| Highly Parallel Genome-wide Expression Profiling of Individual Cells Using Nanoliter Droplets | Cell | 2015 | 3.9K |
| Comprehensive Classification of Retinal Bipolar Neurons by Single-Cell Transcriptomics | Cell | 2016 | 675 |
| Analysis of shared heritability in common disorders of the brain | Science | 2018 | 666 |
| Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations | American Journal of Human Genetics | 2017 | 665 |
| Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores | American Journal of Human Genetics | 2015 | 649 |
| Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism | Cell | 2020 | 578 |
| Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases | American Journal of Human Genetics | 2014 | 411 |
| Exploring Comorbidity Within Mental Disorders Among a Danish National Population | JAMA Psychiatry | 2019 | 188 |
| Predicting Polygenic Risk of Psychiatric Disorders | Biological Psychiatry | 2019 | 170 |
| Genome-wide Association Study Identifies 27 Loci Influencing Concentrations of Circulating Cytokines and Growth Factors | American Journal of Human Genetics | 2017 | 133 |
| Polygenic and clinical risk scores and their impact on age at onset and prediction of cardiometabolic diseases and common cancers | Nature Medicine | 2020 | 109 |
| Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation | Molecular Psychiatry | 2020 | 106 |
| Genetic variation in human DNA replication timing | Cell | 2014 | 102 |
| Genetically Distinct Parallel Pathways in the Entopeduncular Nucleus for Limbic and Sensorimotor Output of the Basal Ganglia | Neuron | 2017 | 95 |
| Polygenic risk of Alzheimer disease is associated with early- and late-life processes | Neurology | 2016 | 86 |
| An Unexpectedly Complex Architecture for Skin Pigmentation in Africans | Cell | 2017 | 85 |
| Mutations in PAX2 associate with adult-onset FSGS | Journal of the American Society of Nephrology: JASN | 2014 | 76 |
| Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum | American Journal of Human Genetics | 2018 | 59 |
| Leveraging Distant Relatedness to Quantify Human Mutation and Gene-Conversion Rates | American Journal of Human Genetics | 2015 | 56 |
| Functional Architectures of Local and Distal Regulation of Gene Expression in Multiple Human Tissues | American Journal of Human Genetics | 2017 | 50 |
| Geographic Variation and Bias in the Polygenic Scores of Complex Diseases and Traits in Finland | American Journal of Human Genetics | 2019 | 50 |
| Random replication of the inactive X chromosome | Genome Research | 2014 | 50 |
| Fine-Scale Genetic Structure in Finland | G3: Genes, Genomes, Genetics | 2017 | 50 |
| Biallelic Variants in UBA5 Link Dysfunctional UFM1 Ubiquitin-like Modifier Pathway to Severe Infantile-Onset Encephalopathy | American Journal of Human Genetics | 2016 | 43 |
| De Novo Truncating Variants in ASXL2 Are Associated with a Unique and Recognizable Clinical Phenotype | American Journal of Human Genetics | 2016 | 42 |
