Inferring mechanisms of copy number change from haplotype structures at the human DEFA1A3 locus

Por Black, Holly A, Khan, Fayeza F, Tyson, Jess, Armour, John AL
Publicado em 2014

Accurate measurement of gene copy number for human alpha-defensin DEFA1A3

Por Khan, Fayeza F, Carpenter, Danielle, Mitchell, Laura, Mansouri, Omniah, Black, Holly A, Tyson, Jess, Armour, John AL
Publicado em 2013

De novo mutations in autosomal recessive congenital malformations

Por Black, Holly A., Parry, David, Atanur, Santosh S., Ross, David, Rose, Elaine, Russell, Helen, Stock, Sarah, Warner, Jon, Porteous, Mary, Aitman, Timothy J., Evans, Margaret J.
Publicado no Genet Med (2016)

Absolute measurement of the tissue origins of cell-free DNA in the healthy state and following paracetamol overdose

Por Laurent, Danny, Semple, Fiona, Starkey Lewis, Philip J., Rose, Elaine, Black, Holly A., Coe, Jennifer, Forbes, Stuart J., Arends, Mark J., Dear, James W., Aitman, Timothy J.
Publicado no BMC Med Genomics (2020)

Genetic epidemiology of motor neuron disease-associated variants in the Scottish population

Por Black, Holly A., Leighton, Danielle J., Cleary, Elaine M., Rose, Elaine, Stephenson, Laura, Colville, Shuna, Ross, David, Warner, Jon, Porteous, Mary, Gorrie, George H., Swingler, Robert, Goldstein, David, Harms, Matthew B., Connick, Peter, Pal, Suvankar, Aitman, Timothy J., Chandran, Siddharthan
Publicado no Neurobiol Aging (2017)

Corrigendum to “Genetic epidemiology of motor neuron disease-associated variants in the Scottish population.” [Neurobiol. Aging 51 (2017) 178.e11–178.e20]

Por Black, Holly A., Leighton, Danielle J., Cleary, Elaine M., Rose, Elaine, Stephenson, Laura, Colville, Shuna, Ross, David, Warner, Jon, Porteous, Mary, Gorrie, George H., Swingler, Robert, Goldstein, David, Harms, Matthew B., Connick, Peter, Pal, Suvankar, Aitman, Timothy J., Chandran, Siddharthan
Publicado no Neurobiol Aging (2017)