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Michael S. Watson

1973–2023 年に発表

56
論文数
19,330
被引用数
46
h 指数
54
i10 指数

被引用数

Michael S. Watson の年別被引用数1959 年: 被引用 1 件1975 年: 被引用 2 件1976 年: 被引用 2 件1978 年: 被引用 2 件1980 年: 被引用 1 件1982 年: 被引用 1 件1984 年: 被引用 1 件1985 年: 被引用 1 件1986 年: 被引用 3 件1987 年: 被引用 6 件1988 年: 被引用 8 件1989 年: 被引用 6 件1990 年: 被引用 2 件1991 年: 被引用 6 件1992 年: 被引用 4 件1993 年: 被引用 7 件1994 年: 被引用 4 件1995 年: 被引用 7 件1996 年: 被引用 8 件1997 年: 被引用 9 件1998 年: 被引用 11 件1999 年: 被引用 7 件2000 年: 被引用 20 件2001 年: 被引用 29 件2002 年: 被引用 29 件2003 年: 被引用 31 件2004 年: 被引用 39 件2005 年: 被引用 32 件2006 年: 被引用 31 件2007 年: 被引用 52 件2008 年: 被引用 49 件2009 年: 被引用 52 件2010 年: 被引用 69 件2011 年: 被引用 92 件2012 年: 被引用 86 件2013 年: 被引用 103 件2014 年: 被引用 125 件2015 年: 被引用 163 件2016 年: 被引用 163 件2017 年: 被引用 157 件2018 年: 被引用 207 件2019 年: 被引用 647 件2020 年: 被引用 629 件2021 年: 被引用 625 件2022 年: 被引用 528 件2023 年: 被引用 317 件2024 年: 被引用 488 件2025 年: 被引用 184 件2026 年: 被引用 9 件1960〜1974 年は被引用が無いため表示していません1977 年は被引用が無いため表示していません1979 年は被引用が無いため表示していません1981 年は被引用が無いため表示していません1983 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 2,520 件、この内訳の 30.7%イギリス: 引用元論文 707 件、この内訳の 8.6%カナダ: 引用元論文 468 件、この内訳の 5.7%ドイツ: 引用元論文 372 件、この内訳の 4.5%オランダ: 引用元論文 351 件、この内訳の 4.3%オーストラリア: 引用元論文 348 件、この内訳の 4.2%イタリア: 引用元論文 310 件、この内訳の 3.8%中国: 引用元論文 295 件、この内訳の 3.6%フランス: 引用元論文 271 件、この内訳の 3.3%スペイン: 引用元論文 198 件、この内訳の 2.4%ベルギー: 引用元論文 151 件、この内訳の 1.8%日本: 引用元論文 137 件、この内訳の 1.7%
0%30.7%その他 25.4%

機関

分野

  • Biochemistry, Genetics and Molecular Biology53.7%
  • Medicine33.8%
  • Immunology and Microbiology4.2%
  • Neuroscience3.2%
  • Pharmacology, Toxicology and Pharmaceutics1.3%
  • Engineering0.7%
  • その他3.1%

トピック

  • Genomics and Rare Diseases12.6%
  • Genomic variations and chromosomal abnormalities6.4%
  • BRCA gene mutations in cancer4.1%
  • Prenatal Screening and Diagnostics4%
  • Cancer Genomics and Diagnostics3.4%
  • Congenital heart defects research3%
  • その他66.5%

共著者

全論文

検索で開く
  1. ClinGen — The Clinical Genome Resource

    著者: Heidi L. Rehm, Jonathan S. Berg, Lisa Brooks, Carlos D. Bustamante, James P. Evans, Melissa Landrum, David H. Ledbetter, Donna Maglott, Christa Lese Martin, Robert L. Nussbaum, Sharon E. Plon, Erin M. Ramos, Stephen T. Sherry, Michael S. Watson - New England Journal of Medicine 2015 被引用: 1,537

  2. Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies

    著者: David T. Miller, Margaret P Adam, Swaroop Aradhya, Leslie G. Biesecker, Arthur R. Brothman, Nigel P. Carter, Deanna M. Church, John A. Crolla, Evan E. Eichler, Charles J. Epstein, W. Andrew Faucett, Lars Feuk, Jan M. Friedman, Ada Hamosh, Laird Jackson, Erin B. Kaminsky, Klaas Kok, Ian D. Krantz, Robert M. Kuhn, Charles Lee, James M. Ostell, Carla Rosenberg, Stephen W. Scherer, Nancy B. Spinner, Dimitri J. Stavropoulos, James Tepperberg, Erik C. Thorland, Joris Vermeesch, Darrel Waggoner, Michael S. Watson, Christa Lese Martin, David H. Ledbetter - The American Journal of Human Genetics 2010 被引用: 2,873

