Renius Owen

811 total citations
23 papers, 329 citations indexed

About

Renius Owen is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Renius Owen has authored 23 papers receiving a total of 329 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 11 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Renius Owen's work include Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers) and Metabolism and Genetic Disorders (6 papers). Renius Owen is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Prenatal Screening and Diagnostics (8 papers) and Metabolism and Genetic Disorders (6 papers). Renius Owen collaborates with scholars based in United States, United Kingdom and Lebanon. Renius Owen's co-authors include Terence R. Flotte, Peter W. Stacpoole, David A. Flockhart, John Dikran Balian, S.K. Willsie, John Foxworth, Trilochan Sahoo, Jia‐Chi Wang, Jacqueline S. Marinac and Jane McPheat and has published in prestigious journals such as PLoS ONE, Scientific Reports and Antioxidants and Redox Signaling.

In The Last Decade

Renius Owen

23 papers receiving 295 citations

Peers

Renius Owen

GENET

PPCH

PHARM

Kristen Wigby United States

Mara Marongiu Italy

Chayanon Peerapittayamongkol Thailand

Boris Zagradišnik Slovenia

Mathilde Lefebvre France

Miguel Angel Alcántara‐Ortigoza Mexico

Nick Giannoukakis United States

Elizabeth G. Ames United States

Allan Daly United Kingdom

Manuel Méndez Spain

Kristen Wigby United States

Renius Owen

190 ×1.4

GENET

163 ×1.3

52 ×0.6

PPCH

18 ×0.5

4 ×0.1

PHARM

Citations per year, relative to Renius Owen Renius Owen (= 1×) peers Kristen Wigby

Countries citing papers authored by Renius Owen

Since Specialization

Citations

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

Fields of papers citing papers by Renius Owen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Renius Owen

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

All Works

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20 of 20 papers shown

Герасимова, Анна, Ron M. Kagan, Yan Liu, et al.. (2022). Development and validation of a high throughput SARS-CoV-2 whole genome sequencing workflow in a clinical laboratory. Scientific Reports. 12(1). 2054–2054. 15 indexed citations

Герасимова, Анна, Marie‐Aline Charles, Hairong Li, et al.. (2021). Analytical validation and performance characteristics of a 48-gene next-generation sequencing panel for detecting potentially actionable genomic alterations in myeloid neoplasms. PLoS ONE. 16(4). e0243683–e0243683. 5 indexed citations

Sun, Weimin, Ke Zhang, Yan Liu, et al.. (2020). Development and Validation of a 34‐Gene Inherited Cancer Predisposition Panel Using Next‐Generation Sequencing. BioMed Research International. 2020(1). 3289023–3289023. 5 indexed citations

Strom, Charles M., Ben Anderson, David Tsao, et al.. (2017). Improving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS). PLoS ONE. 12(3). e0167130–e0167130. 11 indexed citations

Luskin, Marlise R., et al.. (2017). Maternal iAMP21 acute lymphoblastic leukemia detected on prenatal cell-free DNA genetic screening. Blood Advances. 1(19). 1491–1494. 5 indexed citations

Wang, Jia‐Chi, et al.. (2016). Enrichment of small pathogenic deletions at chromosome 9p24.3 and 9q34.3 involving DOCK8, KANK1, EHMT1 genes identified by using high-resolution oligonucleotide-single nucleotide polymorphism array analysis. Molecular Cytogenetics. 9(1). 82–82. 7 indexed citations

Habbal, Zuheir, et al.. (2014). First Report of a Deletion Encompassing an Entire Exon in the Homogentisate 1,2-Dioxygenase Gene Causing Alkaptonuria. PLoS ONE. 9(9). e106948–e106948. 7 indexed citations

Singh, Kathryn, et al.. (2014). Amelioration of the typical cognitive phenotype in a patient with the 5pter deletion associated with Cri‐du‐chat syndrome in addition to a partial duplication of CTNND2. American Journal of Medical Genetics Part A. 164(7). 1761–1764. 20 indexed citations

Boyar, Fatih Z, Trilochan Sahoo, Jia‐Chi Wang, et al.. (2014). Abnormalities in spontaneous abortions detected by G-banding and chromosomal microarray analysis (CMA) at a national reference laboratory. Molecular Cytogenetics. 7(1). 33–33. 50 indexed citations

10.

Hemmat, Morteza, Arturo Anguiano, Fatih Z Boyar, et al.. (2013). Genotype-phenotype analysis of recombinant chromosome 4 syndrome: an array-CGH study and literature review. Molecular Cytogenetics. 6(1). 17–17. 9 indexed citations

11.

Simon, Julie, et al.. (2013). Deletion Xq27.3q28 in female patient with global developmental delays and skewed X-inactivation. BMC Medical Genetics. 14(1). 49–49. 21 indexed citations

12.

Owen, Renius, et al.. (2012). Characterization of a complex rearrangement involving duplication and deletion of 9p in an infant with craniofacial dysmorphism and cardiac anomalies. Molecular Cytogenetics. 5(1). 31–31. 8 indexed citations

13.

Conlon, Thomas J., Glenn A. Walter, Renius Owen, et al.. (2006). Systemic Correction of a Fatty Acid Oxidation Defect by Intramuscular Injection of a Recombinant Adeno-Associated Virus Vector. Human Gene Therapy. 17(1). 71–80. 14 indexed citations

14.

Conlon, Thomas J., Glenn A. Walter, Renius Owen, et al.. (2005). Systemic Correction of a Fatty Acid Oxidation Defect by Intramuscular Injection of a Recombinant Adeno-Associated Virus Vector. Human Gene Therapy. 0(0). 880211497–880211497. 1 indexed citations

15.

Stacpoole, Peter W., Renius Owen, & Terence R. Flotte. (2003). The Pyruvate Dehydrogenase Complex as a Target for Gene Therapy. Current Gene Therapy. 3(3). 239–245. 13 indexed citations

16.

Owen, Renius, Ronald J. Mandel, Thomas J. Conlon, et al.. (2002). Gene Therapy for Pyruvate Dehydrogenase E1α Deficiency Using Recombinant Adeno-Associated Virus 2 (rAAV2) Vectors. Molecular Therapy. 6(3). 394–399. 11 indexed citations

17.

Owen, Renius & Terence R. Flotte. (2001). Approaches and Limitations to Gene Therapy for Mitochondrial Diseases. Antioxidants and Redox Signaling. 3(3). 451–460. 4 indexed citations

18.

Owen, Renius, Alfred S. Lewin, Alyson Peel, et al.. (2000). Recombinant Adeno-Associated Virus Vector-Based Gene Transfer for Defects in Oxidative Metabolism. Human Gene Therapy. 11(15). 2067–2078. 27 indexed citations

19.

Marinac, Jacqueline S., John Dikran Balian, John Foxworth, et al.. (1996). Determination of CYP2C19 phenotype in black Americans with omeprazole: Correlation with genotype*. Clinical Pharmacology & Therapeutics. 60(2). 138–144. 46 indexed citations

20.

Pope, F M, A C Nicholls, Jane McPheat, Philippa J. Talmud, & Renius Owen. (1985). Collagen genes and proteins in osteogenesis imperfecta.. Journal of Medical Genetics. 22(6). 466–478. 29 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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