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Joanne Doherty

Cardiff University

17H指数
48论文数
1.7K被引数
收录论文 25
发表时间
Penetrance of neurodevelopmental copy number variants is associated with variations in cortical morphology神经发育性拷贝数变异的穿透性与皮层形态变异相关
err2025-05-23
err0
PREAI
errAna I. Silva; Ida E. Sønderby; George Kirov; Abdel Abdellaoui; Ingrid Agartz; David Ames; Nicola J. Armstrong; Eric Artiges; Tobias Banaschewski; Anne S. Bassett; Carrie E. Bearden; John Blangero; Rune Boen; Dorret I. Boomsma; Robin Bülow; Nancy J. Butcher; Vince Calhoun; Linda E. Campbell; Eva W.C. Chow; Simone Ciufolini; Michael C. Craig; Benedicto Crespo-Farroco; Adam C. Cunningham; Shareefa Dalvie; Eileen Daly; Paola Dazzan; Eco J.C. de Geus; Greig I. de Zubicaray; Joanne L. Doherty; Gary Donohoe; Mark Drakesmith; Thomas Espeseth; Vincent Frouin; Hugh Garavan; David C. Glahn; Naomi J. Goodrich-Hunsaker; Penny A. Gowland; Hans J. Grabe; Antoine Grigis; Maria Gudbrandsen; Boris A. Gutman; Jan Haavik; Asta K. Håberg; Jeremy Hall; Andreas Heinz; Sarah Hohmann; Jouke-Jan Hottenga; Sébastien Jacquemont; Neda Jahanshad; Rachel K. Jonas; Derek K. Jones; Erik G. Jönsson; Sanne Koops; Kuldeep Kumar; Stephanie Le Hellard; Herve Lemaitre; Jingyu Liu; Astri J. Lundervold; Jean-Luc Martinot; Karen A. Mather; Donna M. McDonald-McGinn; Katie L. McMahon; Allan F. McRae; Sarah E. Medland; Clara A. Moreau; Kieran C. Murphy; Declan Murphy; Robin M. Murray; Frauke Nees; Michael J. Owen; Marie-Laure Paillère Martinot; Diimitri Papadopoulos Orfanos; Tomas Paus; Luise Poustka; Tiago Reis Marques; David R. Roalf; Perminder S. Sachdev; Freda Scheffler; J. Eric Schmitt; Gunter Schumann; Vidar M. Steen; Dan J. Stein; Lachlan T. Strike; Alexander Teumer; Anbupalam Thalamuthu; Sophia I. Thomopoulos; Diana Tordesillas-Gutiérrez; Julian N. Trollor; Anne Uhlmann; Ariana Vajdi; Dennis van ’t Ent; Therese van Amelsvoort; Marianne B.M. van den Bree; Dennis van der Meer; Javier Vázquez-Bourgon; Julio E. Villalón-Reina; Uwe Völker; Henry Völzke; Jacob A.S. Vorstman; Lars T. Westlye; Nigel Williams; Katharina Wittfeld; Margaret J. Wright; Paul M. Thompson; Ole A. Andreassen; David E.J. Linden
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The translation of psychiatric genetic findings to the clinic
err2024-05-01
err1
errOAAI
errKendall, Kimberley Marie; Duffin, Donna; Doherty, Joanne; Irving, Rachel; Procter, Annie; Walters, James Tynan Rhys
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Source-based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome基于源的形态计量学揭示了22 q11.2缺失综合征的结构性脑模式异常
err2024-01-12
err4
errOAAI
errGe, Ruiyang; Ching, Christopher R. K.; Bassett, Anne S.; Kushan, Leila; Antshel, Kevin M.; van Amelsvoort, Therese; Bakker, Geor; Butcher, Nancy J.; Campbell, Linda E.; Chow, Eva W. C.; Craig, Michael; Crossley, Nicolas A.; Cunningham, Adam; Daly, Eileen; Doherty, Joanne L.; Durdle, Courtney A.; Emanuel, Beverly S.; Fiksinski, Ania; Forsyth, Jennifer K.; Fremont, Wanda; Goodrich-Hunsaker, Naomi J.; Gudbrandsen, Maria; Gur, Raquel E.; Jalbrzikowski, Maria; Kates, Wendy R.; Lin, Amy; Linden, David E. J.; Mccabe, Kathryn L.; McDonald-McGinn, Donna; Moss, Hayley; Murphy, Declan G.; Murphy, Kieran C.; Owen, Michael J.; Villalon-Reina, Julio E.; Repetto, Gabriela M.; Roalf, David R.; Ruparel, Kosha; Schmitt, J. Eric; Schuite-Koops, Sanne; Angkustsiri, Kathleen; Sun, Daqiang; Vajdi, Ariana; van den Bree, Marianne; Vorstman, Jacob; Thompson, Paul M.; Vila-Rodriguez, Fidel; Bearden, Carrie E.
