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John B. Vincent

1987–2025 年に発表

101
論文数
22,719
被引用数
81
h 指数
98
i10 指数

被引用数

John B. Vincent の年別被引用数1966 年: 被引用 1 件1988 年: 被引用 4 件1989 年: 被引用 23 件1990 年: 被引用 12 件1991 年: 被引用 13 件1992 年: 被引用 8 件1993 年: 被引用 11 件1994 年: 被引用 18 件1995 年: 被引用 17 件1996 年: 被引用 33 件1997 年: 被引用 21 件1998 年: 被引用 32 件1999 年: 被引用 32 件2000 年: 被引用 41 件2001 年: 被引用 43 件2002 年: 被引用 52 件2003 年: 被引用 64 件2004 年: 被引用 89 件2005 年: 被引用 89 件2006 年: 被引用 87 件2007 年: 被引用 110 件2008 年: 被引用 212 件2009 年: 被引用 246 件2010 年: 被引用 282 件2011 年: 被引用 290 件2012 年: 被引用 330 件2013 年: 被引用 322 件2014 年: 被引用 292 件2015 年: 被引用 253 件2016 年: 被引用 207 件2017 年: 被引用 203 件2018 年: 被引用 166 件2019 年: 被引用 442 件2020 年: 被引用 455 件2021 年: 被引用 453 件2022 年: 被引用 322 件2023 年: 被引用 201 件2024 年: 被引用 313 件2025 年: 被引用 135 件2026 年: 被引用 3 件1967〜1987 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 2,614 件、この内訳の 25.8%イギリス: 引用元論文 862 件、この内訳の 8.5%ドイツ: 引用元論文 605 件、この内訳の 6%カナダ: 引用元論文 557 件、この内訳の 5.5%中国: 引用元論文 486 件、この内訳の 4.8%フランス: 引用元論文 454 件、この内訳の 4.5%オランダ: 引用元論文 375 件、この内訳の 3.7%イタリア: 引用元論文 370 件、この内訳の 3.6%オーストラリア: 引用元論文 339 件、この内訳の 3.3%スペイン: 引用元論文 240 件、この内訳の 2.4%スウェーデン: 引用元論文 237 件、この内訳の 2.3%日本: 引用元論文 226 件、この内訳の 2.2%
0%25.8%その他 27.4%

機関

分野

  • Biochemistry, Genetics and Molecular Biology50%
  • Neuroscience17.2%
  • Medicine14.2%
  • Materials Science5.9%
  • Environmental Science3.1%
  • Psychology2.8%
  • その他6.8%

トピック

  • 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%
  • その他72.3%

共著者

全論文

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  1. Structural Variation of Chromosomes in Autism Spectrum Disorder

    著者: Christian R. Marshall, Abdul Noor, John B. Vincent, Anath C. Lionel, Lars Feuk, Jennifer Skaug, Mary Shago, Rainald Moessner, Dalila Pinto, Yan Ren, Bhooma Thiruvahindrapduram, Andreas Fiebig, Stefan Schreiber, Jan M. Friedman, Cees Ketelaars, Yvonne J. Vos, Can Fıçıcıoğlu, Susan J. Kirkpatrick, Rob Nicolson, Leon Sloman, Anne Summers, Clare Gibbons, Ahmad S. Teebi, David Chitayat, Rosanna Weksberg, Ann Thompson, Cathy Vardy, Vicki Crosbie, Sandra Luscombe, Rebecca Baatjes, Lonnie Zwaigenbaum, Wendy Roberts, Bridget A. Fernandez, Péter Szatmári, Stephen W. Scherer - The American Journal of Human Genetics 2008 被引用: 1,843

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

    著者: Taimoor I. Sheikh, Nasim Vasli, Stephen F. Pastore, Kimia Kharizi, Ricardo Harripaul, Zohreh Fattahi, Shruti Pande, Farooq Naeem, A. Hussain, Asif Mir, Omar Islam, Katta M. Girisha, Muhammad Irfan, Muhammad Ayub, Christoph Schwarzer, Hossein Najmabadi, Anju Shukla, Valentina C. Sladky, Vincent Z. Braun, Irmina García-Carpio, Andreas Villunger, John B. Vincent - Translational Psychiatry 2021 被引用: 149

