Options
REPETTO LISBOA, MARIA GABRIELA
Preferred name
REPETTO LISBOA, MARIA GABRIELA
Main Affiliation
Email
grepetto@udd.cl
ORCID
Scopus Author ID
57198456305
Now showing
1 - 10 of 13
-
PublicationRare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome( 2017)
;Anne S. Bassett ;Chelsea Lowther ;Daniele Merico ;Gregory Costain ;Eva W. C. Chow ;Therese van Amelsvoort ;Donna McDonald-McGinn ;Raquel E. Gur ;Ann Swillen ;Marianne Van den Bree ;Kieran Murphy ;Doron Gothelf ;Carrie E. Bearden ;Stephan Eliez ;Wendy Kates ;Nicole Philip ;Vandana Sashi ;Linda Campbell ;Jacob Vorstman ;Joseph Cubells ;Tony Simon ;Erik Boot ;Tracy Heung ;Rens Evers ;Claudia Vingerhoets ;Esther van Duin ;Elaine Zackai ;Elfi Vergaelen ;Koen Devriendt ;Joris R. Vermeesch ;Michael Owen ;Clodagh Murphy ;Elena Michaelovosky ;Leila Kushan ;Maude Schneider ;Wanda Fremont ;Tiffany Busa ;Stephen Hooper ;Kathryn McCabe ;Sasja Duijff ;Karin Isaev ;Giovanna Pellecchia ;John Wei ;Matthew J. Gazzellone ;Stephen W. Scherer ;Beverly S. Emanuel ;Tingwei Guo ;Bernice E. MorrowChristian R. MarshallScopus© Citations 71 -
PublicationChromatin regulators in the TBX1 network confer risk for conotruncal heart defects in 22q11.2DS( 2023)
;Yingjie Zhao ;Yujue Wang ;Lijie Shi ;Donna M. McDonald-McGinn ;T. Blaine Crowley ;Daniel E. McGinn ;Oanh T. Tran ;Daniella Miller ;Jhih-Rong Lin ;Elaine Zackai ;H. Richard Johnston ;Eva W. C. Chow ;Jacob A. S. Vorstman ;Claudia Vingerhoets ;Therese van Amelsvoort ;Doron Gothelf ;Ann Swillen ;Jeroen Breckpot ;Joris R. Vermeesch ;Stephan Eliez ;Maude Schneider ;Marianne B. M. van den Bree ;Michael J. Owen ;Wendy R. Kates ;Vandana Shashi ;Kelly Schoch ;Carrie E. Bearden ;M. Cristina Digilio ;Marta Unolt ;Carolina Putotto ;Bruno Marino ;Maria Pontillo ;Marco Armando ;Stefano Vicari ;Kathleen Angkustsiri ;Linda Campbell ;Tiffany Busa ;Damian Heine-Suñer ;Kieran C. Murphy ;Declan Murphy ;Sixto García-Miñaúr ;Luis Fernández ;Tiffany Busa ;Zhengdong D. Zhang ;Elizabeth Goldmuntz ;Raquel E. Gur ;Beverly S. Emanuel ;Deyou Zheng ;Christian R. Marshall ;Anne S. Bassett ;Tao WangBernice E. MorrowScopus© Citations 2 4 -
PublicationGenome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3( 2017)
;Tingwei Guo ;Donna M. McDonald McGinn ;Jonathan H. Chung ;Hiroko Nomaru ;Christopher L. Campbell ;Anna Blonska ;Anne S. Bassett ;Eva W.C. Chow ;Elisabeth E. Mlynarski ;Ann Swillen ;Joris Vermeesch ;Koen Devriendt ;Doron Gothelf ;Miri Carmel ;Elena Michaelovsky ;Maude Schneider ;Stephan Eliez ;Stylianos E. Antonarakis ;Karlene Coleman ;Aoy Tomita-Mitchell ;Michael E. Mitchell ;M. Cristina Digilio ;Bruno Dallapiccola ;Bruno Marino ;Nicole Philip ;Tiffany Busa ;Leila Kushan-Wells ;Carrie E. Bearden ;Małgorzata Piotrowicz ;Wanda Hawuła ;Amy E. Roberts ;Flora Tassone ;Tony J. Simon ;Esther D.A. van Duin ;Thérèse A. van Amelsvoort ;Wendy R. Kates ;Elaine Zackai ;H. Richard Johnston ;David J. Cutler ;A.J. Agopian ;Elizabeth Goldmuntz ;Laura E. Mitchell ;Tao Wang ;Beverly S. EmanuelBernice E. MorrowScopus© Citations 19 9 -
PublicationSource‐based morphometry reveals structural brain pattern abnormalities in 22q11.2 deletion syndrome( 2024)
