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Annals of Human Genetics|June 10, 2010
Evaluating differences in linkage disequilibrium between populationsBirgir Hrafnkelsson, Agnar Helgason, Gudbjorn F Jonsson, et al.Journal of Medical Genetics|January 8, 2008
CDKN2A mutations and melanoma risk in the Icelandic populationA M Goldstein, S N Stacey, J H Olafsson, et al.Research Square|February 15, 2023
Intravenous functional gene transfer throughout the brain of non-human primates using AAVMiguel R Chuapoco, Nicholas C Flytzanis, Nick Goeden, et al.Nature Nanotechnology|July 10, 2023
Adeno-associated viral vectors for functional intravenous gene transfer throughout the non-human primate brainMiguel R Chuapoco, Nicholas C Flytzanis, Nick Goeden, et al.Plos One|August 20, 2011
Large scale replication study of the association between HLA class II/BTNL2 variants and osteoarthritis of the knee in European-descent populationsAna M Valdes, Unnur Styrkarsdottir, Michael Doherty, et al.Translational Psychiatry|October 19, 2019
Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorderOlafur O Gudmundsson, G Bragi Walters, Andres Ingason, et al.Nature|December 20, 2013
CNVs conferring risk of autism or schizophrenia affect cognition in controlsHreinn Stefansson, Andreas Meyer-Lindenberg, Stacy Steinberg, et al.Nature Genetics|October 14, 2008
Common variants on 1p36 and 1q42 are associated with cutaneous basal cell carcinoma but not with melanoma or pigmentation traitsSimon N Stacey, Daniel F Gudbjartsson, Patrick Sulem, et al.Nature Genetics|April 29, 2008
Common variants on chromosome 5p12 confer susceptibility to estrogen receptor-positive breast cancerSimon N Stacey, Andrei Manolescu, Patrick Sulem, et al.Pageof 5