Sanjeev S. Bhaskar

6.1k total citations
31 papers, 1.6k citations indexed

About

Sanjeev S. Bhaskar is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sanjeev S. Bhaskar has authored 31 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 17 papers in Genetics and 3 papers in Genetics. Recurrent topics in Sanjeev S. Bhaskar's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Retinal Development and Disorders (5 papers). Sanjeev S. Bhaskar is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Retinal Development and Disorders (5 papers). Sanjeev S. Bhaskar collaborates with scholars based in United Kingdom, United States and India. Sanjeev S. Bhaskar's co-authors include James O’Sullivan, Graeme C. Black, Simon G. Williams, William G. Newman, Simon Ramsden, Jill Urquhart, Sarah B. Daly, D. Gareth Evans, Georgina Hall and Miriam J. Smith and has published in prestigious journals such as The Lancet, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Sanjeev S. Bhaskar

30 papers receiving 1.6k citations

Peers

Sanjeev S. Bhaskar

GENET

OPHTH

EPIDE

NEURO

James O’Sullivan United Kingdom

Allan J. Richards United Kingdom

Pierre Bitoun France

Annemarie H. van der Hout Netherlands

Hardeep Singh Mudhar United Kingdom

Rahat Perveen United Kingdom

Lesley C. Adès Australia

B S Emanuel United States

Luitgard M. Neumann Germany

Jan M. Cobben Netherlands

James O’Sullivan United Kingdom

Sanjeev S. Bhaskar

1.4k ×1.2

510 ×0.8

GENET

324 ×1.3

OPHTH

214 ×1.1

EPIDE

197 ×1.1

NEURO

Citations per year, relative to Sanjeev S. Bhaskar Sanjeev S. Bhaskar (= 1×) peers James O’Sullivan

Countries citing papers authored by Sanjeev S. Bhaskar

Since Specialization

Citations

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

Fields of papers citing papers by Sanjeev S. Bhaskar

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sanjeev S. Bhaskar. 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 Sanjeev S. Bhaskar. The network helps show where Sanjeev S. Bhaskar may publish in the future.

Co-authorship network of co-authors of Sanjeev S. Bhaskar

This figure shows the co-authorship network connecting the top 25 collaborators of Sanjeev S. Bhaskar. A scholar is included among the top collaborators of Sanjeev S. Bhaskar 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 Sanjeev S. Bhaskar. Sanjeev S. Bhaskar 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

Beaman, Glenda M., Keng Wee Teik, Jill Urquhart, et al.. (2019). A homozygous missense variant in CHRM3 associated with familial urinary bladder disease. Clinical Genetics. 96(6). 515–520. 9 indexed citations

Sharkia, Rajech, Stavit A. Shalev, Nathan Watemberg, et al.. (2017). Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy. American Journal of Medical Genetics Part A. 173(4). 1051–1055. 9 indexed citations

Elalaoui, Siham Chafai, Ilham Ratbi, Jill Urquhart, et al.. (2016). Non lethal Raine syndrome and differential diagnosis. European Journal of Medical Genetics. 59(11). 577–583. 32 indexed citations

Urquhart, Jill, R. C. Roberts, Stavit A. Shalev, et al.. (2016). Exploring the genetic basis of 3MC syndrome: Findings in 12 further families. American Journal of Medical Genetics Part A. 170(5). 1216–1224. 22 indexed citations

Ellingford, Jamie M., Stephanie Barton, Sanjeev S. Bhaskar, et al.. (2016). Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease. Ophthalmology. 123(5). 1143–1150. 93 indexed citations

Lennon, Rachel, et al.. (2015). Pinpointing clinical diagnosis through whole exome sequencing to direct patient care.. The Lancet. 1 indexed citations

Sergouniotis, Panagiotis I., Jill Urquhart, Simon G. Williams, et al.. (2015). Agnathia-otocephaly complex and asymmetric velopharyngeal insufficiency due to an in-frame duplication in OTX2. Journal of Human Genetics. 60(4). 199–202. 11 indexed citations

Ellison, Gillian, Shuwen Huang, T. Hedley Carr, et al.. (2015). A reliable method for the detection of BRCA1 and BRCA2 mutations in fixed tumour tissue utilising multiplex PCR-based targeted next generation sequencing. BMC Clinical Pathology. 15(1). 5–5. 41 indexed citations

Urquhart, Jill, Simon G. Williams, Sanjeev S. Bhaskar, et al.. (2015). Deletion of 19q13 reveals clinical overlap with Dubowitz syndrome. Journal of Human Genetics. 60(12). 781–785. 22 indexed citations

10.

Ellingford, Jamie M., Panagiotis I. Sergouniotis, Rachel Lennon, et al.. (2015). Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome. The Lancet. 385(9980). 1916–1916. 21 indexed citations

11.

Daly, Sarah B., Hitesh Shah, James O’Sullivan, et al.. (2014). Exome Sequencing Identifies a Dominant <b><i>TNNT3</i></b> Mutation in a Large Family with Distal Arthrogryposis. Molecular Syndromology. 5(5). 218–228. 14 indexed citations

12.

Gillespie, Rachel, James O’Sullivan, Jane Ashworth, et al.. (2014). Personalized Diagnosis and Management of Congenital Cataract by Next-Generation Sequencing. Ophthalmology. 121(11). 2124–2137.e2. 130 indexed citations

13.

Smith, Miriam J., Christian Beetz, Simon G. Williams, et al.. (2014). Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis. Neurology. 84(2). 141–147. 78 indexed citations

14.

Smith, Miriam J., James O’Sullivan, Sanjeev S. Bhaskar, et al.. (2013). Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas. Nature Genetics. 45(3). 295–298. 168 indexed citations

15.

O’Sullivan, James, Sanjeev S. Bhaskar, Jonathan E. Dickerson, et al.. (2012). A paradigm shift in the delivery of services for diagnosis of inherited retinal disease. Journal of Medical Genetics. 49(5). 322–326. 124 indexed citations

16.

Mitchell, Karen S., James O’Sullivan, Caterina Missero, et al.. (2011). Exome Sequence Identifies RIPK4 as the Bartsocas- Papas Syndrome Locus. The American Journal of Human Genetics. 90(1). 69–75. 73 indexed citations

17.

Hanson, Dan, Philip Murray, James O’Sullivan, et al.. (2011). Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth. The American Journal of Human Genetics. 89(1). 148–153. 88 indexed citations

18.

Raffan, Eleanor, Liam A. Hurst, Saeed Al Turki, et al.. (2011). Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient. SHILAP Revista de lepidopterología. 2. 8–8. 9 indexed citations

19.

O’Sullivan, James, Carolina Cavalcante Bitu, Sarah B. Daly, et al.. (2011). Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome. The American Journal of Human Genetics. 88(5). 616–620. 126 indexed citations

20.

Bhaskar, Sanjeev S., et al.. (2005). Expansion of GAA trinucleotide repeats in mammals. Genomics. 87(1). 57–67. 27 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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