Swapan Nath to Phenotype
This is a "connection" page, showing publications Swapan Nath has written about Phenotype.
Connection Strength
0.493
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PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes. PLoS One. 2013; 8(8):e69404.
Score: 0.092
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Gene network analysis of small molecules with autoimmune disease associated genes predicts a novel strategy for drug efficacy. Autoimmun Rev. 2013 Feb; 12(4):510-22.
Score: 0.086
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Confirmation of an association between rs6822844 at the Il2-Il21 region and multiple autoimmune diseases: evidence of a general susceptibility locus. Arthritis Rheum. 2010 Feb; 62(2):323-9.
Score: 0.072
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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: 0.041
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Biallelic variants in KARS1 are associated with neurodevelopmental disorders and hearing loss recapitulated by the knockout zebrafish. Genet Med. 2021 10; 23(10):1933-1943.
Score: 0.040
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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: 0.029
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Expanding the spectrum of ?-secretase gene mutation-associated phenotypes: two novel mutations segregating with familial hidradenitis suppurativa (acne inversa) and acne conglobata. Exp Dermatol. 2016 Apr; 25(4):314-6.
Score: 0.027
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Genetic epidemiology of vitiligo: multilocus recessivity cross-validated. Am J Hum Genet. 1994 Nov; 55(5):981-90.
Score: 0.025
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Rh segregation distortion: an artifact of ascertainment bias? Am J Hum Genet. 1992 Jun; 50(6):1328-32.
Score: 0.021
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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: 0.019
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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: 0.017
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Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis. Am J Med Genet A. 2006 Jul 01; 140(13):1440-6.
Score: 0.014
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Thrombocytopenia identifies a severe familial phenotype of systemic lupus erythematosus and reveals genetic linkages at 1q22 and 11p13. Blood. 2003 Feb 01; 101(3):992-7.
Score: 0.011