Nabil Moghrabi - Concepedia

Author

Nabil Moghrabi

King Faisal Specialist Hospital & Research Centre

Also Known As

N Moghrabi, N. MOGHRABI, N. Moghrabi, N. N. Moghrabi, Nabil Moghrabi, Nabil N Moghrabi, Nabil N. Moghrabi

Publications

Citations

H-Index

Concepts

All Affiliations

King Faisal Specialist Hospital & Research Centre The University of Texas Southwestern Medical Center Alfaisal University King Abdulaziz City for Science and Technology Ninewells Hospital

About

Nabil Moghrabi is an author at King Faisal Specialist Hospital & Research Centre specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	906
2	Health Sciences	2	2	33
3	Biology	2	2	256
4	Natural Sciences	1	1	139
5	Biochemistry	1	1	41

Nabil Moghrabi

Publications

1.8K

Citations

H-Index

Page 1

	Year	Citations
Deficient 17β-Hydroxysteroid Dehydrogenase Type 2 Expression in Endometriosis: Failure to Metabolize 17β-Estradiol<sup>1</sup> Khaled Zeitoun, Kazuto Takayama, Hironobu Sasano, The Journal of Clinical Endocrinology & Metabolism	1998	312
The landscape of genetic diseases in Saudi Arabia based on the first 1000 diagnostic panels and exomes Dorota Monies, Mohamed Abouelhoda, Moeenaldeen AlSayed, Human Genetics	2017	296
Lessons Learned from Large-Scale, First-Tier Clinical Exome Sequencing in a Highly Consanguineous Population Dorota Monies, Mohammed Abouelhoda, Mirna Assoum, The American Journal of Human Genetics SequencingNext-generation SequencingGeneticsPathologyOmics	2019	276
A Role for the deep orange and carnation Eye Color Genes in Lysosomal Delivery in Drosophila Evgueni A. Sevrioukov, Jing-Ping He, Nabil Moghrabi, Molecular Cell BiologyGeneticsGenomic MechanismGenetic EngineeringGenetic Mechanism	1999	206
Genetic defects of the UDP-glucuronosyltransferase-1 (UGT1) gene that cause familial non-haemolytic unconjugated hyperbilirubinaemias Douglas J. Clarke, Nabil Moghrabi, Gemma Monaghan, Clinica Chimica Acta Allelic VariantMendelian DisorderGenetic DisorderMedicineGenetics	1997	139
Identification of an A-to-G Missense Mutation in Exon 2 of the UGT1 Gene Complex That Causes Crigler-Najjar Syndrome Type 2 Nabil Moghrabi, Douglas J. Clarke, Maureen Boxer, Genomics A-to-g Missense MutationMendelian DisorderUgt1 Gene ComplexGenetic DisorderGenetics	1993	83
Deleterious Missense Mutations and Silent Polymorphism in the Human 17β-Hydroxysteroid Dehydrogenase 3 Gene (HSD17B3)1 Nabil Moghrabi, Ieuan A. Hughes, Andrea Dunaif, The Journal of Clinical Endocrinology & Metabolism	1998	78
Cosegregation of intragenic markers with a novel mutation that causes Crigler-Najjar syndrome type I: implication in carrier detection and prenatal diagnosis. Nabil Moghrabi, Douglas J. Clarke, Brian Burchell, PubMed	1993	53
Cell Type-Specific Expression of 17β-Hydroxysteroid Dehydrogenase Type 2 in Human Placenta and Fetal Liver<sup>1</sup> Nabil Moghrabi, Judith R. Head, Stefan Andersson The Journal of Clinical Endocrinology & Metabolism	1997	53
A Mutation in<i>dVps28</i>Reveals a Link between a Subunit of the Endosomal Sorting Complex Required for Transport-I Complex and the Actin Cytoskeleton in<i>Drosophila</i> Evgueni A. Sevrioukov, Nabil Moghrabi, Mary Kuhn, Molecular Biology of the Cell Viral ReplicationGeneticsMolecular GeneticsCytoskeletonEndosomal Sorting Complex	2005	50

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