;Ruiyang Ge ;Christopher R. K. Ching ;Anne S. Bassett ;Leila Kushan ;Kevin M. Antshel ;Therese van Amelsvoort ;Geor Bakker ;Nancy J. Butcher ;Linda E. Campbell ;Eva W. C. Chow ;Michael Craig ;Nicolas A. Crossley ;Adam Cunningham ;Eileen Daly ;Joanne L. Doherty ;Courtney A. Durdle ;Beverly S. Emanuel ;Ania Fiksinski ;Jennifer K. Forsyth ;Wanda Fremont ;Naomi J. Goodrich‐Hunsaker ;Maria Gudbrandsen ;Raquel E. Gur ;Maria Jalbrzikowski ;Wendy R. Kates ;Amy Lin ;David E. J. Linden ;Kathryn L. McCabe ;Donna McDonald‐McGinn ;Hayley Moss ;Declan G. Murphy ;Kieran C. Murphy ;Michael J. Owen ;Julio E. Villalon‐Reina ;David R. Roalf ;Kosha Ruparel ;J. Eric Schmitt ;Sanne Schuite‐Koops ;Kathleen Angkustsiri ;Daqiang Sun ;Ariana Vajdi ;Marianne van den Bree ;Jacob Vorstman ;Paul M. Thompson ;Fidel Vila‐RodriguezCarrie E. Bearden2 -
PublicationMapping Subcortical Brain Alterations in 22q11.2 Deletion Syndrome: Effects of Deletion Size and Convergence With Idiopathic Neuropsychiatric Illness( 2020)
;Christopher R.K. Ching ;Boris A. Gutman ;Daqiang Sun ;Julio Villalon Reina ;Anjanibhargavi Ragothaman ;Dmitry Isaev ;Artemis Zavaliangos-Petropulu ;Amy Lin ;Rachel K. Jonas ;Leila Kushan ;Laura Pacheco-Hansen ;Ariana Vajdi ;Jennifer K. Forsyth ;Maria Jalbrzikowski ;Geor Bakker ;Therese van Amelsvoort ;Kevin M. Antshel ;Wanda Fremont ;Wendy R. Kates ;Linda E. Campbell ;Kathryn L. McCabe ;Michael C. Craig ;Eileen Daly ;Maria Gudbrandsen ;Clodagh M. Murphy ;Declan G. Murphy ;Kieran C. Murphy ;Ania Fiksinski ;Sanne Koops ;Jacob Vorstman ;T. Blaine Crowley ;Beverly S. Emanuel ;Raquel E. Gur ;Donna M. McDonald-McGinn ;David R. Roalf ;Kosha Ruparel ;J. Eric Schmitt ;Elaine H. Zackai ;Courtney A. Durdle ;Naomi J. Goodrich-Hunsaker ;Tony J. Simon ;Anne S. Bassett ;Nancy J. Butcher ;Eva W.C. Chow ;Fidel Vila-Rodriguez ;Adam Cunningham ;Joanne Doherty ;David E. Linden ;Hayley Moss ;Michael J. Owen ;Marianne van den Bree ;Nicolas A. Crossley ;Paul M. ThompsonCarrie E. BeardenScopus© Citations 44 7 -
PublicationRobust and replicable functional brain signatures of 22q11.2 deletion syndrome and associated psychosis: a deep neural network-based multi-cohort study( 2024)
;Kaustubh Supekar ;Carlo de los Angeles ;Srikanth Ryali ;Leila Kushan ;Charlie Schleifer ;Nicolas A. Crossley ;Tony Simon ;Carrie E. BeardenVinod Menon7 -
PublicationVariance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects( 2018)
;Yingjie Zhao ;Tingwei Guo ;Ania Fiksinski ;Elemi Breetvelt ;Donna M. McDonald-McGinn ;Terrence B. Crowley ;Alexander Diacou ;Maude Schneider ;Stephan Eliez ;Ann Swillen ;Jeroen Breckpot ;Joris Vermeesch ;Eva W. C. Chow ;Doron Gothelf ;Sasja Duijff ;Rens Evers ;Thérèse A. van Amelsvoort ;Marianne van den Bree ;Michael Owen ;Maria Niarchou ;Carrie E. Bearden ;Claudia Ornstein ;Maria Pontillo ;Antonino Buzzanca ;Stefano Vicari ;Marco Armando ;Kieran C. Murphy ;Clodagh Murphy ;Sixto Garcia-Minaur ;Nicole Philip ;Linda Campbell ;Jaume Morey-Cañellas ;Jasna Raventos ;Jordi Rosell ;Damian Heine-Suner ;Robert J. Shprintzen ;Raquel E. Gur ;Elaine Zackai ;Beverly S. Emanuel ;Tao Wang ;Wendy R. Kates ;Anne S. Bassett ;Jacob A. S. Vorstman ;Bernice E. MorrowScopus© Citations 30 12 -
