Raveen Basran

1.4k total citations
19 papers, 398 citations indexed

About

Raveen Basran is a scholar working on Genetics, Genetics and Molecular Biology. According to data from OpenAlex, Raveen Basran has authored 19 papers receiving a total of 398 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 9 papers in Genetics and 8 papers in Molecular Biology. Recurrent topics in Raveen Basran's work include Hemoglobinopathies and Related Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Prenatal Screening and Diagnostics (5 papers). Raveen Basran is often cited by papers focused on Hemoglobinopathies and Related Disorders (9 papers), Genomics and Rare Diseases (6 papers) and Prenatal Screening and Diagnostics (5 papers). Raveen Basran collaborates with scholars based in Canada, United States and Switzerland. Raveen Basran's co-authors include Stephanie Newton, Nancy F. Olivieri, Zhenyuan Wang, Peter N. Ray, Seema M. Jamal, Rita Selby, Christian R. Marshall, Jeff M. Milunsky, Eric Nisbet‐Brown and Thomas A. Maher and has published in prestigious journals such as Blood, Molecular and Cellular Biology and Annals of the New York Academy of Sciences.

In The Last Decade

Raveen Basran

19 papers receiving 393 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Raveen Basran Canada 12 197 164 116 99 73 19 398
R.N. Simmers Australia 9 205 1.0× 158 1.0× 24 0.2× 70 0.7× 37 0.5× 10 389
Ivy Ng Singapore 10 120 0.6× 147 0.9× 84 0.7× 141 1.4× 55 0.8× 19 375
Matthew Cannon United States 10 133 0.7× 50 0.3× 41 0.4× 10 0.1× 51 0.7× 20 417
N.J. Barton United Kingdom 7 264 1.3× 303 1.8× 53 0.5× 51 0.5× 24 0.3× 10 453
Ronald F. Carter Canada 8 104 0.5× 99 0.6× 13 0.1× 22 0.2× 65 0.9× 17 247
Stephanie Dallaire United States 5 274 1.4× 476 2.9× 26 0.2× 96 1.0× 12 0.2× 7 630
L. Alexander Liggett United States 7 193 1.0× 92 0.6× 26 0.2× 26 0.3× 79 1.1× 7 446
Kumi Ubukawa Japan 12 84 0.4× 21 0.1× 31 0.3× 34 0.3× 38 0.5× 21 349
Olivier Nègre France 13 429 2.2× 232 1.4× 198 1.7× 91 0.9× 84 1.2× 24 596
Kristen S. Jahn United States 5 440 2.2× 52 0.3× 78 0.7× 37 0.4× 72 1.0× 5 530

