Wendy Chung
Columbia University in the City of New York
H-index: 122
North America-United States
Top articles of Wendy Chung
Title | Journal | Author(s) | Publication Date |
|---|---|---|---|
An Overview of GeneticTesting | Wendy K Chung John P Schacht Haluk Kavus | 2024/1/1 | |
Improvement of Variant Reclassification in Genetic Neurodevelopmental Conditions | Genetics in Medicine Open | Michelle Kowanda Rebecca Sheedy Smith Jamie Atondo Catherine Kentros Elisheva Kleinman | 2024/4/9 |
Evidence-Based Recruitment Strategies for Clinical Research: Study Personnel’s and Research Participants’ Perceptions About Successful Methods of Outreach for a US Autism … | Journal of clinical and translational science | Robin P Goin-Kochel Ivana Lozano Gabrielle Duhon Gabriela Marzano Amy Daniels | 2024/4/2 |
Selection, optimization and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse US populations | Nature Medicine | Niall J Lennon Leah C Kottyan Christopher Kachulis Noura S Abul-Husn Josh Arias | 2024/2/19 |
Heterogeneity of comprehensive clinical phenotype and longitudinal adaptive function and correlation with computational predictions of severity of missense genotypes in KIF1A … | medRxiv | Khemika K Sudnawa Wenxing Li Sean Calamia Cara H Kanner Jennifer M Bain | 2024 |
Receiving de novo genetic diagnoses for autism with intellectual disability: parents’ views of impacts on families’ reproductive decisions | Journal of Community Genetics | Robert Klitzman Ekaterina Bezborodko Wendy K Chung Paul S Appelbaum | 2024/2 |
O35: Feasibility of expanded newborn screening using genome sequencing for early actionable conditions in a diverse city | Genetics in Medicine Open | Wendy Chung Alban Ziegler Carrie Koval-Burt Denise Kay Sharon Suchy | 2024/1/1 |
PreMode predicts mode of action of missense variants by deep graph representation learning of protein sequence and structural context | bioRxiv | Guojie Zhong Yige Zhao Demi Zhuang Wendy K Chung Yufeng Shen | 2024 |
FOXP1 Haploinsufficiency Contributes to the Development of Congenital Diaphragmatic Hernia | Journal of Pediatric Genetics | Katherine E Pendleton Andres Hernandez-Garcia Jennifer M Lyu Ian M Campbell Chad A Shaw | 2024/3 |
Urinary Androgens Provide Additional Evidence Related to Metabolism and Are Correlated With Serum Androgens in Girls | Journal of the Endocrine Society | Sasinya N Scott Marvin Siguencia Frank Z Stanczyk Michaela F Hartmann Stefan A Wudy | 2024/3 |
Abstract PO1-08-10: Impact of Oncologist-Led Genetic Counseling and Testing on Prophylactic Mastectomy Rates Among Multi-Ethnic Women with Operable Breast Cancer | Cancer Research | Alissa Michel Kelly Luo Vicky Ro Matthew Fine Meghna Trivedi | 2024/5/2 |
SPARKing New Insight Into Autism Across the Lifespan | American Journal on Intellectual and Developmental Disabilities | Khemika K Sudnawa Wendy K Chung | 2024/3/1 |
An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders | International Journal of Neonatal Screening | Wendy K Chung Stephen M Kanne Zhanzhi Hu | 2024/4/16 |
LHX2 haploinsufficiency causes a variable neurodevelopmental disorder | Genetics in Medicine | Cosima M Schmid Anne Gregor Gregory Costain Chantal F Morel Lauren Massingham | 2023/7/1 |
Rescuing lung development through embryonic inhibition of histone acetylation | Science Translational Medicine | Giangela Stokes Zhuowei Li Nicole Talaba William Genthe Maria B Brix | 2024/1/31 |
Resúmenes al Espanol | American Journal on Intellectual and Developmental Disabilities | Exploracion de la Capacidad de Comunicacion Christina K Zigler Nicole Lucas Molly McFatrich Kelly L Gordon | 2023 |
169 Curating the fetal genome: experience of the ClinGen prenatal gene curation expert panel (GCEP) | American Journal of Obstetrics & Gynecology | Stephanie Galloway Jessica L Giordano Amanda Thomas-Wilson Volkan Okur Carrie J Shawber | 2024/1/1 |
Automated Identification of Germline de novo Mutations in Family Trios: A Consensus-Based Informatic Approach | bioRxiv | Mariya Shadrina Ozem Kalay Sinem Demirkaya-Budak Charles A LeDuc Wendy K Chung | 2024 |
Association of genetic and sulcal traits with executive function in congenital heart disease | Annals of clinical and translational neurology | Lara Maleyeff Jane W Newburger David Wypij Nina H Thomas Evdokia Anagnoustou | 2024/2 |
Homozygous missense variants in YKT6 result in loss of function and are associated with developmental delay, with or without severe infantile liver disease and risk for … | Genetics in Medicine | Mengqi Ma Mythily Ganapathi Yiming Zheng Kai-Li Tan Oguz Kanca | 2024/3/21 |
