Phelelani Thokozani Mpangase (Phelelani T Mpangase, Phelelani Mpangase)

Publication Activity (10 Years)

Years Active: 2021-2024
Publications (10 Years): 9

Top Topics

Peritoneal Dialysis

African American

Dna Methylation

Top Venues

European journal of human genetics : EJHG

medRxiv : the preprint server for health sciences

BMJ global health

South African computer journal = Suid-Afrikaanse rekenaartydskrif

This page only lists publications with an associated author ORCID identifier.

Publications

Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
Correction: STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Musalula Sinkala, Gaone Retshabile, Phelelani Thokozani Mpangase, Salia Bamba, Modibo K Goita, Victoria Nembaware, Samar S M Elsheikh, Jeannine M Heckmann, Kevin Kum Esoh, Mogomotsi Matshaba, Clement A Adebamowo, Sally N Adebamowo, Ofon E Amih, Ambroise Wonkam, Michelle Ramsay, Nicola M Mulder
Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations. medRxiv : the preprint server for health sciences (2024)
Fahmida Essop, Bronwyn Dillon, Felicity Mhlongo, Louisa Bhengu, Thirona Naicker, Lindsay Lambie, Liani Smit, Karen Fieggen, Anneline Lochan, Jessica Dawson, Phelelani Thokozani Mpangase, Marc Hauptfleisch, Gail Scher, Odirile Tabane, Marelize Immelman, Michael Urban, Amanda Krause
STAC3 disorder: a common cause of congenital hypotonia in Southern African patients. European journal of human genetics : EJHG (2024)
Michelle Kamp, Okechinyere J Achilonu, Isaac Kisiangani, Daniel Maina Nderitu, Phelelani Thokozani Mpangase, Girmaw Abebe Tadesse, Kayode Adetunji, Samuel Iddi, Skyler Speakman, Scott Hazelhurst, Gershim Asiki, Michelle Ramsay, null null
Multimorbidity in African ancestry populations: a scoping review. BMJ global health 8 (12) (2023)
Phelelani Thokozani Mpangase, Jacqueline Frost, Mohammed Tikly, Michelle Ramsay, Scott Hazelhurst
nf-rnaSeqCount: A Nextflow pipeline for obtaining raw read counts from RNA-seq data. South African computer journal = Suid-Afrikaanse rekenaartydskrif 33 (2) (2021)
Jenny Mary Mathew, Phelelani Thokozani Mpangase, Dhriti Sengupta, Stanford Kwanda, Demetra Mavri-Damelin, Michelle Ramsay
UGT1A1 regulatory variant with potential effect on efficacy of HIV and cancer drugs commonly prescribed in South Africa. Pharmacogenomics 22 (15) (2021)