  3. Contribution of SHANK3 Mutations to Autism Spectrum Disorder

    著者: Rainald Moessner, Christian R. Marshall, James S. Sutcliffe, Jennifer Skaug, Dalila Pinto, John B. Vincent, Lonnie Zwaigenbaum, Bridget A. Fernandez, Wendy Roberts, Péter Szatmári, Stephen W. Scherer - The American Journal of Human Genetics 2007 被引用: 691

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

    著者: Liyun Sang, Julie J. Miller, Kevin C. Corbit, Rachel H. Giles, Matthew J. Brauer, Edgar A. Otto, Lisa M. Baye, Xiaohui Wen, Suzie J. Scales, Mandy Kwong, Erik G. Huntzicker, Mindan K. Sfakianos, Wendy Sandoval, J. Fernando Bazán, Priya Kulkarni, Francesc R. García-Gonzalo, Allen D Seol, John F. O’Toole, Susanne Held, Heiko Reutter, William S. Lane, Muhammad Rafiq, Abdul Noor, Muhammad Ansar, Akella Radha Rama Devi, Val C. Sheffield, Diane C. Slusarski, John B. Vincent, Daniel Doherty, Friedhelm Hildebrandt, Jeremy F. Reiter, Peter K. Jackson - Cell 2011 被引用: 630

  5. MeCP2: The Genetic Driver of Rett Syndrome Epigenetics

    著者: Katrina Good, John B. Vincent, Juan Ausió - Frontiers in Genetics 2021 被引用: 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

    著者: Patrick Rossignol, Daniela Dobre, John J.V. McMurray, Karl Swedberg, Henry Krum, Dirk J. van Veldhuisen, Harry Shi, Michael Messig, John B. Vincent, Nicolas Girerd, George L. Bakris, Bertram Pitt, Faı̈ez Zannad - Circulation Heart Failure 2013 被引用: 254

  7. Mutations disrupting neuritogenesis genes confer risk for cerebral palsy

    著者: Sheng Chih Jin, Sara A. Lewis, Somayeh Bakhtiari, Xue Zeng, Michael C. Sierant, Sheetal Shetty, Sandra M. Nordlie, Aureliane Elie, Mark Corbett, Bethany Y. Norton, Clare L. van Eyk, Shozeb Haider, Brandon S. Guida, Helen Magee, James H. Liu, Stephen F. Pastore, John B. Vincent, Janice Brunstrom-Hernandez, Antigone Papavasileiou, Michael Fahey, Jesia G. Berry, Kelly Harper, Chongchen Zhou, Junhui Zhang, Boyang Li, Hongyu Zhao, Jennifer Heim, Dani L. Webber, Mahalia S. B. Frank, Lei Xia, 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 被引用: 175

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

    著者: Niamh Mullins, Tim B. Bigdeli, Anders D. Børglum, Jonathan R. I. Coleman, Ditte Demontis, Divya Mehta, Robert A. Power, Stephan Ripke, Eli A. Stahl, Anna Starnawska, Adebayo Anjorin, M.R.C.Psych, Aiden Corvin, Alan R. Sanders, Andreas J. Forstner, Andreas Reif, Anna C. Koller, Beata Świątkowska, Bernhard T. Baune, Bertram Müller-Myhsok, Brenda W.J.H. Penninx, Carlos N. Pato, Clement C. Zai, Dan Rujescu, David M. Hougaard, Digby Quested, Douglas F. Levinson, Elisabeth B. Binder, Enda M. Byrne, Esben Agerbo, 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 ほか 23 名 - American Journal of Psychiatry 2019 被引用: 285

  9. New Evidence against Chromium as an Essential Trace Element

    著者: John B. Vincent - Journal of Nutrition 2017 被引用: 224

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

    著者: Roberta Sessoli, Hui Lien Tsai, Ann R. Schake, Sheyi Wang, John B. Vincent, Kirsten Folting, Dante Gatteschi, George Christou, David N. Hendrickson - Journal of the American Chemical Society 1993 被引用: 2,266

