Nancy Hamel

6.3k citations

58 papers · 2.4k indexed · h-index 25

Impact in

Cancer Research top 2%
- Cancer Genomics and Diagnostics
- Breast Cancer Treatment Studies
Genetics top 1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities

Papers in ⓘ

Genetics 31
- BRCA gene mutations in cancer 27
- Genomic variations and chromosomal abnormalities 8
Cancer Research 11
- Cancer Genomics and Diagnostics 7

Co-authors: William D. Foulkes (52 shared papers)Pierre O. Chappuis (5 shared papers)Nora Wong (7 shared papers)Jean‐Sébastien Brunet (4 shared papers)Marc Tischkowitz (12 shared papers)Nelly Sabbaghian (8 shared papers)Louis R. Bégin (4 shared papers)John R. Goffin (2 shared papers)
Journals: British Journal of Cancer (5 papers)Cancer Research (4 papers)Clinical Genetics (4 papers)Journal of Medical Genetics (3 papers)Scientific Reports (2 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Nancy Hamel

54 papers receiving 2.4k citations

Peers

Countries citing papers authored by Nancy Hamel

Since Specialization

Citations

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

Fields of papers citing papers by Nancy Hamel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Showing the 20 most-cited of 58 papers — load more, or switch the sort, to bring in the rest.

