Salma M. Wakil

3.1k total citations
67 papers, 1.2k citations indexed

About

Salma M. Wakil is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Salma M. Wakil has authored 67 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Molecular Biology, 22 papers in Genetics and 14 papers in Cell Biology. Recurrent topics in Salma M. Wakil's work include Congenital heart defects research (7 papers), Genetic Associations and Epidemiology (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Salma M. Wakil is often cited by papers focused on Congenital heart defects research (7 papers), Genetic Associations and Epidemiology (7 papers) and Genomic variations and chromosomal abnormalities (7 papers). Salma M. Wakil collaborates with scholars based in Saudi Arabia, Austria and United States. Salma M. Wakil's co-authors include Brian F. Meyer, Seyed E. Hasnain, Shiv Kumar Sarin, Syed Naqui Kazim, Sheikh Raisuddin, Saeed Bohlega, R C Guptan, Nduna Dzimiri, Luqman Ahmad Khan and Osama Alsmadi and has published in prestigious journals such as The Lancet, SHILAP Revista de lepidopterología and Molecular and Cellular Biology.

In The Last Decade

Salma M. Wakil

65 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Salma M. Wakil Saudi Arabia 19 517 293 268 220 154 67 1.2k
Ross Dobie United Kingdom 16 571 1.1× 239 0.8× 73 0.3× 212 1.0× 385 2.5× 30 1.4k
Barbara D. Wright United States 6 1.1k 2.0× 416 1.4× 130 0.5× 82 0.4× 394 2.6× 13 2.1k
Yuki Hitomi Japan 16 444 0.9× 227 0.8× 279 1.0× 154 0.7× 267 1.7× 39 1.1k
S Sekiguchi Japan 17 300 0.6× 107 0.4× 109 0.4× 74 0.3× 167 1.1× 51 935
Lijiang Ma United States 20 1.2k 2.4× 296 1.0× 312 1.2× 39 0.2× 312 2.0× 33 2.3k
Yume T. Phung United States 9 486 0.9× 112 0.4× 92 0.3× 112 0.5× 75 0.5× 12 1.1k
Lucie Poupel France 17 414 0.8× 252 0.9× 53 0.2× 86 0.4× 630 4.1× 30 1.4k
Cécile Cazeneuve France 24 975 1.9× 182 0.6× 115 0.4× 69 0.3× 349 2.3× 44 1.9k
Gary Elliott United States 16 930 1.8× 52 0.2× 233 0.9× 190 0.9× 612 4.0× 22 1.8k
Marzena Zdanowicz United States 12 990 1.9× 525 1.8× 209 0.8× 331 1.5× 42 0.3× 14 1.4k

Countries citing papers authored by Salma M. Wakil

Since Specialization
Citations

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

Fields of papers citing papers by Salma M. Wakil

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Salma M. Wakil. 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 Salma M. Wakil. The network helps show where Salma M. Wakil may publish in the future.

