Thomas Liehr

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

Research Profile (preview)

Procedures

Disorders

Physiology

Anatomy

Concepts & Ideas

Interphase

Sign-in to see full Profile

Sign-in to see all Coauthors

Publications

TOP 3
de Figueiredo Amanda Faria; Mkrtchyan Hasmik; Liehr Thomas; Soares Ventura Eliane Maria; de Jesus Marques-Salles Terezinha; Santos Neide; Ribeiro Raul Corrêa; Abdelhay Eliana; Macedo Silva Maria Luiza
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.
Manvelyan Marina; Kempf Philipp; Weise Anja; Mrasek Kristin; Heller Anita; Lier Amelie; Höffken Klaus; Fricke Hans-Jörg; Sayer Herbert G; Liehr Thomas; Mkrtchyan Hasmik
Preferred co-localization of chromosome 8 and 21 in myeloid bone marrow cells detected by three dimensional molecular cytogenetics.
Manolakos Emmanouil; Vetro Annalisa; Kitmirides Stylianos; Papoulidis Ioannis; Kosyakova Nadezda; Mrasek Kristin; Weise Anja; Agapitos Emmanouil; Orru Sandro; Peitsidis Panagiotis; Liehr Thomas; Petersen Michael B
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH.

Sign-in to see all Publications

Sign in free and see...

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the visualized research activity
of experts around the globe

Sign-in to see more

Geonetwork of Thomas Liehr (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

