Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Wendy K. Chung

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

American Journal of Human Genetics

Genetics

2018

English

De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

American Journal of Human Genetics

Genetics

2019

English

Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects

American Journal of Human Genetics

Genetics

2016

English

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

American Journal of Human Genetics

Genetics

2018

English

Novel Risk Genes and Mechanisms Implicated by Exome Sequencing of 2572 Individuals With Pulmonary Arterial Hypertension

English

The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population

Biological Psychiatry

2015

English

Should Life Insurers Have Access to Genetic Test Results?

JAMA - Journal of the American Medical Association

Medicine

2014

English

Clinical Application of Whole-Exome Sequencing

JAMA Neurology

Neurology

2013

English

Development of a Tiered and Binned Genetic Counseling Model for Informed Consent in the Era of Multiplex Testing for Cancer Susceptibility

English

Informed Consent for Return of Incidental Findings in Genomic Research

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Wendy K. Chung

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia

Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects

Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated With Craniofacial, Neurological, Cardiovascular, and Skeletal Features

Novel Risk Genes and Mechanisms Implicated by Exome Sequencing of 2572 Individuals With Pulmonary Arterial Hypertension

The Cognitive and Behavioral Phenotype of the 16p11.2 Deletion in a Clinically Ascertained Population

Should Life Insurers Have Access to Genetic Test Results?

Clinical Application of Whole-Exome Sequencing

Development of a Tiered and Binned Genetic Counseling Model for Informed Consent in the Era of Multiplex Testing for Cancer Susceptibility

Informed Consent for Return of Incidental Findings in Genomic Research