J. Gilbert

J. Gilbert, J. Haines, M. Pericak-Vance, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Physical and cDNA Mapping in the DBH Region of Human Chromosome 9q34

J. Gilbert, M. Pericak-Vance, P. Xu, 2000, Human Heredity.

Fine mapping of autistic disorder to chromosome 15q11‐q13 by use of phenotypic subtypes.

M A Pericak-Vance, J. Gilbert, M. Cuccaro, 2003, American journal of human genetics.

Phenotypic homogeneity provides increased support for linkage on chromosome 2 in autistic disorder.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2001, American journal of human genetics.

Genome-wide association study implicates a chromosome 12 risk locus for late-onset Alzheimer disease.

Eden R Martin, John R Gilbert, Jonathan L Haines, 2009, American journal of human genetics.

Evaluating Mitochondrial DNA Variation in Autism Spectrum Disorders

J. Gilbert, M. Cuccaro, J. Haines, 2013, Annals of human genetics.

Age at onset in two common neurodegenerative diseases is genetically controlled.

Rajesh Pahwa, Fengyu Zhang, Kristin K Nicodemus, 2002, American journal of human genetics.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

High Density SNP Screen in A Large Multiplex Neural Tube Defect Family Refines Linkage to Loci at 7p21-Pter And 2q33.1-35

J. Gilbert, D. Stephan, Diane Hu-Lince, 2014 .

Linkage and association of successful aging to the 6q25 region in large Amish kindreds

J. Gilbert, J. Haines, M. Pericak-Vance, 2012, AGE.

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

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2020, Nature Communications.

Mutation analysis of presenillin 1 gene in Alzheimer's disease.

J. Gilbert, G. Small, P. Xu, 1996, Lancet.

Mutation analysis of presenilin 1 gene in Alzheimer's disease

J. Gilbert, P. Xu, K. Boteva, 1996, The Lancet.

Dementia revealed: Novel chromosome 6 locus for late-onset Alzheimer's disease provides genetic evidence for folate-pathway abnormalities

J. Gilbert, J. Buxbaum, J. Haines, 2010, Alzheimer's & Dementia.

Mitochondrial Haplogroup X is associated with successful aging in the Amish

J. Gilbert, J. Haines, M. Pericak-Vance, 2011, Human Genetics.

Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Nick C Fox, Michelle K. Lupton, Charles C. White, 2019, Nature Genetics.

Assignment of the human slow skeletal troponin T gene to 19q13.4 using somatic cell hybrids and fluorescence in situ hybridization analysis.

B. Trask, J. Gilbert, P. D. de Jong, 1992, Genomics.

Supervised Machine Learning for Risk Stratification of Influenza-Like Illness: A Model to Prioritize Emerging Infectious Disease Disaster Responses

J. Gilbert, Y. Oyang, F. Shih, 2021 .

Isolation and localization of a slow troponin (TnT) gene on chromosome 19 by subtraction hybridization of a cDNA muscle library using myotonic dystrophy muscle cDNA

J. Gilbert, W. Hung, A. Roses, 1990, Journal of Neuroscience Research.

Linkage studies in facioscapulohumeral muscular dystrophy (FSHD).

J. Gilbert, A. Roses, J. Vance, 1992, American journal of human genetics.

Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD).

J. Gilbert, M. Pericak-Vance, J. Vance, 1993, American journal of human genetics.

The gene encoding ganglioside- induced differentiation-associated protein 1 is mutated in axonal Charcot-Marie-Tooth type 4A disease

J. Gilbert, M. Pericak-Vance, J. Vance, 2001 .

Differential neurotrophic effects of apolipoprotein E in aged transgenic mice

J. Gilbert, E. Masliah, M. Mallory, 1999, Neuroscience Letters.

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

J. Gilbert, M. Cuccaro, J. Haines, 2009, Annals of human genetics.

Ganglioside-induced differentiation-associated protein-1 is mutant in Charcot-Marie-Tooth disease type 4A/8q21

J. Gilbert, M. Pericak-Vance, J. Vance, 2002, Nature Genetics.

Linkage studies of late-onset familial Alzheimer's disease.

J. Gilbert, M. Pericak-Vance, A. Roses, 1990, Advances in neurology.

Exploring the Relationship Between Autism Spectrum Disorder and Epilepsy Using Latent Class Cluster Analysis

J. Gilbert, M. Cuccaro, J. Haines, 2011, Journal of Autism and Developmental Disorders.

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study.

