Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distributionCommon genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studiesGenetic structure of Europeans: a view from the North-EastMutations in ATP2A2, encoding a Ca2+ pump, cause Darier diseaseGenome-wide association defines more than 30 distinct susceptibility loci for Crohn's diseaseGenome-wide association study of glioma and meta-analysisImputation and subset based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairmentsMutations in the gene encoding SLURP-1 in Mal de MeledaMutations in CERS3 cause autosomal recessive congenital ichthyosis in humansPhenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controlsPNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humansCCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogsSHANK1 Deletions in Males with Autism Spectrum DisorderMutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathologyCombined analysis of three genome-wide association studies on vWF and FVIII plasma levelsHLA antigens and seronegative rheumatoid arthritis.A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT projectMutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndromeRefined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region.Common variants at 30 loci contribute to polygenic dyslipidemiaCommon variants at five new loci associated with early-onset inflammatory bowel diseaseInternational network of cancer genome projects.Isolation and mapping of a polymorphic DNA sequence (pMCT108.2) on chromosome 18 [D18S24]Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskBlood pressure loci identified with a gene-centric arrayHundreds of variants clustered in genomic loci and biological pathways affect human heightCoordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigreesGenome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorderGenetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosisGenome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemiaThe European dimension for the mouse genome mutagenesis programLung cancer susceptibility locus at 5p15.33Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathwaysA genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinomaEvaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistypingA novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness lociFamilial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16
P50
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P50
description
Canadees onderzoeker
@nl
Canadian scientist
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Canadian scientist
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Canadian scientist
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eolaí Ceanadach
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investigador canadianu
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investigador canadiense
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kanadischer Forscher
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عالم كندي
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name
Mark Lathrop
@ast
Mark Lathrop
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Mark Lathrop
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Mark Lathrop
@de
Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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type
label
Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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altLabel
G M Lathrop
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G Mark Lathrop
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G. M. Lathrop
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G. Mark Lathrop
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Lathrop G. M.
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Lathrop G.
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Lathrop GM
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Lathrop M
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Lathrop M.
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Lathrop
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prefLabel
Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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Mark Lathrop
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1950-01-01T00:00:00Z
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