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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 16
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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 -
PublicationGathering the Stakeholder’s Perspective: Experiences and Opportunities in Rare Genetic Disease Research( 2023)
;Lauren K. White ;T. Blaine Crowley ;Brenda Finucane ;Emily J. McClellan ;Sarah Donoghue ;Sixto Garcia-Minaur ;Matthias Fischer ;Sebastien Jacquemont ;Raquel E. Gur ;Anne M. Maillard ;Kirsten A. Donald ;Anne S. Bassett ;Ann SwillenDonna M. McDonald-McGinnScopus© Citations 1 3 -
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 GarcÃa-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 -
PublicationPEMapper and PECaller provide a simplified approach to whole-genome sequencing( 2017)
;H. Richard Johnston ;Pankaj Chopra ;Thomas S. Wingo ;Viren Patel ;Michael P. Epstein ;Jennifer G. Mulle ;Stephen T. Warren ;Michael E. Zwick ;David J. Cutler ;Bernice Morrow ;Beverly Emanuel ;Donna M. McDonald-McGinn ;Steve Scherer ;Anne Bassett ;Eva Chow ;Joris Vermeesch ;Ann Swillen ;Raquel Gur ;Carrie Bearden ;Wendy Kates ;Vandana Shashi ;Tony Simon ;Pankj Chopra ;Joseph Cubells ;David J. Cutler ;Michael P. Epstein ;H. Richard Johnston ;Jennifer Mulle ;Viren Patel ;Stephen T. Warren ;Thomas S. Wingo ;Michael E. Zwick ;Linda Campbell ;Jacob Vorstman ;Therese Van Amelsvoort ;Stephen Eliez ;Nicole Philip ;Doron Gothelf ;Marianne Van Den Bree ;Michael Owen ;Clodagh Murphy ;Declan Murphy ;Sixto Garcia-Minaur ;Damian Neine-Suner ;Kieran Murphy ;Marco ArmandoStefano Vicari7 -
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 -
PublicationRETRACTED: Nested Inversion Polymorphisms Predispose Chromosome 22q11.2 to Meiotic Rearrangements( 2017)
;Wolfram Demaerel ;Matthew S. Hestand ;Elfi Vergaelen ;Ann Swillen ;Marcos López-Sánchez ;Luis A. Pérez-Jurado ;Donna M. McDonald-McGinn ;Elaine Zackai ;Beverly S. Emanuel ;Bernice E. Morrow ;Jeroen Breckpot ;Koenraad Devriendt ;Joris R. Vermeesch ;Kevin Antshel ;Celso Arango ;Marco Armando ;Anne Bassett ;Carrie Bearden ;Erik Boot ;Marta Bravo-Sanchez ;Elemi Breetvelt ;Tiffany Busa ;Nancy Butcher ;Linda Campbell ;Miri Carmel ;Eva Chow ;T. Blaine Crowley ;Joseph Cubells ;David Cutler ;Wolfram Demaerel ;Maria Cristina Digilio ;Sasja Duijff ;Stephan Eliez ;Beverly Emanuel ;Michael Epstein ;Rens Evers ;Luis Fernandez Garcia-Moya ;Ania Fiksinski ;David Fraguas ;Wanda Fremont ;Rosemarie Fritsch ;Sixto Garcia-Minaur ;Aaron Golden ;Doron Gothelf ;Tingwei Guo ;Ruben Gur ;Raquel Gur ;Damian Heine-Suner ;Matthew Hestand ;Stephen Hooper ;Wendy Kates ;Leila Kushan ;Alejandra Laorden-Nieto ;Johanna Maeder ;Bruno Marino ;Christian Marshall ;Kathryn McCabe ;Donna McDonald-McGinn ;Elena Michaelovosky ;Bernice Morrow ;Edward Moss ;Jennifer Mulle ;Declan Murphy ;Kieran Murphy ;Clodagh Murphy ;Maria Niarchou ;Claudia Ornstein ;Michael Owen ;Nicole Philip ;Maude Schneider ;Vandana Shashi ;Tony Simon ;Ann Swillen ;Flora Tassone ;Marta Unolt ;Therese van Amelsvoort ;Marianne van den Bree ;Esther Van Duin ;Elfi Vergaelen ;Joris Vermeesch ;Stefano Vicari ;Claudia Vingerhoets ;Jacob Vorstman ;Steve Warren ;Ronnie Weinberger ;Omri Weisman ;Abraham Weizman ;Elaine Zackai ;Zhengdong ZhangMichael Zwick8 -
