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Thomas Illig

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Genes & Molecular Sequences

Physiology

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Ramesh Chandra Pandey; Ernst Rietschel; Maximilian Schieck; Burkhard Simma; Andrea von Berg; Norman Klopp; Otto Laub; Liming Liang; Sven Michel; Aristea Binia; Albrecht Bufe; Andre Franke; Thomas Frischer; Jon Genuneit; Andrea Heinzmann; Thomas Illig; Michael Kabesch
Polymorphisms in extracellular signal-regulated kinase family influence genetic susceptibility to asthma.
Diana Raedler; Erika von Mutius; Sabina Illi; Thomas Illig; Michael Kabesch; Leonardo Araujo Pinto; Bianca Schaub
IL10 polymorphisms influence neonatal immune responses, atopic dermatitis, and wheeze at age 3 years.
Ramesh Chandra Pandey; Ernst Rietschel; Michaela Schedel; Burkhard Simma; Riccardina Tesse; Andrea von Berg; Norman Klopp; Otto Laub; Liming Liang; Sven Michel; Aristea Binia; Albrecht Bufe; Andre Franke; Thomas Frischer; Jon Genuneit; Andrea Heinzmann; Thomas Illig; Michael Kabesch
Genetic variation in the Toll-like receptor signaling pathway is associated with childhood asthma.

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All Publications

2013: Ramesh Chandra Pandey; Ernst Rietschel; Maximilian Schieck; Burkhard Simma; Andrea von Berg; Norman Klopp; Otto Laub; Liming Liang; Sven Michel; Aristea Binia; Albrecht Bufe; Andre Franke; Thomas Frischer; Jon Genuneit; Andrea Heinzmann; Thomas Illig; Michael Kabesch
Polymorphisms in extracellular signal-regulated kinase family influence genetic susceptibility to asthma.
The Journal of allergy and clinical immunology 2013;131(4):1245-7.
2013: Diana Raedler; Erika von Mutius; Sabina Illi; Thomas Illig; Michael Kabesch; Leonardo Araujo Pinto; Bianca Schaub
IL10 polymorphisms influence neonatal immune responses, atopic dermatitis, and wheeze at age 3 years.
The Journal of allergy and clinical immunology 2013;131(3):789-96.
2013: Ramesh Chandra Pandey; Ernst Rietschel; Michaela Schedel; Burkhard Simma; Riccardina Tesse; Andrea von Berg; Norman Klopp; Otto Laub; Liming Liang; Sven Michel; Aristea Binia; Albrecht Bufe; Andre Franke; Thomas Frischer; Jon Genuneit; Andrea Heinzmann; Thomas Illig; Michael Kabesch
Genetic variation in the Toll-like receptor signaling pathway is associated with childhood asthma.
The Journal of allergy and clinical immunology 2013;131(2):602-5.
2013: Anna Floegel; Andreas Fritsche; Hans-Ulrich Häring; Thomas Illig; Hans-Georg Joost; Kristin Mühlenbruch; Annette Peters; Cornelia Prehn; Michael Roden; Matthias B Schulze; Norbert Stefan; Rui Wang-Sattler; Zhonghao Yu; Martin Hrabe de Angelis; Jerzy Adamski; Heiner Boeing; Dagmar Drogan; Tobias Pischon
Identification of serum metabolites associated with risk of type 2 diabetes using a targeted metabolomic approach.
Diabetes 2013;62(2):639-48.
2013: Sonja Zeilinger; Jerzy Adamski; Hansjörg Baurecht; Christian Gieger; Anja Kleinschmidt; Norman Klopp; Brigitte Kühnel; Eva Lattka; Annette Peters; Konstantin Strauch; Melanie Waldenberger; Stephan Weidinger; Thomas Illig
Tobacco smoking leads to extensive genome-wide changes in DNA methylation.
PloS one 2013;8(5):e63812.
2013: Tao Xu; Zhonghao Yu; H-Erich Wichmann; Jerzy Adamski; Erik Bader; Xiao Dong; Christina Holzapfel; Thomas Illig; Marta Jaremek; Karl H Ladwig; Yixue Li; Katrin Perstorfer; Annette Peters; Cornelia Prehn; Wolfgang Rathmann; Werner Roemisch-Margl; Karsten Suhre; Fabian Theis; Henri Wallaschofski; Rui Wang-Sattler
Effects of smoking and smoking cessation on human serum metabolite profile: results from the KORA cohort study.
BMC medicine 2013;11():60.
2013: Nadja Knoll; Annette Peters; André Scherag; Anna-Lena Volckmar; Heinz-Erich Wichmann; Christian Gieger; Harald Grallert; Johannes Hebebrand; Thomas Illig; Ivonne Jarick; Martin Klingenspor; Anke Hinney
Gene set of nuclear-encoded mitochondrial regulators is enriched for common inherited variation in obesity.
PloS one 2013;8(2):e55884.
2013: Andreas Hector; Thomas Illig; Julia Kammermeier; Matthias Kappler; Norman Klopp; Michael Kormann; Veronica Marcos; Lauren Mays; Nikolaus Rieber; Joachim Riethmueller; Friederike Serve; Martin Stern; Stefan Zielen; Sofia Burdi; Gerd Döring; Olaf Eickmeier; Fabian Falkenstein; Ute Graepler-Mainka; Matthias Griese; Dominik Hartl
Expression and regulation of interferon-related development regulator-1 in cystic fibrosis neutrophils.
American journal of respiratory cell and molecular biology 2013;48(1):71-7.
2013: Divya Mehta; Thomas Meitinger; Matthias Nauck; Maren Carstensen; Gertrud Eckstein; Christian Gieger; Katharina Heim; Christian Herder; Georg Homuth; Thomas Illig; Michael Roden; Claudia Schurmann; Uwe Völker; Holger Prokisch
Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood.
European journal of human genetics : EJHG 2013;21(1):48-54.
2012: Zhonghao Yu; Guangju Zhai; Heinz-Erich Wichmann; Tao Xu; Jerzy Adamski; Christian Gieger; Ying He; Joachim Heinrich; Thomas Illig; Eva Lattka; Yixue Li; Kirstin Mittelstraß; Annette Peters; Cornelia Prehn; Werner Römisch-Margl; Paula Singmann; Nicole Soranzo; Tim D Spector; Marie Standl; Karsten Suhre; Elisabeth Thiering; Rui Wang-Sattler
Human serum metabolic profiles are age dependent.
Aging cell 2012;11(6):960-7.
2012: Oemer-Necmi Goek; Margit Heier; Thomas Illig; Wolfgang Koenig; Anna Köttgen; Cornelia Prehn; Werner Römisch-Margl; Peggy Sekula; Karsten Suhre; Rui Wang-Sattler; Guangju Zhai; Jerzy Adamski; Angela Döring; Christian Gieger; Christa Meisinger
Serum metabolite concentrations and decreased GFR in the general population.
American journal of kidney diseases : the official journal of the National Kidney Foundation 2012;60(2):197-206.
2012: Mascha C Schmied; Karl Vass; H-Erich Wichmann; Karin Zebenholzer; Sonja Zehetmayer; Eduard Auff; Barbara Bajer-Kornek; Thomas Berger; Rainer Ehling; Franz Fazekas; Sigrid Fuchs; Christian Gieger; Christoph Hotzy; Klaus Huber; Thomas Illig; Michael Khalil; W Kristoferitsch; Fritz Leutmezer; Peter Lichtner; Thomas Meitinger; Markus Reindl; Helena Schmidt; Alexander Zimprich
Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients.
Neurogenetics 2012;13(2):181-7.
2012: André Scherag; Thorkild I A Sørensen; André M Toschke; Anne Ruth; Tanja Boes; Harald Grallert; Katrine Grau; Johannes Hebebrand; Iris M Heid; Anke Hinney; Thomas Illig; Michaela Kleber; Andreea-Liliana Kolbe; Thomas Reinehr
SDCCAG8 obesity alleles and reduced weight loss after a lifestyle intervention in overweight children and adolescents.
Obesity (Silver Spring, Md.) 2012;20(2):466-70.
2012: Mahir Karakas; Marcus E Kleber; Jens Baumert; Dhayana Dallmeier; Tanja B Grammer; Thomas Illig; Winfried März; Christa Meisinger; Wolfgang Rottbauer; Günther Silbernagel; Barbara Thorand; Wolfgang Koenig
A variant in the Abo gene explains the variation in soluble E-selectin levels-results from dense genotyping in two independent populations.
PloS one 2012;7(12):e51441.
2012: Anna-Lena Volckmar; Martin Wabitsch; Heinz-Erich Wichmann; Susanna Wiegand; Heike Biebermann; Florian Bolze; Pamela Fischer-Posovszky; Harald Grallert; Johannes Hebebrand; Thomas Illig; Ivonne Jarick; Martin Klingenspor; Nadja Knoll; Heiko Krude; Thomas Reinehr; Winfried Rief; André Scherag; Anke Hinney
Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants.
BMC medical genomics 2012;5():65.
2012: Simone Wahl; Rui Wang-Sattler; Zhonghao Yu; Werner Römisch-Margl; Paula Singmann; Karsten Suhre; Jerzy Adamski; Harald Grallert; Ying He; Christina Holzapfel; Thomas Illig; Michaela Kleber; Kirstin Mittelstrass; Alexey Polonikov; Cornelia Prehn; Thomas Reinehr
Childhood obesity is associated with changes in the serum metabolite profile.
