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The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy

Circulation research, 2021-05, Vol.128 (10), p.1514-1532

2021

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The central role of family-based approaches in understanding the genetic architecture of left ventricular noncompaction

International journal of cardiology, 2022-04, Vol.353, p.75-76

Kinnamon, Daniel D.

2022

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Antenatal hydronephrosis as a predictor of postnatal outcome: a meta-analysis

Pediatrics (Evanston), 2006-08, Vol.118 (2), p.586-593

2006

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Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy

JAMA : the journal of the American Medical Association, 2022-02, Vol.327 (5), p.454

2022

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Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants

PloS one, 2012-02, Vol.7 (2), p.e30238-e30238

2012

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Expanded newborn screening for biochemical disorders: the effect of a false-positive result

Pediatrics (Evanston), 2006-06, Vol.117 (6), p.1915-1921

2006

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Screening for Dilated Cardiomyopathy in At-Risk First-Degree Relatives

Journal of the American College of Cardiology, 2023-05, Vol.81 (21), p.2059-2071

2023

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Response to "assessment of risk of ALS conferred by the GGGGCC hexanucleotide expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion"

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-06, p.1-3

2024

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Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry

JAMA : the journal of the American Medical Association, 2023-08, Vol.330 (5), p.432

2023

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Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study

Circulation (New York, N.Y.), 2023-09, Vol.148 (11), p.872-881

2023

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Attitudes of Dilated Cardiomyopathy Patients and Investigators Toward Genomic Study Enrollment, Consent Process, and Return of Genetic Results

Clinical and translational science, 2021-03, Vol.14 (2), p.550-557

2021

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Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees

Circulation. Genomic and precision medicine, 2018-07, Vol.11 (7), p.e002038-e002038

2018

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TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study

Genetics in medicine, 2022-07, Vol.24 (7), p.1495-1502

2022

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Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

Neurology, 2013-03, Vol.80 (11), p.982-989

2013

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Associations between neurohormonal and inflammatory activation and heart failure in children

The American heart journal, 2008-03, Vol.155 (3), p.527-533

2008

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Understanding BRCA Mutation Carriers' Preferences for Communication of Genetic Modifiers of Breast Cancer Risk

Journal of health communication, 2019-04, Vol.24 (4), p.377-384

2019

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Single Marker Family-Based Association Analysis Conditional on Parental Information

Methods in molecular biology (Clifton, N.J.), 2017-01, Vol.1666, p.391

2017

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Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study

Circulation. Cardiovascular genetics, 2017-12, Vol.10 (6)

2017

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Cerebellar hemorrhage in the preterm infant: ultrasonographic findings and risk factors

Pediatrics (Evanston), 2005-09, Vol.116 (3), p.717-724

2005

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Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy

Circulation. Genomic and precision medicine, 2022-06, Vol.15 (3), p.e003541-e003541

2022

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Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura

Blood, 2006-04, Vol.107 (7), p.2639-2642

2006

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Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy

JAMA cardiology, 2023-01, Vol.8 (1), p.33

2023

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Valid Monte Carlo Permutation Tests for Genetic Case-Control Studies With Missing Genotypes

Genetic epidemiology, 2014-05, Vol.38 (4), p.325-344

2014

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SOS1 Gain-of-Function Variants in Dilated Cardiomyopathy

Circulation. Genomic and precision medicine, 2020-08, Vol.13 (4), p.e002892-e002892

2020

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The Complex and Diverse Genetic Architecture of Dilated Cardiomyopathy

The central role of family-based approaches in understanding the genetic architecture of left ventricular noncompaction

Antenatal hydronephrosis as a predictor of postnatal outcome: a meta-analysis

Prevalence and Cumulative Risk of Familial Idiopathic Dilated Cardiomyopathy

Reconsidering association testing methods using single-variant test statistics as alternatives to pooling tests for sequence data with rare variants

Expanded newborn screening for biochemical disorders: the effect of a false-positive result

Screening for Dilated Cardiomyopathy in At-Risk First-Degree Relatives

Response to "assessment of risk of ALS conferred by the GGGGCC hexanucleotide expansion in C9orf72 among first-degree relatives of patients with ALS carrying the repeat expansion"

Effectiveness of the Family Heart Talk Communication Tool in Improving Family Member Screening for Dilated Cardiomyopathy: Results of a Randomized Trial

Genetic Architecture of Dilated Cardiomyopathy in Individuals of African and European Ancestry

Rare Variant Genetics and Dilated Cardiomyopathy Severity: The DCM Precision Medicine Study

Attitudes of Dilated Cardiomyopathy Patients and Investigators Toward Genomic Study Enrollment, Consent Process, and Return of Genetic Results

Multigenic Disease and Bilineal Inheritance in Dilated Cardiomyopathy Is Illustrated in Nonsegregating LMNA Pedigrees

TTR variants in patients with dilated cardiomyopathy: An investigation of the DCM Precision Medicine Study

Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease

Associations between neurohormonal and inflammatory activation and heart failure in children

Understanding BRCA Mutation Carriers' Preferences for Communication of Genetic Modifiers of Breast Cancer Risk

Single Marker Family-Based Association Analysis Conditional on Parental Information

Toward Genetics-Driven Early Intervention in Dilated Cardiomyopathy: Design and Implementation of the DCM Precision Medicine Study

Cerebellar hemorrhage in the preterm infant: ultrasonographic findings and risk factors

Communal Coping as a Strategy to Enhance Family Engagement in Dilated Cardiomyopathy

Prospective phase 1/2 study of rituximab in childhood and adolescent chronic immune thrombocytopenic purpura

Knowledge of Genome Sequencing and Trust in Medical Researchers Among Patients of Different Racial and Ethnic Groups With Idiopathic Dilated Cardiomyopathy

Valid Monte Carlo Permutation Tests for Genetic Case-Control Studies With Missing Genotypes

SOS1 Gain-of-Function Variants in Dilated Cardiomyopathy

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