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Beyond the Global Brain Differences: Intraindividual Variability Differences in 1q21.1 Distal and 15q11.2 BP1-BP2 Deletion Carriers超越全局大脑差异: 1 q21.1远端和15 q11.2 BP1-BP2缺失携带者的个体内变异性差异
err2024-01-01
err0
errOAAI
errBoen, Rune; Kaufmann, Tobias; van der Meer, Dennis; Frei, Oleksandr; Agartz, Ingrid; Ames, David; Andersson, Micael; Armstrong, Nicola J.; Artiges, Eric; Atkins, Joshua R.; Bauer, Jochen; Benedetti, Francesco; Boomsma, Dorret I.; Brodaty, Henry; Brosch, Katharina; Buckner, Randy L.; Cairns, Murray J.; Calhoun, Vince; Caspers, Svenja; Cichon, Sven; Corvin, Aiden P.; Crespo-Facorro, Benedicto; Dannlowski, Udo; David, Friederike S.; de Geus, Eco J. C.; de Zubicaray, Greig I.; Desrivieres, Sylvane; Doherty, Joanne L.; Donohoe, Gary; Ehrlich, Stefan; Eising, Else; Espeseth, Thomas; Fisher, Simon E.; Forstner, Andreas J.; Fortaner-Uya, Lidia; Frouin, Vincent; Fukunaga, Masaki; Ge, Tian; Glahn, David C.; Goltermann, Janik; Grabe, Hans J.; Green, Melissa J.; Groenewold, Nynke A.; Grotegerd, Dominik; Grontvedt, Goril Rolfseng; Hahn, Tim; Hashimoto, Ryota; Hehir-Kwa, Jayne Y.; Henskens, Frans A.; Holmes, Avram J.; Haberg, Asta K.; Haavik, Jan; Jacquemont, Sebastien; Jansen, Andreas; Jockwitz, Christiane; Joensson, Erik G.; Kikuchi, Masataka; Kircher, Tilo; Kumar, Kuldeep; Le Hellard, Stephanie; Leu, Costin; Linden, David E.; Liu, Jingyu; Loughnan, Robert; Mather, Karen A.; Mcmahon, Katie L.; Mcrae, Allan F.; Medland, Sarah E.; Meinert, Susanne; Moreau, Clara A.; Morris, Derek W.; Mowry, Bryan J.; Muehleisen, Thomas W.; Nenadic, Igor; Noethen, Markus M.; Nyberg, Lars; Ophoff, Roel A.; Owen, Michael J.; Pantelis, Christos; Paolini, Marco; Paus, Tomas; Pausova, Zdenka; Persson, Karin; Quide, Yann; Marques, Tiago Reis; Sachdev, Perminder S.; Sando, Sigrid B.; Schall, Ulrich; Scott, Rodney J.; Selbaek, Geir; Shumskaya, Elena; Silva, Ana I.; Sisodiya, Sanjay M.; Stein, Frederike; Stein, Dan J.; Straube, Benjamin; Streit, Fabian; Strike, Lachlan T.; Teumer, Alexander; Teutenberg, Lea; Thalamuthu, Anbupalam; Tooney, Paul A.; Tordesillas-Gutierrez, Diana; Trollor, Julian N.; Van't Ent, Dennis; van den Bree, Marianne B. M.; van Haren, Neeltje E. M.; Vazquez-Bourgon, Javier; Voelzke, Henry; Wen, Wei; Wittfeld, Katharina; Ching, Christopher R. K.; Westlye, Lars T.; Thompson, Paul M.; Bearden, Carrie E.; Selmer, Kaja K.; Alnaes, Dag; Andreassen, Ole A.; Sonderby, Ida E.
