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| 36601918 | Genetically Predicted Differences in Systolic Blood Pressure and Risk of Cardiovascular and Noncardiovascular Diseases: A Mendelian Randomization Study in Chinese Adults. | | 2023 |
| 37749248 | Author Correction: Multi-ancestry genome-wide association analyses improve resolution of genes and pathways influencing lung function and chronic obstructive pulmonary disease risk. | Nat Genet | 2023 |
| 37676424 | Conventional and genetic associations of adiposity with 1463 proteins in relatively lean Chinese adults. | | 2023 |
| 37582581 | Psychosis Endophenotypes: A Gene-Set-Specific Polygenic Risk Score Analysis. | | 2023 |
| 37503126 | Understanding the genetic complexity of puberty timing across the allele frequency spectrum. | medRxiv | 2023 |
| 37392542 | Associations of alcohol intake with subclinical carotid atherosclerosis in 22,000 Chinese adults. | | 2023 |
| 37292977 | Genetics of skeletal proportions in two different populations. | bioRxiv | 2023 |
| 37034649 | Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications. | medRxiv | 2023 |
| 36925053 | The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases. | Neurobiol Dis | 2023 |
| 36726144 | Mendelian randomisation study of body composition and depression in people of East Asian ancestry highlights potential setting-specific causality. | BMC Med | 2023 |
| 36240095 | Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke. | Neurology | 2022 |
| 35840665 | Conventional and genetic risk factors for chronic Hepatitis B virus infection in a community-based study of 0.5 million Chinese adults. | Scientific Reports | 2022 |
| 35551307 | Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation. | Nat Genet | 2022 |
| 35534559 | Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. | Nat Genet | 2022 |
| 35513594 | Investigation into the Health Effects of Reduced Chymase Function Using Predicted Loss-of-Function Mutations in CMA1. | Journal of Cardiovascular Translational Research | 2022 |
| 35452448 | Genetic associations of adult height with risk of cardioembolic and other subtypes of ischemic stroke: A mendelian randomization study in multiple ancestries. | PLoS Medicine | 2022 |
| 35048370 | Alcohol metabolism genes and risks of site-specific cancers in Chinese adults: An 11-year prospective study. | International Journal of Cancer | 2022 |
| 34995520 | Limb development genes underlie variation in human fingerprint patterns. | Cell | 2022 |
| 34906514 | Polygenic risk scores for prediction of breast cancer risk in Asian populations. | Genet Med | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 33766948 | A large-scale genome-wide association analysis of lung function in the Chinese population identifies novel loci and highlights shared genetic aetiology with obesity. | Eur Respir J | 2021 |
| 33536041 | Improved prediction of fracture risk leveraging a genome-wide polygenic risk score. | Genome Med | 2021 |
| 32719466 | Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study. | Mol Psychiatry | 2021 |
| 34851696 | Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics". | Sci Transl Med | 2021 |
| 34586374 | The Genetic Architecture of Depression in Individuals of East Asian Ancestry: A Genome-Wide Association Study. | JAMA Psychiatry | 2021 |
| 31901293 | Dysregulated Fc gamma receptor-mediated phagocytosis pathway in Alzheimer's disease: network-based gene expression analysis. | Neurobiol Aging | 2020 |
| 33239672 | The genetic architecture of sporadic and multiple consecutive miscarriage. | Nat Commun | 2020 |
| 32755048 | Genome-wide transcriptome analysis identifies novel dysregulated genes implicated in Alzheimer's pathology. | Alzheimers Dement | 2020 |
| 32581134 | Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics. | Sci Transl Med | 2020 |
| 31399431 | Genetic Predisposition to Type 2 Diabetes and Risk of Subclinical Atherosclerosis and Cardiovascular Diseases Among 160,000 Chinese Adults. | Diabetes | 2019 |
| 30804560 | New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries. | Nat Genet | 2019 |
| 29094675 | Associations between psychosis endophenotypes across brain functional, structural, and cognitive domains. | Psychological Medicine | 2018 |
| 28851104 | A polygenic risk score analysis of psychosis endophenotypes across brain functional, structural, and cognitive domains. | Am J Med Genet B Neuropsychiatr Genet | 2018 |
| 30524137 | Metabolomic consequences of genetic inhibition of PCSK9 compared with statin treatment. | Circulation | 2018 |
| 30487518 | Interethnic analyses of blood pressure loci in populations of East Asian and European descent. | Nat Commun | 2018 |
| 30290141 | Genomic Analyses from Non-invasive Prenatal Testing Reveal Genetic Associations, Patterns of Viral Infections, and Chinese Population History. | Cell | 2018 |
| 30113282 | Use of schizophrenia and bipolar disorder polygenic risk scores to identify psychotic disorders. | Br J Psychiatry | 2018 |
| 28010125 | Proposed association between the hexanucleotide repeat of C9orf72 and opposability index of the thumb. | Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration | 2017 |
| 28241208 | Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study. | JAMA Oncol | 2017 |
| 26858977 | Evidence for Dsg3 in regulating Src signaling by competing with it for binding to caveolin-1. | Data in Brief | 2016 |
| 27455348 | Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis. | Nat Genet | 2016 |
| 27244217 | Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral Sclerosis. | JAMA Neurol | 2016 |
| 24081377 | The role of ABCA1 gene sequence variants on risk of Alzheimer's disease. | Journal of Alzheimer's Disease | 2014 |
| 23871474 | A genome-wide association analysis of a broad psychosis phenotype identifies three loci for further investigation. | Biol Psychiatry | 2014 |
| 23164818 | Common variant at 16p11.2 conferring risk of psychosis. | Mol Psychiatry | 2014 |
| 25150574 | Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease. | Neurobiol Aging | 2014 |
| 24256812 | A genome-wide association meta-analysis identifies a novel locus at 17q11.2 associated with sporadic amyotrophic lateral sclerosis. | Hum Mol Genet | 2014 |
| 23974872 | Genome-wide association analysis identifies 13 new risk loci for schizophrenia. | Nat Genet | 2013 |
| 22294297 | Non-junctional human desmoglein 3 acts as an upstream regulator of Src in E-cadherin adhesion, a pathway possibly involved in the pathogenesis of pemphigus vulgaris. | Journal of Pathology | 2012 |
| 22766072 | C9ORF72 repeat expansion in a large Italian ALS cohort: evidence of a founder effect. | Neurobiology of Aging | 2012 |