Sign-in to see more

All Publications

2009: de Figueiredo Amanda Faria; Mkrtchyan Hasmik; Liehr Thomas; Soares Ventura Eliane Maria; de Jesus Marques-Salles Terezinha; Santos Neide; Ribeiro Raul Corrêa; Abdelhay Eliana; Macedo Silva Maria Luiza
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: Manvelyan Marina; Kempf Philipp; Weise Anja; Mrasek Kristin; Heller Anita; Lier Amelie; Höffken Klaus; Fricke Hans-Jörg; Sayer Herbert G; Liehr Thomas; Mkrtchyan Hasmik
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: Manolakos Emmanouil; Vetro Annalisa; Kitmirides Stylianos; Papoulidis Ioannis; Kosyakova Nadezda; Mrasek Kristin; Weise Anja; Agapitos Emmanouil; Orru Sandro; Peitsidis Panagiotis; Liehr Thomas; Petersen Michael B
Prenatal diagnosis of a fetus with ring chromosome 15 characterized by array-CGH.
Prenatal diagnosis 2009;29(9):884-8.
2009: Uroz L; Liehr T; Mrasek K; Templado C
Centromere-specific multicolour fluorescence in situ hybridization on human spermatocyte I and II metaphases.
Human reproduction (Oxford, England) 2009;24(8):2029-33.
2009: Iourov Ivan Y; Vorsanova Svetlana G; Liehr Thomas; Kolotii Alexei D; Yurov Yuri B
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: Polityko Anna D; Khurs Olga M; Kulpanovich Anna I; Mosse Konstantin A; Solntsava Angelica V; Rumyantseva Natalia V; Naumchik Irina V; Liehr Thomas; Weise Anja; Mkrtchyan Hasmik
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: Liehr Thomas; Ewers Elisabeth; Kosyakova Nadezda; Klaschka Vivian; Rietz Franziska; Wagner Rebecca; Weise Anja
Handling small supernumerary marker chromosomes in prenatal diagnostics.
Expert review of molecular diagnostics 2009;9(4):317-24.
2009: de Jesus Marques-Salles Terezinha; Liehr Thomas; Mkrtchyan Hasmik; Raimondi Susana C; Tavares de Souza Mariana; de Figueiredo Amanda Faria; Rouxinol Soraia; Jordy Macedo Fernanda C; Abdelhay Eliana; Santos Neide; Macedo Silva Maria Luiza
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: Gross Madeleine; Mkrtchyan Hasmik; Glaser Melanie; Fricke Hans Jörg; Höffken Klaus; Heller Anita; Weise Anja; Liehr Thomas
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: Al Achkar Walid; Wafa Abdulsamad; Mkrtchyan Hasmik; Moassass Faten; Liehr Thomas
Novel complex translocation involving 5 different chromosomes in a chronic myeloid leukemia with Philadelphia chromosome: a case report.
Molecular Cytogenetics 2009;2():21.
2009: Melo J B; Matoso E; Polityko A; Saraiva J; Backx L; Vermeesch J R; Kosyakova N; Ewers E; Liehr T; Carreira I M
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: Erlecke Jörn; Hartmann Isabell; Hoffmann Martin; Kroll Torsten; Starke Heike; Heller Anita; Gloria Alexander; Sayer Herbert G; Johannes Tilman; Claussen Uwe; Liehr Thomas; Loncarevic Ivan F
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: Liehr T; Stumm M; Wegner R D; Bhatt S; Hickmann P; Patsalis P C; Meins M; Morlot S; Klaschka V; Ewers E; Hinreiner S; Mrasek K; Kosyakova N; Cai W W; Cheung S W; Weise A
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: Auber Bernd; Bruemmer Verena; Zoll Barbara; Burfeind Peter; Boehm Detlef; Liehr Thomas; Brockmann Knut; Wilichowski Ekkehard; Argyriou Loukas; Bartels Iris
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: Kitsiou-Tzeli Sofia; Manolakos Emmanouil; Lagou Magdalini; Anagnostopoulou Katerina; Kontodiou Maria; Kosyakova Nadezda; Ewers Elisabeth; Weise Anja; Garas Antonios; Orru Sandro; Liehr Thomas; Metaxotou Aikaterini
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.
Molecular Cytogenetics 2009;2():8.
2009: Silva Maria Luiza Macedo; do Socorro Pombo-de-Oliveira Maria; Raimondi Susana C; Mkrtchyan Hasmik; Abdelhay Eliana; de Figueiredo Amanda Faria; de Souza Mariana Tavares; Garcia Daniela Ribeiro Ney; de Ventura Eliane Maria Soares; de Sousa Adriana Martins; Liehr Thomas
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: Kosyakova Nadezda; Weise Anja; Mrasek Kristin; Claussen Uwe; Liehr Thomas; Nelle Heike
The hierarchically organized splitting of chromosomal bands for all human chromosomes.
Molecular Cytogenetics 2009;2():4.
2009: Kitsiou-Tzeli Sofia; Manolakos Emmanouil; Lagou Magdalini; Kontodiou Maria; Kosyakova Nadezda; Ewers Elisabeth; Weise Anja; Garas Antonios; Orru Sandro; Liehr Thomas; Metaxotou Aikaterini
Characterization of a prenatally assessed de novo supernumerary minute ring chromosome 20 in a phenotypically normal male.
Molecular Cytogenetics 2009;2():1.
2008: Mkrtchyan Hasmik; Ghazaryan Seda; Avetisyan Gayane; Hovhannisyan Anna; Muradyan Laura; Daghbashyan Smbat; Karst Constanze; Gross Madeleine; Hinreiner Sophie; Aroutiounian Rouben; Liehr Thomas
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: Manvelyan Marina; Riegel Mariluce; Santos Monica; Fuster Carme; Pellestor Franck; Mazaurik Marie-Luise; Schulze Bernt; Polityko Anna; Tittelbach Hanne; Reising-Ackermann Gisela; Belitz Britta; Hehr Ute; Kelbova Christina; Volleth Marianne; Gödde Elisabeth; Anderson Jasen; Küpferling Peter; Köhler Sigrid; Duba Hans-Christoph; Dufke Andreas; Aktas Dilek; Martin Thomas; Schreyer Isolde; Ewers Elisabeth; Reich Daniela; Mrasek Kristin; Weise Anja; Liehr Thomas
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: Weise Anja; Mrasek Kristin; Fickelscher Ina; Claussen Uwe; Cheung Sau Wai; Cai Wei Wen; Liehr Thomas; Kosyakova Nadezda
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: Macedo Silva Maria Luiza; Raimondi Susana C; Abdelhay Eliana; Gross Madeleine; Mkrtchyan Hasmik; de Figueiredo Amanda Faria; Ribeiro Raul C; de Jesus Marques-Salles Terezinha; Sobral Elaine S; Gerardin Land Marcelo Poirot; Liehr Thomas
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: Weise A; Gross M; Mrasek K; Mkrtchyan H; Horsthemke B; Jonsrud C; Von Eggeling F; Hinreiner S; Witthuhn V; Claussen U; Liehr T
