Julia Wynn

4.5k total citations
61 papers, 1.7k citations indexed

About

Julia Wynn is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Surgery. According to data from OpenAlex, Julia Wynn has authored 61 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 34 papers in Genetics, 19 papers in Pediatrics, Perinatology and Child Health and 15 papers in Surgery. Recurrent topics in Julia Wynn's work include BRCA gene mutations in cancer (24 papers), Genomics and Rare Diseases (22 papers) and Congenital Diaphragmatic Hernia Studies (14 papers). Julia Wynn is often cited by papers focused on BRCA gene mutations in cancer (24 papers), Genomics and Rare Diseases (22 papers) and Congenital Diaphragmatic Hernia Studies (14 papers). Julia Wynn collaborates with scholars based in United States, Canada and Israel. Julia Wynn's co-authors include Wendy K. Chung, Lan Yu, Yufeng Shen, Heidi Lumish, Paul S. Appelbaum, Guðrún Aspelund, Jacqueline T. Hecht, Michael J. Gambello, D. Kim Waller and Wendy K. Chung and has published in prestigious journals such as SHILAP Revista de lepidopterología, Annals of Internal Medicine and Circulation Research.

In The Last Decade

Julia Wynn

60 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Julia Wynn United States 25 805 555 456 449 295 61 1.7k
R. Coutant France 32 812 1.0× 681 1.2× 116 0.3× 677 1.5× 491 1.7× 119 2.3k
Andrea Corrias Italy 39 1.1k 1.4× 722 1.3× 125 0.3× 591 1.3× 593 2.0× 98 3.3k
Chirag Patel Australia 23 516 0.6× 228 0.4× 243 0.5× 644 1.4× 136 0.5× 99 1.4k
Susumu Yokoya Japan 23 667 0.8× 221 0.4× 87 0.2× 683 1.5× 399 1.4× 130 2.1k
Nathalie Alos Canada 21 283 0.4× 266 0.5× 261 0.6× 240 0.5× 239 0.8× 67 1.4k
Evelien Gevers United Kingdom 27 449 0.6× 239 0.4× 396 0.9× 700 1.6× 86 0.3× 69 2.2k
Alessandra Carnevale Mexico 20 522 0.6× 184 0.3× 108 0.2× 377 0.8× 204 0.7× 98 1.2k
B Boscherini Italy 23 460 0.6× 266 0.5× 188 0.4× 659 1.5× 193 0.7× 87 1.6k
Roland Schweizer Germany 27 681 0.8× 230 0.4× 69 0.2× 620 1.4× 411 1.4× 88 1.8k
Kirk Aleck United States 18 566 0.7× 323 0.6× 135 0.3× 775 1.7× 815 2.8× 31 2.0k

Countries citing papers authored by Julia Wynn

Since Specialization
Citations

This map shows the geographic impact of Julia Wynn's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Julia Wynn with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Julia Wynn more than expected).

Fields of papers citing papers by Julia Wynn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Julia Wynn. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Julia Wynn. The network helps show where Julia Wynn may publish in the future.

