Peter N. Robinson

1996–2026 年に発表

別表記
Peter N Robinson
258
論文数
28,454
被引用数
89
h 指数
205
i10 指数

被引用数

Peter N. Robinson の年別被引用数1967 年: 被引用 1 件1981 年: 被引用 1 件1982 年: 被引用 1 件1984 年: 被引用 1 件1987 年: 被引用 4 件1988 年: 被引用 2 件1991 年: 被引用 1 件1996 年: 被引用 1 件1998 年: 被引用 2 件1999 年: 被引用 11 件2000 年: 被引用 15 件2001 年: 被引用 24 件2002 年: 被引用 31 件2003 年: 被引用 27 件2004 年: 被引用 24 件2005 年: 被引用 46 件2006 年: 被引用 48 件2007 年: 被引用 64 件2008 年: 被引用 81 件2009 年: 被引用 112 件2010 年: 被引用 166 件2011 年: 被引用 232 件2012 年: 被引用 241 件2013 年: 被引用 264 件2014 年: 被引用 278 件2015 年: 被引用 455 件2016 年: 被引用 527 件2017 年: 被引用 497 件2018 年: 被引用 558 件2019 年: 被引用 1,033 件2020 年: 被引用 1,036 件2021 年: 被引用 1,111 件2022 年: 被引用 1,170 件2023 年: 被引用 944 件2024 年: 被引用 1,303 件2025 年: 被引用 723 件2026 年: 被引用 98 件1968〜1980 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1985〜1986 年は被引用が無いため表示していません1989〜1990 年は被引用が無いため表示していません1992〜1995 年は被引用が無いため表示していません1997 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 3,515 件、この内訳の 23.6%イギリス: 引用元論文 1,393 件、この内訳の 9.3%ドイツ: 引用元論文 1,096 件、この内訳の 7.3%中国: 引用元論文 987 件、この内訳の 6.6%カナダ: 引用元論文 635 件、この内訳の 4.3%フランス: 引用元論文 622 件、この内訳の 4.2%イタリア: 引用元論文 575 件、この内訳の 3.9%オランダ: 引用元論文 556 件、この内訳の 3.7%オーストラリア: 引用元論文 536 件、この内訳の 3.6%スペイン: 引用元論文 466 件、この内訳の 3.1%日本: 引用元論文 307 件、この内訳の 2.1%スイス: 引用元論文 290 件、この内訳の 1.9%
0%23.6%その他 26.4%

分野

  • Biochemistry, Genetics and Molecular Biology60.9%
  • Medicine18.9%
  • Computer Science8.9%
  • Immunology and Microbiology2.9%
  • Neuroscience1.8%
  • Agricultural and Biological Sciences1.4%
  • その他5.2%

トピック

  • Bioinformatics and Genomic Networks6.8%
  • Genomics and Rare Diseases6.6%
  • Biomedical Text Mining and Ontologies5.9%
  • Gene expression and cancer classification2.8%
  • Genetic Associations and Epidemiology1.9%
  • Connective tissue disorders research1.9%
  • その他74.1%

共著者

全論文

検索で開く
  1. The Human Phenotype Ontology in 2021

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David Lagorce, Julie A. McMurry, Jillian A. Miller, Monica C. Munoz-Torres, Rebecca L. Peters, Christina K. Rapp, Ana Rath, Shahmir A. Rind, Avi Z. Rosenberg, Michael M. Segal, Markus G. Seidel, Damian Smedley, Tomer Talmy, Yarlalu Thomas, Samuel A. Wiafe, Julie Xian, Zafer Yüksel, Ingo Helbig, Christopher J. Mungall, Melissa A. Haendel, Peter N. Robinson - Nucleic Acids Research, Nucleic Acids Res. 2020 被引用: 1,240

  2. How many rare diseases are there?

    著者: , , , , , , , , , , , , , , , , , , - Nature Reviews Drug Discovery 2019 被引用: 586

  3. The National COVID Cohort Collaborative (N3C): Rationale, design, infrastructure, and deployment

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Adam M. Lee, Harold P. Lehmann, Lora Lingrey, Robert T. Miller, Michele Morris, Shawn N. Murphy, Karthik Natarajan, Matvey B. Palchuk, Usman Sheikh, Harold Solbrig, Shyam Visweswaran, Anita Walden, Kellie M. Walters, Griffin M. Weber, Xiaohan Tanner Zhang, Richard L. Zhu, Benjamin R. C. Amor, Andrew T. Girvin, Amin Manna, Nabeel Qureshi, Michael G. Kurilla, Sam G. Michael, Lili M. Portilla, Joni L. Rutter, Christopher P. Austin, Kenneth R. Gersing - Journal of the American Medical Informatics Association, J. Am. Medical Informatics Assoc. 2020 被引用: 588