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: Balikova Irina; Martens Kevin; Melotte Cindy; Amyere Mustapha; Van Vooren Steven; Moreau Yves; Vetrie David; Fiegler Heike; Carter Nigel P; Liehr Thomas; Vikkula Miikka; Matthijs Gert; Fryns Jean-Pierre; Casteels Ingele; Devriendt Koen; Vermeesch Joris Robert
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: Manvelyan Marina; Hunstig Friederike; Bhatt Samarth; Mrasek Kristin; Pellestor Franck; Weise Anja; Simonyan Isabella; Aroutiounian Rouben; Liehr Thomas
Chromosome distribution in human sperm - a 3D multicolor banding-study.
Molecular Cytogenetics 2008;1():25.
2008: Manolakos Emmanouil; Kosyakova Nadezda; Thomaidis Loreta; Neroutsou Rozita; Weise Anja; Mihalatos Markos; Orru Sandro; Kokotas Haris; Kitsos George; Liehr Thomas; Petersen Michael B
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(1):24.
2008: Mrasek K; Krüger G; Bauer I; Müller-Navia J; Liehr T; Weise A
A new unbalanced chromosomal abnormality in 1q31.1 to 1q32 without phenotypic consequences.
Cytogenetic and genome research 2008;121(3-4):286-7.
2008: Vorsanova Svetlana G; Iourov Ivan Y; Voinova-Ulas Victoria Y; Weise Anja; Monakhov Victor V; Kolotii Alexei D; Soloviev Ilia V; Novikov Petr V; Yurov Yuri B; Liehr Thomas
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(1):13.
2008: Liehr Thomas; Mrasek Kristin; Kosyakova Nadezda; Ogilvie Caroline Mackie; Vermeesch Joris; Trifonov Vladimir; Rubtsov Nikolai
Small supernumerary marker chromosomes (sSMC) in humans; are there B chromosomes hidden among them.
Molecular Cytogenetics 2008;1(1):12.
2008: Trifonov Vladimir; Fluri Simon; Binkert Franz; Nandini Adayapalam; Anderson Jasen; Rodriguez Laura; Gross Madeleine; Kosyakova Nadezda; Mkrtchyan Hasmik; Ewers Elisabeth; Reich Daniela; Weise Anja; Liehr Thomas
Complex rearranged small supernumerary marker chromosomes (sSMC), three new cases; evidence for an underestimated entity?
Molecular Cytogenetics 2008;1(1):6.
2008: Manvelyan Marina; Hunstig Friederike; Mrasek Kristin; Bhatt Samarth; Pellestor Franck; Weise Anja; Liehr Thomas
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(1):9.
2008: Weise Anja; Liehr Thomas
Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH).
Methods in molecular biology (Clifton, N.J.) 2008;444():39-47.
2008: Liehr Thomas
Characterization of prenatally assessed de novo small supernumerary marker chromosomes by molecular cytogenetics.
Methods in molecular biology (Clifton, N.J.) 2008;444():27-38.
2007: Carreira Isabel M; Mascarenhas Alexandra; Matoso Eunice; Couceiro Ana B; Ramos Lina; Dufke Andreas; Mazauric Marie; Stressig Rüdiger; Kosyakova Nadezda; Melo Joana B; Liehr Thomas
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: Fickelscher Ina; Liehr Thomas; Watts Kathryn; Bryant Victoria; Barber John C K; Heidemann Simone; Siebert Reiner; Hertz Jens Michael; Tumer Zeynep; Simon Thomas N
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: Santos Mònica; Mrasek Kristin; Rigola Maria Angels; Starke Heike; Liehr Thomas; Fuster Carme
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: Utine G E; Aktas D; Alanay Y; Gücer S; Tuncbilek E; Mrasek K; Liehr T
Distal partial trisomy 1q: report of two cases and a review of the literature.
Prenatal diagnosis 2007;27(9):865-71.
2007: Fickelscher Ina; Starke Heike; Schulze Eberhard; Ernst Günther; Kosyakova Nadezda; Mkrtchyan Hasmik; MacDermont Kay; Sebire Neil; Liehr Thomas
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: Rosenhahn Julia; Weise Anja; Michel Susanne; Hennig Katrin; Hartmann Isabell; Schiefner Jana; Schubert Katrin; Liehr Thomas; von Eggeling Ferdinand; Loncarevic Ivan F
Cytogenetic characterisation and proteomic profiling of the Imatinib-resistant cell line KCL22-R.
International journal of oncology 2007;31(1):121-8.
2007: Manvelyan M; Schreyer I; Höls-Herpertz I; Köhler S; Niemann R; Hehr U; Belitz B; Bartels I; Götz J; Huhle D; Kossakiewicz M; Tittelbach H; Neubauer S; Polityko A; Mazauric M-L; Wegner R; Stumm M; Küpferling P; Süss F; Kunze H; Weise A; Liehr T; Mrasek K
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: Tönnies Holger; Pietrzak Joanna; Bocian Ewa; MacDermont Kay; Kuechler Alma; Belitz Britta; Trautmann Udo; Schmidt Angela; Schulze Berndt; Rodríguez Laura; Binkert Franz; Yardin Catharine; Kosyakova Nadezda; Volleth Marianne; Mkrtchyan Hasmik; Schreyer Isolde; von Eggeling Ferdinand; Weise Anja; Mrasek Kristin; Liehr Thomas
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: Sauter S M; Böhm Detlef; Bartels Iris; Burfeind Peter; Laccone Franco A; Neesen Jürgen; Wilken Bernd; Liehr Thomas; Zoll Barbara
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: Liehr Thomas; Weise Anja
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: Glei Michael; Schaeferhenrich Anja; Claussen Uwe; Kuechler Alma; Liehr Thomas; Weise Anja; Marian Brigitte; Sendt Wolfgang; Pool-Zobel Beatrice L
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: Weise Anja; Gross Madeleine; Schmidt Sabine; Reichelt Franziska; Claussen Uwe; Liehr Thomas
New aspects of chromosomal evolution in the gorilla and the orangutan.
International journal of molecular medicine 2007;19(3):437-43.
2007: Bartels Iris; Starke Heike; Argyriou Loukas; Sauter Simone M; Zoll Barbara; Liehr Thomas
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: Liehr T; Mrasek K; Hinreiner S; Reich D; Ewers E; Bartels I; Seidel J; Emmanuil N; Petesen M; Polityko A; Dufke A; Iourov I; Trifonov V; Vermeesch J; Weise A
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: Sun F; Oliver-Bonet M; Liehr T; Starke H; Ko E; Rademaker A; Martin R H
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: Felka T; Lemke J; Lemke C; Michel S; Liehr T; Claussen U
DNA degradation during maturation of erythrocytes - molecular cytogenetic characterization of Howell-Jolly bodies.
