Olga Jarinova

2.3k total citations
19 papers, 695 citations indexed

About

Olga Jarinova is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Olga Jarinova has authored 19 papers receiving a total of 695 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 8 papers in Genetics and 4 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Olga Jarinova's work include Genomics and Rare Diseases (7 papers), RNA modifications and cancer (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Olga Jarinova is often cited by papers focused on Genomics and Rare Diseases (7 papers), RNA modifications and cancer (4 papers) and Cardiomyopathy and Myosin Studies (4 papers). Olga Jarinova collaborates with scholars based in Canada, United States and United Kingdom. Olga Jarinova's co-authors include Robert Roberts, Alexandre F.R. Stewart, Christine Buerki, Bradley W. McLean, Joel S. Parker, Ruth McPherson, Thet Naing, Richard Cook, George A. Wells and Paulina Lau and has published in prestigious journals such as Development, Genome Research and Arteriosclerosis Thrombosis and Vascular Biology.

In The Last Decade

Olga Jarinova

18 papers receiving 684 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olga Jarinova Canada 10 439 300 151 59 53 19 695
Christopher R. Futtner United States 12 695 1.6× 232 0.8× 164 1.1× 30 0.5× 80 1.5× 16 983
Jennifer E. Posey United States 16 481 1.1× 394 1.3× 83 0.5× 31 0.5× 47 0.9× 61 813
Rocío Acuña‐Hidalgo United States 7 443 1.0× 340 1.1× 162 1.1× 22 0.4× 23 0.4× 8 824
Shehla Mohammed United Kingdom 12 497 1.1× 248 0.8× 92 0.6× 34 0.6× 42 0.8× 25 680
Ruen Yao China 15 385 0.9× 334 1.1× 61 0.4× 43 0.7× 44 0.8× 64 657
Jeroen Breckpot Belgium 19 562 1.3× 392 1.3× 52 0.3× 96 1.6× 75 1.4× 56 900
Katherine Holman Australia 15 529 1.2× 522 1.7× 74 0.5× 76 1.3× 58 1.1× 31 911
Rodger Palmer United Kingdom 13 397 0.9× 494 1.6× 51 0.3× 27 0.5× 76 1.4× 20 915
Bernd Auber Germany 13 194 0.4× 223 0.7× 40 0.3× 38 0.6× 53 1.0× 48 492
Elisa Tassano Italy 15 310 0.7× 272 0.9× 58 0.4× 17 0.3× 85 1.6× 54 596

Countries citing papers authored by Olga Jarinova

Since Specialization
Citations

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

Fields of papers citing papers by Olga Jarinova

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olga Jarinova

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

All Works

19 of 19 papers shown
1.
Ungar, Wendy J., Robin Z. Hayeems, Christian R. Marshall, et al.. (2023). Protocol for a Prospective, Observational Cost-effectiveness Analysis of Returning Secondary Findings of Genome Sequencing for Unexplained Suspected Genetic Conditions. Clinical Therapeutics. 45(8). 702–709. 1 indexed citations
2.
Hartley, Taila, Marije Bartels, David A. Dyment, et al.. (2022). Heterozygous Variants in the DNA-binding Domain of c-Myb May Affect Normal B/T Cell Development. HemaSphere. 6(10). e774–e774. 2 indexed citations
3.
Hayeems, Robin Z., Christian R. Marshall, Anna Szuto, et al.. (2022). Comparing genome sequencing technologies to improve rare disease diagnostics: a protocol for the evaluation of a pilot project, Genome-wide Sequencing Ontario. CMAJ Open. 10(2). E460–E465. 9 indexed citations
4.
Alkhunaizi, Ebba, Nicole Martin, Angie C. Jelin, et al.. (2022). Fetal akinesia deformation sequence syndrome associated with recessive TTN variants. American Journal of Medical Genetics Part A. 191(3). 760–769. 3 indexed citations
5.
Daoud, Hussein, Mahdi Ghani, Nasim Vasli, et al.. (2019). Genetic Diagnostic Testing for Inherited Cardiomyopathies. Journal of Molecular Diagnostics. 21(3). 437–448. 3 indexed citations
6.
Dyment, David A., Asuri N. Prasad, Kym M. Boycott, et al.. (2019). Implementation of Epilepsy Multigene Panel Testing in Ontario, Canada. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 47(1). 61–68. 5 indexed citations
7.
Pranckevičienė, Erinija, et al.. (2019). Validation of bcbio-nextgen Pipeline Based on NextSeq500 Exome Sequencing. Vytautas Magnus University. 1–6.
8.
Huang, Lijia, Nancy Carson, Jean McGowan‐Jordan, et al.. (2019). ALU transposition induces familial hypertrophic cardiomyopathy. Molecular Genetics & Genomic Medicine. 8(1). e951–e951. 1 indexed citations
9.
Ghani, Mahdi, Hussein Daoud, Nasim Vasli, et al.. (2018). Leveraging the power of new molecular technologies in the clinical setting requires unprecedented awareness of limitations and drawbacks: experience of one diagnostic laboratory. Journal of Medical Genetics. 56(6). 408–412. 2 indexed citations
10.
Daoud, Hussein, Mahdi Ghani, Gabrielle Mettler, et al.. (2017). Reinterpretation of sequence variants: one diagnostic laboratory’s experience, and the need for standard guidelines. Genetics in Medicine. 20(3). 365–368. 32 indexed citations
11.
Daoud, Hussein, Rui Li, Eric Bareke, et al.. (2016). Next-generation sequencing for diagnosis of rare diseases in the neonatal intensive care unit. Canadian Medical Association Journal. 188(11). E254–E260. 68 indexed citations
12.
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
13.
Daoud, Hussein, Dong Zhang, Fiona McMurray, et al.. (2015). Identification of a pathogenic FTO mutation by next-generation sequencing in a newborn with growth retardation and developmental delay. Journal of Medical Genetics. 53(3). 200–207. 50 indexed citations
14.
Smith, Amanda, Kym M. Boycott, & Olga Jarinova. (2013). Lake Louise Mutation Detection Meeting 2013: Clinical Translation of Next-Generation Sequencing Requires Optimization of Workflows and Interpretation of Variants. Human Mutation. 35(2). 265–269. 9 indexed citations
15.
Jarinova, Olga & Marc Ekker. (2012). Regulatory variations in the era of next-generation sequencing: Implications for clinical molecular diagnostics. Human Mutation. 33(7). 1021–1030. 11 indexed citations
16.
Armour, Christine M., Dennis E. Bulman, Olga Jarinova, et al.. (2011). 17p13.3 microduplications are associated with split-hand/foot malformation and long-bone deficiency (SHFLD). European Journal of Human Genetics. 19(11). 1144–1151. 28 indexed citations
17.
Jarinova, Olga, Alexandre F.R. Stewart, Robert Roberts, et al.. (2009). Functional Analysis of the Chromosome 9p21.3 Coronary Artery Disease Risk Locus. Arteriosclerosis Thrombosis and Vascular Biology. 29(10). 1671–1677. 294 indexed citations
18.
Jarinova, Olga, Gary Hatch, Luc Poitras, et al.. (2008). Functional resolution of duplicatedhoxb5genes in teleosts. Development. 135(21). 3543–3553. 20 indexed citations
19.
Ghanem, Noël, Olga Jarinova, Angel Amores, et al.. (2003). Regulatory Roles of Conserved Intergenic Domains in Vertebrate Dlx Bigene Clusters. Genome Research. 13(4). 533–543. 145 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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