Joseph W. Ray

490 total citations
16 papers, 116 citations indexed

About

Joseph W. Ray is a scholar working on Surgery, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Joseph W. Ray has authored 16 papers receiving a total of 116 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Surgery, 7 papers in Genetics and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Joseph W. Ray's work include Congenital Anomalies and Fetal Surgery (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Joseph W. Ray is often cited by papers focused on Congenital Anomalies and Fetal Surgery (4 papers), Prenatal Screening and Diagnostics (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Joseph W. Ray collaborates with scholars based in United States, Germany and Poland. Joseph W. Ray's co-authors include Sunil K. Jain, Laura S. Farach, Mark A. Canfield, A. J. Agopian, Christian P. Schaaf, Jianli Dong, Han Chen, Renata H. Benjamin, Peter H. Langlois and Michael D. Swartz and has published in prestigious journals such as Pediatric Research, Molecular Genetics and Metabolism and The Cleft Palate-Craniofacial Journal.

In The Last Decade

Joseph W. Ray

16 papers receiving 115 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joseph W. Ray United States 8 56 52 35 22 20 16 116
Laura Konczal United States 6 119 2.1× 77 1.5× 19 0.5× 13 0.6× 6 0.3× 13 185
Katharina Löhner Netherlands 4 87 1.6× 59 1.1× 16 0.5× 28 1.3× 11 0.6× 5 137
Willa Thorson United States 5 50 0.9× 54 1.0× 39 1.1× 26 1.2× 5 0.3× 12 132
Shahida Moosa South Africa 10 91 1.6× 96 1.8× 16 0.5× 7 0.3× 8 0.4× 29 169
Ignacio Arroyo Spain 6 57 1.0× 74 1.4× 36 1.0× 57 2.6× 9 0.5× 17 183
Odile Boute‐Bénéjean France 7 64 1.1× 75 1.4× 35 1.0× 22 1.0× 7 0.3× 13 147
Sara Caylor United States 4 109 1.9× 44 0.8× 9 0.3× 34 1.5× 18 0.9× 4 139
Rob Hastings United Kingdom 5 26 0.5× 94 1.8× 16 0.5× 9 0.4× 9 0.5× 9 136
Nakamichi Saito Japan 6 47 0.8× 71 1.4× 47 1.3× 30 1.4× 31 1.6× 12 147
Edith Said Malta 8 44 0.8× 67 1.3× 23 0.7× 11 0.5× 12 0.6× 13 122

Countries citing papers authored by Joseph W. Ray

Since Specialization
Citations

This map shows the geographic impact of Joseph W. Ray'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 Joseph W. Ray with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Joseph W. Ray more than expected).

Fields of papers citing papers by Joseph W. Ray

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Joseph W. Ray. 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 Joseph W. Ray. The network helps show where Joseph W. Ray may publish in the future.

Co-authorship network of co-authors of Joseph W. Ray

This figure shows the co-authorship network connecting the top 25 collaborators of Joseph W. Ray. A scholar is included among the top collaborators of Joseph W. Ray 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 Joseph W. Ray. Joseph W. Ray is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

