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Genetics|May 5, 2010
Whole-genome profiling of mutagenesis in Caenorhabditis elegansStephane Flibotte, Mark L Edgley, Iasha Chaudhry, et al.
Genes, Chromosomes & Cancer|March 23, 2004
Delineation of a minimal region of deletion at 6q16.3 in follicular lymphoma and construction of a bacterial artificial chromosome contig spanning a 6-megabase region of 6q16-q21Laura-Jane Henderson, Ichiro Okamoto, Valia S Lestou, et al.
Plos One|August 24, 2012
Mutation discovery in regions of segmental cancer genome amplifications with CoNAn-SNV: a mixture model for next generation sequencing of tumorsAnamaria Crisan, Rodrigo Goya, Gavin Ha, et al.
Cancer Cell|March 18, 2022
Single-cell landscapes of primary glioblastomas and matched explants and cell lines show variable retention of inter- and intratumor heterogeneityVéronique G LeBlanc, Diane L Trinh, Shaghayegh Aslanpour, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|August 26, 2025
The cost and cost trajectory of genome sequencing and bioinformatics analysis for Indigenous children with suspected rare diseasesMorgan Ehman, Kartik Sharma, Deirdre Weymann, et al.
BMC Cancer|July 14, 2007
Correlations of EGFR mutations and increases in EGFR and HER2 copy number to gefitinib response in a retrospective analysis of lung cancer patientsTrevor J Pugh, Gwyn Bebb, Lorena Barclay, et al.
BMC Genomics|January 31, 2008
Analysis of 4,664 high-quality sequence-finished poplar full-length cDNA clones and their utility for the discovery of genes responding to insect feedingSteven G Ralph, Hye Jung E Chun, Dawn Cooper, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 30, 2009
Sequence variant discovery in DNA repair genes from radiosensitive and radiotolerant prostate brachytherapy patientsTrevor J Pugh, Mira Keyes, Lorena Barclay, et al.
Genome Research|April 20, 2005
Analysis of long-lived C. elegans daf-2 mutants using serial analysis of gene expressionJulius Halaschek-Wiener, Jaswinder S Khattra, Sheldon McKay, et al.
Journal of Human Genetics|January 24, 2019
A distinct neurodevelopmental syndrome with intellectual disability, autism spectrum disorder, characteristic facies, and macrocephaly is caused by defects in CHD8Heba Yasin, William T Gibson, Sylvie Langlois, et al.
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