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Experimental Dermatology|April 19, 2012
Selected variants of the steroid-5-alpha-reductase isoforms SRD5A1 and SRD5A2 and the sex steroid hormone receptors ESR1, ESR2 and PGR: no association with female pattern hair loss identifiedSilke Redler, Rachid Tazi-Ahnini, Dmitriy Drichel, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|November 21, 2009
A systematic association mapping on chromosome 6q in bipolar affective disorder--evidence for the melanin-concentrating-hormone-receptor-2 gene as a risk factor for bipolar affective disorderRami Abou Jamra, Thomas G Schulze, Tim Becker, et al.Psychiatric Genetics|November 16, 2006
No association between genetic variants at the ASCT1 gene and schizophrenia or bipolar disorder in a German sampleMarkus H Skowronek, Alexander Georgi, Rami Abou Jamra, et al.Plos One|October 14, 2009
CFH, C3 and ARMS2 are significant risk loci for susceptibility but not for disease progression of geographic atrophy due to AMDHendrik P N Scholl, Monika Fleckenstein, Lars G Fritsche, et al.Neurobiology of Aging|February 10, 2015
Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's diseaseEva Louwersheimer, Alfredo Ramirez, Carlos Cruchaga, et al.Human Molecular Genetics|May 6, 2009
The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populationsJohannes Schumacher, Gonzalo Laje, Rami Abou Jamra, et al.Archives of Dermatological Research|November 6, 2012
Selected variants of the melanocortin 4 receptor gene (MC4R) do not confer susceptibility to female pattern hair lossHassnaa Mahmoudi, Silke Redler, Pattie Birch, et al.Familial Cancer|January 19, 2016
Exome sequencing identifies potential novel candidate genes in patients with unexplained colorectal adenomatous polyposisIsabel Spier, Martin Kerick, Dmitriy Drichel, et al.Journal of Medical Genetics|November 29, 2015
Low-level APC mutational mosaicism is the underlying cause in a substantial fraction of unexplained colorectal adenomatous polyposis casesIsabel Spier, Dmitriy Drichel, Martin Kerick, et al.The Journal of Investigative Dermatology|April 27, 2012
Follow-up study of the first genome-wide association scan in alopecia areata: IL13 and KIAA0350 as susceptibility loci supported with genome-wide significanceDagny Jagielska, Silke Redler, Felix F Brockschmidt, et al.Pageof 23