Stigma in African genomics research: Gendered blame, polygamy, ancestry and disease causal beliefs impact on the risk of harm

por de Vries, Jantina, Landouré, Guida, Wonkam, Ambroise
Publicado 2020

Fahr's syndrome with hyperparathyroidism revealed by seizures and proximal weakness

por Dembélé, Kékouta, Cissé, Lassana, Djimdé, Samba, Coulibaly, Youlouza, Diarra, Salimata, Yalcouyé, Abdoulaye, Maiga, Boubacar, Guinto, Cheick O., Landouré, Guida
Publicado 2019

Genetics and genomic medicine in Mali: challenges and future perspectives

por Landouré, Guida, Samassékou, Oumar, Traoré, Mahamadou, Meilleur, Katherine G., Guinto, Cheick Oumar, Burnett, Barrington G., Sumner, Charlotte J., Fischbeck, Kenneth H.
Publicado 2016

An unusual case of Dyke–Davidoff–Masson syndrome revealed by status epilepticus in a Malian patient

por Djimdé, Samba O., Yalcouyé, Abdoulaye, Koïta, Abdou, Samir, Hassana, Kebkiba, Pofinet, Gueli, Chrystelle Awovi, Maïga, Alassane B., Sissoko, Adama S., Landouré, Guida
Publicado 2022

Antiretroviral-induced adverse drug reactions in HIV-infected patients in Mali: a resource-limited setting experience

por Oumar, Aboubacar Alassane, Dakouo, Mamadou, Tchibozo, Anicet, Maiga, Mamoudou, Landouré, Guida, Abdi-Bogoreh, Raysso, Tulkens, Paul M., Dao, Sounkalo, Yombi, Jean Cyr
Publicado 2019

Increasing African genomic data generation and sharing to resolve rare and undiagnosed diseases in Africa: a call-to-action by the H3Africa rare diseases working group

por Lumaka, Aimé, Carstens, Nadia, Devriendt, Koenraad, Krause, Amanda, Kulohoma, Benard, Kumuthini, Judit, Mubungu, Gerrye, Mukisa, John, Nel, Melissa, Olanrewaju, Timothy O., Lombard, Zané, Landouré, Guida
Publicado 2022

A novel mutation in the GARS gene in a Malian family with Charcot‐Marie‐Tooth disease

por Yalcouyé, Abdoulaye, Diallo, Seybou H., Coulibaly, Thomas, Cissé, Lassana, Diallo, Salimata, Samassékou, Oumar, Diarra, Salimata, Coulibaly, Dramane, Keita, Mohamed, Guinto, Cheick O., Fischbeck, Kenneth, Landouré, Guida
Publicado 2019

Socio-cultural adaptation and standardization of Dubois' five words testing in a population of normal subject in Mali, West Africa

por Guinto, Cheick O., Coulibaly, Toumany, Koné, Zeinab, Coulibaly, Souleymane, Maiga, Boubacar, Dembélé, Kekouta, Cissé, Lassana, Konaté, Mamadou, Coulibaly, Thomas, Sissoko, Adama S., Karambé, Mamadou, Burnett, Barrington, Landouré, Guida, Traoré, Moussa
Publicado 2016

Etiologies of Childhood Hearing Impairment in Schools for the Deaf in Mali

por Yalcouyé, Abdoulaye, Traoré, Oumou, Taméga, Abdoulaye, Maïga, Alassane B., Kané, Fousseyni, Oluwole, Oluwafemi G., Guinto, Cheick Oumar, Kéita, Mohamed, Timbo, Samba Karim, DeKock, Carmen, Landouré, Guida, Wonkam, Ambroise
Publicado 2021

A monoallelic variant in EYA1 is associated with Branchio‐Otic syndrome in a Malian family

por Yalcouyé, Abdoulaye, Traoré, Oumou, Diarra, Salimata, Schrauwen, Isabelle, Esoh, Kevin, Kadlubowska, Magda Kamila, Bharadwaj, Thashi, Adadey, Samuel Mawuli, Kéita, Mohamed, Guinto, Cheick O., Leal, Suzanne M., Landouré, Guida, Wonkam, Ambroise
Publicado 2022

A novel mutation in KIF5A in a Malian family with spastic paraplegia and sensory loss

por Guinto, Cheick O., Diarra, Salimata, Diallo, Salimata, Cissé, Lassana, Coulibaly, Thomas, Diallo, Seybou H., Taméga, Abdoulaye, Chen, Ke‐Lian, Schindler, Alice B., Bagayoko, Koumba, Simaga, Assiatou, Blackstone, Craig, Fischbeck, Kenneth H., Landouré, Guida
Publicado 2017

“Black Lives Matter and Black Research Matters”: the African Society of Human Genetics’ call to halt racism in science

por Wonkam, Ambroise, Bardien, Soraya, Diallo, Rokhaya Ndiaye, Gaye, Amadou, Alimohamed, Mohamed Zahir, Kya, Siana, Makani, Julie, Landoure, Guida, Mutesa, Leon, El-Kamah, Ghada, Mohamed, Amal, Newport, Melanie, Williams, Scott M., Ramsay, Michele, Nembaware, Victoria
Publicado 2022

Implementation of genomics research in Africa: challenges and recommendations

por Adebamowo, Sally N., Francis, Veronica, Tambo, Ernest, Diallo, Seybou H., Landouré, Guida, Nembaware, Victoria, Dareng, Eileen, Muhamed, Babu, Odutola, Michael, Akeredolu, Teniola, Nerima, Barbara, Ozumba, Petronilla J., Mbhele, Slee, Ghanash, Anita, Wachinou, Ablo P., Ngomi, Nicholas
Publicado 2018

