Common variants at 12ql5 and 12q24 are associated with infant head circumferenceTAAL, H. Rob; ST POURCAIN, Beate; GELLER, Frank et al.Nature genetics. 2012, Vol 44, Num 5, pp 532-538, issn 1061-4036, 7 p.Article

Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populationsGUDMUNDSSON, Julius; SULEM, Patrick; MAGNUSDOTTIR, Droplaug N et al.Nature genetics. 2009, Vol 41, Num 4, pp 460-464, issn 1061-4036, 5 p.Article

Ghrelin gene: Identification of missense variants and a frameshift mutation in extremely obese children and adolescents and healthy normal weight students : The impact of the human genome on endocrinology: Special featuresHINNEY, Anke; HOCH, Anne; GELLER, Frank et al.The Journal of clinical endocrinology and metabolism. 2002, Vol 87, Num 6, pp 2716-2719, issn 0021-972XArticle

Replication of a Genome-Wide Association Study of Birth Weight in Preterm NeonatesRYCKMAN, Kelli K; FEENSTRA, Bjarke; SIMHAN, Hyagriv N et al.The Journal of pediatrics. 2012, Vol 160, Num 1, pp 19-24, issn 0022-3476, 6 p.Article

Human galanin (GAL) and galanin 1 receptor (GALR1) variations are not involved in fat intake and early onset obesitySCHÄUBLE, Nadine; REICHWALD, Kathrin; BLUNDELL, John et al.The Journal of nutrition. 2005, Vol 135, Num 6, pp 1387-1392, issn 0022-3166, 6 p.Article

Ghrelin receptor gene: Identification of several sequence variants in extremely obese children and adolescents, healthy normal-weight and underweight students, and children with short normal statureWANG, Hai-Jun; GELLER, Frank; HUSE, Klaus et al.The Journal of clinical endocrinology and metabolism. 2004, Vol 89, Num 1, pp 157-162, issn 0021-972X, 6 p.Article

Dopamine receptor gene polymorphisms in Parkinson's disease patients reporting sleep attacksRISSLING, Ida; GELLER, Frank; BANDMANN, Oliver et al.Movement disorders. 2004, Vol 19, Num 11, pp 1279-1284, issn 0885-3185, 6 p.Article

Sequence variant on 8q24 confers susceptibility to urinary bladder cancerKIEMENEY, Lambertus A; THORLACIUS, Steinunn; BLONDAL, Thorarinn et al.Nature genetics. 2008, Vol 40, Num 11, pp 1307-1312, issn 1061-4036, 6 p.Article

Preprohypocretin plymorphisms in Parkinson disease patients reporting sleep attacksRISSLING, Ida; KÖRNER, Yvonne; GELLER, Frank et al.Sleep (New York, NY). 2005, Vol 28, Num 7, pp 871-875, issn 0161-8105, 5 p.Article

Melanocortin-4 receptor gene: Case-control study and transmission disequilibrium test confirm that functionally relevant mutations are compatible with a major gene effect for extreme obesityHINNEY, Anke; HOHMANN, Sarah; SCHÄFER, Helmut et al.The Journal of clinical endocrinology and metabolism. 2003, Vol 88, Num 9, pp 4258-4267, issn 0021-972X, 10 p.Article

Serotonergic effects of clozapine and its metabolites in hippocampal HT22 cellsHEISER, Philip; HAUSMANN, Christiane; FREY, Joachim et al.Psychiatry research. 2002, Vol 112, Num 3, pp 221-229, issn 0165-1781, 9 p.Article

Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5― CHRNA3―CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weightTYRRELL, Jessica; HUIKARI, Ville; JOHNSON, Paul C. D et al.Human molecular genetics (Print). 2012, Vol 21, Num 24, pp 5344-5358, issn 0964-6906, 15 p.Article

Sequence variants at the TERT-CLPTM1L locus associate with many cancer typesRAFNAR, Thorunn; SULEM, Patrick; BLÖNDAL, Thorarinn et al.Nature genetics. 2009, Vol 41, Num 2, pp 221-227, issn 1061-4036, 7 p.Article

