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Laboratory Investigation; a Journal of Technical Methods and Pathology|October 2, 2024
Epigenomic and Transcriptomic Profiling of Solitary Fibrous Tumors Identifies Site-Specific Patterns and Candidate Genes Regulated by DNA MethylationHannah C Beird, Jeffrey M Cloutier, Nalan Gokgoz, et al.
Bioinformatics (Oxford, England)|December 14, 2023
Assigning mutational signatures to individual samples and individual somatic mutations with SigProfilerAssignmentMarcos Díaz-Gay, Raviteja Vangara, Mark Barnes, et al.
Cell Stem Cell|November 3, 2018
PPM1D Mutations Drive Clonal Hematopoiesis in Response to Cytotoxic ChemotherapyJoanne I Hsu, Tajhal Dayaram, Ayala Tovy, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 11, 2020
Proteogenomic Analysis of Salivary Adenoid Cystic Carcinomas Defines Molecular Subtypes and Identifies Therapeutic TargetsRenata Ferrarotto, Yoshitsugu Mitani, Daniel J McGrail, et al.
American Journal of Human Genetics|September 26, 2003
Mutations in the gene encoding capillary morphogenesis protein 2 cause juvenile hyaline fibromatosis and infantile systemic hyalinosisSandra Hanks, Sarah Adams, Jenny Douglas, et al.
Blood|September 20, 2014
Differential and limited expression of mutant alleles in multiple myelomaNaim U Rashid, Adam S Sperling, Niccolo Bolli, et al.
Nature Genetics|October 13, 2006
Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility allelesSheila Seal, Deborah Thompson, Anthony Renwick, et al.
Nature Genetics|January 4, 2007
PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility geneNazneen Rahman, Sheila Seal, Deborah Thompson, et al.
Nature|January 21, 2011
Exome sequencing identifies frequent mutation of the SWI/SNF complex gene PBRM1 in renal carcinomaIgnacio Varela, Patrick Tarpey, Keiran Raine, et al.
Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.
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