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Reinhard Ullmann

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.

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Haensel Jennifer; Kohlschmidt Nicolai; Pitz Susanne; Keilmann Annerose; Zenker Martin; Ullmann Reinhard; Haaf Thomas; Bartsch Oliver
Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder.
Hilhorst-Hofstee Yvonne; Tümer Zeynep; Born Peter; Knijnenburg Jeroen; Hansson Kerstin; Yatawara Vindhya; Steensberg Jesper; Ullmann Reinhard; Arkesteijn Ger; Tommerup Niels; Larsen Lars Allan
Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24.
Zhang Litu; Tümer Zeynep; Møllgård Kjeld; Barbi Gotthold; Rossier Eva; Bendsen Eske; Møller Rikke Steensbjerre; Ullmann Reinhard; He Jian; Papadopoulos Nickolas; Tommerup Niels; Larsen Lars Allan
Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.

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2009: Haensel Jennifer; Kohlschmidt Nicolai; Pitz Susanne; Keilmann Annerose; Zenker Martin; Ullmann Reinhard; Haaf Thomas; Bartsch Oliver
Case report supporting that the Barber-Say and ablepharon macrostomia syndromes could represent one disorder.
American journal of medical genetics. Part A 2009;149A(10):2236-40.
2009: Hilhorst-Hofstee Yvonne; Tümer Zeynep; Born Peter; Knijnenburg Jeroen; Hansson Kerstin; Yatawara Vindhya; Steensberg Jesper; Ullmann Reinhard; Arkesteijn Ger; Tommerup Niels; Larsen Lars Allan
Molecular characterization of two patients with de novo interstitial deletions in 4q22-q24.
American journal of medical genetics. Part A 2009;149A(8):1830-3.
2009: Zhang Litu; Tümer Zeynep; Møllgård Kjeld; Barbi Gotthold; Rossier Eva; Bendsen Eske; Møller Rikke Steensbjerre; Ullmann Reinhard; He Jian; Papadopoulos Nickolas; Tommerup Niels; Larsen Lars Allan
Characterization of a t(5;8)(q31;q21) translocation in a patient with mental retardation and congenital heart disease: implications for involvement of RUNX1T1 in human brain and heart development.
European journal of human genetics : EJHG 2009;17(8):1010-8.
2009: Raile Klemens; Klopocki Eva; Holder Martin; Wessel Theda; Galler Angela; Deiss Dorothee; Müller Dominik; Riebel Thomas; Horn Denise; Maringa Monika; Weber Jürgen; Ullmann Reinhard; Grüters Annette
Expanded clinical spectrum in hepatocyte nuclear factor 1b-maturity-onset diabetes of the young.
The Journal of clinical endocrinology and metabolism 2009;94(7):2658-64.
2009: Zatkova Andrea; Merk Sylvia; Wendehack Melanie; Bilban Martin; Muzik Eva Maria; Muradyan Artur; Haferlach Claudia; Haferlach Torsten; Wimmer Katharina; Fonatsch Christa; Ullmann Reinhard
AML/MDS with 11q/MLL amplification show characteristic gene expression signature and interplay of DNA copy number changes.
Genes, chromosomes & cancer 2009;48(6):510-20.
2009: Shoichet Sarah A; Waibel Stefan; Endruhn Sonja; Sperfeld Anne D; Vorwerk Brita; Müller Ines; Erdogan Fikret; Ludolph Albert C; Ropers Hans-Hilger; Ullmann Reinhard
Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridization.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2009;10(3):162-9.
2009: Tzschach A; Ramel C; Kron A; Seipel B; Wüster C; Cordes U; Liehr T; Hoeltzenbein M; Menzel C; Ropers H-H; Ullmann R; Kalscheuer V; Decker J; Steinberger D
Hypergonadotropic hypogonadism in a patient with inv ins (2;4).
International journal of andrology 2009;32(3):226-30.
2009: Tzschach Andreas; Graul-Neumann Luitgard M; Konrat Kateryna; Richter Reyk; Ebert Grit; Ullmann Reinhard; Neitzel Heidemarie
Interstitial deletion 2p11.2-p12: report of a patient with mental retardation and review of the literature.
American journal of medical genetics. Part A 2009;149A(2):242-5.
