Works matching AU Baker, Mei W.

Results: 13

Missed Cystic Fibrosis Newborn Screening Cases due to Immunoreactive Trypsinogen Levels below Program Cutoffs: A National Survey of Risk Factors.

Published in:

International Journal of Neonatal Screening (IJNS), 2022, v. 8, n. 4, p. 58, doi. 10.3390/ijns8040058

By:

Kharrazi, Martin;
Sacramento, Charlene;
Comeau, Anne Marie;
Hale, Jaime E.;
Caggana, Michele;
Kay, Denise M.;
Lee, Rachel;
Reilly, Brendan;
Thompson, John D.;
Nasr, Samya Z.;
Kleyn, Mary;
Hoffman, Gary;
Baker, Mei W.;
Clarke, Colleen;
Harris, Cheryl L.;
Dorley, M. Christine;
Fryman, Hilary;
Sutaria, Ankit;
Hietala, Amy;
Winslow, Holly

Publication type:

Article

Newborn Screen for X-Linked Adrenoleukodystrophy Using Flow Injection Tandem Mass Spectrometry in Negative Ion Mode.

Published in:

International Journal of Neonatal Screening (IJNS), 2022, v. 8, n. 2, p. 27, doi. 10.3390/ijns8020027

By:

Teber, Tarek A.;
Conti, Brian J.;
Haynes, Christopher A.;
Hietala, Amy;
Baker, Mei W.

Publication type:

Article

Correction: Furnier et al. Translating Molecular Technologies into Routine Newborn Screening Practice. Int. J. Neonatal Screen. 2020, 6 , 80.

Published in:

2021

By:

Furnier, Sarah M.;
Durkin, Maureen S.;
Baker, Mei W.

Publication type:

Correction Notice

Newborn Screening for Severe Combined Immunodeficiency: Do Preterm Infants Require Special Consideration?

Published in:

International Journal of Neonatal Screening (IJNS), 2021, v. 7, n. 3, p. 1, doi. 10.3390/ijns7030040

By:

Atkins, Anne E.;
Cogley, Michael F.;
Baker, Mei W.

Publication type:

Article

Newborn Screening for Severe Combined Immunodeficiency Using the Multiple of the Median Values of T-Cell Receptor Excision Circles.

Published in:

International Journal of Neonatal Screening (IJNS), 2021, v. 7, n. 3, p. 1, doi. 10.3390/ijns7030043

By:

Cogley, Michael F.;
Wiberley-Bradford, Amy E.;
Mochal, Sean T.;
Dawe, Sandra J.;
Piro, Zachary D.;
Baker, Mei W.

Publication type:

Article

The Impact of the CFTR Gene Discovery on Cystic Fibrosis Diagnosis, Counseling, and Preventive Therapy.

Published in:

Genes, 2020, v. 11, n. 4, p. 1, doi. 10.3390/genes11040401

By:

Farrell, Philip M.;
Rock, Michael J.;
Baker, Mei W.

Publication type:

Article

Low-normal FMR1 CGG repeat length: phenotypic association.

Published in:

Frontiers in Genetics, 2014, v. 5, p. 1, doi. 10.3389/fgene.2014.00309

By:

Mailick, Marsha R.;
Jinkuk Hong;
Rathouz, Paul;
Baker, Mei W.;
Greenberg, Jan S.;
Smith, Leann;
Maenner, Matthew

Publication type:

Article

Novel mutation in TP 63 associated with ectrodactyly ectodermal dysplasia and clefting syndrome and T cell lymphopenia.

Published in:

American Journal of Medical Genetics. Part A, 2013, v. 161A, n. 6, p. 1432, doi. 10.1002/ajmg.a.35885

By:

Giampietro, Philip F.;
Baker, Mei W.;
Basehore, Monica J.;
Jones, Julie R.;
Seroogy, Christine M.

Publication type:

Article

FMR1 CGG Expansions: Prevalence and Sex Ratios.

Published in:

American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2013, v. 162B, n. 5, p. 466, doi. 10.1002/ajmg.b.32176

By:

Maenner, Matthew J.;
Baker, Mei W.;
Broman, Karl W.;
Tian, Jianan;
Barnes, Janel K.;
Atkins, Anne;
McPherson, Elizabeth;
Hong, Jinkuk;
Brilliant, Murray H.;
Mailick, Marsha R.

Publication type:

Article

CGG Repeats in the 5’UTR of FMR1 RNA Regulate Translation of Other RNAs Localized in the Same RNA Granules.

Published in:

PLoS ONE, 2016, v. 11, n. 12, p. 1, doi. 10.1371/journal.pone.0168204

By:

Rovozzo, René;
Korza, George;
Baker, Mei W.;
Li, Meng;
Bhattacharyya, Anita;
Barbarese, Elisa;
Carson, John H.

Publication type:

Article

Microarray analysis of retinoid-dependent gene activity during rat embryogenesis: Increased collagen fibril production in a model of retinoid insufficiency.

Published in:

Developmental Dynamics, 2004, v. 229, n. 4, p. 886

By:

George R. Flentke;
Mei W. Baker;
Kimberly E. Docterman;
Susan Power;
John Lough;
Susan M. Smith

Publication type:

Article

Health Profiles of Mosaic Versus Non-mosaic FMR1 Premutation Carrier Mothers of Children With Fragile X Syndrome.

Published in:

Frontiers in Genetics, 2018, p. 1, doi. 10.3389/fgene.2018.00173

By:

Mailick, Marsha R.;
Movaghar, Arezoo;
Jinkuk Hong;
Greenberg, Jan S.;
DaWalt, Leann S.;
Lili Zhou;
Jackson, Jonathan;
Rathouz, Paul J.;
Baker, Mei W.;
Brilliant, Murray;
Page, David;
Berry-Kravis, Elizabeth

Publication type:

Article

Statewide Newborn Screening for Severe T-Cell Lymphopenia.

Published in:

JAMA: Journal of the American Medical Association, 2009, v. 302, n. 22, p. 2465, doi. 10.1001/jama.2009.1806

By:

Routes, John M.;
Grossman, William J.;
Verbsky, James;
Laessig, Ronald H.;
Hoffman, Gary L.;
Brokopp, Charles D.;
Baker, Mei W.

Publication type:

Article