  3. ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing

    著者: Robert C. Green, Jonathan S. Berg, Wayne W. Grody, Sarah S. Kalia, Bruce R. Korf, Christa Lese Martin, Amy L. McGuire, Robert L. Nussbaum, Julianne O’Daniel, Kelly E. Ormond, Heidi L. Rehm, Michael S. Watson, Marc S. Williams, Leslie G. Biesecker - Genetics in Medicine 2013 被引用: 2,518

  4. ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

    著者: David T. Miller, Kristy Lee, Wendy K. Chung, Allan Gordon, Gail E. Herman, Teri E. Klein, Douglas R. Stewart, Laura M. Amendola, Kathy Adelman, Sherri J. Bale, Michael H. Gollob, Steven M. Harrison, Ray E. Hershberger, Kent D. McKelvey, C. Sue Richards, Christopher N. Vlangos, Michael S. Watson, Christa Lese Martin - Genetics in Medicine 2021 被引用: 562

  5. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics

    著者: Sarah S. Kalia, Kathy Adelman, Sherri J. Bale, Wendy K. Chung, Christine M. Eng, James P. Evans, Gail E. Herman, Sophia B. Hufnagel, Teri E. Klein, Bruce R. Korf, Kent D. McKelvey, Kelly E. Ormond, C. Sue Richards, Christopher N. Vlangos, Michael S. Watson, Christa Lese Martin, David T. Miller - Genetics in Medicine 2016 被引用: 1,700

  6. Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG)

    著者: David T. Miller, Kristy Lee, Allan Gordon, Laura M. Amendola, Kathy Adelman, Sherri J. Bale, Wendy K. Chung, Michael H. Gollob, Steven M. Harrison, Gail E. Herman, Ray E. Hershberger, Teri E. Klein, Kent D. McKelvey, C. Sue Richards, Christopher N. Vlangos, Douglas R. Stewart, Michael S. Watson, Christa Lese Martin - Genetics in Medicine 2021 被引用: 263

  7. ClinGen Variant Curation Expert Panel experiences and standardized processes for disease and gene‐level specification of the ACMG/AMP guidelines for sequence variant interpretation

    著者: E. Andres Rivera-Munoz, Laura V. Milko, Steven M. Harrison, Danielle R. Azzariti, C. Lisa Kurtz, Kristy Lee, Jessica L. Mester, Meredith Weaver, Erin Currey, William Craigen, Charis Eng, Birgit Funke, Madhuri Hegde, Ray E. Hershberger, Rong Mao, Robert D. Steiner, Lisa M. Vincent, Christa Lese Martin, Sharon E. Plon, Erin M. Ramos, Heidi L. Rehm, Michael S. Watson, Jonathan S. Berg - Human Mutation 2018 被引用: 219

  8. Newborn Screening for Severe Combined Immunodeficiency in 11 Screening Programs in the United States

    著者: Antonia Kwan, Roshini S. Abraham, Robert J. Currier, Amy Brower, Karen Andruszewski, Jordan K. Abbott, Mei Baker, Mark Ballow, Louis Bartoshesky, Francisco A. Bonilla, Charles D. Brokopp, Edward G. Brooks, Michele Caggana, Jocelyn Celestin, Joseph A. Church, Anne Marie Comeau, James A. Connelly, Morton J. Cowan, Charlotte Cunningham‐Rundles, Trivikram Dasu, Nina Dave, M. Teresa de la Morena, Ulrich Duffner, Chin-To Fong, Lisa R. Forbes, Debra Freedenberg, Erwin W. Gelfand, Jaime E. Hale, I. Celine Hanson, Beverly N. Hay, Diana Hu, Anthony J. Infante, Daisy Johnson, Neena Kapoor, Denise M. Kay, Donald B. Kohn, Rachel Lee, Heather K. Lehman, Zhili Lin, Fred Lorey, Aly Abdel‐Mageed, Adrienne Manning, Sean McGhee, Theodore B. Moore, Stanley J. Naides, Luigi D. Notarangelo, Jordan S. Orange, Sung‐Yun Pai, Matthew H. Porteus, Ray Rodríguez, Neil Romberg, John M. Routes, Mary Ruehle, Arye Rubenstein, Carlos A. Saavedra‐Matiz, G. E. M. Scott, Patricia M. Scott, Elizabeth Secord, Christine M. Seroogy, William T. Shearer, Subhadra Siegel, Stacy K. Silvers, E. Richard Stiehm, Robert W. Sugerman, John L. Sullivan, Susan Tanksley, Millard L. Tierce, James Verbsky, Beth Vogel, Rosalyn Walker, Kelly Walkovich, Jolán E. Walter, Richard L. Wasserman, Michael S. Watson, Geoffrey A. Weinberg, Leonard B. Weiner, Heather Wood, Anne Yates, Jennifer M. Puck - JAMA 2014 被引用: 673

