kConFab

583 total citations
10 papers, 161 citations indexed

About

kConFab is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, kConFab has authored 10 papers receiving a total of 161 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Pathology and Forensic Medicine. Recurrent topics in kConFab's work include BRCA gene mutations in cancer (8 papers), DNA Repair Mechanisms (3 papers) and Cancer Genomics and Diagnostics (3 papers) kConFab is often cited by papers focused on BRCA gene mutations in cancer (8 papers), DNA Repair Mechanisms (3 papers) and Cancer Genomics and Diagnostics (3 papers) kConFab collaborates with scholars based in Australia, United States and France kConFab's co-authors include Georgia Chenevix‐Trench, Melissa C. Southey, Sarah Sawyer, Gillian Mitchell, Ian Campbell, Ella R. Thompson, Paul A. James, Alison H. Trainer, Ee Ming Wong and John L. Hopper and has published in prestigious journals such as PLoS ONE, International Journal of Molecular Sciences and Journal of Medical Genetics.

In The Last Decade

kConFab

10 papers receiving 158 citations

Peers

Countries citing papers authored by kConFab

Since Specialization

Citations

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

Fields of papers citing papers by kConFab

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of kConFab

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

All Works

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10 of 10 papers shown

#	Work	Indexed citations
1	VTRNA2-1: Genetic Variation, Heritable Methylation and Disease Association 2021 ·International Journal of Molecular Sciences ·Pierre‐Antoine Dugué, Chenglong Yu, (unknown), Ee Ming Wong, Jihoon E. Joo, Helen Tsimiklis, Fleur Hammet, Maryam Mahmoodi, (unknown), kConFab, John L. Hopper, Graham G. Giles, Roger L. Milne, Jason A. Steen, James G. Dowty, Tú Nguyen‐Dumont, Melissa C. Southey	16
2	Analysis of RAD51D in Ovarian Cancer Patients and Families with a History of Ovarian or Breast Cancer 2013 ·PLoS ONE ·Ella R. Thompson, Simone M. Rowley, Sarah Sawyer, kConFab, Diana Eccles, Alison H. Trainer, Gillian Mitchell, Paul A. James, Ian Campbell	30
3	Analysis of RAD51C germline mutations in high-risk breast and ovarian cancer families and ovarian cancer patients 2011 ·Human Mutation ·Ella R. Thompson, Samantha E. Boyle, Julie K. Johnson, Georgina L. Ryland, Sarah Sawyer, David Y.H. Choong, kConFab, Georgia Chenevix‐Trench, Alison H. Trainer, Geoffrey J. Lindeman, Gillian Mitchell, Paul A. James, Ian Campbell	53
4	A BRCA1 promoter variant (rs11655505) and breast cancer risk 2010 ·Journal of Medical Genetics ·Paolo Verderio, Sara Pizzamiglio, Melissa C. Southey, Amanda B. Spurdle, John L. Hopper, (unknown), Jonathan Beesley, kConFab, (unknown), R Schmutzler, Christoph Engel, Barbara Burwinkel, Peter Bugert, Filomena Ficarazzi, Siranoush Manoukian, Monica Barile, Barbara Wappenschmidt, Georgia Chenevix‐Trench, Paolo Radice, Paolo Peterlongo	6
5	Is MSH2 a breast cancer susceptibility gene? 2007 ·Familial Cancer ·Ee Ming Wong, Andrea Tesoriero, Gulietta M. Pupo, kConFab, (unknown), (unknown), Graham G. Giles, John L. Hopper, Graham J. Mann, David E. Goldgar, Melissa C. Southey	5
6	Chromosome 2q24.2 is lost in sporadic but not in BRCA1-associated ovarian carcinomas 2006 ·Pathology ·Morteza Aghmesheh, (unknown), Michael Friedländer, Jahn M. Nesland, J. Kærn, Michael Stewart, kConFab, Anne Dørum, Kathy Tucker, Michael F. Buckley	2
7	Ratio of male to female births in the offspring of BRCA1 and BRCA2 carriers 2005 ·Familial Cancer ·Georgia Chenevix‐Trench, Olga M. Sinilnikova, Graeme Suthers, Nirmala Pandeya, Sylvie Mazoyer, Joseph Sambrook, (unknown), David E. Goldgar, Henry T. Lynch, Gilbert Lenoir, (unknown), kConFab	2
8	Molecular characterization and cancer risk associated withBRCA1 andBRCA2 splice site variants identified in multiple-case breast cancer families 2005 ·Human Mutation ·Andrea Tesoriero, Ee Ming Wong, Mark A. Jenkins, John L. Hopper, kConFab, Melissa A. Brown, Georgia Chenevix‐Trench, Amanda B. Spurdle, Melissa C. Southey	39
9	027. Mapping novel breast cancer susceptibility genes by linkage analysis of Australian multiple case kindreds 2004 ·Reproduction Fertility and Development ·Graham J. Mann, Gulietta M. Pupo, Beth Newman, Deon J. Venter, John L. Hopper, Georgia Chenevix‐Trench, kConFab	1
10	A specific GFP expression assay, penetrance estimate, and histological assessment for a putative splice site mutation inBRCA1 2003 ·Human Mutation ·Melissa C. Southey, Andrea Tesoriero, Matthew A. Young, Andrew J. Holloway, Mark A. Jenkins, (unknown), (unknown), kConFab, Sue Anne McLachlan, Deon J. Venter, Jane E. Armes	7

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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