Neda Gharani

44.1k total citations
32 papers, 1.9k citations indexed

About

Neda Gharani is a scholar working on Public Health, Environmental and Occupational Health, Reproductive Medicine and Genetics. According to data from OpenAlex, Neda Gharani has authored 32 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Public Health, Environmental and Occupational Health, 13 papers in Reproductive Medicine and 12 papers in Genetics. Recurrent topics in Neda Gharani's work include Ovarian function and disorders (13 papers), Reproductive Biology and Fertility (9 papers) and Pharmacogenetics and Drug Metabolism (5 papers). Neda Gharani is often cited by papers focused on Ovarian function and disorders (13 papers), Reproductive Biology and Fertility (9 papers) and Pharmacogenetics and Drug Metabolism (5 papers). Neda Gharani collaborates with scholars based in United States, United Kingdom and Australia. Neda Gharani's co-authors include Mark I. McCarthy, Davinia White, Dawn Waterworth, Stephen Franks, James H. Millonig, Linda M. Brzustowicz, R. Williamson, Gerard S. Conway, Stephen Franks and Carole Gilling‐Smith and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Neda Gharani

32 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Neda Gharani United States 22 926 778 648 436 328 32 1.9k
Kathryn A. Martin United States 26 1.7k 1.9× 933 1.2× 757 1.2× 661 1.5× 37 0.1× 46 2.9k
Doris Gruber Austria 20 193 0.2× 190 0.2× 261 0.4× 196 0.4× 102 0.3× 56 1.4k
Carl‐Joachim Partsch Germany 29 747 0.8× 193 0.2× 637 1.0× 1.1k 2.5× 33 0.1× 81 2.4k
J. Neulen Germany 23 903 1.0× 604 0.8× 314 0.5× 355 0.8× 16 0.0× 75 1.8k
Séverine Trabado France 21 361 0.4× 121 0.2× 275 0.4× 424 1.0× 79 0.2× 70 1.4k
Caroline Dalton United Kingdom 21 410 0.4× 265 0.3× 156 0.2× 305 0.7× 36 0.1× 71 1.4k
Barbara Roland United States 16 135 0.1× 543 0.7× 69 0.1× 834 1.9× 112 0.3× 20 2.5k
Teófilo Gautier United States 22 527 0.6× 143 0.2× 666 1.0× 1.8k 4.1× 24 0.1× 31 3.2k
C. Martín United Kingdom 17 294 0.3× 258 0.3× 49 0.1× 339 0.8× 40 0.1× 25 948
M. A. F. Murray United Kingdom 19 350 0.4× 167 0.2× 149 0.2× 220 0.5× 43 0.1× 30 1.3k

Countries citing papers authored by Neda Gharani

Since Specialization
Citations

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

Fields of papers citing papers by Neda Gharani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Neda Gharani

