Deborah McEldrew

434 total citations
8 papers, 234 citations indexed

About

Deborah McEldrew is a scholar working on Surgery, Pulmonary and Respiratory Medicine and Genetics. According to data from OpenAlex, Deborah McEldrew has authored 8 papers receiving a total of 234 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Surgery, 4 papers in Pulmonary and Respiratory Medicine and 3 papers in Genetics. Recurrent topics in Deborah McEldrew's work include Congenital Anomalies and Fetal Surgery (3 papers), Pediatric Hepatobiliary Diseases and Treatments (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Deborah McEldrew is often cited by papers focused on Congenital Anomalies and Fetal Surgery (3 papers), Pediatric Hepatobiliary Diseases and Treatments (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Deborah McEldrew collaborates with scholars based in United States, Italy and Israel. Deborah McEldrew's co-authors include Ramakrishnan Rajagopalan, Nancy B. Spinner, Melissa A. Gilbert, Kathleen M. Loomes, Ian D. Krantz, Christopher M. Grochowski, David A. Piccoli, Laura K. Conlin, Bryan L. Krock and Grace F. Chao and has published in prestigious journals such as Scientific Reports, The Journal of Pediatrics and PLoS Genetics.

In The Last Decade

Deborah McEldrew

8 papers receiving 230 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah McEldrew United States 7 125 94 77 76 20 8 234
Anne Hutchinson United States 5 173 1.4× 121 1.3× 47 0.6× 84 1.1× 18 0.9× 6 263
Nicole Raynaud France 9 166 1.3× 117 1.2× 50 0.6× 84 1.1× 14 0.7× 17 276
Eriko Nishi Japan 9 78 0.6× 40 0.4× 84 1.1× 113 1.5× 47 2.4× 32 252
Rocío Mena Spain 7 20 0.2× 48 0.5× 75 1.0× 65 0.9× 32 1.6× 16 182
Avinash V. Dharmadhikari United States 8 58 0.5× 80 0.9× 61 0.8× 143 1.9× 20 1.0× 15 222
Aline Receveur France 9 20 0.2× 21 0.2× 109 1.4× 81 1.1× 50 2.5× 22 200
Guillermo Lay‐Son Chile 9 38 0.3× 42 0.4× 133 1.7× 128 1.7× 15 0.8× 24 239
Abbas Rizvi United States 5 61 0.5× 47 0.5× 20 0.3× 67 0.9× 9 0.5× 6 201
Carole Goumy France 11 75 0.6× 41 0.4× 185 2.4× 125 1.6× 100 5.0× 36 324
Donna K. Mahnke United States 11 82 0.7× 44 0.5× 70 0.9× 300 3.9× 19 0.9× 14 392

Countries citing papers authored by Deborah McEldrew

Since Specialization
Citations

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

Fields of papers citing papers by Deborah McEldrew

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah McEldrew. 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 Deborah McEldrew. The network helps show where Deborah McEldrew may publish in the future.

Co-authorship network of co-authors of Deborah McEldrew

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

All Works

8 of 8 papers shown
1.
Wild, K. Taylor, Deborah McEldrew, Maninder Kaur, et al.. (2022). Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases. The Journal of Pediatrics. 246. 251–265.e2. 3 indexed citations
2.
Conlin, Laura K., Erfan Aref‐Eshghi, Deborah McEldrew, Minjie Luo, & Ramakrishnan Rajagopalan. (2022). Long‐read sequencing for molecular diagnostics in constitutional genetic disorders. Human Mutation. 43(11). 1531–1544. 31 indexed citations
3.
Rajagopalan, Ramakrishnan, Melissa A. Gilbert, Deborah McEldrew, et al.. (2020). Genome sequencing increases diagnostic yield in clinically diagnosed Alagille syndrome patients with previously negative test results. Genetics in Medicine. 23(2). 323–330. 12 indexed citations
4.
Gilbert, Melissa A., Robert C. Bauer, Ramakrishnan Rajagopalan, et al.. (2019). Alagille syndrome mutation update: Comprehensive overview ofJAG1andNOTCH2mutation frequencies and insight into missense variant classification. Human Mutation. 40(12). 2197–2220. 89 indexed citations
5.
Gilbert, Melissa A., Christopher M. Grochowski, Deborah McEldrew, et al.. (2018). A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1. PLoS Genetics. 14(8). e1007532–e1007532. 47 indexed citations
6.
Mills, Jason A., Pamela S. Herrera, Maninder Kaur, et al.. (2018). NIPBL+/− haploinsufficiency reveals a constellation of transcriptome disruptions in the pluripotent and cardiac states. Scientific Reports. 8(1). 1056–1056. 23 indexed citations
7.
Kaur, Maninder, Alessandro Rocca, G Cocchi, et al.. (2018). Prenatal profile of Pallister‐Killian syndrome: Retrospective analysis of 114 pregnancies, literature review and approach to prenatal diagnosis. American Journal of Medical Genetics Part A. 176(12). 2575–2586. 17 indexed citations
8.
Spinner, Nancy B., Roy D. Schmickel, Elaine H. Zackai, et al.. (1989). The role of cytologic NOR variants in the etiology of trisomy 21.. PubMed. 44(5). 631–8. 12 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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2026