Murray Feingold

4.5k total citations
111 papers, 2.6k citations indexed

About

Murray Feingold is a scholar working on Genetics, Surgery and Molecular Biology. According to data from OpenAlex, Murray Feingold has authored 111 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 22 papers in Surgery and 22 papers in Molecular Biology. Recurrent topics in Murray Feingold's work include Craniofacial Disorders and Treatments (13 papers), Cleft Lip and Palate Research (10 papers) and Metabolism and Genetic Disorders (7 papers). Murray Feingold is often cited by papers focused on Craniofacial Disorders and Treatments (13 papers), Cleft Lip and Palate Research (10 papers) and Metabolism and Genetic Disorders (7 papers). Murray Feingold collaborates with scholars based in United States, United Kingdom and Netherlands. Murray Feingold's co-authors include William H. Bossert, Jules Baum, Louis Bartoshesky, Sydney S. Gellis, Marilyn J. Bull, Allen C. Crocker, Jürgen W. Spranger, Jules G. Leroy, John M. Opitz and Rosalie Goldberg and has published in prestigious journals such as New England Journal of Medicine, The Lancet and PEDIATRICS.

In The Last Decade

Murray Feingold

102 papers receiving 2.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Murray Feingold United States 28 1.2k 1.0k 531 243 239 111 2.6k
Leonard O. Langer United States 31 1.5k 1.3× 879 0.9× 532 1.0× 210 0.9× 204 0.9× 77 2.7k
R. Neil Schimke United States 27 699 0.6× 882 0.9× 418 0.8× 336 1.4× 207 0.9× 76 2.4k
Richard M. Goodman Israel 26 889 0.8× 611 0.6× 340 0.6× 127 0.5× 236 1.0× 121 2.2k
H. ‐R. Wiedemann Germany 24 923 0.8× 856 0.8× 572 1.1× 112 0.5× 253 1.1× 137 2.2k
David Bixler United States 29 1.3k 1.1× 1.1k 1.1× 523 1.0× 89 0.4× 188 0.8× 135 3.1k
Ahmad S. Teebi Canada 31 1.3k 1.1× 1.3k 1.3× 522 1.0× 172 0.7× 323 1.4× 111 3.2k
Eberhard Passarge Germany 34 1.3k 1.1× 2.2k 2.2× 620 1.2× 155 0.6× 554 2.3× 158 4.1k
Yoshikazu Kuroki Japan 26 1.4k 1.2× 835 0.8× 284 0.5× 139 0.6× 400 1.7× 106 2.2k
Miriam G. Wilson United States 24 829 0.7× 592 0.6× 292 0.5× 193 0.8× 478 2.0× 82 1.9k
Thaddeus E. Kelly United States 28 1.3k 1.1× 1.1k 1.1× 357 0.7× 215 0.9× 482 2.0× 90 4.7k

Countries citing papers authored by Murray Feingold

Since Specialization
Citations

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

Fields of papers citing papers by Murray Feingold

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Murray Feingold

This figure shows the co-authorship network connecting the top 25 collaborators of Murray Feingold. A scholar is included among the top collaborators of Murray Feingold 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 Murray Feingold. Murray Feingold 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.
Boyle, Lia, Mirjam M. C. Wamelink, Gajja S. Salomons, et al.. (2016). Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects. The American Journal of Human Genetics. 98(6). 1235–1242. 33 indexed citations
2.
Zárate, Yuri A., Hazel Perry, Tawfeg Ben‐Omran, et al.. (2015). Further supporting evidence for the SATB2‐associated syndrome found through whole exome sequencing. American Journal of Medical Genetics Part A. 167(5). 1026–1032. 37 indexed citations
3.
Feingold, Murray. (2008). Random Thoughts Continued. Archives of Pediatrics and Adolescent Medicine. 162(1). 8–8.
4.
Feingold, Murray. (1999). Costello syndrome and rhabdomyosarcoma.. PubMed. 36(7). 582–3. 22 indexed citations
5.
Hoyme, H. Eugene, et al.. (1998). Isolated hemihyperplasia (hemihypertrophy): Report of a prospective multicenter study of the incidence of neoplasia and review. American Journal of Medical Genetics. 79(4). 274–278. 109 indexed citations
6.
Feingold, Murray, Bryan D. Hall, Yves Lacassie, & María‐Luisa Martínez‐Frías. (1997). Syndrome of microcephaly, facial and hand abnormalities, tracheoesophageal fistula, duodenal atresia, and developmental delay. American Journal of Medical Genetics. 69(3). 245–249. 37 indexed citations
7.
Lewanda, Amy Feldman, E D Green, Jean Weissenbach, et al.. (1994). Evidence that the Saethre-Chotzen syndrome locus lies between D7S664 and D7S507, by genetic analysis and detection of a microdeletion in a patient.. PubMed. 55(6). 1195–201. 20 indexed citations
8.
Robinson, Paul, Mordechai Shohat, Robin M. Winter, et al.. (1988). A unique association of short stature, dysmorphic features, and speech impairment (Floating-harbor syndrome). The Journal of Pediatrics. 113(4). 703–706. 41 indexed citations
9.
Zippin, Calvin & Murray Feingold. (1985). Service role of the hospital tumour registry in the USA.. PubMed. 121–31. 1 indexed citations
10.
Feingold, Murray. (1985). Picture of the Month. Archives of Pediatrics and Adolescent Medicine. 139(3). 319–319.
11.
Feingold, Murray & Hermine M. Pashayan. (1983). Genetics and birth defects in clinical practice. Little, Brown eBooks. 1 indexed citations
12.
Feingold, Murray, et al.. (1980). Picture of the month. Metaphyseal chondrodysplasia, Schmid type.. PubMed. 134(7). 699–700. 2 indexed citations
13.
Feingold, Murray, et al.. (1978). Picture of the month: hemangiomas with osteolysis (Gorham's disease, vanishing bone disease).. Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 132(7). 715–6. 4 indexed citations
14.
Feingold, Murray, et al.. (1978). Picture of the month. Nager's syndrome (Nager's acrofacial dystosis). Munich Personal RePEc Archive (Ludwig Maximilian University of Munich). 132(5). 519–20. 11 indexed citations
15.
Feingold, Murray, et al.. (1974). Picture of the month. Pseudoachondroplasia (pseudoachondroplastic spondlyloepiphyseal dysplasia).. PubMed. 128(6). 833–4. 4 indexed citations
16.
Leroy, Jules G., Jürgen W. Spranger, Murray Feingold, John M. Opitz, & Allen C. Crocker. (1971). I-cell disease: A clinical picture. The Journal of Pediatrics. 79(3). 360–365. 128 indexed citations
17.
Feingold, Murray. (1971). FAMILIAL NEUROBLASTOMA AND TRISOMY 13. Archives of Pediatrics and Adolescent Medicine. 121(5). 451–451. 21 indexed citations
18.
Feingold, Murray, et al.. (1971). Congenital brevicollis--(Klippel-Feil syndrome).. PubMed. 121(6). 501–2. 4 indexed citations
19.
Feingold, Murray, et al.. (1970). State-wide information center for handicapped children. The Journal of Pediatrics. 77(5). 830–832.
20.
Atkins, L. & Murray Feingold. (1969). 46,XY,21qi-46,XY,21p- mosaicism in a child with Down's syndrome.. Journal of Medical Genetics. 6(2). 206–208. 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.

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