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Thomas Wienker

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Elisabeth Mangold; Sergio G Muñoz-Jiménez; Markus M Nöthen; Stefanie Nowak; Rocío Ortiz-López; Mario Paredes-Zenteno; Heiko Reutter; Abelardo Arizpe-Cantú; Stefan Herms; Michael Knapp; Franz-Josef Kramer; Rafael B R León-Cachón; Kerstin U Ludwig; Thomas F Wienker; Óscar Chacón-Camacho; Augusto Rojas-Martínez
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate.
Boris B Quednow; Noah Savary; Katja N Spreckelmeyer; Holger Thiele; Norbert Thuerauf; Mohammad R Toliat; Michael Wagner; Thomas F Wienker; Jürgen Brinkmeyer; Marion Clepce; Norbert Dahmen; Amalia Diaz-Lacava; Ingo Frommann; Jürgen Gallinat; Gerhard Gründer; Falk Kiefer; Leonhard Lennertz; Wolfgang Maier; Tomislav Majic; Arian Mobascher; Rainald Mössner; Francesco Musso; Michael Nothnagel; Peter Nürnberg; Nadine Petrovsky; Georg Winterer
Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating.
Amalia Diaz-Lacava; Maja Walier; Gustavo Penacino; Thomas F Wienker; Max P Baur
Spatial assessment of Argentinean genetic admixture with geographical information systems.

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All Publications

2012: Elisabeth Mangold; Sergio G Muñoz-Jiménez; Markus M Nöthen; Stefanie Nowak; Rocío Ortiz-López; Mario Paredes-Zenteno; Heiko Reutter; Abelardo Arizpe-Cantú; Stefan Herms; Michael Knapp; Franz-Josef Kramer; Rafael B R León-Cachón; Kerstin U Ludwig; Thomas F Wienker; Óscar Chacón-Camacho; Augusto Rojas-Martínez
Evaluating SKI as a candidate gene for non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2012;120(5):373-7.
2012: Boris B Quednow; Noah Savary; Katja N Spreckelmeyer; Holger Thiele; Norbert Thuerauf; Mohammad R Toliat; Michael Wagner; Thomas F Wienker; Jürgen Brinkmeyer; Marion Clepce; Norbert Dahmen; Amalia Diaz-Lacava; Ingo Frommann; Jürgen Gallinat; Gerhard Gründer; Falk Kiefer; Leonhard Lennertz; Wolfgang Maier; Tomislav Majic; Arian Mobascher; Rainald Mössner; Francesco Musso; Michael Nothnagel; Peter Nürnberg; Nadine Petrovsky; Georg Winterer
Schizophrenia risk polymorphisms in the TCF4 gene interact with smoking in the modulation of auditory sensory gating.
Proceedings of the National Academy of Sciences of the United States of America 2012;109(16):6271-6.
2011: Amalia Diaz-Lacava; Maja Walier; Gustavo Penacino; Thomas F Wienker; Max P Baur
Spatial assessment of Argentinean genetic admixture with geographical information systems.
Forensic science international. Genetics 2011;5(4):297-302.
2011: Stefan Pabst; M Golebiewski; S Herms; A Karpushova; A Díaz-Lacava; M Walier; S Zimmer; Sven Cichon; Thomas F Wienker; Markus M Nöthen; Georg Nickenig; R Meyer; Dirk Skowasch; Christian Grohé
Caspase recruitment domain 15 gene haplotypes in sarcoidosis.
Tissue antigens 2011;77(4):333-7.
2011: Amalia Diaz-Lacava; Maja Walier; Sascha Willuweit; Thomas F Wienker; Rolf Fimmers; Max P Baur; Lutz Roewer
Geostatistical inference of main Y-STR-haplotype groups in Europe.
Forensic science international. Genetics 2011;5(2):91-4.
2011: Osman El-Maarri; Maja Walier; Frank Behne; Jan van Üüm; Heike Singer; Amalia Diaz-Lacava; Nicole Nüsgen; Barbara Niemann; Matthias Watzka; Jochen Reinsberg; Hans van der Ven; Thomas F Wienker; Birgit Stoffel-Wagner; Rainer Schwaab; Johannes Oldenburg
Methylation at global LINE-1 repeats in human blood are affected by gender but not by age or natural hormone cycles.
PloS one 2011;6(1):e16252.
2011: Nilma Almeida de Assis; Stefanie Nowak; Kerstin U Ludwig; Heiko Reutter; Jennifer Vollmer; Stefanie Heilmann; Nadine Kluck; Carola Lauster; Bert Braumann; Rudolf H Reich; Alexander Hemprich; Michael Knapp; Thomas F Wienker; Franz-Josef Kramer; Per Hoffmann; Markus M Nöthen; Elisabeth Mangold
SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: no evidence for the involvement of common or rare variants in Central European patients.
International journal of pediatric otorhinolaryngology 2011;75(1):49-52.
2011: Frauke Stanke; Tim Becker; Vinod Kumar; Silke Hedtfeld; Christian Becker; Harry Cuppens; Stephanie Tamm; Jennifer Yarden; Ulrike Laabs; Benny Siebert; Luis Fernandez; Milan Macek Jr.; Dragica Radojkovic; Manfred Ballmann; Joachim Greipel; Jean-Jacques Cassiman; Thomas F Wienker; Burkhard Tümmler
Genes that determine immunology and inflammation modify the basic defect of impaired ion conductance in cystic fibrosis epithelia.
Journal of medical genetics 2011;48(1):24-31.
2010: Ulrike Hüffmeier; Steffen Uebe; Arif B Ekici; John Bowes; Emiliano Giardina; Eleanor Korendowych; Kristina Juneblad; Maria Apel; Ross McManus; Pauline Ho; Ian N Bruce; Anthony Ryan; Frank Behrens; Jesús Lascorz; Beate Böhm; Heiko Traupe; Jörg Lohmann; Christian Gieger; Heinz-Erich Wichmann; Christine Herold; Michael Steffens; Lars Klareskog; Thomas F Wienker; Oliver Fitzgerald; Gerd-Marie Alenius; Neil J McHugh; Giuseppe Novelli; Harald Burkhardt; Anne Barton; André Reis
Common variants at TRAF3IP2 are associated with susceptibility to psoriatic arthritis and psoriasis.
