Guiqing Cai
Active 1997–2024
- 32
- Papers
- 19,783
- Citations
- 29
- h-index
- 32
- i10-index
Citations
Citation sources
Countries
Institutions
Fields
- Biochemistry, Genetics and Molecular Biology54.7%
- Neuroscience23.5%
- Medicine14.7%
- Psychology3.3%
- Immunology and Microbiology0.8%
- Environmental Science0.6%
- Other2.4%
Topics
- Genetic Associations and Epidemiology10.6%
- Genetics and Neurodevelopmental Disorders6.6%
- Autism Spectrum Disorder Research5.1%
- Genomic variations and chromosomal abnormalities4%
- Genomics and Rare Diseases3.3%
- Tryptophan and brain disorders3.2%
- Other67.2%
Coauthors
- Joseph D. Buxbaum12
- Stephan Ripke10
- Benjamin M. Neale7
- Ingrid Agartz7
- Aiden Corvin6
- Brendan Bulik‐Sullivan6
- David Collier6
- Farooq Amin6
- Hailiang Huang6
- Kai-How Farh6
- Madeline Alexander6
- Margot Albus6
- Peter Holmans6
- Richard A. Belliveau6
- Silviu‐Alin Bacanu6
- Eli A. Stahl5
- Elizabeth Bevilacqua5
- Esben Agerbo5
- James Walters5
- Phil Lee5
- Sarah E. Bergen5
- Tim B. Bigdeli5
- Catalina Betancur4
- Donald W. Black4
All papers
- Biological insights from 108 schizophrenia-associated genetic loci
Authors: Jacqueline I. Goldstein, Benjamin M. Neale, Stephan Ripke, Hailiang Huang, Kai-How Farh, Hailiang Huang, Menachem Fromer, Brendan Bulik‐Sullivan, Mark J. Daly, Kimberly D. Chambert, Giulio Genovese, Jordan W. Smoller, Phil Lee, Edward M. Scolnick, Stephan Ripke, Elizabeth Bevilacqua, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Richard A. Belliveau, Steven A. McCarroll, Sarah E. Bergen, Joel N. Hirschhorn, Alkes Price, Eli A. Stahl, Tõnu Esko, Aiden Corvin, Paul Cormican, Jacqueline I. Goldstein, Derek W. Morris, Benjamin M. Neale, James T. R. Walters, Hailiang Huang, Noa Carrera, Alkes L. Price, Mark J. Daly, Lyudmila Georgieva, Marian L. Hamshere, Benjamin M. Neale, Jordan W. Smoller, Andrew J. Pocklington, Paul Cormican, Aiden Corvin, Michael Gill, Gary Donohoe, Michael J. Owen, Alexander Richards, David A. Collier, Michael J. Owen, Noa Carrera, Marian L. Hamshere, Nick Craddock, David Kavanagh, Morten Mattingsdal, Peter Holmans, George Kirov, Sophie E. Legge, Valentina Escott‐Price, Nigel Williams, Andrew Pocklington, Lyudmila Georgieva, James Walters, Nick Craddock, Henrik B. Rasmussen, Michael J. Owen, Peter Holmans, David Collier, Younes Mokrab, David Collier, Tune H. Pers, Farooq Amin, Silviu A. Bacanu, Tim B. Bigdeli, Erik Söderman, Brandon K. Wormley, Martin Begemann, Christian Hammer, Srdjan Djurovic, Morten Mattingsdal, Judit Bene, Ole A. Andreassen, Anna K. Kähler, Ingrid Melle, Esben Agerbo, Preben Bo Mortensen, Esben Agerbo, Preben Bo Mortensen, Preben Bo Mortensen, Randy L. Buckner, Henrik B. Rasmussen, Ditte Demontis, Esben Agerbo, Line Olsen, Eric Strengman, Roel A. Ophoff, Guiqing Cai, Thomas Folkmann Hansen, Margot Albus, Madeline Alexander, Claudine Laurent and 197 more - Nature 2014 cited by 8,166
- Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores
