Swapan Nath to Pedigree
This is a "connection" page, showing publications Swapan Nath has written about Pedigree.
Connection Strength
0.712
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Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing. Invest Ophthalmol Vis Sci. 2011 Aug 29; 52(9):6814-9.
Score: 0.093
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Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34. Am J Hum Genet. 2006 Sep; 79(3):580-5.
Score: 0.066
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Linkage at 5q14.3-15 in multiplex systemic lupus erythematosus pedigrees stratified by autoimmune thyroid disease. Arthritis Rheum. 2005 Nov; 52(11):3646-50.
Score: 0.062
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Genetics of human systemic lupus erythematosus: the emerging picture. Curr Opin Immunol. 2004 Dec; 16(6):794-800.
Score: 0.059
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Linkage analysis of SLE susceptibility: confirmation of SLER1 at 5p15.3. Genes Immun. 2004 May; 5(3):209-14.
Score: 0.056
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Mapping the systematic lupus erythematosus susceptibility genes. Methods Mol Med. 2004; 102:11-29.
Score: 0.055
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SLEB3 in systemic lupus erythematosus (SLE) is strongly related to SLE families ascertained through neuropsychiatric manifestations. Hum Genet. 2002 Jul; 111(1):54-8.
Score: 0.049
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Evidence for a susceptibility gene, SLEV1, on chromosome 17p13 in families with vitiligo-related systemic lupus erythematosus. Am J Hum Genet. 2001 Dec; 69(6):1401-6.
Score: 0.047
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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: 0.024
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. J Med Genet. 2012 Apr; 49(4):270-6.
Score: 0.024
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Identification of novel suggestive loci for high-grade myopia in Polish families. Mol Vis. 2011; 17:2028-39.
Score: 0.023
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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: 0.019
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Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1. Am J Hum Genet. 2007 Jul; 81(1):180-8.
Score: 0.017
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Current status of lupus genetics. Arthritis Res Ther. 2007; 9(3):210.
Score: 0.017
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Genomewide linkage scan for split-hand/foot malformation with long-bone deficiency in a large Arab family identifies two novel susceptibility loci on chromosomes 1q42.2-q43 and 6q14.1. Am J Hum Genet. 2007 Jan; 80(1):105-11.
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: 0.016
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Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region. Am J Med Genet A. 2006 Jul 01; 140(13):1384-95.
Score: 0.016
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Genetic linkage of systemic lupus erythematosus with chromosome 11q14 (SLEH1) in African-American families stratified by a nucleolar antinuclear antibody pattern. Genes Immun. 2002 Oct; 3 Suppl 1:S31-4.
Score: 0.013
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Genome scan stratified by the presence of anti-double-stranded DNA (dsDNA) autoantibody in pedigrees multiplex for systemic lupus erythematosus (SLE) establishes linkages at 19p13.2 (SLED1) and 18q21.1 (SLED2). Genes Immun. 2002 Oct; 3 Suppl 1:S35-41.
Score: 0.013
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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: 0.013
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Evidence for a susceptibility gene (SLEH1) on chromosome 11q14 for systemic lupus erythematosus (SLE) families with hemolytic anemia. Proc Natl Acad Sci U S A. 2002 Sep 03; 99(18):11766-71.
Score: 0.012