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Thomas Liehr

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Walid Al-Achkar; Manar Assaad; Christian Ehlers; Abdulsamad Wafa; Thomas Liehr
A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7.
Thomas Liehr; Kristin Mrasek; Moneeb Ak Othman; Anja Weise; Nadine Aust; Xiaobo Fan; Ahmed B Hamid; Elisabeth Klein; Nadezda Kosyakova
Multicolor FISH methods in current clinical diagnostics.
Christine Leibiger; Michael Glei; Nadezda Kosyakova; Hasmik Mkrtchyan; Vladimir Trifonov; Thomas Liehr
First molecular cytogenetic high resolution characterization of the NIH 3T3 cell line by murine multicolor banding.

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2013: Walid Al-Achkar; Manar Assaad; Christian Ehlers; Abdulsamad Wafa; Thomas Liehr
A unique case of female pseudohermaphroditism with 21-hydroxylase deficiency and small supernumerary marker chromosome 7.
Molecular medicine reports 2013;7(5):1545-8.
2013: Thomas Liehr; Kristin Mrasek; Moneeb Ak Othman; Anja Weise; Nadine Aust; Xiaobo Fan; Ahmed B Hamid; Elisabeth Klein; Nadezda Kosyakova
Multicolor FISH methods in current clinical diagnostics.
Expert review of molecular diagnostics 2013;13(3):251-5.
2013: Christine Leibiger; Michael Glei; Nadezda Kosyakova; Hasmik Mkrtchyan; Vladimir Trifonov; Thomas Liehr
First molecular cytogenetic high resolution characterization of the NIH 3T3 cell line by murine multicolor banding.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2013;61(4):306-12.
2013: Daniela Ribeiro Ney-Garcia; Raul Correa Ribeiro; Társis Paiva Vieira; Samarth Bhatt; Amanda Faria de Figueiredo; Mariana Tavares de Souza; Thomas Liehr; Maria Luiza Macedo Silva
A case of childhood T cell acute lymphoblastic leukemia with a complex t(9;9) and homozygous deletion of CDKN2A gene associated with a Philadelphia-positive minor subclone.
Blood cells, molecules & diseases 2013;50(2):131-3.
2013: John C K Barber; Mark Bateman; Beverley Bewes; Angela F Brady; Nicki Foulds; Victoria Hall; Shuwen Huang; Thomas Liehr; Viv K Maloney; Karl Mehnert; Angharad M Roberts; Marianne Volleth; Helen White
16p11.2-p12.2 duplication syndrome; a genomic condition differentiated from euchromatic variation of 16p11.2.
European journal of human genetics : EJHG 2013;21(2):182-9.
2013: Thomas Liehr; Henry Heng; Yuri Yurov
Reviewer acknowledgement 2013.
Molecular cytogenetics 2013;6(1):9.
2013: Nadezda Kosyakova; Katharina Kreskowski; Anna I Kulpanovich; Thomas Liehr; Marina Manvelyan; Thomas Martin; Martina Merkas; Hasmik Mkrtchyan; Irina V Naumchik; Heike Nelle; Anna D Polityko; Gisela Reising-Ackermann; Laura Rodríguez; Ali Sazci; Isolde Schreyer; Natalia Shorokh; Isabella Simonyan; Markus Stumm; Marianne Volleth; Svetlana Vorsanova; Rolf-Dieter Wegner; Anja Weise; Monika Ziegler; Rouben Aroutiounian; Samarth Bhatt; Lukretija Brecevic; Marcelo de Bello Cioffi; Tatiana Egorova; Alla Frolova; Ani Grigorian; Evgenia Jaroshevich; Emel Ergul
Heteromorphic variants of chromosome 9.
Molecular cytogenetics 2013;6(1):14.
2013: Thomas Liehr; Kristin Mrasek; C Venner; Anja Weise; N Aust; R S Guilherme; E Klein; Nadezda Kosyakova; A B Hamid
Clinical impact of somatic mosaicism in cases with small supernumerary marker chromosomes.
Cytogenetic and genome research 2013;139(3):158-63.
2013: T Schmidt; Iris Bartels; P Burfeind; Thomas Liehr; Barbara Zoll; M Shoukier
A family with an inverted tandem duplication 5q22.1q23.2.
Cytogenetic and genome research 2013;139(1):65-70.
2013: Jian Ou; Fuxin Wang; Wei Wang; Thomas Liehr; Chengying Duan; Ahmed B Hamid; Elisabeth Klein; Hong Li
Characterization of three small supernumerary marker chromosomes (sSMC) in humans.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2013;26(1):106-8.
2012: Roberta Santos Guilherme; Ahmed B Hamid; Elisabeth Klein; Nadezda Kosyakova; Anna Kulpanovich; Maria Isabel Melaragno; Anna Polityko; Claudia Venner; Marianne Volleth; Samarth Bhatt; Thomas Liehr
Human ring chromosomes and small supernumerary marker chromosomes-do they have telomeres?
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2012;20(7):825-35.
2012: Nestor L Lopez Corrales; Thomas Liehr; Kristin Mrasek; Martin Voigt; Nadezda Kosyakova
Copy number variations (CNVs) in human pluripotent cell-derived neuroprogenitors.
Gene 2012;506(2):377-9.
2012: Walid Al-Achkar; Elisabeth Klein; Thomas Liehr; Abdulsamad Wafa; Faten Moassass
Detailed analysis of an idic(Y)(q11.21) in a mosaic karyotype.
Molecular medicine reports 2012;6(2):293-6.
2012: Ahmed B Hamid; David Hardekopf; Tatyana Karamysheva; Roberta Santos Guilherme; Nadezda Kosayakova; Katharina Kreskowski; Thomas Liehr; Kristin Mrasek; Sona Pekova; Martin Voigt; Rebecca Wagner; Anja Weise; Elisabeth Klein
How to narrow down chromosomal breakpoints in small and large derivative chromosomes--a new probe set.
Journal of applied genetics 2012;53(3):259-69.
2012: Maria Bucksch; Wolfgang Fischer; Britta Belitz; Nadezda Kosayakova; Anna I Kulpanovich; Thomas Liehr; Juan C Llerena; Susanne Morlot; Milene V Mulhatino; Michael B Petersen; Anna Polityko; Vladimir Trifonov; Anja Weise; Monika Ziegler; Milene V Mulatinho; Ahmed B Hamid
A new multicolor fluorescence in situ hybridization probe set directed against human heterochromatin: HCM-FISH.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2012;60(7):530-6.
2012: Anja Weise; samarth Bhatt; David Hardekopf; Elisabeth Klein; Nadezda Kosyakova; Juan C Llerena; Kristin Mrasek; Milene Mulatinho; Sona Pekova; Thomas Liehr
Microdeletion and microduplication syndromes.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2012;60(5):346-58.
2012: Emmanouil Manolakos; Vassilis Mersinias; Makarios Eleftheriades; George Kitsos; Thomas Liehr; Ioannis Papoulidis; Panagiotis Peitsidis; Michael B Petersen; Stavros Sifakis; Sotirios Sotiriou; Loretta Thomaidis; Sandro Orru
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature.
Clinical dysmorphology 2012;21(2):101-5.
2012: Amanda Faria de Figueiredo; Mariana Tavares de Souza; Thomas Liehr; Terezinha de Jesus Marques-Salles; Raul C Ribeiro; Maria Luiza Macedo Silva; Tarsis Paiva Vieira; samarth Bhatt; Renata Binato; Edna Carboni; Eliana Abdelhay
A rare cryptic and complex rearrangement leading to MLL-MLLT10 gene fusion masked by del(10)(p12) in a child with acute monoblastic leukemia (AML-M5).
Leukemia research 2012;36(4):e74-7.
2012: Galina Hovhannisyan; Rouben Aroutiounian; Thomas Liehr
Chromosomal composition of micronuclei in human leukocytes exposed to mitomycin C.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2012;60(4):316-22.
2012: Annalisa Vetro; Giulia Arrigo; Stefania Cesari; Gianfranco Croci; Barbara Dal Bello; Fabrizia Franchi; Angela Iasci; Thomas Liehr; Emmanouil Manolakos; Maria Marinelli; Emanuela Meneghelli; Michael B Petersen; Loretta Thomaidis; Orsetta Zuffardi
Unexpected results in the constitution of small supernumerary marker chromosomes.
European journal of medical genetics 2012;55(3):185-90.
2012: Daniela R Ney-Garcia; Raul C Ribeiro; Roberto R Capela de Matos; Eliana Abdelhay; samarth Bhatt; Renata Binato; Mariana T de Souza; Fernanda C Jordy; Thomas Liehr; Maria Luiza M Silva
Molecular cytogenetics studies reveal unexpected chromosomal inversion as variant of t(12;21)(p13;q22) in child with B-cell precursor acute lymphoblastic leukemia.
Leukemia & lymphoma 2012;53(2):342-4.
2012: Christel Eckmann-Scholz; Stefan Gesk; Walter Jonat; Holger Tönnies; Thomas Liehr; Almuth Caliebe
Normal prenatal ultrasound findings in a case with de novo mosaic small supernumerary marker chromosome 18--how to counsel?
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2012;25(2):200-2.
2012: FRENNY SHETH; Olawaleye Adeteye; Olakanmi Akinde; Manisha Desai; Naresh Gohel; Thomas Liehr; Jayesh Sheth
Gain of chromosome 4qter and loss of 5pter: an unusual case with features of cri du chat syndrome.
Case reports in genetics 2012;2012():153405.
2012: Ke Ma; Kristin Mrasek; Li Qiu; Luciana Gonçalves Quintana; Jun Zhang; Thomas Liehr; Zheng Li
Common fragile sites: genomic hotspots of DNA damage and carcinogenesis.
International journal of molecular sciences 2012;13(9):11974-99.
2012: Marina Araújo Fonzar Hernandes; Edinalva Pereira Leite; Thomas Liehr; Terezinha de Jesus Marques-Salles; Hasmik Mkrtchyan; Maria Tereza Cartaxo Muniz; Neide Santos; Maria Teresa Marquim Nogueira Cornélio; Eliane Maria Soares-Ventura; Maria Luiza Macedo Silva
Extra Copies of der(21)t(12;21) plus Deletion of ETV6 Gene due to dic(12;18) in B-Cell Precursor ALL with Poor Outcome.
Case reports in genetics 2012;2012():186532.
2012: Milene Vianna Mulatinho; Sona Pekova; Nagesh Rao; Fernanda Scalco; Anja Weise; Cassio Luiz de Carvalho Serao; David Hardekopf; Thomas Liehr; Kristin Mrasek; Juan Clinton Llerena
Severe intellectual disability, omphalocele, hypospadia and high blood pressure associated to a deletion at 2q22.1q22.3: case report.
Molecular cytogenetics 2012;5(1):30.
2012: I Papoulidis; M B Petersen; I Saitis; E Siomou; L Thomaidis; M Tzimina; P Nicolaides; S Orru; A B Hamid; E Klein; M Kontodiou; U Kordass; Nadezda Kosyakova; J Kunz; Thomas Liehr; E Manolakos
Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.
Cytogenetic and genome research 2012;136(4):237-41.
2012: Elisabeth Klein; Thomas Liehr; Marina Manvelyan; Isabella Simonyan; Roberta Santos Guilherme; Ahmed B Hamid; Tatyana Karamysheva
Centromeric association of small supernumerary marker chromosomes with their sister-chromosomes detected by three dimensional molecular cytogenetics.
Molecular cytogenetics 2012;5():15.
2012: E Klein; Nadezda Kosyakova; C Kraus; W Fischer; M Meins; S Morlot; C Mackie Ogilvie; A Ovens-Raeder; Anna Polityko; M Rocchi; Marianne Volleth; Anja Weise; M Ziegler; Thomas Liehr
Five novel locations of Neocentromeres in human: 18q22.1, Xq27.1∼27.2, Acro p13, Acro p12, and heterochromatin of unknown origin.
Cytogenetic and genome research 2012;136(3):163-6.
2012: D R Ney-Garcia; G Pimenta; Wolmar Pulcheri; R C Ribeiro; Eliana Abdelhay; samarth Bhatt; M T de Souza; Thomas Liehr; R R Capela de Matos; Maria Luiza Macedo Silva
Childhood B-cell progenitor acute lymphoblastic leukemia presenting a three-way t(11;12;21)(q14;p13;q22) with a RUNX1 gene signal on chromosome 11.
International journal of hematology 2012;95(1):112-4.
2011: Cornelius Woelfel; Waleed Amin Kotb; Anja Weise; Detlef Katenkamp; Jan Langrehr; Thomas Liehr; Manuela Pacyna-Gengelbach; Iver Petersen
Molecular cytogenetic characterization of epithelioid hemangioendothelioma.
Cancer genetics 2011;204(12):671-6.
2011: Claudia Backsch; Andreas Clad; Mieczyslaw Gajda; Thomas Liehr; Melanie Liesenfeld; Kristin Mrasek; Birgit Pauly; Ingo B Runnebaum; Cornelia Scheungraber; Evelin Schrock; Matthias Dürst
Two novel unbalanced whole arm translocations are frequently detected in cervical squamous cell carcinoma.
Cancer genetics 2011;204(12):646-53.
2011: Gisela Dobbernack; Simone Florian; Madeleine Gross; Heinz Himmelbauer; Thomas Liehr; Walter Meinl; Nicole Schade; Ingo Voigt; Korinna Wend; Hansruedi Glatt
Altered tissue distribution of 2-amino-1-methyl-6-phenylimidazo[4,5-b]pyridine-DNA adducts in mice transgenic for human sulfotransferases 1A1 and 1A2.
Carcinogenesis 2011;32(11):1734-40.
2011: Olaya Villa; Arenillas Leonor; Beatriz Bellosillo; Ivon Cuscó; Blanca Espinet; Lourdes Florensa; Manel García-Aragonés; Luis A Pérez Jurado; Nadezda Kosyakova; Thomas Liehr; Mar Mallo; Luz Martínez-Avilés; Carmen Pedro; Marta Salido; Francesc Solé
Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array.
Leukemia research 2011;35(9):e161-3.
2011: Thomas Liehr; Elisabeth Ewers; Ahmed B Hamid; Nadezda Kosyakova; Martin Voigt; Anja Weise; Marina Manvelyan
Small supernumerary marker chromosomes and uniparental disomy have a story to tell.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2011;59(9):842-8.
2011: Friederike Braulke; Ilse Chudoba; Thomas Liehr; Marina Manvelyan; Julie Schanz; Rainer Steffens; Detlef Haase
Two different del(5q) clones in a patient with myelodysplastic syndrome.
Leukemia & lymphoma 2011;52(9):1811-4.
2011: Marcelo de Bello Cioffi; Nadezda Kosyakova; Thomas Liehr; Juan Alberto Marchal; Antonio Sánchez; Vladimir Trifonov; L A C Bertollo
Whole chromosome painting reveals independent origin of sex chromosomes in closely related forms of a fish species.
Genetica 2011;139(8):1065-72.
2011: Amanda Faria De Figueiredo; Roberto Rodrigues Capela De Matos; Mariana Tavares De Souza; Terezinha De Jesus Marques Salles; Eliana Abdelhay; samarth Bhatt; Renata Binato; Fernanda C Jordy; Thomas Liehr; Raul C Ribeiro; Maria Luiza Macedo Silva
A complex karyotype masked a cryptic variant t(8;21)(q22;q22) in a child with acute myeloid leukemia.