Obesity facts 2012;5(5):660-70.
2012: Jan Krumsiek; Michael V Milburn; Matthew W Mitchell; Robert P Mohney; Werner Römisch-Margl; Karsten Suhre; Fabian J Theis; Brigitte Wägele; Jerzy Adamski; Anne M Evans; Christian Gieger; Thomas Illig; Gabi Kastenmüller
Mining the unknown: a systems approach to metabolite identification combining genetic and metabolic information.
PLoS genetics 2012;8(10):e1003005.
2012: Matthias Arnold; Hansjörg Baurecht; Andre Franke; Mara L Hartsperger; Thomas Illig; Michael Kabesch; Hans-Werner Mewes; Arne Pfeufer; Elke Rodríguez; Marcel Romanos; Volker Stümpflen; Benedikt Wachinger; Juliane Winkelmann; Stephan Weidinger
Network-based SNP meta-analysis identifies joint and disjoint genetic features across common human diseases.
BMC genomics 2012;13():490.
2012: Timo D Müller; Benedetta Nacmias; Marta Ribasés; valdo ricca; Helmut Schäfer; André Scherag; Susann Scherag; Sandro Sorbi; Heinz-Erich Wichmann; Thomas Illig; Ulrike Lehmkuhl; Laura Bellodi; Maria C Cavallini; Elena Cellini; Daniela Di Bella; Stefan Ehrlich; Stefano Erzegovesi; Xavier Estivill; Fernando Fernández-Aranda; Manfred Fichter; Christian Fleischhaker; Harald Grallert; Monica Gratacòs; Brandon H Greene; Johannes Hebebrand; Beate Herpertz-Dahlmann; Wolfgang Herzog; Anke Hinney
Fat mass and obesity-associated gene (FTO) in eating disorders: evidence for association of the rs9939609 obesity risk allele with bulimia nervosa and anorexia nervosa.
Obesity facts 2012;5(3):408-19.
2012: Carolin Jourdan; Gabi Kastenmüller; Jan Krumsiek; Jerzy Adamski; Elisabeth Altmaier; Angela Döring; Christian Gieger; Thomas Illig; Christa Meisinger; Annette Peters; Ann-Kristin Petersen; Cornelia Prehn; Werner Römisch-Margl; Karsten Suhre; Fabian J Theis; Rui Wang-Sattler; H-Erich Wichmann; Jakob Linseisen
Body fat free mass is associated with the serum metabolite profile in a population-based study.
PloS one 2012;7(6):e40009.
2012: Jessica Mühlhaus; Wilfried Pott; Carolin Pütter; Thomas Reinehr; Susann Scherag; Hai-Jun Wang; Susanna Wiegand; Özgür Albayrak; Anne-Madeleine Bau; Heike Biebermann; Harald Brumm; Harald Grallert; Annette Grüters; Johannes Hebebrand; Anke Hinney; Thomas Illig; Heiko Krude; André Scherag
Do common variants separate between obese melanocortin-4 receptor gene mutation carriers and non-carriers? The impact of cryptic relatedness.
Hormone research in pædiatrics 2012;77(6):358-68.
2011: Claudia Lamina; Stefan Coassin; Thomas Illig; Florian Kronenberg
Look beyond one's own nose: combination of information from publicly available sources reveals an association of GATA4 polymorphisms with plasma triglycerides.
Atherosclerosis 2011;219(2):698-703.
2011: Laura Maintz; Hansjörg Baurecht; Thomas Bieber; Thomas Illig; E Rodríguez; Stephan Weidinger; C-F Yu; Natalija Novak
Association of single nucleotide polymorphisms in the diamine oxidase gene with diamine oxidase serum activities.
Allergy 2011;66(7):893-902.
2011: Rubén Fernández-Santiago; Manu Sharma; Daniela Berg; Thomas Illig; Johanna Anneser; Thomas Meyer; Albert Ludolph; Thomas Gasser
No evidence of association of FLJ10986 and ITPR2 with ALS in a large German cohort.
Neurobiology of aging 2011;32(3):551.e1-4.
2011: Eva Lattka; Peter Rzehak; Éva Szabó; Viktoria Jakobik; Melanie Weck; Maria Weyermann; Harald Grallert; Dietrich Rothenbacher; Joachim Heinrich; Hermann Brenner; Tamás Decsi; Thomas Illig; Berthold Koletzko
Genetic variants in the FADS gene cluster are associated with arachidonic acid concentrations of human breast milk at 1.5 and 6 mo postpartum and influence the course of milk dodecanoic, tetracosenoic, and trans-9-octadecenoic acid concentrations over the duration of lactation.
The American journal of clinical nutrition 2011;93(2):382-91.
2011: Christina Holzapfel; Harald Grallert; Jens Baumert; Barbara Thorand; Angela Döring; H-Erich Wichmann; Hans Hauner; Thomas Illig; Andreas Mielck
First investigation of two obesity-related loci (TMEM18, FTO) concerning their association with educational level as well as income: the MONICA/KORA study.
Journal of epidemiology and community health 2011;65(2):174-6.
2011: Anna Floegel; Thomas Illig; Hans-Georg Joost; Jerzy Adamski; Heiner Boeing; Dagmar Drogan; Cornelia Prehn; Rui Wang-Sattler; Tobias Pischon
Reliability of serum metabolite concentrations over a 4-month period using a targeted metabolomic approach.
PloS one 2011;6(6):e21103.
2011: Berthold Koletzko; Eva Lattka; Sonja Zeilinger; Thomas Illig; Colin Steer
Genetic variants of the fatty acid desaturase gene cluster predict amounts of red blood cell docosahexaenoic and other polyunsaturated fatty acids in pregnant women: findings from the Avon Longitudinal Study of Parents and Children.
The American journal of clinical nutrition 2011;93(1):211-9.
2010: Denise Horn; Johannes Kapeller; Núria Rivera-Brugués; Ute Moog; Bettina Lorenz-Depiereux; Sebastian Eck; Maja Hempel; Janine Wagenstaller; Alex Gawthrope; Anthony P Monaco; Michael Bonin; Olaf Riess; Eva Wohlleber; Thomas Illig; Connie R Bezzina; Andre Franke; Stephanie Spranger; Pablo Villavicencio-Lorini; Wenke Seifert; Jochen Rosenfeld; Eva Klopocki; Gudrun A Rappold; Tim M Strom
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits.
Human mutation 2010;31(11):E1851-60.
2010: Jeannine Sauber; Jessica Grothe; Maria Behm; André Scherag; Harald Grallert; Thomas Illig; Anke Hinney; Johannes Hebebrand; Susanna Wiegand; Annette Grüters; Heiko Krude; Heike Biebermann
Association of variants in gastric inhibitory polypeptide receptor gene with impaired glucose homeostasis in obese children and adolescents from Berlin.
European journal of endocrinology / European Federation of Endocrine Societies 2010;163(2):259-64.
2010: Claudia Cramer; Elke Link; Maike Horster; Sibylle Koletzko; Carl-P Bauer; Dietrich Berdel; Andrea von Berg; Irina Lehmann; Olf Herbarth; Michael Borte; Beate Schaaf; Heidrun Behrendt; Chih-Mei Chen; Stefanie Sausenthaler; Thomas Illig; H-Erich Wichmann; Joachim Heinrich; Ursula Krämer
Elder siblings enhance the effect of filaggrin mutations on childhood eczema: results from the 2 birth cohort studies LISAplus and GINIplus.
The Journal of allergy and clinical immunology 2010;125(6):1254-1260.e5.
2010: Sylvia Rabstein; Thomas Brüning; Volker Harth; Hans-Peter Fischer; Susanne Haas; Tobias Weiss; Anne Spickenheuer; Christiane Pierl; Christina Justenhoven; Thomas Illig; Caren Vollmert; Christian Baisch; Yon-Dschun Ko; Ute Hamann; Hiltrud Brauch; Beate Pesch
N-acetyltransferase 2, exposure to aromatic and heterocyclic amines, and receptor-defined breast cancer.
European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) 2010;19(2):100-9.
2010: Sathiyavedu T Santhiya; Ganesan Senthil Kumar; Pridhvi Sudhakar; Navnit Gupta; Norman Klopp; Thomas Illig; Torben Söker; Marco Groth; Matthias Platzer; Puthiya M Gopinath; Jochen Graw
Molecular analysis of cataract families in India: new mutations in the CRYBB2 and GJA3 genes and rare polymorphisms.
Molecular vision 2010;16():1837-47.
2010: Susanne Tan; André Scherag; Onno Eilard Janssen; Susanne Hahn; Harald Lahner; Tiina Dietz; Susann Scherag; Harald Grallert; Carla Ivane Ganz Vogel; Rainer Kimmig; Thomas Illig; Klaus Mann; Johannes Hebebrand; Anke Hinney
Large effects on body mass index and insulin resistance of fat mass and obesity associated gene (FTO) variants in patients with polycystic ovary syndrome (PCOS).
BMC medical genetics 2010;11():12.
2010: Timo D Müller; Günter Brönner; Melanie Wandolski; Jophia Carrie; Trang T Nguyen; Brandon H Greene; André Scherag; Harald Grallert; Carla Ig Vogel; Susann Scherag; Winfried Rief; Hans-Erich Wichmann; Thomas Illig; Helmut Schäfer; Johannes Hebebrand; Anke Hinney
Mutation screen and association studies for the fatty acid amide hydrolase (FAAH) gene and early onset and adult obesity.
