Ieda Maria Orioli

Instituição:

Universidade Federal do Rio de Janeiro

Centro:

Centro de Ciências da Saúde

Unidade:

Instituto de Biologia

Departamento:

Departamento de Genética/IB

ORCID:

não disponível no Lattes


Formação:

  • Children's Hospital Of Philadelphia

    | Pós-Doutorado | 1999 - 2000

  • Sociedade Brasileira de Genética Clínica

    Especialista Em Genética Médica | Especialização | 1997 - 1997

  • Universidade de São Paulo

    Ciências Biológicas (Genética) | Doutorado | 1973 - 1976

  • Universidade de São Paulo

    Instituto de Biociências | Mestrado | 1970 - 1973

  • Universidade Federal Fluminense

    Medicina | Graduação | 1964 - 1969
Laboratórios:
Nuvens de Palavras:
Artigos:

(57.45% artigos com DOI)

Titulo DOI Ano
A large, ten-generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studies 10.1002/ajmg.a.62994 2023
The burden, prevention and care of infants and children with congenital anomalies in sub-Saharan Africa: A scoping review 10.1371/journal.pgph.0001850 2023
Genome-wide association study of multiethnic nonsyndromic orofacial cleft families identifies novel loci specific to family and phenotypic subtypes 10.1002/gepi.22447 2022
Genetic Analyses of Enamel Hypoplasia in Multiethnic Cohorts 10.1159/000522642 2022
Mothers of children with Down syndrome: a clinical and epidemiological study 10.1007/s12687-022-00627-7 2022
Dental anomaly detection using intraoral photos via deep learning 10.1038/s41598-022-15788-1 2022
Multivariate GWAS of Structural Dental Anomalies and Dental Caries in a Multi-Ethnic Cohort 10.3389/fdmed.2021.771116 2022
Author Correction: Dental anomaly detection using intraoral photos via deep learning 10.1038/s41598-022-17668-0 2022
Tooth Agenesis Patterns in Orofacial Clefting Using Tooth Agenesis Code: A Meta-Analysis 10.3390/dj10070128 2022
Global birth defects app: An innovative tool for describing and coding congenital anomalies at birth in low resource settings 10.1002/bdr2.1898 2021
Genome-Wide Association Study (GWAS) of dental caries in diverse populations 10.1186/s12903-021-01670-5 2021
Genome-Wide Association Study of Non-syndromic Orofacial Clefts in a Multiethnic Sample of Families and Controls Identifies Novel Regions 10.3389/fcell.2021.621482 2021
Prevalence of microcephaly: the Latin American Network of Congenital Malformations 2010-2017 10.1136/bmjpo-2021-001235 2021
The legacy of ZikaPLAN: a transnational research consortium addressing Zika 10.1080/16549716.2021.2008139 2021
New SHH and Known SIX3 Variants in a Series of Latin American Patients with Holoprosencephaly 10.1159/000515044 2021
Differential expression of the IRF6 gene in the signs of Van der Woude Syndrome: Are distinct genetic modifiers operating? 10.5195/d3000.2021.164 2021
Individuals with nonsyndromic orofacial clefts have increased asymmetry of fingerprint patterns 10.1371/journal.pone.0230534 2020
The Latin American network for congenital malformation surveillance: ReLAMC 10.1002/ajmg.c.31872 2020
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 10.1136/bmjopen-2020-042869 2020
Association of low-frequency genetic variants in regulatory regions with nonsyndromic orofacial clefts 10.1002/ajmg.a.61002 2019
A systematic genetic analysis and visualization of phenotypic heterogeneity among orofacial cleft GWAS signals 10.1002/gepi.22214 2019
ZikaPLAN: addressing the knowledge gaps and working towards a research preparedness network in the Americas 10.1080/16549716.2019.1666566 2019
ICD-10 impact on ascertainment and accuracy of oral cleft cases as recorded by the Brazilian national live birth information system 10.1002/ajmg.a.38634 2018
PVR/CD155 Ala67Thr Mutation and Cleft Lip/Palate 10.1097/SCS.0000000000004159 2018
