Liam Crapper

824 total citations
9 papers, 483 citations indexed

About

Liam Crapper is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Liam Crapper has authored 9 papers receiving a total of 483 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Cognitive Neuroscience. Recurrent topics in Liam Crapper's work include Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (3 papers) and Congenital heart defects research (2 papers). Liam Crapper is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Autism Spectrum Disorder Research (3 papers) and Congenital heart defects research (2 papers). Liam Crapper collaborates with scholars based in Canada, Brazil and United States. Liam Crapper's co-authors include Juan Pablo López, Gilles Maussion, Carl Ernst, Gustavo Turecki, Naguib Mechawar, Volodymyr Yerko, Érika Vigneault, Caroline Fasano, Jennie Yang and Benoît Labonté and has published in prestigious journals such as Nature Medicine, The American Journal of Human Genetics and Human Genetics.

In The Last Decade

Liam Crapper

9 papers receiving 474 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Liam Crapper Canada 8 312 174 134 82 66 9 483
Patricia Damschroder‐Williams United States 7 247 0.8× 158 0.9× 141 1.1× 41 0.5× 49 0.7× 7 452
John Bohnsack United States 13 238 0.8× 68 0.4× 41 0.3× 42 0.5× 30 0.5× 17 430
Michael P. Geaghan Australia 10 211 0.7× 163 0.9× 101 0.8× 21 0.3× 48 0.7× 15 378
Genni Desiato Italy 9 169 0.5× 58 0.3× 41 0.3× 47 0.6× 62 0.9× 12 449
Tessa Sipilä Finland 7 180 0.6× 124 0.7× 43 0.3× 36 0.4× 26 0.4× 8 400
Mareen Engel Germany 8 442 1.4× 211 1.2× 81 0.6× 23 0.3× 23 0.3× 10 607
Anderson A. Butler United States 8 259 0.8× 109 0.6× 85 0.6× 29 0.4× 8 0.1× 10 369
Bisrat T. Woldemichael Switzerland 7 202 0.6× 63 0.4× 77 0.6× 22 0.3× 15 0.2× 7 338
Sonia I Lombroso United States 6 331 1.1× 25 0.1× 95 0.7× 29 0.4× 59 0.9× 8 480
Erica Shen United States 10 317 1.0× 36 0.2× 197 1.5× 22 0.3× 19 0.3× 21 541

Countries citing papers authored by Liam Crapper

Since Specialization
Citations

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

Fields of papers citing papers by Liam Crapper

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Liam Crapper

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

All Works

9 of 9 papers shown
1.
Bell, Scott C., et al.. (2016). Lesch-Nyhan Syndrome: Models, Theories, and Therapies. Molecular Syndromology. 7(6). 302–311. 46 indexed citations
2.
Merner, Nancy D., Baudouin Forgeot d’Arc, Scott C. Bell, et al.. (2016). A de novo frameshift mutation in chromodomain helicase DNA‐binding domain 8 (CHD8): A case report and literature review. American Journal of Medical Genetics Part A. 170(5). 1225–1235. 26 indexed citations
3.
Bell, Scott C., Huashan Peng, Liam Crapper, et al.. (2016). A Rapid Pipeline to Model Rare Neurodevelopmental Disorders with Simultaneous CRISPR/Cas9 Gene Editing. Stem Cells Translational Medicine. 6(3). 886–896. 18 indexed citations
4.
Gigek, Carolina Oliveira, Elizabeth Chen, Vanessa Ota, et al.. (2015). A molecular model for neurodevelopmental disorders. Translational Psychiatry. 5(5). e565–e565. 28 indexed citations
5.
Maussion, Gilles, Alpha Diallo, Carolina Oliveira Gigek, et al.. (2015). Investigation of genes important in neurodevelopment disorders in adult human brain. Human Genetics. 134(10). 1037–1053. 23 indexed citations
6.
López, Juan Pablo, et al.. (2015). MicroRNA regulation of central glial cell line-derived neurotrophic factor (GDNF) signalling in depression. Translational Psychiatry. 5(2). e511–e511. 49 indexed citations
7.
Crapper, Liam & Carl Ernst. (2015). Comparative Analysis of Self-Injury in People with Psychopathology or Neurodevelopmental Disorders. Pediatric Clinics of North America. 62(3). 619–631. 5 indexed citations
8.
López, Juan Pablo, Raymond S. Lim, Cristiana Cruceanu, et al.. (2014). miR-1202 is a primate-specific and brain-enriched microRNA involved in major depression and antidepressant treatment. Nature Medicine. 20(7). 764–768. 236 indexed citations
9.
Chen, Elizabeth, Carolina Oliveira Gigek, Jill A. Rosenfeld, et al.. (2014). Molecular Convergence of Neurodevelopmental Disorders. The American Journal of Human Genetics. 95(5). 490–508. 52 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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