BMC medical genetics 2010;11():2.
2010: Christoph B Lücking; Peter Lichtner; E R Kramer; C Gieger; Thomas Illig; Martin Dichgans; Daniela Berg; Thomas Gasser
Polymorphisms in the receptor for GDNF (RET) are not associated with Parkinson's disease in Southern Germany.
Neurobiology of aging 2010;31(1):167-8.
2009: S Zeilinger; L A Pinto; W A Nockher; Martin Depner; Norman Klopp; Thomas Illig; Erika von Mutius; H Renz; Michael Kabesch
The effect of BDNF gene variants on asthma in German children.
Allergy 2009;64(12):1790-4.
2009: Eva Fisher; Harald Grallert; Maja Klapper; Albrecht Pfäfflin; Jürgen Schrezenmeir; Thomas Illig; Heiner Boeing; Frank Döring
Evidence for the Thr79Met polymorphism of the ileal fatty acid binding protein (FABP6) to be associated with type 2 diabetes in obese individuals.
Molecular genetics and metabolism 2009;98(4):400-5.
2009: Christiane Winkler; Thomas Illig; Kerstin Koczwara; Ezio Bonifacio; Anette-G Ziegler
HHEX-IDE polymorphism is associated with low birth weight in offspring with a family history of type 1 diabetes.
The Journal of clinical endocrinology and metabolism 2009;94(10):4113-5.
2009: Manu Sharma; Peter Lichtner; Rejko Kruger; Daniela Berg; Claudia Schulte; Thomas Illig; Olaf Riess; Thomas Gasser
Further delineation of the association signal on chromosome 5 from the first whole genome association study in Parkinson's disease.
Neurobiology of aging 2009;30(10):1706-9.
2009: chih-mei Chen; S Weidinger; N Klopp; Stefanie Sausenthaler; W Bischof; Olf Herbarth; M Bauer; Michael Borte; B Schaaf; Irina Lehmann; Heidrun Behrendt; U Krämer; D Berdel; Andrea Von Berg; C P Bauer; Sibylle Koletzko; Thomas Illig; H-Erich Wichmann; Joachim Heinrich
Common variants in FCER1A influence total serum IgE levels from cord blood up to six years of life.
Allergy 2009;64(9):1327-32.
2009: Rubén Fernández-Santiago; Sabine Hoenig; Peter Lichtner; Anne-Dorte Sperfeld; Manu Sharma; Daniela Berg; Oliver Weichenrieder; Thomas Illig; Katharina Eger; Thomas Meyer; Johanna Anneser; Christoph Münch; Stephan Zierz; Thomas Gasser; Albert Ludolph
Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosis.
Journal of neurology 2009;256(8):1337-42.
2009: Mike Böhme; Harald Grallert; Maja Klapper; Christian Gieger; Alexandra Fischer; Iris Heid; H-Erich Wichmann; Frank Döring; Thomas Illig
Association between functional FABP2 promoter haplotypes and body mass index: analyses of 8072 participants of the KORA cohort study.
Molecular nutrition & food research 2009;53(6):681-5.
2009: Jorge Esparza-Gordillo; Stephan Weidinger; Regina Fölster-Holst; Anja Bauerfeind; Franz Ruschendorf; Giannino Patone; Klaus Rohde; Ingo Marenholz; Florian Schulz; Tamara Kerscher; Norbert Hubner; Ulrich Wahn; Stefan Schreiber; Andre Franke; Rainer Vogler; Simon Heath; Hansjörg Baurecht; Natalija Novak; Elke Rodriguez; Thomas Illig; Min Ae Lee-Kirsch; Andrzej Ciechanowicz; Michael Kurek; Tereza Piskackova; Milan Macek Jr.; Young-Ae Lee; Andreas Ruether
A common variant on chromosome 11q13 is associated with atopic dermatitis.
Nature genetics 2009;41(5):596-601.
2009: Christina Justenhoven; Christiane Pierl; Susanne Haas; Hans-Peter Fischer; Ute Hamann; Christian Baisch; Volker Harth; Anne Spickenheuer; Sylvia Rabstein; Caren Vollmert; Thomas Illig; Beate Pesch; Thomas Brüning; Jürgen Dippon; Yon-Dschun Ko; Hiltrud Brauch
Polymorphic loci of E2F2, CCND1 and CCND3 are associated with HER2 status of breast tumors.
International journal of cancer. Journal international du cancer 2009;124(9):2077-81.
2009: Julia Fuchs; Jakob C Mueller; Peter Lichtner; Claudia Schulte; Marita Munz; Daniela Berg; Ullrich Wüllner; Thomas Illig; Manu Sharma; Thomas Gasser
The transcription factor PITX3 is associated with sporadic Parkinson's disease.
Neurobiology of aging 2009;30(5):731-8.
2009: Alexandra Fischer; Harald Grallert; Mike Böhme; Christian Gieger; Inka Boomgaarden; Iris Heid; H-Erich Wichmann; Frank Döring; Thomas Illig
Association analysis between the prostaglandin E synthase 2 R298H polymorphism and body mass index in 8079 participants of the KORA study cohort.
Genetic testing and molecular biomarkers 2009;13(2):223-6.
2009: M S D Kormann; R Ferstl; Martin Depner; Norman Klopp; S Spiller; Thomas Illig; Christian Vogelberg; Erika von Mutius; C J Kirschning; Michael Kabesch
Rare TLR2 mutations reduce TLR2 receptor function and can increase atopy risk.
Allergy 2009;64(4):636-42.
2009: L A Pinto; Martin Depner; L Steudemann; Norman Klopp; Thomas Illig; Erika von Mutius; Michael Kabesch
IL15 gene variants are not associated with asthma and atopy.
Allergy 2009;64(4):643-6.
2009: Annette Peters; Sonja Greven; Iris M Heid; Fiammetta Baldari; Susanne Breitner; tom bellander; Christina Chrysohoou; Thomas Illig; Bénédicte Jacquemin; Wolfgang Koenig; Timo Lanki; Fredrik Nyberg; Juha Pekkanen; Riccardo Pistelli; Regina Rückerl; Christodoulos I Stefanadis; Alexandra Schneider; Jordi Sunyer; H-Erich Wichmann
Fibrinogen genes modify the fibrinogen response to ambient particulate matter.
American journal of respiratory and critical care medicine 2009;179(6):484-91.
2009: Mahir Karakas; Michael M Hoffmann; Caren Vollmert; Dietrich Rothenbacher; Christa Meisinger; Bernhard R Winkelmann; Natalie Khuseyinova; Bernhard O Böhm; Thomas Illig; Winfried März; Wolfgang Koenig
Genetic variation in Fc gamma receptor IIa and risk of coronary heart disease: negative results from two large independent populations.
BMC medical genetics 2009;10():46.
2009: Carla I G Vogel; André Scherag; Günter Brönner; Thuy T Nguyen; Hai-Jun Wang; Harald Grallert; Alexa Bornhorst; Dieter Rosskopf; Henry Völzke; Thomas Reinehr; Winfried Rief; Thomas Illig; H-Erich Wichmann; Helmut Schäfer; Johannes Hebebrand; Anke Hinney
Gastric inhibitory polypeptide receptor: association analyses for obesity of several polymorphisms in large study groups.
BMC medical genetics 2009;10():19.
2009: Carla I G Vogel; Brandon Greene; André Scherag; Timo D Müller; Susann Friedel; Harald Grallert; Iris M Heid; Thomas Illig; H-Erich Wichmann; Helmut Schäfer; Johannes Hebebrand; Anke Hinney
Non-replication of an association of CTNNBL1 polymorphisms and obesity in a population of Central European ancestry.
BMC medical genetics 2009;10():14.
2009: Kathrin Suttner; Isabell Ruoss; Philip Rosenstiel; Martin Depner; Leonardo A Pinto; Michaela Schedel; Jerzy Adamski; Thomas Illig; Stefan Schreiber; Erika von Mutius; Michael Kabesch
HLX1 gene variants influence the development of childhood asthma.
The Journal of allergy and clinical immunology 2009;123(1):82-88.e6.
2008: Iris M Heid; Claudia Lamina; Helmut Küchenhoff; Guido Fischer; Norman Klopp; Melanie Kolz; Harald Grallert; Caren Vollmert; Stefanie Wagner; Cornelia Huth; Julia Müller; Martina Müller; Steven C Hunt; Annette Peters; Bernhard Paulweber; H-Erich Wichmann; Florian Kronenberg; Thomas Illig
Estimating the single nucleotide polymorphism genotype misclassification from routine double measurements in a large epidemiologic sample.
American journal of epidemiology 2008;168(8):878-89.
2008: C Holzapfel; Jens Baumert; H Grallert; A M Müller; Barbara Thorand; Natalie Khuseyinova; C Herder; Christa Meisinger; H Hauner; H E Wichmann; W Koenig; Thomas Illig; N Klopp
Genetic variants in the USF1 gene are associated with low-density lipoprotein cholesterol levels and incident type 2 diabetes mellitus in women: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.
European journal of endocrinology / European Federation of Endocrine Societies 2008;159(4):407-16.
