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Mary‐Claire King

Active 1973–2025

152
Papers
47,423
Citations
108
h-index
151
i10-index

Citations

Citations per year for Mary‐Claire King1974: 3 citations1975: 8 citations1976: 16 citations1977: 20 citations1978: 10 citations1979: 14 citations1980: 13 citations1981: 16 citations1982: 10 citations1983: 13 citations1984: 12 citations1985: 11 citations1986: 10 citations1987: 16 citations1988: 22 citations1989: 16 citations1990: 32 citations1991: 44 citations1992: 76 citations1993: 119 citations1994: 142 citations1995: 156 citations1996: 208 citations1997: 239 citations1998: 217 citations1999: 162 citations2000: 219 citations2001: 195 citations2002: 221 citations2003: 244 citations2004: 224 citations2005: 216 citations2006: 226 citations2007: 250 citations2008: 360 citations2009: 440 citations2010: 506 citations2011: 602 citations2012: 551 citations2013: 505 citations2014: 503 citations2015: 527 citations2016: 487 citations2017: 423 citations2018: 354 citations2019: 1,164 citations2020: 1,241 citations2021: 969 citations2022: 701 citations2023: 451 citations2024: 646 citations2025: 272 citations2026: 7 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 6,350 citing papers, 33.3% of this breakdownUnited Kingdom: 1,636 citing papers, 8.6% of this breakdownCanada: 881 citing papers, 4.6% of this breakdownGermany: 873 citing papers, 4.6% of this breakdownChina: 852 citing papers, 4.5% of this breakdownFrance: 734 citing papers, 3.9% of this breakdownItaly: 673 citing papers, 3.5% of this breakdownAustralia: 621 citing papers, 3.3% of this breakdownNetherlands: 615 citing papers, 3.2% of this breakdownSpain: 446 citing papers, 2.3% of this breakdownJapan: 427 citing papers, 2.2% of this breakdownSweden: 354 citing papers, 1.9% of this breakdown
0%33.3%Other 24.1%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology54.9%
  • Medicine29.3%
  • Neuroscience9%
  • Immunology and Microbiology1.9%
  • Agricultural and Biological Sciences1.4%
  • Psychology0.8%
  • Other2.7%

Topics

  • BRCA gene mutations in cancer6.1%
  • Genomic variations and chromosomal abnormalities4.3%
  • Genomics and Rare Diseases3.2%
  • DNA Repair Mechanisms3%
  • Genetics and Neurodevelopmental Disorders2.6%
  • Cancer Genomics and Diagnostics2.6%
  • Other78.2%

Coauthors

All papers

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  1. Evolution at Two Levels in Humans and Chimpanzees

    Authors: Mary‐Claire King, Allan C. Wilson - Science 1975 cited by 2,921

  2. Strong Association of De Novo Copy Number Mutations with Autism

    Authors: Jonathan Sebat, B. Lakshmi, Dheeraj Malhotra, Jennifer Troge, Christa Lese‐Martin, Tom Walsh, Boris Yamrom, Seungtai Yoon, A. Krasnitz, Jude Kendall, Anthony Leotta, Deepa Pai, Ray Zhang, Yoonha Lee, James Hicks, Sarah Spence, Annette T. Lee, Kaija Puura, Terho Lehtimäki, David H. Ledbetter, Peter K. Gregersen, Joel D. Bregman, James S. Sutcliffe, Vaidehi Jobanputra, Wendy K. Chung, Dorothy Warburton, Mary‐Claire King, David Skuse, Daniel H. Geschwind, T. Conrad Gilliam, Kenny Ye, Michael Wigler - Science 2007 cited by 2,849

  3. Targeted long-read sequencing identifies missing disease-causing variation

    Authors: Danny E. Miller, Arvis Sulovari, Tianyun Wang, Hailey Loucks, Kendra Hoekzema, Katherine M. Munson, Alexandra P. Lewis, Edith P. Almanza Fuerte, Catherine R. Paschal, Tom Walsh, Jenny Thies, James T. Bennett, Ian A. Glass, Katrina M. Dipple, Karynne Patterson, Emily Bonkowski, Zoe Nelson, Audrey Squire, Megan Sikes, Erika Beckman, Robin L. Bennett, Dawn Earl, Winston Lee, Rando Allikmets, Seth J. Perlman, Penny Chow, Anne Hing, Tara Wenger, Margaret P Adam, Angela Sun, Christina Lam, Irene J. Chang, Xue Zou, Stephanie Austin, Erin Huggins, Alexias Safi, Apoorva K. Iyengar, Timothy E. Reddy, William H. Majoros, Andrew S. Allen, Gregory E. Crawford, Priya S. Kishnani, Mary‐Claire King, Tim Cherry, Jessica X. Chong, Michael J. Bamshad, Deborah A. Nickerson, Heather C. Mefford, Dan Doherty, Evan E. Eichler - The American Journal of Human Genetics 2021 cited by 239

