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Year | Number of Results |
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2018 | 2 |
2019 | 3 |
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Page 1
Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
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.
The psychological impact of cryptic chromosomal abnormalities diagnosis announcement.
Houdayer F, Gargiulo M, Frischmann M, Labalme A, Decullier E, Cordier MP, Dupuis-Girod S, Lesca G, Till M, Sanlaville D, Edery P, Rossi M.
Houdayer F, et al.
Eur J Med Genet. 2013 Nov;56(11):585-90. doi: 10.1016/j.ejmg.2013.09.002. Epub 2013 Sep 17.
Eur J Med Genet. 2013.
PMID: 24055527
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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.
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
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10 years of CEMARA database in the AnDDI-Rares network: a unique resource facilitating research and epidemiology in developmental disorders in France.
Messiaen C, Racine C, Khatim A, Soussand L, Odent S, Lacombe D, Manouvrier S, Edery P, Sigaudy S, Geneviève D, Thauvin-Robinet C, Pasquier L, Petit F, Rossi M, Willems M, Attié-Bitach T, Roux-Levy PH, Demougeot L, Slama LB, Landais P; AnDDI-Rares network; Jannot AS, Binquet C, Sandrin A, Verloes A, Faivre L.
Messiaen C, et al.
Orphanet J Rare Dis. 2021 Aug 4;16(1):345. doi: 10.1186/s13023-021-01957-4.
Orphanet J Rare Dis. 2021.
PMID: 34348744
Free PMC article.
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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: houdayer f.
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.
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[Changes in clinical practice related to the arrival of next-generation sequencing in the genetic diagnosis of developmental diseases].
Demougeot L, Houdayer F, Pélissier A, Mohrez F, Thevenon J, Duffourd Y, Nambot S, Gautier E, Binquet C, Rossi M, Sanlaville D, Béjean S, Peyron C, Thauvin-Robinet C, Faivre L.
Demougeot L, et al. Among authors: houdayer f.
Arch Pediatr. 2018 Feb;25(2):77-83. doi: 10.1016/j.arcped.2017.12.006. Epub 2018 Feb 12.
Arch Pediatr. 2018.
PMID: 29395884
French.
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