S.S. Bhattacharya

1.1k total citations
38 papers, 933 citations indexed

About

S.S. Bhattacharya is a scholar working on Molecular Biology, Genetics and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, S.S. Bhattacharya has authored 38 papers receiving a total of 933 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 8 papers in Genetics and 7 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in S.S. Bhattacharya's work include Retinal Development and Disorders (13 papers), RNA regulation and disease (5 papers) and Photoreceptor and optogenetics research (4 papers). S.S. Bhattacharya is often cited by papers focused on Retinal Development and Disorders (13 papers), RNA regulation and disease (5 papers) and Photoreceptor and optogenetics research (4 papers). S.S. Bhattacharya collaborates with scholars based in United Kingdom, Mexico and United States. S.S. Bhattacharya's co-authors include Peng T. Khaw, Gregory S. Schultz, M. Francesca Cordeiro, D. Gardner‐Medwin, Anna M. Rose, Mark A. Johnson, J.B. Harris, L. V. B. Nicholson, Kay E. Davies and P. Pearson and has published in prestigious journals such as Nucleic Acids Research, European Heart Journal and Human Molecular Genetics.

In The Last Decade

S.S. Bhattacharya

36 papers receiving 892 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
S.S. Bhattacharya United Kingdom 17 593 201 193 148 98 38 933
Sunil K. Parapuram Canada 17 937 1.6× 321 1.6× 385 2.0× 232 1.6× 72 0.7× 24 1.5k
Е. В. Семина Russia 14 531 0.9× 80 0.4× 182 0.9× 61 0.4× 146 1.5× 62 862
April C. Carpenter United States 12 747 1.3× 44 0.2× 104 0.5× 39 0.3× 117 1.2× 17 1.1k
Mei Cheng United States 16 382 0.6× 230 1.1× 44 0.2× 125 0.8× 78 0.8× 32 727
Lyndsay L. Leach United States 11 464 0.8× 122 0.6× 101 0.5× 73 0.5× 84 0.9× 15 647
Kimberly C. Sippel United States 16 276 0.5× 305 1.5× 75 0.4× 451 3.0× 112 1.1× 31 960
Cataldo Schietroma United States 13 694 1.2× 40 0.2× 47 0.2× 34 0.2× 154 1.6× 17 955
Pilar Villacampa Spain 13 344 0.6× 141 0.7× 200 1.0× 84 0.6× 37 0.4× 21 762
Igor O. Nasonkin United States 20 993 1.7× 159 0.8× 208 1.1× 125 0.8× 398 4.1× 38 1.4k
Jennifer T. Durham United States 11 320 0.5× 177 0.9× 19 0.1× 140 0.9× 36 0.4× 12 735

