Kimberly F. Doheny

Active 1993–2024

72
Papers
22,578
Citations
64
h-index
72
i10-index

Citations

Citations per year for Kimberly F. Doheny1993: 2 citations1994: 7 citations1995: 9 citations1996: 9 citations1997: 4 citations1998: 7 citations1999: 14 citations2000: 1 citations2001: 4 citations2002: 8 citations2003: 6 citations2004: 14 citations2005: 6 citations2006: 9 citations2007: 88 citations2008: 247 citations2009: 219 citations2010: 248 citations2011: 278 citations2012: 280 citations2013: 244 citations2014: 234 citations2015: 230 citations2016: 248 citations2017: 275 citations2018: 273 citations2019: 770 citations2020: 825 citations2021: 728 citations2022: 606 citations2023: 397 citations2024: 697 citations2025: 296 citations2026: 17 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,992 citing papers, 24% of this breakdownUnited Kingdom: 1,572 citing papers, 9.5% of this breakdownChina: 909 citing papers, 5.5% of this breakdownGermany: 825 citing papers, 5% of this breakdownCanada: 702 citing papers, 4.2% of this breakdownAustralia: 672 citing papers, 4% of this breakdownFrance: 585 citing papers, 3.5% of this breakdownNetherlands: 571 citing papers, 3.4% of this breakdownSweden: 520 citing papers, 3.1% of this breakdownItaly: 506 citing papers, 3.1% of this breakdownSpain: 446 citing papers, 2.7% of this breakdownDenmark: 321 citing papers, 1.9% of this breakdown
0%24%Other 30.1%

Fields

  • Biochemistry, Genetics and Molecular Biology54.3%
  • Medicine34.8%
  • Neuroscience3.7%
  • Immunology and Microbiology1.2%
  • Pharmacology, Toxicology and Pharmaceutics1%
  • Nursing1%
  • Other4%

Topics

  • Genetic Associations and Epidemiology10.3%
  • Genomics and Rare Diseases3.5%
  • BRCA gene mutations in cancer2.5%
  • Epigenetics and DNA Methylation2.3%
  • Parkinson's Disease Mechanisms and Treatments2%
  • Genomic variations and chromosomal abnormalities2%
  • Other77.4%

Coauthors

All papers

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  1. Genomic data in the All of Us Research Program

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Samantha J. Wirkus, Victoria A. Wagner, Jeffrey G. Meyer, Mine Cicek, Donna M. Muzny, Eric Venner, Michelle Mawhinney, Sean Griffith, Elvin Hsu, Hua Ling, Marcia K. Adams, Kimberly Walker, Taobo Hu, HarshaVardhan Doddapaneni, Christie Kovar, Mullai Murugan, Shannon Dugan, Ziad Khan, Eric Boerwinkle, Niall J. Lennon, Christina Austin‐Tse, Eric Banks, Michael Gatzen, Namrata Gupta, Emma Henricks, Katie Larsson, Sheli McDonough, Steven M. Harrison, Christopher Kachulis, Matthew S. Lebo, Cynthia L. Neben, Marcie Steeves, Alicia Y. Zhou, Joshua D. Smith, Christian D. Frazar, Colleen Davis, Karynne Patterson, Marsha M. Wheeler, Sean McGee, Christina M. Lockwood, Brian H. Shirts, Colin C. Pritchard, Mitzi L. Murray, Valeria Vasta, Dru F. Leistritz, M Richardson, Jillian G. Buchan, Aparna Radhakrishnan, Niklas Krumm, Brenna Ehmen, Sophie Schwartz, M. Morgan T. Aster, Kristian Cibulskis, Andrea Haessly, Rebecca Asch, Aurora Cremer, Kylee Degatano, Akum Shergill, Laura D. Gauthier, Samuel K. Lee, Aaron Hatcher, George Grant, Genevieve R. Brandt, Miguel Covarrubias, Eric Banks, Ashley Able, Ashley E. Green, Robert J. Carroll, Jennifer Zhang, Henry Robert Condon and 15 more - Nature 2024 cited by 795

