John B. Vincent

Active 1987–2025

101
Papers
22,719
Citations
81
h-index
98
i10-index

Citations

Citations per year for John B. Vincent1966: 1 citations1988: 4 citations1989: 23 citations1990: 12 citations1991: 13 citations1992: 8 citations1993: 11 citations1994: 18 citations1995: 17 citations1996: 33 citations1997: 21 citations1998: 32 citations1999: 32 citations2000: 41 citations2001: 43 citations2002: 52 citations2003: 64 citations2004: 89 citations2005: 89 citations2006: 87 citations2007: 110 citations2008: 212 citations2009: 246 citations2010: 282 citations2011: 290 citations2012: 330 citations2013: 322 citations2014: 292 citations2015: 253 citations2016: 207 citations2017: 203 citations2018: 166 citations2019: 442 citations2020: 455 citations2021: 453 citations2022: 322 citations2023: 201 citations2024: 313 citations2025: 135 citations2026: 3 citations1967–1987: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 2,614 citing papers, 25.8% of this breakdownUnited Kingdom: 862 citing papers, 8.5% of this breakdownGermany: 605 citing papers, 6% of this breakdownCanada: 557 citing papers, 5.5% of this breakdownChina: 486 citing papers, 4.8% of this breakdownFrance: 454 citing papers, 4.5% of this breakdownNetherlands: 375 citing papers, 3.7% of this breakdownItaly: 370 citing papers, 3.6% of this breakdownAustralia: 339 citing papers, 3.3% of this breakdownSpain: 240 citing papers, 2.4% of this breakdownSweden: 237 citing papers, 2.3% of this breakdownJapan: 226 citing papers, 2.2% of this breakdown
0%25.8%Other 27.4%

Fields

  • Biochemistry, Genetics and Molecular Biology50%
  • Neuroscience17.2%
  • Medicine14.2%
  • Materials Science5.9%
  • Environmental Science3.1%
  • Psychology2.8%
  • Other6.8%

Topics

  • Genetics and Neurodevelopmental Disorders8.3%
  • Autism Spectrum Disorder Research6.3%
  • Genomic variations and chromosomal abnormalities4.6%
  • Genetic Associations and Epidemiology3.6%
  • Genomics and Rare Diseases2.6%
  • Congenital heart defects research2.3%
  • Other72.3%

Coauthors

All papers

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  1. Structural Variation of Chromosomes in Autism Spectrum Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lonnie Zwaigenbaum, Wendy Roberts, Bridget A. Fernandez, Péter Szatmári, Stephen W. Scherer - The American Journal of Human Genetics 2008 cited by 1,843

  2. Biallelic mutations in the death domain of PIDD1 impair caspase-2 activation and are associated with intellectual disability

    Authors: , , , , , , , , , , , , , , , , , , , , , - Translational Psychiatry 2021 cited by 149

  3. Contribution of SHANK3 Mutations to Autism Spectrum Disorder

    Authors: , , , , , , , , , , - The American Journal of Human Genetics 2007 cited by 691

  4. Mapping the NPHP-JBTS-MKS Protein Network Reveals Ciliopathy Disease Genes and Pathways

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jeremy F. Reiter, Peter K. Jackson - Cell 2011 cited by 630

  5. MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

    Authors: , , - Frontiers in Genetics 2021 cited by 147

  6. Incidence, Determinants, and Prognostic Significance of Hyperkalemia and Worsening Renal Function in Patients With Heart Failure Receiving the Mineralocorticoid Receptor Antagonist Eplerenone or Placebo in Addition to Optimal Medical Therapy

