Rohini Rau‐Murthy

3.5k total citations
14 papers, 256 citations indexed

About

Rohini Rau‐Murthy is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Rohini Rau‐Murthy has authored 14 papers receiving a total of 256 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 5 papers in Molecular Biology and 4 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Rohini Rau‐Murthy's work include BRCA gene mutations in cancer (6 papers), Renal and related cancers (3 papers) and Genetic factors in colorectal cancer (3 papers). Rohini Rau‐Murthy is often cited by papers focused on BRCA gene mutations in cancer (6 papers), Renal and related cancers (3 papers) and Genetic factors in colorectal cancer (3 papers). Rohini Rau‐Murthy collaborates with scholars based in United States. Rohini Rau‐Murthy's co-authors include Kenneth Offit, Zsofia K. Stadler, Mark E. Robson, Erin Salo‐Mullen, Lauren Jacobs, Leonard B. Saltz, David P. Kelsen, Maeve A. Lowery, Kenneth H. Yu and Amethyst Saldia and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Cancer.

In The Last Decade

Rohini Rau‐Murthy

14 papers receiving 251 citations

Peers

Rohini Rau‐Murthy

ONCOL

GENET

PFM

María Carolina Sanabria‐Salas Colombia

Chantal Perret Canada

Rosaria Cesaraccio Italy

Kristen Hanson United States

Ashley Woodson United States

Salina Chan United States

Julio E. Abugattas Peru

Sue Gerty United Kingdom

Neal Clark Norway

Amal Yussuf United States

María Carolina Sanabria‐Salas Colombia

Rohini Rau‐Murthy

131 ×1.0

ONCOL

110 ×0.9

66 ×0.7

91 ×1.2

GENET

55 ×0.9

PFM

Citations per year, relative to Rohini Rau‐Murthy Rohini Rau‐Murthy (= 1×) peers María Carolina Sanabria‐Salas

Countries citing papers authored by Rohini Rau‐Murthy

Since Specialization

Citations

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

Fields of papers citing papers by Rohini Rau‐Murthy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rohini Rau‐Murthy. 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 Rohini Rau‐Murthy. The network helps show where Rohini Rau‐Murthy may publish in the future.

Co-authorship network of co-authors of Rohini Rau‐Murthy

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

All Works

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14 of 14 papers shown

Rau‐Murthy, Rohini, et al.. (2017). Community-based asthma education.. PubMed. 23(2). e67–e69. 9 indexed citations

Kopp, Ryan, Kelly Stratton, Emily Glogowski, et al.. (2017). Utility of prospective pathologic evaluation to inform clinical genetic testing for hereditary leiomyomatosis and renal cell carcinoma. Cancer. 123(13). 2452–2458. 13 indexed citations

Corines, Marina, Jada G. Hamilton, Emily Glogowski, et al.. (2016). Educational and Psychosocial Support Needs in Lynch Syndrome: Implementation and Assessment of an Educational Workshop and Support Group. Journal of Genetic Counseling. 26(2). 232–243. 12 indexed citations

Gany, Francesca, et al.. (2015). Increasing influenza vaccination in New York City taxi drivers: A community driven approach. Vaccine. 33(22). 2521–2523. 5 indexed citations

Sullivan, John, Ryan Kopp, Kelly Stratton, et al.. (2015). An analysis of the association between prostate cancer risk loci, PSA levels, disease aggressiveness and disease-specific mortality. British Journal of Cancer. 113(1). 166–172. 10 indexed citations

Stratton, Kelly, Shaheen Alanee, Emily Glogowski, et al.. (2015). Outcome of genetic evaluation of patients with kidney cancer referred for suspected hereditary cancer syndromes. Urologic Oncology Seminars and Original Investigations. 34(5). 238.e1–238.e7. 16 indexed citations

Salo‐Mullen, Erin, Eileen M. O’Reilly, David P. Kelsen, et al.. (2015). Identification of germline genetic mutations in patients with pancreatic cancer. Cancer. 121(24). 4382–4388. 142 indexed citations

Stratton, Kelly, Kasmintan A. Schrader, Christopher Manschreck, et al.. (2014). MP30-12 RENAL CELL CARCINOMA AND NON-HODGKIN’S LYMPHOMA: GENOMIC APPROACHES TO IDENTIFICATION OF SHARED SUSCEPTIBILITY. The Journal of Urology. 191(4S). 2 indexed citations

Kopp, Ryan, Kelly Stratton, Emily Glogowski, et al.. (2014). MP36-06 UTILITY OF PROSPECTIVE PATHOLOGIC EVALUATION TO INFORM CLINICAL GENETIC TESTING FOR HEREDITARY LEIOMYOMATOSIS AND RENAL CELL CARCINOMA. The Journal of Urology. 191(4S). 1 indexed citations

10.

Alanee, Shaheen, Sohela Shah, Joseph Vijai, et al.. (2013). Prevalence of HOXB13 mutation in a population of Ashkenazi Jewish men treated for prostate cancer. Familial Cancer. 12(4). 597–600. 7 indexed citations

11.

Shah, Sohela, Yonghwan Kim, Irina Ostrovnaya, et al.. (2013). Assessment of SLX4 Mutations in Hereditary Breast Cancers. PLoS ONE. 8(6). e66961–e66961. 34 indexed citations

12.

Salo‐Mullen, Erin, Eileen M. O’Reilly, David P. Kelsen, et al.. (2013). Identification of germline genetic mutations in patients with pancreatic adenocarcinoma.. Journal of Clinical Oncology. 31(4_suppl). 159–159. 1 indexed citations

13.

Shah, Sohela, Yonghwan Kim, Kara Sarrel, et al.. (2012). Abstract 2600: SLX4 mutation in hereditary breast cancer. Cancer Research. 72(8_Supplement). 2600–2600. 1 indexed citations

14.

Alanee, Shaheen, Sohela Shah, Rajmohan Murali, et al.. (2012). Absence of loss of heterozygosity of BRCA1 in a renal tumor from a BRCA1 germline mutation carrier. Familial Cancer. 12(1). 125–127. 3 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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