Eric Crawford

815 total citations
12 papers, 609 citations indexed

About

Eric Crawford is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Eric Crawford has authored 12 papers receiving a total of 609 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Surgery and 3 papers in Molecular Biology. Recurrent topics in Eric Crawford's work include Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Reproductive Biology and Fertility (2 papers). Eric Crawford is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Genomic variations and chromosomal abnormalities (3 papers) and Reproductive Biology and Fertility (2 papers). Eric Crawford collaborates with scholars based in United States, Australia and Canada. Eric Crawford's co-authors include Mary C. Phelan, K. Lenahan, Sherman J. Silber, Michael J. Friez, David J. Levine, Roger G. Gosden, Jorge A. Pineda, Cindy Skinner, Steven A. Skinner and Richard J. Schroer and has published in prestigious journals such as New England Journal of Medicine, Blood and Genomics.

In The Last Decade

Eric Crawford

12 papers receiving 579 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric Crawford United States 7 343 260 195 192 166 12 609
Jean‐Pierre Frijns Belgium 17 328 1.0× 300 1.2× 57 0.3× 114 0.6× 36 0.2× 23 670
Karen Kowal United States 18 984 2.9× 806 3.1× 56 0.3× 91 0.5× 251 1.5× 23 1.3k
Tsvia Frumkin Israel 9 198 0.6× 294 1.1× 121 0.6× 64 0.3× 44 0.3× 16 505
Anne Maddalena United States 17 736 2.1× 411 1.6× 40 0.2× 375 2.0× 160 1.0× 27 1.1k
Antonia Paula Marques‐de‐Faria Brazil 15 391 1.1× 383 1.5× 34 0.2× 65 0.3× 81 0.5× 51 617
S. L. Sherman United States 11 642 1.9× 424 1.6× 156 0.8× 199 1.0× 71 0.4× 18 1.0k
Yotam Kaufman Israel 11 335 1.0× 390 1.5× 96 0.5× 89 0.5× 26 0.2× 14 599
Babett Heye Germany 7 206 0.6× 147 0.6× 77 0.4× 48 0.3× 61 0.4× 7 365
Ilia V. Soloviev Russia 14 579 1.7× 356 1.4× 48 0.2× 79 0.4× 46 0.3× 26 788
Amal Abu Rayyan Palestinian Territory 12 228 0.7× 356 1.4× 82 0.4× 45 0.2× 57 0.3× 18 632

Countries citing papers authored by Eric Crawford

Since Specialization
Citations

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

Fields of papers citing papers by Eric Crawford

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Crawford

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

All Works

12 of 12 papers shown
1.
Crawford, Eric, et al.. (2020). Efficacy of a Bioresorbable Matrix in Healing Complex Chronic Wounds: An Open-Label Prospective Pilot Study. WOUNDS A Compendium of Clinical Research and Practice. 32(11). 309–318. 1 indexed citations
2.
3.
Lillicrap, David, et al.. (2009). The Prevalence of Non-Neutralizing Anti-FVIII Antibodies in the Canadian Hemophilia Population.. Blood. 114(22). 1291–1291. 2 indexed citations
4.
Silber, Sherman J., K. Lenahan, David J. Levine, et al.. (2005). Ovarian Transplantation between Monozygotic Twins Discordant for Premature Ovarian Failure. New England Journal of Medicine. 353(1). 58–63. 178 indexed citations
5.
Silber, Sherman J., K. Lenahan, David J. Levine, et al.. (2005). Ovarian Transplantation Between Monozygotic Twins Discordant for Premature Ovarian Failure. Obstetrical & Gynecological Survey. 61(1). 29–30. 34 indexed citations
6.
Phelan, Mary C., R. Curtis Rogers, Eric Crawford, Laura G. Brown, & David C. Page. (2002). Velocardiofacial syndrome in an unexplained XX male. American Journal of Medical Genetics Part A. 116A(1). 77–79. 4 indexed citations
7.
Davids, Matthew S., Eric Crawford, Stanislawa Weremowicz, et al.. (2001). STK25 Is a Candidate Gene for Pseudopseudohypoparathyroidism. Genomics. 77(1-2). 2–4. 13 indexed citations
8.
Schroer, Richard J., Mary C. Phelan, Ron C. Michaelis, et al.. (1998). Autism and maternally derived aberrations of chromosome 15q. American Journal of Medical Genetics. 76(4). 327–336. 284 indexed citations
9.
Phelan, Mary C., Will R. Blackburn, R. Curtis Rogers, et al.. (1998). FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16. Prenatal Diagnosis. 18(11). 1174–1180. 1 indexed citations
10.
Phelan, Mary C., Will R. Blackburn, R. Curtis Rogers, et al.. (1998). FISH analysis of a complex chromosome rearrangement involving nine breakpoints on chromosomes 6, 12, 14 and 16. Prenatal Diagnosis. 18(11). 1174–1180. 19 indexed citations
11.
Chenevix‐Trench, Georgia, Terry Hurst, David Purdie, et al.. (1997). Analysis of loss of heterozygosity andKRAS2 mutations in ovarian neoplasms: Clinicopathological correlations. Genes Chromosomes and Cancer. 18(2). 75–83. 44 indexed citations
12.
Brown, Angela M., Mary C. Phelan, Shivanand R. Patil, et al.. (1996). Two patients with duplication of 17p11.2: The reciprocal of the Smith-Magenis syndrome deletion?. American Journal of Medical Genetics. 63(2). 373–377. 25 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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