This figure shows the co-authorship network connecting the top 25 collaborators of Neda Gharani. A scholar is included among the top collaborators of Neda Gharani 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 Neda Gharani. Neda Gharani 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.
Kusic, Dara, et al.. (2024). ursaPGx: a new R package to annotate pharmacogenetic star alleles using phased whole-genome sequencing data. SHILAP Revista de lepidopterología. 4. 1351620–1351620. 2 indexed citations
2.
Kusic, Dara, Stefan Zajic, Neda Gharani, et al.. (2023). Genome-wide Association Study of Caffeine Consumption Using Coriell Personalized Medicine Collaborative Data. 5(1). 1 indexed citations
3.
Shahabi, Payman, Laura Scheinfeldt, D.E. Lynch, et al.. (2016). An expanded pharmacogenomics warfarin dosing table with utility in generalised dosing guidance. Thrombosis and Haemostasis. 116(8). 337–348. 14 indexed citations
4.
Scheinfeldt, Laura, Neda Gharani, Rachel Kasper, et al.. (2015). Using the Coriell Personalized Medicine Collaborative Data to conduct a genome‐wide association study of sleep duration. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 168(8). 697–705. 28 indexed citations
5.
Gharani, Neda, Margaret Keller, Catharine B. Stack, et al.. (2013). The Coriell personalized medicine collaborative pharmacogenomics appraisal, evidence scoring and interpretation system. Genome Medicine. 5(10). 93–93. 33 indexed citations
6.
Stack, Catharine B., Neda Gharani, Erynn S. Gordon, et al.. (2011). Genetic risk estimation in the Coriell Personalized Medicine Collaborative. Genetics in Medicine. 13(2). 131–139. 35 indexed citations
7.
Choi, Jiyeon, et al.. (2009). Autism-Associated Haplotype Affects the Regulation of the Homeobox Gene, ENGRAILED 2. Biological Psychiatry. 66(10). 911–917. 56 indexed citations
8.
Buyske, Steven, Marsha E. Bates, Neda Gharani, et al.. (2005). Cognitive Traits Link to Human Chromosomal Regions. Behavior Genetics. 36(1). 65–76. 27 indexed citations
9.
Gharani, Neda, Ian Rossman, Shannon Bruse, et al.. (2005). Support for the Homeobox Transcription Factor Gene ENGRAILED 2 as an Autism Spectrum Disorder Susceptibility Locus. The American Journal of Human Genetics. 77(5). 851–868. 135 indexed citations
10.
Gaasenbeek, Michelle, Brenda L. Powell, Ulla Sovio, et al.. (2004). Large-Scale Analysis of the Relationship betweenCYP11APromoter Variation, Polycystic Ovarian Syndrome, and Serum Testosterone. The Journal of Clinical Endocrinology & Metabolism. 89(5). 2408–2413. 74 indexed citations
11.
Gharani, Neda, et al.. (2004). Association of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorder. Molecular Psychiatry. 9(5). 474–484. 168 indexed citations
12.
Whittaker, John C., Neda Gharani, Peter C. Hindmarsh, & Mark I. McCarthy. (2003). Estimation and Testing of Parent-of-Origin Effects for Quantitative Traits. The American Journal of Human Genetics. 72(4). 1035–1039. 19 indexed citations
13.
Haddad, Lema, Julie Evans, Neda Gharani, et al.. (2002). Variation within the Type 2 Diabetes Susceptibility Gene Calpain-10 and Polycystic Ovary Syndrome. The Journal of Clinical Endocrinology & Metabolism. 87(6). 2606–2610. 60 indexed citations
14.
Franks, Stephen, Neda Gharani, & Mark I. McCarthy. (2001). Candidate genes in polycystic ovary syndrome. Human Reproduction Update. 7(4). 405–410. 107 indexed citations
15.
Franks, Stephen, Carole Gilling‐Smith, Neda Gharani, & Mark I. McCarthy. (2000). Pathogenesis of polycystic ovary syndrome: Evidence for a genetically determined disorder of ovarian androgen production. Human Fertility. 3(2). 77–79. 21 indexed citations
16.
Franks, Stephen, Neda Gharani, & Carole Gilling‐Smith. (1999). Polycystic ovary syndrome: evidence for a primary disorder of ovarian steroidogenesis. The Journal of Steroid Biochemistry and Molecular Biology. 69(1-6). 269–272. 20 indexed citations
17.
Franks, Stephen, Neda Gharani, Dawn Waterworth, et al.. (1998). Current Developments in the Molecular Genetics of the Polycystic Ovary Syndrome. Trends in Endocrinology and Metabolism. 9(2). 51–54. 10 indexed citations
18.
Franks, Stephen, Neda Gharani, Dawn Waterworth, et al.. (1998). Genetics of polycystic ovary syndrome. Molecular and Cellular Endocrinology. 145(1-2). 123–128. 36 indexed citations
19.
Waterworth, Dawn, Simon T. Bennett, Neda Gharani, et al.. (1997). Linkage and association of insulin gene VNTR regulatory polymorphism with polycystic ovary syndrome. The Lancet. 349(9057). 986–990. 254 indexed citations
20.
Franks, S., Neda Gharani, Dawn Waterworth, et al.. (1997). The genetic basis of polycystic ovary syndrome. Human Reproduction. 12(12). 2641–2648. 233 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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