PublicationPrenatal vs postnatal diagnosis of 22q11.2 deletion syndrome: cardiac and noncardiac outcomes through 1 year of age( 2023)
;Lindsay R. Freud ;Stephanie Galloway ;T. Blaine Crowley ;Julie Moldenhauer ;Ann Swillen ;Jeroen Breckpot ;Antoni Borrell ;Neeta L. Vora ;Bettina Cuneo ;Hilary Hoffman ;Lisa Gilbert ;Beata Nowakowska ;Maciej Geremek ;Anna Kutkowska-Kaźmierczak ;Joris R. Vermeesch ;Koen Devriendt ;Tiffany Busa ;Sabine Sigaudy ;Trisha Vigneswaran ;John M. Simpson ;Jeffrey Dungan ;Nina Gotteiner ;Karl-Philipp Gloning ;Maria Cristina Digilio ;Marta Unolt ;Carolina Putotto ;Bruno Marino ;Magdalena Fadic ;Sixto Garcia-Minaur ;Ana Achón Buil ;Mary Ann Thomas ;Deborah Fruitman ;Taylor Beecroft ;Pui Wah Hui ;Solveig Oskarsdottir ;Rachael Bradshaw ;Amanda Criebaum ;Mary E. Norton ;Tiffany Lee ;Miwa Geiger ;Leslie Dunnington ;Jacqueline Isaac ;Louise Wilkins-Haug ;Lindsey Hunter ;Claudia Izzi ;Marika Toscano ;Tullio Ghi ;Julie McGlynn ;Francesca Romana Grati ;Beverly S. Emanuel ;Kimberly Gaiser ;J. William Gaynor ;Elizabeth Goldmuntz ;Daniel E. McGinn ;Erica Schindewolf ;Oanh Tran ;Elaine H. Zackai ;Qi Yan ;Anne S. Bassett ;Ronald WapnerDonna M. McDonald-McGinnScopus© Citations 2 22 -
PublicationUpdated clinical practice recommendations for managing children with 22q11.2 deletion syndrome( 2023)
;Sólveig Óskarsdóttir ;Erik Boot ;Terrence Blaine Crowley ;Joanne C.Y. Loo ;Jill M. Arganbright ;Marco Armando ;Adriane L. Baylis ;Elemi J. Breetvelt ;René M. Castelein ;Madeline Chadehumbe ;Christopher M. Cielo ;Steven de Reuver ;Stephan Eliez ;Ania M. Fiksinski ;Brian J. Forbes ;Emily Gallagher ;Sarah E. Hopkins ;Oksana A. Jackson ;Lorraine Levitz-Katz ;Gunilla Klingberg ;Michele P. Lambert ;Bruno Marino ;Maria R. Mascarenhas ;Julie Moldenhauer ;Edward M. Moss ;Beata Anna Nowakowska ;Ani Orchanian-Cheff ;Carolina Putotto ;Erica Schindewolf ;Maude Schneider ;Cynthia B. Solot ;Kathleen E. Sullivan ;Ann Swillen ;Marta Unolt ;Jason P. Van Batavia ;Claudia Vingerhoets ;Jacob Vorstman ;Anne S. BassettDonna M. McDonald-McGinnScopus© Citations 5 5 -
PublicationDeletion size analysis of 1680 22q11.2DS subjects identifies a new recombination hotspot on chromosome 22q11.2( 2018)
;Tingwei Guo ;Alexander Diacou ;Hiroko Nomaru ;Donna M McDonald-McGinn ;Matthew Hestand ;Wolfram Demaerel ;Liangtian Zhang ;Yingjie Zhao ;Francisco Ujueta ;Jidong Shan ;Cristina Montagna ;Deyou Zheng ;Terrence B Crowley ;Leila Kushan-Wells ;Carrie E Bearden ;Wendy R Kates ;Doron Gothelf ;Maude Schneider ;Stephan Eliez ;Jeroen Breckpot ;Ann Swillen ;Jacob Vorstman ;Elaine Zackai ;Beverly S Emanuel ;Anne S Bassett ;Joris R Vermeesch ;Christian R MarshallBernice E MorrowScopus© Citations 16 15 -
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