Raj Ramesar

15.1k citations
224 papers · 5.3k · h-index 40

Impact in

Papers in

    • Retinal Development and Disorders 27
    • Genetic Associations and Epidemiology 19
    • Genomics and Rare Diseases 13
    • Connective tissue disorders research 9

Raj Ramesar

217 papers receiving 5.2k citations

Peers

Raj Ramesar
Comparison fields: 5 of 163
  • Sensory Systems 219
  • Psychiatry and Mental health 629
  • Genetics 1.2k
  • Cellular and Molecular Neuroscience 556
  • Genetics 290
Replace Stacey S. Cherny with:
Stacey S. Cherny Hong Kong
Michel Guipponi Switzerland
A.J. Pakstis United States
Eden R. Martin United States
Hans Eiberg Denmark
Dale R. Nyholt Australia
David Curtis United Kingdom
David L. Duffy Australia
Joseph D. Terwilliger United States
Anjali K. Henders Australia
Raj Ramesar relative to Stacey S. Cherny Hong Kong Stacey S. Cherny's profile →
Citations per field
00.5×1.5×2.3×
Stacey S. Cherny · 1×
Citations per year

Countries citing papers authored by Raj Ramesar

Since Specialization
Citations

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

Fields of papers citing papers by Raj Ramesar

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Raj Ramesar, 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 Raj Ramesar Line = papers co-authored together Raj Ramesar links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 224 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2005245
2 2000148
3 2001144
4 2005140
5
Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.
1994138
6 2004127
7 2005118
8 2006117
9 1994108
10 200099
11 200487
12 201485
13 199983
14 200882
15 200877
16 201475
17 200575
18
Mutations of the KIT (mast/stem cell growth factor receptor) proto-oncogene account for a continuous range of phenotypes in human piebaldism.
199272
19 200365
20 200864

About Raj Ramesar

Raj Ramesar is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Oncology and Psychiatry and Mental health, having authored 224 papers that have together received 5.3k indexed citations. Recurring topics across this work include Genetic factors in colorectal cancer (37 papers), Retinal Development and Disorders (27 papers), Genetic Associations and Epidemiology (19 papers), Colorectal Cancer Screening and Detection (16 papers), Bipolar Disorder and Treatment (14 papers), Genomics and Rare Diseases (13 papers), Cancer Genomics and Diagnostics (12 papers) and Connective tissue disorders research (9 papers). The work is most often cited by research in Sensory Systems (219 citations), Psychiatry and Mental health (629 citations), Genetics (1.2k citations), Cellular and Molecular Neuroscience (556 citations) and Genetics (290 citations). Raj Ramesar has collaborated with scholars based in South Africa, United States and United Kingdom. Frequent co-authors include Jonathan Savitz, Mark Solms, Peter Beighton, Lize van der Merwe, Dan J. Stein, Jacquie Greenberg, Paul Goldberg, Ambroise Wonkam, Denis Viljoen and Timothy K. Newman. Their work appears in journals such as Clinical Genetics, Human Genetics, PLoS ONE, The American Journal of Human Genetics and Human Mutation.

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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