Shibu John

1.1k total citations
16 papers, 429 citations indexed

About

Shibu John is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Shibu John has authored 16 papers receiving a total of 429 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 10 papers in Cardiology and Cardiovascular Medicine and 4 papers in Genetics. Recurrent topics in Shibu John's work include Cardiomyopathy and Myosin Studies (6 papers), RNA and protein synthesis mechanisms (4 papers) and Genomics and Rare Diseases (2 papers). Shibu John is often cited by papers focused on Cardiomyopathy and Myosin Studies (6 papers), RNA and protein synthesis mechanisms (4 papers) and Genomics and Rare Diseases (2 papers). Shibu John collaborates with scholars based in United Kingdom, Singapore and India. Shibu John's co-authors include Stuart A. Cook, James S. Ware, Jayashree Shanker, Vijay V. Kakkar, Paul J.R. Barton, Roddy Walsh, Rachel Buchan, Veena S. Rao, Chee Jian Pua and Sanjay Prasad and has published in prestigious journals such as PLoS ONE, European Heart Journal and Heart.

In The Last Decade

Shibu John

16 papers receiving 418 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Shibu John United Kingdom	11	253	199	88	71	55	16	429
Hugo R. Martinez United States	11	152 0.6×	135 0.7×	74 0.8×	31 0.4×	46 0.8×	38	301
Anna‐Maria Müller Germany	8	103 0.4×	139 0.7×	15 0.2×	31 0.4×	26 0.5×	10	330
Sonny Dandona Canada	12	159 0.6×	163 0.8×	186 2.1×	31 0.4×	217 3.9×	21	497
P. Fain United States	9	315 1.2×	219 1.1×	124 1.4×	15 0.2×	63 1.1×	10	542
Yumiko Ikemoto Japan	8	138 0.5×	116 0.6×	20 0.2×	39 0.5×	72 1.3×	16	282
Fabiana Cerrato Italy	8	106 0.4×	229 1.2×	54 0.6×	177 2.5×	51 0.9×	8	375
Ruo-Gu Li China	11	132 0.5×	270 1.4×	51 0.6×	137 1.9×	43 0.8×	14	365
Marcel M. Levi Netherlands	4	77 0.3×	89 0.4×	99 1.1×	20 0.3×	50 0.9×	5	283
Lina Cordeddu Sweden	8	73 0.3×	325 1.6×	84 1.0×	14 0.2×	28 0.5×	12	418
Maria Grazia Franzosi Italy	5	89 0.4×	284 1.4×	199 2.3×	28 0.4×	94 1.7×	8	537

Countries citing papers authored by Shibu John

Since Specialization

Citations

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

Fields of papers citing papers by Shibu John

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Shibu John

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

All Works

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16 of 16 papers shown

Raju, Hariharan, James S. Ware, Jonathan R. Skinner, et al.. (2019). Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy. BMC Cardiovascular Disorders. 19(1). 174–174. 11 indexed citations

Walsh, Roddy, Paul J.R. Barton, Rachel Buchan, et al.. (2017). A comparative study of mutation screening of sarcomeric genes ( MYBPC3 , MYH7 , TNNT2 ) using single gene approach versus targeted gene panel next generation sequencing in a cohort of HCM patients in Egypt. Egyptian Journal of Medical Human Genetics. 18(4). 381–387. 1 indexed citations

Rea, Gillian, Tessa Homfray, Jan Till, et al.. (2016). Histiocytoid cardiomyopathy and microphthalmia with linear skin defects syndrome: phenotypes linked by truncating variants in NDUFB11. Molecular Case Studies. 3(1). a001271–a001271. 11 indexed citations

Pua, Chee Jian, Jaydutt Bhalshankar, Kui Miao, et al.. (2016). Development of a Comprehensive Sequencing Assay for Inherited Cardiac Condition Genes. Journal of Cardiovascular Translational Research. 9(1). 3–11. 53 indexed citations

Walsh, Roddy, Rachel Buchan, Alicja Wilk, et al.. (2016). Defining the genetic architecture of hypertrophic cardiomyopathy: re-evaluating the role of non-sarcomeric genes. European Heart Journal. 38(46). ehw603–ehw603. 139 indexed citations

Francis, Catherine, Antonio de Marvao, Declan P. O’Regan, et al.. (2015). 175 Aortopathy-causing mutations increase aortic stiffness in healthy individuals. A99.1–A99. 1 indexed citations

Francis, Catherine, Shibu John, Rachel Buchan, et al.. (2014). 95 Identification Of Likely Pathogenic Variants In Patients With Bicuspid Aortic Valve: Correlation Of Complex Genotype With A More Severe Aortic Phenotype. Heart. 100(Suppl 3). A55–A56. 4 indexed citations

Baksi, A. John, Angharad M. Roberts, James S. Ware, et al.. (2014). Titin: a phenotype-genotype descriptive comparison of dilated cardiomyopathy. Journal of Cardiovascular Magnetic Resonance. 16. O89–O89. 3 indexed citations

Li, Man, Andrew Buckton, Stephen Wilkinson, et al.. (2013). Towards Clinical Molecular Diagnosis of Inherited Cardiac Conditions: A Comparison of Bench-Top Genome DNA Sequencers. PLoS ONE. 8(7). e67744–e67744. 44 indexed citations

10.

Ware, James S., Shibu John, Angharad M. Roberts, et al.. (2012). Next Generation Diagnostics in Inherited Arrhythmia Syndromes. Journal of Cardiovascular Translational Research. 6(1). 94–103. 28 indexed citations

11.

Shanker, Jayashree, et al.. (2010). Polymorphisms in the pituitary growth hormone gene and its receptor associated with coronary artery disease in a predisposed cohort from India. Journal of Genetics. 89(4). 437–447. 4 indexed citations

12.

Rao, Veena S., et al.. (2010). Usefulness of C-Reactive Protein as a Marker for Prediction of Future Coronary Events in the Asian Indian Population: Indian Atherosclerosis Research Study. International Journal of Vascular Medicine. 2010. 1–8. 14 indexed citations

13.

Shanker, Jayashree, et al.. (2009). Genotype-phenotype relationship of F7 R353Q polymorphism and plasma factor VII coagulant activity in Asian Indian families predisposed to coronary artery disease. Journal of Genetics. 88(3). 291–297. 12 indexed citations

14.

Dash, Debabrata, et al.. (2009). A common variant in chromosome 9p21 associated with coronary artery disease in Asian Indians. Journal of Genetics. 88(1). 113–118. 20 indexed citations

15.

Shanker, Jayashree, et al.. (2008). Polymorphisms in the IL6 gene in Asian Indian families with premature coronary artery disease – The Indian Atherosclerosis Research Study. Thrombosis and Haemostasis. 99(11). 944–950. 48 indexed citations

16.

Shanker, Jayashree, et al.. (2008). Genetic studies on the APOA1-C3-A5 gene cluster in Asian Indians with premature coronary artery disease. Lipids in Health and Disease. 7(1). 33–33. 36 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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