about
Current limitations of SNP data from the public domain for studies of complex disorders: a test for ten candidate genes for obesity and osteoporosisGenomewide significant linkage to stuttering on chromosome 12.Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locusA locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10Paget disease of bone: mapping of two loci at 5q35-qter and 5q31.Handling marker-marker linkage disequilibrium: pedigree analysis with clustered markersFunctional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence.Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample.A mutation in the LDL receptor-related protein 5 gene results in the autosomal dominant high-bone-mass traitWaardenburg syndrome (WS) type I is caused by defects at multiple loci, one of which is near ALPP on chromosome 2: first report of the WS consortiumThe gene for autosomal dominant craniometaphyseal dysplasia maps to chromosome 5p and is distinct from the growth hormone-receptor genePharmacogenetic association of the APOA1/C3/A4/A5 gene cluster and lipid responses to fenofibrate: the genetics of lipid-lowering drugs and diet network studyDescription of the data from the Collaborative Study on the Genetics of Alcoholism (COGA) and single-nucleotide polymorphism genotyping for Genetic Analysis Workshop 14Chromosome 18 DNA markers and manic-depressive illness: evidence for a susceptibility geneGenome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22.Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependenceAssociation of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependenceA genomewide search finds major susceptibility loci for gallbladder disease on chromosome 1 in Mexican Americans.Statistical tests for detection of misspecified relationships by use of genome-screen data.PedGenie: an analysis approach for genetic association testing in extended pedigrees and genealogies of arbitrary size.Design considerations in a sib-pair study of linkage for susceptibility loci in cancer.Diabetes-specific genetic effects on obesity traits in American Indian populations: the Strong Heart Family StudyAn evaluation of inflammatory gene polymorphisms in sibships discordant for premature coronary artery disease: the GRACE-IMMUNE studyA genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish.Genome-wide linkage analysis of carotid artery lumen diameter: the strong heart family study.GABRR1 and GABRR2, encoding the GABA-A receptor subunits rho1 and rho2, are associated with alcohol dependenceHaplotype association analyses in resources of mixed structure using Monte Carlo testingA susceptibility locus on chromosome 6q greatly increases lung cancer risk among light and never smokersGenome-wide significant loci for addiction and anxietyA novel non-parametric regression reveals linkage on chromosome 4 for the number of externalizing symptoms in sib-pairs.Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.Genetics of microstructure of cerebral white matter using diffusion tensor imaging.Genome-wide significant localization for working and spatial memory: Identifying genes for psychosis using models of cognition.Two quantitative trait loci influence whipworm (Trichuris trichiura) infection in a Nepalese populationA schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.Linkage analysis of a complex pedigree with severe bipolar disorder, using a Markov chain Monte Carlo method.Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters.Incorporating genotypes of relatives into a test of linkage disequilibriumAutosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11Identification of a novel germline missense mutation of the androgen receptor in African American men with familial prostate cancer.
P2860
Q21283795-BECA817F-7B85-48FF-BB11-14F1935764F6Q24531471-18061A52-6399-4A01-8698-B176FE43A55CQ24531544-CE9A122F-FF86-418B-9F88-8F5E3E33C9FCQ24533527-0FEADF48-870E-4D28-9154-3A73269F6427Q24535825-B8253348-3DA4-4111-80BD-1CE4487308A3Q24535870-17DBDE86-B9A1-4493-A764-EFA703C658A7Q24540485-63BED5C1-3BCF-49CB-A555-0EF69365DF99Q24540539-2D37DE91-592C-4D88-82F0-6F65BC58FCA7Q24561917-369B5FE9-8D0D-4046-8E91-5F1241302783Q24670212-C9FF9C01-CCAD-4950-97F7-0ACE68B5E41DQ24677660-56B556E6-FBBF-4E7B-844B-52C218103ABDQ28302934-FEFC4C8F-1313-4661-B026-1234B5995BD4Q28757788-7F5FD04E-7892-452F-B9B3-8AD4A6FE865FQ28775974-74336E1E-BA98-4305-9F83-F1377D75E9DAQ30368930-E8C49D75-4168-487B-994C-4D476F66E7B3Q30471884-0BF6AF35-90BE-474B-8079-3310B14E5A0CQ30482193-A67B7619-8255-4322-9FDA-FEB5E416B7D6Q30498786-3F4FD765-F2DE-497F-BA4F-162B680003D8Q30587143-56A6B859-0EE5-49C0-81AA-2C451F4A421AQ33240164-DF4C2C27-47A0-45EA-A4FC-85A022CEE75DQ33350691-FDB91225-2390-4302-AE64-F0D4E4662789Q33375836-1267313A-0FF9-4B72-899D-BA8959FBF741Q33523617-D83D0809-CF6E-4EDE-ACB4-DC050E49648EQ33595430-E3830D7B-A688-433D-A692-F79028EB98FBQ33637407-760DB167-5129-4056-8158-6B1C6501EAF7Q33691260-099E3093-F3E5-4379-81DA-703DC6EE69BDQ33766979-2832190B-9C7C-40D8-BA04-004CC5DA4827Q33793537-49F6C4CB-3BBF-461F-A2F7-00A14AFA107EQ33832991-FDC37C12-2AE5-4863-A208-B0B3BF3C65CBQ33888169-655F7219-CF22-4303-8351-041E0D69A53FQ33905879-543E5018-B54B-44A0-A99D-702C33A4B29CQ33925803-DAE4C8BE-3E5F-4A28-A90A-19C2C49C282BQ33930490-1B77271B-A05D-402C-B456-0682265F1108Q34004434-EDB49350-8417-4E5B-A437-C795EFC71EAEQ34020480-FC896B3E-72BC-4CA9-86B7-79C014A86692Q34114601-3F255F4A-260D-4356-BBFB-909D03F59605Q34145558-38C514BD-B3CF-43BA-8BBC-2ED8ADC29DC9Q34384182-43365AE4-53F0-4DC7-BD32-14691C00D307Q34387769-71FAD665-5A87-4597-8CDD-AF793AD9BD7CQ34432522-49CEA6DC-D8B7-4C1F-BF70-AE6DC7D2E882
P2860
description
1991 nî lūn-bûn
@nan
1991 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
1991 թվականի հունվարին հրատարակված գիտական հոդված
@hy
1991年の論文
@ja
1991年論文
@yue
1991年論文
@zh-hant
1991年論文
@zh-hk
1991年論文
@zh-mo
1991年論文
@zh-tw
1991年论文
@wuu
name
Allele frequency estimation from data on relatives
@ast
Allele frequency estimation from data on relatives
@en
Allele frequency estimation from data on relatives.
@nl
type
label
Allele frequency estimation from data on relatives
@ast
Allele frequency estimation from data on relatives
@en
Allele frequency estimation from data on relatives.
@nl
prefLabel
Allele frequency estimation from data on relatives
@ast
Allele frequency estimation from data on relatives
@en
Allele frequency estimation from data on relatives.
@nl
P2860
P1476
Allele frequency estimation from data on relatives
@en
P2093
P2860
P407
P577
1991-01-01T00:00:00Z