Leukemia & lymphoma 2011;52(8):1593-6.
2011: Lilia Kraoua; Thomas Liehr; Faouzi Maazoul; Ines Ouertani; Lamia Ben Jemaa; Mohamed Chaabouni; Imen Chelly; Elisabeth Ewers; Habiba Chaabouni
Hexasomy of the Prader-Willi/Angelman critical region, including the OCA2 gene, in a patient with pigmentary dysplasia: case report.
European journal of medical genetics 2011;54(4):e446-50.
2011: Franck Pellestor; Jacques Puechberty; Tal Anahory; B Hédon; Geneviève Lefort; Thomas Liehr; Pierre Sarda
Complex chromosomal rearrangements: origin and meiotic behavior.
Human reproduction update 2011;17(4):476-94.
2011: Emmanouil Manolakos; Annalisa Vetro; Konstantinos Kefalas; Loretta Thomaidis; Georgios Aperis; Sotirios Sotiriou; George Kitsos; Martina Merkas; Stavros Sifakis; Ioannis Papoulidis; Thomas Liehr; Orsetta Zuffardi; Michael B Petersen
Deletion 2q31.2-q31.3 in a 4-year-old girl with microcephaly and severe mental retardation.
American journal of medical genetics. Part A 2011;155A(6):1476-82.
2011: Franck Pellestor; Jacques Puechberty; Anja Weise; Geneviève Lefort; Tal Anahory; Thomas Liehr; Pierre Sarda
Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier.
Fertility and sterility 2011;95(7):2433.e17-22.
2011: Joana Barbosa Melo; Liesbeth Backx; Joris R Vermeesch; Heloisa G Santos; Ana C Sousa; Nadezda Kosyakova; Anja Weise; Ferdinand von Eggeling; Thomas Liehr; Isabel Marques Carreira
Chromosome 5 derived small supernumerary marker: towards a genotype/phenotype correlation of proximal chromosome 5 imbalances.
Journal of applied genetics 2011;52(2):193-200.
2011: Eliane Maria Soares-Ventura; Hasmik Mkrtchyan; Terezinha de Jesus Marques-Salles; Mariluze Silva; Neide Santos; Bethania de Araujo Silva Amaral; Thomas Liehr; Eliana Abdelhay; Maria Luiza Macedo Silva; Maria Tereza Cartaxo Muniz
Molecular cytogenetics reveals complex karyotype in apparent t(8;13) therapy-related acute myeloid leukemia M2 after fibrosarcoma.
Leukemia research 2011;35(5):e27-9.
2011: FRENNY SHETH; Joris Andrieux; Elisabeth Ewers; Nadezda Kosyakova; Anja Weise; Harsh Sheth; Serge-Pierrick Romana; Marc Lelorc'h; Bruno Delobel; Olivier Theisen; Thomas Liehr; Sheela Nampoothiri; Jayesh Sheth
Characterization of sSMC by FISH and molecular techniques.
European journal of medical genetics 2011;54(3):247-55.
2011: Mariana Tavares de Souza; Hasmik Mkrtchyan; Rocio Hassan; Daniela Ribeiro Ney-Garcia; Alice Maria Boulhosa de Azevedo; Elaine Sobral da Costa; Amanda Faria de Figueiredo; Thomas Liehr; Eliana Abdelhay; Maria Luiza Macedo Silva
Secondary abnormalities involving 1q or 13q and poor outcome in high stage Burkitt leukemia/lymphoma cases with 8q24 rearrangement at diagnosis.
International journal of hematology 2011;93(2):232-6.
2011: Marcelo B Cioffi; Nadezda Kosyakova; Thomas Liehr; Juan A Marchal; Antonio Sánchez; Vladimir Trifonov; L A C Bertollo
Cross-species chromosome painting tracks the independent origin of multiple sex chromosomes in two cofamiliar Erythrinidae fishes.
BMC evolutionary biology 2011;11():186.
2011: Marina Manvelyan; Friedrich W Cremer; Jeannette Lancé; Rüdiger Kläs; Christina Kelbova; Christian Ramel; Herbert Reichenbach; Catharina Schmidt; Elisabeth Ewers; Katharina Kreskowski; Monika Ziegler; Nadezda Kosyakova; Thomas Liehr
New cytogenetically visible copy number variant in region 8q21.2.
Molecular cytogenetics 2011;4(1):1.
2011: Bernhard Horsthemke; Michaela Wawrzik; Stephanie Gross; Christina Lich; Birgitta Sauer; Imma Rost; Ernst Krasemann; Nadezda Kosyakova; Thomas Liehr; Anja Weise; J Nikolaj Dybowski; Daniel Hoffmann; Dagmar Wieczorek
Parental origin and functional relevance of a de novo UBE3A variant.
European journal of medical genetics 2011;54(1):19-24.
2011: Thomas Liehr; I Bartels; B Zoll; E Ewers; Kristin Mrasek; Nadezda Kosyakova; M Merkas; A B Hamid; Ferdinand von Eggeling; N Posorski; Anja Weise
Is there a yet unreported unbalanced chromosomal abnormality without phenotypic consequences in proximal 4p?
Cytogenetic and genome research 2011;132(1-2):121-3.
2010: Walid Al-Achkar; Abdulsamad Wafa; Marina Manvelyan; Adnan Ikhtiar; Thomas Liehr
De novo translocation involving two chromosomes in adult prolymphocytic leukemia--a rare case.
Leukemia research 2010;34(12):e345-7.
2010: E Manolakos; K Kefalas; R Neroutsou; M Lagou; Nadezda Kosyakova; E Ewers; M Ziegler; A Weise; P Tsoplou; S M Rapti; I Papoulidis; E Anastasakis; A Garas; S Sotiriou; M Eleftheriades; P Peitsidis; D Malathrakis; L Thomaidis; G Kitsos; S Orru; Thomas Liehr; M B Petersen; S Kitsiou-Tzeli
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization.
Molecular medicine reports 2010;3(6):1015-22.
2010: Odul Egritas; Busranur Cavdarli; Buket Dalgic; mehmet ergun; Ferda Percin; Monika Ziegler; Beate Pohle; Thomas Liehr
Duplication 4q associated with chronic cholestatic changes in liver biopsy.
European journal of medical genetics 2010;53(6):411-4.
2010: Amanda Faria de Figueiredo; Thomas Liehr; Samarth Bath; Renata Binato; Eliane Maria Soares Ventura; Mariana Tavares de Souza; Roberto Rodrigues Capela de Matos; Raul Correa Ribeiro; Eliana Abdelhay; Maria Luiza Macedo Silva
A new cryptic ins(11;1)(q23;q21q31) detected in a t(1;8;11)(q21;p21;q23) in a baby with acute myeloid leukemia FAB AML-M5.
Blood cells, molecules & diseases 2010;45(3):197-8.
2010: M Santos; Kristin Mrasek; I Madrigal; M R Martorell; A González-Meneses; G Rodríguez-Criado; M Milà; Thomas Liehr; C Fuster
Characterization of a complex cryptic mosaicism for an sSMC derived from the X chromosome present in a boy with congenital malformations.
American journal of medical genetics. Part A 2010;152A(10):2661-3.
2010: Thomas Liehr; Tatyana Karamysheva; Martina Merkas; Lukrecija Brecevic; Ahmed B Hamid; Elisabeth Ewers; Kristin Mrasek; Nadezda Kosyakova; Anja Weise
Somatic mosaicism in cases with small supernumerary marker chromosomes.
Current genomics 2010;11(6):432-9.
2010: Hasmik Mkrtchyan; Madeleine Gross; Sophie Hinreiner; Anna Polytiko; Marina Manvelyan; Kristin Mrasek; Nadezda Kosyakova; Elisabeth Ewers; Heike Nelle; Thomas Liehr; samarth Bhatt; Karen Thoma; Erich Gebhart; Sylvia Wilhelm; Raimund Fahsold; Marianne Volleth; Anja Weise
The human genome puzzle - the role of copy number variation in somatic mosaicism.
Current genomics 2010;11(6):426-31.
2010: Terezinha de Jesus Marques-Salles; Jemima Eline Xavier da Silva Barros; Eliane Maria Soares-Ventura; Maria Tereza Cartaxo Muniz; Neide Santos; Elizangela Ferreira da Silva; Maria Luiza Macedo Silva; Thomas Liehr; Hasmik Mkrtchyan
Unusual childhood biphenotypic acute leukemia with a yet unreported t(3;13)(p25.1;q13).
Leukemia research 2010;34(8):e206-7.
2010: Terezinha de Jesus Marques-Salles; Hasmik Mkrtchyan; Edinalva Pereira Leite; Eliane Maria Soares-Ventura; Maria Tereza Cartaxo Muniz; Elizangela Ferreira Silva; Thomas Liehr; Maria Luiza Macedo Silva; Neide Santos
Complex karyotype defined by molecular cytogenetic FISH and M-FISH in an infant with acute megakaryoblastic leukemia and neurofibromatosis.
Cancer genetics and cytogenetics 2010;200(2):167-9.
2010: Heike Nelle; Isolde Schreyer; Elisabeth Ewers; Kristin Mrasek; Nadezda Kosyakova; Martina Merkas; Ahmed Basheer Hamid; Raimund Fahsold; Anikó Ujfalusi; Jasen Anderson; Nikolai Rubtsov; Alma Küchler; Ferdinand von Eggeling; Julia Hentschel; Anja Weise; Thomas Liehr
Presence of harmless small supernumerary marker chromosomes hampers molecular genetic diagnosis: a case report.
Molecular medicine reports 2010;3(4):571-4.
2010: Elisabeth Ewers; Kinya Yoda; Ahmed B Hamid; Anja Weise; Marina Manvelyan; Thomas Liehr
Centromere activity in dicentric small supernumerary marker chromosomes.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2010;18(5):555-62.
2010: Ioannis Papoulidis; Emmanouil Manolakos; Elisavet Siomou; Kostantinos Kefalas; Loretta Thomaidis; Thomas Liehr; Annalisa Vetro; Apostolos Athanasiadis; Orsetta Zuffardi; Michael B Petersen
A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth.
Prenatal diagnosis 2010;30(6):586-8.
2010: Bernd Auber; Peter Burfeind; C Thiels; E A Alsat; M Shoukier; Thomas Liehr; H Nelle; Iris Bartels; G Salinas-Riester; Franco Laccone
An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patient.
Clinical genetics 2010;77(6):593-7.
2010: Thomas Liehr; Nadezda Kosyakova; Anja Weise; M Ziegler; G Raabe-Meyer
First case of a neocentromere formation in an otherwise normal chromosome 7.
Cytogenetic and genome research 2010;128(4):189-91.
2010: Eleni Ktistaki; Anna Garefalaki; Adam Williams; Simon R Andrews; Donald M Bell; Katie E Foster; Charalampos G Spilianakis; Richard A Flavell; Nadezda Kosyakova; Vladmir Trifonov; Thomas Liehr; Dimitris Kioussis
CD8 locus nuclear dynamics during thymocyte development.
Journal of immunology (Baltimore, Md. : 1950) 2010;184(10):5686-95.
2010: Elif Uz; Yasemin Alanay; Dilek Aktas; Ibrahim Vargel; Safak Gucer; Gokhan Tuncbilek; Ferdinand von Eggeling; Engin Yilmaz; Ozgur Deren; Nicole Posorski; Hilal Ozdag; Thomas Liehr; Sevim Balci; Mehmet Alikasifoglu; Bernd Wollnik; Nurten A Akarsu
Disruption of ALX1 causes extreme microphthalmia and severe facial clefting: expanding the spectrum of autosomal-recessive ALX-related frontonasal dysplasia.
American journal of human genetics 2010;86(5):789-96.
2010: Zhuoya Li; Q Zhang; J-H Mao; A Weise; K Mrasek; X Fan; Xueping Zhang; Thomas Liehr; K H Lu; A Balmain; W-W Cai
An HDAC1-binding domain within FATS bridges p21 turnover to radiation-induced tumorigenesis.
Oncogene 2010;29(18):2659-71.
2010: Emmanouil Manolakos; Panagiotis Peitsidis; Makarios Eleftheriades; Evaggelos Dedoulis; Monika Ziegler; Sandro Orru; Thomas Liehr; Michael B Petersen
Prenatal detection of full monosomy 21 in a fetus with increased nuchal translucency: molecular cytogenetic analysis and review of the literature.
The journal of obstetrics and gynaecology research 2010;36(2):435-40.
2010: Thomas Liehr; Rolf-Dieter Wegner; Markus Stumm; Thomas Martin; Gabriele Gillessen-Kaesbach; Nadezda Kosyakova; Elisabeth Ewers; Ahmed Basheer Hamid; Ferdinand von Eggeling; Julia Hentschel; Monika Ziegler; Anja Weise
Small supernumerary marker chromosomes 1 with a normal phenotype.
Journal of the Chinese Medical Association : JCMA 2010;73(4):205-7.
2010: Kristin Mrasek; Christiane Schoder; Anne-Christin Teichmann; Katja Behr; Britta Franze; Kathleen Wilhelm; Nancy Blaurock; Uwe Claussen; Thomas Liehr; Anja Weise
Global screening and extended nomenclature for 230 aphidicolin-inducible fragile sites, including 61 yet unreported ones.
International journal of oncology 2010;36(4):929-40.
2010: Anja Weise; Bernd Timmermann; Manfred Grabherr; Martin Werber; Patricia Heyn; Nadezda Kosyakova; Thomas Liehr; Heidemarie Neitzel; Kateryna Konrat; Christiane Bommer; Carola Dietrich; Anna Rajab; Richard Reinhardt; Stefan Mundlos; Tom H Lindner; Katrin Hoffmann
High-throughput sequencing of microdissected chromosomal regions.
European journal of human genetics : EJHG 2010;18(4):457-62.
2010: Vladimir A Trifonov; Nadezda Kosyakova; Svetlana A. Romanenko; Roscoe Stanyon; Alexander Graphodatsky ; Thomas Liehr
New insights into the karyotypic evolution in muroid rodents revealed by multicolor banding applying murine probes.
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2010;18(2):265-75.
2010: Hasmik Mkrtchyan; Daniela Ribeiro Garcia Ney; Eliane Soares de Ventura; Thomas Liehr; Gabriel Rafael Felix; Terezinha de Jesus Marques-Salles; Eliana Abdelhay; Maria Luiza Macedo Silva
Molecular cytogenetic studies characterize a near-triploid complex karyotype in a child with acute lymphoblastic leukemia.
Cancer genetics and cytogenetics 2010;197(1):71-4.
2010: Christiane Schoder; Thomas Liehr; Eunike Velleuer; Kathleen Wilhelm; Nancy Blaurock; Anja Weise; Kristin Mrasek
New aspects on chromosomal instability: chromosomal break-points in Fanconi anemia patients co-localize on the molecular level with fragile sites.
International journal of oncology 2010;36(2):307-12.
2010: Fabio E da Silva; Ana B Cordeiro; Cleusa Y Nagamachi; Julio C Pieczarka; Willen Rens; Anja Weise; Thomas Liehr; Hasmik Mkrtchyan; Nilson P Anselmo; Edivaldo H C de Oliveira
A case of aggressive medulloblastoma with multiple recurrent chromosomal alterations.
