Works by Chung, Wendy

Results: 376

Founder Fukutin mutation causes Walker-Warburg syndrome in four Ashkenazi Jewish families.

Published in:

Prenatal Diagnosis, 2009, v. 29, n. 6, p. 560, doi. 10.1002/pd.2238

By:

Chung, Wendy;
Winder, Thomas L.;
LeDuc, Charles A.;
Simpson, Lynn L.;
Millar, William S.;
Dungan, Jeffrey;
Ginsberg, Norman;
Plaga, Stacey;
Moore, Steven A.;
Chung, Wendy K.

Publication type:

Article

Two Novel PNLIP Mutations Causing Congenital Lipase Deficiency in Identical Twin Boys.

Published in:

2020

By:

Gottesman-Katz, Lena;
Wendy Chung;
Hernan, Rebecca;
DeFelice, Amy R.;
Chung, Wendy

Publication type:

Letter

Comparison of endoscopic and clinical characteristics of patients with familial and sporadic Barrett's esophagus.

Published in:

2011

By:

Ash, Samuel;
Vaccaro, Benjamin;
Dabney, Mary;
Chung, Wendy;
Lightdale, Charles;
Abrams, Julian;
Vaccaro, Benjamin J;
Dabney, Mary Kay;
Chung, Wendy K;
Lightdale, Charles J;
Abrams, Julian A

Publication type:

journal article

Proprioceptive synaptic dysfunction is a key feature in mice and humans with spinal muscular atrophy.

Published in:

Brain: A Journal of Neurology, 2025, v. 148, n. 8, p. 2797, doi. 10.1093/brain/awaf074

By:

Simon, Christian M;
Delestrée, Nicolas;
Montes, Jacqueline;
Sowoidnich, Leonie;
Gerstner, Florian;
Carranza, Erick;
Buettner, Jannik M;
Pagiazitis, John G;
Prat-Ortega, Genis;
Ensel, Scott;
Donadio, Serena;
Dreilich, Vanessa;
Carlini, Maria J;
Garcia, Jose L;
Kratimenos, Panagiotis;
Chung, Wendy K;
Sumner, Charlotte J;
Weimer, Louis H;
Pirondini, Elvira;
Capogrosso, Marco

Publication type:

Article

PreMode predicts mode-of-action of missense variants by deep graph representation learning of protein sequence and structural context.

Published in:

Nature Communications, 2025, v. 16, n. 1, p. 1, doi. 10.1038/s41467-025-62318-4

By:

Zhong, Guojie;
Zhao, Yige;
Zhuang, Demi;
Chung, Wendy K.;
Shen, Yufeng

Publication type:

Article

Deep Genetic Connection Between Cancer and Developmental Disorders.

Published in:

Human Mutation, 2016, v. 37, n. 10, p. 1042, doi. 10.1002/humu.23040

By:

Qi, Hongjian;
Dong, Chengliang;
Chung, Wendy K.;
Wang, Kai;
Shen, Yufeng

Publication type:

Article

Pulmonary Arterial Hypertension: A Current Perspective on Established and Emerging Molecular Genetic Defects.

Published in:

Human Mutation, 2015, v. 36, n. 12, p. 1113, doi. 10.1002/humu.22904

By:

Machado, Rajiv D.;
Southgate, Laura;
Eichstaedt, Christina A.;
Aldred, Micheala A.;
Austin, Eric D.;
Best, D. Hunter;
Chung, Wendy K.;
Benjamin, Nicola;
Elliott, C. Gregory;
Eyries, Mélanie;
Fischer, Christine;
Gräf, Stefan;
Hinderhofer, Katrin;
Humbert, Marc;
Keiles, Steven B.;
Loyd, James E.;
Morrell, Nicholas W.;
Newman, John H.;
Soubrier, Florent;
Trembath, Richard C.

Publication type:

Article

Molecular and functional analysis of SLC25A20 mutations causing carnitine-acylcarnitine translocase deficiency.

