Pages that link to "Q6768494"
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The following pages link to Mark Lathrop (Q6768494):
Displayed 50 items.
- Wellcome Centre for Human Genetics (Q7981196) (← links)
- Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution (Q21092459) (← links)
- Common genetic variation near the phospholamban gene is associated with cardiac repolarisation: meta-analysis of three genome-wide association studies (Q21143760) (← links)
- Genetic structure of Europeans: a view from the North-East (Q21143785) (← links)
- Mutations in ATP2A2, encoding a Ca2+ pump, cause Darier disease (Q22009038) (← links)
- Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease (Q22251067) (← links)
- Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (Q22251069) (← links)
- Genome-wide association study of glioma and meta-analysis (Q23919638) (← links)
- Imputation and subset-based association analysis across different cancer types identifies multiple independent risk loci in the TERT-CLPTM1L region on chromosome 5p15.33 (Q23924183) (← links)
- Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments (Q23936599) (← links)
- Mutations in the gene encoding SLURP-1 in Mal de Meleda (Q24291082) (← links)
- Mutations in CERS3 cause autosomal recessive congenital ichthyosis in humans (Q24294868) (← links)
- Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls (Q24300678) (← links)
- PNPLA1 mutations cause autosomal recessive congenital ichthyosis in golden retriever dogs and humans (Q24301980) (← links)
- CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs (Q24312161) (← links)
- SHANK1 Deletions in Males with Autism Spectrum Disorder (Q24313471) (← links)
- Mutations in the transporter ABCA12 are associated with lamellar ichthyosis type 2 (Q24315044) (← links)
- Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology (Q24316259) (← links)
- Combined analysis of three genome-wide association studies on vWF and FVIII plasma levels (Q24318690) (← links)
- HLA antigens and seronegative rheumatoid arthritis (Q24514541) (← links)
- A genomewide exploration suggests a new candidate gene at chromosome 11q23 as the major determinant of plasma homocysteine levels: results from the GAIT project (Q24530955) (← links)
- Mutations in CGI-58, the gene encoding a new protein of the esterase/lipase/thioesterase subfamily, in Chanarin-Dorfman syndrome (Q24536104) (← links)
- Refined 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 (Q24538880) (← links)
- Common variants at 30 loci contribute to polygenic dyslipidemia (Q24598765) (← links)
- Common variants at five new loci associated with early-onset inflammatory bowel disease (Q24600801) (← links)
- International network of cancer genome projects (Q24611474) (← links)
- Isolation and mapping of a polymorphic DNA sequence (pMCT108.2) on chromosome 18 [D18S24] (Q24613472) (← links)
- Genome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controls (Q24628710) (← links)
- Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk (Q24630394) (← links)
- Blood pressure loci identified with a gene-centric array (Q24630508) (← links)
- Hundreds of variants clustered in genomic loci and biological pathways affect human height (Q24630979) (← links)
- Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigrees (Q24633174) (← links)
- Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder (Q24634497) (← links)
- Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (Q24635370) (← links)
- Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia (Q24643127) (← links)
- The European dimension for the mouse genome mutagenesis program (Q24644441) (← links)
- Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants (Q24646663) (← links)
- Lung cancer susceptibility locus at 5p15.33 (Q24649980) (← links)
- Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways (Q24653432) (← links)
- A genome-wide association study of lung cancer identifies a region of chromosome 5p15 associated with risk for adenocarcinoma (Q24657797) (← links)
- Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping (Q24675178) (← links)
- A novel locus for autosomal dominant nonsyndromic hearing loss, DFNA50, maps to chromosome 7q32 between the DFNB17 and DFNB13 deafness loci (Q24675917) (← links)
- Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16 (Q24678116) (← links)
- A detailed multipoint map of human chromosome 4 provides evidence for linkage heterogeneity and position-specific recombination rates (Q24679121) (← links)
- Strategies for multilocus linkage analysis in humans (Q27860521) (← links)
- A comprehensive genetic map of the human genome based on 5,264 microsatellites (Q27860812) (← links)
- EIF2AK3, encoding translation initiation factor 2-alpha kinase 3, is mutated in patients with Wolcott-Rallison syndrome (Q28142981) (← links)
- Lymphotoxin-alpha gene and risk of myocardial infarction in 6,928 cases and 2,712 controls in the ISIS case-control study (Q28199426) (← links)
- A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29 (Q28217708) (← links)
- European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy (Q28241180) (← links)