Skip to Main Content

Author Details

Julia Wynn
Vagelos College of Physicians and Surgeons, Columbia University
2007
84
27
PMIDPaper TitleJournal TitlePublished Year
37860921Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study.J Am Med Inform Assoc2024
36385723Measuring quality and value in genetic counseling: The current landscape and future directions.J Genet Couns2023
37751738PLS3 missense variants affecting the actin-binding domains cause X-linked congenital diaphragmatic hernia and body-wall defects.Am J Hum Genet2023
37522894Response to Benn et al.Genet Med2023
37611220Uptake of Genetic Research Results and Patient-Reported Outcomes With Return of Results Incorporating Web-Based Predisclosure Education.J Clin Oncol2023
37350320Newborn screening for Duchenne muscular dystrophy: A two-year pilot study.Ann Clin Transl Neurol2023
37246632Education and electronic medical records and genomics network, challenges, and lessons learned from a large-scale clinical trial using polygenic risk scores.Genet Med2023
36803080Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study.Circ Genom Precis Med2023
36454238Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions.Genet Med2023
36416152Development of Competency-based Online Genomic Medicine Training (COGENT).Per Med2023
34002349Questioning the validity of clinically available breast cancer polygenic risk scores: comparison of two labs reveals discrepancies.Fam Cancer2022
35476893Information is power: The experiences, attitudes and needs of individuals who chose to have prenatal genomic sequencing for fetal anomalies.Prenat Diagn2022
35840571SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.Nat Commun2022
35767006Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines.Genet Med2022
35466194Improving Recruitment for a Newborn Screening Pilot Study with Adaptations in Response to the COVID-19 Pandemic.Int J Neonatal Screen2022
35777474Mother and Daughter Perspectives on Genetic Counseling and Testing of Adolescents for Hereditary Breast Cancer Risk.J Pediatr2022
36108601Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing.Public Health Genomics2022
36278620Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot.Int J Neonatal Screen2022
35216901The reckoning: The return of genomic results to 1444 participants across the eMERGE3 Network.Genet Med2022
34665896Do research participants share genomic screening results with family members?J Genet Couns2022
33368851GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing.J Genet Couns2021
36046768Returning negative results from large-scale genomic screening: Experiences from the eMERGE III network.Am J Med Genet A2021
33734519COVID contingencies: Early epicenter experiences of different genetics clinics at a New York City institution inform emergency adaptation strategies.J Genet Couns2021
33709066An electronic health record (EHR) log analysis shows limited clinician engagement with unsolicited genetic test results.JAMIA Open2021
34377931Penetrance of Breast Cancer Susceptibility Genes From the eMERGE III Network.JNCI Cancer Spectr2021
34547244Rare and de novo variants in 827 congenital diaphragmatic hernia probands implicate LONP1 as candidate risk gene.Am J Hum Genet2021
34255550Impact of Genetic Testing for Cardiomyopathy on Emotional Well-Being and Family Dynamics: A Study of Parents and Adolescents.Circ Genom Precis Med2021
31443905The influence of genetics in congenital diaphragmatic hernia.Semin Perinatol2020
31677822Comparative outcomes of right versus left congenital diaphragmatic hernia: A multicenter analysis.J Pediatr Surg2020
33263113Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias.HGG Adv2020
32719394Likely damaging de novo variants in congenital diaphragmatic hernia patients are associated with worse clinical outcomes.Genet Med2020
32969094Advancing the genetic counseling profession through research: Identification of priorities by the National Society of Genetic Counselors research task force.J Genet Couns2020
32669677Participant choices for return of genomic results in the eMERGE Network.Genet Med2020
32555418Ethical conflicts in translational genetic research: lessons learned from the eMERGE-III experience.Genet Med2020
32308889User engagement with web-based genomics education videos and implications for designing scalable patient education materials.AMIA Annu Symp Proc2020
32413979Understanding the Return of Genomic Sequencing Results Process: Content Review of Participant Summary Letters in the eMERGE Research Network.J Pers Med2020
32382939Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals.J Community Genet2020
32298033A qualitative study of Latinx parents' experiences of clinical exome sequencing.J Genet Couns2020
32349224Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network.J Pers Med2020
31521424Impact of patient education videos on genetic counseling outcomes after exome sequencing.Patient Educ Couns2020
30930462Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study.Genet Med2019
32016023Developing effective and efficient genomic educational tools for our diverse population.Ann Transl Med2019
31040387Correction: Evaluation of the cost and effectiveness of diverse recruitment methods for a genetic screening study.Genet Med2019
27550844De novo and inherited mutations in the X-linked gene CLCN4 are associated with syndromic intellectual disability and behavior and seizure disorders in males and females.Mol Psychiatry2018
30035818Parental perceptions of prenatal whole exome sequencing (PPPWES) study.Prenat Diagn2018
30532227De novo variants in congenital diaphragmatic hernia identify MYRF as a new syndrome and reveal genetic overlaps with other developmental disorders.PLoS Genet2018
29497922Why Patients Decline Genomic Sequencing Studies: Experiences from the CSER Consortium.J Genet Couns2018
29739461Clinical providers' experiences with returning results from genomic sequencing: an interview study.BMC Med Genomics2018
29301385Ethical Considerations Related to Return of Results from Genomic Medicine Projects: The eMERGE Network (Phase III) Experience.J Pers Med2018
29168042Impact of Receiving Secondary Results from Genomic Research: A 12-Month Longitudinal Study.J Genet Couns2018
  • 1 - 50 of 84

