|
| 36807635 | Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2023 |
| 36408616 | Use of Whole-Genome Sequencing to Estimate the Contribution of Immune Evasion and Waning Immunity on Decreasing COVID-19 Vaccine Effectiveness. | J Infect Dis | 2023 |
| 36807635 | Author Correction: Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2023 |
| 36408616 | Use of Whole-Genome Sequencing to Estimate the Contribution of Immune Evasion and Waning Immunity on Decreasing COVID-19 Vaccine Effectiveness. | J Infect Dis | 2023 |
| 34634447 | Clinical Implications of the Amyloidogenic V122I Transthyretin Variant in the General Population. | J Card Fail | 2022 |
| 35999217 | Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. | Nat Commun | 2022 |
| 35939579 | Germline Mutations in <i>CIDEB</i> and Protection against Liver Disease. | N Engl J Med | 2022 |
| 36450978 | Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2022 |
| 35534559 | Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. | Nat Genet | 2022 |
| 34634447 | Clinical Implications of the Amyloidogenic V122I Transthyretin Variant in the General Population. | J Card Fail | 2022 |
| 35149777 | UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. | Pharmacogenomics J | 2022 |
| 35534559 | Within-sibship genome-wide association analyses decrease bias in estimates of direct genetic effects. | Nat Genet | 2022 |
| 36450978 | Common and rare variant associations with clonal haematopoiesis phenotypes. | Nature | 2022 |
| 35939579 | Germline Mutations in <i>CIDEB</i> and Protection against Liver Disease. | N Engl J Med | 2022 |
| 35999217 | Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes. | Nat Commun | 2022 |
| 35149777 | UGT1A1 genetic variants are associated with increases in bilirubin levels in rheumatoid arthritis patients treated with sarilumab. | Pharmacogenomics J | 2022 |
| 33441424 | Kidney disease genetic risk variants alter lysosomal beta-mannosidase (<i>MANBA</i>) expression and disease severity. | Sci Transl Med | 2021 |
| 33542107 | Heterozygosity for a Pathogenic Variant in <i>SLC12A3</i> That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium. | J Am Soc Nephrol | 2021 |
| 34120448 | Causal Effect of Adiposity Measures on Blood Pressure Traits in 2 Urban Swedish Cohorts: A Mendelian Randomization Study. | J Am Heart Assoc | 2021 |
| 33692434 | Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease. | Sci Rep | 2021 |
| 34115965 | Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. | Am J Hum Genet | 2021 |
| 33619501 | Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease. | medRxiv | 2021 |
| 34210852 | Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity. | Science | 2021 |
| 33655273 | A catalog of associations between rare coding variants and COVID-19 outcomes. | medRxiv | 2021 |
| 33441424 | Kidney disease genetic risk variants alter lysosomal beta-mannosidase (<i>MANBA</i>) expression and disease severity. | Sci Transl Med | 2021 |
| 34184762 | Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals. | Genet Epidemiol | 2021 |
| 33222547 | Clinical Evaluation of the Polygenetic Background of Blood Pressure in the Population-Based Setting. | Hypertension | 2021 |
| 33432171 | Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. | Nat Med | 2021 |
| 34727153 | ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers. | Invest Ophthalmol Vis Sci | 2021 |
| 34662886 | Exome sequencing and analysis of 454,787 UK Biobank participants. | Nature | 2021 |
| 34945778 | Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization. | J Pers Med | 2021 |
| 33655273 | A catalog of associations between rare coding variants and COVID-19 outcomes. | medRxiv | 2021 |
| 33542107 | Heterozygosity for a Pathogenic Variant in <i>SLC12A3</i> That Causes Autosomal Recessive Gitelman Syndrome Is Associated with Lower Serum Potassium. | J Am Soc Nephrol | 2021 |
| 33619501 | Genome-wide analysis in 756,646 individuals provides first genetic evidence that <i>ACE2</i> expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease. | medRxiv | 2021 |
| 33692434 | Mutation spectrum of NOD2 reveals recessive inheritance as a main driver of Early Onset Crohn's Disease. | Sci Rep | 2021 |
| 34945778 | Association of Thyroid Function with Blood Pressure and Cardiovascular Disease: A Mendelian Randomization. | J Pers Med | 2021 |
| 34727153 | ERAP1, ERAP2, and Two Copies of HLA-Aw19 Alleles Increase the Risk for Birdshot Chorioretinopathy in HLA-A29 Carriers. | Invest Ophthalmol Vis Sci | 2021 |
| 34662886 | Exome sequencing and analysis of 454,787 UK Biobank participants. | Nature | 2021 |
| 34184762 | Genome-wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals. | Genet Epidemiol | 2021 |
| 34210852 | Sequencing of 640,000 exomes identifies <i>GPR75</i> variants associated with protection from obesity. | Science | 2021 |
| 34120448 | Causal Effect of Adiposity Measures on Blood Pressure Traits in 2 Urban Swedish Cohorts: A Mendelian Randomization Study. | J Am Heart Assoc | 2021 |
| 34115965 | Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals. | Am J Hum Genet | 2021 |
| 33432171 | Exome-wide evaluation of rare coding variants using electronic health records identifies new gene-phenotype associations. | Nat Med | 2021 |
| 33222547 | Clinical Evaluation of the Polygenetic Background of Blood Pressure in the Population-Based Setting. | Hypertension | 2021 |
| 32498804 | Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease. | J Am Coll Cardiol | 2020 |
| 31836692 | Clinical and Molecular Prevalence of Lipodystrophy in an Unascertained Large Clinical Care Cohort. | Diabetes | 2020 |
| 31923704 | Biallelic variants in KYNU cause a multisystemic syndrome with hand hyperphalangism. | Bone | 2020 |
| 31707832 | Patients With High Genome-Wide Polygenic Risk Scores for Coronary Artery Disease May Receive Greater Clinical Benefit From Alirocumab Treatment in the ODYSSEY OUTCOMES Trial. | Circulation | 2020 |
| 33087929 | Exome sequencing and characterization of 49,960 individuals in the UK Biobank. | Nature | 2020 |
| 32498804 | Limitations of Contemporary Guidelines for Managing Patients at High Genetic Risk of Coronary Artery Disease. | J Am Coll Cardiol | 2020 |