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Aubrey Milunsky
Researcher at Tufts University
Publications - 284
Citations - 9773
Aubrey Milunsky is an academic researcher from Tufts University. The author has contributed to research in topics: Prenatal diagnosis & Amniotic fluid. The author has an hindex of 47, co-authored 283 publications receiving 9502 citations. Previous affiliations of Aubrey Milunsky include Queen Mary University of London & University of the Witwatersrand.
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Journal ArticleDOI
Multivitamin/Folic Acid Supplementation in Early Pregnancy Reduces the Prevalence of Neural Tube Defects
Aubrey Milunsky,Hershel Jick,Susan S. Jick,Carol L. Bruell,Dean S. MacLaughlin,Kenneth J. Rothman,Walter C. Willett +6 more
TL;DR: The relation of multivitamin intake in general, and folic acid in particular, to the risk of neural tube defects in a cohort of 23,491 women undergoing maternal serum alpha-fetoprotein screening or amniocentesis around 16 weeks of gestation was examined.
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Teratogenicity of High Vitamin A Intake
Kenneth J. Rothman,Lynn L. Moore,Martha R. Singer,Uyen-Sa D. T. Nguyen,Salvatore Mannino,Aubrey Milunsky +5 more
TL;DR: Of the 22,748 pregnant women identified between October 1984 and June 1987, 339 had babies with birth defects; 121 of these babies had defects occurring in sites that originated in the cranial neural crest.
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Congenital bilateral absence of the vas deferens. A primarily genital form of cystic fibrosis
Arturo Anguiano,Robert D. Oates,Jean A. Amos,Michael Dean,Bernard Gerrard,Claudia Stewart,Thomas A. Maher,Marga Belle White,Aubrey Milunsky +8 more
TL;DR: Some, if not all, otherwise healthy men with CBAVD reflect a newly recognized, primarily genital, phenotype of CF, and CF mutation analysis should be recommended for them and their partners, as well as for their relatives.
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An exonic mutation in the HuP2 paired domain gene causes Waardenburg's syndrome
TL;DR: A mutation causing Waardenburg's syndrome as well as a mutation causing a form of congenital deafness was found in the HuP2 gene, a member of the paired domain family of proteins that bind DNA and regulate gene expression.
Journal ArticleDOI
Methotrexate-induced congenital malformations.
Aubrey Milunsky,Aubrey Milunsky,John W. Graef,John W. Graef,Martin F. Gaynor,Martin F. Gaynor +5 more
TL;DR: The case of an infant born after the unsuccessful abortifacient use of methotrexate, with resulting multiple congenital anomalies included absence of the frontal bone, synostosis of the lambdoid and coronal sutures, multiple anomalous ribs, unusual facies, and absence of digits on the left foot with only one digit on the right foot.