  4. Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas

    Authors: Kathryn P. Pennington, Tom Walsh, Maria I. Harrell, Ming K. Lee, Christopher C. Pennil, Mara H. Rendi, Anne Thornton, Barbara M. Norquist, Silvia Casadei, Alex S. Nord, Kathy Agnew, Colin C. Pritchard, Sheena Scroggins, Rochelle L. Garcia, Mary‐Claire King, Elizabeth M. Swisher - Clinical Cancer Research 2013 cited by 1,053

  5. Breast and Ovarian Cancer Risks Due to Inherited Mutations in BRCA1 and BRCA2

    Authors: Mary‐Claire King, Joan H. Marks, Jessica B. Mandell - Science 2003 cited by 2,244

  6. Inherited Mutations in Women With Ovarian Carcinoma

    Authors: Barbara M. Norquist, Maria I. Harrell, Mark F. Brady, Tom Walsh, Ming K. Lee, Süleyman Gülsüner, Sarah S. Bernards, Silvia Casadei, Yi Qian, Robert A. Burger, John K. Chan, Susan A. Davidson, Robert S. Mannel, Paul DiSilvestro, Heather A. Lankes, Nilsa C. Ramirez, Mary‐Claire King, Elizabeth M. Swisher, Michael J. Birrer - JAMA Oncology 2015 cited by 764

  7. Breast-Cancer Risk in Families with Mutations in PALB2

    Authors: Antonis C. Antoniou, Silvia Casadei, Tuomas Heikkinen, Daniel Barrowdale, Katri Pylkäs, Jonathan Roberts, Andrew Lee, Deepak Subramanian, Kim De Leeneer, Florentia Fostira, Eva Tomiak, Susan L. Neuhausen, Zhi L. Teo, Sofia Khan, Kristiina Aittomäki, Jukka S. Moilanen, Clare Turnbull, Sheila Seal, Arto Mannermaa, Anne Kallioniemi, Geoffrey J. Lindeman, Saundra S. Buys, Irene L. Andrulis, Paolo Radice, Carlo Tondini, Siranoush Manoukian, Amanda E. Toland, Penelope Miron, Jeffrey N. Weitzel, Susan M. Domchek, Bruce Poppe, Kathleen Claes, Drakoulis Yannoukakos, Patrick Concannon, Jonine L. Bernstein, Paul A. James, Douglas F. Easton, David E. Goldgar, John L. Hopper, Nazneen Rahman, Paolo Peterlongo, Heli Nevanlinna, Mary‐Claire King, Fergus J. Couch, Melissa C. Southey, Robert Winqvist, William D. Foulkes, Marc Tischkowitz - New England Journal of Medicine 2014 cited by 855

  8. Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia

    Authors: Tom Walsh, Jon McClellan, Shane McCarthy, Anjené Addington, Sarah B. Pierce, Gregory M. Cooper, Alex S. Nord, Mary Kusenda, Dheeraj Malhotra, Abhishek Bhandari, Sunday M. Stray, Caitlin Rippey, Patricia Roccanova, Vlad Makarov, B. Lakshmi, Robert L. Findling, Linmarie Sikich, T Stromberg, Barry Merriman, Nitin Gogtay, Philip Butler, Kristen Eckstrand, Laila Noory, Peter Gochman, Robert T. Long, Zugen Chen, Sean Davis, Carl Baker, Evan E. Eichler, Paul S. Meltzer, Stanley F. Nelson, Andrew Singleton, Ming K. Lee, Judith L. Rapoport, Mary‐Claire King, Jonathan Sebat - Science 2008 cited by 1,832

  9. Linkage of Early-Onset Familial Breast Cancer to Chromosome 17q21

    Authors: Jeff Hall, Ming K. Lee, Beth Newman, Jan E. Morrow, Lee Anderson, Bing Huey, Mary‐Claire King - Science 1990 cited by 2,547

  10. Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing

    Authors: Tom Walsh, Silvia Casadei, Ming K. Lee, Christopher C. Pennil, Alex S. Nord, Anne Thornton, Wendy Roeb, Kathy Agnew, Sunday M. Stray, Anneka Wickramanayake, Barbara M. Norquist, Kathryn P. Pennington, Rochelle L. Garcia, Mary‐Claire King, Elizabeth M. Swisher - National Academy of Sciences, Proceedings of the National Academy of Sciences 2011 cited by 936

  11. The lta4h Locus Modulates Susceptibility to Mycobacterial Infection in Zebrafish and Humans

    Authors: David M. Tobin, Jay C. Vary, John P. Ray, Gregory S. Walsh, Sarah J. Dunstan, Nguyen Duc Bang, Deanna A. Hagge, Saraswoti Khadge, Mary‐Claire King, Thomas R. Hawn, Cecilia B. Moens, Lalita Ramakrishnan - Cell 2010 cited by 535