Published in:

Human Mutation, 2004, v. 24, n. 4, p. 312, doi. 10.1002/humu.20085

By:

Iacobazzi, Vito;
Invernizzi, Federica;
Baratta, Silvia;
Pons, Roser;
Chung, Wendy;
Garavaglia, Barbara;
Dionisi-Vici, Carlo;
Ribes, Antonia;
Parini, Rossella;
Huertas, Maria Dolores;
Roldan, Susana;
Lauria, Graziantonio;
Palmieri, Ferdinando;
Taroni, Franco

Publication type:

Article

Comparing 5-Year and Lifetime Risks of Breast Cancer using the Prospective Family Study Cohort.

Published in:

2021

By:

MacInnis, Robert J;
Knight, Julia A;
Chung, Wendy K;
Milne, Roger L;
Whittemore, Alice S;
Buchsbaum, Richard;
Liao, Yuyan;
Zeinomar, Nur;
Dite, Gillian S;
Southey, Melissa C;
Goldgar, David;
Giles, Graham G;
Kurian, Allison W;
Investigators, kConFab;
Andrulis, Irene L;
John, Esther M;
Daly, Mary B;
Buys, Saundra S;
Phillips, Kelly-Anne;
Hopper, John L

Publication type:

journal article

Considerations When Using Breast Cancer Risk Models for Women with Negative BRCA1/BRCA2 Mutation Results.

Published in:

2020

By:

MacInnis, Robert J;
Liao, Yuyan;
Knight, Julia A;
Milne, Roger L;
Whittemore, Alice S;
Chung, Wendy K;
Leoce, Nicole;
Buchsbaum, Richard;
Zeinomar, Nur;
Dite, Gillian S;
Southey, Melissa C;
Goldgar, David;
Giles, Graham G;
McLachlan, Sue-Anne;
Weideman, Prue C;
Nesci, Stephanie;
Friedlander, Michael L;
Glendon, Gord;
Investigators, kConFab;
Andrulis, Irene L

Publication type:

journal article

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study.

Published in:

2019

By:

Qian, Frank;
Wang, Shengfeng;
Mitchell, Jonathan;
McGuffog, Lesley;
Barrowdale, Daniel;
Leslie, Goska;
Oosterwijk, Jan C;
Chung, Wendy K;
Evans, D Gareth;
Engel, Christoph;
Kast, Karin;
Aalfs, Cora M;
Adank, Muriel A;
Adlard, Julian;
Agnarsson, Bjarni A;
Aittomäki, Kristiina;
Alducci, Elisa;
Andrulis, Irene L;
Arun, Banu K;
Ausems, Margreet G E M

Publication type:

journal article

Risk-Reducing Oophorectomy and Breast Cancer Risk Across the Spectrum of Familial Risk.

Published in:

2019

By:

Terry, Mary Beth;
Daly, Mary B;
Phillips, Kelly Anne;
Ma, Xinran;
Zeinomar, Nur;
Leoce, Nicole;
Dite, Gillian S;
MacInnis, Robert J;
Chung, Wendy K;
Knight, Julia A;
Southey, Melissa C;
Milne, Roger L;
Goldgar, David;
Giles, Graham G;
Weideman, Prue C;
Glendon, Gord;
Buchsbaum, Richard;
Andrulis, Irene L;
John, Esther M;
Buys, Saundra S

Publication type:

journal article

Pathogenic heterozygous TRPM7 variants and hypomagnesemia with developmental delay.

Published in:

Clinical Kidney Journal, 2024, v. 17, n. 8, p. 1, doi. 10.1093/ckj/sfae211

By:

Bosman, Willem;
Butler, Kameryn M;
Chang, Caitlin A;
Ganapathi, Mythily;
Guzman, Edwin;
Latta, Femke;
Chung, Wendy K;
Claverie-Martin, Felix;
Davis, Jessica M;
Hoenderop, Joost G J;
Baaij, Jeroen H F de

Publication type:

Article

Solid phase capturable dideoxynucleotides for multiplex genotyping using mass spectrometry.