PublicationComplete Sequence of the 22q11.2 Allele in 1,053 Subjects with 22q11.2 Deletion Syndrome Reveals Modifiers of Conotruncal Heart Defects( 2020)
;Yingjie Zhao ;Alexander Diacou ;H. Richard Johnston ;Fadi I. Musfee ;Donna M. McDonald-McGinn ;Daniel McGinn ;T. Blaine Crowley ;Ann Swillen ;Jeroen Breckpot ;Joris R. Vermeesch ;Wendy R. Kates ;M. Cristina Digilio ;Marta Unolt ;Bruno Marino ;Maria Pontillo ;Marco Armando ;Fabio Di Fabio ;Stefano Vicari ;Marianne van den Bree ;Hayley Moss ;Michael J. Owen ;Kieran C. Murphy ;Clodagh M. Murphy ;Declan Murphy ;Kelly Schoch ;Vandana Shashi ;Flora Tassone ;Tony J. Simon ;Robert J. Shprintzen ;Linda Campbell ;Nicole Philip ;Damian Heine-Suñer ;Sixto García-Miñaúr ;Luis Fernández ;Carrie E. Bearden ;Claudia Vingerhoets ;Therese van Amelsvoort ;Stephan Eliez ;Maude Schneider ;Jacob A.S. Vorstman ;Doron Gothelf ;Elaine Zackai ;A.J. Agopian ;Raquel E. Gur ;Anne S. Bassett ;Beverly S. Emanuel ;Elizabeth Goldmuntz ;Laura E. Mitchell ;Tao Wang ;Bernice E. Morrow ;Stylianos E. Antonarakis ;Massimo Biondi ;Erik Boot ;Elemi Breetvelt ;Tiffany Busa ;Nancy Butcher ;Antonino Buzzanca ;Miri Carmel ;Isabelle Cleynen ;David Cutler ;Bruno Dallapiccola ;María Angeles de la Fuente Sanches ;Michael P. Epstein ;Rens Evers ;Luis Fernandez ;Rosemarie Fritsch ;Fernando García Algas ;Tingwei Guo ;Raquel Gur ;Matthew S. Hestand ;Tracy Heung ;Stephen Hooper ;Andrea Jin ;Leila Kushan-Wells ;Alejandra Teresa Laorden-Nieto ;Guido Lattanzi ;Christian Marshall ;Kathryn McCabe ;Elena Michaelovsky ;Claudia Ornstein ;Candice Silversides ;Oanh Tran ;Esther D.A. van Duin ;Elfi Vergaelen ;Steve T. Warren ;Ronnie Weinberger ;Abraham Weizman ;Zhengdong ZhangMichael ZwickScopus© Citations 36 5 -
PublicationA normative chart for cognitive development in a genetically selected population( 2021)
;Ania M. Fiksinski ;Carrie E. Bearden ;Anne S. Bassett ;René S. Kahn ;Janneke R. Zinkstok ;Stephen R. Hooper ;Wanda Tempelaar ;Donna McDonald-McGinn ;Ann Swillen ;Beverly Emanuel ;Bernice Morrow ;Raquel Gur ;Eva Chow ;Marianne van den Bree ;Joris Vermeesch ;Stephen Warren ;Michael Owen ;Therese van Amelsvoort ;Stephan Eliez ;Doron Gothelf ;Celso Arango ;Wendy Kates ;Tony Simon ;Kieran Murphy ;Damian Heine Suner ;Stefano Vicari ;Joseph Cubells ;Marco Armando ;Nicole Philip ;Linda Campbell ;Sixto Garcia-Minaur ;Maude Schneider ;Vandana Shashi ;Jacob VorstmanElemi J. BreetveltScopus© Citations 11 15 -
PublicationUsing common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome( 2020)
;Robert W. Davies ;Ania M. Fiksinski ;Elemi J. Breetvelt ;Nigel M. Williams ;Stephen R. Hooper ;Thomas Monfeuga ;Anne S. Bassett ;Michael J. Owen ;Raquel E. Gur ;Bernice E. Morrow ;Donna M. McDonald-McGinn ;Ann Swillen ;Eva W. C. Chow ;Marianne van den Bree ;Beverly S. Emanuel ;Joris R. Vermeesch ;Therese van Amelsvoort ;Celso Arango ;Marco Armando ;Linda E. Campbell ;Joseph F. Cubells ;Stephan Eliez ;Sixto Garcia-Minaur ;Doron Gothelf ;Wendy R. Kates ;Kieran C. Murphy ;Clodagh M. Murphy ;Declan G. Murphy ;Nicole Philip ;Vandana Shashi ;Tony J. Simon ;Damiàn Heine Suñer ;Stefano Vicari ;Stephen W. Scherer ;Carrie E. BeardenJacob A. S. VorstmanScopus© Citations 71 8