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Journal of Clinical Medicine
|
August 21, 2019
<i>APOE</i> Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of <i>APOE</i> ε4 on Alzheimer's Disease Risk in a Multiracial Sample
Kyu Yeong Choi, Jang Jae Lee, Tamil Iniyan Gunasekaran, et al.
Nature
|
May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang, Haitao Zhang, Deqiong Ma, et al.
Clinical Pharmacology and Therapeutics
|
June 25, 2014
Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems
L J Rasmussen-Torvik, S C Stallings, A S Gordon, et al.
Blood Advances
|
November 25, 2025
Outcomes Following Matched Sibling Donor Transplantation for Severe Combined Immunodeficiency: A Report from the PIDTC
Ahmad Rayes, Brent R Logan, Xuerong Liu, et al.
Nature Genetics
|
November 13, 2012
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
David C Whitcomb, Jessica LaRusch, Alyssa M Krasinskas, et al.
Nature Genetics
|
January 22, 2020
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
Jamie E Craig, Xikun Han, Ayub Qassim, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
June 21, 2015
Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk
Timothy J Hohman, Jessica N Cooke-Bailey, Christiane Reitz, et al.
Nature Genetics
|
September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
Xiaowei Zhan, David E Larson, Chaolong Wang, et al.
Neurobiology of Aging
|
September 11, 2012
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1
Kreshnik B Ahmeti, Senda Ajroud-Driss, Ammar Al-Chalabi, et al.
Nature Communications
|
May 16, 2018
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Adriana I Iglesias, Aniket Mishra, Veronique Vitart, et al.
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of 91
Search research articles
Search
Showing results (851-860 of 908) with videos related to
Sort By:
Page
of 91
Journal of Clinical Medicine
|
August 21, 2019
<i>APOE</i> Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of <i>APOE</i> ε4 on Alzheimer's Disease Risk in a Multiracial Sample
Kyu Yeong Choi, Jang Jae Lee, Tamil Iniyan Gunasekaran, et al.
Nature
|
May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disorders
Kai Wang, Haitao Zhang, Deqiong Ma, et al.
Clinical Pharmacology and Therapeutics
|
June 25, 2014
Design and anticipated outcomes of the eMERGE-PGx project: a multicenter pilot for preemptive pharmacogenomics in electronic health record systems
L J Rasmussen-Torvik, S C Stallings, A S Gordon, et al.
Blood Advances
|
November 25, 2025
Outcomes Following Matched Sibling Donor Transplantation for Severe Combined Immunodeficiency: A Report from the PIDTC
Ahmad Rayes, Brent R Logan, Xuerong Liu, et al.
Nature Genetics
|
November 13, 2012
Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis
David C Whitcomb, Jessica LaRusch, Alyssa M Krasinskas, et al.
Nature Genetics
|
January 22, 2020
Multitrait analysis of glaucoma identifies new risk loci and enables polygenic prediction of disease susceptibility and progression
Jamie E Craig, Xikun Han, Ayub Qassim, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
June 21, 2015
Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk
Timothy J Hohman, Jessica N Cooke-Bailey, Christiane Reitz, et al.
Nature Genetics
|
September 17, 2013
Identification of a rare coding variant in complement 3 associated with age-related macular degeneration
Xiaowei Zhan, David E Larson, Chaolong Wang, et al.
Neurobiology of Aging
|
September 11, 2012
Age of onset of amyotrophic lateral sclerosis is modulated by a locus on 1p34.1
Kreshnik B Ahmeti, Senda Ajroud-Driss, Ammar Al-Chalabi, et al.
Nature Communications
|
May 16, 2018
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases
Adriana I Iglesias, Aniket Mishra, Veronique Vitart, et al.
Page
of 91