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Genomics|April 16, 2013
Increased CNV-region deletions in mild cognitive impairment (MCI) and Alzheimer's disease (AD) subjects in the ADNI sampleGuia Guffanti, Federica Torri, Jerod Rasmussen, et al.Nature Communications|July 29, 2025
Cas13d-mediated isoform-specific RNA knockdown with a unified computational and experimental toolboxMegan D Schertzer, Andrew Stirn, Keren Isaev, et al.Nature Genetics|February 14, 1998
TULP1 mutation in two extended Dominican kindreds with autosomal recessive retinitis pigmentosaP Banerjee, P W Kleyn, J A Knowles, et al.Gene|January 13, 1998
Identification of a novel member of the TGF-beta superfamily highly expressed in human placentaL N Lawton, M F Bonaldo, P C Jelenc, et al.American Journal of Human Genetics|January 23, 1999
A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locusV M Aita, J Liu, J A Knowles, et al.Genes, Chromosomes & Cancer|February 9, 2010
Deletion at chromosome arm 9p in relation to BRAF/NRAS mutations and prognostic significance for primary melanomaCaroline Conway, Samantha Beswick, Faye Elliott, et al.Gastroenterology|March 30, 2010
Genetic risk factors for hepatopulmonary syndrome in patients with advanced liver diseaseKari E Roberts, Steven M Kawut, Michael J Krowka, et al.European Journal of Cancer (Oxford, England : 1990)|February 26, 2013
Expression of Engrailed-2 (EN2) protein in bladder cancer and its potential utility as a urinary diagnostic biomarkerRichard Morgan, Richard T Bryan, Saqib Javed, et al.Circulation|October 26, 2011
Distinct epigenomic features in end-stage failing human heartsMehregan Movassagh, Mun-Kit Choy, David A Knowles, et al.Chest|January 15, 2009
Serotonin transporter polymorphisms in patients with portopulmonary hypertensionKari E Roberts, Michael B Fallon, Michael J Krowka, et al.Pageof 66