Rezultati - Steve McCarroll

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  1. 1
    Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p

    Statistical and functional convergence of common and rare variant risk for autism spectrum disorders at chromosome 16p od Daniel J. Weiner, Emi Ling, Serkan Erdin, Derek J.C. Tai, Rachita Yadav, Jakob Grove, Jack Fu, Ajay Nadig, Caitlin E. Carey, Nikolas Baya, Jonas Bybjerg‐Grauholm, Sabina Berretta, Evan Z. Macosko, Jonathan Sebat, Luke J. O’Connor, David M. Hougaard, Anders D. Børglum, Michael E. Talkowski, Steve McCarroll, Elise Robinson

    Izdano 2022
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  2. 2
    The genomic psychiatry cohort: Partners in discovery

    The genomic psychiatry cohort: Partners in discovery od Michele T. Pato, Janet L. Sobell, Helena Medeiros, Colony Abbott, Brooke M. Sklar, P.F. Buckley, Evelyn J. Bromet, Michael Escamilla, Ayman H. Fanous, Douglas S. Lehrer, Fabìo Macciardi, Dolores Malaspina, Steve McCarroll, Stephen R. Marder, Jennifer L. Moran, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Shaun M. Purcell, Mark Hyman Rapaport, Pamela Sklar, Jordan W. Smoller, James A. Knowles, Carlos N. Pato

    Izdano 2013
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  3. 3
    Implication of <i>LRRC4C</i> and <i>DPP6</i> in neurodevelopmental disorders

    Implication of <i>LRRC4C</i> and <i>DPP6</i> in neurodevelopmental disorders od Gilles Maussion, Cristiana Cruceanu, Jill A. Rosenfeld, Scott C. Bell, Fabrice Jollant, Jin Szatkiewicz, Ryan L. Collins, Carrie Hanscom, Ilaria Kolobova, Nicolas Menjot de Champfleur, Ian Blumenthal, Colby Chiang, Vanessa Kiyomi Ota, Christina M. Hultman, Colm O’Dushlaine, Steve McCarroll, Martin Alda, Sébastien Jacquemont, Zehra Ordulu, Christian R. Marshall, Melissa T. Carter, Lisa G. Shaffer, Pamela Sklar, Santhosh Girirajan, Cynthia C. Morton, James F. Gusella, Gustavo Turecki, Dimitri J. Stavropoulos, Patrick F. Sullivan, Stephen W. Scherer, Michael E. Talkowski, Carl Ernst

    Izdano 2016
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  4. 4
    Genome-wide Comparison of African-Ancestry Populations from CARe and Other Cohorts Reveals Signals of Natural Selection

    Genome-wide Comparison of African-Ancestry Populations from CARe and Other Cohorts Reveals Signals of Natural Selection od Gaurav Bhatia, Nick Patterson, Bogdan Paşaniuc, Noah Zaitlen, Giulio Genovese, Samuela Pollack, Swapan Mallick, Simon Myers, Arti Tandon, Chris C. A. Spencer, Lyle J. Palmer, Adebowale Adeyemo, Ermeg L. Akylbekova, L. Adrienne Cupples, Jasmin Divers, Myriam Fornage, W.H. Linda Kao, Leslie A. Lange, Mingyao Li, Solomon K. Musani, Josyf C. Mychaleckyj, Adesola Ogunniyi, George Papanicolaou, Charles N. Rotimi, Jerome I. Rotter, Ingo Ruczinski, Babatunde Salako, David S. Siscovick, Bamidele O. Tayo, Qiong Yang, Steve McCarroll, Pardis C. Sabeti, Guillaume Lettre, Phil De Jager, Joel N. Hirschhorn, Xiaofeng Zhu, Stephen S. Rich, David Reich, James G. Wilson, Alkes L. Price

    Izdano 2011
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  5. 5
    Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

    Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders od Tarjinder Singh, Mitja Kurki, David Curtis, Shaun Purcell, Lucy Crooks, Jeremy F. McRae, Jaana Suvisaari, Himanshu Chheda, Douglas Blackwood, Gerome Breen, Olli Pietiläinen, Sebastian S. Gerety, Muhammad Ayub, Moira Blyth, Trevor Cole, David Collier, Eve L. Coomber, Nick Craddock, Mark J. Daly, John Danesh, Marta Di Forti, Alison Foster, Nelson B. Freimer, Daniel H. Geschwind, Mandy Johnstone, Shelagh Joss, George Kirov, Jarmo Körkkö, Outi Kuismin, Peter Holmans, Christina M. Hultman, Conrad Iyegbe, Jouko Lönnqvist, Minna Männikkö, Steve McCarroll, Peter McGuffin, Andrew M. McIntosh, Andrew McQuillin, Jukka S. Moilanen, Carmel Moore, Robin Murray, Ruth Newbury‐Ecob, Willem H. Ouwehand, Tiina Paunio, Elena Prigmore, Elliott Rees, David J. Roberts, Jennifer Sambrook, Pamela Sklar, David St Clair, Juha Veijola, James Walters, Hywel Williams, Patrick F. Sullivan, Matthew E. Hurles, Michael O’Donovan, Aarno Palotie, Michael J. Owen, Jeffrey C. Barrett

    Izdano 2016
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  6. 6
    A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

    A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder od Jubao Duan, Jianxin Shi, Alessia Fiorentino, Catherine Leites, Xiangning Chen, Winton Moy, Jingchun Chen, Boian S. Alexandrov, Anny Usheva, Deli He, Jessica Freda, Niamh L. O’Brien, Andrew McQuillin, Alan R. Sanders, Elliot S. Gershon, Lynn E. DeLisi, A. R. Bishop, Hugh Gurling, Michele T. Pato, Douglas F. Levinson, Kenneth S. Kendler, Carlos N. Pato, Pablo V. Gejman, Pablo V. Gejman, Alan R. Sanders, Jubao Duan, Douglas F. Levinson, Jianxin Shi, Nancy G. Buccola, Bryan Mowry, Robert Freedman, Ann Olincy, Farooq Amin, Donald W. Black, Jeremy M. Silverman, William Byerley, Dragan M. Švrakić, C. Robert Cloninger, Michele T. Pato, Janet L. Sobell, Helena Medeiros, Colony Abbott, Brooke Skar, P.F. Buckley, Evelyn J. Bromet, Michael Escamilla, Ayman H. Fanous, Douglas S. Lehrer, Fabìo Macciardi, Dolores Malaspina, Steve McCarroll, Stephen R. Marder, Jennifer L. Moran, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Shaun Purcell, Mark Hyman Rapaport, Pamela Sklar, Jordan W. Smoller, James A. Knowles, Carlos N. Pato

    Izdano 2014
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  7. 7
    Rare chromosomal deletions and duplications increase risk of schizophrenia

    Rare chromosomal deletions and duplications increase risk of schizophrenia od Jennifer Stone, Michael O’Donovan, Hugh Gurling, George Kirov, Douglas H. R. Blackwood, Aiden Corvin, Nick Craddock, Michael Gill, Christina M. Hultman, Paul Lichtenstein, Andrew McQuillin, Carlos N. Pato, Douglas M. Ruderfer, Michael J. Owen, David St Clair, Patrick F. Sullivan, Pamela Sklar, Shaun Purcell, Joshua M. Korn, Stuart MacGregor, Derek W. Morris, Colm Ó'Dúshláine, Mark Daly, Peter M. Visscher, Peter Holmans, Edward M. Scolnick, Nigel Williams, L. Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Vihra Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, John L. Waddington, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, David Curtis, Caroline Crombie, Gillian Fraser, Soh Leh Kwan, Nicholas Walker, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, Maria Helena Pinto de Azevedo, Steve McCarroll, Mark Daly, Kimberly Chambert, Casey Gates, Stacey B. Gabriel, Scott Mahon, Kristen Ardlie

    Izdano 2008
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  8. 8
    Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms

    Leveraging Cross-Species Transcription Factor Binding Site Patterns: From Diabetes Risk Loci to Disease Mechanisms od Melina Claussnitzer, Simon N. Dankel, Bernward Klocke, Harald Grallert, Viktoria Glunk, Tea Berulava, Heekyoung Lee, Nikolay Oskolkov, João Fadista, Kerstin Ehlers, Simone Wahl, Christoph Hoffmann, Kun Qian, Tina Rönn, Helene Riess, Martina Müller‐Nurasyid, Nancy Bretschneider, Timm Schroeder, Thomas Skurk, Bernhard Horsthemke, Derek Spieler, Martin Klingenspor, Martin Seifert, Michael J. Kern, Niklas Mejhert, Ingrid Dahlman, Ola Hansson, Stefanie M. Hauck, Matthias Blüher, Peter Arner, Leif Groop, Thomas Illig, Karsten Suhre, Yi‐Hsiang Hsu, Gunnar Mellgren, Hans Hauner, Helmut Laumen, Benjamin F. Voight, Laura J. Scott, Valgerður Steinthórsdóttir, Andrew P. Morris, Christian Dina, Ryan Welch, Eleftheria Zeggini, Cornelia Huth, Yurii S. Aulchenko, Guðmar Þorleifsson, Laura McCulloch, Teresa Ferreira, Harald Grallert, Najaf Amin, Guanming Wu, Cristen J. Willer, Soumya Raychaudhuri, Steve McCarroll, Claudia Langenberg, Oliver Hofmann, Josée Dupuis, Lu Qi, Ayellet V. Segrè, Mandy van Hoek, Pau Navarro, Kristin Ardlie, Beverley Balkau, Rafn Benediktsson, Amanda J. Bennett, Roza Blagieva, Eric Boerwinkle, Lori L. Bonnycastle, Kristina Bengtsson Boström, Bert Bravenboer, Suzannah Bumpstead, Noël P. Burtt, G. Charpentier, Peter S. Chines, Marilyn C. Cornelis, David Couper, Gabe Crawford, Alex S. F. Doney, Katherine S. Elliott, Amanda L. Elliott, Michael R. Erdos, Caroline S. Fox, Christopher S. Franklin, Martha Ganser, Christian Gieger, Niels Grarup, Todd J. Green, Simon J. Griffin, Christopher J. Groves, Candace Guiducci, Samy Hadjadj, Neelam Hassanali, Christian Herder, Bo Isomaa, Anne Jackson, Paul R V Johnson, Torben Jørgensen, Wen H. Kao, Norman Klopp

    Izdano 2014
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  9. 9
    Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis

    Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis od Benjamin F. Voight, Laura J. Scott, Valgerður Steinthórsdóttir, Andrew P. Morris, Christian Dina, Ryan Welch, Eleftheria Zeggini, Cornelia Huth, Yurii S. Aulchenko, Guðmar Þorleifsson, Laura McCulloch, Teresa Ferreira, Harald Grallert, Najaf Amin, Guanming Wu, Cristen J. Willer, Soumya Raychaudhuri, Steve McCarroll, Claudia Langenberg, Oliver Hofmann, Josée Dupuis, Lu Qi, Ayellet V. Segrè, Mandy van Hoek, Pau Navarro, Kristin Ardlie, Beverley Balkau, Rafn Benediktsson, Amanda J. Bennett, Roza Blagieva, Eric Boerwinkle, Lori L. Bonnycastle, Kristina Bengtsson Boström, Bert Bravenboer, Suzannah Bumpstead, Noisël P Burtt, G. Charpentier, Peter S. Chines, Marilyn C. Cornelis, David Couper, Gabe Crawford, Alex S. F. Doney, Katherine S. Elliott, Amanda L. Elliott, Michael R. Erdos, Caroline S. Fox, Christopher S. Franklin, Martha Ganser, Christian Gieger, Niels Grarup, Todd J. Green, Simon J. Griffin, Christopher J. Groves, Candace Guiducci, Samy Hadjadj, Neelam Hassanali, Christian Herder, Bo Isomaa, Anne Jackson, Paul R V Johnson, Torben Jørgensen, Wen H. Kao, Norman Klopp, Augustine Kong, Peter Kraft, Johanna Kuusisto, Torsten Lauritzen, Man Li, Aloysius G. Lieverse, Cecilia M. Lindgren, Valeriya Lyssenko, Michel Marre, Thomas Meitinger, Kristian Midthjell, Mario A. Morken, Narisu Narisu, Peter M. Nilsson, Katharine R. Owen, Felicity Payne, John R. B. Perry, Ann-Kristin Petersen, Carl G. P. Platou, Christine Proença, Inga Prokopenko, Wolfgang Rathmann, Nigel W. Rayner, Neil R. Robertson, Ghislain Rocheleau, Michael Roden, Michael Sampson, Richa Saxena, Beverley M. Shields, Peter Shrader, Gunnar Sigurðsson, Thomas Sparsø, Klaus Straßburger, Heather M. Stringham, Qi Sun, Amy J. Swift, Barbara Thorand

    Izdano 2010
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  10. 10
    Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores od 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, Hon‐Cheong So, 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