Cytogenetic and genome research 2007;119(1-2):2-8.
2007: Liehr T; Utine G E; Trautmann U; Rauch A; Kuechler A; Pietrzak J; Bocian E; Kosyakova N; Mrasek K; Boduroglu K; Weise A; Aktas D
Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature.
Cytogenetic and genome research 2007;118(1):31-7.
2007: Pietrzak Joanna; Mrasek Kristin; Obersztyn Ewa; Stankiewicz Pawel; Kosyakova Nadezda; Weise Anja; Cheung Sau Wai; Cai Wei Wen; von Eggeling Ferdinand; Mazurczak Tadeusz; Bocian Ewa; Liehr Thomas
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: Backx L; Van Esch H; Melotte C; Kosyakova N; Starke H; Frijns J-P; Liehr T; Vermeesch J R
Array painting using microdissected chromosomes to map chromosomal breakpoints.
Cytogenetic and genome research 2007;116(3):158-66.
2006: Mitter Diana; Buiting Karin; von Eggeling Ferdinand; Kuechler Alma; Liehr Thomas; Mau-Holzmann Ulrike Angelika; Prott Eva-Christina; Wieczorek Dagmar; Gillessen-Kaesbach Gabriele
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: Sun Fei; Oliver-Bonet M; Liehr T; Starke H; Turek P; Ko E; Rademaker A; Martin R H
Analysis of non-crossover bivalents in pachytene cells from 10 normal men.
Human reproduction (Oxford, England) 2006;21(9):2335-9.
2006: Sun Fei; Oliver-Bonet Maria; Liehr Thomas; Starke Heike; Turek Paul; Ko Evelyn; Rademaker Alfred; Martin Renée H
Variation in MLH1 distribution in recombination maps for individual chromosomes from human males.
Human molecular genetics 2006;15(15):2376-91.
2006: Karst Constanze; Gross Madeleine; Haase Detlef; Wedding Ulrich; Höffken Klaus; Liehr Thomas; Mkrtchyan Hasmik
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: Stankiewicz Pawel; Kuechler Alma; Eller C Daniel; Sahoo Trilochan; Baldermann Christiane; Lieser Ulla; Hesse Martin; Gläser Christiane; Hagemann Monika; Yatsenko Svetlana A; Liehr Thomas; Horsthemke Bernhard; Claussen Uwe; Marahrens York; Lupski James R; Hansmann Ingo
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: Karst Constanze; Trifonov Vladimir; Romanenko Svetlana A; Claussen Uwe; Mrasek Kristin; Michel Susanne; Avner Philip; Liehr Thomas
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: Liehr Thomas; Gross Madeleine; Karst Constanze; Glaser Melanie; Mrasek Kristin; Starke Heike; Weise Anja; Mkrtchyan Hasmik; Kuechler Alma
FISH banding in tumor cytogenetics.
Cancer genetics and cytogenetics 2006;164(1):88-9.
2006: Liehr Thomas; Starke Heike; Senger Gabriele; Melotte Cindy; Weise Anja; Vermeesch Joris Robert
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: Liehr Thomas
Application of yeast artificial chromosomes in fluorescence in situ hybridization.
Methods in molecular biology (Clifton, N.J.) 2006;349():175-86.
2006: Brecevic L; Michel S; Starke H; Müller K; Kosyakova N; Mrasek K; Weise A; Liehr T
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: Mkrtchyan H; Glaser M; Gross M; Wedding U; Hoffken K; Liehr T; Karst C; Aroutiounian R
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: Liehr T; Starke H; Heller A; Kosyakova N; Mrasek K; Gross M; Karst C; Steinhaeuser U; Hunstig F; Fickelscher I; Kuechler A; Trifonov V; Romanenko S A; Weise A
Multicolor fluorescence in situ hybridization (FISH) applied to FISH-banding.
Cytogenetic and genome research 2006;114(3-4):240-4.
2006: Gross M; Starke H; Trifonov V; Claussen U; Liehr T; Weise A
A molecular cytogenetic study of chromosome evolution in chimpanzee.
Cytogenetic and genome research 2006;112(1-2):67-75.
2006: Liehr T; Mrasek K; Weise A; Dufke A; Rodríguez L; Martínez Guardia N; Sanchís A; Vermeesch J R; Ramel C; Polityko A; Haas O A; Anderson J; Claussen U; von Eggeling F; Starke H
Small supernumerary marker chromosomes--progress towards a genotype-phenotype correlation.
Cytogenetic and genome research 2006;112(1-2):23-34.
2005: Gutiérrez-Mateo C; Benet J; Starke H; Oliver-Bonet M; Munné S; Liehr T; Navarro J
Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique.
Human reproduction (Oxford, England) 2005;20(12):3395-401.
2005: Sun Fei; Oliver-Bonet Maria; Liehr Thomas; Starke Heike; Trpkov Kiril; Ko Evelyn; Rademaker Alfred; Martin Renée H
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: Kautenburger Tanja; Beyer-Sehlmeyer Gabriele; Festag Grit; Haag Natja; Kühler Stephanie; Küchler Alma; Weise Anja; Marian Brigitte; Peters Wilbert H M; Liehr Thomas; Claussen Uwe; Pool-Zobel Beatrice L
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: Barber John C K; Maloney Viv; Hollox Edward J; Stuke-Sontheimer Annegret; du Bois Gabi; Daumiller Eva; Klein-Vogler Ute; Dufke Andreas; Armour John A L; Liehr Thomas
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: Weise Anja; Liehr Thomas; Claussen Uwe; Halbhuber Karl-Jürgen
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: Karst Constanze; Heller Anita; Claussen Uwe; Gebhart Erich; Liehr Thomas
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: von Beust G; Sauter S M; Liehr T; Burfeind P; Bartels I; Starke H; von Eggeling F; Zoll B
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: Vermeesch Joris Robert; Melotte Cindy; Salden Ivo; Riegel Mariluce; Trifnov Vladimir; Polityko Anna; Rumyantseva Natalia; Naumchik Irina; Starke Heike; Matthijs Gert; Schinzel Albert; Fryns Jean-Pierre; Liehr Thomas
Tetrasomy 12pter-12p13.31 in a girl with partial Pallister-Killian syndrome phenotype.
European journal of medical genetics 2005;48(3):319-27.
2005: Schmidt S; Claussen U; Liehr T; Weise A
Evolution versus constitution: differences in chromosomal inversion.
Human genetics 2005;117(2-3):213-9.
2005: Trifonov Vladimir; Karst Constanze; Claussen Uwe; Mrasek Kristin; Michel Susanne; Avner Philip; Liehr Thomas
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: Liehr Thomas; Brude Elke; Gillessen-Kaesbach Gabriele; König Rainer; Mrasek Kristin; von Eggeling Ferdinand; Starke Heike
