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Guillaume Cogan

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Comptes Rendus Biologies|February 13, 2025
[Parkinson's disease: from genetics to targeted therapies]Guillaume Cogan, Alexis Brice
Current Opinion in Neurobiology|November 18, 2025
The genetics of autosomal recessive early-onset Parkinson's diseaseGuillaume Cogan, Suzanne Lesage, Alexis Brice
Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2025
Exploration of Neurodegenerative Diseases Using Long-Read Sequencing and Optical Genome Mapping TechnologiesGuillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2024
Confirmation of RAB32 Ser71Arg Involvement in Parkinson's DiseaseGuillaume Cogan, Christelle Tesson, Christine Brefel-Courbon, et al.
NPJ Parkinson'S Disease|October 17, 2025
Should ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel familiesGuillaume Cogan, Christelle Tesson, Lisa Welment, et al.
Molecular Genetics & Genomic Medicine|June 24, 2023
Diagnosis of Menke-Hennekam syndrome by prenatal whole exome sequencing and review of prenatal signsGuillaume Cogan, Nicolas Bourgon, Roxana Borghese, et al.
Prenatal Diagnosis|November 12, 2024
Use of Prenatal Exome Sequencing: Opinion Statement of the French Federation of Human Genetics Working GroupGuillaume Cogan, Marie-Bérengère Troadec, Françoise Devillard, et al.
Clinical Genetics|December 14, 2021
Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorderJonathan Lévy, Guillaume Cogan, Anna Maruani, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2024
Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's DiseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Comptes Rendus Biologies|February 13, 2025
[Parkinson's disease: from genetics to targeted therapies]Guillaume Cogan, Alexis Brice
Current Opinion in Neurobiology|November 18, 2025
The genetics of autosomal recessive early-onset Parkinson's diseaseGuillaume Cogan, Suzanne Lesage, Alexis Brice
Movement Disorders : Official Journal of the Movement Disorder Society|March 3, 2025
Exploration of Neurodegenerative Diseases Using Long-Read Sequencing and Optical Genome Mapping TechnologiesGuillaume Cogan, Kensuke Daida, Cornelis Blauwendraat, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 23, 2024
Confirmation of RAB32 Ser71Arg Involvement in Parkinson's DiseaseGuillaume Cogan, Christelle Tesson, Christine Brefel-Courbon, et al.
NPJ Parkinson'S Disease|October 17, 2025
Should ITSN1 be considered as a Mendelian Parkinson's disease gene? Description of three novel familiesGuillaume Cogan, Christelle Tesson, Lisa Welment, et al.
Molecular Genetics & Genomic Medicine|June 24, 2023
Diagnosis of Menke-Hennekam syndrome by prenatal whole exome sequencing and review of prenatal signsGuillaume Cogan, Nicolas Bourgon, Roxana Borghese, et al.
Prenatal Diagnosis|November 12, 2024
Use of Prenatal Exome Sequencing: Opinion Statement of the French Federation of Human Genetics Working GroupGuillaume Cogan, Marie-Bérengère Troadec, Françoise Devillard, et al.
Clinical Genetics|December 14, 2021
Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorderJonathan Lévy, Guillaume Cogan, Anna Maruani, et al.
Medrxiv : the Preprint Server for Health Sciences|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's diseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 29, 2024
Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's DiseaseGuillaume Cogan, Kensuke Daida, Kimberley J Billingsley, et al.
Pageof 2