Search Results - Stacey B. Gabriel
Stacey Gabriel
Stacey B. Gabriel is an American geneticist and Senior Director of the Genomics Platform at the Broad Institute. With Eric Lander, she is also the co-director of the National Human Genome Research Institute's sequencing center at the Broad Institute. She was named the "hottest researcher" on Thomson Reuters' list of the World's Most Influential Scientific Minds in 2014. She was given this honor because she published twenty-three of the most cited papers of 2013, more than any other single researcher recorded by Thomson Reuters. She topped the same list again in 2015. She is also an ISI Highly Cited Researcher.In 2020, Gabriel helped create and organize a high-throughput COVID-19 testing facility based out of the Broad Institute. Under her guidance, the institute has processed over 10 million tests as of April 2021. Provided by Wikipedia
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Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci by John B. Harley, Marta E. Alarcón‐Riquelme, Lindsey A. Criswell, Chaim O. Jacob, Robert P. Kimberly, Kathy L. Moser, Betty P. Tsao, Timothy J. Vyse, Carl D. Langefeld, Swapan K. Nath, Joel M. Guthridge, Beth L. Cobb, Daniel B. Mirel, Miranda C. Marion, Adrienne H. Williams, Jasmin Divers, Wei Wang, Summer G Frank-Pearce, Bahram Namjou, Stacey B. Gabriel, Annette T. Lee, Peter K. Gregersen, Timothy W. Behrens, Robert P. Kimberly, Michelle M. A. Fernando, Raphael Zidovetzki, Patrick M. Gaffney, Jeffrey C. Edberg, John D. Rioux, Joshua O. Ojwang, Judith A. James, Joan T. Merrill, Gary S. Gilkeson, Michael F. Seldin, Hong Yin, Emily C. Baechler, Quan Zhen Li, Edward K. Wakeland, Gail R. Bruner, Kenneth M. Kaufman, Jennifer A. Kelly
Published 2008Artigo -
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Biallelic mutations in the 3′ exonuclease TOE1 cause pontocerebellar hypoplasia and uncover a role in snRNA processing by Rea M. Lardelli, Ashleigh E. Schaffer, Veerle Rc Eggens, Maha S. Zaki, Stephanie Grainger, Shashank Sathe, Eric L. Van Nostrand, Zinayida Schlachetzki, Başak Rosti, Naiara Akizu, Eric Scott, Jennifer L. Silhavy, Laura D. Heckman, Rasim Özgür Rosti, Esra Dikoglu, Anne Gregor, Alicia Guemez‐Gamboa, Damir Musaev, Rohit Mande, Ari Widjaja, Timothy Shaw, Sebastian Markmiller, Isaac Marin‐Valencia, Justin H. Davies, Linda De Meırleır, Hülya Kayserili, Umut Altunoğlu, Mary Louise Freckmann, Linda Warwick, David Chitayat, Susan Blasér, Ahmet Okay Çağlayan, Kaya Bilgüvar, Hüseyin Per, Christina Fagerberg, Henrik Thybo Christesen, Maria Kibæk, Kimberly A. Aldinger, David K. Manchester, Naomichi Matsumoto, Kazuhiro Muramatsu, Hirotomo Saitsu, Masaaki Shiina, Kazuhiro Ogata, Nicola Foulds, William B. Dobyns, C. Neil, David Traver, Luigina Spaccini, Stefania Maria Bova, Stacey B. Gabriel, Murat Günel, Enza Maria Valente, Marie‐Cécile Nassogne, Eric J. Bennett, G Yeo, Frank Baas, Jens Lykke‐Andersen, Joseph G. Gleeson
Published 2017Artigo -
23