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

    著者: Pamela Sklar, Stephan Ripke, Laura J. Scott, Ole A. Andreassen, Sven Cichon, Nick Craddock, Howard J. Edenberg, John I. Nürnberger, Marcella Rietschel, Douglas Blackwood, Aiden Corvin, Matthew Flickinger, Weihua Guan, Morten Mattingsdal, Andrew McQuillin, Phoenix Kwan, Thomas F. Wienker, Mark J. Daly, Frank Dudbridge, Peter Holmans, Danyu Lin, Margit Burmeister, Tiffany A. Greenwood, Marian L. Hamshere, Pierandrea Muglia, Erin N. Smith, Peter P. Zandi, Caroline M. Nievergelt, R. Anne McKinney, Paul D. Shilling, 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 ほか 72 名 - Nature Genetics 2011 被引用: 1,412

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

    著者: Muzammil Ahmad Khan, Muhammad Rafiq, Abdul Noor, Shobbir Hussain, Joana V. Flores, Verena Rupp, Akshita K. Vincent, Roland Malli, Ghazanfar Ali, Falak Sher Khan, Gisele E. Ishak, Dan Doherty, Rosanna Weksberg, Muhammad Ayub, Christian Windpassinger, Shahnaz Ibrahim, Michaela Frye, Muhammad Ansar, John B. Vincent - The American Journal of Human Genetics 2012 被引用: 231

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

    著者: Mark A. Ditmer, John B. Vincent, Leland K. Werden, Jessie C. Tanner, Timothy G. Laske, Paul A. Iaizzo, David L. Garshelis, John Fieberg - Current Biology 2015 被引用: 345

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

    著者: Jason Z. Liu, Federica Tozzi, Dawn Waterworth, Sreekumar Pillai, Pierandrea Muglia, Lefkos Middleton, Wade H. Berrettini, Christopher W. Knouff, Xin Yuan, Gérard Waeber, Péter Vollenweider, Martin Preisig, Nicholas J. Wareham, Jing Hua Zhao, Ruth J. F. Loos, Inês Barroso, Kay‐Tee Khaw, Scott M. Grundy, Philip J. Barter, Robert W. Mahley, Antero Kesäniemi, Ruth McPherson, John B. Vincent, John S. Strauss, James L. Kennedy, Anne Farmer, Peter McGuffin, Richard Day, K. Matthews, Per Bakke, 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 ほか 6 名 - Nature Genetics 2010 被引用: 618

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

    著者: Jedidiah Carlson, Adam E. Locke, Matthew Flickinger, Matthew Zawistowski, Shawn Levy, R Myers, Michael Boehnke, Hyun Min Kang, Laura J. Scott, Jun Z. Li, Sebastian Zöllner, Devin Absher, Huda Akil, Gerome Breen, Margit Burmeister, Sarah Cohen‐Woods, William G. Iacono, James A. Knowles, Lisa N. Legrand, Qing Lu, Matthew McGue, Melvin G. McInnis, Carlos N. Pato, Michele T. Pato, Margarita Rivera, Janet L. Sobell, John B. Vincent, Stanley J. Watson - Nature Communications 2018 被引用: 160

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

    著者: Dévina C. Ung, Giovanni Iacono, Hamid Méziane, Edward Blanchard, M-A Papon, Martijn Selten, J-R van Rhijn, Rodrick Montjean, J. Rucci, Stéphane Martin, Andrew Fleet, M-C Birling, Sylviane Marouillat, Ronald Roepman, Mohammed Selloum, Aline Lux, R-A Thépault, Paul A. Hamel, Kirti Mittal, John B. Vincent, Olivier Dorseuil, H.G. Stunnenberg, Pierre Billuart, Nael Nadif Kasri, Yann Hérault, Frédéric Laumonnier - Molecular Psychiatry 2017 被引用: 89

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

    著者: Péter Szatmári, Ping G. Tepper, Ann Thompson, Jennifer Skaug, Andrew D. Paterson, Lars Feuk, Qian Cheng, Christian R. Marshall, Christian R Marshall, Stephen W. Scherer, Lonnie Zwaigenbaum, Jessica Brian, Lili Senman, Wendy Roberts, John B. Vincent, Susan E. Bryson, Marshall B. Jones, Veronica J. Vieland, La Vonne Mangin, Christopher W. Bartlett, Alberto M. Segre, Rhinda Goedken, Michael L. Cuccaro, Margaret A. Pericak‐Vance, John R. Gilbert, Harry H. Wright, Ruth K. Abramson, Catalina Betancur, Marion Leboyer, Thomas Bourgeron, 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 ほか 38 名 - Nature Genetics 2007 被引用: 1,416