2009: Kalscheuer Vera M; Musante Luciana; Fang Cheng; Hoffmann Kirsten; Fuchs Celine; Carta Eloisa; Deas Emma; Venkateswarlu Kanamarlapudi; Menzel Corinna; Ullmann Reinhard; Tommerup Niels; Dalprà Leda; Tzschach Andreas; Selicorni Angelo; Lüscher Bernhard; Ropers Hans-Hilger; Harvey Kirsten; Harvey Robert J
A balanced chromosomal translocation disrupting ARHGEF9 is associated with epilepsy, anxiety, aggression, and mental retardation.
Human mutation 2009;30(1):61-8.
2008: Erdogan F; Larsen L A; Zhang L; Tümer Z; Tommerup N; Chen W; Jacobsen J R; Schubert M; Jurkatis J; Tzschach A; Ropers H-H; Ullmann R
High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.
Journal of medical genetics 2008;45(11):704-9.
2008: Busche Andreas; Klopocki Eva; Ullmann Reinhard; Mundlos Stefan; Horn Denise
A cryptic unbalanced translocation t(2;9)(p25.2;q34.3) causes the phenotype of 9q subtelomeric deletion syndrome and additional exophthalmos and joint contractures.
European journal of medical genetics 2008;51(6):615-21.
2008: Muradyan Artur; Boldt Vivien; Steininger Anne; Stabentheiner Stephanie; Tebel Katrin; Kreutzberger Jürgen; Müller Ines; Madle Hannelore; Popper Helmut H; Ullmann Reinhard
An integrative approach for analyzing the interplay of genetic and epigenetic changes in tumors.
Archives of pathology & laboratory medicine 2008;132(10):1557-61.
2008: Najm Juliane; Horn Denise; Wimplinger Isabella; Golden Jeffrey A; Chizhikov Victor V; Sudi Jyotsna; Christian Susan L; Ullmann Reinhard; Kuechler Alma; Haas Carola A; Flubacher Armin; Charnas Lawrence R; Uyanik Gökhan; Frank Ulrich; Klopocki Eva; Dobyns William B; Kutsche Kerstin
Mutations of CASK cause an X-linked brain malformation phenotype with microcephaly and hypoplasia of the brainstem and cerebellum.
Nature genetics 2008;40(9):1065-7.
2008: Kaalund S S; Møller R S; Tészás A; Miranda M; Kosztolanyi G; Ullmann R; Tommerup N; Tümer Z
Investigation of 4q-deletion in two unrelated patients using array CGH.
American journal of medical genetics. Part A 2008;146A(18):2431-4.
2008: Kalscheuer Vera M; Feenstra Ilse; Van Ravenswaaij-Arts Conny M A; Smeets Dominique F C M; Menzel Corinna; Ullmann Reinhard; Musante Luciana; Ropers Hans-Hilger
Disruption of the TCF4 gene in a girl with mental retardation but without the classical Pitt-Hopkins syndrome.
American journal of medical genetics. Part A 2008;146A(16):2053-9.
2008: Klopocki Eva; Graul-Neumann Luitgard M; Grieben Ulrike; Tönnies Holger; Ropers Hans-Hilger; Horn Denise; Mundlos Stefan; Ullmann Reinhard
A further case of the recurrent 15q24 microdeletion syndrome, detected by array CGH.
European journal of pediatrics 2008;167(8):903-8.
2008: Chen Wei; Kalscheuer Vera; Tzschach Andreas; Menzel Corinna; Ullmann Reinhard; Schulz Marcel Holger; Erdogan Fikret; Li Na; Kijas Zofia; Arkesteijn Ger; Pajares Isidora Lopez; Goetz-Sothmann Margret; Heinrich Uwe; Rost Imma; Dufke Andreas; Grasshoff Ute; Glaeser Birgitta; Vingron Martin; Ropers H Hilger
Mapping translocation breakpoints by next-generation sequencing.
Genome research 2008;18(7):1143-9.
2008: Engenheiro E; Møller R S; Pinto M; Soares G; Nikanorova M; Carreira I M; Ullmann R; Tommerup N; Tümer Z
Mowat-Wilson syndrome: an underdiagnosed syndrome?
Clinical genetics 2008;73(6):579-84.
2008: Klopocki E; Ott C-E; Benatar N; Ullmann R; Mundlos S; Lehmann K
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome.