  9. The 2019 US medical genetics workforce: a focus on clinical genetics

    著者: Brittany D. Jenkins, Catherine G. Fischer, Curt A. Polito, Deborah Maiese, Alisha Keehn, Megan Lyon, Mathew J. Edick, Matthew R.G. Taylor, Hans C. Andersson, Joann Bodurtha, Miriam G. Blitzer, Maximilian Muenke, Michael S. Watson - Genetics in Medicine 2021 被引用: 170

  10. Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics

    著者: Anthony R. Gregg, Brian G. Skotko, Judith Benkendorf, Kristin G. Monaghan, Komal Bajaj, Robert G. Best, Susan Klugman, Michael S. Watson - Genetics in Medicine 2016 被引用: 692

  11. Pompe disease diagnosis and management guideline

    著者: Priya S. Kishnani, Robert D. Steiner, Deeksha Bali, Kenneth I. Berger, Barry J. Byrne, Laura E. Case, John F. Crowley, Steven M. Downs, R. Rodney Howell, Richard M. Kravitz, Joanne Mackey, Deborah Marsden, Anna Maria Martins, David S. Millington, Marc Nicolino, Gwen O’grady, Marc C. Patterson, David M. Rapoport, Alfred E. Slonim, Carolyn T. Spencer, Cynthia J. Tifft, Michael S. Watson - Genetics in Medicine 2006 被引用: 628

  12. Newborn Sequencing in Genomic Medicine and Public Health

    著者: Jonathan S. Berg, Pankaj B. Agrawal, Donald B. Bailey, Alan H. Beggs, Steven E. Brenner, Amy Brower, Julie A. Cakici, Ozge Ceyhan‐Birsoy, Kee Chan, Flavia Chen, Robert J. Currier, Dmitry Dukhovny, Robert C. Green, Julie Harris-Wai, Ingrid A. Holm, Brenda Iglesias, Galen Joseph, Stephen F. Kingsmore, Barbara A. Koenig, Pui–Yan Kwok, John D. Lantos, Steven J. Leeder, Megan A. Lewis, Amy L. McGuire, Laura V. Milko, Sean D. Mooney, Richard B. Parad, Stacey Pereira, Joshua E. Petrikin, Bradford C. Powell, Cynthia M. Powell, Jennifer M. Puck, Heidi L. Rehm, Neil Risch, Myra I. Roche, Joseph T.C. Shieh, Narayanan Veeraraghavan, Michael S. Watson, Laurel K. Willig, Timothy W. Yu, Tiina K. Urv, Anastasia L. Wise - PEDIATRICS 2017 被引用: 235

  13. Newborn Screening: Toward a Uniform Screening Panel and System—Executive Summary

    著者: Michael S. Watson, Marie Y. Mann, Michele A. Lloyd-Puryear, Piero Rinaldo, R. Rodney Howell - PEDIATRICS 2006 被引用: 501

  14. Diagnosis and management of glycogen storage disease type I: a practice guideline of the American College of Medical Genetics and Genomics

    著者: Priya S. Kishnani, Stephanie Austin, José E. Abdenur, Pamela Arn, Deeksha Bali, Anne Boney, Wendy K. Chung, Aditi I Dagli, David C. Dale, Dwight D. Koeberl, Michael J.G. Somers, Stephanie Burns Wechsler, David A. Weinstein, Joseph I. Wolfsdorf, Michael S. Watson - Genetics in Medicine 2014 被引用: 495