Authors: Bjarni J. Vilhjálmsson, Jian Yang, Hilary K. Finucane, Alexander Gusev, Sara Lindström, Stephan Ripke, Giulio Genovese, Po‐Ru Loh, Gaurav Bhatia, Ron Do, Tristan J. Hayeck, Hong‐Hee Won, Sekar Kathiresan, Michele T. Pato, Carlos N. Pato, Rulla M. Tamimi, Eli A. Stahl, Noah Zaitlen, Bogdan Paşaniuc, Gillian M. Belbin, Eimear E. Kenny, Mikkel Heide Schierup, Philip L. De Jager, Nikolaos A. Patsopoulos, Steve McCarroll, Mark J. Daly, Shaun Purcell, Daniel I. Chasman, Benjamin M. Neale, Michael E. Goddard, Peter M. Visscher, Peter Kraft, Nick Patterson, Alkes L. Price, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price and 302 more - The American Journal of Human Genetics 2015 cited by 1,489
- Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Authors: Christian R. Marshall, Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, Peter Holmans, Dalila Pinto, Madhusudan Gujral, William M. Brandler, Dheeraj Malhotra, Zhouzhi Wang, Karin V. Fuentes Fajarado, Michelle S. Maile, Stephan Ripke, Ingrid Agartz, Margot Albus, Madeline Alexander, Farooq Amin, Joshua Atkins, Silviu‐Alin Bacanu, Richard A. Belliveau, Sarah E. Bergen, Marcelo Bertalan, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, Brendan Bulik‐Sullivan, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J. Cairns, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Wei Cheng, C. Robert Cloninger, David Cohen, Paul Cormican, Nick Craddock, Benedicto Crespo‐Facorro, James J Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Kai-How Farh, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Joseph I. Friedman, Andreas J. Forstner, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Elliot S. Gershon, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, Jacob Gratten, Lieuwe de Haan, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Hailiang Huang, Masashi Ikeda, Inge Joa, Anna K. Kähler and 163 more - Nature Genetics 2016 cited by 1,142
- Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes
Authors: Douglas M. Ruderfer, Stephan Ripke, Andrew McQuillin, James Boocock, Eli A. Stahl, Jennifer M. Whitehead Pavlides, Niamh Mullins, Alexander W. Charney, Anil P. S. Ori, Loes M. Olde Loohuis, Enrico Domenici, Arianna Di Florio, Sergi Papiol, János Kálmán, Vassily Trubetskoy, Rolf Adolfsson, Ingrid Agartz, Esben Agerbo, Huda Akil, Diego Albani, Margot Albus, Martin Alda, Madeline Alexander, Ney Alliey‐Rodriguez, Thomas D. Als, Farooq Amin, Adebayo Anjorin, María J. Arranz, Swapnil Awasthi, Silviu‐Alin Bacanu, Judith A. Badner, Marie Bækvad‐Hansen, Steven C. Bakker, Gavin Band, Jack D. Barchas, Inês Barroso, Nicholas Bass, Michael Bauer, Bernhard T. Baune, Martin Begemann, Céline Bellenguez, Richard A. Belliveau, Frank Bellivier, Stephan Bender, Judit Bene, Sarah E. Bergen, Wade H. Berrettini, Elizabeth Bevilacqua, Joanna M. Biernacka, Tim B. Bigdeli, Donald W. Black, Hannah Blackburn, Jenefer M. Blackwell, Douglas Blackwood, Carsten Bøcker Pedersen, Michael Boehnke, Marco P. Boks, Anders D. Børglum, Elvira Bramon, Gerome Breen, Matthew A. Brown, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, Monika Budde, Brendan Bulik‐Sullivan, Suzannah J. Bumpstead, William E. Bunney, Margit Burmeister, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J. Cairns, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Juan P. Casas, Miguel Casas, Stanley V. Catts, Pablo Cervantes, Kimberley D. Chambert, Raymond C. K. Chan, Eric Chen, Ronald Y.L. Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, Toni‐Kim Clarke, C. Robert Cloninger, David Cohen, Nadine Cohen, Jonathan R. I. Coleman, David Collier, Paul Cormican, William Coryell, Nicholas Craddock, David W. Craig and 440 more - Cell 2018 cited by 821
