Molly Sheridan

Assistant Professor

20052018
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Fingerprint Dive into the research topics where Molly Sheridan is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 2 Similar Profiles
DiGeorge Syndrome Medicine & Life Sciences
Cystic Fibrosis Medicine & Life Sciences
Genes Medicine & Life Sciences
Mutation Medicine & Life Sciences
Congenital Heart Defects Medicine & Life Sciences
Genetic Association Studies Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Cystic Fibrosis Transmembrane Conductance Regulator Medicine & Life Sciences

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Research Output 2005 2018

Functional Assays Are Essential for Interpretation of Missense Variants Associated with Variable Expressivity

Raraigh, K. S., Han, S. T., Davis, E., Evans, T. A., Pellicore, M. J., McCague, A. F., Joynt, A. T., Lu, Z., Atalar, M., Sharma, N., Sheridan, M., Sosnay, P. R. & Cutting, G. R., Jun 7 2018, In : American Journal of Human Genetics. 102, 6, p. 1062-1077 16 p.

Research output: Contribution to journalArticle

Cystic Fibrosis
Virulence
Molecular Pathology
Human Genome
Genomics

Rare copy number variants and congenital heart defects in the 22q11.2 deletion syndrome

Mlynarski, E. E., Xie, M., Taylor, D., Sheridan, M., Guo, T., Racedo, S. E., McDonald-McGinn, D. M., Chow, E. W. C., Vorstman, J., Swillen, A., Devriendt, K., Breckpot, J., Digilio, M. C., Marino, B., Dallapiccola, B., Philip, N., Simon, T. J., Roberts, A. E., Piotrowicz, M., Bearden, C. E. & 11 others, Eliez, S., Gothelf, D., Coleman, K., Kates, W. R., Devoto, M., Zackai, E., Heine- Suñer, D., Goldmuntz, E., Bassett, A. S., Morrow, B. E. & Emanuel, B. S., Mar 1 2016, In : Human Genetics. 135, 3, p. 273-285 13 p.

Research output: Contribution to journalArticle

DiGeorge Syndrome
Congenital Heart Defects
Genes
Thoracic Aorta
Single Nucleotide Polymorphism

Copy-number variation of the glucose transporter gene SLC2A3 and congenital heart defects in the 22q11.2 deletion syndrome

Mlynarski, E. E., Sheridan, M., Xie, M., Guo, T., Racedo, S. E., McDonald-Mcginn, D. M., Gai, X., Chow, E. W. C., Vorstman, J., Swillen, A., Devriendt, K., Breckpot, J., Digilio, M. C., Marino, B., Dallapiccola, B., Philip, N., Simon, T. J., Roberts, A. E., Piotrowicz, M., Bearden, C. E. & 12 others, Eliez, S., Gothelf, D., Coleman, K., Kates, W. R., Devoto, M., Zackai, E., Heine-Suñer, D., Shaikh, T. H., Bassett, A. S., Goldmuntz, E., Morrow, B. E. & Emanuel, B. S., May 7 2015, In : American Journal of Human Genetics. 96, 5, p. 753-764 12 p.

Research output: Contribution to journalArticle

DiGeorge Syndrome
Facilitative Glucose Transport Proteins
Congenital Heart Defects
Thoracic Aorta
Genes

Analysis of the t(3;8) of hereditary renal cell carcinoma: A palindrome-mediated translocation

Kato, T., Franconi, C. P., Sheridan, M., Hacker, A. M., Inagakai, H., Glover, T. W., Arlt, M. F., Drabkin, H. A., Gemmill, R. M., Kurahashi, H. & Emanuel, B. S., 2014, In : Cancer genetics. 207, 4, p. 133-140 8 p.

Research output: Contribution to journalArticle

Chromosome Breakpoints
Chromosomes, Human, Pair 22
Chromosomes, Human, Pair 3
Renal Cell Carcinoma
Introns

The impact of chromosomal microarray on clinical management: A retrospective analysis

Henderson, L. B., Applegate, C. D., Wohler, E., Sheridan, M., Hoover Fong, J. E. & Batista, D., Sep 11 2014, In : Genetics in Medicine. 16, 9, p. 657-664 8 p.

Research output: Contribution to journalArticle

Viverridae
Insurance Carriers
Electronic Health Records
Early Detection of Cancer
Cytogenetics