Journal of medical genetics 2008;45(6):370-5.
2008: Møller Rikke S; Kübart Sabine; Hoeltzenbein Maria; Heye Babett; Vogel Ida; Hansen Christian P; Menzel Corinna; Ullmann Reinhard; Tommerup Niels; Ropers Hans-Hilger; Tümer Zeynep; Kalscheuer Vera M
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephaly.
American journal of human genetics 2008;82(5):1165-70.
2008: Tzschach Andreas; Kelbova Christina; Weidensee Sabine; Peters Hartmut; Ropers Hans-Hilger; Ullmann Reinhard; Erdogan Fikret; Jurkatis Jan; Menzel Corinna; Kalscheuer Vera; Demuth Stephanie
Blepharophimosis-ptosis-epicanthus inversus syndrome in a girl with chromosome translocation t(2;3)(q33;q23).
Ophthalmic genetics 2008;29(1):37-40.
2008: Gilling Mette; Lauritsen Marlene Briciet; Møller Morten; Henriksen Karen Friis; Vicente Astrid; Oliveira Guiomar; Cintin Christina; Eiberg Hans; Andersen Paal Skyt; Mors Ole; Rosenberg Thomas; Brøndum-Nielsen Karen; Cotterill Rodney M J; Lundsteen Claes; Ropers Hans-Hilger; Ullmann Reinhard; Bache Iben; Tümer Zeynep; Tommerup Niels
A 3.2 Mb deletion on 18q12 in a patient with childhood autism and high-grade myopia.
European journal of human genetics : EJHG 2008;16(3):312-9.
2008: Walczak-Sztulpa Joanna; Wisniewska Marzena; Latos-Bielenska Anna; Linné Maja; Kelbova Christina; Belitz Britta; Pfeiffer Lutz; Kalscheuer Vera; Erdogan Fikret; Kuss Andreas W; Ropers Hans-Hilger; Ullmann Reinhard; Tzschach Andreas
Chromosome deletions in 13q33-34: report of four patients and review of the literature.
American journal of medical genetics. Part A 2008;146(3):337-42.
2008: Kirov George; Gumus Dilihan; Chen Wei; Norton Nadine; Georgieva Lyudmila; Sari Murat; O'Donovan Michael C; Erdogan Fikret; Owen Michael J; Ropers Hans-Hilger; Ullmann Reinhard
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
Human molecular genetics 2008;17(3):458-65.
2008: Tzschach Andreas; Chen Wei; Erdogan Fikret; Hoeller Adelheid; Ropers Hans-Hilger; Castellan Claudio; Ullmann Reinhard; Schinzel Albert
Characterization of interstitial Xp duplications in two families by tiling path array CGH.
American journal of medical genetics. Part A 2008;146A(2):197-203.
2008: So Joyce; Müller Ines; Kunath Melanie; Herrmann Susanne; Ullmann Reinhard; Schweiger Susann
Diagnosis of a terminal deletion of 4p with duplication of Xp22.31 in a patient with findings of Opitz G/BBB syndrome and Wolf-Hirschhorn syndrome.
American journal of medical genetics. Part A 2008;146A(1):103-9.
2008: Erdogan F; Belloso J M; Gabau E; Ajbro K D; Guitart M; Ropers H H; Tommerup N; Ullmann R; Tümer Z; Larsen L A
Fine mapping of a de novo interstitial 10q22-q23 duplication in a patient with congenital heart disease and microcephaly.
European journal of medical genetics 2008;51(1):81-6.
2007: Møller R S; Hansen C P; Jackson G D; Ullmann R; Ropers H H; Tommerup N; Tümer Z
Interstitial deletion of chromosome 4p associated with mild mental retardation, epilepsy and polymicrogyria of the left temporal lobe.
Clinical genetics 2007;72(6):593-8.
2007: Jakobsen Linda P; Ullmann Reinhard; Kjaer Klaus W; Knudsen Mary A; Tommerup Niels; Eiberg Hans
Suggestive linkage to a neighboring region of IRF6 in a cleft lip and palate multiplex family.
American journal of medical genetics. Part A 2007;143A(22):2716-21.