  2. Genetic analyses of diverse populations improves discovery for complex traits

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alexandra Sockell, Karan Vahi, Marie Verbanck, Abhishek Vishnu, Ryan W. Walker, Kristin L. Young, Niha Zubair, Victor Acuña-Alonso, José Luis Ambite, Kathleen C. Barnes, Eric Boerwinkle, Erwin P. Böttinger, Carlos D. Bustamante, Christian Caberto, Samuel Canizales‐Quinteros, Matthew P. Conomos, Ewa Deelman, Ron Do, Kimberly F. Doheny, Lindsay Fernández‐Rhodes, Myriam Fornage, Benyam Hailu, Gerardo Heiss, Brenna M. Henn, Lucia A. Hindorff, Rebecca D. Jackson, Cecelia Laurie, Cathy C. Laurie, Yuqing Li, Dan-Yu Lin, Andrés Moreno‐Estrada, Girish N. Nadkarni, Paul J. Norman, Loreall Pooler, Alex P. Reiner, Jane Romm, Chiara Sabatti, Karla Sandoval, Xin Sheng, Eli A. Stahl, Daniel O. Stram, Timothy A. Thornton, Christina L. Wassel, Lynne R. Wilkens, Cheryl A. Winkler, Sachi Yoneyama, Steven Buyske, Christopher A. Haiman, Charles Kooperberg, Loı̈c Le Marchand, Ruth J. F. Loos, Tara C. Matise, Kari E. North, Ulrike Peters, Eimear E. Kenny, Christopher S. Carlson - Nature 2019 cited by 1,151

  3. Association analysis identifies 65 new breast cancer risk loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Habibul Ahsan, Kristiina Aittomäki, Hoda Anton‐Culver, Natalia Antonenkova, Volker Arndt, Kristan J. Aronson, Banu Arun, Paul L. Auer, François Bacot, Myrto Barrdahl, Caroline Baynes, Matthias W. Beckmann, Sabine Behrens, Javier Benı́tez, Marina Bermisheva, Leslie Bernstein, Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Bernardo Bonanni, Anne‐Lise Børresen‐Dale, Judith S. Brand, Hiltrud Brauch, Paul Brennan, Hermann Brenner, Louise A. Brinton, Per Broberg, Ian W. Brock, Annegien Broeks, Angela Brooks‐Wilson, Sara Y. Brucker, Thomas Brüning, Barbara Burwinkel, Katja Butterbach, Qiuyin Cai, Hui Cai, Trinidad Caldés, Federico Canzian, Ángel Carracedo, Brian D. Carter, Jose E. Castelao, Tsun Leung Chan, Ting‐Yuan David Cheng, Kee Seng Chia, Ji‐Yeob Choi, Hans Christiansen, Christine L. Clarke, NBCS Collaborators, Margriet Collée, Don Conroy, Emilie Cordina‐Duverger, Sten Cornelissen, David G. Cox, Angela Cox, Simon S. Cross, Julie M. Cunningham, Kamila Czene, Mary B. Daly, Peter Devilee, Kimberly F. Doheny, Thilo Dörk, Isabel dos‐Santos‐Silva, Martine Dumont, Lorraine Durcan, Miriam Dwek, Diana M. Eccles, Arif B. Ekici, A. Heather Eliassen, Carolina Ellberg, Mingajeva Elvira and 262 more - Nature 2017 cited by 1,598

  4. Discovery of common and rare genetic risk variants for colorectal cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hermann Brenner, Stefanie Brezina, Stephan Buch, Daniel D. Buchanan, Andrea N. Burnett‐Hartman, Katja Butterbach, Bette J. Caan, Peter T. Campbell, Christopher S. Carlson, Sergi Castellvı́-Bel, Andrew T. Chan, Jenny Chang-Claude, Stephen J. Chanock, María‐Dolores Chirlaque, Sang‐Hee Cho, Charles M. Connolly, Amanda J. Cross, Katarina Ćuk, Keith R. Curtis, Albert de la Chapelle, Kimberly F. Doheny, David Duggan, Douglas F. Easton, Sjoerd G. Elias, Faye Elliott, Dallas R. English, Edith J. M. Feskens, Jane C. Figueiredo, Rocky Fischer, Liesel M. FitzGerald, David Forman, Manish Gala, Steven Gallinger, W. James Gauderman, Graham G. Giles, Elizabeth M. Gillanders, Jian Gong, Phyllis J. Goodman, William M. Grady, John Grove, Andrea Gsur, Marc J. Gunter, Robert W. Haile, Jochen Hampe, Heather Hampel, Sophia Harlid, Richard B. Hayes, Philipp Hofer, Michael Hoffmeister, John L. Hopper, Wan‐Ling Hsu, Wen‐Yi Huang, Thomas J. Hudson, David J. Hunter, Gemma Ibáñez‐Sanz, Gregory Idos, Roxann Ingersoll, Rebecca D. Jackson, Eric J. Jacobs, Mark A. Jenkins, Amit D. Joshi, Corinne E. Joshu, Temitope O. Keku, Timothy J. Key, Hyeong Rok Kim, Emiko Kobayashi, Laurence N. Kolonel, Charles Kooperberg, Tilman Kühn, Sébastien Küry and 99 more - Nature Genetics 2018 cited by 605

