Laura K. Conlin, Ph.D.
Affiliations: | 2007 | University of Pennsylvania, Philadelphia, PA, United States |
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"Laura Conlin"Parents
Sign in to add mentorHillary C. Nelson | grad student | 2007 | Penn | |
(Trehalose is a positive regulator of the heat-induced activity of yeast heat shock transcription factor.) |
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Publications
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Larson DP, Akkari YM, Van Dyke DL, et al. (2020) Conventional Cytogenetic Analysis of Hematologic Neoplasms: A 20-Year Review of Proficiency Test Results From the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee. Archives of Pathology & Laboratory Medicine |
Rentas S, Pillai V, Wertheim GB, et al. (2020) Evolution of histomorphologic, cytogenetic, and genetic abnormalities in an untreated patient with MIRAGE syndrome. Cancer Genetics. 245: 42-48 |
Kawamura R, Kato T, Miyai S, et al. (2020) A case of a parthenogenetic 46,XX/46,XY chimera presenting ambiguous genitalia. Journal of Human Genetics |
Rajagopalan R, Murrell JR, Luo M, et al. (2020) A highly sensitive and specific workflow for detecting rare copy-number variants from exome sequencing data. Genome Medicine. 12: 14 |
Gilbert MA, Schultz-Rogers L, Rajagopalan R, et al. (2020) Protein-elongating mutations in MYH11 are implicated in a dominantly-inherited smooth muscle dysmotility syndrome with severe esophageal, gastric, and intestinal disease. Human Mutation |
Sheppard SE, Lalonde E, Adzick NS, et al. (2019) Androgenetic chimerism as an etiology for Beckwith-Wiedemann syndrome: diagnosis and management. Genetics in Medicine : Official Journal of the American College of Medical Genetics |
Wu C, Devkota B, Evans P, et al. (2019) Rapid and accurate interpretation of clinical exomes using Phenoxome: a computational phenotype-driven approach. European Journal of Human Genetics : Ejhg |
Correll-Tash S, Conlin L, Mininger BA, et al. (2018) The Recurrent t(11;22)(q23;q11.2) Can Occur as a Post-Zygotic Event. Cytogenetic and Genome Research |
Carson JC, Hoffner L, Conlin L, et al. (2018) Diploid/triploid mixoploidy: A consequence of asymmetric zygotic segregation of parental genomes. American Journal of Medical Genetics. Part A |
Salzano E, Raible SE, Kaur M, et al. (2018) Prenatal profile of Pallister-Killian syndrome: Retrospective analysis of 114 pregnancies, literature review and approach to prenatal diagnosis. American Journal of Medical Genetics. Part A |