- A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts
Authors: Guiyan Ni, Jian Zeng, Joana Revez, Ying Wang, Zhili Zheng, Tian Ge, Restuadi Restuadi, Jacqueline Kiewa, Dale R. Nyholt, Jonathan R. I. Coleman, Jordan W. Smoller, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Raymond C. K. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian and 391 more - Biological Psychiatry 2021 cited by 207
- Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases
Authors: Alexander Gusev, Sang Lee, Gosia Trynka, Hilary K. Finucane, Bjarni J. Vilhjálmsson, Han Xu, Chongzhi Zang, Stephan Ripke, Brendan Bulik‐Sullivan, Eli A. Stahl, Anna K. Kähler, Christina M. Hultman, Shaun Purcell, Steven A. McCarroll, Mark J. Daly, Bogdan Paşaniuc, Patrick F. Sullivan, Benjamin M. Neale, Naomi R. Wray, Soumya Raychaudhuri, Alkes L. Price, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Anders D. Børglum, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael H. Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva and 245 more - The American Journal of Human Genetics 2014 cited by 654
- Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders
Authors: Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang, Jacob Vorstman, Ann Thompson, Regina Regan, Marion Pilorge, Giovanna Pellecchia, Alistair T. Pagnamenta, Bárbara Oliveira, Christian R. Marshall, Tiago R. Magalhães, Jennifer K. Lowe, Jennifer Howe, Anthony J. Griswold, John R. Gilbert, Eftichia Duketis, Beth A. Dombroski, Maretha Jonge, Michael L. Cuccaro, Emily L. Crawford, Catarina Correia, Judith Conroy, 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
- Autism genome-wide copy number variation reveals ubiquitin and neuronal genes
Authors: Joseph Glessner, Kai Wang, Guiqing Cai, Olena Korvatska, Cecilia E. Kim, Shawn Wood, Haitao Zhang, Annette Estes, Camille W. Brune, Jonathan P. Bradfield, Marcin Imieliński, Edward C. Frackelton, Jennifer Reichert, Emily L. Crawford, Jeffrey Munson, Patrick Sleiman, Rosetta Chiavacci, Kiran Annaiah, Kelly Thomas, Cuiping Hou, Wendy Glaberson, James H. Flory, F. George Otieno, Maria Garris, Latha Soorya, Lambertus Klei, Joseph Piven, Kacie J. Meyer, Evdokia Anagnostou, Takeshi Sakurai, 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
- Patterns and rates of exonic de novo mutations in autism spectrum disorders
Authors: Benjamin M. Neale, Yan Kou, Li Liu, Avi Ma’ayan, Kaitlin E. Samocha, Aniko Sabo, Chiao‐Feng Lin, Christine Stevens, Li-San Wang, Vladimir Makarov, Paz Polak, Seungtai Yoon, Jared Maguire, Emily L. Crawford, Nicholas G. Campbell, Evan Geller, Otto Valladares, Chad Schafer, Han Liu, Tuo Zhao, Guiqing Cai, Jayon Lihm, Ruth Dannenfelser, Omar Jabado, Zuleyma Peralta, Uma Nagaswamy, Donna M. Muzny, Jeffrey G. Reid, Irene Newsham, Yuanqing Wu, Lora Lewis, Yi Han, Benjamin F. Voight, Elaine T. Lim, Elizabeth J. Rossin, Andrew Kirby, Jason Flannick, Menachem Fromer, Khalid Shakir, Tim Fennell, Kiran Garimella, Eric Banks, Ryan Poplin, Stacey Gabriel, Mark A. DePristo, Jack R. Wimbish, Braden Boone, Shawn Levy, Catalina Betancur, Shamil Sunyaev, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Bernie Devlin, Richard A. Gibbs, Kathryn Roeder, Gerard D. Schellenberg, James S. Sutcliffe, Mark J. Daly - Nature 2012 cited by 1,808
- Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia
Authors: Antonio F. Pardiñas, Sophie E. Smart, Isabella Willcocks, Peter Holmans, Charlotte Dennison, Amy Lynham, Sophie E. Legge, Bernhard T. Baune, Tim B. Bigdeli, Murray J. Cairns, Aiden Corvin, Ayman H. Fanous, Josef Frank, Brian Kelly, Andrew McQuillin, Ingrid Melle, Preben Bo Mortensen, Bryan Mowry, Carlos N. Pato, Sathish Periyasamy, Marcella Rietschel, Dan Rujescu, Carmen Simonsen, David St Clair, Paul A. Tooney, Jing Wu, Ole A. Andreassen, Kaarina Kowalec, Patrick F. Sullivan, Robin Murray, Michael J. Owen, James H. MacCabe, Michael O‘Donovan, James Walters, Stephan Ripke, Benjamin M. Neale, Kai-How Farh, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond C. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Martilias S. Farrell, Lude Franke, Robert Freedman and 261 more - JAMA Psychiatry 2022 cited by 106
- Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders
Authors: Gabriëlla A.M. Blokland, Jakob Grove, Chia‐Yen Chen, Chris Cotsapas, Stuart Tobet, Robert J. Handa, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond C. K. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn and 861 more - Biological Psychiatry 2021 cited by 139
- Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood
Authors: Guiyan Ni, G. Möser, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, В. Е. Голимбет, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Mads V. Hollegaard, David M. Hougaard and 202 more - The American Journal of Human Genetics 2018 cited by 202
- Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency
Authors: Latha Soorya, A lexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, Lily Schwartz, Yitzchak Frank, A. Ting Wang, Guiqing Cai, Elena Parkhomenko, Danielle Halpern, David Grodberg, Benjamin Angarita, Judith P. Willner, Amy Yang, Roberto Canitano, William F. Chaplin, Catalina Betancur, Joseph D. Buxbaum - Molecular Autism 2013 cited by 349
- ABCA7 frameshift deletion associated with Alzheimer disease in African Americans
Authors: Holly N. Cukier, Brian W. Kunkle, Badri N. Vardarajan, Sophie Rolati, Kara L. Hamilton‐Nelson, Martin Kohli, Patrice L. Whitehead, Beth A. Dombroski, Derek Van Booven, Rosalyn Lang, Derek M. Dykxhoorn, Lindsay A. Farrer, Michael L. Cuccaro, Jeffery M. Vance, John R. Gilbert, Gary W. Beecham, Eden R. Martin, Regina M. Carney, Richard Mayeux, Gerard D. Schellenberg, Goldie S. Byrd, Jonathan L. Haines, Margaret A. Pericak‐Vance, Marilyn S. Albert, Roger L. Albin, Liana G. Apostolova, Steven E. Arnold, Sanjay Asthana, Craig Atwood, Clinton T. Baldwin, M. Michael Barmada, Lisa L. Barnes, Sandra Barral, Thomas G. Beach, James T. Becker, Gary W. Beecham, Duane Beekly, David A. Bennett, Eileen H. Bigio, Thomas D. Bird, Deborah Blacker, Bradley F. Boeve, Adam Boxer, James R. Burke, Jeffrey M. Burns, Joseph D. Buxbaum, Goldie S. Byrd, Guiqing Cai, Nigel J. Cairns, Laura B. Cantwell, Chuanhai Cao, Cynthia M. Carlsson, Regina M. Carney, Minerva M. Carrasquillo, Steven L. Carroll, Helena C. Chui, David G. Clark, David H. Cribbs, Elizabeth Crocco, Carlos