Sanjeev S. Bhaskar

6.1k citations

31 papers · 1.6k indexed · h-index 20

Co-authors: James O’Sullivan Graeme C. Black Simon G. Williams William G. Newman Simon Ramsden Jill Urquhart Sarah B. Daly D. Gareth Evans
Topics: Genomics and Rare Diseases (5 papers)Genomic variations and chromosomal abnormalities (5 papers)Retinal Development and Disorders (5 papers)
Cited by: Ophthalmology Genetics Molecular Biology
Journals: The Lancet Nature Genetics Journal of Clinical Oncology
Partner nations: United Kingdom United States India

In The Last Decade

Sanjeev S. Bhaskar

30 papers receiving 1.6k citations

Peers

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

#	Work	Indexed citations
1	A homozygous missense variant in CHRM3 associated with familial urinary bladder disease 2019 ·Clinical Genetics ·Glenda M. Beaman,(unknown),Keng Wee Teik,Jill Urquhart,(unknown),James O’Sullivan,Sanjeev S. Bhaskar,K Wood,Huw B. Thomas,Raymond T. O’Keefe,Adrian S. Woolf,Helen M. Stuart,William G. Newman	9
2	Homozygous mutation in PTRH2 gene causes progressive sensorineural deafness and peripheral neuropathy 2017 ·American Journal of Medical Genetics Part A ·Rajech Sharkia,Stavit A. Shalev,(unknown),(unknown),Nathan Watemberg,Jill Urquhart,Sarah B. Daly,Sanjeev S. Bhaskar,Simon G. Williams,William G. Newman,Ronen Spiegel,Abdussalam Azem,Orly Elpeleg,Muhammad Mahajnah	9
3	Non lethal Raine syndrome and differential diagnosis 2016 ·European Journal of Medical Genetics ·Siham Chafai Elalaoui,(unknown),Ilham Ratbi,Jill Urquhart,James O’Sullivan,Sanjeev S. Bhaskar,Simon G. Williams,(unknown),Jaber Lyahyai,(unknown),Imane Cherkaoui Jaouad,(unknown),William G. Newman,Abdelaziz Sefiani	32
4	Exploring the genetic basis of 3MC syndrome: Findings in 12 further families 2016 ·American Journal of Medical Genetics Part A ·Jill Urquhart,R. C. Roberts,(unknown),Stavit A. Shalev,(unknown),Sheela Nampoothiri,Yves Sznajer,Nicole Revençu,(unknown),Mohnish Suri,Jamie M. Ellingford,Simon G. Williams,Sanjeev S. Bhaskar,Jill Clayton‐Smith	22
5	Whole Genome Sequencing Increases Molecular Diagnostic Yield Compared with Current Diagnostic Testing for Inherited Retinal Disease 2016 ·Ophthalmology ·Jamie M. Ellingford,Stephanie Barton,Sanjeev S. Bhaskar,Simon G. Williams,Panagiotis I. Sergouniotis,James O’Sullivan,Janine A. Lamb,Rahat Perveen,Georgina Hall,William G. Newman,Richard D. Unwin,Stephen A. Roberts,(unknown),Rick Tearle,S. C. Bayliss,Simon Ramsden,Andrea H. Németh,Graeme C. Black	93
6	Pinpointing clinical diagnosis through whole exome sequencing to direct patient care. 2015 ·The Lancet ·(unknown),(unknown),Rachel Lennon,Sanjeev S. Bhaskar,(unknown),(unknown),(unknown),Georgina Hall,(unknown),(unknown),Adrian S. Woolf,Graeme C. Black	1
7	Agnathia-otocephaly complex and asymmetric velopharyngeal insufficiency due to an in-frame duplication in OTX2 2015 ·Journal of Human Genetics ·Panagiotis I. Sergouniotis,Jill Urquhart,Simon G. Williams,Sanjeev S. Bhaskar,Graeme C. Black,Simon C. Lovell,David J. Whitby,William G. Newman,Jill Clayton‐Smith	11
8	A reliable method for the detection of BRCA1 and BRCA2 mutations in fixed tumour tissue utilising multiplex PCR-based targeted next generation sequencing 2015 ·BMC Clinical Pathology ·Gillian Ellison,Shuwen Huang,T. Hedley Carr,Andrew J. Wallace,Miika Ahdesmäki,Sanjeev S. Bhaskar,John Mills	41
9	Deletion of 19q13 reveals clinical overlap with Dubowitz syndrome 2015 ·Journal of Human Genetics ·Jill Urquhart,Simon G. Williams,Sanjeev S. Bhaskar,Naomi L. Bowers,Jill Clayton‐Smith,William G. Newman	22
10	Pinpointing clinical diagnosis through whole exome sequencing to direct patient care: a case of Senior-Loken syndrome 2015 ·The Lancet ·Jamie M. Ellingford,Panagiotis I. Sergouniotis,Rachel Lennon,Sanjeev S. Bhaskar,Simon G. Williams,(unknown),James O’Sullivan,Georgina Hall,Simon Ramsden,I. Christopher Lloyd,Adrian S. Woolf,Graeme C. Black	21
