Khalda Amr - Concepedia

Author

Khalda Amr

National Research Centre ORCID

Also Known As

Amr, khalda, Christian Beetz, K Amr, K. Amr, K. S. Amr, K.S. Amr, KHALDA S AMR, Khalda Amr, Khalda S Amr, Khalda S. Amr

142

Publications

2.4K

Citations

H-Index

100

Concepts

All Affiliations

National Research Centre National Water Research Center Al-Azhar University Cairo University Ain Shams University

About

Khalda Amr is an author at National Research Centre specializing in medicine, pathology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	27	1.2K
2	Public Health	5	5	133
3	Health Sciences	2	2	130
4	Engineering	1	1	38
5	Social Sciences	1	1	28

Khalda Amr

Publications

Citations

H-Index

Page 1

	Year	Citations
Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta Pablo Lapunzina, Mona Aglan, Samia A. Temtamy, The American Journal of Human Genetics Bone DiseaseRecessive Osteogenesis ImperfectaDevelopmental BiologyOsteopathyGenetics	2010	283
LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome Yun Li, Barbara Pawlik, Nursel Elçioğlu, The American Journal of Human Genetics	2010	163
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
Early diagnostic evaluation of miR-122 and miR-224 as biomarkers for hepatocellular carcinoma Khalda Amr, Hanan Abd Elmawgoud Atia, Rehab Abd Elazeem Elbnhawy, Genes & Diseases	2017	96
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum Maria Trinidad Puig-Hervás, Samia A. Temtamy, Mona Aglan, Human Mutation	2012	95
Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling Yun Li, Kathrin Laue, Samia A. Temtamy, The American Journal of Human Genetics Developmental BiologyMendelian DisorderBone Morphogenic ProteinGenetic DisorderGenetics	2010	94
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
Expanding the phenome and variome of skeletal dysplasia Sateesh Maddirevula, Saud Alsahli, Lamees Alhabeeb, Genetics in Medicine Developmental BiologyBone Morphogenic ProteinDistraction OsteogenesisBone RemodelingMorphogenesis	2018	69
Association of vitamin D receptor gene polymorphism (VDR) with vitamin D deficiency, metabolic and inflammatory markers in Egyptian obese women Moushira Zaki, Sanaa Kamal, Walaa A. Basha, Genes & Diseases ObesityNutritionMetabolic SyndromeInsulin ResistanceBody Composition	2017	62
The potential role of miRNAs 21 and 199-a in early diagnosis of hepatocellular carcinoma Khalda Amr, Wafaa M. Ezzat, Yasser A. Elhosary, Gene Early DiagnosisHepatologyHepatocellular CarcinomaMedicineHistopathology	2015	61

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