Oana Caluseriu

3.6k total citations
37 papers, 876 citations indexed

About

Oana Caluseriu is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Oana Caluseriu has authored 37 papers receiving a total of 876 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 20 papers in Genetics and 10 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Oana Caluseriu's work include Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital heart defects research (6 papers). Oana Caluseriu is often cited by papers focused on Prenatal Screening and Diagnostics (9 papers), Genomic variations and chromosomal abnormalities (8 papers) and Congenital heart defects research (6 papers). Oana Caluseriu collaborates with scholars based in Canada, United States and Italy. Oana Caluseriu's co-authors include Rosanna Weksberg, Anne S. Bassett, Eva W.C. Chow, Michael Α. Gatzoulis, Gary D. Webb, Janice Husted, Donald A. Young, Consolato Sergi, David D. Eisenstat and Jillian S. Parboosingh and has published in prestigious journals such as SHILAP Revista de lepidopterología, Biological Psychiatry and Journal of the American Society of Nephrology.

In The Last Decade

Oana Caluseriu

36 papers receiving 860 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Oana Caluseriu Canada 14 583 389 208 138 116 37 876
Erawati V. Bawle United States 17 562 1.0× 442 1.1× 82 0.4× 82 0.6× 91 0.8× 38 1.1k
Elisabetta Lapi Italy 18 534 0.9× 477 1.2× 67 0.3× 61 0.4× 70 0.6× 48 957
Maria Descartes United States 16 399 0.7× 431 1.1× 72 0.3× 62 0.4× 72 0.6× 34 720
Angélica Oviedo United States 13 273 0.5× 133 0.3× 66 0.3× 108 0.8× 232 2.0× 27 923
Emmanuelle Lemyre Canada 22 550 0.9× 879 2.3× 86 0.4× 67 0.5× 129 1.1× 52 1.3k
Miranda Splitt United Kingdom 15 598 1.0× 435 1.1× 192 0.9× 104 0.8× 173 1.5× 29 1.1k
Rena E. Falk United States 19 408 0.7× 447 1.1× 84 0.4× 75 0.5× 137 1.2× 39 1.0k
Cheryl Cytrynbaum Canada 16 636 1.1× 435 1.1× 207 1.0× 149 1.1× 67 0.6× 36 991
Camelia V. Marcos-Gutierrez Netherlands 10 857 1.5× 281 0.7× 115 0.6× 61 0.4× 593 5.1× 10 1.8k
Zhishuo Ou United States 14 602 1.0× 862 2.2× 95 0.5× 44 0.3× 80 0.7× 26 1.1k

Countries citing papers authored by Oana Caluseriu

Since Specialization
Citations

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

Fields of papers citing papers by Oana Caluseriu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Oana Caluseriu