Third molar agenesis as a potential marker for craniofacial deformities 10.1016/j.archoralbio.2018.01.010 2018
Genome-wide interaction studies identify sex-specific risk alleles for nonsyndromic orofacial clefts 10.1002/gepi.22158 2018
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate 10.1007/s00439-016-1754-7 2017
Association studies of low-frequency coding variants in nonsyndromic cleft lip with or without cleft palate 10.1002/ajmg.a.38210 2017
Identification of 16q21 as a modifier of nonsyndromic orofacial cleft phenotypes 10.1002/gepi.22090 2017
Prevalence and clinical profile of microcephaly in South America pre-Zika, 2005-14: prevalence and case-control study 10.1136/bmj.j5018 2017
Analysis of the genetic ancestry of patients with oral clefts from South American admixed populations 10.1111/eos.12275 2016
A multi-ethnic genome-wide association study identifies novel loci for non-syndromic cleft lip with or without cleft palate on 2p24.2, 17q23 and 19q13 10.1093/hmg/ddw104 2016
A Genome-wide Association Study of Nonsyndromic Cleft Palate Identifies an Etiologic Missense Variant in GRHL3 10.1016/j.ajhg.2016.02.014 2016
Uniparental ancestry markers in Chilean populations 10.1590/1678-4685-GMB-2015-0273 2016
Family-based genome-wide association study in Patagonia confirms the association of the DMD locus and cleft lip and palate 10.1111/eos.12212 2015
Aquaporin 5 Interacts with Fluoride and Possibly Protects against Caries 10.1371/journal.pone.0143068 2015
Rare nasal cleft in a patient with holoprosencephaly due to a mutation in the ZIC2 gene 10.1002/bdra.23216 2014
Role of estrogen related receptor beta (ESRRB) in DFN35B hearing impairment and dental decay 10.1186/1471-2350-15-81 2014
Molecular analysis of holoprosencephaly in South America 10.1590/s1415-47572014000200011 2014
Genealogical data in population medical genetics: field guidelines 10.1590/S1415-47572014000200004 2014
Fine-Mapping of 5q12.1?13.3 Unveils New Genetic Contributors to Caries 10.1159/000346278 2013
Association of methylenetetrahydrofolate reductase gene 677C > T polymorphism and Down syndrome 10.1007/s11033-012-2270-z 2013
Role of TRAV locus in low caries experience 10.1007/s00439-013-1313-4 2013
Genetic mapping of high caries experience on human chromosome 13 10.1186/1471-2350-14-116 2013
Clinical epidemiology of skeletal dysplasias in South America 10.1002/ajmg.a.35246 2012
Association of AXIN2 with Non-syndromic Oral Clefts in Multiple Populations 10.1177/0022034512440578 2012
Interaction between IRF6 and TGFA Genes Contribute to the Risk of Nonsyndromic Cleft Lip/Palate 10.1371/journal.pone.0045441 2012
The effect of systematic pediatric care on neonatal mortality and hospitalizations of infants born with oral clefts 10.1186/1471-2431-11-121 2011
Women Are More Susceptible to Caries but Individuals Born with Clefts Are Not 10.1155/2011/454532 2011
Effects of folic acid fortification on spina bifida prevalence in Brazil 10.1002/bdra.20830 2011
Cyclopia: An epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research 10.1002/ajmg.c.30323 2011
Sirenomelia: An epidemiologic study in a large dataset from the International Clearinghouse of Birth Defects Surveillance and Research, and literature review 10.1002/ajmg.c.30324 2011
Prenatal Diagnosis of Skeletal Dysplasias: Contribution of Three-Dimensional Computed Tomography 10.1159/000322212 2011
CRISPLD2 Variants Including a C471T Silent Mutation May Contribute to Nonsyndromic Cleft Lip With or Without Cleft Palate 10.1597/09-227 2011
Detection of Streptococcus mutans Genomic DNA in Human DNA Samples Extracted from Saliva and Blood 10.5402/2011/543561 2011
Sentinel phenotype for rubella embryopathy: time-space distribution in Brazil. 2011
