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Scientific Reports (2)
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Showing 1–5 of 5 results

Advanced filters: Author: Kevin K. Esoh Clear advanced filters

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

Here, the authors perform a genome-wide association study of fetal haemoglobin (HbF) levels in Africans with sickle cell disease replicating known loci, identifing 14 candidate loci, and highlighting FLT1’s role in hypoxia-associated HbF induction.

Ambroise Wonkam
Kevin Esoh
Stylianos E. Antonarakis
ResearchOpen Access01 Mar 2025
Nature Communications

Volume: 16, P: 1-21
Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

Samuel M. Adadey
Isabelle Schrauwen
Ambroise Wonkam
ResearchOpen Access05 Jul 2021
Journal of Human Genetics

Volume: 66, P: 1169-1175
Fine scale human genetic structure in three regions of Cameroon reveals episodic diversifying selection

Kevin K. Esoh
Tobias O. Apinjoh
Eric A. Achidi
ResearchOpen Access13 Jan 2021
Scientific Reports

Volume: 11, P: 1-13
Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

Whole-exome sequencing for 51 families in Ghana reveals 7 candidate genes associated with hearing impairment, 6 of which have previously been demonstrated to be expressed in the mouse inner ear.

Ambroise Wonkam
Samuel Mawuli Adadey
Suzanne M. Leal
ResearchOpen Access19 Apr 2022
Communications Biology

Volume: 5, P: 1-16
In-silico design of a multi-epitope vaccine candidate against onchocerciasis and related filarial diseases

Robert Adamu Shey
Stephen Mbigha Ghogomu
Jacob Souopgui
ResearchOpen Access13 Mar 2019
Scientific Reports

Volume: 9, P: 1-18