  4. The Human Phenotype Ontology: A Tool for Annotating and Analyzing Human Hereditary Disease

    著者: , , , , , - The American Journal of Human Genetics 2008 被引用: 1,057

  5. Next-generation diagnostics and disease-gene discovery with the Exomiser

    著者: , , , , , , , , , , , , - Nature Protocols 2015 被引用: 466

  6. Mondo: Unifying diseases for the world, by the world

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Charles Tapley Hoyt, Megan Kane, Sebastian Köhler, David Lagorce, Abbe Lai, Martin Larralde, Antonia Lock, Irene López Santiago, Donna Maglott, Adriana J Malheiro, Birgit Meldal, Mónica Muñoz-Torres, Tristan Nelson, F. W. Nicholas, David Ochoa, Daniel Olson, Tudor I. Oprea, David Osumi-Sutherland, Helen Parkinson, Zoë May Pendlington, Ana Rath, Heidi L. Rehm, Lyubov Remennik, Erin Rooney Riggs, Paola Roncaglia, Justyne Ross, Marion Shadbolt, Kent Shefchek, Morgan Similuk, Nicholas Sioutos, Damian Smedley, Rachel Sparks, Ray Stefancsik, Ralf Stephan, Andrea L. Storm, Doron Stupp, Gregory S. Stupp, Jagadish Chandrabose Sundaramurthi, Imke Tammen, D. K. C. Tay, Courtney Thaxton, Eloise Valasek, Jordi Valls-Margarit, Alex H. Wagner, Danielle Welter, Patricia L. Whetzel, Lori Whiteman, Valerie Wood, Colleen Xu, Andreas Zankl, Xingmin Zhang, Christopher G. Chute, Peter N. Robinson, Chris Mungall, Ada Hamosh, Melissa Haendel - medRxiv 2022 被引用: 102

  7. Walking the Interactome for Prioritization of Candidate Disease Genes

    著者: , , , - The American Journal of Human Genetics 2008 被引用: 1,298

  8. The Monarch Initiative: an integrative data and analytic platform connecting phenotypes to genotypes across species

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , - Nucleic Acids Research, Nucleic Acids Res. 2016 被引用: 486

  9. Generalisable long COVID subtypes: findings from the NIH N3C and RECOVER programmes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter N. Robinson, Heidi Spratt, Shyam Visweswaran, Joseph E Flack, Yun Jae Yoo, Davera Gabriel, G. Caleb Alexander, Hemalkumar B. Mehta, Feifan Liu, Robert Miller, Rachel Wong, Elaine Hill, Lorna E. Thorpe, Jasmin Divers - EBioMedicine 2022 被引用: 177

  10. The Monarch Initiative in 2019: an integrative data and analytic platform connecting phenotypes to genotypes across species

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marcin P. Joachimiak, Simon Jupp, Kenneth B. Lett, Suzanna E. Lewis, Craig McNamara, Zoë May Pendlington, Clare Pilgrim, Tim E. Putman, Vida Ravanmehr, Justin T. Reese, Erin Rooney Riggs, Sofia M. C. Robb, Paola Roncaglia, James Seager, Erik Segerdell, Morgan Similuk, Andrea L. Storm, Courtney Thaxon, Anne E. Thessen, Julius O. B. Jacobsen, Julie A. McMurry, Tudor Groza, Sebastian Köhler, Damian Smedley, Peter N. Robinson, Christopher J. Mungall, Melissa A. Haendel, Monica C. Munoz-Torres, David Osumi-Sutherland - Nucleic Acids Research, Nucleic Acids Res. 2019 被引用: 265

  11. Classification, Ontology, and Precision Medicine

    著者: , , - New England Journal of Medicine 2018 被引用: 329

  12. The Human Phenotype Ontology in 2017

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gholson J. Lyon, Soichi Ogishima, Annie Olry, Willem H. Ouwehand, Nikolas Pontikos, Ana Rath, Franz Schaefer, Richard H. Scott, Michael Segal, Panagiotis I. Sergouniotis, Richard Sever, Cynthia L. Smith, Volker Straub, Rachel Thompson, Catherine Turner, Ernest Turro, Marijcke W. M. Veltman, Tom Vulliamy, Jing Yu, Julie von Ziegenweidt, Andreas Zankl, Stephan Züchner, Tomasz Zemojtel, Julius O. B. Jacobsen, Tudor Groza, Damian Smedley, Christopher J. Mungall, Melissa A. Haendel, Peter N. Robinson - Nucleic Acids Research, Nucleic Acids Res. 2016 被引用: 801

