K. Holman
GlaxoSmithKline (India)(IN)
Publications by Year
Research Areas
Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities, Autism Spectrum Disorder Research, Alzheimer's disease research and treatments, DNA Repair Mechanisms
Most-Cited Works
- → Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease(1995)4,041 cited
- → Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene(1995)2,060 cited
- → Mapping of DNA Instability at the Fragile X to a Trinucleotide Repeat Sequence P(CCG) n(1991)922 cited
- → Fragile X Genotype Characterized by an Unstable Region of DNA(1991)798 cited
- → Implications of FRA16A Structure for the Mechanism of Chromosomal Fragile Site Genesis(1994)139 cited
- → Fragile X syndrome: genetic localisation by linkage mapping of two microsatellite repeats FRAXAC1 and FRAXAC2 which immediately flank the fragile site.(1991)138 cited
- → Fragile X syndrome unstable element, p(CCG)n, and other simple tandem repeat sequences are binding sites for specific nuclear proteins(1993)131 cited
- → Analysis of the 5′ Sequence, Genomic Structure, and Alternative Splicing of thepresenilin-1Gene (PSEN1) Associated with Early Onset Alzheimer Disease(1997)128 cited
- → Isolation and characterisation of (AC)n microsatellite genetic markers from human chromosome 16(1992)91 cited
- → Dinucleotide repeat polymorphism at the D16S288 locus(1991)51 cited