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Kemal Azibi

Affiliation : National Higher School of Statistics and Applied Economy · Azienda Ospedaliera Bolognini Seriate

• 4Publications (affiliation in Algeria)
• 28Total publications
• 1171Citations
• 15h-index

OpenAlex

Research profile

Kemal Azibi has 4 indexed publications (1994–1996). Their work appears mainly in “FEBS Letters”, “Nature Genetics” and “Journal of Medical Genetics”. Their most cited article, “Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity” (1995), has been cited 188 times.

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Research areas

• Muscle Physiology and Disorders
• Genomics and Rare Diseases
• Cardiomyopathy and Myosin Studies
• Reproductive Biology and Fertility
• Ovarian function and disorders

Publications (4)

• Absence of γ‐sarcoglycan (35 DAG) in autosomal recessive muscular dystrophy linked to chromosome 13q12
  1996 · FEBS Letters · cited 53 times
• Primary adhalinopathy: a common cause of autosomal recessive muscular dystrophy of variable severity
  1995 · Nature Genetics · cited 188 times
• Linkage analysis of families with severe childhood autosomal recessive muscular dystrophy in Morocco indicates genetic homogeneity of the disease in north Africa.
  1994 · Journal of Medical Genetics · cited 30 times
• Adhalin gene polymorphism
  1994 · Human Molecular Genetics · cited 8 times

Publication venues

• FEBS Letters × 1
• Nature Genetics × 1
• Journal of Medical Genetics × 1
• Human Molecular Genetics × 1

Publications per year

• 19961
• 19951
• 19942

Collaborations

Partner institutions : Institut National d'Hygiène du Maroc · Inserm · Hôpital Cochin · Fondation Jean Dausset-CEPH · Genethon (France)

Co-authors’ countries : France · Morocco · Italy

Bibliographic data from OpenAlex (open database).