Steven A. Narod

1.4k total citations
11 papers, 772 citations indexed

About

Steven A. Narod is a scholar working on Oncology, Genetics and Cancer Research. According to data from OpenAlex, Steven A. Narod has authored 11 papers receiving a total of 772 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Oncology, 4 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Steven A. Narod's work include Cancer Genomics and Diagnostics (4 papers), BRCA gene mutations in cancer (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Steven A. Narod is often cited by papers focused on Cancer Genomics and Diagnostics (4 papers), BRCA gene mutations in cancer (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Steven A. Narod collaborates with scholars based in Canada, United States and France. Steven A. Narod's co-authors include Henry T. Lynch, William D. Foulkes, Gilbert Lenoir, Joseph Marcus, David L. Page, Jean‐Sébastien Brunet, Weiva Sieh, Barry P. Rosen, S Gershman and Ping Sun and has published in prestigious journals such as Neurology, Cancer and The American Journal of Human Genetics.

In The Last Decade

Steven A. Narod

11 papers receiving 744 citations

Peers

Countries citing papers authored by Steven A. Narod

Since Specialization

Citations

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

Fields of papers citing papers by Steven A. Narod

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Steven A. Narod. 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 Steven A. Narod. The network helps show where Steven A. Narod may publish in the future.

Co-authorship network of co-authors of Steven A. Narod

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

All Works

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11 of 11 papers shown

#	Work	Indexed citations
1	Survival in women with ovarian cancer with and without microsatellite instability. 2015 ·PubMed ·Yakir Segev, (unknown), (unknown), (unknown), Thomas A. Sellers, (unknown), Harvey A. Risch, Barry P. Rosen, Peter Shaw, Joellen Schildkraut, Steven A. Narod, Tuya Pal	4
2	Contralateral mastectomy and survival after breast cancer in carriers of BRCA1 and BRCA2 mutations: retrospective analysis 2014 ·BMJ ·Kelly Metcalfe, S Gershman, P Ghadirian, Henry T. Lynch, C. Snyder, Nadine Tung, Charmaine Kim‐Sing, Andrea Eisen, William D. Foulkes, Barry P. Rosen, Ping Sun, Steven A. Narod	196
3	Host Susceptibility to Cancer Progression 1998 ·The American Journal of Human Genetics ·Steven A. Narod	12
4	Hereditary breast cancer: Pathobiology, prognosis, and BRCA1 and BRCA2 gene linkage 1996 ·Cancer ·Joseph Marcus, (unknown), David L. Page, Steven A. Narod, Gilbert Lenoir, (unknown), (unknown), (unknown), (unknown), Henry T. Lynch	322
5	Familial risks of squamous cell carcinoma of the head and neck: retrospective case-control study 1996 ·BMJ ·William D. Foulkes, Jean‐Sébastien Brunet, Weiva Sieh, (unknown), (unknown), Steven A. Narod	121
6	Hereditary breast and ovarian cancer: epidemiology, genetics, screening and predictive testing. 1995 ·PubMed ·William D. Foulkes, Steven A. Narod	21
7	Genetic mapping of the breast-ovarian cancer syndrome to a small interval on chromosome 17q12–21: exclusion of candidate genes EDH17B2 and RARA 1993 ·Human Molecular Genetics ·Jacques Simard, Jean Feunteun, Gilbert Lenoir, (unknown), (unknown), Van Luu The, (unknown), Dana D. Lasko, Kenneth Morgan, Guy A. Rouleau, (unknown), (unknown), Steven A. Narod	45
8	Presymptomatic diagnosis for neurofibromatosis 2 with chromosome 22 markers 1993 ·Neurology ·Martin Ruttledge, Steven A. Narod, Jan P. Dumanski, Dilys M. Parry, R Eldridge, Wladimir Wertelecki, Jillian S. Parboosingh, (unknown), G M Lenoir, V. Peter Collins, Magnus Nordenskjöld, Guy A. Rouleau	28
9	A preliminary analysis of consortium data for markers tightly linked to multiple endocrine neoplasia type 2A. 1992 ·PubMed ·Jay B. Lichter, (unknown), (unknown), D.F. Easton, Steven A. Narod, G M Lenoir, Robert F. Gagel, Nancy E. Simpson, Emily Gardner, Paul J. Goodfellow	1
10	The gene for mannose-binding protein maps to chromosome 10 and is a marker for multiple endocrine neoplasia type 2 1991 ·Cytogenetic and Genome Research ·Isabelle Schuffenecker, Steven A. Narod, R. Alan B. Ezekowitz, Hagay Sobol, Jean Feunteun, G M Lenoir	11
11	Radiation, genetics and childhood leukaemia 1990 ·European Journal of Cancer and Clinical Oncology ·Steven A. Narod	11

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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