Concept, Design and Implementation of a Cardiovascular Gene-Centric 50 K SNP Array for Large-Scale Genomic Association Studies by Brendan J. Keating, Sam E. Tischfield, Sarah S. Murray, Tushar Bhangale, Thomas S. Price, Joseph Glessner, Luana Galver, Jeffrey C. Barrett, Struan F.A. Grant, Deborah Farlow, Hareesh Chandrupatla, Thomas Hansen, Saad Ajmal, George Papanicolaou, Yiran Guo, Mingyao Li, Stephanie DerOhannessian, Paul I. W. de Bakker, Swneke D. Bailey, Alexandre Montpetit, Andrew C. Edmondson, Kent D. Taylor, Xiaowu Gai, Susanna S. Wang, Myriam Fornage, Tamim H. Shaikh, Per‐Henrik Groop, Michael Boehnke, Alistair S. Hall, Andrew T. Hattersley, Edward C. Frackelton, Nick Patterson, Charleston W. K. Chiang, Cecelia E. Kim, Richard R. Fabsitz, Willem H. Ouwehand, Alkes L. Price, Patricia B. Munroe, Mark J. Caulfield, Thomas A. Drake, Eric Boerwinkle, David Reich, A.S. Whitehead, Thomas P. Cappola, Nilesh J. Samani, Aldons J. Lusis, Eric E. Schadt, James G. Wilson, Wolfgang Köenig, Mark I. McCarthy, Sekar Kathiresan, Stacey B. Gabriel, Hákon Hákonarson, Sonia S. Anand, Muredach P. Reilly, James C. Engert, Deborah A. Nickerson, Daniel J. Rader, Joel N. Hirschhorn, Garret A. FitzGerald
Published 2008Artigo -
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Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism by Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Lambertus Klei, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Alfredo Brusco, Brian Hon‐Yin Chung, Michael L. Cuccaro, 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, Flora Tassone, Elisabetta Trabetti, Gabriele da Silva Campos, Marcus C.Y. Chan, Chiara Fallerini, Elisa Giorgio, Ana Cristina Girard, Emily Hansen‐Kiss, So Lun Lee, Carla Lintas, Yunin Ludeña, Rachel Nguyen, Lisa Pavinato, Margaret A. Pericak‐Vance, Isaac N. Pessah, Evelise Riberi, Rebecca J. Schmidt, Moyra Smith, Claudia I.C. Souza, Slavica Trajkova, Jaqueline Y. T. Wang, Mullin H.C. Yu, David J. Cutler, Silvia De Rubeis, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Stephan Sanders, Michael E. Talkowski
Published 2021Pré-impressão -
25
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder by Shaun Purcell, Naomi R. Wray, Jennifer Stone, Peter M. Visscher, Michael O’Donovan, Patrick F. Sullivan, Pamela Sklar, Douglas M. Ruderfer, Andrew McQuillin, Derek W. Morris, Colm O’Dushlaine, Aiden Corvin, Peter Holmans, Stuart MacGregor, Hugh Gurling, Douglas Blackwood, Nick Craddock, Michael Gill, Christina M. Hultman, George Kirov, Paul Lichtenstein, Walter Muir, Michael J. Owen, Carlos N. Pato, Edward M. Scolnick, David St Clair, Nigel Williams, Lyudmila Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Mariofanna Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, Emma M. Quinn, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, Caroline Crombie, Gillian Fraser, Soh Leh Kuan, Nicholas Walker, 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, M.H. Azevedo, Andrew Kirby, Manuel A. R. Ferreira, Mark Daly, Kimberly Chambert, Finny G. Kuruvilla, Stacey B. Gabriel, Kristin Ardlie, Jennifer L. Moran
Published 2009Artigo -
26
Prepublication data sharing by Ewan Birney, Thomas J. Hudson, Green Green, Carl A. Gunter, Sean R. Eddy, Jane Rogers, Harris, S. Dusko Ehrlich, Rolf Apweiler, Christopher P. Austin, Leif Berglund, Martin Bobrow, C. Bountra, Anthony J. Brookes, Anne Cambon‐Thomsen, Emma Carter, Rex L. Chisholm, Juan L. Contreras, Roger Cooke, William L. Crosby, Ken Dewar, Richard Durbin, Dyke Som., Ecker, Khaled El Emam, Lars Feuk, Stacey B. Gabriel, Jim Gallacher, William M Gelbart, Antonio Granell, Francisco Guarner, Tim Hubbard, Sara Jackson, Jennifer L. Jennings, Yann Joly, Steven J.M. Jones, Jane Kaye, Karen L. Kennedy, Bartha Maria Knoppers, Nikos C. Kyrpides, William W. Lowrance, Jingchu Luo, John Mackay, L Martín-Rivera, W. Richard McCombie, John D. McPherson, Luke E. Miller, Wendy R. Miller, Daniel E. Moerman, Vincent Mooser, Cynthia C. Morton, James M. Ostell, B. F. Francis Ouellette, Julian Parkhill, Parminder Raina, Chris Rawlings, Steven E. Scherer, Stephen W. Scherer, Paul N. Schofield, Christoph W. Sensen, Victoria Stodden, Michael R. Sussman, Toshio Tanaka, Janet M. Thornton, Tatsuhiko Tsunoda, David Valle, Eero Vuorio, Neil Walker, Steven Wallace, George M. Weinstock, William B. Whitman, Kim C. Worley, Chin‐Lee Wu, Juan Wu, Jiyeon Yu