Published in:

Nucleic Acids Research, 2002, v. 30, n. 16, p. e85, doi. 10.1093/nar/gnf084

By:

Kim, Sobin;
Edwards, John R.;
Deng, Liyong;
Chung, Wendy;
Ju, Jingyue

Publication type:

Article

REGIONAL INTERDEPENDENCE OF THE HIP AND LUMBO-PELVIC REGION IN DIVISON II COLLEGIATE LEVEL BASEBALL PITCHERS: A PRELIMINARY STUDY.

Published in:

International Journal of Sports Physical Therapy, 2015, v. 10, n. 1, p. 1

By:

Kumagai Shimamura, Kathryn;
Cheatham, Scott;
Chung, Wendy;
Farwel, Daniel;
De la Cruz, Francisco;
Goetz, Jennifer;
Lindblom, Kaleigh;
Powers, Darcy

Publication type:

Article

Regular use of aspirin and other non-steroidal anti-inflammatory drugs and breast cancer risk for women at familial or genetic risk: a cohort study.

Published in:

2019

By:

Kehm, Rebecca D.;
Hopper, John L.;
John, Esther M.;
Phillips, Kelly-Anne;
MacInnis, Robert J.;
Dite, Gillian S.;
Milne, Roger L.;
Liao, Yuyan;
Zeinomar, Nur;
Knight, Julia A.;
Southey, Melissa C.;
Vahdat, Linda;
Kornhauser, Naomi;
Cigler, Tessa;
Chung, Wendy K.;
Giles, Graham G.;
McLachlan, Sue-Anne;
Friedlander, Michael L.;
Weideman, Prue C.;
Glendon, Gord

Publication type:

journal article

Age-specific breast cancer risk by body mass index and familial risk: prospective family study cohort (ProF-SC).

Published in:

2018

By:

Hopper, John L.;
Dite, Gillian S.;
MacInnis, Robert J.;
Liao, Yuyan;
Zeinomar, Nur;
Knight, Julia A.;
Southey, Melissa C.;
Milne, Roger L.;
Chung, Wendy K.;
Giles, Graham G.;
Genkinger, Jeanine M.;
McLachlan, Sue-Anne;
Friedlander, Michael L.;
Antoniou, Antonis C.;
Weideman, Prue C.;
Glendon, Gord;
Nesci, Stephanie;
Andrulis, Irene L.;
Buys, Saundra S.;
Daly, Mary B.

Publication type:

journal article

Comparison of methods to assess onset of breast development in the LEGACY Girls Study: methodological considerations for studies of breast cancer.

Published in:

2018

By:

Houghton, Lauren C.;
Knight, Julia A.;
De Souza, Mary Jane;
Goldberg, Mandy;
White, Melissa L.;
O'Toole, Karen;
Chung, Wendy K.;
Bradbury, Angela R.;
Daly, Mary B.;
Andrulis, Irene L.;
John, Esther M.;
Buys, Saundra S.;
Terry, Mary Beth

Publication type:

journal article

Pubertal development in girls by breast cancer family history: the LEGACY girls cohort.

Published in:

2017

By:

Terry, Mary Beth;
Keegan, Theresa H. M.;
Houghton, Lauren C.;
Goldberg, Mandy;
Andrulis, Irene L.;
Daly, Mary B.;
Buys, Saundra S.;
Ying Wei;
Whittemore, Alice S.;
Protacio, Angeline;
Bradbury, Angela R.;
Chung, Wendy K.;
Knight, Julia A.;
John, Esther M.;
Wei, Ying

Publication type:

journal article

Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing.

Published in:

Public Health Genomics, 2022, v. 25, n. 5/6, p. 185, doi. 10.1159/000526382

By:

Timmins, George Thomas;
Wynn, Julia;
Saami, Akilan Murugesan;
Espinal, Aileen;
Chung, Wendy K.

Publication type:

Article

Understanding Factors Associated with Uptake of BRCA1/2 Genetic Testing among Orthodox Jewish Women in the USA Using a Mixed-Methods Approach.

Published in:

Public Health Genomics, 2018, v. 21, n. 5/6, p. 186, doi. 10.1159/000499852

By:

Trivedi, Meghna S.;
Colbeth, Hilary;
Yi, Haeseung;
Vanegas, Alejandro;
Starck, Rebecca;
Chung, Wendy K.;
Appelbaum, Paul S.;
Kukafka, Rita;
Schechter, Isaac;
Crew, Katherine D.

