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
6 results
Filters applied: . Clear all
Results are displayed in a computed author sort order.
The Results By Year timeline is not available.
Page 1
Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
Eur J Med Genet. 2019 Oct;62(10):103711. doi: 10.1016/j.ejmg.2019.103711. Epub 2019 Jun 29.
Eur J Med Genet. 2019.
PMID: 31265899
Exome sequencing in clinical settings: preferences and experiences of parents of children with rare diseases (SEQUAPRE study).
Chassagne A, Pélissier A, Houdayer F, Cretin E, Gautier E, Salvi D, Kidri S, Godard A, Thauvin-Robinet C, Masurel A, Lehalle D, Jean-Marçais N, Thevenon J, Lesca G, Putoux A, Cordier MP, Dupuis-Girod S, Till M, Duffourd Y, Rivière JB, Joly L, Juif C, Putois O, Ancet P, Lapointe AS, Morin P, Edery P, Rossi M, Sanlaville D, Béjean S, Peyron C, Faivre L.
Chassagne A, et al. Among authors: juif c.
Eur J Hum Genet. 2019 May;27(5):701-710. doi: 10.1038/s41431-018-0332-y. Epub 2019 Feb 1.
Eur J Hum Genet. 2019.
PMID: 30710147
Free PMC article.
Item in Clipboard
Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
Delanne J, Nambot S, Chassagne A, Putois O, Pelissier A, Peyron C, Gautier E, Thevenon J, Cretin E, Bruel AL, Goussot V, Ghiringhelli F, Boidot R, Tran Mau-Them F, Philippe C, Vitobello A, Demougeot L, Vernin C, Lapointe AS, Bardou M, Luu M, Binquet C, Lejeune C, Joly L, Juif C, Baurand A, Sawka C, Bertolone G, Duffourd Y, Sanlaville D, Pujol P, Geneviève D, Houdayer F, Thauvin-Robinet C, Faivre L.
Delanne J, et al. Among authors: juif c.
Eur J Med Genet. 2019 Jun;62(6):103529. doi: 10.1016/j.ejmg.2018.08.010. Epub 2018 Aug 28.
Eur J Med Genet. 2019.
PMID: 30165243
Review.
Item in Clipboard
Neuropsychological study in 19 French patients with White-Sutton syndrome and POGZ mutations.
Garde A, Cornaton J, Sorlin A, Moutton S, Nicolas C, Juif C, Geneviève D, Perrin L, Khau-Van-Kien P, Smol T, Vincent-Delorme C, Isidor B, Cogné B, Afenjar A, Keren B, Coubes C, Prieur F, Toutain A, Trousselet Y, Bourgouin S, Gonin-Olympiade C, Giraudat K, Piton A, Gérard B, Odent S, Tessier F, Lemasson L, Heide S, Gelineau AC, Sarret C, Miret A, Schaefer E, Piard J, Mathevet R, Boucon M, Bruel AL, Mau-Them FT, Chevarin M, Vitobello A, Philippe C, Thauvin-Robinet C, Faivre L.
Garde A, et al. Among authors: juif c.
Clin Genet. 2021 Mar;99(3):407-417. doi: 10.1111/cge.13894. Epub 2020 Dec 15.
Clin Genet. 2021.
PMID: 33277917
Item in Clipboard
[Studying dysfunctional personality trends among sex offenders].
Perrot M, Bénony H, Chahraoui K, Juif C.
Perrot M, et al. Among authors: juif c.
Encephale. 2014 Oct;40(5):366-72. doi: 10.1016/j.encep.2014.01.003. Epub 2014 Apr 1.
Encephale. 2014.
PMID: 24703787
French.
Item in Clipboard
Esterase phenotyping in human liver in vitro: specificity of carboxylesterase inhibitors.
Umehara K, Zollinger M, Kigondu E, Witschi M, Juif C, Huth F, Schiller H, Chibale K, Camenisch G.
Umehara K, et al. Among authors: juif c.
Xenobiotica. 2016 Oct;46(10):862-7. doi: 10.3109/00498254.2015.1133867. Epub 2016 Feb 18.
Xenobiotica. 2016.
PMID: 26887925
Item in Clipboard
Cite
Cite