  5. Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gerasimos Aravantinos, Norbert Arnold, Banu Arun, Brita Arver, Jacopo Azzollini, Judith Balmañà, Susana Banerjee, Laure Barjhoux, Rósa B. Barkardóttir, Yukie T. Bean, Matthias W Beckmann, Alicia Beeghly-Fadiel, Javier Benı́tez, Marina Bermisheva, Marcus Q. Bernardini, Michael J. Birrer, Line Bjorge, Amanda Black, Kenneth B. Blankstein, Marinus J. Blok, Clara Bodelón, Natalia Bogdanova, Anders Bojesen, Bernardo Bonanni, Åke Borg, Angela R. Bradbury, James D. Brenton, Carole Brewer, Louise A. Brinton, Per Broberg, Angela Brooks‐Wilson, Fiona Bruinsma, Joan Brunet, Bruno Buecher, Ralf Butzow, Saundra S. Buys, Trinidad Caldés, Maria A. Caligo, Ian Campbell, Rikki Cannioto, Michael E. Carney, Terence Cescon, Salina B Chan, Jenny Chang-Claude, Stephen J. Chanock, Xiao Qing Chen, Yoke-Eng Chiew, Jocelyne Chiquette, Wendy K. Chung, Kathleen Claes, Thomas Conner, Linda S. Cook, Jackie Cook, Daniel W. Cramer, Julie M. Cunningham, Aimee A. D’Aloisio, Mary B Daly, Francesca Damiola, Sakaeva Dina Damirovna, Agnieszka Dansonka‐Mieszkowska, Fanny Dao, Rosemarie Davidson, Anna DeFazio, Capucine Delnatte, Kimberly F. Doheny, Orland Dı́ez, Yuan Chun Ding, Jennifer A. Doherty, Susan M. Domchek, Cecilia M. Dorfling and 320 more - Nature Genetics 2017 cited by 553

  6. Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data

    Authors: , , , , , , , - The American Journal of Human Genetics 2012 cited by 551

  7. Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease

    Authors: , , , , , , , , , , , , , , , , , , - Nature Genetics 2010 cited by 814

  8. A Genome-Wide Association Study of Type 2 Diabetes in Finns Detects Multiple Susceptibility Variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Thomas A. Buchanan, Richard M. Watanabe, Timo T. Valle, Leena Kinnunen, Gonçalo R. Abecasis, Elizabeth Pugh, Kimberly F. Doheny, Richard N. Bergman, Jaakko Tuomilehto, Francis S. Collins, Michael Boehnke - Science 2007 cited by 2,781

  9. Detectable clonal mosaicism from birth to old age and its relationship to cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , William J. Blot, Lisa B. Signorello, Sue A. Ingles, Stephen J. Chanock, Sonja I. Berndt, Loı̈c Le Marchand, Brian E. Henderson, Kristine R. Monroe, John A. Heit, Mariza de Andrade, Sebastian M. Armasu, C Régnier, William L. Lowe, M. Geoffrey Hayes, Mary L. Marazita, Eleanor Feingold, Jeffrey C. Murray, Mads Melbye, Bjarke Feenstra, Jae H. Kang, Janey L. Wiggs, Gail P. Jarvik, Andrew McDavid, Venkatraman Seshan, Daniel B. Mirel, Andrew Crenshaw, Nataliya Sharopova, Anastasia L. Wise, Jess Shen, David R. Crosslin, David Levine, Xiuwen Zheng, Jenna Udren, Siiri Bennett, Sarah C. Nelson, Stephanie M. Gogarten, Matthew P. Conomos, Patrick J. Heagerty, Teri A. Manolio, Louis R. Pasquale, Christopher A. Haiman, Neil E. Caporaso, Bruce S. Weir - Nature Genetics 2012 cited by 599

  10. The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Suzanne M. Leal, Murat Günel, Shrikant Mane, Richard A. Gibbs, Eric Boerwinkle, Ada Hamosh, Jay Shendure, James R. Lupski, Richard P. Lifton, David Valle, Deborah A. Nickerson, Michael J. Bamshad - The American Journal of Human Genetics 2015 cited by 688

  11. Quality control and quality assurance in genotypic data for genome‐wide association studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Genetic Epidemiology 2010 cited by 498

