Lambertus Klei

2003–2025 年に発表

62
論文数
29,742
被引用数
50
h 指数
60
i10 指数

被引用数

Lambertus Klei の年別被引用数1989 年: 被引用 1 件1992 年: 被引用 1 件1995 年: 被引用 2 件2000 年: 被引用 1 件2002 年: 被引用 1 件2003 年: 被引用 1 件2005 年: 被引用 1 件2006 年: 被引用 2 件2007 年: 被引用 45 件2008 年: 被引用 93 件2009 年: 被引用 120 件2010 年: 被引用 197 件2011 年: 被引用 250 件2012 年: 被引用 310 件2013 年: 被引用 329 件2014 年: 被引用 375 件2015 年: 被引用 474 件2016 年: 被引用 420 件2017 年: 被引用 476 件2018 年: 被引用 460 件2019 年: 被引用 1,285 件2020 年: 被引用 1,407 件2021 年: 被引用 1,540 件2022 年: 被引用 1,144 件2023 年: 被引用 805 件2024 年: 被引用 1,140 件2025 年: 被引用 494 件2026 年: 被引用 27 件1990〜1991 年は被引用が無いため表示していません1993〜1994 年は被引用が無いため表示していません1996〜1999 年は被引用が無いため表示していません2001 年は被引用が無いため表示していません2004 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 4,349 件、この内訳の 28.1%イギリス: 引用元論文 1,388 件、この内訳の 9%中国: 引用元論文 978 件、この内訳の 6.3%ドイツ: 引用元論文 772 件、この内訳の 5%カナダ: 引用元論文 751 件、この内訳の 4.8%オランダ: 引用元論文 596 件、この内訳の 3.8%イタリア: 引用元論文 555 件、この内訳の 3.6%フランス: 引用元論文 528 件、この内訳の 3.4%オーストラリア: 引用元論文 504 件、この内訳の 3.3%スウェーデン: 引用元論文 395 件、この内訳の 2.5%日本: 引用元論文 363 件、この内訳の 2.3%スペイン: 引用元論文 347 件、この内訳の 2.2%
0%28.1%その他 25.7%

分野

  • Biochemistry, Genetics and Molecular Biology49.6%
  • Neuroscience29.3%
  • Medicine14.2%
  • Psychology2.8%
  • Immunology and Microbiology0.9%
  • Nursing0.6%
  • その他2.6%

トピック

  • Genetics and Neurodevelopmental Disorders9.9%
  • Autism Spectrum Disorder Research9.6%
  • Genetic Associations and Epidemiology4.9%
  • Genomic variations and chromosomal abnormalities4.8%
  • Genomics and Rare Diseases3.6%
  • Congenital heart defects research2.7%
  • その他64.5%

共著者

全論文

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  1. Identification of common genetic risk variants for autism spectrum disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2019 被引用: 2,632

  2. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Ángel Carracedo, Marcus C.Y. Chan, Andreas G. Chiocchetti, Brian Hon‐Yin Chung, Hilary Coon, Michael L. Cuccaro, Aurora Currò, Bernardo Dalla Bernardina, Ryan N. Doan, Enrico Domenici, Shan Dong, Chiara Fallerini, Montse Fernández‐Prieto, Giovanni Battista Ferrero, Christine M. Freitag, Menachem Fromer, J. Jay Gargus, Daniel H. Geschwind, Elisa Giorgio, Javier González‐Peñas, Stephen J. Guter, Danielle Halpern, Emily Hansen‐Kiss, Xin He, Gail E. Herman, Irva Hertz‐Picciotto, David M. Hougaard, Christina M. Hultman, Iuliana Ionita‐Laza, Suma Jacob, Jesslyn Jamison, Astanand Jugessur, Miia Kaartinen, Gun Peggy Knudsen, A lexander Kolevzon, Itaru Kushima, So Lun Lee, Terho Lehtimäki, Elaine T. Lim, Carla Lintas, W. Ian Lipkin, Diego Lopergolo, Fátima Lopes, Yunin Ludeña, Patrı́cia Maciel, Per Magnus, Behrang Mahjani, Nell Maltman, Dara S. Manoach, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Eduarda Morgana Silva Montenegro, Danielle de Paula Moreira, Eric M. Morrow, Ole Mors, Preben Bo Mortensen, Matthew W. Mosconi, Pierandrea Muglia, Benjamin M. Neale, Merete Nordentoft, Norio Ozaki, Aarno Palotie, Mara Parellada, Maria Rita Passos‐Bueno, Margaret A. Pericak‐Vance, Antonio M. Persico, Isaac N. Pessah, Kaija Puura ほか 90 名 - Cell 2020 被引用: 2,501

