# Khalda Amr

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/khalda-amr/

## Facts

| Field | Value |
| --- | --- |
| Citations | 2,516 |
| Field | MicroRNA in disease regulation |
| h-index | 25 |
| i10-index | 57 |
| OpenAlex ID | https://openalex.org/A5034047313 |
| ORCID iD | 0000-0001-8472-5911 |
| Works | 142 |

## Researcher papers

- [Identification of a Frameshift Mutation in Osterix in a Patient with Recessive Osteogenesis Imperfecta](https://scholariq.org/papers/identification-of-a-frameshift-mutation-in-osterix-in-a-patient-with-recessive/)
- [LRP4 Mutations Alter Wnt/β-Catenin Signaling and Cause Limb and Kidney Malformations in Cenani-Lenz Syndrome](https://scholariq.org/papers/lrp4-mutations-alter-wnt-catenin-signaling-and-cause-limb-and-kidney/)
- [A novel homozygous missense mutation of the leptin gene (N103K) in an obese Egyptian patient](https://scholariq.org/papers/a-novel-homozygous-missense-mutation-of-the-leptin-gene-n103k-in-an-obese/)
- [Mutations in PLOD2 cause autosomal-recessive connective tissue disorders within the Bruck syndrome-Osteogenesis imperfecta phenotypic spectrum](https://scholariq.org/papers/mutations-in-plod2-cause-autosomal-recessive-connective-tissue-disorders-within/)
- [Early diagnostic evaluation of miR-122 and miR-224 as biomarkers for hepatocellular carcinoma](https://scholariq.org/papers/early-diagnostic-evaluation-of-mir-122-and-mir-224-as-biomarkers-for/)
- [Temtamy Preaxial Brachydactyly Syndrome Is Caused by Loss-of-Function Mutations in Chondroitin Synthase 1, a Potential Target of BMP Signaling](https://scholariq.org/papers/temtamy-preaxial-brachydactyly-syndrome-is-caused-by-loss-of-function-mutations/)
- [Homozygosity for a novel missense mutation in the leptin receptor gene (P316T) in two Egyptian cousins with severe early onset obesity](https://scholariq.org/papers/homozygosity-for-a-novel-missense-mutation-in-the-leptin-receptor-gene-p316t-in/)
- [Expanding the phenome and variome of skeletal dysplasia](https://scholariq.org/papers/expanding-the-phenome-and-variome-of-skeletal-dysplasia/)
- [Association of vitamin D receptor gene polymorphism (VDR) with vitamin D deficiency, metabolic and inflammatory markers in Egyptian obese women](https://scholariq.org/papers/association-of-vitamin-d-receptor-gene-polymorphism-vdr-with-vitamin-d/)
- [The potential role of miRNAs 21 and 199-a in early diagnosis of hepatocellular carcinoma](https://scholariq.org/papers/the-potential-role-of-mirnas-21-and-199-a-in-early-diagnosis-of-hepatocellular/)
- [Outlining the Clinical Profile of TCIRG1 14 Variants including 5 Novels with Overview of ARO Phenotype and Ethnic Impact in 20 Egyptian Families](https://scholariq.org/papers/outlining-the-clinical-profile-of-tcirg1-14-variants-including-5-novels-with/)

## Researcher topics

- [MicroRNA in disease regulation](https://scholariq.org/topics/microrna-in-disease-regulation/)
- [Connective tissue disorders research](https://scholariq.org/topics/connective-tissue-disorders-research/)
- [Hepatitis C virus research](https://scholariq.org/topics/hepatitis-c-virus-research/)
- [Psoriasis: Treatment and Pathogenesis](https://scholariq.org/topics/psoriasis-treatment-and-pathogenesis/)
- [Cancer-related molecular mechanisms research](https://scholariq.org/topics/cancer-related-molecular-mechanisms-research/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.