Ieda Orioli

9PUBLICATIONS
49CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Development cooperationInfant and child healthDisease surveillanceGene expression (incl. microarray and other genome-wide approaches)
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Publications (9)

|Sep 30, 2025
Variants in CALD1, ESRP1, and RBFOX1 are associated with orofacial cleft risk.

Jenna C Carlson, Xinyi Zhang, Zeynep Erdogan-Yildirim

|Oct 29, 2022
A large, ten-generation family with autosomal dominant preaxial polydactyly/triphalangeal thumb: Historical, clinical, genealogical, and molecular studies.

Luis Francisco González Álvarez, Jair Tenorio-Castaño, Fernando A Poletta

|Apr 04, 2022
The legacy of ZikaPLAN: a transnational research consortium addressing Zika.

Annelies Wilder-Smith, Elizabeth B Brickley, Ricardo Arraes de Alencar Ximenes

|May 05, 2021
Global birth defects app: An innovative tool for describing and coding congenital anomalies at birth in low resource settings.

Helen Dolk, Aminkeng Zawuo Leke, Phil Whitfield

|Dec 15, 2020
The Latin American network for congenital malformation surveillance: ReLAMC.

Iêda Maria Orioli, Helen Dolk, Jorge Lopez-Camelo

|Oct 24, 2019
ZikaPLAN: addressing the knowledge gaps and working towards a research preparedness network in the Americas.

Annelies Wilder-Smith, Raman Preet, Elizabeth B Brickley

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Frequent Collaborators

4 joint publications

Helen Dolk

2 joint publications

Elizabeth J Leslie-Clarkson

2 joint publications

John R Shaffer

2 joint publications

Annelies Wilder-Smith