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Showing results (561-570 of 599) with videos related to

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JAMA|March 13, 2014
Clinical interpretation and implications of whole-genome sequencingFrederick E Dewey, Megan E Grove, Cuiping Pan, et al.
Circulation. Heart Failure|May 9, 2025
Proteomic Analysis of Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Clinical TrialConstantin-Cristian Topriceanu, Christoffer Rasmus Vissing, Anna Axelsson Raja, et al.
American Journal of Human Genetics|March 21, 2020
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic DecompensationDongxue Mao, Chloe M Reuter, Maura R Z Ruzhnikov, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2026
Temporal Multi-Omic Analysis Uncovers Sex-Biased Molecular Programs Underlying Skeletal Muscle Adaptation to Endurance TrainingGina M Many, Christopher Jin, Nicholas Day, et al.
Circulation|March 20, 2023
Effectiveness of the <i>Family Heart Talk</i> Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized TrialDaniel D Kinnamon, Elizabeth Jordan, Garrie J Haas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2024
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorderJennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature Medicine|June 5, 2019
Identification of rare-disease genes using blood transcriptome sequencing and large control cohortsLaure Frésard, Craig Smail, Nicole M Ferraro, et al.
Circulation|December 5, 2024
Low Penetrance Sarcomere Variants Contribute to Additive Risk in Hypertrophic CardiomyopathyJoshua K Meisner, Aaron Renberg, Eric D Smith, et al.
Nature Communications|June 26, 2019
Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failurePablo Cordero, Victoria N Parikh, Elizabeth T Chin, et al.
Pageof 60

Showing results (561-570 of 599) with videos related to

Sort By:
Pageof 60
JAMA|March 13, 2014
Clinical interpretation and implications of whole-genome sequencingFrederick E Dewey, Megan E Grove, Cuiping Pan, et al.
Circulation. Heart Failure|May 9, 2025
Proteomic Analysis of Valsartan for Attenuating Disease Evolution in Early Sarcomeric Hypertrophic Cardiomyopathy (VANISH) Clinical TrialConstantin-Cristian Topriceanu, Christoffer Rasmus Vissing, Anna Axelsson Raja, et al.
American Journal of Human Genetics|March 21, 2020
De novo EIF2AK1 and EIF2AK2 Variants Are Associated with Developmental Delay, Leukoencephalopathy, and Neurologic DecompensationDongxue Mao, Chloe M Reuter, Maura R Z Ruzhnikov, et al.
Biorxiv : the Preprint Server for Biology|January 7, 2026
Temporal Multi-Omic Analysis Uncovers Sex-Biased Molecular Programs Underlying Skeletal Muscle Adaptation to Endurance TrainingGina M Many, Christopher Jin, Nicholas Day, et al.
Circulation|March 20, 2023
Effectiveness of the <i>Family Heart Talk</i> Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized TrialDaniel D Kinnamon, Elizabeth Jordan, Garrie J Haas, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 20, 2024
Loss of function of FAM177A1, a Golgi complex localized protein, causes a novel neurodevelopmental disorderJennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Arxiv|January 7, 2025
GREGoR: Accelerating Genomics for Rare DiseasesMoez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Nature Medicine|June 5, 2019
Identification of rare-disease genes using blood transcriptome sequencing and large control cohortsLaure Frésard, Craig Smail, Nicole M Ferraro, et al.
Circulation|December 5, 2024
Low Penetrance Sarcomere Variants Contribute to Additive Risk in Hypertrophic CardiomyopathyJoshua K Meisner, Aaron Renberg, Eric D Smith, et al.
Nature Communications|June 26, 2019
Pathologic gene network rewiring implicates PPP1R3A as a central regulator in pressure overload heart failurePablo Cordero, Victoria N Parikh, Elizabeth T Chin, et al.
Pageof 60