Shipra Bhatia

819 total citations
17 papers, 497 citations indexed

About

Shipra Bhatia is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Shipra Bhatia has authored 17 papers receiving a total of 497 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Shipra Bhatia's work include Genomics and Chromatin Dynamics (10 papers), Developmental Biology and Gene Regulation (6 papers) and Animal Genetics and Reproduction (5 papers). Shipra Bhatia is often cited by papers focused on Genomics and Chromatin Dynamics (10 papers), Developmental Biology and Gene Regulation (6 papers) and Animal Genetics and Reproduction (5 papers). Shipra Bhatia collaborates with scholars based in United Kingdom, India and Singapore. Shipra Bhatia's co-authors include Dirk A. Kleinjan, Veronica van Heyningen, Hemant Bengani, Robert M. Grainger, Alison Brown, Maria Teresa Divizia, Riccardo De Marco, Giuseppe Damante, Margaret B. Fish and Pedro M. Coutinho and has published in prestigious journals such as Nucleic Acids Research, PLoS ONE and Scientific Reports.

In The Last Decade

Shipra Bhatia

17 papers receiving 483 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shipra Bhatia United Kingdom	12	377	192	73	59	26	17	497
Katerina Kraft United States	8	533 1.4×	184 1.0×	37 0.5×	123 2.1×	14 0.5×	15	626
Arnaud Kress France	9	276 0.7×	202 1.1×	65 0.9×	24 0.4×	19 0.7×	17	437
Beate Wittbrodt Germany	9	367 1.0×	64 0.3×	185 2.5×	45 0.8×	51 2.0×	12	472
Roya Hosseini United States	8	503 1.3×	192 1.0×	56 0.8×	66 1.1×	12 0.5×	14	623
Jacqueline C. Pulido United States	10	271 0.7×	225 1.2×	23 0.3×	67 1.1×	20 0.8×	12	482
Leath A. Tonkin United States	8	785 2.1×	152 0.8×	60 0.8×	128 2.2×	20 0.8×	8	913
Olga Medina-Martínez United States	12	346 0.9×	148 0.8×	31 0.4×	15 0.3×	50 1.9×	18	468
Darren Grafham United Kingdom	10	425 1.1×	171 0.9×	15 0.2×	94 1.6×	80 3.1×	11	553
Sophie Remacle Belgium	10	276 0.7×	82 0.4×	40 0.5×	15 0.3×	48 1.8×	13	375
Svetlana Zhenilo Russia	10	450 1.2×	142 0.7×	49 0.7×	32 0.5×	32 1.2×	30	542

Countries citing papers authored by Shipra Bhatia

Since Specialization

Citations

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

Fields of papers citing papers by Shipra Bhatia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shipra Bhatia

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

All Works

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17 of 17 papers shown

Papanastasiou, Andrew S., et al.. (2023). Unique activities of two overlappingPAX6retinal enhancers. Life Science Alliance. 6(11). e202302126–e202302126. 5 indexed citations

Parry, David, Mihail Halachev, Kathleen A. Williamson, et al.. (2023). Short-read whole genome sequencing identifies causative variants in most individuals with previously unexplained aniridia. Journal of Medical Genetics. 61(3). 250–261. 4 indexed citations

Ravi, Vydianathan, Shipra Bhatia, Prashant Shingate, et al.. (2019). Lampreys, the jawless vertebrates, contain three Pax6 genes with distinct expression in eye, brain and pancreas. Scientific Reports. 9(1). 19559–19559. 11 indexed citations

Mann, Anita & Shipra Bhatia. (2019). Zebrafish: A Powerful Model for Understanding the Functional Relevance of Noncoding Region Mutations in Human Genetic Diseases. Biomedicines. 7(3). 71–71. 3 indexed citations

Pradeepa, Madapura M., Gillian C.A. Taylor, Hemant Bengani, et al.. (2017). Psip1/p52 regulates posterior Hoxa genes through activation of lncRNA Hottip. PLoS Genetics. 13(4). e1006677–e1006677. 20 indexed citations

Bhatia, Shipra, et al.. (2016). Interaction of the Chromatin Remodeling Protein hINO80 with DNA. PLoS ONE. 11(7). e0159370–e0159370. 6 indexed citations

Benabdallah, Nezha S., et al.. (2016). SBE6: a novel long-range enhancer involved in driving sonic hedgehog expression in neural progenitor cells. Open Biology. 6(11). 160197–160197. 16 indexed citations

Bhatia, Shipra, Christopher T. Gordon, Véronique Abadie, et al.. (2015). Functional Assessment of Disease-Associated Regulatory Variants In Vivo Using a Versatile Dual Colour Transgenesis Strategy in Zebrafish. PLoS Genetics. 11(6). e1005193–e1005193. 18 indexed citations

Bhatia, Shipra, Jack Monahan, Vydianathan Ravi, et al.. (2014). A survey of ancient conserved non-coding elements in the PAX6 locus reveals a landscape of interdigitated cis-regulatory archipelagos. Developmental Biology. 387(2). 214–228. 31 indexed citations

10.

Bhatia, Shipra & Dirk A. Kleinjan. (2014). Disruption of long-range gene regulation in human genetic disease: a kaleidoscope of general principles, diverse mechanisms and unique phenotypic consequences. Human Genetics. 133(7). 815–845. 22 indexed citations

11.

Gordon, Christopher T., Catia Attanasio, Shipra Bhatia, et al.. (2014). Identification of Novel Craniofacial Regulatory Domains Located far Upstream ofSOX9and Disrupted in Pierre Robin Sequence. Human Mutation. 35(8). 1011–1020. 67 indexed citations

12.

Bhatia, Shipra, Hemant Bengani, Margaret B. Fish, et al.. (2013). Disruption of Autoregulatory Feedback by a Mutation in a Remote, Ultraconserved PAX6 Enhancer Causes Aniridia. The American Journal of Human Genetics. 93(6). 1126–1134. 135 indexed citations

13.

Ravi, Vydianathan, Shipra Bhatia, Philippe Gautier, et al.. (2013). Sequencing of Pax6 Loci from the Elephant Shark Reveals a Family of Pax6 Genes in Vertebrate Genomes, Forged by Ancient Duplications and Divergences. PLoS Genetics. 9(1). e1003177–e1003177. 36 indexed citations

14.

Soni, Kartik, Ashwani Choudhary, Ashok Patowary, et al.. (2013). miR-34 is maternally inherited in Drosophila melanogaster and Danio rerio. Nucleic Acids Research. 41(8). 4470–4480. 58 indexed citations

15.

Coutinho, Pedro M., et al.. (2011). Discovery and assessment of conserved Pax6 target genes and enhancers. Genome Research. 21(8). 1349–1359. 37 indexed citations

16.

Bhatia, Shipra, et al.. (2010). Chromatin remodeling protein INO80 has a role in regulation of homeotic gene expression in Drosophila. Genes to Cells. 15(7). 725–735. 17 indexed citations

17.

Bhatia, Shipra, et al.. (2010). Functional analysis of an intergenic non-coding sequence within mce1 operon of M.tuberculosis. BMC Microbiology. 10(1). 128–128. 11 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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