    Authors: , , , , , , , , , , , , - Circulation Heart Failure 2013 cited by 254

  7. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yiran Xu, Dengna Zhu, Bohao Zhang, Amar H. Sheth, James Knight, Christopher Castaldi, Irina R. Tikhonova, Francesc López‐Giráldez, Boris Keren, Sandra Whalen, Julien Buratti, Diane Doummar, Megan Cho, Kyle Retterer, Francisca Millan, Yangong Wang, Jeff L. Waugh, Lance H. Rodan, Julie S. Cohen, Ali Fatemi, Angela E. Lin, J. P. Phillips, Timothy Feyma, Suzanna C. MacLennan, Spencer Vaughan, Kylie Crompton, Susan Reid, Dinah Reddihough, Qing Shang, Chao Gao, Iona Novak, Nadia Badawi, Yana A. Wilson, Sarah McIntyre, Shrikant Mane, Xiaoyang Wang, David J. Amor, Daniela C. Zarnescu, Qiongshi Lu, Qinghe Xing, Changlian Zhu, Kaya Bilgüvar, Sergio Padilla‐Lopez, Richard P. Lifton, Jozef Gécz, Alastair H. MacLennan, Michael C. Kruer - Nature Genetics 2020 cited by 175

  8. GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Dr.Med.Sc, Fabian Streit, Fermín Mayoral, Frank Bellivier, Franziska Degenhardt, Gerome Breen, Gunnar Morken, Gustavo Turecki, Guy A. Rouleau, Hans J. Grabe, Henry Völzke, Ian Jones, Ina Giegling, Ingrid Agartz, Ingrid Melle, Jacob Lawrence, M.R.C.Psych, James Walters, Jana Strohmaier, Jianxin Shi, Joanna Hauser, Joanna M. Biernacka, John B. Vincent, John R. Kelsoe, John S. Strauss, Jolanta Lissowska, Jonathan Pimm, M.R.C.Psych, Jordan W. Smoller, José Guzmán‐Parra, Klaus Berger, Laura J. Scott, Lisa Jones, Maria Helena Pinto de Azevedo, Maciej Trzaskowski, Manolis Kogevinas, Marcella Rietschel, Marco P. Boks, Marcus Ising, Maria Grigoroiu‐Serbânescu, Marian L. Hamshere, Marion Leboyer, Mark A. Frye, Markus M. Nöthen, Martin Alda, Martin Preisig, Merete Nordentoft, Michael Boehnke, Michael O‘Donovan, Michael J. Owen, Michele T. Pato, Miguel E. Rentería, Monika Budde, Dipl.-Psych, Myrna M. Weissman, Naomi R. Wray, Nicholas Bass, M.R.C.Psych, Nicholas Craddock, Olav B. Smeland, Ole A. Andreassen, Ole Mors, Pablo V. Gejman, Pamela Sklar, Patrick J. McGrath, Per Hoffmann, Peter McGuffin, Phil H. Lee, Preben Bo Mortensen, René S. Kahn and 23 more - American Journal of Psychiatry 2019 cited by 285

  9. New Evidence against Chromium as an Essential Trace Element

    Authors: - Journal of Nutrition 2017 cited by 224

  10. High-spin molecules: [Mn12O12(O2CR)16(H2O)4]

    Authors: , , , , , , , , - Journal of the American Chemical Society 1993 cited by 2,266

