François Muratet

Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations

Silvia De Rubeis, Paige M. Siper, Allison Durkin et al. · Molecular Autism · 2018 · 213 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Prospective investigation of FOXP1 syndrome

Paige M. Siper, Silvia De Rubeis, Maria del Pilar Trelles et al. · Molecular Autism · 2017 · 98 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Salim Megat, Natalia Mora, Jason Sanogo et al. · Nature Communications · 2023 · 43 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis

Elisa Teyssou, François Muratet, Maria del Mar Amador et al. · Neurobiology of Aging · 2020 · 40 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Spastic paraplegia due to recessive or dominant mutations in <i>ERLIN2</i> can convert to ALS

Maria del Mar Amador, François Muratet, Elisa Teyssou et al. · Neurology Genetics · 2019 · 21 citations · Full text

Life Sciences, Genetics, Neurology +17