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CALDERON GIADROSIC, JUAN FRANCISCO
Preferred name
CALDERON GIADROSIC, JUAN FRANCISCO
Main Affiliation
Email
juancalderon@udd.cl
ORCID
Scopus Author ID
57190044311
Now showing
1 - 10 of 18
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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 -
ProductDataset - ICTD-Seq: Exome sequencing of patients with Inheritable Connective Tissue Disorders(National Library of Medicine, 2022)
;YANIRETH JIMENEZ ;OSCAR CUEVAS HERREROS ;MARCELO ALEXIS ROJAS HERRERA28 -
PublicationCervical Artery Dissection in Postpartum Women after Cesarean and Vaginal Delivery( 2022)
;Francisca Urrutia ;Tomas Bernstein ;Paulo ZuñigaScopus© Citations 3 7 -
PublicationLineage-specific events underlie aortic root aneurysm pathogenesis in Loeys-Dietz syndrome( 2019)
;Elena Gallo MacFarlane ;Sarah J. Parker ;Joseph Y. Shin ;Shira G. Ziegler ;Tyler J. Creamer ;Rustam Bagirzadeh ;Djahida Bedja ;Yichun Chen ;Katherine Weissler ;Pamela A. Frischmeyer-Guerrerio ;Mark E. Lindsay ;Jennifer P. HabashiHarry C. DietzScopus© Citations 71 35 -
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Scopus© Citations 12 42 -
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Scopus© Citations 15 3 -
PublicationExome Sequencing Identifies Genetic Variants Associated with Extreme Manifestations of the Cardiovascular Phenotype in Marfan Syndrome( 2022)
;Yanireth Jimenez ;Cesar Paulsen ;Eduardo Turner ;Sebastian Iturra ;Oscar Cuevas ;Guillermo Lay-son ;Marcelo RojasScopus© Citations 1 37 -
PublicationIdentification of genetic modifiers of murine hepatic β-glucocerebrosidase activity( 2021)
;Anyelo Durán ;Boris Rebolledo-Jaramillo ;Valeria Olguin ;Marcelo Rojas-Herrera ;Macarena Las Heras ;Silvana Zanlungo ;David A. Priestman ;Frances M. PlattScopus© Citations 5 19 -
PublicationCurrent Controversies in Diagnosis and Management of Cleft Palate and Velopharyngeal Insufficiency( 2015)
;Pablo Antonio Ysunza ;Maria Carmen Pamplona ;Kenneth Shaheen ;Konkgrit ChaiyasateMatthew RontalScopus© Citations 23 8 -
PublicationClinical features of chromosome 22q11.2 microdeletion syndrome in 208 Chilean patients( 2009)
;Guzmán, María Luisa ;Puga, Alonso R. ;Astete A., Carmen Paz ;Aracena, Mariana I. ;Arriaza, Marta I. ;Aravena, TeresaSanz, PatriciaScopus© Citations 24 6