Mona El Gammal - Concepedia

Author

Mona El Gammal

Also Known As

El Gammal, Mona, M A El-Gammal, M A el-Gammal, M. El Gammal, M. El-Gammal, M.A. El Gammal, Mona A. El Gammal, Mona A. El-Gammal, Mona El Gammal, Mona El-Gammal

Publications

798

Citations

H-Index

Concepts

All Affiliations

National Research Centre National Water Research Center Institut Pasteur National Human Genome Research Institute University of Cambridge

About

Mona El Gammal is an author at National Research Centre specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	401
2	Public Health	2	2	67
3	Education	1	1	40
4	Health Sciences	1	1	114
5	Social Sciences	1	1	28

Mona El Gammal

Publications

774

Citations

H-Index

Page 1

	Year	Citations
A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient Inas Mazen, Mona El Gammal, Mohamed S. Abdel‐Hamid, Molecular Genetics and Metabolism ObesityMetabolic SyndromeObese Egyptian PatientGenetic DisorderGenetics	2009	114
Severe Early-Onset Obesity Due to Bioinactive Leptin Caused by a p.N103K Mutation in the Leptin Gene Martin Wabitsch, Jan‐Bernd Funcke, Julia von Schnurbein, The Journal of Clinical Endocrinology & Metabolism	2015	99
Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity Inas Mazen, Mona El Gammal, Mohamed S. Abdel‐Hamid, Molecular Genetics and Metabolism ObesityMetabolic SyndromeAllelic VariantDevelopmental BiologyLeptin Receptor Gene	2011	71
Long interspersed nuclear element-1 (LINE1)-mediated deletion ofEVC,EVC2,C4orf6, andSTK32B in Ellis–van Creveld syndrome with borderline intelligence Samia A. Temtamy, Mona Aglan, Guido Cocchi, Human Mutation ChromatinDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2008	58
Differential Diagnosis of Disorders of Sex Development in Egypt Inas Mazen, Olaf Hiort, R. Bassiouny, Hormone Research in Paediatrics	2008	52
Identification of <b><i>NR5A1</i></b> Mutations and Possible Digenic Inheritance in 46,XY Gonadal Dysgenesis Inas Mazen, Mohamed S. Abdel‐Hamid, Mona K. Mekkawy, Sexual Development GeneticsMolecular GeneticsGenomicsReproductive BiologyMendelian Disorder	2016	48
Phenotypic and cytogenetic spectrum of 9p trisomy Samia A. Temtamy, Alaa K. Kamel, Samira Ismail, PubMed	2007	48
Assessment of Pubertal Development in Egyptian Girls Laila Hosny, Mona El‐Ruby, Moushira Zaki, Journal of Pediatric Endocrinology and Metabolism InfertilityBody CompositionFertilityTeenage PregnancyHuman Growth	2005	40
Analysis of the gene coding for steroidogenic factor 1 (SF1, NR5A1) in a cohort of 50 Egyptian patients with 46,XY disorders of sex development Sally Tantawy, Inas Mazen, Hala Soliman, European Journal of Endocrinology	2014	38
Indicators of the metabolic syndrome in obese adolescents Moushira Zaki, Hala T. El‐Bassyouni, Mona El Gammal, Archives of Medical Science	2015	34

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