Athar Khalil

953 total citations
37 papers, 542 citations indexed

About

Athar Khalil is a scholar working on Molecular Biology, Pulmonary and Respiratory Medicine and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Athar Khalil has authored 37 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 5 papers in Pulmonary and Respiratory Medicine and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Athar Khalil's work include Congenital heart defects research (6 papers), RNA modifications and cancer (5 papers) and Pregnancy and preeclampsia studies (3 papers). Athar Khalil is often cited by papers focused on Congenital heart defects research (6 papers), RNA modifications and cancer (5 papers) and Pregnancy and preeclampsia studies (3 papers). Athar Khalil collaborates with scholars based in Lebanon, United States and United Kingdom. Athar Khalil's co-authors include Georges Nemer, Nehmé El-Hachem, Firas Kobeissy, Benjamin Haibe‐Kains, Mahmoud Hassoun, Rita Feghali, Nerea Maíz, K. H. Nicolaides, Mazen Kurban and F. D’Antonio and has published in prestigious journals such as PLoS ONE, Cancer Research and Scientific Reports.

In The Last Decade

Athar Khalil

37 papers receiving 531 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Athar Khalil Lebanon 13 177 133 77 66 55 37 542
Qingqing Cai China 18 174 1.0× 36 0.3× 36 0.5× 32 0.5× 28 0.5× 53 696
Mona Høysæter Fenstad Norway 11 111 0.6× 241 1.8× 320 4.2× 53 0.8× 28 0.5× 21 661
Alfons C. Wouterse Netherlands 12 267 1.5× 176 1.3× 38 0.5× 42 0.6× 24 0.4× 30 659
Suhua Chen China 15 168 0.9× 207 1.6× 280 3.6× 36 0.5× 20 0.4× 53 694
Marco Brughera Italy 12 113 0.6× 61 0.5× 25 0.3× 13 0.2× 23 0.4× 21 390
Teklie Mengie Ayele Ethiopia 10 112 0.6× 26 0.2× 31 0.4× 51 0.8× 20 0.4× 24 440
Nataša Karas Kuželički Slovenia 14 156 0.9× 150 1.1× 9 0.1× 19 0.3× 53 1.0× 42 489
Nathan A. Brooks United States 16 159 0.9× 38 0.3× 45 0.6× 69 1.0× 25 0.5× 41 775
Feng‐Shu Hsieh Taiwan 12 210 1.2× 90 0.7× 45 0.6× 27 0.4× 10 0.2× 19 494
Yuji Morikawa Japan 11 256 1.4× 85 0.6× 17 0.2× 45 0.7× 17 0.3× 23 499

Countries citing papers authored by Athar Khalil

Since Specialization
Citations

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

Fields of papers citing papers by Athar Khalil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Athar Khalil