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

    著者: Gevork N. Mnatzakanian, Hannes Lohi, Iulia Munteanu, Simon E. Alfred, Takahiro Yamada, Patrick J. M. MacLeod, Julie R. Jones, Stephen W. Scherer, N. Carolyn Schanen, Michael J. Friez, John B. Vincent, Berge A. Minassian - Nature Genetics 2004 被引用: 346

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

    著者: Alexia Martínez de Paz, Leila Khajavi, Hélène Martin, Rafael Claveria‐Gimeno, Susanne tom Dieck, Manjinder S. Cheema, José V. Sánchez‐Mut, Malgorzata M. Moksa, Annaïck Carles, Nick I. Brodie, Taimoor I. Sheikh, Melissa E. Freeman, Evgeniy V. Petrotchenko, Christoph H. Borchers, Erin M. Schuman, Matthias Zytnicki, Adrián Velázquez‐Campoy, Olga Abián, Martin Hirst, Manel Esteller, John B. Vincent, Cécile E. Malnou, Juan Ausió - Epigenetics & Chromatin 2019 被引用: 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

    著者: Andreea Manole, Stéphanie Efthymiou, Emer O’Connor, Marisa I. Mendes, Matthew J. Jennings, Reza Maroofian, Indran Davagnanam, Kshitij Mankad, Maria Rodríguez‐López, Vincenzo Salpietro, Ricardo Harripaul, Lauren Badalato, Jagdeep S. Walia, Christopher S. Francklyn, Alkyoni Athanasiou‐Fragkouli, Roisin Sullivan, Sonal Desai, Kristin Barañano, Faisal Zafar, Nuzhat Rana, Muhammad Ilyas, Alejandro Horga, Majdi Kara, Francesca Mattioli, Alice Goldenberg, Helen Griffin, Amélie Piton, Lindsay B. Henderson, Benyekhlef Kara, Ayça Dilruba Aslanger, 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 被引用: 64

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

    著者: Ricardo Harripaul, Nasim Vasli, А. О. Михайлов, Muhammad Rafiq, Kirti Mittal, Christian Windpassinger, Taimoor I. Sheikh, Abdul Noor, Hina Mahmood, Samantha I Downey, Maneesha Johnson, Kayla Vleuten, Lauren Bell, Muhammad Ilyas, Falak Sher Khan, Valeed Khan, Mohammad Moradi, M. Ayaz, Farooq Naeem, Asieh Heidari, Iqra I. Ahmed, Shirin Ghadami, Zehra Agha, Sirous Zeinali, Raheel Qamar, Hossein Mozhdehipanah, Peter John, Asif Mir, Muhammad Ansar, Leon French, Muhammad Ayub, John B. Vincent - Molecular Psychiatry 2017 被引用: 183

  22. The Biochemistry of Chromium

    著者: John B. Vincent - Journal of Nutrition 2000 被引用: 452

  23. Chromium

    著者: John B. Vincent, Henry C. Lukaski - Advances in Nutrition 2018 被引用: 85

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

    著者: Laura J. Scott, Pierandrea Muglia, Xiangyang Kong, Weihua Guan, Matthew Flickinger, Ruchi Upmanyu, Federica Tozzi, Jun Z. Li, Margit Burmeister, Devin Absher, Robert C. Thompson, Clyde Francks, Fan Meng, Άθως Αντωνιάδης, Audrey M. Southwick, Alan F. Schatzberg, William E. Bunney, Jack D. Barchas, Edward G. Jones, Richard Day, K. Matthews, Peter McGuffin, John S. Strauss, James L. Kennedy, Lefkos Middleton, Allen D. Roses, Stanley J. Watson, John B. Vincent, R Myers, Ann E. Farmer, Huda Akil, Daniel K. Burns, Michael Boehnke - National Academy of Sciences, Proceedings of the National Academy of Sciences 2009 被引用: 320