Jeffrey C. Murray

1984–2025 年に発表

162
論文数
27,463
被引用数
97
h 指数
154
i10 指数

被引用数

Jeffrey C. Murray の年別被引用数1969 年: 被引用 1 件1973 年: 被引用 1 件1974 年: 被引用 1 件1977 年: 被引用 1 件1985 年: 被引用 3 件1986 年: 被引用 7 件1987 年: 被引用 5 件1988 年: 被引用 7 件1989 年: 被引用 7 件1990 年: 被引用 11 件1991 年: 被引用 12 件1992 年: 被引用 17 件1993 年: 被引用 21 件1994 年: 被引用 22 件1995 年: 被引用 48 件1996 年: 被引用 75 件1997 年: 被引用 81 件1998 年: 被引用 53 件1999 年: 被引用 91 件2000 年: 被引用 135 件2001 年: 被引用 110 件2002 年: 被引用 131 件2003 年: 被引用 154 件2004 年: 被引用 173 件2005 年: 被引用 184 件2006 年: 被引用 161 件2007 年: 被引用 175 件2008 年: 被引用 236 件2009 年: 被引用 243 件2010 年: 被引用 142 件2011 年: 被引用 225 件2012 年: 被引用 211 件2013 年: 被引用 213 件2014 年: 被引用 180 件2015 年: 被引用 212 件2016 年: 被引用 217 件2017 年: 被引用 209 件2018 年: 被引用 175 件2019 年: 被引用 657 件2020 年: 被引用 583 件2021 年: 被引用 534 件2022 年: 被引用 373 件2023 年: 被引用 257 件2024 年: 被引用 394 件2025 年: 被引用 158 件2026 年: 被引用 2 件1970〜1972 年は被引用が無いため表示していません1975〜1976 年は被引用が無いため表示していません1978〜1984 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 2,710 件、この内訳の 30.6%イギリス: 引用元論文 821 件、この内訳の 9.3%中国: 引用元論文 429 件、この内訳の 4.8%カナダ: 引用元論文 393 件、この内訳の 4.4%ドイツ: 引用元論文 387 件、この内訳の 4.4%フランス: 引用元論文 309 件、この内訳の 3.5%オランダ: 引用元論文 298 件、この内訳の 3.4%オーストラリア: 引用元論文 295 件、この内訳の 3.3%イタリア: 引用元論文 241 件、この内訳の 2.7%日本: 引用元論文 217 件、この内訳の 2.5%スウェーデン: 引用元論文 186 件、この内訳の 2.1%スペイン: 引用元論文 175 件、この内訳の 2%
0%30.6%その他 27%

分野

  • Biochemistry, Genetics and Molecular Biology49.5%
  • Medicine37.4%
  • Neuroscience4.3%
  • Immunology and Microbiology2%
  • Agricultural and Biological Sciences1.2%
  • Dentistry0.8%
  • その他4.8%

トピック

  • 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%
  • その他83.7%

共著者

全論文

検索で開く
  1. Cleft lip and palate: understanding genetic and environmental influences

    著者: , , , - Nature Reviews Genetics 2011 被引用: 1,969

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

    著者: , , , , , , , , , , , , , , , , - New England Journal of Medicine 2015 被引用: 658

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 599

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

    著者: , , , , , , , , , , , - The Journal of Experimental Medicine 2014 被引用: 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

    著者: , , , , , , , , , , , , , , , , , - PLoS Medicine 2020 被引用: 88

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 105

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

    著者: , , , , , , , , , , , - Nature Genetics 2006 被引用: 363

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 8 名 - Nature Genetics 2011 被引用: 351

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 290

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

    著者: , , , , - The American Journal of Human Genetics 1998 被引用: 1,097

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 ほか 74 名 - Nature Genetics 2010 被引用: 511

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2002 被引用: 901

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2020 被引用: 96

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

    著者: , , , , , , , , , , , , - Transfusion 2015 被引用: 82

  15. Noninvasive Whole-Genome Sequencing of a Human Fetus

    著者: , , , , , , , , , , , , , - Science Translational Medicine 2012 被引用: 413

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

    著者: , , , , , , , , , , - The Cleft Palate-Craniofacial Journal 2015 被引用: 110

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

    著者: , , , , , , , , , , - PLoS Genetics 2021 被引用: 52

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 198

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 103

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - Journal of Medical Genetics 2022 被引用: 78

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 34

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

    著者: , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2008 被引用: 427

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

    著者: , , , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2013 被引用: 230