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Items: 1 to 20 of 116

1.

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.

Musanabaganwa C, Mihigo B, Tumusime R, Uwanyirigira M, da Rocha J, Hayat M, Govender M, Buto P, Nyunga T, Ramesar RS, Rotimi C, Souopgui J, Wonkam A, Williams SM, Jansen S, Ramsay M, Mutesa L.

Am J Trop Med Hyg. 2020 Mar 23. doi: 10.4269/ajtmh.19-0837. [Epub ahead of print]

PMID:
32207403
2.

Lived Experiences of Fragile X Syndrome Caregivers: A Scoping Review of Qualitative Studies.

Kamga KK, De Vries J, Nguefack S, Munung SN, Wonkam A.

Front Neurol. 2020 Feb 27;11:128. doi: 10.3389/fneur.2020.00128. eCollection 2020. Review.

3.

Hearing Impairment Overview in Africa: the Case of Cameroon.

Wonkam Tingang E, Noubiap JJ, F Fokouo JV, Oluwole OG, Nguefack S, Chimusa ER, Wonkam A.

Genes (Basel). 2020 Feb 22;11(2). pii: E233. doi: 10.3390/genes11020233. Review.

4.

MECP2 duplication syndrome in a patient from Cameroon.

Tekendo-Ngongang C, Dahoun S, Nguefack S, Moix I, Gimelli S, Zambo H, Morris MA, Sloan-Béna F, Wonkam A.

Am J Med Genet A. 2020 Apr;182(4):619-622. doi: 10.1002/ajmg.a.61510. Epub 2020 Feb 13.

PMID:
32052928
5.

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

Kengne Kamga K, Nguefack S, Minka K, Wonkam Tingang E, Esterhuizen A, Nchangwi Munung S, De Vries J, Wonkam A.

Genes (Basel). 2020 Jan 28;11(2). pii: E136. doi: 10.3390/genes11020136.

6.

Enhancing Genetic Medicine: Rapid and Cost-Effective Molecular Diagnosis for a GJB2 Founder Mutation for Hearing Impairment in Ghana.

Adadey SM, Tingang Wonkam E, Twumasi Aboagye E, Quansah D, Asante-Poku A, Quaye O, Amedofu GK, Awandare GA, Wonkam A.

Genes (Basel). 2020 Jan 27;11(2). pii: E132. doi: 10.3390/genes11020132.

7.

SickleInAfrica.

Makani J, Sangeda RZ, Nnodu O, Nembaware V, Osei-Akoto A, Paintsil V, Balandya E, Kent J, Luzzatto L, Ofori-Acquah S, Olopade OI, Pallangyo K, Minja IK, Jonas M, Mazandu GK, Mulder N, Ohene-Frempong K, Wonkam A.

Lancet Haematol. 2020 Feb;7(2):e98-e99. doi: 10.1016/S2352-3026(20)30006-5. No abstract available.

PMID:
32004491
8.

The African Genomic Medicine Training Initiative (AGMT): Showcasing a Community and Framework Driven Genomic Medicine Training for Nurses in Africa.

Nembaware V; African Genomic Medicine Training Initiative, Mulder N.

Front Genet. 2019 Dec 20;10:1209. doi: 10.3389/fgene.2019.01209. eCollection 2019.

9.

Turner syndrome in diverse populations.

Kruszka P, Addissie YA, Tekendo-Ngongang C, Jones KL, Savage SK, Gupta N, Sirisena ND, Dissanayake VHW, Paththinige CS, Aravena T, Nampoothiri S, Yesodharan D, Girisha KM, Patil SJ, Jamuar SS, Goh JC, Utari A, Sihombing N, Mishra R, Chitrakar NS, Iriele BC, Lulseged E, Megarbane A, Uwineza A, Oyenusi EE, Olopade OB, Fasanmade OA, Duenas-Roque MM, Thong MK, Tung JYL, Mok GTK, Fleischer N, Rwegerera GM, de Herreros MB, Watts J, Fieggen K, Huckstadt V, Moresco A, Obregon MG, Hussen DF, Ashaat NA, Ashaat EA, Chung BHY, Badoe E, Faradz SMH, El Ruby MO, Shotelersuk V, Wonkam A, Ekure EN, Phadke SR, Richieri-Costa A, Muenke M.

Am J Med Genet A. 2020 Feb;182(2):303-313. doi: 10.1002/ajmg.a.61461. Epub 2019 Dec 19.