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In vivo evidence of microstructural hypo-connectivity of brain white matter in 22q11.2 deletion syndrome
err2023-07-26
err3
errOAAI
errRaven, Erika P. P.; Veraart, Jelle; Kievit, Rogier A. A.; Genc, Sila; Ward, Isobel L. L.; Hall, Jessica; Cunningham, Adam; Doherty, Joanne; van den Bree, Marianne B. M.; Jones, Derek K.
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Atypical cortical networks in children at high-genetic risk of psychiatric and neurodevelopmental disorders
err2023-07-04
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errOAAI
errDoherty, Joanne L.; Cunningham, Adam C.; Chawner, Samuel J. R. A.; Moss, Hayley M.; Dima, Diana C.; Linden, David E. J.; Owen, Michael J.; van den Bree, Marianne B. M.; Singh, Krish D.
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Detecting microstructural deviations in individuals with deep diffusion MRI tractometry
err2021-09-22
err27
errOAAI
errChamberland, Maxime; Genc, Sila; Tax, Chantal M. W.; Shastin, Dmitri; Koller, Kristin; Raven, Erika P.; Cunningham, Adam; Doherty, Joanne; van den Bree, Marianne B. M.; Parker, Greg D.; Hamandi, Khalid; Gray, William P.; Jones, Derek K.
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1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans1 q21.1远端拷贝数变异与人类大脑和认知改变有关
err2021-03-22
err26
errOAAI
errSonderby, Ida E.; van der Meer, Dennis; Moreau, Clara; Kaufmann, Tobias; Walters, G. Bragi; Ellegaard, Maria; Abdellaoui, Abdel; Ames, David; Amunts, Katrin; Andersson, Micael; Armstrong, Nicola J.; Bernard, Manon; Blackburn, Nicholas B.; Blangero, John; Boomsma, Dorret I.; Brodaty, Henry; Brouwer, Rachel M.; Buelow, Robin; Boen, Rune; Cahn, Wiepke; Calhoun, Vince D.; Caspers, Svenja; Ching, Christopher R. K.; Cichon, Sven; Ciufolini, Simone; Crespo-Facorro, Benedicto; Curran, Joanne E.; Dale, Anders M.; Dalvie, Shareefa; Dazzan, Paola; de Geus, Eco J. C.; de Zubicaray, Greig I.; de Zwarte, Sonja M. C.; Desrivieres, Sylvane; Doherty, Joanne L.; Donohoe, Gary; Draganski, Bogdan; Ehrlich, Stefan; Eising, Else; Espeseth, Thomas; Fejgin, Kim; Fisher, Simon E.; Fladby, Tormod; Frei, Oleksandr; Frouin, Vincent; Fukunaga, Masaki; Gareau, Thomas; Ge, Tian; Glahn, David C.; Grabe, Hans J.; Groenewold, Nynke A.; Gustafsson, Omar; Haavik, Jan; Haberg, Asta K.; Hall, Jeremy; Hashimoto, Ryota; Hehir-Kwa, Jayne Y.; Hibar, Derrek P.; Hillegers, Manon H. J.; Hoffmann, Per; Holleran, Laurena; Holmes, Avram J.; Homuth, Georg; Hottenga, Jouke-Jan; Hulshoff Pol, Hilleke E.; Ikeda, Masashi; Jahanshad, Neda; Jockwitz, Christiane; Johansson, Stefan; Joensson, Erik G.; Jorgensen, Niklas R.; Kikuchi, Masataka; Knowles, Emma E. M.; Kumar, Kuldeep; Le Hellard, Stephanie; Leu, Costin; Linden, David E. J.; Liu, Jingyu; Lundervold, Arvid; Lundervold, Astri Johansen; Maillard, Anne M.; Martin, Nicholas G.; Martin-Brevet, Sandra; Mather, Karen A.; Mathias, Samuel R.; McMahon, Katie L.; McRae, Allan F.; Medland, Sarah E.; Meyer-Lindenberg, Andreas; Moberget, Torgeir; Modenato, Claudia; Sanchez, Jennifer Monereo; Morris, Derek W.; Muehleisen, Thomas W.; Murray, Robin M.; Nielsen, Jacob; Nordvik, Jan E.; Nyberg, Lars; Loohuis, Loes M. Olde; Ophoff, Roel A.; Owen, Michael J.; Paus, Tomas; Pausova, Zdenka; Peralta, Juan M.; Pike, G. Bruce; Prieto, Carlos; Quinlan, Erin B.; Reinbold, Celine S.; Marques, Tiago Reis; Rucker, James J. H.; Sachdev, Perminder S.; Sando, Sigrid B.; Schofield, Peter R.; Schork, Andrew J.; Schumann, Gunter; Shin, Jean; Shumskaya, Elena; Silva, Ana I.; Sisodiya, Sanjay M.; Steen, Vidar M.; Stein, Dan J.; Strike, Lachlan T.; Suzuki, Ikuo K.; Tamnes, Christian K.; Teumer, Alexander; Thalamuthu, Anbupalam; Tordesillas-Gutierrez, Diana; Uhlmann, Anne; Ulfarsson, Magnus O.; van 't Ent, Dennis; van den Bree, Marianne B. M.; Vanderhaeghen, Pierre; Vassos, Evangelos; Wen, Wei; Wittfeld, Katharina; Wright, Margaret J.; Agartz, Ingrid; Djurovic, Srdjan; Westlye, Lars T.; Stefansson, Hreinn; Stefansson, Kari; Jacquemont, Sebastien; Thompson, Paul M.; Andreassen, Ole A.
