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Vera Lúcia Gil-da-silva-Lopes
Vera Lúcia Gil-da-silva-Lopes
Livre Docente em Genética Clínica na Universidade Estadual de Campinas
Verified email at fcm.unicamp.br
Title
Cited by
Cited by
Year
Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)
M Zenker, J Mayerle, MM Lerch, A Tagariello, K Zerres, PR Durie, M Beier, ...
Nature genetics 37 (12), 1345-1350, 2005
2942005
Recessive and dominant de novo ITPR1 mutations cause Gillespie syndrome
S Gerber, KJ Alzayady, L Burglen, D Brémond-Gignac, V Marchesin, ...
The American Journal of Human Genetics 98 (5), 971-980, 2016
1482016
22q11. 2 deletion syndrome in diverse populations
P Kruszka, YA Addissie, DE McGinn, AR Porras, E Biggs, M Share, ...
American Journal of Medical Genetics Part A 173 (4), 879-888, 2017
1392017
Anomalias craniofaciais: descrição e avaliação das características gerais da atenção no Sistema Único de Saúde
IL Monlleó, VL Gil-da-Silva-Lopes
Cadernos de saúde pública 22, 913-922, 2006
113*2006
Neonatal care of infants with cleft lip and/or palate: feeding orientation and evolution of weight gain in a nonspecialized Brazilian hospital
LG Amstalden-Mendes, LA Magna, VL Gil-da-Silva-Lopes
The Cleft palate-craniofacial journal 44 (3), 329-334, 2007
932007
Defining new guidelines for screening the 22q11. 2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature
FP Monteiro, TP Vieira, IC Sgardioli, MC Molck, AP Damiano, J Souza, ...
European journal of pediatrics 172, 927-945, 2013
842013
Planning the human variome project: the Spain report
J Kaput, RGH Cotton, L Hardman, M Watson, AI Al Aqeel, JY Al‐Aama, ...
Human mutation 30 (4), 496-510, 2009
652009
A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population
TK de Araujo, R Secolin, TM Félix, LT De Souza, MÍB Fontes, IL Monlleó, ...
Journal of Cranio-Maxillofacial Surgery 44 (1), 16-20, 2016
602016
DLX4 is associated with orofacial clefting and abnormal jaw development
D Wu, S Mandal, A Choi, A Anderson, M Prochazkova, H Perry, ...
Human molecular genetics 24 (15), 4340-4352, 2015
512015
Risk factors and the prevention of oral clefts
VL Gil-da-Silva-Lopes, IL Monlleó
Brazilian oral research 28, 1-5, 2014
472014
Variants in members of the cadherin–catenin complex, CDH1 and CTNND1, cause blepharocheilodontic syndrome
A Kievit, F Tessadori, H Douben, I Jordens, M Maurice, J Hoogeboom, ...
European journal of human genetics 26 (2), 210-219, 2018
432018
Temporomandibular ganglion or synovial cyst?: A case report and literature review
V Lopes, JAH Jones, P Sloan, L McWilliam
Oral surgery, oral medicine, oral pathology 77 (6), 627-630, 1994
421994
Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation
M Simioni, TK Araujo, IL Monlleo, CV Maurer-Morelli, ...
Journal of human genetics 60 (1), 17-25, 2015
412015
Feeding infants with cleft lip and/or palate in Brazil: suggestions to improve health policy and research
VL Gil-da-Silva-Lopes, AC Xavier, D Klein-Antunes, ACRG Ferreira, ...
The Cleft Palate-Craniofacial Journal 50 (5), 577-590, 2013
382013
Genomic imbalances in syndromic congenital heart disease,
MC Molck, M Simioni, TP Vieira, IC Sgardioli, FP Monteiro, J Souza, ...
Jornal de pediatria 93, 497-507, 2017
322017
Diagnostic implications of associated defects in patients with typical orofacial clefts
IL Monlleó, AGR Barros, MIB Fontes, AKM Andrade, GM Brito, ...
Jornal de pediatria 91 (5), 485-492, 2015
322015
Distal deletion at 22q11. 2 as differential diagnosis in craniofacial microsomia: case report and literature review
S Spineli-Silva, LM Bispo, VL Gil-da-Silva-Lopes, TP Vieira
European journal of medical genetics 61 (5), 262-268, 2018
302018
Fenda de lábio e ou palato: recursos para alimentação antes da correção cirúrgica
LG Amstalden-Mendes, VL Gil-da-Silva-Lopes
Revista de Ciências Médicas 15 (5), 2006
292006
Q289P mutation in FGFR2 gene causes Saethre-Chotzen syndrome: some considerations about familial heterogeneity
ECLB de Freitas, SRD Nascimento, MP de Mello, VL Gil-da-Silva-Lopes
The Cleft palate-craniofacial journal 43 (2), 142-147, 2006
282006
Preliminary analysis of the nonsynonymous polymorphism rs17563 in BMP4 gene in Brazilian population suggests protection for nonsyndromic cleft lip and palate
TK Araujo, M Simioni, TM Félix, LT de Souza, MÍB Fontes, IL Monlleo, ...
Plastic Surgery International 2012, 2012
262012
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