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Molly B. Sheridan, Ph.D. - Publications

Affiliations: 
2008 Johns Hopkins University, Baltimore, MD 
Area:
Genetics, Molecular Biology
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8 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2021 Collaco JM, Raraigh KS, Betz J, Aksit MA, Blau N, Brown J, Dietz HC, MacCarrick G, Nogee LM, Sheridan MB, Vernon HJ, Beaty TH, Louis TA, Cutting GR. Accurate assignment of disease liability to genetic variants using only population data. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 34906463 DOI: 10.1016/j.gim.2021.08.012  0.428
2018 Raraigh KS, Han ST, Davis E, Evans TA, Pellicore MJ, McCague AF, Joynt AT, Lu Z, Atalar M, Sharma N, Sheridan MB, Sosnay PR, Cutting GR. Functional Assays Are Essential for Interpretation of Missense Variants Associated with Variable Expressivity. American Journal of Human Genetics. PMID 29805046 DOI: 10.1016/J.Ajhg.2018.04.003  0.602
2015 Sheridan MB, Wohler E, Batista DA, Applegate C, Hoover-Fong J. The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome. Case Reports in Genetics. 2015: 169482. PMID 26664771 DOI: 10.1155/2015/169482  0.644
2014 Henderson LB, Applegate CD, Wohler E, Sheridan MB, Hoover-Fong J, Batista DA. The impact of chromosomal microarray on clinical management: a retrospective analysis. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 657-64. PMID 24625444 DOI: 10.1038/Gim.2014.18  0.504
2011 Sheridan MB, Hefferon TW, Wang N, Merlo C, Milla C, Borowitz D, Green ED, Mogayzel PJ, Cutting GR. CFTR transcription defects in pancreatic sufficient cystic fibrosis patients with only one mutation in the coding region of CFTR. Journal of Medical Genetics. 48: 235-41. PMID 21097845 DOI: 10.1136/Jmg.2010.083287  0.721
2006 Férec C, Casals T, Chuzhanova N, Macek M, Bienvenu T, Holubova A, King C, McDevitt T, Castellani C, Farrell PM, Sheridan M, Pantaleo SJ, Loumi O, Messaoud T, Cuppens H, et al. Gross genomic rearrangements involving deletions in the CFTR gene: characterization of six new events from a large cohort of hitherto unidentified cystic fibrosis chromosomes and meta-analysis of the underlying mechanisms. European Journal of Human Genetics : Ejhg. 14: 567-76. PMID 16493442 DOI: 10.1038/Sj.Ejhg.5201590  0.624
2005 Sheridan MB, Fong P, Groman JD, Conrad C, Flume P, Diaz R, Harris C, Knowles M, Cutting GR. Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. Human Molecular Genetics. 14: 3493-8. PMID 16207733 DOI: 10.1093/Hmg/Ddi374  0.649
2005 Groman JD, Karczeski B, Sheridan M, Robinson TE, Fallin MD, Cutting GR. Phenotypic and genetic characterization of patients with features of "nonclassic" forms of cystic fibrosis. The Journal of Pediatrics. 146: 675-80. PMID 15870673 DOI: 10.1016/J.Jpeds.2004.12.020  0.659
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