Personal information

Activities

Works (43)

Whole exome sequencing in 18 Brazilian families with vertical transmission of non-syndromic oral clefts

Journal of Cranio-Maxillofacial Surgery
2024-12 | Journal article
Contributors: Matheus de Mello Copelli; Milena Atique-Tacla; Eleonore Pairet; Gabriela Roldão Correia-Costa; Tiago Henrique de Souza; Isabella Lopes Monlleó; Társis Paiva Vieira; Raphaël Helaers; Miikka Vikkula; Vera Lúcia Gil-da-Silva-Lopes
Source: check_circle
Crossref

Access to genetic evaluation of 1463 individuals with orofacial cleft in Brazil

Jornal de Pediatria
2024-11 | Journal article
Contributors: Isabela Mayá Wayhs Silva; Milena Atique Tacla; Erlane Marques Ribeiro; Elaine Lustosa-Mendes; Agnes Cristina Fett-Conte; Têmis Maria Félix; Ana Carolina Xavier; Isabella Lopes Monlleó; Vera Lúcia Gil-da-Silva-Lopes
Source: check_circle
Crossref

22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity

Genes
2024-04 | Journal article | Author
Contributors: Melissa Wallau; Ana Carolina Xavier; Carolina Araújo Moreno; Chong Kim; Elaine Lustosa Mendes; Erlane Marques Ribeiro; Amanda Oliveira; Têmis Maria Félix; Agnes Cristina Fett-Conte; Luciana Cardoso Bonadia et al.
Source: check_circle
Multidisciplinary Digital Publishing Institute

Craniofacial microsomia: Reflections on diagnosis and severity assessment based on a series of cases

Congenital Anomalies
2021-09 | Journal article
Contributors: Luna Lira Bergamini; Samira Spineli‐Silva; Têmis Maria Félix; Vera L. Gil‐da‐Silva‐Lopes; Tarsis P. Vieira; Erlane Marques Ribeiro; Ana Carolina Xavier; Elaine Lustosa‐Mendes; Marshall Ítalo Barros Fontes; Isabella L. Monlleó
Source: check_circle
Crossref

Prevalência de cárie e fatores relacionados em pacientes com fibrose cística

Research, Society and Development
2021-07-19 | Journal article
Part of ISSN: 2525-3409
Source: Self-asserted source
Isabella Monlleó

Brazil's Craniofacial Project: Different approaches on orofacial clefts and 22q11.2 deletion syndrome

American Journal of Medical Genetics Part C: Seminars in Medical Genetics
2020-10-28 | Journal article
Part of ISSN: 1552-4868
Part of ISSN: 1552-4876
Source: Self-asserted source
Isabella Monlleó

Identification of genomic imbalances in oral clefts

Jornal de Pediatria
2020-07-01 | Journal article
Part of ISSN: 0021-7557
Source: Self-asserted source
Isabella Monlleó

An invincible memory: what surname analysis tells us about history, health and population medical genetics in the Brazilian Northeast

Journal of Biosocial Science
2020-03-16 | Journal article
Part of ISSN: 0021-9320
Part of ISSN: 1469-7599
Source: Self-asserted source
Isabella Monlleó

Syndromic Oral Clefts: Challenges of Genetic Assessment in Brazil and Suggestions to Improve Health Policies

Public Health Genomics
2019-07-07 | Journal article
Part of ISSN: 1662-4246
Part of ISSN: 1662-8063
Source: Self-asserted source
Isabella Monlleó

CranFlow : An Application for Record-Taking and Management Through the Brazilian Database on Craniofacial Anomalies

Birth Defects Research
2018-01-15 | Journal article
Part of ISSN: 2472-1727
Source: Self-asserted source
Isabella Monlleó

Functional characterization of five NR5A1 gene mutations found in patients with 46,XY disorders of sex development

Human Mutation
2018-01-10 | Journal article
Part of ISSN: 1059-7794
Source: Self-asserted source
Isabella Monlleó

Genomic imbalances in syndromic congenital heart disease

Jornal de Pediatria
2017-09 | Journal article
Part of ISSN: 0021-7557
Source: Self-asserted source
Isabella Monlleó

Genomic Investigation of Balanced Chromosomal Rearrangements in Patients with Abnormal Phenotypes

Source: Self-asserted source
Isabella Monlleó

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population

Journal of Cranio-Maxillo-Facial Surgery
2015 | Journal article
Source: Self-asserted source
Isabella Monlleó

Diagnostic implications of associated defects in patients with typical orofacial clefts

Jornal de Pediatria
2015 | Journal article
Source: Self-asserted source
Isabella Monlleó

Perfil de pacientes com anormalidades geniturinárias atendidos em serviço de genética clínica no sistema único de saúde

Revista Paulista de Pediatria
2015 | Journal article
Source: Self-asserted source
Isabella Monlleó

Clinical Features in Patients With 22q11. 2 Deletion Syndrome Ascertained by Palatal Abnormalities

The Cleft Palate-Craniofacial Journal
2014 | Journal article
WOSUID:

WOS:000357696000009

Contributors: Vieira, T\'arsis P; Monteiro, Fab\'\\iola P; Sgardioli, Il\'aria C; Souza, Josiane; Fett-Conte, Agnes C; Monlle\'o, Isabella L; Fontes, Marshall B; F\'elix, T\^emis M; Leal, Gabriela F; Ribeiro, Erlane Marques et al.
Source: Self-asserted source
Isabella Monlleó via ResearcherID

Investigation of genetic factors underlying typical orofacial clefts: mutational screening and copy number variation

Journal of human genetics
2014 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Mucopolysaccharidosis type II: Identification of 30 novel mutations among Latin American patients

Molecular genetics and metabolism
2014 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Ocular and craniofacial phenotypes in a large Brazilian family with congenital aniridia

Clinical genetics
2014 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Risk factors and the prevention of oral clefts

Brazilian oral research
2014 | Journal article
Contributors: Gil-da-Silva-Lopes, Vera Lucia; Monlleo, Isabella Lopes
Source: Self-asserted source
Isabella Monlleó via ResearcherID

Family care practitioners experience with individuals with orofacial clefts in Brazil

Cadernos Saúde Coletiva
2013 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Implementing the Brazilian Database on Orofacial Clefts

Plastic surgery international
2013 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Defining new guidelines for screening the 22q11. 2 deletion based on a clinical and dysmorphologic evaluation of 194 individuals and review of the literature

European journal of pediatrics
2013-02-26 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Preliminary analysis of the nonsynonymous polymorphism rs17563 in bmp4 gene in brazilian population suggests protection for nonsyndromic cleft lip and palate

Plastic surgery international
2012 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Prevalence of genital abnormalities in neonates

Jornal de pediatria
2012 | Journal article
Source: Self-asserted source
Isabella Monlleó

Clinical and molecular spectrum of patients with 17β-hydroxysteroid dehydrogenase type 3 (17-β-HSD3) deficiency

Arquivos Brasileiros de Endocrinologia & Metabologia
2012-11 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Local Strategies to Address Health Needs of Individuals with Orofacial Clefts in Alagoas, Brazil

2012-01-11 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Adequação da demanda de crianças e adolescentes atendidos na Unidade de Emergencia em Maceió, Alagoas, Brasil

Rev. bras. saúde matern. infant
2010 | Journal article
Source: Self-asserted source
Isabella Monlleó

Evaluation of Craniofacial Care Outside The Brazilian Reference Network for Craniofacial Treatment

2009-03 | Journal article
Contributors: Isabella Monlleó
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Aten\c{c}ao a pessoas com anomalias craniofaciais no Brasil: avalia\c{c}ao e propostas para o Sistema Unico de Sa\'ude

2008 | Other
SOURCE-WORK-ID:

070616183993-26

Contributors: Monlleo, Isabella Lopes
Source: Self-asserted source
Isabella Monlleó via ResearcherID

A clinical study of 77 patients with mucopolysaccharidosis type II

Acta Paediatrica
2007-03-23 | Journal article
Contributors: Isabella Monlleó
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Brazil's Craniofacial Project: genetic evaluation and counseling in the Reference Network for Craniofacial Treatment

The Cleft palate-craniofacial journal
2006 | Journal article
Source: Self-asserted source
Isabella Monlleó

Craniofacial anomalies: description and evaluation of treatment under the Brazilian Unified Health System

Cadernos de Saúde Pública
2006 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Mucopolysaccharidosis type II: a clinical study of 77 Brazilian patients

Acta Paediatrica
2006 | Journal article
WOSUID:

WOS:000237456700027

Contributors: Schwartz, I; Ribeiro, M; Mota, J; Toralles, M; Correia, P; Horovitz, D; Santos, E; Monlleo, I; Fett-Conte, A; Oliveira, R et al.
Source: Self-asserted source
Isabella Monlleó via ResearcherID

Similar interstitial deletions of the KAL-1 gene in two Brazilian families with X-linked Kallmann Syndrome

Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

Craniofacial Brazil Project: preliminary results of a long term health program.

American Journal of Human Genetics
2003 | Journal article
WOSUID:

WOS:000185599701453

Contributors: Monlleo, IL; Lopes, VLGS
Source: Self-asserted source
Isabella Monlleó via ResearcherID

Blomstrand chondrodysplasia: a lethal sclerosing skeletal dysplasia

1999-10-25 | Journal article
Source: Self-asserted source
Isabella Monlleó
grade
Preferred source (of 2)‎

17p13.3 Microdeletion: Insights on Genotype-Phenotype Correlation

Source: Self-asserted source
Isabella Monlleó

A Cytogenomic Approach in a Case of Syndromic XY Gonadal Dysgenesis

Sexual Development
Journal article
Source: Self-asserted source
Isabella Monlleó

ANOMALIAS CRANIOFACIAIS, GEN\'ETICA E SA\'UDE

Other
SOURCE-WORK-ID:

070616183995-11

Contributors: MONLLE\'O, ISABELLA LOPES
Source: Self-asserted source
Isabella Monlleó via ResearcherID
grade
Preferred source (of 2)‎

Genotype-phenotype correlation of 16p13.3 terminal duplication and 22q13.33 deletion: Natural history of a patient and review of the literatur

Source: Self-asserted source
Isabella Monlleó

Study of IRF6 and 8q24 region in non-syndromic oral clefts in the Brazilian population

Oral diseases
Journal article
Source: Self-asserted source
Isabella Monlleó