  12. Perrault Syndrome Is Caused by Recessive Mutations in CLPP, Encoding a Mitochondrial ATP-Dependent Chambered Protease

    Authors: Emma M. Jenkinson, Atteeq U. Rehman, Tom Walsh, Jill Clayton‐Smith, Kwanghyuk Lee, Robert J. Morell, Meghan C. Drummond, Shaheen N. Khan, Muhammad Asif Naeem, Bushra Rauf, Neil Billington, Julie M. Schultz, Jill Urquhart, Ming K. Lee, Andrew Berry, Neil A. Hanley, Sarju Mehta, Deirdre Cilliers, Peter Clayton, Helen Kingston, Miriam J. Smith, Thomas T. Warner, Graeme C. Black, Dorothy Trump, J.R. Davis, Wasim Ahmad, Suzanne M. Leal, Sheikh Riazuddin, Mary‐Claire King, Thomas B. Friedman, William G. Newman - The American Journal of Human Genetics 2013 cited by 245

  13. Genetic Heterogeneity in Human Disease

    Authors: Jon McClellan, Mary‐Claire King - Cell 2010 cited by 1,012

  14. Host Genotype-Specific Therapies Can Optimize the Inflammatory Response to Mycobacterial Infections

    Authors: David M. Tobin, Francisco J. Roca, Sungwhan F. Oh, Ross McFarland, Thad W. Vickery, John P. Ray, Dennis C. Ko, Yuxia Zou, Nguyen Duc Bang, Tran Thi Hong Chau, Jay C. Vary, Thomas R. Hawn, Sarah J. Dunstan, Jeremy Farrar, Guy Thwaites, Mary‐Claire King, Charles N. Serhan, Lalita Ramakrishnan - Cell 2012 cited by 578

  15. Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy

    Authors: Paulina Navon Elkan, Sarah B. Pierce, Reeval Segel, Tom Walsh, Judith Barash, Shai Padeh, Abraham Zlotogorski, Yackov Berkun, Joseph J. Press, M Mukamel, Isabel Voth, Philip J. Hashkes, Liora Harel, Vered Hoffer, Eduard Ling, Fatoş Yalçınkaya, Özgür Kasapçopur, Ming K. Lee, Rachel E. Klevit, Paul Renbaum, Ariella Weinberg‐Shukron, Elif Funda Şener, Barbara Schormair, Sharon Zeligson, Dina Marek‐Yagel, Tim M. Strom, Mordechai Shohat, Amihood Singer, Alan Rubinow, Elon Pras, Juliane Winkelmann, Mustafa Tekin, Yair Anikster, Mary‐Claire King, Ephrat Levy‐Lahad - New England Journal of Medicine 2014 cited by 706

  16. Inherited predisposition to malignant mesothelioma and overall survival following platinum chemotherapy

    Authors: Raffit Hassan, Betsy Morrow, Anish Thomas, Tom Walsh, Ming K. Lee, Süleyman Gülsüner, Meghana Gadiraju, Vasiliki Panou, Shaojian Gao, Idrees Mian, Javed Khan, Mark Raffeld, Snehal Patel, Liqiang Xi, Jun S. Wei, Mary Hesdorffer, Jingli Zhang, Kathleen Calzone, Arpita Desai, Emerson Padiernos, Christine Alewine, David S. Schrump, Seth M. Steinberg, Hedy L. Kindler, Mary‐Claire King, Jane Churpek - National Academy of Sciences, Proceedings of the National Academy of Sciences 2019 cited by 156

  17. Structure of a BRCA1-BARD1 heterodimeric RING-RING complex.

    Authors: Peter S. Brzović, Ponni Rajagopal, David Hoyt, Mary‐Claire King, Rachel E. Klevit - Nature Structural Biology 2001 cited by 499

  18. Mutations in Homologous Recombination Genes and Outcomes in Ovarian Carcinoma Patients in GOG 218: An NRG Oncology/Gynecologic Oncology Group Study

    Authors: Barbara M. Norquist, Mark F. Brady, Maria I. Harrell, Tom Walsh, Ming K. Lee, Süleyman Gülsüner, Sarah S. Bernards, Silvia Casadei, Robert A. Burger, Krishnansu S. Tewari, Floor Backes, Robert S. Mannel, Gretchen Glaser, Cheryl L. Bailey, Stephen C. Rubin, John T. Soper, Heather A. Lankes, Nilsa C. Ramirez, Mary‐Claire King, Michael J. Birrer, Elizabeth M. Swisher - Clinical Cancer Research 2017 cited by 235

