Roxana Moslehi

3.7k citations
48 papers · 3.0k · h-index 23

Impact in

    • Ovarian cancer diagnosis and treatment
  • Genetics top 1%
    • BRCA gene mutations in cancer
    • Genomic variations and chromosomal abnormalities
    • Genetic Associations and Epidemiology
    • Nutrition, Genetics, and Disease

Papers in

    • BRCA gene mutations in cancer 19
    • Genomic variations and chromosomal abnormalities 5
    • Genetic Associations and Epidemiology 4

Roxana Moslehi

48 papers receiving 2.8k citations

Peers

Roxana Moslehi
Comparison fields: 5 of 104
  • Reproductive Medicine 649
  • Genetics 1.7k
  • Pathology and Forensic Medicine 611
  • Cancer Research 414
  • Oncology 598
Replace Laurence Faivre with:
Laurence Faivre France
Thea M. Mooij Netherlands
Kai-Ren Ong United Kingdom
Eva Macháčková Czechia
Tara M. Friebel United States
Andrew Shenton United Kingdom
Carolien M. Kets Netherlands
Moraima Zelada-Hedman Sweden
Carrie Snyder United States
Barbara Weber United States
Roxana Moslehi relative to Laurence Faivre France Laurence Faivre's profile →
Citations per field
00.5×1.5×1.8×
Laurence Faivre · 1×
Citations per year

Countries citing papers authored by Roxana Moslehi

Since Specialization
Citations

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

Fields of papers citing papers by Roxana Moslehi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Roxana Moslehi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Roxana Moslehi Line = papers co-authored together Roxana Moslehi links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1998471
2 2003363
3 1999341
4 2000257
5 1996223
6 1995143
7 2006128
8 2006125
9 1998115
10 199954
11 200649
12 200946
13 201346
14 200144
15 200941
16 199840
17 199936
18 200633
19 200933
20 199530

About Roxana Moslehi

Roxana Moslehi is a scholar working on Genetics, Cancer Research, Oncology, Pathology and Forensic Medicine and Reproductive Medicine, having authored 48 papers that have together received 3.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (19 papers), DNA Repair Mechanisms (8 papers), Genomic variations and chromosomal abnormalities (5 papers), Lymphoma Diagnosis and Treatment (5 papers), Prenatal Screening and Diagnostics (4 papers), Genetic Associations and Epidemiology (4 papers), Ovarian cancer diagnosis and treatment (3 papers) and Viral-associated cancers and disorders (3 papers). The work is most often cited by research in Reproductive Medicine (649 citations), Genetics (1.7k citations), Pathology and Forensic Medicine (611 citations), Cancer Research (414 citations) and Oncology (598 citations). Roxana Moslehi has collaborated with scholars based in United States, Canada and United Kingdom. Frequent co-authors include Steven Alexander Narod, Beth Y. Karlan, Jean‐Sébastien Brunet, Rae Lynn Baldwin, Ilana A. Cass, Harvey A. Risch, Diane Michele Provencher, Susan L. Neuhausen, Hakan Lars Olsson and Paolo Radice. Their work appears in journals such as JNCI Journal of the National Cancer Institute, Clinical Genetics, The American Journal of Human Genetics, International Journal of Cancer and Expert Review of Ophthalmology.

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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