Harsh Sheth

1.3k total citations
34 papers, 277 citations indexed

About

Harsh Sheth is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Harsh Sheth has authored 34 papers receiving a total of 277 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 9 papers in Molecular Biology and 6 papers in Pathology and Forensic Medicine. Recurrent topics in Harsh Sheth's work include Genomic variations and chromosomal abnormalities (8 papers), Genetic factors in colorectal cancer (6 papers) and Genomics and Rare Diseases (5 papers). Harsh Sheth is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetic factors in colorectal cancer (6 papers) and Genomics and Rare Diseases (5 papers). Harsh Sheth collaborates with scholars based in India, Poland and United Kingdom. Harsh Sheth's co-authors include John Burn, Thomas Liehr, Frenny Sheth, Mauro Santibanez‐Koref, Jayesh Sheth, Michael S. Jackson, Robert I. McLachlan, Moira K. O’Bryan, Soon Lee and David O. Hooks and has published in prestigious journals such as PLoS ONE, Gene and Human Reproduction.

In The Last Decade

Harsh Sheth

30 papers receiving 266 citations

Peers

Countries citing papers authored by Harsh Sheth

Since Specialization

Citations

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

Fields of papers citing papers by Harsh Sheth

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Harsh Sheth

This figure shows the co-authorship network connecting the top 25 collaborators of Harsh Sheth. A scholar is included among the top collaborators of Harsh Sheth 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 Harsh Sheth. Harsh Sheth 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	Uniform Reporting of Next Generation Sequencing: Indian Society of Medical and Pediatric Oncology 2025 ·Indian Journal of Medical and Paediatric Oncology ·(unknown), (unknown), (unknown), Prashant Mehta, Anuradha Choughule, Harsh Sheth, (unknown), (unknown), Vineet Govinda Gupta, Umut Dişel, TVSVGK Tilak, Amit Dutt, Anguraj Sadanandam, Bhawna Sirohi, (unknown)	0
2	Lysosomal storage disorders identified in adult population from India: Experience of a tertiary genetic centre and review of literature 2024 ·JIMD Reports ·Jayesh Sheth, (unknown), (unknown), Koumudi Godbole, Chaitanya Datar, Sheela Nampoothiri, Inusha Panigrahi, (unknown), (unknown), (unknown), (unknown), Harsh Sheth	1
3	Complex chromosomal rearrangements in female carriers experiencing recurrent pregnancy loss or poor obstetric history and literature review 2024 ·Journal of Assisted Reproduction and Genetics ·Frenny Sheth, (unknown), Thomas Liehr, Manisha Desai, Himanshu K. Patel, Jayesh Sheth, Harsh Sheth	1
4	Late infantile and adult‐onset metachromatic leukodystrophy due to novel missense variants in the PSAP gene: Case report from India 2023 ·JIMD Reports ·Jayesh Sheth, (unknown), (unknown), (unknown), (unknown), C. Ratna Prabha, Frenny Sheth, Harsh Sheth	2
5	Comparative yield of molecular diagnostic algorithms for autism spectrum disorder diagnosis in India: evidence supporting whole exome sequencing as first tier test 2023 ·BMC Neurology ·Frenny Sheth, (unknown), Deepika Jain, Siddharth Shah, Harshkumar Patel, Ketan J. Patel, (unknown), Anand Iyer, (unknown), (unknown), (unknown), (unknown), Vishal Patel, (unknown), (unknown), Darshan Patel, Jayesh Sheth, Harsh Sheth	12
6	A novel case of two siblings harbouring homozygous variant in the NEUROG1 gene with autism as an additional phenotype: a case report 2023 ·BMC Neurology ·Frenny Sheth, (unknown), Ketan Patel, Darshan Patel, Deepika Jain, Jayesh Sheth, Harsh Sheth	2