2008: Christian Herder; Thomas Illig; Jens Baumert; Martina Müller; Norman Klopp; Natalie Khuseyinova; Christa Meisinger; Stephan Martin; Barbara Thorand; Wolfgang Koenig
Macrophage migration inhibitory factor (MIF) and risk for coronary heart disease: results from the MONICA/KORA Augsburg case-cohort study, 1984-2002.
Atherosclerosis 2008;200(2):380-8.
2008: Stephan Weidinger; Hansjörg Baurecht; Stefan Wagenpfeil; John Henderson; Natalija Novak; Aileen Sandilands; Huijia Chen; Elke Rodriguez; Grainne M O'Regan; Rosemarie Watson; Haihui Liao; Yiwei Zhao; Jonathan N W N Barker; Michael Allen; Nick Reynolds; Simon Meggitt; Kate Northstone; George D Smith; Carolin Strobl; Caroline Stahl; Thomas Kneib; Norman Klopp; Thomas Bieber; Heidrun Behrendt; Colin N A Palmer; H-Erich Wichmann; Johannes Ring; Thomas Illig; W H Irwin McLean; Alan D Irvine
Analysis of the individual and aggregate genetic contributions of previously identified serine peptidase inhibitor Kazal type 5 (SPINK5), kallikrein-related peptidase 7 (KLK7), and filaggrin (FLG) polymorphisms to eczema risk.
The Journal of allergy and clinical immunology 2008;122(3):560-8.e4.
2008: Christina Justenhoven; Christiane Pierl; Susanne Haas; Hans-Peter Fischer; Christian Baisch; Ute Hamann; Volker Harth; Beate Pesch; Thomas Brüning; Caren Vollmert; Thomas Illig; Jürgen Dippon; Yon-Dschun Ko; Hiltrud Brauch
The CYP1B1_1358_GG genotype is associated with estrogen receptor-negative breast cancer.
Breast cancer research and treatment 2008;111(1):171-7.
2008: Anita Brandstätter; Stefan Kiechl; Barbara Kollerits; Steven C Hunt; Iris M Heid; Stefan Coassin; Johann Willeit; Ted D Adams; Thomas Illig; Paul N Hopkins; Florian Kronenberg
Sex-specific association of the putative fructose transporter SLC2A9 variants with uric acid levels is modified by BMI.
Diabetes care 2008;31(8):1662-7.
2008: Michael S D Kormann; Martin Depner; Dominik Hartl; Norman Klopp; Thomas Illig; Jerzy Adamski; Christian Vogelberg; Stephan K Weiland; Erika von Mutius; Michael Kabesch
Toll-like receptor heterodimer variants protect from childhood asthma.
The Journal of allergy and clinical immunology 2008;122(1):86-92, 92.e1-8.
2008: Natalija Novak; Hansjörg Baurecht; Torsten Schäfer; Elke Rodriguez; Stefan Wagenpfeil; Norman Klopp; Joachim Heinrich; Heidrun Behrendt; Johannes Ring; Erich Wichmann; Thomas Illig; Stephan Weidinger
Loss-of-function mutations in the filaggrin gene and allergic contact sensitization to nickel.
The Journal of investigative dermatology 2008;128(6):1430-5.
2008: Wiebke Sauter; Albert Rosenberger; Lars Beckmann; Silke Kropp; Kirstin Mittelstrass; Maria Timofeeva; Gabi Wölke; Angelika Steinwachs; Daniela Scheiner; Eckart Meese; Gerhard Sybrecht; Florian Kronenberg; Hendrik Dienemann; Jenny Chang-Claude; Thomas Illig; Heinz-Erich Wichmann; Heike Bickeböller; Angela Risch
Matrix metalloproteinase 1 (MMP1) is associated with early-onset lung cancer.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2008;17(5):1127-35.
2008: Stephan Weidinger; Maureen O'Sullivan; Thomas Illig; Hansjörg Baurecht; Martin Depner; Elke Rodriguez; Andreas Ruether; Norman Klopp; Christian Vogelberg; Stephan K Weiland; W H Irwin McLean; Erika von Mutius; Alan D Irvine; Michael Kabesch
Filaggrin mutations, atopic eczema, hay fever, and asthma in children.
The Journal of allergy and clinical immunology 2008;121(5):1203-1209.e1.
2008: Melanie Kolz; Wolfgang Koenig; Martina Müller; Mariarita Andreani; Sonja Greven; Thomas Illig; Natalie Khuseyinova; Demosthenes B Panagiotakos; Göran Pershagen; Veikko Salomaa; Jordi Sunyer; Annette Peters
DNA variants, plasma levels and variability of C-reactive protein in myocardial infarction survivors: results from the AIRGENE study.
European heart journal 2008;29(10):1250-8.
2008: Elke Rodríguez; Thomas Illig; Stephan Weidinger
Filaggrin loss-of-function mutations and association with allergic diseases.
Pharmacogenomics 2008;9(4):399-413.
2008: Moritz F Sinner; Arne Pfeufer; Mahmut Akyol; britt beckmann; Martin Hinterseer; Annette Wacker; Siegfried Perz; Wiebke Sauter; Thomas Illig; Michael Näbauer; Claus Schmitt; H-Erich Wichmann; Albert Schömig; Gerhard Steinbeck; Thomas Meitinger; Stefan Kääb
The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).
European heart journal 2008;29(7):907-14.
2008: Michaela Schedel; Leonardo A Pinto; Bianca Schaub; Philip Rosenstiel; Dmitry Cherkasov; Lisa Cameron; Norman Klopp; Thomas Illig; Christian Vogelberg; Stephan K Weiland; Erika von Mutius; Michael Lohoff; Michael Kabesch
IRF-1 gene variations influence IgE regulation and atopy.
American journal of respiratory and critical care medicine 2008;177(6):613-21.
2008: Christina Justenhoven; Ute Hamann; Falk Schubert; Marc Zapatka; Christiane Pierl; Sylvia Rabstein; Silvia Selinski; Tina Mueller; Katja Ickstadt; Michael Gilbert; Yon-Dschun Ko; Christian Baisch; Beate Pesch; Volker Harth; Hermann M Bolt; Caren Vollmert; Thomas Illig; Roland Eils; Jürgen Dippon; Hiltrud Brauch
Breast cancer: a candidate gene approach across the estrogen metabolic pathway.
Breast cancer research and treatment 2008;108(1):137-49.
2008: Juliane Winkelmann; Peter Lichtner; Barbara Schormair; Manfred Uhr; Stephanie Hauk; Karin Stiasny-Kolster; Claudia Trenkwalder; Walter Paulus; Ines Peglau; Ilonka Eisensehr; Thomas Illig; H-Erich Wichmann; Hildegard Pfister; Jelena Golic; Thomas Bettecken; Benno Pütz; Florian Holsboer; Thomas Meitinger; Bertram Müller-Myhsok
Variants in the neuronal nitric oxide synthase (nNOS, NOS1) gene are associated with restless legs syndrome.
Movement disorders : official journal of the Movement Disorder Society 2008;23(3):350-8.
2008: Iris M Heid; Caren Vollmert; Florian Kronenberg; Cornelia Huth; Donna P Ankerst; Andreas Luchner; Anke Hinney; Günter Brönner; H-Erich Wichmann; Thomas Illig; Angela Döring; Johannes Hebebrand
Association of the MC4R V103I polymorphism with the metabolic syndrome: the KORA Study.
Obesity (Silver Spring, Md.) 2008;16(2):369-76.
2008: Joachim Schneider; Thomas Illig; Albert Rosenberger; Heike Bickeböller; Hans-Erich Wichmann
Detection of ATM gene mutations in young lung cancer patients: a population-based control study.
Archives of medical research 2008;39(2):226-31.
2008: Sylvia Rabstein; Klaus Unfried; Ulrich Ranft; Thomas Illig; Melanie Kolz; Chinara Mambetova; Mariana Vlad; Cecilia Roman; Tobias Weiss; Doreen Becker; Thomas Brüning; Beate Pesch
Lack of association of delta-aminolevulinate dehydratase polymorphisms with blood lead levels and hemoglobin in Romanian women from a lead-contaminated region.
Journal of toxicology and environmental health. Part A 2008;71(11-12):716-24.
2008: Sigrun Roeber; Eva Grasbon-Frodl; Otto Windl; Bjarne Krebs; Wei Xiang; Caren Vollmert; Thomas Illig; Andreas Schröter; Thomas Arzberger; Petra Frick; Inga Zerr; Hans A Kretzschmar
Evidence for a pathogenic role of different mutations at codon 188 of PRNP.
PloS one 2008;3(5):e2147.
2008: Albert Rosenberger; Thomas Illig; Katrin Korb; Norman Klopp; Vera Zietemann; Gabi Wölke; Eckart Meese; Gerhard Sybrecht; Florian Kronenberg; Matthias Cebulla; Maria Degen; Peter Drings; Andreas Gröschel; Nikolaus Konietzko; Karsten Grosse Kreymborg; Karl Häußinger; Gerd Höffken; Bettina Jilge; You-Dschun Ko; Harald Morr; Christine Schmidt; E-Wilhelm Schmidt; Dagmar Täuscher; Heike Bickeböller; H-Erich Wichmann
Do genetic factors protect for early onset lung cancer? A case control study before the age of 50 years.
BMC cancer 2008;8():60.
