Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Chinyere, Adeleke"'
Autor:
Abimbola Oladayo, Lord Jephthah Joojo Gowans, Waheed Awotoye, Azeez Alade, Tamara Busch, Thirona Naicker, Mekonen A. Eshete, Wasiu L. Adeyemo, Jacqueline B. Hetmanski, Erliang Zeng, Olawale Adamson, Chinyere Adeleke, Mary Li, Veronica Sule, Sami Kayali, Joy Olotu, Peter A. Mossey, Solomon Obiri‐Yeboah, Carmen J. Buxo, Terri Beaty, Margaret Taub, Peter Donkor, Mary L. Marazita, Oluwakemi Odukoya, Adebowale A. Adeyemo, Jeffrey C. Murray, Anya Prince, Azeez Butali
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 10, Pp n/a-n/a (2023)
Abstract Introduction The frequency and implications of secondary findings (SFs) from genomic testing data have been extensively researched. However, little is known about the frequency or reporting of SFs in Africans, who are underrepresented in lar
Externí odkaz:
https://doaj.org/article/4d477af3634b4221a6b0a0f3e5017d57
Autor:
Waheed Awotoye, Peter A. Mossey, Jacqueline B. Hetmanski, Lord J. J. Gowans, Mekonen A. Eshete, Wasiu L. Adeyemo, Azeez Alade, Erliang Zeng, Olawale Adamson, Thirona Naicker, Deepti Anand, Chinyere Adeleke, Tamara Busch, Mary Li, Aline Petrin, Babatunde S. Aregbesola, Ramat O. Braimah, Fadekemi O. Oginni, Ayodeji O. Oladele, Abimbola Oladayo, Sami Kayali, Joy Olotu, Mohaned Hassan, John Pape, Peter Donkor, Fareed K. N. Arthur, Solomon Obiri-Yeboah, Daniel K. Sabbah, Pius Agbenorku, Gyikua Plange-Rhule, Alexander Acheampong Oti, Rose A. Gogal, Terri H. Beaty, Margaret Taub, Mary L. Marazita, Michael J. Schnieders, Salil A. Lachke, Adebowale A. Adeyemo, Jeffrey C. Murray, Azeez Butali
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-14 (2022)
Abstract The majority (85%) of nonsyndromic cleft lip with or without cleft palate (nsCL/P) cases occur sporadically, suggesting a role for de novo mutations (DNMs) in the etiology of nsCL/P. To identify high impact protein-altering DNMs that contrib
Externí odkaz:
https://doaj.org/article/0796813889b94d029ee132863003d559
Autor:
Thirona Naicker, Azeez Alade, Chinyere Adeleke, Peter A. Mossey, Waheed A. Awotoye, Tamara Busch, Mary Li, Joy Olotu, Colleen Aldous, Azeez Butali
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 5, Pp n/a-n/a (2023)
Abstract Background To date, there are over 320 variants identified in the IRF6 gene that cause Van der Woude syndrome or popliteal pterygium syndrome. We sequenced this gene in a South African orofacial cleft cohort to identify the causal IRF6 varia
Externí odkaz:
https://doaj.org/article/16b5325fa2e94735863b62ff394ec388
Autor:
Azeez Fashina, Tamara Busch, Mary Young, Olawale Adamson, Waheed Awotoye, Azeez Alade, Chinyere Adeleke, Mohaned Hassan, Abimbola M. Oladayo, Lord J. J. Gowans, Mekonen Eshete, Thirona Naicker, Joy Olotu, Wasiu L. Adeyemo, Azeez Butali
Publikováno v:
Frontiers in Oral Health, Vol 3 (2022)
BackgroundSeveral population-based case-control studies have reported concurrent presentation of cancer and congenital malformations. Many associations have been made between oral clefting and cancers, though some of these results are conflicting. So
Externí odkaz:
https://doaj.org/article/8401929f8bf54390bcae430901aae6cc
Autor:
Olubukola O. Olatosi, Mary Li, Azeez A. Alade, Afolabi Oyapero, Tamara Busch, John Pape, Joy Olotu, Waheed Awotoye, Mohaned Hassan, Chinyere Adeleke, Wasiu L. Adeyemo, Elizabeth O. Sote, John R. Shaffer, Mary Marazita, Azeez Butali
Publikováno v:
BMC Oral Health, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Early childhood caries (ECC) is a rapidly progressing form of dental infection and a significant public health problem, especially among socially and economically disadvantaged populations. This study aimed to assess the risk fact
Externí odkaz:
https://doaj.org/article/41b5720f0b9a4d998085be8ae9dfb998
Autor:
Azeez A. Alade, Carmen J. Buxo‐Martinez, Peter A. Mossey, Lord J.J. Gowans, Mekonen A. Eshete, Wasiu L. Adeyemo, Thirona Naicker, Waheed A. Awotoye, Chinyere Adeleke, Tamara Busch, Ada M. Toraño, Carolina A. Bello, Mairim Soto, Marilyn Soto, Ricardo Ledesma, Myrellis Marquez, Jose F. Cordero, Lydia M. Lopez‐Del Valle, Maria I. Salcedo, Natalio Debs, Mary Li, Aline Petrin, Joy Olotu, Colleen Aldous, James Olutayo, Modupe O. Ogunlewe, Fekir Abate, Taye Hailu, Ibrahim Muhammed, Paul Gravem, Milliard Deribew, Mulualem Gesses, Mohaned Hassan, John Pape, Oluwole A. Adeniyan, Solomon Obiri‐Yeboah, Fareed K.N. Arthur, Alexander A. Oti, Olubukola Olatosi, Sara E. Miller, Peter Donkor, Martine M. Dunnwald, Mary L. Marazita, Adebowale A. Adeyemo, Jeffrey C. Murray, Azeez Butali
