Mor Hanany

About Mor Hanany

Mor Hanany, With an exceptional h-index of 7 and a recent h-index of 7 (since 2020), a distinguished researcher at Hebrew University of Jerusalem, specializes in the field of Genetics, Bioinformatics, Population analysis.

His recent articles reflect a diverse array of research interests and contributions to the field:

Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation Considerations

Simultaneous Detection of Common Founder Mutations using a Cost-Effective Deep Sequencing Panel

An in-depth single-gene worldwide carrier frequency and genetic prevalence analysis of CYP4V2 as the cause of Bietti crystalline dystrophy

Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily

Inherited retinal diseases: linking genes, disease-causing variants, and relevant therapeutic modalities

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children

SENIOR–LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis

Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations

Mor Hanany Information

University

Position

___

Citations(all)

358

Citations(since 2020)

345

Cited By

64

hIndex(all)

7

hIndex(since 2020)

7

i10Index(all)

6

i10Index(since 2020)

6

Email

University Profile Page

Google Scholar

Mor Hanany Skills & Research Interests

Genetics

Bioinformatics

Population analysis

Top articles of Mor Hanany

Comparison of Worldwide Disease Prevalence and Genetic Prevalence of Inherited Retinal Diseases and Variant Interpretation Considerations

2024/2/1

Mor Hanany
Mor Hanany

H-Index: 4

Dror Sharon
Dror Sharon

H-Index: 31

Simultaneous Detection of Common Founder Mutations using a Cost-Effective Deep Sequencing Panel

2023/8/1

Mor Hanany
Mor Hanany

H-Index: 4

Dror Sharon
Dror Sharon

H-Index: 31

An in-depth single-gene worldwide carrier frequency and genetic prevalence analysis of CYP4V2 as the cause of Bietti crystalline dystrophy

Translational Vision Science & Technology

2023/2/1

Mor Hanany
Mor Hanany

H-Index: 4

Dror Sharon
Dror Sharon

H-Index: 31

Identification of autosomal recessive novel genes and retinal phenotypes in members of the solute carrier (SLC) superfamily

Genetics in Medicine

2022/7/1

Inherited retinal diseases: linking genes, disease-causing variants, and relevant therapeutic modalities

2022/7/1

Variable phenotype of Knobloch syndrome due to biallelic COL18A1 mutations in children

European Journal of Ophthalmology

2021/11

Mor Hanany
Mor Hanany

H-Index: 4

Dror Sharon
Dror Sharon

H-Index: 31

SENIOR–LØKEN SYNDROME: A Case Series and Review of the Renoretinal Phenotype and Advances of Molecular Diagnosis

2021/10/1

Unique combination of clinical features in a large cohort of 100 patients with retinitis pigmentosa caused by FAM161A mutations

Scientific reports

2020/9/16

Worldwide carrier frequency and genetic prevalence of autosomal recessive inherited retinal diseases

Proceedings of the National Academy of Sciences

2020/2/4

Mor Hanany
Mor Hanany

H-Index: 4

Dror Sharon
Dror Sharon

H-Index: 31

See List of Professors in Mor Hanany University(Hebrew University of Jerusalem)