Jeffrey C. Murray

Active 1984–2025

162
Papers
27,463
Citations
97
h-index
154
i10-index

Citations

Citations per year for Jeffrey C. Murray1969: 1 citations1973: 1 citations1974: 1 citations1977: 1 citations1985: 3 citations1986: 7 citations1987: 5 citations1988: 7 citations1989: 7 citations1990: 11 citations1991: 12 citations1992: 17 citations1993: 21 citations1994: 22 citations1995: 48 citations1996: 75 citations1997: 81 citations1998: 53 citations1999: 91 citations2000: 135 citations2001: 110 citations2002: 131 citations2003: 154 citations2004: 173 citations2005: 184 citations2006: 161 citations2007: 175 citations2008: 236 citations2009: 243 citations2010: 142 citations2011: 225 citations2012: 211 citations2013: 213 citations2014: 180 citations2015: 212 citations2016: 217 citations2017: 209 citations2018: 175 citations2019: 657 citations2020: 583 citations2021: 534 citations2022: 373 citations2023: 257 citations2024: 394 citations2025: 158 citations2026: 2 citations1970–1972: no citations, so these years are not shown1975–1976: no citations, so these years are not shown1978–1984: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,710 citing papers, 30.6% of this breakdownUnited Kingdom: 821 citing papers, 9.3% of this breakdownChina: 429 citing papers, 4.8% of this breakdownCanada: 393 citing papers, 4.4% of this breakdownGermany: 387 citing papers, 4.4% of this breakdownFrance: 309 citing papers, 3.5% of this breakdownNetherlands: 298 citing papers, 3.4% of this breakdownAustralia: 295 citing papers, 3.3% of this breakdownItaly: 241 citing papers, 2.7% of this breakdownJapan: 217 citing papers, 2.5% of this breakdownSweden: 186 citing papers, 2.1% of this breakdownSpain: 175 citing papers, 2% of this breakdown
0%30.6%Other 27%

Fields

  • Biochemistry, Genetics and Molecular Biology49.5%
  • Medicine37.4%
  • Neuroscience4.3%
  • Immunology and Microbiology2%
  • Agricultural and Biological Sciences1.2%
  • Dentistry0.8%
  • Other4.8%

Topics

  • Cleft Lip and Palate Research5.2%
  • Craniofacial Disorders and Treatments3%
  • Genetic Associations and Epidemiology2.3%
  • dental development and anomalies2.2%
  • Genomic variations and chromosomal abnormalities1.9%
  • Neonatal Respiratory Health Research1.7%
  • Other83.7%

Coauthors

All papers

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  1. Cleft lip and palate: understanding genetic and environmental influences

    Authors: , , , - Nature Reviews Genetics 2011 cited by 1,969

  2. Between-Hospital Variation in Treatment and Outcomes in Extremely Preterm Infants

    Authors: , , , , , , , , , , , , , , , , - New England Journal of Medicine 2015 cited by 658

  3. 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

  4. Siglec-5 and Siglec-14 are polymorphic paired receptors that modulate neutrophil and amnion signaling responses to group B Streptococcus

    Authors: , , , , , , , , , , , - The Journal of Experimental Medicine 2014 cited by 195

  5. Dissecting maternal and fetal genetic effects underlying the associations between maternal phenotypes, birth outcomes, and adult phenotypes: A mendelian-randomization and haplotype-based genetic score analysis in 10,734 mother–infant pairs

    Authors: , , , , , , , , , , , , , , , , , - PLoS Medicine 2020 cited by 88

  6. Multiomics Characterization of Preterm Birth in Low- and Middle-Income Countries

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Fahad Aftab, Abdul Quaiyum, Alexander Manu, Sachiyo Yoshida, Rajiv Bahl, Anisur Rahman, Jesmin Pervin, Jennifer Winston, Patrick Musonda, Jeffrey S. A. Stringer, James A. Litch, Mohammad Sajjad Ghaemi, Mira N. Moufarrej, Kévin Contrepois, Songjie Chen, Ina A. Stelzer, Natalie Stanley, Alan L. Chang, Ghaith Bany Hammad, Ronald J. Wong, Candace Liu, Cecele C. Quaintance, Anthony Culos, Camilo Espinosa, Maria Xenochristou, Martin Becker, Ramin Fallahzadeh, Edward A. Ganio, Amy S. Tsai, Dyani Gaudillière, Eileen S. Tsai, Xiaoyuan Han, Kazuo Ando, Martha Tingle, Ivana Marić, Paul H. Wise, Virginia D. Winn, Maurice L. Druzin, Ronald S. Gibbs, Gary L. Darmstadt, Jeffrey C. Murray, Gary M. Shaw, David K. Stevenson, M Snyder, Stephen R. Quake, Martin S. Angst, Brice Gaudillière, Nima Aghaeepour - JAMA Network Open 2020 cited by 105

