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European Journal of Human Genetics : EJHG
|
May 10, 2012
PITX2 and FOXC1 spectrum of mutations in ocular syndromes
Linda M Reis, Rebecca C Tyler, Bethany A Volkmann Kloss, et al.
Circulation Research
|
January 8, 2011
Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families
Donna K Arnett, Kristin J Meyers, Richard B Devereux, et al.
European Journal of Human Genetics : EJHG
|
June 16, 2011
Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study
Nathan E Wineinger, Nicholas M Pajewski, Richard E Kennedy, et al.
Human Genetics
|
February 23, 2011
BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome
Linda M Reis, Rebecca C Tyler, Kala F Schilter, et al.
Pediatrics
|
June 24, 2016
Pharmacogenetics for Safe Codeine Use in Sickle Cell Disease
Roseann S Gammal, Kristine R Crews, Cyrine E Haidar, et al.
Frontiers in Genetics
|
April 24, 2015
PCSK9 variation and association with blood pressure in African Americans: preliminary findings from the HyperGEN and REGARDS studies
Ngan T Tran, Stella Aslibekyan, Hemant K Tiwari, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
March 28, 2024
Predicting oncology drug-induced cardiotoxicity with donor-specific iPSC-CMs-a proof-of-concept study with doxorubicin
Li Pang, Chengzhong Cai, Praful Aggarwal, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 26, 2025
Improving performance of polygenic risk scores for hypertension across two ancestry groups
Marguerite R Irvin, Vinodh Srinivasasainagendra, Nicole D Armstrong, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2014
Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes
Philip F Giampietro, Linlea Armstrong, Alex Stoddard, et al.
International Journal of Cardiology
|
July 27, 2018
Clinical correlates and heritability of cardiac mechanics: The HyperGEN study
Sadiya S Khan, Kwang-Youn A Kim, Jie Peng, et al.
Page
of 13
Search research articles
Search
Showing results (71-80 of 125) with videos related to
Sort By:
Page
of 13
European Journal of Human Genetics : EJHG
|
May 10, 2012
PITX2 and FOXC1 spectrum of mutations in ocular syndromes
Linda M Reis, Rebecca C Tyler, Bethany A Volkmann Kloss, et al.
Circulation Research
|
January 8, 2011
Genetic variation in NCAM1 contributes to left ventricular wall thickness in hypertensive families
Donna K Arnett, Kristin J Meyers, Richard B Devereux, et al.
European Journal of Human Genetics : EJHG
|
June 16, 2011
Characterization of autosomal copy-number variation in African Americans: the HyperGEN Study
Nathan E Wineinger, Nicholas M Pajewski, Richard E Kennedy, et al.
Human Genetics
|
February 23, 2011
BMP4 loss-of-function mutations in developmental eye disorders including SHORT syndrome
Linda M Reis, Rebecca C Tyler, Kala F Schilter, et al.
Pediatrics
|
June 24, 2016
Pharmacogenetics for Safe Codeine Use in Sickle Cell Disease
Roseann S Gammal, Kristine R Crews, Cyrine E Haidar, et al.
Frontiers in Genetics
|
April 24, 2015
PCSK9 variation and association with blood pressure in African Americans: preliminary findings from the HyperGEN and REGARDS studies
Ngan T Tran, Stella Aslibekyan, Hemant K Tiwari, et al.
Toxicological Sciences : an Official Journal of the Society of Toxicology
|
March 28, 2024
Predicting oncology drug-induced cardiotoxicity with donor-specific iPSC-CMs-a proof-of-concept study with doxorubicin
Li Pang, Chengzhong Cai, Praful Aggarwal, et al.
Medrxiv : the Preprint Server for Health Sciences
|
November 26, 2025
Improving performance of polygenic risk scores for hypertension across two ancestry groups
Marguerite R Irvin, Vinodh Srinivasasainagendra, Nicole D Armstrong, et al.
American Journal of Medical Genetics. Part A
|
October 29, 2014
Whole exome sequencing identifies a POLRID mutation segregating in a father and two daughters with findings of Klippel-Feil and Treacher Collins syndromes
Philip F Giampietro, Linlea Armstrong, Alex Stoddard, et al.
International Journal of Cardiology
|
July 27, 2018
Clinical correlates and heritability of cardiac mechanics: The HyperGEN study
Sadiya S Khan, Kwang-Youn A Kim, Jie Peng, et al.
Page
of 13