Epidemiology of holoprosencephaly: Prevalence and risk factors 10.1002/ajmg.c.30233 2010
Follow-up association studies of chromosome region 9q and nonsyndromic cleft lip/palate 10.1002/ajmg.a.33482 2010
Folic acid flour fortification: Impact on the frequencies of 52 congenital anomaly types in three South American countries 10.1002/ajmg.a.33479 2010
Síndrome do incisivo central superior mediano: relato de caso 2010
Novel Cleft Susceptibility Genes in Chromosome 6q 10.1177/0022034510370004 2010
Clusters of sirenomelia in South America 10.1002/bdra.20492 2009
Letter to the Editor 10.1597/07-235.1 2009
Second case of Beare-Stevenson syndrome with anFGFR2 Ser372Cys mutation 10.1002/ajmg.a.32176 2008
No association of the polyhistidine tract polymorphism of ZIC2 gene with neural tube defects in a South American (ECLAMC) population 2008
Beare-Stevenson cutis gyrata syndrome: A new case of a c.1124C-G (Y375C) mutation in the FGFR2 gene 10.3892/mmr_00000024 2008
Gastroschisis: International epidemiology and public health perspectives 10.1002/ajmg.c.30181 2008
Frequency of holoprosencephaly in the International Clearinghouse Birth Defects Surveillance Systems: Searching for population variations 10.1002/bdra.20479 2008
Reduced folate carrier 1 (RFC1) is associated with cleft of the lip only. 2008
Sirenomelia and cyclopia cluster in Cali, Colombia 10.1002/ajmg.a.32506 2008
MTHFR 677C→T And 1298A→C POLYMORPHISMS IN CHILDREN WITH DOWN SYNDROME AND ACUTE MYELOID LEUKEMIA IN BRAZIL 10.1080/08880010802435104 2008
Functional analysis of mutations in TGIF associated with holoprosencephaly 2007
Single median maxillary central incisor: New data and mutation review 10.1002/bdra.20380 2007
Non-Latin European descent could be a requirement for association of NTDs andMTHFR variant 677C->-T: A meta-analysis 10.1002/ajmg.a.31812 2007
Interferon regulatory factor 6 (IRF6) is associated with oral-facial cleft in individuals that originate in South America 10.1002/ajmg.a.31884 2007
Clinical epidemiologic study of holoprosencephaly in South America 10.1002/ajmg.a.32104 2007
Regional analysis on the occurrence of oral clefts in South America 10.1002/ajmg.a.32076 2007
Genetic evidence for the role of loci at 19q13 in cleft and palate 2006
Intrauterine growth restriction in like-sex twins discordant for structural defects 2006
PVRL1 variants contribute to non-syndromic cleft lip and palate in multiple populations 10.1002/ajmg.a.31367 2006
Studies of reduced folate carrier 1 (RFC1) A80G and 5,10-methylenetetrahydrofolate reductase (MTHFR) C677T polymorphisms with neural tube and orofacial cleft defects 10.1002/ajmg.a.30705 2005
Reduction of birth prevalence rates of neural tube defects after folic acid fortification in Chile 10.1002/ajmg.a.30651 2005
SHH Ile111Asp in alobar holoprosencephaly in a proposita, whose mother had only a solitary median maxillary incisor 10.1002/ajmg.a.30624 2005
Medical Sequencing of Candidate Genes for Nonsyndromic Cleft Lip and Palate 10.1371/journal.pgen.0010064 2005
Is there a familial link between Down´s syndrome and neural tube defects? Population and familial survey. 2004
ECLAMC: the Latin-American collaborative study of congenital malformations. 2004
Interferon regulatory factor 6 (IRF6) gene variants and the risk of isolate lip or palate. 2004
MSX1 and TGFB3 contribute to clefting in South America 2003
Complex segregation analysis of 1,792 cleft lip and palate families in South America:1967-1997 2003
Preliminary data on changes in neural tube defect prevalence rates after folic acid fortification in South America 10.1002/ajmg.a.20230 2003
Complete sequencing shows a role for MSX1 in non-syndromic cleft lip and palate. 2003
Inheritance of cleft palate in South America: evidence for a major locus recessive. 2003