Nature genetics 2010;42(11):996-9.
2010: Frauke Stanke; Tim Becker; Silke Hedtfeld; Stephanie Tamm; Thomas F Wienker; Burkhard Tümmler
Hierarchical fine mapping of the cystic fibrosis modifier locus on 19q13 identifies an association with two elements near the genes CEACAM3 and CEACAM6.
Human genetics 2010;127(4):383-94.
2010: Ulrike Hüffmeier; Judith G M Bergboer; Tim Becker; John A Armour; Heiko Traupe; Xavier Estivill; Eva Riveira-Munoz; Rotraut Mössner; Kristian Reich; Werner Kurrat; Thomas F Wienker; Joost Schalkwijk; Patrick L J M Zeeuwen; André Reis
Replication of LCE3C-LCE3B CNV as a risk factor for psoriasis and analysis of interaction with other genetic risk factors.
The Journal of investigative dermatology 2010;130(4):979-84.
2010: Eva Drews; Ildiko Rácz; Amalia Diaz Lacava; Alexander Barth; Andras Bilkei-Gorzó; Thomas F Wienker; Andreas Zimmer
Quantitative trait loci contributing to physiological and behavioural ethanol responses after acute and chronic treatment.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2010;13(2):155-69.
2010: Michael Steffens; Tim Becker; Thomas Sander; Rolf Fimmers; Christine Herold; Daniela A Holler; Costin Leu; Stefan Herms; Sven Cichon; Bastian Bohn; Thomas Gerstner; Michael Griebel; Markus M Nöthen; Thomas F Wienker; Max P Baur
Feasible and successful: genome-wide interaction analysis involving all 1.9 x 10(11) pair-wise interaction tests.
Human heredity 2010;69(4):268-84.
2010: Stefan Pabst; Anna Karpushova; Amalia Diaz-Lacava; Stefan Herms; Maja Walier; Sebastian Zimmer; Sven Cichon; Georg Nickenig; Markus M Nöthen; Thomas F Wienker; Christian Grohé
VEGF gene haplotypes are associated with sarcoidosis.
Chest 2010;137(1):156-63.
2009: Stefanie Birnbaum; Kerstin U Ludwig; Heiko Reutter; Stefan Herms; Nilma A de Assis; Amalia Diaz-Lacava; Sandra Barth; Carola Lauster; Gül Schmidt; Martin Scheer; Mitra Saffar; Markus Martini; Rudolf H Reich; Franziska Schiefke; Alexander Hemprich; Simone Pötzsch; Bernd Pötzsch; Thomas F Wienker; Per Hoffmann; Michael Knapp; Franz-Josef Kramer; Markus M Nöthen; Elisabeth Mangold
IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate.
European journal of oral sciences 2009;117(6):766-9.
2009: Elisabeth Mangold; Heiko Reutter; Stefanie Birnbaum; Maja Walier; Manuel Mattheisen; Henning Henschke; Carola Lauster; Gül Schmidt; Franziska Schiefke; Rudolf H Reich; Martin Scheer; Alexander Hemprich; Markus Martini; Bert Braumann; Michael Krimmel; Charlotte Opitz; Jan-Hendrik Lenz; Franz-Josef Kramer; Thomas F Wienker; Markus M Nöthen; Amalia Diaz-Lacava
Genome-wide linkage scan of nonsyndromic orofacial clefting in 91 families of central European origin.
American journal of medical genetics. Part A 2009;149A(12):2680-94.
2009: Ulrike Hüffmeier; Jesús Lascorz; T Becker; F Schürmeier-Horst; A Magener; Arif B Ekici; S Endele; Christian T Thiel; S Thoma-Uszynski; Rotraut Mössner; Kristian Reich; W Kurrat; Thomas F Wienker; Heiko Traupe; André Reis
Characterisation of psoriasis susceptibility locus 6 (PSORS6) in patients with early onset psoriasis and evidence for interaction with PSORS1.
Journal of medical genetics 2009;46(11):736-44.
2009: Jens Treutlein; Sven Cichon; Monika Ridinger; Norbert Wodarz; Michael Soyka; Peter Zill; Wolfgang Maier; Rainald Moessner; Wolfgang Gaebel; Norbert Dahmen; Christoph Fehr; Norbert Scherbaum; Michael Steffens; Kerstin U Ludwig; Josef Frank; H-Erich Wichmann; Stefan Schreiber; Nico Dragano; Wolfgang Sommer; Fernando Leonardi-Essmann; Anbarasu Lourdusamy; Peter J Gebicke-Haerter; Thomas F Wienker; Patrick F Sullivan; Markus M Nöthen; Falk Kiefer; Rainer Spanagel; Karl Mann; Marcella Rietschel
Genome-wide association study of alcohol dependence.
Archives of general psychiatry 2009;66(7):773-84.
2009: Osman El-Maarri; Michael S Kareta; Thomas Mikeska; Tim Becker; Amalia Diaz-Lacava; Judith Junen; Nicole Nüsgen; Frank Behne; Thomas F Wienker; Andreas Waha; Johannes Oldenburg; Frédéric Chédin
A systematic search for DNA methyltransferase polymorphisms reveals a rare DNMT3L variant associated with subtelomeric hypomethylation.
Human molecular genetics 2009;18(10):1755-68.
2009: Katrin Hoffmann; Christian Planitz; Franz Rüschendorf; Bertram Müller-Myhsok; Hans H Stassen; Barbara Lucke; Manuel Mattheisen; Michael Stumvoll; Rolf Bochmann; Martin Zschornack; Thomas F Wienker; Peter Nürnberg; André Reis; Friedrich C Luft; Tom H Lindner
A novel locus for arterial hypertension on chromosome 1p36 maps to a metabolic syndrome trait cluster in the Sorbs, a Slavic population isolate in Germany.
Journal of hypertension 2009;27(5):983-90.