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: Mrasek Kristin; Starke Heike; Liehr Thomas
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: Schreyer Isolde; Neumann Annett; Beensen Volkmar; Eichhorn Karl-Heinz; Heller Anita; Claussen Uwe; Liehr Thomas
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: Starke Heike; Mrasek Kristin; Liehr Thomas
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: Kuechler Alma; Ziegler Monika; Blank Cornelia; Rommel Birgit; Bullerdiek Joern; Ahrens Jochen; Claussen Uwe; Liehr Thomas
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: Trimborn M; Liehr T; Belitz B; Pfeiffer L; Varon R; Neitzel H; Tönnies H
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: Liehr Thomas; Ziegler Monika
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: Oliver-Bonet M; Benet J; Sun F; Navarro J; Abad C; Liehr T; Starke H; Greene C; Ko E; Martin R H
Meiotic studies in two human reciprocal translocations and their association with spermatogenic failure.
Human reproduction (Oxford, England) 2005;20(3):683-8.
2005: Barber John C K; Thomas N Simon; Collinson Morag N; Dennis Nick R; Liehr Thomas; Weise Anja; Belitz Britta; Pfeiffer Lutz; Kirchhoff Maria; Krag-Olsen Bente; Lundsteen Claes
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: Liehr T; Mrasek K; Starke H; Claussen U; Schreiber G
Unusual small supernumerary marker chromosome (sSMC) 9 in a Klinefelter patient.
Cytogenetic and genome research 2005;111(2):179-81.
2005: Polityko A; Starke H; Rumyantseva N; Claussen U; Liehr T; Raskin S
Three cases with rare interstitial rearrangements of chromosome 1 characterized by multicolor banding.
Cytogenetic and genome research 2005;111(2):171-4.
2005: Weise A; Starke H; Mrasek K; Claussen U; Liehr T
New insights into the evolution of chromosome 1.
Cytogenetic and genome research 2005;108(1-3):217-22.
2004: Liehr Thomas; Heller Anita; Eichhorn Karl-Heinz; Beensen Volkmar; Schulze Eberhart; Starke Heike; Claussen Uwe; Schreyer Isolde
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: Polityko Anna; Maltseva Olga; Rumyantseva Natalia; Khurs Olga; Seidel Jörg; Claussen Uwe; Weise Anja; Liehr Thomas; Starke Heike
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: Gebhart Erich; Ries Jutta; Wiltfang Jörg; Liehr Thomas; Efferth Thomas
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: Zumkeller Walter; Volleth Marianne; Muschke Petra; Tönnies Holger; Heller Anita; Liehr Thomas; Wieacker Peter; Stumm Markus
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: Codina-Pascual M; Oliver-Bonet M; Navarro J; Starke H; Liehr T; Gutiérrez-Mateo C; Sánchez-García J F; Arango O; Egozcue J; Benet J
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: Camps Jordi; Mrasek Kristin; Prat Esther; Weise Anja; Starke Heike; Egozcue Josep; Miró Rosa; Liehr Thomas
Molecular cytogenetic characterisation of the colorectal cancer cell line SW480.
Oncology reports 2004;11(6):1215-8.
2004: Keller Ulrike; Kuechler Alma; Liehr Thomas; Müller Elisabeth; Grabenbauer Gerhard; Sauer Rolf; Distel Luitpold
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: Boehm Detlef; Herold Sabine; Kuechler Alma; Liehr Thomas; Laccone Franco
Rapid detection of subtelomeric deletion/duplication by novel real-time quantitative PCR using SYBR-green dye.
Human mutation 2004;23(4):368-78.
2004: Sun Fei; Oliver-Bonet Maria; Liehr Thomas; Starke Heike; Ko Evelyn; Rademaker Alfred; Navarro Joaquima; Benet Jordi; Martin Renée H
Human male recombination maps for individual chromosomes.
American journal of human genetics 2004;74(3):521-31.
2004: Liehr T; Starke H; Weise A; Lehrer H; Claussen U
Multicolor FISH probe sets and their applications.
Histology and histopathology 2004;19(1):229-37.
2004: Heller Anita; Loncarevic Ivan F; Glaser Melanie; Gebhart Erich; Trautmann Udo; Claussen Uwe; Liehr Thomas
Breakpoint differentiation in chromosomal aberrations of hematological malignancies: Identification of 33 previously unrecorded breakpoints.
International journal of oncology 2004;24(1):127-36.
2004: Heller Anita; Fricke Hans-Joerg; Starke Heike; Loncarevic Ivan F; Claussen Uwe; Liehr Thomas
Characterization of a highly aberrant plasma cell leukemia karyotype: a case report.
Oncology reports 2004;11(1):89-92.
2004: Liehr T; Claussen U; Starke H
Small supernumerary marker chromosomes (sSMC) in humans.
Cytogenetic and genome research 2004;107(1-2):55-67.
2004: Lehrer H; Weise A; Michel S; Starke H; Mrasek K; Heller A; Kuechler A; Claussen U; Liehr T
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: Liehr T; Hickmann G; Kozlowski P; Claussen U; Starke H
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.
2003: Starke Heike; Nietzel Angela; Weise Anja; Heller Anita; Mrasek Kristin; Belitz Britta; Kelbova Christine; Volleth Marianne; Albrecht Beate; Mitulla Beate; Trappe Ralf; Bartels Iris; Adolph Sabine; Dufke Andreas; Singer Sylke; Stumm Markus; Wegner Rolf-Dieter; Seidel Jörg; Schmidt Angela; Kuechler Alma; Schreyer Isolde; Claussen Uwe; von Eggeling Ferdinand; Liehr Thomas
Small supernumerary marker chromosomes (SMCs): genotype-phenotype correlation and classification.
Human genetics 2003;114(1):51-67.
2003: Oliver-Bonet Maria; Liehr Thomas; Nietzel Angela; Heller Anita; Starke Heike; Claussen Uwe; Codina-Pascual Montserrat; Pujol Aïda; Abad Carlos; Egozcue Josep; Navarro Joaquima; Benet Jordi
Karyotyping of human synaptonemal complexes by cenM-FISH.
European journal of human genetics : EJHG 2003;11(11):879-83.
2003: Heller Anita; Trifonov Vladimir; Rubtsov Nikolai; Sauerbrey Axel; Starke Heike; Loncarevic Ivan F; Claussen Uwe; Liehr Thomas
Complex chromosomal rearrangements in a secondary acute myeloblastic leukemia after chemotherapy in TRAPS.