Clinical and epidemiological studies of amniotic deformity, adhesion, and mutilation (ADAM) sequence in a South American (ECLAMC) population 10.1002/ajmg.a.10194 2003
Mutational analysis of theSonic Hedgehog gene in 220 newborns with oral clefts in a South American (ECLAMC) population 10.1002/ajmg.10204 2002
Birth order and oral clefts: a meta analysis 2002
Genetic origins in a South American clefting population 2002
Maternal Age and oral clefts: A reappraisal 2002
Correlation between molecular and conventional genealogies in Aicuna: A rural population from Northwestern Argentina 2001
Candidate genes for nonsyndromic cleft lip and palate. 2001
Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly. 2001
Epidemiological assessment of misoprostol teratogenicity 2000
Isolated small intestinal atresias in Latin America and Spain: epidemiological analysis 2000
Awareness of the benefit of periconceptional folic acid supplementation in South America 2000
Availability of teratogens in Brazil: misoprostol and thalidomide 2000
Thumb/Hallux Duplication And Preaxial Polydactyly Type I 1999
Principais Dúvidas das Gestantes Em Relação À Odontologia 1999
Pregnancy Outcome After Exposure To Misoprostol In Brazil: A Prospective, Controlled Study 1999
Survival Of Children With Down Syndrome In South America 1998
Male To Male Transmission Of Supernumerary Nipples 1997
Thalidomide, a Current Teratogen In South America. 1996
Heterogeneous Rates For Birth Defects In Latin America: Hints On Causality 1996
Segregation Distortion In The Offspring Of Afroamerican Fathers With Postaxial Polydactyly 1995
The Effect Of Paternal Age In Achondroplasia, Thanatophoric Dysplasia And Osteogenesis Imperfecta 1995
Achondrogenesis Type Ii With Polydactyly 1995
Malformation surveillance and maternal drug exposure. The MADRE project. 1994
Teratogenicity of misoprostol: Data from the Latin-American Collaborative study of Congenital Malformations 1994
El ECLAMC: Estudio Colaborativo Latinoamericano de Malformaciones Congenitas. 1994
Seasonal variation in the frequency of congenital malformations. 1990
The epidemiology of conjoined twins in Latin America. 1988
Epidemiology of Ambiguous Genitalia in South America. 1987
The Birth Prevalence Rates For Skeletal Dysplasias 1986
Prevalence Rates of microtia in South America. 1986
Epidemiology of Neural tube defects in South America. 1985
On monitoring the multiply malformed infant I: Case-finding, case-recording, and dta handling in a Latin American Program. 1985
El Estudio Colaborativo Latinoamericano de Malformaciones Congénitas:ECLAMC / MONITOR 1983
Colaboración Internacional en la Monitorización de Defectos congénitos. 1983
Malformations and inbreeding. 1982
Inbreeding in South-American newborn series. 1982
Epidemiologia de los nevos pigmentados congénitos: III- Herdabilidad. 1982
Epidemiology of congenital pigmented naevi: I-Incidence rates and relative frequencies. 1981
Epidemiology of congenital pigmented naevi: II-Risk factors. 1981
Syndactyly: frequency of specif types. 1980
Vigilância Epidemiológica em Malformações Múltiplas. 1980
Síndrome de la feminización testicular o de la insensibilidad a los andrógenos. 1980
Estudio de factores de riesgo en el síndrome de Down. 1980
Metrorragia y antecedentes de aborto como factores de riesgo para malformaciones. 1980
Variação geográfica de malformações do sistema nervoso central. 1980
Pectoralis major muscle defect and Poland complex 10.1002/ajmg.1320040309 1979
Herdabilidade em malformações de membros segundo a lateralidade. 1979
Características morfológicas dos nevos pigmentados no recém-nascido. 1979
Location of the gene for testicular feminization on the chromosome X in man. 1971
Eventos:

(0.00% eventos com DOI)

Titulo DOI Ano
Mapeamento fino e estudo de associação entre variantes comuns no gene BHMT e fenda labial com ou sem fenda palatina 2023
Mapeamento fino e estudo de associação entre variantes comuns no gene NOS3 e CBS e fenda labial com ou sem fenda palatina 2023
Ausência de associação entre gene nectin1 e fenda labial com ou sem fenda palatina não sindrômica em uma região de alta prevalência 2022
Mapeamento fino dos genes NOS3, CBS e BHMT do ciclo do folato em busca de variantes comuns para estudo de associação de fenda labial com ou sem fenda palatina 2022
Ausência de associação entre polimorfismos do ciclo do folato e fenda oral com ou sem fenda palatina não sindrômica em uma população da Patagônia Argentina. 2021
Variantes de GHRL3 em pacientes com fenda palatina 2021
Ancestry analysis of BrazilianNortheast?s population by uniparental markers 2019
Ancestrality analysis for cleft lip with or without cleft palate in medium prevalence regions identify by ECLAMC in Brazil. 2019
Uso de álcool na gravidezcomo fator de risco após infecção por Vírus Zika 2018
Saúde bucal de crianças nascidas de mães com sintomas de Zika-vírus durante a gravidez 2018
Exposição ao Vírus Zika em mães de recém nascidos com microcefalia, outros defeitos ou sem defeitos. 2018
Incidencia de ZIKA-VÍRUS na população e razão observado/esperado de casos de microcefalia no Brasil 2017
Incidencia de ZIKA-VÍRUS na população e razão observado/esperado de casos de microcefalia no Brasil 2017
Análise de ancestralidade a partir de marcadores uniparentais em uma população do nordeste brasileiro 2017
Dental anomalies in children born with microcephaly 2017
Análise de ancestralidade a partir de marcadores uniparentais em uma população do nordeste brasileiro 2017
Incidência de Zika-virus na população e razão observado/esperado de casos de microcefalia no Brasil. 2017
O papel do gene Geminina na etiologia da holoprosencefalia 2017
28 de novo CNVs suggested as candidate regions for CL ±P in a high prevalence area in South America 2016
28 de novo CNVs suggested as candidate regions for CL ±P in a high prevalence area in South America 2016
28 de novo CNVs suggested as candidate regions for CL ±P in a high prevalence area in South America 2016
CNVS and loh suggested as candidate regions for CL+P: discussing, calling and filtering 2016
FAM110B on 8q12.1 as a new candidate gene for CL P in a highprevalence area in South America. 2015
Análisis de asociación entre marcadores moleculares en el gen DMD y labio leporino con o sin paladar hendido en una población de Patagonia 2015
Contribuição da ancestralidade africana em regiões de prevalência alta ou usual de fenda labial com ou sem fenda palatina identificadas pelo ECLAMC 2015
Ancestralidade em hospitais argentinos e chilenos com prevalência usual para fendas labiopalatinas 2015
A family-based genone-wide scan shows 10q25.2, LRFN2, TGFB2 and CRISPLD2 loci associated with cleft lip with or without cleft palat in high-prevalence cluster in South America 2014
Análise de ancestralidade para fenda labial com ou sem fenda palatina em regiões de prevalência usual identificadas pelo ECLAMC 2014
Family-based genomewide association study in Patagonia, a region with high prevalence of oral clefts: preliminary results 2013
X-linked genes associated with cleft lip with or without palate in a family-based genome wide association study in Patagonia 2013
Uniparental markers of ancestry in usual prevalence areas of cleft lip with or without cleft palate identified by ECLAMC in Argentina 2013
