FLT1 and other candidate fetal haemoglobin modifying loci in sickle cell disease in African ancestries.

Journal: Nature communications

Publication Year: 2025

Authors & Co-authors:  Wonkam Ambroise A Esoh Kevin K Levine Rachel M RM Ngo Bitoungui Valentina Josiane VJ Mnika Khuthala K Nimmagadda Nikitha N Dempsey Erin A D EAD Nkya Siana S Sangeda Raphael Z RZ Nembaware Victoria V

Mapping Epigenetic Gene Variant Dynamics: Comparative Analysis of Frequency, Functional Impact and Trait Associations in African and European Populations.

Journal: medRxiv : the preprint server for health sciences

Publication Year: 

Authors & Co-authors:  Sinkala Musalula M Retshabile Gaone G Mpangase Phelelani T PT Bamba Salia S Goita Modibo K MK Nembaware Vicky V Elsheikh Samar S M SSM Heckmann Jeannine J Esoh Kevin K Matshaba Mogomotsi M

Post genome-wide association analysis: dissecting computational pathway/network-based approaches.

Journal: Briefings in bioinformatics

Publication Year: 2020

Authors & Co-authors:  Chimusa Emile R ER Dalvie Shareefa S Dandara Collet C Wonkam Ambroise A Mazandu Gaston K GK

Perceptions of parents of children with hearing loss of genetic origin in South Africa.

Journal: Journal of community genetics

Publication Year: 

Authors & Co-authors:  Gardiner Sinead Amber SA Laing Nakita N Mall Sumaya S Wonkam Ambroise A

Cascade Testing for Fragile X Syndrome in a Rural Setting in Cameroon (Sub-Saharan Africa).

Journal: Genes

Publication Year: 2020

Authors & Co-authors:  Kengne Kamga Karen K Nguefack Séraphin S Minka Khuthala K Wonkam Tingang Edmond E Esterhuizen Alina A Nchangwi Munung Syntia S De Vries Jantina J Wonkam Ambroise A

MECP2 duplication syndrome in a patient from Cameroon.

Journal: American journal of medical genetics. Part A

Publication Year: 2021

Authors & Co-authors:  Tekendo-Ngongang Cedrik C Dahoun Sophie S Nguefack Séraphin S Moix Isabelle I Gimelli Stefania S Zambo Huguette H Morris Michael A MA Sloan-Béna Frédérique F Wonkam Ambroise A

Explanatory models for the cause of Fragile X Syndrome in rural Cameroon.

Journal: Journal of genetic counseling

Publication Year: 2022

Authors & Co-authors:  Kengne Kamga Karen K De Vries Jantina J Nguefack Séraphin S Munung Nchangwi Syntia NS Wonkam Ambroise A

Building Skills and Resources for Genomics, Epigenetics, and Bioinformatics Research for Africa: Report of the Joint 11th Conference of the African Society of Human Genetics and 12th H3Africa Consortium, 2018.

Journal: The American journal of tropical medicine and hygiene

Publication Year: 2020

Authors & Co-authors:  Musanabaganwa Clarisse C Mihigo Bonaventure B Tumusime Robert R Uwanyirigira Mediatrice M da Rocha Jorge J Hayat Mahtaab M Govender Melanie M Buto Peace P Nyunga Tina T Ramesar Raj S RS