Publication type:

Article

Identifying Interdisciplinary Research Priorities to Prevent and Treat Pediatric Obesity in New York City.

Published in:

CTS: Clinical & Translational Science, 2010, v. 3, n. 4, p. 172, doi. 10.1111/j.1752-8062.2010.00210.x

By:

Gallagher, Dympna;
Larson, Elaine L.;
Yun-Hsin Claire Wang;
Richards, Boyd;
Chunhua Weng;
Hametz, Patricia;
Begg, Melissa D.;
Chung, Wendy K.;
Boden-Albala, Bernadette;
Akabas, Sharon R.

Publication type:

Article

Maternal Germline Mosaicism in Dominant Dystrophic Epidermolysis Bullosa.

Published in:

Journal of Investigative Dermatology, 2001, v. 117, n. 5, p. 1327, doi. 10.1046/j.0022-202x.2001.01558.x

By:

Cserhalmi-Friedman, Peter B;
Garzon, Maria C;
Guzman, Edwin;
Martinez-Mir, Amalia;
Chung, Wendy K;
Anyane-Yeboa, Kwame;
Christiano, Angela M

Publication type:

Article

Choroidal metastasis in breast cancer.

Published in:

Surgical Practice, 2023, v. 27, n. 3, p. 190, doi. 10.1111/1744-1633.12618

By:

Siu Yuk Wo, Aaron;
Mak Yan Sin, Rita;
Au‐Yeung Chung Ling, Karen;
Yeuk‐hei, Ling;
Lai Yee Tak, Alta;
Wong Wai Chung, Wendy

Publication type:

Article

A pathogenic CtBP1 missense mutation causes altered cofactor binding and transcriptional activity.

Published in:

Neurogenetics, 2019, v. 20, n. 3, p. 129, doi. 10.1007/s10048-019-00578-1

By:

Beck, David B.;
Subramanian, T.;
Vijayalingam, S.;
Ezekiel, Uthayashankar R.;
Donkervoort, Sandra;
Yang, Michele L.;
Dubbs, Holly A.;
Ortiz-Gonzalez, Xilma R.;
Lakhani, Shenela;
Segal, Devorah;
Au, Margaret;
Graham, John M.;
Verma, Sumit;
Waggoner, Darrel;
Shinawi, Marwan;
Bönnemann, Carsten G.;
Chung, Wendy K.;
Chinnadurai, G.

Publication type:

Article

Mutations in HIVEP2 are associated with developmental delay, intellectual disability, and dysmorphic features.

Published in:

Neurogenetics, 2016, v. 17, n. 3, p. 159, doi. 10.1007/s10048-016-0479-z

By:

Steinfeld, Hallie;
Cho, Megan;
Retterer, Kyle;
Person, Rick;
Schaefer, G.;
Danylchuk, Noelle;
Malik, Saleem;
Wechsler, Stephanie;
Wheeler, Patricia;
Gassen, Koen;
Terhal, P.A.;
Verhoeven, Virginie;
Slegtenhorst, Marjon;
Monaghan, Kristin;
Henderson, Lindsay;
Chung, Wendy

Publication type:

Article

A recurrent de novo CTBP1 mutation is associated with developmental delay, hypotonia, ataxia, and tooth enamel defects.

Published in:

Neurogenetics, 2016, v. 17, n. 3, p. 173, doi. 10.1007/s10048-016-0482-4

By:

Beck, David;
Cho, Megan;
Millan, Francisca;
Yates, Carin;
Hannibal, Mark;
O'Connor, Bridget;
Shinawi, Marwan;
Connolly, Anne;
Waggoner, Darrel;
Halbach, Sara;
Angle, Brad;
Sanders, Victoria;
Shen, Yufeng;
Retterer, Kyle;
Begtrup, Amber;
Bai, Renkui;
Chung, Wendy

Publication type:

Article

De novo missense variants in PPP2R5D are associated with intellectual disability, macrocephaly, hypotonia, and autism.