D. G. Clark, C. Carlson, K. Lunetta, 2014, JAMA neurology.

The Expanding Role of MBD Genes in Autism: Identification of a MECP2 Duplication and Novel Alterations in MBD5, MBD6, and SETDB1

Juan I. Young, John R Gilbert, Jonathan L Haines, 2012, Autism research : official journal of the International Society for Autism Research.

Novel variants identified in methyl-CpG-binding domain genes in autistic individuals

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2010, neurogenetics.

Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in Iceland.

J. Gilbert, J. Vance, F. Jónasson, 2000, Molecular vision.

Physical and genetic mapping of the macular corneal dystrophy locus on chromosome 16q and exclusion of TAT and LCAT as candidate genes.

J. Gilbert, J. Vance, F. Jónasson, 2000, Molecular vision.

Lewy body and Alzheimer pathology in a family with the amyloid-β precursor protein APP717 gene mutation

J. Gilbert, M. Pericak-Vance, A. Saunders, 2000, Acta Neuropathologica.

Association and gene–gene interaction of SLC6A4 and ITGB3 in autism

E R Martin, M A Pericak-Vance, J. Gilbert, 2010, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Convergent genetic and expression data implicate immunity in Alzheimer's disease

J. Gallacher, K. Lunetta, M. Nalls, 2014, Alzheimer's & Dementia.

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

Genetic studies of autistic disorder and chromosome 7.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 1999, Genomics.

Analysis of association at single nucleotide polymorphisms in the APOE region.

J. Gilbert, M. Pericak-Vance, A. Roses, 2000, Genomics.

T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families.

J. Gilbert, E. Rampersaud, K. Viles, 2002, American journal of medical genetics.

Three Brothers With Autism Carry a Stop‐Gain Mutation in the HPA‐Axis Gene NR3C2

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2020, Autism research : official journal of the International Society for Autism Research.

Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants

Derek J Van Booven, J. Gilbert, M. Cuccaro, 2015, Molecular Autism.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

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

Eden R Martin, Derek Van Booven, Susan H Slifer, 2014, Molecular Autism.

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

Joseph T. Glessner, Stephen J. Guter, D. Pinto, 2011, Human Genetics.

A new human slow skeletal troponin T (TnTs) mRNA isoform derived from alternative splicing of a single gene.

J. Gilbert, A. Roses, F. Samson, 1994, Biochemical and biophysical research communications.

EXCEPTIONALLY LOW LIKELIHOOD OF ALZHEIMER'S DEMENTIA IN APOE2 HOMOZYGOTES

C. Carlson, Jonathan, K. Lunetta, 2019, medRxiv.

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

Nick C Fox, Michelle K. Lupton, Charles C. White, 2019, Nature Genetics.

Genomic screen and follow-up analysis for autistic disorder.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2002, American journal of medical genetics.

Copy Number Variants in Extended Autism Spectrum Disorder Families Reveal Candidates Potentially Involved in Autism Risk

Scott M. Williams, J. Gilbert, M. Cuccaro, 2011, PloS one.

Retrospective analysis of The Two Sister Study using haplotype-based association testing to identify loci associated with early-onset breast cancer

J. Gilbert, G. Cooper, J. Losee, 2020, medRxiv.

Association Analysis of Chromosome 15 GABAA Receptor Subunit Genes in Autistic Disorder

E R Martin, M A Pericak-Vance, J. Gilbert, 2001, Journal of neurogenetics.

No association between the APOE gene and autism

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Three probands with autistic disorder and isodicentric chromosome 15.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2000, American journal of medical genetics.

Genetic linkage studies in Alzheimer's disease families

J. M. Vance, J. L. Haines, A. D. Roses, 1988, Experimental Neurology.

Segregation of a rare TTC3 variant in an extended family with late-onset Alzheimer disease

Margaret A. Pericak-Vance, Jonathan L. Haines, Lindsay A. Farrer, 2016, Neurology: Genetics.

SNPs in the neural cell adhesion molecule 1 gene (NCAM1) may be associated with human neural tube defects

J. Gilbert, D. McClay, A. Bassuk, 2005, Human Genetics.

Autistic disorder and chromosome 15q11-q13: construction and analysis of a BAC/PAC contig.

