Megan Priston
North York General Hospital(CA)
Publications by Year
Research Areas
Prenatal Screening and Diagnostics, Pregnancy and preeclampsia studies, Connexins and lens biology, Glaucoma and retinal disorders, Corneal surgery and disorders
Most-Cited Works
- → Digenic Inheritance of Early-Onset Glaucoma: CYP1B1, a Potential Modifier Gene(2002)308 cited
- → The γ-Crystallins and Human Cataracts: A Puzzle Made Clearer(1999)250 cited
- Genetic heterogeneity of the Coppock-like cataract: a mutation in CRYBB2 on chromosome 22q11.2.(2000)
- → Phenotypic heterogeneity of CYP1B1: mutations in a patient with Peters' anomaly(2001)110 cited
- → Functional analyses of two newly identified PITX2 mutants reveal a novel molecular mechanism for Axenfeld-Rieger syndrome(2001)105 cited
- Further support of the role of CYP1B1 in patients with Peters anomaly.(2006)
- CRYBB1 mutation associated with congenital cataract and microcornea.(2005)
- → A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22(2001)52 cited
- → Prenatal screening for trisomy 21: a comparative performance and cost analysis of different screening strategies(2020)27 cited
- → Modified multiple marker aneuploidy screening as a primary screening test for preeclampsia(2022)13 cited