Ancestry markers in regions of high frequency for oral clefts 2013
Known Holoprosencephaly mutation found in a gingival fibromatosis case 2012
Ancestry analysis of usual prevalence regions for cleft lip with or without cleft palate identified by ECLAMC in South America 2012
TCOF1 gene analysis in a patiente with Treacher Collins syndrome 2012
Haplotypes in MTHFR gene are associated with oral clefts 2012
Ancestry Markers in Regions of High Frequency for Oral Clefts 2012
Análise de Ancestralidade em Populações de Regiões com Alta Prevalência de Fendas Orais Identificadas Pelo ECLAMC - Patagônia Argentina 2012
Cleft palate prevalence with data from the Brazilian Live Births Information System, 2006 ? 2010 2012
Association between rs642961 and cleft lip and palate in Patagonia ECLAMC) population. 2011
IRF6, SNAP91, PRSS35 and CRISPLD2 contribute to the etiology of oral clefts in a Latin American population (ECLAMC). 2011
Segregation Analysis of Isolated Cleft Lip in a high-prevalence cluster of South America: uncommon high-risk allele and implications for genetic association studies 2011
Análises de erros mendelianos no estudo de marcadores polimórficos em tríades da população ECLAMC 2011
Molecular anallysis of MTHFD1 1958G>A and MTHFR 677C>T SNPs in patients with neural tube defects in the Latin American population 2010
Positive selection of oral cleft candidate Genes could explain ethnic differences in prevalence: a model 2010
SHH, ZIC2, SIX3 and TGIF Mutations in a South-American (ECLAMC) population with holoprosencephaly 2010
Association between rs642961 and cleft lip and palate in a Patagonian population (ECLAMC). 2010
Using dental anomalies to subphenotype clefts in Patagonia 2010
Análises de erros mendelianos no estudo de marcadores polimórficos em tríades (mãe, pai, filho) na população do ECLAMC 2010
High Frequency of Amerindian MtDNA Haplogroups in Oral Clefts 2010
Análise de Ancestralidade em Regiões de Alta Prevalência de Fendas Orais no ECLAMC: Equador 2010
Prevalência de fenda labial e fenda palatina no Brasil usando dados da DNV 2009
Microdeletions seem a more common of holoprocenphaly than point mutations. 2009
Brazilian Live Birth Declaration as a Source for a National Birth Defects Registry 2009
Variação na frequência de espinha bífida antes e depois da fortificação do acido fólico no Brasil usando dados da Declaração de Nascidos Vivos. 2009
Análise de Ancestralidade (DNA Mitocondrial) na Região da Patagônia Argentina Estudada pelo ECLAMC 2009
Análise da Ancestralidade (DNA do Cromossomo Y) em Regiões com Alta Prevalência de Fendas Orais no ECLAMC 2009
Interferon regulatory factor 6 (IRF6) variation contributes to oral clefts in South America 2008
Análise Molecular da Variante 677C>T do Gene MTHFR em Pacientes com Fenda Palatina na América do Sul 2008
Interaction between IRF6 and TGFA contributes to the risk of cleft lip/palate. 2008
Variante 677C>T do Gene MTHFR em Pacientes com Fendas Orais na América Latina. 2008
Gene Sumo-1 em Pacientes com Fendas Orais. 2008
Rubella vaccination campaigns in Brazil, impact on the birth prevalence rates of congenital anomalies, and on induced abortions 2008
Surveillance and prevention of birth defects in Brazil: The ECLAMC and the brazilian birth notification certificate 2007
Frequencies of 4 allelic variants for NAT2 in 6 hospitals from ECLAMC 2007
Highly prevalence of mucopolyssaccharidosis VI in Monte Santo, a city in the state of Bahia ? northeast of Brazil 2007
S372 Mutation in the FGFR-2 in a beare-stevenson cutis gyrate syndrome patient 2007
Six3 mutation in a patent with single median maxillary central incisor (SMMCI) and normal brain. 2007
