D. Gareth Evans

Active 1960–2025

Also published as
D Gareth Evans
631
Papers
107,640
Citations
175
h-index
580
i10-index

Citations

Citations per year for D. Gareth Evans1962: 2 citations1965: 1 citations1966: 1 citations1968: 1 citations1970: 1 citations1971: 2 citations1973: 12 citations1974: 17 citations1975: 18 citations1976: 22 citations1977: 66 citations1978: 83 citations1979: 65 citations1980: 75 citations1981: 51 citations1982: 64 citations1983: 41 citations1984: 68 citations1985: 53 citations1986: 35 citations1987: 48 citations1988: 46 citations1989: 25 citations1990: 54 citations1991: 67 citations1992: 70 citations1993: 122 citations1994: 96 citations1995: 111 citations1996: 150 citations1997: 169 citations1998: 191 citations1999: 179 citations2000: 237 citations2001: 212 citations2002: 266 citations2003: 290 citations2004: 343 citations2005: 345 citations2006: 423 citations2007: 529 citations2008: 568 citations2009: 600 citations2010: 730 citations2011: 682 citations2012: 646 citations2013: 718 citations2014: 795 citations2015: 707 citations2016: 828 citations2017: 788 citations2018: 724 citations2019: 2,422 citations2020: 3,034 citations2021: 2,775 citations2022: 2,323 citations2023: 1,667 citations2024: 2,745 citations2025: 1,087 citations2026: 26 citations1963–1964: no citations, so these years are not shown1967: no citations, so this year is not shown1969: no citations, so this year is not shown1972: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 7,581 citing papers, 23.9% of this breakdownUnited Kingdom: 3,243 citing papers, 10.2% of this breakdownGermany: 1,575 citing papers, 5% of this breakdownCanada: 1,512 citing papers, 4.8% of this breakdownChina: 1,451 citing papers, 4.6% of this breakdownItaly: 1,377 citing papers, 4.4% of this breakdownAustralia: 1,288 citing papers, 4.1% of this breakdownNetherlands: 1,225 citing papers, 3.9% of this breakdownFrance: 1,149 citing papers, 3.6% of this breakdownSpain: 925 citing papers, 2.9% of this breakdownSweden: 741 citing papers, 2.3% of this breakdownJapan: 611 citing papers, 1.9% of this breakdown
0%23.9%Other 28.4%

Fields

  • Medicine50.6%
  • Biochemistry, Genetics and Molecular Biology39.7%
  • Computer Science2.3%
  • Neuroscience1.4%
  • Immunology and Microbiology1.1%
  • Materials Science0.6%
  • Other4.3%

Topics

  • BRCA gene mutations in cancer7.2%
  • Genetic factors in colorectal cancer3.6%
  • Cancer Genomics and Diagnostics2.6%
  • Neurofibromatosis and Schwannoma Cases2.4%
  • DNA Repair Mechanisms2.2%
  • Breast Cancer Treatment Studies2%
  • Other80%

Coauthors

All papers

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  1. Risks of Breast, Ovarian, and Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jean‐Pierre Fricker, Laurence Faivre, Pascaline Berthet, Maartje J. Hooning, Lizet E. van der Kolk, Carolien M. Kets, Muriel A. Adank, Esther M. John, Wendy K. Chung, Irene L. Andrulis, Melissa C. Southey, Mary B. Daly, Saundra S. Buys, Ana Osório, Christoph Engel, Karin Kast, Rita K. Schmutzler, Trinidad Caldés, Anna Jakubowska, Jacques Simard, Michael Friedländer, Sue‐Anne McLachlan, Eva Macháčková, Lenka Foretová, Yen Y. Tan, Christian F. Singer, Edith Oláh, Anne‐Marie Gerdes, Brita Arver, Håkan Olsson - JAMA 2017 cited by 2,863

