Amal Alhashem

5.2k total citations
76 papers, 1.1k citations indexed

About

Amal Alhashem is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Amal Alhashem has authored 76 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 29 papers in Genetics and 13 papers in Clinical Biochemistry. Recurrent topics in Amal Alhashem's work include Genomics and Rare Diseases (13 papers), Metabolism and Genetic Disorders (13 papers) and Genetic and Kidney Cyst Diseases (7 papers). Amal Alhashem is often cited by papers focused on Genomics and Rare Diseases (13 papers), Metabolism and Genetic Disorders (13 papers) and Genetic and Kidney Cyst Diseases (7 papers). Amal Alhashem collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Amal Alhashem's co-authors include Fowzan S. Alkuraya, Brahim Tabarki, Amer Ammari, Saad AlShahwan, Ranad Shaheen, Nouran Adly, Majid Alfadhel, Mais Hashem, Giulio Zuccoli and Yong Xiong and has published in prestigious journals such as SHILAP Revista de lepidopterología, Hepatology and Neurology.

In The Last Decade

Amal Alhashem

63 papers receiving 1.1k citations

Peers

Amal Alhashem

GENET

SURGE

Caroline Sevin France

Reeval Segel Israel

Brendan C. Lanpher United States

Elżbieta Ciara Poland

Carolina Fischinger Moura de Souza Brazil

Anne-Sophie Lèbre France

Matias Wagner Germany

Duangrurdee Wattanasirichaigoon Thailand

Toshiki Takenouchi Japan

Argirios Dinopoulos Greece

Caroline Sevin France

Amal Alhashem

551 ×0.9

268 ×0.6

GENET

121 ×0.7

163 ×1.3

SURGE

120 ×1.0

Citations per year, relative to Amal Alhashem Amal Alhashem (= 1×) peers Caroline Sevin

Countries citing papers authored by Amal Alhashem

Since Specialization

Citations

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

Fields of papers citing papers by Amal Alhashem

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amal Alhashem

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

All Works

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20 of 20 papers shown

Khan, Arif O., et al.. (2025). Congenital glaucoma associated with high hyperopia, an ophthalmic phenotypical manifestation for GLIS3 deletion: case report and review of literature. Ophthalmic Genetics. 46(6). 646–657. 1 indexed citations

Alhashem, Amal, et al.. (2024). Clinical, biochemical and molecular characteristics of classic homocystinuria in Saudi Arabia and the impact of newborn screening on prevention of the complications: A tertiary center experience. JIMD Reports. 66(1). e12454–e12454. 1 indexed citations

Sudhakar, Sniya, Asthik Biswas, Jessica Rosenblum, et al.. (2024). Sotos Syndrome: Deep Neuroimaging Phenotyping Reveals a High Prevalence of Malformations of Cortical Development. American Journal of Neuroradiology. 45(10). 1570–1577.

Johari, Mridul, Ana Töpf, Jennifer Duff, et al.. (2024). Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement. Journal of Medical Genetics. 61(10). 992–998.

AlAbdi, Lama, Zuhair Rahbeeni, Sateesh Maddirevula, et al.. (2024). A founder variant expands the phenotype of WNT7B ‐related PDAC syndrome. Clinical Genetics. 106(1). 66–71.

Alhashem, Amal, et al.. (2023). Variable phenotype of a null PPP1R13L allele in children with dilated cardiomyopathy. American Journal of Medical Genetics Part A. 194(1). 59–63. 1 indexed citations

Alhashem, Amal, et al.. (2022). A Biallelic Variant in FRA10AC1 Is Associated With Neurodevelopmental Disorder and Growth Retardation. Neurology Genetics. 8(4). e200010–e200010. 3 indexed citations

Altassan, Ruqaiah, Riyadh Alokaili, Khalid Alhasan, et al.. (2022). Further delineation of GEMIN4 related neurodevelopmental disorder with microcephaly, cataract, and renal abnormalities syndrome. American Journal of Medical Genetics Part A. 188(10). 2932–2940. 1 indexed citations

Marais, Anett, Aida M. Bertoli‐Avella, Christian Beetz, et al.. (2022). Further clinical and genetic evidence of ASC-1 complex dysfunction in congenital neuromuscular disease. European Journal of Medical Genetics. 65(8). 104537–104537. 4 indexed citations

10.

Alghamdi, Malak, Nouran Adly, Amal Alhashem, et al.. (2021). Molecular autopsy by proxy in preconception counseling. Clinical Genetics. 100(6). 678–691. 6 indexed citations

11.

Fletcher, Emily V., Ranad Shaheen, Michael S. Nahorski, et al.. (2021). Mutations in phospholipase C eta-1 (PLCH1) are associated with holoprosencephaly. Journal of Medical Genetics. 59(4). 358–365. 2 indexed citations

12.

Shamseldin, Hanan E., Amal Alhashem, Brahim Tabarki, et al.. (2021). Mitochondrial “dysmorphology” in variant classification. Human Genetics. 141(1). 55–64. 3 indexed citations

13.

Shamseldin, Hanan E., Muslim M. Alsaadi, Amal Alhashem, et al.. (2020). An exome-first approach to aid in the diagnosis of primary ciliary dyskinesia. Human Genetics. 139(10). 1273–1283. 16 indexed citations

14.

Hashem, Mais, et al.. (2020). Survey of disorders of sex development in a large cohort of patients with diverse Mendelian phenotypes. American Journal of Medical Genetics Part A. 185(9). 2789–2800. 8 indexed citations

15.

Shamseldin, Hanan E., Amal Alhashem, Mais Hashem, et al.. (2019). MDH1 deficiency is a metabolic disorder of the malate–aspartate shuttle associated with early onset severe encephalopathy. Human Genetics. 138(11-12). 1247–1257. 40 indexed citations

16.

Kurdi, Ahmed M, et al.. (2019). Congenital anomalies and associated risk factors in a Saudi population: a cohort study from pregnancy to age 2 years. BMJ Open. 9(9). e026351–e026351. 27 indexed citations

17.

Alhashem, Amal, et al.. (2019). A de novo splicing variant supports the candidacy of TLL1 in ASD pathogenesis. European Journal of Human Genetics. 28(4). 525–528. 5 indexed citations

18.

Alhashem, Amal, Eissa Faqeih, Majid Alfadhel, et al.. (2017). Congenital disorders of glycosylation: The Saudi experience. American Journal of Medical Genetics Part A. 173(10). 2614–2621. 29 indexed citations

19.

Patel, Nisha, et al.. (2016). Distal acroosteolysis, poikiloderma and joint stiffness: a novel laminopathy?. European Journal of Human Genetics. 24(8). 1220–1222. 4 indexed citations

20.

Tabarki, Brahim, Amal Alhashem, & Majid Alfadhel. (2013). Biotin-Thiamine-Responsive Basal Ganglia Disease. 12 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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