PMID:
31854143
10.

Urinary Transforming Growth Factor-Beta 1 (uTGF-β1) and Prevalent CKD Risk in HIV-Positive Patients in West Africa.

Ekrikpo UE, Okuku CN, Ajayi SO, Ayodele OE, Bello AK, Wonkam A, Dandara C, Kengne AP, Okpechi I.

Kidney Int Rep. 2019 Jul 27;4(12):1698-1704. doi: 10.1016/j.ekir.2019.07.011. eCollection 2019 Dec.

11.

Returning incidental findings in African genomics research.

Wonkam A, de Vries J.

Nat Genet. 2020 Jan;52(1):17-20. doi: 10.1038/s41588-019-0542-4. No abstract available.

PMID:
31768070
12.

The Hearing Impairment Ontology: A Tool for Unifying Hearing Impairment Knowledge to Enhance Collaborative Research.

Hotchkiss J, Manyisa N, Adadey SM, Oluwole OG, Wonkam E, Mnika K, Yalcouye A, Nembaware V, Haendel M, Vasilevsky N, Mulder NJ, Jupp S, Wonkam A, Mazandu GK.

Genes (Basel). 2019 Nov 21;10(12). pii: E960. doi: 10.3390/genes10120960.

13.

GJB2 and GJB6 Mutations in Hereditary Recessive Non-Syndromic Hearing Impairment in Cameroon.

Tingang Wonkam E, Chimusa E, Noubiap JJ, Adadey SM, F Fokouo JV, Wonkam A.

Genes (Basel). 2019 Oct 25;10(11). pii: E844. doi: 10.3390/genes10110844.

14.

Establishing a Multi-Country Sickle Cell Disease Registry in Africa: Ethical Considerations.

Munung NS, Nembaware V, de Vries J, Bukini D, Tluway F, Treadwell M, Sangeda RZ, Mazandu G, Jonas M, Paintsil V, Nnodu OE, Balandya E, Makani J, Wonkam A.

Front Genet. 2019 Oct 10;10:943. doi: 10.3389/fgene.2019.00943. eCollection 2019.

15.

GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana.

Adadey SM, Manyisa N, Mnika K, de Kock C, Nembaware V, Quaye O, Amedofu GK, Awandare GA, Wonkam A.

Front Genet. 2019 Sep 18;10:841. doi: 10.3389/fgene.2019.00841. eCollection 2019. Erratum in: Front Genet. 2019 Nov 26;10:1151.

16.

Implementing Artificial Intelligence and Digital Health in Resource-Limited Settings? Top 10 Lessons We Learned in Congenital Heart Defects and Cardiology.

Thomford NE, Bope CD, Agamah FE, Dzobo K, Owusu Ateko R, Chimusa E, Mazandu GK, Ntumba SB, Dandara C, Wonkam A.

OMICS. 2019 Oct 8. doi: 10.1089/omi.2019.0142. [Epub ahead of print]

PMID:
31592719
17.

Sickle cell disease in Africa: an urgent need for longitudinal cohort studies.

Wonkam A, Makani J.

Lancet Glob Health. 2019 Oct;7(10):e1310-e1311. doi: 10.1016/S2214-109X(19)30364-X. Epub 2019 Aug 23. No abstract available.

18.

Exploring the Role of Shared Decision Making in the Consent Process for Pediatric Genomics Research in Cameroon, Tanzania, and Ghana.

Bukini D, deVries J, Treadwell M, Anie K, Dennis-Antwi J, Kamga KK, McCurdy S, Ohene-Frempong K, Makani J, Wonkam A.

AJOB Empir Bioeth. 2019 Jul-Sep;10(3):182-189. doi: 10.1080/23294515.2019.1645759. Epub 2019 Aug 5.

PMID:
31379268
19.

Dissecting in silico Mutation Prediction of Variants in African Genomes: Challenges and Perspectives.

Bope CD, Chimusa ER, Nembaware V, Mazandu GK, de Vries J, Wonkam A.

Front Genet. 2019 Jun 25;10:601. doi: 10.3389/fgene.2019.00601. eCollection 2019.

20.

Hydroxyurea-Induced miRNA Expression in Sickle Cell Disease Patients in Africa.

Mnika K, Mazandu GK, Jonas M, Pule GD, Chimusa ER, Hanchard NA, Wonkam A.

Front Genet. 2019 May 28;10:509. doi: 10.3389/fgene.2019.00509. eCollection 2019.

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