Taimoor I. Sheikh

729 total citations
11 papers, 135 citations indexed

About

Taimoor I. Sheikh is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Taimoor I. Sheikh has authored 11 papers receiving a total of 135 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cognitive Neuroscience. Recurrent topics in Taimoor I. Sheikh's work include Genetics and Neurodevelopmental Disorders (6 papers), RNA modifications and cancer (3 papers) and Autism Spectrum Disorder Research (3 papers). Taimoor I. Sheikh is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), RNA modifications and cancer (3 papers) and Autism Spectrum Disorder Research (3 papers). Taimoor I. Sheikh collaborates with scholars based in Canada, Pakistan and United States. Taimoor I. Sheikh's co-authors include John B. Vincent, Muhammad Ayub, Juan Ausió, Kirti Mittal, Mary Willis, Ricardo Harripaul, Alexia Martínez de Paz, Ishtiaq Qadri, Nidhi Aggarwal and James H. Eubanks and has published in prestigious journals such as Scientific Reports, Human Molecular Genetics and Human Mutation.

In The Last Decade

Taimoor I. Sheikh

11 papers receiving 134 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Taimoor I. Sheikh Canada 7 82 77 32 12 11 11 135
Nathalie Fieremans Belgium 9 162 2.0× 154 2.0× 28 0.9× 11 0.9× 14 1.3× 10 264
J Gauthier Canada 3 96 1.2× 98 1.3× 49 1.5× 38 3.2× 5 0.5× 5 187
Sarah Romero United States 5 60 0.7× 122 1.6× 42 1.3× 33 2.8× 6 0.5× 11 189
Stefanie Belet Belgium 9 153 1.9× 148 1.9× 19 0.6× 22 1.8× 15 1.4× 10 252
Denis A. Reshetov Russia 8 83 1.0× 185 2.4× 11 0.3× 19 1.6× 4 0.4× 18 237
Erin K. Roney United States 8 161 2.0× 172 2.2× 17 0.5× 21 1.8× 10 0.9× 11 279
Arjan PM de Brouwer Netherlands 7 125 1.5× 170 2.2× 17 0.5× 12 1.0× 27 2.5× 7 247
Jamie B. Littleboy Australia 5 50 0.6× 144 1.9× 37 1.2× 30 2.5× 8 0.7× 5 225
María J. Guillen Sacoto United States 10 121 1.5× 118 1.5× 14 0.4× 10 0.8× 2 0.2× 17 203
Melanie Leffler Australia 4 46 0.6× 58 0.8× 7 0.2× 12 1.0× 5 0.5× 9 161

Countries citing papers authored by Taimoor I. Sheikh

Since Specialization
Citations

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

Fields of papers citing papers by Taimoor I. Sheikh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Taimoor I. Sheikh. 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 Taimoor I. Sheikh. The network helps show where Taimoor I. Sheikh may publish in the future.

Co-authorship network of co-authors of Taimoor I. Sheikh

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

All Works

11 of 11 papers shown
1.
Sheikh, Taimoor I., et al.. (2023). Emerging molecular subtypes and therapies in acute lymphoblastic leukemia. Seminars in Diagnostic Pathology. 40(3). 202–215. 10 indexed citations
2.
Mok, Rebecca S.F., Taimoor I. Sheikh, Isabella Rodrigues Fernandes, et al.. (2022). Wide spectrum of neuronal and network phenotypes in human stem cell-derived excitatory neurons with Rett syndrome-associated MECP2 mutations. Translational Psychiatry. 12(1). 450–450. 15 indexed citations
3.
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
4.
Epp, Jonathan R., Kirti Mittal, Taimoor I. Sheikh, et al.. (2019). Ptchd1 exon3 truncating mutations recapitulate more clinically relevant autistic-like traits in mice. IBRO Reports. 6. S507–S507. 1 indexed citations
5.
Sheikh, Taimoor I., Ricardo Harripaul, Muhammad Ayub, & John B. Vincent. (2018). MeCP2 AT-Hook1 mutations in patients with intellectual disability and/or schizophrenia disrupt DNA binding and chromatin compaction in vitro. Human Mutation. 39(5). 717–728. 20 indexed citations
6.
Sheikh, Taimoor I., et al.. (2017). MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation. Human Molecular Genetics. 26(21). 4132–4141. 20 indexed citations
7.
Sheikh, Taimoor I., Juan Ausió, Josh Silver, et al.. (2016). From Function to Phenotype: Impaired DNA Binding and Clustering Correlates with Clinical Severity in Males with Missense Mutations in MECP2. Scientific Reports. 6(1). 38590–38590. 19 indexed citations
8.
Sheikh, Taimoor I., et al.. (2015). Upregulated hepatic expression of mitochondrial PEPCK triggers initial gluconeogenic reactions in the HCV-3 patients. Asian Pacific Journal of Tropical Medicine. 8(8). 618–623. 5 indexed citations
9.
10.
Sheikh, Taimoor I., Kirti Mittal, Mary Willis, & John B. Vincent. (2013). A synonymous change, p.Gly16Gly in MECP2 Exon 1, causes a cryptic splice event in a Rett syndrome patient. Orphanet Journal of Rare Diseases. 8(1). 108–108. 20 indexed citations
11.

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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2026