Co-authorship network of co-authors of Julia Wynn

This figure shows the co-authorship network connecting the top 25 collaborators of Julia Wynn. A scholar is included among the top collaborators of Julia Wynn based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Julia Wynn. Julia Wynn is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Wynn, Julia, et al.. (2025). Clinical Performance of Cell-Free DNA for Fetal RhD Detection in RhD-Negative Pregnant Individuals in the United States. Obstetrics and Gynecology. 145(4). 402–408. 2 indexed citations
2.
Wynn, Julia, Benjamin Huber, L. Casey White, et al.. (2024). Impact of a Genetic Diagnosis for a Child’s Autism on Parental Perceptions. Journal of Autism and Developmental Disorders. 55(5). 1809–1823. 6 indexed citations
3.
Wynn, Julia, et al.. (2023). Performance of single‐gene noninvasive prenatal testing for autosomal recessive conditions in a general population setting. Prenatal Diagnosis. 43(10). 1344–1354. 6 indexed citations
4.
Bakken, Suzanne, John Lynch, Wendy K. Chung, et al.. (2023). Participant-guided development of bilingual genomic educational infographics for Electronic Medical Records and Genomics Phase IV study. Journal of the American Medical Informatics Association. 31(2). 306–316. 2 indexed citations
5.
Moses, Rachel Gore, et al.. (2023). Performance of the shared decision‐making process scale for use in evaluation of hereditary cancer genetic testing decisions. Journal of Genetic Counseling. 32(5). 957–964. 2 indexed citations
6.
Hartnett, M. J., Michele A. Lloyd-Puryear, Norma P. Tavakoli, et al.. (2022). Newborn Screening for Duchenne Muscular Dystrophy: First Year Results of a Population-Based Pilot. International Journal of Neonatal Screening. 8(4). 50–50. 12 indexed citations
7.
Appelbaum, Paul S., Karolynn Siegel, Julia Wynn, et al.. (2022). Challenges of variant reinterpretation: Opinions of stakeholders and need for guidelines. Genetics in Medicine. 24(9). 1878–1887. 19 indexed citations
8.
Wynn, Julia, et al.. (2022). Diverse Parental Perspectives of the Social and Educational Needs for Expanding Newborn Screening through Genomic Sequencing. Public Health Genomics. 25(5-6). 185–192. 6 indexed citations
9.
Hoskovec, Jennifer, et al.. (2022). Maternal carrier screening with single-gene NIPS provides accurate fetal risk assessments for recessive conditions. Genetics in Medicine. 25(2). 100334–100334. 21 indexed citations
10.
Hoell, Christin, Julia Wynn, Luke V. Rasmussen, et al.. (2020). Participant choices for return of genomic results in the eMERGE Network. Genetics in Medicine. 22(11). 1821–1829. 24 indexed citations
11.
Farrell, Andrew, Julia Wynn, Barry Moore, et al.. (2020). Deep whole-genome sequencing of multiple proband tissues and parental blood reveals the complex genetic etiology of congenital diaphragmatic hernias. SHILAP Revista de lepidopterología. 1(1). 100008–100008. 5 indexed citations
12.
Chiuzan, Codruța, Gabriel A. Lazarin, Chunhua Weng, et al.. (2020). Choices, attitudes, and experiences of genetic screening in Latino/a and Ashkenazi Jewish individuals. Journal of Community Genetics. 11(4). 391–403. 5 indexed citations
13.
Yu, Lan, Rebecca Hernan, Julia Wynn, & Wendy K. Chung. (2019). The influence of genetics in congenital diaphragmatic hernia. Seminars in Perinatology. 44(1). 151169–151169. 38 indexed citations
14.
Robinson, Jill O., Julia Wynn, Barbara B. Biesecker, et al.. (2019). 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. 21(12). 2781–2790. 51 indexed citations
15.
Ma, Lijiang, Julia Wynn, Usha Krishnan, et al.. (2017). Mutations in BMPR2 are not present in patients with pulmonary hypertension associated with congenital diaphragmatic hernia. Journal of Pediatric Surgery. 52(11). 1747–1750. 3 indexed citations
16.
Lumish, Heidi, Julia Wynn, Orrin Devinsky, & Wendy K. Chung. (2015). Brief Report: SETD2 Mutation in a Child with Autism, Intellectual Disabilities and Epilepsy. Journal of Autism and Developmental Disorders. 45(11). 3764–3770. 49 indexed citations
17.
Azarow, Kenneth S., Julia Wynn, Wendy K. Chung, et al.. (2015). The association between congenital diaphragmatic hernia and undescended testes. Journal of Pediatric Surgery. 50(5). 744–745. 6 indexed citations
18.
Wynn, Julia, Lan Yu, & Wendy K. Chung. (2014). Genetic causes of congenital diaphragmatic hernia. Seminars in Fetal and Neonatal Medicine. 19(6). 324–330. 71 indexed citations
19.
Yu, Lan, James T. Bennett, Julia Wynn, et al.. (2014). Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia. Journal of Medical Genetics. 51(3). 197–202. 48 indexed citations
20.
Wynn, Julia, Guðrún Aspelund, Annette Zygmunt, et al.. (2013). Developmental outcomes of children with congenital diaphragmatic hernia: A multicenter prospective study. Journal of Pediatric Surgery. 48(10). 1995–2004. 62 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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