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    The African Coelecanth genome provides insights into tetrapod evolution 

    Christoffels, Alan; Hesse, Uljana; Gamieldien, Junaid; Panji, Sumir; Picone, Barbara; Van Heusden, Peter (Macmillan Publishers, 2013)
    The discovery of a living coelacanth specimen in 1938 was remarkable, as this lineage of lobe-finned fish was thought to have become extinct 70 million years ago. The modern coelacanth looks remarkably similar to many of ...
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    Self-similarity of human protein interaction networks: a novel strategy of distinguishing proteins 

    Fadhal, Emad; Gamieldien, Junaid; Mwambene, Eric (2015)
    The successful determination of reliable protein interaction networks (PINs) in several species in the post-genomic era has hitherto facilitated the quest to understanding systems and structural properties of such networks. ...
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    Whole-genome sequencing for an enhanced understanding of genetic variation among South Africans 

    Choudhury, Ananyo; Christoffels, Alan; Gamieldien, Junaid; Sefid-Dashti, Mahjoubeh J. (Nature Publishing Group, 2017)
    The Southern African Human Genome Programme is a national initiative that aspires to unlock the unique genetic character of southern African populations for a better understanding of human genetic diversity. In this pilot ...
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    A 35-gene signature discriminates between rapidly- and slowly-progressing glioblastoma multiforme and predicts survival in known subtypes of the cancer 

    Fatai, Azeez A.; Gamieldien, Junaid (BioMed Central, 2018)
    BACKGROUND: Gene expression can be employed for the discovery of prognostic gene or multigene signatures cancer. In this study, we assessed the prognostic value of a 35-gene expression signature selected by pathway ...
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    Exome sequencing identifies novel dysferlin mutation in a family with paucisymptomatic heterozygous carriers 

    Jalali-Sefid-Dashti, Mahjoubeh; Nel, Melissa; Heckmann, Jeannine M.; Gamieldien, Junaid (BioMed Central, 2018)
    BACKGROUND: We investigated a South African family of admixed ancestry in which the first generation (G1) developed insidious progressive distal to proximal weakness in their twenties, while their offspring (G2) experienced ...
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    Defining the molecular signatures of Achilles tendinopathy and anterior cruciate ligament ruptures: A whole-exome sequencing approach 

    Gibbon, Andrea; Saunders, Colleen J.; Collins, Malcolm; Gamieldien, Junaid; September, Alison V. (Public Library of Science, 2018)
    Musculoskeletal soft tissue injuries are complex phenotypes with genetics being one of many proposed risk factors. Case-control association studies using the candidate gene approach have predominately been used to identify ...
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    Defining the molecular signatures of Achilles tendinopathy and anterior cruciate ligament ruptures: A whole-exome sequencing approach 

    Gibbon, Andrea; Saunders, Colleen J.; Collins, Malcolm; Gamieldien, Junaid; September, Alison V. (Public Library of Science, 2018)
    Musculoskeletal soft tissue injuries are complex phenotypes with genetics being one of many proposed risk factors. Case-control association studies using the candidate gene approach have predominately been used to identify ...
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    Exome sequencing identifies novel dysferlin mutation in a family with pauci-symptomatic heterozygous carriers 

    Jalali-Sefid-Dashti, Mahjoubeh; Nel, Melissa; Heckmann, Jeannine M.; Gamieldien, Junaid (Springer Nature, 2018)
    Background: We investigated a South African family of admixed ancestry in which the first generation (G1) developed insidious progressive distal to proximal weakness in their twenties, while their offspring (G2) experienced ...
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    Identification of novel prognostic markers of survival time in high-risk neuroblastoma using gene expression profiles 

    Giwa, Abdulazeez; Fatai, Azeez A.; Gamieldien, Junaid (Impact Journals, 2020)
    Neuroblastoma is the most common extracranial solid tumor in childhood. Patients in high-risk group often have poor outcomes with low survival rates despite several treatment options. This study aimed to identify a genetic ...

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    Gamieldien, Junaid (9)
    Christoffels, Alan (2)Collins, Malcolm (2)Fatai, Azeez A. (2)Gibbon, Andrea (2)Heckmann, Jeannine M. (2)Jalali-Sefid-Dashti, Mahjoubeh (2)Nel, Melissa (2)Saunders, Colleen J. (2)September, Alison V. (2)... View MoreSubjectCramps (2)Dysferlinopathy (2)Exome (2)Musculoskeletal soft tissue injuries (2)Myalgia (2)Pauci-symptomatic carriers (2)African populations (1)Chemoradiation resistance pathways (1)Coelecanth genome (1)Complex phenotypes (1)... View MoreDate Issued2020 (1)2018 (5)2017 (1)2015 (1)2013 (1)

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