2009: Antonia Flaquer; Christine Fischer; Thomas F Wienker
A new sex-specific genetic map of the human pseudoautosomal regions (PAR1 and PAR2).
Human heredity 2009;68(3):192-200.
2008: Ildiko Racz; Britta Schürmann; Anna Karpushova; Martin Reuter; Sven Cichon; Christian Montag; Robert Fürst; Christian Schütz; Petra Franke; Jana Strohmaier; Thomas F Wienker; Lars Terenius; Urban Osby; Agneta Gunnar; Wolfgang Maier; Andras Bilkei-Gorzó; Markus Nöthen; Andreas Zimmer
The opioid peptides enkephalin and beta-endorphin in alcohol dependence.
Biological psychiatry 2008;64(11):989-97.
2008: Axel M Hillmer; Felix F Brockschmidt; Sandra Hanneken; Sibylle Eigelshoven; Michael Steffens; Antonia Flaquer; Stefan Herms; Tim Becker; Anne-Katrin Kortüm; Dale R Nyholt; Zhen Zhen Zhao; Grant W Montgomery; Nicholas G Martin; Thomas W Mühleisen; Margrieta A Alblas; Susanne Moebus; Karl-Heinz Jöckel; Martina Bröcker-Preuss; Raimund Erbel; Roman Reinartz; Regina C Betz; Sven Cichon; Peter Propping; Max P Baur; Thomas F Wienker; Roland Kruse; Markus M Nöthen
Susceptibility variants for male-pattern baldness on chromosome 20p11.
Nature genetics 2008;40(11):1279-81.
2008: Antonia Flaquer; Gudrun A Rappold; Thomas F Wienker; Christine Fischer
The human pseudoautosomal regions: a review for genetic epidemiologists.
European journal of human genetics : EJHG 2008;16(7):771-9.
2008: Markus Mezger; Michael Steffens; Melanie Beyer; Carolin Manger; Johannes Eberle; Mohammad R Toliat; Thomas F Wienker; Per Ljungman; Holger Hebart; Hans Jürgen Dornbusch; Hermann Einsele; Juergen Loeffler
Polymorphisms in the chemokine (C-X-C motif) ligand 10 are associated with invasive aspergillosis after allogeneic stem-cell transplantation and influence CXCL10 expression in monocyte-derived dendritic cells.
Blood 2008;111(2):534-6.
2008: Marc Fatar; Mark Stroick; Michael Steffens; Eva Senn; Bjoern Reuter; Simone Bukow; Martin Griebe; Angelika Alonso; Peter Lichtner; Peter Bugert; Thomas Meitinger; Thomas F Wienker; Michael G Hennerici
Single-nucleotide polymorphisms of MMP-2 gene in stroke subtypes.
Cerebrovascular diseases (Basel, Switzerland) 2008;26(2):113-9.
2007: Osman El-Maarri; Tim Becker; Judith Junen; Syed Saadi Manzoor; Amalia Diaz-Lacava; Rainer Schwaab; Thomas F Wienker; Johannes Oldenburg
Gender specific differences in levels of DNA methylation at selected loci from human total blood: a tendency toward higher methylation levels in males.
Human genetics 2007;122(5):505-14.
2007: Rami Abou Jamra; Robert Fuerst; RAdka Kaneva; Guillermo Orozco Diaz; Fabio Rivas; Fermin Mayoral; Eudoxia Gay; Sebastian Sans; Maria Jose Gonzalez; Susana Gil; Francisco Cabaleiro; Francisco Del Rio; Fermin Perez; Jesus Haro; Georg Auburger; vihra milanova; Christian Kostov; Vesselin Chorbov; Vessela Stoyanova; Amelia Nikolova-Hill; Georgi Onchev; Ivo Kremensky; Assen Jablensky; Thomas G. Schulze; Peter Propping; Marcella Rietschel; Markus M Nothen; Sven Cichon; Thomas F Wienker; Johannes Schumacher
The first genomewide interaction and locus-heterogeneity linkage scan in bipolar affective disorder: strong evidence of epistatic effects between loci on chromosomes 2q and 6q.
American journal of human genetics 2007;81(5):974-86.
2007: Regina C Betz; Jana Pforr; Antonia Flaquer; Silke Redler; Sandra Hanneken; Sibylle Eigelshoven; Anne-Katrin Kortüm; Thomas Tüting; Julien Lambert; Jozef De Weert; Axel M Hillmer; Christine Schmael; Thomas F Wienker; Roland Kruse; Gerhard Lutz; Bettina Blaumeiser; Markus M Nöthen
Loss-of-function mutations in the filaggrin gene and alopecia areata: strong risk factor for a severe course of disease in patients comorbid for atopic disease.
The Journal of investigative dermatology 2007;127(11):2539-43.
2007: Frank Grünhage; Monica Acalovschi; Simona Tirziu; Maja Walier; Thomas F Wienker; Anca Ciocan; Ofelia Mosteanu; Tilman Sauerbruch; Frank Lammert
Increased gallstone risk in humans conferred by common variant of hepatic ATP-binding cassette transporter for cholesterol.
Hepatology (Baltimore, Md.) 2007;46(3):793-801.
2007: K Hoffmann; Manuel Mattheisen; S Dahm; P Nürnberg; C Roe; J Johnson; N J Cox; H E Wichmann; Thomas F Wienker; J Schulze; P E H Schwarz; T H Lindner
A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
Diabetologia 2007;50(7):1418-22.
2007: Tim Becker; Silke Jansen; Stephanie Tamm; Thomas F Wienker; Burkhard Tümmler; Frauke Stanke
Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13.
European journal of human genetics : EJHG 2007;15(7):774-8.
2007: Gudrun Schneider; Teresa C Paus; Gerd A Kullak-Ublick; Peter J Meier Abt; Thomas F Wienker; Thomas Lang; Patricia Van de Vondel; Tilman Sauerbruch; Christoph Reichel
Linkage between a new splicing site mutation in the MDR3 alias ABCB4 gene and intrahepatic cholestasis of pregnancy.
