Eric Bareke

2.3k total citations
42 papers, 639 citations indexed

About

Eric Bareke is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Eric Bareke has authored 42 papers receiving a total of 639 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 9 papers in Genetics and 5 papers in Pathology and Forensic Medicine. Recurrent topics in Eric Bareke's work include Epigenetics and DNA Methylation (7 papers), RNA modifications and cancer (7 papers) and Gene expression and cancer classification (6 papers). Eric Bareke is often cited by papers focused on Epigenetics and DNA Methylation (7 papers), RNA modifications and cancer (7 papers) and Gene expression and cancer classification (6 papers). Eric Bareke collaborates with scholars based in Canada, United States and Belgium. Eric Bareke's co-authors include Jacek Majewski, Martine Tétreault, Kym M. Boycott, Najmeh Alirezaie, Cynthia Horth, Eric Depiereux, Benjamin A. Garcia, Javad Nadaf, Dennis E. Bulman and Bertrand De Meulder and has published in prestigious journals such as Journal of Clinical Oncology, PLoS ONE and Brain.

In The Last Decade

Eric Bareke

39 papers receiving 631 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eric Bareke Canada 14 403 167 129 61 57 42 639
Dorota Piekutowska‐Abramczuk Poland 17 773 1.9× 181 1.1× 86 0.7× 34 0.6× 67 1.2× 59 1.0k
Xuyun Hu China 18 484 1.2× 327 2.0× 72 0.6× 35 0.6× 47 0.8× 54 801
Guoqing Tong China 10 766 1.9× 118 0.7× 98 0.8× 25 0.4× 66 1.2× 30 939
Kihyun Park South Korea 5 809 2.0× 110 0.7× 108 0.8× 44 0.7× 60 1.1× 7 943
Jongcheol Jeon South Korea 7 936 2.3× 114 0.7× 104 0.8× 37 0.6× 64 1.1× 10 1.1k
Je Yeong Ko South Korea 15 544 1.3× 171 1.0× 250 1.9× 39 0.6× 107 1.9× 38 749
Anthony O. Fedele Australia 10 282 0.7× 71 0.4× 197 1.5× 29 0.5× 29 0.5× 17 692
Jayanth Krishnan United States 3 541 1.3× 71 0.4× 135 1.0× 57 0.9× 79 1.4× 5 736
Archana Dhasarathy United States 18 799 2.0× 137 0.8× 142 1.1× 59 1.0× 229 4.0× 31 1.0k
Jenny Lord United Kingdom 16 410 1.0× 409 2.4× 67 0.5× 42 0.7× 30 0.5× 33 813