Published in:

Neurogenetics, 2016, v. 17, n. 1, p. 43, doi. 10.1007/s10048-015-0466-9

By:

Shang, Linshan;
Henderson, Lindsay;
Cho, Megan;
Petrey, Donald;
Fong, Chin-To;
Haude, Katrina;
Shur, Natasha;
Lundberg, Julie;
Hauser, Natalie;
Carmichael, Jason;
Innis, Jeffrey;
Schuette, Jane;
Wu, Yvonne;
Asaikar, Shailesh;
Pearson, Margaret;
Folk, Leandra;
Retterer, Kyle;
Monaghan, Kristin;
Chung, Wendy

Publication type:

Article

Mutations in ARID2 are associated with intellectual disabilities.

Published in:

Neurogenetics, 2015, v. 16, n. 4, p. 307, doi. 10.1007/s10048-015-0454-0

By:

Shang, Linshan;
Cho, Megan;
Retterer, Kyle;
Folk, Leandra;
Humberson, Jennifer;
Rohena, Luis;
Sidhu, Alpa;
Saliganan, Sheila;
Iglesias, Alejandro;
Vitazka, Patrik;
Juusola, Jane;
O'Donnell-Luria, Anne;
Shen, Yufeng;
Chung, Wendy

Publication type:

Article

Glucokinase mutations in young children with hyperglycemia.

Published in:

Diabetes/Metabolism Research & Reviews, 2006, v. 22, n. 5, p. 348, doi. 10.1002/dmrr.622

By:

Codner, Ethel;
Deng, Liyong;
Pérez-Bravo, Francisco;
Román, Rossana;
Lanzano, Patricia;
Cassorla, Fernando;
Chung, Wendy K.

Publication type:

Article

An Opportunity to Fill a Gap for Newborn Screening of Neurodevelopmental Disorders.

Published in:

International Journal of Neonatal Screening (IJNS), 2024, v. 10, n. 2, p. 33, doi. 10.3390/ijns10020033

By:

Chung, Wendy K.;
Kanne, Stephen M.;
Hu, Zhanzhi

Publication type:

Article

Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot.

Published in:

International Journal of Neonatal Screening (IJNS), 2022, v. 8, n. 4, p. 50, doi. 10.3390/ijns8040050

By:

Hartnett, Michael J.;
Lloyd-Puryear, Michele A.;
Tavakoli, Norma P.;
Wynn, Julia;
Koval-Burt, Carrie L.;
Gruber, Dorota;
Trotter, Tracy;
Caggana, Michele;
Chung, Wendy K.;
Armstrong, Niki;
Brower, Amy M.

Publication type:

Article

Frequency of GBA Variants in Autopsy-proven Multiple System Atrophy.

Published in:

Movement Disorders Clinical Practice, 2017, v. 4, n. 4, p. 574, doi. 10.1002/mdc3.12481

By:

Sklerov, Miriam;
Kang, Un J.;
Liong, Christopher;
Clark, Lorraine;
Marder, Karen;
Pauciulo, Michael;
Nichols, William C.;
Chung, Wendy K.;
Honig, Lawrence S.;
Cortes, Etty;
Vonsattel, Jean Paul;
Alcalay, Roy N.

Publication type:

Article

Nonspecific phenotype of Noonan syndrome diagnosed by whole exome sequencing.

Published in:

Clinical Case Reports, 2015, v. 3, n. 4, p. 237, doi. 10.1002/ccr3.205

By:

Coromilas, Alexandra;
Wynn, Julia;
Haverfield, Eden;
Chung, Wendy K.

Publication type:

Article

Motor phenotypes associated with genetic neurodevelopmental disorders.

Published in:

Annals of Clinical & Translational Neurology, 2024, v. 11, n. 12, p. 3238, doi. 10.1002/acn3.52231

By:

Santana Almansa, Alexandra;
Snyder, LeeAnne Green;
Chung, Wendy K.;
Bain, Jennifer M.;
Srivastava, Siddharth

Publication type:

Article

Association of genetic and sulcal traits with executive function in congenital heart disease.

