Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Iêda M Orioli"'
Autor:
Helen Dolk, Boris Groisman, Joan Morris, Rosa Pardo, Elizabeth Limb, Iêda M Orioli, Adriana Benavides-Lara, María de la Paz Barboza-Arguello, Maria Aurora Canessa Tapia, Giovanny Vinícius Araújo de França, Jorge Holguin, Paula Margarita Hurtado-Villa, Marisol Ibarra Ramirez, Cecilia Mellado, Dania Maria Pastora Bucardo, Catherin Rodríguez, Ignacio Zarante
Publikováno v:
BMJ Paediatrics Open, Vol 5, Iss 1 (2021)
Objective The Latin American Network of Congenital Malformations: ReLAMC was established in 2017 to provide accurate congenital anomaly surveillance. This study used data from ReLAMC registries to quantify the prevalence of microcephaly from 2010 to
Externí odkaz:
https://doaj.org/article/5b0400fc4d8a4c33a2ef2fc7f22012d7
Autor:
Katherine Neiswanger, Nandita Mukhopadhyay, Shwetha Rajagopalan, Elizabeth J Leslie, Carla A Sanchez, Jacqueline T Hecht, Iêda M Orioli, Fernando A Poletta, Javier Enríquez de Salamanca, Seth M Weinberg, Mary L Marazita
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0230534 (2020)
Dermatoglyphic patterns on the fingers often differ in syndromes and other conditions with a developmental component, compared to the general population. Previous literature on the relationship between orofacial clefts-the most common craniofacial bi
Externí odkaz:
https://doaj.org/article/dd806ce1c31549b188c19881c86818ad
Autor:
Ida Anjomshoaa, Jessica Briseño-Ruiz, Kathleen Deeley, Fernardo A Poletta, Juan C Mereb, Aline L Leite, Priscila A T M Barreta, Thelma L Silva, Piper Dizak, Timothy Ruff, Asli Patir, Mine Koruyucu, Zerrin Abbasoğlu, Priscila L Casado, Andrew Brown, Samer H Zaky, Merve Bayram, Erika C Küchler, Margaret E Cooper, Kai Liu, Mary L Marazita, İlknur Tanboğa, José M Granjeiro, Figen Seymen, Eduardo E Castilla, Iêda M Orioli, Charles Sfeir, Hongjiao Owyang, Marília A R Buzalaf, Alexandre R Vieira
Publikováno v:
PLoS ONE, Vol 10, Iss 12, p e0143068 (2015)
Aquaporins (AQP) are water channel proteins and the genes coding for AQP2, AQP5, and AQP6 are clustered in 12q13. Since AQP5 is expressed in serous acinar cells of salivary glands, we investigated its involvement in caries. DNA samples from 1,383 ind
Externí odkaz:
https://doaj.org/article/fa8123d599924aa0ac391f8900899508
Autor:
Takehiko Shimizu, Bao Ho, Kathleen Deeley, Jessica Briseño-Ruiz, Italo M Faraco, Brett I Schupack, João A Brancher, Giovana D Pecharki, Erika C Küchler, Patricia N Tannure, Andrea Lips, Thays C S Vieira, Asli Patir, Mine Yildirim, Fernando A Poletta, Juan C Mereb, Judith M Resick, Carla A Brandon, Iêda M Orioli, Eduardo E Castilla, Mary L Marazita, Figen Seymen, Marcelo C Costa, José M Granjeiro, Paula C Trevilatto, Alexandre R Vieira
Publikováno v:
PLoS ONE, Vol 7, Iss 9, p e45022 (2012)
There is evidence for a genetic component in caries susceptibility, and studies in humans have suggested that variation in enamel formation genes may contribute to caries. For the present study, we used DNA samples collected from 1,831 individuals fr
Externí odkaz:
https://doaj.org/article/efa7b4edc0da4918b87bf70c99598838
Autor:
Alexandre R Vieira, Joseph R Avila, Sandra Daack-Hirsch, Ecaterina Dragan, Têmis M Félix, Fedik Rahimov, Jill Harrington, Rebecca R Schultz, Yoriko Watanabe, Marla Johnson, Jennifer Fang, Sarah E O'Brien, Iêda M Orioli, Eduardo E Castilla, David R Fitzpatrick, Rulang Jiang, Mary L Marazita, Jeffrey C Murray
Publikováno v:
PLoS Genetics, Vol 1, Iss 6, p e64 (2005)
Nonsyndromic or isolated cleft lip with or without cleft palate (CL/P) occurs in wide geographic distribution with an average birth prevalence of 1/700. We used direct sequencing as an approach to study candidate genes for CL/P. We report here the re
