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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 98
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PublicationNistagmo secundario a albinismo con compromiso ocular en paciente femenina( 2020)
;Luisa Schonhaut B. ;Joanna Britzmann L. ;Mario Zanolli S. ;Jovanka Pavlov N. ;Trinidad Hasbun Z. -
PublicationAbnormal nodal and global network organization in resting state functional MRI from subjects with the 22q11 deletion syndrome( 2021)
;Teuntje A. D. Pelgrim ;Matthijs G. Bossong ;Analía Cuiza ;Luz María Alliende ;Carlos Mena ;Angeles Tepper ;Juan Pablo Ramirez-Mahaluf ;Barbara Iruretagoyena ;Claudia Ornstein ;Rosemarie Fritsch ;Juan Pablo Cruz ;Cristian TejosNicolas CrossleyScopus© Citations 2 1 -
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 -
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 -
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 -
PublicationPalate abnormalities in Chilean patients with chromosome 22q11 microdeletion syndrome( 2012)
;Guillermo Lay-Son ;Mirta Palomares ;M. Luisa Guzman ;Marcos Vasquez ;Alonso PugaScopus© Citations 10 2 -
PublicationClinical, neuroimaging, and molecular spectrum of TECPR2 ‐associated hereditary sensory and autonomic neuropathy with intellectual disability( 2021)
;Sonja Neuser ;Barbara Brechmann ;Gali Heimer ;Ines Brösse ;Susanna Schubert ;Lauren O'Grady ;Michael Zech ;Siddharth Srivastava ;David A. Sweetser ;Yasemin Dincer ;Volker Mall ;Juliane Winkelmann ;Christian Behrends ;Basil T. Darras ;Robert J. Graham ;Parul Jayakar ;Barry Byrne ;Bat El Bar‐Aluma ;Yael Haberman ;Amir Szeinberg ;Hesham M. Aldhalaan ;Mais Hashem ;Amal Al Tenaiji ;Omar Ismayl ;Asma E. Al Nuaimi ;Karima Maher ;Shahnaz Ibrahim ;Fatima Khan ;Henry Houlden ;Vijayalakshmi S. Ramakumaran ;Alistair T. Pagnamenta ;Jennifer E. Posey ;James R. Lupski ;Wen‐Hann Tan ;Gehad ElGhazali ;Isabella Herman ;Tatiana Muñoz ;Angelika Seitz ;Mandy Krumbiegel ;Usha Kini ;Stephanie Efthymiou ;Jens Meiler ;Reza Maroofian ;Fowzan S. Alkuraya ;Rami Abou Jamra ;Bernt Popp ;Bruria Ben‐ZeevDarius Ebrahimi‐FakhariScopus© Citations 15 25 -
PublicationA neurogenetic model for the study of schizophrenia spectrum disorders: the International 22q11.2 Deletion Syndrome Brain Behavior Consortium( 2017)
;R E Gur ;A S Bassett ;D M McDonald-McGinn ;C E Bearden ;E Chow ;B S Emanuel ;M Owen ;A Swillen ;M Van den Bree ;J Vermeesch ;J A S Vorstman ;S Warren ;T Lehner ;B Morrow14 -
PublicationVEGFA polymorphisms and cardiovascular anomalies in 22q11 microdeletion syndrome: a case-control and family-based study( 2009)
;ALONSO R PUGA ;M. LUISA GUZMÁN ;CARMEN PAZ ASTETE ;MARTA ARRIAZA ;MARIANA ARACENA ;TERESA ARAVENA ;PATRICIA SANZScopus© Citations 6