Alison Brebner

Prevalence and predictors of mortality in gastroschisis: a population-based study of 4803 cases in the USA

H. Abenhaim, N. Czuzoj-Shulman, Alison Brebner, 2018, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

A PRDX1 mutant allele causes a MMACHC secondary epimutation in cblC patients

W. Chung, M. Baumgartner, A. Montpetit, 2018, Nature Communications.

High resolution melting analysis of the MMAB gene in cblB patients and in those with undiagnosed methylmalonic aciduria.

C. Wittwer, D. Watkins, D. Rosenblatt, 2013, Molecular genetics and metabolism.

Mutations in THAP11 cause an inborn error of cobalamin metabolism and developmental abnormalities

Warren A. Cheung, T. Shaikh, T. Pastinen, 2017, Human molecular genetics.

High resolution melting analysis of the MMAA gene in patients with cblA and in those with undiagnosed methylmalonic aciduria.

C. Wittwer, D. Watkins, D. Rosenblatt, 2012, Molecular genetics and metabolism.

An X-linked cobalamin disorder caused by mutations in transcriptional coregulator HCFC1.

T. Shaikh, M. Baumgartner, T. Suormala, 2013, American journal of human genetics.

A Patient With an Inborn Error of Vitamin B12 Metabolism (cblF) Detected by Newborn Screening

M. Geraghty, D. Watkins, D. Rosenblatt, 2013, Pediatrics.

High resolution melting analysis of the MMAB gene in cblB patients and in those with undiagnosed methylmalonic aciduria.

C. Wittwer, D. Watkins, D. Rosenblatt, 2013, Molecular genetics and metabolism.

A Patient With an Inborn Error of Vitamin B12 Metabolism (cblF) Detected by Newborn Screening

M. Geraghty, D. Watkins, D. Rosenblatt, 2013, Pediatrics.