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Jason J. Corneveaux · SciRah

Researcher profile · Semantic Scholar

Jason J. Corneveaux

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Jason J. Corneveaux — researcher profile on SciRah

h-index: 43
Works: 86
Citations: 8,026

Most-cited papers

Common variants in MS4A4/MS4A6E, CD2uAP, CD33, and EPHA1 are associated with late-onset Alzheimer’s disease
A. Naj, G. Jun, G. Beecham, Li-San Wang +151 more
2011Nature Genetics1,897 citations Open access
Semantic Scholar
Common Kibra Alleles Are Associated with Human Memory Performance
A. Papassotiropoulos, D. Stephan, M. Huentelman, F. Hoerndli +16 more
2006Science433 citations Open access
Semantic Scholar
Small cell carcinoma of the ovary, hypercalcemic type, displays frequent inactivating germline and somatic mutations in SMARCA4
Pilar Ramos, A. Karnezis, David W. Craig, A. Sekulic +23 more
2014Nature Genetics350 citations Open access
Semantic Scholar
Genome-Wide Association Meta-analysis of Neuropathologic Features of Alzheimer's Disease and Related Dementias
G. Beecham, K. Hamilton, A. Naj, Eden R. Martin +32 more
2014PLoS Genetics345 citations Open access
Semantic Scholar
Voxelwise genome-wide association study (vGWAS)
J. Stein, Xue Hua, Suh Lee, A. J. Ho +16 more
2010NeuroImage297 citations Open access
Semantic Scholar
IDENTIFICATION OF GENETIC VARIANTS USING BARCODED MULTIPLEXED SEQUENCING
David W. Craig, John V. Pearson, S. Szelinger, Aswin Sekar +8 more
2008Nature Methods267 citations Open access
Semantic Scholar
A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly
A. J. Ho, J. Stein, Xue Hua, Suh Lee +24 more
2010Proceedings of the National Academy of Sciences of the United States of America263 citations Open access
Semantic Scholar
Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.
Jason J. Corneveaux, Amanda J. Myers, April N. Allen, J. Pruzin +24 more
2010Human Molecular Genetics257 citations Open access
Semantic Scholar
GRM7 variants confer susceptibility to age-related hearing impairment.
R. Friedman, L. Van Laer, M. Huentelman, Sonal S. Sheth +28 more
2009Human Molecular Genetics214 citations Open access
Semantic Scholar
A genome-wide scan for common variants affecting the rate of age-related cognitive decline
P. De Jager, J. Shulman, Lori B. Chibnik, B. Keenan +16 more
2011Neurobiology of Aging193 citations Open access
Semantic Scholar
CR1 is associated with amyloid plaque burden and age-related cognitive decline
Lori B. Chibnik, Joshua M. Shulman, S. Leurgans, J. Schneider +13 more
2011Annals of Neurology184 citations Open access
Semantic Scholar
Genome-wide association between DNA methylation and alternative splicing in an invertebrate
Kevin B. Flores, F. Wolschin, Jason J. Corneveaux, April N. Allen +2 more
2012BMC Genomics171 citations Open access
Semantic Scholar
Genetic Susceptibility for Alzheimer’s Disease Neuritic Plaque Pathology
J. Shulman, Ke-Wei Chen, B. Keenan, Lori B. Chibnik +13 more
2013JAMA Neurology169 citations Open access
Semantic Scholar
Genome-Wide Analysis Reveals Novel Genes Influencing Temporal Lobe Structure with Relevance to Neurodegeneration in Alzheimer’s Disease
J. Stein, Xue Hua, J. Morra, Suh Lee +23 more
2010NeuroImage154 citations Open access
Semantic Scholar
Reduced Posterior Cingulate Mitochondrial Activity in Expired Young Adult Carriers of the APOE ε4 Allele, the Major Late-Onset Alzheimer's Susceptibility Gene
J. Valla, R. Yaari, Andrew B. Wolf, Yael Kusne +6 more
2010Journal of Alzheimer's Disease150 citations Open access
Semantic Scholar
Variants in triggering receptor expressed on myeloid cells 2 are associated with both behavioral variant frontotemporal lobar degeneration and Alzheimer’s disease
M. Giraldo, F. Lopera, A. Siniard, Jason J. Corneveaux +10 more
2013Neurobiology of Aging146 citations Open access
Semantic Scholar