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Effects of copy number variations on brain structure and risk for psychiatric illness: Large-scale studies from the ENIGMA working groups on CNVs拷贝数变化对大脑结构和精神疾病风险的影响: ENIGMA CNVs工作组的大规模研究
err2021-02-21
err35
errOAAI
errSonderby, Ida E.; Ching, Christopher R. K.; Thomopoulos, Sophia I.; van Der Meer, Dennis; Sun, Daqiang; Villalon-Reina, Julio E.; Agartz, Ingrid; Amunts, Katrin; Arango, Celso; Armstrong, Nicola J.; Ayesa-Arriola, Rosa; Bakker, Geor; Bassett, Anne S.; Boomsma, Dorret I.; Bulow, Robin; Butcher, Nancy J.; Calhoun, Vince D.; Caspers, Svenja; Chow, Eva W. C.; Cichon, Sven; Ciufolini, Simone; Craig, Michael C.; Crespo-Facorro, Benedicto; Cunningham, Adam C.; Dale, Anders M.; Dazzan, Paola; de Zubicaray, Greig I.; Djurovic, Srdjann; Doherty, Joanne L.; Donohoe, Gary; Draganski, Bogdan; Durdle, Courtney A.; Ehrlich, Stefan; Emanuel, Beverly S.; Espeseth, Thomas; Fisher, Simon E.; Ge, Tian; Glahn, David C.; Grabe, Hans J.; Gur, Raquel E.; Gutman, Boris A.; Haavik, Jan; Haberg, Asta K.; Hansen, Laura A.; Hashimoto, Ryota; Hibar, Derrek P.; Holmes, Avram J.; Hottenga, Jouke-Jan; Hulshoff Pol, Hilleke E.; Jalbrzikowski, Maria; Knowles, Emma E. M.; Kushan, Leila; Linden, David E. J.; Liu, Jingyu; Lundervold, Astri J.; Martin-Brevet, Sandra; Martinez, Kenia; Mather, Karen A.; Mathias, Samuel R.; McDonald-McGinn, Donna M.; McRae, Allan F.; Medland, Sarah E.; Moberget, Torgeir; Modenato, Claudia; Monereo Sanchez, Jennifer; Moreau, Clara A.; Muhleisen, Thomas W.; Paus, Tomas; Pausova, Zdenka; Prieto, Carlos; Ragothaman, Anjanibhargavi; Reinbold, Celine S.; Reis Marques, Tiago; Repetto, Gabriela M.; Reymond, Alexandre; Roalf, David R.; Rodriguez-Herreros, Borja; Rucker, James J.; Sachdev, Perminder S.; Schmitt, James E.; Schofield, Peter R.; Silva, Ana I.; Stefansson, Hreinn; Stein, Dan J.; Tamnes, Christian K.; Tordesillas-Gutierrez, Diana; Ulfarsson, Magnus O.; Vajdi, Ariana; van 't Ent, Dennis; van den Bree, Marianne B. M.; Vassos, Evangelos; Vazquez-Bourgon, Javier; Vila-Rodriguez, Fidel; Walters, G. Bragi; Wen, Wei; Westlye, Lars T.; Wittfeld, Katharina; Zackai, Elaine H.; Stefansson, Kari; Jacquemont, Sebastien; Thompson, Paul M.; Bearden, Carrie E.; Andreassen, Ole A.
