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Showing results (11-20 of 18) with videos related to

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JAMA Network Open|December 15, 2025
Genomic Ascertainment of CHEK2-Related Cancer PredispositionSun Young Kim, Jung Kim, Mark Ramos, et al.
Nature Communications|February 28, 2024
Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritisPavel Loginovic, Feiyi Wang, Jiang Li, et al.
Genetics in Medicine Open|May 8, 2026
Evidence of variations in genetic prevalence for loss-of-function <i>PKP2</i> variants between individuals with European and African ancestryAlexandra Winters, Renae Judy, Choudhary Anwar A Chahal, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Genomic ascertainment to quantify prevalence and cancer risk in adults with pathogenic and likely pathogenic germline variants in RASopathy genesJung Kim, Gina Ney, Megan N Frone, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2026
Cancer risk in adults with pathogenic germline variants in RAS/MAPK genes using genomic ascertainmentJung Kim, Gina Ney, Megan N Frone, et al.
Plos Genetics|January 10, 2020
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseasesSylvia T Nurnberg, Marie A Guerraty, Robert C Wirka, et al.
JAMA Dermatology|May 27, 2026
Prevalence of Familial Melanoma Genes and Cancer Risk Among Genomically Ascertained IndividualsAlisa M Goldstein, Jung Kim, Jeremy S Haley, et al.
American Journal of Human Genetics|June 18, 2019
Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human LiverMinal Çalışkan, Elisabetta Manduchi, H Shanker Rao, et al.
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Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
JAMA Network Open|December 15, 2025
Genomic Ascertainment of CHEK2-Related Cancer PredispositionSun Young Kim, Jung Kim, Mark Ramos, et al.
Nature Communications|February 28, 2024
Applying a genetic risk score model to enhance prediction of future multiple sclerosis diagnosis at first presentation with optic neuritisPavel Loginovic, Feiyi Wang, Jiang Li, et al.
Genetics in Medicine Open|May 8, 2026
Evidence of variations in genetic prevalence for loss-of-function <i>PKP2</i> variants between individuals with European and African ancestryAlexandra Winters, Renae Judy, Choudhary Anwar A Chahal, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
Genomic ascertainment to quantify prevalence and cancer risk in adults with pathogenic and likely pathogenic germline variants in RASopathy genesJung Kim, Gina Ney, Megan N Frone, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 29, 2026
Cancer risk in adults with pathogenic germline variants in RAS/MAPK genes using genomic ascertainmentJung Kim, Gina Ney, Megan N Frone, et al.
Plos Genetics|January 10, 2020
Genomic profiling of human vascular cells identifies TWIST1 as a causal gene for common vascular diseasesSylvia T Nurnberg, Marie A Guerraty, Robert C Wirka, et al.
JAMA Dermatology|May 27, 2026
Prevalence of Familial Melanoma Genes and Cancer Risk Among Genomically Ascertained IndividualsAlisa M Goldstein, Jung Kim, Jeremy S Haley, et al.
American Journal of Human Genetics|June 18, 2019
Genetic and Epigenetic Fine Mapping of Complex Trait Associated Loci in the Human LiverMinal Çalışkan, Elisabetta Manduchi, H Shanker Rao, et al.
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