Hearing loss in Africa: current genetic profile

por Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Aboagye, Elvis Twumasi, Quaye, Osbourne, Awandare, Gordon A., Wonkam, Ambroise
Publicado 2021

Global Distribution of Founder Variants Associated with Non-Syndromic Hearing Impairment

por Aboagye, Elvis Twumasi, Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Amenga-Etego, Lucas, Awandare, Gordon A., Wonkam, Ambroise
Publicado 2023

Clinical and therapeutic outcomes of COVID-19 intensive care units (ICU) patients: a retrospective study in Ghana

por Afriyie-Mensah, Jane, Aboagye, Elvis Twumasi, Ganu, Vincent Jessey, Bondzi, Samuel, Tetteh, Dennis, Kwarteng, Ernest, Akamah, Joseph, Doku, Alfred, Adjei, Patrick
Publicado 2021

Age Estimate of GJB2-p.(Arg143Trp) Founder Variant in Hearing Impairment in Ghana, Suggests Multiple Independent Origins across Populations

por Aboagye, Elvis Twumasi, Adadey, Samuel Mawuli, Esoh, Kevin, Jonas, Mario, de Kock, Carmen, Amenga-Etego, Lucas, Awandare, Gordon A., Wonkam, Ambroise
Publicado 2022

Connexin Genes Variants Associated with Non-Syndromic Hearing Impairment: A Systematic Review of the Global Burden

por Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Twumasi Aboagye, Elvis, Nayo-Gyan, Daniel Wonder, Boatemaa Ansong, Maame, Quaye, Osbourne, Awandare, Gordon A., Wonkam, Ambroise
Publicado 2020

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

por M. Adadey, Samuel, Tingang Wonkam, Edmond, Twumasi Aboagye, Elvis, Quansah, Darius, Asante-Poku, Adwoa, Quaye, Osbourne, K. Amedofu, Geoffrey, A. Awandare, Gordon, Wonkam, Ambroise
Publicado 2020

Catheter-Related Bloodstream Infections among patients on maintenance haemodialysis: a cross-sectional study at a tertiary hospital in Ghana

por Opoku-Asare, Bismark, Boima, Vincent, Ganu, Vincent Jessey, Aboagye, Elvis, Asafu-Adjaye, Olive, Asare, Anita Ago, Kyeremateng, Isaac, Kwakyi, Edward, Agyei, Adwoa, Sampane-Donkor, Eric, Puplampu, Peter
Publicado 2023

A novel autosomal dominant GREB1L variant associated with non-syndromic hearing impairment in Ghana

por Adadey, Samuel Mawuli, Aboagye, Elvis Twumasi, Esoh, Kevin, Acharya, Anushree, Bharadwaj, Thashi, Lin, Nicole S., Amenga-Etego, Lucas, Awandare, Gordon A., Schrauwen, Isabelle, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2022

Cell-based analysis of CLIC5A and SLC12A2 variants associated with hearing impairment in two African families

por Adadey, Samuel Mawuli, Wonkam-Tingang, Edmond, Alves de Souza Rios, Leonardo, Aboagye, Elvis Twumasi, Esoh, Kevin, Manyisa, Noluthando, De Kock, Carmen, Awandare, Gordon A., Mowla, Shaheen, Wonkam, Ambroise
Publicado 2022

Association between eNOS Gene Polymorphism (T786C and VNTR) and Sickle Cell Disease Patients in Ghana

por Antwi-Boasiako, Charles, Dzudzor, Bartholomew, Kudzi, William, Doku, Alfred, Dale, Campbell Andrew, Sey, Fredericka, Otu, Kate Hgar, Boatemaa, Gifty Dankwah, Ekem, Ivy, Ahenkorah, John, Achel, Daniel Gyingiri, Aboagye, Elvis Twumasi, Donkor, Eric S.
Publicado 2018

Further confirmation of the association of SLC12A2 with non-syndromic autosomal-dominant hearing impairment

por Adadey, Samuel M., Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Bharadwaj, Thashi, Esoh, Kevin K., Basit, Sulman, Acharya, Anushree, Nouel-Saied, Liz M., Liaqat, Khurram, Wonkam-Tingang, Edmond, Mowla, Shaheen, Awandare, Gordon A., Ahmad, Wasim, Leal, Suzanne M., Wonkam, Ambroise
Publicado 2021

GJB2 Is a Major Cause of Non-Syndromic Hearing Impairment in Senegal

por Dia, Yacouba, Adadey, Samuel Mawuli, Diop, Jean Pascal Demba, Aboagye, Elvis Twumasi, Ba, Seydi Abdoul, De Kock, Carmen, Ly, Cheikh Ahmed Tidjane, Oluwale, Oluwafemi Gabriel, Sène, Andrea Regina Gnilane, Sarr, Pierre Diaga, Diallo, Bay Karim, Diallo, Rokhaya Ndiaye, Wonkam, Ambroise
Publicado 2022

Childhood Hearing Impairment in Senegal

por Dia, Yacouba, Loum, Birame, Dieng, Yaay Joor Koddu Biigé, Diop, Jean Pascal Demba, Adadey, Samuel Mawuli, Aboagye, Elvis Twumasi, Ba, Seydi Abdoul, Touré, Abdoul Aziz, Niang, Fallou, Diaga Sarr, Pierre, Tidiane Ly, Cheikh Ahmed, Sène, Andrea Regina Gnilane, Kock, Carmen De, Bassier, Rhiyana, Popel, Kalinka, Ndiaye Diallo, Rokhaya, Wonkam, Ambroise, Diallo, Bay Karim
Publicado 2023

Exome sequencing of families from Ghana reveals known and candidate hearing impairment genes

por Wonkam, Ambroise, Adadey, Samuel Mawuli, Schrauwen, Isabelle, Aboagye, Elvis Twumasi, Wonkam-Tingang, Edmond, Esoh, Kevin, Popel, Kalinka, Manyisa, Noluthando, Jonas, Mario, deKock, Carmen, Nembaware, Victoria, Cornejo Sanchez, Diana M., Bharadwaj, Thashi, Nasir, Abdul, Everard, Jenna L., Kadlubowska, Magda K., Nouel-Saied, Liz M., Acharya, Anushree, Quaye, Osbourne, Amedofu, Geoffrey K., Awandare, Gordon A., Leal, Suzanne M.
Publicado 2022