Transcriptomic Analysis of Tail Regeneration in the Lizard Anolis carolinensis Reveals Activation of Conserved Vertebrate Developmental and Repair Mechanisms
Elizabeth D. Hutchins, Glenn J. Markov, W. Eckalbar, Rajani M. George +15 more
2014PLoS ONE137 citations Open access
Semantic Scholar
Evidence for an association between KIBRA and late-onset Alzheimer’s disease
Jason J. Corneveaux, W. Liang, E. Reiman, Jennifer Webster +29 more
2008Neurobiology of Aging115 citations Open access
Semantic Scholar
Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment
E. Fransen, Sarah Bonneux, Jason J. Corneveaux, I. Schrauwen +8 more
2014European Journal of Human Genetics106 citations Open access
Semantic Scholar
Mechanisms of CO2/H+ Sensitivity of Astrocytes
E. Turovsky, Shefeeq M. Theparambil, V. Kasymov, J. Deitmer +8 more
2016Journal of Neuroscience104 citations Open access
Semantic Scholar
Hypometabolism in Alzheimer's-Affected Brain Regions in Cognitively Normal Latinos Carrying the Apolipoprotein E ε4 Allele
J. Langbaum, Ke-Wei Chen, R. Caselli, Wendy Lee +12 more
2010Archives of Neurology101 citations Open access
Semantic Scholar
Peripheral Delivery of a ROCK Inhibitor Improves Learning and Working Memory
M. Huentelman, D. Stephan, J. Talboom, Jason J. Corneveaux +6 more
2009Behavioral Neuroscience99 citations Open access
Semantic Scholar
Analysis of Copy Number Variation in Alzheimer’s Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals
S. Swaminathan, M. Huentelman, Jason J. Corneveaux, Amanda J. Myers +9 more
2012PLoS ONE95 citations Open access
Semantic Scholar
DNA Diagnostics of Hereditary Hearing Loss: A Targeted Resequencing Approach Combined with a Mutation Classification System
M. Sommen, I. Schrauwen, G. Vandeweyer, N. Boeckx +16 more
2016Human Mutation88 citations Open access
Semantic Scholar
Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance.
M. Huentelman, A. Papassotiropoulos, David W. Craig, F. Hoerndli +10 more
2007Human Molecular Genetics88 citations Open access
Semantic Scholar
A coding variant in CR1 interacts with APOE-1 4 to inﬂuence cognitive decline
B. Keenan, J. Shulman, Lori B. Chibnik, T. Raj +13 more
201287 citations
Semantic Scholar
2014 ACVIM Forum Research Abstracts Program
Ashley Taylor, C. Welsh, C. E. Young, Erich Spoor +15 more
2014Journal of Veterinary Internal Medicine82 citations Open access
Semantic Scholar
Genome reannotation of the lizard Anolis carolinensis based on 14 adult and embryonic deep transcriptomes
W. Eckalbar, Elizabeth D. Hutchins, Glenn J. Markov, April N. Allen +6 more
2013BMC Genomics77 citations Open access
Semantic Scholar
A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.
I. Schrauwen, M. Ealy, M. Huentelman, M. Thys +13 more
2009American Journal of Human Genetics77 citations Open access
Semantic Scholar
Plasma cytokine profiling in sibling pairs discordant for autism spectrum disorder
V. Napolioni, Benjamin Ober-Reynolds, S. Szelinger, Jason J. Corneveaux +8 more
2013Journal of Neuroinflammation74 citations Open access
Semantic Scholar
Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.
S. Melquist, David W. Craig, M. Huentelman, R. Crook +24 more
2007American Journal of Human Genetics74 citations Open access
Semantic Scholar
Tonic Premarin dose-dependently enhances memory, affects neurotrophin protein levels and alters gene expression in middle-aged rats
E. Engler-Chiurazzi, C. W. S. Tsang, Sean Nonnenmacher, W. Liang +4 more
2009Neurobiology of Aging73 citations Open access
Semantic Scholar
Comparison against 186 canid whole-genome sequences reveals survival strategies of an ancient clonally transmissible canine tumor
B. Decker, B. Davis, M. Rimbault, Adrienne H. Long +13 more
2015Genome Research71 citations Open access
Semantic Scholar
A sensitive and specific diagnostic test for hearing loss using a microdroplet PCR‐based approach and next generation sequencing
