Guy Helman

3.2k total citations
41 papers, 1.0k citations indexed

About

Guy Helman is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Guy Helman has authored 41 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Immunology. Recurrent topics in Guy Helman's work include RNA regulation and disease (22 papers), RNA modifications and cancer (9 papers) and RNA Research and Splicing (8 papers). Guy Helman is often cited by papers focused on RNA regulation and disease (22 papers), RNA modifications and cancer (9 papers) and RNA Research and Splicing (8 papers). Guy Helman collaborates with scholars based in United States, Australia and Netherlands. Guy Helman's co-authors include Adeline Vanderver, Marjo S. van der Knaap, Cas Simons, Nicole I. Wolf, Ryan J. Taft, Raphael Schiffmann, Marc C. Patterson, Johanna Schmidt, Amy Pizzino and Geneviève Bernard and has published in prestigious journals such as PLoS ONE, Brain and Neurology.

In The Last Decade

Guy Helman

39 papers receiving 985 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Guy Helman United States 19 692 156 156 120 113 41 1.0k
Sumita Danda India 16 489 0.7× 128 0.8× 78 0.5× 49 0.4× 62 0.5× 122 1.0k
Asaf Ta‐Shma Israel 16 450 0.7× 61 0.4× 126 0.8× 205 1.7× 47 0.4× 19 988
Haike Reznik‐Wolf Israel 15 554 0.8× 49 0.3× 128 0.8× 37 0.3× 40 0.4× 39 888
Ghada M. H. Abdel‐Salam Egypt 20 895 1.3× 69 0.4× 119 0.8× 47 0.4× 38 0.3× 89 1.4k
Tae Kwann Park South Korea 18 654 0.9× 45 0.3× 85 0.5× 70 0.6× 28 0.2× 80 1.4k
Pilar Camaño Spain 11 1.1k 1.5× 45 0.3× 36 0.2× 77 0.6× 192 1.7× 22 1.3k
Olga Criado‐García Spain 13 339 0.5× 43 0.3× 140 0.9× 208 1.7× 45 0.4× 18 1.1k
Reeval Segel Israel 18 649 0.9× 32 0.2× 50 0.3× 53 0.4× 174 1.5× 40 1.1k
Pagon Ra United States 6 450 0.7× 29 0.2× 86 0.6× 37 0.3× 59 0.5× 291 791
Shravani Mukherjee India 5 555 0.8× 38 0.2× 59 0.4× 35 0.3× 74 0.7× 5 806