  3. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Enrico Domenici, Giovanni Battista Ferrero, J. Jay Gargus, Gail E. Herman, Irva Hertz‐Picciotto, Patrı́cia Maciel, Dara S. Manoach, Maria Rita Passos‐Bueno, Antonio M. Persico, Alessandra Renieri, James S. Sutcliffe, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Simona Cardaropoli, Diana Carli, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina De Sanctis Girardi, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Rebecca J. Schmidt, Moyra Smith, Claudia Ismania Samogy Costa, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, Branko Aleksić, Mykyta Artomov, Elisa Benetti, Monica Biscaldi-Schafer, Anders D. Børglum, Ángel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montse Fernández‐Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, A lexander Kolevzon, Itaru Kushima, Terho Lehtimäki, Caterina Lo Rizzo, Nell Maltman, Marianna Manara, Gal Meiri, Idan Menashe, Judith Miller, Nancy J. Minshew, Matthew W. Mosconi, Norio Ozaki, Aarno Palotie, Mara Parellada, Kaija Puura, Abraham Reichenberg, Sven Sandin, Stephen W. Scherer, Sabine Schlitt ほか 17 名 - Nature Genetics 2022 被引用: 617

  4. Synaptic, transcriptional and chromatin genes disrupted in autism

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Eftichia Duketis, Bridget A. Fernandez, Louise Gallagher, Evan Geller, Stephen J. Guter, R. Sean Hill, Iuliana Ionita‐Laza, Patricia González, Helena Kilpinen, Sabine M. Klauck, A lexander Kolevzon, Irene Lee, Jing Lei, Terho Lehtimäki, Chiao‐Feng Lin, Avi Ma’ayan, Christian R. Marshall, Alison McInnes, Benjamin M. Neale, Michael J. Owen, Norio Ozaki, Mara Parellada, Jeremy Parr, Shaun Purcell, Kaija Puura, Deepthi Rajagopalan, Karola Rehnström, Abraham Reichenberg, Aniko Sabo, Michael Sachse, Stephan Sanders, Chad Schafer, Martin Schulte‐Rüther, David Skuse, Christine Stevens, Péter Szatmári, Kristiina Tammimies, Otto Valladares, Annette Voran, Li‐San Wang, Lauren A. Weiss, A. Jeremy Willsey, Timothy W. Yu, Ryan K. C. Yuen, Edwin H. Cook, Christine M. Freitag, Michael Gill, Christina M. Hultman, Thomas Lehner, Aarno Palotie, Gerard D. Schellenberg, Pamela Sklar, Matthew W. State, James S. Sutcliffe, Christopher A. Walsh, Stephen W. Scherer, Michael E. Zwick, Jeffrey C. Barrett, David J. Cutler, Kathryn Roeder, Bernie Devlin, Mark J. Daly, Joseph D. Buxbaum - Nature 2014 被引用: 2,974

  5. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Jennifer K. Lowe, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Michael E. Talkowski, James S. Sutcliffe, Christopher A. Walsh, Timothy W. Yu, David H. Ledbetter, Christa Lese Martin, Edwin H. Cook, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Matthew W. State - Neuron 2015 被引用: 1,547