Mitochondrial ancestry and susceptibility to clefting in South American population. 2007
High prevalence of mucopolysaccharidosis VI in a northeastern brazilian town 2007
No association of ZIC2 10H allele and neural tube defects in a South American (ECLAMC) population 2007
Distribution of 5,10 methylenetetrahydrofolate reductase (MTHFR) C.677C>T and C. polymorphisms in Latin America. 2007
Genetics in the ?Sertão?: study frequent monogenic genetic disorders in Monte Santo ? A small city of the state of Bahia ? Northeast of Brazil 2007
Misoprostol use in South American countries. 2007
Molecular analysis of a methylene-tetrahydrofolate-dehydrogenase 1958> a polymorphism in patients with neural tube defects 2007
Geographic analysis of oral cleft birth prevalence rates in South America 2007
Isocromossomo 18q- relato de um caso com manifestações leves 2006
Criação de página na internet para o Serviço de Informação Teratogênica do Rio de Janeiro 2006
Síndrome de Goltz associada a craniossinostose e ossos Wormianos 2006
Coarctação da aorta - Um achado raro na sequência de Klippel-Feel 2006
Perfil no Atendimento do Disque Gestante 2005
Estudo Molecular da Variante c.677C>T da 5,10 Metilenotetrahidrofolato Redutase (MTHFR) em Diferentes Maternidades Latino-Americanas. 2005
Misoprostol e Defeitos Congênitos: Uso no Brasil e em Outro Países da América do Sul. 2005
Agenesias dentárias múltiplas ? Relato de Caso Clínico 2005
Advances in research conducted through birth defects surveillance network: The ECLAMC experience 2005
Misoprostol e Defeitos Congênitos. 2004
Consultas sobre rubéola do Disque Gestante antes e depois da campanha de vacinação contra a rubéola. 2004
Definição fenotípica e epidemiológica do Complexo de ADAM. 2003
Riscos desnecessários na gravidez. 2003
Gestação e Doenças Infecciosas 2003
Retinóides - Risco do Uso na Gestação. 2003
Misoprostol and Teratogenicity: Reviewing the evidence. 2003
Potential mechanism regarding growth disparity in like-sex twins discordant for hypospadias 2003
MSX1 and TGFB3 are associated to nonsyndromic oral-facial clefts in South America. 2002
Frequency of mtDNA population-specific variants in a nonsyndromic clefting South American population. 2002
Nos Dez Anos do Disque-Gestante (SIT-RJ)-I 2002
Nos Dez Anos do Disque-Gestante (SIT-RJ) ? II. 2002
Genetic origins of a South American clefting population. 2002
Neural tube defects in Hispanics ? The situation in South America 2002
Frecuencias de las mutaciones C677T y A1298C de MHTFR en LatinoAmérica. 2001
MSX1 Variant is associated with Cleft Lip/Palate in a South American Population. 2001
Conhecimento da população do Rio de Janeiro sobre os teratógenos talidomida e misoprostol 2000
Principais dúvidas das gestantes em relação à dermatologia no Serviço de Informação Teratogênica do Rio de Janeiro 2000
Anomalias de couro cabeludo: análise dos casos do ECLAMC. 2000
Prevalência dos defeitos congênitos na sequência de bridas amnióticas 2000
MSX1 mutation research in diverse populations of individuals with clefting. Analysis of Sonic hedgehog in 217 newborns with nonsyndromic oral clefts 2000
Association of MSX1 with nonsyndromic orofacial clefting in ECLAMC. 2000
New associations between prenatal exposure to drugs and malformations. 2000
Fatores de risco na gravidez no serviço de infromação teratogênica do Rio de Janeiro 2000
Continuing And Distance Education And Prevention Of Congenital Malformations 1998
Análise das Consulentes Com Mais de Uma Consulta Ao Disque-Gestante No Período 1992-1997 1998
