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Showing results (51-60 of 59) with videos related to

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Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2017
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigreesGoo Jun, Alisa Manning, Marcio Almeida, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
Diabetes|March 26, 2017
A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes RiskAlisa Manning, Heather M Highland, Jessica Gasser, et al.
Nature|July 12, 2016
The genetic architecture of type 2 diabetesChristian Fuchsberger, Jason Flannick, Tanya M Teslovich, et al.
Scientific Data|January 24, 2018
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.
Scientific Data|December 20, 2017
Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Nature|April 13, 2012
Patterns and rates of exonic de novo mutations in autism spectrum disordersBenjamin M Neale, Yan Kou, Li Liu, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 28, 2017
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigreesGoo Jun, Alisa Manning, Marcio Almeida, et al.
Nature|August 19, 2016
Analysis of protein-coding genetic variation in 60,706 humansMonkol Lek, Konrad J Karczewski, Eric V Minikel, et al.
The New England Journal of Medicine|June 19, 2014
Loss-of-function mutations in APOC3, triglycerides, and coronary disease, Jacy Crosby, Gina M Peloso, et al.
Nature|December 10, 2014
Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarctionRon Do, Nathan O Stitziel, Hong-Hee Won, et al.
Diabetes|March 26, 2017
A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes RiskAlisa Manning, Heather M Highland, Jessica Gasser, et al.
Nature|July 12, 2016
The genetic architecture of type 2 diabetesChristian Fuchsberger, Jason Flannick, Tanya M Teslovich, et al.
Scientific Data|January 24, 2018
Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.
Scientific Data|December 20, 2017
Sequence data and association statistics from 12,940 type 2 diabetes cases and controlsJason Flannick, Christian Fuchsberger, Anubha Mahajan, et al.
Pageof 6