Amal Hashem

1.0k total citations
11 papers, 354 citations indexed

About

Amal Hashem is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Amal Hashem has authored 11 papers receiving a total of 354 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cell Biology. Recurrent topics in Amal Hashem's work include RNA modifications and cancer (3 papers), Renal and related cancers (3 papers) and Genomics and Rare Diseases (2 papers). Amal Hashem is often cited by papers focused on RNA modifications and cancer (3 papers), Renal and related cancers (3 papers) and Genomics and Rare Diseases (2 papers). Amal Hashem collaborates with scholars based in Saudi Arabia, United States and Germany. Amal Hashem's co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Anas M. Alazami, Hanan E. Shamseldin, Ahmed M Kurdi, Mais Hashem, Mustafa A. Salih, Mohammed S. Al‐Dosari, Mohammed A. Aldahmesh and Tariq Masoodi and has published in prestigious journals such as SHILAP Revista de lepidopterología, The American Journal of Human Genetics and Human Molecular Genetics.

In The Last Decade

Amal Hashem

11 papers receiving 352 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Amal Hashem Saudi Arabia 9 236 138 54 46 32 11 354
Eyby Leon United States 9 263 1.1× 104 0.8× 41 0.8× 32 0.7× 11 0.3× 29 379
Mahmoud Taleb Al‐Ali United Arab Emirates 10 174 0.7× 150 1.1× 38 0.7× 44 1.0× 13 0.4× 34 312
Hande Kaymakçalan Türkiye 9 187 0.8× 133 1.0× 114 2.1× 36 0.8× 18 0.6× 14 337
Jonathan J. Wilde United States 7 305 1.3× 114 0.8× 101 1.9× 54 1.2× 14 0.4× 7 429
Kavita Narwani United States 8 283 1.2× 100 0.7× 48 0.9× 66 1.4× 27 0.8× 11 421
Francesco Benedicenti Italy 10 165 0.7× 123 0.9× 28 0.5× 43 0.9× 21 0.7× 21 417
Naiara Akizu United States 11 380 1.6× 229 1.7× 44 0.8× 50 1.1× 9 0.3× 19 484
Anouck Schneider France 12 134 0.6× 199 1.4× 27 0.5× 62 1.3× 63 2.0× 21 355
Sonia Nizard France 10 131 0.6× 227 1.6× 62 1.1× 87 1.9× 21 0.7× 12 357
Mary Haddadin United States 6 210 0.9× 103 0.7× 24 0.4× 56 1.2× 60 1.9× 7 343

Countries citing papers authored by Amal Hashem

Since Specialization
Citations

This map shows the geographic impact of Amal Hashem'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 Amal Hashem with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Amal Hashem more than expected).

Fields of papers citing papers by Amal Hashem

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Amal Hashem. 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 Amal Hashem. The network helps show where Amal Hashem may publish in the future.

Co-authorship network of co-authors of Amal Hashem

This figure shows the co-authorship network connecting the top 25 collaborators of Amal Hashem. A scholar is included among the top collaborators of Amal Hashem 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 Amal Hashem. Amal Hashem is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
Ramzan, Khushnooda, Mohammed Al‐Owain, Nouf S. Al‐Numair, et al.. (2019). Identification of TMC1 as a relatively common cause for nonsyndromic hearing loss in the Saudi population. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 183(3). 172–180. 14 indexed citations
2.
Hundallah, Khalid, et al.. (2018). A novel variant in ATM gene causes ataxia telangiectasia revealed by whole-exome sequencing. Neurosciences. 23(2). 162–164. 4 indexed citations
3.
Suleiman, Jehan, Amal Hashem, Brahim Tabarki, et al.. (2018). PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities. Clinical Genetics. 94(3-4). 351–355. 8 indexed citations
4.
Shamseldin, Hanan E., Toma A. Yakulov, Amal Hashem, Gerd Walz, & Fowzan S. Alkuraya. (2016). ANKS3 is mutated in a family with autosomal recessive laterality defect. Human Genetics. 135(11). 1233–1239. 15 indexed citations
5.
Shaheen, Ranad, et al.. (2016). Mutations in CIT, encoding citron rho-interacting serine/threonine kinase, cause severe primary microcephaly in humans. Human Genetics. 135(10). 1191–1197. 25 indexed citations
6.
El‐Hattab, Ayman W., Mohammed A. Saleh, Amal Hashem, et al.. (2016). ADAT3‐related intellectual disability: Further delineation of the phenotype. American Journal of Medical Genetics Part A. 170(5). 1142–1147. 26 indexed citations
7.
Shamseldin, Hanan E., Maha Tulbah, Wesam Kurdi, et al.. (2015). Identification of embryonic lethal genes in humans by autozygosity mapping and exome sequencing in consanguineous families. Genome Biology. 16(1). 116–116. 78 indexed citations
8.
Kurdi, Ahmed M, et al.. (2015). Patterns of folic acid use in pregnant Saudi women and prevalence of neural tube defects — Results from a nested case–control study. SHILAP Revista de lepidopterología. 2. 572–576. 21 indexed citations
9.
Shamseldin, Hanan E., Anas M. Alazami, Melanie Manning, et al.. (2015). RTTN Mutations Cause Primary Microcephaly and Primordial Dwarfism in Humans. The American Journal of Human Genetics. 97(6). 862–868. 31 indexed citations
10.
Shaheen, Ranad, Miriam Schmidts, Eissa Faqeih, et al.. (2014). A founder CEP120 mutation in Jeune asphyxiating thoracic dystrophy expands the role of centriolar proteins in skeletal ciliopathies. Human Molecular Genetics. 24(5). 1410–1419. 53 indexed citations
11.
Alazami, Anas M., Hadia Hijazi, Mohammed S. Al‐Dosari, et al.. (2013). Mutation in ADAT3, encoding adenosine deaminase acting on transfer RNA, causes intellectual disability and strabismus. Journal of Medical Genetics. 50(7). 425–430. 79 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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