Countries citing papers authored by Eric Bareke

Since Specialization
Citations

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

Fields of papers citing papers by Eric Bareke

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eric Bareke

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Bareke. A scholar is included among the top collaborators of Eric Bareke 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 Eric Bareke. Eric Bareke 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.
Gao, Zheng, Eric Bareke, Ebtesam Abdalla, et al.. (2025). Two Novel Protein‐Truncating Variants in NLRP2 and Their Functional Impacts on the Subcortical Maternal Complex. Clinical Genetics. 108(2). 179–183.
2.
Cheung, Anthony, Erminia Di Pietro, Eric Bareke, et al.. (2025). Using multiple modalities to confirm diagnosis in patients with suspected peroxisome biogenesis disorders. Molecular Genetics and Metabolism. 145(1). 109080–109080.
3.
Bareke, Eric, Sanaa Choufani, Sujatha Jagadeesh, et al.. (2024). A homozygous stop codon in HORMAD2 in a patient with recurrent digynic triploid miscarriage. Molecular Genetics & Genomic Medicine. 12(2). e2402–e2402. 1 indexed citations
4.
Horth, Cynthia, Bo Hu, Eric Bareke, et al.. (2024). Systematic perturbations of SETD2, NSD1, NSD2, NSD3, and ASH1L reveal their distinct contributions to H3K36 methylation. Genome biology. 25(1). 263–263. 6 indexed citations
5.
Bareke, Eric, et al.. (2023). Sf3b4 regulates chromatin remodeler splicing and Hox expression. Differentiation. 131. 59–73. 6 indexed citations
6.
Chen, Haifeng, Bo Hu, Cynthia Horth, et al.. (2022). H3K36 dimethylation shapes the epigenetic interaction landscape by directing repressive chromatin modifications in embryonic stem cells. Genome Research. 32(5). 825–837. 28 indexed citations
7.
Xiao, Shangxi, Nicolás Gómez, Elizabeth M.H. Tank, et al.. (2021). TDP-43 stabilizes G3BP1 mRNA: relevance to amyotrophic lateral sclerosis/frontotemporal dementia. Brain. 144(11). 3461–3476. 38 indexed citations
8.
Gayden, Tenzin, Eric Bareke, Jean Nunes dos Santos, et al.. (2020). Whole‐exome sequencing reveals novel vacuolar ATPase genes’ variants and variants in genes involved in lysosomal biology and autophagosomal formation in oral granular cell tumors. Journal of Oral Pathology and Medicine. 50(4). 410–417. 7 indexed citations
9.
Nicolau, Stefan, Karine Choquet, Eric Bareke, et al.. (2020). A Molecular Diagnosis of LGMDR1 Established by RNA Sequencing. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 48(2). 293–296. 2 indexed citations
10.
Harutyunyan, Ashot S., Haifeng Chen, Tianyuan Lu, et al.. (2020). H3K27M in Gliomas Causes a One-Step Decrease in H3K27 Methylation and Reduced Spreading within the Constraints of H3K36 Methylation. Cell Reports. 33(7). 108390–108390. 47 indexed citations
11.
Cavallone, Luca, Adriana Aguilar‐Mahecha, Josiane Lafleur, et al.. (2020). Prognostic and predictive value of circulating tumor DNA during neoadjuvant chemotherapy for triple negative breast cancer. Scientific Reports. 10(1). 14704–14704. 65 indexed citations
12.
Bourque, Danielle K., M. Cloutier, Kristin D. Kernohan, et al.. (2019). Neu–Laxova syndrome presenting prenatally with increased nuchal translucency and cystic hygroma: The utility of exome sequencing in deciphering the diagnosis. American Journal of Medical Genetics Part A. 179(5). 813–816. 12 indexed citations
13.
Hartley, Taila, Eric Bareke, Kym M. Boycott, et al.. (2017). Autosomal dominant cutis laxa with progeroid features due to a novel, de novo mutation in ALDH18A1. Journal of Human Genetics. 62(6). 661–663. 11 indexed citations
14.
Richer, Julie, Hussein Daoud, Pavel Geier, et al.. (2015). Resolution of refractory hypotension and anuria in a premature newborn with loss‐of‐function of ACE. American Journal of Medical Genetics Part A. 167(7). 1654–1658. 12 indexed citations
15.
Mendoza‐Londono, Roberto, Lucie Dupuis, Pekka Kannus, et al.. (2015). MG-109 Revisiting a clinical diagnosis 15 years later with the aid of whole exome sequencing: Osteopetrosis versus harderophorphyria. Clinical Genetics. A4.1–A4. 1 indexed citations
16.
Smith, Amanda, Dennis E. Bulman, Eric Bareke, et al.. (2014). Meconium ileus in a Lebanese family secondary to mutations in the GUCY2C gene. European Journal of Human Genetics. 23(7). 990–992. 25 indexed citations
17.
Bareke, Eric, Virginie Saillour, Jean-François Spinella, et al.. (2013). Joint genotype inference with germline and somatic mutations. BMC Bioinformatics. 14(S5). S3–S3. 4 indexed citations
18.
Helaers, Raphaël, Eric Bareke, Bertrand De Meulder, et al.. (2011). gViz, a novel tool for the visualization of co-expression networks. BMC Research Notes. 4(1). 452–452. 8 indexed citations
19.
Bareke, Eric, Michael St.Pierre, Anthoula Gaigneaux, et al.. (2010). PathEx: a novel multi factors based datasets selector web tool. BMC Bioinformatics. 11(1). 528–528. 5 indexed citations
20.
Meulder, Bertrand De, Anthoula Gaigneaux, Eric Bareke, et al.. (2010). Functional Analysis: Evaluation of Response Intensities - Tailoring ANOVA for Lists of Expression Subsets. BMC Bioinformatics. 11(1). 510–510. 7 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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