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Plos One
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March 27, 2010
Genome-wide association of lipid-lowering response to statins in combined study populations
Mathew J Barber, Lara M Mangravite, Craig L Hyde, et al.
Blood
|
May 22, 2013
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project
Jill M Johnsen, Paul L Auer, Alanna C Morrison, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us Participants
Andrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology
|
February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Communications Biology
|
June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Human Molecular Genetics
|
February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish
Regie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
The Journal of Molecular Diagnostics : JMD
|
February 8, 2022
CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project
Andrea Gaedigk, Erin C Boone, Steven E Scherer, et al.
International Journal of Obesity (2005)
|
December 3, 2022
Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis
Luciana B Vargas, Leslie A Lange, Kendra Ferrier, et al.
Journal of the American College of Cardiology
|
February 25, 2014
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome
Peter Weeke, Jonathan D Mosley, David Hanna, et al.
American Journal of Human Genetics
|
April 9, 2013
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation
Bobby G Ng, Kati J Buckingham, Kimiyo Raymond, et al.
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of 20
Search research articles
Search
Showing results (111-120 of 194) with videos related to
Sort By:
Page
of 20
Plos One
|
March 27, 2010
Genome-wide association of lipid-lowering response to statins in combined study populations
Mathew J Barber, Lara M Mangravite, Craig L Hyde, et al.
Blood
|
May 22, 2013
Common and rare von Willebrand factor (VWF) coding variants, VWF levels, and factor VIII levels in African Americans: the NHLBI Exome Sequencing Project
Jill M Johnsen, Paul L Auer, Alanna C Morrison, et al.
Medrxiv : the Preprint Server for Health Sciences
|
July 1, 2024
Frequency of pharmacogenomic variation and medication exposures among All of Us Participants
Andrew Haddad, Aparna Radhakrishnan, Sean McGee, et al.
Communications Biology
|
February 20, 2024
The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Communications Biology
|
June 10, 2024
Author Correction: The frequency of pathogenic variation in the All of Us cohort reveals ancestry-driven disparities
Eric Venner, Karynne Patterson, Divya Kalra, et al.
Human Molecular Genetics
|
February 1, 2014
Adenylate cyclase 1 (ADCY1) mutations cause recessive hearing impairment in humans and defects in hair cell function and hearing in zebrafish
Regie Lyn P Santos-Cortez, Kwanghyuk Lee, Arnaud P Giese, et al.
The Journal of Molecular Diagnostics : JMD
|
February 8, 2022
CYP2C8, CYP2C9, and CYP2C19 Characterization Using Next-Generation Sequencing and Haplotype Analysis: A GeT-RM Collaborative Project
Andrea Gaedigk, Erin C Boone, Steven E Scherer, et al.
International Journal of Obesity (2005)
|
December 3, 2022
Gene expression associations with body mass index in the Multi-Ethnic Study of Atherosclerosis
Luciana B Vargas, Leslie A Lange, Kendra Ferrier, et al.
Journal of the American College of Cardiology
|
February 25, 2014
Exome sequencing implicates an increased burden of rare potassium channel variants in the risk of drug-induced long QT interval syndrome
Peter Weeke, Jonathan D Mosley, David Hanna, et al.
American Journal of Human Genetics
|
April 9, 2013
Mosaicism of the UDP-galactose transporter SLC35A2 causes a congenital disorder of glycosylation
Bobby G Ng, Kati J Buckingham, Kimiyo Raymond, et al.
Page
of 20