  6. Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gregory E. Crawford, Pat Sullivan, Wesley K. Thompson, Preben Bo Mortensen, Esben Agerbo, Marianne Giørtz Pedersen, Carsten Bøcker Pedersen, Ole Mors, Anders D. Børglum, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Alicia R. Martin, Ashley Dumont, Christine Stevens, Claire Churchhouse, Daniel P. Howrigan, Duncan S. Palmer, Elise Robinson, Kyle Satterstrom, Felecia Cerrato, Hailiang Huang, Jacqueline I. Goldstein, Jennifer L. Moran, Joanna Martin Julian, M. Alonge Kimberly, C. Seed Patrick, Patrick Turley, Raymond K. Walters, Rich Belliveau, Stephan Ripke, Timothy Poterba, Mark J. Daly, Benjamin M. Neale, Menachem Fromer, Panos Roussos, Jessica Johnson, Hardik Shah, Milind Mahajan, Eric E. Schadt, Vahram Haroutunian, Douglas M. Ruderfer, Joseph D. Buxbaum, Solveig K. Sieberts, Kristen K. Dang, Ben Logsdon, Lara M. Mangravite, Mette A. Peters, Raquel E. Gur, Chang-Gyu Hahn, Bernie Devlin, Lambertus Klei, David A. Lewis, Barbara K. Lipska, Keisuke Hirai, Hiroyoshi Toyoshiba, Enrico Domenici - Science 2018 被引用: 1,177

  7. Gene expression elucidates functional impact of polygenic risk for schizophrenia

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Benjamin A. Logsdon, Konrad Talbot, Towfique Raj, David A. Bennett, Philip L. De Jager, Jun Zhu, Bin Zhang, Patrick F. Sullivan, Andrew Chess, Shaun Purcell, Leslie A. Shinobu, Lara M. Mangravite, Hiroyoshi Toyoshiba, Raquel E. Gur, Chang-Gyu Hahn, David A. Lewis, Vahram Haroutunian, Mette A. Peters, Barbara K. Lipska, Joseph D. Buxbaum, Eric E. Schadt, Keisuke Hirai, Kathryn Roeder, Kristen Brennand, Nicholas Katsanis, Enrico Domenici, Bernie Devlin, Pamela Sklar - Nature Neuroscience 2016 被引用: 1,217

  8. Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , James P. Noonan, Kathryn Roeder, Bernie Devlin, Nenad Šestan, Matthew W. State - Cell 2013 被引用: 1,000

  9. Most genetic risk for autism resides with common variation

    著者: , , , , , , , , , , , , , , , , , , - Nature Genetics 2014 被引用: 1,286

  10. Functional impact of global rare copy number variation in autism spectrum disorders

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emily L. Crawford, Andrew Crossett, Cheryl Cytrynbaum, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Håkon Håkonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, A lexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Anath C. Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge ほか 77 名 - Nature 2010 被引用: 2,066

  11. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , A. Jeremy Willsey, Michael E. Talkowski, Bernie Devlin, Kathryn Roeder, Stephan Sanders - Science 2018 被引用: 362

  12. Identification of common variants influencing risk of the tauopathy progressive supranuclear palsy

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrew Singleton, Matthew J. Farrer, Chang-En Yu, Lawrence I. Golbe, Tamás Révész, John Hardy, Andrew J. Lees, Bernie Devlin, Håkon Håkonarson, Ulrich Müller, Gerard D Schellenberg - Nature Genetics 2011 被引用: 632

