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About the database ScholarIQanswers from OpenAlex & ORCID
How has Khalda Amr's publication output changed over time?
ScholarIQpublication output · 2009–2023
Output grew0% over the shown period — from 1 works in 2009 to 1 in 2023.
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1
1
1
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1
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20092010201120122015201720182023
What are the most-cited papers on Khalda Amr?
ScholarIQmost cited works
Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta
Pablo Lapunzina, Mona Aglan, Samia A. Temtamy, José A. Caparrós‐Martín, Maria Valencia, Rocío Letón, Víctor Martínez‐Glez, Rasha M. Elhossini, Khalda Amr, Nuria Vilaboa, Víctor L. Ruiz‐Pérez
S134425043. 2010289 CitationsOPEN ACCESS
LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome
Yun Li, Barbara Pawlik, Nursel Elçioğlu, Mona Aglan, Hülya Kayserili, Gökhan Yigit, E. Ferda Perçin, Frances R. Goodman, Gudrun Nürnberg, Asım Cenani, Jill Urquhart, Boi-Dinh Chung, Samira Ismail, Khalda Amr, Ayça Dilruba Aslanger, Christian Becker, Christian Netzer, Peter Scambler, Wafaa Eyaid, Hanan Hamamy, Jill Clayton‐Smith, Raoul C. M. Hennekam, Peter Nürnberg, Joachim Herz, Samia A. Temtamy, Bernd Wollnik
S134425043. 2010169 CitationsOPEN ACCESS
A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient
Inas Mazen, Mona El Gammal, Mohamed S. Abdel‐Hamid, Khalda Amr
S42433034. 2009117 Citations
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, Maria Valencia, Víctor Martínez‐Glez, María Juliana Ballesta‐Martínez, Vanesa López‐González, Adel M. Ashour, Khalda Amr, Verónica Pulido, Encarna Guillén‐Navarro, Pablo Lapunzina, José A. Caparrós‐Martín, Víctor L. Ruiz‐Pérez
S98809561. 201299 Citations
Early diagnostic evaluation of miR-122 and miR-224 as biomarkers for hepatocellular carcinoma
Khalda Amr, Hanan Abd Elmawgoud Atia, Rehab Abd Elazeem Elbnhawy, Wafaa M. Ezzat
S2764642421. 201798 CitationsOPEN ACCESS
Related on ScholarIQ
Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta
Paper
LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome
Paper
A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient
Paper
Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum
Paper
Early diagnostic evaluation of miR-122 and miR-224 as biomarkers for hepatocellular carcinoma
Paper
Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling
Paper