Cancer genetics and cytogenetics 2010;196(2):198-200.
2010: K Karaer; mehmet ergun; A Weise; E Ewers; Thomas Liehr; N Kosyakova; H Mkrtchyan
The case of an infertile male with an uncommon reciprocal X-autosomal translocation: how does this affect male fertility?
Genetic counseling (Geneva, Switzerland) 2010;21(4):397-404.
2010: Emmanouil Manolakos; Annalisa Vetro; Konstantinos Kefalas; Stamatia-Maria Rapti; eirini louizou; Antonios Garas; George Kitsos; Lefteris Vasileiadis; Panagiota Tsoplou; Makarios Eleftheriades; Panagiotis Peitsidis; Sandro Orru; Thomas Liehr; Michael B Petersen; Loretta Thomaidis
The use of array-CGH in a cohort of Greek children with developmental delay.
Molecular cytogenetics 2010;3():22.
2010: K Gersak; K Writzl; A Veble; Thomas Liehr
Primary amenorrhoea in a patient with mosaicism for monosomy X and a derivative X-chromosome.
Genetic counseling (Geneva, Switzerland) 2010;21(3):335-42.
2010: S Balci; B Yuksel Konuk; F Atik; A K Oguz; mehmet ergun; Volkan Baltaci; N Kosyakova; Thomas Liehr
Partial deletion of the long arm of chromosome 13 (q32q33.2) associated with mental retardation, choanal atresia and fish mouth.
Genetic counseling (Geneva, Switzerland) 2010;21(3):317-24.
2010: Walid Al Achkar; Abdulsamad Wafa; Faten Moassass; Thomas Liehr
Partial trisomy 9p22 to 9p24.2 in combination with partial monosomy 9pter in a Syrian girl.
Molecular cytogenetics 2010;3():18.
2010: Anja Weise; Madeleine Gross; Sophie Hinreiner; Vera Witthuhn; Hasmik Mkrtchyan; Thomas Liehr
POD-FISH: a new technique for parental origin determination based on copy number variation polymorphism.
Methods in molecular biology (Clifton, N.J.) 2010;659():291-8.
2010: Thomas Liehr; Anja Weise; Sophie Hinreiner; Hasmik Mkrtchyan; Kristin Mrasek; Nadezda Kosyakova
Characterization of chromosomal rearrangements using multicolor-banding (MCB/m-band).
Methods in molecular biology (Clifton, N.J.) 2010;659():231-8.
2010: Joaquín Fernández-Toral; Laura Rodríguez; Ana Plasencia; María Luisa Martínez-Frías; Elisabeth Ewers; Ahmed B Hamid; Monika Ziegler; Thomas Liehr
Four small supernumerary marker chromosomes derived from chromosomes 6, 8, 11 and 12 in a patient with minimal clinical abnormalities: a case report.
Journal of medical case reports 2010;4():239.
2010: Susana I Ferreira; Eunice Matoso; Marta Pinto; Joana Almeida; Thomas Liehr; Joana Melo; Isabel M Carreira
X-chromosome terminal deletion in a female with premature ovarian failure: Haploinsufficiency of X-linked genes as a possible explanation.
Molecular cytogenetics 2010;3():14.
2010: Dilek Aktas; Eda G Utine; Kristin Mrasek; Anja Weise; Ferdinand von Eggeling; Kalbiye Yalaz; Nicole Posorski; Nurten Akarsu; Mehmet Alikasifoglu; Thomas Liehr; Ergul Tuncbilek
Derivative chromosome 1 and GLUT1 deficiency syndrome in a sibling pair.
Molecular cytogenetics 2010;3(1):10.
2010: P Burégio-Frota; L Valença; G F Leal; AR Duarte; A V S Bispo-Brito; E M Soares-Ventura; T J Marques-Salles; M T M C Nogueira; M T C Muniz; M L M Silva; F Hunstig; Thomas Liehr; N Santos
Identification of a de novo inv dup(X)(pter--> q22) by multicolor banding in a girl with Turner syndrome.
Genetics and molecular research : GMR 2010;9(2):780-4.
2010: Thomas Liehr
Cytogenetic contribution to uniparental disomy (UPD).
Molecular cytogenetics 2010;3():8.
2010: Walid Al Achkar; Abdulsamad Wafa; Hasmik Mkrtchyan; Faten Moassass; Thomas Liehr
A rare case of chronic myeloid leukemia with secondary chromosomal changes including partial trisomy 17q21 to 17qter and partial monosomy of 16p13.3.
Molecular cytogenetics 2010;3():6.
2010: Hasmik Mkrtchyan; Madeleine Gross; Sophie Hinreiner; Anna Polytiko; Marina Manvelyan; Kristin Mrasek; Nadezda Kosyakova; Elisabeth Ewers; Heike Nelle; Thomas Liehr; Marianne Volleth; Anja Weise
Early embryonic chromosome instability results in stable mosaic pattern in human tissues.
PloS one 2010;5(3):e9591.
2010: Anna Polityko; Olga Khurs; Natalia Rumyantseva; Irina Naumchik; Nadezda Kosyakova; Holger Tönnies; Karl Sperling; Heidemarie Neitzel; Anja Weise; Thomas Liehr
Two siblings with immunodeficiency, facial abnormalities and chromosomal instability without mutation in DNMT3B gene but liability towards malignancy; a new chromatin disorder delineation?
Molecular cytogenetics 2010;3():5.
2010: John Ck Barber; Dave Bunyan; Merryl Curtis; Denise Robinson; Susanne Morlot; Anette Dermitzel; Thomas Liehr; Claudia Alves; Joana Trindade; Ana I Paramos; Clare Cooper; Kevin Ocraft; Emma-Jane Taylor; Viv K Maloney
8p23.1 duplication syndrome differentiated from copy number variation of the defensin cluster at prenatal diagnosis in four new families.
Molecular cytogenetics 2010;3():3.
2009: Yasemin Soysal; Sevim Balci; Kuyaş Hekimler; Thomas Liehr; Elisabeth Ewers; Jacqueline Schoumans; The-Hung Bui; Fadime Mutlu Içduygu; Nadezda Kosyakova; Necat Imirzalioğlu
Characterization of double ring chromosome 4 mosaicism associated with bilateral hip dislocation, cortical dysgenesis, and epilepsy.
American journal of medical genetics. Part A 2009;149A(12):2782-7.
2009: Thomas Liehr
Small supernumerary marker chromosomes (sSMCs): a spotlight on some nomenclature problems.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2009;57(11):991-3.
2009: Amanda Faria de Figueiredo; Hasmik Mkrtchyan; Thomas Liehr; Eliane Maria Soares Ventura; Terezinha de Jesus Marques-Salles; Neide Santos; Raul Corrêa Ribeiro; Eliana Abdelhay; Maria Luiza Macedo Silva
A case of childhood acute myeloid leukemia AML (M5) with a neocentric chromosome neo(1)(qter-->q23 approximately 24::q23 approximately 24-->q43-->neo-->q43-->qter) and tetrasomy of chromosomes 8 and 21.
Cancer genetics and cytogenetics 2009;193(2):123-6.
2009: Marina Manvelyan; Philipp Kempf; Anja Weise; Kristin Mrasek; Anita Heller; Amelie Lier; Klaus Höffken; Hans-Jörg Fricke; Herbert G Sayer; Thomas Liehr; Hasmik Mkrtchyan
Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics.
International journal of molecular medicine 2009;24(3):335-41.
2009: Emmanouil Manolakos; Annalisa Vetro; Stylianos Kitmirides; Ioannis Papoulidis; Nadezda Kosyakova; Kristin Mrasek; Anja Weise; Emmanouil Agapitos; Sandro Orru; Panagiotis Peitsidis; Thomas Liehr; Michael B Petersen
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH.
Prenatal diagnosis 2009;29(9):884-8.
2009: L Uroz; Thomas Liehr; Kristin Mrasek; Cristina Templado
Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases.
Human reproduction (Oxford, England) 2009;24(8):2029-33.
2009: Ivan Y Iourov; Svetlana G Vorsanova; Thomas Liehr; Alexei D Kolotii; Yuri B Yurov
Increased chromosome instability dramatically disrupts neural genome integrity and mediates cerebellar degeneration in the ataxia-telangiectasia brain.
Human molecular genetics 2009;18(14):2656-69.
2009: Anja Weise; Elisabeth Ewers; Nadezda Kosyakova; Hasmik Mkrtchyan; Kristin Mrasek; Thomas Liehr
Diagnostic applications of fluorescence in situ hybridization.
Expert opinion on medical diagnostics 2009;3(4):453-60.
2009: Anna Polityko; Olga M Khurs; Anna I Kulpanovich; Konstantin A Mosse; Angelica V Solntsava; Natalia Rumyantseva; Irina V Naumchik; Thomas Liehr; Anja Weise; Hasmik Mkrtchyan
Paternally derived der(7)t(Y;7)(p11.1 approximately 11.2;p22.3)dn in a mosaic case with Turner syndrome.
European journal of medical genetics 2009;52(4):207-10.
2009: Emel Ergul; Thomas Liehr; Kristin Mrasek; Ali Sazci
A de novo complex chromosome rearrangement involving three chromosomes (2, 13, and 18) in an oligospermic male.
Fertility and sterility 2009;92(1):391.e9-391.e12.
2009: Andreas Tzschach; C Ramel; A Kron; B Seipel; C Wüster; U Cordes; Thomas Liehr; Maria Hoeltzenbein; Corinna Menzel; Hans-Hilger Ropers; Reinhard Ullmann; Vera Kalscheuer; J Decker; D Steinberger
Hypergonadotropic hypogonadism in a patient with inv ins (2;4).
International journal of andrology 2009;32(3):226-30.
2009: Ana Patrícia Barros Cordeiro; Fábio P E da Silva; Julio Cesar Pieczarka; Cleusa Yoshiko Nagamachi; Nilson Praia Anselmo; José Reginaldo Brito; Douglas S Vasconcelos; Thomas Liehr; Anja Weise; Edivaldo H C de Oliveira
Comparative analysis of proliferative and genetic alterations in a primary chordoid meningioma and its recurrence using locus-specific probes and AgNOR.
Molecular medicine reports 2009;2(3):449-54.
2009: Thomas Liehr; Elisabeth Ewers; Nadezda Kosyakova; Vivian Klaschka; Franziska Rietz; Rebecca Wagner; Anja Weise
Handling small supernumerary marker chromosomes in prenatal diagnostics.
Expert review of molecular diagnostics 2009;9(4):317-24.
2009: Ivan Y Iourov; Svetlana G Vorsanova; Thomas Liehr; Yuri B Yurov
Aneuploidy in the normal, Alzheimer's disease and ataxia-telangiectasia brain: differential expression and pathological meaning.
Neurobiology of disease 2009;34(2):212-20.
2009: Hendryk Aurich; M Sgodda; Petra Kaltwasser; M Vetter; A Weise; Thomas Liehr; Marc Brulport; Jan G Hengstler; Matthias M Dollinger; Wolfgang E Fleig; Bruno Christ
Hepatocyte differentiation of mesenchymal stem cells from human adipose tissue in vitro promotes hepatic integration in vivo.
Gut 2009;58(4):570-81.
2009: Terezinha de Jesus Marques-Salles; Thomas Liehr; Hasmik Mkrtchyan; Susana C Raimondi; Mariana Tavares de Souza; Amanda Faria de Figueiredo; Soraia Rouxinol; Fernanda C Jordy Macedo; Eliana Abdelhay; Neide Santos; Maria Luiza Macedo Silva
A new chromosomal three-way rearrangement involving MLL masked by a t(9;19)(p11;p13) in an infant with acute myeloid leukemia.
Cancer genetics and cytogenetics 2009;189(1):59-62.
2009: Madeleine Gross; Hasmik Mkrtchyan; Melanie Glaser; Hans Jörg Fricke; Klaus Höffken; Anita Heller; Anja Weise; Thomas Liehr
Delineation of yet unknown cryptic subtelomere aberrations in 50% of acute myeloid leukemia with normal GTG-banding karyotype.
International journal of oncology 2009;34(2):417-23.
2009: FRENNY SHETH; Elisabeth Ewers; Nadezda Kosyakova; Anja Weise; Jayesh Sheth; Manisha Desai; Joris Andrieux; Joris R Vermeesch; Ahmed B Hamid; Monika Ziegler; Thomas Liehr
A small supernumerary marker chromosome present in a Turner syndrome patient not derived from X- or Y-chromosome: a case report.
Molecular cytogenetics 2009;2():22.
2009: Walid Al Achkar; Abdulsamad Wafa; Hasmik Mkrtchyan; Faten Moassass; Thomas Liehr
Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report.
Molecular cytogenetics 2009;2():21.
2009: Hasmik Mkrtchyan; S Scheler; I Klein; A Fahr; P O Couraud; Ignacio Romero; B Weksler; Thomas Liehr
Molecular cytogenetic characterization of the human cerebral microvessel endothelial cell line hCMEC/D3.
Cytogenetic and genome research 2009;126(4):313-7.
2009: FRENNY SHETH; E Ewers; N Kosyakova; A Weise; J Sheth; S Patil; M Ziegler; Thomas Liehr
A neocentric isochromosome Yp present as additional small supernumerary marker chromosome--evidence against U-type exchange mechanism?
Cytogenetic and genome research 2009;125(2):115-6.
2009: Joana Melo; E Matoso; A Polityko; J Saraiva; L Backx; Joris R Vermeesch; Nadezda Kosyakova; E Ewers; Thomas Liehr; Isabel M Carreira
Molecular cytogenetic characterization of two cases with de novo small mosaic supernumerary marker chromosomes derived from chromosome 16: towards a genotype/phenotype correlation.
Cytogenetic and genome research 2009;125(2):109-14.
2009: Dilek Aktas; Anja Weise; Eda Utine; Dursun Alehan; Kristin Mrasek; Ferdinand von Eggeling; Heike Thieme; Ergul Tuncbilek; Thomas Liehr
Clinically abnormal case with paternally derived partial trisomy 8p23.3 to 8p12 including maternal isodisomy of 8p23.3: a case report.
Molecular cytogenetics 2009;2():14.
2009: Jörn Erlecke; Isabell Hartmann; Martin Hoffmann; Torsten Kroll; Heike Starke; Anita Heller; Alexander Gloria; Herbert G Sayer; Tilman Johannes; Uwe Claussen; Thomas Liehr; Ivan F Loncarevic
Automated detection of residual cells after sex-mismatched stem-cell transplantation - evidence for presence of disease-marker negative residual cells.
Molecular cytogenetics 2009;2():12.
2009: Thomas Liehr; Markus Stumm; Rolf-Dieter Wegner; S Bhatt; P Hickmann; P C Patsalis; M Meins; S Morlot; V Klaschka; E Ewers; S Hinreiner; Kristin Mrasek; Nadezda Kosyakova; W W Cai; Sau Wai Cheung; Anja Weise
10p11.2 to 10q11.2 is a yet unreported region leading to unbalanced chromosomal abnormalities without phenotypic consequences.
Cytogenetic and genome research 2009;124(1):102-5.