  7. Abnormal skin, limb and craniofacial morphogenesis in mice deficient for interferon regulatory factor 6 (Irf6)

    Authors: , , , , , , , , , , , - Nature Genetics 2006 cited by 363

  8. Meta-analysis of genome-wide association studies identifies three new risk loci for atopic dermatitis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Juha Pekkanen, Alexandra I. F. Blakemore, Jessica L. Buxton, Marika Kaakinen, David L Duffy, Pamela A. F. Madden, Andrew C. Heath, Grant W. Montgomery, Philip J. Thompson, Melanie C. Matheson, Peter N. Le Souëf, Beaté St Pourcain, George Davey Smith, John Henderson, John P. Kemp, Nicholas J. Timpson, Panos Deloukas, Susan M. Ring, H‐Erich Wichmann, Martina Müller‐Nurasyid, Natalija Novak, Norman Klopp, Elke Rodríguez, Wendy L. McArdle, Allan Linneberg, Torkil Menné, Ellen A. Nøhr, Albert Hofman, André G. Uitterlinden, Cornelia M. van Duijn, Fernando Rivadeneira, Johan C. de Jongste, Ralf J.P. van der Valk, Matthias Wjst, Rain Jögi, Frank Geller, Heather A. Boyd, Jeffrey C. Murray, Cecilia Kim, Frank Mentch, Michael March, Massimo Mangino, Tim D. Spector, Véronique Bataille, Craig E. Pennell, Patrick G. Holt, Peter D. Sly, Carla M. T. Tiesler, Elisabeth Thiering, Thomas Illig, Medea Imboden, Wenche Nystad, Angela Simpson, Jouke‐Jan Hottenga, Dirkje S. Postma, Gerard H. Koppelman, Henriëtte A. Smit, Cilla Söderhäll, Bo Chawes, Eskil Kreiner‐Møller, Hans Bisgaard, Erik Melén, Dorret I. Boomsma, Adnan Čustović, Bo Jacobsson, Nicole Probst‐Hensch, Lyle J. Palmer, Daniel Glass, Håkon Håkonarson, Mads Melbye and 8 more - Nature Genetics 2011 cited by 351

  9. Genetic Evidence for Causal Relationships Between Maternal Obesity-Related Traits and Birth Weight

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mark I. McCarthy, George McMahon, Sarah E. Medland, Mads Melbye, Andrew P. Morris, Michael Nodzenski, Christoph Reichetzeder, Susan M. Ring, Sylvain Sebért, Verena Sengpiel, Thorkild I. A. Sørensen, Gonneke Willemsen, Eco J. C. de Geus, Nicholas G. Martin, Tim D. Spector, Christopher Power, Marjo‐Riitta Järvelin, Hans Bisgaard, Struan F.A. Grant, Ellen A. Nøhr, Vincent W. V. Jaddoe, Bo Jacobsson, Jeffrey C. Murray, Berthold Hocher, Andrew T. Hattersley, Denise Scholtens, George Davey Smith, Marie‐France Hivert, Janine F. Felix, Elina Hyppönen, William L. Lowe, Timothy M. Frayling, Debbie A. Lawlor, Rachel M. Freathy - JAMA 2016 cited by 290

  10. Comprehensive Human Genetic Maps: Individual and Sex-Specific Variation in Recombination

    Authors: , , , , - The American Journal of Human Genetics 1998 cited by 1,097

  11. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Shelia Ulivi, Nicole M. Warrington, Lina Zgaga, Helen Alavere, Najaf Amin, Thor Aspelund, Stefania Bandinelli, Inês Barroso, Gerald S. Berenson, Sven Bergmann, Hannah Blackburn, Eric Boerwinkle, Julie E. Buring, Fabio Busonero, Harry Campbell, Stephen J. Chanock, Wei Chen, Marilyn C. Cornelis, David Couper, Andrea D. Coviello, Pio D’Adamo, Ulf dé Fairé, Eco J. C. de Geus, Panos Deloukas, Angela Döring, George Davey Smith, Douglas F. Easton, Guðný Eiríksdóttir, Valur Emilsson, Johan G. Eriksson, Luigi Ferrucci, Aaron R. Folsom, Tatiana Foroud, Melissa Garcia, Paolo Gasparini, Frank Geller, Christian Gieger, Vilmundur Guðnason, Per Hall, Susan E. Hankinson, Liana Ferreli, Andrew C. Heath, Dena G. Hernandez, Albert Hofman, Frank B. Hu, Thomas Illig, Marjo‐Riitta Järvelin, Andrew D. Johnson, David Karasik, Kay‐Tee Khaw, Douglas P. Kiel, Tuomas O. Kilpeläinen, Ivana Kolčić, Peter Kraft, Lenore J. Launer, Joop S.E. Laven, Shengxu Li, Jianjun Liu, Daniel Levy, Nicholas G. Martin, Wendy L. McArdle, Mads Melbye, Vincent Mooser, Jeffrey C. Murray, Sarah S. Murray, Michael A. Nalls, Pau Navarro, Mari Nelis, Andrew R Ness, Kate Northstone and 74 more - Nature Genetics 2010 cited by 511

  12. Mutations in IRF6 cause Van der Woude and popliteal pterygium syndromes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2002 cited by 901

