James V. Higgins

1.4k total citations
39 papers, 927 citations indexed

About

James V. Higgins is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, James V. Higgins has authored 39 papers receiving a total of 927 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Molecular Biology and 9 papers in Surgery. Recurrent topics in James V. Higgins's work include Cleft Lip and Palate Research (4 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). James V. Higgins is often cited by papers focused on Cleft Lip and Palate Research (4 papers), Congenital Anomalies and Fetal Surgery (4 papers) and Genomic variations and chromosomal abnormalities (4 papers). James V. Higgins collaborates with scholars based in United States and Canada. James V. Higgins's co-authors include Helga V. Toriello, John M. Opitz, James F. Reynolds, Thomas W. Glover, Diane E. Miller, Daniel S. Greenspan, Kazuhiko Takahara, Peter H. Byers, James F. Reynolds and Cathy A. Stevens and has published in prestigious journals such as Science, Nature Genetics and Gastroenterology.

In The Last Decade

James V. Higgins

39 papers receiving 872 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
James V. Higgins United States 18 414 332 241 182 109 39 927
Juan Chemke Israel 20 327 0.8× 365 1.1× 152 0.6× 220 1.2× 72 0.7× 64 1.1k
M. H. K. Shokeir Canada 19 355 0.9× 557 1.7× 191 0.8× 178 1.0× 45 0.4× 48 1.3k
Boris G. Kousseff United States 25 785 1.9× 603 1.8× 307 1.3× 276 1.5× 143 1.3× 83 1.6k
M Super United Kingdom 18 453 1.1× 526 1.6× 184 0.8× 129 0.7× 111 1.0× 47 1.6k
Naomi Fitch Canada 22 585 1.4× 479 1.4× 262 1.1× 186 1.0× 119 1.1× 44 1.1k
Mark Lubinsky United States 25 577 1.4× 734 2.2× 399 1.7× 401 2.2× 149 1.4× 73 1.6k
M Shohat Israel 15 387 0.9× 329 1.0× 88 0.4× 134 0.7× 105 1.0× 29 911
María‐Luisa Martínez‐Frías Spain 16 327 0.8× 251 0.8× 267 1.1× 155 0.9× 93 0.9× 22 801
D L Rimoin United States 19 860 2.1× 504 1.5× 170 0.7× 96 0.5× 314 2.9× 43 1.3k
J. Spranger Germany 19 508 1.2× 407 1.2× 103 0.4× 93 0.5× 154 1.4× 55 930

Countries citing papers authored by James V. Higgins

Since Specialization
Citations

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

Fields of papers citing papers by James V. Higgins

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by James V. Higgins. 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 James V. Higgins. The network helps show where James V. Higgins may publish in the future.

Co-authorship network of co-authors of James V. Higgins

This figure shows the co-authorship network connecting the top 25 collaborators of James V. Higgins. A scholar is included among the top collaborators of James V. Higgins 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 James V. Higgins. James V. Higgins 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.
Warzynski, Michael J., et al.. (2002). Flow cytometric immunophenotyping test for staging/monitoring neuroblastoma patients. Cytometry. 50(6). 298–304. 27 indexed citations
2.
Heubi, James E., James V. Higgins, Eric A. Argào, Rosa I. Sierra, & Bonny Specker. (1997). The Role of Magnesium in the Pathogenesis of Bone Disease in Childhood Cholestatic Liver Disease: A Preliminary Report. Journal of Pediatric Gastroenterology and Nutrition. 25(3). 301–306. 30 indexed citations
3.
Toriello, Helga V., Thomas W. Glover, Kazuhiko Takahara, et al.. (1996). A translocation interrupts the COL5A1 gene in a patient with Ehlers–Danlos syndrome and hypomelanosis of Ito. Nature Genetics. 13(3). 361–365. 105 indexed citations
4.
Dewald, Gordon W., et al.. (1995). Clinical phenotype associated with terminal 2q37 deletion. Clinical Genetics. 48(3). 134–139. 45 indexed citations
5.
Johnson, Judith A., et al.. (1994). Prenatal diagnosis of Smith–Lemli–Opitz syndrome, type II. American Journal of Medical Genetics. 49(2). 240–243. 18 indexed citations
6.
Glover, Thomas W., et al.. (1993). Translocation breakpoint in Aarskog syndrome maps to Xp11.21 between ALAS2 and DXS323. Human Molecular Genetics. 2(10). 1717–1718. 13 indexed citations
7.
Toriello, Helga V., Yves Lacassie, Patrick J. Droste, & James V. Higgins. (1993). Provisionally unique syndrome of ocular and ectodermal defects in two unrelated boys. American Journal of Medical Genetics. 45(6). 764–766. 32 indexed citations
8.
Toriello, Helga V., et al.. (1993). Provisionally unique autosomal recessive chondrodysplasia punctata syndrome. American Journal of Medical Genetics. 47(5). 797–799. 7 indexed citations
9.
El‐Fouly, Mohamed H., et al.. (1991). Digeorge anomaly in an infant with deletion of chromosome 22 and dup(9p) due to adjacent type II disjunction. American Journal of Medical Genetics. 38(4). 569–573. 27 indexed citations
10.
Higgins, James V., et al.. (1990). Two siblings with tel Hashomer camptodactyly and mitral valve prolapse. American Journal of Medical Genetics. 36(4). 398–403. 6 indexed citations
11.
Bernstein, Jay, et al.. (1989). Renal tubular dysgenesis: Delayed onset of oligohydramnios. American Journal of Medical Genetics. 32(1). 127–132. 49 indexed citations
12.
Metheny, William P., et al.. (1988). Amniocentesis use and risk awareness: Comparison of knowledge and beliefs among older Gravida. Social Biology. 35(1-2). 50–61. 6 indexed citations
13.
O’Malley, Daniel P., Roshni Kulkarni, Martin K. Oaks, & James V. Higgins. (1988). Acute lymphoblastic leukemia with a unique rearrangement between chromosomes 4 and 11. Cancer Genetics and Cytogenetics. 31(2). 291–294. 10 indexed citations
14.
Toriello, Helga V., et al.. (1986). Sibs with the polyasplenia developmental field defect. American Journal of Medical Genetics. 25(S2). 31–36. 13 indexed citations
15.
Higgins, James V., et al.. (1986). Isolated diaphragmatic defect in three sibs. American Journal of Medical Genetics. 25(S2). 177–181. 8 indexed citations
16.
Toriello, Helga V., et al.. (1985). Sibs with the fetal akinesia sequence, fetal edema, and malformations: A new syndrome?. American Journal of Medical Genetics. 21(2). 271–277. 40 indexed citations
17.
Higgins, James V., et al.. (1985). X‐linked syndrome of branchial arch and other defects. American Journal of Medical Genetics. 21(1). 137–142. 17 indexed citations
18.
Higgins, James V., et al.. (1983). Ring‐11 chromosome: Phenotype‐karyotype correlation with deletions of 11q. American Journal of Medical Genetics. 14(1). 29–35. 22 indexed citations
19.
Valenta, Lubomir J., James V. Higgins, & Gerald B. Holzman. (1977). Ovarian Dysgenesis Due to 45 X, 0/46 Dic (X) Mosaicism. The Journal of Clinical Endocrinology & Metabolism. 45(4). 702–706. 4 indexed citations
20.
Hecht, Frederick, et al.. (1968). Nonrandomness of Translocations in Man: Preferential Entry of Chromosomes into 13-15/21 Translocations. Science. 161(3839). 371–372. 42 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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