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American Journal of Human Genetics
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August 5, 2014
Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results
Holly K Tabor, Paul L Auer, Seema M Jamal, et al.
Circulation. Genomic and Precision Medicine
|
November 7, 2025
Functional Profiling of <i>KCNE1</i> Variants Informs Population Carrier Frequency of Jervell and Lange-Nielsen Syndrome Type 2
Carlos G Vanoye, Reshma R Desai, Jordan D John, et al.
Biorxiv : the Preprint Server for Biology
|
April 16, 2025
Functional profiling of <i>KCNE1</i> variants informs population carrier frequency of Jervell and Lange-Nielsen syndrome type 2
Carlos G Vanoye, Reshma R Desai, Jordan D John, et al.
Journal of the American Heart Association
|
March 24, 2022
Practitioners' Confidence and Desires for Education in Cardiovascular and Sudden Cardiac Death Genetics
Laura Lopez Santibanez Jacome, Lisa M Dellefave-Castillo, Catherine A Wicklund, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2024
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Adam S Gordon, Kristy Lee, Noura S Abul-Husn, et al.
American Journal of Human Genetics
|
August 20, 2019
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting
Adam S Gordon, Elisabeth A Rosenthal, David S Carrell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 22, 2023
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Lupus
|
May 12, 2021
Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis
Vivian K Kawai, Mingjian Shi, Ge Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 8, 2022
ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 26, 2025
ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Kristy Lee, Noura S Abul-Husn, Laura M Amendola, et al.
Page
of 5
Search research articles
Search
Showing results (11-20 of 45) with videos related to
Sort By:
Page
of 5
American Journal of Human Genetics
|
August 5, 2014
Pathogenic variants for Mendelian and complex traits in exomes of 6,517 European and African Americans: implications for the return of incidental results
Holly K Tabor, Paul L Auer, Seema M Jamal, et al.
Circulation. Genomic and Precision Medicine
|
November 7, 2025
Functional Profiling of <i>KCNE1</i> Variants Informs Population Carrier Frequency of Jervell and Lange-Nielsen Syndrome Type 2
Carlos G Vanoye, Reshma R Desai, Jordan D John, et al.
Biorxiv : the Preprint Server for Biology
|
April 16, 2025
Functional profiling of <i>KCNE1</i> variants informs population carrier frequency of Jervell and Lange-Nielsen syndrome type 2
Carlos G Vanoye, Reshma R Desai, Jordan D John, et al.
Journal of the American Heart Association
|
March 24, 2022
Practitioners' Confidence and Desires for Education in Cardiovascular and Sudden Cardiac Death Genetics
Laura Lopez Santibanez Jacome, Lisa M Dellefave-Castillo, Catherine A Wicklund, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
May 31, 2024
Consideration of disease penetrance in the selection of secondary findings gene-disease pairs: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Adam S Gordon, Kristy Lee, Noura S Abul-Husn, et al.
American Journal of Human Genetics
|
August 20, 2019
Rates of Actionable Genetic Findings in Individuals with Colorectal Cancer or Polyps Ascertained from a Community Medical Setting
Adam S Gordon, Elisabeth A Rosenthal, David S Carrell, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 22, 2023
ACMG SF v3.2 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Lupus
|
May 12, 2021
Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis
Vivian K Kawai, Mingjian Shi, Ge Liu, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
July 8, 2022
ACMG SF v3.1 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
David T Miller, Kristy Lee, Noura S Abul-Husn, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 26, 2025
ACMG SF v3.3 list for reporting of secondary findings in clinical exome and genome sequencing: A policy statement of the American College of Medical Genetics and Genomics (ACMG)
Kristy Lee, Noura S Abul-Husn, Laura M Amendola, et al.
Page
of 5