11	Exome Sequencing Identifies a Dominant <b><i>TNNT3</i></b> Mutation in a Large Family with Distal Arthrogryposis 2014 ·Molecular Syndromology ·Sarah B. Daly,Hitesh Shah,James O’Sullivan,Beverley Anderson,Sanjeev S. Bhaskar,Simon Williams,(unknown),(unknown),Siddharth Banka,William G. Newman,Katta M. Girisha	14
12	Personalized Diagnosis and Management of Congenital Cataract by Next-Generation Sequencing 2014 ·Ophthalmology ·Rachel Gillespie,James O’Sullivan,Jane Ashworth,Sanjeev S. Bhaskar,Simon G. Williams,Susmito Biswas,(unknown),Simon Ramsden,Jill Clayton‐Smith,Graeme C. Black,I. Christopher Lloyd	130
13	Mutations in LZTR1 add to the complex heterogeneity of schwannomatosis 2014 ·Neurology ·Miriam J. Smith,(unknown),Christian Beetz,Simon G. Williams,Sanjeev S. Bhaskar,Wilfrid Richer,James O’Sullivan,Beverly Anderson,Sarah B. Daly,Jill Urquhart,Alan Fryer,Cecilie F. Rustad,Samantha J. Mills,Amir Samii,Daniel du Plessis,Dorothy Halliday,S. Barbarot,Franck Bourdeaut,William G. Newman,D. Gareth Evans	78
14	Loss-of-function mutations in SMARCE1 cause an inherited disorder of multiple spinal meningiomas 2013 ·Nature Genetics ·Miriam J. Smith,James O’Sullivan,Sanjeev S. Bhaskar,Kristen D. Hadfield,Gemma Poke,John Caird,Saba Sharif,Diana Eccles,David Fitzpatrick,Daniel Rawluk,Daniel du Plessis,William G. Newman,D. Gareth Evans	168
15	A paradigm shift in the delivery of services for diagnosis of inherited retinal disease 2012 ·Journal of Medical Genetics ·James O’Sullivan,(unknown),Sanjeev S. Bhaskar,Jonathan E. Dickerson,Georgina Hall,Anna O’Grady,Andrew R. Webster,Simon Ramsden,Graeme C. Black	124
16	Exome Sequence Identifies RIPK4 as the Bartsocas- Papas Syndrome Locus 2011 ·The American Journal of Human Genetics ·Karen S. Mitchell,James O’Sullivan,Caterina Missero,Ed Blair,Rose Richardson,Beverley Anderson,Dario Antonini,Jeffrey C. Murray,Alan Shanske,Brian C. Schutte,Rose-Anne Romano,Satrajit Sinha,Sanjeev S. Bhaskar,Graeme C. Black,Jill Dixon,Michael J. Dixon	73
17	Exome Sequencing Identifies CCDC8 Mutations in 3-M Syndrome, Suggesting that CCDC8 Contributes in a Pathway with CUL7 and OBSL1 to Control Human Growth 2011 ·The American Journal of Human Genetics ·Dan Hanson,Philip Murray,James O’Sullivan,Jill Urquhart,Sarah B. Daly,Sanjeev S. Bhaskar,Leslie G. Biesecker,Mars Skae,Claire E. L. Smith,Trevor Cole,Jeremy Kirk,Kate Chandler,Helen Kingston,Dian Donnai,Peter Clayton,Graeme C. Black	88
18	Early Diagnosis of Werner's Syndrome Using Exome-Wide Sequencing in a Single, Atypical Patient 2011 ·SHILAP Revista de lepidopterología ·Eleanor Raffan,Liam A. Hurst,Saeed Al Turki,Gillian Carpenter,Carol Scott,Allan Daly,Alison J. Coffey,Sanjeev S. Bhaskar,Eleanor Howard,Naz Khan,Helen Kingston,Aarno Palotie,David B. Savage,Mark O’Driscoll,Claire E. L. Smith,Stephen O’Rahilly,Inês Barroso,Robert K. Semple	9
19	Whole-Exome Sequencing Identifies FAM20A Mutations as a Cause of Amelogenesis Imperfecta and Gingival Hyperplasia Syndrome 2011 ·The American Journal of Human Genetics ·James O’Sullivan,Carolina Cavalcante Bitu,Sarah B. Daly,Jill Urquhart,Martin Barron,Sanjeev S. Bhaskar,Hercílio Martelli‐Júnior,(unknown),M. Adela Mansilla,Jeffrey C. Murray,Ricardo D. Coletta,Graeme C. Black,Michael J. Dixon	126
20	Expansion of GAA trinucleotide repeats in mammals 2005 ·Genomics ·(unknown),Sanjeev S. Bhaskar,Masaki Miyahara,Gillian L. Dalgliesh,Sanjay I. Bidichandani	27

About Sanjeev S. Bhaskar

Sanjeev S. Bhaskar is a scholar working on Genetics, Developmental Biology and Molecular Biology, having authored 31 papers that have together received 1.6k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Retinal Development and Disorders (5 papers). The work is most often cited by research in Ophthalmology (252 citations), Genetics (609 citations) and Molecular Biology (1.1k citations). Sanjeev S. Bhaskar has collaborated with scholars based in United Kingdom, United States and India. Frequent 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. Their work appears in journals such as The Lancet, Nature Genetics and Journal of Clinical Oncology.

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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