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Medrxiv : the Preprint Server for Health Sciences
|
December 9, 2024
Implementing Precision Medicine for Dilated Cardiomyopathy: Insights from The DCM Consortium
Elizabeth Jordan, Hanyu Ni, Patricia Parker, et al.
Circulation
|
August 29, 2023
Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study
Mark Hofmeyer, Garrie J Haas, Elizabeth Jordan, et al.
JAMA
|
March 13, 2014
Clinical interpretation and implications of whole-genome sequencing
Frederick 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 Trial
Constantin-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 Decompensation
Dongxue Mao, Chloe M Reuter, Maura R Z Ruzhnikov, et al.
Circulation. Genomic and Precision Medicine
|
June 18, 2025
Implementing Precision Medicine for Dilated Cardiomyopathy: Insights From the DCM Consortium
Elizabeth Jordan, Hanyu Ni, Patricia Parker, 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 Training
Gina 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 Trial
Daniel 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 disorder
Jennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Arxiv
|
January 7, 2025
GREGoR: Accelerating Genomics for Rare Diseases
Moez Dawood, Ben Heavner, Marsha M Wheeler, et al.
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of 20
Search research articles
Search
Showing results (151-160 of 191) with videos related to
Sort By:
Page
of 20
Medrxiv : the Preprint Server for Health Sciences
|
December 9, 2024
Implementing Precision Medicine for Dilated Cardiomyopathy: Insights from The DCM Consortium
Elizabeth Jordan, Hanyu Ni, Patricia Parker, et al.
Circulation
|
August 29, 2023
Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study
Mark Hofmeyer, Garrie J Haas, Elizabeth Jordan, et al.
JAMA
|
March 13, 2014
Clinical interpretation and implications of whole-genome sequencing
Frederick 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 Trial
Constantin-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 Decompensation
Dongxue Mao, Chloe M Reuter, Maura R Z Ruzhnikov, et al.
Circulation. Genomic and Precision Medicine
|
June 18, 2025
Implementing Precision Medicine for Dilated Cardiomyopathy: Insights From the DCM Consortium
Elizabeth Jordan, Hanyu Ni, Patricia Parker, 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 Training
Gina 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 Trial
Daniel 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 disorder
Jennefer N Kohler, Nicole R Legro, Dustin Baldridge, et al.
Arxiv
|
January 7, 2025
GREGoR: Accelerating Genomics for Rare Diseases
Moez Dawood, Ben Heavner, Marsha M Wheeler, et al.
Page
of 20