  12. Quality Control Procedures for Genome‐Wide Association Studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Current Protocols in Human Genetics 2011 cited by 378

  13. Centers for Mendelian Genomics: A decade of facilitating gene discovery

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Harindra Arachchi, Mehmed M. Atik, Christina Austin‐Tse, Larry Babb, Tamara Bacus, Vahid Bahrambeigi, Suganthi Balasubramanian, Yavuz Bayram, Arthur L. Beaudet, Christine R. Beck, John W. Belmont, Jennifer E. Below, Kaya Bilgüvar, Corinne D. Boehm, Eric Boerwinkle, Philip M. Boone, Sara J. Bowne, Harrison Brand, Kati J. Buckingham, Alicia B. Byrne, Daniel G. Calame, Ian M. Campbell, Xiaolong Cao, Claudia M.B. Carvalho, Varuna Chander, Jaime Chang, Katherine R. Chao, Iván K. Chinn, Declan Clarke, Ryan L. Collins, Beryl B. Cummings, Zain Dardas, Moez Dawood, Kayla Delano, Stephanie DiTroia, HarshaVardhan Doddapaneni, Haowei Du, Renqian Du, Ruizhi Duan, Mohammad K. Eldomery, Christine M. Eng, Eleina England, Emily Evangelista, Selin Everett, Jawid M. Fatih, Adam L. Felsenfeld, Laurent C. Francioli, Christian D. Frazar, Jack Fu, Emmanuel Gamarra, Tomasz Gambin, Weiniu Gan, Mira Gandhi, Vijay Ganesh, Kiran Garimella, Laura D. Gauthier, Danielle Giroux, Claudia Gonzaga‐Jauregui, Julia K. Goodrich, William W. Gordon, Sean Griffith, Christopher M. Grochowski, Shen Gu, Sanna Gudmundsson, Stacey Hall, Adam Hansen, Tamar Harel, Arif Harmanci, Isabella Herman, Kurt N. Hetrick and 142 more - Genetics in Medicine 2022 cited by 80

  14. A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marina Bermisheva, Carl Blomqvist, Natalia Bogdanova, Stig E. Bojesen, Hiltrud Brauch, Hermann Brenner, Louise A. Brinton, Per Broberg, Sara Y. Brucker, Barbara Burwinkel, Trinidad Caldés, Federico Canzian, Brian D. Carter, Jose E. Castelao, Jenny Chang‐Claude, Xiaoqing Chen, Ting‐Yuan David Cheng, Hans Christiansen, Christine L. Clarke, Margriet Collée, Sten Cornelissen, Fergus J. Couch, David G. Cox, Angela Cox, Simon S. Cross, Julie M. Cunningham, Kamila Czene, Mary B. Daly, Peter Devilee, Kimberly F. Doheny, Thilo Dörk, Isabel dos‐Santos‐Silva, Martine Dumont, Miriam Dwek, Diana M. Eccles, Ursula Eilber, A. Heather Eliassen, Christoph Engel, Mikael Eriksson, Laura Fachal, Peter A. Fasching, Jonine D. Figueroa, Dieter Flesch‐Janys, Olivia Fletcher, Henrik Flyger, Lin Fritschi, Marike Gabrielson, Manuela Gago-Domínguez, Susan M. Gapstur, Montserrat García‐Closas, Mia M. Gaudet, Maya Ghoussaini, Graham G. Giles, Mark S. Goldberg, David E. Goldgar, Anna González‐Neira, Pascal Guénel, Eric Hahnen, Christopher A. Haiman, Niclas Håkansson, Per Hall, Emily Hallberg, Ute Hamann, Patricia Harrington, Alexander Hein, Belynda Hicks, Peter Hillemanns, Antoinette Hollestelle, Robert N. Hoover, John L. Hopper and 112 more - Nature Genetics 2018 cited by 246