This figure shows the co-authorship network connecting the top 25 collaborators of Oana Caluseriu. A scholar is included among the top collaborators of Oana Caluseriu 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 Oana Caluseriu. Oana Caluseriu 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.
Caluseriu, Oana, et al.. (2024). P520: The Translational Genomics Hub (TGH): A new precision medicine tool at the University of Alberta. SHILAP Revista de lepidopterología. 2. 101419–101419. 1 indexed citations
2.
Mórotz, Gábor M., Neil A. Bradbury, Oana Caluseriu, et al.. (2024). A revised nomenclature for the lemur family of protein kinases. Communications Biology. 7(1). 57–57. 5 indexed citations
3.
Timberlake, Andrew T., Garrett Allington, Emre Kiziltug, et al.. (2023). De novo variants implicate chromatin modification, transcriptional regulation, and retinoic acid signaling in syndromic craniosynostosis. The American Journal of Human Genetics. 110(5). 846–862. 11 indexed citations
4.
Fraser, Sherri D., Oana Caluseriu, Claudia Vivori, et al.. (2022). Hnrnpul1 controls transcription, splicing, and modulates skeletal and limb development in vivo. G3 Genes Genomes Genetics. 12(5). 5 indexed citations
5.
Eaton, Alison, et al.. (2022). Prenatal Genetic Testing in the Era of Next Generation Sequencing: A One-Center Canadian Experience. Genes. 13(11). 2019–2019. 2 indexed citations
6.
Doucette, Lance P., et al.. (2021). Whole exome sequencing reveals putatively novel associations in retinopathies and drusen formation. European Journal of Human Genetics. 29(8). 1171–1185. 2 indexed citations
7.
McBrien, Angela, et al.. (2021). Fetal double outlet right ventricle without heterotaxy syndrome: Diagnostic spectrum, associated extracardiac pathology and clinical outcomes. Prenatal Diagnosis. 41(9). 1118–1126. 3 indexed citations
8.
Banerjee, Mayukh, Denis Arutyunov, Hanna Kolski, et al.. (2019). The novel p.Ser263Phe mutation in the human high‐affinity choline transporter 1 (CHT1/ SLC5A7 ) causes a lethal form of fetal akinesia syndrome. Human Mutation. 40(10). 1676–1683. 14 indexed citations
9.
Butcher, Darci T., Andrei L. Turinsky, Cheryl Cytrynbaum, et al.. (2019). Functional DNA methylation signatures for autism spectrum disorder genomic risk loci: 16p11.2 deletions and CHD8 variants. Clinical Epigenetics. 11(1). 103–103. 43 indexed citations
10.
Eaton, Alison, François P. Bernier, Oana Caluseriu, et al.. (2018). Is PNPT1‐related hearing loss ever non‐syndromic? Whole exome sequencing of adult siblings expands the natural history of PNPT1‐related disorders. American Journal of Medical Genetics Part A. 176(11). 2487–2493. 13 indexed citations
11.
Bramswig, Nuria C., Oana Caluseriu, H.‐J. Lüdecke, et al.. (2017). Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin–Siris syndrome-like phenotype. Human Genetics. 136(3). 297–305. 46 indexed citations
12.
Lazier, Joanna, Deborah Fruitman, Julie Lauzon, et al.. (2016). Prenatal Array Comparative Genomic Hybridization in Fetuses With Structural Cardiac Anomalies. Journal of Obstetrics and Gynaecology Canada. 38(7). 619–626. 11 indexed citations
13.
14.
Bassett, Anne S., Oana Caluseriu, Rosanna Weksberg, Donald A. Young, & Eva W.C. Chow. (2007). Catechol-O-methyl Transferase and Expression of Schizophrenia in 73 Adults with 22q11 Deletion Syndrome. Biological Psychiatry. 61(10). 1135–1140. 77 indexed citations
15.
Caluseriu, Oana, Ghazala Mirza, Jiannis Ragoussis, et al.. (2006). Schizophrenia in an adult with 6p25 deletion syndrome. American Journal of Medical Genetics Part A. 140A(11). 1208–1213. 23 indexed citations
16.
Bassett, Anne S., Eva W.C. Chow, Janice Husted, et al.. (2005). Clinical features of 78 adults with 22q11 deletion syndrome. American Journal of Medical Genetics Part A. 138A(4). 307–313. 337 indexed citations
17.
18.
Caluseriu, Oana, et al.. (2003). Clozapine-associated seizures in a 22Q deletion syndrome subtype of schizophrenia. Schizophrenia Research. 60(1). 79–79. 2 indexed citations
19.
Goldman, Michaël, Adam C. Smith, Cheryl Shuman, et al.. (2002). Renal Abnormalities in Beckwith-Wiedemann Syndrome Are Associated with 11p15.5 Uniparental Disomy. Journal of the American Society of Nephrology. 13(8). 2077–2084. 40 indexed citations
20.
Caluseriu, Oana, Emanuela Lucci‐Cordisco, Alessandra Viel, et al.. (2001). Four novelMSH2 andMLH1 frameshift mutations and occurrence of a breast cancer phenocopy in hereditary nonpolyposis colorectal cancer. Human Mutation. 17(6). 521–521. 18 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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