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Page 1
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: lapointe as. 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.
Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
Houdayer F, Putois O, Babonneau ML, Chaumet H, Joly L, Juif C, Michon CC, Staraci S, Cretin E, Delanoue S, Charron P, Chassagne A, Edery P, Gautier E, Lapointe AS, Thauvin-Robinet C, Sanlaville D, Gargiulo M, Faivre L. Houdayer F, et al. Among authors: lapointe as. 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: lapointe as. 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.
Guidelines for reporting secondary findings of genome sequencing in cancer genes: the SFMPP recommendations.
Pujol P, Vande Perre P, Faivre L, Sanlaville D, Corsini C, Baertschi B, Anahory M, Vaur D, Olschwang S, Soufir N, Bastide N, Amar S, Vintraud M, Ingster O, Richard S, Le Coz P, Spano JP, Caron O, Hammel P, Luporsi E, Toledano A, Rebillard X, Cambon-Thomsen A, Putois O, Rey JM, Hervé C, Zorn C, Baudry K, Galibert V, Gligorov J, Azria D, Bressac-de Paillerets B, Burnichon N, Spielmann M, Zarca D, Coupier I, Cussenot O, Gimenez-Roqueplo AP, Giraud S, Lapointe AS, Niccoli P, Raingeard I, Le Bidan M, Frebourg T, Rafii A, Geneviève D. Pujol P, et al. Among authors: lapointe as. Eur J Hum Genet. 2018 Dec;26(12):1732-1742. doi: 10.1038/s41431-018-0224-1. Epub 2018 Aug 8. Eur J Hum Genet. 2018. PMID: 30089825 Free PMC article.
Transition from child to adult health care for patients with lysosomal storage diseases in France: current status and priorities-the TENALYS study, a patient perspective survey.
Genevaz D, Arnoux A, Marcel C, Brassier A, Pichard S, Feillet F, Labarthe F, Chabrol B, Berger M, Lapointe AS, Frigout Y, Héron B, Chatellier G, Belmatoug N. Genevaz D, et al. Among authors: lapointe as. Orphanet J Rare Dis. 2022 Feb 21;17(1):68. doi: 10.1186/s13023-022-02232-w. Orphanet J Rare Dis. 2022. PMID: 35189927 Free PMC article.
[The Pneumococcal Observatory for the Central Region, 1 April 1999 to 31 March 2000].
Cattier B, Lempérière S, Gallois I, Adam MN, Akli J, Amirault P, Bret L, Cahiez M, Carbonnelle J, Cartron JC, Gavignet M, Graveron JL, Harriau P, Lapointe A, Laudat P, Loulergue J, Secher A. Cattier B, et al. Pathol Biol (Paris). 2002 Apr;50(3):178-83. doi: 10.1016/s0369-8114(02)00285-7. Pathol Biol (Paris). 2002. PMID: 11980331 French.