  15. Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Larry A. Donoso, Lifeng Tian, Brian Kaderli, Dexter Hadley, Stephanie A. Hagstrom, Neal S. Peachey, Ronald Klein, Barbara E.K. Klein, Norimoto Gotoh, Kenji Yamashiro, Frederick L. Ferris, Jesen Fagerness, Robyn Reynolds, Lindsay A. Farrer, Ivana K. Kim, Joan W. Miller, Marta Cortón, Ángel Carracedo, Manuel Sánchez‐Salorio, Elizabeth Pugh, Kimberly F. Doheny, Marı́a Brión, Margaret M. DeAngelis, Daniel E. Weeks, Donald J. Zack, Emily Y. Chew, John R. Heckenlively, Nagahisa Yoshimura, Sudha K. Iyengar, Peter J. Francis, Nicholas Katsanis, Johanna M. Seddon, Jonathan L. Haines, Michael B. Gorin, Gonçalo R. Abecasis, Anand Swaroop, Robert N. Johnson, Everett Ai, H. Richard McDonald, Margaret Stolarczuk, Peter R. Pavan, Karina K. Billiris, Mohan Iyer, Matthew M. Menosky, Scott E. Pautler, Sharon M. Millard, G. Baker Hubbard, Thomas Aaberg, Lindy DuBois, Alice T. Lyon, Susan Anderson-Nelson, Lee M. Jampol, David V. Weinberg, Annie Muñana, Zuzanna Rozenbajgier, David H. Orth, Jack Cohen, Matthew MacCumber, Matthew MacCumber, Celeste Figliulo, Liz Porcz, James C. Folk, H. Culver Boldt, Stephen R. Russell, Rachel Ivins, Connie J. Hinz, Charles C. Barr, Steve Bloom, Ken Jaegers, Brian Kritchman and 68 more - National Academy of Sciences, Proceedings of the National Academy of Sciences 2010 cited by 516

  16. The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Stefanie A. Nelson, Stephen Demetriades, David E. Goldgar, Fergus J. Couch, Judith L. Forman, Graham G. Giles, David V. Conti, Heike Bickeböller, Angela Risch, Mélanie Waldenberger, Irene Brüske‐Hohlfeld, Belynda Hicks, Hua Ling, Lesley McGuffog, Andrew Lee, Karoline Kuchenbaecker, Penny Soucy, Judith Manz, Julie M. Cunningham, Katja Butterbach, Zsofia Kote‐Jarai, Peter Kraft, Liesel M. FitzGerald, Sara Lindström, Marcia Adams, James McKay, Catherine M. Phelan, Sara Benlloch, Linda E. Kelemen, Paul Brennan, Marjorie J. Riggan, Tracy A. O’Mara, Hongbing Shen, Yongyong Shi, Deborah J. Thompson, Marc T. Goodman, Sune F. Nielsen, Andrew Berchuck, Sylvie LaBoissière, Stephanie L. Schmit, Tameka Shelford, Christopher K. Edlund, Jack A. Taylor, John K. Field, Sue K. Park, Kenneth Offit, Mads Thomassen, Rita K. Schmutzler, Laura Ottini, Rayjean J. Hung, Jonathan Marchini, Ali Amin Al Olama, Ulrike Peters, Rosalind A. Eeles, Michael F. Seldin, Elizabeth M. Gillanders, Daniela Seminara, Antonis C. Antoniou, Paul D.P. Pharoah, Georgia Chenevix‐Trench, Stephen J. Chanock, Jacques Simard, Douglas F. Easton - Cancer Epidemiology Biomarkers & Prevention 2016 cited by 393

  17. Germline Sequencing Analysis to Inform Clinical Gene Panel Testing for Aggressive Prostate Cancer

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Robert J. MacInnis, Melissa C. Southey, Rosalind A. Eeles, Fredrik Wiklund, David V. Conti, Zsofia Kote‐Jarai, Christopher A. Haiman - JAMA Oncology 2023 cited by 51

  18. Whole-genome sequencing as an investigational device for return of hereditary disease risk and pharmacogenomic results as part of the All of Us Research Program

    Authors: , , , , , , , , , , , , , , , , , , , , - Genome Medicine 2022 cited by 63

  19. Genome‐Wide Association Analysis Reveals Genetic Heterogeneity of Sjögren's Syndrome According to Ancestry

    Authors: , , , , , , , , , , , , , , , , , , , - Arthritis & Rheumatology 2017 cited by 131

  20. Genomewide association study for susceptibility genes contributing to familial Parkinson disease

    Authors: , , , , , , , , , , , - Human Genetics 2008 cited by 444

  21. Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Annals of Neurology 2011 cited by 299

  22. Insights into genetics, human biology and disease gleaned from family based genomic studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tara C. Matise, Heidi L. Rehm, Mark Gerstein, Michael J. Bamshad, David Valle, James R. Lupski - Genetics in Medicine 2019 cited by 211

  23. Identification of HKDC1 and BACE2 as Genes Influencing Glycemic Traits During Pregnancy Through Genome-Wide Association Studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Diabetes 2013 cited by 154

  24. Variant‐level matching for diagnosis and discovery: Challenges and opportunities

    Authors: , , , , , , , , , , , , , , , , - Human Mutation 2022 cited by 44