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One or more keywords matched the following items that are connected to Nath, Swapan
Item TypeName
Concept Chromosome Aberrations
Concept Chromosome Mapping
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 10
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 16
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 18
Concept Chromosomes, Human, Pair 19
Concept Chromosomes, Human, Pair 3
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 7
Concept Chromosomes, Human, Pair 8
Concept Physical Chromosome Mapping
Concept Chromosome Duplication
Academic Article Evidence for a susceptibility gene, SLEV1, on chromosome 17p13 in families with vitiligo-related systemic lupus erythematosus.
Academic Article SLEB3 in systemic lupus erythematosus (SLE) is strongly related to SLE families ascertained through neuropsychiatric manifestations.
Academic Article Evidence for a susceptibility gene (SLEH1) on chromosome 11q14 for systemic lupus erythematosus (SLE) families with hemolytic anemia.
Academic Article Linkage at 12q24 with systemic lupus erythematosus (SLE) is established and confirmed in Hispanic and European American families.
Academic Article Autosomal dominant nonsyndromic cleft lip and palate: significant evidence of linkage at 18q21.1.
Academic Article Genome-wide association scan of Dupuytren's disease.
Academic Article A candidate region on 11p13 for systemic lupus erythematosus: a linkage identified in African-American families.
Academic Article Mapping the systematic lupus erythematosus susceptibility genes.
Academic Article Systemic lupus erythematosus susceptibility loci defined by genome scan meta-analysis.
Academic Article Linkage at 5q14.3-15 in multiplex systemic lupus erythematosus pedigrees stratified by autoimmune thyroid disease.
Academic Article Split-hand/split-foot malformation 3 (SHFM3) at 10q24, development of rapid diagnostic methods and gene expression from the region.
Academic Article 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.
Academic Article Localization of a gene for keratoconus to a 5.6-Mb interval on 13q32.
Academic Article Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21.
Academic Article Genetic linkage of systemic lupus erythematosus with chromosome 11q14 (SLEH1) in African-American families stratified by a nucleolar antinuclear antibody pattern.
Academic Article 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).
Academic Article Linkage analysis of SLE susceptibility: confirmation of SLER1 at 5p15.3.
Academic Article Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region.
Academic Article Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele.
Academic Article Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production.
Academic Article Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4.
Academic Article Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription.
Academic Article Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects.
Academic Article Two-trait-locus linkage analyses of asthma susceptibility.
Academic Article Comparison of three methods for obtaining principal components from family data in genetic analysis of complex disease.
Academic Article Thrombocytopenia identifies a severe familial phenotype of systemic lupus erythematosus and reveals genetic linkages at 1q22 and 11p13.
Academic Article Stratification of pedigrees multiplex for systemic lupus erythematosus and for self-reported rheumatoid arthritis detects a systemic lupus erythematosus susceptibility gene (SLER1) at 5p15.3.
Academic Article Systemic lupus erythematosus (SLE) and chromosome 16: confirmation of linkage to 16q12-13 and evidence for genetic heterogeneity.
Academic Article Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34.
Academic Article Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
Academic Article A nonsynonymous functional variant in integrin-alpha(M) (encoded by ITGAM) is associated with systemic lupus erythematosus.
Academic Article Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing.
Academic Article Fine-mapping and transethnic genotyping establish IL2/IL21 genetic association with lupus and localize this genetic effect to IL21.
Academic Article Identification of novel suggestive loci for high-grade myopia in Polish families.
Academic Article Genome-Wide Association Study in an Amerindian Ancestry Population Reveals Novel Systemic Lupus Erythematosus Risk Loci and the Role of European Admixture.
Academic Article miR-125b promotes cell death by targeting spindle assembly checkpoint gene MAD1 and modulating mitotic progression.
Search Criteria
  • Chromosomes Human Pair 1