  2. Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Natalia Bogdanova, Stig E. Bojesen, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Hiltrud Brauch, Michael Bremer, Hermann Brenner, Adam R. Brentnall, Ian W. Brock, Angela Brooks‐Wilson, Sara Y. Brucker, Thomas Brüning, Barbara Burwinkel, Daniele Campa, Brian D. Carter, Jose E. Castelao, Stephen J. Chanock, Rowan T. Chlebowski, Hans Christiansen, Christine L. Clarke, J. Margriet Collée, Emilie Cordina‐Duverger, Sten Cornelissen, Fergus J. Couch, Angela Cox, Simon S. Cross, Kamila Czene, Mary B. Daly, Peter Devilee, Thilo Dörk, Isabel dos‐Santos‐Silva, Martine Dumont, Lorraine Durcan, Miriam Dwek, Diana M. Eccles, Arif B. Ekici, A. Heather Eliassen, Carolina Ellberg, Christoph Engel, Mikael Eriksson, D. Gareth Evans, Peter A. Fasching, Jonine D. Figueroa, Olivia Fletcher, Henrik Flyger, Asta Försti, Lin Fritschi, Marike Gabrielson, Manuela Gago-Domínguez, Susan M. Gapstur, José Á. García-Sáenz, Mia M. Gaudet, V. Georgoulias, Graham G. Giles, I. R. Gilyazova, Gord Glendon, Mark S. Goldberg, David E. Goldgar, Anna González‐Neira, Grethe I.G. Alnæs, Mervi Grip, Jacek Gronwald, Anne Grundy, Pascal Guénel, Lothar Haeberle, Eric Hahnen, Christopher A. Haiman, Niclas Håkansson, Ute Hamann, Susan E. Hankinson and 169 more - The American Journal of Human Genetics 2018 cited by 1,183

  3. Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Bernardo Bonanni, Davide Bondavalli, Åke Borg, Hiltrud Brauch, Hermann Brenner, Ignacio Briceño, Annegien Broeks, Sara Y. Brucker, Thomas Brüning, Barbara Burwinkel, Saundra S. Buys, Helen Byers, Trinidad Caldés, Maria A. Caligo, Mariarosaria Calvello, Daniele Campa, Jose E. Castelao, Jenny Chang‐Claude, Stephen J. Chanock, Melissa Christiaens, Hans Christiansen, Wendy K. Chung, Kathleen Claes, Christine L. Clarke, Sten Cornelissen, Fergus J. Couch, Angela Cox, Simon S. Cross, Kamila Czene, Mary B. Daly, Peter Devilee, Orland Dı́ez, Susan M. Domchek, Thilo Dörk, Miriam Dwek, Diana M. Eccles, Arif B. Ekici, D. Gareth Evans, Peter A. Fasching, Jonine D. Figueroa, Lenka Foretová, Florentia Fostira, Eitan Friedman, Debra Frost, Manuela Gago-Domínguez, Susan M. Gapstur, Judy E. Garber, José Á. García-Sáenz, Mia M. Gaudet, Simon A. Gayther, Graham G. Giles, Andrew K. Godwin, Mark S. Goldberg, David E. Goldgar, Anna González‐Neira, Mark H. Greene, Jacek Gronwald, Pascal Guénel, Lothar Häberle, Eric Hahnen, Christopher A. Haiman, Christopher R. Hake, Per Hall, Ute Hamann, Elaine F. Harkness, Bernadette A. M. Heemskerk‐Gerritsen, Peter Hillemanns and 176 more - Nature Genetics 2020 cited by 567

  4. Personalized early detection and prevention of breast cancer: ENVISION consensus statement

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter Devilee, Suzette Delaloge, Marjanka K. Schmidt, Martin Widschwendter - Nature Reviews Clinical Oncology 2020 cited by 439

  5. Decoding the transcriptome of calcified atherosclerotic plaque at single-cell resolution

    Authors: , , , - Communications Biology 2022 cited by 199

  6. Germline BRCA Mutations Are Associated With Higher Risk of Nodal Involvement, Distant Metastasis, and Poor Survival Outcomes in Prostate Cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lucy Side, Jacqueline Eason, Alex Murray, Antonis C. Antoniou, Douglas F. Easton, Zsofia Kote‐Jarai, Rosalind A. Eeles - Journal of Clinical Oncology 2013 cited by 824