  19. Microduplications of 16p11.2 are associated with schizophrenia

    Authors: Shane McCarthy, Vladimir Makarov, George Kirov, Anjené Addington, Jon McClellan, Seungtai Yoon, Diana O. Perkins, Diane E. Dickel, Mary Kusenda, Olga Krastoshevsky, Verena Krause, Ravinesh A. Kumar, Detelina Grozeva, Dheeraj Malhotra, Tom Walsh, Elaine H. Zackai, Paige Kaplan, Jaya Ganesh, Ian D. Krantz, Nancy B. Spinner, Patricia Roccanova, Abhishek Bhandari, Kevin Pavon, B. Lakshmi, Anthony Leotta, Jude Kendall, Yoon-ha Lee, Vladimir Vacic, Sydney Gary, Lilia M. Iakoucheva, Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimäki, Kaija Puura, Chad Haldeman‐Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nöthen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael O‘Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith L. Rapoport, Deborah L. Levy, Mary‐Claire King, Jonathan Sebat - Nature Genetics 2009 cited by 736

  20. Atherogenic lipoprotein phenotype. A proposed genetic marker for coronary heart disease risk.

    Authors: M A Austin, Mary‐Claire King, K M Vranizan, R.M. Krauss - Circulation 1990 cited by 1,421

  21. Germline ETV6 mutations in familial thrombocytopenia and hematologic malignancy

    Authors: Michael Y. Zhang, Jane E. Churpek, Sioḃán Keel, Tom Walsh, Ming K. Lee, Keith R. Loeb, Süleyman Gülsüner, Colin C. Pritchard, Marilyn Sánchez-Bonilla, Jeffrey J. Delrow, Ryan Basom, Melissa Forouhar, Boglarka Gyurkocza, Bradford S. Schwartz, Barbara Neistadt, Rafael Márquez, Christopher J. Mariani, Scott A. Coats, Inga Hofmann, R. Coleman Lindsley, David A. Williams, Janis L. Abkowitz, Marshall S. Horwitz, Mary‐Claire King, Lucy A. Godley, Akiko Shimamura - Nature Genetics 2015 cited by 362

  22. Population-based screening for breast and ovarian cancer risk due to BRCA1 and BRCA2

    Authors: Efrat Gabai-Kapara, Amnon Lahad, Bella Kaufman, Eitan Friedman, Shlomo Segev, Paul Renbaum, Rachel Beeri, Moran Gal, Julia Grinshpun‐Cohen, Karen Djemal, Jessica B. Mandell, Ming K. Lee, Uziel Beller, Raphael Catane, Mary‐Claire King, Ephrat Levy‐Lahad - National Academy of Sciences, Proceedings of the National Academy of Sciences 2014 cited by 345

  23. Mutations in LARS2, Encoding Mitochondrial Leucyl-tRNA Synthetase, Lead to Premature Ovarian Failure and Hearing Loss in Perrault Syndrome

    Authors: Sarah B. Pierce, Ksenija Geršak, Rachel Michaelson‐Cohen, Tom Walsh, Ming K. Lee, Daniel Malach, Rachel E. Klevit, Mary‐Claire King, Ephrat Levy‐Lahad - The American Journal of Human Genetics 2013 cited by 219

  24. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

    Authors: Santhosh Girirajan, Jill A. Rosenfeld, Gregory M. Cooper, Francesca Antonacci, Priscillia Siswara, Andy Itsara, Laura Vives, Tom Walsh, Shane McCarthy, Carl Baker, Heather C. Mefford, Jeffrey M. Kidd, Sharon R. Browning, Brian L. Browning, Diane E. Dickel, Deborah L. Levy, Blake C. Ballif, Kathryn Platky, Darren Farber, Gordon C. Gowans, Jessica J Wetherbee, Alexander Asamoah, David D. Weaver, Paul R. Mark, Jennifer A. Dickerson, Bhuwan P. Garg, Sara Ellingwood, Rosemarie Smith, Valerie Banks, Wendy E. Smith, Marie McDonald, Joe J. Hoo, Beatrice N. French, Cindy Hudson, John P. Johnson, Jillian R. Ozmore, John B. Moeschler, Urvashi Surti, Luis Escobar, Dima El‐Khechen, Jerome L. Gorski, Jennifer Kussmann, Bonnie Anne Salbert, Yves Lacassie, Alisha Biser, Donna M. McDonald‐McGinn, Elaine H. Zackai, Matthew A. Deardorff, Tamim H. Shaikh, Eric Haan, Kathryn Friend, Marco Fichera, Corrado Romano, Jozef Gécz, Lynn E. DeLisi, Jonathan Sebat, Mary‐Claire King, Lisa G. Shaffer, Evan E. Eichler - Nature Genetics 2010 cited by 674