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Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|July 8, 2026
Polygenic scores in psychiatric research and clinical practiceLeonard Frach, Friederike S David, Markus M Nöthen, et al.European Journal of Human Genetics : EJHG|August 18, 2011
A systematic eQTL study of cis-trans epistasis in 210 HapMap individualsJessica Becker, Jens R Wendland, Britta Haenisch, et al.Plos One|October 8, 2013
Familial occurrence of systemic mast cell activation diseaseGerhard J Molderings, Britta Haenisch, Manuela Bogdanow, et al.Journal of Medical Genetics|February 20, 2007
Genetics of dyslexia: the evolving landscapeJohannes Schumacher, Per Hoffmann, Christine Schmäl, et al.Plos One|May 14, 2024
Genetic polymorphisms affecting telomere length and their association with cardiovascular disease in the Heinz-Nixdorf-Recall studyNico Tannemann, Raimund Erbel, Markus M Nöthen, et al.European Journal of Nutrition|September 24, 2022
Analysis of associations between dietary patterns, genetic disposition, and cognitive function in data from UK BiobankChristina-Alexandra Schulz, Leonie Weinhold, Matthias Schmid, et al.Experimental Dermatology|September 18, 2020
Hormonal regulation in male androgenetic alopecia-Sex hormones and beyond: Evidence from recent genetic studiesStefanie Heilmann-Heimbach, Lara M Hochfeld, Sabrina K Henne, et al.European Journal of Nutrition|April 27, 2023
Association between urinary iodine excretion, genetic disposition and fluid intelligence in children, adolescents and young adults: the DONALD studyChristina-Alexandra Schulz, Leonie Weinhold, Matthias Schmid, et al.Human Heredity|April 4, 1998
A novel missense mutation in the DNA mismatch repair gene hMLH1 present among East Asians but not among EuropeansY Wang, W Friedl, C Lamberti, et al.Psychiatric Genetics|November 5, 1997
Association study of schizophrenia and the histidase geneM Nobile, P Maffei, M M Nöthen, et al.Pageof 88