  7. Average Risks of Breast and Ovarian Cancer Associated with BRCA1 or BRCA2 Mutations Detected in Case Series Unselected for Family History: A Combined Analysis of 22 Studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Fiona Lalloo, D. Gareth Evans, Douglas F. Easton - The American Journal of Human Genetics 2003 cited by 3,685

  8. The effects of intermittent or continuous energy restriction on weight loss and metabolic disease risk markers: a randomized trial in young overweight women

    Authors: , , , , , , , , , , , , , , , - International Journal of Obesity 2010 cited by 813

  9. Revised diagnostic criteria for neurofibromatosis type 1 and Legius syndrome: an international consensus recommendation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Vanessa L. Merker, Miriam J. Smith, David A. Stevenson, Monique Anten, Arthur S. Aylsworth, Diana Baralle, S. Barbarot, Fred G. Barker, Shay Ben‐Shachar, Amanda L. Bergner, D. Bessis, Ignacio Blanco, Cathérine Cassiman, Patricia Ciavarelli, Maurizio Clementi, Thierry Frébourg, Marco Giovannini, Dorothy Halliday, Chris Hammond, C. Oliver Hanemann, Helen Hanson, Arvid Heiberg, K.H. Ly, Michel Kalamarides, Matthias A. Karajannis, Daniela Kroshinsky, Margarita Larralde, Conxi Lázaro, Lu Q. Le, Michael P. Link, Robert Listernick, Mia MacCollin, Conor Mallucci, Christopher L. Moertel, Amy Mueller, Joanne Ngeow, Rianne Oostenbrink, Roger J. Packer, Laura Papi, Allyson Parry, Juha Peltonen, Dominique C. Pichard, Bruce Poppe, Nilton Alves de Rezende, Luiz Oswaldo Carneiro Rodrigues, Tena Rosser, Martino Ruggieri, Eduard Serra, Verena Steinke‐Lange, Stavros Stivaros, Amy Taylor, Jaan Toelen, James H. Tonsgard, Eva Trevisson, Meena Upadhyaya, Ali Varan, Meredith Wilson, Hao Wu, Gelareh Zadeh, Susan Huson, D. Gareth Evans, Scott R. Plotkin - Genetics in Medicine 2021 cited by 771

  10. Cancer Risks Associated With BRCA1 and BRCA2 Pathogenic Variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tanja N. Fehm, Florentia Fostira, George Fountzilas, Megan Frone, Vanesa Garcia-Barberan, Pilar Garre, Marion Gauthier-Villars, Andrea Gehrig, Gord Glendon, David E. Goldgar, Lisa Golmard, Mark H. Greene, Eric Hahnen, Ute Hamann, Helen Hanson, Tiara Hassan, Julia Hentschel, Judit Horvath, Louise Izatt, Ramunas Janavicius, Yue Jiao, Esther M. John, Beth Y. Karlan, Sung-Won Kim, Irene Konstantopoulou, Ava Kwong, Anthony Laugé, Jong Won Lee, Fabienne Lesueur, Noura Mebirouk, Alfons Meindl, Emmanuelle Mouret-Fourme, Hannah Musgrave, Joanne Ngeow Yuen Yie, Dieter Niederacher, Sue K. Park, Inge Sokilde Pedersen, Juliane Ramser, Susan J. Ramus, Johanna Rantala, Muhammad U. Rashid, Florian Reichl, Julia Ritter, Andreas Rump, Marta Santamariña, Claire Saule, Gunnar Schmidt, Rita K. Schmutzler, Leigha Senter, Saba Shariff, Christian F. Singer, Melissa C. Southey, Dominique Stoppa-Lyonnet, Christian Sutter, Yen Tan, Soo Hwang Teo, Mary Beth Terry, Mads Thomassen, Marc Tischkowitz, Amanda E. Toland, Diana Torres, Ana Vega, Sebastian A. Wagner, Shan Wang-Gohrke, Barbara Wappenschmidt, Bernhard H. F. Weber, Drakoulis Yannoukakos, Amanda B. Spurdle, Douglas F. Easton, Georgia Chenevix-Trench and 2 more - Journal of Clinical Oncology 2022 cited by 275

