SA Narod

2.0k citations

18 papers · 1.0k indexed · h-index 13

Impact in

Genetics top 2%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Nutrition, Genetics, and Disease
Reproductive Medicine top 5%
- Ovarian cancer diagnosis and treatment

Papers in ⓘ

Genetics 16
- BRCA gene mutations in cancer 15
- Genomic variations and chromosomal abnormalities 4
- Estrogen and related hormone effects 2
Cancer Research 8
- Cancer Genomics and Diagnostics 5
- Breast Cancer Treatment Studies 2

Co-authors: Alexander Liede (2 shared papers)William D. Foulkes (3 shared papers)Jan Lubiński (5 shared papers)Cezary Cybulski (4 shared papers)Joanne Honeyford (1 shared paper)Jean‐Sébastien Brunet (1 shared paper)Elizabeth Warner (1 shared paper)Nancy Hamel (1 shared paper)
Journals: Clinical Genetics (9 papers)JNCI Journal of the National Cancer Institute (2 papers)Prostate Cancer and Prostatic Diseases (1 paper)Breast Cancer Research and Treatment (1 paper)Cancer Research (1 paper)
Partner nations: Canada United States Poland

In The Last Decade

SA Narod

18 papers receiving 982 citations

Peers

Countries citing papers authored by SA Narod

Since Specialization

Citations

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

Fields of papers citing papers by SA Narod

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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18 of 18 papers shown

