N. White

Direct sequencing of bacterial and P1 artificial chromosome-nested deletions for identifying position-specific single-nucleotide polymorphisms.

J. Riley, D. Yarnall, H. E. Davies, 1999, Proceedings of the National Academy of Sciences of the United States of America.

A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p

M. Pericak-Vance, J. Riley, J. Vance, 2006, European Journal of Human Genetics.

Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine.

P. R. Boyd, A. Roses, J. Riley, 2001, Genomics.

Effectiveness of computational methods in haplotype prediction

Dmitri V. Zaykin, Chun-Fang Xu, P. R. Boyd, 2002, Human Genetics.

Identification of a novel asthma susceptibility gene on chromosome 1qter and its functional evaluation.

J. Vestbo, J. Riley, M. Wigglesworth, 2008, Human molecular genetics.

Identification, genomic structure, and screening of the vacuolar proton-ATPase membrane sector-associated protein M8-9 gene within the COD1 critical region (Xp11.4).

M. Gorin, F. Demirci, M B Gorin, 2001, Molecular vision.

A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p

M. Pericak-Vance, J. Riley, J. Vance, 2007, European Journal of Human Genetics.

Refinement of the Physical Location and the Genomic Characterization of the CRSP2 (EXLM1) Gene on Xp11.4

J. Ramser, A. Meindl, M. Gorin, 2003, DNA sequence : the journal of DNA sequencing and mapping.

Susceptibility Genes: Detection

J. Riley, N. White, 2006 .