W. Hulme

Comparison of Three Targeted Enrichment Strategies on the SOLiD Sequencing Platform

J. Gilbert, M. Pericak-Vance, Shan Yang, 2011, PloS one.

Identification of New Viral Genes and Transcript Isoforms during Epstein-Barr Virus Reactivation using RNA-Seq

D. Hedges, E. Flemington, W. Hulme, 2011, Journal of Virology.

Variants in toll-like receptors 2 and 9 influence susceptibility to pulmonary tuberculosis in Caucasians, African-Americans, and West Africans

J. Gilbert, G. Sirugo, C. Hamilton, 2009, Human Genetics.

Mutations in phospholipase DDHD2 cause autosomal recessive hereditary spastic paraplegia (SPG54)

S. Züchner, R. Schüle, L. Schöls, 2013, European Journal of Human Genetics.

Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families

S. Züchner, W. Brown, Michael A. Gonzalez, 2012, PloS one.

Correction: Mutations in the Gene DNAJC5 Cause Autosomal Dominant Kufs Disease in a Proportion of Cases: Study of the Parry Family and 8 Other Families

S. Züchner, W. Brown, Michael A. Gonzalez, 2012, PLoS ONE.

Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variants

Derek J Van Booven, J. Gilbert, M. Cuccaro, 2015, Molecular Autism.

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders

Eden R Martin, Derek Van Booven, Susan H Slifer, 2014, Molecular Autism.

Whole-exome sequencing links a variant in DHDDS to retinitis pigmentosa.

Juan I. Young, J. Buxbaum, J. Haines, 2011, American journal of human genetics.

Whole-Genome Sequencing of the Akata and Mutu Epstein-Barr Virus Strains

D. Hedges, E. Flemington, W. Hulme, 2012, Journal of Virology.

Exome sequencing allows for rapid gene identification in a Charcot‐Marie‐Tooth family

Stephan Züchner, William Hulme, S. Züchner, 2011, Annals of neurology.

Whole Genome Sequencing and a New Bioinformatics Platform Allow for Rapid Gene Identification in D. melanogaster EMS Screens

Derek J. Van Booven, Michael A. Gonzalez, M. Logan, 2012, Biology.

Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and Caucasians.

J. Gilbert, C. Hamilton, W. Scott, 2009, The international journal of tuberculosis and lung disease : the official journal of the International Union against Tuberculosis and Lung Disease.

NOS2A, TLR4, and IFNGR1 interactions influence pulmonary tuberculosis susceptibility in African-Americans

Carol D. Hamilton, John R. Gilbert, William K. Scott, 2009, Human Genetics.