Julia Wynn (J Wynn)

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 19

Top Topics

Intellectual Disability

Hepatitis C Virus

Congenital Heart Disease

Top Venues

Prenatal diagnosis

Circulation. Genomic and precision medicine

Journal of genetic counseling

Journal of community genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Julia Wynn, Shannon Rego O'Rourke, Jennifer Hoskovec, Sriram C Perni
Response to the correspondence on "Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting". Prenatal diagnosis 44 (4) (2024)
Julia Wynn, Jennifer Hoskovec
Correspondence on "Current Controversy in Prenatal Diagnosis: The Use of cfDNA to Screen for Monogenic Conditions in Low Risk Populations Is Ready for Clinical Use". Prenatal diagnosis (2024)
Julia Wynn, Shannon Rego O'Rourke, Jennifer Hoskovec, Sriram C Perni
Response to the correspondence on "Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting". Prenatal diagnosis 44 (4) (2024)
Julia Wynn, Anna Karlsen, Benjamin Huber, Alina Levine, Amanie Salem, L Casey White, Marti Luby, Ekaterina Bezborodko, Sabrina Xiao, Wendy K Chung, Robert L Klitzman, Paul S Appelbaum
Impact of a Genetic Diagnosis for a Child's Autism on Parental Perceptions. Journal of autism and developmental disorders (2024)
Julia Wynn, Shannon Rego O'Rourke, Jennifer Hoskovec, Sriram C Perni
Response to the correspondence on "Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting". Prenatal diagnosis 44 (4) (2024)
Julia Wynn, Shannon Rego O'Rourke, Jennifer Hoskovec, Sriram C Perni
Response to the correspondence on "Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting". Prenatal diagnosis (2024)
Julia Wynn, Jennifer Hoskovec, Rebecca D Carter, Meredith J Ross, Sriram C Perni
Performance of single-gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting. Prenatal diagnosis (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Emily L Griffin, Shannon N Nees, Sarah U Morton, Julia Wynn, Nihir Patel, Vaidehi Jobanputra, Scott Robinson, Stephanie M Kochav, Alice Tao, Carli Andrews, Nancy Cross, Judith Geva, Kristen Lanzilotta, Alyssa L Ritter, Eileen Taillie, Alexandra Thompson, Chris Meyer, Rachel Akers, Eileen C King, James F Cnota, Richard W Kim, George A Porter, Martina Brueckner, Christine E Seidman, Yufeng Shen, Bruce D Gelb, Elizabeth Goldmuntz, Jane W Newburger, Amy E Roberts, Wendy K Chung
Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study. Circulation. Genomic and precision medicine (2023)
Susanne B Haga, Wendy K Chung, Luis A Cubano, Timothy B Curry, Philip E Empey, Geoffrey S Ginsburg, Kara Mangold, Christina Y Miyake, Siddharth K Prakash, Laura B Ramsey, Robb Rowley, Carolyn R Rohrer Vitek, Todd C Skaar, Julia Wynn, Teri A Manolio
Development of Competency-based Online Genomic Medicine Training (COGENT). Personalized medicine (2022)
Julia Wynn, Elana Levinson, Carrie Koval, Michelle E Ernst, Wendy K Chung
Questioning the validity of clinically available breast cancer polygenic risk scores: comparison of two labs reveals discrepancies. Familial cancer (2021)
Anne E Reed-Weston, Aileen Espinal, Bianca Hasar, Codruta Chiuzan, Gabriel Lazarin, Chunhua Weng, Paul S Appelbaum, Wendy K Chung, Julia Wynn
Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals. Journal of community genetics 11 (4) (2020)
Daniel Luksic, Radha Sukhu, Carrie Koval, Megan T Cho, Aileen Espinal, Katiana Rufino, Tania Vasquez Loarte, Wendy K Chung, Julia Wynn
A qualitative study of Latinx parents' experiences of clinical exome sequencing. Journal of genetic counseling 29 (4) (2020)
Hila Milo Rasouly, Nicole Cuneo, Maddalena Marasà, Natalia DeMaria, Debanjana Chatterjee, Jacqueline J Thompson, David A Fasel, Julia Wynn, Wendy K Chung, Paul S Appelbaum, Chunhua Weng, Suzanne R Bakken, Ali G Gharavi
GeneLiFT: A novel test to facilitate rapid screening of genetic literacy in a diverse population undergoing genetic testing. Journal of genetic counseling 30 (3) (2020)
Jill O Robinson, Julia Wynn, Barbara Biesecker, Leslie G Biesecker, Barbara Bernhardt, Kyle Bertram Brothers, Wendy K Chung, Kurt D Christensen, Robert C Green, Amy L McGuire, M Ragan Hart, Ida Griesemer, Donald L Patrick, Christine Rini, David Veenstra, Angel M Cronin, Stacy W Gray
Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies. Genetics in medicine : official journal of the American College of Medical Genetics 21 (12) (2019)
Julia Wynn, R Ottman, J Duong, A L Wilson, P Ahimaz, J Martinez, R Rabin, E Rosen, R Webster, C Au, M T Cho, C Egan, E Guzman, M Primiano, J E Shaw, R Sisson, R L Klitzman, P S Appelbaum, U Lichter-Konecki, K Anyane-Yeboa, A Iglesias, W K Chung
Diagnostic exome sequencing in children: A survey of parental understanding, experience and psychological impact. Clinical genetics 93 (5) (2018)
Julia Wynn, David T Holland, Jimmy Duong, Priyanka Ahimaz, Wendy K Chung
Examining the Psychosocial Impact of Genetic Testing for Cardiomyopathies. Journal of genetic counseling 27 (4) (2017)
Julia Wynn
Genomic Testing: a Genetic Counselor's Personal Reflection on Three Years of Consenting and Testing. Journal of genetic counseling 25 (4) (2015)