Jaime L. Frías

Medicine · Health Sciences

39h-index4.7kcitations140works0.02yr avg
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Research Topics

Congenital Anomalies and Fetal Surgery(18), Folate and B Vitamins Research(14), Craniofacial Disorders and Treatments(14), Cleft Lip and Palate Research(13), Genomic variations and chromosomal abnormalities(12)

Publications140 total

Serbia’s New Growth Agenda
World Bank, Washington, DC eBooks·2020
A Practitioner's Guide to Innovation Policy
World Bank, Washington, DC eBooks·2020· 25 cited
Two unrelated patients with autosomal dominant omodysplasia and <i>FRIZZLED2</i> mutations
Clinical Case Reports·2018· 13 citedOpen Access
David Weyhe Smith, MD (1926–1981)—The Father of Dysmorphology
Advances in Pediatrics·2015· 4 cited
Methods for surveillance of fetal alcohol syndrome: The fetal alcohol syndrome surveillance network II (FASSNetII) – Arizona, Colorado, New York, 2009 ‐ 2014
Birth Defects Research Part A Clinical and Molecular Teratology·2015· 10 citedOpen Access
Fetal alcohol syndrome among children aged 7-9 years - Arizona, Colorado, and New York, 2010.
PubMed·2015· 48 cited
Laterality defects in the national birth defects prevention study (1998–2007): Birth prevalence and descriptive epidemiology
American Journal of Medical Genetics Part A·2014· 210 citedOpen Access
In Memoriam: Lew Barness
Advances in Pediatrics·2014
Exploring the feasibility of using electronic health records in the surveillance of fetal alcohol syndrome
Birth Defects Research Part A Clinical and Molecular Teratology·2014· 4 citedOpen Access
Long‐term observation of a patient with dominant omodysplasia
American Journal of Medical Genetics Part A·2014· 8 cited
A pilot study using residual newborn dried blood spots to assess the potential role of cytomegalovirus and <i>Toxoplasma gondii</i> in the etiology of congenital hydrocephalus
Birth Defects Research Part A Clinical and Molecular Teratology·2013· 16 citedOpen Access
Neural tube defects in Latin America and the impact of fortification: a literature review
Public Health Nutrition·2013· 87 citedOpen Access
Two extraordinarily severe cases of Treacher Collins syndrome
American Journal of Medical Genetics Part A·2013· 8 cited
Maternal age and prevalence of isolated congenital heart defects in an urban area of the United States
American Journal of Medical Genetics Part A·2011· 122 cited
Table of Contents, Volume 155, Number 3, March 2011
American Journal of Medical Genetics Part A·2011Open Access
Congenital Heart Defects and Major Structural Noncardiac Anomalies, Atlanta, Georgia, 1968 to 2005
The Journal of Pediatrics·2011· 66 cited
Descriptive study of nonsyndromic atrioventricular septal defects in the National Birth Defects Prevention Study, 1997–2005
American Journal of Medical Genetics Part A·2011· 23 cited
Effect of specimen storage conditions on newborn dried blood spots used to assess Toxoplasma gondii immunoglobulin M (IgM)
Clinica Chimica Acta·2010· 19 cited
Long-Term Survival of Infants with Atrioventricular Septal Defects
The Journal of Pediatrics·2010· 47 cited
Risk factors for non‐syndromic holoprosencephaly in the National Birth Defects Prevention Study
American Journal of Medical Genetics Part C Seminars in Medical Genetics·2010· 70 cited
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Frequent Co-authors

Sonja A. Rasmussen(7), Margaret A. Honein(5), M. L. Martínez‐Frías(5), Tiffany Riehle‐Colarusso(4), I. T. Thomas(4), Eva Bermejo(4), John M. Opitz(4), Assia Miller(3), Adolfo Correa(3), Elvira Rodríguez‐Pinilla(3), María Luisa Martínez‐Frías(3), Mahsa M. Yazdy(3), Charlotte Z. Lafer(2), Csaba Siffel(2), María Luisa Martínez‐Frías(2), Juan P. Frías(2), Charles A. Williams(2), Arlan L. Rosenbloom(2), Owen M. Rennert(2), Kimberlea W. Hauser(2)