Swapan Nath to Middle Aged
This is a "connection" page, showing publications Swapan Nath has written about Middle Aged.
Connection Strength
0.400
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Impaired Molecular Mechanisms Contributing to Chronic Pain in Patients with Hidradenitis Suppurativa: Exploring Potential Biomarkers and Therapeutic Targets. Int J Mol Sci. 2025 Jan 25; 26(3).
Score: 0.108
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The intravenous adenosine test: a new test for the identification of bradycardia pacing indications? A pilot study in subjects with bradycardia pacing indications, vasovagal syncope and controls. QJM. 2009 Jul; 102(7):461-8.
Score: 0.036
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Empyema thoracis. Kathmandu Univ Med J (KUMJ). 2007 Oct-Dec; 5(4):521-5.
Score: 0.033
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Segregation analysis of blood pressure and body mass index in a rural US community. Hum Biol. 2002 Feb; 74(1):11-23.
Score: 0.022
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Impact of functional IL-18 polymorphisms on genetic predisposition and diverse clinical manifestations of the disease in Indian SLE patients. Lupus. 2019 Apr; 28(4):545-554.
Score: 0.018
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A Rare Variant (rs933717) at FBXO31-MAP1LC3B in Chinese Is Associated With Systemic Lupus Erythematosus. Arthritis Rheumatol. 2018 02; 70(2):287-297.
Score: 0.017
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Genotype-Phenotype Study of the Middle Gangetic Plain in India Shows Association of rs2470102 with Skin Pigmentation. J Invest Dermatol. 2017 03; 137(3):670-677.
Score: 0.015
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Novel identified associations of RGS1 and RASGRP1 variants in IgA Nephropathy. Sci Rep. 2016 11 02; 6:35781.
Score: 0.015
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Association of variants in CCR6 with susceptibility to lupus nephritis in Chinese. Arthritis Rheumatol. 2015 Nov; 67(11):3091-3.
Score: 0.014
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GDF15(MIC1) H6D Polymorphism Does Not Influence Cardiovascular Disease in a Latin American Population with Rheumatoid Arthritis. J Immunol Res. 2015; 2015:270763.
Score: 0.014
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Genetic epidemiology of vitiligo: multilocus recessivity cross-validated. Am J Hum Genet. 1994 Nov; 55(5):981-90.
Score: 0.013
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High-density genotyping of immune loci in Koreans and Europeans identifies eight new rheumatoid arthritis risk loci. Ann Rheum Dis. 2015 Mar; 74(3):e13.
Score: 0.013
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Novel homozygous, heterozygous and hemizygous FRMD7 gene mutations segregated in the same consanguineous family with congenital X-linked nystagmus. Eur J Hum Genet. 2012 Oct; 20(10):1032-6.
Score: 0.011
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Right hemicolectomy is not routinely indicated in pseudomyxoma peritonei. Am Surg. 2012 Feb; 78(2):171-7.
Score: 0.011
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Genome-wide association scan of Dupuytren's disease. J Hand Surg Am. 2010 Dec; 35(12):2039-45.
Score: 0.010
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Early disease onset is predicted by a higher genetic risk for lupus and is associated with a more severe phenotype in lupus patients. Ann Rheum Dis. 2011 Jan; 70(1):151-6.
Score: 0.010
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Replication of association between a common variant near melanocortin-4 receptor gene and obesity-related traits in Asian Sikhs. Obesity (Silver Spring). 2010 Feb; 18(2):425-9.
Score: 0.009
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Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32. Invest Ophthalmol Vis Sci. 2009 Apr; 50(4):1531-9.
Score: 0.009
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Impact of nine common type 2 diabetes risk polymorphisms in Asian Indian Sikhs: PPARG2 (Pro12Ala), IGF2BP2, TCF7L2 and FTO variants confer a significant risk. BMC Med Genet. 2008 Jul 03; 9:59.
Score: 0.009
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TCF7L2 polymorphisms are associated with type 2 diabetes in Khatri Sikhs from North India: genetic variation affects lipid levels. Ann Hum Genet. 2008 Jul; 72(Pt 4):499-509.
Score: 0.008
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Sustained wide complex tachycardia resulting in myocardial injury in a patient with apical hypertrophic cardiomyopathy. Pacing Clin Electrophysiol. 1997 Jul; 20(7):1866-9.
Score: 0.004