    Izdano 2015
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  11. 11
    Clonal haematopoiesis and risk of chronic liver disease

    Clonal haematopoiesis and risk of chronic liver disease od Waihay J. Wong, Connor A. Emdin, Alexander G. Bick, Seyedeh M. Zekavat, Abhishek Niroula, James P. Pirruccello, Laura E. Dichtel, Gabriel K. Griffin, Md Mesbah Uddin, Christopher J. Gibson, Veronica Kovalcik, Amy Lin, Marie McConkey, Amélie Vromman, Rob S. Sellar, Peter G. Kim, Mridul Agrawal, Joshua S. Weinstock, Michelle T. Long, Bing Yu, Rajarshi Banerjee, Rowan C. Nicholls, Andrea Dennis, Matt Kelly, Po‐Ru Loh, Steve McCarroll, Eric Boerwinkle, Ramachandran S. Vasan, Siddhartha Jaiswal, Andrew D. Johnson, Raymond T. Chung, Kathleen E. Corey, Daniel Levy, Christie M. Ballantyne, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Nathan R. Blue, Donald W. Bowden, Russell P. Bowler, Jennifer A. Brody, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban G. Burchard, Carlos D. Bustamante, Erin Buth, Brian E. Cade, Jonathan Cardwell, Vincent J. Carey, Julie Carrier, April P. Carson, Cara L. Carty, Richard Casaburi, Juan P. Romero, James F. Casella, Peter J. Castaldi, Mark Chaffin, Christy Chang, Yi‐Cheng Chang, Daniel I. Chasman, Sameer Chavan, Bo-Juen Chen, Wei‐Min Chen

    Izdano 2023
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  12. 12
    Author Correction: Clonal haematopoiesis and risk of chronic liver disease

    Author Correction: Clonal haematopoiesis and risk of chronic liver disease od Waihay J. Wong, Connor A. Emdin, Alexander G. Bick, Seyedeh M. Zekavat, Abhishek Niroula, James P. Pirruccello, Laura E. Dichtel, Gabriel K. Griffin, Md Mesbah Uddin, Christopher J. Gibson, Veronica Kovalcik, Amy Lin, Marie McConkey, Amélie Vromman, Rob S. Sellar, Peter G. Kim, Mridul Agrawal, Joshua S. Weinstock, Michelle T. Long, Bing Yu, Rajarshi Banerjee, Rowan C. Nicholls, Andrea Dennis, Matt Kelly, Po‐Ru Loh, Steve McCarroll, Eric Boerwinkle, Ramachandran S. Vasan, Siddhartha Jaiswal, Andrew D. Johnson, Raymond T. Chung, Kathleen E. Corey, Daniel Levy, Christie M. Ballantyne, Namiko Abe, Gonçalo R. Abecasis, François Aguet, Christine M. Albert, Laura Almasy, Álvaro Alonso, Seth A. Ament, Peter H. Anderson, Pramod Anugu, Deborah Applebaum‐Bowden, Kristin Ardlie, Dan E. Arking, Donna K. Arnett, Allison E. Ashley‐Koch, Stella Aslibekyan, Tim Assimes, Paul L. Auer, Dimitrios Avramopoulos, Najib Ayas, Adithya Balasubramanian, John Barnard, Kathleen C. Barnes, R. Graham Barr, Emily Barron‐Casella, Lucas Barwick, Terri H. Beaty, Gerald J. Beck, Diane M. Becker, Lewis C. Becker, Rebecca Beer, Amber L. Beitelshees, Emelia J. Benjamin, Takis Benos, Marcos Bezerra, Larry Bielak, Joshua C. Bis, Thomas W. Blackwell, John Blangero, Nathan R. Blue, Donald W. Bowden, Russell P. Bowler, Jennifer A. Brody, Ulrich Broeckel, Jai Broome, Deborah Brown, Karen Bunting, Esteban G. Burchard, Carlos D. Bustamante, Erin Buth, Brian E. Cade, Jonathan Cardwell, Vincent J. Carey, Julie Carrier, April P. Carson, Cara L. Carty, Richard Casaburi, Juan Pablo Casas Romero, James F. Casella, Peter J. Castaldi, Mark Chaffin, Christy Chang, Yi‐Cheng Chang, Daniel I. Chasman, Sameer Chavan, Bo‐Juen Chen, Wei‐Min Chen

    Izdano 2023
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