2007: Rokavec Matjaz; Christina Justenhoven; Werner Schroth; Monica Istrate; Susanne Haas; Hans-Peter Fischer; Caren Vollmert; Thomas Illig; Ute Hamann; Yon-Dschun Ko; Damjan Glavac; Hiltrud Brauch
A novel polymorphism in the promoter region of ERBB4 is associated with breast and colorectal cancer risk.
Clinical cancer research : an official journal of the American Association for Cancer Research 2007;13(24):7506-14.
2007: Jan Heidrich; Jürgen Wellmann; Angela Döring; Thomas Illig; Ulrich Keil
Alcohol consumption, alcohol dehydrogenase and risk of coronary heart disease in the MONICA/KORA-Augsburg cohort 1994/1995-2002.
European journal of cardiovascular prevention and rehabilitation : official journal of the European Society of Cardiology, Working Groups on Epidemiology & Prevention and Cardiac Rehabilitation and Exercise Physiology 2007;14(6):769-74.
2007: L A Pinto; L Steudemann; Martin Depner; Norman Klopp; Thomas Illig; Stephan K Weiland; Erika von Mutius; Michael Kabesch
STAT1 gene variations, IgE regulation and atopy.
Allergy 2007;62(12):1456-61.
2007: Hansjörg Baurecht; Alan D Irvine; Natalija Novak; Thomas Illig; Bettina Bühler; Johannes Ring; Stefan Wagenpfeil; Stephan Weidinger
Toward a major risk factor for atopic eczema: meta-analysis of filaggrin polymorphism data.
The Journal of allergy and clinical immunology 2007;120(6):1406-12.
2007: Harald Grallert; Eva-Maria Sedlmeier; Cornelia Huth; Melanie Kolz; Iris M Heid; Christa Meisinger; Christian Herder; Klaus Strassburger; Anke Gehringer; Markus Haak; Guido Giani; Florian Kronenberg; H-Erich Wichmann; Jerzy Adamski; Bernhard Paulweber; Thomas Illig; Wolfgang Rathmann
APOA5 variants and metabolic syndrome in Caucasians.
Journal of lipid research 2007;48(12):2614-21.
2007: Veit Schoenborn; Henning Gohlke; Iris M Heid; Thomas Illig; Gerd Utermann; Florian Kronenberg
Sample selection algorithm to improve quality of genotyping from plasma-derived DNA: to separate the wheat from the chaff.
Human mutation 2007;28(11):1141-9.
2007: Alexander Georgi; Rami Abou Jamra; Katrin Klein; Angela Wolf Villela; Johannes Schumacher; Tim Becker; Torsten Paul; Christine Schmael; Susanne Höfels; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Thomas G. Schulze; Marcella Rietschel
Possible association between genetic variants at the GRIN1 gene and schizophrenia with lifetime history of depressive symptoms in a German sample.
Psychiatric genetics 2007;17(5):308-10.
2007: C Holzapfel; N Klopp; Harald Grallert; Cornelia Huth; Christian Gieger; Christa Meisinger; Klaus Strassburger; Guido Giani; H-Erich Wichmann; Helmut Laumen; Hans Hauner; Christian Herder; Wolfgang Rathmann; Thomas Illig
Genetic variants in the leukemia-associated Rho guanine nucleotide exchange factor (ARHGEF12) gene are not associated with T2DM and related parameters in Caucasians (KORA study).
European journal of endocrinology / European Federation of Endocrine Societies 2007;157(3):R1-5.
2007: Juliane Winkelmann; Barbara Schormair; Peter Lichtner; Stephan Ripke; Lan Xiong; Shapour Jalilzadeh; Stephany Fulda; Benno Pütz; Gertrud Eckstein; Stephanie Hauk; Claudia Trenkwalder; Alexander Zimprich; Karin Stiasny-Kolster; Wolfgang H Oertel; Cornelius G Bachmann; Walter Paulus; Ines Peglau; Ilonka Eisensehr; Jacques Montplaisir; Gustavo Turecki; Guy Rouleau; Christian Gieger; Thomas Illig; H-Erich Wichmann; Florian Holsboer; Bertram Müller-Myhsok; Thomas Meitinger
Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions.
Nature genetics 2007;39(8):1000-6.
2007: Inke Nitz; Eva Fisher; Harald Grallert; Yun Li; Christian Gieger; Diana Rubin; Heiner Boeing; Joachim Spranger; Inka Lindner; Stefan Schreiber; Wolfgang Rathmann; Henning Gohlke; Angela Döring; H-Erich Wichmann; Jürgen Schrezenmeir; Frank Döring; Thomas Illig
Association of prostaglandin E synthase 2 (PTGES2) Arg298His polymorphism with type 2 diabetes in two German study populations.
The Journal of clinical endocrinology and metabolism 2007;92(8):3183-8.
2007: Miriam F Moffatt; Michael Kabesch; Liming Liang; Anna Dixon; David Strachan; Simon Heath; Martin Depner; Andrea Von Berg; Albrecht Bufe; Ernst Rietschel; Andrea Heinzmann; Burkard Simma; Thomas Frischer; Saffron A G Willis-Owen; Kenny C C Wong; Thomas Illig; Christian Vogelberg; Stephan K Weiland; Erika von Mutius; Goncalo Abecasis; Martin Farrall; Ivo Gut; G Mark Lathrop; William O C M Cookson
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.
Nature 2007;448(7152):470-3.
2007: Natalija Novak; C-F Yu; Caroline Bussmann; Laura Maintz; Wenming M Peng; J Hart; Tobias Hagemann; Amalia Diaz-Lacava; Hansjörg Baurecht; Norman Klopp; Stefan Wagenpfeil; Heidrun Behrendt; Thomas Bieber; Johannes Ring; Thomas Illig; Stephan Weidinger
Putative association of a TLR9 promoter polymorphism with atopic eczema.
Allergy 2007;62(7):766-72.
2007: Malgorzata Jaremko; Christina Justenhoven; Werner Schroth; Benny K Abraham; Peter Fritz; Caren Vollmert; Thomas Illig; Wolfgang Simon; Matthias Schwab; Hiltrud Brauch
Polymorphism of the DNA repair enzyme XRCC1 is associated with treatment prediction in anthracycline and cyclophosphamide/methotrexate/5-fluorouracil-based chemotherapy of patients with primary invasive breast cancer.
Pharmacogenetics and genomics 2007;17(7):529-38.
2007: Jakob C Mueller; Matthias Riemenschneider; Andreas Schoepfer-Wendels; Henning Gohlke; Lidija Konta; Patricia Friedrich; Thomas Illig; Simon Laws; hans förstl; Alexander Kurz
Weak independent association signals between IDE polymorphisms, Alzheimer's disease and cognitive measures.
Neurobiology of aging 2007;28(5):727-34.
2007: Frederike Schirmbeck; Alexander Georgi; Jana Strohmaier; Christine Schmael; Carolin Knorr; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Norman Klopp; Thomas Illig; Maren Wulf; Markus Schwarz; Wolfgang Maier; Peter Propping; Sven Cichon; Markus M Nöthen; Thomas G. Schulze; Marcella Rietschel
No association between the serine racemase gene (SRR) and bipolar disorder in a German case-control sample.
Psychiatric genetics 2007;17(2):127.
2007: Jana Strohmaier; Alexander Georgi; Frederike Schirmbeck; Christine Schmael; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Susanne Höfels; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Marcella Rietschel; Thomas G. Schulze
No association between the serine racemase gene (SRR) and schizophrenia in a German case-control sample.
Psychiatric genetics 2007;17(2):125.
2007: Michael Kabesch; Martin Depner; I Dahmen; Stephan K Weiland; Christian Vogelberg; Bodo Niggemann; S Lau; Thomas Illig; Norman Klopp; U Wahn; D Reinhardt; Erika von Mutius; R Nickel
Polymorphisms in eosinophil pathway genes, asthma and atopy.
Allergy 2007;62(4):423-8.
2007: Eva-Maria Sedlmeier; Harald Grallert; Cornelia Huth; Hannelore Löwel; Christian Herder; Klaus Strassburger; Guido Giani; H-Erich Wichmann; Hans Hauner; Thomas Illig; Wolfgang Rathmann
Gene variants of monocyte chemoattractant protein 1 and components of metabolic syndrome in KORA S4, Augsburg.
European journal of endocrinology / European Federation of Endocrine Societies 2007;156(3):377-85.
2007: Caren Vollmert; Susanne Hahn; Claudia Lamina; Cornelia Huth; Melanie Kolz; Andreas Schöpfer-Wendels; Klaus Mann; Friedhelm Bongardt; Jakob C Mueller; Florian Kronenberg; H-Erich Wichmann; Christian Herder; Rolf Holle; Hannelore Löwel; Thomas Illig; Onno Eilard Janssen
Calpain-10 variants and haplotypes are associated with polycystic ovary syndrome in Caucasians.
American journal of physiology. Endocrinology and metabolism 2007;292(3):E836-44.
2007: Eva Fisher; Inke Nitz; Christian Gieger; Harald Grallert; Henning Gohlke; Inka Lindner; Stefan Dahm; Heiner Boeing; Barbara Burwinkel; Wolfgang Rathmann; H-Erich Wichmann; Jürgen Schrezenmeir; Thomas Illig; Frank Döring
Association of acyl-CoA-binding protein (ACBP) single nucleotide polymorphisms and type 2 diabetes in two German study populations.
