
Wendy Kay Chung MD PhD
Clinical Genetics, Clinical Molecular Genetics
Chair, Department of Pediatrics, Boston Childrens Hospital and Harvard Medical School
Join to View Full Profile
300 Longwood AvenueBoston, MA 02115
Phone+1 617-355-5022
Dr. Chung is on Doximity
As a Doximity member you'll join over two million verified healthcare professionals in a private, secure network.
- Gain access to free telehealth tools, such as our “call shielding” and one-way patient texting.
- Connect with colleagues in the same hospital or clinic.
- Read the latest clinical news, personalized to your specialty.
Summary
- Dr. Wendy Chung is a medical geneticist and Chair of Pediatrics at Boston Children's Hospital in Boston, MA. She received her medical degree from Weill Cornell Medicine and has been in practice 23 years. She specializes in clinical genetics and clinical molecular genetics and is experienced in inborn errors of metabolism. She has more than 600 publications. She is a member of the National Academy of Medicine.
Education & Training
- Weill Cornell MedicineClass of 1998
Certifications & Licensure
- MA State Medical License 2023 - 2025
- NJ State Medical License 2006 - 2025
- NY State Medical License 2000 - 2025
- American Board of Medical Genetics and Genomics Clinical Molecular Genetics
- American Board of Medical Genetics and Genomics Clinical Genetics and Genomics
Awards, Honors, & Recognition
- America's Top Doctors Castle Connolly, 2014
- New York Magazine: Top Doctors Castle Connolly, 2012-2014
- Top Doctors: New York Metro Area Castle Connolly, 2012-2014
- Join now to see all
Clinical Trials
- Pancreatic Cancer Genetics Start of enrollment: 2008 Jan 01
- Validation of a Mouse Model of Pancreatic Carcinogenesis Start of enrollment: 2009 Mar 01
- Family and Personal History of Malignancy in Intraductal Papillary Mucinous Neoplasm (IPMN) Start of enrollment: 2008 Nov 17
- Join now to see all
Publications & Presentations
PubMed
- Newborn Screening Using Genome Sequencing for Early Actionable Conditions-Reply.Alban Ziegler, Wendy K Chung
JAMA. 2025-03-25 - A toxic gain of function variant in MAPK8IP3 provides novel insights into JIP3 cellular roles.Wei Zhang, Swapnil Mittal, Ria Thomas, Anahid Foroughishafiei, Ricardo Nunes Bastos
JCI Insight. 2025-03-20 - GATA6 regulates WNT and BMP programs to pattern precardiac mesoderm during the earliest stages of human cardiogenesis.Joseph A Bisson, Miriam Gordillo, Ritu Kumar, Neranjan de Silva, Ellen Yang
Elife. 2025-03-13
Journal Articles
- Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization StudySusan M Domchek, Wendy K Chung, Patricia A Ganz, Robert L Nussbaum, Journal of the National Cancer Institute
- Rare Variants in SOX17 Are Associated with Pulmonary Arterial Hypertension with Congenital Heart DiseaseUsha Krishnan, Eric D Austin, Frederick E Dewey, D Dunbar Ivy, Wendy K Chung, Rizwan Hamid, BioMed Central
Press Mentions
- Hidden Genetic Causes of Congenital Heart Disease IdentifiedFebruary 20th, 2025
- GeneDx to Highlight Key Research Findings at American Society of Human Genetics (ASHG) Annual MeetingNovember 4th, 2024
- Groundbreaking GUARDIAN Study Shows Benefits of Adding Genome Sequencing to Newborn Screening; Augments and Improves Standard Newborn ScreeningOctober 24th, 2024
- Join now to see all
Grant Support
- Fair Phenotype Annotation and Genomic ReinterpretationCOLUMBIA UNIVERSITY HEALTH SCIENCES2023–2028
- Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in AutismCOLUMBIA UNIVERSITY HEALTH SCIENCES2022–2027
- Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in AutismCOLUMBIA UNIVERSITY HEALTH SCIENCES2022–2027
- Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in AutismCOLUMBIA UNIVERSITY HEALTH SCIENCES2022–2027
- Prospective Genetic Risk Evaluation and Assessment (PROGRESS) in AutismCOLUMBIA UNIVERSITY HEALTH SCIENCES2022–2027
- CLEAR Consortium: Discovering the Developmental Mechanisms of Trachea-Esophageal Birth DefectsCINCINNATI CHILDRENS HOSP MED CTR2017–2027
- CLEAR Consortium: Discovering the Developmental Mechanisms of Trachea-Esophageal Birth DefectsCINCINNATI CHILDRENS HOSP MED CTR2017–2027
- CLEAR Consortium: Discovering the Developmental Mechanisms of Trachea-Esophageal Birth DefectsCINCINNATI CHILDRENS HOSP MED CTR2017–2027
- CLEAR Consortium: Discovering the Developmental Mechanisms of Trachea-Esophageal Birth DefectsCINCINNATI CHILDRENS HOSP MED CTR2017–2027
- CLEAR Consortium: Discovering the Developmental Mechanisms of Trachea-Esophageal Birth DefectsCINCINNATI CHILDRENS HOSP MED CTR2017–2027
- Child Health Research Career Development Award (CHRCDA) Program (K12)BOSTON CHILDREN'S HOSPITAL2007–2027
- Child Health Research Career Development Award (CHRCDA) Program (K12)BOSTON CHILDREN'S HOSPITAL2007–2027
- Child Health Research Career Development Award (CHRCDA) Program (K12)BOSTON CHILDREN'S HOSPITAL2007–2027
- Child Health Research Career Development Award (CHRCDA) Program (K12)BOSTON CHILDREN'S HOSPITAL2007–2027
- Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart diseaseCOLUMBIA UNIVERSITY HEALTH SCIENCES2020–2025
- Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart diseaseCOLUMBIA UNIVERSITY HEALTH SCIENCES2020–2025
- Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart diseaseCOLUMBIA UNIVERSITY HEALTH SCIENCES2020–2025
- Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart diseaseCOLUMBIA UNIVERSITY HEALTH SCIENCES2020–2025
- Identifying and applying genetic variation relevant to clinical outcomes for individuals with congenital heart diseaseCOLUMBIA UNIVERSITY HEALTH SCIENCES2020–2025
- EHR-based Genomic Risk Assessment and Management for Diverse PopulationsCOLUMBIA UNIVERSITY HEALTH SCIENCES2015–2025
- Role of the Kinesin KIF1A in Neurological DiseaseCOLUMBIA UNIVERSITY HEALTH SCIENCES2020–2024
- Molecular Genetic Analysis Of Human ObesityNational Institute Of Diabetes And Digestive And Kidney Diseases2009–2012
- Impact Of Return Of Incidental Genetic Test Results To Research Participants In TNational Human Genome Research Institute2011
- Molecular Approaches To Gene Identification In Congenital Heart DiseaseNational Heart, Lung, And Blood Institute2009–2011
- Identification Of Novel Genes For Congenital Diaphragmatic HerniaEunice Kennedy Shriver National Institute Of Child Health &Human Development2008–2011
Viewing the full profile is available to verified healthcare professionals only.
Find your profile and take control of your online presence: