Iêda M. Orioli

Universidade Federal do Rio de Janeiro — Brazil

Biochemistry, Genetics and Molecular Biology · Life Sciences

34h-index4.5kcitations103works0.02yr avg
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Research Topics

Cleft Lip and Palate Research(57), Craniofacial Disorders and Treatments(36), Congenital Anomalies and Fetal Surgery(18), dental development and anomalies(15), Folate and B Vitamins Research(12)

Publications102 total

Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk
PLoS Genetics·2025Open Access
Variants in <i>CALD1</i> , <i>ESRP1</i> , and <i>RBFOX1</i> are associated with orofacial cleft risk
2025Open Access
The burden, prevention and care of infants and children with congenital anomalies in sub-Saharan Africa: A scoping review
PLOS Global Public Health·2023· 11 citedOpen Access
Mothers of children with Down syndrome: a clinical and epidemiological study
Journal of Community Genetics·2022· 11 citedOpen Access
A large, ten‐generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studies
American Journal of Medical Genetics Part A·2022· 3 cited
Dental anomaly detection using intraoral photos via deep learning
Scientific Reports·2022· 28 citedOpen Access
Tooth Agenesis Patterns in Orofacial Clefting Using Tooth Agenesis Code: A Meta-Analysis
Dentistry Journal·2022· 2 citedOpen Access
Genome‐wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes
Genetic Epidemiology·2022· 12 citedOpen Access
Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort
Frontiers in Dental Medicine·2022· 16 citedOpen Access
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts
Human Heredity·2022· 6 citedOpen Access
Differential expression of the IRF6 gene in the signs of Van der Woude Syndrome: Are distinct genetic modifiers operating?
Dentistry 3000·2021Open Access
Prevalence of microcephaly: the Latin American Network of Congenital Malformations 2010–2017
BMJ Paediatrics Open·2021· 8 citedOpen Access
The legacy of ZikaPLAN: a transnational research consortium addressing Zika
Global Health Action·2021· 12 citedOpen Access
Genome-wide association study of multiethnic non-syndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes
2021· 2 citedOpen Access
Genome-Wide Association Study (GWAS) of dental caries in diverse populations
BMC Oral Health·2021· 39 citedOpen Access
Global birth defects app: An innovative tool for describing and coding congenital anomalies at birth in low resource settings
Birth Defects Research·2021· 17 citedOpen Access
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions
Frontiers in Cell and Developmental Biology·2021· 31 citedOpen Access
New &lt;b&gt;&lt;i&gt;SHH&lt;/i&gt;&lt;/b&gt; and Known &lt;b&gt;&lt;i&gt;SIX3&lt;/i&gt;&lt;/b&gt; Variants in a Series of Latin American Patients with Holoprosencephaly
Molecular Syndromology·2021· 2 citedOpen Access
Use of infectious disease surveillance reports to monitor the Zika virus epidemic in Latin America and the Caribbean from 2015 to 2017: strengths and deficiencies
BMJ Open·2020· 15 citedOpen Access
The Latin American network for congenital malformation surveillance: <scp>ReLAMC</scp>
American Journal of Medical Genetics Part C Seminars in Medical Genetics·2020· 30 citedOpen Access
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Frequent Co-authors

Eduardo E. Castilla(39), Alexandre R. Vieira(22), Mary L. Marazita(19), Jorge S. López‐Camelo(16), Jeffrey C. Murray(11), Fernando A. Poletta(10), Jacqueline T. Hecht(9), George L. Wehby(8), Margaret E. Cooper(7), Kaare Christensen(7), Carmencita D. Padilla(7), Carmen J. Buxó(7), Seth M. Weinberg(7), José Mauro Granjeiro(7), Lina M. Moreno(6), John R. Shaffer(6), Ariadne Letra(6), Elizabeth J. Leslie(5), Eleanor Feingold(5), Frederic W.‐B. Deleyiannis(5)