| A high-density whole-genome association study reveals that APOE is the major susceptibility gene for sporadic late-onset Alzheimer's disease KD Coon, AJ Myers, DW Craig, JA Webster, JV Pearson, DH Lince, ... Journal of Clinical Psychiatry 68 (4), 613, 2007 | 713 | 2007 |
| GAB2 alleles modify Alzheimer's risk in APOE ɛ4 carriers EM Reiman, JA Webster, AJ Myers, J Hardy, T Dunckley, VL Zismann, ... Neuron 54 (5), 713-720, 2007 | 572 | 2007 |
| A survey of genetic human cortical gene expression AJ Myers, JR Gibbs, JA Webster, K Rohrer, A Zhao, L Marlowe, M Kaleem, ... Nature genetics 39 (12), 1494-1499, 2007 | 569 | 2007 |
| Microarray and genetic analysis of electron transfer to electrodes in Geobacter sulfurreducens DE Holmes, SK Chaudhuri, KP Nevin, T Mehta, BA Methé, A Liu, JE Ward, ... Environmental Microbiology 8 (10), 1805-1815, 2006 | 421 | 2006 |
| Genetic control of human brain transcript expression in Alzheimer disease JA Webster, JR Gibbs, J Clarke, M Ray, W Zhang, P Holmans, K Rohrer, ... The American Journal of Human Genetics 84 (4), 445-458, 2009 | 330 | 2009 |
| Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide–polymorphism association studies JV Pearson, MJ Huentelman, RF Halperin, WD Tembe, S Melquist, ... The American Journal of Human Genetics 80 (1), 126-139, 2007 | 184 | 2007 |
| Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease JL Stein, X Hua, JH Morra, S Lee, DP Hibar, AJ Ho, AD Leow, AW Toga, ... Neuroimage 51 (2), 542-554, 2010 | 175 | 2010 |
| Mutations in LOXHD1, an evolutionarily conserved stereociliary protein, disrupt hair cell function in mice and cause progressive hearing loss in humans N Grillet, M Schwander, MS Hildebrand, A Sczaniecka, A Kolatkar, ... The American Journal of Human Genetics 85 (3), 328-337, 2009 | 158 | 2009 |
| Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42 G Borck, AU Rehman, K Lee, HM Pogoda, N Kakar, S Von Ameln, ... The American Journal of Human Genetics 88 (2), 127-137, 2011 | 130 | 2011 |
| Evidence for an association between KIBRA and late-onset Alzheimer's disease JJ Corneveaux, WS Liang, EM Reiman, JA Webster, AJ Myers, ... Neurobiology of aging 31 (6), 901-909, 2010 | 127 | 2010 |
| Adaptation to Disruption of the Electron Transfer Pathway for Fe(III) Reduction in Geobacter sulfurreducens C Leang, LA Adams, KJ Chin, KP Nevin, BA Methe, J Webster, ... Journal of bacteriology 187 (17), 5918-5926, 2005 | 103 | 2005 |
| DNA Microarray Analysis of Nitrogen Fixation and Fe(III) Reduction in Geobacter sulfurreducens BA Methé, J Webster, K Nevin, J Butler, DR Lovley Applied and environmental microbiology 71 (5), 2530-2538, 2005 | 102 | 2005 |
| Sorl1 as an Alzheimer’s Disease Predisposition Gene? JA Webster, AJ Myers, JV Pearson, DW Craig, D Hu-Lince, KD Coon, ... Neurodegenerative Diseases 5 (2), 60-64, 2008 | 97 | 2008 |
| Underutilization of Lynch syndrome screening in a multisite study of patients with colorectal cancer DS Cross, AK Rahm, TL Kauffman, J Webster, AQ Le, ... Genetics in Medicine 15 (12), 933-940, 2013 | 56 | 2013 |
| SNiPer-HD: improved genotype calling accuracy by an expectation-maximization algorithm for high-density SNP arrays J Hua, DW Craig, M Brun, J Webster, V Zismann, W Tembe, K Joshipura, ... Bioinformatics 23 (1), 57-63, 2007 | 56 | 2007 |
| Mutations in the first MyTH4 domain of MYO15A are a common cause of DFNB3 hearing loss AE Shearer, MS Hildebrand, JA Webster, K Kahrizi, NC Meyer, ... The Laryngoscope 119 (4), 727-733, 2009 | 55 | 2009 |
| Community oncology medical homes: Physician-driven change to improve patient care and reduce costs TM Waters, JA Webster, LA Stevens, T Li, CM Kaplan, I Graetz, ... Journal of oncology practice 11 (6), 462-467, 2015 | 49 | 2015 |
| Description and pilot results from a novel method for evaluating return of incidental findings from next-generation sequencing technologies KAB Goddard, EP Whitlock, JS Berg, MS Williams, EM Webber, ... Genetics in Medicine 15 (9), 721-728, 2013 | 48 | 2013 |
| Use of real‐world evidence to drive drug development strategy and inform clinical trial design S Dagenais, L Russo, A Madsen, J Webster, L Becnel Clinical Pharmacology & Therapeutics 111 (1), 77-89, 2022 | 46 | 2022 |
| Variable hearing impairment in a DFNB2 family with a novel MYO7A missense mutation MS Hildebrand, NP Thorne, CJ Bromhead, K Kahrizi, JA Webster, ... Clinical genetics 77 (6), 563-571, 2010 | 44 | 2010 |
Dietrich A. StephanProfessor and Chairman, Human Genetics Department, University of PittsburghVerified email at pitt.edu