Recommended Authors

Whitley V Kelley
HudsonAlpha Institute for Biotechnology
Career Start Year 2017
Number of shared co-authors 28
Hadley Stevens Smith
Center for Medical Ethics and Health Policy, Baylor College of Medicine
Career Start Year 2017
Number of shared co-authors 24
Jennefer N Kohler
Stanford Center for Undiagnosed Diseases
Career Start Year 2017
Number of shared co-authors 11
Morgan Similuk
National Institute of Allergy and Infectious Diseases, National Institutes of Health
Career Start Year 2016
Number of shared co-authors 2
Stacey Pereira
Baylor College of Medicine.
Career Start Year 2013
Number of shared co-authors 18
Leila Jamal
Center for Cancer Research, National Cancer Institute
Career Start Year 2012
Number of shared co-authors 12
Megan E Grove
Stanford Medicine Clinical Genomics Program
Career Start Year 2011
Number of shared co-authors 2
Seema M Jamal
Division of Clinical and Metabolic Genetics (R.K., The Hospital for Sick Children
Career Start Year 2010
Number of shared co-authors 37
Kandamurugu Manickam
Nationwide Children's Hospital, The Ohio State University College of Medicine
Career Start Year 2010
Number of shared co-authors 19
Lauren Chad
Hospital for Sick Children, Canada University of Toronto
Career Start Year 2008
Number of shared co-authors 4
Amanda L Bergner
Vagelos College of Physicians and Surgeons, Columbia University
Career Start Year 2006
Number of shared co-authors 4
Aaron J Goldenberg
Case Western Reserve University
Career Start Year 2005
Number of shared co-authors 18
Danya F Vears
University of Melbourne
Career Start Year 2004
Number of shared co-authors 6
Flavia M Facio
Invitae Corporation
Career Start Year 2004
Number of shared co-authors 3
Caroline F Wright
University of Exeter, Royal Devon and Exeter Hospital
Career Start Year 2003
Number of shared co-authors 7
Michael J Szego
University of Toronto.
Career Start Year 2003
Number of shared co-authors 2
Noura S Abul-Husn
Institute for Genomic Health, Icahn School of Medicine at Mount Sinai
Career Start Year 2002
Number of shared co-authors 66
Zornitza Stark
Murdoch Children's Research Institute
Career Start Year 2001
Number of shared co-authors 19
Peter J Hulick
Neaman Center for Personalized Medicine, NorthShore University HealthSystem
Career Start Year 2000
Number of shared co-authors 14
Michael F Murray
Yale School of Medicine
Career Start Year 1999
Number of shared co-authors 31
Cinnamon Bloss
University of California
Career Start Year 1998
Number of shared co-authors 9
Kelly E Ormond
Stanford University School of Medicine
Career Start Year 1996
Number of shared co-authors 22
Christine Patch
Queen Mary University of London, United Kingdom Society and Ethics Research
Career Start Year 1994
Number of shared co-authors 1
William Gregory Feero
Dartmouth Geisel School of Medicine
Career Start Year 1993
Number of shared co-authors 9
Anne-Marie Laberge
UNIVERSITY OF MONTREAL
Career Start Year 1991
Number of shared co-authors 9
William A Faucett
Genomic Medicine Institute
Career Start Year 1991
Number of shared co-authors 33
Clara Gaff
Murdoch Children's Research Institute
Career Start Year 1990
Number of shared co-authors 5
Wendy R Uhlmann
University of Michigan School of Medicine ann arbor
Career Start Year 1989
Number of shared co-authors 16
Barbara B Biesecker
and Translational Research Center
Career Start Year 1987
Number of shared co-authors 43
Joann Bodurtha
Johns Hopkins McKusick-Nathans Department of Genetic Medicine
Career Start Year 1974
Number of shared co-authors 10