2009: Bernd Auber; Verena Bruemmer; Barbara Zoll; Peter Burfeind; Detlef Boehm; Thomas Liehr; Knut Brockmann; Ekkehard Wilichowski; Loukas Argyriou; Iris Bartels
Identification of subtelomeric genomic imbalances and breakpoint mapping with quantitative PCR in 296 individuals with congenital defects and/or mental retardation.
Molecular cytogenetics 2009;2():10.
2009: Sophia Kitsiou-Tzeli; Emmanouil Manolakos; Magdalini Lagou; Katerina Anagnostopoulou; Maria Kontodiou; Nadezda Kosyakova; Elisabeth Ewers; Anja Weise; Antonios Garas; Sandro Orru; Thomas Liehr; Aikaterini Metaxotou
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.
Molecular cytogenetics 2009;2():8.
2009: Maria Luiza Macedo Silva; Maria do Socorro Pombo-de-Oliveira; Susana C Raimondi; Hasmik Mkrtchyan; Eliana Abdelhay; Amanda Faria de Figueiredo; Mariana Tavares de Souza; Daniela Ribeiro Ney Garcia; Eliane Maria Soares de Ventura; Adriana Martins de Sousa; Thomas Liehr
Unbalanced chromosome 1 abnormalities leading to partial trisomy 1q in four infants with Down syndrome and acute megakaryocytic leukemia.
Molecular cytogenetics 2009;2():7.
2009: Nadezda Kosyakova; Anja Weise; Kristin Mrasek; Uwe Claussen; Thomas Liehr; Heike Nelle
The hierarchically organized splitting of chromosomal bands for all human chromosomes.
Molecular cytogenetics 2009;2():4.
2009: Sophia Kitsiou-Tzeli; Emmanouil Manolakos; Magdalini Lagou; Maria Kontodiou; Nadezda Kosyakova; Elisabeth Ewers; Anja Weise; Antonios Garas; Sandro Orru; Thomas Liehr; Aikaterini Metaxotou
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.
Molecular cytogenetics 2009;2():1.
2009: samarth Bhatt; Kamran Moradkhani; Kristin Mrasek; Jacques Puechberty; Marina Manvelyan; Friederike Hunstig; Genevieve Lefort; Anja Weise; James Lespinasse; Pierre Sarda; Thomas Liehr; Samir Hamamah; Franck Pellestor
Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions.
European journal of human genetics : EJHG 2009;17(1):44-50.
2008: Jie Lian; Yimeng Yin; Maria Oliver-Bonet; Thomas Liehr; Evelyn Ko; Paul Turek; Fei Sun; Renée H Martin
Variation in crossover interference levels on individual chromosomes from human males.
Human molecular genetics 2008;17(17):2583-94.
2008: Anja Weise; Thomas Liehr
Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies.
Expert review of molecular diagnostics 2008;8(4):355-7.
2008: Hasmik Mkrtchyan; Seda Ghazaryan; Gayane Avetisyan; Anna Hovhannisyan; Laura Muradyan; Smbat Daghbashyan; Constanze Karst; Madeleine Gross; Sophie Hinreiner; Rouben Aroutiounian; Thomas Liehr
Novel complex t(V;9;22) rearrangements in three cases with chronic myeloid leukemia and a rare translocation in a case with classical Philadelphia chromosome.
Oncology reports 2008;20(1):99-104.
2008: Tiziano Pramparo; Manuela De Gregori; stefania gimelli; Roberto Ciccone; Domenico Frondizi; Thomas Liehr; Simona Pellacani; Gabriele Masi; Paola Brovedani; Orsetta Zuffardi; Renzo Guerrini
A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation.
American journal of medical genetics. Part A 2008;146A(13):1754-60.
2008: Marina Manvelyan; Mariluce Riegel; Monica Santos; Carme Fuster; Franck Pellestor; Marie-Luise Mazaurik; Bernt Schulze; Anna Polityko; Hanne Tittelbach; Gisela Reising-Ackermann; Britta Belitz; Ute Hehr; Christine Kelbova; Marianne Volleth; Elisabeth Gödde; Jasen Anderson; Peter Küpferling; Sigrid Köhler; Hans-Christoph Duba; Andreas Dufke; Dilek Aktas; Thomas Martin; Isolde Schreyer; Elisabeth Ewers; Daniela Reich; Kristin Mrasek; Anja Weise; Thomas Liehr
Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.
International journal of molecular medicine 2008;21(6):705-14.
2008: Altuğ Koç; Derya Kan; Kadri Karaer; mehmet ergun; Meral Yirmibeş Karaoğuz; Kivilcim Gücüyener; Sophie Hinreiner; Thomas Liehr; E Ferda Perçin
An unexpected finding in a child with neurological problems: mosaic ring chromosome 18.
European journal of pediatrics 2008;167(6):655-9.
2008: Anja Weise; Kristin Mrasek; Ina Fickelscher; Uwe Claussen; Sau Wai Cheung; Wei Wen Cai; Thomas Liehr; Nadezda Kosyakova
Molecular definition of high-resolution multicolor banding probes: first within the human DNA sequence anchored FISH banding probe set.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2008;56(5):487-93.
2008: Maria Luiza Macedo Silva; Susana C Raimondi; Eliana Abdelhay; Madeleine Gross; Hasmik Mkrtchyan; Amanda Faria de Figueiredo; Raul C Ribeiro; Terezinha de Jesus Marques-Salles; Elaine Costa; Marcelo Poirot Gerardin Land; Thomas Liehr
Banding and molecular cytogenetic studies detected a CBFB-MYH11 fusion gene that appeared as abnormal chromosomes 1 and 16 in a baby with acute myeloid leukemia FAB M4-Eo.
Cancer genetics and cytogenetics 2008;182(1):56-60.
2008: Anja Weise; Madeleine Gross; Kristin Mrasek; Hasmik Mkrtchyan; B Horsthemke; C Jonsrud; Ferdinand von Eggeling; S Hinreiner; V Witthuhn; Uwe Claussen; Thomas Liehr
Parental-origin-determination fluorescence in situ hybridization distinguishes homologous human chromosomes on a single-cell level.
International journal of molecular medicine 2008;21(2):189-200.
2008: Marina Manvelyan; Friederike Hunstig; samarth Bhatt; Kristin Mrasek; Franck Pellestor; Anja Weise; Isabella Simonyan; Rouben Aroutiounian; Thomas Liehr
Chromosome distribution in human sperm - a 3D multicolor banding-study.
Molecular cytogenetics 2008;1():25.
2008: Emmanouil Manolakos; Nadezda Kosyakova; Loreta Thomaidis; Rozita Neroutsou; Anja Weise; Markos Mihalatos; Sandro Orru; Haris Kokotas; George Kitsos; Thomas Liehr; Michael B Petersen
Complex chromosome rearrangement in a child with microcephaly, dysmorphic facial features and mosaicism for a terminal deletion del(18)(q21.32-qter) investigated by FISH and array-CGH: Case report.
Molecular cytogenetics 2008;1():24.
2008: Ivan Y Iourov; Svetlana G Vorsanova; Thomas Liehr; V V Monakhov; Ilia V Soloviev; Yuri B Yurov
Dynamic mosaicism manifesting as loss, gain and rearrangement of an isodicentric Y chromosome in a male child with growth retardation and abnormal external genitalia.
Cytogenetic and genome research 2008;121(3-4):302-6.
2008: Kristin Mrasek; G Krüger; I Bauer; J Müller-Navia; Thomas Liehr; Anja Weise
A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences.
Cytogenetic and genome research 2008;121(3-4):286-7.
2008: Svetlana G Vorsanova; Ivan Y Iourov; Victoria Y Voinova-Ulas; Anja Weise; Victor V Monakhov; Alexei D Kolotii; Ilia V Soloviev; Petr V Novikov; Yuri B Yurov; Thomas Liehr
Partial monosomy 7q34-qter and 21pter-q22.13 due to cryptic unbalanced translocation t(7;21) but not monosomy of the whole chromosome 21: a case report plus review of the literature.
Molecular cytogenetics 2008;1():13.
2008: Thomas Liehr; Kristin Mrasek; Nadezda Kosyakova; Caroline Mackie Ogilvie; Joris R Vermeesch; Vladimir Trifonov; Nikolai Rubtsov
Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them.
Molecular cytogenetics 2008;1():12.
2008: Vladimir Trifonov; Simon Fluri; Franz Binkert; Adayapalam Nandini; Jasen Anderson; Laura Rodriguez; Madeleine Gross; Nadezda Kosyakova; Hasmik Mkrtchyan; Elisabeth Ewers; Daniela Reich; Anja Weise; Thomas Liehr
Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?
Molecular cytogenetics 2008;1():6.
2008: Laura Rodríguez; Thomas Liehr; María-Luisa Martínez-Fernández; Ana Lara; Antonio Torres; María Luisa Martínez-Frías
A new small supernumerary marker chromosome, generating mosaic pure trisomy 16q11.1-q12.1 in a healthy man.
Molecular cytogenetics 2008;1():4.
2008: Yuri B Yurov; Thomas Liehr; Lisa Shaffer; Ivan Y Iourov; Svetlana G Vorsanova
A new open access journal for a rapidly evolving biomedical field: introducing Molecular Cytogenetics.
Molecular cytogenetics 2008;1():1.
2008: Marina Manvelyan; Friederike Hunstig; Kristin Mrasek; samarth Bhatt; Franck Pellestor; Anja Weise; Thomas Liehr
Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon.
Molecular cytogenetics 2008;1():9.
2008: Anja Weise; Thomas Liehr
Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH).
Methods in molecular biology (Clifton, N.J.) 2008;444():39-47.
2008: Thomas Liehr
Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.
Methods in molecular biology (Clifton, N.J.) 2008;444():27-38.
2008: Irina Balikova; Kevin Martens; Cindy Melotte; Mustapha Amyere; Steven Van Vooren; Yves Moreau; David Vetrie; Heike Fiegler; Nigel P Carter; Thomas Liehr; Miikka Vikkula; Gert Matthijs; Jean-Pierre Fryns; Ingele Casteels; koenraad devriendt; Joris R Vermeesch
Autosomal-dominant microtia linked to five tandem copies of a copy-number-variable region at chromosome 4p16.
American journal of human genetics 2008;82(1):181-7.
2008: Yuri B Yurov; Ivan Y Iourov; Svetlana G Vorsanova; Irina A Demidova; Viktor S Kravetz; Alphia K Beresheva; Alexei D Kolotii; Viktor V Monakchov; Natalya A Uranova; Victor M Vostrikov; Ilia V Soloviev; Thomas Liehr
The schizophrenia brain exhibits low-level aneuploidy involving chromosome 1.
Schizophrenia research 2008;98(1-3):139-47.
2007: Laura Rodríguez; Thomas Liehr; K Mrasek; Elena Mansilla; María-Luisa Martínez-Fernández; A Garcia; María Luisa Martínez-Frías
Small supernumerary chromosome marker generating complete and pure trisomy 18p, characterized by molecular cytogenetic techniques and review.
American journal of medical genetics. Part A 2007;143A(22):2727-32.
2007: Isabel M Carreira; Alexandra Mascarenhas; Eunice Matoso; Ana Bela Couceiro; Lina Ramos; Andreas Dufke; Marie Mazauric; Rüdiger Stressig; Nadezda Kosyakova; Joana Melo; Thomas Liehr
Three unusual but cytogenetically similar cases with up to five different cell lines involving structural and numerical abnormalities of chromosome 18.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2007;55(11):1123-8.
2007: bhatt samarth; Kamran Moradkhani; K Mrasek; Jacques Puechberty; Geneviève Lefort; James Lespinasse; Pierre Sarda; Thomas Liehr; Samir Hamamah; Franck Pellestor
Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm.
Molecular human reproduction 2007;13(10):751-6.
2007: Ina Fickelscher; Thomas Liehr; Kathryn Watts; Victoria Bryant; John C K Barber; Simone Heidemann; Reiner Siebert; Jens Michael Hertz; Zeynep Tumer; N Simon Thomas
The variant inv(2)(p11.2q13) is a genuinely recurrent rearrangement but displays some breakpoint heterogeneity.
American journal of human genetics 2007;81(4):847-56.
2007: Ivan Y Iourov; Thomas Liehr; Svetlana G Vorsanova; Yuri B Yurov
Interphase chromosome-specific multicolor banding (ICS-MCB): a new tool for analysis of interphase chromosomes in their integrity.
Biomolecular engineering 2007;24(4):415-7.
2007: Mònica Santos; Kristin Mrasek; Maria Angels Rigola; Heike Starke; Thomas Liehr; Carme Fuster
Identification of a "cryptic mosaicism" involving at least four different small supernumerary marker chromosomes derived from chromosome 9 in a woman without reproductive success.
Fertility and sterility 2007;88(4):969.e11-7.
2007: Joerg Mattes; Bruce Whitehead; Thomas Liehr; Ian Wilkinson; John Bear; Kerry Fagan; Paul Craven; Bruce Bennetts; Matthew Edwards
Paternal uniparental isodisomy for chromosome 14 with mosaicism for a supernumerary marker chromosome 14.
American journal of medical genetics. Part A 2007;143A(18):2165-71.
2007: G Eda Utine; D Aktas; Yasemin Alanay; S Gücer; Ergul Tuncbilek; Kristin Mrasek; Thomas Liehr
Distal partial trisomy 1q: report of two cases and a review of the literature.
Prenatal diagnosis 2007;27(9):865-71.
2007: Ina Fickelscher; Heike Starke; Eberhard Schulze; Günther Ernst; Nadezda Kosyakova; Hasmik Mkrtchyan; Kay MacDermont; Neil J Sebire; Thomas Liehr
A further case with a small supernumerary marker chromosome (sSMC) derived from chromosome 1--evidence for high variability in mosaicism in different tissues of sSMC carriers.
Prenatal diagnosis 2007;27(8):783-5.
2007: Alexandre Serra; Hans K Schackert; Brigitte Mohr; Anja Weise; Thomas Liehr; Guido Fitze
t(11;19)(q21;p12~p13.11) and MECT1-MAML2 fusion transcript expression as a prognostic marker in infantile lung mucoepidermoid carcinoma.
Journal of pediatric surgery 2007;42(7):E23-9.
2007: Julia Rosenhahn; Anja Weise; Susanne Michel; Katrin Hennig; Isabell Hartmann; Jana Schiefner; Katrin Schubert; Thomas Liehr; Ferdinand von Eggeling; Ivan F Loncarevic
Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R.
International journal of oncology 2007;31(1):121-8.
2007: M Manvelyan; Isolde Schreyer; I Höls-Herpertz; S Köhler; R Niemann; U Hehr; Britta Belitz; Iris Bartels; J Götz; D Huhle; M Kossakiewicz; H Tittelbach; S Neubauer; Anna Polityko; M-L Mazauric; Rolf-Dieter Wegner; Markus Stumm; P Küpferling; F Süss; H Kunze; Anja Weise; Thomas Liehr; Kristin Mrasek
Forty-eight new cases with infertility due to balanced chromosomal rearrangements: detailed molecular cytogenetic analysis of the 90 involved breakpoints.
International journal of molecular medicine 2007;19(6):855-64.