Oncology reports 2003;10(6):1789-92.
2003: Heller Anita; Brecevic Lukrecija; Glaser Melanie; Loncarevic Ivan; Gebhart Erich; Claussen Uwe; Liehr Thomas
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: Starke Heike; Mitulla Beate; Beensen Volkmar; Trifonov Vladimir; Rubtsov Nikolai; Heller Anita; Ziegler Monika; Neumann Annett; Claussen Uwe; Liehr Thomas
First postnatal case of mosaic del(22)/r(22).
Prenatal diagnosis 2003;23(9):765-7.
2003: Kinne Raimund W; Kunisch Elke; Beensen Volkmar; Zimmermann Thomas; Emmrich Frank; Petrow Peter; Lungershausen Wolfgang; Hein Gert; Braun Rudolf K; Foerster Martin; Kroegel Claus; Winter Rando; Liesaus Eckehard; Fuhrmann Renée A; Roth Andreas; Claussen Uwe; Liehr Thomas
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: Seidel Jörg; Heller Anita; Senger Gabriele; Starke Heike; Chudoba Ilse; Kelbova Christina; Tönnies Holger; Neitzel Heidemarie; Haase Claudia; Beensen Volkmar; Zintl Felix; Claussen Uwe; Liehr Thomas
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: Sauter S; von Beust G; Burfeind P; Weise A; Starke H; Liehr T; Zoll B
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: Liehr T; Ziegler M; Starke H; Heller A; Kuechler A; Kittner G; Beensen V; Seidel J; Hässler H; Müsebeck J; Claussen U
Conspicuous GTG-banding results of the centromere-near region can be caused by alphoid DNA heteromorphism.
Clinical genetics 2003;64(2):166-7.
2003: Mrasek Kristin; Heller Anita; Rubtsov Nikolai; Trifonov Vladimir; Starke Heike; Claussen Uwe; Liehr Thomas
Detailed Hylobates lar karyotype defined by 25-color FISH and multicolor banding.
International journal of molecular medicine 2003;12(2):139-46.
2003: Kuechler Alma; Dreidax Mareike; Pigorsch Steffi U; Liehr Thomas; Claussen Uwe; Wendt Thomas G; Dunst Jürgen
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: Heller Anita; Rubtsov Nikolai; Kytölä Soili; Karamysheva Tatyana V; Sablina Olga V; Degtyareva Marina M; Starke Heike; Metzke Hermann; Claussen Uwe; Liehr Thomas
Highly complex karyotypic changes in acute myelogenous leukemia: a case report.
International journal of oncology 2003;23(1):139-43.
2003: Trifonov Vladimir; Seidel Jörg; Starke Heike; Martina Prechtel; Beensen Volkmar; Ziegler Monika; Hartmann Isabell; Heller Anita; Nietzel Angela; Claussen Uwe; Liehr Thomas
Enlarged chromosome 13 p-arm hiding a cryptic partial trisomy 6p22.2-pter.
Prenatal diagnosis 2003;23(5):427-30.
2003: Schaeferhenrich Anja; Beyer-Sehlmeyer Gabriele; Festag Grit; Kuechler Alma; Haag Natja; Weise Anja; Liehr Thomas; Claussen Uwe; Marian Brigitte; Sendt Wolfgang; Scheele Johannes; Pool-Zobel Beatrice Louise
Human adenoma cells are highly susceptible to the genotoxic action of 4-hydroxy-2-nonenal.
Mutation research 2003;526(1-2):19-32.
2003: Liehr T; Starke H; Heller A; Weise A; Beensen V; Senger G; Kittner G; Prechtel M; Claussen U; Seidel J
Evidence for a new microdeletion syndrome in 15q21.
International journal of molecular medicine 2003;11(5):575-7.
2003: Schaeferhenrich A; Sendt W; Scheele J; Kuechler A; Liehr T; Claussen U; Rapp A; Greulich K-O; Pool-Zobel B L
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: Weise Anja; Harbarth Peter; Claussen Uwe; Liehr Thomas
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: Nietzel A; Albrecht B; Starke H; Heller A; Gillessen-Kaesbach G; Claussen U; Liehr T
Partial hexasomy 15pter-->15q13 including SNRPN and D15S10: first molecular cytogenetically proven case report.
Journal of medical genetics 2003;40(3):e28.
2003: Kuechler Alma; Weise Anja; Michel Susanne; Schaeferhenrich Anja; Pool-Zobel Beatrice L; Claussen Uwe; Liehr Thomas
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: Starke Heike; Mitulla Beate; Nietzel Angela; Heller Anita; Beensen Volkmar; Grosswendt Gisela; Claussen Uwe; von Eggeling Ferdinand; Liehr Thomas
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.
2003: Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Pool-Zobel B L; Claussen U; Liehr T
Multitude multicolor chromosome banding (mMCB) - a comprehensive one-step multicolor FISH banding method.
Cytogenetic and genome research 2003;103(1-2):34-9.
2003: Grasshoff U; Singer S; Liehr T; Starke H; Fode B; Schöning M; Dufke A
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: Weise A; Rittinger O; Starke H; Ziegler M; Claussen U; Liehr T
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: Gebhart E; Liehr T; Wolff E; Wiltfang J; Koscielny S; Ries J
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: Bartels I; Schlueter G; Liehr T; von Eggeling F; Starke H; Glaubitz R; Burfeind P
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.
2002: Steinhaeuser Ulf; Starke Heike; Nietzel Angela; Lindenau Joerg; Ullmann Peter; Claussen Uwe; Liehr Thomas
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: Starke Heike; Seidel Jörg; Henn Wolfram; Reichardt Sylvia; Volleth Marianne; Stumm Markus; Behrend Christine; Sandig Klaus R; Kelbova Christine; Senger Gabriele; Albrecht Beate; Hansmann Ingo; Heller Anita; Claussen Uwe; Liehr Thomas
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: Lemke Johannes; Claussen Jan; Michel Susanne; Chudoba Ilse; Mühlig Peter; Westermann Martin; Sperling Karl; Rubtsov Nikolai; Grummt Ulrich-Walter; Ullmann Peter; Kromeyer-Hauschild Katrin; Liehr Thomas; Claussen Uwe
The DNA-based structure of human chromosome 5 in interphase.
American journal of human genetics 2002;71(5):1051-9.
2002: Liehr Thomas; Schreyer Isolde; Neumann Annett; Beensen Volkmar; Ziegler Monika; Hartmann Isabell; Starke Heike; Heller Anita; Nietzel Angela; Claussen Uwe
Two more possible pitfalls of rapid prenatal diagnostics using interphase nuclei.
Prenatal diagnosis 2002;22(6):497-9.
2002: Weise A; Starke H; Heller A; Tönnies H; Volleth M; Stumm M; Gabriele S; Nietzel A; Claussen U; Liehr T