  11. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nicholas J. Schork, Cinnamon S. Bloss, Tatiana Foroud, Daniel L. Koller, Elliot S. Gershon, Chunyu Liu, Judith A. Badner, William A. Scheftner, William Lawson, Evaristus Nwulia, Maria Hipolito, William Coryell, John Rice, William Byerley, Francis J. McMahon, Thomas G. Schulze, Wade H. Berrettini, Falk W. Lohoff, James B. Potash, Pamela B. Mahon, Melvin G. McInnis, Sebastian Zöllner, Peng Zhang, David W. Craig, Szabocls Szelinger, Thomas B. Barrett, René Breuer, Sandra Meier, Jana Strohmaier, Stephanie H. Witt, Federica Tozzi, Anne Farmer, Peter McGuffin, John S. Strauss, Wei Xu, James L Kennedy, John B. Vincent, K. Matthews, Richard Day, Manuel A. R. Ferreira, Colm Ó'Dúshláine, Roy H. Perlis, Soumya Raychaudhuri, Douglas M. Ruderfer, Phil H Lee, Jordan W. Smoller, Jun Li, Devin Absher, William E. Bunney, Jack D. Barchas, Alan F. Schatzberg, Edward G. Jones, Fan Meng, Robert C. Thompson, Stanley J. Watson, Richard M. Myers, Huda Akil, Michael Boehnke, Kim Chambert, Jennifer L. Moran, Ed Scolnick, Srdjan Djurovic, Ingrid Melle, Gunnar Morken, Michael Gill, Derek W. Morris, Emma M. Quinn, Thomas W. Mühleisen, Franziska Degenhardt, Manuel Mattheisen and 72 more - Nature Genetics 2011 cited by 1,412

  12. Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

    Authors: , , , , , , , , , , , , , , , , , , - The American Journal of Human Genetics 2012 cited by 231

  13. Bears Show a Physiological but Limited Behavioral Response to Unmanned Aerial Vehicles

    Authors: , , , , , , , - Current Biology 2015 cited by 345

  14. Meta-analysis and imputation refines the association of 15q25 with smoking quantity

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Amund Gulsvik, Susanne Lucae, Marcus Ising, T. Brueckl, Sonja Horstmann, H‐Erich Wichmann, Rajesh Rawal, Norbert Dahmen, Claudia Lamina, Ozren Polašek, Lina Zgaga, Jennifer E. Huffman, Susan Campbell, Jaspal S. Kooner, John C. Chambers, Mary Susan Burnett, Joseph M. Devaney, Augusto D. Pichard, Kenneth M. Kent, Lowell Satler, Joseph Lindsay, Ron Waksman, Stephen E. Epstein, James F. Wilson, Sarah H. Wild, Harry Campbell, Véronique Vitart, Muredach P. Reilly, Mingyao Li, Liming Qu, Robert Wilensky, William Matthai, Håkon Håkonarson, Daniel J. Rader, André Franke, Michael Wittig, Arne Schäfer, Manuela Uda, Antonio Terracciano, Xiangjun Xiao, Fabio Busonero, Paul Scheet, David Schlessinger, David St Clair, Dan Rujescu, Gonçalo R. Abecasis, Hans J. Grabe, Alexander Teumer, Henry Völzke, Astrid Petersmann, Ulrich John, Igor Rudan, Caroline Hayward, Alan F. Wright, Ivana Kolčić, Benjamin J. Wright, John R. Thompson, Anthony J. Balmforth, Alistair S. Hall, Nilesh J. Samani, Carl A. Anderson, Tariq Ahmad, Christopher G. Mathew, Miles Parkes, Jack Satsangi, Mark J. Caulfield, Patricia B. Munroe, Martin Farrall, Anna F. Dominiczak, Jane Worthington and 6 more - Nature Genetics 2010 cited by 618