2007: Mefford Heather C; Clauin Severine; Sharp Andrew J; Moller Rikke S; Ullmann Reinhard; Kapur Raj; Pinkel Dan; Cooper Gregory M; Ventura Mario; Ropers H Hilger; Tommerup Niels; Eichler Evan E; Bellanne-Chantelot Christine
Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy.
American journal of human genetics 2007;81(5):1057-69.
2007: Motazacker Mohammad Mahdi; Rost Benjamin Rainer; Hucho Tim; Garshasbi Masoud; Kahrizi Kimia; Ullmann Reinhard; Abedini Seyedeh Sedigheh; Nieh Sahar Esmaeeli; Amini Saeid Hosseini; Goswami Chandan; Tzschach Andreas; Jensen Lars Riff; Schmitz Dietmar; Ropers Hans Hilger; Najmabadi Hossein; Kuss Andreas Walter
A defect in the ionotropic glutamate receptor 6 gene (GRIK2) is associated with autosomal recessive mental retardation.
American journal of human genetics 2007;81(4):792-8.
2007: Bisgaard Anne-Marie; Kirchhoff Maria; Nielsen Jens Erik; Brandt Carsten; Hove Hanne; Jepsen Birgit; Jensen Tim; Ullmann Reinhard; Skovby Flemming
Transmitted cytogenetic abnormalities in patients with mental retardation: pathogenic or normal variants?
European journal of medical genetics 2007;50(4):243-55.
2007: Ullmann Reinhard; Turner Gillian; Kirchhoff Maria; Chen Wei; Tonge Bruce; Rosenberg Carla; Field Michael; Vianna-Morgante Angela M; Christie Louise; Krepischi-Santos Ana C; Banna Lynn; Brereton Avril V; Hill Alyssa; Bisgaard Anne-Marie; Müller Ines; Hultschig Claus; Erdogan Fikret; Wieczorek Georg; Ropers H Hilger
Array CGH identifies reciprocal 16p13.1 duplications and deletions that predispose to autism and/or mental retardation.
Human mutation 2007;28(7):674-82.
2007: Jakobsen Linda P; Ullmann Reinhard; Christensen Steen B; Jensen Karl Erik; Mølsted Kirsten; Henriksen Karen F; Hansen Claus; Knudsen Mary A; Larsen Lars A; Tommerup Niels; Tümer Zeynep
Pierre Robin sequence may be caused by dysregulation of SOX9 and KCNJ2.
Journal of medical genetics 2007;44(6):381-6.
2007: Kalscheuer Vera M; FitzPatrick David; Tommerup Niels; Bugge Merete; Niebuhr Erik; Neumann Luitgard M; Tzschach Andreas; Shoichet Sarah A; Menzel Corinna; Erdogan Fikret; Arkesteijn Ger; Ropers Hans-Hilger; Ullmann Reinhard
Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation.
Human genetics 2007;121(3-4):501-9.
2007: Meyer Stefan; Fergusson William D; Whetton Anthony D; Moreira-Leite Flavia; Pepper Stuart D; Miller Crispin; Saunders Emma K; White Daniel J; Will Andrew M; Eden Tim; Ikeda Hideyuki; Ullmann Reinhard; Tuerkmen Seval; Gerlach Antje; Klopocki Eva; Tönnies Holger
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption.
Genes, chromosomes & cancer 2007;46(4):359-72.
2007: Klopocki Eva; Schulze Harald; Strauss Gabriele; Ott Claus-Eric; Hall Judith; Trotier Fabienne; Fleischhauer Silke; Greenhalgh Lynn; Newbury-Ecob Ruth A; Neumann Luitgard M; Habenicht Rolf; König Rainer; Seemanova Eva; Megarbane André; Ropers Hans-Hilger; Ullmann Reinhard; Horn Denise; Mundlos Stefan
Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius syndrome.
American journal of human genetics 2007;80(2):232-40.
2007: Tzschach Andreas; Menzel Corinna; Erdogan Fikret; Schubert Marei; Hoeltzenbein Maria; Barbi Gotthold; Petzenhauser Christine; Ropers Hans-Hilger; Ullmann Reinhard; Kalscheuer Vera
Characterization of a 16 Mb interstitial chromosome 7q21 deletion by tiling path array CGH.
American journal of medical genetics. Part A 2007;143(4):333-7.
