Graham Lamb
Publications by Year
Research Areas
Genetic Associations and Epidemiology, Autism Spectrum Disorder Research, Cardiac electrophysiology and arrhythmias, Ion channel regulation and function, Immunodeficiency and Autoimmune Disorders
Most-Cited Works
- → The Epsin 4 Gene on Chromosome 5q, Which Encodes the Clathrin-Associated Protein Enthoprotin, Is Involved in the Genetic Susceptibility to Schizophrenia(2005)70 cited
- → Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G‐protein signaling 4 protein (RGS4)(2006)33 cited
- → Failure to Confirm Allelic Association Between Markers at the CAPON Gene Locus and Schizophrenia in a British Sample(2005)32 cited
- → Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1)(2001)29 cited
- → Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia(2007)23 cited
- → A novel polymorphism in exon 11 of the WKL1 gene, shows no association with schizophrenia(2002)16 cited
- Hyper-IgE syndrome: fatal progressive multifocal leukoencephalopathy in an Italian child with DOCK8 mutation(2010)
- Exon 11 of the chromosome 22 gene WKL1, previously shown to exhibit a base pair mutation in rare cases of schizophrenia, was found to contain an insertion/deletion polymorphism, affecting the receptor channel amino acid sequence.(2001)
- → A Haploview generated diagram of the location of SNPs in the DNTBP1 gene that were genotyped in this study(2011)
- Thirty-eight of 47 patients with autosomal-recessive hyper-IgE syndrome carry deletions and point mutations in Dock8(2010)