2007: Holger Tönnies; Joanna Pietrzak; Ewa Bocian; Kay MacDermont; Alma Kuechler; Britta Belitz; Udo Trautmann; Angela Schmidt; Berndt Schulze; Laura Rodríguez; Franz Binkert; Catharine Yardin; Nadezda Kosyakova; Marianne Volleth; Hasmik Mkrtchyan; Isolde Schreyer; Ferdinand von Eggeling; Anja Weise; Kristin Mrasek; Thomas Liehr
New immortalized cell lines of patients with small supernumerary marker chromosome: towards the establishment of a cell bank.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2007;55(6):651-60.
2007: Simone M Sauter; Detlef Böhm; Iris Bartels; Peter Burfeind; Franco Laccone; Juergen Neesen; Bernd Wilken; Thomas Liehr; Barbara Zoll
Partial trisomy of distal 19q detected by quantitative real-time PCR and FISH in a girl with mild facial dysmorphism, hypotonia and developmental delay.
American journal of medical genetics. Part A 2007;143A(10):1091-9.
2007: Thomas Liehr; Anja Weise
Frequency of small supernumerary marker chromosomes in prenatal, newborn, developmentally retarded and infertility diagnostics.
International journal of molecular medicine 2007;19(5):719-31.
2007: Michael Glei; Anja Schaeferhenrich; Uwe Claussen; Alma Kuechler; Thomas Liehr; Anja Weise; Brigitte Marian; Wolfgang Sendt; Beatrice L Pool-Zobel
Comet fluorescence in situ hybridization analysis for oxidative stress-induced DNA damage in colon cancer relevant genes.
Toxicological sciences : an official journal of the Society of Toxicology 2007;96(2):279-84.
2007: Sevim Balci; Aysun Unal; Ozlem Engiz; Dilek Aktas; Thomas Liehr; Madelaine Gross; Kristin Mrasek; Serap Saygi
Bilateral periventricular nodular heterotopia, severe learning disability, and epilepsy in a male patient with 46,XY,der(19)t(X;19) (q11.1-11.2;p13.3).
Developmental medicine and child neurology 2007;49(3):219-24.
2007: Anja Weise; Madeleine Gross; Sabine Schmidt; Franziska Reichelt; Uwe Claussen; Thomas Liehr
New aspects of chromosomal evolution in the gorilla and the orangutan.
International journal of molecular medicine 2007;19(3):437-43.
2007: Iris Bartels; Heike Starke; Loukas Argyriou; Simone M Sauter; Barbara Zoll; Thomas Liehr
An exceptional complex chromosomal rearrangement (CCR) with eight breakpoints involving four chromosomes (1;3;9;14) in an azoospermic male with normal phenotype.
European journal of medical genetics 2007;50(2):133-8.
2007: Thomas Liehr; Kristin Mrasek; S Hinreiner; D Reich; E Ewers; I Bartels; J Seidel; N Emmanuil; M Petesen; A Polityko; A Dufke; I Iourov; V Trifonov; J Vermeesch; Anja Weise
Small supernumerary marker chromosomes (sSMC) in patients with a 45,X/46,X,+mar karyotype - 17 new cases and a review of the literature.
Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2007;1(6):353-62.
2007: Fei Sun; Maria Oliver-Bonet; Thomas Liehr; Heike Starke; Evelyn Ko; Alfred Rademaker; Renée H Martin
Discontinuities and unsynapsed regions in meiotic chromosomes have a trans effect on meiotic recombination of some chromosomes in human males.
Cytogenetic and genome research 2007;119(1-2):27-32.
2007: T Felka; Johannes Lemke; Cornelius Lemke; Susanne Michel; Thomas Liehr; Uwe Claussen
DNA degradation during maturation of erythrocytes - molecular cytogenetic characterization of Howell-Jolly bodies.
Cytogenetic and genome research 2007;119(1-2):2-8.
2007: NP Bochkov; E S Voronina; N V Kosyakova; Thomas Liehr; AA Rzhaninova; LD Katosova; VI Platonova; DV Gol'dshtein
Chromosome variability of human multipotent mesenchymal stromal cells.
Bulletin of experimental biology and medicine 2007;143(1):122-6.
2007: Thomas Liehr; G Eda Utine; Udo Trautmann; A Rauch; Alma Kuechler; Joanna Pietrzak; J Pietracz; Ewa Bocian; Nadezda Kosyakova; Kristin Mrasek; Koray Boduroglu; Anja Weise; Dilek Aktas
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Cytogenetic and genome research 2007;118(1):31-7.
2007: Yuri B Yurov; Ivan Y Iourov; Svetlana G Vorsanova; Thomas Liehr; Alexei D Kolotii; Sergei I Kutsev; Franck Pellestor; Alphia K Beresheva; Irina A Demidova; Viktor S Kravets; Viktor V Monakhov; Ilia V Soloviev
Aneuploidy and confined chromosomal mosaicism in the developing human brain.
PloS one 2007;2(6):e558.
2007: Joanna Pietrzak; Kristin Mrasek; Ewa Obersztyn; Pawel Stankiewicz; Nadezda Kosyakova; Anja Weise; Sau Wai Cheung; Wei-Wen Cai; Ferdinand von Eggeling; Tadeusz Mazurczak; Ewa Bocian; Thomas Liehr
Molecular cytogenetic characterization of eight small supernumerary marker chromosomes originating from chromosomes 2, 4, 8, 18, and 21 in three patients.
Journal of applied genetics 2007;48(2):167-75.
2007: liesbeth backx; Hilde Van Esch; Cindy Melotte; Nadezda Kosyakova; Heike Starke; JP Frijns; Thomas Liehr; Joris R Vermeesch
Array painting using microdissected chromosomes to map chromosomal breakpoints.
Cytogenetic and genome research 2007;116(3):158-66.
2006: Eleftheria Papadopoulou; Stavros Sifakis; Catherine Sarri; Jolanda Gyftodimou; Thomas Liehr; Kristin Mrasek; Maria Kalmanti; Michael B Petersen
A report of pure 7p duplication syndrome and review of the literature.
American journal of medical genetics. Part A 2006;140(24):2802-6.
2006: Diana Mitter; Karin Buiting; Ferdinand von Eggeling; Alma Kuechler; Thomas Liehr; Ulrike Angelika Mau-Holzmann; Eva-Christina Prott; Dagmar Wieczorek; Gabriele Gillessen-Kaesbach
Is there a higher incidence of maternal uniparental disomy 14 [upd(14)mat]? Detection of 10 new patients by methylation-specific PCR.
American journal of medical genetics. Part A 2006;140(19):2039-49.
2006: Fei Sun; Maria Oliver-Bonet; Thomas Liehr; Heike Starke; Paul Turek; Evelyn Ko; Alfred Rademaker; Renée H Martin
Analysis of non-crossover bivalents in pachytene cells from 10 normal men.
Human reproduction (Oxford, England) 2006;21(9):2335-9.
2006: Fei Sun; Maria Oliver-Bonet; Thomas Liehr; Heike Starke; Paul Turek; Evelyn Ko; Alfred Rademaker; Renée H Martin
Variation in MLH1 distribution in recombination maps for individual chromosomes from human males.
Human molecular genetics 2006;15(15):2376-91.
2006: Thomas Liehr
Familial small supernumerary marker chromosomes are predominantly inherited via the maternal line.
Genetics in medicine : official journal of the American College of Medical Genetics 2006;8(7):459-62.
2006: Constanze Karst; Madeleine Gross; Detlef Haase; Ulrich Wedding; Klaus Höffken; Thomas Liehr; Hasmik Mkrtchyan
Novel cryptic chromosomal rearrangements detected in acute lymphoblastic leukemia detected by application of new multicolor fluorescent in situ hybridization approaches.
International journal of oncology 2006;28(4):891-7.
2006: Sevim Balci; Ozlem Engiz; Dilek Aktaş; Ibrahim Vargel; M Sinan Beksaç; Kristin Mrasek; Joris R Vermeesch; Thomas Liehr
Ring chromosome 4 and Wolf-Hirschhorn syndrome (WHS) in a child with multiple anomalies.
American journal of medical genetics. Part A 2006;140(6):628-32.
2006: Pawel Stankiewicz; Alma Kuechler; C Daniel Eller; Trilochan Sahoo; Christiane Baldermann; Ulla Lieser; Martin Hesse; Christiane Gläser; Monika Hagemann; Svetlana A Yatsenko; Thomas Liehr; Bernhard Horsthemke; Uwe Claussen; York Marahrens; James R Lupski; Ingo Hansmann
Minimal phenotype in a girl with trisomy 15q due to t(X;15)(q22.3;q11.2) translocation.
American journal of medical genetics. Part A 2006;140(5):442-52.
2006: Constanze Karst; Vladimir Trifonov; Svetlana A. Romanenko; Uwe Claussen; Kristin Mrasek; Susanne Michel; Philip Avner; Thomas Liehr
Molecular cytogenetic characterization of the mouse cell line WMP2 by spectral karyotyping and multicolor banding applying murine probes.
International journal of molecular medicine 2006;17(2):209-13.
2006: Thomas Liehr
Application of yeast artificial chromosomes in fluorescence in situ hybridization.
Methods in molecular biology (Clifton, N.J.) 2006;349():175-86.
2006: Lukrecija Brecevic; S Michel; Heike Starke; K Müller; Nadezda Kosyakova; Kristin Mrasek; Anja Weise; Thomas Liehr
Multicolor FISH used for the characterization of small supernumerary marker chromosomes (sSMC) in commercially available immortalized cell lines.
Cytogenetic and genome research 2006;114(3-4):319-24.
2006: Hasmik Mkrtchyan; M Glaser; Madeleine Gross; Ulrich Wedding; K Hoffken; Thomas Liehr; Constanze Karst; R Aroutiounian
Multicolor-FISH applied to resolve complex chromosomal changes in a case of T-ALL (FAB L2).
Cytogenetic and genome research 2006;114(3-4):270-3.
2006: Thomas Liehr; Heike Starke; Anita Heller; Nadezda Kosyakova; Kristin Mrasek; Madeleine Gross; Constanze Karst; U Steinhaeuser; F Hunstig; Ina Fickelscher; Alma Kuechler; Vladimir Trifonov; Svetlana A. Romanenko; Anja Weise
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding.
Cytogenetic and genome research 2006;114(3-4):240-4.
2006: Ivan Y Iourov; Thomas Liehr; Svetlana G Vorsanova; Alexei D Kolotii; Yuri B Yurov
Visualization of interphase chromosomes in postmitotic cells of the human brain by multicolour banding (MCB).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2006;14(3):223-9.
2006: Cornelia Rudolph; Thomas Liehr; Doris Steinemann; Makito Emura; M Daibata; Y Matsuo; N Emi; M Abe; R Lai; K Mrasek; U Claussen; Brigitte Schlegelberger
Different breakage-prone regions on chromosome 1 detected in t(11;14)-positive mantle cell lymphoma cell lines and multiple myeloma cell lines are associated with different tumor progression-related mechanisms.
Cytogenetic and genome research 2006;112(3-4):213-21.
2006: Thomas Liehr; Madeleine Gross; Constanze Karst; Melanie Glaser; Kristin Mrasek; Heike Starke; Anja Weise; Hasmik Mkrtchyan; Alma Kuechler
FISH banding in tumor cytogenetics.
Cancer genetics and cytogenetics 2006;164(1):88-9.
2006: Thomas Liehr; Heike Starke; Gabriele Senger; Cindy Melotte; Anja Weise; Joris R Vermeesch
Overrepresentation of small supernumerary marker chromosomes (sSMC) from chromosome 6 origin in cases with multiple sSMC.
American journal of medical genetics. Part A 2006;140(1):46-51.
2006: Madeleine Gross; Heike Starke; Vladimir Trifonov; Uwe Claussen; Thomas Liehr; Anja Weise
A molecular cytogenetic study of chromosome evolution in chimpanzee.
Cytogenetic and genome research 2006;112(1-2):67-75.
2006: Thomas Liehr; Kristin Mrasek; Anja Weise; Andreas Dufke; L Rodríguez; N Martínez Guardia; A Sanchís; Joris R Vermeesch; C Ramel; Anna Polityko; O A Haas; J Anderson; Uwe Claussen; Ferdinand von Eggeling; Heike Starke
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
Cytogenetic and genome research 2006;112(1-2):23-34.
2005: Cristina Gutiérrez-Mateo; Jordi Benet; Heike Starke; Maria Oliver-Bonet; Santiago Munné; Thomas Liehr; Joaquima Navarro
Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique.
Human reproduction (Oxford, England) 2005;20(12):3395-401.
2005: Fei Sun; Maria Oliver-Bonet; Thomas Liehr; Heike Starke; Kiril Trpkov; Evelyn Ko; Alfred Rademaker; Renée H Martin
Discontinuities and unsynapsed regions in meiotic chromosomes have a cis effect on meiotic recombination patterns in normal human males.
Human molecular genetics 2005;14(20):3013-8.
2005: Laura Rodríguez; Heike Starke; Nieves Martínez Guardia; Holger Tönnies; Heidemarie Neitzel; Peter Kozlowski; M-L Mazauric; Anita Heller; Fermina López Grondona; Elena Mansilla; M José Santos Muñoz; Thomas Liehr; María Luisa Martínez-Frías
Three new cases with a supernumerary ring chromosome 1.
Clinical dysmorphology 2005;14(4):169-75.
2005: Tanja Kautenburger; Gabriele Beyer-Sehlmeyer; Grit Festag; Natja Haag; Stephanie Kühler; Alma Küchler; Anja Weise; Brigitte Marian; Wilbert H M Peters; Thomas Liehr; Uwe Claussen; Beatrice L Pool-Zobel
The gut fermentation product butyrate, a chemopreventive agent, suppresses glutathione S-transferase theta (hGSTT1) and cell growth more in human colon adenoma (LT97) than tumor (HT29) cells.
Journal of cancer research and clinical oncology 2005;131(10):692-700.
2005: John C K Barber; Vivienne Maloney; Ed Hollox; Annegret Stuke-Sontheimer; Gabi du Bois; Eva Daumiller; Ute Klein-Vogler; Andreas Dufke; John A L Armour; Thomas Liehr
Duplications and copy number variants of 8p23.1 are cytogenetically indistinguishable but distinct at the molecular level.
European journal of human genetics : EJHG 2005;13(10):1131-6.
2005: Anja Weise; Thomas Liehr; Uwe Claussen; Karl-Jürgen Halbhuber
Increased efficiency of fluorescence in situ hybridization (FISH) using the microwave.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(10):1301-3.
2005: Maria Luiza Macedo Silva; Marcelo Gerardin Poirot Land; Anita Heller; Eliana Abdelhay; Maria do Socorro Pombo-de-Oliveira; Raul Ribeiro; Gilda Alves; Décio Lerner; Thomas Liehr
New rearrangement t(3;17)(q26.3;q12) in an AML patient with a poor outcome.
Oncology reports 2005;14(3):663-6.
2005: G Von Beust; Simone M Sauter; Thomas Liehr; Peter Burfeind; Iris Bartels; Heike Starke; Ferdinand von Eggeling; Barbara Zoll
Molecular cytogenetic characterization of a de novo supernumerary ring chromosome 7 resulting in partial trisomy, tetrasomy, and hexasomy in a child with dysmorphic signs, congenital heart defect, and developmental delay.
