Gregory J. Pelka

1.3k total citations
14 papers, 1.0k citations indexed

About

Gregory J. Pelka is a scholar working on Molecular Biology, Genetics and Cognitive Neuroscience. According to data from OpenAlex, Gregory J. Pelka has authored 14 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 13 papers in Genetics and 2 papers in Cognitive Neuroscience. Recurrent topics in Gregory J. Pelka's work include Genetics and Neurodevelopmental Disorders (11 papers), RNA modifications and cancer (5 papers) and Chromatin Remodeling and Cancer (3 papers). Gregory J. Pelka is often cited by papers focused on Genetics and Neurodevelopmental Disorders (11 papers), RNA modifications and cancer (5 papers) and Chromatin Remodeling and Cancer (3 papers). Gregory J. Pelka collaborates with scholars based in Australia, United Kingdom and Russia. Gregory J. Pelka's co-authors include Patrick Tam, John Christodoulou, Catherine M. Watson, Hooshang Lahooti, Sarah Williamson, Anthony J. Hannan, Laura Gray, Tania Radziewic, Mari Kondo and Carolyn Ellaway and has published in prestigious journals such as Journal of Neuroscience, Blood and Molecular and Cellular Biology.

In The Last Decade

Gregory J. Pelka

14 papers receiving 994 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gregory J. Pelka Australia 14 783 597 347 101 82 14 1.0k
SakkuBai Naidu United States 15 643 0.8× 483 0.8× 354 1.0× 87 0.9× 92 1.1× 18 991
Amber Hogart United States 10 1.2k 1.5× 972 1.6× 627 1.8× 115 1.1× 67 0.8× 10 1.5k
Claudio Toma Spain 21 527 0.7× 359 0.6× 359 1.0× 153 1.5× 151 1.8× 41 1.0k
Holly N. Cukier United States 16 518 0.7× 525 0.9× 403 1.2× 147 1.5× 84 1.0× 26 1.0k
Reymundo Lozano United States 20 819 1.0× 552 0.9× 519 1.5× 100 1.0× 81 1.0× 44 1.1k
Tychele N. Turner United States 20 1.1k 1.4× 915 1.5× 530 1.5× 82 0.8× 65 0.8× 47 1.7k
Sakkubai Naidu United States 18 1.0k 1.3× 731 1.2× 665 1.9× 123 1.2× 88 1.1× 25 1.3k
Hayley Archer United Kingdom 14 1.0k 1.3× 558 0.9× 407 1.2× 69 0.7× 133 1.6× 17 1.1k
James Jaworski United States 17 588 0.8× 372 0.6× 546 1.6× 153 1.5× 69 0.8× 19 951
Vijayendran Chandran United States 11 542 0.7× 709 1.2× 379 1.1× 169 1.7× 26 0.3× 16 1.1k

Countries citing papers authored by Gregory J. Pelka

Since Specialization
Citations

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

Fields of papers citing papers by Gregory J. Pelka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory J. Pelka. 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 Gregory J. Pelka. The network helps show where Gregory J. Pelka may publish in the future.

Co-authorship network of co-authors of Gregory J. Pelka

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

All Works

14 of 14 papers shown
1.
Kondo, Mari, Laura Gray, Gregory J. Pelka, et al.. (2015). Affective dysfunction in a mouse model ofRett syndrome: Therapeutic effects of environmental stimulation and physical activity. Developmental Neurobiology. 76(2). 209–224. 20 indexed citations
2.
Williamson, Sarah, Carolyn Ellaway, Greg B. Peters, et al.. (2014). Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype. European Journal of Human Genetics. 23(9). 1171–1175. 13 indexed citations
3.
Gold, Wendy, Sarah Williamson, Simranpreet Kaur, et al.. (2014). Mitochondrial dysfunction in the skeletal muscle of a mouse model of Rett syndrome (RTT): Implications for the disease phenotype. Mitochondrion. 15. 10–17. 52 indexed citations
4.
Maxwell, Scott, Gregory J. Pelka, Patrick Tam, & Assam El‐Osta. (2013). Chromatin context and ncRNA highlight targets of MeCP2 in brain. RNA Biology. 10(11). 1741–1757. 40 indexed citations
5.
Funnell, Alister P. W., Ka Sin Mak, Natalie A. Twine, et al.. (2013). Generation of Mice Deficient in both KLF3/BKLF and KLF8 Reveals a Genetic Interaction and a Role for These Factors in Embryonic Globin Gene Silencing. Molecular and Cellular Biology. 33(15). 2976–2987. 39 indexed citations
6.
Williamson, Sarah, Charlotte Kilstrup‐Nielsen, Wendy Gold, et al.. (2011). A novel transcript of cyclin-dependent kinase-like 5 (CDKL5) has an alternative C-terminus and is the predominant transcript in brain. Human Genetics. 131(2). 187–200. 44 indexed citations
7.
KN, Harikrishnan, Richard Bayles, Giuseppe D. Ciccotosto, et al.. (2010). Alleviating Transcriptional Inhibition of the NorepinephrineSlc6a2Transporter Gene in Depolarized Neurons. Journal of Neuroscience. 30(4). 1494–1501. 24 indexed citations
8.
Kondo, Mari, Laura Gray, Gregory J. Pelka, et al.. (2008). Environmental enrichment ameliorates a motor coordination deficit in a mouse model of Rett syndrome –Mecp2gene dosage effects and BDNF expression. European Journal of Neuroscience. 27(12). 3342–3350. 153 indexed citations
9.
Watson, Catherine M., Paul A. Trainor, Tania Radziewic, et al.. (2008). Application of lacZ Transgenic Mice to Cell Lineage Studies. Methods in molecular biology. 461. 149–164. 20 indexed citations
10.
Pelka, Gregory J., Catherine M. Watson, Tania Radziewic, et al.. (2006). Mecp2 deficiency is associated with learning and cognitive deficits and altered gene activity in the hippocampal region of mice. Brain. 129(4). 887–898. 160 indexed citations
11.
Watson, Catherine M., Gregory J. Pelka, Mona D. Shahbazian, et al.. (2005). Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactivation. Human Molecular Genetics. 14(13). 1851–1861. 15 indexed citations
12.
Pelka, Gregory J., Catherine M. Watson, John Christodoulou, & Patrick Tam. (2005). Distinct expression profiles of Mecp2 transcripts with different lengths of 3′UTR in the brain and visceral organs during mouse development. Genomics. 85(4). 441–452. 33 indexed citations
13.
Weaving, Linda S., John Christodoulou, Sarah Williamson, et al.. (2004). Mutations of CDKL5 Cause a Severe Neurodevelopmental Disorder with Infantile Spasms and Mental Retardation. The American Journal of Human Genetics. 75(6). 1079–1093. 375 indexed citations
14.
Ho, P. Joy, Ross Brown, Gregory J. Pelka, et al.. (2001). Illegitimate switch recombinations are present in approximately half of primary myeloma tumors, but do not relate to known prognostic indicators or survival. Blood. 97(2). 490–495. 21 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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