J. Webster

发表

A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease.

Rebecca F. Halperin, D. Stephan, A. Myers, 2007, The Journal of clinical psychiatry.

GAB2 Alleles Modify Alzheimer's Risk in APOE ɛ4 Carriers

Winnie S. Liang, G. Alexander, D. Stephan, 2007, Neuron.

GAB2 alleles modify Alzheimer's risk in APOE epsilon4 carriers.

Winnie S. Liang, G. Alexander, D. Stephan, 2007, Neuron.

Genetic control of human brain transcript expression in Alzheimer disease.

D. Stephan, P. Holmans, A. Myers, 2009, American journal of human genetics.

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies.

Rebecca F. Halperin, Nils Homer, D. Stephan, 2007, American journal of human genetics.

Genome-wide analysis reveals novel genes in fl uencing temporal lobe structure with relevance to neurodegeneration in Alzheimer ' s disease

Michael W. Weiner, Andrew J. Saykin, Paul M. Thompson, 2010 .

Evidence for an association between KIBRA and late-onset Alzheimer's disease

Richard J. Caselli, Gene E. Alexander, Daniel Bandy, 2010, Neurobiology of Aging.

Whole genome association analysis shows that ACE is a risk factor for Alzheimer's disease and fails to replicate most candidates from Meta-analysis.

D. Stephan, S. Melquist, A. Myers, 2010, International journal of molecular epidemiology and genetics.

A survey of genetic human cortical gene expression

D. Stephan, P. Holmans, A. Myers, 2007, Nature Genetics.

Altered TMPRSS2 usage by SARS-CoV-2 Omicron impacts tropism and fusogenicity

Eleanor, Joy, Josh, 2022 .

Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.

S. Leal, D. Stephan, M. Schiller, 2011, American journal of human genetics.

Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans.

D. Stephan, L. Tarantino, T. Wiltshire, 2009, American journal of human genetics.

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

Edward R. Dougherty, Marcel Brun, Jianping Hua, 2007, Bioinform..

Mutations in TMC1 are a Common Cause of DFNB7/11 Hearing Loss in the Iranian Population

D. Stephan, J. Webster, M. Bahlo, 2010, The Annals of otology, rhinology, and laryngology.

A novel splice site mutation in the RDX gene causes DFNB24 hearing loss in an Iranian family

D. Stephan, J. Webster, M. Bahlo, 2009, American journal of medical genetics. Part A.

Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss

D. Stephan, J. Webster, M. Bahlo, 2009, The Laryngoscope.

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

Michael Weiner, Andrew J. Saykin, Paul M. Thompson, 2010, NeuroImage.

A novel mutation in COCH—implications for genotype‐phenotype correlations in DFNA9 hearing loss

D. Stephan, J. Webster, M. Bahlo, 2010, The Laryngoscope.

Sorl1 as an Alzheimer’s Disease Predisposition Gene?

D. Stephan, A. Myers, J. Hardy, 2007, Neurodegenerative Diseases.

Evidence for an association between KIBRA and late-onset Alzheimer's disease

Jason J. Corneveaux, Winnie S. Liang, G. Alexander, 2010, Neurobiology of Aging.

SNiPer 500K: A Novel SNP Genotype Calling Algorithm

E. Dougherty, D. Stephan, D. Craig, 2006, 2006 IEEE/NLM Life Science Systems and Applications Workshop.

SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

M. Huentelman, J. Webster, V. Zismann, 2007, Bioinform..

Genetics and population analysis SNiPer-HD : improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays

E. Dougherty, D. Stephan, D. Craig, 2006 .

Sniper-hd: Improved Genotype Calling Accuracy by an Expecta- Tion-maximization Algorithm for High-density Snp Arrays

M. Huentelman, J. Webster, V. Zismann, 2022 .