American journal of medical genetics. Part A 2005;137(1):59-64.
2005: Constanze Karst; Anita Heller; Uwe Claussen; Erich Gebhart; Thomas Liehr
Detection of cryptic chromosomal aberrations in the in vitro non-proliferating cells of acute myeloid leukemia.
International journal of oncology 2005;27(2):355-9.
2005: Tiziano Pramparo; Teresa Mattina; stefania gimelli; Thomas Liehr; Orsetta Zuffardi
Narrowing the deleted region associated with the 15q21 syndrome.
European journal of medical genetics 2005;48(3):346-52.
2005: Joris R Vermeesch; Cindy Melotte; Ivo Salden; Mariluce Riegel; Vladimir Trifnov; Anna Polityko; Natalia Rumyantseva; Irina Naumchik; Heike Starke; Gert Matthijs; Albert Schinzel; Jean-Pierre Fryns; Thomas Liehr
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
European journal of medical genetics 2005;48(3):319-27.
2005: S Schmidt; Uwe Claussen; Thomas Liehr; Anja Weise
Evolution versus constitution: differences in chromosomal inversion.
Human genetics 2005;117(2-3):213-9.
2005: Vladimir Trifonov; Constanze Karst; Uwe Claussen; Kristin Mrasek; Susanne Michel; Philip Avner; Thomas Liehr
Microdissection-derived murine mcb probes from somatic cell hybrids.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(6):791-2.
2005: Thomas Liehr; Elke Brude; Gabriele Gillessen-Kaesbach; Rainer König; Kristin Mrasek; Ferdinand von Eggeling; Heike Starke
Prader-Willi syndrome with a karyotype 47,XY,+min(15)(pter->q11.1:) and maternal UPD 15--case report plus review of similar cases.
European journal of medical genetics 2005;48(2):175-81.
2005: Kristin Mrasek; Heike Starke; Thomas Liehr
Another small supernumerary marker chromosome (sSMC) derived from chromosome 2: towards a genotype/phenotype correlation.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):367-70.
2005: Isolde Schreyer; Annett Neumann; Volkmar Beensen; Karl-Heinz Eichhorn; Anita Heller; Uwe Claussen; Thomas Liehr
Dup(13)(q14.2-q14.3): yet another new differential diagnostic aspect for short stature-like phenotype.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):365-6.
2005: Heike Starke; Kristin Mrasek; Thomas Liehr
Three cases with enlarged acrocentric p-arms and two cases with cryptic partial trisomies.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):359-60.
2005: Alma Kuechler; Monika Ziegler; Cornelia Blank; Birgit Rommel; Jörn Bullerdiek; Jochen Ahrens; Uwe Claussen; Thomas Liehr
A highly complex chromosomal rearrangement between five chromosomes in a healthy female diagnosed in preparation for intracytoplasmatic sperm injection.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):355-7.
2005: Marc Trimborn; Thomas Liehr; Britta Belitz; Lutz Pfeiffer; Raymonda Varon; Heidemarie Neitzel; Holger Tönnies
Prenatal diagnosis and molecular cytogenetic characterization of an unusual complex structural rearrangement in a pregnancy following intracytoplasmic sperm injection (ICSI).
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):351-4.
2005: Thomas Liehr; Monika Ziegler
Rapid prenatal diagnostics in the interphase nucleus: procedure and cut-off rates.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):289-91.
2005: Thomas Liehr; Heinz-Ulrich G Weier
14th workshop on fetal cells and fetal DNA.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2005;53(3):253-4.
2005: Maria Oliver-Bonet; Jordi Benet; Fei Sun; J Navarro; Carlos Abad; Thomas Liehr; Heike Starke; Calvin Greene; Evelyn Ko; Renée H Martin
Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure.
Human reproduction (Oxford, England) 2005;20(3):683-8.
2005: John C K Barber; N Simon Thomas; Morag N Collinson; Nicholas R Dennis; Thomas Liehr; Anja Weise; Britta Belitz; Lutz Pfeiffer; Maria Kirchhoff; Bente Krag-Olsen; Claes Lundsteen
Segmental haplosufficiency: transmitted deletions of 2p12 include a pancreatic regeneration gene cluster and have no apparent phenotypic consequences.
European journal of human genetics : EJHG 2005;13(3):283-91.
2005: Thomas Liehr; Kristin Mrasek; Heike Starke; Uwe Claussen; G Schreiber
Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
Cytogenetic and genome research 2005;111(2):179-81.
2005: Anna Polityko; Heike Starke; Natalia Rumyantseva; Uwe Claussen; Thomas Liehr; S Raskin
Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.
Cytogenetic and genome research 2005;111(2):171-4.
2005: Anja Weise; Heike Starke; Kristin Mrasek; Uwe Claussen; Thomas Liehr
New insights into the evolution of chromosome 1.
Cytogenetic and genome research 2005;108(1-3):217-22.
2004: Thomas Liehr; Anita Heller; Karl-Heinz Eichhorn; Volkmar Beensen; Eberhart Schulze; Heike Starke; Uwe Claussen; Isolde Schreyer
Inherited cryptic chromosomal aberrations may be more easily detected in their balanced forms: a case report with hidden der(1)t(1;17)(q44;p13.2).
Prenatal diagnosis 2004;24(12):1022-4.
2004: Anna Polityko; Olga Maltseva; Natalia Rumyantseva; Olga Khurs; Jörg Seidel; Uwe Claussen; Anja Weise; Thomas Liehr; Heike Starke
Two further AHO-like syndrome patients with deletion of glypican 1 gene region in 2q37.2-q37.3.
International journal of molecular medicine 2004;14(6):977-9.
2004: Erich Gebhart; Jutta Ries; Jörg Wiltfang; Thomas Liehr; Thomas Efferth
Genomic gain of the epidermal growth factor receptor harboring band 7p12 is part of a complex pattern of genomic imbalances in oral squamous cell carcinomas.
Archives of medical research 2004;35(5):385-94.
2004: Cornelia Rudolph; Doris Steinemann; Nils von neuhoff; Dorothea Gadzicki; T Ripperger; H G Drexler; K Mrasek; Thomas Liehr; U Claussen; Makito Emura; E Schrock; Brigitte Schlegelberger
Molecular cytogenetic characterization of the mantle cell lymphoma cell line GRANTA-519.
Cancer genetics and cytogenetics 2004;153(2):144-50.
2004: Walter Zumkeller; Marianne Volleth; Petra Muschke; Holger Tönnies; Anita Heller; Thomas Liehr; Peter Wieacker; Markus Stumm
Genotype/phenotype analysis in a patient with pure and complete trisomy 12p.
American journal of medical genetics. Part A 2004;129A(3):261-4.
2004: Montserrat Codina-Pascual; Maria Oliver-Bonet; Joaquima Navarro; Heike Starke; Thomas Liehr; Cristina Gutiérrez-Mateo; Jorge Fernando Sánchez-García; Octavio Arango; Josep Egozcue; Jordi Benet
FISH characterization of a dicentric Yq (p11.32) isochromosome in an azoospermic male.
American journal of medical genetics. Part A 2004;127A(3):302-6.
2004: Jordi Camps; Kristin Mrasek; Esther Prat; Anja Weise; Heike Starke; Josep Egozcue; Rosa Miró; Thomas Liehr
Molecular cytogenetic characterisation of the colorectal cancer cell line SW480.
Oncology reports 2004;11(6):1215-8.
2004: Ulrike Keller; Alma Kuechler; Thomas Liehr; Elisabeth Müller; Gerhard Grabenbauer; Rolf Sauer; Luitpold Distel
Impact of various parameters in detecting chromosomal aberrations by FISH to describe radiosensitivity.
Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2004;180(5):289-96.
2004: Detlef Boehm; Sabine Herold; Alma Kuechler; Thomas Liehr; Franco Laccone
Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
Human mutation 2004;23(4):368-78.
2004: Fei Sun; Maria Oliver-Bonet; Thomas Liehr; Heike Starke; Evelyn Ko; Alfred Rademaker; Joaquima Navarro; Jordi Benet; Renée H Martin
Human male recombination maps for individual chromosomes.
American journal of human genetics 2004;74(3):521-31.
2004: Thomas Liehr; Uwe Claussen; Heike Starke
Small supernumerary marker chromosomes (sSMC) in humans.
Cytogenetic and genome research 2004;107(1-2):55-67.
2004: H Lehrer; Anja Weise; Susanne Michel; Heike Starke; Kristin Mrasek; Anita Heller; Alma Kuechler; Uwe Claussen; Thomas Liehr
The hierarchically organized splitting of chromosome bands into sub-bands analyzed by multicolor banding (MCB).
Cytogenetic and genome research 2004;105(1):25-8.
2004: Thomas Liehr; Gabriele Hickmann; Peter Kozlowski; Uwe Claussen; Heike Starke
Molecular-cytogenetic characterization of the origin and the presence of pericentromeric euchromatin on minute supernumerary marker chromosomes (SMCs).
Chromosome research : an international journal on the molecular, supramolecular and evolutionary aspects of chromosome biology 2004;12(3):239-44.
2004: Thomas Liehr; Heike Starke; Anja Weise; H Lehrer; Uwe Claussen
Multicolor FISH probe sets and their applications.
Histology and histopathology 2004;19(1):229-37.
2004: Anita Heller; Ivan F Loncarevic; Melanie Glaser; Erich Gebhart; Udo Trautmann; Uwe Claussen; Thomas Liehr
Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints.
International journal of oncology 2004;24(1):127-36.
2004: Anita Heller; Hans-Joerg Fricke; Heike Starke; Ivan F Loncarevic; Uwe Claussen; Thomas Liehr
Characterization of a highly aberrant plasma cell leukemia karyotype: a case report.
Oncology reports 2004;11(1):89-92.
2003: Heike Starke; Angela Nietzel; Anja Weise; Anita Heller; Kristin Mrasek; Britta Belitz; Christine Kelbova; Marianne Volleth; Beate Albrecht; Beate Mitulla; Ralf Trappe; Iris Bartels; Sabine Adolph; Andreas Dufke; Sylke Singer; Markus Stumm; Rolf-Dieter Wegner; Jörg Seidel; Angela Schmidt; Alma Kuechler; Isolde Schreyer; Uwe Claussen; Ferdinand von Eggeling; Thomas Liehr
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Human genetics 2003;114(1):51-67.
2003: Maria Oliver-Bonet; Thomas Liehr; Angela Nietzel; Anita Heller; Heike Starke; Uwe Claussen; Montserrat Codina-Pascual; Aïda Pujol; Carlos Abad; Josep Egozcue; Joaquima Navarro; Jordi Benet
Karyotyping of human synaptonemal complexes by cenM-FISH.
European journal of human genetics : EJHG 2003;11(11):879-83.
2003: Anita Heller; Vladimir Trifonov; Nikolai Rubtsov; Axel Sauerbrey; Heike Starke; Ivan F Loncarevic; Uwe Claussen; Thomas Liehr
Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS.
Oncology reports 2003;10(6):1789-92.
2003: Anita Heller; Lukrecija Brecevic; Melanie Glaser; Ivan F Loncarevic; Erich Gebhart; Uwe Claussen; Thomas Liehr
Trisomy 8 as the sole chromosomal aberration in myelocytic malignancies: a comprehensive molecular cytogenetic analysis reveals no cryptic aberrations.
Cancer genetics and cytogenetics 2003;146(1):81-3.
2003: Heike Starke; Beate Mitulla; Volkmar Beensen; Vladimir Trifonov; Nikolai Rubtsov; Anita Heller; Monika Ziegler; Annett Neumann; Uwe Claussen; Thomas Liehr
First postnatal case of mosaic del(22)/r(22).
Prenatal diagnosis 2003;23(9):765-7.
2003: Raimund W Kinne; Elke Kunisch; Volkmar Beensen; Thomas Zimmermann; Frank Emmrich; Peter Petrow; Wolfgang Lungershausen; Gert Hein; Ruedi K Braun; Martin Foerster; Claus Kroegel; Rando Winter; Eckehard Liesaus; Renée A Fuhrmann; Andreas Roth; Uwe Claussen; Thomas Liehr
Synovial fibroblasts and synovial macrophages from patients with rheumatoid arthritis and other inflammatory joint diseases show chromosomal aberrations.
Genes, chromosomes & cancer 2003;38(1):53-67.
2003: Jörg Seidel; Anita Heller; Gabriele Senger; Heike Starke; Ilse Chudoba; Christine Kelbova; Holger Tönnies; Heidemarie Neitzel; Claudia Haase; Volkmar Beensen; Felix Zintl; Uwe Claussen; Thomas Liehr
A multiple translocation event in a patient with hexadactyly, facial dysmorphism, mental retardation and behaviour disorder characterised comprehensively by molecular cytogenetics. Case report and review of the literature.
European journal of pediatrics 2003;162(9):582-8.
2003: Simone M Sauter; G Von Beust; Peter Burfeind; Anja Weise; Heike Starke; Thomas Liehr; Barbara Zoll
Autistic disorder and chromosomal mosaicism 46,XY[123]/46,XY,del(20)(pter --> p12.2)[10].
American journal of medical genetics. Part A 2003;120A(4):533-6.
2003: Ferdinand von Eggeling; S Langer; C Hoppe; Thomas Liehr; A Weise; Gaby Lederer; Dieter Kotzot
Presumed mutation in a microsatellite marker mimicking segmental uniparental disomy in a case of a small supernumerary marker chromosome detected at prenatal diagnosis.
Clinical genetics 2003;64(2):168-71.
2003: Thomas Liehr; Monika Ziegler; Heike Starke; Anita Heller; Alma Kuechler; Gabriele Kittner; Volkmar Beensen; Jörg Seidel; H Hässler; J Müsebeck; Uwe Claussen
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism.
Clinical genetics 2003;64(2):166-7.
2003: Kristin Mrasek; Anita Heller; Nikolai Rubtsov; Vladimir Trifonov; Heike Starke; Uwe Claussen; Thomas Liehr
Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding.
International journal of molecular medicine 2003;12(2):139-46.
2003: Alma Kuechler; Mareike Dreidax; Steffi U Pigorsch; Thomas Liehr; Uwe Claussen; Thomas G Wendt; Jürgen Dunst
Residual chromosomal damage after radiochemotherapy with and without amifostine detected by 24-color FISH.
Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2003;179(7):493-8.
2003: Anita Heller; Nikolai Rubtsov; Soili Kytölä; Tatiana V Karamysheva; Olga V Sablina; Marina M Degtyareva; Heike Starke; Hermann Metzke; Uwe Claussen; Thomas Liehr
Highly complex karyotypic changes in acute myelogenous leukemia: a case report.
International journal of oncology 2003;23(1):139-43.
2003: Anja Schaeferhenrich; Gabriele Beyer-Sehlmeyer; Grit Festag; Alma Kuechler; Natja Haag; Anja Weise; Thomas Liehr; Uwe Claussen; Brigitte Marian; Wolfgang Sendt; Johannes Scheele; Beatrice L Pool-Zobel
Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal.
Mutation research 2003;526(1-2):19-32.
2003: Vladimir Trifonov; Jörg Seidel; Heike Starke; Prechtel Martina; Volkmar Beensen; Monika Ziegler; Isabell Hartmann; Anita Heller; Angela Nietzel; Uwe Claussen; Thomas Liehr
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter.