Molecular nutrition & food research 2007;51(2):178-84.
2007: Mahmut Akyol; Shapour Jalilzadeh; Moritz F Sinner; Siegfried Perz; britt beckmann; Christian Gieger; Thomas Illig; H-Erich Wichmann; Thomas Meitinger; Stefan Kääb; Arne Pfeufer
The common non-synonymous variant G38S of the KCNE1-(minK)-gene is not associated to QT interval in Central European Caucasians: results from the KORA study.
European heart journal 2007;28(3):305-9.
2007: Rami Abou Jamra; Tim Becker; Norman Klopp; Faten Dahdouh; Thomas G. Schulze; Magdalena Gross; Monika Deschner; Christine Schmäl; Thomas Illig; Marcella Rietschel; Peter Propping; Sven Cichon; Markus M Nöthen; Johannes Schumacher
No evidence for an association between variants at the gamma-amino-n-butyric acid type A receptor beta2 locus and schizophrenia.
Psychiatric genetics 2007;17(1):43-5.
2007: Anke Hinney; Thuy Trang Nguyen; André Scherag; Susann Friedel; Günter Brönner; Timo Dirk Müller; Harald Grallert; Thomas Illig; H-Erich Wichmann; Winfried Rief; Helmut Schäfer; Johannes Hebebrand
Genome wide association (GWA) study for early onset extreme obesity supports the role of fat mass and obesity associated gene (FTO) variants.
PloS one 2007;2(12):e1361.
2007: Annette Peters; Alexandra Schneider; Sonja Greven; tom bellander; Francesco Forastiere; Angela Ibald-Mulli; Thomas Illig; Bénédicte Jacquemin; Klea Katsouyanni; Wolfgang Koenig; Timo Lanki; Juha Pekkanen; Göran Pershagen; Sally Picciotto; Regina Rückerl; Angelika Schaffrath Rosario; Christodoulos I Stefanadis; Jordi Sunyer
Air pollution and inflammatory response in myocardial infarction survivors: gene-environment interactions in a high-risk group.
Inhalation toxicology 2007;19 Suppl 1():161-75.
2007: Silke Pauli; Torben Söker; Norman Klopp; Thomas Illig; Wolfgang Engel; Jochen Graw
Mutation analysis in a German family identified a new cataract-causing allele in the CRYBB2 gene.
Molecular vision 2007;13():962-7.
2007: Martin Depner; Michael S D Kormann; Norman Klopp; Thomas Illig; Christian Vogelberg; Stephan K Weiland; Erika von Mutius; Christophe Combadière; Michael Kabesch
CX3CR1 polymorphisms are associated with atopy but not asthma in German children.
International archives of allergy and immunology 2007;144(1):91-4.
2007: C Marzi; Cornelia Huth; Melanie Kolz; Harald Grallert; Christa Meisinger; H-Erich Wichmann; Wolfgang Rathmann; Christian Herder; Thomas Illig
Variants of the transcription factor 7-like 2 gene (TCF7L2) are strongly associated with type 2 diabetes but not with the metabolic syndrome in the MONICA/KORA surveys.
Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et métabolisme 2007;39(1):46-52.
2006: Markus H Skowronek; Alexander Georgi; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Christine Schmael; Torsten Paul; Monika Deschner; Susanne Höfels; Maren Wulff; Markus Schwarz; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Thomas G. Schulze; Marcella Rietschel
No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sample.
Psychiatric genetics 2006;16(6):233-4.
2006: C Vollmert; Otto Windl; Wei Xiang; Albert Rosenberger; I Zerr; H-E Wichmann; Heike Bickeböller; Thomas Illig; Hans A Kretzschmar
Significant association of a M129V independent polymorphism in the 5' UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study.
Journal of medical genetics 2006;43(10):e53.
2006: Alexander Georgi; Rami Abou Jamra; Johannes Schumacher; Tim Becker; Christine Schmael; Monika Deschner; Susanne Höfels; Maren Wulff; Markus Schwarz; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Markus M Nöthen; Marcella Rietschel; Thomas G. Schulze
No association between genetic variants at the GRIN1 gene and bipolar disorder in a German sample.
Psychiatric genetics 2006;16(5):183-4.
2006: Rami Abou Jamra; Katrin Klein; Angela Wolf Villela; Tim Becker; Thomas G. Schulze; Christine Schmael; Monika Deschner; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
Association study between genetic variants at the PIP5K2A gene locus and schizophrenia and bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006;141B(6):663-5.
2006: Matthias Riemenschneider; Lidija Konta; Patricia Friedrich; Sandra Schwarz; Kevin Taddei; Frauke Neff; Alessandro Padovani; Heike Kölsch; Simon Laws; Norman Klopp; Heike Bickeböller; Stefan Wagenpfeil; Jakob C Mueller; Albert Rosenberger; Janine Diehl-Schmid; Silvana Archetti; Nicola T Lautenschlager; Barbara Borroni; Ulrich Müller; Thomas Illig; Reinhard Heun; Rupert Egensperger; Jürgen Schlegel; hans förstl; Ralph N Martins; Alexander Kurz
A functional polymorphism within plasminogen activator urokinase (PLAU) is associated with Alzheimer's disease.
Human molecular genetics 2006;15(16):2446-56.
2006: Harald Grallert; Cornelia Huth; Melanie Kolz; Christa Meisinger; Christian Herder; Klaus Strassburger; Guido Giani; H-Erich Wichmann; Jerzy Adamski; Thomas Illig; Wolfgang Rathmann
IL-6 promoter polymorphisms and quantitative traits related to the metabolic syndrome in KORA S4.
Experimental gerontology 2006;41(8):737-45.
2006: Jochen Graw; Norman Klopp; Thomas Illig; Markus N Preising; Birgit Lorenz
Congenital cataract and macular hypoplasia in humans associated with a de novo mutation in CRYAA and compound heterozygous mutations in P.
Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv für klinische und experimentelle Ophthalmologie 2006;244(8):912-9.
2006: Stephan Weidinger; Natalija Novak; Norman Klopp; Hansjörg Baurecht; Stefan Wagenpfeil; Lars Rummler; Johannes Ring; Heidrun Behrendt; Thomas Illig
Lack of association between Toll-like receptor 2 and Toll-like receptor 4 polymorphisms and atopic eczema.
The Journal of allergy and clinical immunology 2006;118(1):277-9.
2006: Stephan Weidinger; Thomas Illig; Hansjörg Baurecht; Alan D Irvine; Elke Rodriguez; Amalia Diaz-Lacava; Norman Klopp; Stefan Wagenpfeil; Yiwei Zhao; Haihui Liao; Simon P Lee; Colin N A Palmer; Claudia Jenneck; Laura Maintz; Tobias Hagemann; Heidrun Behrendt; Johannes Ring; Markus M Nothen; W H Irwin McLean; Natalija Novak
Loss-of-function variations within the filaggrin gene predispose for atopic dermatitis with allergic sensitizations.
The Journal of allergy and clinical immunology 2006;118(1):214-9.
2006: Rami Abou Jamra; Angela Wolf Villela; Katrin Klein; Tim Becker; Thomas G. Schulze; Christine Schmael; Monika Deschner; Norman Klopp; Thomas Illig; Peter Propping; Sven Cichon; Marcella Rietschel; Markus M Nöthen; Johannes Schumacher
No association between genetic variants at the GLYT2 gene and bipolar affective disorder and schizophrenia.
Psychiatric genetics 2006;16(3):91.
2006: Linda Schaeffer; Henning Gohlke; Martina Müller; Iris M Heid; Lyle Palmer; Iris Kompauer; Hans Demmelmair; Thomas Illig; Berthold Koletzko; Joachim Heinrich
Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids.
Human molecular genetics 2006;15(11):1745-56.
2006: Dan E Arking; Arne Pfeufer; Wendy S Post; WEN KAO; Christopher Newton-Cheh; Morna Ikeda; Kristen West; Carl S Kashuk; Mahmut Akyol; Siegfried Perz; Shapour Jalilzadeh; Thomas Illig; Christian Gieger; Chao-Yu Guo; Martin G Larson; H-Erich Wichmann; Eduardo Marban; Christopher J O'Donnell; Joel N Hirschhorn; Stefan Kääb; PETER SPOONER; Thomas Meitinger; Aravinda Chakravarti
A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization.
Nature genetics 2006;38(6):644-51.
2006: Veit Schoenborn; Iris M Heid; Caren Vollmert; Arno Lingenhel; Ted D Adams; Paul N Hopkins; Thomas Illig; Robert Zimmermann; Rudolf Zechner; Steven C Hunt; Florian Kronenberg
The ATGL gene is associated with free fatty acids, triglycerides, and type 2 diabetes.
Diabetes 2006;55(5):1270-5.
2006: Anke Hinney; Thomas Bettecken; Patrick Tarnow; Harald Brumm; Kathrin Reichwald; Peter Lichtner; André Scherag; Thuy Trang Nguyen; Pia Schlumberger; Winfried Rief; Caren Vollmert; Thomas Illig; H-Erich Wichmann; Helmut Schäfer; Matthias Platzer; Heike Biebermann; Thomas Meitinger; Johannes Hebebrand
Prevalence, spectrum, and functional characterization of melanocortin-4 receptor gene mutations in a representative population-based sample and obese adults from Germany.
The Journal of clinical endocrinology and metabolism 2006;91(5):1761-9.