Hepatology (Baltimore, Md.) 2007;45(1):150-8.
2007: Johannes Dietter; Manuel Mattheisen; Robert Fürst; Franz Rüschendorf; Thomas F Wienker; Konstantin Strauch
Linkage analysis using sex-specific recombination fractions with GENEHUNTER-MODSCORE.
Bioinformatics (Oxford, England) 2007;23(1):64-70.
2006: Reinhard Schneppenheim; Johanna A Kremer-Hovinga; Tim Becker; Ulrich Budde; Diana Karpman; Wolfgang Brockhaus; Ingrid Hrachovinová; Bartosz Korczowski; Florian Oyen; Simon Rittich; Johannes von Rosen; Geir Tjønnfjord; John E Pimanda; Thomas F Wienker; Bernhard Lämmle
A common origin of the 4143insA ADAMTS13 mutation.
Thrombosis and haemostasis 2006;96(1):3-6.
2006: Ulrike Hüffmeier; M Steffens; Harald Burkhardt; Jesús Lascorz; Funda Schürmeier-Horst; Markward Ständer; Reinhard Kelsch; Claudia Baumann; Wolfgang Küster; R Mössner; K Reich; Thomas F Wienker; Heiko Traupe; André Reis
Evidence for susceptibility determinant(s) to psoriasis vulgaris in or near PTPN22 in German patients.
Journal of medical genetics 2006;43(6):517-22.
2006: Juergen Loeffler; Michael Steffens; Eva-Maria Arlt; Mohammad R Toliat; Markus Mezger; Anita Suk; Thomas F Wienker; Holger Hebart; Peter Nürnberg; Michael Boeckh; Per Ljungman; Rudolf Trenschel; Hermann Einsele
Polymorphisms in the genes encoding chemokine receptor 5, interleukin-10, and monocyte chemoattractant protein 1 contribute to cytomegalovirus reactivation and disease after allogeneic stem cell transplantation.
Journal of clinical microbiology 2006;44(5):1847-50.
2006: Bettina Blaumeiser; Ineke van der Goot; Rolf Fimmers; Sandra Hanneken; Sibylle Ritzmann; Katia Seymons; Regina C Betz; Thomas Ruzicka; Thomas F Wienker; Jozef De Weert; Julien Lambert; Roland Kruse; Markus M Nöthen
Familial aggregation of alopecia areata.
Journal of the American Academy of Dermatology 2006;54(4):627-32.
2006: Frauke Stanke; Tim Becker; Harry Cuppens; Vinod Kumar; Jean-Jacques Cassiman; Silke Jansen; Dragica Radojkovic; Benny Siebert; Jennifer Yarden; David W Ussery; Thomas F Wienker; Burkhard Tümmler
The TNFalpha receptor TNFRSF1A and genes encoding the amiloride-sensitive sodium channel ENaC as modulators in cystic fibrosis.
Human genetics 2006;119(3):331-43.
2006: Ulrike Hüffmeier; André Reis; Michael Steffens; Jesús Lascorz; Beate Böhm; Jörg Lohmann; Jörg Wendler; Heiko Traupe; Wolfgang Küster; Thomas F Wienker; Harald Burkhardt
Male restricted genetic association of variant R620W in PTPN22 with psoriatic arthritis.
The Journal of investigative dermatology 2006;126(4):932-5.
2006: Andreas Reif; Sabine Herterich; Alexander Strobel; Ann-Christine Ehlis; D Saur; Christian P Jacob; Thomas F Wienker; Theresia Töpner; Sabrina Fritzen; Ulrich Walter; Angelika Schmitt; Andreas J Fallgatter; Klaus-Peter Lesch
A neuronal nitric oxide synthase (NOS-I) haplotype associated with schizophrenia modifies prefrontal cortex function.
Molecular psychiatry 2006;11(3):286-300.
2006: Michael Steffens; Claudia Lamina; Thomas Illig; Thomas Bettecken; Rainer Vogler; Patricia Entz; Eun-Kyung Suk; Mohammad R Toliat; Norman Klopp; Almuth Caliebe; Inke R König; Karola Köhler; Jan Ludemann; Amalia Diaz-Lacava; Rolf Fimmers; Peter Lichtner; Andreas Ziegler; Andreas Wolf; Michael Krawczak; Peter Nūrnberg; Jochen Hampe; Stefan Schreiber; Thomas Meitinger; H-Erich Wichmann; Kathryn Roeder; Thomas F Wienker; Max P Baur
SNP-based analysis of genetic substructure in the German population.
Human heredity 2006;62(1):20-9.
2005: Jobst Meyer; Kirsten Johannssen; Christine M Freitag; Kerstin Schraut; Isabel Teuber; Astrid Hahner; Christian Mainhardt; Rainald Mössner; Hans-Peter Volz; Thomas F Wienker; Darleen McKeane; Dietrich A Stephan; Guy Rouleau; Andreas Reif; Klaus-Peter Lesch
Rare variants of the gene encoding the potassium chloride co-transporter 3 are associated with bipolar disorder.
The international journal of neuropsychopharmacology / official scientific journal of the Collegium Internationale Neuropsychopharmacologicum (CINP) 2005;8(4):495-504.
2005: Christof Geisen; Matthias Watzka; Katja Sittinger; Michael Steffens; Laurynas Daugela; Erhard Seifried; Clemens R Müller; Thomas F Wienker; Johannes Oldenburg
VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation.
Thrombosis and haemostasis 2005;94(4):773-9.
2005: Axel M Hillmer; Sandra Hanneken; Sibylle Ritzmann; Tim Becker; Jan Freudenberg; Felix F Brockschmidt; Antonia Flaquer; Yun Freudenberg-Hua; Rami Abou Jamra; Christine Metzen; Uwe Heyn; Nadine Schweiger; Regina C Betz; Bettina Blaumeiser; Jochen Hampe; Stefan Schreiber; Thomas G. Schulze; Hans Christian Hennies; Johannes Schumacher; Peter Propping; Thomas Ruzicka; Sven Cichon; Thomas F Wienker; Roland Kruse; Markus M Nothen
Genetic variation in the human androgen receptor gene is the major determinant of common early-onset androgenetic alopecia.