Externí odkaz:
https://doaj.org/article/58a2334e6b2f4ca5a3ac6d4a04816e34
Autor:
Joissy Aprigio, Carolina M. L. de Castro, Marcelo A. Costa Lima, Márcia G. Ribeiro, Iêda M. Orioli, Márcia R. Amorim
Publikováno v:
J Community Genet
Down syndrome is the main genetic cause of intellectual disability. Many studies describe the clinical characteristics of DS patients; however, few have investigated the clinical profile of mothers who have children with DS. Advanced maternal age (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a403ad9135987d9b3b30b653aef287a3
https://europepmc.org/articles/PMC10104982/
https://europepmc.org/articles/PMC10104982/
Autor:
Ronilo Ragodos, Tong Wang, Carmencita Padilla, Jacqueline T. Hecht, Fernando A. Poletta, Iêda M. Orioli, Carmen J. Buxó, Azeez Butali, Consuelo Valencia-Ramirez, Claudia Restrepo Muñeton, George L. Wehby, Seth M. Weinberg, Mary L. Marazita, Lina M. Moreno Uribe, Brian J. Howe
Publikováno v:
Scientific Reports. 12
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dce3acddfe7afb1ee64deefe038efad5
https://doi.org/10.1038/s41598-022-17668-0
https://doi.org/10.1038/s41598-022-17668-0
Autor:
Ana Maria Bolognese, Milagros M. Duenas-Roque, Viviane Freitas de Castro, Maria Teresa Vieira Sanseverino, Viviana Cosentino, Rachel Sayuri Honjo, Larissa Souza Mario Bueno, Juan C. Llerena, Luiz Carlos Santana da Silva, Júlio César Loguercio Leite, Daniel Mattos, Márcia Pereira Alves de Souza, Denise P. Cavalcanti, Pablo Barbero, Pricila Bernardi, Flávia Martinez de Carvalho, Patrícia Santana Correia, Clarice Pagani Savastano, Iêda M. Orioli
Publikováno v:
Molecular Syndromology. 12:219-233
Holoprosencephaly (HPE) is the failure of the embryonic forebrain to develop into 2 hemispheres promoting midline cerebral and facial defects. The wide phenotypic variability and causal heterogeneity make genetic counseling difficult. Heterozygous va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ba2f0476a84a943b99e0e9ec2a83f4e
https://doi.org/10.1159/000515044
https://doi.org/10.1159/000515044
Autor:
Lucas Gabriel Gimenez, Marta Ascurra, Paula Hurtado-Villa, Jorge S. Lopez-Camelo, Maria Aurora Canessa‐Tapia, Dania Maria Pastora, Flávia Martinez de Carvalho, Daniel Mattos Correa, Iêda M. Orioli, Adriana Benavides-Lara, Boris Groisman, Flávia Schneider Soares, Giovanny Vinícius Araújo de França, Marisol Ibarra-Ramírez, Mariana Piola, Rosa Pardo, Helen Dolk, Ignacio Zarante, Eliana de Aquino Bonilha
Publikováno v:
American Journal of Medical Genetics Part C: Seminars in Medical Genetics. 184:1078-1091
The early detection of congenital anomaly epidemics occurs when comparing current with previous frequencies in the same population. The success of epidemiologic surveillance depends on numerous factors, including the accuracy of the rates available i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26b277a7c232a409c943ffd94f340b68
https://doi.org/10.1002/ajmg.c.31872
https://doi.org/10.1002/ajmg.c.31872
Autor:
Jacqueline T. Hecht, Carmencita D. Padilla, Lina M. Moreno Uribe, Consuelo Valencia-Ramirez, Tong Wang, Iêda M. Orioli, Seth M. Weinberg, Carmen J. Buxó, Azeez Butali, Fernando A. Poletta, B.J. Howe, George L. Wehby, Mary L. Marazita, Ronilo Ragodos, Claudia P. Restrepo Muñeton
Children with orofacial clefting (OFC) present with a wide range of dental anomalies. Identifying these anomalies is vital to understand their etiology and to discern the complex phenotypic spectrum of OFC. Such anomalies are currently identified usi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c64bb247e93ba4ba06b4aac6d67cb7b
https://doi.org/10.21203/rs.3.rs-1061414/v1
https://doi.org/10.21203/rs.3.rs-1061414/v1