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Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go
84 auth.
T. Dangouloff,
E. Vrščaj,
L. Servais,
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T. Adoukonou,
O. Aryani,
N. Barišić,
F. Bashiri,
L. Bastaki,
A. Benitto,
T. Omran,
G. Bernert,
E. Bertini,
P. Borde,
Peter Born,
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N. Butoianu,
C. Castiglioni,
F. Catibusic,
S. Chan,
Y. Chien,
K. Christodoulou,
Donniphat Dejsuphong,
M. Farrar,
Duma Filip,
N. Goemans,
K. Guinhouya,
J. Haberlova,
K. Hadzsiev,
Kristine Hovhannesyan,
P. Isohanni,
Nelica Ivanović Radović,
D. Jacquier,
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M. Jędrzejowska,
Gwendolene Q Kandawasvika,
C. Kaputu,
Nfwama Kawatu,
K. Kernohan,
J. Kirschner,
B. Klink,
S. Kodsy,
A. Kouamé-Assouan,
R. Kravljanac,
M. Kreile,
I. Litvinenko,
H. McMillan,
S. Mesa,
Inaam Mohamed,
Liljana Muaremoska Kanzoska,
Y. Nevo,
S. Nguefack,
K. Nkole,
G. O'grady,
D. O'Rourke,
M. Oskoui,
F. Piazzon,
D. Poddighe,
A. Prasauskienė,
J. Prieto,
M. Rasmussen,
Santara Razafindrasata,
Narayan Saha,
Kayoko Saito,
Foksouna Sakadi,
M. Sangare,
M. Schroth,
L. Shalkevich,
A. Shatillo,
R. Suthar,
L. Szabó,
N. Tatishvili,
M. Tazir,
E. Tizzano,
H. Topaloğlu,
M. Tulinius,
L. Pol,
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J. Wanigasinghe,
J. Wilmshurst,
H. Xiong,
D. Zafeiriou,
E. Zamba
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6 |
2021 |
6
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🐜
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Hereditary Spastic Paraplegia Type 43 (SPG43) is Caused by Mutation in C19orf12
31 auth.
G. Landouré,
P. Zhu,
Charles M Lourenço,
Janel O. Johnson,
C. Toro,
Katherine V. Bricceno,
C. Rinaldi,
K. Meilleur,
M. Sangare,
O. Diallo,
T. Pierson,
H. Ishiura,
S. Tsuji,
N. Hein,
J. Fink,
...
Marion Stoll,
G. Nicholson,
Michael A. Gonzalez,
Fiorella Speziani,
A. Dürr,
G. Stevanin,
L. Biesecker,
J. Accardi,
Dennis Landis,
W. Gahl,
B. Traynor,
W. Marques,
S. Züchner,
C. Blackstone,
K. Fischbeck,
Barrington G. Burnett
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6 |
2013 |
6
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|
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Expanding Research Capacity in Sub-Saharan Africa Through Informatics, Bioinformatics, and Data Science Training Programs in Mali
23 auth.
J. Shaffer,
Frances J. Mather,
Mamadou Wélé,
Jian Li,
C. Tangara,
Y. Kassogue,
S. Srivastav,
O. Thiero,
M. Diakité,
M. Sangare,
...
D. Dabitao,
Mahamoudou Touré,
A. Djimde,
S. Traore,
B. Diakite,
M. Coulibaly,
Yao-Zhong Liu,
M. Lacey,
J. Lefante,
O. Koita,
J. Schieffelin,
D. Krogstad,
S. Doumbia
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5 |
2019 |
5
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A comprehensive analysis of drug resistance molecular markers and Plasmodium falciparum genetic diversity in two malaria endemic sites in Mali
19 auth.
S. Diakité,
K. Traore,
I. Sanogo,
T. Clark,
S. Campino,
M. Sangare,
D. Dabitao,
Antoine Dara,
D. Konate,
Fousseyni Doucouré,
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A. Cissé,
Bourama Keita,
M. Doumbouya,
M. Guindo,
Mahamoudou Touré,
N. Sogoba,
S. Doumbia,
G. Awandare,
M. Diakité
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5 |
2019 |
5
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|
🦁
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Genetics of low spinal muscular atrophy carrier frequency in sub‐Saharan Africa
36 auth.
M. Sangare,
B. Hendrickson,
Hammadoun A Sango,
Ke‐lian Chen,
J. Nofziger,
A. Amara,
A. Dutra,
A. Schindler,
A. Guindo,
M. Traore,
G. Harmison,
E. Pak,
F. Yaro,
Katherine V. Bricceno,
C. Grunseich,
...
Guibin Chen,
M. Boehm,
K. Zukosky,
Nouhoum Bocoum,
K. Meilleur,
Fatoumata Daou,
Koumba Bagayogo,
Y. Coulibaly,
M. Diakité,
M. Fay,
Hee‐Suk Lee,
A. Saâd,
M. Gribaa,
A. Singleton,
Y. Maiga,
S. Auh,
G. Landouré,
R. Fairhurst,
Barrington G. Burnett,
T. Scholl,
K. Fischbeck
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5 |
2014 |
5
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Serosurvey of Crimean-Congo Hemorrhagic Fever Virus in Cattle, Mali, West Africa.
15 auth.
Ousmane Maiga,
M. Sas,
K. Rosenke,
B. Kamissoko,
M. Mertens,
N. Sogoba,
A. Traoré,
M. Sangare,
M. Niang,
T. Schwan,
...
H. Maiga,
S. Traore,
H. Feldmann,
D. Safronetz,
M. Groschup
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4 |
2017 |
4
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|
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Hereditary spastic paraplegia and amyotrophy associated with a novel locus on chromosome 19
18 auth.
K. G. Meilleur,
K. G. Meilleur,
Mamadou Traoré,
M. Sangare,
Angela Britton,
G. Landouré,
G. Landouré,
S. Coulibaly,
B. Niaré,
Fanny Mochel,
...
A. Pean,
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C. Watts,
D. Shriner,
M. Littleton-Kearney,
Craig Blackstone,
AB Singleton,
K. Fischbeck
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4 |
2010 |
4
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|
🐜
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Genetic testing and counseling for hereditary neurological diseases in Mali
10 auth.
K. Meilleur,
S. Coulibaly,
M. Traoré,
G. Landouré,
A. Pean,
M. Sangare,
...
F. Mochel,
S. Traoré,
K. Fischbeck,
Hae-Ra Han
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4 |
2011 |
4
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|
