Matthew J Huentelman

发表

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

Eden R Martin, Seth Love, Brian Lawlor, 2019, Nature Genetics.

Identification of a novel risk locus for progressive supranuclear palsy by a pooled genomewide scan of 500,288 single-nucleotide polymorphisms.

Richard J Caselli, John V Pearson, Irene Litvan, 2007, American journal of human genetics.

Calmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performance.

Andreas Buchmann, Eric M Reiman, Katharina Henke, 2007, Human molecular genetics.

Brain imaging and fluid biomarker analysis in young adults at genetic risk for autosomal dominant Alzheimer's disease in the presenilin 1 E280A kindred: a case-control study

Kewei Chen, Eric M Reiman, Francisco Lopera, 2012, The Lancet Neurology.

Peripheral Biomarkers in Schizophrenia: A Meta-Analysis of Microarray Gene Expression Datasets

Mirko Manchia, Bernardo Carpiniello, J. Kennedy, 2018, The international journal of neuropsychopharmacology.

Association of CR1, CLU and PICALM with Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals.

Kewei Chen, Eric M Reiman, Wendy Lee, 2010, Human molecular genetics.

Hypometabolism in Alzheimer-affected brain regions in cognitively healthy Latino individuals carrying the apolipoprotein E epsilon4 allele.

Daniel Bandy, Eric M Reiman, Richard J Caselli, 2010, Archives of neurology.

Identification of disease causing loci using an array-based genotyping approach on pooled DNA

David W Craig, D. Stephan, D. Craig, 2005, BMC Genomics.

Brain differences in infants at differential genetic risk for late-onset Alzheimer disease: a cross-sectional imaging study.

Xue Hua, Kewei Chen, Eric M Reiman, 2014, JAMA neurology.

Efficient large-scale production and concentration of HIV-1-based lentiviral vectors for use in vivo.

Sergey Kasparov, Julian F R Paton, J. Paton, 2003, Physiological genomics.

SNiPer: Improved SNP genotype calling for Affymetrix 10K GeneChip microarray data

John V Pearson, Albert D. Shieh, Jason J. Corneveaux, 2005, BMC Genomics.

Protective variant for hippocampal atrophy identified by whole exome sequencing

Li Shen, Magda Tsolaki, Clifford R Jack, 2015, Annals of neurology.

Whole-genome analysis of sporadic amyotrophic lateral sclerosis.

Kuixing Zhang, Hiroshi Mitsumoto, Richard Barohn, 2007, The New England journal of medicine.

Peripheral delivery of a ROCK inhibitor improves learning and working memory.

Carol A Barnes, Eric M Reiman, Jason J. Corneveaux, 2009, Behavioral neuroscience.

A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.

Ingeborg Dhooge, Paul Van de Heyning, Nils Homer, 2009, American journal of human genetics.

Big data collision: the internet of things, wearable devices and genomics in the study of neurological traits and disease.

M. Huentelman, J. Talboom, Matthew J Huentelman, 2018, Human molecular genetics.

Genome-wide association analysis demonstrates the highly polygenic character of age-related hearing impairment

Umberto Ambrosetti, Guy Van Camp, Erik Fransen, 2014, European Journal of Human Genetics.

Florbetapir PET analysis of amyloid-β deposition in the presenilin 1 E280A autosomal dominant Alzheimer's disease kindred: a cross-sectional study

Eric M Reiman, Kewei Chen, Napatkamon Ayutyanont, 2012, The Lancet Neurology.