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Toni I Pollin

Showing results (121-130 of 148) with videos related to

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Archives of Internal Medicine|November 10, 2010
Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amishHaiqing Shen, Coleen M Damcott, Evadnie Rampersaud, et al.
Molecular Psychiatry|March 7, 2023
Genome-wide significant risk loci for mood disorders in the Old Order Amish founder populationElizabeth M Humphries, Kwangmi Ahn, Rachel L Kember, et al.
Human Genetics|July 8, 2026
Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot projectYasas D Kolambage, Claudia Gonzaga-Jauregui, Guillermo Lay-Son, et al.
Circulation. Genomic and Precision Medicine|November 3, 2020
<i>KCNQ1</i> and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision MedicineElizabeth A Streeten, Vincent Y See, Linda B J Jeng, et al.
Nature Communications|December 18, 2013
A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolatesIoanna Tachmazidou, George Dedoussis, Lorraine Southam, et al.
Journal of Diabetes Science and Technology|January 9, 2025
Advancing Monogenic Diabetes Research and Clinical Care by Creating a Data Commons: The Precision Diabetes Consortium (PREDICT)Michael E McCullough, Lisa R Letourneau-Freiberg, Rochelle N Naylor, et al.
American Journal of Medical Genetics. Part A|August 6, 2025
Exonic Variation and Its Clinical Impact in 7221 Old Order AmishBraxton D Mitchell, Ebuka Onyenobi, Joshua P Lewis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Implementation of pharmacogenetics: the University of Maryland Personalized Anti-platelet Pharmacogenetics ProgramAlan R Shuldiner, Kathleen Palmer, Ruth E Pakyz, et al.
Circulation. Cardiovascular Genetics|February 9, 2013
Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomesJoshua P Lewis, Kathleen Ryan, Jeffrey R O'Connell, et al.
Diabetes|December 16, 2022
Identification of Genetic Variation Influencing Metformin Response in a Multiancestry Genome-Wide Association Study in the Diabetes Prevention Program (DPP)Josephine H Li, James A Perry, Kathleen A Jablonski, et al.
Pageof 15

Showing results (121-130 of 148) with videos related to

Sort By:
Pageof 15
Archives of Internal Medicine|November 10, 2010
Familial defective apolipoprotein B-100 and increased low-density lipoprotein cholesterol and coronary artery calcification in the old order amishHaiqing Shen, Coleen M Damcott, Evadnie Rampersaud, et al.
Molecular Psychiatry|March 7, 2023
Genome-wide significant risk loci for mood disorders in the Old Order Amish founder populationElizabeth M Humphries, Kwangmi Ahn, Rachel L Kember, et al.
Human Genetics|July 8, 2026
Implementation of exome sequencing for rare undiagnosed diseases in LMICs: the G2MC rare diseases exome sequencing pilot projectYasas D Kolambage, Claudia Gonzaga-Jauregui, Guillermo Lay-Son, et al.
Circulation. Genomic and Precision Medicine|November 3, 2020
<i>KCNQ1</i> and Long QT Syndrome in 1/45 Amish: The Road From Identification to Implementation of Culturally Appropriate Precision MedicineElizabeth A Streeten, Vincent Y See, Linda B J Jeng, et al.
Nature Communications|December 18, 2013
A rare functional cardioprotective APOC3 variant has risen in frequency in distinct population isolatesIoanna Tachmazidou, George Dedoussis, Lorraine Southam, et al.
Journal of Diabetes Science and Technology|January 9, 2025
Advancing Monogenic Diabetes Research and Clinical Care by Creating a Data Commons: The Precision Diabetes Consortium (PREDICT)Michael E McCullough, Lisa R Letourneau-Freiberg, Rochelle N Naylor, et al.
American Journal of Medical Genetics. Part A|August 6, 2025
Exonic Variation and Its Clinical Impact in 7221 Old Order AmishBraxton D Mitchell, Ebuka Onyenobi, Joshua P Lewis, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 12, 2014
Implementation of pharmacogenetics: the University of Maryland Personalized Anti-platelet Pharmacogenetics ProgramAlan R Shuldiner, Kathleen Palmer, Ruth E Pakyz, et al.
Circulation. Cardiovascular Genetics|February 9, 2013
Genetic variation in PEAR1 is associated with platelet aggregation and cardiovascular outcomesJoshua P Lewis, Kathleen Ryan, Jeffrey R O'Connell, et al.
Diabetes|December 16, 2022
Identification of Genetic Variation Influencing Metformin Response in a Multiancestry Genome-Wide Association Study in the Diabetes Prevention Program (DPP)Josephine H Li, James A Perry, Kathleen A Jablonski, et al.
Pageof 15