I. Schrauwen, M. Sommen, Jason J. Corneveaux, R. Reiman +7 more
2013American Journal of Medical Genetics. Part A68 citations
Semantic Scholar
A comprehensive catalogue of the coding and non-coding transcripts of the human inner ear
I. Schrauwen, Yehudit Hasin-Brumshtein, Jason J. Corneveaux, J. Ohmen +6 more
2015Hearing Research60 citations Open access
Semantic Scholar
Somitogenesis in the anole lizard and alligator reveals evolutionary convergence and divergence in the amniote segmentation clock.
W. Eckalbar, Eris Lasku, C. Infante, R. Elsey +9 more
2012Developmental Biology60 citations Open access
Semantic Scholar
Age-at-Onset in Late Onset Alzheimer Disease is Modified by Multiple Genetic Loci
A. Naj, G. Jun, Christiane Reitz, Brian W. Kunkle +170 more
2014JAMA Neurology57 citations Open access
Semantic Scholar
Protective Variant for Hippocampal Atrophy Identified by Whole Exome Sequencing
K. Nho, Sungeun Kim, S. Risacher, Li Shen +30 more
2015Annals of Neurology56 citations Open access
Semantic Scholar
Initial Assessment of the Pathogenic Mechanisms of the recently identified Alzheimer Risk Loci
P. Holton, M. Ryten, M. Nalls, D. Trabzuni +20 more
2013Annals of Human Genetics56 citations Open access
Semantic Scholar
Association of SNPs in EGR3 and ARC with Schizophrenia Supports a Biological Pathway for Schizophrenia Risk
M. Huentelman, Leela Muppana, Jason J. Corneveaux, V. Dinu +10 more
2015PLoS ONE50 citations Open access
Semantic Scholar
Genetic implication of a novel thiamine transporter in human hypertension
Kuixing Zhang, M. Huentelman, Fangwen Rao, Eric I. Sun +15 more
2014Journal of the American College of Cardiology47 citations Open access
Semantic Scholar
Novel pathogenic variants and genes for myopathies identified by whole exome sequencing
Jesse M. Hunter, M. E. Ahearn, Chris Balak, W. Liang +11 more
2015Molecular Genetics & Genomic Medicine46 citations Open access
Semantic Scholar
Identification of risk loci for necrotizing meningoencephalitis in Pug dogs.
R. Barber, S. Schatzberg, Jason J. Corneveaux, April N. Allen +5 more
2011Journal of Heredity46 citations
Semantic Scholar
A Frame-Shift Mutation in CAV1 Is Associated with a Severe Neonatal Progeroid and Lipodystrophy Syndrome
I. Schrauwen, S. Szelinger, A. Siniard, Ahmet A. Kurdoglu +11 more
2015PLoS ONE41 citations Open access
Semantic Scholar
Identification of Novel Genetic Risk Loci in Maltese Dogs with Necrotizing Meningoencephalitis and Evidence of a Shared Genetic Risk across Toy Dog Breeds
I. Schrauwen, R. Barber, S. Schatzberg, A. Siniard +11 more
2014PLoS ONE37 citations Open access
Semantic Scholar
SNiPer: Improved SNP genotype calling for Affymetrix 10K GeneChip microarray data
M. Huentelman, David W. Craig, Albert D. Shieh, Jason J. Corneveaux +3 more
2005BMC Genomics36 citations Open access
Semantic Scholar
Next-generation profiling to identify the molecular etiology of Parkinson dementia
Adrienne Henderson-Smith, Jason J. Corneveaux, M. D. De Both, Lori Cuyugan +6 more
2016Neurology: Genetics30 citations Open access
Semantic Scholar
Whole transcriptome profiling of the human hippocampus suggests an involvement of the KIBRA rs17070145 polymorphism in differential activation of the MAPK signaling pathway
I. Piras, Jonida Krate, I. Schrauwen, Jason J. Corneveaux +4 more
2017Hippocampus27 citations Open access
Semantic Scholar
A de novo missense mutation in ZMYND11 is associated with global developmental delay, seizures, and hypotonia
A. Moskowitz, N. Belnap, A. Siniard, S. Szelinger +14 more
2016Cold Spring Harbor molecular case studies27 citations Open access
Semantic Scholar
A De Novo Mutation in TEAD1 Causes Non-X-Linked Aicardi Syndrome.
I. Schrauwen, S. Szelinger, A. Siniard, Jason J. Corneveaux +13 more
2015Investigative Ophthalmology and Visual Science27 citations
Semantic Scholar

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