Countries citing papers authored by S.S. Bhattacharya

Since Specialization
Citations

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

Fields of papers citing papers by S.S. Bhattacharya

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of S.S. Bhattacharya

This figure shows the co-authorship network connecting the top 25 collaborators of S.S. Bhattacharya. A scholar is included among the top collaborators of S.S. Bhattacharya 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 S.S. Bhattacharya. S.S. Bhattacharya 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.
Bhattacharya, S.S., et al.. (2013). Effects of cisplatin on testes and chromosome of rats: A histological and chromosomal study. Journal of Pharmacovigilance. 1 indexed citations
2.
MacDonald, et al.. (2007). Epiblastic Cited2 function explains pleiotropy and penetrance of cardiac malformation resulting from its deficiency. European Heart Journal. 28. 123–123. 1 indexed citations
3.
Arora, Anita, Peter J. Francis, Alexander Ionides, et al.. (2004). A CRYGD mutation is associated with familial coralliform cataract. Investigative Ophthalmology & Visual Science. 45(13). 374–374.
4.
Chakarova, Christina, et al.. (2004). Can the stability of a mutant mRNA copy of PRPF31 with an 11bp deletion be compromised through alternative splicing. Investigative Ophthalmology & Visual Science. 45(13). 2484–2484. 1 indexed citations
5.
El-Ashry, Mohamed F., Mai M. Abd El-Aziz, Linda Ficker, et al.. (2004). BIGH3 mutation in a Bangladeshi family with a variable phenotype of LCDI. Eye. 18(7). 723–728. 8 indexed citations
6.
Aung, Tin, Richard Bowman, Paul Chew, et al.. (2003). Genome-wide Linkage Scan for Primary Angle Closure Glaucoma. Investigative Ophthalmology & Visual Science. 44(13). 3224–3224.
7.
Wilkins, Simon, et al.. (2002). Novel Mutations in CHST6 Gene Causing Macular Corneal Dystrophy. Investigative Ophthalmology & Visual Science. 43(13). 1655–1655. 18 indexed citations
8.
Kučinskas, Vaidutis, et al.. (1999). Mutations in the human rhodopsin gene and polymorphisms in peripherin/RDS gene in Lithuanian autosomal dominant retinitis pigmentosa patients. Journal of Applied Genetics. 40(1). 53–61. 1 indexed citations
9.
Votruba, Marcela, A. T. Moore, & S.S. Bhattacharya. (1998). Physical mapping of the OPA1 region and linkage disequilibrium analysis in dominant optic atrophy. 39(4). 51215. 1 indexed citations
10.
Ali, Robin R., et al.. (1997). Gene Therapy for Retinal Degeneration. Ophthalmic Research. 29(5). 261–268. 11 indexed citations
11.
Sargan, David R., et al.. (1994). Progressive retinal atrophy: a model for retinitis pigmentosa in companion animals.. PubMed. 1 Suppl 1(9). S89–S89. 7 indexed citations
12.
Al-Maghtheh, Mai, Richard Kim, Alison J. Hardcastle, C.F. Inglehearn, & S.S. Bhattacharya. (1994). A 150 bp insertion in the rhodopsin gene of an autosomal dominant retinitis pigmentosa family. Human Molecular Genetics. 3(1). 205–206. 23 indexed citations
13.
Fuchs, Sigrid, M. J. Denton, Eberhart Zrenner, et al.. (1994). Three novel rhodopsin mutations (C110F, L131P, A164V) in patients with autosomal dominant retinitis pigmentosa. Human Molecular Genetics. 3(7). 1203–1203. 28 indexed citations
14.
Curtis, Ann, et al.. (1993). Absence of cystic fibrosis mutations in a large Asian population sample and occurrence of a homozygous S549N mutation in an inbred Pakistani family.. Journal of Medical Genetics. 30(2). 164–166. 24 indexed citations
15.
Thiselton, Dawn L., Smaragda Kamakari, Michel P. Coleman, et al.. (1993). Dinucleotide repeat polymorphism at the DXS556 locus. Human Molecular Genetics. 2(5). 613–613. 3 indexed citations
16.
Al-Maghtheh, Mai, et al.. (1993). Variation in DNA Polymorphisms of the Short Arm of the Human X Chromosome: Genetic Affinity of Parsi from Western India. Human Heredity. 43(4). 239–243. 3 indexed citations
17.
Bashir, R., C.F. Inglehearn, T J Keen, et al.. (1992). Exclusion of chromosome 6 and 8 locations in nonrhodopsin autosomal dominant retinitis pigmentosa families: Further locus heterogeneity in adRP. Genomics. 14(1). 191–193. 4 indexed citations
18.
Nicholson, L. V. B., Mark A. Johnson, D. Gardner‐Medwin, S.S. Bhattacharya, & J.B. Harris. (1990). Heterogeneity of dystrophin expression in patients with Duchenne and Becker muscular dystrophy. Acta Neuropathologica. 80(3). 239–250. 127 indexed citations
19.
Papiha, S.S., S.S. Bhattacharya, & D. F. Roberts. (1988). DNA Polymorphisms, Identified by an X-Chromosome Short-Arm Probe L 1.28 (DXS7), in Different Racial Groups. Human Heredity. 38(2). 72–75. 5 indexed citations
20.
Wieacker, Peter, Kay E. Davies, Howard J. Cooke, et al.. (1984). Toward a complete linkage map of the human X chromosome: regional assignment of 16 cloned single-copy DNA sequences employing a panel of somatic cell hybrids.. PubMed. 36(2). 265–76. 137 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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