Cruchaga, Philip L. De Jager, Charles DeCarli, F. Yesim Demirci, Malcolm Dick, Dennis W. Dickson, Ranjan Duara, Nilüfer Ertekin‐Taner, Denis A. Evans, Kelley Faber, M. Daniele Fallin, Kenneth B. Fallon, David W. Fardo, Martin R. Farlow, Lindsay A. Farrer, Steven H. Ferris, Tatiana Foroud, Matthew P. Frosch, Douglas Galasko, Marla Gearing, Daniel H. Geschwind, Bernardino Ghetti, John R. Gilbert, Rodney C.P. Go, Alison Goate, Neill R. Graff‐Radford, Robert C. Green, Patrick Griffith, John H. Growdon, Jonathan L. Haines, Håkon Håkonarson, Ronald L. Hamilton, Kara L. Hamilton‐Nelson, Vahram Haroutunian, Lindy E. Harrell, Lawrence S. Honig, Ryan Huebinger, Christine M. Hulette, Bradley T. Hyman, Gregory A. Jicha, Lee‐Way Jin and 97 more - Neurology Genetics 2016 cited by 107
- A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism
Authors: Patrícia B. S. Celestino-Soper, Sara Violante, Emily L. Crawford, Rui Luo, Anath C. Lionel, Elsa Delaby, Guiqing Cai, Bekim Sadiković, Kwanghyuk Lee, Charlene Lo, Kun Gao, Richard Person, Timothy J. M. Moss, Jennifer R. German, Ni Huang, Marwan Shinawi, Diane Treadwell‐Deering, Péter Szatmári, Wendy Roberts, Bridget A. Fernandez, Richard J. Schroer, Roger E. Stevenson, Joseph D. Buxbaum, Catalina Betancur, Stephen W. Scherer, Stephan Sanders, Daniel H. Geschwind, James S. Sutcliffe, Matthew E. Hurles, Ronald J. A. Wanders, Chad A. Shaw, Suzanne M. Leal, Edwin H. Cook, Robin P. Goin‐Kochel, Frédéric M. Vaz, Arthur L. Beaudet - National Academy of Sciences, Proceedings of the National Academy of Sciences 2012 cited by 142
- Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
Authors: Eduardo A. Maury, Maxwell A. Sherman, Giulio Genovese, Thomas G. Gilgenast, Tushar Kamath, S.J. Burris, Prashanth Rajarajan, Erin Flaherty, Schahram Akbarian, Andrew Chess, Steven A. McCarroll, Po‐Ru Loh, Jennifer E. Phillips‐Cremins, Kristen Brennand, Evan Z. Macosko, James Walters, Michael O‘Donovan, Patrick F. Sullivan, Christian R. Marshall, Daniele Merico, Bhooma Thiruvahindrapuram, Zhouzhi Wang, Stephen W. Scherer, Daniel P. Howrigan, Stephan Ripke, Brendan Bulik‐Sullivan, Kai-How Farh, Menachem Fromer, Jacqueline I. Goldstein, Hailiang Huang, Phil Lee, Mark J. Daly, Benjamin M. Neale, Richard A. Belliveau, Sarah E. Bergen, Elizabeth Bevilacqua, Kimberley D. Chambert, Colm Ó'Dúshláine, Edward M. Scolnick, Jordan W. Smoller, Jennifer L. Moran, Aarno Palotie, Tracey L. Petryshen, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, Madhusudan Gujral, William M. Brandler, Dheeraj Malhotra, Karin V. Fuentes Fajarado, Michelle S. Maile, Peter Holmans, Noa Carrera, Nick Craddock, Valentina Escott‐Price, Lyudmila Georgieva, Marian L. Hamshere, David Kavanagh, Sophie E. Legge, Andrew Pocklington, Alexander Richards, Douglas M. Ruderfer, Nigel Williams, George Kirov, Michael J. Owen, Dalila Pinto, Guiqing Cai, Kenneth L. Davis, Elodie Drapeau, Joseph I. Friedman, Vahram Haroutunian, Elena Parkhomenko, Abraham Reichenberg, Jeremy M. Silverman, Joseph D. Buxbaum, Enrico Domenici, Ingrid Agartz, Srdjan Djurovic, Morten Mattingsdal, Ingrid Melle, Ole A. Andreassen, Erik G. Jönsson, Erik Söderman, Margot Albus, Madeline Alexander, Claudine Laurent, Douglas F. Levinson, Farooq Amin, Joshua Atkins, Murray J. Cairns, Rodney J. Scott, Paul A. Tooney, Jing Wu, Silviu‐Alin Bacanu, Tim B. Bigdeli, Mark A. Reimers, Bradley T. Webb, Aaron R. Wolen, Brandon K. Wormley and 268 more - Cell Genomics 2023 cited by 43
