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BMC Genomics|November 20, 2016
Pooled genome wide association detects association upstream of FCRL3 with Graves' diseaseJwu Jin Khong, Kathryn P Burdon, Yi Lu, et al.
Journal of Alzheimer'S Disease : JAD|June 6, 2018
Accuracy of Inferred APOE Genotypes for a Range of Genotyping Arrays and Imputation Reference PanelsMichelle K Lupton, Sarah E Medland, Scott D Gordon, et al.
Investigative Ophthalmology & Visual Science|May 31, 2018
Family-Based Genome-Wide Association Study of South Indian Pedigrees Supports WNT7B as a Central Corneal Thickness LocusBao Jian Fan, Xueli Chen, Nisha Sondhi, et al.
Nature Genetics|August 1, 2017
A common intronic variant of PARP1 confers melanoma risk and mediates melanocyte growth via regulation of MITFJiyeon Choi, Mai Xu, Matthew M Makowski, et al.
Investigative Ophthalmology & Visual Science|January 17, 2013
Identification of a candidate gene for astigmatismMargarida C Lopes, Pirro G Hysi, Virginie J M Verhoeven, et al.
BMJ Open|March 29, 2020
Rationale and protocol for the 7- and 8-year longitudinal assessments of eye health in a cohort of young adults in the Raine StudySamantha Sze-Yee Lee, Gareth Lingham, Seyhan Yazar, et al.
Ophthalmology. Glaucoma|December 14, 2020
A Polygenic Risk Score Predicts Intraocular Pressure Readings Outside Office Hours and Early Morning Spikes as Measured by Home TonometryAyub Qassim, Sean Mullany, Mona S Awadalla, et al.
Carcinogenesis|January 8, 2013
Association between functional polymorphisms in genes involved in the MAPK signaling pathways and cutaneous melanoma riskHongliang Liu, Li-E Wang, Zhensheng Liu, et al.
Plos Genetics|May 21, 2010
Common genetic variants near the Brittle Cornea Syndrome locus ZNF469 influence the blinding disease risk factor central corneal thicknessYi Lu, David P Dimasi, Pirro G Hysi, et al.
Haematologica|March 31, 2022
Acute central nervous system toxicity during treatment of pediatric acute lymphoblastic leukemia: phenotypes, risk factors and genotypesStavroula Anastasopoulou, Rikke Linnemann Nielsen, Bodil Als-Nielsen, et al.
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