Annette Abel
Publications by Year
Research Areas
Hereditary Neurological Disorders, Neurogenetic and Muscular Disorders Research, Neurological diseases and metabolism, Amyotrophic Lateral Sclerosis Research, Genetic Neurodegenerative Diseases
Most-Cited Works
- → DNA/RNA Helicase Gene Mutations in a Form of Juvenile Amyotrophic Lateral Sclerosis (ALS4)(2004)810 cited
- → Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V(2003)559 cited
- → The Role of the Gap Junction Protein Connexin32 in the Pathogenesis of X‐Linked Charcot‐Marie‐Tooth Disease(2007)50 cited
- → Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A(2004)49 cited
- → Androgen receptor mutation in Kennedy'sdisease(1999)47 cited
- → Studies in Transgenic Mice Indicate a Loss of Connexin32 Function in X-Linked Charcot-Marie-Tooth Disease(1999)36 cited
- → A gene for autosomal dominant juvenile amyotrophic lateral sclerosis (ALS4 ) localizes to a 500-kb interval on chromosome 9q34(2000)35 cited
- → X‐linked Charcot‐Marie‐Tooth Disease and Connexin32(1999)22 cited
- → ACADEMICALLY AT-RISK HIGH SCHOOL(2019)
- → Identification of Finite‐Motion Parameters of Serial Chains via Measurement of 6 × 6 Stiffness Matrices(2005)