American journal of human genetics 2005;77(1):140-8.
2005: Vytautas Ivaskevicius; Egle Jusciute; Michael Steffens; Christof Geisen; Peter Hanfland; Thomas F Wienker; Erhard Seifried; Johannes Oldenburg
gammaAla82Gly represents a common fibrinogen gamma-chain variant in Caucasians.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2005;16(3):205-8.
2005: Konstantin Strauch; Robert Fürst; Franz Rüschendorf; Christine Windemuth; Johannes Dietter; Antonia Flaquer; Max P Baur; Thomas F Wienker
Linkage analysis of alcohol dependence using MOD scores.
BMC genetics 2005;6 Suppl 1():S162.
2005: Ulrike Hüffmeier; Heiko Traupe; Harald Burkhardt; Funda Schürmeier-Horst; Jesús Lascorz; Beate Böhm; Jörg Lohmann; Markward Ständer; Jörg Wendler; Reinhard Kelsch; Claudia Baumann; Wolfgang Küster; Thomas F Wienker; André Reis
Lack of evidence for genetic association to RUNX1 binding site at PSORS2 in different German psoriasis cohorts.
The Journal of investigative dermatology 2005;124(1):107-10.
2004: Johannes Dietter; Alexander Spiegel; Dieter an Mey; Hans-Joachim Pflug; Hussam Al-Kateb; Katrin Hoffmann; Thomas F Wienker; Konstantin Strauch
Efficient two-trait-locus linkage analysis through program optimization and parallelization: application to hypercholesterolemia.
European journal of human genetics : EJHG 2004;12(7):542-50.
2004: Thorsten Kurz; Konstantin Strauch; Henriette Dietrich; Sandra Braun; Steffen Hierl; Silvija-Pera Jerkic; Thomas F Wienker; Klaus A Deichmann; Andrea Heinzmann
Multilocus haplotype analyses reveal association between 5 novel IL-15 polymorphisms and asthma.
The Journal of allergy and clinical immunology 2004;113(5):896-901.
2004: Alexandra Weber; Klaus-Peter Wandinger; Wolf Mueller; Orhan Aktas; Oliver Wengert; Eva Grundström; Stefan Ehrlich; Christine Windemuth; Tanja Kuhlmann; Thomas F Wienker; Wolfgang Brück; Frauke Zipp
Identification and functional characterization of a highly polymorphic region in the human TRAIL promoter in multiple sclerosis.
Journal of neuroimmunology 2004;149(1-2):195-201.
2004: Konstantin Strauch; Max P Baur; Thomas F Wienker
A recoding scheme for X-linked and pseudoautosomal loci to be used with computer programs for autosomal LOD-score analysis.
Human heredity 2004;58(1):55-8.
2003: Johannes Schumacher; Andreas C J Otte; Tim Becker; Yuli Sun; Thomas F Wienker; Brunhilde Wirth; Petra Franke; Rami Abou Jamra; Peter Propping; Jürgen Deckert; Markus M Nöthen; Sven Cichon
No evidence for DUP25 in patients with panic disorder using a quantitative real-time PCR approach.
Human genetics 2003;114(1):115-7.
2003: Peter Hensen; Christine Windemuth; Ulrike Hüffmeier; Franz Rüschendorf; Antje Stadelmann; V Hoppe; D Fenneker; Markward Ständer; M Schmitt-Egenolf; Thomas F Wienker; Heiko Traupe; André Reis
Association scan of the novel psoriasis susceptibility region on chromosome 19: evidence for both susceptible and protective loci.
Experimental dermatology 2003;12(4):490-6.
2003: Rainer G Ruf; Arno Fuchshuber; Stephanie M Karle; Arnaud Lemainque; Kirsten Huck; Thomas F Wienker; Edgar Otto; Friedhelm Hildebrandt
Identification of the first gene locus (SSNS1) for steroid-sensitive nephrotic syndrome on chromosome 2p.
Journal of the American Society of Nephrology : JASN 2003;14(7):1897-900.
2003: Konstantin Strauch; Rolf Fimmers; Max P Baur; Thomas F Wienker
How to model a complex trait. 2. Analysis with two disease loci.
Human heredity 2003;56(4):200-11.
2003: Konstantin Strauch; Rolf Fimmers; Max P Baur; Thomas F Wienker
How to model a complex trait. 1. General considerations and suggestions.
Human heredity 2003;55(4):202-10.
2002: Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Amedeo Bianchi; Federico Zara; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; R Nabbout-Tarantino; Jean-François Prud'homme; Olivier Dulac; Louise Bate; R Mark Gardiner; Dick Lindhout; Thomas F Wienker; Dieter Janz; Thomas Sander
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizures.
Epilepsy research 2002;51(1-2):23-9.
2002: Thomas Sander; Christine Windemuth; Herbert Schulz; Kathrin Saar; Elena Gennaro; Amedeo Bianchi; Federico Zara; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; Jean-François Prud'homme; Olivier Dulac; Louise Bate; R Mark Gardiner; Gerrit-Jan de Haan; Guus A M A J Janssen; Jorine Witte; D J J Halley; Dick Lindhout; Thomas F Wienker; Dieter Janz
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
American journal of medical genetics 2002;114(6):673-8.
2002: Jobst Meyer; W Saam; Rainald Mössner; O Cangir; Gabriela Ortega; Thomas Tatschner; Peter Riederer; Thomas F Wienker; Klaus-Peter Lesch
Evolutionary conserved microsatellites in the promoter region of the 5-hydroxytryptamine receptor 2C gene (HTR2C) are not associated with bipolar disorder in females.
Journal of neural transmission (Vienna, Austria : 1996) 2002;109(5-6):939-46.
2002: Markus Feldkötter; Verena Schwarzer; Radu Wirth; Thomas F Wienker; Brunhilde Wirth
Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy.
American journal of human genetics 2002;70(2):358-68.