J. Gilbert, M. Pericak-Vance, J. Vance, 1999, Genomics.

Integrated whole transcriptome and DNA methylation analysis identifies gene networks specific to late-onset Alzheimer's disease.

Eden Martin, Deborah C Mash, J. Gilbert, 2015, Journal of Alzheimer's disease : JAD.

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation

J. Gilbert, M. Pericak-Vance, S. Züchner, 2014, Alzheimer's & Dementia.

Genetic Linkage Studies in Late-Onset Alzheimer’s Disease Families

J. Gilbert, J. Haines, M. Pericak-Vance, 1988 .

Identification of chromosome 7 inversion breakpoints in an autistic family narrows candidate region for autism susceptibility

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2009, Autism research : official journal of the International Society for Autism Research.

Two knockdown models of the autism genes SYNGAP1 and SHANK3 in zebrafish produce similar behavioral phenotypes associated with embryonic disruptions of brain morphogenesis.

J. Gilbert, J. Buxbaum, M. Cuccaro, 2015, Human molecular genetics.

Glutathione S-transferase omega-1 modifies age-at-onset of Alzheimer disease and Parkinson disease.

Eden R Martin, Rajesh Pahwa, Clemens R Scherzer, 2003, Human molecular genetics.

Alzheimer disease (AD) specific transcription, DNA methylation and splicing in twenty AD associated loci

J. Gilbert, M. Pericak-Vance, D. Mash, 2015, Molecular and Cellular Neuroscience.

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2.

J. Gilbert, A. Bassuk, E. Linney, 2005, Birth defects research. Part A, Clinical and molecular teratology.

Exploring the Relationship Between Autism Spectrum Disorder and Epilepsy Using Latent Class Cluster Analysis

Jonathan L. Haines, John R. Gilbert, Ruth K. Abramson, 2011, Journal of Autism and Developmental Disorders.

A Comparison of Repetitive Behaviors in Aspergers Disorder and High Functioning Autism

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2007, Child psychiatry and human development.

A new probe for the diagnosis of myotonic muscular dystrophy.

J. Gilbert, M. Pericak-Vance, T. Mohandas, 1987, Science.

Variants in several genomic regions associated with asperger disorder

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2010, Autism research : official journal of the International Society for Autism Research.

Lack of association between autism and SLC25A12.

Eden R Martin, John R Gilbert, Jonathan L Haines, 2006, The American journal of psychiatry.

An Analysis Paradigm for Investigating Multi‐locus Effects in Complex Disease: Examination of Three GABAA Receptor Subunit Genes on 15q11‐q13 as Risk Factors for Autistic Disorder.

E R Martin, M A Pericak-Vance, J. Gilbert, 2006, Annals of human genetics.

Identification of significant association and gene-gene interaction of GABA receptor subunit genes in autism.

E R Martin, M A Pericak-Vance, J. Gilbert, 2005, American journal of human genetics.

Ordered‐subset analysis of savant skills in autism for 15q11‐q13

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes

J. Sutcliffe, J. Gilbert, M. Cuccaro, 2004, Neuroscience Letters.

No association between the WNT2 gene and autistic disorder.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2002, American journal of medical genetics.

Linkage disequilibrium at the Angelman syndrome gene UBE3A in autism families.

J. Sutcliffe, S. Folstein, J. Gilbert, 2001, Genomics.

Analysis of linkage disequilibrium in gamma-aminobutyric acid receptor subunit genes in autistic disorder.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2000, American journal of medical genetics.

Microduplications in an autism multiplex family narrow the region of susceptibility for developmental disorders on 15q24 and implicate 7p21

Scott M. Williams, J. Gilbert, M. Cuccaro, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1

J. Gilbert, D. Stephan, V. Zismann, 2008, Neurology.

A duplication in chromosome 4q35 is associated with hereditary benign intraepithelial dyskeratosis.

J. Gilbert, M. Pericak-Vance, J. Vance, 2001, American journal of human genetics.

Refinement of 2q and 7p loci in a large multiplex NTD family.

J. Gilbert, D. Stephan, J. Connelly, 2008, Birth defects research. Part A, Clinical and molecular teratology.

Detailed analysis of allelic variation in the ABCA4 gene in age-related maculopathy.

J. Gilbert, J. Haines, M. Pericak-Vance, 2003, Investigative ophthalmology & visual science.

Analysis of the Stargardt disease gene (ABCR) in age-related macular degeneration.