  15. Expanded Carrier Screening in Reproductive Medicine—Points to Consider

    著者: Janice G. Edwards, Gerald L. Feldman, James Goldberg, Anthony R. Gregg, Mary E. Norton, Nancy C. Rose, Adele Schneider, Katie Stoll, Ronald J. Wapner, Michael S. Watson - Obstetrics and Gynecology 2015 被引用: 368

  16. Current conditions in medical genetics practice

    著者: Deborah Maiese, Alisha Keehn, Megan Lyon, David B. Flannery, Michael S. Watson - Genetics in Medicine 2019 被引用: 161

  17. Newborn screening for neurodevelopmental diseases: Are we there yet?

    著者: Wendy K. Chung, Jonathan S. Berg, Jeffrey R. Botkin, Steven E. Brenner, Jeffrey P. Brosco, Kyle B. Brothers, Robert J. Currier, Amy Gaviglio, Walter E. Kowtoniuk, Colleen Olson, Michele A. Lloyd-Puryear, Annamarie Saarinen, Mustafa Şahin, Yufeng Shen, Elliott H. Sherr, Michael S. Watson, Zhanzhi Hu - American Journal of Medical Genetics Part C Seminars in Medical Genetics 2022 被引用: 27

  18. Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathways

    著者: D. Woodrow Benson, G. Michael Silberbach, Ann Kavanaugh‐McHugh, Carol M. Cottrill, Yizhong Zhang, Steve Riggs, Octavia Smalls, Mark C. Johnson, Michael S. Watson, Jonathan G. Seidman, Christine E. Seidman, John S. Plowden, John D. Kugler - Journal of Clinical Investigation 1999 被引用: 687

  19. Empowering newborn screening programs in African countries through establishment of an international collaborative effort

    著者: Bradford L. Therrell, Michele A. Lloyd-Puryear, Kwaku Ohene‐Frempong, Russell E. Ware, Carmencita D. Padilla, Emmanuela E. Ambrose, Amina Barkat, Hassan Ghazal, Charles Kiyaga, Tisungane Mvalo, Obiageli Nnodu, Karim Ouldim, Mohamed Chérif Rahimy, Brígida Santos, Léon Tshilolo, Careema Yusuf, Guisou Zarbalian, Michael S. Watson - Journal of Community Genetics 2020 被引用: 69

  20. Glycogen Storage Disease Type III diagnosis and management guidelines

    著者: Priya S. Kishnani, Stephanie Austin, Pamela Arn, Deeksha Bali, Anne Boney, Laura E. Case, Wendy K. Chung, Dev M. Desai, Areeg El‐Gharbawy, Ronald G. Haller, Gerrit Smit, Alastair D. Smith, Lisa D. Hobson‐Webb, Stephanie Burns Wechsler, David A. Weinstein, Michael S. Watson - Genetics in Medicine 2010 被引用: 305

  21. Executive Summary

    著者: Michael S. Watson, Marie Y. Mann, Michele A. Lloyd-Puryear, Piero Rinaldo, R. Rodney Howell - Genetics in Medicine 2006 被引用: 487

  22. The Progress and Future of US Newborn Screening

    著者: Michael S. Watson, Michele A. Lloyd-Puryear, R. Rodney Howell - International Journal of Neonatal Screening 2022 被引用: 50

  23. Cystic fibrosis population carrier screening: 2004 revision of American College of Medical Genetics mutation panel

    著者: Michael S. Watson, Garry R. Cutting, Robert J. Desnick, Deborah A. Driscoll, K. Klinger, Michael T. Mennuti, Glenn E. Palomaki, Bradley W. Popovich, Victoria M. Pratt, Elizabeth M. Rohlfs, Charles M. Strom, C. Sue Richards, David R. Witt, Wayne W. Grody - Genetics in Medicine 2004 被引用: 479

  24. Diagnosis and management of glycogen storage diseases type VI and IX: a clinical practice resource of the American College of Medical Genetics and Genomics (ACMG)

    著者: Priya S. Kishnani, Jennifer Goldstein, Stephanie Austin, Pamela Arn, Bert Bachrach, Deeksha Bali, Wendy K. Chung, Areeg El‐Gharbawy, Laurie M. Brown, Stephen G. Kahler, Surekha Pendyal, Katalin M. Ross, Laurie A. Tsilianidis, David A. Weinstein, Michael S. Watson - Genetics in Medicine 2019 被引用: 138