Molly B. Sheridan, Ph.D.
Affiliations: | 2008 | Johns Hopkins University, Baltimore, MD |
Area:
Genetics, Molecular BiologyGoogle:
"Molly Sheridan"Parents
Sign in to add mentor| Garry R. Cutting | grad student | 2008 | Johns Hopkins | |
| (Genetic heterogeneity in cystic fibrosis.) | ||||
BETA: Related publications
See more...
Publications
|
You can help our author matching system! If you notice any publications incorrectly attributed to this author, please sign in and mark matches as correct or incorrect. |
| Collaco JM, Raraigh KS, Betz J, et al. (2021) Accurate assignment of disease liability to genetic variants using only population data. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
| Raraigh KS, Han ST, Davis E, et al. (2018) Functional Assays Are Essential for Interpretation of Missense Variants Associated with Variable Expressivity. American Journal of Human Genetics |
| Sheridan MB, Wohler E, Batista DA, et al. (2015) 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 |
| Henderson LB, Applegate CD, Wohler E, et al. (2014) 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 |
| Sheridan MB, Hefferon TW, Wang N, et al. (2011) 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 |
| Férec C, Casals T, Chuzhanova N, et al. (2006) 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 |
| Sheridan MB, Fong P, Groman JD, et al. (2005) Mutations in the beta-subunit of the epithelial Na+ channel in patients with a cystic fibrosis-like syndrome. Human Molecular Genetics. 14: 3493-8 |
| Groman JD, Karczeski B, Sheridan M, et al. (2005) Phenotypic and genetic characterization of patients with features of "nonclassic" forms of cystic fibrosis. The Journal of Pediatrics. 146: 675-80 |