J. Gilbert, J. Haines, M. Pericak-Vance, 1999, Ophthalmology.

Phenotypic definition of Chiari type I malformation coupled with high‐density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15

J. Gilbert, D. Stephan, B. Green, 2006, American journal of medical genetics. Part A.

Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14

J. Gilbert, M. Cuccaro, J. Haines, 2007, Molecular Psychiatry.

Duchenne muscular dystrophy

J. Gilbert, M. Pericak-Vance, R. Bartlett, 1988, Neurology.

Neural Tube Defects and Folate Pathway Genes: Family-Based Association Tests of Gene–Gene and Gene–Environment Interactions

J. Gilbert, H. Nijhout, M. Reed, 2006, Environmental health perspectives.

TERC is not a major gene in human neural tube defects.

J. Gilbert, A. Bassuk, J. Kessler, 2004, Birth defects research. Part A, Clinical and molecular teratology.

MCP1 SNPs and Pulmonary Tuberculosis in Cohorts from West Africa, the USA and Argentina: Lack of Association or Epistasis with IL12B Polymorphisms

Scott M. Williams, J. Gilbert, G. Sirugo, 2012, PloS one.

A de novo 1.5 Mb microdeletion on chromosome 14q23.2‐23.3 in a patient with autism and spherocytosis

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2011, Autism research : official journal of the International Society for Autism Research.

Evidence for locus heterogeneity in the Bethlem myopathy and linkage to 2q37.

J. Gilbert, M. Pericak-Vance, J. Vance, 1996, Human molecular genetics.

Hypothesis: Microtubule Instability and Paired Helical Filament Formation in the Alzheimer Disease Brain Are Related to Apolipoprotein E Genotype

Margaret A. Pericak-Vance, Seol-Heui Han, John R. Gilbert, 1994, Experimental Neurology.

Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4

J. Gilbert, J. Stajich, R. Frants, 2007, Neurology.

Investigation of potential gene–gene interactions between apoe and reln contributing to autism risk

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2007, Psychiatric genetics.

Sample degradation leads to false-positive copy number variation calls in multiplex real-time polymerase chain reaction assays.

J. Gilbert, M. Pericak-Vance, D. Hedges, 2009, Analytical biochemistry.

An X chromosome-wide association study in autism families identifies TBL1X as a novel autism spectrum disorder candidate gene in males

J. Gilbert, H. Hakonarson, Kai Wang, 2011, Molecular autism.

C9ORF72 Intermediate Repeat Copies Are a Significant Risk Factor for Parkinson Disease

Juan I. Young, J. Gilbert, J. Haines, 2013, Annals of human genetics.

Genetic studies in autistic disorder and chromosome 15

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2000, Neurogenetics.

Examination of tetrahydrobiopterin pathway genes in autism

J. Gilbert, M. Pericak-Vance, N. Schnetz-Boutaud, 2009, Genes, brain, and behavior.

Examination of association of genes in the serotonin system to autism

J. L. Haines, J. Gilbert, M. Cuccaro, 2009, neurogenetics.

Examination of association to autism of common genetic variationin genes related to dopamine

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2008, Autism research : official journal of the International Society for Autism Research.

Autism in African American Families: Clinical‐phenotypic findings

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Female with autistic disorder and monosomy X (Turner syndrome): parent-of-origin effect of the X chromosome.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2000, American journal of medical genetics.

A role for apoE in regulating the levels of alpha-1-antichymotrypsin in the aging mouse brain and in Alzheimer's disease.

J. Gilbert, E. Masliah, M. Mallory, 1999, The American journal of pathology.

Shared genetic contribution to ischemic stroke and Alzheimer's disease

Nick C Fox, C. Sudlow, J. Gallacher, 2016, Annals of neurology.

Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease

J. Gilbert, M. Cuccaro, J. Haines, 2017, Neuroscience Letters.

Vitamin D receptor and Alzheimer's disease: a genetic and functional study

J. Gilbert, J. Haines, M. Pericak-Vance, 2012, Neurobiology of Aging.

Mitochondrial Haplogroup X is associated with successful aging in the Amish

J. Gilbert, J. Haines, M. Pericak-Vance, 2012, Human Genetics.

Rarity of the Alzheimer disease-protective APP A673T variant in the United States.

