Kolexia
Gautier Evelyne Génétique médicale
Gautier Evelyne
Génétique médicale
CHU Dijon-Bourgogne
Dijon, France
16 Activités
0 Followers
Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Maladies génétiques congénitales Syndrome de Marfan Maladies rares Syndactylie Polydactylie Maladies génétiques liées au chromosome X Malformations multiples Syndrome de Pallister-Hall {{person.topmesh10.name}}

Collaborateurs

Voir plus
Olivier-Faivre Laurence
Olivier-Faivre Laurence
Hôpital François Mitterrand, Dijon, France
Thauvin-Robinet Christel
Thauvin-Robinet Christel
Hôpital François Mitterrand, Dijon, France
Thevenon Julien
Thevenon Julien
Hôpital Nord Grenoble, La Tronche, France
Sanlaville Damien
Sanlaville Damien
Hôpital Femme Mère Enfant, Bron, France

Industries

Voir plus
{{person.topindus1.name}}
{{person.topindus1.tot}} collaboration(s)
Dernière en {{person.topindus1.last}}
{{person.topindus2.name}}
{{person.topindus2.tot}} collaboration(s)
Dernière en {{person.topindus2.last}}
{{person.topindus3.name}}
{{person.topindus3.tot}} collaboration(s)
Dernière en {{person.topindus3.last}}
{{person.topindus4.name}}
{{person.topindus4.tot}} collaboration(s)
Dernière en {{person.topindus4.last}}

Dernières activités

Voir plus
French FIND study (preliminary results). Psychological effects of actionable secondary findings obtained from exome sequencing in patients/families with undiagnosed rare diseases
Abstracts from the 52nd European Society of Human Genetics (ESHG) Conference   01 octobre 2019
Preferences and representations from patients and parents with regard to the use of Next-Generation Sequencing technologies in medical genetics. The case of development anomalies
Abstracts from the 50th European Society of Human Genetics Conference   01 juillet 2019
The evolving role of the clinical geneticist facing new technologies: the opinion of patients from the AnDDI-Rares network
Abstracts from the 51st European Society of Human Genetics (ESHG) Conference, in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)   01 juillet 2019
The evolving role of the clinical geneticist facing new technologies: the opinion of French clinical geneticists, molecular biologists and specialists, and the views of the European Reference Network ITHACA
Abstracts from the 51st European Society of Human Genetics (ESHG) Conference, in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)   01 juillet 2019
Secondary findings from whole exome or genome sequencing: psychological and ethical Issues. Patient point of view
Abstracts from the 51st European Society of Human Genetics (ESHG) Conference, in conjunction with the European Meeting on Psychosocial Aspects of Genetics (EMPAG)   01 juillet 2019
actionable findings identified by whole-exome sequencing from 693 consecutive tests: implications for organization of care and patients?
Abstracts from the 50th European Society of Human Genetics Conference   01 juillet 2019
Secondary findings from next generation sequencing: Psychological and ethical issues. Family and patient perspectives.
European journal of medical genetics   29 juin 2019
Secondary findings from whole-exome/genome sequencing evaluating stakeholder perspectives. A review of the literature.
European journal of medical genetics   28 août 2018
Changes in clinical practice related to the arrival of next-generation sequencing in the genetic diagnosis of developmental diseases.
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie   12 février 2018
Genetic counselling difficulties and ethical implications of incidental findings from array-CGH: a 7-year national survey.
Clinical genetics   04 janvier 2016