2002: Jobst Meyer; Gabriela Ortega; K Schraut; G Nürnberg; Franz Rüschendorf; Kathrin Saar; Rainald Mössner; Thomas F Wienker; André Reis; Gerald Stöber; Klaus-Peter Lesch
Exclusion of the neuronal nicotinic acetylcholine receptor alpha7 subunit gene as a candidate for catatonic schizophrenia in a large family supporting the chromosome 15q13-22 locus.
Molecular psychiatry 2002;7(2):220-3.
2002: Heymut Omran; Gürsel Sasmaz; Karsten Häffner; Andreas Volz; Heike Olbrich; Rachid Melkaoui; Edgar Otto; Thomas F Wienker; Rudolf Korinthenberg; Matthias Brandis; Corinne Antignac; Friedhelm Hildebrandt
Identification of a gene locus for Senior-Løken syndrome in the region of the nephronophthisis type 3 gene.
Journal of the American Society of Nephrology : JASN 2002;13(1):75-9.
2001: Sven Cichon; Johannes Schumacher; Daniel J Müller; M Hürter; Christine Windemuth; Konstantin Strauch; S Hemmer; Thomas G. Schulze; Gabriele D Schmidt-Wolf; Margot Albus; Margitta Borrmann-Hassenbach; E Franzek; Mario Lanczik; J Fritze; R Kreiner; U Reuner; B Weigelt; J Minges; Dirk Lichtermann; Bernard Lerer; Kyra Sarner Kanyas; Max P Baur; Thomas F Wienker; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen
A genome screen for genes predisposing to bipolar affective disorder detects a new susceptibility locus on 8q.
Human molecular genetics 2001;10(25):2933-44.
2001: Katja Grohmann; Markus Schuelke; Alexander Diers; K Hoffmann; B Lucke; C Adams; Enrico Bertini; H Leonhardt-Horti; Francesco Muntoni; Robert Ouvrier; A Pfeufer; Rainer Rossi; Lionel Van Maldergem; Jo Wilmshurst; Thomas F Wienker; Michael Sendtner; Sabine Rudnik-Schöneborn; Klaus Zerres; Christoph Hübner
Mutations in the gene encoding immunoglobulin mu-binding protein 2 cause spinal muscular atrophy with respiratory distress type 1.
Nature genetics 2001;29(1):75-7.
2001: Frauke Zipp; Christine Windemuth; J Dichgans; Thomas F Wienker; R Martin; C Müller
Peripheral blood cell bulk cultures are not suitable for the analysis of the genetic control of T-cell cytokine function.
Immunology letters 2001;78(1):21-7.
2001: Regina C Betz; Benedikt Schoser; D Kasper; Kenneth Ricker; A Ramírez; Valentin Stein; Torberg Torbergsen; YA Lee; Markus M Nöthen; Thomas F Wienker; Jean-Pierre Malin; Peter Propping; A Reis; Wilhelm Mortier; Thomas J Jentsch; Matthias Vorgerd; Christian Kubisch
Mutations in CAV3 cause mechanical hyperirritability of skeletal muscle in rippling muscle disease.
Nature genetics 2001;28(3):218-9.
2001: Sven Cichon; Gabriele D Schmidt-Wolf; Johannes Schumacher; Daniel J Müller; M Hürter; Thomas G. Schulze; Margot Albus; Margitta Borrmann-Hassenbach; E Franzek; Mario Lanczik; J Fritze; R Kreiner; B Weigelt; J Minges; Dirk Lichtermann; Bernard Lerer; Kyra Sarner Kanyas; Konstantin Strauch; Christine Windemuth; Max P Baur; Thomas F Wienker; Wolfgang Maier; Marcella Rietschel; Peter Propping; Markus M Nöthen
A possible susceptibility locus for bipolar affective disorder in chromosomal region 10q25--q26.
Molecular psychiatry 2001;6(3):342-9.
2001: Konstantin Strauch; Manuela Bogdanow; Rolf Fimmers; Max P Baur; Thomas F Wienker
Linkage analysis of asthma and atopy including models with genomic imprinting.
Genetic epidemiology 2001;21 Suppl 1():S204-9.
2001: Gerald Stöber; Bruno Pfuhlmann; G Nürnberg; Armin Schmidtke; André Reis; E Franzek; Thomas F Wienker
Towards the genetic basis of periodic catatonia: pedigree sample for genome scan I and II.
European archives of psychiatry and clinical neuroscience 2001;251 Suppl 1():I25-30.
2001: S Niemann; J Becker-Follmann; G Nürnberg; Franz Rüschendorf; N Sieweke; Monika Hügens-Penzel; Heiko Traupe; Thomas F Wienker; André Reis; Ulrich Müller
Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma.
American journal of medical genetics 2001;98(1):32-6.
2000: Thorsten Kurz; Konstantin Strauch; Andrea Heinzmann; Sandra Braun; M Jung; Franz Rüschendorf; M F Moffatt; William O C M Cookson; F Inacio; A Ruffilli; G Nordskov-Hansen; G Peltre; Johannes Forster; Joachim Kuehr; A Reis; Thomas F Wienker; Klaus A Deichmann
A European study on the genetics of mite sensitization.
The Journal of allergy and clinical immunology 2000;106(5):925-32.
2000: Heymut Omran; Karsten Häffner; A Völkel; Joachim Kuehr; U P Ketelsen; U H Ross; Nikolaus Konietzko; Thomas F Wienker; Matthias Brandis; Friedhelm Hildebrandt
Homozygosity mapping of a gene locus for primary ciliary dyskinesia on chromosome 5p and identification of the heavy dynein chain DNAH5 as a candidate gene.
American journal of respiratory cell and molecular biology 2000;23(5):696-702.
2000: Gerald Stöber; Kathrin Saar; Franz Rüschendorf; Jobst Meyer; G Nürnberg; Susanne Jatzke; E Franzek; André Reis; Klaus-Peter Lesch; Thomas F Wienker; Helmut Beckmann
Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
American journal of human genetics 2000;67(5):1201-7.