D. G. Clark, C. Carlson, K. Lunetta, 2015, JAMA neurology.

De novo partial duplication of chromosome 7p in a male with autistic disorder.

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2001, American journal of medical genetics.

Award Number: W81XWH-12-1-0013 TITLE: Whole Exome Analysis of Early Onset Alzheimer’s Disease PRINCIPAL INVESTIGATOR: Margaret Pericak-Vance CONTRACTING ORGANIZATION: University of Miami

J. Gilbert, E. Martin, J. Vance, 2016 .

Human Apolipoprotein E Isoform‐Specific Differences in Neuronal Sprouting in Organotypic Hippocampal Culture

J. Gilbert, A. Roses, D. Galasko, 1999, Journal of neurochemistry.

Disease Expression and Gene Expression Can Be Quite Distinct: Modulation of Skeletal Muscle Sodium Channels by the Human Myotonin Dystrophy Protein Kinase (HMPK)*

J. Gilbert, A. Roses, P. Xu, 1996 .

Modulation of skeletal muscle sodium channels by human myotonin protein kinase.

J. Gilbert, A. Roses, J. Mounsey, 1995, The Journal of clinical investigation.

Interleukin 12B (IL12B) Genetic Variation and Pulmonary Tuberculosis: A Study of Cohorts from The Gambia, Guinea-Bissau, United States and Argentina

Scott M. Williams, J. Gilbert, G. Sirugo, 2011, PloS one.

Screening for MECP2 mutations in females with autistic disorder

J. Gilbert, M. Cuccaro, M. Pericak-Vance, 2001 .

The identification and characterization of KRAB-domain-containing zinc finger proteins.

J. Gilbert, R. Bartlett, A. Roses, 1992, Genomics.

Autism, Stress, and Chromosome 7 Genes

J. Gilbert, M. Shapira, H. Soreq, 2002 .

Repeat expansions in the C9ORF72 gene contribute to Alzheimer's disease in Caucasians

J. Gilbert, J. Haines, M. Pericak-Vance, 2013, Neurobiology of Aging.

Defectiv eNeurona lSproutin gb yHuman Apolipoprotei nE 4I sa Gain-of-Negative Function

J. Gilbert, A. Roses, D. Galasko, 2002 .

Model of Genetic Susceptibility to Late-Onset Alzheimer’s Disease: Mice Transgenic for Human Apolipoprotein E Alleles

J. Gilbert, A. Roses, P. Xu, 1999 .

Ordered-subsets linkage analysis detects novel Alzheimer disease loci on chromosomes 2q34 and 15q22.

J. Gilbert, J. Haines, M. Pericak-Vance, 2003, American journal of human genetics.

Independent effects of complement factor H Y402H polymorphism and cigarette smoking on risk of age-related macular degeneration.

J. Gilbert, J. Haines, M. Pericak-Vance, 2007, Ophthalmology.

Effect of heterogeneity on the chromosome 10 risk in late‐onset Alzheimer disease

J. Gilbert, J. Haines, M. Pericak-Vance, 2007, Human mutation.

Lack of association between UBQLN1 and Alzheimer disease

J. Gilbert, M. Pericak-Vance, P. Doraiswamy, 2006, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics.

Genomic convergence to identify candidate genes for Alzheimer Disease on chromosome 10

Stephan Züchner, J. Gilbert, J. Haines, 2009, Human mutation.

Covariate analysis of late-onset Alzheimer disease refines the chromosome 12 locus

J. Gilbert, J. Haines, M. Pericak-Vance, 2006, Molecular Psychiatry.

Linkage and association of successful aging to the 6q25 region in large Amish kindreds

J. Gilbert, J. Haines, M. Pericak-Vance, 2013, AGE.

Isolation of a cytochrome oxidase gene overexpressed in Alzheimer's disease brain

J. Gilbert, A. Roses, L. Middleton, 1992, Molecular and Cellular Neuroscience.

Functional candidate genes in age-related macular degeneration: significant association with VEGF, VLDLR, and LRP6.

