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Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans.

Human molecular genetics

Fatumo S, Chikowore T, Kalyesubula R, Nsubuga RN, Asiki G, Nashiru O, Seeley J, Crampin AC, Nitsch D, Smeeth L, Kaleebu P, Burgess S, Nyirenda M, Franceschini N, Morris AP, Tomlinson L, Newton R.
PMID: 33783510
Hum Mol Genet. 2021 Jul 28;30(16):1559-1568. doi: 10.1093/hmg/ddab088.

Genome-wide association studies (GWAS) of kidney function have uncovered hundreds of loci, primarily in populations of European ancestry. We have undertaken the first continental African GWAS of estimated glomerular filtration rate (eGFR), a measure of kidney function used to...

Cite
Fatumo S, Chikowore T, Kalyesubula R, et al. Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Hum Mol Genet. 2021;30(16):1559-1568doi: 10.1093/hmg/ddab088.
Fatumo, S., Chikowore, T., Kalyesubula, R., Nsubuga, R. N., Asiki, G., Nashiru, O., Seeley, J., Crampin, A. C., Nitsch, D., Smeeth, L., Kaleebu, P., Burgess, S., Nyirenda, M., Franceschini, N., Morris, A. P., Tomlinson, L., & Newton, R. (2021). Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Human molecular genetics, 30(16), 1559-1568. https://doi.org/10.1093/hmg/ddab088
Fatumo, Segun, et al. "Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans." Human molecular genetics vol. 30,16 (2021): 1559-1568. doi: https://doi.org/10.1093/hmg/ddab088
Fatumo S, Chikowore T, Kalyesubula R, Nsubuga RN, Asiki G, Nashiru O, Seeley J, Crampin AC, Nitsch D, Smeeth L, Kaleebu P, Burgess S, Nyirenda M, Franceschini N, Morris AP, Tomlinson L, Newton R. Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Hum Mol Genet. 2021 Jul 28;30(16):1559-1568. doi: 10.1093/hmg/ddab088. PMID: 33783510; PMCID: PMC8330895.
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Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits.

Frontiers in genetics

Fatumo S, Carstensen T, Nashiru O, Gurdasani D, Sandhu M, Kaleebu P.
PMID: 31080455
Front Genet. 2019 Apr 26;10:334. doi: 10.3389/fgene.2019.00334. eCollection 2019.

Genome-wide association studies (GWAS) have found hundreds of novel loci associated with full blood count (FBC) phenotypes. However, most of these studies were performed in a single phenotype framework without putting into consideration the clinical relatedness among traits. In...

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Fatumo S, Carstensen T, Nashiru O, et al. Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Front Genet. 2019;10:334doi: 10.3389/fgene.2019.00334.
Fatumo, S., Carstensen, T., Nashiru, O., Gurdasani, D., Sandhu, M., & Kaleebu, P. (2019). Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Frontiers in genetics, 10334. https://doi.org/10.3389/fgene.2019.00334
Fatumo, Segun, et al. "Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits." Frontiers in genetics vol. 10 (2019): 334. doi: https://doi.org/10.3389/fgene.2019.00334
Fatumo S, Carstensen T, Nashiru O, Gurdasani D, Sandhu M, Kaleebu P. Complimentary Methods for Multivariate Genome-Wide Association Study Identify New Susceptibility Genes for Blood Cell Traits. Front Genet. 2019 Apr 26;10:334. doi: 10.3389/fgene.2019.00334. eCollection 2019. PMID: 31080455; PMCID: PMC6497788.
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Leukocyte methylomic imprints of exposure to the genocide against the Tutsi in Rwanda: a pilot epigenome-wide analysis.

Epigenomics

Musanabaganwa C, Wani AH, Donglasan J, Fatumo S, Jansen S, Mutabaruka J, Rutembesa E, Uwineza A, Hermans EJ, Roozendaal B, Wildman DE, Mutesa L, Uddin M.
PMID: 34875875
Epigenomics. 2022 Jan;14(1):11-25. doi: 10.2217/epi-2021-0310. Epub 2021 Dec 08.

No abstract available.

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Musanabaganwa C, Wani AH, Donglasan J, et al. Leukocyte methylomic imprints of exposure to the genocide against the Tutsi in Rwanda: a pilot epigenome-wide analysis. Epigenomics. 2021;14(1):11-25doi: 10.2217/epi-2021-0310.
Musanabaganwa, C., Wani, A. H., Donglasan, J., Fatumo, S., Jansen, S., Mutabaruka, J., Rutembesa, E., Uwineza, A., Hermans, E. J., Roozendaal, B., Wildman, D. E., Mutesa, L., & Uddin, M. (2022). Leukocyte methylomic imprints of exposure to the genocide against the Tutsi in Rwanda: a pilot epigenome-wide analysis. Epigenomics, 14(1), 11-25. https://doi.org/10.2217/epi-2021-0310
Musanabaganwa, Clarisse, et al. "Leukocyte methylomic imprints of exposure to the genocide against the Tutsi in Rwanda: a pilot epigenome-wide analysis." Epigenomics vol. 14,1 (2022): 11-25. doi: https://doi.org/10.2217/epi-2021-0310
Musanabaganwa C, Wani AH, Donglasan J, Fatumo S, Jansen S, Mutabaruka J, Rutembesa E, Uwineza A, Hermans EJ, Roozendaal B, Wildman DE, Mutesa L, Uddin M. Leukocyte methylomic imprints of exposure to the genocide against the Tutsi in Rwanda: a pilot epigenome-wide analysis. Epigenomics. 2022 Jan;14(1):11-25. doi: 10.2217/epi-2021-0310. Epub 2021 Dec 08. PMID: 34875875; PMCID: PMC8672329.
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Traumatic Stress Epigenetics.