Published in:

Annals of Clinical & Translational Neurology, 2024, v. 11, n. 2, p. 278, doi. 10.1002/acn3.51950

By:

Maleyeff, Lara;
Newburger, Jane W.;
Wypij, David;
Thomas, Nina H.;
Anagnoustou, Evdokia;
Brueckner, Martina;
Chung, Wendy K.;
Cleveland, John;
Cunningham, Sean;
Gelb, Bruce D.;
Goldmuntz, Elizabeth;
Hagler, Donald J;
Huang, Hao;
King, Eileen;
McQuillen, Patrick;
Miller, Thomas A.;
Norris‐Brilliant, Ami;
Porter, George A.;
Roberts, Amy E.;
Grant, P. Ellen

Publication type:

Article

Newborn screening for Duchenne muscular dystrophy: A two‐year pilot study.

Published in:

Annals of Clinical & Translational Neurology, 2023, v. 10, n. 8, p. 1383, doi. 10.1002/acn3.51829

By:

Tavakoli, Norma P.;
Gruber, Dorota;
Armstrong, Niki;
Chung, Wendy K.;
Maloney, Breanne;
Park, Sunju;
Wynn, Julia;
Koval‐Burt, Carrie;
Verdade, Lorraine;
Tegay, David H.;
Cohen, Lilian L.;
Shapiro, Natasha;
Kennedy, Annie;
Noritz, Garey;
Ciafaloni, Emma;
Weinberger, Barry;
Ellington, Marty;
Schleien, Charles;
Spinazzola, Regina;
Sood, Sunil

Publication type:

Article

Advances in the Understanding of the Genetic Determinants of Congenital Heart Disease and Their Impact on Clinical Outcomes.

Published in:

2018

By:

Russell, Mark W.;
Chung, Wendy K.;
Kaltman, Jonathan R.;
Miller, Thomas A.

Publication type:

journal article

The Impact of Heterozygous KCNK3 Mutations Associated With Pulmonary Arterial Hypertension on Channel Function and Pharmacological Recovery.

Published in:

Journal of the American Heart Association, 2017, v. 6, n. 9, p. 1, doi. 10.1161/JAHA.117.006465

By:

Bohnen, Michael S.;
Roman-Campos, Danilo;
Terrenoire, Cecile;
Jnani, Jack;
Sampson, Kevin J.;
Chung, Wendy K.;
Kass, Robert S.

Publication type:

Article

Mild fasting hyperglycemia in children: high rate of glucokinase mutations and some risk of developing type 1 diabetes mellitus.

Published in:

Pediatric Diabetes, 2009, v. 10, n. 6, p. 382, doi. 10.1111/j.1399-5448.2009.00499.x

By:

Codner, Ethel;
Rocha, Ana;
Liyong Deng;
Martínez-Aguayo, Alejandro;
Godoy, Claudia;
Mericq, Verónica;
Chung, Wendy K.

Publication type:

Article

Dual Optical Recordings for Action Potentials and Calcium Handling in Induced Pluripotent Stem Cell Models of Cardiac Arrhythmias Using Genetically Encoded Fluorescent Indicators.

Published in:

Stem Cells Translational Medicine, 2015, v. 4, n. 5, p. 468, doi. 10.5966/sctm.2014-0245

By:

LOUJIN SONG;
AWARI, DANIEL W.;
HAN, ELIZABETH Y.;
UCHE-ANYA, EUGENIA;
PARK, SEON-HYE E.;
YABE, YOKO A.;
CHUNG, WENDY K.;
MASAYUKI YAZAWA

Publication type:

Article

Evaluation of the CAV1 gene in clinically, sonographically and histologically proven morphea patients.

Published in:

Experimental Dermatology, 2015, v. 24, n. 9, p. 718, doi. 10.1111/exd.12743

By:

Wortsman, Ximena;
Ma, Lijiang;
Chung, Wendy K.;
Wortsman, Jacobo

Publication type:

Article

Motor pool selectivity of neuromuscular degeneration in type I spinal muscular atrophy is conserved between human and mouse.

