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Showing results (751-760 of 897) with videos related to

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Nature Genetics|January 9, 2007
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionAgnar Helgason, Snaebjörn Pálsson, Gudmar Thorleifsson, et al.
JAMA Oncology|January 25, 2019
Association of Inherited Pathogenic Variants in Checkpoint Kinase 2 (CHEK2) With Susceptibility to Testicular Germ Cell TumorsSaud H AlDubayan, Louise C Pyle, Marija Gamulin, et al.
Circulation. Cardiovascular Imaging|May 20, 2018
Effect of 2 Psoriasis Treatments on Vascular Inflammation and Novel Inflammatory Cardiovascular Biomarkers: A Randomized Placebo-Controlled TrialNehal N Mehta, Daniel B Shin, Aditya A Joshi, et al.
Cell Stem Cell|April 8, 2017
Large, Diverse Population Cohorts of hiPSCs and Derived Hepatocyte-like Cells Reveal Functional Genetic Variation at Blood Lipid-Associated LociEvanthia E Pashos, YoSon Park, Xiao Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2010
Strong synaptic transmission impact by copy number variations in schizophreniaJoseph T Glessner, Muredach P Reilly, Cecilia E Kim, et al.
Journal of Clinical Lipidology|September 29, 2016
US physician practices for diagnosing familial hypercholesterolemia: data from the CASCADE-FH registryZahid S Ahmad, Rolf L Andersen, Lars H Andersen, et al.
American Journal of Human Genetics|June 18, 2021
Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylationDaniel L Polla, Andrew C Edmondson, Sandrine Duvet, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 17, 2022
Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infectionChao Zhang, Anurag Verma, Yuanqing Feng, et al.
JAMA|December 11, 2019
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino AncestryScott M Damrauer, Kumardeep Chaudhary, Judy H Cho, et al.
Nature|August 6, 2010
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locusKiran Musunuru, Alanna Strong, Maria Frank-Kamenetsky, et al.
Pageof 90

Showing results (751-760 of 897) with videos related to

Sort By:
Pageof 90
Nature Genetics|January 9, 2007
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionAgnar Helgason, Snaebjörn Pálsson, Gudmar Thorleifsson, et al.
JAMA Oncology|January 25, 2019
Association of Inherited Pathogenic Variants in Checkpoint Kinase 2 (CHEK2) With Susceptibility to Testicular Germ Cell TumorsSaud H AlDubayan, Louise C Pyle, Marija Gamulin, et al.
Circulation. Cardiovascular Imaging|May 20, 2018
Effect of 2 Psoriasis Treatments on Vascular Inflammation and Novel Inflammatory Cardiovascular Biomarkers: A Randomized Placebo-Controlled TrialNehal N Mehta, Daniel B Shin, Aditya A Joshi, et al.
Cell Stem Cell|April 8, 2017
Large, Diverse Population Cohorts of hiPSCs and Derived Hepatocyte-like Cells Reveal Functional Genetic Variation at Blood Lipid-Associated LociEvanthia E Pashos, YoSon Park, Xiao Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 22, 2010
Strong synaptic transmission impact by copy number variations in schizophreniaJoseph T Glessner, Muredach P Reilly, Cecilia E Kim, et al.
Journal of Clinical Lipidology|September 29, 2016
US physician practices for diagnosing familial hypercholesterolemia: data from the CASCADE-FH registryZahid S Ahmad, Rolf L Andersen, Lars H Andersen, et al.
American Journal of Human Genetics|June 18, 2021
Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylationDaniel L Polla, Andrew C Edmondson, Sandrine Duvet, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 17, 2022
Impact of natural selection on global patterns of genetic variation and association with clinical phenotypes at genes involved in SARS-CoV-2 infectionChao Zhang, Anurag Verma, Yuanqing Feng, et al.
JAMA|December 11, 2019
Association of the V122I Hereditary Transthyretin Amyloidosis Genetic Variant With Heart Failure Among Individuals of African or Hispanic/Latino AncestryScott M Damrauer, Kumardeep Chaudhary, Judy H Cho, et al.
Nature|August 6, 2010
From noncoding variant to phenotype via SORT1 at the 1p13 cholesterol locusKiran Musunuru, Alanna Strong, Maria Frank-Kamenetsky, et al.
Pageof 90