Ghada A. Otaify

1.0k total citations
31 papers, 453 citations indexed

About

Ghada A. Otaify is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Ghada A. Otaify has authored 31 papers receiving a total of 453 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 20 papers in Molecular Biology and 6 papers in Oncology. Recurrent topics in Ghada A. Otaify's work include Connective tissue disorders research (12 papers), Bone health and treatments (6 papers) and Bone and Dental Protein Studies (4 papers). Ghada A. Otaify is often cited by papers focused on Connective tissue disorders research (12 papers), Bone health and treatments (6 papers) and Bone and Dental Protein Studies (4 papers). Ghada A. Otaify collaborates with scholars based in Egypt, United States and Spain. Ghada A. Otaify's co-authors include Mona Aglan, Samia A. Temtamy, Mohamed S. Abdel‐Hamid, Stylianos E. Antonarakis, Víctor L. Ruiz‐Pérez, Periklis Makrythanasis, Hanan Hamamy, Maha S. Zaki, Antonella Forlino and Pablo Lapunzina and has published in prestigious journals such as The American Journal of Human Genetics, Human Molecular Genetics and Journal of Bone and Mineral Research.

In The Last Decade

Ghada A. Otaify

31 papers receiving 450 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Ghada A. Otaify Egypt 11 253 250 107 57 44 31 453
Elena Gallo MacFarlane United States 11 242 1.0× 177 0.7× 64 0.6× 39 0.7× 40 0.9× 22 560
Ok-Hwa Kim South Korea 11 270 1.1× 153 0.6× 119 1.1× 76 1.3× 45 1.0× 15 458
Siham Chafai Elalaoui Morocco 14 158 0.6× 262 1.0× 47 0.4× 35 0.6× 23 0.5× 41 525
Michaela Durigova Canada 10 218 0.9× 104 0.4× 173 1.6× 74 1.3× 80 1.8× 11 441
Riikka E. Mäkitie Finland 16 306 1.2× 386 1.5× 79 0.7× 134 2.4× 28 0.6× 38 616
D. Sillence Australia 10 310 1.2× 181 0.7× 116 1.1× 80 1.4× 43 1.0× 22 451
Pamela Poblete‐Gutiérrez Netherlands 12 151 0.6× 400 1.6× 122 1.1× 34 0.6× 66 1.5× 48 653
Danese M. Joiner United States 10 88 0.3× 334 1.3× 65 0.6× 111 1.9× 19 0.4× 11 491
Björn‐Anders Jonsson Sweden 10 135 0.5× 214 0.9× 52 0.5× 49 0.9× 18 0.4× 11 448

Countries citing papers authored by Ghada A. Otaify

Since Specialization
Citations

This map shows the geographic impact of Ghada A. Otaify's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ghada A. Otaify with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ghada A. Otaify more than expected).

Fields of papers citing papers by Ghada A. Otaify

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ghada A. Otaify. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ghada A. Otaify. The network helps show where Ghada A. Otaify may publish in the future.

