Whole-exon sequencing of human myeloma cell lines shows mutations related to myeloma patients at relapse with major hits in the DNA regulation and repair pathways.
Journal Of Hematology & Oncology
Tessoulin, Benoît B; Moreau-Aubry, Agnès A; Descamps, Géraldine G; Gomez-Bougie, Patricia P; Maïga, Sophie S; Gaignard, Alban A; Chiron, David D; Ménoret, Emmanuelle E; Le Gouill, Steven S; Moreau, Philippe P; Amiot, Martine M; Pellat-Deceunynck, Catherine C
The impact of tumor profiling approaches and genomic data strategies for cancer precision medicine.
Genome Medicine
Garofalo, Andrea A; Sholl, Lynette L; Reardon, Brendan B; Taylor-Weiner, Amaro A; Amin-Mansour, Ali A; Miao, Diana D; Liu, David D; Oliver, Nelly N; MacConaill, Laura L; Ducar, Matthew M; Rojas-Rudilla, Vanesa V; Giannakis, Marios M; Ghazani, Arezou A; Gray, Stacy S; Janne, Pasi P; Garber, Judy J; Joffe, Steve S; Lindeman, Neal N; Wagle, Nikhil N; Garraway, Levi A LA; Van Allen, Eliezer M EM
Publication Date: 2016-07-26
Variant appearance in text: CSMD1: 6784C>G; P2262A
Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.
Molecular Autism
Cukier, Holly N HN; Dueker, Nicole D ND; Slifer, Susan H SH; Lee, Joycelyn M JM; Whitehead, Patrice L PL; Lalanne, Eminisha E; Leyva, Natalia N; Konidari, Ioanna I; Gentry, Ryan C RC; Hulme, William F WF; Booven, Derek Van DV; Mayo, Vera V; Hofmann, Natalia K NK; Schmidt, Michael A MA; Martin, Eden R ER; Haines, Jonathan L JL; Cuccaro, Michael L ML; Gilbert, John R JR; Pericak-Vance, Margaret A MA