Steven A. Narod

9.2k total citations
9 papers, 489 citations indexed

About

Steven A. Narod is a scholar working on Genetics, Reproductive Medicine and Molecular Biology. According to data from OpenAlex, Steven A. Narod has authored 9 papers receiving a total of 489 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 4 papers in Reproductive Medicine and 2 papers in Molecular Biology. Recurrent topics in Steven A. Narod's work include BRCA gene mutations in cancer (7 papers), Ovarian cancer diagnosis and treatment (4 papers) and Genetic factors in colorectal cancer (2 papers). Steven A. Narod is often cited by papers focused on BRCA gene mutations in cancer (7 papers), Ovarian cancer diagnosis and treatment (4 papers) and Genetic factors in colorectal cancer (2 papers). Steven A. Narod collaborates with scholars based in Canada, United States and France. Steven A. Narod's co-authors include Olga Serova, Gilbert Lenoir, Caryn Lerman, Carolyn Durham, Susan Tinley, Beth Y. Karlan, Lawrence D. Platt, Denise Barbuto, Leslie J. Raffel and Rae Lynn Baldwin and has published in prestigious journals such as Cancer, Human Molecular Genetics and American Journal of Obstetrics and Gynecology.

In The Last Decade

Steven A. Narod

8 papers receiving 471 citations

Peers

Steven A. Narod

GENET

RM

PFM

MB

CR

D. G. Crüger Denmark

Steven A. Narod Canada

Anne‐Bine Skytte Denmark

R.I. Olivier Netherlands

Jeanna McCuaig Canada

M. Daly United States

Sue Friedman United States

Faiza Gaba United Kingdom

Fiona Lalloo United Kingdom

Julie Erlichman United States

D. G. Crüger Denmark

Steven A. Narod

339 ×0.9

GENET

141 ×0.8

RM

97 ×0.8

PFM

156 ×1.6

MB

100 ×1.1

CR

Citations per year, relative to Steven A. Narod Steven A. Narod (= 1×) peers D. G. Crüger

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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9 of 9 papers shown

1.

Reid, Brett M., Jennifer B. Permuth, Y. Ann Chen, et al.. (2019). Genome-wide Analysis of Common Copy Number Variation and Epithelial Ovarian Cancer Risk. Cancer Epidemiology Biomarkers & Prevention. 28(7). 1117–1126. 18 indexed citations

2.

Stevens, Kristen N., Linda E. Kelemen, Xianshu Wang, et al.. (2012). Common Variation in Nemo-Like Kinase Is Associated with Risk of Ovarian Cancer. Cancer Epidemiology Biomarkers & Prevention. 21(3). 523–528. 8 indexed citations

3.

Goshen, Ran, William Chu, Laurie Elit, et al.. (2000). Is Uterine Papillary Serous Adenocarcinoma a Manifestation of the Hereditary Breast–Ovarian Cancer Syndrome?. Gynecologic Oncology. 79(3). 477–481. 88 indexed citations

4.

Narod, Steven A.. (1999). Genetic epidemiology of prostate cancer. Biochimica et Biophysica Acta (BBA) - Reviews on Cancer. 1423(1). F1–F13. 26 indexed citations

5.

Lynch, Henry T., Patrice Watson, Susan Tinley, et al.. (1999). An Update on DNA-Based BRCA1/BRCA2 Genetic Counseling in Hereditary Breast Cancer. Cancer Genetics and Cytogenetics. 109(2). 91–98. 61 indexed citations

6.

Karlan, Beth Y., Rae Lynn Baldwin, Leslie J. Raffel, et al.. (1999). Peritoneal serous papillary carcinoma, a phenotypic variant of familial ovarian cancer: Implications for ovarian cancer screening. American Journal of Obstetrics and Gynecology. 180(4). 917–928. 92 indexed citations

7.

Lynch, H., Stephen J. Lemon, Carolyn Durham, et al.. (1997). A descriptive study of BRCA1 testing and reactions to disclosure of test results. Cancer. 79(11). 2219–2228. 181 indexed citations

8.

Phelan, Catherine M., Catharina Larsson, Stephen Baird, et al.. (1996). The Human Mammary-Derived Growth Inhibitor (MDGI) Gene: Genomic Structure and Mutation Analysis in Human Breast Tumors. Genomics. 36(2). 377–377.

9.

Tonin, Patricia N., Olga Serova, Jacques Simard, et al.. (1994). The gene for hereditary breast-ovarian cancer, BRCA1, maps distal to EDH17B2 in chromosome region 17q12–q21. Human Molecular Genetics. 3(9). 1679–1682. 15 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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