  15. Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2018 cited by 160

  16. Ptchd1 deficiency induces excitatory synaptic and cognitive dysfunctions in mouse

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2017 cited by 89

  17. Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Christopher Gillberg, Marion Leboyer, Eric Hollander, Jeremy M. Silverman, Kenneth L. Davis, Joseph D. Buxbaum, Linda Lotspeich, Joachim Hallmayer, James S. Sutcliffe, James S. Sutcliffe, Jonathan L. Haines, Susan E. Folstein, Joseph Piven, Val C. Sheffield, Kacie J. Meyer, Thomas H. Wassink, Daniel H. Geschwind, Maja Bućan, W. Ted Brown, Rita M. Cantor, Stan F. Nelson, John N. Constantino, T. Conrad Gilliam, Martha R. Herbert, Janet Miller, Clara Lajonchere, David H. Ledbetter, Christa Lese‐Martin, Carol A Samango-Sprouse, Sarah Spence, Fred R. Volkmar, Matthew W. State, Rudolph E. Tanzi, Hilary Coon, William M. McMahon, Jeff Munson, Géraldine Dawson, Géraldine Dawson, Annette Estes, Lambertus Klei, Nancy J. Minshew, Bernie Devlin, Pamela Flodman, Moyra Smith, M. Anne Spence, Chang-En Yu, Gerard D. Schellenberg, Elena Korvatska, Bernadette Rogé, Gerard D. Schellenberg, Elena Korvatska, Patricia M. Rodier, Chris Stodgell, Gerard D. Schellenberg, Ellen M. Wijsman, Ellen M. Wijsman, Kerstin Wittemeyer, Bernadette Rogé, Carine Mantoulan, Bärbel Felder, Sabine M. Klauck, Annemarie Poustka, Claudia Schuster, Gabi Schmötzer, Sven Bölte, Fritz Poustka, Sabine Feineis-Matthews, Evelyn Herbrecht, Κaterina Papanikolaou, John Tsiantis and 38 more - Nature Genetics 2007 cited by 1,416

  18. A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome

    Authors: , , , , , , , , , , , - Nature Genetics 2004 cited by 346

  19. MeCP2-E1 isoform is a dynamically expressed, weakly DNA-bound protein with different protein and DNA interactions compared to MeCP2-E2

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Epigenetics & Chromatin 2019 cited by 72

  20. De Novo and Bi-allelic Pathogenic Variants in NARS1 Cause Neurodevelopmental Delay Due to Toxic Gain-of-Function and Partial Loss-of-Function Effects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Joost Raaphorst, Rolph Pfundt, R Portier, Marwan Shinawi, Amelia Kirby, Katherine Christensen, Lu Wang, Rasim Özgür Rosti, Sohail Aziz Paracha, Muhammad Tahir Sarwar, Dagan Jenkins, Jawad Ahmed, Federico Santoni, Emmanuelle Ranza, Justyna Iwaszkiewicz, Cheryl Cytrynbaum, Rosanna Weksberg, Ingrid M. Wentzensen, María J. Guillen Sacoto, Yue Si, Aida Telegrafi, Marisa V. Andrews, Dustin Baldridge, Heinz Gabriel, Julia Mohr, Barbara Oehl‐Jaschkowitz, Sylvain Debard, Bruno Senger, Frédéric Fischer, Conny van Ravenwaaij, Annemarie Fock, Servi J.C. Stevens, Jürg Bähler, Amina Nasar, John F. Mantovani, Adnan Manzur, Anna Sarkozy, Desirée E.C. Smith, Gajja S. Salomons, Zubair M. Ahmed, S. Riazuddin, Saima Riazuddin, Muhammad A. Usmani, Annette Seibt, Muhammad Ansar, Stylianos E. Antonarakis, John B. Vincent, Muhammad Ayub, Mona Grimmel, Anne Marie Jelsig, Tina Duelund Hjortshøj, Helena Gásdal Karstensen, Marybeth Hummel, Tobias B. Haack, Yalda Jamshidi, Felix Distelmaier, Rita Horváth, Joseph G. Gleeson, H. D. Becker, Jean-Louis Mandel, David A. Koolen, Henry Houlden - The American Journal of Human Genetics 2020 cited by 64

  21. Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Muhammad Ayub, John B. Vincent - Molecular Psychiatry 2017 cited by 183

  22. The Biochemistry of Chromium

    Authors: - Journal of Nutrition 2000 cited by 452

  23. Chromium

    Authors: , - Advances in Nutrition 2018 cited by 85

  24. Genome-wide association and meta-analysis of bipolar disorder in individuals of European ancestry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Huda Akil, Daniel K. Burns, Michael Boehnke - National Academy of Sciences, Proceedings of the National Academy of Sciences 2009 cited by 320