2006: Henning Gohlke; Thomas Illig; Norman Klopp; Stefan Wagenpfeil; Lidija Konta; Simon Laws; Alexander Kurz; Matthias Riemenschneider
Association study between the D10S1423 microsatellite marker and Alzheimer's disease.
Neurobiology of aging 2006;27(5):776.e1-776.e3.
2006: Alan Herbert; Norman P Gerry; Matthew B McQueen; Iris M Heid; Arne Pfeufer; Thomas Illig; H-Erich Wichmann; Thomas Meitinger; David Hunter; Frank B Hu; GRaham Colditz; Anke Hinney; Johannes Hebebrand; Kerstin Koberwitz; Xiaofeng Zhu; Richard Cooper; Kristin G Ardlie; Helen N Lyon; Joel N Hirschhorn; Nan M Laird; Marc E Lenburg; Christoph Lange; Michael F Christman
A common genetic variant is associated with adult and childhood obesity.
Science (New York, N.Y.) 2006;312(5771):279-83.
2006: Vitolds Mackevics; Iris M Heid; Stefanie A Wagner; Paula Cip; Hildegard Doppelmayr; Aivars Lejnieks; Henning Gohlke; Gunther Ladurner; Thomas Illig; Bernhard Iglseder; Florian Kronenberg; Bernhard Paulweber
The adiponectin gene is associated with adiponectin levels but not with characteristics of the insulin resistance syndrome in healthy Caucasians.
European journal of human genetics : EJHG 2006;14(3):349-56.
2006: Christian Herder; Sylvia Müller-Scholze; Philipp Rating; Wolfgang Koenig; Barbara Thorand; Burkhard Haastert; Rolf Holle; Thomas Illig; Wolfgang Rathmann; Jochen Seissler; H-Erich Wichmann; Hubert Kolb
Systemic monocyte chemoattractant protein-1 concentrations are independent of type 2 diabetes or parameters of obesity: results from the Cooperative Health Research in the Region of Augsburg Survey S4 (KORA S4).
European journal of endocrinology / European Federation of Endocrine Societies 2006;154(2):311-7.
2006: Iris M Heid; Stefanie A Wagner; Henning Gohlke; Bernhard Iglseder; Jakob C Mueller; Paula Cip; Gunther Ladurner; Raphael Reiter; Andreas Stadlmayr; Vitolds Mackevics; Thomas Illig; Florian Kronenberg; Bernhard Paulweber
Genetic architecture of the APM1 gene and its influence on adiponectin plasma levels and parameters of the metabolic syndrome in 1,727 healthy Caucasians.
Diabetes 2006;55(2):375-84.
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.
2006: Sathiyavedu T Santhiya; Torben Soker; Norman Klopp; Thomas Illig; M V S Prakash; Bhavani Selvaraj; Puthiya M Gopinath; Jochen Graw
Identification of a novel, putative cataract-causing allele in CRYAA (G98R) in an Indian family.
Molecular vision 2006;12():768-73.
2006: Michaela Schedel; Martin Depner; Carola Schoen; Stephan K Weiland; Christian Vogelberg; Bodo Niggemann; Susanne Lau; Thomas Illig; Norman Klopp; Ulrich Wahn; Erika von Mutius; Renate Nickel; Michael Kabesch
The role of polymorphisms in ADAM33, a disintegrin and metalloprotease 33, in childhood asthma and lung function in two German populations.
Respiratory research 2006;7():91.
2006: Marie-Hélène Metzger; Margit Heier; Markku Mäki; Enzo Bravi; Andrea Schneider; Hannelore Löwel; Thomas Illig; Detlef Schuppan; H-Erich Wichmann
Mortality excess in individuals with elevated IgA anti-transglutaminase antibodies: the KORA/MONICA Augsburg cohort study 1989-1998.
European journal of epidemiology 2006;21(5):359-65.
2006: Sylvia Rabstein; Klaus Unfried; Ulrich Ranft; Thomas Illig; Melanie Kolz; Hans-Peter Rihs; Chinara Mambetova; Mariana Vlad; Thomas Brüning; Beate Pesch
Variation of the N-acetyltransferase 2 gene in a Romanian and a Kyrgyz population.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2006;15(1):138-41.
2005: Christina Justenhoven; Ute Hamann; Christiane Pierl; Sylvia Rabstein; Beate Pesch; Volker Harth; Christian Baisch; Caren Vollmert; Thomas Illig; Thomas Brüning; Yon Ko; Hiltrud Brauch
One-carbon metabolism and breast cancer risk: no association of MTHFR, MTR, and TYMS polymorphisms in the GENICA study from Germany.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2005;14(12):3015-8.
2005: Saskia Biskup; Jakob C Mueller; Manu Sharma; Peter Lichtner; Alexander Zimprich; Daniela Berg; Ullrich Wüllner; Thomas Illig; Thomas Meitinger; Thomas Gasser
Common variants of LRRK2 are not associated with sporadic Parkinson's disease.
Annals of neurology 2005;58(6):905-8.
2005: Thomas G. Schulze; Stephanie Ohlraun; Piotr M Czerski; Johannes Schumacher; Layla Kassem; Monika Deschner; Magdalena Gross; Monja Tullius; Vivien Heidmann; Svetlana Kovalenko; Rami Abou Jamra; Tim Becker; Anna Leszczynska-Rodziewicz; Joanna Hauser; Thomas Illig; Norman Klopp; Stefan Wellek; Sven Cichon; Fritz A Henn; Francis McMajon; Wolfgang Maier; Peter Propping; Markus M Nöthen; Marcella Rietschel
Genotype-phenotype studies in bipolar disorder showing association between the DAOA/G30 locus and persecutory delusions: a first step toward a molecular genetic classification of psychiatric phenotypes.
The American journal of psychiatry 2005;162(11):2101-8.
2005: Barbara Thorand; Hubert Kolb; Jens Baumert; Wolfgang Koenig; Lloyd E Chambless; Christa Meisinger; Thomas Illig; Stephan Martin; Christian Herder
Elevated levels of interleukin-18 predict the development of type 2 diabetes: results from the MONICA/KORA Augsburg Study, 1984-2002.
Diabetes 2005;54(10):2932-8.
2005: Stephan Weidinger; L Rümmler; Norman Klopp; Stefan Wagenpfeil; Hansjörg Baurecht; G Fischer; Rolf Holle; Anke Gauger; T Schäfer; Thilo Jakob; Markus Ollert; Heidrun Behrendt; H E Wichmann; Johannes Ring; Thomas Illig
Association study of mast cell chymase polymorphisms with atopy.
Allergy 2005;60(10):1256-61.
2005: Johannes Schumacher; Rami Abou Jamra; Tim Becker; Stephanie Ohlraun; Norman Klopp; Elisabeth B Binder; Thomas G. Schulze; Monika Deschner; Christine Schmäl; Susanne Höfels; Astrid Zobel; Thomas Illig; Peter Propping; Florian Holsboer; Marcella Rietschel; Markus M Nöthen; Sven Cichon
Evidence for a relationship between genetic variants at the brain-derived neurotrophic factor (BDNF) locus and major depression.
Biological psychiatry 2005;58(4):307-14.
2005: Iris M Heid; Claudia Lamina; Friedhelm Bongardt; G Fischer; N Klopp; Cornelia Huth; Helmut Küchenhoff; Florian Kronenberg; H-Erich Wichmann; Thomas Illig
[How about the uncertainty in the haplotypes in the population-based KORA studies?].
Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)) 2005;67 Suppl 1():S132-6.
2005: Thomas Illig; Friedhelm Bongardt; Andreas Schöpfer-Wendels; Cornelia Huth; Iris M Heid; Wolfgang Rathmann; S Martin; Caren Vollmert; Rolf Holle; Barbara Thorand; H-Erich Wichmann; Wolfgang Koenig; Hubert Kolb; Christian Herder
Genetics of type 2 diabetes: impact of interleukin-6 gene variants.
Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)) 2005;67 Suppl 1():S122-6.
2005: Christian Herder; Thomas Illig; Wolfgang Rathmann; Stephan Martin; Burkhard Haastert; Sylvia Müller-Scholze; Rolf Holle; Barbara Thorand; Wolfgang Koenig; H-Erich Wichmann; Hubert Kolb
Inflammation and type 2 diabetes: results from KORA Augsburg.
Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)) 2005;67 Suppl 1():S115-21.
2005: H-Erich Wichmann; Christian Gieger; Thomas Illig
KORA-gen--resource for population genetics, controls and a broad spectrum of disease phenotypes.
Gesundheitswesen (Bundesverband der Ärzte des Öffentlichen Gesundheitsdienstes (Germany)) 2005;67 Suppl 1():S26-30.
2005: Stephan Weidinger; Norman Klopp; L Rümmler; Stefan Wagenpfeil; Hansjörg Baurecht; Anke Gauger; Ulf Darsow; Thilo Jakob; Natalija Novak; T Schäfer; J Heinrich; Heidrun Behrendt; H E Wichmann; Johannes Ring; Thomas Illig
Association of CARD15 polymorphisms with atopy-related traits in a population-based cohort of Caucasian adults.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2005;35(7):866-72.