Collaborators

Wendy K Chung
Boston Children's Hospital, Harvard Medical School
Co-authored papers 64
Paul S Appelbaum
Center for Law, Columbia University Irving Medical Center
Co-authored papers 17
Yufeng Shen
Columbia University
Co-authored papers 11
Ingrid A Holm
Harvard Medical School
Co-authored papers 11
Hila Milo Rasouly
Center for Precision Medicine and Genomics, Columbia University Irving Medical Center
Co-authored papers 10
Richard R Sharp
Biomedical Ethics, Mayo Clinic and Foundation
Co-authored papers 9
Gail P Jarvik
University of Washington Medical Center
Co-authored papers 9
Maureen E Smith
Center for Genetic Medicine, Feinberg School of Medicine, Northwestern University
Co-authored papers 9
Kathleen A Leppig
Kaiser Permanente Washington
Co-authored papers 9
Maddalena Marasa
Columbia University College of Physicians and Surgeons
Co-authored papers 8
E Clayton
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 7
Margaret Harr
Center for Applied Genomics, Children's Hospital of Philadelphia
Co-authored papers 7
Chunhua Weng
Columbia University Irving Medical Center
Co-authored papers 7
Melanie F Myers
Cincinnati Children's Hospital Medical Center
Co-authored papers 7
Janet L Williams
Genomic Medicine Institute
Co-authored papers 7
Iftikhar J Kullo
Mayo Clinic
Co-authored papers 7
Cynthia A Prows
Cincinnati Children's Hospital Medical Center
Co-authored papers 7
Christin Hoell
Northwestern University, Center for Genetic Medicine
Co-authored papers 7
Megan T Cho
Co-authored papers 6
Sharon Aufox
Northwestern University, Center for Genetic Medicine
Co-authored papers 6
Georgia L Wiesner
Vanderbilt Genetics Institute, Vanderbilt University Medical Center
Co-authored papers 6
Ali G Gharavi
Columbia University College of Physicians and Surgeons
Co-authored papers 6
Barbara A Bernhardt
Thomas Jefferson University
Co-authored papers 5
Laura M Amendola
Illumina Inc.
Co-authored papers 5
Sarah Scollon
Texas Children's Cancer Center, Texas Children's Hospital
Co-authored papers 5
Carrie L Blout
Department of Medicine Brigham and Women's Hospital and Harvard Medical School
Co-authored papers 5
Robert C Green
Brigham and Women's Hospital, Broad Institute Ariadne Labs and Harvard Medical School
Co-authored papers 5
Sawona Biswas
University of California San Francisco
Co-authored papers 5
Eric B Larson
University of Washington
Co-authored papers 4
Josh F Peterson
Vanderbilt University Medical Center
Co-authored papers 4
Release 1.2