Published in:

Human Molecular Genetics, 2025, v. 34, n. 4, p. 347, doi. 10.1093/hmg/ddae190

By:

Lee, Justin C;
Chung, Wendy K;
Pisapia, David J;
Henderson, Christopher E

Publication type:

Article

Melatonin receptor 1A variants as genetic cause of idiopathic osteoporosis.

Published in:

Science Translational Medicine, 2024, v. 16, n. 769, p. 1, doi. 10.1126/scitranslmed.adj0085

By:

Bisikirska, Brygida;
Labella, Rossella;
Cuesta-Dominguez, Alvaro;
Luo, Na;
De Angelis, Jessica;
Mosialou, Ioanna;
Lin, Chyuan-Sheng;
Beck, David;
Lata, Sneh;
Shyu, Peter Timothy;
McMahon, Donald J.;
Guo, Edward;
Hagen, Jacob;
Chung, Wendy K.;
Shane, Elizabeth;
Cohen, Adi;
Kousteni, Stavroula

Publication type:

Article

PH Roundtable: Genetics and Pulmonary Hypertension.

Published in:

Advances in Pulmonary Hypertension, 2021, v. 20, n. 5, p. 168, doi. 10.21693/1933-088X-20.5.168

By:

Elliott, Greg;
Krishnan, Usha S.;
Chung, Wendy K.;
Yu, Paul;
Austin, Eric D

Publication type:

Article

Genomics of Pulmonary Hypertension.

Published in:

Advances in Pulmonary Hypertension, 2021, v. 20, n. 5, p. 142, doi. 10.21693/1933-088X-20.5.142

By:

Welch, Carrie Lynn;
Chung, Wendy K.

Publication type:

Article

Becoming Agents of Change: Contextual Influences on Medical Educator Professionalization and Practice in a LMIC Context.

Published in:

Teaching & Learning in Medicine, 2023, v. 35, n. 3, p. 323, doi. 10.1080/10401334.2022.2056743

By:

Hu, Wendy Chung-Ya;
Nguyen, Van Anh Thi;
Nguyen, Nga Thanh;
Stalmeijer, Renée E

Publication type:

Article

The Congenital Heart Disease Genetic Network Study: Cohort description.

Published in:

PLoS ONE, 2018, v. 13, n. 1, p. 1, doi. 10.1371/journal.pone.0191319

By:

Hoang, Thanh T.;
Goldmuntz, Elizabeth;
Roberts, Amy E.;
Chung, Wendy K.;
Kline, Jennie K.;
Deanfield, John E.;
Giardini, Alessandro;
Aleman, Adolfo;
Gelb, Bruce D.;
Mac Neal, Meghan;
Jr.Porter, George A.;
Kim, Richard;
Brueckner, Martina;
Lifton, Richard P.;
Edman, Sharon;
Woyciechowski, Stacy;
Mitchell, Laura E.;
Agopian, A. J.

Publication type:

Article

Reimbursement for Genetic Variant Reinterpretation: Five Questions Payers Should Ask.

Published in:

American Journal of Managed Care, 2021, v. 27, n. 10, p. e336, doi. 10.37765/ajmc.2021.88763

By:

Veenstra, David L.;
Rowe, John W.;
Pagán, José A.;
Brown, H. Shelton;
Schneider, John E.;
Gupta, Avni;
Berger, Sara M.;
Chung, Wendy K.;
Appelbaum, Paul S.

Publication type:

Article

Human iPSC-Derived Neuronal Cells From CTBP1 -Mutated Patients Reveal Altered Expression of Neurodevelopmental Gene Networks.

Published in:

Frontiers in Neuroscience, 2020, p. N.PAG, doi. 10.3389/fnins.2020.562292

By:

Vijayalingam, S.;
Ezekiel, Uthayashanker R.;
Xu, Fenglian;
Subramanian, T.;
Geerling, Elizabeth;
Hoelscher, Brittany;
San, KayKay;
Ganapathy, Aravinda;
Pemberton, Kyle;
Tycksen, Eric;
Pinto, Amelia K.;
Brien, James D.;
Beck, David B.;
Chung, Wendy K.;
Gurnett, Christina A.;
Chinnadurai, G.

Publication type:

Article