  11. Cancer Risks Associated With GermlinePALB2Pathogenic Variants: An International Study of 524 Families

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Antoine De Pauw, Orland Dı́ez, Jill S. Dolinsky, Susan M. Domchek, Christoph Engel, D. Gareth Evans, Florentia Fostira, Judy E. Garber, Lisa Golmard, Ellen L. Goode, Stephen B. Gruber, Eric Hahnen, Christopher R. Hake, Tuomas Heikkinen, Judith Hurley, Ramūnas Janavičius, Zdeněk Kleibl, Petra Kleiblová, Irene Konstantopoulou, Anders Kvist, Holly LaDuca, Ann S. G. Lee, Fabienne Lesueur, Eamonn R. Maher, Arto Mannermaa, Siranoush Manoukian, Rachel McFarland, Wendy McKinnon, Alfons Meindl, Kelly Metcalfe, Nur Aishah Mohd Taib, Jukka S. Moilanen, Katherine L. Nathanson, Susan L. Neuhausen, Pei Sze Ng, Tú Nguyen‐Dumont, Sarah M. Nielsen, Florian Obermair, Kenneth Offit, Olufunmilayo I. Olopade, Laura Ottini, Judith Penkert, Katri Pylkäs, Paolo Radice, Susan J. Ramus, Vilius Rudaitis, Lucy Side, Rachel Silva‐Smith, Valentina Silvestri, Anne‐Bine Skytte, Thomas Slavin, Jana Soukupová, Carlo Tondini, Alison H. Trainer, Gary Unzeitig, Lydia Usha, Thomas van Overeem Hansen, James Whitworth, Marie Wood, Cheng Har Yip, Sook‐Yee Yoon, Amal Yussuf, George Zogopoulos, David E. Goldgar, John L. Hopper, Georgia Chenevix‐Trench, Paul D.P. Pharoah, Sophia George, Judith Balmañà, Claude Houdayer and 19 more - Journal of Clinical Oncology 2019 cited by 418

  12. Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Reinhard Büttner, Heike Görgens, Elke Holinski‐Feder, Monika Morak, Stefanie Holzapfel, Robert Hüneburg, Magnus von Knebel Doeberitz, Markus Loeffler, Nils Rahner, Hans K. Schackert, Verena Steinke‐Lange, Wolff Schmiegel, Deepak Vangala, Kirsi Pylvänäinen, Laura Renkonen‐Sinisalo, John L. Hopper, Aung Ko Win, Robert W. Haile, Noralane M. Lindor, Steven Gallinger, Loı̈c Le Marchand, Polly A. Newcomb, Jane C. Figueiredo, Stephen N. Thibodeau, Karin Wadt, Christina Therkildsen, Henrik Okkels, Zohreh Ketabi, Leticia Moreira, Ariadna Sánchez, Miquel Serra‐Burriel, Marta Pineda, Matilde Navarro, Ignacio Blanco, Kate Green, Fiona Lalloo, Emma J. Crosbie, James Hill, Oliver G. Denton, Ian M. Frayling, Einar Andreas Rødland, Hans F. A. Vasen, Miriam Mints, Florencia Neffa, Patricia Esperón, Karin Álvarez, Revital Kariv, Guy Rosner, Tamara Alejandra Piñero, María Laura González, Pablo Kalfayan, Douglas Tjandra, Ingrid Winship, Finlay Macrae, Gabriela Möslein, Jukka‐Pekka Mecklin, Maartje Nielsen, Pål Møller - Genetics in Medicine 2019 cited by 649

  13. Cancer prevention with aspirin in hereditary colorectal cancer (Lynch syndrome), 10-year follow-up and registry-based 20-year data in the CAPP2 study: a double-blind, randomised, placebo-controlled trial

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mary Porteous, Julian R. Sampson, Rodney J. Scott, Lucy Side - The Lancet 2020 cited by 403

