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Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 16, 2018
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Kidney360
|
September 21, 2022
The KIDNEYCODE Program: Diagnostic Yield and Clinical Features of Individuals with CKD
Kenneth V Lieberman, Alexander R Chang, Geoffrey A Block, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
January 25, 2026
High Sensitisation but Low Clinical Reactivity to Edible Insects in Shellfish-Allergic Individuals
Marta Perez-Montoya, Ana Morales-Hidalgo, Alicia Gomez-Lopez, et al.
Journal of the Peripheral Nervous System : JPNS
|
August 14, 2024
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy
Jennifer Roggenbuck, Ana Morales, Colin A Ellis, et al.
Circulation. Genomic and Precision Medicine
|
December 13, 2023
Real-World Genetic Testing Utilization Among Patients With Cardiomyopathy
Ana Morales, Chad Moretz, Sheng Ren, et al.
JAMA Cardiology
|
May 26, 2021
Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis
Amy C Sturm, Rebecca Truty, Thomas E Callis, et al.
Neurology. Genetics
|
December 20, 2021
Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings
Dianalee McKnight, Sara L Bristow, Rebecca M Truty, et al.
Circulation. Cardiovascular Genetics
|
February 19, 2013
Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy
Nadine Norton, Duanxiang Li, Evadnie Rampersaud, et al.
Frontiers in Neuroscience
|
February 27, 2018
The Decrease in Mitochondrial DNA Mutation Load Parallels Visual Recovery in a Leber Hereditary Optic Neuropathy Patient
Sonia Emperador, Mariona Vidal, Carmen Hernández-Ainsa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 11, 2021
Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program
Eric T Rush, Britt Johnson, Swaroop Aradhya, et al.
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of 20
Search research articles
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Showing results (131-140 of 196) with videos related to
Sort By:
Page
of 20
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
June 16, 2018
Genetic evaluation of cardiomyopathy: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)
Ray E Hershberger, Michael M Givertz, Carolyn Y Ho, et al.
Kidney360
|
September 21, 2022
The KIDNEYCODE Program: Diagnostic Yield and Clinical Features of Individuals with CKD
Kenneth V Lieberman, Alexander R Chang, Geoffrey A Block, et al.
Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology
|
January 25, 2026
High Sensitisation but Low Clinical Reactivity to Edible Insects in Shellfish-Allergic Individuals
Marta Perez-Montoya, Ana Morales-Hidalgo, Alicia Gomez-Lopez, et al.
Journal of the Peripheral Nervous System : JPNS
|
August 14, 2024
Diagnostic and clinical utility of comprehensive multigene panel testing for patients with neuropathy
Jennifer Roggenbuck, Ana Morales, Colin A Ellis, et al.
Circulation. Genomic and Precision Medicine
|
December 13, 2023
Real-World Genetic Testing Utilization Among Patients With Cardiomyopathy
Ana Morales, Chad Moretz, Sheng Ren, et al.
JAMA Cardiology
|
May 26, 2021
Limited-Variant Screening vs Comprehensive Genetic Testing for Familial Hypercholesterolemia Diagnosis
Amy C Sturm, Rebecca Truty, Thomas E Callis, et al.
Neurology. Genetics
|
December 20, 2021
Multigene Panel Testing in a Large Cohort of Adults With Epilepsy: Diagnostic Yield and Clinically Actionable Genetic Findings
Dianalee McKnight, Sara L Bristow, Rebecca M Truty, et al.
Circulation. Cardiovascular Genetics
|
February 19, 2013
Exome sequencing and genome-wide linkage analysis in 17 families illustrate the complex contribution of TTN truncating variants to dilated cardiomyopathy
Nadine Norton, Duanxiang Li, Evadnie Rampersaud, et al.
Frontiers in Neuroscience
|
February 27, 2018
The Decrease in Mitochondrial DNA Mutation Load Parallels Visual Recovery in a Leber Hereditary Optic Neuropathy Patient
Sonia Emperador, Mariona Vidal, Carmen Hernández-Ainsa, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research
|
October 11, 2021
Molecular Diagnoses of X-Linked and Other Genetic Hypophosphatemias: Results From a Sponsored Genetic Testing Program
Eric T Rush, Britt Johnson, Swaroop Aradhya, et al.
Page
of 20