Search Results - "Ojewunmi, Oyesola"

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    A survey of genetic fetal-haemoglobin modifiers in Nigerian patients with sickle cell anaemia by Adeyemo, Titilope A, Ojewunmi, Oyesola O, Oyetunji, Idat A, Rooks, Helen, Rees, David C, Akinsulie, Adebola O, Akanmu, Alani S, Thein, Swee Lay, Menzel, Stephan

    Published in PloS one (07-06-2018)
    “…Genetic variants at three quantitative trait loci (QTL) for fetal haemoglobin (HbF), BCL11A, HBS1L-MYB and the β-globin gene cluster, have attracted interest…”
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    Journal Article
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    Health related quality of life and perception of stigmatisation in adolescents living with sickle cell disease in Nigeria: A cross sectional study by Adeyemo, Titilope A., Ojewunmi, Oyesola O., Diaku-Akinwumi, Ijeoma N., Ayinde, Oluwaseyi C., Akanmu, Alani S.

    Published in Pediatric blood & cancer (01-07-2015)
    “…Background Sickle cell disease impacts the physical, emotional and psychological aspects of life of the affected persons, often times exposing them to disease…”
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    Journal Article
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    Accounting for heterogeneity due to environmental sources in meta-analysis of genome-wide association studies by Wang, Siru, Ojewunmi, Oyesola O., Kamiza, Abram, Ramsay, Michele, Morris, Andrew P., Chikowore, Tinashe, Fatumo, Segun, Asimit, Jennifer L.

    Published in Communications biology (14-11-2024)
    “…Meta-analysis of genome-wide association studies (GWAS) across diverse populations offers power gains to identify loci associated with complex traits and…”
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    Journal Article
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    Current perspectives of sickle cell disease in Nigeria: changing the narratives by Ojewunmi, Oyesola O, Adeyemo, Titilope A, Ayinde, Oluseyi C, Iwalokun, Bamidele, Adekile, Adekunle

    Published in Expert review of hematology (03-08-2019)
    “…: Sickle cell disease (SCD) is an inherited blood disorder characterized by clinical heterogeneity that may be influenced by environmental factors, ethnicity,…”
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    Journal Article
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    Barriers to the use of hydroxyurea in the management of sickle cell disease in Nigeria by Adeyemo, Titilope A., Diaku-Akinwunmi, Ijeoma N., Ojewunmi, Oyesola O., Bolarinwa, Abiola B., Adekile, Adekunle D.

    Published in Hemoglobin (04-05-2019)
    “…Hydroxyurea (HU) is a well-known Hb F-inducing agent with proven clinical and laboratory efficacy for patients with sickle cell disease. However, concerns…”
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    Journal Article
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    Fetal-haemoglobin enhancing genotype at BCL11A reduces HbA 2 levels in patients with sickle cell anaemia by Adeyemo, Titilope A, Ojewunmi, Oyesola O, Oyetunji, Idayat Ajoke, Kalejaiye, Olufunto Olufela, Menzel, Stephan

    Published in EJHaem (01-08-2021)
    “…Understanding the interplay of genetic factors with haemoglobin expression and pathological processes in sickle cell disease is important for pharmacological…”
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    Journal Article
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    Fetal‐haemoglobin enhancing genotype at BCL11A reduces HbA2 levels in patients with sickle cell anaemia by Adeyemo, Titilope A., Ojewunmi, Oyesola O., Oyetunji, Idayat Ajoke, Kalejaiye, Olufunto Olufela, Menzel, Stephan

    Published in EJHaem (01-08-2021)
    “…Understanding the interplay of genetic factors with haemoglobin expression and pathological processes in sickle cell disease is important for pharmacological…”
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    Journal Article
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    Prevalence, Determinants and Impact of Haemoglobin Phenotype Misdiagnosis Among Parents of Children Living with Sickle Cell Disease in Nigeria by Adekunle, Motunrayo Oluwabukola, Ojewunmi, Oyesola, Animasahun, Adeola Barakat, Lawani, Faith Ozavisa, Ubuane, Peter Odion

