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🦁
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A human homologue of the Drosophila eyes absent gene underlies Branchio-Oto-Renal (BOR) syndrome and identifies a novel gene family
20 auth.
S. Abdelhak,
V. Kalatzis,
R. Heilig,
S. Compain,
D. Samson,
C. Vincent,
D. Weil,
C. Cruaud,
I. Sahly,
M. Leibovici,
...
M. Bitner-Glindzicz,
M. Francis,
D. Lacombe,
J. Vigneron,
R. Charachon,
K. Boven,
P. Bedbeder,
N. Regemorter,
J. Weissenbach,
C. Petit
|
9 |
1997 |
9
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Gene for chronic proximal spinal muscular atrophies maps to chromosome 5q
25 auth.
J. Melki,
S. Abdelhak,
P. Sheth,
M. Bachelot,
P. Burlet,
A. Marcadet,
J. Aicardi,
A. Barois,
J. Carriere,
M. Fardeau,
D. Fontán,
G. Ponsot,
T. Billette,
C. Angelini,
C. Barbosa,
...
G. Ferrière,
G. Lanzi,
A. Ottolini,
M. Babron,
D. Cohen,
A. Hanauer,
F. Clerget-Darpoux,
M. Lathrop,
A. Munnich,
J. Frézal
|
8 |
1990 |
8
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Systems medicine and integrated care to combat chronic noncommunicable diseases
64 auth.
J. Bousquet,
J. Antó,
P. Sterk,
I. Adcock,
K. Chung,
J. Roca,
A. Agustí,
C. Brightling,
A. Cambon-Thomsen,
A. Cesario,
S. Abdelhak,
S. Antonarakis,
A. Avignon,
A. Ballabio,
E. Baraldi,
...
A. Baranov,
T. Bieber,
J. Bockaert,
S. Brahmachari,
C. Brambilla,
J. Bringer,
M. Dauzat,
I. Ernberg,
L. Fabbri,
P. Froguel,
D. Galas,
T. Gojobori,
P. Hunter,
Christian Jorgensen,
F. Kauffmann,
P. Kourilsky,
M. Kowalski,
D. Lancet,
C. Pen,
J. Mallet,
B. Mayosi,
J. Mercier,
A. Metspalu,
J. Nadeau,
G. Ninot,
D. Noble,
Mehmet Öztürk,
S. Palkonen,
C. Prefaut,
K. Rabe,
E. Renard,
R. Roberts,
B. Samolinski,
H. Schünemann,
H. Simon,
M. Soares,
G. Superti-Furga,
J. Tegnér,
S. Verjovski-Almeida,
P. Wellstead,
O. Wolkenhauer,
E. Wouters,
R. Balling,
A. Brookes,
D. Charron,
C. Pison,
Zhu Chen,
L. Hood,
C. Auffray
|
7 |
2011 |
7
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Clustering of mutations responsible for branchio-oto-renal (BOR) syndrome in the eyes absent homologous region (eyaHR) of EYA1.
15 auth.
S. Abdelhak,
V. Kalatzis,
R. Heilig,
S. Compain,
D. Samson,
C. Vincent,
Fabienne L evi-Acobas,
C. Cruaud,
M. Merrer,
M. Mathieu,
...
R. König,
J. Vigneron,
J. Weissenbach,
C. Petit,
D. Weil
|
7 |
1997 |
7
🦁
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|
🐜
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BOR and BO Syndromes Are Allelic Defects of EYA1
8 auth.
C. Vincent,
V. Kalatzis,
S. Abdelhak,
H. Chaïb,
S. Compain,
J. Hélias,
...
F. Vaneecloo,
C. Petit
|
7 |
1997 |
7
🐜
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|
🐜
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Cancer in Africa: The Untold Story
7 auth.
Y. Hamdi,
Ines Abdeljaoued-Tej,
Afzal Ali Zatchi,
S. Abdelhak,
S. Boubaker,
Joel s. Brown,
...
Alia Benkahla
|
6 |
2021 |
6
🐜
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|
🐜
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Deficiency for the ubiquitin ligase UBE3B in a blepharophimosis-ptosis-intellectual-disability syndrome.
36 auth.
L. Basel‐Vanagaite,
B. Dallapiccola,
R. Ramírez‐Solís,
A. Segref,
H. Thiele,
Andrew Edwards,
M. Arends,
X. Miró,
Jacqueline K. White,
J. Désir,
M. Abramowicz,
M. Dentici,
F. Lepri,
K. Hofmann,
Adi Har‐Zahav,
...
E. Ryder,
N. Karp,
J. Estabel,
Anna-Karin B Gerdin,
C. Podrini,
N. Ingham,
J. Altmüller,
G. Nürnberg,
P. Frommolt,
S. Abdelhak,
M. Pasmanik-Chor,
O. Konen,
R. Kelley,
M. Shohat,
P. Nürnberg,
J. Flint,
K. Steel,
T. Hoppe,
C. Kubisch,
D. Adams,
G. Borck
|
6 |
2012 |
6
🐜
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|
🐢
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Consanguinity, endogamy, and genetic disorders in Tunisia
24 auth.
N. Ben Halim,
N. Ben Alaya Bouafif,
Lilia Romdhane,
Rym Kefi Ben Atig,
Ibtissem Chouchane,
Y. Bouyacoub,
I. Arfa,
W. Cherif,
Sonia Nouira,
Faten Talmoudi,
...
Khaled Lasram,
S. Hsouna,
Welid Ghazouani,
H. Azaiez,
L. el Matri,
A. Abid,
N. Tebib,
M. B. Ben Dridi,
S. Kachboura,
A. Amouri,
M. Mokni,
S. Ben Arab,
K. Dellagi,
S. Abdelhak
|
6 |
2012 |
6
🐢
|
|
🐜
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Clinical and genetic heterogeneity of inherited autosomal recessive susceptibility to disseminated Mycobacterium bovis bacille calmette-guérin infection.
8 auth.
H. Elloumi-Zghal,
M. Barbouche,
J. Chemli,
M. Bejaoui,
A. Harbi,
N. Snoussi,
...
S. Abdelhak,
K. Dellagi
|
6 |
2002 |
6
🐜
|
|
🐜
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Genome-Wide Association Studies (GWAS) breast cancer susceptibility loci in Arabs: susceptibility and prognostic implications in Tunisians
13 auth.
Jingxuan Shan,
W. Mahfoudh,
Shoba P. Dsouza,
E. Hassen,
N. Bouaouina,
S. Abdelhak,
Ahlem Benhadjayed,
Hager Memmi,
R. Mathew,
I. Aigha,
...
S. Gabbouj,
Yassmine Remadi,
L. Chouchane
|
6 |
2012 |
6
🐜
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|
🐢
|
Founder mutations in Tunisia: implications for diagnosis in North Africa and Middle East
Lilia Romdhane,
R. Kefi,
H. Azaiez,
N. B. Halim,
K. Dellagi,
S. Abdelhak
|
6 |
2012 |
6
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