This figure shows the co-authorship network connecting the top 25 collaborators of Athar Khalil. A scholar is included among the top collaborators of Athar Khalil 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 Athar Khalil. Athar Khalil 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.
Wang, Yuxiang, et al.. (2023). Unveiling immune checkpoint regulation: exploring the power of in vivo CRISPR screenings in cancer immunotherapy. Frontiers in Genetics. 14. 1304425–1304425. 3 indexed citations
2.
Wang, Zhenghe, et al.. (2023). Exploring the molecular landscape of NNK-induced transformation: A comprehensive genome-wide CRISPR/Cas9 screening. Genes & Diseases. 11(4). 101131–101131. 1 indexed citations
3.
Nemer, Georges, et al.. (2022). Novel genes linked to Class II Division 1 malocclusion with mandibular micrognathism. American Journal of Orthodontics and Dentofacial Orthopedics. 163(5). 667–676.e3. 1 indexed citations
4.
Dawy, Zaher, et al.. (2021). Mutational signatures in GATA3 transcription factor and its DNA binding domain that stimulate breast cancer and HDR syndrome. Scientific Reports. 11(1). 22762–22762. 2 indexed citations
5.
Khalil, Athar, et al.. (2021). The Digenic Causality in Familial Hypercholesterolemia: Revising the Genotype–Phenotype Correlations of the Disease. Frontiers in Genetics. 11. 572045–572045. 13 indexed citations
6.
Khalil, Athar, et al.. (2021). Congenital Heart Disease in Syrian Refugee Children: The Experience at a Tertiary Care Center in a Developing Country. Pediatric Cardiology. 42(5). 1010–1017. 5 indexed citations
7.
Khalil, Athar, et al.. (2021). Questioning the sex-specific differences in the association of smoking on the survival rate of hospitalized COVID-19 patients. PLoS ONE. 16(8). e0255692–e0255692. 8 indexed citations
8.
Nemer, Georges, Nehmé El-Hachem, Tara Bardawil, et al.. (2020). A novel TRAF3IP2 variant causing familial scarring alopecia with mixed features of discoid lupus erythematosus and folliculitis decalvans. Clinical Genetics. 98(2). 116–125. 11 indexed citations
9.
Nour, Afif M. Abdel, Georges Nemer, & Athar Khalil. (2020). The MIQE Guidelines' tenth anniversary: The good and bad students. Gene Reports. 19. 100630–100630. 3 indexed citations
10.
Khalil, Athar, et al.. (2020). Post-lingual non-syndromic hearing loss phenotype: a polygenic case with 2 biallelic mutations in MYO15A and MITF. BMC Medical Genetics. 21(1). 1–1. 4 indexed citations
11.
Khalil, Athar, Rita Feghali, & Mahmoud Hassoun. (2020). The Lebanese COVID-19 Cohort; A Challenge for the ABO Blood Group System. Frontiers in Medicine. 7. 585341–585341. 25 indexed citations
12.
Khalil, Athar, et al.. (2020). Thalidomide-Revisited: Are COVID-19 Patients Going to Be the Latest Victims of Yet Another Theoretical Drug-Repurposing?. Frontiers in Immunology. 11. 1248–1248. 35 indexed citations
13.
Refaat, Marwan M., Athar Khalil, Fadi Bitar, et al.. (2019). Non-familial cardiomyopathies in Lebanon: exome sequencing results for five idiopathic cases. BMC Medical Genomics. 12(1). 33–33. 7 indexed citations
14.
Khalil, Athar, Fouad Boulos, Avrum Spira, et al.. (2018). Transcriptomic Alterations in Lung Adenocarcinoma Unveil New Mechanisms Targeted by the TBX2 Subfamily of Tumor Suppressor Genes. Frontiers in Oncology. 8. 482–482. 11 indexed citations
15.
Kurban, Mazen, Christiane Al‐Haddad, Akl C. Fahed, et al.. (2018). Degenerated hair follicle cells and partial loss of sebaceous and eccrine glands in a familial case of axenfeld-rieger syndrome: An emerging role for the FOXC1/NFATC1 genetic axis. Journal of Dermatological Science. 92(3). 237–244. 4 indexed citations
16.
Khalil, Athar, Christiane Al‐Haddad, Kamel Shibbani, et al.. (2017). A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations. Frontiers in Cardiovascular Medicine. 4. 58–58. 12 indexed citations
17.
Khalil, Athar, et al.. (2017). A HAND to TBX5 Explains the Link Between Thalidomide and Cardiac Diseases. Scientific Reports. 7(1). 1416–1416. 28 indexed citations
18.
Khalil, Athar, Smruthy Sivakumar, F Anthony San Lucas, et al.. (2017). TBX2subfamily suppression in lung cancer pathogenesis: a high-potential marker for early detection. Oncotarget. 8(40). 68230–68241. 16 indexed citations
19.
Deraz, Sahar F., et al.. (2011). Estimating the genetic purity in cytoplasmic male sterile (CMS) lines of Egyptian rice.. Australian Journal of Crop Science. 5(3). 251–261. 1 indexed citations
20.
Khalil, Athar, et al.. (1998). Bernard-Soulier Syndrome in pregnancy: case report and review of the literature. Clinical & Laboratory Haematology. 20(2). 125–128. 20 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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