2000: Frauke Zipp; Christine Windemuth; H Pankow; J Dichgans; Thomas F Wienker; R Martin; C Müller
Multiple sclerosis associated amino acids of polymorphic regions relevant for the HLA antigen binding are confined to HLA-DR2.
Human immunology 2000;61(10):1021-30.
2000: Y A Lee; Franz Rüschendorf; Christine Windemuth; M Schmitt-Egenolf; Antje Stadelmann; G Nürnberg; Markward Ständer; Thomas F Wienker; André Reis; Heiko Traupe
Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13.
American journal of human genetics 2000;67(4):1020-4.
2000: Kristin Bosse; Regina C Betz; YA Lee; Thomas F Wienker; A Reis; H Kleen; Peter Propping; Sven Cichon; Markus M Nöthen
Localization of a gene for syndactyly type 1 to chromosome 2q34-q36.
American journal of human genetics 2000;67(2):492-7.
2000: Gerald Stöber; Jobst Meyer; Indrajit Nanda; Thomas F Wienker; Kathrin Saar; Michael Knapp; Susanne Jatzke; Michael Schmid; Klaus-Peter Lesch; Helmut Beckmann
Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13.
American journal of medical genetics 2000;96(3):392-7.
2000: Thomas Sander; Herbert Schulz; Kathrin Saar; Elena Gennaro; M C Riggio; Amedeo Bianchi; Federico Zara; D Luna; Christine Bulteau; Anna Kaminska; Dorothée Ville; Cécile Cieuta; F Picard; Jean-François Prud'homme; Louise Bate; A Sundquist; R Mark Gardiner; Guus A M A J Janssen; Gerrit-Jan de Haan; Dorothée G A Kasteleijn-Nolst Trenité; Adri Bader; Dick Lindhout; Olaf Riess; Thomas F Wienker; Dieter Janz; A Reis
Genome search for susceptibility loci of common idiopathic generalised epilepsies.
Human molecular genetics 2000;9(10):1465-72.
2000: Konstantin Strauch; Rolf Fimmers; Thorsten Kurz; Klaus A Deichmann; Thomas F Wienker; Max P Baur
Parametric and nonparametric multipoint linkage analysis with imprinting and two-locus-trait models: application to mite sensitization.
American journal of human genetics 2000;66(6):1945-57.
2000: Regina C Betz; YA Lee; Anette Bygum; Flemming Brandrup; A I Bernal; J Toribio; J I Alvarez; Guido Kukuk; H H Ibsen; H B Rasmussen; Thomas F Wienker; A Reis; Peter Propping; Roland Kruse; Sven Cichon; Markus M Nöthen
A gene for hypotrichosis simplex of the scalp maps to chromosome 6p21.3.
American journal of human genetics 2000;66(6):1979-83.
2000: Peter Propping; Waltraut Friedl; Thomas F Wienker; Siegfried Uhlhaas; Klaus Zerres
ADULT syndrome allelic to limb mammary syndrome (LMS)?
American journal of medical genetics 2000;90(2):179-82.
2000: Gerald Stöber; Jobst Meyer; Indrajit Nanda; Thomas F Wienker; Kathrin Saar; Susanne Jatzke; Michael Schmid; Klaus-Peter Lesch; Helmut Beckmann
hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia.
European archives of psychiatry and clinical neuroscience 2000;250(4):163-8.
1999: Katja Grohmann; Thomas F Wienker; Kathrin Saar; Sabine Rudnik-Schöneborn; Gisela Stoltenburg-Didinger; Rainer Rossi; G Novelli; G Nürnberg; A Pfeufer; B Wirth; André Reis; Klaus Zerres; Christoph Hübner
Diaphragmatic spinal muscular atrophy with respiratory distress is heterogeneous, and one form Is linked to chromosome 11q13-q21.
American journal of human genetics 1999;65(5):1459-62.
1999: Thomas Sander; Herbert Schulz; A M Vieira-Saeker; A Bianchi; U Sailer; Gerhard Bauer; A Scaramelli; Thomas F Wienker; Kathrin Saar; André Reis; Dieter Janz; JT Epplen; Olaf Riess
Evaluation of a putative major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q14.
American journal of medical genetics 1999;88(2):182-7.
1999: N Jacob; Franz Rüschendorf; M Schmitt-Egenolf; H C Hennies; G Friedl; Markward Ständer; Thomas F Wienker; André Reis; Heiko Traupe
Promoter polymorphism at -238 of the tumor necrosis factor alpha gene is not associated with early onset psoriasis when tested by the transmission disequilibrium test.
The Journal of investigative dermatology 1999;112(4):514-6.
1999: Christine Windemuth; A Hahn; Konstantin Strauch; Max P Baur; Thomas F Wienker
Linkage analysis in alcohol dependence.
Genetic epidemiology 1999;17 Suppl 1():S403-7.
1999: Konstantin Strauch; Rolf Fimmers; Christine Windemuth; A Hahn; Thomas F Wienker; Max P Baur
Linkage analysis with adequate modeling of a parent-of-origin effect.
Genetic epidemiology 1999;17 Suppl 1():S331-6.
1998: Martin Vollmer; M Jung; Franz Rüschendorf; Rainer G Ruf; Thomas F Wienker; A Reis; R Krapf; Friedhelm Hildebrandt
The gene for human fibronectin glomerulopathy maps to 1q32, in the region of the regulation of complement activation gene cluster.
American journal of human genetics 1998;63(6):1724-31.
1998: Kathrin Saar; Detlev Schindler; Rolf-Dieter Wegner; A Reis; Thomas F Wienker; Holger Hoehn; Hans Joenje; Karl Sperling; Martin Digweed
Localisation of a Fanconi anaemia gene to chromosome 9p.
European journal of human genetics : EJHG 1998;6(5):501-8.
1998: Hakan R Toka; Sylvia Bähring; David Chitayat; J C Melby; R Whitehead; E Jeschke; Thomas F Wienker; Okan Toka; Herbert Schuster; Friedrich C Luft
Families with autosomal dominant brachydactyly type E, short stature, and severe hypertension.
Annals of internal medicine 1998;129(3):204-8.