Variações de Cordão Umbilical e de Placenta 1998
Pregnancy Outcome After Abortion Attempt With Misoprostol 1997
Exercício Epidemiológico Para Detecção de Riscos Teratogênicos 1997
Perfil das Gestantes Consulentes No Sit-Rj e Riscos Na Gravidez 1997
Perfil das Gestantes Consulentes do Sit-Rj e Resultados Adversos 1997
Conhecimento de Estudantes da Área de Saúde Em Prevenção Primária de Defeitos Congênitos 1996
Teratogenicity Of Misoprostol 1996
Hábitos de Vida Como Fatores de Risco Na Gravidez 1996
Avaliação da Teratogenicidade do Misoprostol 1996
Fatores Assiociados Às Dificuldades de Seguimento das Gestantes Orientadas Pelo Serviço e Registro de Informação do Rio de Janeiro 1996
Genetic Background Influence On Environmental Risk Factors For Neural Tube Defects 1995
Uso de Medicamentos Na Gravidez 1995
Peso Placentário e Fetal Em Populações Latino-Americanas 1995
Há Significado Patológico Nas Variações Observadas Em Cordão Umbilical e Placenta? 1995
Significado do grupo nativo em populaçõs urbanas latino-americanas. 1989
Genética Molecular. 1988
El estudio prospectivo de displasias esqueléticas. 1987
Dados dos sistemas ABO e Rh em amostras hospitalares sul-americanas 1986
Frecuencias de base por diagnóstico: datos ECLAMC 1982-1983. 1984
La edad reproductiva como factor de riesgo para malformaciones. 1984
Displasias esqueléticas. 1984
Relacion entre gemelaridad Y edad materna 1983
Frequências de anencefalia, espinha bífida e cefalocele em cidades sul-americanas. 1982
Heredabilidad de los nevos pigmentados congenitos 1982
Programa para la monitorizacion de los polimalformados 1982
Frequências de anencefalia, espinha bífida e cafalocele em cidades Sul-Americanas 1982
Defeitos congênitos associados. 1982
Estudo de peso ao nascimento e da idade gestacional em populações da América do Sul. 1980
Correlação entre idade materna e fatores de risco na Síndrome de Down. 1980
Variação temporal de espinha bífida, hidrocefalia e microcefalia. 1980
Estudo de fatores de risco em nevos pigmentados congênitos. 1980
Utilidad de algunas variables como indicadores de endocria en poblaciones urbanas 1980
Analisis de etnicidad en poblaciones racionalmente estratificadas. 1980
Efectos de la endocria en productos de uniones fertiles. 1980
Vigilância epidemiológica de malformações múltiplas 1980
Epidemiologia de los Malformados Múltiples 1980
Genitales ambiguos en el recien nacido 1980
Malformaciones Congenitas del Sistema Nervoso Central 1980
significado de la Consanguinidad Paterna 1980
Distribuição de variáveis genéticas em populações da América do Sul. 1979
Classificação dos defeitos de fechamento do tubo neural. 1979
Incidência da síndorme de Down na América do Sul. 1979
Estudo do cromossomo Y em bovinos com 5-BUdR. 1979
Consaguinidade em nascimentos hospitalares na América do Sul. 1979
Levantamento dos casos atendidos no ambulatório de genética médica (HC-FMRPUSP) no período de 1974 a 1976 1977
Fundamentos Epidemiológicos para los Complejos Malformativos 1977
Revisión de los patrones de herencia en las sindactilias 1977
Patrones de recurrencia familiar de malformaciones 1977
Experiência de um serviço de aconselhamento genético integrado a um registro de malformações congenitas 1977
Inbreeding and outcrossing data form malformed and non malformed newborns. 1976
Cariótipo 46,XY,t (7;15) (p15;q15) em paciente com má história reprodutiva. 1975
Família com dois casos de glicose tipo II (Von Gierke): detecção de heterozigotos. 1974
Síndrome de feminização testicular. 1972
Amiloidose portuguesa. 1972
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