Nasim Vasli

1.5k total citations
16 papers, 466 citations indexed

About

Nasim Vasli is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Nasim Vasli has authored 16 papers receiving a total of 466 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Genetics and 5 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Nasim Vasli's work include Muscle Physiology and Disorders (6 papers), Genomics and Rare Diseases (5 papers) and Cardiomyopathy and Myosin Studies (5 papers). Nasim Vasli is often cited by papers focused on Muscle Physiology and Disorders (6 papers), Genomics and Rare Diseases (5 papers) and Cardiomyopathy and Myosin Studies (5 papers). Nasim Vasli collaborates with scholars based in France, United States and Canada. Nasim Vasli's co-authors include Jocelyn Laporte, Johann Böhm, Jean Muller, Cécile Pizot, Perry B. Shieh, Lindsay C. Swanson, Susan T. Iannaccone, Kyriacos Markianos, Alan H. Beggs and Carlos Hidalgo and has published in prestigious journals such as PLoS ONE, Neurology and PLoS Genetics.

In The Last Decade

Nasim Vasli

15 papers receiving 463 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nasim Vasli France	10	353	203	125	109	87	16	466
Leigh B. Waddell Australia	14	536 1.5×	317 1.6×	90 0.7×	217 2.0×	89 1.0×	20	648
Elizabeth T. DeChene United States	10	405 1.1×	283 1.4×	170 1.4×	118 1.1×	76 0.9×	14	575
Jaya Punetha United States	11	319 0.9×	94 0.5×	139 1.1×	85 0.8×	46 0.5×	15	437
C. Bönnemann United States	8	256 0.7×	123 0.6×	95 0.8×	115 1.1×	55 0.6×	17	346
Christoffer Jonsrud Norway	10	246 0.7×	83 0.4×	94 0.8×	55 0.5×	48 0.6×	19	409
Nathalie Deburgrave France	13	461 1.3×	109 0.5×	91 0.7×	76 0.7×	91 1.0×	26	567
Gina O’Grady New Zealand	10	282 0.8×	106 0.5×	137 1.1×	125 1.1×	26 0.3×	22	480
Lidia González‐Quereda Spain	13	476 1.3×	156 0.8×	59 0.5×	109 1.0×	58 0.7×	35	540
Roula Ghaoui Australia	10	300 0.8×	96 0.5×	115 0.9×	121 1.1×	39 0.4×	22	486
Anni Evilä Finland	12	525 1.5×	322 1.6×	57 0.5×	186 1.7×	75 0.9×	20	644

Countries citing papers authored by Nasim Vasli

Since Specialization

Citations

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

Fields of papers citing papers by Nasim Vasli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nasim Vasli

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

All Works

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16 of 16 papers shown

Sheikh, Taimoor I., Ricardo Harripaul, Nasim Vasli, et al.. (2021). Heterozygous De Novo Truncating Mutation of Nucleolin in an ASD Individual Disrupts Its Nucleolar Localization. Genes. 13(1). 51–51. 2 indexed citations

Daoud, Hussein, Mahdi Ghani, Nasim Vasli, et al.. (2019). Genetic Diagnostic Testing for Inherited Cardiomyopathies. Journal of Molecular Diagnostics. 21(3). 437–448. 3 indexed citations

Harripaul, Ricardo, Nasim Vasli, Saqib Mahmood, et al.. (2019). WHOLE EXOME TRIO SEQUENCING IDENTIFIES NOVEL VARIANTS FOR AUTISM SPECTRUM DISORDER. European Neuropsychopharmacology. 29. S829–S830.

Ghani, Mahdi, Hussein Daoud, Nasim Vasli, et al.. (2018). Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory. Journal of Medical Genetics. 56(6). 408–412. 2 indexed citations

Vasli, Nasim, Kirti Mittal, Anna Mikhailov, et al.. (2015). Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability. Psychiatric Genetics. 26(2). 66–73. 17 indexed citations

Geoffroy, Véronique, Cécile Pizot, Claire Redin, et al.. (2015). VaRank: a simple and powerful tool for ranking genetic variants. PeerJ. 3. e796–e796. 47 indexed citations

Mittal, Kirti, Taimoor I. Sheikh, Nasim Vasli, et al.. (2014). Identification of a homozygous splice site mutation in the dynein axonemal light chain 4 gene on 22q13.1 in a large consanguineous family from Pakistan with congenital mirror movement disorder. Human Genetics. 133(11). 1419–1429. 18 indexed citations

Mir, Asif, Kirti Mittal, Nasim Vasli, et al.. (2014). Truncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani family. Human Genetics. 133(8). 975–984. 17 indexed citations

Böhm, Johann, Nasim Vasli, Edoardo Malfatti, et al.. (2013). An Integrated Diagnosis Strategy for Congenital Myopathies. PLoS ONE. 8(6). e67527–e67527. 43 indexed citations

10.

Vasli, Nasim, Marie Maurer, Belinda S. Cowling, et al.. (2013). Correction: Altered Splicing of the BIN1 Muscle-Specific Exon in Humans and Dogs with Highly Progressive Centronuclear Myopathy. PLoS Genetics. 9(6). 5 indexed citations

11.

Böhm, Johann, Nasim Vasli, Marie Maurer, et al.. (2013). Altered Splicing of the BIN1 Muscle-Specific Exon in Humans and Dogs with Highly Progressive Centronuclear Myopathy. PLoS Genetics. 9(6). e1003430–e1003430. 51 indexed citations

12.

Ceyhan‐Birsoy, Ozge, Pankaj B. Agrawal, Carlos Hidalgo, et al.. (2013). Recessive truncating titin gene, TTN , mutations presenting as centronuclear myopathy. Neurology. 81(14). 1205–1214. 147 indexed citations

13.

Vasli, Nasim & Jocelyn Laporte. (2012). Impacts of massively parallel sequencing for genetic diagnosis of neuromuscular disorders. Acta Neuropathologica. 125(2). 173–185. 29 indexed citations

14.

Vasli, Nasim, Johann Böhm, Stéphanie Le Gras, et al.. (2012). Next generation sequencing for molecular diagnosis of neuromuscular diseases. Acta Neuropathologica. 124(2). 273–283. 57 indexed citations

15.

Vasli, Nasim, Vincent Laugel, Johann Böhm, et al.. (2012). Myotubular myopathy caused by multiple abnormal splicing variants in the MTM1 RNA in a patient with a mild phenotype. European Journal of Human Genetics. 20(6). 701–704. 2 indexed citations

16.

Tosch, Valérie, Nasim Vasli, Christine Kretz, et al.. (2010). Novel molecular diagnostic approaches for X-linked centronuclear (myotubular) myopathy reveal intronic mutations. Neuromuscular Disorders. 20(6). 375–381. 26 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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