L.I. Al-Gazali - Concepedia

Author

L.I. Al-Gazali

Also Known As

L I AL-GAZALI, L I AL-Gazali, L I Al-Gazali, L I al-Gazali, L I. Al‐Gazali, L. I. AL-GAZALI, L. I. Al-Gazali, L.I Al-Gazali, L.I. Al-Gazali, L. I. Al-Gazali

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

United Arab Emirates University Al Ain Hospital Tawam Hospital Hôpital Necker-Enfants Malades Inserm

About

L.I. Al-Gazali is an author at United Arab Emirates University specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	21	31	1.8K
2	Health Sciences	3	3	89
3	Public Health	2	2	72
4	Natural Sciences	1	1	71
5	Biochemistry	1	1	29

L.I. Al-Gazali

Publications

2.5K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the Transmembrane Natriuretic Peptide Receptor NPR-B Impair Skeletal Growth and Cause Acromesomelic Dysplasia, Type Maroteaux Cynthia F. Bartels, Hülya Bükülmez, Pius S. Padayatti, The American Journal of Human Genetics SclerostinSignal TransductionMolecular PhysiologyBone Morphogenic ProteinGenetic Disorder	2004	363
Mutations in FAM20C Are Associated with Lethal Osteosclerotic Bone Dysplasia (Raine Syndrome), Highlighting a Crucial Molecule in Bone Development Michael A. Simpson, Ray C. J. Hsu, Lindsay Keir, The American Journal of Human Genetics Bone DiseaseGenetic DisorderGeneticsFam20c Are AssociatedBone Development	2007	225
Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome Nathalie Dagoneau, Déborah Scheffer, Céline Huber, The American Journal of Human Genetics Genetic DisorderGeneticsPathologyDisease Gene IdentificationMedicine	2004	183
The profile of major congenital abnormalities in the United Arab Emirates (UAE) population. L.I. Al-Gazali, Adekunle Dawodu, K Sabarinathan, Journal of Medical Genetics Down SyndromeDevelopmental AnomalyMajor MalformationsUnited Arab EmiratesPediatrics	1995	124
Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome? Tamás Révész, Sophie Fletcher, L.I. Al-Gazali, Journal of Medical Genetics	1992	118
A study of possible deleterious effects of consanguinity Yousef M. Abdulrazzaq, Abdülbari Bener, L.I. Al-Gazali, Clinical Genetics	1997	104
Identification of CANT1 Mutations in Desbuquois Dysplasia Céline Huber, Bénédicte Oulès, Marta Bértoli, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsPathologyMolecular Genetics	2009	103
FREM1 Mutations Cause Bifid Nose, Renal Agenesis, and Anorectal Malformations Syndrome Anas M. Alazami, Ranad Shaheen, Fatema Alzahrani, The American Journal of Human Genetics Developmental AnomalyDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2009	90
Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect L.I. Al-Gazali, R. Padmanabhan, Stepan Melnyk, American Journal of Medical Genetics	2001	85
Homozygous Nonsense Mutations in TWIST2 Cause Setleis Syndrome Turgut Tükel, Dražen Šošić, L.I. Al-Gazali, The American Journal of Human Genetics Genome InstabilityGenetic DisorderNatural SciencesGeneticsMolecular Biology	2010	71

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