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: Heller Anita; Starke Heike; Trifonov Vladimir; Rubtsov Nikolai; Wedding Ulrich; Loncarevic Ivan; Bleck Cordula; Claussen Uwe; Liehr Thomas
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: Loncarevic Ivan F; Römer Jennifer; Starke Heike; Heller Anita; Bleck Cordula; Ziegler Monika; Fiedler Wolfgang; Liehr Thomas; Clement Joachim H; Claussen Uwe
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: Liehr Thomas; Heller Anita; Starke Heike; Claussen Uwe
FISH banding methods: applications in research and diagnostics.
Expert review of molecular diagnostics 2002;2(3):217-25.
2002: Liehr Thomas; Claussen Uwe
Current developments in human molecular cytogenetic techniques.
Current molecular medicine 2002;2(3):283-97.
2002: Liehr Thomas; Schmidt Matthias; Starke Heike; Ziegler Monika; Kittner Gabriele; Heller Anita; Rubtsov Nikolai; Trifonov Vladimir; Claussen Uwe
First case of trisomy 13 plus mosaic trisomy 1q.
Fetal diagnosis and therapy 2002;17(3):133-6.
2002: Kuechler Alma; Neubauer Susann; Grabenbauer Gerhard G; Claussen Uwe; Liehr Thomas; Sauer Rolf; Wendt Thomas G
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: Weise Anja; Starke Heike; Heller Anita; Uwe Claussen; Liehr Thomas
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: Liehr Thomas; Heller Anita; Starke Heike; Rubtsov Nikolai; Trifonov Vladimir; Mrasek Kristin; Weise Anja; Kuechler Alma; Claussen Uwe
Microdissection based high resolution multicolor banding for all 24 human chromosomes.
International journal of molecular medicine 2002;9(4):335-9.
2002: Claussen U; Michel S; Mühlig P; Westermann M; Grummt U-W; Kromeyer-Hauschild K; Liehr T
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: Weise A; Liehr T; Efferth T; Kuechler A; Gebhart E
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: Trappe R; Böhm D; Kohlhase J; Weise A; Liehr T; Essers G; Meins M; Zoll B; Bartels I; Burfeind P
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: Liehr T; Weise A; Heller A; Starke H; Mrasek K; Kuechler A; Weier H-U G; Claussen U
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: Starke H; Senger G; Kossakiewicz M; Tittelbach H; Rau D; Rubtsov N; Trifonov V; Heller A; Hartmann I; Claussen U; Liehr T
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: Dufke A; Walczak C; Liehr T; Starke H; Trifonov V; Rubtsov N; Schöning M; Enders H; Eggermann T
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: Liehr T; Beensen V; Starke H; Hauschild R; Hempell E; Fritsche V; Hoppe C; Grosswendt G; Prechtel M; Ziegler M; Claussen U; von Eggeling F
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: Bleichert A; Fiedler W; Claussen U; Ernst G; Loncarevic I F; Heller A; Liehr T; Kunert C; von Eggeling F
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: Starke H; Raida M; Trifonov V; Clement J H; Loncarevic I F; Heller A; Bleck C; Nietzel A; Rubtsov N; Claussen U; Liehr T
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: Liehr T; Beensen V; Hauschild R; Ziegler M; Hartmann I; Starke H; Heller A; Kähler C; Schmidt M; Reiber W; Hesse M; Claussen U
Pitfalls of rapid prenatal diagnosis using the interphase nucleus.
Prenatal diagnosis 2001;21(5):419-21.
2001: Liehr T; Reiter L T; Lupski J R; Murakami T; Claussen U; Rautenstrauss B
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: Nietzel A; Rocchi M; Starke H; Heller A; Fiedler W; Wlodarska I; Loncarevic I F; Beensen V; Claussen U; Liehr T
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: Kuechler A; Mueller C R; Liehr T; Claussen U
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: Kinne R W; Liehr T; Beensen V; Kunisch E; Zimmermann T; Holland H; Pfeiffer R; Stahl H D; Lungershausen W; Hein G; Roth A; Emmrich F; Claussen U; Froster U G
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: Mrasek K; Heller A; Rubtsov N; Trifonov V; Starke H; Rocchi M; Claussen U; Liehr T
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: Jakubiczka S; Mitulla B; Liehr T; Arnemann J; Lehrach H; Sudbrak R; Stumm M; Wieacker P F; Bettecken T
Incidental prenatal detection of an Xp deletion using an anonymous primer pair for fetal sexing.
Prenatal diagnosis 2000;20(10):842-6.
2000: Heller A; Seidel J; Hübler A; Starke H; Beensen V; Senger G; Rocchi M; Wirth J; Chudoba I; Claussen U; Liehr T
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: Hübler A; Seidel J; Kauf E; Schramm D; Beensen V; Heller A; Liehr T; Zintl F
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: Heller A; Chudoba I; Bleck C; Senger G; Claussen U; Liehr T
Microdissection based comparative genomic hybridization analysis (micro-CGH) of secondary acute myelogenous leukemias.
International journal of oncology 2000;16(3):461-8.
2000: Gebhart E; Liehr T
Patterns of genomic imbalances in human solid tumors (Review).
International journal of oncology 2000;16(2):383-99.
2000: Bayerlein K; Rith T; Verdorfer I; Liehr T; Wolff E; Girod S; Gebhart E
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.
2000: Dufke A; Seidel J; Schöning M; Döbler-Neumann M; Kelbova C; Liehr T; Beensen V; Backsch C; Klein-Vogler U; Enders H
Microdeletion 4p16.3 in three unrelated patients with Wolf-Hirschhorn syndrome.
Cytogenetics and cell genetics 2000;91(1-4):81-4.
1999: Starke H; Schreyer I; Kähler C; Fiedler W; Beensen V; Heller A; Nietzel A; Claussen U; Liehr T
Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8.
Prenatal diagnosis 1999;19(12):1169-74.
1999: Hühne K; Park O; Liehr T; Rautenstrauss B
Expression analysis of the PMP22 gene in glioma and osteogenic sarcoma cell lines.
Journal of neuroscience research 1999;58(5):624-31.
1999: Reiter L T; Liehr T; Rautenstrauss B; Robertson H M; Lupski J R
Localization of mariner DNA transposons in the human genome by PRINS.
