Dania S. Khalil

490 total citations
11 papers, 322 citations indexed

About

Dania S. Khalil is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Dania S. Khalil has authored 11 papers receiving a total of 322 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Pathology and Forensic Medicine and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Dania S. Khalil's work include Ophthalmology and Eye Disorders (6 papers), Hedgehog Signaling Pathway Studies (3 papers) and Mitochondrial Function and Pathology (2 papers). Dania S. Khalil is often cited by papers focused on Ophthalmology and Eye Disorders (6 papers), Hedgehog Signaling Pathway Studies (3 papers) and Mitochondrial Function and Pathology (2 papers). Dania S. Khalil collaborates with scholars based in Saudi Arabia, United States and Oman. Dania S. Khalil's co-authors include Nada Al Tassan, Jameela Shinwari, Prashant Bavi, José Morales, Ali A. Al‐Rajhi, Fowzan S. Alkuraya, Brian F. Meyer, Saeed Bohlega, Arif O. Khan and Thamer Alkhairallah and has published in prestigious journals such as PLoS ONE, Ophthalmology and The American Journal of Human Genetics.

In The Last Decade

Dania S. Khalil

11 papers receiving 316 citations

Peers

Dania S. Khalil

MB

GENET

CR

PFM

NEURO

Teresa Neuhann Germany

Anne Destrèe Belgium

Pavlína Plevová Czechia

Siddharth R. Vora United States

Vera Uliana Italy

T. Schweitzer Germany

Allan H. Friedman United States

Leslie Boghosian-Sell United States

Greg B. Peters Australia

José Antonio Aragon-Martin United Kingdom

Teresa Neuhann Germany

Dania S. Khalil

215 ×1.5

MB

189 ×1.4

GENET

35 ×0.6

CR

32 ×0.7

PFM

22 ×0.5

NEURO

Citations per year, relative to Dania S. Khalil Dania S. Khalil (= 1×) peers Teresa Neuhann

Countries citing papers authored by Dania S. Khalil

Since Specialization

Citations

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

Fields of papers citing papers by Dania S. Khalil

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dania S. Khalil

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

All Works

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11 of 11 papers shown

1.

Bohlega, Saeed, Bashayer Al‐Mubarak, Mohamed Abouelhoda, et al.. (2016). Clinical heterogeneity of PLA2G6-related Parkinsonism: analysis of two Saudi families. BMC Research Notes. 9(1). 295–295. 17 indexed citations

2.

Al‐Mubarak, Bashayer, Saeed Bohlega, Thamer Alkhairallah, et al.. (2015). Parkinson’s Disease in Saudi Patients: A Genetic Study. PLoS ONE. 10(8). e0135950–e0135950. 22 indexed citations

3.

Bohlega, Saeed, et al.. (2011). Clinical and Molecular Characterization of Ataxia with Oculomotor Apraxia Patients In Saudi Arabia. BMC Medical Genetics. 12(1). 27–27. 12 indexed citations

4.

Khan, Arif O., Jameela Shinwari, Dania S. Khalil, et al.. (2011). The Optic Nerve Head in Congenital Fibrosis of the Extraocular Muscles. Ophthalmic Genetics. 32(3). 175–180. 5 indexed citations

5.

Tassan, Nada Al, Dania S. Khalil, Jameela Shinwari, et al.. (2011). A missense mutation in PIK3R5 gene in a family with ataxia and oculomotor apraxia. Human Mutation. 33(2). 351–354. 40 indexed citations

6.

Khan, Arif O., et al.. (2011). Potential linkage of different phenotypic forms of childhood strabismus to a recessive susceptibility locus (16p13.12-p12.3).. PubMed. 17. 971–6. 14 indexed citations

7.

Khan, Arif O., et al.. (2011). Infantile esotropia could be oligogenic and allelic with Duane retraction syndrome.. PubMed. 17. 1997–2002. 7 indexed citations

8.

Khan, Arif O., Jameela Shinwari, Dania S. Khalil, et al.. (2011). Lack of KIF21A mutations in congenital fibrosis of the extraocular muscles type I patients from consanguineous Saudi Arabian families.. PubMed. 17. 218–24. 9 indexed citations

9.

Morales, José, Dania S. Khalil, Jameela Shinwari, et al.. (2009). Homozygous Mutations in ADAMTS10 and ADAMTS17 Cause Lenticular Myopia, Ectopia Lentis, Glaucoma, Spherophakia, and Short Stature. The American Journal of Human Genetics. 85(5). 558–568. 177 indexed citations

10.

Khan, Arif O., et al.. (2009). Germline Mosaicism for KIF21A Mutation (p.R954L) Mimicking Recessive Inheritance for Congenital Fibrosis of the Extraocular Muscles. Ophthalmology. 117(1). 154–158. 13 indexed citations

11.

Khan, Arif O., Dania S. Khalil, & Nada Al Tassan. (2008). Congential Fibrosis of the Extraocular Muscles Type I (CFEOM1) on the Arabian Peninsula. Ophthalmic Genetics. 29(1). 25–28. 6 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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