2007: Gratias Sandrine; Rieder Harald; Ullmann Reinhard; Klein-Hitpass Ludger; Schneider Stephanie; Bölöni Réka; Kappler Martin; Lohmann Dietmar R
Allelic loss in a minimal region on chromosome 16q24 is associated with vitreous seeding of retinoblastoma.
Cancer research 2007;67(1):408-16.
2007: Erdogan Fikret; Ullmann Reinhard; Chen Wei; Schubert Marei; Adolph Sabine; Hultschig Claus; Kalscheuer Vera; Ropers Hans-Hilger; Spaich Christiane; Tzschach Andreas
Characterization of a 5.3 Mb deletion in 15q14 by comparative genomic hybridization using a whole genome "tiling path" BAC array in a girl with heart defect, cleft palate, and developmental delay.
American journal of medical genetics. Part A 2007;143(2):172-8.
2007: Bartsch O; Vlcková Z; Erdogan F; Ullmann R; Novotná D; Spiegel M; Beyer V; Haaf T; Zechner U; Seemanová E
Two independent chromosomal rearrangements, a very small (550 kb) duplication of the 7q subtelomeric region and an atypical 17q11.2 (NF1) microdeletion, in a girl with neurofibromatosis.
Cytogenetic and genome research 2007;119(1-2):158-64.
2006: Klopocki Eva; Neumann Luitgard M; Tönnies Holger; Ropers Hans-Hilger; Mundlos Stefan; Ullmann Reinhard
Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene.
European journal of human genetics : EJHG 2006;14(12):1274-9.
2006: Müller D; Klopocki E; Neumann L M; Mundlos S; Taupitz M; Schulze I; Ropers H-H; Querfeld U; Ullmann R
A complex phenotype with cystic renal disease.
Kidney international 2006;70(9):1656-60.
2006: Klopocki Eva; Fiebig Britta; Robinson Peter; Tönnies Holger; Erdogan Fikret; Ropers Hans-Hilger; Mundlos Stefan; Ullmann Reinhard
A novel 8 Mb interstitial deletion of chromosome 8p12-p21.2.
American journal of medical genetics. Part A 2006;140(8):873-7.
2006: Garshasbi Masoud; Motazacker Mohammad Mahdi; Kahrizi Kimia; Behjati Farkhondeh; Abedini Seyedeh Sedigheh; Nieh Sahar Esmaeeli; Firouzabadi Saghar Ghasemi; Becker Christian; Rüschendorf Franz; Nürnberg Peter; Tzschach Andreas; Vazifehmand Reza; Erdogan Fikret; Ullmann Reinhard; Lenzner Steffen; Kuss Andreas W; Ropers H Hilger; Najmabadi Hossein
SNP array-based homozygosity mapping reveals MCPH1 deletion in family with autosomal recessive mental retardation and mild microcephaly.
Human genetics 2006;118(6):708-15.
2006: Erdogan F; Chen W; Kirchhoff M; Kalscheuer V M; Hultschig C; Müller I; Schulz R; Menzel C; Bryndorf T; Ropers H-H; Ullmann R
Impact of low copy repeats on the generation of balanced and unbalanced chromosomal aberrations in mental retardation.
Cytogenetic and genome research 2006;115(3-4):247-53.
2006: Schwarzbraun T; Ullmann R; Schubert M; Ledinegg M; Ofner L; Windpassinger C; Wagner K; Kroisel P M; Petek E
Characterization of a de novo complex chromosome rearrangement (CCR) involving chromosomes 2 and 12, associated with mental retardation and impaired speech development.
Cytogenetic and genome research 2006;115(1):84-9.
2005: Wieser R; Fritz B; Ullmann R; Müller I; Galhuber M; Storlazzi C T; Ramaswamy A; Christiansen H; Shimizu N; Rehder H
Novel rearrangement of chromosome band 22q11.2 causing 22q11 microdeletion syndrome-like phenotype and rhabdoid tumor of the kidney.
Human mutation 2005;26(2):78-83.
2005: Halbwedl Iris; Ullmann Reinhard; Kremser Marie-Luise; Man Yan Gao; Isadi-Moud Narges; Lax Sigurd; Denk Helmut; Popper Helmut H; Tavassoli Fattaneh A; Moinfar Farid
Chromosomal alterations in low-grade endometrial stromal sarcoma and undifferentiated endometrial sarcoma as detected by comparative genomic hybridization.