Countries citing papers authored by Guy Helman

Since Specialization
Citations

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

Fields of papers citing papers by Guy Helman

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guy Helman

This figure shows the co-authorship network connecting the top 25 collaborators of Guy Helman. A scholar is included among the top collaborators of Guy Helman 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 Guy Helman. Guy Helman 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.
Helman, Guy, Rosalina M.L. van Spaendonk, Cas Simons, et al.. (2024). Megalencephalic leukoencephalopathy with subcortical cysts: a variant update and review of the literature. Frontiers in Genetics. 15. 1352947–1352947. 6 indexed citations
2.
Helman, Guy, Jennifer Orthmann‐Murphy, & Adeline Vanderver. (2024). Approaches to diagnosis for individuals with a suspected inherited white matter disorder. Handbook of clinical neurology. 204. 21–35.
3.
Wu, Kaiyuan, Asako Takanohashi, Sarah Woidill, et al.. (2022). Generation of human induced pluripotential stem cells from individuals with complex heterozygous, isogenic corrected, and homozygous Bloc1s1 mutations. Stem Cell Research. 64. 102905–102905. 2 indexed citations
4.
Takanohashi, Asako, Mohamad‐Gabriel Alameh, Sarah Woidill, et al.. (2022). SARS-CoV-2 mRNA-based vaccines in the Aicardi Goutières Syndrome. Molecular Genetics and Metabolism. 137(4). 320–327. 1 indexed citations
5.
Helman, Guy, Marzena Walkiewicz, Stefanie Eggers, et al.. (2021). Aberrant splicing and transcriptional activity of TPP1 result in CLN2-like disorder. European Journal of Medical Genetics. 64(8). 104259–104259. 2 indexed citations
6.
Helman, Guy, Ayelet Zerem, Sarah Woidill, et al.. (2021). Further Delineation of the Clinical and Pathologic Features of HIKESHI-Related Hypomyelinating Leukodystrophy. Pediatric Neurology. 121. 11–19. 4 indexed citations
7.
Helman, Guy, Alison G. Compton, Daniella H. Hock, et al.. (2020). Multiomic analysis elucidates Complex I deficiency caused by a deep intronic variant in NDUFB10. Human Mutation. 42(1). 19–24. 18 indexed citations
8.
Helman, Guy, Suvasini Sharma, Joanna Crawford, et al.. (2019). Leukoencephalopathy due to variants in GFPT1- associated congenital myasthenic syndrome. Neurology. 92(6). e587–e593. 9 indexed citations
9.
Adang, Laura, David B. Frank, Ahmed Gilani, et al.. (2018). Aicardi goutières syndrome is associated with pulmonary hypertension. Molecular Genetics and Metabolism. 125(4). 351–358. 32 indexed citations
10.
Helman, Guy, Sunita Venkateswaran, & Adeline Vanderver. (2018). The spectrum of adult-onset heritable white-matter disorders. Handbook of clinical neurology. 148. 669–692. 6 indexed citations
11.
Curiel, Julian, Guillermo Rodríguez Bey, Asako Takanohashi, et al.. (2017). TUBB4A mutations result in specific neuronal and oligodendrocytic defects that closely match clinically distinct phenotypes. Human Molecular Genetics. 26(22). 4506–4518. 53 indexed citations
12.
Kevelam, Sietske H., Marjan E. Steenweg, Guy Helman, et al.. (2016). Update on Leukodystrophies: A Historical Perspective and Adapted Definition. Neuropediatrics. 47(6). 349–354. 68 indexed citations
13.
Vanderver, Adeline, Morgan Prust, Davide Tonduti, et al.. (2015). Case definition and classification of leukodystrophies and leukoencephalopathies. Molecular Genetics and Metabolism. 114(4). 494–500. 157 indexed citations
14.
Pacheco‐Colón, Ileana, et al.. (2015). Reduced Functional Connectivity of Default Mode and Set-Maintenance Networks in Ornithine Transcarbamylase Deficiency. PLoS ONE. 10(6). e0129595–e0129595. 4 indexed citations
15.
Helman, Guy, Ileana Pacheco‐Colón, Kyle F. Shattuck, et al.. (2014). Investigating neurological deficits in carriers and affected patients with ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism. 113(1-2). 136–141. 20 indexed citations
16.
Haren, Keith Van, Joshua L. Bonkowsky, Geneviève Bernard, et al.. (2014). Consensus statement on preventive and symptomatic care of leukodystrophy patients. Molecular Genetics and Metabolism. 114(4). 516–526. 29 indexed citations
17.
Helman, Guy, Μαρία Παππά, & Phillip L. Pearl. (2014). Widening Phenotypic Spectrum of AADC Deficiency, a Disorder of Dopamine and Serotonin Synthesis. JIMD Reports. 17. 23–27. 27 indexed citations
18.
Willard, Μ. D., et al.. (2000). Intestinal Crypt Lesions Associated with Protein-Losing Enteropathy in the Dog. Journal of Veterinary Internal Medicine. 14(3). 298–307. 28 indexed citations
19.
Willard, Μ. D., et al.. (2000). Intestinal Crypt Lesions Associated with Protein-Losing Enteropathy in the Dog. Journal of Veterinary Internal Medicine. 14(3). 298–298. 33 indexed citations
20.
Helman, Guy, et al.. (1997). Diagnosing visceral blackleg as a cause of sudden death in cattle.. Veterinary medicine. 92(10). 914–916. 5 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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