Ali Fawaz

487 total citations
10 papers, 298 citations indexed

About

Ali Fawaz is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Clinical Biochemistry. According to data from OpenAlex, Ali Fawaz has authored 10 papers receiving a total of 298 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 2 papers in Pediatrics, Perinatology and Child Health and 2 papers in Clinical Biochemistry. Recurrent topics in Ali Fawaz's work include Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Metabolism and Genetic Disorders (2 papers). Ali Fawaz is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Metabolism and Genetic Disorders (2 papers). Ali Fawaz collaborates with scholars based in Lebanon, France and Canada. Ali Fawaz's co-authors include Sonya A. MacParland, Mario Ostrowski, Ben Ouyang, Anton Zilman, Warren C. W. Chan, Ian D. McGilvray, Justin Manuel, Kim M. Tsoi, Benjamin A. Alman and Xue‐Zhong Ma and has published in prestigious journals such as ACS Nano, PLoS ONE and Seizure.

In The Last Decade

Ali Fawaz

10 papers receiving 295 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ali Fawaz Lebanon 7 97 84 74 67 35 10 298
Zhenghua Wei China 8 161 1.7× 33 0.4× 36 0.5× 30 0.4× 36 1.0× 16 321
Zhenmeng Wang China 12 354 3.6× 22 0.3× 123 1.7× 36 0.5× 26 0.7× 32 548
Xiangbo Xu China 12 40 0.4× 129 1.5× 17 0.2× 20 0.3× 31 0.9× 18 301
Meryem T. Ok United States 6 98 1.0× 27 0.3× 83 1.1× 37 0.6× 44 1.3× 8 311
Pu Shao China 8 111 1.1× 27 0.3× 70 0.9× 38 0.6× 16 0.5× 15 317
Guanlan Fan China 10 169 1.7× 81 1.0× 160 2.2× 90 1.3× 27 0.8× 14 412
Anjan Motamarry United States 8 109 1.1× 25 0.3× 139 1.9× 109 1.6× 20 0.6× 14 303
Ammar Ebrahimi Iran 11 171 1.8× 33 0.4× 46 0.6× 32 0.5× 14 0.4× 26 329
Shiyuan Yang China 12 68 0.7× 179 2.1× 76 1.0× 24 0.4× 18 0.5× 16 427
Fei Yin China 8 173 1.8× 38 0.5× 70 0.9× 43 0.6× 48 1.4× 20 377

Countries citing papers authored by Ali Fawaz

Since Specialization
Citations

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

Fields of papers citing papers by Ali Fawaz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ali Fawaz

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

All Works

10 of 10 papers shown
1.
Leigh, Jennifer, Shing Fung Lee, Ali Fawaz, et al.. (2025). Assessment of the benefits of bone modifying agents in the management of advanced breast, prostate, and lung cancers. Current Opinion in Supportive and Palliative Care. 19(2). 117–129. 1 indexed citations
2.
Nava, Caroline, et al.. (2019). Dravet Syndrome in Lebanon: First Report on Cases with SCN1A Mutations. Case Reports in Medicine. 2019. 1–4. 5 indexed citations
3.
Esfandiari, Babak, et al.. (2018). A case-based reasoning approach to learning state-based behavior. The Florida AI Research Society. 377–382. 2 indexed citations
4.
Haidar, Ziyad S., Nadine Jalkh, Sandra Corbani, et al.. (2018). Atypical pyridoxine dependent epilepsy resulting from a new homozygous missense mutation, in ALDH7A1. Seizure. 57. 32–33. 12 indexed citations
5.
MacParland, Sonya A., Kim M. Tsoi, Ben Ouyang, et al.. (2016). Phenotype Determines Nanoparticle Uptake by Human Macrophages from Liver and Blood. ACS Nano. 11(3). 2428–2443. 186 indexed citations
6.
MacParland, Sonya A., Ali Fawaz, Jun Liu, et al.. (2016). HCV Specific IL-21 Producing T Cells but Not IL-17A Producing T Cells Are Associated with HCV Viral Control in HIV/HCV Coinfection. PLoS ONE. 11(4). e0154433–e0154433. 8 indexed citations
7.
Ghoch, Joelle Abou, Sandra Corbani, Pierre Cacciagli, et al.. (2015). Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients. Molecular Cytogenetics. 8(1). 26–26. 6 indexed citations
8.
Mignon‐Ravix, Cécile, Pierre Cacciagli, Joelle Abou Ghoch, et al.. (2015). Evidence that homozygous PTPRD gene microdeletion causes trigonocephaly, hearing loss, and intellectual disability. Molecular Cytogenetics. 8(1). 39–39. 31 indexed citations
9.
Ghoch, Joelle Abou, et al.. (2015). 10q26.1 Microdeletion: Redefining the critical regions for microcephaly and genital anomalies. American Journal of Medical Genetics Part A. 167(11). 2707–2713. 16 indexed citations
10.
Fawaz, Ali. (2014). Slope Stability Analysis Using Numerical Modelling. American Journal of Civil Engineering. 2(3). 60–60. 31 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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