Prenatal diagnosis 2003;23(5):427-30.
2003: Thomas Liehr; Heike Starke; Anita Heller; Anja Weise; Volkmar Beensen; Gabriele Senger; Gabriele Kittner; M Prechtel; Uwe Claussen; Jörg Seidel
Evidence for a new microdeletion syndrome in 15q21.
International journal of molecular medicine 2003;11(5):575-7.
2003: Anja Schaeferhenrich; Wolfgang Sendt; Johannes Scheele; Alma Kuechler; Thomas Liehr; Uwe Claussen; Alexander Rapp; Karl Otto Greulich; Beatrice L Pool-Zobel
Putative colon cancer risk factors damage global DNA and TP53 in primary human colon cells isolated from surgical samples.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association 2003;41(5):655-64.
2003: Gunnar Houge; Thomas Liehr; Jacqueline Schoumans; Gro Oddveig Ness; Kjetil Solland; Heike Starke; Uwe Claussen; Petter Strømme; Bjug Akre; Stefan Vermeulen
Ten years follow up of a boy with a complex chromosomal rearrangement: going from a > 5 to 15-breakpoint CCR.
American journal of medical genetics. Part A 2003;118A(3):235-40.
2003: Anja Weise; Peter Harbarth; Uwe Claussen; Thomas Liehr
Fluorescence in situ hybridization (FISH) on human chromosomes using photoprobe biotin-labeled probes.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2003;51(4):549-51.
2003: Angela Nietzel; Beate Albrecht; Heike Starke; Anita Heller; G Gillessen-Kaesbach; Uwe Claussen; Thomas Liehr
Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report.
Journal of medical genetics 2003;40(3):e28.
2003: Alma Kuechler; Anja Weise; Susanne Michel; Anja Schaeferhenrich; Beatrice L Pool-Zobel; Uwe Claussen; Thomas Liehr
Precise breakpoint characterization of the colon adenocarcinoma cell line HT-29 clone 19A by means of 24-color fluorescence in situ hybridization and multicolor banding.
Genes, chromosomes & cancer 2003;36(2):207-10.
2003: Anja Weise; Anita Heller; Heike Starke; Kristin Mrasek; Alma Kuechler; Beatrice L Pool-Zobel; Uwe Claussen; Thomas Liehr
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method.
Cytogenetic and genome research 2003;103(1-2):34-9.
2003: U Grasshoff; S Singer; Thomas Liehr; Heike Starke; B Fode; Martin Schöning; Andreas Dufke
A complex chromosomal rearrangement with a translocation 4;10;14 in a fertile male carrier: ascertainment through an offspring with partial trisomy 14q13-->q24.1 and partial monosomy 4q27-->q28 [corrected].
Cytogenetic and genome research 2003;103(1-2):17-23.
2003: Anja Weise; O Rittinger; Heike Starke; M Ziegler; Uwe Claussen; Thomas Liehr
De novo 9-break-event in one chromosome 21 combined with a microdeletion in 21q22.11 in a mentally retarded boy with short stature.
Cytogenetic and genome research 2003;103(1-2):14-6.
2003: Erich Gebhart; Thomas Liehr; E Wolff; Jörg Wiltfang; S Koscielny; Jutta Ries
Loss of 9p21 is embedded in a complex but consistent pattern of genomic imbalances in oral squamous cell carcinomas.
Cytogenetic and genome research 2003;101(2):106-12.
2003: Iris Bartels; G Schlueter; Thomas Liehr; Ferdinand von Eggeling; Heike Starke; R Glaubitz; Peter Burfeind
Supernumerary small marker chromosome (SMC) and uniparental disomy 22 in a child with confined placental mosaicism of trisomy 22: trisomy rescue due to marker chromosome formation.
Cytogenetic and genome research 2003;101(2):103-5.
2003: Heike Starke; Beate Mitulla; Angela Nietzel; Anita Heller; Volkmar Beensen; Gisela Grosswendt; Uwe Claussen; Ferdinand von Eggeling; Thomas Liehr
First patient with trisomy 21 accompanied by an additional der(4)(:p11 --> q11:) plus partial uniparental disomy 4p15-16.
American journal of medical genetics. Part A 2003;116A(1):26-30.
2002: Ulf Steinhaeuser; Heike Starke; Angela Nietzel; Joerg Lindenau; Peter Ullmann; Uwe Claussen; Thomas Liehr
Suspension (S)-FISH, a new technique for interphase nuclei.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society 2002;50(12):1697-8.
2002: Heike Starke; Jörg Seidel; Wolfram Henn; Sylvia Reichardt; Marianne Volleth; Markus Stumm; Christine Behrend; Klaus R Sandig; Christine Kelbova; Gabriele Senger; Beate Albrecht; Ingo Hansmann; Anita Heller; Uwe Claussen; Thomas Liehr
Homologous sequences at human chromosome 9 bands p12 and q13-21.1 are involved in different patterns of pericentric rearrangements.
European journal of human genetics : EJHG 2002;10(12):790-800.
2002: Johannes Lemke; Jan Claussen; Susanne Michel; Ilse Chudoba; Peter Mühlig; Martin Westermann; Karl Sperling; Nikolai Rubtsov; Ulrich-W Grummt; Peter Ullmann; Katrin Kromeyer-Hauschild; Thomas Liehr; Uwe Claussen
The DNA-based structure of human chromosome 5 in interphase.
American journal of human genetics 2002;71(5):1051-9.
2002: Ferdinand von Eggeling; C Hoppe; U Bartz; H Starke; Gunnar Houge; U Claussen; G Ernst; Dieter Kotzot; Thomas Liehr
Maternal uniparental disomy 12 in a healthy girl with a 47,XX,+der(12)(:p11-->q11:)/46,XX karyotype.
Journal of medical genetics 2002;39(7):519-21.
2002: Thomas Liehr; Isolde Schreyer; Annett Neumann; Volkmar Beensen; Monika Ziegler; Isabell Hartmann; Heike Starke; Anita Heller; Angela Nietzel; Uwe Claussen
Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei.
Prenatal diagnosis 2002;22(6):497-9.
2002: Anja Weise; Heike Starke; Anita Heller; Holger Tönnies; Marianne Volleth; Markus Stumm; S Gabriele; Angela Nietzel; Uwe Claussen; Thomas Liehr
Chromosome 2 aberrations in clinical cases characterised by high resolution multicolour banding and region specific FISH probes.
Journal of medical genetics 2002;39(6):434-9.
2002: Anita Heller; Heike Starke; Vladimir Trifonov; Nikolai Rubtsov; Ulrich Wedding; Ivan F Loncarevic; Cordula Bleck; Uwe Claussen; Thomas Liehr
A complex translocation event between the two homologues of chromosomes 5 leading to a del(5)(q21q33) as a sole aberration in a case clinically diagnosed as CML: characterization of the aberration by multicolor banding.
International journal of oncology 2002;20(6):1179-81.
2002: Ivan F Loncarevic; Jennifer Römer; Heike Starke; Anita Heller; Cordula Bleck; Monika Ziegler; Wolfgang Fiedler; Thomas Liehr; Joachim H Clement; Uwe Claussen
Heterogenic molecular basis for loss of ABL1-BCR transcription: deletions in der(9)t(9;22) and variants of standard t(9;22) in BCR-ABL1-positive chronic myeloid leukemia.
Genes, chromosomes & cancer 2002;34(2):193-200.
2002: Thomas Liehr; Anita Heller; Heike Starke; Uwe Claussen
FISH banding methods: applications in research and diagnostics.
Expert review of molecular diagnostics 2002;2(3):217-25.
2002: Thomas Liehr; Uwe Claussen
Current developments in human molecular cytogenetic techniques.
Current molecular medicine 2002;2(3):283-97.
2002: Thomas Liehr; Matthias Schmidt; Heike Starke; Monika Ziegler; Gabriele Kittner; Anita Heller; Nikolai Rubtsov; Vladimir Trifonov; Uwe Claussen
First case of trisomy 13 plus mosaic trisomy 1q.
Fetal diagnosis and therapy 2002;17(3):133-6.
2002: Alma Kuechler; Susann Neubauer; Gerhard G Grabenbauer; Uwe Claussen; Thomas Liehr; Rolf Sauer; Thomas G Wendt
Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity?
Strahlentherapie und Onkologie : Organ der Deutschen Röntgengesellschaft ... [et al] 2002;178(4):209-15.
2002: Anja Weise; Heike Starke; Anita Heller; Claussen Uwe; Thomas Liehr
Evidence for interphase DNA decondensation transverse to the chromosome axis: a multicolor banding analysis.
International journal of molecular medicine 2002;9(4):359-61.
2002: Thomas Liehr; Anita Heller; Heike Starke; Nikolai Rubtsov; Vladimir Trifonov; Kristin Mrasek; Anja Weise; Alma Kuechler; Uwe Claussen
Microdissection based high resolution multicolor banding for all 24 human chromosomes.
International journal of molecular medicine 2002;9(4):335-9.
2002: Uwe Claussen; Susanne Michel; Peter Mühlig; Martin Westermann; Ulrich-W Grummt; Katrin Kromeyer-Hauschild; Thomas Liehr
Demystifying chromosome preparation and the implications for the concept of chromosome condensation during mitosis.
Cytogenetic and genome research 2002;98(2-3):136-46.
2002: Anja Weise; Thomas Liehr; Thomas Efferth; Alma Kuechler; Erich Gebhart
Comparative M-FISH and CGH analyses in sensitive and drug-resistant human T-cell acute leukemia cell lines.
Cytogenetic and genome research 2002;98(2-3):118-25.
2002: Ralf Trappe; Detlef Böhm; Juergen Kohlhase; Anja Weise; Thomas Liehr; G Essers; Moritz Meins; Barbara Zoll; Iris Bartels; Peter Burfeind
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis.
Cytogenetic and genome research 2002;98(1):1-8.
2002: Thomas Liehr; Anja Weise; Anita Heller; Heike Starke; Kristin Mrasek; Alma Kuechler; Heinz-Ulrich G Weier; Uwe Claussen
Multicolor chromosome banding (MCB) with YAC/BAC-based probes and region-specific microdissection DNA libraries.
Cytogenetic and genome research 2002;97(1-2):43-50.
2001: Heike Starke; Gabriele Senger; M Kossakiewicz; H Tittelbach; D Rau; Nikolai Rubtsov; Vladimir Trifonov; Anita Heller; Isabell Hartmann; Uwe Claussen; Thomas Liehr
Maternal insertion of 18q11.2-q12.2 in 18p11.3 of the same chromosome analysed by microdissection and multicolour banding (MCB).
Prenatal diagnosis 2001;21(12):1049-52.
2001: Stefanie Scheil; Silke Brüderlein; Thomas Liehr; H Starke; J Herms; Michael Schulte; Peter Möller
Genome-wide analysis of sixteen chordomas by comparative genomic hybridization and cytogenetics of the first human chordoma cell line, U-CH1.
Genes, chromosomes & cancer 2001;32(3):203-11.
2001: Andreas Dufke; C Walczak; Thomas Liehr; Heike Starke; Vladimir Trifonov; Nikolai Rubtsov; Martin Schöning; Herbert Enders; Thomas Eggermann
Partial tetrasomy 12pter-12p12.3 in a girl with Pallister-Killian syndrome: extraordinary finding of an analphoid, inverted duplicated marker.
European journal of human genetics : EJHG 2001;9(8):572-6.
2001: Thomas Liehr; Volkmar Beensen; Heike Starke; R Hauschild; E Hempell; V Fritsche; C Hoppe; G Grosswendt; M Prechtel; Monika Ziegler; Uwe Claussen; Ferdinand von Eggeling
Tetrasomy 21 due to a de novo Robertsonian translocation t(14;21) and an additional free trisomy 21.
Clinical genetics 2001;60(1):83-5.
2001: A Bleichert; Wolfgang Fiedler; Uwe Claussen; Günther Ernst; Ivan F Loncarevic; Anita Heller; Thomas Liehr; Christa Kunert; Ferdinand von Eggeling
A long distance-PCR derived FISH probe detects a deletion between p15 and p16 in CML and T-ALL patients.
International journal of molecular medicine 2001;7(6):591-5.
2001: Heike Starke; Martin Raida; Vladimir Trifonov; Joachim H Clement; Ivan F Loncarevic; Anita Heller; Cordula Bleck; Angela Nietzel; Nikolai Rubtsov; Uwe Claussen; Thomas Liehr
Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia-negative chronic myelogenous leukaemia.
British journal of haematology 2001;113(2):435-8.
2001: Thomas Liehr; Volkmar Beensen; R Hauschild; Monika Ziegler; Isabell Hartmann; Heike Starke; Anita Heller; Christiane Kähler; M Schmidt; Wolfgang Reiber; M Hesse; Uwe Claussen
Pitfalls of rapid prenatal diagnosis using the interphase nucleus.
Prenatal diagnosis 2001;21(5):419-21.
2001: YANXING YU; A Heller; Thomas Liehr; Cynthia C Smith; Laure Aurelian
Expression analysis and chromosome location of a novel gene (H11) associated with the growth of human melanoma cells.
International journal of oncology 2001;18(5):905-11.
2001: Gilda Alves; A Heller; Wolfgang Fiedler; Mèrcia Mendes Campos; U Claussen; Antonio Augusto Ornellas; Thomas Liehr
Genetic imbalances in 26 cases of penile squamous cell carcinoma.
Genes, chromosomes & cancer 2001;31(1):48-53.
2001: Andreas Rump; Grit Kasper; C Hayes; G Wen; H Starke; Thomas Liehr; R Lehmann; D Lagemann; André Rosenthal
Complex arrangement of genes within a 220-kb region of double-duplicated DNA on human 2q37.1.
Genomics 2001;73(1):50-5.
2001: Thomas Liehr; Lawrence Reiter; James R Lupski; T Murakami; U Claussen; Bernd Rautenstrauss
Regional localization of 10 mariner transposon-like ESTs by means of FISH--evidence for a correlation with fragile sites.
Mammalian genome : official journal of the International Mammalian Genome Society 2001;12(4):326-8.
2001: Angela Nietzel; M Rocchi; Heike Starke; Anita Heller; Wolfgang Fiedler; I Wlodarska; Ivan F Loncarevic; Volkmar Beensen; Uwe Claussen; Thomas Liehr
A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH).
Human genetics 2001;108(3):199-204.
2001: S Stein; Thomas Liehr; Klaus Eschrich
Characterization of the mouse liver fructose-1,6-bisphosphatase gene.
Gene 2001;264(2):215-24.
2001: V Bureau; Séverine Marionneau; Anne THOMAS; Béatrice Le Moullac-Vaidye; Thomas Liehr; Jacques Le Pendu
Comparison of the three rat GDP-L-fucose:beta-D-galactoside 2-alpha-L-fucosyltransferases FTA, FTB and FTC.
European journal of biochemistry / FEBS 2001;268(4):1006-19.
2001: S Neubauer; Thomas Liehr
Interphase cytogenetics in paraffin-embedded ovarian tissue.
Methods in molecular medicine 2001;39():223-8.
2001: Thomas Liehr
Interphase cytogenetics in frozen ovarian tumor tissue.