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A Genetics-First Approach to Dissecting the Heterogeneity of Autism: Phenotypic Comparison of Autism Risk Copy Number Variants剖析自闭症异质性的遗传学优先方法: 自闭症风险拷贝数变异的表型比较
err2021-01-01
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errChawner, Samuel J. R. A.; Doherty, Joanne L.; Anney, Richard J. L.; Antshel, Kevin M.; Bearden, Carrie E.; Bernier, Raphael; Chung, Wendy K.; Clements, Caitlin C.; Curran, Sarah R.; Cuturilo, Goran; Fiksinski, Ania M.; Gallagher, Louise; Goin-Kochel, Robin P.; Gur, Raquel E.; Hanson, Ellen; Jacquemont, Sebastien; Kates, Wendy R.; Kushan, Leila; Maillard, Anne M.; McDonald-McGinn, Donna M.; Mihaljevic, Marina; Miller, Judith S.; Moss, Hayley; Pejovic-Milovancevic, Milica; Schultz, Robert T.; Green-Snyder, Leeanne; Vorstman, Jacob A.; Wenger, Tara L.; Hall, Jeremy; Owen, Michael J.; van den Bree, Marianne B. M.
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Electrophysiological network alterations in adults with copy number variants associated with high neurodevelopmental risk
err2020-09-21
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errOAAI
errDima, Diana C.; Adams, Rachael; Linden, Stefanie C.; Baird, Alister; Smith, Jacqueline; Foley, Sonya; Perry, Gavin; Routley, Bethany C.; Magazzini, Lorenzo; Drakesmith, Mark; Williams, Nigel; Doherty, Joanne; van den Bree, Marianne B. M.; Owen, Michael J.; Hall, Jeremy; Linden, David E. J.; Singh, Krish D.
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Mapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness
err2020-07-01
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errChing, Christopher R. K.; Gutman, Boris A.; Sun, Daqiang; Reina, Julio Villalon; Ragothaman, Anjanibhargavi; Isaev, Dmitry; Zavaliangos-Petropulu, Artemis; Lin, Amy; Jonas, Rachel K.; Kushan, Leila; Pacheco-Hansen, Laura; Vajdi, Ariana; Forsyth, Jennifer K.; Jalbrzikowski, Maria; Bakker, Geor; van Amelsvoort, Therese; Antshel, Kevin M.; Fremont, Wanda; Kates, Wendy R.; Campbell, Linda E.; McCabe, Kathryn L.; Craig, Michael C.; Daly, Eileen; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan G.; Murphy, Kieran C.; Fiksinski, Ania; Koops, Sanne; Vorstman, Jacob; Crowley, T. Blaine; Emanuel, Beverly S.; Gur, Raquel E.; McDonald-McGinn, Donna M.; Roalf, David R.; Ruparel, Kosha; Schmitt, J. Eric; Zackai, Elaine H.; Durdle, Courtney A.; Goodrich-Hunsaker, Naomi J.; Simon, Tony J.; Bassett, Anne S.; Butcher, Nancy J.; Chow, Eva W. C.; Vila-Rodriguez, Fidel; Cunningham, Adam; Doherty, Joanne; Linden, David E.; Moss, Hayley; Owen, Michael J.; van den Bree, Marianne; Crossley, Nicolas A.; Repetto, Gabriela M.; Thompson, Paul M.; Bearden, Carrie E.
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Altered white matter microstructure in 22q11.2 deletion syndrome: a multisite diffusion tensor imaging study
err2019-07-29
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errVillalon-Reina, Julio E.; Martinez, Kenia; Qu, Xiaoping; Ching, Christopher R. K.; Nir, Talia M.; Kothapalli, Deydeep; Corbin, Conor; Sun, Daqiang; Lin, Amy; Forsyth, Jennifer K.; Kushan, Leila; Vajdi, Ariana; Jalbrzikowski, Maria; Hansen, Laura; Jonas, Rachel K.; van Amelsvoort, Therese; Bakker, Geor; Kates, Wendy R.; Antshel, Kevin M.; Fremont, Wanda; Campbell, Linda E.; McCabe, Kathryn L.; Daly, Eileen; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan; Craig, Michael; Emanuel, Beverly; McDonald-McGinn, Donna M.; Vorstman, Jacob A. S.; Fiksinski, Ania M.; Koops, Sanne; Ruparel, Kosha; Roalf, David; Gur, Raquel E.; Schmitt, J. Eric; Simon, Tony J.; Goodrich-Hunsaker, Naomi J.; Durdle, Courtney A.; Doherty, Joanne L.; Cunningham, Adam C.; van den Bree, Marianne; Linden, David E. J.; Owen, Michael; Moss, Hayley; Kelly, Sinead; Donohoe, Gary; Murphy, Kieran C.; Arango, Celso; Jahanshad, Neda; Thompson, Paul M.; Bearden, Carrie E.