Co-authorship network of co-authors of Ghada A. Otaify

This figure shows the co-authorship network connecting the top 25 collaborators of Ghada A. Otaify. A scholar is included among the top collaborators of Ghada A. Otaify based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ghada A. Otaify. Ghada A. Otaify is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Otaify, Ghada A., et al.. (2022). Shohat type-spondyloepimetaphyseal dysplasia: Further phenotypic delineation. European Journal of Medical Genetics. 65(12). 104640–104640. 2 indexed citations
2.
Abdel‐Hamid, Mohamed S., et al.. (2022). Osteoporosis-pseudoglioma syndrome in four new patients: identification of two novel LRP5 variants and insights on patients’ management using bisphosphonates therapy. Osteoporosis International. 33(7). 1501–1510. 6 indexed citations
3.
Flores, Carmen‐Lisset, Ghada A. Otaify, Julián Nevado, et al.. (2022). Mutations in SCNM1 cause orofaciodigital syndrome due to minor intron splicing defects affecting primary cilia. The American Journal of Human Genetics. 109(10). 1828–1849. 8 indexed citations
4.
Kague, Érika, Francesco Turci, Kate Robson Brown, et al.. (2021). 3D assessment of intervertebral disc degeneration in zebrafish identifies changes in bone density that prime disc disease. Bone Research. 9(1). 39–39. 39 indexed citations
5.
Horn, Denise, Julián Nevado, Nadja Ehmke, et al.. (2021). Biallelic truncating variants in MAPKAPK5 cause a new developmental disorder involving neurological, cardiac, and facial anomalies combined with synpolydactyly. Genetics in Medicine. 23(4). 679–688. 5 indexed citations
6.
Ashaat, Engy A., Ghada A. Otaify, Samira Ismail, et al.. (2021). First Report of Two Egyptian Patients with Desbuquois Dysplasia due to Homozygous <b><i>CANT1</i></b> Mutations. Molecular Syndromology. 12(5). 279–288. 5 indexed citations
7.
Khairat, Rabab, Nara Sobreira, Elizabeth Wohler, et al.. (2021). Expansion of the phenotypic and mutational spectrum of Carpenter syndrome. European Journal of Medical Genetics. 65(1). 104377–104377. 6 indexed citations
8.
Besio, Roberta, Laura Leoni, Lina Cipolla, et al.. (2019). Cellular stress due to impairment of collagen prolyl hydroxylation complex is rescued by the chaperone 4-phenylbutyrate. Disease Models & Mechanisms. 12(6). 52 indexed citations
9.
Otaify, Ghada A.. (2019). Bone-specific therapeutic modalities for genetic skeletal diseases. 8(2). 69. 1 indexed citations
10.
11.
Ismail, Somaia, et al.. (2018). ROBERTS SYNDROME: CLINICAL AND CYTOGENETIC STUDIES IN 8 EGYPTIAN PATIENTS AND MOLECULAR STUDIES IN 4 PATIENTS WITH GENOTYPE/PHENOTYPE CORRELATION.. PubMed. 27(3). 305–323. 4 indexed citations
12.
Doyard, Mathilde, Séverine Bacrot, Céline Huber, et al.. (2018). FAM46A mutations are responsible for autosomal recessive osteogenesis imperfecta. Journal of Medical Genetics. 55(4). 278–284. 53 indexed citations
13.
Abdel‐Hamid, Mohamed S., Samira Ismail, Maha S. Zaki, et al.. (2018). GAPO syndrome in seven new patients: Identification of five novel ANTXR1 mutations including the first large intragenic deletion. American Journal of Medical Genetics Part A. 179(2). 237–242. 9 indexed citations
14.
Otaify, Ghada A., et al.. (2018). Genetic study of eight Egyptian patients with pycnodysostosis: identification of novel CTSK mutations and founder effect. Osteoporosis International. 29(8). 1833–1841. 13 indexed citations
15.
Gagliardi, Assunta, Roberta Besio, Claudia Landi, et al.. (2017). Cytoskeleton and nuclear lamina affection in recessive osteogenesis imperfecta: A functional proteomics perspective. Journal of Proteomics. 167. 46–59. 21 indexed citations
16.
Abdel‐Hamid, Mohamed S., Mahmoud Y. Issa, Ghada A. Otaify, & Maha S. Zaki. (2017). A novel frameshift mutation in the sterol 27-hydroxylase gene in an Egyptian family with cerebrotendinous xanthomatosis without cataract. Metabolic Brain Disease. 32(2). 311–315. 3 indexed citations
17.
Otaify, Ghada A., Michael P. Whyte, Gary S. Gottesman, et al.. (2017). Gnathodiaphyseal dysplasia: Severe atypical presentation with novel heterozygous mutation of the anoctamin gene (ANO5). Bone. 107. 161–171. 25 indexed citations
18.
Caparrós‐Martín, José A., Alessandro De Luca, François Cartault, et al.. (2015). Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium. Human Molecular Genetics. 24(14). 4126–4137. 42 indexed citations
19.
Otaify, Ghada A., et al.. (2015). Zoledronic acid in children with osteogenesis imperfecta and Bruck syndrome: a 2-year prospective observational study. Osteoporosis International. 27(1). 81–92. 27 indexed citations
20.
Aglan, Mona, Khalda Amr, Samira Ismail, et al.. (2015). Clinical and molecular characterization of seven Egyptian families with autosomal recessive robinow syndrome: Identification of four novel ROR2 gene mutations. American Journal of Medical Genetics Part A. 167(12). 3054–3061. 6 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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