  14. Risk reduction and screening of cancer in hereditary breast-ovarian cancer syndromes: ESMO Clinical Practice Guideline

    Authors: , , , , , , , , , , , , , , , , , - Annals of Oncology 2022 cited by 276

  15. Cancer risk and survival in path_MMR carriers by gene and gender up to 75 years of age: a report from the Prospective Lynch Syndrome Database

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mev Dominguez–Valentin, Ian M. Frayling, John‐Paul Plazzer, Kirsi Pylvänäinen, Maurizio Genuardi, Jukka‐Pekka Mecklin, Gabriela Moeslein, Julian R. Sampson, Gabriel Capellá - Gut 2017 cited by 573

  16. Specifications of the ACMG/AMP variant interpretation guidelines for germline TP53 variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Human Mutation 2020 cited by 165

  17. Guidelines for the Li–Fraumeni and heritable TP53-related cancer syndromes

    Authors: , , , , , - European Journal of Human Genetics 2020 cited by 329

  18. Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1 / 2 (CIMBA)

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Monica Barile, Sara Volorio, Barbara Pasini, Riccardo Dolcetti, Anna Laura Putignano, Laura Ottini, Paolo Radice, Ute Hamann, Muhammad Usman Rashid, Frans B.L. Hogervorst, Mieke Kriege, Rob B. van der Luijt, Susan Peock, Debra Frost, D. Gareth Evans, Carole Brewer, Lisa Walker, Mark T. Rogers, Lucy Side, Catherine Houghton, JoEllen Weaver, Andrew K. Godwin, Rita K. Schmutzler, Barbara Wappenschmidt, Alfons Meindl, Karin Kast, Norbert Arnold, Dieter Niederacher, Christian Sutter, Helmut Deißler, Doroteha Gadzicki, Sabine Preisler‐Adams, Raymonda Varon-Mateeva, Ines Schönbuchner, Heidrun Gevensleben, Dominique Stoppa‐Lyonnet, Muriel Belotti, Laure Barjhoux, Claudine Isaacs, Beth N. Peshkin, Trinidad Caldés, Miguel de la Hoya, Carmen Cañadas, Tuomas Heikkinen, Päivi Heikkilä, Kristiina Aittomäki, Ignacio Blanco, Conxi Lázaro, Joan Brunet, Bjarni A. Agnarsson, Aðalgeir Arason, Rósa B. Barkardóttir, Martine Dumont, Jacques Simard, Marco Montagna, Simona Agata, Emma D’Andrea, Max Yan, Stephen B. Fox, Timothy R. Rebbeck, Wendy S. Rubinstein, Nadine Tung, Judy E. Garber, Xianshu Wang, Zachary Fredericksen, V. Shane Pankratz, Noralane M. Lindor, Csilla I. Szabo, Kenneth Offit, Rita A. Sakr and 33 more - Cancer Epidemiology Biomarkers & Prevention 2012 cited by 668

  19. Cancer Screening Recommendations for Individuals with Li-Fraumeni Syndrome

    Authors: , , , , , , , , , , , , , , , , , , , , , - Clinical Cancer Research 2017 cited by 521

  20. Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - The Lancet Oncology 2018 cited by 495

  21. EANO guideline on the diagnosis and treatment of vestibular schwannoma

    Authors: , , , , , , , , , , , , , , - Neuro-Oncology 2019 cited by 437

  22. Gene-Panel Sequencing and the Prediction of Breast-Cancer Risk

    Authors: , , , , , , , , , , , , , , , , - New England Journal of Medicine 2015 cited by 937

  23. Birth incidence and prevalence of tumor‐prone syndromes: Estimates from a UK family genetic register service

    Authors: , , , , , , - American Journal of Medical Genetics Part A 2010 cited by 997

  24. The effect of intermittent energy and carbohydrate restrictionv. daily energy restriction on weight loss and metabolic disease risk markers in overweight women

    Authors: , , , , , , , , , , , , , , , - British Journal Of Nutrition 2013 cited by 458