M. Burley

发表

A Gain-of-Function Mutation in TRPA1 Causes Familial Episodic Pain Syndrome

G. Bedoya, A. Ruiz-Linares, C. Woods, 2010, Neuron.

Lack of Support for a Role for RLIP76 (RALBP1) in Response to Treatment or Predisposition to Epilepsy

D. Goldstein, A. Sali, L. Martinian, 2007, Epilepsia.

C4 complement allotypes in juvenile dermatomyositis.

V. Dubowitz, M. Burley, J. Batchelor, 1988, Human immunology.

HLA class III haplotypes in multicase rheumatoid arthritis families.

A. Silman, W. Ollier, M. Burley, 1989, Human immunology.

Admixture in Latin America: Geographic Structure, Phenotypic Diversity and Self-Perception of Ancestry Based on 7,342 Individuals

D. Balding, N. Ray, G. Bedoya, 2014, PLoS genetics.

Contrasting Patterns of Nuclear and mtDNA Diversity in Native American Populations

L. Excoffier, Sijia Wang, N. Ray, 2010, Annals of human genetics.

Failure to replicate previously reported genetic associations with sporadic temporal lobe epilepsy: where to from here?

D. Goldstein, S. Sisodiya, C. Depondt, 2005, Brain : a journal of neurology.

Extensive founder effect for distal renal tubular acidosis (dRTA) with sensorineural deafness in an isolated South American population

G. Bedoya, A. Ruiz-Linares, S. Povey, 2008, American journal of medical genetics. Part A.

The −1021C→T DBH gene variant is not associated with epilepsy or antiepileptic drug response

D. Goldstein, S. Sisodiya, C. Depondt, 2004, Neurology.

Identification of the tuberous sclerosis gene TSC1 on chromosome 9q34.

S Povey, D Ravine, D Lindhout, 1997, Science.

Familial distal renal tubular acidosis is associated with mutations in the red cell anion exchanger (Band 3, AE1) gene.

S. Povey, M. Tanner, M. Burley, 1997, The Journal of clinical investigation.

Extensive founder effect for distal renal tubular acidosis (dRTA) with sensorineural deafness in an isolated South American population

G. Bedoya, A. Ruiz-Linares, S. Povey, 2008, American journal of medical genetics. Part A.