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Publications by Wendy K. Chung

Intragenic Deletion as a Novel Type of Mutation in Wolman Disease

Molecular Genetics and Metabolism

English

De novoPHIPpredicted Deleterious Variants Are Associated With Developmental Delay, Intellectual Disability, Obesity, and Dysmorphic Features

Cold Spring Harbor molecular case studies

English

De Novo Truncating Variants in theAHDC1gene Encoding the AT-hook DNA-binding Motif-Containing Protein 1 Are Associated With Intellectual Disability and Developmental Delay

Cold Spring Harbor molecular case studies

English

An Overview of Mongenic and Syndromic Obesities in Humans

Pediatric Blood and Cancer

English

Natural History and Genotype-Phenotype Correlations in 72 Individuals With SATB2 -Associated Syndrome

American Journal of Medical Genetics, Part A

Genetics

2018

English

Parental Perceptions of Prenatal Whole Exome Sequencing (PPPWES) Study

English

Celiac Disease and Down Syndrome Mortality: A Nationwide Cohort Study

English

EXPRESS: United States Pulmonary Hypertension Scientific Registry (USPHSR): Rationale, Design, and Clinical Implications

Pulmonary Circulation

Pulmonary

Respiratory Medicine

2019

English

Psychiatrists’ Views of the Genetic Bases of Mental Disorders and Behavioral Traits and Their Use of Genetic Tests

Journal of Nervous and Mental Disease

Psychiatry

Mental Health

2014

English

Clinical Presentation and Natural History of Infantile-Onset Ascending Spastic Paralysis From Three Families With an ALS2 Founder Variant

Neurological Sciences

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Wendy K. Chung

Intragenic Deletion as a Novel Type of Mutation in Wolman Disease

De novoPHIPpredicted Deleterious Variants Are Associated With Developmental Delay, Intellectual Disability, Obesity, and Dysmorphic Features

De Novo Truncating Variants in theAHDC1gene Encoding the AT-hook DNA-binding Motif-Containing Protein 1 Are Associated With Intellectual Disability and Developmental Delay

An Overview of Mongenic and Syndromic Obesities in Humans

Natural History and Genotype-Phenotype Correlations in 72 Individuals With SATB2 -Associated Syndrome

Parental Perceptions of Prenatal Whole Exome Sequencing (PPPWES) Study

Celiac Disease and Down Syndrome Mortality: A Nationwide Cohort Study

EXPRESS: United States Pulmonary Hypertension Scientific Registry (USPHSR): Rationale, Design, and Clinical Implications

Psychiatrists’ Views of the Genetic Bases of Mental Disorders and Behavioral Traits and Their Use of Genetic Tests

Clinical Presentation and Natural History of Infantile-Onset Ascending Spastic Paralysis From Three Families With an ALS2 Founder Variant