  13. Genome-wide Enrichment of De Novo Coding Mutations in Orofacial Cleft Trios

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2020 cited by 96

  14. The heritability of hemolysis in stored human red blood cells

    Authors: , , , , , , , , , , , , - Transfusion 2015 cited by 82

  15. Noninvasive Whole-Genome Sequencing of a Human Fetus

    Authors: , , , , , , , , , , , , , - Science Translational Medicine 2012 cited by 413

  16. The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community

    Authors: , , , , , , , , , , - The Cleft Palate-Craniofacial Journal 2015 cited by 110

  17. Pleiotropy method reveals genetic overlap between orofacial clefts at multiple novel loci from GWAS of multi-ethnic trios

    Authors: , , , , , , , , , , - PLoS Genetics 2021 cited by 52

  18. Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Régine P.M. Steegers‐Theunissen, Michele Rubini, Peter Mossey, Per Hoffmann, Christoph Lange, Sven Cichon, Peter Propping, Michael Knapp, Markus M. Nöthen - Nature Genetics 2012 cited by 361

  19. Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Berthold Hocher, Albert Hofman, Hazel Inskip, Samuel E. Jones, Manolis Kogevinas, Penelope A. Lind, Letizia Marullo, Sarah E. Medland, Anna Murray, Jeffrey C. Murray, Pål R. Njølstad, Ellen A. Nøhr, Christoph Reichetzeder, Susan M. Ring, Katherine S. Ruth, Loreto Santa‐Marina, Denise Scholtens, Sylvain Sebért, Verena Sengpiel, Marcus A. Tuke, Marc Vaudel, Michael N. Weedon, Gonneke Willemsen, Andrew R. Wood, Hanieh Yaghootkar, Louis J. Muglia, Meike Bartels, Caroline L. Relton, Craig E. Pennell, Leda Chatzi, Xavier Estivill, John W. Holloway, Dorret I. Boomsma, Grant W. Montgomery, Joanne M. Murabito, Tim D. Spector, Christine Power, Marjo‐Riitta Järvelin, Hans Bisgaard, Struan F.A. Grant, Thorkild I. A. Sørensen, Vincent W.V. Jaddoe, Bo Jacobsson, Mads Melbye, Mark I. McCarthy, Andrew T. Hattersley, M. Geoffrey Hayes, Timothy M. Frayling, Marie‐France Hivert, Janine F. Felix, Elina Hyppönen, William L. Lowe, David M. Evans, Debbie A. Lawlor, Bjarke Feenstra, Rachel M. Freathy - Human Molecular Genetics 2018 cited by 198

  20. Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Håkon Håkonarson, M. Geoffrey Hayes, Denise Scholtens, Fernando Rivadeneira, Vincent W. V. Jaddoe, Rebecca Vinding, Hans Bisgaard, Bridget Knight, Katja Pahkala, Olli T. Raitakari, Øyvind Helgeland, Stefan Johansson, Pål R. Njølstad, João Fadista, Andrew J. Schork, Ron Nudel, Daniel E. Miller, Xiaoting Chen, Matthew T. Weirauch, Preben Bo Mortensen, Anders D. Børglum, Merete Nordentoft, Ole Mors, Ke Hao, Kelli K. Ryckman, David M. Hougaard, Leah C. Kottyan, Craig E. Pennell, Leo‐Pekka Lyytikäinen, Klaus Bønnelykke, Martine Vrijheid, Janine F. Felix, William L. Lowe, Struan F.A. Grant, Elina Hyppönen, Bo Jacobsson, Marjo‐Riitta Järvelin, Louis J. Muglia, Jeffrey C. Murray, Rachel M. Freathy, Thomas Werge, Mads Melbye, Alfonso Buil, Bjarke Feenstra - Nature Communications 2019 cited by 103

  21. Axenfeld-Rieger syndrome: more than meets the eye

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - Journal of Medical Genetics 2022 cited by 78

  22. Multiomic signals associated with maternal epidemiological factors contributing to preterm birth in low- and middle-income countries

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sayedur Rahman, A. S. M. Tarik Hasan, Said M. Ali, Mohamed Hamad Juma, Monjur Rahman, Shaki Aktar, Saikat Deb, Joan T. Price, Paul H. Wise, Virginia D. Winn, Maurice L. Druzin, Ronald S. Gibbs, Gary L. Darmstadt, Jeffrey C. Murray, Jeffrey S. A. Stringer, Brice Gaudillière, M Snyder, Martin S. Angst, Anisur Rahman, Abdullah H Baqui, Fyezah Jehan, Muhammad Imran Nisar, Bellington Vwalika, Sunil Sazawal, Gary M. Shaw, David K. Stevenson, Nima Aghaeepour - Science Advances 2023 cited by 34

  23. Disruption of an AP-2α binding site in an IRF6 enhancer is associated with cleft lip

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2008 cited by 427

  24. Dominant Mutations in GRHL3 Cause Van der Woude Syndrome and Disrupt Oral Periderm Development

    Authors: , , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2013 cited by 230