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Psychiatric disorders in children with 16p11.2 deletion and duplication (vol 9, 8, 2019)
err2019-03-05
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errOAAI
errNiarchou, Maria; Chawner, Samuel J. R. A.; Doherty, Joanne L.; Maillard, Anne M.; Jacquemont, Sebastien; Chung, Wendy K.; Green-Snyder, LeeAnne; Bernier, Raphael A.; Goin-Kochel, Robin P.; Hanson, Ellen; Linden, David E. J.; Linden, Stefanie C.; Raymond, F. Lucy; Skuse, David; Hall, Jeremy; Owen, Michael J.; van den Bree, Marianne B. M.
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The emergence of psychotic experiences in the early adolescence of 22q11.2 Deletion Syndrome
err2019-02-01
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errOAAI
errChawner, Samuel J. R. A.; Niarchou, Maria; Doherty, Joanne L.; Moss, Hayley; Owen, Michael J.; van den Bree, Marianne B. M.
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Psychiatric disorders in children with 16p11.2 deletion and duplication
err2019-01-16
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errNiarchou, Maria; Chawner, Samuel J. R. A.; Doherty, Joanne L.; Maillard, Anne M.; Jacquemont, Sebastien; Chung, Wendy K.; Green-Snyder, LeeAnne; Bernier, Raphael A.; Goin-Kochel, Robin P.; Hanson, Ellen; Linden, David E. J.; Linden, Stefanie C.; Raymond, F. Lucy; Skuse, David; Hall, Jeremy; Owen, Michael J.; van den Bree, Marianne B. M.
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A GENETIC FIRST APPROACH TO DISSECTING THE HETEROGENEITY OF AUTISM: PHENOTYPIC COMPARISON OF AUTISM RISK COPY NUMBER VARIANTS
err2019-01-01
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PREAI
errChawner, Samuel; Doherty, Joanne; Moss, Hayley; Bearden, Carrie; Chung, Wendy; Curran, Sarah; Hall, Jeremy; Jacquemont, Sebastien; Kates, Wendy; Vorstman, Jacob; Owen, Michael; Van den Bree, Marianne
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Large-scale mapping of cortical alterations in 22q11.2 deletion syndrome: Convergence with idiopathic psychosis and effects of deletion size
err2018-06-13
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errSun, Daqiang; Ching, Christopher R. K.; Lin, Amy; Forsyth, Jennifer K.; Kushan, Leila; Vajdi, Ariana; Jalbrzikowski, Maria; Hansen, Laura; Villalon-Reina, Julio E.; Qu, Xiaoping; Jonas, Rachel K.; van Amelsvoort, Therese; Bakker, Geor; Kates, Wendy R.; Antshel, Kevin M.; Fremont, Wanda; Campbell, Linda E.; McCabe, Kathryn L.; Daly, Eileen; Gudbrandsen, Maria; Murphy, Clodagh M.; Murphy, Declan; Craig, Michael; Vorstman, Jacob; Fiksinski, Ania; Koops, Sanne; Ruparel, Kosha; Roalf, David R.; Gur, Raquel E.; Schmitt, J. Eric; Simon, Tony J.; Goodrich-Hunsaker, Naomi J.; Durdle, Courtney A.; Bassett, Anne S.; Chow, Eva W. C.; Butcher, Nancy J.; Vila-Rodriguez, Fidel; Doherty, Joanne; Cunningham, Adam; van den Bree, Marianne B. M.; Linden, David E. J.; Moss, Hayley; Owen, Michael J.; Murphy, Kieran C.; McDonald-McGinn, Donna M.; Emanuel, Beverly; van Erp, Theo G. M.; Turner, Jessica A.; Thompson, Paul M.; Bearden, Carrie E.
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