Gynecologic oncology 2005;97(2):582-7.
2005: Chen Wei; Erdogan Fikret; Ropers H-Hilger; Lenzner Steffen; Ullmann Reinhard
CGHPRO -- a comprehensive data analysis tool for array CGH.
BMC bioinformatics 2005;6():85.
2004: Petzmann Susanna; Ullmann Reinhard; Halbwedl Iris; Popper Helmut H
Analysis of chromosome-11 aberrations in pulmonary and gastrointestinal carcinoids: an array comparative genomic hybridization-based study.
Virchows Archiv : an international journal of pathology 2004;445(2):151-9.
2004: Ullmann Reinhard; Morbini Patrizia; Halbwedl Iris; Bongiovanni Massimo; Gogg-Kammerer Margit; Papotti Mauro; Gabor Sabine; Renner Heiko; Popper Helmut Hans
Protein expression profiles in adenocarcinomas and squamous cell carcinomas of the lung generated using tissue microarrays.
The Journal of pathology 2004;203(3):798-807.
2004: Stacher Elvira; Ullmann Reinhard; Halbwedl Iris; Gogg-Kammerer Margit; Boccon-Gibod Liliane; Nicholson Andrew G; Sheppard Mary N; Carvalho Lina; Franca Maria Teresa; Macsweeney Fergus; Morresi-Hauf Alicia; Popper Helmut H
Atypical goblet cell hyperplasia in congenital cystic adenomatoid malformation as a possible preneoplasia for pulmonary adenocarcinoma in childhood: A genetic analysis.
Human pathology 2004;35(5):565-70.
2004: Zatkova Andrea; Ullmann Reinhard; Rouillard Jean Marie; Lamb Barbara J; Kuick Rork; Hanash Sam M; Schnittger Susanne; Schoch Claudia; Fonatsch Christa; Wimmer Katharina
Distinct sequences on 11q13.5 and 11q23-24 are frequently coamplified with MLL in complexly organized 11q amplicons in AML/MDS patients.
Genes, chromosomes & cancer 2004;39(4):263-76.
2003: Ullmann R; Bongiovanni M; Halbwedl I; Fraire A E; Cagle P T; Mori M; Papotti M; Popper Helmut H
Is high-grade adenomatous hyperplasia an early bronchioloalveolar adenocarcinoma?
The Journal of pathology 2003;201(3):371-6.
2003: Ullmann Reinhard; Bongiovanni Massimo; Halbwedl Iris; Petzmann Susanna; Gogg-Kammerer Margit; Sapino Anna; Papotti Mauro; Bussolati Gianni; Popper Helmut H
Bronchiolar columnar cell dysplasia--genetic analysis of a novel preneoplastic lesion of peripheral lung.
Virchows Archiv : an international journal of pathology 2003;442(5):429-36.
2002: Ullmann Reinhard; Petzmann Susanna; Klemen Huberta; Fraire Armando E; Hasleton Phil; Popper Helmut H
The position of pulmonary carcinoids within the spectrum of neuroendocrine tumors of the lung and other tissues.
Genes, chromosomes & cancer 2002;34(1):78-85.
2001: Ullmann R; Petzmann S; Sharma A; Cagle P T; Popper H H
Chromosomal aberrations in a series of large-cell neuroendocrine carcinomas: unexpected divergence from small-cell carcinoma of the lung.
Human pathology 2001;32(10):1059-63.
2001: Pfragner R; Ullmann R; Behmel A; Popper H H
Comparative genomic hybridization and cytogenetic analysis in a bronchial adenoma: three clones with different chromosomal aberrations.
International journal of oncology 2001;18(5):923-8.
2001: Petzmann S; Ullmann R; Klemen H; Renner H; Popper H H
Loss of heterozygosity on chromosome arm 11q in lung carcinoids.
Human pathology 2001;32(3):333-8.
1998: Ullmann R; Schwendel A; Klemen H; Wolf G; Petersen I; Popper H H
Unbalanced chromosomal aberrations in neuroendocrine lung tumors as detected by comparative genomic hybridization.
Human pathology 1998;29(10):1145-9.

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Reinhard Ullmann

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