1998: J Hampe; Thomas F Wienker; S Schreiber; P Nürnberg
POPSIM: a general population simulation program.
Bioinformatics (Oxford, England) 1998;14(5):458-64.
1998: Thomas Sander; C Peters; Dieter Janz; A Bianchi; Gerhard Bauer; Thomas F Wienker; T Hildmann; JT Epplen; Olaf Riess
The gene encoding the alpha1A-voltage-dependent calcium channel (CACN1A4) is not a candidate for causing common subtypes of idiopathic generalized epilepsy.
Epilepsy research 1998;29(2):115-22.
1998: Herbert Schuster; Okan Toka; Hakan R Toka; Andreas Busjahn; ozgur oztekin; Thomas F Wienker; N Bilginturan; Sylvia Bähring; F Skrabal; Hermann Haller; Friedrich C Luft
A cross-over medication trial for patients with autosomal-dominant hypertension with brachydactyly.
Kidney international 1998;53(1):167-72.
1997: M W Laass; Hans Christian Hennies; S Preis; Howard P Stevens; M Jung; Irene M Leigh; Thomas F Wienker; André Reis
Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping.
Human genetics 1997;101(3):376-82.
1997: Thomas Sander; B Bockenkamp; T Hildmann; R Blasczyk; R Kretz; Thomas F Wienker; Armin Volz; Bettina Schmitz; G Beck-Mannagetta; Olaf Riess; JT Epplen; Dieter Janz; Andreas Ziegler
Refined mapping of the epilepsy susceptibility locus EJM1 on chromosome 6.
Neurology 1997;49(3):842-7.
1997: Ramin Naraghi; Herbert Schuster; Hakan R Toka; Sylvia Bähring; Okan Toka; ozgur oztekin; N Bilginturan; Hans Knoblauch; Thomas F Wienker; Andreas Busjahn; Hermann Haller; Rudolf Fahlbusch; Friedrich C Luft
Neurovascular compression at the ventrolateral medulla in autosomal dominant hypertension and brachydactyly.
Stroke; a journal of cerebral circulation 1997;28(9):1749-54.
1997: Thomas Sander; T Hildmann; R Kretz; R Fürst; U Sailer; Gerhard Bauer; Bettina Schmitz; G Beck-Mannagetta; Thomas F Wienker; Dieter Janz
Allelic association of juvenile absence epilepsy with a GluR5 kainate receptor gene (GRIK1) polymorphism.
American journal of medical genetics 1997;74(4):416-21.
1997: Sylvia Bähring; T Nagai; Hakan R Toka; I Nitz; Okan Toka; Atakan Aydin; Astrid Mühl; Thomas F Wienker; Herbert Schuster; Friedrich C Luft
Deletion at 12p in a Japanese child with brachydactyly overlaps the assigned locus of brachydactyly with hypertension in a Turkish family.
American journal of human genetics 1997;60(3):732-5.
1997: Kathrin Saar; Krystyna H Chrzanowska; Markus Stumm; M Jung; G Nürnberg; Thomas F Wienker; Eva Seemanová; Rolf-Dieter Wegner; André Reis; Karl Sperling
The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21.
American journal of human genetics 1997;60(3):605-10.
1996: Herbert Schuster; Thomas F Wienker; Hakan R Toka; Sylvia Bähring; E Jeschke; Okan Toka; Andreas Busjahn; A Hempel; C Tahlhammer; W Oelkers; J Kunze; N Bilginturan; Hermann Haller; Friedrich C Luft
Autosomal dominant hypertension and brachydactyly in a Turkish kindred resembles essential hypertension.
Hypertension 1996;28(6):1085-92.
1996: A Pfeufer; Karl Josef Osterziel; H Urata; G Borck; Herbert Schuster; Thomas F Wienker; Rainer Dietz; Friedrich C Luft
Angiotensin-converting enzyme and heart chymase gene polymorphisms in hypertrophic cardiomyopathy.
The American journal of cardiology 1996;78(3):362-4.
1996: Thomas Sander; T Hildmann; Dieter Janz; Thomas F Wienker; A Bianchi; Gerhard Bauer; U Sailer; A Scaramelli; Heidemarie Neitzel; Bettina Schmitz; M E Bailey; G Beck-Mannagetta; keith jack johnson; M G Darlison
Exclusion of linkage between idiopathic generalized epilepsies and the GABAA receptor alpha 1 and gamma 2 subunit gene cluster on chromosome 5.
Epilepsy research 1996;23(3):235-44.
1996: Thomas Sander; T Hildmann; Thomas F Wienker; C Ramel; G Beck-Mannagetta; A Bianchi; U Sailer; K Berek; Gerhard Bauer; Heidemarie Neitzel; Bettina Schmitz; Martina Durner; keith jack johnson; Dieter Janz
Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.
American journal of medical genetics 1996;67(1):31-9.
1995: Herbert Schuster; Thomas F Wienker; U Stremmler; B Noll; A Steinmetz; Friedrich C Luft
An angiotensin-converting enzyme gene variant is associated with acute myocardial infarction in women but not in men.
The American journal of cardiology 1995;76(8):601-3.
1995: Thomas Sander; Dieter Janz; C Ramel; Christopher A Ross; W Paschen; T Hildmann; Thomas F Wienker; A Bianchi; Gerhard Bauer; U Sailer
Refinement of map position of the human GluR6 kainate receptor gene (GRIK2) and lack of association and linkage with idiopathic generalized epilepsies.
Neurology 1995;45(9):1713-20.
1995: Thomas Sander; T Hildmann; Dieter Janz; Thomas F Wienker; Heidemarie Neitzel; A Bianchi; Gerhard Bauer; U Sailer; K Berek; Bettina Schmitz
The phenotypic spectrum related to the human epilepsy susceptibility gene "EJM1".
Annals of neurology 1995;38(2):210-7.
1989: Rolf Fimmers; M Neugebauer; J Dennert; Thomas F Wienker; Max P Baur
Association and sibpair analysis for the HLA, Gm, Km, and insulin polymorphisms in multiplex IDDM families.
Genetic epidemiology 1989;6(1):107-12.