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| 36273371 | Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome. | Clin Genet | 2023 |
| 37366597 | Comparison of regmed and BayesNetty for exploring causal models with many variables. | Genet Epidemiol | 2023 |
| 37026715 | Regulation of immune responses in primary biliary cholangitis: a transcriptomic analysis of peripheral immune cells. | Hepatol Commun | 2023 |
| 36922251 | Corrigendum to: "Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically characterised cohort<sup>â¿¿</sup>" [J Hepatol (2020) 505-515]. | J Hepatol | 2023 |
| 36548480 | Rationale, Design, and the Baseline Characteristics of the RHDGen (The Genetics of Rheumatic Heart Disease) Network Studyâ¿ . | Circ Genom Precis Med | 2023 |
| 36639314 | Corrigendum to: "An international genome-wide meta-analysis of primary biliary cholangitis: Novel risk loci and candidate drugs" [J Hepatol 75 (2021) 572-581]. | J Hepatol | 2023 |
| 34656649 | A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers. | J Hepatol | 2022 |
| 35654975 | A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation. | Nat Genet | 2022 |
| 36371989 | Comprehensive genetic and functional analyses of Fc gamma receptors influence on response to rituximab therapy for autoimmunity. | EBioMedicine | 2022 |
| 36072060 | Confirmation of the superior performance of the causal Graphical Analysis Using Genetics (cGAUGE) pipeline in comparison to various competing alternatives. | Wellcome Open Res | 2022 |
| 35930604 | Investigating the prediction of CpG methylation levels from SNP genotype data to help elucidate relationships between methylation, gene expression and complex traits. | Genet Epidemiol | 2022 |
| 34983928 | Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. | Nat Commun | 2022 |
| 35287983 | Corrigendum to: 'A genetic risk score and diabetes predict development of alcohol-related cirrhosis in drinkers' [J Hepatol 2022 (76) 275-282]. | J Hepatol | 2022 |
| 35285476 | Rare complement factor I variants associated with reduced macular thickness and age-related macular degeneration in the UK Biobank. | Hum Mol Genet | 2022 |
| 34886679 | Common Genetic Variants Contribute to Risk of Transposition of the Great Arteries. | Circ Res | 2022 |
| 34864633 | rs9459874 and rs1012656 in CCR6/FGFR1OP confer susceptibility to primary biliary cholangitis. | J Autoimmun | 2022 |
| 34893828 | No Evidence That Genetic Variation at the Klotho Locus Is Associated With Longevity in Caucasians from the Newcastle 85+ Study and the UK Biobank. | J Gerontol A Biol Sci Med Sci | 2022 |
| 32853455 | Genome-wide Association Study and Meta-analysis on Alcohol-Associated Liver Cirrhosis Identifies Genetic Risk Factors. | Hepatology | 2021 |
| 33678471 | Corrigendum to: "Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically characterised cohort"â¿¿ (J Hepatol [2020] 505-515). | J Hepatol | 2021 |
| 33893282 | Publisher Correction: A meta-analysis of genome-wide association studies identifies multiple longevity genes. | Nat Commun | 2021 |
| 33693626 | Common and Rare Genetic Variants That Could Contribute to Severe Otitis Media in an Australian Aboriginal Population. | Clin Infect Dis | 2021 |
| 33808740 | A <i>PDCD1</i> Role in the Genetic Predisposition to NAFLD-HCC? | Cancers (Basel) | 2021 |
| 33607192 | Rationale and design of the African Cardiomyopathy and Myocarditis Registry Program: The IMHOTEP study. | Int J Cardiol | 2021 |
| 34587167 | A Bayesian network approach incorporating imputation of missing data enables exploratory analysis of complex causal biological relationships. | PLoS Genet | 2021 |
| 34106200 | Association of Novel Locus With Rheumatic Heart Disease in Black African Individuals: Findings From the RHDGen Study. | JAMA Cardiol | 2021 |
| 34285246 | Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome. | Sci Rep | 2021 |
| 33437986 | Heritability and family-based GWAS analyses of the N-acyl ethanolamine and ceramide plasma lipidome. | Hum Mol Genet | 2021 |
| 33201861 | Congenital heart disease risk loci identified by genome-wide association study in European patients. | J Clin Invest | 2021 |
| 32830257 | A Genome-wide Association Study Identifies SERPINB10, CRLF3, STX7, LAMP3, IFNG-AS1, and KRT80 As Risk Loci Contributing to Cutaneous Leishmaniasis in Brazil. | Clin Infect Dis | 2021 |
| 32190932 | Investigation of prediction accuracy and the impact of sample size, ancestry, and tissue in transcriptome-wide association studies. | Genet Epidemiol | 2020 |
| 31879347 | Mouse genetics reveals Barttin as a genetic modifier of Joubert syndrome. | Proc Natl Acad Sci U S A | 2020 |
| 33102976 | Early B-cell Factor 3-Related Genetic Disease Can Mimic Urofacial Syndrome. | Kidney Int Rep | 2020 |
| 33268509 | Transcriptomic profiling across the nonalcoholic fatty liver disease spectrum reveals gene signatures for steatohepatitis and fibrosis. | Sci Transl Med | 2020 |
| 33125279 | Cardiac Imaging of Aortic Valve Area From 34 287 UK Biobank Participants Reveals Novel Genetic Associations and Shared Genetic Comorbidity With Multiple Disease Phenotypes. | Circ Genom Precis Med | 2020 |
| 32873833 | Heritability of haemodynamics in the ascending aorta. | Sci Rep | 2020 |
| 32339198 | Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma. | PLoS Genet | 2020 |
| 32119656 | Bayesian network analysis incorporating genetic anchors complements conventional Mendelian randomization approaches for exploratory analysis of causal relationships in complex data. | PLoS Genet | 2020 |
| 32501499 | An Intronic HCP5 Variant Is Associated With Age of Onset and Susceptibility to Graves Disease in UK and Polish Cohorts. | J Clin Endocrinol Metab | 2020 |
| 32203202 | Correction: Comparison of methods for transcriptome imputation through application to two common complex diseases. | Eur J Hum Genet | 2020 |
| 32298765 | Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically characterised cohort<sup>â¿¿</sup>. | J Hepatol | 2020 |
| 29727703 | Statistical methods for genome-wide association studies. | Semin Cancer Biol | 2019 |
| 31413261 | A meta-analysis of genome-wide association studies identifies multiple longevity genes. | Nat Commun | 2019 |
| 31537879 | Marked variation in heritability estimates of left ventricular mass depending on modality of measurement. | Sci Rep | 2019 |
| 31480262 | Exploring Shared Susceptibility between Two Neural Crest Cells Originating Conditions: Neuroblastoma and Congenital Heart Disease. | Genes (Basel) | 2019 |
| 30704525 | A genome-wide association study of mitochondrial DNA copy number in two population-based cohorts. | Hum Genomics | 2019 |
| 30940094 | Haplin power analysis: a software module for power and sample size calculations in genetic association analyses of family triads and unrelated controls. | BMC Bioinformatics | 2019 |
| 30908486 | The Plight of Muntaser Ibrahim. | PLoS Genet | 2019 |
| 30281845 | Analysis of BAFF gene polymorphisms in UK Graves' disease patients. | Clin Endocrinol (Oxf) | 2019 |
| 30582441 | Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot. | Circ Res | 2019 |
| 30556296 | A case-control genome wide association study of substance use disorder (SUD) identifies novel variants on chromosome 7p14.1 in patients from the United Arab Emirates (UAE). | Am J Med Genet B Neuropsychiatr Genet | 2019 |