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JAMA|December 10, 2009
Statewide newborn screening for severe T-cell lymphopeniaJohn M Routes, William J Grossman, James Verbsky, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 7, 2013
FMR1 CGG expansions: prevalence and sex ratiosMatthew J Maenner, Mei W Baker, Karl W Broman, et al.Neuromuscular Disorders : NMD|February 5, 2022
Newborn screening for spinal muscular atrophy: The Wisconsin first year experienceMei W Baker, Sean T Mochal, Sandra J Dawe, et al.The Journal of Allergy and Clinical Immunology|June 2, 2009
Development of a routine newborn screening protocol for severe combined immunodeficiencyMei W Baker, William J Grossman, Ronald H Laessig, et al.Frontiers in Genetics|June 6, 2018
Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X SyndromeMarsha R Mailick, Arezoo Movaghar, Jinkuk Hong, et al.Molecular Genetics and Metabolism|May 29, 2013
Prevalence and mutation analysis of short/branched chain acyl-CoA dehydrogenase deficiency (SBCADD) detected on newborn screening in WisconsinSandra C Van Calcar, Mei W Baker, Phillip Williams, et al.Journal of Clinical Immunology|November 10, 2011
Newborn screening for severe combined immunodeficiency; the Wisconsin experience (2008-2011)James W Verbsky, Mei W Baker, William J Grossman, et al.International Journal of Neonatal Screening|November 22, 2022
Missed Cystic Fibrosis Newborn Screening Cases due to Immunoreactive Trypsinogen Levels below Program Cutoffs: A National Survey of Risk FactorsMartin Kharrazi, Charlene Sacramento, Anne Marie Comeau, et al.Pageof 3