7	An ultra-rare case of immunoskeletal dysplasia with neurodevelopmental abnormalities in an Indian patient with homozygous c.953C > T variant in EXTL3 gene: a case report 2022 ·BMC Pediatrics ·(unknown), (unknown), (unknown), Frenny Sheth, Jayesh Sheth, Harsh Sheth	2
8	Identification of novel exonic variants contributing to hereditary breast and ovarian cancer in west Indian population 2022 ·Gene ·Bhargav N. Waghela, Ramesh Pandit, (unknown), Franky D. Shah, Prabhudas S. Patel, (unknown), Harsh Sheth, (unknown), Shashank Pandya, Chaitanya G. Joshi, Madhvi Joshi	0
9	The GALNS p.P77R variant is a probable Gujarati-Indian founder mutation causing Mucopolysaccharidosis IVA syndrome 2022 ·BMC Genomics ·Harsh Sheth, (unknown), (unknown), (unknown), (unknown), Frenny Sheth, Jayesh Sheth	2
10	Molecular Diagnosis of Muscular Dystrophy Patients in Western Indian Population: A Comprehensive Mutation Analysis Using Amplicon Sequencing 2021 ·Frontiers in Genetics ·(unknown), (unknown), (unknown), Bhargav N. Waghela, Ramesh Pandit, Harsh Sheth, Chaitanya G. Joshi, Madhvi Joshi	2
11	Case Report: Recurrent Variant c.298 TA in CCN6 Gene Found in Progressive Pseudorheumatoid Dysplasia Patients From Patni Community of Gujarat: A Report of Three Cases 2021 ·Frontiers in Genetics ·Harsh Sheth, (unknown), (unknown), (unknown), Jayesh Sheth	1
12	Recurrent variant c.1680C>A in FAM20C gene and genotype-phenotype correlation in a patient with Raine syndrome: a case report 2021 ·BMC Pediatrics ·(unknown), Fazul Nabi, (unknown), Harsh Sheth	5
13	Mosaic chromosome 18 anomaly delineated in a child with dysmorphism using a three-pronged cytogenetic techniques approach: a case report 2020 ·BMC Medical Genomics ·Harsh Sheth, (unknown), Thomas Liehr, Ketan Patel, Deepika Jain, Jayesh Sheth, Frenny Sheth	1
14	Association of stroke and bleed events in non-valvular atrial fibrillation patients with direct oral anticoagulant prescriptions in NHS England between 2013 and 2016 2019 ·PLoS ONE ·Harsh Sheth, (unknown), Mauro Santibanez‐Koref, John Burn	5
15	The role of aspirin in preventing colorectal cancer 2016 ·British Medical Bulletin ·John Burn, Harsh Sheth	25
16	Point of care testing for improving risk- benefit ratio of aspirin and warfarin 2014 ·Molecular Cytogenetics ·Harsh Sheth, (unknown), Faye Elliott, Michael S. Jackson, Mauro Santibáñez Koref, John R. Tyson, Ann K. Daly, (unknown), Jayesh Sheth, Frenny Sheth, Keyur Parikh, D. Timothy Bishop, John Burn	1
17	Chromosomal imbalance letter: Phenotypic consequences of combined deletion 8pter and duplication 15qter 2013 ·Molecular Cytogenetics ·Frenny Sheth, Joris Andrieux, (unknown), Harsh Sheth, Manisha Desai, (unknown), (unknown), Jayesh Sheth	1
18	Chromosomal abnormalities in couples with repeated fetal loss: An Indian retrospective study 2013 ·Indian journal of human genetics ·(unknown), Thomas Liehr, (unknown), (unknown), Harsh Sheth, (unknown)	44
19	Identification of a neuronal transcription factor network involved inmedulloblastoma development 2013 ·Acta Neuropathologica Communications ·Maria Łastowska, Hani Al-Afghani, Haya H. Al‐Balool, Harsh Sheth, (unknown), Jonathan Coxhead, Christopher P.F. Redfern, Heiko Peters, Alastair D. Burt, Mauro Santibanez‐Koref, Chris M. Bacon, Louis Chesler, Alistair G. Rust, David J. Adams, Daniel Williamson, Steven C. Clifford, Michael S. Jackson	34
20	Characterization of sSMC by FISH and molecular techniques 2011 ·European Journal of Medical Genetics ·Frenny Sheth, Joris Andrieux, Elisabeth Ewers, Nadezda Kosyakova, Anja Weise, Harsh Sheth, Serge Romana, (unknown), Bruno Delobel, Olivier Theisen, Thomas Liehr, Sheela Nampoothiri, Jayesh Sheth	14

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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