Published 2009Artigo -
27
Rare chromosomal deletions and duplications increase risk of schizophrenia by 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
Published 2008Artigo -
28
Integrating common and rare genetic variation in diverse human populations by David Altshuler, Richard A Gibbs, Leena Peltonen, David Altshuler, Richard A Gibbs, Leena Peltonen, Emmanouil T. Dermitzakis, S. F. Schaffner, Fuli Yu, Leena Peltonen, Emmanouil T. Dermitzakis, Penelope E. Bonnen, David Altshuler, Richard A Gibbs, Paul I. W. de Bakker, Panos Deloukas, Stacey B. Gabriel, Rhian Gwilliam, Sarah Hunt, Michael Inouye, Xiaoming Jia, Aarno Palotie, Melissa Parkin, Pamela Whittaker, Fuli Yu, Kyle Chang, Alicia Hawes, Lora Lewis, Yanru Ren, David A. Wheeler, Richard A. Gibbs, Donna M. Muzny, C. Barnes, Katayoon Darvishi, Matthew E. Hurles, Joshua M. Korn, Kati Kristiansson, Charles Lee, Steven A. McCarrol, James Nemesh, Emmanouil T. Dermitzakis, Alon Keinan, Stephen B. Montgomery, Samuela Pollack, Alkes L. Price, Nicole Soranzo, Penelope E. Bonnen, Richard A Gibbs, Claudia Gonzaga‐Jauregui, Alon Keinan, Alkes L. Price, Fuli Yu, Verneri Anttila, Wendy Brodeur, Mark J. Daly, Stephen Leslie, Gil McVean, Loukas Moutsianas, Huy Nguyen, S. F. Schaffner, Qingrun Zhang, Mohammed J. R. Ghori, Ralph McGinnis, William McLaren, Samuela Pollack, Alkes L. Price, S. F. Schaffner, Fumihiko Takeuchi, Sharon R. Grossman, Ilya Shlyakhter, Elizabeth Hostetter, Pardis C. Sabeti, Clement Adebamowo, Morris W. Foster, Deborah R Gordon, Júlio Licinio, María Cristina Manca, Patricia A. Marshall, Ichiro Matsuda, Duncan Ngare, Vivian Ota Wang, Deepa Reddy, Charles N. Rotimi, Charmaine Royal, Richard R. Sharp, Changqing Zeng, Lisa Brooks, Jean E. McEwen
Published 2010Artigo -
29
Integrated genomic characterization of endometrial carcinoma by Gad Getz, Stacey B. Gabriel, Kristian Cibulskis, Eric Lander, Andrey Sivachenko, Carrie Sougnez, Robert Lawrence, Cyriac Kandoth, David J. Dooling, Robert W. Fulton, Lucinda Fulton, Joelle Kalicki-Veizer, Michael D. McLellan, Michelle D. O’Laughlin, Heather K. Schmidt, Richard K. Wilson, Kai Ye, Li Ding, Adrian Ally, Miruna Balasundaram, İnanç Birol, Yaron S.N. Butterfield, Rebecca Carlsen, Candace Carter, Andy Chu, Eric Chuah, Hye Jung E. Chun, Noreen Dhalla, Ranabir Guin, Carrie Hirst, Robert A. Holt, Steven J.M. Jones, Darlene Lee, Haiyan I. Li, Marco A. Marra, Michael Mayo, Richard A. Moore, Andrew J. Mungall, Patrick Plettner, Jacqueline E. Schein, Payal Sipahimalani, Angela Tam, Richard Varhol, A. Gordon Robertson, Andrew D. Cherniack, Itai Pashtan, Gordon Saksena, Robert C. Onofrio, Steven E. Schumacher, Barbara Tabak, Scott L. Carter, Bryan Hernandez, Jeff Gentry, Helga B. Salvesen, Kristin Ardlie, Wendy Winckler, Rameen Beroukhim, Matthew Meyerson, Angela Hadjipanayis, Semin Lee, Harshad S. Mahadeshwar, Peter J. Park, Alexei Protopopov, Xiaojia Ren, Sahil Seth, Xingzhi Song, Jiabin Tang, Ruibin Xi, Lixing Yang, Zeng Dong, Raju Kucherlapati, Lynda Chin, Jianhua Zhang, J. Todd Auman, Saianand Balu, Tom Bodenheimer, Elizabeth Buda, D. Neil Hayes, Alan P. Hoyle, Joshua M. Stuart, Corbin D. Jones, Shaowu Meng, Piotr A. Mieczkowski, Lisle E. Mose, Joel S. Parker, Charles M. Perou, Jeffrey Roach, Yan Shi, Janae V. Simons, Mathew G. Soloway, Donghui Tan, Michael D. Topal, Stephen C. Waring, Junyuan Wu, Katherine A. Hoadley, Stephen B. Baylin, Moiz Bootwalla, Phillip H. Lai, Timothy J. Triche, David Van Den Berg
