John R. Gilbert, PhD
Affiliations: | Human Genetics | University of Miami, Coral Gables, FL |
Area:
http://www.researchprofiles.collexis.com/jad/expert.asp?u_id=146Website:
http://www.mihg.org/weblog/people/2008/03/john-r-gilbert.htmlGoogle:
"John Gilbert"Bio:
http://www.dukehealth.org/health_library/news/7174
http://www.researchprofiles.collexis.com/miami/expert.asp?n=John+Gilbert&u_id=758
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Cross-listing: Alzheimer's Tree - GenetiTree
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Publications
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| Rajabli F, Benchek P, Tosto G, et al. (2023) Multi-ancestry genome-wide meta-analysis of 56,241 individuals identifies and nominates ancestry-specific loci , , and as novel risk loci for Alzheimer's disease: the Alzheimer's Disease Genetics Consortium. Medrxiv : the Preprint Server For Health Sciences |
| Cukier HN, Griswold AJ, Hofmann NK, et al. (2020) Three Brothers With Autism Carry a Stop-Gain Mutation in the HPA-Axis Gene NR3C2. Autism Research : Official Journal of the International Society For Autism Research |
| Kunkle BW, Grenier-Boley B, Sims R, et al. (2019) Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nature Genetics. 51: 414-430 |
| Griswold AJ, Van Booven D, Cuccaro ML, et al. (2017) Identification of rare noncoding sequence variants in gamma-aminobutyric acid A receptor, alpha 4 subunit in autism spectrum disorder. Neurogenetics |
| Sims R, van der Lee SJ, Naj AC, et al. (2017) Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease. Nature Genetics |
| Cukier HN, Kunkle BW, Vardarajan BN, et al. (2016) ABCA7 frameshift deletion associated with Alzheimer disease in African Americans. Neurology. Genetics. 2: e79 |
| Kohli MA, Cukier HN, Hamilton-Nelson KL, et al. (2016) Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease. Neurology. Genetics. 2: e41 |
| Hicks JE, Konidari I, Scott BL, et al. (2016) Linkage of familial essential tremor to chromosome 5q35. Movement Disorders : Official Journal of the Movement Disorder Society |
| Cukier HN, Kunkle BW, Rolati S, et al. (2016) O1-09-02: Whole Exome Sequencing of Late Onset Multiplex Families Identifies Rare Coding Variants in Known and Novel Alzheimer’s Disease Genes Alzheimer's & Dementia. 12: P196-P197 |
| Griswold AJ, Dueker ND, Van Booven D, et al. (2015) Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants. Molecular Autism. 6: 43 |