Methods in molecular medicine 2001;39():215-21.
2001: Thomas Liehr
Cytogenetics of ovarian cancer technical overview.
Methods in molecular medicine 2001;39():207-13.
2001: Alma Kuechler; C R Mueller; Thomas Liehr; Uwe Claussen
Detection of microdeletions in the short arm of the X chromosome by chromosome stretching.
Cytogenetics and cell genetics 2001;95(1-2):12-6.
2001: Raimund W Kinne; Thomas Liehr; Volkmar Beensen; Elke Kunisch; Thomas Zimmermann; Heidrun Holland; R Pfeiffer; HD Stahl; Wolfgang Lungershausen; Gert Hein; Andreas Roth; Frank Emmrich; Uwe Claussen; Ursula G Froster
Mosaic chromosomal aberrations in synovial fibroblasts of patients with rheumatoid arthritis, osteoarthritis, and other inflammatory joint diseases.
Arthritis research 2001;3(5):319-30.
2001: Kristin Mrasek; Anita Heller; Nikolai Rubtsov; Vladimir Trifonov; Heike Starke; M Rocchi; Uwe Claussen; Thomas Liehr
Reconstruction of the female Gorilla gorilla karyotype using 25-color FISH and multicolor banding (MCB).
Cytogenetics and cell genetics 2001;93(3-4):242-8.
2000: Christian Kebelmann-Betzing; K Seeger; A Kulozik; G Henze; Thomas Liehr; A Heller; A Teigler-Schlegel
Secondary acute myeloid leukemia after treatment of acute monoblastic leukemia.
The New England journal of medicine 2000;343(25):1897-8.
2000: Sibylle Jakubiczka; Beate Mitulla; Thomas Liehr; Joachim Arnemann; H Lehrach; R Sudbrak; Markus Stumm; Peter Wieacker; Thomas Bettecken
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing.
Prenatal diagnosis 2000;20(10):842-6.
2000: Claudia Helmken; A Wetter; Sabine Rudnik-Schöneborn; Thomas Liehr; Klaus Zerres; Brunhilde Wirth
An essential SMN interacting protein (SIP1) is not involved in the phenotypic variability of spinal muscular atrophy (SMA).
European journal of human genetics : EJHG 2000;8(7):493-9.
2000: Anita Heller; Jörg Seidel; Axel Hübler; Heike Starke; Volkmar Beensen; Gabriele Senger; M Rocchi; Jutta Wirth; Ilse Chudoba; Uwe Claussen; Thomas Liehr
Molecular cytogenetic characterisation of partial trisomy 9q in a case with pyloric stenosis and a review.
Journal of medical genetics 2000;37(7):529-32.
2000: Harald Tillmann; S Stein; Thomas Liehr; Klaus Eschrich
Structure and chromosomal localization of the human and mouse muscle fructose-1,6-bisphosphatase genes.
Gene 2000;247(1-2):241-53.
2000: Axel Hübler; Jörg Seidel; Eberhard Kauf; Dirk Schramm; Volkmar Beensen; Anita Heller; Thomas Liehr; Felix Zintl
Insulin-like growth factor serum concentrations reflect insufficient growth in a hypoplastic infant with partial trisomy 9q in the 12th week of life.
Journal of pediatric endocrinology & metabolism : JPEM 2000;13(4):445-50.
2000: Anita Heller; Ilse Chudoba; C Bleck; Gabriele Senger; Uwe Claussen; Thomas Liehr
Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.
International journal of oncology 2000;16(3):461-8.
2000: Erich Gebhart; Thomas Liehr
Patterns of genomic imbalances in human solid tumors (Review).
International journal of oncology 2000;16(2):383-99.
2000: Andreas Dufke; Jörg Seidel; Martin Schöning; Marion Döbler-Neumann; Christine Kelbova; Thomas Liehr; Volkmar Beensen; C Backsch; Ute Klein-Vogler; Herbert Enders
Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome.
Cytogenetics and cell genetics 2000;91(1-4):81-4.
2000: Nikolai Rubtsov; Tatjana V Karamisheva; Natalia M Astakhova; Thomas Liehr; U Claussen; Natalia S Zhdanova
Zoo-FISH with region-specific paints for mink chromosome 5q: delineation of inter- and intrachromosomal rearrangements in human, pig, and fox.
Cytogenetics and cell genetics 2000;90(3-4):268-70.
2000: Kristina Bayerlein; Torsten Rith; Irmgard Verdorfer; Thomas Liehr; E Wolff; SC Girod; Erich Gebhart
I-FISH control of CGH-detected gain of DNA sequence copy number in oral squamous cell carcinomas (OSCC).
Anticancer research 2000;20(1A):427-32.
1999: Heike Starke; Isolde Schreyer; Christiane Kähler; Wolfgang Fiedler; Volkmar Beensen; Anita Heller; Angela Nietzel; Uwe Claussen; Thomas Liehr
Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.
Prenatal diagnosis 1999;19(12):1169-74.
1999: Kathrin Hühne; O Park; Thomas Liehr; Bernd Rautenstrauss
Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines.
Journal of neuroscience research 1999;58(5):624-31.
1999: Lawrence Reiter; Thomas Liehr; Bernd Rautenstrauss; H M Robertson; James R Lupski
Localization of mariner DNA transposons in the human genome by PRINS.
Genome research 1999;9(9):839-43.
1999: T Gebhart; Thomas Liehr
Clonality determined by fluorescence in situ hybridization of single-cell aberrations in hematopoietic neoplasias.
Cancer genetics and cytogenetics 1999;113(2):193-4.
1999: F von Deimling; JM Scharf; Thomas Liehr; Marcus Rothe; AR Kelter; Peter Albers; William F Dietrich; Louis Kunkel; Nicolas Wernert; Brunhilde Wirth
Human and mouse RAD17 genes: identification, localization, genomic structure and histological expression pattern in normal testis and seminoma.
Human genetics 1999;105(1-2):17-27.
1999: Thomas Liehr; Gregor Kuhlenbäumer; P Wulf; V Taylor; U Suter; Christine Van Broeckhoven; J R Lupski; U Claussen; Bernd Rautenstrauss
Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3.
Genomics 1999;58(1):106-8.
1999: M Dobler; J Schuh; Franklin Kiesewetter; Hermann Schell; Thomas Liehr; Erich Gebhart
Deletion monitoring in skin tumors by interphase-FISH using band-specific DNA probes.
International journal of oncology 1999;14(3):571-6.
1999: Thomas Liehr; Heike Starke; Volkmar Beensen; Christiane Kähler; M Harbich; Elke Brude; Monika Ziegler; Uwe Claussen
Translocation trisomy dup(21q) and free trisomy 21 can be distinguished by interphase-FISH.
International journal of molecular medicine 1999;3(1):11-4.
1998: Christina Fuchs; Thomas Liehr; Sevinc Ozbey; Arif B Ekici; H Grehl; Bernd Rautenstrauss
Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies: a SacI polymorphism in the proximal CMT1A-REP elements may lead to genetic misdiagnosis.
Neurogenetics 1998;2(1):43-6.
1998: A Taubald; Thomas Liehr; Jutta Ries; SC Girod; E Hassfurter; Erich Gebhart
CGH-detected DNA sequence copy number amplifications can be confirmed by interphase-FISH: new possiblities for prognostic approaches in oral squamous cell carcinomas.
International journal of molecular medicine 1998;2(5):555-60.
1998: S Neubauer; Thomas Liehr; S Birkenhake; Erich Gebhart; R Fietkau; R Sauer
Estimation of DNA single-strand breaks by single cells gel electrophoresis in tumor cells.
Genetic analysis : biomolecular engineering 1998;14(4):121-4.
1998: C Lange; Thomas Liehr; M Goen; E Gebhart; Bernhard Fleckenstein; Armin Ensser
New eukaryotic semaphorins with close homology to semaphorins of DNA viruses.
Genomics 1998;51(3):340-50.
1998: E Wolff; SC Girod; Thomas Liehr; U Vorderwülbecke; Jutta Ries; H Steininger; Erich Gebhart
Oral squamous cell carcinomas are characterized by a rather uniform pattern of genomic imbalances detected by comparative genomic hybridisation.
Oral oncology 1998;34(3):186-90.
1998: Erich Gebhart; Thomas Liehr; E Wolff; Jutta Ries; W Fiedler; H Steininger; S Koscielny; SC Girod
Pattern of genomic imbalances in oral squamous cell carcinomas with and without an increased copy number of 11q13.
International journal of oncology 1998;12(5):1151-5.
1998: Thomas Liehr; RA Pfeiffer; Udo Trautmann; Erich Gebhart
Centromeric alphoid DNA heteromorphisms of chromosome 22 revealed by FISH-technique.
Clinical genetics 1998;53(3):231-2.
1998: Bernd Rautenstrauss; Ulrich Zechner; Horst Hameister; H Grehl; Thomas Liehr
Expression pattern of the peripheral myelin protein 22kDa (PMP22) in neural and non-neural tissue types of adult wildtype and Trembler mice--a comparative study.
Journal of the peripheral nervous system : JPNS 1998;3(2):117-24.
1998: Bernd Rautenstrauss; Christina Fuchs; Arif B Ekici; Eva Nelis; Christine Van Broeckhoven; Thomas Liehr
Assay of transfection rate in insect cells on a single cell level.
Genetic analysis : biomolecular engineering 1998;14(3):103-4.
1998: Karin Michels-Rautenstrauss; Christian Y Mardin; W M Budde; Thomas Liehr; J Polansky; T Nguyen; V Timmerman; Christine Van Broeckhoven; Gottfried Naumann; RA Pfeiffer; Bernd Rautenstrauss
Juvenile open angle glaucoma: fine mapping of the TIGR gene to 1q24.3-q25.2 and mutation analysis.
Human genetics 1998;102(1):103-6.
1997: Thomas Liehr; H Grehl; Bernd Rautenstrauss
Accumulation of peripheral myelin protein 22 (PMP22) in onion bulbs of nerves biopsied from patients with different subtypes of Charcot-Marie-Tooth disease type 1.
Acta neuropathologica 1997;94(5):514-6.
1997: B Rautenstrauss; Thomas Liehr; U M Schrell; H Grehl
Use of FISH analysis for prostate tumors and other tissue types.
The American journal of pathology 1997;151(4):1171-2.
1997: Thomas Liehr; H Grehl; Bernd Rautenstrauss
Molecular diagnosis of PMP22-associated neuropathies using fluorescence in situ hybridization (FISH) on archival peripheral nerve tissue preparations.
Acta neuropathologica 1997;94(3):266-71.
1997: Thomas Liehr; F Hallouin; Bernd Rautenstrauss; J LePendu; M G Denis
Mapping of two different alpha-1,2-fucosyltransferase genes to rat chromosome 1q22-q31.
Mammalian genome : official journal of the International Mammalian Genome Society 1997;8(4):297-8.
1997: Bernd Rautenstrauss; Christina Fuchs; Thomas Liehr; H Grehl; T Murakami; James R Lupski
Visualization of the CMT1A duplication and HNPP deletion by FISH on stretched chromosome fibers.
Journal of the peripheral nervous system : JPNS 1997;2(4):319-22.
1997: H Grehl; Bernd Rautenstrauss; Thomas Liehr; Andreas Bickel; Arif B Ekici; KD Bathke; Bernhard Neundörfer
Clinical and morphological phenotype of HMSN 1A mosaicism.
Neuromuscular disorders : NMD 1997;7(1):27-31.
1997: Vincent Timmerman; Bernd Rautenstrauss; Lawrence Reiter; T Koeuth; Ann Löfgren; Thomas Liehr; Eva Nelis; KD Bathke; Peter De Jonghe; H Grehl; Jean-Jacques Martin; James R Lupski; Christine Van Broeckhoven
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent.
Journal of medical genetics 1997;34(1):43-9.
1996: Thomas Liehr; H Grehl; Bernd Rautenstrauss
A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissues.
Trends in genetics : TIG 1996;12(12):505-6.
1996: Felicitas Pröls; Thomas Liehr; M Marx; Bernd Rautenstrauss
Regional localization of rat microvascular endothelial differentiation gene 1 (Mdg1) to chromosome 6q16-23 by means of FISH.
Mammalian genome : official journal of the International Mammalian Genome Society 1996;7(11):867-8.
1996: Thomas Liehr; Bernd Rautenstrauss; H Grehl; K D Bathke; Arif B Ekici; Anita Rauch; Hans-Dieter Rott
Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion.
Human genetics 1996;98(1):22-8.
1995: D Baechner; Thomas Liehr; H Hameister; H Altenberger; H Grehl; Ueli Suter; Bernd Rautenstrauss
Widespread expression of the peripheral myelin protein-22 gene (PMP22) in neural and non-neural tissues during murine development.
Journal of neuroscience research 1995;42(6):733-41.
1995: Thomas Liehr; Arif B Ekici; R Hillenbrand; Bernd Rautenstrauss
Regional localization of rat myelin protein zero Mpz gene to chromosome 13q24-25 by means of FISH.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(11):824-5.
1995: Thomas Liehr; H Grehl; Bernd Rautenstrauss
FISH analysis of interphase nuclei extracted from paraffin-embedded tissue.
Trends in genetics : TIG 1995;11(10):377-8.
1995: Thomas Liehr; Bernd Rautenstrauss
Regional localization of rat peripheral myelin protein 22 (Pmp22) gene to chromosome 10q22 by FISH.
Mammalian genome : official journal of the International Mammalian Genome Society 1995;6(7):489.
1995: Erich Gebhart; Thomas Liehr; P Harrer; S Reichardt; G Schmitt; K Thoma; Martin Gramatzki; Udo Trautmann
Determination by interphase-FISH of the clonality of aberrant karyotypes in human hematopoietic neoplasias.
Leukemia & lymphoma 1995;17(3-4):295-302.
1995: Thomas Liehr; H Altenberger; Bernd Rautenstrauss
Rapid fluorescence in situ detection of heterologous expression in E. coli and counterstaining with diamidinophenylindol.
Trends in genetics : TIG 1995;11(4):129.
1994: Udo Trautmann; Martin Gramatzki; M Krauss; A Friz; Thomas Liehr; Erich Gebhart
Tetrasomy 8 as a clonal anomaly in myeloid neoplasias.
Cancer genetics and cytogenetics 1994;72(2):101-4.
1994: Thomas Liehr; A Stübinger; K Thoma; H A Tulusan; Erich Gebhart
Comparative interphase cytogenetics using FISH on human ovarian carcinomas.
Anticancer research 1994;14(1A):183-8.
1993: Erich Gebhart; Udo Trautmann; S Reichardt; Thomas Liehr
Chromosomal heterogeneity of aneuploid leukemic cell populations detected by conventional karyotyping and by fluorescence in situ hybridization (FISH).
Anticancer research 1993;13(5C):1857-62.
1992: Thomas Liehr; RA Pfeiffer; Udo Trautmann
Typical and partial cat eye syndrome: identification of the marker chromosome by FISH.
Clinical genetics 1992;42(2):91-6.
1992: Anita Rauch; RA Pfeiffer; Udo Trautmann; Thomas Liehr; Hans-Dieter Rott; R Ulmer
A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH).
Clinical genetics 1992;42(2):84-90.