Search Page
Save citations to file
Email citations
Send citations to clipboard
Add to Collections
Add to My Bibliography
Create a file for external citation management software
Your saved search
Your RSS Feed
Search Results
7 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Experience and expectations of pharmacogenetic tests in France.
Therapie. 2023 Jul 17:S0040-5957(23)00103-8. doi: 10.1016/j.therap.2023.07.002. Online ahead of print.
Therapie. 2023.
PMID: 37516659
Stepwise use of genomics and transcriptomics technologies increases diagnostic yield in Mendelian disorders.
Colin E, Duffourd Y, Chevarin M, Tisserant E, Verdez S, Paccaud J, Bruel AL, Tran Mau-Them F, Denommé-Pichon AS, Thevenon J, Safraou H, Besnard T, Goldenberg A, Cogné B, Isidor B, Delanne J, Sorlin A, Moutton S, Fradin M, Dubourg C, Gorce M, Bonneau D, El Chehadeh S, Debray FG, Doco-Fenzy M, Uguen K, Chatron N, Aral B, Marle N, Kuentz P, Boland A, Olaso R, Deleuze JF, Sanlaville D, Callier P, Philippe C, Thauvin-Robinet C, Faivre L, Vitobello A.
Colin E, et al. Among authors: verdez s.
Front Cell Dev Biol. 2023 Feb 28;11:1021920. doi: 10.3389/fcell.2023.1021920. eCollection 2023.
Front Cell Dev Biol. 2023.
PMID: 36926521
Free PMC article.
Item in Clipboard
A second look at exome sequencing data: detecting mobile elements insertion in a rare disease cohort.
Garret P, Chevarin M, Vitobello A, Verdez S, Fournier C, Verloes A, Tisserant E, Vabres P, Prevel O, Philippe C, Denommé-Pichon AS, Bruel AL, Mau-Them FT, Safraou H, Boughalem A, Costa JM, Trost D, Thauvin-Robinet C, Faivre L, Duffourd Y.
Garret P, et al. Among authors: verdez s.
Eur J Hum Genet. 2023 Jul;31(7):761-768. doi: 10.1038/s41431-022-01250-3. Epub 2022 Dec 1.
Eur J Hum Genet. 2023.
PMID: 36450799
Item in Clipboard
Detection of relevant pharmacogenetic information through exome sequencing in oncology.
Verdez S, Albuisson J, Duffourd Y, Boidot R, Reda M, Thauvin-Robinet C, Fumet JD, Ladoire S, Nambot S, Callier P, Faivre L, Ghiringhelli F, Picard N.
Verdez S, et al.
Pharmacogenomics. 2022 Sep;23(14):759-770. doi: 10.2217/pgs-2022-0085. Epub 2022 Aug 31.
Pharmacogenomics. 2022.
PMID: 36043386
Item in Clipboard
Detection of the novel allele, HLA-A*32:165, in a French individual by next-generation sequencing.
Verdez S, Chevarin M, Couturier V, Leleu D, Thauvin-Robinet C.
Verdez S, et al.
HLA. 2022 Dec;100(6):631-632. doi: 10.1111/tan.14783. Epub 2022 Sep 20.
HLA. 2022.
PMID: 35998064
Item in Clipboard
Exome sequencing allows detection of relevant pharmacogenetic variants in epileptic patients.
Verdez S, Thomas Q, Garret P, Verstuyft C, Tisserant E, Vitobello A, Mau-Them FT, Philippe C, Bardou M, Luu M, Bourredjem A, Callier P, Thauvin-Robinet C, Picard N, Faivre L, Duffourd Y.
Verdez S, et al.
Pharmacogenomics J. 2022 Dec;22(5-6):258-263. doi: 10.1038/s41397-022-00280-w. Epub 2022 May 19.
Pharmacogenomics J. 2022.
PMID: 35590072
Item in Clipboard
Copy number variants calling from WES data through eXome hidden Markov model (XHMM) identifies additional 2.5% pathogenic genomic imbalances smaller than 30 kb undetected by array-CGH.
Tisserant E, Vitobello A, Callegarin D, Verdez S, Bruel AL, Aho Glele LS, Sorlin A, Viora-Dupont E, Konyukh M, Marle N, Nambot S, Moutton S, Racine C, Garde A, Delanne J, Tran-Mau-Them F, Philippe C, Kuentz P, Poulleau M, Payet M, Poe C, Thauvin-Robinet C, Faivre L, Mosca-Boidron AL, Thevenon J, Duffourd Y, Callier P.
Tisserant E, et al. Among authors: verdez s.
Ann Hum Genet. 2022 Jul;86(4):171-180. doi: 10.1111/ahg.12459. Epub 2022 Feb 9.
Ann Hum Genet. 2022.
PMID: 35141892
Item in Clipboard
Cite
Cite