16 of 16 papers shown
1.
Chang, Richard, Monica Boyer, Laura Davis‐Keppen, et al.. (2024). Outcomes in 14 live births resulting from Pegvaliase-treated pregnancies in PKU-affected females. Molecular Genetics and Metabolism. 141(3). 108152–108152. 7 indexed citations
2.
DeBarber, Andrea E., Ernst J. Schaefer, Jenny Do, et al.. (2024). Genetically and clinically confirmed atypical cerebrotendinous xanthomatosis with normal cholestanol and marked elevations of bile acid precursors and bile alcohols. Journal of clinical lipidology. 18(3). e465–e476. 1 indexed citations
3.
Ray, Joseph W., et al.. (2023). Novel mosaic TRAF7 likely pathogenic variant in an African American family. American Journal of Medical Genetics Part A. 191(7). 1990–1993. 1 indexed citations
4.
Schraw, Jeremy M., Renata H. Benjamin, Mark A. Canfield, et al.. (2022). Patterns of co‐occurring birth defects in children with anotia and microtia. American Journal of Medical Genetics Part A. 191(3). 805–812. 1 indexed citations
5.
Adams, Darius J., Hans C. Andersson, Kristin Lindstrom, et al.. (2021). Use of pegvaliase in the management of phenylketonuria: Case series of early experience in US clinics. Molecular Genetics and Metabolism Reports. 28. 100790–100790. 14 indexed citations
6.
Benjamin, Renata H., Angela E. Scheuerle, Daryl A. Scott, et al.. (2021). Birth defect co-occurrence patterns in the Texas Birth Defects Registry. Pediatric Research. 91(5). 1278–1285. 8 indexed citations
7.
Louie, Raymond J., Melanie A. Jones, Alka Chaubey, et al.. (2021). Copy neutral absence of heterozygosity on chromosome 15 distal long arm: A surrogate marker for Prader–Willi/Angelman syndromes?. Molecular Cytogenetics. 14(1). 37–37. 2 indexed citations
8.
Benjamin, Renata H., Laura E. Mitchell, Peter H. Langlois, et al.. (2021). Patterns of congenital anomalies among individuals with trisomy 13 in Texas. American Journal of Medical Genetics Part A. 185(6). 1787–1793. 3 indexed citations
9.
Benjamin, Renata H., Laura E. Mitchell, Peter H. Langlois, et al.. (2021). Birth Defect Co-Occurrence Patterns Among Infants With Cleft Lip and/or Palate. The Cleft Palate-Craniofacial Journal. 59(4). 417–426. 12 indexed citations
10.
Benjamin, Renata H., Scott McLean, Hope Northrup, et al.. (2020). Patterns of co-occurring birth defects among infants with hypospadias. Journal of Pediatric Urology. 17(1). 64.e1–64.e8. 2 indexed citations
11.
Schraw, Jeremy M., Renata H. Benjamin, Daryl A. Scott, et al.. (2020). A Comprehensive Assessment of Co-occurring Birth Defects among Infants with Non-Syndromic Anophthalmia or Microphthalmia. Ophthalmic Epidemiology. 28(5). 428–435. 3 indexed citations
12.
Benjamin, Renata H., Angela E. Scheuerle, Christian P. Schaaf, et al.. (2020). Birth defects that co‐occur with non‐syndromic gastroschisis and omphalocele. American Journal of Medical Genetics Part A. 182(11). 2581–2593. 7 indexed citations
13.
Wu, Haotian, Fangling Xu, Joseph W. Ray, et al.. (2020). Phenotypes Associated with 16p11.2 Copy Number Gains and Losses at a Single Institution. Laboratory Medicine. 51(6). 642–648. 3 indexed citations
14.
Xu, Fangling, et al.. (2019). Genotypic and phenotypic variability of 22q11.2 microduplications: An institutional experience. American Journal of Medical Genetics Part A. 179(11). 2178–2189. 26 indexed citations
15.
Benjamin, Renata H., Han Chen, Laura E. Mitchell, et al.. (2019). Co‐occurring defect analysis: A platform for analyzing birth defect co‐occurrence in registries. Birth Defects Research. 111(18). 1356–1364. 12 indexed citations
16.
Ray, Joseph W., et al.. (2019). A De novo HDAC2 variant in a patient with features consistent with Cornelia de Lange syndrome phenotype. American Journal of Medical Genetics Part A. 179(5). 852–856. 14 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Laura Konczal Breakdown of academic impact, for papers by Katharina Löhner Breakdown of academic impact, for papers by Willa Thorson Breakdown of academic impact, for papers by Shahida Moosa Breakdown of academic impact, for papers by Ignacio Arroyo Breakdown of academic impact, for papers by Odile Boute‐Bénéjean Breakdown of academic impact, for papers by Sara Caylor Breakdown of academic impact, for papers by Rob Hastings Breakdown of academic impact, for papers by Nakamichi Saito Breakdown of academic impact, for papers by Edith Said
Rankless by CCL
2026