Semantic interrogation of a multi knowledge domain ontological model of tendinopathy identifies four strong candidate risk genes

Por Saunders, Colleen J., Jalali Sefid Dashti, Mahjoubeh, Gamieldien, Junaid
Publicado no Sci Rep (2016)

Exome sequencing identifies novel dysferlin mutation in a family with pauci-symptomatic heterozygous carriers

Por Jalali-Sefid-Dashti, Mahjoubeh, Nel, Melissa, Heckmann, Jeannine M., Gamieldien, Junaid
Publicado no BMC Med Genet (2018)

Exome sequencing combined with semantic discovery identifies strong disease-associated candidates in a single case of relapsing remitting multiple sclerosis

Por Jalali Sefid Dashti Mahjoubeh, Kotze Maritha, van Rensburg Susan, Christoffels Alan, Gamieldien Junaid
Publicado em 2012-10-01

Exome sequencing combined with semantic discovery identifies strong disease-associated candidates in a single case of relapsing remitting multiple sclerosis

Por Jalali Sefid Dashti, Mahjoubeh, Kotze, Maritha, van Rensburg, Susan Janse, Christoffels, Alan, Gamieldien, Junaid
Publicado em 2012

Population-specific common SNPs reflect demographic histories and highlight regions of genomic plasticity with functional relevance

Por Choudhury, Ananyo, Hazelhurst, Scott, Meintjes, Ayton, Achinike-Oduaran, Ovokeraye, Aron, Shaun, Gamieldien, Junaid, Jalali Sefid Dashti, Mahjoubeh, Mulder, Nicola, Tiffin, Nicki, Ramsay, Michèle
Publicado em 2014