#	Work
1	Prevalence and Penetrance of BRCA1 and BRCA2 Gene Mutations in Unselected Ashkenazi Jewish Women With Breast Cancer JNCI Journal of the National Cancer Institute ·Elizabeth Warner, William D. Foulkes, Pamela J. Goodwin, Wendy S. Meschino, John Blondal, Craig Paterson, H Ozçelik, Paul E. Goss, Diane Allingham‐Hawkins, Nancy Hamel, Lisa Di Prospero, V. Contiga, Corinne Serruya, Martin Klein, Roxana Moslehi, Joanne Honeyford, Alexander Liede, Gord Glendon, Jean‐Sébastien Brunet, SA Narod	1999	306
2	Oral Contraceptives and the Risk of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers JNCI Journal of the National Cancer Institute ·SA Narod	2002	239
3	*NBS1* Is a Prostate Cancer Susceptibility Gene Cancer Research ·Cezary Cybulski, Bohdan Górski, Tadeusz Dębniak, B. Gliniewicz, Marek Mierzejewski, Bartłomiej Masojć, Anna Jakubowska, Joanna Matyjasik, Elżbieta Złowocka, Andrzej Sikorski, SA Narod, Jan Lubiński	2004	111
4	The prevalence of BRCA1 and BRCA2 mutations among young Mexican women with triple-negative breast cancer Breast Cancer Research and Treatment ·Cynthia Villarreal‐Garza, Jeffrey N. Weitzel, M Llacuachaqui, Erika Sifuentes, Maria Cristina Magallanes-Hoyos, Lenny Gallardo, Rosa María Álvarez-Gómez, Josef Herzog, Danielle Castillo, Robert E. Royer, Mohammad R. Akbari, Fernando Lara-Medina, Luis A. Herrera, Alejandro Mohar, SA Narod	2015	60
5	Development and testing of a decision aid for breast cancer prevention for women with a BRCA1 or BRCA2 mutation Clinical Genetics ·Kelly Metcalfe, Aletta Poll, Annette M. O’Connor, S Gershman, Susan Randall Armel, Amy Finch, Rochelle Demsky, Barry P. Rosen, SA Narod	2007	55
6	Estrogen receptor status in CHEK2‐positive breast cancers: implications for chemoprevention Clinical Genetics ·Cezary Cybulski, Tomasz Huzarski, Tomasz Byrski, Jacek Gronwald, Tadeusz Dębniak, Anna Jakubowska, Bohdan Górski, Dominika Wokołorczyk, Bartłomiej Masojć, SA Narod, Jan Lubiński	2008	45
7	Testing for CHEK2 in the cancer genetics clinic: ready for prime time? Clinical Genetics ·SA Narod	2010	41
8	Evaluation of the needs of spouses of female carriers of mutations in BRCA1 and BRCA2 Clinical Genetics ·Kelly Metcalfe, Alexander Liede, Martina Trinkaus, Danielle Hanna, SA Narod	2002	28
9	The contribution of founder mutations to early‐onset breast cancer in French‐Canadian women Clinical Genetics ·P Ghadirian, A. Robidoux, Ping Zhang, Robert E. Royer, Mohammad R. Akbari, S Zhang, Eve Fafard, Maurício Magalhães Costa, G. Martin, Claude Potvin, Érica Patocskai, Nicole Larouche, Rami Younan, Edgard Nassif, Sylvie Giroux, SA Narod, François Rousseau, William D. Foulkes	2009	27
10	BRCA1 and BRCA2 mutations among familial breast cancer patients from Costa Rica Clinical Genetics ·GA Gutiérrez Espeleta, M Llacuachaqui, Lourdes García‐Jiménez, Mercedes Herrera, Kenneth Loáiciga Vega, Adolfo Ortiz Barboza, Robert E. Royer, S Li, SA Narod	2011	24
11	The contribution of founder mutations in BRCA1 to breast cancer in Belarus Clinical Genetics ·N Uglanitsa, Oleg Oszurek, K Uglanitsa, E Savonievich, Jan Lubiński, Cezary Cybulski, Tadeusz Dębniak, SA Narod, Jacek Gronwald	2010	20
12	High risk genes predisposing to prostate cancer development—do they exist? Prostate Cancer and Prostatic Diseases ·Rashmi Singh, Rosalind A. Eeles, Francine Durocher, Jacques Simard, S M Edwards, Michael D. Badzioch, Z. Kote-Jarai, M. Dawn Teare, Deborah Ford, David Dearnaley, Audrey Ardern‐Jones, A Murkin, Anna Dowe, Robert Shearer, Jo A. Kelly, Fernand Labrie, Douglas F. Easton, SA Narod, P Tonin, William D. Foulkes, (unknown)	2000	17
13	Screening for BRCA1 and BRCA2 mutations among French‐Canadian breast cancer cases attending an outpatient clinic in Montreal Clinical Genetics ·P Ghadirian, A. Robidoux, Edgard Nassif, G. Martin, Claude Potvin, Érica Patocskai, Rami Younan, Nicole Larouche, A Venne, S Zhang, Robert E. Royer, SA Narod	2013	12
14	Selenium and the risk of cancer in BRCA1 carriers Hereditary Cancer in Clinical Practice ·Jan Lubiński, Katarzyna Jaworska, Katarzyna Durda, Anna Jakubowska, Tomasz Huzarski, Tomasz Byrski, Małgorzata Stawicka, Jacek Gronwald, Bohdan Górski, Wojciech Wąsowicz, Ewa Kilar, Marek Szwiec, Dariusz Surdyka, Elżbieta Marczyk, Peng Sun, SA Narod	2011	10
15	Earlier Age of Onset in BRCA Carriers—Anticipation or Cohort Effect? Current Oncology ·SA Narod	2011	7
16	Clinical implications of genetic testing for BRCA1 and BRCA2 mutations in Austria Clinical Genetics ·Christian F. Singer, Daniela Muhr, Christine Rappaport, M. Tea, Daphne Gschwantler‐Kaulich, A. Fink-Retter, G Pfeiler, Andreas Berger, Peng Sun, SA Narod	2013	6
17	Neoadjuvant chemotherapy with Cisplatin in BRCA1 mutation carriers – results of treatment Hereditary Cancer in Clinical Practice ·Tomasz Byrski, Jacek Gronwald, Tomasz Huzarski, Elżbieta Marczyk, Paweł Blecharz, Oleg Ashuryk, Cezary Cybulski, Dorota Zuziak, Rafał Wiśniowski, Dariusz Godlewski, SA Narod, Jan Lubiński	2012	4
18	Familial and hormonal risk factors for papillary serous uterine cancer. PubMed ·L. Elit, T. Pal, Ran Goshen, Helena Jernström, Ida Ackerman, Anthony Fyles, Mark Carey, Margot Mitchell, Jennifer Aubé, SA Narod	2002	4

About SA Narod

SA Narod is a scholar working on Genetics, Cancer Research, Reproductive Medicine, Public Health, Environmental and Occupational Health and Oncology, having authored 18 papers that have together received 1.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (15 papers), Cancer Genomics and Diagnostics (5 papers), DNA Repair Mechanisms (5 papers), Genomic variations and chromosomal abnormalities (4 papers), Breast Cancer Treatment Studies (2 papers), Male Breast Health Studies (2 papers), Estrogen and related hormone effects (2 papers) and Ovarian cancer diagnosis and treatment (2 papers). The work is most often cited by research in Genetics (800 citations), Reproductive Medicine (184 citations), Cancer Research (282 citations), Pathology and Forensic Medicine (220 citations) and Oncology (215 citations). SA Narod has collaborated with scholars based in Canada, United States and Poland. Frequent co-authors include Alexander Liede, William D. Foulkes, Jan Lubiński, Cezary Cybulski, Joanne Honeyford, Jean‐Sébastien Brunet, Elizabeth Warner, Nancy Hamel, Paul E. Goss and Wendy S. Meschino. Their work appears in journals such as Clinical Genetics, JNCI Journal of the National Cancer Institute, Prostate Cancer and Prostatic Diseases, Breast Cancer Research and Treatment and Cancer Research.

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