Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 15 publications
Incidence of positive genetic testing among patients referred for cardiac positron emission tomography.
Journal: Journal of medical genetics
Published: January 08, 2025
Intrinsic Atrial Myopathy Precedes Left Ventricular Dysfunction and Predicts Atrial Fibrillation in Lamin A/C Cardiomyopathy.
Journal: Circulation. Genomic and precision medicine
Published: December 22, 2022
Effects of Vigorous Versus Restorative Yoga Practice on Objective Cognition Functions in Sedentary Breast and Ovarian Cancer Survivors: A Randomized Controlled Pilot Trial.
Journal: Integrative cancer therapies
Published: July 21, 2022
Correction to: The genetic architecture of Plakophilin 2 cardiomyopathy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: August 19, 2021
The genetic architecture of Plakophilin 2 cardiomyopathy.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: February 08, 2021
De novo and inherited variants in ZNF292 underlie a neurodevelopmental disorder with features of autism spectrum disorder.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: July 16, 2019
Clinical and genetic risk factors for aromatase inhibitor-associated arthralgia in breast cancer survivors.
Journal: Breast (Edinburgh, Scotland)
Published: July 10, 2019
Yield of whole exome sequencing in undiagnosed patients facing insurance coverage barriers to genetic testing.
Journal: Journal of genetic counseling
Published: March 13, 2019
Extracutaneous manifestations in phacomatosis cesioflammea and cesiomarmorata: Case series and literature review.
Journal: American journal of medical genetics. Part A
Published: October 15, 2018
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
Journal: American journal of human genetics
Published: November 27, 2017
A Patient with Sjogren's Syndrome and Subsequent Diagnosis of Inclusion Body Myositis and Light-Chain Amyloidosis.
Journal: Journal of general internal medicine
Published: October 23, 2017
A New Approach to Rare Diseases of Children: The Undiagnosed Diseases Network.
Journal: The Journal of pediatrics
Published: September 30, 2017
Last Updated: 09/26/2026