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Hadla Hariri
Hadla Hariri
American University of Beirut
Phenotype
Biology
Genetics
Mutation
Missense mutation
5
Papers
29
Citations
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Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis
2018
Journal of Dermatological Science
Hadla Hariri
Mazen Kurban
Christiane Al Haddad
Akl C. Fahed
Sarin Poladian
Athar Khalil
Oussama Abbas
Mariam Arabi
Fadi Bitar
Georges Nemer
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Citations (2)
A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations
2017
Frontiers in Cardiovascular Medicine
Athar Khalil
Christiane Al Haddad
Hadla Hariri
Kamel Shibbani
Fadi Bitar
Mazen Kurban
Georges Nemer
Mariam Arabi
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Citations (9)
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient
2016
Molecular Genetics & Genomic Medicine
Kameel Kassab
Hadla Hariri
Lara Gharibeh
Akl C. Fahed
Manal Zein
Inaam El‐Rassy
Mona Nemer
Issam El-Rassi
Fadi Bitar
Georges Nemer
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Citations (18)
P569A novel role for NFATC1 in patients with both congenital heart disease and glaucoma
2014
Cardiovascular Research
Hadla Hariri
Theresa Farhat
Ruby Khalaf
Akl C. Fahed
Christiane Al Haddad
Mariam Arabi
Fadi Bitar
Georges Nemer
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P329GATA5: a key player in congenital heart diseases
2014
Cardiovascular Research
K Kassab
Hadla Hariri
Akl C. Fahed
Issam El-Rassi
Fadi Bitar
Georges Nemer
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