Current behavioral neuroscience reports

Pfeiffer JR, Mutesa L, Uddin M.
PMID: 30225184
Curr Behav Neurosci Rep. 2018 Mar;5(1):81-93. doi: 10.1007/s40473-018-0143-z. Epub 2018 Feb 13.

PURPOSE OF REVIEW: Traumatic stress has profound impacts on many domains of life, yet the mechanisms that confer risk for or resilience to the development of traumatic stress-related psychopathologies are still very much under investigation. The current review highlights...

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Pfeiffer JR, Mutesa L, Uddin M. Traumatic Stress Epigenetics. Curr Behav Neurosci Rep. 2018;5(1):81-93doi: 10.1007/s40473-018-0143-z.
Pfeiffer, J. R., Mutesa, L., & Uddin, M. (2018). Traumatic Stress Epigenetics. Current behavioral neuroscience reports, 5(1), 81-93. https://doi.org/10.1007/s40473-018-0143-z
Pfeiffer, John R, et al. "Traumatic Stress Epigenetics." Current behavioral neuroscience reports vol. 5,1 (2018): 81-93. doi: https://doi.org/10.1007/s40473-018-0143-z
Pfeiffer JR, Mutesa L, Uddin M. Traumatic Stress Epigenetics. Curr Behav Neurosci Rep. 2018 Mar;5(1):81-93. doi: 10.1007/s40473-018-0143-z. Epub 2018 Feb 13. PMID: 30225184; PMCID: PMC6138446.
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Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans.

Human molecular genetics

Fatumo S, Chikowore T, Kalyesubula R, Nsubuga RN, Asiki G, Nashiru O, Seeley J, Crampin AC, Nitsch D, Smeeth L, Kaleebu P, Burgess S, Nyirenda M, Franceschini N, Morris AP, Tomlinson L, Newton R.
PMID: 33783510
Hum Mol Genet. 2021 Jul 28;30(16):1559-1568. doi: 10.1093/hmg/ddab088.

Genome-wide association studies (GWAS) of kidney function have uncovered hundreds of loci, primarily in populations of European ancestry. We have undertaken the first continental African GWAS of estimated glomerular filtration rate (eGFR), a measure of kidney function used to...

Cite
Fatumo S, Chikowore T, Kalyesubula R, et al. Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Hum Mol Genet. 2021;30(16):1559-1568doi: 10.1093/hmg/ddab088.
Fatumo, S., Chikowore, T., Kalyesubula, R., Nsubuga, R. N., Asiki, G., Nashiru, O., Seeley, J., Crampin, A. C., Nitsch, D., Smeeth, L., Kaleebu, P., Burgess, S., Nyirenda, M., Franceschini, N., Morris, A. P., Tomlinson, L., & Newton, R. (2021). Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Human molecular genetics, 30(16), 1559-1568. https://doi.org/10.1093/hmg/ddab088
Fatumo, Segun, et al. "Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans." Human molecular genetics vol. 30,16 (2021): 1559-1568. doi: https://doi.org/10.1093/hmg/ddab088
Fatumo S, Chikowore T, Kalyesubula R, Nsubuga RN, Asiki G, Nashiru O, Seeley J, Crampin AC, Nitsch D, Smeeth L, Kaleebu P, Burgess S, Nyirenda M, Franceschini N, Morris AP, Tomlinson L, Newton R. Discovery and fine-mapping of kidney function loci in first genome-wide association study in Africans. Hum Mol Genet. 2021 Jul 28;30(16):1559-1568. doi: 10.1093/hmg/ddab088. PMID: 33783510; PMCID: PMC8330895.
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Transcription-translation error: .

Informatics in medicine unlocked

Soremekun OS, Ezenwa C, Soliman M, Chikowore T, Nashiru O, Fatumo S.
PMID: 33665355
Inform Med Unlocked. 2021;22. doi: 10.1016/j.imu.2020.100503. Epub 2020 Dec 24.

Nonsynonymous single nucleotide polymorphisms (nsSNPs) are one of the most common forms of mutations known to disrupt the product of translation thereby altering the protein structure-function relationship.

Cite
Soremekun OS, Ezenwa C, Soliman M, et al. Transcription-translation error: . Inform Med Unlocked. 2020;22doi: 10.1016/j.imu.2020.100503.
Soremekun, O. S., Ezenwa, C., Soliman, M., Chikowore, T., Nashiru, O., & Fatumo, S. (2021). Transcription-translation error: . Informatics in medicine unlocked, 22. https://doi.org/10.1016/j.imu.2020.100503
Soremekun, Opeyemi S, et al. "Transcription-translation error: ." Informatics in medicine unlocked vol. 22 (2021). doi: https://doi.org/10.1016/j.imu.2020.100503
Soremekun OS, Ezenwa C, Soliman M, Chikowore T, Nashiru O, Fatumo S. Transcription-translation error: . Inform Med Unlocked. 2021;22. doi: 10.1016/j.imu.2020.100503. Epub 2020 Dec 24. PMID: 33665355; PMCID: PMC7928429.
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