Lambertus Klei

Active 2003–2025

62
Papers
29,742
Citations
50
h-index
60
i10-index

Citations

Citations per year for Lambertus Klei1989: 1 citations1992: 1 citations1995: 2 citations2000: 1 citations2002: 1 citations2003: 1 citations2005: 1 citations2006: 2 citations2007: 45 citations2008: 93 citations2009: 120 citations2010: 197 citations2011: 250 citations2012: 310 citations2013: 329 citations2014: 375 citations2015: 474 citations2016: 420 citations2017: 476 citations2018: 460 citations2019: 1,285 citations2020: 1,407 citations2021: 1,540 citations2022: 1,144 citations2023: 805 citations2024: 1,140 citations2025: 494 citations2026: 27 citations1990–1991: no citations, so these years are not shown1993–1994: no citations, so these years are not shown1996–1999: no citations, so these years are not shown2001: no citations, so this year is not shown2004: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 4,349 citing papers, 28.1% of this breakdownUnited Kingdom: 1,388 citing papers, 9% of this breakdownChina: 978 citing papers, 6.3% of this breakdownGermany: 772 citing papers, 5% of this breakdownCanada: 751 citing papers, 4.8% of this breakdownNetherlands: 596 citing papers, 3.8% of this breakdownItaly: 555 citing papers, 3.6% of this breakdownFrance: 528 citing papers, 3.4% of this breakdownAustralia: 504 citing papers, 3.3% of this breakdownSweden: 395 citing papers, 2.5% of this breakdownJapan: 363 citing papers, 2.3% of this breakdownSpain: 347 citing papers, 2.2% of this breakdown
0%28.1%Other 25.7%

Fields

  • Biochemistry, Genetics and Molecular Biology49.6%
  • Neuroscience29.3%
  • Medicine14.2%
  • Psychology2.8%
  • Immunology and Microbiology0.9%
  • Nursing0.6%
  • Other2.6%

Topics

  • 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%
  • Other64.5%

Coauthors

All papers

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 2,632

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 90 more - Cell 2020 cited by 2,501

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 17 more - Nature Genetics 2022 cited by 617

  4. Synaptic, transcriptional and chromatin genes disrupted in autism

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 2,974

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 1,547

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 1,177

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 1,217

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , James P. Noonan, Kathryn Roeder, Bernie Devlin, Nenad Šestan, Matthew W. State - Cell 2013 cited by 1,000

  9. Most genetic risk for autism resides with common variation

    Authors: , , , , , , , , , , , , , , , , , , - Nature Genetics 2014 cited by 1,286

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 77 more - Nature 2010 cited by 2,066

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , A. Jeremy Willsey, Michael E. Talkowski, Bernie Devlin, Kathryn Roeder, Stephan Sanders - Science 2018 cited by 362

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 632

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 12 more - The American Journal of Human Genetics 2014 cited by 1,028

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 1,448

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 345

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 1,292

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

    Authors: , , , , , , , , , , , , , , , , , , - Nature Communications 2015 cited by 372

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 and 86 more - Scientific Data 2020 cited by 330

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 152

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 68

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 172

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 52

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

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 cited by 360

  24. Genetic risk for schizophrenia and psychosis in Alzheimer disease

    Authors: , , , , , , , , , , , , , , , , , , , - Molecular Psychiatry 2017 cited by 77