  13. International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter N. Robinson, Pak C. Sham, Румен Стефанов, Domenica Taruscio, Divya Unni, Megan R. Vanstone, Feng Zhang, Han G. Brunner, Michael J. Bamshad, Hanns Lochmüller - The American Journal of Human Genetics 2017 被引用: 453

  14. The GA4GH Phenopacket schema defines a computable representation of clinical data

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anastasios Papakonstantinou, Davide Piscia, Nikolas Pontikos, Núria Queralt-Rosiñach, Marco Roos, Julian Saß, Paul N. Schofield, Dominik Seelow, Anastasios Siapos, Damian Smedley, Lindsay Smith, Robin Steinhaus, Jagadish Chandrabose Sundaramurthi, Emilia M. Swietlik, Sylvia Thun, Nicole Vasilevsky, Alex H. Wagner, Jeremy L. Warner, Claus Weiland, Myles Axton, Lawrence Babb, Cornelius F. Boerkoel, Bimal P. Chaudhari, Hui‐Lin Chin, Michel Dumontier, Nour Gazzaz, David P. Hansen, Harry Hochheiser, Veronica A. Kinsler, Hanns Lochmüller, Alexander Mankovich, Gary Saunders, Panagiotis I. Sergouniotis, Rachel Thompson, Andreas Zankl, Melissa Haendel, Peter N. Robinson - Nature Biotechnology 2022 被引用: 111

  15. The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nara Sobreira, G. Jawahar Swaminathan, Peter E.M. Taschner, Sharon F. Terry, Nicole Washington, Stephan Züchner, Kym M. Boycott, Heidi L. Rehm - Human Mutation 2015 被引用: 488

  16. Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrea L. Storm, Marc Hanauer, Michael Brudno, Susan M. Bello, Murat Sincan, Kayli Rageth, Matthew T. Wheeler, Renske Oegema, Halima Lourghi, Maria G. Della Rocca, Rachel Thompson, Francisco Castellanos, James Priest, Charlotte Cunningham-Rundles, Ayushi Hegde, Ruth C. Lovering, Catherine Hajek, Annie Olry, Luigi Notarangelo, Morgan Similuk, Xingmin Aaron Zhang, David Gómez-Andrés, Hanns Lochmüller, Hélène Dollfus, Sergio Rosenzweig, Shruti Marwaha, Ana Rath, Kathleen Sullivan, Cynthia L. Smith, Joshua D. Milner, Dorothée Leroux, Cornelius F. Boerkoel, Amy Klion, Melody C. Carter, Tudor Groza, Damian Smedley, Melissa A. Haendel, Chris Mungall, Peter N. Robinson - Nucleic Acids Research, Nucleic Acids Res. 2018 被引用: 737

  17. Deep phenotyping for precision medicine

    著者: - Human Mutation 2012 被引用: 482

  18. The Monarch Initiative in 2024: an analytic platform integrating phenotypes, genes and diseases across species

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathleen R. Mullen, Shawn T. O’Neil, Kent Shefchek, Ray Stefancsik, Sabrina Toro, Nicole Vasilevsky, Ramona Walls, Patricia L. Whetzel, David Osumi-Sutherland, Damian Smedley, Peter N. Robinson, Chris Mungall, Melissa Haendel, Mónica Muñoz-Torres - Nucleic Acids Research 2023 被引用: 105

  19. Whole-exome sequencing for finding de novo mutations in sporadic mental retardation

    著者: - Genome Biology 2010 被引用: 214

  20. Clinical Diagnostics in Human Genetics with Semantic Similarity Searches in Ontologies

    著者: , , , , , , , , , - The American Journal of Human Genetics 2009 被引用: 623

  21. A Whole-Genome Analysis Framework for Effective Identification of Pathogenic Regulatory Variants in Mendelian Disease

    著者: , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2016 被引用: 295

  22. Structured Prompt Interrogation and Recursive Extraction of Semantics (SPIRES): a method for populating knowledge bases using zero-shot learning

    著者: , , , , , , , , , , , - Bioinformatics, Bioinform. 2024 被引用: 104

  23. PhenoTagger: A Hybrid Method for Phenotype Concept Recognition using Human Phenotype Ontology

    著者: , , , , , , , , , - Bioinformatics, Bioinform. 2021 被引用: 77

  24. Phenolyzer: phenotype-based prioritization of candidate genes for human diseases

    著者: , , - Nature Methods 2015 被引用: 439