about
GENLIB: an R package for the analysis of genealogical dataIsolated populations and complex disease gene identificationGenetic studies of the Roma (Gypsies): a reviewConstrained spherical deconvolution-based tractography and tract-based spatial statistics show abnormal microstructural organization in Asperger syndromeABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosisA population-specific HTR2B stop codon predisposes to severe impulsivitySerial audiometry and speech recognition findings in Finnish Usher syndrome type III patientsThe spectrum of SLC17A5-gene mutations resulting in free sialic acid-storage diseases indicates some genotype-phenotype correlation.GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1LA genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyX-linked retinoschisis: an updateGenetics of impulsive behaviourReplication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia familiesGenetics of hypertrophic cardiomyopathy in eastern Finland: few founder mutations with benign or intermediary phenotypesInfantile onset spinocerebellar ataxia is caused by recessive mutations in mitochondrial proteins Twinkle and TwinkyA genome-wide search for alleles and haplotypes associated with autism and related pervasive developmental disorders on the Faroe IslandsSearching for Grendel: origin and global spread of the C9ORF72 repeat expansionThe genome-wide patterns of variation expose significant substructure in a founder populationASPM is a major determinant of cerebral cortical sizeVariance in disease risk: rural populations and genetic diversity.The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population.A system for specific, high-throughput genotyping by allele-specific primer extension on microarrays.Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland.Detecting population growth, selection and inherited fertility from haplotypic data in humans.Constrained hidden Markov models for population-based haplotyping.Genetic influences on hand osteoarthritis in Finnish women--a replication study of candidate genesX-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypesLinkage analysis of schizophrenia controlling for population substructure.Saturation of the human phenomeMutation history of the roma/gypsies.A population-specific reference panel empowers genetic studies of Anabaptist populations.Antenatal gene tests in low-risk pregnancies: molecular screening for aspartylglucosaminuria (AGU) and infantile neuronal ceroid lipofuscinosis (INCL) in Finland.Population-genetic comparison of the Sorbian isolate population in Germany with the German KORA population using genome-wide SNP arraysFine-scale estimation of location of birth from genome-wide single-nucleotide polymorphism dataTwo exonic single nucleotide polymorphisms in the microsomal epoxide hydrolase gene are jointly associated with preeclampsia.The extent of linkage disequilibrium in four populations with distinct demographic histories.Assignment of a novel locus for autosomal recessive congenital ichthyosis to chromosome 19p13.1-p13.2.Founder population-specific HapMap panel increases power in GWA studies through improved imputation accuracy and CNV tagging.Variations in the TNFα gene and their interactions with the IL4R and IL10 genes in relation to hand osteoarthritis.
P2860
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P2860
description
1999 nî lūn-bûn
@nan
1999 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年論文
@yue
1999年論文
@zh-hant
1999年論文
@zh-hk
1999年論文
@zh-mo
1999年論文
@zh-tw
1999年论文
@wuu
name
Molecular genetics of the Finnish disease heritage.
@ast
Molecular genetics of the Finnish disease heritage.
@en
type
label
Molecular genetics of the Finnish disease heritage.
@ast
Molecular genetics of the Finnish disease heritage.
@en
prefLabel
Molecular genetics of the Finnish disease heritage.
@ast
Molecular genetics of the Finnish disease heritage.
@en
P356
P1476
Molecular genetics of the Finnish disease heritage
@en
P2093
P304
P356
10.1093/HMG/8.10.1913
P50
P577
1999-01-01T00:00:00Z