Countries citing papers authored by Raveen Basran

Since Specialization
Citations

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

Fields of papers citing papers by Raveen Basran

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Raveen Basran

This figure shows the co-authorship network connecting the top 25 collaborators of Raveen Basran. A scholar is included among the top collaborators of Raveen Basran 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 Raveen Basran. Raveen Basran 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.
Alekseyev, Yuriy O., Roghayeh Fazeli, Yang Shi, et al.. (2018). A Next-Generation Sequencing Primer—How Does It Work and What Can It Do?. Academic Pathology. 5. 1532766649–1532766649. 53 indexed citations
2.
Cohn, Iris, Tara Paton, Christian R. Marshall, et al.. (2017). Genome sequencing as a platform for pharmacogenetic genotyping: a pediatric cohort study. npj Genomic Medicine. 2(1). 19–19. 38 indexed citations
3.
Hayeems, Robin Z., Jasmin Bhawra, Kate Tsiplova, et al.. (2017). Care and cost consequences of pediatric whole genome sequencing compared to chromosome microarray. European Journal of Human Genetics. 25(12). 1303–1312. 27 indexed citations
4.
Brzezinski, Jack, Cheryl Shuman, Sanaa Choufani, et al.. (2017). Wilms tumour in Beckwith–Wiedemann Syndrome and loss of methylation at imprinting centre 2: revisiting tumour surveillance guidelines. European Journal of Human Genetics. 25(9). 1031–1039. 21 indexed citations
5.
Cytrynbaum, Cheryl, Karen Chong, Vickie Hannig, et al.. (2016). Genomic imbalance in the centromeric 11p15 imprinting center in three families: Further evidence of a role for IC2 as a cause of Russell–Silver syndrome. American Journal of Medical Genetics Part A. 170(10). 2731–2739. 14 indexed citations
6.
Grafodatskaya, Daria, Sanaa Choufani, Raveen Basran, & Rosanna Weksberg. (2016). An Update on Molecular Diagnostic Testing of Human Imprinting Disorders. Journal of Pediatric Genetics. 6(1). 3–17. 18 indexed citations
7.
Gonorazky, Hernán, Minggao Liang, Beryl B. Cummings, et al.. (2015). RNA seq analysis for the diagnosis of muscular dystrophy. Annals of Clinical and Translational Neurology. 3(1). 55–60. 59 indexed citations
8.
Basran, Raveen, Christian R. Marshall, Adam Shlien, et al.. (2015). MG-129 Our experience ofin silicogene panel testing for clinically heterogeneous disorders using exome sequencing. Journal of Medical Genetics. 52(Suppl 2). A11.1–A11. 1 indexed citations
9.
Maher, Thomas A., Raveen Basran, Aubrey Milunsky, et al.. (2011). Fraternal twins with Aarskog–Scott syndrome due to maternal germline mosaicism. American Journal of Medical Genetics Part A. 155(8). 1987–1990. 7 indexed citations
10.
Jamal, Seema M., Raveen Basran, Stephanie Newton, Zhenyuan Wang, & Jeff M. Milunsky. (2010). Novel de novo PCDH19 mutations in three unrelated females with epilepsy female restricted mental retardation syndrome. American Journal of Medical Genetics Part A. 152A(10). 2475–2481. 45 indexed citations
11.
Schmugge, Markus, et al.. (2008). THE Hb S/β+-Thalassemia Phenotype Demonstrates that the IVS-I (−2) (A>C) Mutation is a Mild β-Thalassemia Allele. Hemoglobin. 32(3). 303–307. 6 indexed citations
12.
Luo, Hongyuan, Raveen Basran, Tien Hsu, et al.. (2008). A T-to-G Transversion at Nucleotide −567 Upstream of HBG2 in a GATA-1 Binding Motif Is Associated with Elevated Hemoglobin F. Molecular and Cellular Biology. 28(13). 4386–4393. 32 indexed citations
13.
Luo, Hongyuan, Adeboye H. Adewoye, Monika Pilichowska, et al.. (2007). Two New α-Thalassemia Frameshift Mutations. Hemoglobin. 31(2). 135–139. 5 indexed citations
14.
Basran, Raveen, Ulrike M. Reiss, Hongyuan Luo, Russell E. Ware, & David H.K. Chui. (2006). β‐thalassemia intermedia due to compound heterozygosity for two β‐globin gene promoter mutations, including a novel TATA box deletion. Pediatric Blood & Cancer. 50(2). 363–366. 5 indexed citations
15.
Luo, Hongyuan, et al.. (2006). Sickle cell disease due to compound heterozygosity for Hb S and a novel 7.7‐kb β‐globin gene deletion. European Journal Of Haematology. 78(1). 82–85. 6 indexed citations
16.
Basran, Raveen, M Patterson, L. R. Walker, et al.. (2005). Prenatal Diagnosis of Hemoglobinopathies in Ontario, Canada. Annals of the New York Academy of Sciences. 1054(1). 507–510. 13 indexed citations
17.
Basran, Raveen, et al.. (1998). Genetic influences on bone disease in thalassemia.. Blood. 92. 2 indexed citations
18.
Selby, Rita, et al.. (1997). Valproic Acid and Augmentation of Fetal Hemoglobin in Individuals With and Without Sickle Cell Disease. Blood. 90(2). 891–892. 25 indexed citations
19.
Selby, Rita, et al.. (1997). Valproic Acid and Augmentation of Fetal Hemoglobin in Individuals With and Without Sickle Cell Disease. Blood. 90(2). 891–892. 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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