Sakthivel Murugan

914 total citations
28 papers, 416 citations indexed

About

Sakthivel Murugan is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Sakthivel Murugan has authored 28 papers receiving a total of 416 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 9 papers in Genetics and 3 papers in Genetics. Recurrent topics in Sakthivel Murugan's work include Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Metabolism and Genetic Disorders (3 papers). Sakthivel Murugan is often cited by papers focused on Genetics and Neurodevelopmental Disorders (5 papers), Genomics and Rare Diseases (4 papers) and Metabolism and Genetic Disorders (3 papers). Sakthivel Murugan collaborates with scholars based in India, United States and Australia. Sakthivel Murugan's co-authors include Vedam L. Ramprasad, Ravi Gupta, Ashwin Dalal, Shagun Aggarwal, Govindasamy Kumaramanickavel, Aneek Das Bhowmik, Manoj Shanmugamoorthy, Sampathkumar Velusamy, Lokesh Lingappa and M. S. P. Subathra and has published in prestigious journals such as Blood, PLoS ONE and Scientific Reports.

In The Last Decade

Sakthivel Murugan

27 papers receiving 404 citations

Peers

Countries citing papers authored by Sakthivel Murugan

Since Specialization

Citations

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

Fields of papers citing papers by Sakthivel Murugan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sakthivel Murugan