Non-motor signs in patients with Parkinson's disease at the University Hospital of Point “G”, Mali

por Maïga, Boubacar, Koné, Aïssata, Landouré, Guida, Coulibaly, Toumany, Sangaré, Modibo, Dembélé, Kekouta, Diop, Marième Soda, Cissé, Lassana, Dadah, Sami Mohamed Lemine, Konaté, Mamadou, Coulibaly, Catherine, Sissoko, Adama Seydou, Coulibaly, Thomas, Karambé, Mamadou, Guinto, Cheick Oumar, Moustapha Ndiaye, M., Ndiaye, Mouhamadou Mansour, Traoré, Moussa
Publicado 2016

Friedreich ataxia in a family from Mali, West Africa/Friedreich ataxia in a Malian family

por Cissé, Cheick A. K., Cissé, Lassana, Ba, Hamidou O., Samassékou, Oumar, Simaga, Assiatou, Taméga, Abdoulaye, Diarra, Salimata, Diallo, Seybou H., Coulibaly, Thomas, Diallo, Salimata, Yalcouyé, Abdoulaye, Maiga, Alassane B., Keita, Mohamed, Fischbeck, Kenneth H., Traoré, Sékou F., Guinto, Cheick O., Landouré, Guida
Publicado 2021

Undiagnosed diseases: Needs and opportunities in 20 countries participating in the Undiagnosed Diseases Network International

por Taruscio, Domenica, Salvatore, Marco, Lumaka, Aimè, Carta, Claudio, Cellai, Laura L., Ferrari, Gianluca, Sciascia, Savino, Groft, Stephen, Alanay, Yasemin, Azam, Maleeha, Baynam, Gareth, Cederroth, Helene, Cutiongco-de la Paz, Eva Maria, Dissanayake, Vajira Harshadeva Weerabaddana, Giugliani, Roberto, Gonzaga-Jauregui, Claudia, Hettiarachchi, Dineshani, Kvlividze, Oleg, Landoure, Guida, Makay, Prince, Melegh, Béla, Ozbek, Ugur, Puri, Ratna Dua, Romero, Vanessa, Scaria, Vinod, Jamuar, Saumya S., Shotelersuk, Vorasuk, Roccatello, Dario, Gahl, William A., Wiafe, Samuel A., Bodamer, Olaf, Posada, Manuel
Publicado 2023

Does the survival motor neuron copy number variation play a role in the onset and severity of sporadic amyotrophic lateral sclerosis in Malians?

por Sangare, Modibo, Dicko, Ilo, Guinto, Cheick Oumar, Sissoko, Adama, Dembele, Kekouta, Coulibaly, Youlouza, Coulibaly, Siaka Y., Landoure, Guida, Diallo, Abdallah, Dolo, Mamadou, Dolo, Housseini, Maiga, Boubacar, Traore, Moussa, Karembe, Mamadou, Traore, Kadiatou, Toure, Amadou, Sylla, Mariam, Togora, Arouna, Coulibaly, Souleymane, Traore, Sékou Fantamady, Hendrickson, Brant, Bricceno, Katherine, Schindler, Alice B., Kokkinis, Angela, Meilleur, Katherine G., Sangho, Hammadoun Ali, Diakite, Brehima, Kassogue, Yaya, Coulibaly, Yaya Ibrahim, Burnett, Barrington, Maiga, Youssoufa, Doumbia, Seydou, Fischbeck, Kenneth H.
Publicado 2016

Unmet needs in countries participating in the undiagnosed diseases network international: an international survey considering national health care and economic indicators

por Sciascia, Savino, Roccatello, Dario, Salvatore, Marco, Carta, Claudio, Cellai, Laura L., Ferrari, Gianluca, Lumaka, Aimè, Groft, Stephen, Alanay, Yasemin, Azam, Maleeha, Baynam, Gareth, Cederroth, Helene, Cutiongco-de la Paz, Eva Maria, Dissanayake, Vajira Harshadeva Weerabaddana, Giugliani, Roberto, Gonzaga-Jauregui, Claudia, Hettiarachchi, Dineshani, Kvlividze, Oleg, Landoure, Guida, Makay, Prince, Melegh, Béla, Ozbek, Ugur, Puri, Ratna Dua, Romero, Vanessa I., Scaria, Vinod, Jamuar, Saumya S., Shotelersuk, Vorasuk, Gahl, William A., Wiafe, Samuel A., Bodamer, Olaf, Posada, Manuel, Taruscio, Domenica
Publicado 2023

Genetics of low spinal muscular atrophy carrier frequency in sub‐Saharan Africa

por Sangaré, Modibo, Hendrickson, Brant, Sango, Hammadoun Ali, Chen, Kelian, Nofziger, Jonathan, Amara, Abdelbasset, Dutra, Amalia, Schindler, Alice B., Guindo, Aldiouma, Traoré, Mahamadou, Harmison, George, Pak, Evgenia, Yaro, Fatoumata N'Go, Bricceno, Katherine, Grunseich, Christopher, Chen, Guibin, Boehm, Manfred, Zukosky, Kristen, Bocoum, Nouhoum, Meilleur, Katherine G., Daou, Fatoumata, Bagayogo, Koumba, Coulibaly, Yaya Ibrahim, Diakité, Mahamadou, Fay, Michael P., Lee, Hee‐Suk, Saad, Ali, Gribaa, Moez, Singleton, Andrew B., Maiga, Youssoufa, Auh, Sungyoung, Landouré, Guida, Fairhurst, Rick M., Burnett, Barrington G., Scholl, Thomas, Fischbeck, Kenneth H.
Publicado 2014