Genome research 1999;9(9):839-43.
1999: Liehr T; Kuhlenbäumer G; Wulf P; Taylor V; Suter U; Van Broeckhoven C; Lupski J R; Claussen U; Rautenstrauss B
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: Dobler M; Schuh J; Kiesewetter F; Schell H; Liehr T; Gebhart E
Deletion monitoring in skin tumors by interphase-FISH using band-specific DNA probes.
International journal of oncology 1999;14(3):571-6.
1999: Liehr T; Starke H; Beensen V; Kähler C; Harbich M; Brude E; Ziegler M; Claussen U
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: Fuchs C; Liehr T; Ozbey S; Ekici A; Grehl H; Rautenstrauss B
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: Taubald A; Liehr T; Ries J; Girod S; Hassfurter E; Gebhart E
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: Neubauer S; Liehr T; Birkenhake S; Gebhart E; Fietkau R; Sauer R
Estimation of DNA single-strand breaks by single cells gel electrophoresis in tumor cells.
Genetic analysis : biomolecular engineering 1998;14(4):121-4.
1998: Lange C; Liehr T; Goen M; Gebhart E; Fleckenstein B; Ensser A
New eukaryotic semaphorins with close homology to semaphorins of DNA viruses.
Genomics 1998;51(3):340-50.
1998: Wolff E; Girod S; Liehr T; Vorderwülbecke U; Ries J; Steininger H; Gebhart E
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: Gebhart E; Liehr T; Wolff E; Ries J; Fiedler W; Steininger H; Koscielny S; Girod S
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: Liehr T; Pfeiffer R A; Trautmann U; Gebhart E
Centromeric alphoid DNA heteromorphisms of chromosome 22 revealed by FISH-technique.
Clinical genetics 1998;53(3):231-2.
1998: Rautenstrauss B; Fuchs C; Ekici A; Nelis E; Van Broeckhoven C; Liehr T
Assay of transfection rate in insect cells on a single cell level.
Genetic analysis : biomolecular engineering 1998;14(3):103-4.
1998: Michels-Rautenstrauss K G; Mardin C Y; Budde W M; Liehr T; Polansky J; Nguyen T; Timmerman V; Van Broeckhoven C; Naumann G O; Pfeiffer R A; Rautenstrauss B W
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.
1998: Rautenstrauss B; Zechner U; Hameister H; Grehl H; Liehr T
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.
1997: Liehr T; Grehl H; Rautenstrauss B
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: Rautenstrauss B; Liehr T; Schrell U M; Grehl H
Use of FISH analysis for prostate tumors and other tissue types.
The American journal of pathology 1997;151(4):1171-2.
1997: Liehr T; Grehl H; Rautenstrauss B
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: Liehr T; Hallouin F; Rautenstrauss B; LePendu J; Denis M G
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: Grehl H; Rautenstrauss B; Liehr T; Bickel A; Ekici A; Bathke K; Neundörfer B
Clinical and morphological phenotype of HMSN 1A mosaicism.
Neuromuscular disorders : NMD 1997;7(1):27-31.
1997: Timmerman V; Rautenstrauss B; Reiter L T; Koeuth T; Löfgren A; Liehr T; Nelis E; Bathke K D; De Jonghe P; Grehl H; Martin J J; Lupski J R; Van Broeckhoven C
Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent.
Journal of medical genetics 1997;34(1):43-9.
1997: Rautenstrauss B; Fuchs C; Liehr T; Grehl H; Murakami T; Lupski J R
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.
1996: Liehr T; Grehl H; Rautenstrauss B
A rapid method for FISH analysis on interphase nuclei extracted from cryofixed tissues.
Trends in genetics : TIG 1996;12(12):505-6.
1996: Pröls F; Liehr T; Marx M; Rautenstrauss B
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: Liehr T; Rautenstrauss B; Grehl H; Bathke K D; Ekici A; Rauch A; Rott H D
Mosaicism for the Charcot-Marie-Tooth disease type 1A duplication suggests somatic reversion.
Human genetics 1996;98(1):22-8.
1995: Baechner D; Liehr T; Hameister H; Altenberger H; Grehl H; Suter U; Rautenstrauss B
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: Liehr T; Ekici A; Hillenbrand R; Rautenstrauss B
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: Liehr T; Grehl H; Rautenstrauss B
FISH analysis of interphase nuclei extracted from paraffin-embedded tissue.
Trends in genetics : TIG 1995;11(10):377-8.
1995: Liehr T; Rautenstrauss B
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: Gebhart E; Liehr T; Harrer P; Reichardt S; Schmitt G; Thoma K; Gramatzki M; Trautmann U
Determination by interphase-FISH of the clonality of aberrant karyotypes in human hematopoietic neoplasias.
Leukemia & lymphoma 1995;17(3-4):295-302.
1995: Liehr T; Altenberger H; Rautenstrauss B
Rapid fluorescence in situ detection of heterologous expression in E. coli and counterstaining with diamidinophenylindol.
Trends in genetics : TIG 1995;11(4):129.
1994: Trautmann U; Gramatzki M; Krauss M; Friz A; Liehr T; Gebhart E
Tetrasomy 8 as a clonal anomaly in myeloid neoplasias.
Cancer genetics and cytogenetics 1994;72(2):101-4.
1994: Liehr T; Stübinger A; Thoma K; Tulusan H A; Gebhart E
Comparative interphase cytogenetics using FISH on human ovarian carcinomas.
Anticancer research 1994;14(1A):183-8.
1993: Gebhart E; Trautmann U; Reichardt S; Liehr T
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: Liehr T; Pfeiffer R A; Trautmann U
Typical and partial cat eye syndrome: identification of the marker chromosome by FISH.
Clinical genetics 1992;42(2):91-6.
1992: Rauch A; Pfeiffer R A; Trautmann U; Liehr T; Rott H D; Ulmer R
A study of ten small supernumerary (marker) chromosomes identified by fluorescence in situ hybridization (FISH).
Clinical genetics 1992;42(2):84-90.

Sign-in to see more

Sign-in free and Explore the Exciting World of BiomedExperts:

NetworkView

Thomas Liehr

Research Profile (preview)

Procedures

Disorders

Physiology

Anatomy

Concepts & Ideas

Network (preview)

Publications

Sign in free and see...

Visualized networks:

GeoTargeted Searches:

Research Profiles:

Geonetwork of Thomas Liehr (preview)

All Publications