Leen Abu Safieh - Concepedia

Author

Leen Abu Safieh

Also Known As

Abdolmajid Hosseini, Igor Kozak, L Abu Safieh, L. Abu Safieh, Leen Abu Safieh, Leen Safieh, Mohammad Pakravan, Pattama Torvorapanit

Publications

1.4K

Citations

H-Index

Concepts

All Affiliations

King Khaled Eye Specialist Hospital King Faisal Specialist Hospital & Research Centre King Saud University Alfaisal University King Khalid University Hospital

About

Leen Abu Safieh is an author at King Khaled Eye Specialist Hospital specializing in medicine, molecular genetics, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	340
2	Natural Sciences	1	1	209
3	Biology	1	1	209
4	Cell Biology	1	1	58
5	Molecular Biology	1	1	14

Leen Abu Safieh

Publications

747

Citations

H-Index

Page 1

	Year	Citations
EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa Mai M. Abd El-Aziz, Isabel Barragán, C. O'Driscoll, Nature Genetics BiologyDevelopmental BiologyDevelopmental GeneticsGeneticsMedicine	2008	209
Clinical and molecular characterisation of Bardet–Biedl syndrome in consanguineous populations: the power of homozygosity mapping Leen Abu Safieh, Mohammed A. Aldahmesh, Hanan E. Shamseldin, Journal of Medical Genetics	2009	86
Molecular characterization of retinitis pigmentosa in Saudi Arabia. Mohammed A. Aldahmesh, Leen Abu Safieh, Hisham Alkuraya, PubMed	2009	80
Molecular characterization of Joubert syndrome in Saudi Arabia Anas M. Alazami, Muneera Alshammari, Mustafa A. Salih, Human Mutation Mendelian DisorderJoubert SyndromeSaudi ArabiaGeneticsInherited Metabolic Disease	2012	59
ACVR1C/SMAD2 signaling promotes invasion and growth in retinoblastoma Laura Asnaghi, David T. White, Nolan Key, Oncogene Developmental BiologyCell RegulationMedicineCell ProliferationTumor Suppressor	2018	58
SARS-CoV-2 susceptibility and COVID-19 disease severity are associated with genetic variants affecting gene expression in a variety of tissues Matteo D’Antonio, Jennifer Nguyen, Timothy D. Arthur, Cell Reports	2021	46
Identification of a novel CRYAB mutation associated with autosomal recessive juvenile cataract in a Saudi family. Leen Abu Safieh, A.O. Khan, Fowzan S. Alkuraya PubMed	2009	44
RP1 and retinitis pigmentosa: report of novel mutations and insight into mutational mechanism May Alrashed, Leen Abu Safieh, Hisham Alkuraya, British Journal of Ophthalmology	2012	29
Later retinal degeneration following childhood surgical aphakia in a family with recessive CRYAB mutation (p.R56W) Arif O. Khan, Leen Abu Safieh, Fowzan S. Alkuraya Ophthalmic Genetics	2010	23
Methylation Profiling of Medulloblastoma in a Clinical Setting Permits Sub-classification and Reveals New Outcome Predictions Musa Alharbi, Nahla Ali Mobark, Yara Bashawri, Frontiers in Neurology	2020	20

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