#	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	The Prognostic Implication of the Basal-Like (Cyclin Ehigh/p27low/p53+/Glomeruloid-Microvascular-Proliferation+) Phenotype of *BRCA1* -Related Breast Cancer Cancer Research ·William D. Foulkes, Jean‐Sébastien Brunet, Ingunn M. Stefansson, Oddbjørn Straume, Pierre O. Chappuis, Louis R. Bégin, Nancy Hamel, John R. Goffin, Nora Wong, Michel Trudel, Linda Kapusta, Peggy L. Porter, Lars A. Akslen	2004	300
3	Analysis ofPALB2/FANCN-associated breast cancer families Proceedings of the National Academy of Sciences ·Marc Tischkowitz, Bing Xia, Nelly Sabbaghian, Jorge S. Reis‐Filho, Nancy Hamel, Guilan Li, Erik H. van Beers, Lili Li, Tayma Khalil, Louise Quenneville, Atilla Ömeroğlu, Aletta Poll, Patricia Lepage, Nora Wong, Petra M. Nederlof, Alan Ashworth, Patricia N. Tonin, Steven A. Narod, David M. Livingston, William D. Foulkes	2007	160
4	TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations: distinctive spectrum and structural distribution. PubMed ·Marc S. Greenblatt, Pierre O. Chappuis, Jeffrey P. Bond, Nancy Hamel, William D. Foulkes	2001	151
5	Extending the phenotypes associated withDICER1mutations Human Mutation ·William D. Foulkes, Amin Bahubeshi, Nancy Hamel, Barbara Pasini, Sofia Asioli, Gareth Baynam, Catherine S. Choong, Adrian Charles, Richard P. Frieder, Megan K. Dishop, Nicole Graf, Mesiha Ekim, Dorothée Bouron‐Dal Soglio, Jocelyne Arseneau, Robert H. Young, Nelly Sabbaghian, Archana Srivastava, Marc Tischkowitz, John R. Priest	2011	143
6	Identification of a novel truncating PALB2mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women Breast Cancer Research ·William D. Foulkes, Parviz Ghadirian, Mohammed Reza Akbari, Nancy Hamel, Sylvie Giroux, Nelly Sabbaghian, Andrew D. Darnel, Robert E. Royer, Aletta Poll, Eve Fafard, André Robidoux, G. Martin, Tarek A. Bismar, Marc Tischkowitz, François Rousseau, Steven A. Narod	2007	107
7	Biallelic Deleterious BRCA1 Mutations in a Woman with Early-Onset Ovarian Cancer Cancer Discovery ·Susan M. Domchek, Jiang-bo Tang, Jill E. Stopfer, Dana R. Lilli, Nancy Hamel, Marc Tischkowitz, Álvaro N.A. Monteiro, Troy E. Messick, Jacquelyn M. Powers, Alexandria Yonker, Fergus J. Couch, David E. Goldgar, H. Rosemarie Davidson, Katherine L. Nathanson, William D. Foulkes, Roger A. Greenberg	2012	101
8	Germline DICER1 mutations and familial cystic nephroma Journal of Medical Genetics ·Amin Bahubeshi, Nebıl Bal, Thomas Rio Frio, Nancy Hamel, Carly Pouchet, Ahmet Yılmaz, Dorothée Bouron‐Dal Soglio, Gretchen M. Williams, M Tischkowitz, John R. Priest, William D. Foulkes	2010	87
9	Impact of germline BRCA1 mutations and overexpression of p53 on prognosis and response to treatment following breast carcinoma Cancer ·John R. Goffin, Pierre O. Chappuis, Louis R. Bégin, Nora Wong, Jean‐Sébastien Brunet, Nancy Hamel, Ann‐Josée Paradis, Jeff Boyd, William D. Foulkes	2003	80
10	Impaired RASGRF1/ERK–mediated GM-CSF response characterizes CARD9 deficiency in French-Canadians Journal of Allergy and Clinical Immunology ·Christina Gavino, Nancy Hamel, Ji Zeng, Catherine Legault, Marie‐Christine Guiot, Jeffrey Chankowsky, Duncan Lejtenyi, Martine Lemire, Isabelle Alarie, Simon F. Dufresne, Jean-Nicolas Boursiquot, Fiona McIntosh, Mélanie J. Langelier, Marcel A. Behr, Donald C. Sheppard, William D. Foulkes, Donald C. Vinh	2015	63
11	Homozygous BUB1B Mutation and Susceptibility to Gastrointestinal Neoplasia New England Journal of Medicine ·Thomas Rio Frio, Josée N. Lavoie, Nancy Hamel, Felipe C. Geyer, Yaël B. Kushner, David J. Novak, Landon Wark, Cristian Capelli, Jorge S. Reis‐Filho, Sabine Mai, Tomi Pastinen, Marc Tischkowitz, Victoria Marcus, William D. Foulkes	2010	60
12	No association between P53 codon 72 polymorphism and risk of squamous cell carcinoma of the head and neck British Journal of Cancer ·Nancy Hamel, Martin J. Black, P Ghadirian, William D. Foulkes	2000	53
13	SWI/SNF-Compromised Cancers Are Susceptible to Bromodomain Inhibitors Cancer Research ·Tatiana Shorstova, Maud Marques, Jie Su, Jake Johnston, Claudia L. Kleinman, Nancy Hamel, Sidong Huang, Moulay A. Alaoui‐Jamali, William D. Foulkes, Michael Witcher	2019	52
14	Nuclear Genes Associated With a Single Brassica CMS Restorer Locws Influence Transcripts of Three Different Mitochondrial Gene Regions Genetics ·Mahipal Singh, Nancy Hamel, Rima Menasaa, Xu-Qing Li, Barbara Young, Martine Jean, Benoit Landry, Gregory G. Brown	1996	51
15	Familial rhabdoid tumour 'avant la lettre'—from pathology review to exome sequencing and back again The Journal of Pathology ·Leora Witkowski, Emilie Lalonde, Jian Zhang, Steffen Albrecht, Nancy Hamel, Luca Cavallone, Sandra May, James C. Nicholson, Nicholas Coleman, Matthew J. Murray, P. F. Tauber, David G. Huntsman, Stefan Schönberger, David W. Yandell, Martin Hasselblatt, Marc Tischkowitz, Jacek Majewski, William D. Foulkes	2013	51
16	Germline DICER1 mutation and associated loss of heterozygosity in a pineoblastoma: Figure 1 Journal of Medical Genetics ·Nelly Sabbaghian, Nancy Hamel, Archana Srivastava, Steffen Albrecht, John R. Priest, William D. Foulkes	2012	44
17	Frequency of the CHEK2 1100delC Mutation among Women with Breast Cancer: An International Study Cancer Research ·Shiyu Zhang, Catherine M. Phelan, Phil Zhang, François Rousseau, Parviz Ghadirian, André Robidoux, William D. Foulkes, Nancy Hamel, David R. McCready, Maureen Trudeau, Henry T. Lynch, Douglas E. Horsman, Maria Lourdes Leon De Matsuda, Zeba Aziz, Magda Conceição Barbosa Gomes, Maurício Magalhães Costa, Alexander Liede, Aletta Poll, Ping Sun, Steven A. Narod	2008	44
18	Glomeruloid microvascular proliferation is associated with p53 expression, germline BRCA1 mutations and an adverse outcome following breast cancer British Journal of Cancer ·JR Goffin, Oddbjørn Straume, Pierre O. Chappuis, JS Brunet, L R Bégin, Nancy Hamel, Nora Wong, LA Akslen, William D. Foulkes	2003	42
19	Ovarian embryonal rhabdomyosarcoma is a rare manifestation of the DICER1 syndrome Human Pathology ·Leanne de Kock, Harriet Druker, Evan Weber, Nancy Hamel, Jeffrey Traubici, David Malkin, Jocelyne Arseneau, Colin J.R. Stewart, Dorothée Bouron‐Dal Soglio, John R. Priest, William D. Foulkes	2015	40
20	Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach European Journal of Human Genetics ·(unknown), Marc Tischkowitz, Nancy Hamel, Marcelo A. Carvalho, Gabriel Birrane, Aditi Soni, Erik H. van Beers, Simon A. Joosse, Nora Wong, David J. Novak, Louise Quenneville, Scott Grist, Petra M. Nederlof, (unknown), Sean V. Tavtigian, Álvaro N.A. Monteiro, John A. A. Ladias, William D. Foulkes	2008	38

About Nancy Hamel

Nancy Hamel is a scholar working on Genetics, Cancer Research, Pathology and Forensic Medicine, Oncology and Molecular Biology, having authored 58 papers that have together received 2.4k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (27 papers), DNA Repair Mechanisms (18 papers), Genomic variations and chromosomal abnormalities (8 papers), Genetic factors in colorectal cancer (7 papers), Cancer Genomics and Diagnostics (7 papers), Congenital Diaphragmatic Hernia Studies (7 papers), CRISPR and Genetic Engineering (4 papers) and Chromatin Remodeling and Cancer (3 papers). The work is most often cited by research in Cancer Research (650 citations), Genetics (1.2k citations), Pathology and Forensic Medicine (494 citations), Oncology (633 citations) and Molecular Biology (1.3k citations). Nancy Hamel has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include William D. Foulkes, Pierre O. Chappuis, Nora Wong, Jean‐Sébastien Brunet, Marc Tischkowitz, Nelly Sabbaghian, Louis R. Bégin, John R. Goffin, Jeffrey P. Bond and Marc S. Greenblatt. Their work appears in journals such as British Journal of Cancer, Cancer Research, Clinical Genetics, Journal of Medical Genetics and Scientific Reports.

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.

Explore authors with similar magnitude of impact