Concepedia
Statistics
Publications
92
Citations
4.3K
H-Index
40
Active since
2015
Affiliations
Inserm(Current)
Centre National de la Recherche Scientifique
Institut du Thorax
Génétique Médicale & Génomique Fonctionelle
Nantes Université
Benjamin Cogné is an author at Inserm specializing in life sciences, genetics, and molecular genetics.
Publications per year
2015–2025
Pathogenic DDX3X Mutations Impair RNA Metabolism and Neurogenesis during Fetal Cortical Development
Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang et al. · Neuron · 2020 · 222 citations · Full text
Life Sciences, Genetics, Molecular Genetics +12
De Novo Mutations in Protein Kinase Genes CAMK2A and CAMK2B Cause Intellectual Disability
Sébastien Küry, Geeske M. van Woerden, Thomas Besnard et al. · The American Journal of Human Genetics · 2017 · 201 citations · Full text
Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway
Justyna A. Karolak, Marie Vincent, Gail Deutsch et al. · The American Journal of Human Genetics · 2019 · 183 citations · Full text
Life Sciences, Developmental Biology, Genetics +15
Germline De Novo Mutations in GNB1 Cause Severe Neurodevelopmental Disability, Hypotonia, and Seizures
Slavé Petrovski, Sébastien Küry, Candace T. Myers et al. · The American Journal of Human Genetics · 2016 · 119 citations · Full text
Life Sciences, Genetics, Molecular Genetics +14
KAT6A Syndrome: genotype–phenotype correlation in 76 patients with pathogenic KAT6A variants
Joanna Kennedy, David Goudie, Edward Blair et al. · Genetics in Medicine · 2018 · 111 citations · Full text
Life Sciences, Genetics, Molecular Genetics +9
1–5 of 92