Duncan P. McHale
Pfizer (United Kingdom)(GB)
Publications by Year
Research Areas
Genomics and Phylogenetic Studies, Pain Mechanisms and Treatments, Chromosomal and Genetic Variations, Microtubule and mitosis dynamics, Ion channel regulation and function
Most-Cited Works
- → An SCN9A channelopathy causes congenital inability to experience pain(2006)1,562 cited
- → Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease(2001)539 cited
- → Pain perception is altered by a nucleotide polymorphism in SCN9A(2010)300 cited
- → Primary Autosomal Recessive Microcephaly (MCPH1) Maps to Chromosome 8p22-pter(1998)168 cited
- → The second locus for autosomal recessive primary microcephaly (MCPH2) maps to chromosome 19q13.1–13.2(1999)108 cited
- → A new locus for non-syndromal, autosomal recessive, sensorineural hearing loss (DFNB16) maps to human chromosome 15q21-q22.(1997)57 cited
- → A Gene for Autosomal Recessive Symmetrical Spastic Cerebral Palsy Maps to Chromosome 2q24-25(1999)52 cited
- → Autozygosity Mapping, to Chromosome 11q25, of a Rare Autosomal Recessive Syndrome Causing Histiocytosis, Joint Contractures, and Sensorineural Deafness(1998)32 cited
- → Association between neprilysin polymorphisms and sporadic Alzheimer's disease(2007)23 cited
- → A Syndrome of Severe Mental Retardation, Spasticity, and Tapetoretinal Degeneration Linked to Chromosome 15q24(1998)16 cited