This figure shows the co-authorship network connecting the top 25 collaborators of Sakthivel Murugan. A scholar is included among the top collaborators of Sakthivel Murugan 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 Sakthivel Murugan. Sakthivel Murugan 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	Neonatal hypoglycaemic brain injury, a common cause of early‐childhood epilepsy in India: A prospective longitudinal study on aetiologies and outcomes 2025 ·Developmental Medicine & Child Neurology ·(unknown), (unknown), (unknown), (unknown), (unknown), Vedam L. Ramprasad, Sakthivel Murugan, Pradeep Goyal, (unknown), Vivek Jain	0
2	GIS based landslide susceptibility mapping and assessment using weighted overlay method in Wayanad: A part of Western Ghats, Kerala 2023 ·Urban Climate ·(unknown), (unknown), Sampathkumar Velusamy, Manoj Shanmugamoorthy, Sakthivel Murugan	27
3	Early-infantile developmental and epileptic encephalopathy: the aetiologies, phenotypic differences and outcomes—a prospective observational study 2023 ·Brain Communications ·(unknown), (unknown), (unknown), Nilesh Kurwale, (unknown), (unknown), (unknown), Vedam L. Ramprasad, Sakthivel Murugan, (unknown), Pradeep Goyal, Vivek Jain	5
4	Solar Energy Forecasting Using Machine Learning and Deep Learning Techniques 2023 ·Archives of Computational Methods in Engineering ·(unknown), (unknown), Sakthivel Murugan, M. S. P. Subathra, (unknown)	22
5	Metabolic and Genetic Evaluation in Children with Nephrolithiasis 2022 ·The Indian Journal of Pediatrics ·(unknown), Priyanka Khandelwal, (unknown), Sakthivel Murugan, Jitendra Meena, Manisha Jana, Aditi Sinha, (unknown), Amlesh Seth, Pankaj Hari, Arvind Bagga	4
6	Growth and neurodevelopmental disorder with arthrogryposis, microcephaly and structural brain anomalies caused by Bi-allelic partial deletion of SMPD4 gene 2021 ·Journal of Human Genetics ·Sunita Bijarnia‐Mahay, (unknown), Parneet Kaur, (unknown), Vedam L. Ramprasad, Sakthivel Murugan, (unknown), Anju Shukla	5
7	Retinoblastoma genetics screening and clinical management 2021 ·BMC Medical Genomics ·Himika Gupta, Sivasankar Malaichamy, Ashwin Mallipatna, Sakthivel Murugan, Nallathambi Jeyabalan, (unknown), Anuprita Ghosh, Arkasubhra Ghosh, Sam Santhosh, Somasekar Seshagiri, Vedam L. Ramprasad, Govindasamy Kumaramanickavel	9
8	Seven novel genetic variants in a North Indian cohort with classical homocystinuria 2020 ·Scientific Reports ·(unknown), Savita Verma Attri, Arushi Gahlot Saini, Naveen Sankhyan, Satwinder Singh, Mohammed Faruq, Vedam L. Ramprasad, Sheetal Sharda, Sakthivel Murugan	6
9	Whole genome enrichment approach for rapid detection of Mycobacterium tuberculosis and drug resistance-associated mutations from direct sputum sequencing 2020 ·Tuberculosis ·(unknown), Priti Kambli, (unknown), (unknown), Sakthivel Murugan, (unknown), Jeffrey A. Tornheim, Camilla Rodrigues, Ravi Gupta, Vedam L. Ramprasad	23
10	Infantile spasms: Etiology, lead time and treatment response in a resource limited setting 2020 ·Epilepsy & Behavior Reports ·(unknown), Joseph D. Symonds, (unknown), (unknown), (unknown), (unknown), Sakthivel Murugan, (unknown), Vivek Bhargava, Pradeep Goyal, Sameer M. Zuberi, Vivek Jain	28
11	Mutational Landscape of Esophageal Squamous Cell Carcinoma in an Indian Cohort 2020 ·Frontiers in Oncology ·Kiran K. Mangalaparthi, Krishna Patel, Aafaque Ahmad Khan, (unknown), Karunakaran Coral, Sakthivel Murugan, Ravi Gupta, Rohit Gupta, Arati Khanna‐Gupta, Amitabha Chaudhuri, Prashant Kumar, (unknown), Rekha V. Kumar, Thottethodi Subrahmanya Keshava Prasad, Aditi Chatterjee, Akhilesh Pandey, Harsha Gowda	20
12	A newly recognized multiple malformation syndrome with caudal regression associated with a biallelic c.402G>A variant in TBX4 2020 ·European Journal of Human Genetics ·Prajnya Ranganath, (unknown), (unknown), (unknown), Aparna Shankar, Sakthivel Murugan, Ashwin Dalal	9
13	Next-Generation Sequencing in a Cohort of Asian Indian Patients with the Duchenne Muscular Dystrophy Phenotype: Diagnostic Yield and Mutation Spectrum 2020 ·Journal of Pediatric Genetics ·(unknown), Prajnya Ranganath, Sakthivel Murugan	5
14	Immunodeficiency, Motor Delay, and Hypouricemia Caused by a Novel Mutation of Purine Nucleoside Phosphorylase Gene in an Indian Infant 2018 ·Annals of Indian Academy of Neurology ·(unknown), Lokesh Lingappa, Ramesh Konanki, (unknown), Vedam L. Ramprasad, Sakthivel Murugan	5
15	A neoepitope derived from a novel human germline APC gene mutation in familial adenomatous polyposis shows selective immunogenicity 2018 ·PLoS ONE ·(unknown), (unknown), (unknown), Yogesh Mistry, (unknown), Priyanka Shah, (unknown), Bharti Mittal, (unknown), Sakthivel Murugan, Lakshmi Shree Kulumani Mahadevan, (unknown), (unknown), Papia Chakraborty, Ravi Gupta, Amitabha Chaudhuri, Arati Khanna‐Gupta	4
16	Asparagine Synthetase deficiency-report of a novel mutation and review of literature 2017 ·Metabolic Brain Disease ·Neerja Gupta, (unknown), Manoj Kumar, (unknown), Aditi Gupta, Pallavi Mishra, Punit Kaur, Vedam L. Ramprasad, Sakthivel Murugan, (unknown), Manisha Jana, Madhulika Kabra	23
17	A novel splice variant in EMC1 is associated with cerebellar atrophy, visual impairment, psychomotor retardation with epilepsy 2017 ·Molecular Genetics & Genomic Medicine ·(unknown), Lokesh Lingappa, (unknown), (unknown), (unknown), Sakthivel Murugan, Ravi Gupta, Vedam L. Ramprasad	31
18	Underwater Acoustic Modem- Challenges, Technology and Applications - A Review Survey 2017 ·Oceanography & Fisheries Open access Journal ·Sakthivel Murugan	4
19	A splice site mutation in HERC1 leads to syndromic intellectual disability with macrocephaly and facial dysmorphism: Further delineation of the phenotypic spectrum 2016 ·American Journal of Medical Genetics Part A ·Shagun Aggarwal, Aneek Das Bhowmik, Vedam L. Ramprasad, Sakthivel Murugan, Ashwin Dalal	29
20	Retinoblastoma in India 2007 ·Molecular Diagnosis & Therapy ·Vedam L. Ramprasad, Jagadeesan Madhavan, Sakthivel Murugan, Sujatha Jagadeesh, Suresh Seshadri, Tarun Sharma, Govindasamy Kumaramanickavel	12

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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