Leona Fishman

1.3k total citations
9 papers, 366 citations indexed

About

Leona Fishman is a scholar working on Molecular Biology, Reproductive Medicine and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Leona Fishman has authored 9 papers receiving a total of 366 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 4 papers in Reproductive Medicine and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Leona Fishman's work include Hypothalamic control of reproductive hormones (4 papers), Congenital heart defects research (3 papers) and Ovarian function and disorders (2 papers). Leona Fishman is often cited by papers focused on Hypothalamic control of reproductive hormones (4 papers), Congenital heart defects research (3 papers) and Ovarian function and disorders (2 papers). Leona Fishman collaborates with scholars based in Canada, Australia and Chile. Leona Fishman's co-authors include F John Holland, A.T.A. Fazekas, John D. Bailey, Cheryl Cytrynbaum, Andrea Shugar, Susan R. George, Wai Lun Alan Fung, Gregory Costain, Hanna Faghfoury and Eva W.C. Chow and has published in prestigious journals such as New England Journal of Medicine, The Journal of Clinical Endocrinology & Metabolism and Pediatric Research.

In The Last Decade

Leona Fishman

7 papers receiving 343 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Leona Fishman Canada 5 233 137 134 78 63 9 366
Carolina Putotto Italy 11 156 0.7× 129 0.9× 55 0.4× 66 0.8× 9 0.1× 38 288
Shaoxing Wu United States 7 68 0.3× 46 0.3× 72 0.5× 14 0.2× 12 0.2× 10 383
Joachim Wölfle Germany 10 116 0.5× 28 0.2× 155 1.2× 9 0.1× 42 0.7× 24 335
Rieko Tadokoro‐Cuccaro United Kingdom 10 212 0.9× 24 0.2× 100 0.7× 43 0.6× 18 0.3× 19 305
G. H. Newns United Kingdom 11 129 0.6× 31 0.2× 63 0.5× 26 0.3× 12 0.2× 17 354
Anne Lise Delezoïde France 9 58 0.2× 42 0.3× 43 0.3× 57 0.7× 25 0.4× 12 175
Barry A. Warner United States 5 44 0.2× 28 0.2× 56 0.4× 83 1.1× 99 1.6× 8 317
Diana Caprau United States 9 92 0.4× 95 0.7× 60 0.4× 53 0.7× 8 0.1× 10 321
Elizabeth Eklund United States 11 58 0.2× 20 0.1× 31 0.2× 27 0.3× 206 3.3× 27 449
Horst Seithe Germany 4 79 0.3× 14 0.1× 166 1.2× 83 1.1× 14 0.2× 6 247

Countries citing papers authored by Leona Fishman

Since Specialization
Citations

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

Fields of papers citing papers by Leona Fishman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leona Fishman

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

All Works

9 of 9 papers shown
1.
Choufani, Sanaa, et al.. (2021). Paternal Uniparental Disomy of the Entire Chromosome 20 in a Child with Beckwith-Wiedemann Syndrome. Genes. 12(2). 172–172. 3 indexed citations
2.
Shugar, Andrea, et al.. (2015). An increased prevalence of thyroid disease in children with 22q11.2 deletion syndrome. American Journal of Medical Genetics Part A. 167(7). 1560–1564. 15 indexed citations
3.
Fung, Wai Lun Alan, Nancy J. Butcher, Gregory Costain, et al.. (2015). Practical guidelines for managing adults with 22q11.2 deletion syndrome. Genetics in Medicine. 17(8). 599–609. 194 indexed citations
4.
Baskin, Berivan, Adam C. Smith, Andrea Shugar, et al.. (2007). Molecular diagnosis of 22q11.2 deletion and duplication by multiplex ligation dependent probe amplification. American Journal of Medical Genetics Part A. 143A(24). 2924–2930. 39 indexed citations
6.
Holland, F John, Leona Fishman, John D. Bailey, & Sang Whay Kooh. (1985). 455 KETOCONAZOLE TREATMENT IN BOYS WITH PRECOCIOUS PUBERTY. Pediatric Research. 19(4). 186A–186A.
7.
Holland, F John, Leona Fishman, D. COLM COSTIGAN, J. Steven Leeder, & A.T.A. Fazekas. (1985). 178 D-SER(TBU)6EA9lHRH IN PRECOCIOUS PUBERTY: PHARMACO-KINEIICS OF SC IV AND INTRANASAL USE. Pediatric Research. 19(6). 633–633. 1 indexed citations
8.
Holland, F John, Leona Fishman, John D. Bailey, & A.T.A. Fazekas. (1985). Ketoconazole in the Management of Precocious Puberty Not Responsive to LHRH-Analogue Therapy. New England Journal of Medicine. 312(16). 1023–1028. 84 indexed citations
9.
Fishman, Leona, et al.. (1984). Subcutaneous and intranasal use of D-ser (TBU)6 LHRH 1–9 EA10 (HOE 766) in precocious puberty (PP). Journal of Steroid Biochemistry. 20(6). 1380–1380.

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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