Published 2013Artigo -
30
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants by Sekar Kathiresan, Benjamin F. Voight, Shaun Purcell, Kiran Musunuru, Diego Ardissino, Pier M Mannucci, Sonia Anand, James C. Engert, Nilesh J Samani, Heribert Schunkert, Jeanette Erdmann, Muredach P. Reilly, Daniel J. Rader, Thomas Morgan, John A. Spertus, Monika Stoll, Domenico Girelli, Pascal McKeown, Chris C Patterson, David S Siscovick, Christopher J O'Donnell, Roberto Elosúa, Leena Peltonen, Veikko Salomaa, Stephen M Schwartz, Olle Melander, David Altshuler, Pier Angelica Merlini, Carlo Berzuini, Luisa Bernardinelli, Flora Peyvandi, Marco Tubaro, Patrizia Celli, Maurizio Ferrario, Raffaela Fetiveau, Nicola Marziliano, Giorgio Casari, Michele Galli, Flavio Ribichini, Marco Rossi, Francesco Bernardi, Pietro Zonzin, Alberto Piazza, Jean Yee, Yechiel Friedlander, Jaume Marrugat, Gavin Lucas, Isaac Subirana, Joan Sala, Rafel Ramos, James B Meigs, Gordon Williams, David M Nathan, Calum A. MacRae, Aki S Havulinna, Göran Berglund, Joel N. Hirschhorn, Rosanna Asselta, Stefano Duga, Marta Spreafico, Mark Daly, James Nemesh, Joshua M. Korn, Steven A. McCarroll, Aarti Surti, Candace Guiducci, Lauren Gianniny, Daniel B. Mirel, Melissa Parkin, Noël P. Burtt, Stacey B. Gabriel, John R Thompson, Peter S. Braund, Benjamin J. Wright, Anthony J Balmforth, Stephen G. Ball, Alistair S. Hall, Patrick Linsel‐Nitschke, Wolfgang Lieb, Andreas Ziegler, Inke R. König, Christian Hengstenberg, Marcus Fischer, Klaus Stark, Anika Grosshennig, Michael Preuß, H‐Erich Wichmann, Stefan Schreiber, Willem H. Ouwehand, Panos Deloukas, Michael Scholz, Francois Cambien, Mingyao Li, Zhen Chen, Robert Wilensky, William Matthai, Atif Qasim, Hákon Hákonarson, Joe Devaney, Mary-Susan Burnett
Published 2009Artigo -
31
A genome-wide linkage and association scan reveals novel loci for autism by Lauren A. Weiss, Dan E. Arking, Mark J. Daly, Aravinda Chakravarti, Camille W. Brune, Kristen M. West, Ashley O’Connor, Gina M. Hilton, R Tomlinson, Andrew B. West, Edwin H. Cook, Todd Green, Shun-Chiao Chang, Stacey B. Gabriel, Casey Gates, Ellen Hanson, Andrew Kirby, Joshua M. Korn, Finny G. Kuruvilla, Steven McCarroll, Eric M. Morrow, Benjamin M. Neale, Shaun Purcell, Roksana Sasanfar, Carrie Sougnez, Christine Stevens, David Altshuler, James F. Gusella, Susan L. Santangelo, Pamela Sklar, Rudolph E. Tanzi, Richard Anney, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Catalina Betancur, Sven Bölte, Patrick Bolton, Jessica Brian, Susan E. Bryson, Joseph D. Buxbaum, Ines Cabrito, Guiqing Cai, Rita M. Cantor, Hilary Coon, Judith Conroy, Catarina Correia, Christina Corsello, Emily L. Crawford, Michael L. Cuccaro, Géraldine Dawson, Maretha Jonge, Bernie Devlin, Eftichia Duketis, Sean Ennis, Annette Estes, Penny Farrar, Éric Fombonne, Christine M. Freitag, Louise Gallagher, Daniel H. Geschwind, John R. Gilbert, Michael Gill, Christopher