| 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 |
| 37968452 | Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37898691 | Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37348055 | Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. | Genetics | 2023 |
| 37196047 | Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. | PLoS One | 2023 |
| 37126548 | The genetic determinants of recurrent somatic mutations in 43,693 blood genomes. | Sci Adv | 2023 |
| 37046083 | Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis. | Nature | 2023 |
| 36960714 | Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program. | Circ Genom Precis Med | 2023 |
| 36778406 | Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. | bioRxiv | 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 |
| 37898691 | Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37968452 | Author Correction: Genetic variation in the human leukocyte antigen region confers susceptibility to Clostridioides difficile infection. | Sci Rep | 2023 |
| 37348055 | Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. | Genetics | 2023 |
| 37046083 | Aberrant activation of TCL1A promotes stem cell expansion in clonal haematopoiesis. | Nature | 2023 |
| 37196047 | Multi-ancestry genome- and phenome-wide association studies of diverticular disease in electronic health records with natural language processing enriched phenotyping algorithm. | PLoS One | 2023 |
| 37126548 | The genetic determinants of recurrent somatic mutations in 43,693 blood genomes. | Sci Adv | 2023 |
| 36960714 | Whole Genome Analysis of Venous Thromboembolism: the Trans-Omics for Precision Medicine Program. | Circ Genom Precis Med | 2023 |
| 36778406 | Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants. | bioRxiv | 2023 |
| 35915169 | Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. | Nat Genet | 2022 |
| 35927319 | Rare genetic variants explain missing heritability in smoking. | Nat Hum Behav | 2022 |
| 35915169 | Cross-ancestry genome-wide meta-analysis of 61,047 cases and 947,237 controls identifies new susceptibility loci contributing to lung cancer. | Nat Genet | 2022 |
| 35592775 | The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. | Front Endocrinol (Lausanne) | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 36568030 | Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. | HGG Adv | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 36154123 | Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. | Circulation | 2022 |
| 35592775 | The Value of Rare Genetic Variation in the Prediction of Common Obesity in European Ancestry Populations. | Front Endocrinol (Lausanne) | 2022 |
| 35385311 | Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential. | Sci Adv | 2022 |
| 36477530 | Genetic diversity fuels gene discovery for tobacco and alcohol use. | Nature | 2022 |
| 36568030 | Whole-exome sequence analysis of anthropometric traits illustrates challenges in identifying effects of rare genetic variants. | HGG Adv | 2022 |
| 35927319 | Rare genetic variants explain missing heritability in smoking. | Nat Hum Behav | 2022 |
| 36154123 | Cross-Ancestry Investigation of Venous Thromboembolism Genomic Predictors. | Circulation | 2022 |
| 34282949 | Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry. | Circ Genom Precis Med | 2021 |
| 33720349 | Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. | Genetics | 2021 |
| 33594163 | Rare deleterious germline variants and risk of lung cancer. | NPJ Precis Oncol | 2021 |
| 34282949 | Associations of Genetically Predicted Lp(a) (Lipoprotein [a]) Levels With Cardiovascular Traits in Individuals of European and African Ancestry. | Circ Genom Precis Med | 2021 |
| 34125579 | Outcomes of COVID-19 in Patients With Cancer: A Closer Look at Pre-Emptive Routine Screening Strategies. | JCO Oncol Pract | 2021 |
| 33853833 | Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. | Cancer Res | 2021 |
| 33720349 | Robust, flexible, and scalable tests for Hardy-Weinberg equilibrium across diverse ancestries. | Genetics | 2021 |
| 33853833 | Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer. | Cancer Res | 2021 |
| 33594163 | Rare deleterious germline variants and risk of lung cancer. | NPJ Precis Oncol | 2021 |
| 34125579 | Outcomes of COVID-19 in Patients With Cancer: A Closer Look at Pre-Emptive Routine Screening Strategies. | JCO Oncol Pract | 2021 |
| 32374294 | Bivariate traits association analysis using generalized estimating equations in family data. | Stat Appl Genet Mol Biol | 2020 |
| 32952248 | COVID-19 pandemic and pediatric dentistry: Fear, eating habits and parent's oral health perceptions. | Child Youth Serv Rev | 2020 |
| 32374345 | Identification of Susceptibility Loci for Spontaneous Coronary Artery Dissection. | JAMA Cardiol | 2020 |
| 32374294 | Bivariate traits association analysis using generalized estimating equations in family data. | Stat Appl Genet Mol Biol | 2020 |
| 32300485 | A Digital Health Weight Loss Program in 250,000 Individuals. | J Obes | 2020 |
| 32180992 | A digital health weight-loss intervention in severe obesity. | Digit Health | 2020 |
| 31826912 | Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q. | Cancer Epidemiol Biomarkers Prev | 2020 |
| 31826912 | Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q. | Cancer Epidemiol Biomarkers Prev | 2020 |