J. Gilbert, J. Haines, M. Pericak-Vance, 2006, Investigative ophthalmology & visual science.

Association Analysis of Genetic Polymorphisms in the CDC2 Gene with Late-Onset Alzheimer Disease

J. Gilbert, J. Haines, M. Pericak-Vance, 2006, Dementia and Geriatric Cognitive Disorders.

Clinical Studies in Non-chromosome 4-Linked Facioscapulohumeral Muscular Dystrophy

J. Gilbert, M. Pericak-Vance, E. Rampersaud, 2001, Journal of clinical neuromuscular disease.

Human Apolipoprotein E2, E3, and E4 Isoform-Specific Transgenic Mice: Human-like Pattern of GlialandNeuronal Immunoreactivity in Central Nervous System Not Observed in Wild-Type Mice

J. Gilbert, A. Roses, P. Xu, 1996, Neurobiology of Disease.

Association of the apolipoprotein E gene with age-related macular degeneration: possible effect modification by family history, age, and gender.

J L Haines, M A Pericak-Vance, S Schmidt, 2000, Molecular vision.

Comparing age-related macular degeneration phenotype in probands from singleton and multiplex families.

J. Gilbert, J. Haines, M. Pericak-Vance, 2005, American journal of ophthalmology.

Parsing the genetic heterogeneity of chromosome 12q susceptibility genes for Alzheimer disease by family-based association analysis

Margaret A. Pericak-Vance, P. Murali Doraiswamy, Jonathan L. Haines, 2006, Neurogenetics.

Morphological, Biochemical, and Genetic Support for an Apolipoprotein E Effect on Microtubular Metabolism a

J. Gilbert, M. Pericak-Vance, A. Roses, 1996, Annals of the New York Academy of Sciences.

Joint effects of smoking history and APOE genotypes in age-related macular degeneration.

J. Gilbert, J. Haines, M. Pericak-Vance, 2005, Molecular vision.

Manifestations of Alzheimer’s disease genetic risk in the blood are evident in a multiomic analysis in healthy adults aged 18 to 90

Benjamin A. Logsdon, Cory C. Funk, John C. Earls, 2022, Scientific Reports.

Sialylated Human Apolipoprotein E (apoEs) Is Preferentially Associated with Neuron-Enriched Cultures from APOE Transgenic Mice

J. Gilbert, A. Roses, P. Xu, 1999, Neurobiology of Disease.

Linkage of familial essential tremor to chromosome 5q35

J. Gilbert, W. Scott, A. Ashley-Koch, 2016, Movement disorders : official journal of the Movement Disorder Society.

Specific regional transcription of apolipoprotein E in human brain neurons.

J. Gilbert, P. Xu, C. Hulette, 1999, The American journal of pathology.

PCDH11X variation is not associated with late-onset Alzheimer disease susceptibility

J. Gilbert, J. Buxbaum, J. Haines, 2010, Psychiatric genetics.

ABCA7 frameshift deletion associated with Alzheimer disease in African Americans

Derek J Van Booven, J. Gilbert, M. Cuccaro, 2016, Neurology: Genetics.

Exploring the association of glyceraldehyde-3-phosphate dehydrogenase gene and Alzheimer disease

J. Gilbert, J. Haines, M. Pericak-Vance, 2006, Neurology.

Resolving the relationship between ApolipoproteinE and depression

J. Gilbert, J. Haines, M. Pericak-Vance, 2009, Neuroscience Letters.

Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians.

J. Gilbert, C. Hamilton, W. Scott, 2009, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

NOS2A, TLR4, and IFNGR1 interactions influence pulmonary tuberculosis susceptibility in African-Americans

Carol D. Hamilton, John R. Gilbert, William K. Scott, 2009, Human Genetics.

Regionally specific neuronal expression of human APOE gene in transgenic mice

J. Gilbert, A. Roses, P. Xu, 1998, Neuroscience Letters.

Cis-Acting Human ApoE Tissue Expression Element is Associated with Human Pattern of Intraneuronal ApoE in Transgenic Mice

J. Gilbert, A. Roses, P. Xu, 1998, Neurobiology of Aging.

No Association between SNP rs498055 on Chromosome 10 and Late‐Onset Alzheimer Disease in Multiple Datasets

J. Gilbert, J. Haines, M. Pericak-Vance, 2007, Annals of human genetics.

Interaction between the α-T catenin gene (VR22) and APOE in Alzheimer’s disease

J. Gilbert, M. Pericak-Vance, N. Schnetz-Boutaud, 2005, Journal of Medical Genetics.

TO JMG Interaction between the a-T catenin gene ( VR 22 ) and APOE in Alzheimer ’ s disease

J. Gilbert, J. Haines, M. Pericak-Vance, 2005 .