  13. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Inês C. Conceição, Andreas G. Chiocchetti, Jillian P. Casey, Guiqing Cai, Christelle Cabrol, Nadia Bolshakova, Elena Bacchelli, Richard Anney, Steven Gallinger, Michelle Cotterchio, Graham Casey, Lonnie Zwaigenbaum, Kerstin Wittemeyer, Kirsty Wing, Simon Wallace, Hermán van Engeland, Ana Tryfon, Susanne Thomson, Latha Soorya, Bernadette Rogé, Wendy Roberts, Fritz Poustka, Susana Mouga, Nancy J. Minshew, L. Alison McInnes, Susan G. McGrew, Catherine Lord, Marion Leboyer, Ann S. Couteur, A lexander Kolevzon, Patricia González, Suma Jacob, Richard Holt, Stephen J. Guter, Jonathan Green, Andrew Green, Christopher Gillberg, Bridget A. Fernandez, Frederico Duque, Richard Delorme, Géraldine Dawson, Pauline Chaste, Cátia Café, S. Brennan, Thomas Bourgeron, Patrick Bolton, Sven Bölte, Raphael Bernier, Gillian Baird, Anthony Bailey, Evdokia Anagnostou, Joana Almeida, Ellen M. Wijsman, Veronica J. Vieland, Astrid M. Vicente, Gerard D. Schellenberg, Margaret A. Pericak‐Vance, Andrew D. Paterson, Jeremy Parr, Guiomar Oliveira, John I. Nürnberger, Anthony P. Monaco, Elena Maestrini, Sabine M. Klauck, Håkon Håkonarson, Jonathan L. Haines, Daniel H. Geschwind, Christine M. Freitag, Susan E. Folstein, Sean Ennis ほか 12 名 - The American Journal of Human Genetics 2014 被引用: 1,028

  14. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Rachel M. Game, Danielle S. Rudd, Danielle Zurawiecki, Christopher J. McDougle, Lea K. Davis, Judith Miller, David J. Posey, Shana M. Michaels, A lexander Kolevzon, Jeremy M. Silverman, Raphael Bernier, Susan E. Levy, Robert T. Schultz, Géraldine Dawson, Thomas Owley, William M. McMahon, Thomas H. Wassink, John A. Sweeney, John I. Nürnberger, Hilary Coon, James S. Sutcliffe, Nancy J. Minshew, Struan F.A. Grant, Maja Bućan, Edwin H. Cook, Joseph D. Buxbaum, Bernie Devlin, Gerard D. Schellenberg, Håkon Håkonarson - Nature 2009 被引用: 1,448

  15. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Xin He, Arnold R. Kriegstein, John L.R. Rubenstein, Nenad Šestan, Steven A. McCarroll, Benjamin M. Neale, Hilary Coon, A. Jeremy Willsey, Joseph D. Buxbaum, Mark J. Daly, Matthew W. State, Aaron R. Quinlan, Gábor Marth, Kathryn Roeder, Bernie Devlin, Michael E. Talkowski, Stephan Sanders - Nature Genetics 2018 被引用: 345

  16. Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State - Neuron 2011 被引用: 1,292

  17. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment

    著者: , , , , , , , , , , , , , , , , , , - Nature Communications 2015 被引用: 372

  18. Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nancy Francoeur, John F. Fullard, Sergio Espeso‐Gil, Kiran Girdhar, Attila Gulyás-Kovács, Raquel E. Gur, Chang-Gyu Hahn, Vahram Haroutunian, Mads E. Hauberg, Laura M. Huckins, Rivky Jacobov, Yan Jiang, Jessica Johnson, Bibi Kassim, Yungil Kim, Lambertus Klei, Robin S. S. Kramer, Mario Lauria, Thomas Lehner, David A. Lewis, Barbara K. Lipska, Kelsey S. Montgomery, Royce Park, Chaggai Rosenbluh, Panagiotis Roussos, Douglas M. Ruderfer, Geetha Senthil, Hardik Shah, Laura Sloofman, Lingyun Song, Eli Stahl, Patrick Sullivan, Roberto Visintainer, Jiebiao Wang, Ying‐Chih Wang, Jennifer Wiseman, Eva Xia, Wen Zhang, Elizabeth Zharovsky, Laura Addis, Sadiya N. Addo, David Airey, Matthias Arnold, David A. Bennett, Yingtao Bi, Knut Biber, Colette Blach, Elizabeth Bradhsaw, Paul E. Brennan, Rosa Canet-Aviles, Sherry Cao, Anna Cavalla, Yooree Chae, William W. Chen, Jie Cheng, David Collier, Jeffrey L. Dage, Eric B. Dammer, J. Wade Davis, John B. Davis, Derek Drake, Duc M. Duong, Brian J. Eastwood, Michelle E. Ehrlich, Benjamin M. Ellingson, Brett W. Engelmann, Sahar Esmaeeli-Nieh, Daniel Felsky, Cory C. Funk, Chris Gaiteri ほか 86 名 - Scientific Data 2020 被引用: 330

