Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)
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Systematic association mapping identifies NELL1 as a novel IBD disease genePopulation structure and eigenanalysisPolymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryEvidence of a linkage between matrilin-1 gene (MATN1) and idiopathic scoliosisThe serotonin 1A receptor C(-1019)G polymorphism in relation to suicide attemptAssociation study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotypingExamination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genesGenome-wide association study of bipolar disorder in Canadian and UK populations corroborates disease loci including SYNE1 and CSMD1Are rare variants responsible for susceptibility to complex diseases?Tests and estimates of allelic association in complex inheritanceMissense mutations in the MEFV gene are associated with fibromyalgia syndrome and correlate with elevated IL-1beta plasma levelsStrong evidence of linkage disequilibrium between polymorphisms at the IRF6 locus and nonsyndromic cleft lip with or without cleft palate, in an Italian population.Genetic variation at the 22q11 PRODH2/DGCR6 locus presents an unusual pattern and increases susceptibility to schizophreniaPolymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree seriesStudies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United KingdomA sibship test for linkage in the presence of association: the sib transmission/disequilibrium testAssociation of MSX1 and TGFB3 with nonsyndromic clefting in humansA genomic screen of autism: evidence for a multilocus etiology.A fifth locus for Bardet-Biedl syndrome maps to chromosome 2q31The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysmsAn allele of IKZF1 (Ikaros) conferring susceptibility to childhood acute lymphoblastic leukemia protects against type 1 diabetesGenetics and visceral leishmaniasis: of mice and manNeuregulin 1 and susceptibility to schizophrenia.Genetic variations in the receptor-ligand pair CCR5 and CCL3L1 are important determinants of susceptibility to Kawasaki diseaseThe role of the GABRA2 polymorphism in multiplex alcohol dependence families with minimal comorbidity: within-family association and linkage analysesCorrelated genotypes in friendship networksMaternal genetic effects, exerted by genes involved in homocysteine remethylation, influence the risk of spina bifidaA polymorphism, R653Q, in the trifunctional enzyme methylenetetrahydrofolate dehydrogenase/methenyltetrahydrofolate cyclohydrolase/formyltetrahydrofolate synthetase is a maternal genetic risk factor for neural tube defects: report of the Birth DefecFine mapping on chromosome 10q22-q23 implicates Neuregulin 3 in schizophreniaA human type 1 diabetes susceptibility locus maps to chromosome 21q22.3The human GIMAP5 gene has a common polyadenylation polymorphism increasing risk to systemic lupus erythematosusAssociation of the oxytocin receptor gene (OXTR) in Caucasian children and adolescents with autismHigh throughput SNP and expression analyses of candidate genes for non-syndromic oral cleftsThe transmission/disequilibrium test: history, subdivision, and admixtureEvidence for linkage disequilibrium in chromosome 13-linked Duchenne-like muscular dystrophy (LGMD2C)Aryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetesThe TDT and other family-based tests for linkage disequilibrium and associationGenomewide scan for linkage reveals evidence of several susceptibility loci for alopecia areataIL-23 receptor (IL-23R) gene protects against pediatric Crohn's disease
P2860
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P2860
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)
description
1993 nî lūn-bûn
@nan
1993 թուականի Մարտին հրատարակուած գիտական յօդուած
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1993 թվականի մարտին հրատարակված գիտական հոդված
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1993年の論文
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1993年学术文章
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1993年学术文章
@zh-cn
1993年学术文章
@zh-hans
1993年学术文章
@zh-my
1993年学术文章
@zh-sg
1993年學術文章
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name
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@ast
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@en
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@nl
type
label
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@ast
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@en
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@nl
prefLabel
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@ast
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@en
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@nl
P2093
P2860
P3181
P1476
Transmission test for linkage ...... ndent diabetes mellitus (IDDM)
@en
P2093
R E McGinnis
R S Spielman
P2860
P304
P3181
P407
P577
1993-03-01T00:00:00Z