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| 27461236 | A family-based genome-wide association study reveals an association of spondyloarthritis with MAPK14. | Ann Rheum Dis | 2017 |
| 27519970 | Variations of SOST mRNA expression in human bone are associated with DNA polymorphism and DNA methylation in the SOST gene. | | 2016 |
| 25778476 | A novel Alzheimer disease locus located near the gene encoding tau protein. | Mol Psychiatry | 2016 |
| 27266705 | Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia. | BMC Genet | 2016 |
| 26275432 | Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13. | Ann Rheum Dis | 2016 |
| 26633630 | Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma. | Nature | 2016 |
| 26068201 | TCF12 is mutated in anaplastic oligodendroglioma. | Nat Commun | 2015 |
| 25420145 | Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection. | Nat Genet | 2015 |
| 26301497 | Genetic association analyses highlight biological pathways underlying mitral valve prolapse. | Nat Genet | 2015 |
| 26156739 | Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trial. | Am J Clin Nutr | 2015 |
| 24922517 | Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease. | PLoS One | 2014 |
| 25261932 | Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma. | Nat Genet | 2014 |
| 23892592 | Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families. | J Invest Dermatol | 2014 |
| 23756445 | AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome). | Eur J Hum Genet | 2014 |
| 25188300 | Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments. | PLoS Genet | 2014 |
| 24716566 | Association between circadian genes, bipolar disorders and chronotypes. | Chronobiol Int | 2014 |
| 25111785 | Common and rare variant analysis in early-onset bipolar disorder vulnerability. | PLoS One | 2014 |
| 25069958 | Global genetic architecture of an erythroid quantitative trait locus, HMIP-2. | Ann Hum Genet | 2014 |
| 23708188 | Combined sequence-based and genetic mapping analysis of complex traits in outbred rats. | Nat Genet | 2013 |
| 24162737 | Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease. | Nat Genet | 2013 |
| 23937567 | Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus. | Annals of Human Genetics | 2013 |
| 23876493 | Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls. | Circ Cardiovasc Genet | 2013 |
| 23874506 | CpG methylation changes within the IL2RA promoter in type 1 diabetes of childhood onset. | PLoS ONE | 2013 |
| 23603762 | Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly. | Nature Genetics | 2013 |
| 23404349 | Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms. | Cancer Causes and Control | 2013 |
| 23399914 | Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology. | Mol Psychiatry | 2013 |
| 23399484 | Deciphering the 8q24.21 association for glioma. | Hum Mol Genet | 2013 |
| 23680914 | Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice. | Diabetologia | 2013 |
| 23583980 | Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis. | Nat Genet | 2013 |
| 23297363 | Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. | Hum Mol Genet | 2013 |
| 23455637 | A variant in FTO shows association with melanoma risk not due to BMI. | Nat Genet | 2013 |
| 23455636 | Seven new loci associated with age-related macular degeneration. | Nat Genet | 2013 |
| 23571737 | Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222. | Br J Cancer | 2013 |
| 23708191 | Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16. | Nat Genet | 2013 |
| 22262880 | Genetic variants of FOXP2 and KIAA0319/TTRAP/THEM2 locus are associated with altered brain activation in distinct language-related regions. | J Neurosci | 2012 |
| 22939634 | Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. | Am J Hum Genet | 2012 |
| 22479202 | Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals. | PLoS Genet | 2012 |
| 22745674 | Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis. | PLoS One | 2012 |
| 22694956 | Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3. | Hum Mol Genet | 2012 |
| 22346768 | Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders. | PLoS Genet | 2012 |
| 22297974 | Serial translocation by means of circular intermediates underlies colour sidedness in cattle. | Nature | 2012 |
| 22581228 | A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. | Nat Genet | 2012 |
| 22466613 | Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis. | Nat Genet | 2012 |
| 22286212 | Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups. | J Natl Cancer Inst | 2012 |
| 22675575 | Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis. | PLoS One | 2012 |
| 22567146 | Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes. | PLoS One | 2012 |
| 22662130 | Using prior information from the medical literature in GWAS of oral cancer identifies novel susceptibility variant on chromosome 4--the AdAPT method. | PLoS One | 2012 |
| 22443383 | Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project. | Br J Haematol | 2012 |
| 23153393 | High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly. | BMC Genomics | 2012 |
| 22010048 | A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. | Hum Mol Genet | 2012 |