Stéphanie Millecamps
Centre National de la Recherche Scientifique(FR)Inserm(FR)Sorbonne Université(FR)Assistance Publique – Hôpitaux de Paris(FR)Pitié-Salpêtrière Hospital(FR)Institut du Cerveau(FR)
Publications by Year
Research Areas
Amyotrophic Lateral Sclerosis Research, Neurogenetic and Muscular Disorders Research, Neurological diseases and metabolism, Parkinson's Disease Mechanisms and Treatments, Alzheimer's disease research and treatments
Most-Cited Works
- → Haploinsufficiency of TBK1 causes familial ALS and fronto-temporal dementia(2015)775 cited
- → Axonal transport deficits and neurodegenerative diseases(2013)735 cited
- → Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis(2016)620 cited
- → Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology(2021)522 cited
- → SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations(2010)293 cited
- → Mutations in SQSTM1 encoding p62 in amyotrophic lateral sclerosis: genetics and neuropathology(2013)231 cited