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 74
-
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. -
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 -
Publication
4 -
Publication
Scopus© Citations 5 2 -
PublicationSociodemographic risk factors of hantavirus cardiopulmonary syndrome ^[Factores de riesgo socio-demográficos del síndrome]( 2019)
;Francisca Valdivieso R. ;Analía Cuiza V. ;Iris Delgado B. ;Grazielle Ribeiro E. ;Elena Llop R. ;Marcela Ferrés G. ;Raúl Riquelme O. ;M. Luisa Rioseco Z. ;Mario Calvo A. ;Gregory MertzScopus© Citations 4 25 -
PublicationChromosomal microarrays testing in children with developmental disabilities and congenital anomalies( 2015)
;GUILLERMO ROBERTO LAY SON RODRIGUEZ ;Karena Espinoza ;Juan C. Rivera ;María L. GuzmánScopus© Citations 13 18 -
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 -
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 8 -
PublicationCleft Palate, Interdisciplinary Diagnosis, and Treatment( 2015)
;Pablo Antonio Ysunza ;Maria Carmen PamplonaScopus© Citations 5 10 -
PublicationCystic fibrosis in Chilean patients: Analysis of 36 common CFTR gene mutations( 2011)
;Guillermo Lay-Son ;Alonso Puga ;Pedro AstudilloScopus© Citations 19 3