  19. A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn’s Disease and Human Gut Microbiome Composition

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Håkon Håkonarson, Ramnik J. Xavier, Mark J. Daly, Steven R. Brant, John D. Rioux, Mark S. Silverberg, Judy H. Cho, Jonathan Braun, Dermot McGovern, Richard H. Duerr - Gastroenterology 2016 被引用: 152

  20. Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Patrizia Mecocci, Alessandro Serretti, Diana De Ronchi, Antonis Politis, Julie Williams, Richard Mayeux, Tatiana Foroud, Agustı́n Ruiz, Clive Ballard, Peter Holmans, Oscar L. López, M. Ilyas Kamboh, Bernie Devlin, Robert A. Sweet - Molecular Psychiatry 2021 被引用: 68

  21. Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathryn Roeder, Lu Xie, Konrad Talbot, Scott E. Hemby, Laurent Essioux, Andrew Browne, Andrew Chess, Aaron Topol, Alexander W. Charney, Amanda Dobbyn, Ben Readhead, Bin Zhang, Dalila Pinto, David A. Bennett, David H. Kavanagh, Douglas M. Ruderfer, Eli A. Stahl, Eric E. Schadt, Gabriel E. Hoffman, Hardik Shah, Jun Zhu, Jessica Johnson, John F. Fullard, Joel T. Dudley, Kiran Girdhar, Kristen Brennand, Laura G. Sloofman, Laura M. Huckins, Menachem Fromer, Milind Mahajan, Panos Roussos, Schahram Akbarian, Shaun Purcell, Tymor Hamamsy, Towfique Raj, Vahram Haroutunian, Ying‐Chih Wang, Zeynep H. Gümüş, Geetha Senthil, Robin S. S. Kramer, Benjamin A. Logsdon, Jonathan M.J. Derry, Kristen K. Dang, Solveig K. Sieberts, Thanneer M. Perumal, Roberto Visintainer, Leslie A. Shinobu, Patrick F. Sullivan, Lambertus Klei, Schahram Akbarian, Panos Roussos, Enrico Domenici, Bernie Devlin, Pamela Sklar, Eli A. Stahl, Solveig K. Sieberts - The American Journal of Human Genetics 2018 被引用: 172

  22. Population-level variation in enhancer expression identifies disease mechanisms in the human brain

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Barbara K. Lipska, Francis J. McMahon, Pavan K. Auluck, Stefano Marenco, Kelsey S. Montgomery, Mette A. Peters, Solveig K. Sieberts, Chang-Gyu Hahn, Raquel E. Gur, Jiebiao Wang, Bernie Devlin, David A. Lewis, Lambertus Klei, Enrico Domenici, Michele Filosi, Roberto Visintainer, Douglas M. Ruderfer, Lide Han, Kristen Brennand, Vahram Haroutunian, Georgios Voloudakis, John F. Fullard, Panos Roussos - Nature Genetics 2022 被引用: 52

  23. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Christopher Lawrence, Michele D. Lewis, Julia Mayerle, Richard Mayeux, Nadine M Melhem, Mary E. Money, Thiruvengadam Muniraj, Georgios I. Papachristou, Margaret A. Pericak‐Vance, Joseph Romagnuolo, Gerard D. Schellenberg, Stuart Sherman, Péter Simon, Vijay Singh, Adam Slivka, Donna B. Stolz, Robert Sutton, Frank Ulrich Weiß, C. Mel Wilcox, Narcis Zarnescu, Stephen R. Wisniewski, Michael R. O’Connell, Michelle L. Kienholz, Kathryn Roeder, M. Michael Barmada, Dhiraj Yadav, Bernie Devlin - Nature Genetics 2012 被引用: 360

  24. Genetic risk for schizophrenia and psychosis in Alzheimer disease

    著者: , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2017 被引用: 77