S. Sharif

653 total citations
7 papers, 374 citations indexed

About

S. Sharif is a scholar working on Neurology, Epidemiology and Genetics. According to data from OpenAlex, S. Sharif has authored 7 papers receiving a total of 374 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Neurology, 3 papers in Epidemiology and 3 papers in Genetics. Recurrent topics in S. Sharif's work include Meningioma and schwannoma management (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Genetic Syndromes and Imprinting (2 papers). S. Sharif is often cited by papers focused on Meningioma and schwannoma management (3 papers), Neurofibromatosis and Schwannoma Cases (3 papers) and Genetic Syndromes and Imprinting (2 papers). S. Sharif collaborates with scholars based in United Kingdom, Iran and United States. S. Sharif's co-authors include D. Gareth Evans, A Shenton, Rosalie E. Ferner, S M Huson, Elizabeth Howard, Anthony Moran, David H. Gutmann, Linda Piersall, Joel Charrow and Robert Listernick and has published in prestigious journals such as The Lancet, Neurology and Journal of Medical Genetics.

In The Last Decade

S. Sharif

7 papers receiving 355 citations

Peers

S. Sharif

NEURO

EPIDE

RHEUM

GENET

PPCH

Irene Paganini Italy

G Stark United Kingdom

Joan Tamburro United States

L. Musset France

Sahag A. Baghdassarian Lebanon

Mona S. Jahromi United States

Alfredo Pinto Canada

Robin A. Vora United States

Corinne Jeanne‐Pasquier France

Caroline Thomas France

Irene Paganini Italy

S. Sharif

144 ×0.6

NEURO

125 ×0.9

EPIDE

32 ×0.4

RHEUM

41 ×0.7

GENET

5 ×0.1

PPCH

Citations per year, relative to S. Sharif S. Sharif (= 1×) peers Irene Paganini

Countries citing papers authored by S. Sharif

Since Specialization

Citations

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

Fields of papers citing papers by S. Sharif

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S. Sharif

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

All Works

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7 of 7 papers shown

1.

Sharif, S., et al.. (2024). Evaluation of mtDNA common deletion in esophageal squamous cell carcinoma. Indian Journal of Cancer. 61(2). 363–367. 1 indexed citations

2.

Sharif, S., Meena Upadhyaya, Rosalie E. Ferner, et al.. (2011). A molecular analysis of individuals with neurofibromatosis type 1 (NF1) and optic pathway gliomas (OPGs), and an assessment of genotype–phenotype correlations. Journal of Medical Genetics. 48(4). 256–260. 63 indexed citations

3.

Sharif, S., Anthony Moran, S M Huson, et al.. (2007). Women with neurofibromatosis 1 are at a moderately increased risk of developing breast cancer and should be considered for early screening. Journal of Medical Genetics. 44(8). 481–484. 147 indexed citations

4.

Sharif, S., et al.. (2006). Non‐mosaic trisomy 22: a report of 2 cases. Prenatal Diagnosis. 26(10). 962–965. 19 indexed citations

5.

Sharif, S. & Dian Donnai. (2004). Filippi syndrome: two cases with ectodermal features, expanding the phenotype. Clinical Dysmorphology. 13(4). 221–226. 9 indexed citations

6.

Listernick, Robert, Rosalie E. Ferner, Linda Piersall, et al.. (2004). Late-onset optic pathway tumors in children with neurofibromatosis 1. Neurology. 63(10). 1944–1946. 85 indexed citations

7.

Adinolfí, Matteo, Alisha Davies, S. Sharif, Peter Soothill, & CH Rodeck. (1993). Detection of trisomy 18 and Y-derived sequences in fetal nucleated cells obtained by transcervical flushing. The Lancet. 342(8868). 403–404. 50 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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