Gillberg, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Jonathan L. Haines, Joachim Hallmayer, Vanessa Hus, Sabine M. Klauck, Olena Korvatska, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett L. Leventha, Xiaoqing Liu, Catherine Lord, Linda Lotspeich, Elena Maestrini, Tiago R. Magalhães, William J. Mahoney, Carine Mantoulan, Helen McConachie, Christopher J. McDougle, William M. McMahon, Christian R. Marshall, Judith Miller, Nancy J. Minshew, Anthony P. Monaco, Jeff Munson, John I. Nürnberger, Guiomar Oliveira, Alistair T. Pagnamenta, Katerina Papanikolaou, Jeremy Parr, Andrew D. Paterson
Published 2009Artigo -
32
Highly evolvable malaria vectors: The genomes of 16 <i>Anopheles</i> mosquitoes by Daniel E. Neafsey, Robert M. Waterhouse, Mohammad Reza Abai, Sergey Aganezov, Max A. Alekseyev, James E. Allen, James Amon, Bruno Arcà, Peter Arensburger, Gleb N. Artemov, Lauren A. Assour, Hamidreza Basseri, Aaron Berlin, Bruce W. Birren, Stéphanie Blandin, Andrew I. Brockman, Thomas R. Burkot, Austin Burt, Clara S. Chan, Cédric Chauve, Joanna C. Chiu, Mikkel Christensen, Carlo Costantini, Victoria L M Davidson, Elena Deligianni, Tania Dottorini, Vicky Dritsou, Stacey B. Gabriel, Wamdaogo M. Guelbéogo, A. Brantley Hall, Mira V. Han, Thaung Hlaing, Daniel Hughes, Adam M. Jenkins, Xiaofang Jiang, Irwin Jungreis, Evdoxia G. Kakani, Maryam Kamali, Petri Kemppainen, Ryan Kennedy, Ioannis Kirmitzoglou, Lizette L. Koekemoer, Njoroge Laban, Nicholas Langridge, Mara Lawniczak, Manolis Lirakis, Neil F. Lobo, Ernesto Lowy, Robert M. MacCallum, Chunhong Mao, G. Maslen, Charles Mbogo, Jennifer B. McCarthy, Kristin Michel, Sara N. Mitchell, Wendy Moore, Katherine A. Murphy, Anastasia N. Naumenko, Tony Nolan, Eva Maria Novoa, Samantha M. O’Loughlin, Chioma Oringanje, Mohammad Ali Oshaghi, Nazzy Pakpour, Philippos Aris Papathanos, Ashley Peery, Michael Povelones, Anil Prakash, David P. Price, Ashok Rajaraman, Lisa Reimer, David C. Rinker, Antonis Rokas, Tanya L. Russell, N’Falé Sagnon, Maria V. Sharakhova, Terrance Shea, Felipe A. Simão, Frédéric Simard, Michel A. Slotman, Pradya Somboon, V. N. Stegniy, Cláudio J. Struchiner, Gregg W.C. Thomas, Marta Tojo, Pantelis Topalis, José M. C. Tubío, Maria Unger, John Vontas, Catherine Walton, Craig S. Wilding, Judith H. Willis, Yi-Chieh Wu, Guiyun Yan, Evgeny M. Zdobnov, Xiaofan Zhou, Flaminia Catteruccia, George K. Christophides, Frank H. Collins, Robert S. Cornman
Published 2014Artigo -
33
Rare coding variation provides insight into the genetic architecture and phenotypic context of autism by Jack Fu, F. Kyle Satterstrom, Minshi Peng, Harrison Brand, Ryan L. Collins, Shan Dong, Brie Wamsley, Lambertus Klei, Lily Wang, Stephanie P. Hao, Christine Stevens, Caroline Cusick, Mehrtash Babadi, Eric Banks, Brett Collins, Sheila Dodge, Stacey B. Gabriel, Laura D. Gauthier, Samuel K. Lee, Lindsay Liang, Alicia Ljungdahl, Behrang Mahjani, Laura Sloofman, Andrey N. Smirnov, Mafalda Barbosa, Catalina Betancur, Alfredo Brusco, Brian Hon‐Yin Chung, Edwin H. Cook, Michael L. Cuccaro, 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, Ãngel Carracedo, Andreas G. Chiocchetti, Hilary Coon, Ryan N. Doan, Montserrat Fernández Prieto, Christine M. Freitag, Sherif Gerges, Stephen J. Guter, David M. Hougaard, Christina M. Hultman, Suma Jacob, Miia Kaartinen, Alexander 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
Published 2022Revisão
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