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Abstract Background The development of the face occurs during the early days of intrauterine life by the formation of facial processes from the first Pharyngeal arch. Derangement in these well‐organized fusion events results in Orofacial clefts (OF
Externí odkaz:
https://doaj.org/article/0abb9e91af0b4d64a4c82a601537aef8
Autor:
Carissa L Comnick, Deepti Anand, Mary Li, John Pape, Mary L. Marazita, P Donkor, Mekonen Eshete, Aline da Silva Petrin, M Hassan, Adebowale A. Adeyemo, Jeffrey C. Murray, Thirona Naicker, S E Miller, Tamara Busch, Peter A. Mossey, D Albokhari, Salil A. Lachke, Wasiu Lanre Adeyemo, C. Pendleton, Nara Sobreira, Azeez Alade, Joy Olotu, Azeez Butali, Chinyere Adeleke, Waheed O Awotoye, Erliang Zeng, Lord J.J. Gowans
Publikováno v:
J Dent Res
Risk loci identified through genome-wide association studies have explained about 25% of the phenotypic variations in nonsyndromic orofacial clefts (nsOFCs) on the liability scale. Despite the notable sex differences in the incidences of the differen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e05984760aa0a8ee7a0563f36a86037c
https://doi.org/10.1177/00220345211046614
https://doi.org/10.1177/00220345211046614
Autor:
Waheed, Awotoye, Peter A, Mossey, Jacqueline B, Hetmanski, Lord J J, Gowans, Mekonen A, Eshete, Wasiu L, Adeyemo, Azeez, Alade, Erliang, Zeng, Olawale, Adamson, Olutayo, James, Azeez, Fashina, Modupe O, Ogunlewe, Thirona, Naicker, Chinyere, Adeleke, Tamara, Busch, Mary, Li, Aline, Petrin, Abimbola, Oladayo, Sami, Kayali, Joy, Olotu, Veronica, Sule, Mohaned, Hassan, John, Pape, Emmanuel T, Aladenika, Peter, Donkor, Fareed K N, Arthur, Solomon, Obiri-Yeboah, Daniel K, Sabbah, Pius, Agbenorku, Debashree, Ray, Gyikua, Plange-Rhule, Alexander Acheampong, Oti, Daniah, Albokhari, Nara, Sobreira, Martine, Dunnwald, Terri H, Beaty, Margaret, Taub, Mary L, Marazita, Adebowale A, Adeyemo, Jeffrey C, Murray, Azeez, Butali
Publikováno v:
The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.
Novel or rare damaging mutations have been implicated in the developmental pathogenesis of nonsyndromic cleft lip with or without cleft palate (nsCL ± P). Thus, we investigated the human genome for high-impact mutations that could explain the risk o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3fa4a289fcd107e9235534380a98ae23
https://pubmed.ncbi.nlm.nih.gov/36384317
https://pubmed.ncbi.nlm.nih.gov/36384317
Autor:
Azeez Alade, Chinyere Adeleke, Tamara Busch, Azeez Butali, Colleen Aldous, Joy Olotu, Thirona Naicker, Waheed A. Awotoye, Peter A. Mossey, Mary Li, Lord J.J. Gowans
Publikováno v:
The Cleft Palate-Craniofacial Journal. 59:1125-1130
Objective The etiology of cleft palate (CP) is poorly understood compared with that of cleft lip with or without palate (CL ± P). Recently, variants in Grainyhead like transcription factor 3 ( GRHL3) were reported to be associated with a risk for CP
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bafb60fd5c823acee5f0b685da94afc2
https://doi.org/10.1177/10556656211038453
https://doi.org/10.1177/10556656211038453
Autor:
Waheed Awotoye, Peter A. Mossey, Jacqueline B. Hetmanski, Lord J. J. Gowans, Mekonen A. Eshete, Wasiu L. Adeyemo, Azeez Alade, Erliang Zeng, Olawale Adamson, Thirona Naicker, Deepti Anand, Chinyere Adeleke, Tamara Busch, Mary Li, Aline Petrin, Babatunde S. Aregbesola, Ramat O. Braimah, Fadekemi O. Oginni, Ayodeji O. Oladele, Abimbola Oladayo, Sami Kayali, Joy Olotu, Mohaned Hassan, John Pape, Peter Donkor, Fareed K. N. Arthur, Solomon Obiri-Yeboah, Daniel K. Sabbah, Pius Agbenorku, Gyikua Plange-Rhule, Alexander Acheampong Oti, Rose A. Gogal, Terri H. Beaty, Margaret Taub, Mary L. Marazita, Michael J. Schnieders, Salil A. Lachke, Adebowale A. Adeyemo, Jeffrey C. Murray, Azeez Butali
Publikováno v:
Scientific reports. 12(1)
The majority (85%) of nonsyndromic cleft lip with or without cleft palate (nsCL/P) cases occur sporadically, suggesting a role for de novo mutations (DNMs) in the etiology of nsCL/P. To identify high impact DNMs that contribute to the risk of nsCL/P,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bca60bf22dd1ae7c8e9c204f53777c1e
https://pubmed.ncbi.nlm.nih.gov/35817949
https://pubmed.ncbi.nlm.nih.gov/35817949