Co-authorship network of co-authors of Salma M. Wakil

This figure shows the co-authorship network connecting the top 25 collaborators of Salma M. Wakil. A scholar is included among the top collaborators of Salma M. Wakil 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 Salma M. Wakil. Salma M. Wakil 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.
AlBakheet, Albandary, Rawan Almass, Alya Qari, et al.. (2024). Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population. Clinical Dysmorphology. 33(2). 55–62. 1 indexed citations
2.
Al-Harbi, Najla, et al.. (2023). Multivariate piecewise linear regression model to predict radiosensitivity using the association with the genome-wide copy number variation. Frontiers in Oncology. 13. 1154222–1154222. 2 indexed citations
3.
Aldughaim, Mohammed S., Mashael R. Al‐Anazi, Marie Fe F. Bohol, et al.. (2021). Gene Expression and Transcriptome Profiling of Changes in a Cancer Cell Line Post-Exposure to Cadmium Telluride Quantum Dots: Possible Implications in Oncogenesis. Dose-Response. 19(2). 1485769832–1485769832. 7 indexed citations
4.
Afzal, Sibtain, Khushnooda Ramzan, Salma M. Wakil, et al.. (2020). A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients. BMC Medical Genetics. 21(1). 20–20. 4 indexed citations
5.
Żyła, Joanna, Sylwia Kabacik, Gráinne O’Brien, et al.. (2019). Combining CDKN1A gene expression and genome-wide SNPs in a twin cohort to gain insight into the heritability of individual radiosensitivity. Functional & Integrative Genomics. 19(4). 575–585. 10 indexed citations
6.
Meyer, Brian F., et al.. (2019). A novel KIT mutation in a family with expanded syndrome of piebaldism. JAAD Case Reports. 5(7). 627–631. 5 indexed citations
7.
Altassan, Ruqaiah, Tariq Masoodi, Ola Khalifa, et al.. (2017). Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype. American Journal of Medical Genetics Part A. 173(4). 1009–1016. 15 indexed citations
8.
Patel, Nisha, Hanan E. Shamseldin, Nadia Sakati, et al.. (2017). GZF1 Mutations Expand the Genetic Heterogeneity of Larsen Syndrome. The American Journal of Human Genetics. 100(5). 831–836. 13 indexed citations
9.
Monies, Dorota, Hindi Al‐Hindi, Mohamed Abouelhoda, et al.. (2016). A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies. Human Genomics. 10(1). 32–32. 29 indexed citations
10.
Shamseldin, Hanan E., Shams Anazi, Salma M. Wakil, et al.. (2016). Novel copy number variants and major limb reduction malformation: Report of three cases. American Journal of Medical Genetics Part A. 170(5). 1245–1250. 8 indexed citations
11.
Finsterer, Josef & Salma M. Wakil. (2016). Stroke-like episodes, peri-episodic seizures, and MELAS mutations. European Journal of Paediatric Neurology. 20(6). 824–829. 13 indexed citations
12.
Wakil, Salma M., et al.. (2016). Novel mutations in TGM1 and ABCA12 cause autosomal recessive congenital ichthyosis in five Saudi families. International Journal of Dermatology. 55(6). 673–679. 7 indexed citations
13.
Shaheen, Ranad, Mohammed Hussien Alghamdi, Salma M. Wakil, et al.. (2015). Positional mapping of PRKD1 , NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosus. Journal of Medical Genetics. 52(5). 322–329. 27 indexed citations
14.
Wakil, Salma M., Shamsa Anazi, Anas M. Alazami, et al.. (2014). The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population. Genetics in Medicine. 17(9). 719–725. 11 indexed citations
15.
Wakil, Salma M., Asma I. Tahir, Batoul Baz, et al.. (2014). A study of the role of GATA2 gene polymorphism in coronary artery disease risk traits. Gene. 544(2). 152–158. 33 indexed citations
16.
Wakil, Salma M., Khushnooda Ramzan, Rana Alomar, et al.. (2013). Infantile-onset ascending hereditary spastic paraplegia with bulbar involvement due to the novel ALS2 mutation c.2761C > T. Gene. 536(1). 217–220. 21 indexed citations
17.
Zargar, Seema, et al.. (2013). Involvement of ATP-binding cassette, subfamily A polymorphism with susceptibility to coronary artery disease. Biomedical Reports. 1(6). 883–888. 18 indexed citations
18.
Alsmadi, Osama, Brian F. Meyer, Fowzan S. Alkuraya, et al.. (2008). Syndromic congenital sensorineural deafness, microtia and microdontia resulting from a novel homoallelic mutation in fibroblast growth factor 3 (FGF3). European Journal of Human Genetics. 17(1). 14–21. 32 indexed citations
19.
Wakil, Salma M., Syed Naqui Kazim, Luqman Ahmad Khan, et al.. (2002). Prevalence and profile of mutations associated with lamivudine therapy in Indian patients with chronic hepatitis B in the surface and polymerase genes of hepatitis B virus. Journal of Medical Virology. 68(3). 311–318. 42 indexed citations
20.
Kapoor, Dharmesh, R C Guptan, Salma M. Wakil, et al.. (2000). Beneficial effects of lamivudine in hepatitis B virus-related decompensated cirrhosis. Journal of Hepatology. 33(2). 308–312. 123 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Ross Dobie Breakdown of academic impact, for papers by Barbara D. Wright Breakdown of academic impact, for papers by Yuki Hitomi Breakdown of academic impact, for papers by S Sekiguchi Breakdown of academic impact, for papers by Lijiang Ma Breakdown of academic impact, for papers by Yume T. Phung Breakdown of academic impact, for papers by Lucie Poupel Breakdown of academic impact, for papers by Cécile Cazeneuve Breakdown of academic impact, for papers by Gary Elliott Breakdown of academic impact, for papers by Marzena Zdanowicz
Rankless by CCL
2026