ScholarIQanswers from OpenAlex & ORCID
Khalda Amr
ResearcherPublications, citations & collaboration network
Khalda Amr is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Khalda Amr have?
ScholarIQindexed works
Khalda Amr has 142 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Khalda Amr have?
ScholarIQcitation count
Khalda Amr has 2,516 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Khalda Amr?
ScholarIQh-index
Khalda Amr has an h-index of 25 in OpenAlex.
What is the i10-index of Khalda Amr?
ScholarIQi10-index
Khalda Amr has an i10-index of 57 in OpenAlex.
What is the ORCID of Khalda Amr?
ScholarIQorcid
The ORCID for Khalda Amr is on the source record.
What is the OpenAlex record for Khalda Amr?
ScholarIQopenalex
The OpenAlex for Khalda Amr is on the source record.
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
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
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
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
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