Absence of the wild-type allele (192 Base Pairs) of a polymorphism in the promoter region of the IGF-I gene but not a polymorphism in the insulin gene variable number of tandem repeat locus is associated with accelerated weight gain in infancyLANDMANN, Eva; GELLER, Frank; SCHILLING, Jutta et al.Pediatrics (Evanston). 2006, Vol 118, Num 6, pp 2374-2379, issn 0031-4005, 6 p.Article

Mutation analysis of the MCHR1 gene in human obesityWERMTER, Anne-Kathrin; REICHWALD, Kathrin; SIEGFRIED, Wolfgang et al.European journal of endocrinology. 2005, Vol 152, Num 6, pp 851-862, issn 0804-4643, 12 p.Article

GSTP1 A¹⁵⁷⁸G (Ile¹⁰⁵Val) polymorphism in benzidine-exposed workers: an association with cytological grading of exfoliated urothelial cellsQINGWEN MA; GUOFANG LIN; YIQIU QIN et al.Pharmacogenetics (London). 2003, Vol 13, Num 7, pp 409-415, issn 0960-314X, 7 p.Article

Genome scan for childhood and adolescent obesity in German familiesSAAR, Kathrin; GELLER, Frank; ZIEGLER, Andreas et al.Pediatrics (Evanston). 2003, Vol 111, Num 2, pp 321-327, issn 0031-4005, 7 p.Article

Sequence variants at CHRNB3―CHRNA6 and CYP2A6 affect smoking behaviorTHORGEIRSSON, Thorgeir E; GUDBJARTSSON, Daniel F; GIEGER, Christian et al.Nature genetics. 2010, Vol 42, Num 5, pp 448-453, issn 1061-4036, 6 p.Article

A variant associated with nicotine dependence, lung cancer and peripheral arterial diseaseTHORGEIRSSON, Thorgeir E; GELLER, Frank; STACEY, Simon N et al.Nature (London). 2008, Vol 452, Num 7187, pp 638-641, issn 0028-0836, 4 p.Article

Male-pattern baldness susceptibility locus at 20pllRICHARDS, J. Brent; XIN YUAN; KIEMENEY, Lambertus A et al.Nature genetics. 2008, Vol 40, Num 11, pp 1284-1286, issn 1061-4036, 3 p.Article

Common variants on chromosomes 2q35 and 16q12 confer susceptibility to estrogen receptor-positive breast cancerSTACEY, Simon N; MANOLESCU, Andrei; ABEN, Katja K et al.Nature genetics. 2007, Vol 39, Num 7, pp 865-869, issn 1061-4036, 5 p.Article

Secular trends in body mass index measurements in preschool children from the City of Aachen, GermanyHERPERTZ-DAHLMANN, Beate; GELLER, Frank; BÖHLE, Corinna et al.European journal of pediatrics. 2003, Vol 162, Num 2, pp 104-109, issn 0340-6199, 6 p.Article

Prevalence of obesity in adolescent and young adult patients with and without schizophrenia and in relationship to antipsychotic medicationTHEISEN, Frank M; LINDEN, André; GELLER, Frank et al.Journal of psychiatric research. 2001, Vol 35, Num 6, pp 339-345, issn 0022-3956Article

Plasma Lipids, Genetic Variants Near APOA1, and the Risk of Infantile Hypertrophic Pyloric StenosisFEENSTRA, Bjarke; GELLER, Frank; NORDENSKJÖLD, Agneta et al.JAMA, the journal of the American Medical Association. 2013, Vol 310, Num 7, pp 714-721, issn 0098-7484, 8 p.Article

Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosisFEENSTRA, Bjarke; GELLER, Frank; KROGH, Camilla et al.Nature genetics. 2012, Vol 44, Num 3, pp 334-337, issn 1061-4036, 4 p.Article