John R. Gilbert

Research interests

Publications

• Exceptionally low likelihood of Alzheimer’s dementia in APOE2 homozygotes from a 5,000-person neuropathological study

  Nature Communications · 2020 · https://doi.org/10.1038/s41467-019-14279-8

• Transethnic genome‐wide scan identifies novel Alzheimer's disease loci

  Alzheimer s & Dementia · 2017 · https://doi.org/10.1016/j.jalz.2016.12.012

• Assessment of the genetic variance of late-onset Alzheimer's disease

  Neurobiology of Aging · 2016 · https://doi.org/10.1016/j.neurobiolaging.2016.02.024

• Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

  Molecular Autism · 2014 · https://doi.org/10.1186/2040-2392-5-1

• Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

  The American Journal of Human Genetics · 2014 · https://doi.org/10.1016/j.ajhg.2014.03.018

• Effects of Multiple Genetic Loci on Age at Onset in Late-Onset Alzheimer Disease

  JAMA Neurology · 2014 · https://doi.org/10.1001/jamaneurol.2014.1491

• Individual common variants exert weak effects on the risk for autism spectrum disorders

  Human Molecular Genetics · 2012 · https://doi.org/10.1093/hmg/dds301

• A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

  Human Genetics · 2011 · https://doi.org/10.1007/s00439-011-1094-6

• Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

  Nature Genetics · 2011 · https://doi.org/10.1038/ng.801

• A noise-reduction GWAS analysis implicates altered regulation of neurite outgrowth and guidance in autism

  Molecular Autism · 2011 · https://doi.org/10.1186/2040-2392-2-1

• Functional impact of global rare copy number variation in autism spectrum disorders

  Nature · 2010 · https://doi.org/10.1038/nature09146

• Common genetic variants on 5p14.1 associate with autism spectrum disorders

  Nature · 2009 · https://doi.org/10.1038/nature07999

• A Genome‐wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1

  Annals of Human Genetics · 2009 · https://doi.org/10.1111/j.1469-1809.2009.00523.x

• Mapping autism risk loci using genetic linkage and chromosomal rearrangements

  Nature Genetics · 2007 · https://doi.org/10.1038/ng1985

• Approximating Treewidth, Pathwidth, Frontsize, and Shortest Elimination Tree

  Journal of Algorithms · 1995 · https://doi.org/10.1006/jagm.1995.1009

Current projects

No projects listed.