    Published in The journal of pediatric research (01-09-2021)
    “…Aim: Nigeria has the highest number of children with sickle cell disease (SCD) with a consistent prevalence of 2 to 3% despite increased awareness and…”
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    Journal Article
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    Contribution of single-nucleotide polymorphism in transcription factor 7-like 2 gene to cardiometabolic risk in adult Nigerians by Udenze, Ifeoma, Taiwo, Idowu, Ojewunmi, Oyesola

    “…Background: Single-nucleotide polymorphism in the gene, transcription factor 7-like 2 (TCF7L2), shows the strongest and most consistent association with risk…”
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    Serum concentrations of IL-16 and its genetic polymorphism rs4778889 affect the susceptibility and severity of endometriosis in Nigerian women by Babah, Ochuwa Adiketu, Ojewunmi, Oyesola Oyewole, Onwuamah, Chika Kingsley, Udenze, Ifeoma Christiana, Osuntoki, Akinniyi Adediran, Afolabi, Bosede Bukola

    Published in BMC women's health (11-05-2023)
    “…Endometriosis is the presence of active ectopic endometrial glands and stroma at other sites outside the uterine cavity. It is a common cause of chronic pelvic…”
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    Journal Article
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    Genetic Polymorphisms of Glucose-6-Phosphate Dehydrogenase in Lagos, Nigeria by Babalola, Musa O., Imaga, Ngozi A., Samuel, Titilola A., Diriwari, Iyanu P., Kolade, Olajumoke, Ezeamalu, Irene, Laoye, Adefioye O., Ojewunmi, Oyesola O.

    Published in Hemoglobin (02-01-2018)
    “…Glucose-6-phosphate dehydrogenase (G6PD) is an essential enzyme in the pentose phosphate pathway that prevents oxidative damage to cells. This study determined…”
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    Journal Article
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    Genetic polymorphisms of Vascular Endothelial Growth Factor (VEGF) associated with endometriosis in Nigerian women by Babah, Ochuwa Adiketu, Ojewunmi, Oyesola Oyewole, Osuntoki, Akinniyi Adediran, Simon, Melissa A, Afolabi, Bosede Bukola

    Published in Human genomics (30-10-2021)
    “…To determine if genetic polymorphism of VEGF is associated with the development of endometriosis in Nigerian women. Case control study of 100 women (50 healthy…”
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    Journal Article
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    Capacity building and stroke risk assessment in Nigerian children with sickle cell anaemia by Soyebi, Kofo, Adeyemo, Titilope, Ojewunmi, Oyesola, James, Funmi, Adefalujo, Kunle, Akinyanju, Olu

    Published in Pediatric blood & cancer (01-12-2014)
    “…Background Transcranial Doppler ultrasonography (TCD) measures blood flow velocities in the large cerebral vessels and thus, detects the risk of stroke. This…”
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    The COPILOT Raw Illumina Genotyping QC Protocol by Patel, Hamel, Lee, Sang-Hyuck, Breen, Gerome, Menzel, Stephen, Ojewunmi, Oyesola, Dobson, Richard J B

    Published in Current protocols (01-04-2022)
    “…The Illumina genotyping microarrays generate data in image format, which is processed by the platform-specific software GenomeStudio, followed by an array of…”
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    Evaluation of high performance liquid chromatography (HPLC) pattern and prevalence of beta-thalassaemia trait among sickle cell disease patients in Lagos, Nigeria by Adeyemo, Titilope, Ojewunmi, Oyesola, Oyetunji, Ajoke

    Published in The Pan African medical journal (2014)
    “…Sickle cell disease (SCD) is the most common inherited disorder of haemoglobin worldwide. This study evaluated the chromatographic patterns and red blood cell…”
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