- Personalized medicine of non-gene-specific chemotherapies for non-small cell lung cancer
Authors: Wenxiao Jiang, Guiqing Cai, Peter Hu, Yue Wang - Acta Pharmaceutica Sinica B 2021 cited by 29
- Gene Expression Patterns Associated with Posttraumatic Stress Disorder Following Exposure to the World Trade Center Attacks
Authors: Rachel Yehuda, Guiqing Cai, Julia A. Golier, Casey Sarapas, Sandro Galea, Marcus Ising, Theo Rein, James Schmeidler, Bertram Müller‐Myhsok, Florian Holsboer, Joseph D. Buxbaum - Biological Psychiatry 2009 cited by 300
- Dementia Revealed: Novel Chromosome 6 Locus for Late-Onset Alzheimer Disease Provides Genetic Evidence for Folate-Pathway Abnormalities
Authors: Adam C. Naj, Gary W. Beecham, Eden R. Martin, Paul J. Gallins, Eric Powell, Ioanna Konidari, Patrice L. Whitehead, Guiqing Cai, Vahram Haroutunian, William K. Scott, Jeffery M. Vance, Michael A. Slifer, Harry E. Gwirtsman, John R. Gilbert, Jonathan L. Haines, Joseph D. Buxbaum, Margaret A. Pericak‐Vance - PLoS Genetics 2010 cited by 152
- High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L–DOCK4 gene region in autism susceptibility
Authors: IMGSAC, Elena Maestrini, Alistair T. Pagnamenta, Janine A. Lamb, Elena Bacchelli, Nuala Sykes, Inês Sousa, Claudio Toma, Gabrielle Barnby, Helen Butler, Laura Winchester, Thomas Scerri, Fiorella Minopoli, Jennifer Reichert, Guiqing Cai, Joseph D. Buxbaum, Olena Korvatska, Gerry Schellenberg, Géraldine Dawson, Annelies de Bildt, Ruud B. Minderaa, E Mulder, Andrew P. Morris, Anthony Bailey, Anthony P. Monaco - Molecular Psychiatry 2009 cited by 144
- Expression profiling associates blood and brain glucocorticoid receptor signaling with trauma-related individual differences in both sexes
Authors: Nikolaos P. Daskalakis, Hagit Cohen, Guiqing Cai, Joseph D. Buxbaum, Rachel Yehuda - National Academy of Sciences, Proceedings of the National Academy of Sciences 2014 cited by 131
- Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis
Authors: Robert A. Kozol, Holly N. Cukier, Bing Zou, Vera Mayo, Silvia De Rubeis, Guiqing Cai, Anthony J. Griswold, Patrice L. Whitehead, Jonathan L. Haines, John R. Gilbert, Michael L. Cuccaro, Eden R. Martin, James D. Baker, Joseph D. Buxbaum, Margaret A. Pericak‐Vance, Julia E. Dallman - Human Molecular Genetics 2015 cited by 89
- Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly
Authors: Joseph D. Buxbaum, Guiqing Cai, Pauline Chaste, Gudrun Nygren, Juliet Goldsmith, Jennifer Reichert, Henrik Anckarsäter, Maria Råstam, Christopher J. Smith, Jeremy M. Silverman, Eric Hollander, Marion Leboyer, Christopher Gillberg, Alain Verloès, Catalina Betancur - American Journal of Medical Genetics Part B Neuropsychiatric Genetics 2007 cited by 274
- Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT
Authors: Guiqing Cai, Lisa Edelmann, Juliet Goldsmith, Ninette Cohen, Alisa Nakamine, Jennifer Reichert, Ellen J. Hoffman, Danielle Zurawiecki, Jeremy M. Silverman, Eric Hollander, Latha Soorya, Evdokia Anagnostou, Catalina Betancur, Joseph D. Buxbaum - BMC Medical Genomics 2008 cited by 94
