Ali Awaji

475 total citations
6 papers, 265 citations indexed

About

Ali Awaji is a scholar working on Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Ali Awaji has authored 6 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Ali Awaji's work include Connective tissue disorders research (2 papers), Cardiovascular Effects of Exercise (2 papers) and Genetic Syndromes and Imprinting (1 paper). Ali Awaji is often cited by papers focused on Connective tissue disorders research (2 papers), Cardiovascular Effects of Exercise (2 papers) and Genetic Syndromes and Imprinting (1 paper). Ali Awaji collaborates with scholars based in Saudi Arabia, United States and Kuwait. Ali Awaji's co-authors include Fowzan S. Alkuraya, Ranad Shaheen, Mohammed A. Aldahmesh, Mohammed Al‐Owain, Mais Hashem, Nadia Alhashmi, Zayed Al‐Zayed, Eissa Faqeih, Amal Hashem and Anas M. Alazami and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and British Journal of Haematology.

In The Last Decade

Ali Awaji

6 papers receiving 264 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ali Awaji Saudi Arabia	4	178	170	27	24	19	6	265
Kristen L. Sund United States	9	193 1.1×	171 1.0×	19 0.7×	19 0.8×	28 1.5×	15	326
Joyce Andrade Brazil	7	195 1.1×	126 0.7×	39 1.4×	52 2.2×	17 0.9×	14	331
Kim Jenny United States	4	188 1.1×	160 0.9×	18 0.7×	10 0.4×	10 0.5×	6	265
Jeannette Connerney United States	6	249 1.4×	137 0.8×	43 1.6×	32 1.3×	10 0.5×	8	354
Ronny Derks Netherlands	10	221 1.2×	130 0.8×	19 0.7×	40 1.7×	13 0.7×	15	326
Anna Hammarsjö Sweden	9	164 0.9×	115 0.7×	16 0.6×	59 2.5×	8 0.4×	21	264
Jennifer McDaid United Kingdom	8	271 1.5×	99 0.6×	21 0.8×	29 1.2×	17 0.9×	8	325
Maha Faden Saudi Arabia	6	93 0.5×	100 0.6×	31 1.1×	12 0.5×	20 1.1×	9	178
Teresa Vendrell Spain	12	160 0.9×	143 0.8×	25 0.9×	12 0.5×	19 1.0×	25	310
Clémentine Mahaut France	5	98 0.6×	122 0.7×	16 0.6×	20 0.8×	17 0.9×	5	196

Countries citing papers authored by Ali Awaji

Since Specialization

Citations

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

Fields of papers citing papers by Ali Awaji

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ali Awaji

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

All Works

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6 of 6 papers shown

1.

Marafi, Dana, Mais Hashem, Firdous Abdulwahab, et al.. (2023). Human ‘knockouts’ of CSF3 display severe congenital neutropenia. British Journal of Haematology. 203(3). 477–480. 3 indexed citations

2.

Awaji, Ali, et al.. (2023). Dilated cardiomyopathy associated with NRAP gene: a case series. SHILAP Revista de lepidopterología. 6(1). 70–74. 1 indexed citations

3.

Aldahmesh, Mohammed A., Yuanyuan Li, Amal Alhashem, et al.. (2014). IFT27, encoding a small GTPase component of IFT particles, is mutated in a consanguineous family with Bardet-Biedl syndrome. Human Molecular Genetics. 23(12). 3307–3315. 109 indexed citations

4.

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

5.

Shaheen, Ranad, Mohammed Al‐Owain, Eissa Faqeih, et al.. (2011). Mutations in FKBP10 cause both Bruck syndrome and isolated osteogenesis imperfecta in humans. American Journal of Medical Genetics Part A. 155(6). 1448–1452. 55 indexed citations

6.

Al‐Owain, Mohammed, Salma M. Wakil, Mansoor A. Haider, et al.. (2010). Novel homozygous mutation in DSP causing skin fragility-woolly hair syndrome: report of a large family and review of the desmoplakin-related phenotypes. Clinical Genetics. 80(1). 50–58. 18 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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