2005: Beate Glaser; Johannes Schumacher; Hywel J Williams; Rami Abou Jamra; Nikolai Ianakiev; Radoi Milev; Stephanie Ohlraun; Thomas G. Schulze; Piotr M Czerski; Joanna Hauser; Erik G Jönsson; Göran C Sedvall; Norman Klopp; Thomas Illig; Tim Becker; Peter Propping; Nigel M Williams; Sven Cichon; George Kirov; Marcella Rietschel; Kieran C Murphy; Michael C O'Donovan; Markus M Nöthen; Michael J Owen
No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples.
Biological psychiatry 2005;58(1):78-80.
2005: Stephan Weidinger; Norman Klopp; Lars Rummler; Stefan Wagenpfeil; Natalija Novak; Hansjörg Baurecht; Werner Groer; Ulf Darsow; Joachim Heinrich; Anke Gauger; Torsten Schafer; Thilo Jakob; Heidrun Behrendt; Hans-Erich Wichmann; Johannes Ring; Thomas Illig
Association of NOD1 polymorphisms with atopic eczema and related phenotypes.
The Journal of allergy and clinical immunology 2005;116(1):177-84.
2005: Michael S D Kormann; David Carr; Norman Klopp; Thomas Illig; Wolfgang Leupold; Christian Fritzsch; Stephan K Weiland; Erika von Mutius; Michael Kabesch
G-Protein-coupled receptor polymorphisms are associated with asthma in a large German population.
American journal of respiratory and critical care medicine 2005;171(12):1358-62.
2005: Johannes Schumacher; Rami Abou Jamra; Tim Becker; Norman Klopp; Petra Franke; Christian Jacob; Philipp Sand; Jürgen Fritze; Stephanie Ohlraun; Thomas G. Schulze; Marcella Rietschel; Thomas Illig; Peter Propping; Sven Cichon; Jürgen Deckert; Markus M Nöthen
Investigation of the DAOA/G30 locus in panic disorder.
Molecular psychiatry 2005;10(5):428-9.
2005: Iris M Heid; Caren Vollmert; Anke Hinney; A Döring; Frank Geller; H Löwel; H-Erich Wichmann; Thomas Illig; Johannes Hebebrand; F Kronenberg
Association of the 103I MC4R allele with decreased body mass in 7937 participants of two population based surveys.
Journal of medical genetics 2005;42(4):e21.
2005: Arne Pfeufer; Shapour Jalilzadeh; Siegfried Perz; Jakob C Mueller; Martin Hinterseer; Thomas Illig; Mahmut Akyol; Cornelia Huth; Andreas Schöpfer-Wendels; Bernhard Kuch; Gerhard Steinbeck; Rolf Holle; Michael Näbauer; H-Erich Wichmann; Thomas Meitinger; Stefan Kääb
Common variants in myocardial ion channel genes modify the QT interval in the general population: results from the KORA study.
Circulation research 2005;96(6):693-701.
2005: Malgorzata Jaremko; Christina Justenhoven; Benny K Abraham; Werner Schroth; Peter Fritz; Sandra Brod; Caren Vollmert; Thomas Illig; Hiltrud Brauch
MALDI-TOF MS and TaqMan assisted SNP genotyping of DNA isolated from formalin-fixed and paraffin-embedded tissues (FFPET).
Human mutation 2005;25(3):232-8.
2005: Jakob C Mueller; Elin Lõhmussaar; Reedik Mägi; Maido Remm; Thomas Bettecken; Peter Lichtner; Saskia Biskup; Thomas Illig; Arne Pfeufer; Jan Luedemann; Stefan Schreiber; Peter P Pramstaller; Irene Pichler; Giovanni Romeo; Anthony Gaddi; Alessandra Testa; H-Erich Wichmann; Andres Metspalu; Thomas Meitinger
Linkage disequilibrium patterns and tagSNP transferability among European populations.
American journal of human genetics 2005;76(3):387-98.
2004: Caren Vollmert; Thomas Illig; Janine Altmüller; S Klugbauer; Sabine Loesgen; L Dumitrescu; Matthias Wjst
Single nucleotide polymorphism screening and association analysis--exclusion of integrin beta 7 and vitamin D receptor (chromosome 12q) as candidate genes for asthma.
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology 2004;34(12):1841-50.
2004: Christina Justenhoven; Ute Hamann; Beate Pesch; Volker Harth; Sylvia Rabstein; Christian Baisch; Caren Vollmert; Thomas Illig; Yon-Dschun Ko; Thomas Brüning; Hiltrud Brauch
ERCC2 genotypes and a corresponding haplotype are linked with breast cancer risk in a German population.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2004;13(12):2059-64.
2004: Michaela Schedel; David Carr; Norman Klopp; Bernd Woitsch; Thomas Illig; Daniel Stachel; Irene Schmid; Christian Fritzsch; Stephan K Weiland; Erika von Mutius; Michael Kabesch
A signal transducer and activator of transcription 6 haplotype influences the regulation of serum IgE levels.
The Journal of allergy and clinical immunology 2004;114(5):1100-5.
2004: Matthias Riemenschneider; Shokoufeh Mahmoodzadeh; Tamara Eisele; Norman Klopp; S Schwarz; Stefan Wagenpfeil; Janine Diehl; U Mueller; hans förstl; Thomas Illig; Alexander Kurz
Association analysis of genes involved in cholesterol metabolism located within the linkage region on chromosome 10 and Alzheimer's disease.
Neurobiology of aging 2004;25(10):1305-8.
2004: Thomas Illig; Friedhelm Bongardt; A Schöpfer; Sylvia Müller-Scholze; Wolfgang Rathmann; Wolfgang Koenig; Barbara Thorand; Caren Vollmert; Rolf Holle; Hubert Kolb; Christian Herder
Significant association of the interleukin-6 gene polymorphisms C-174G and A-598G with type 2 diabetes.
The Journal of clinical endocrinology and metabolism 2004;89(10):5053-8.
2004: Stephan Weidinger; Norman Klopp; S Wagenpfeil; L Rümmler; Michaela Schedel; Michael Kabesch; T Schäfer; Ulf Darsow; Thilo Jakob; Heidrun Behrendt; H E Wichmann; Johannes Ring; Thomas Illig
Association of a STAT 6 haplotype with elevated serum IgE levels in a population based cohort of white adults.
Journal of medical genetics 2004;41(9):658-63.
2004: Matthias Riemenschneider; Norman Klopp; W Xiang; Stefan Wagenpfeil; C Vollmert; U Müller; hans förstl; Thomas Illig; Hans A Kretzschmar; Alexander Kurz
Prion protein codon 129 polymorphism and risk of Alzheimer disease.
Neurology 2004;63(2):364-6.
2004: Henning Gohlke; Thomas Illig; Margret Bahnweg; Norman Klopp; Elisabeth André; Janine Altmüller; Nicole Herbon; Monika Werner; Michael Knapp; Lydia Pescollderungg; Attilio L Boner; Giovanni Malerba; Pier Franco Pignatti; Matthias Wjst
Association of the interleukin-1 receptor antagonist gene with asthma.
American journal of respiratory and critical care medicine 2004;169(11):1217-23.
2004: Frank Geller; Kathrin Reichwald; Astrid Dempfle; Thomas Illig; Caren Vollmert; Stephan Herpertz; Winfried Siffert; Matthias Platzer; Claudia Hess; Thomas Gudermann; Heike Biebermann; H-Erich Wichmann; Helmut Schäfer; Anke Hinney; Johannes Hebebrand
Melanocortin-4 receptor gene variant I103 is negatively associated with obesity.
American journal of human genetics 2004;74(3):572-81.
2003: Thomas Illig; Friedhelm Bongardt; Andreas Schöpfer; Rolf Holle; Sylvia Müller; Wolfgang Rathmann; Wolfgang Koenig; Christa Meisinger; H-Erich Wichmann; Hubert Kolb
The endotoxin receptor TLR4 polymorphism is not associated with diabetes or components of the metabolic syndrome.
Diabetes 2003;52(11):2861-4.
2003: Nicole Herbon; Monika Werner; Christine Braig; Henning Gohlke; Gaby Dütsch; Thomas Illig; Janine Altmüller; Jochen Hampe; Annette Lantermann; Stefan Schreiber; Ezio Bonifacio; Annette Ziegler; Sibylle Schwab; Dieter B Wildenauer; Dirk van den Boom; Andreas Braun; Michael Knapp; Peter Reitmeir; Matthias Wjst
High-resolution SNP scan of chromosome 6p21 in pooled samples from patients with complex diseases.
Genomics 2003;81(5):510-8.
2003: Norman Klopp; Elise Héon; Gail Billingsley; Thomas Illig; Matthias Wjst; Günther Rudolph; Jochen Graw
Further genetic heterogeneity for autosomal dominant human sutural cataracts.
Ophthalmic research 2003;35(2):71-7.
2002: Monika Werner; Michael Sych; Nicole Herbon; Thomas Illig; Inke R König; Matthias Wjst
Large-scale determination of SNP allele frequencies in DNA pools using MALDI-TOF mass spectrometry.
Human mutation 2002;20(1):57-64.
2002: Gabriele Duetsch; Thomas Illig; Sabine Loesgen; Klaus Rohde; Norman Klopp; Nicole Herbon; Henning Gohlke; Janine Altmueller; Matthias Wjst
STAT6 as an asthma candidate gene: polymorphism-screening, association and haplotype analysis in a Caucasian sib-pair study.
Human molecular genetics 2002;11(6):613-21.