| human | Q5 |
| P6178 | Dimensions author ID | 01167035545.46 |
| P496 | ORCID iD | 0000-0001-7496-2075 |
| P69 | educated at | University of Oxford | Q34433 |
| University of Cambridge | Q35794 | ||
| P108 | employer | Helmholtz Zentrum München | Q878592 |
| Wellcome Sanger Institute | Q1142544 | ||
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | female | Q6581072 |
| Q37162971 | A Genome-Wide Association Study for Regulators of Micronucleus Formation in Mice |
| Q115038468 | Analysis of independent cohorts of outbred CFW mice reveals novel loci for behavioral and physiological traits and identifies factors determining reproducibility |
| Q39825160 | CHRONICITY OF DEPRESSION AND MOLECULAR MARKERS IN A LARGE SAMPLE OF HAN CHINESE WOMEN. |
| Q36404519 | Genetic Control over mtDNA and Its Relationship to Major Depressive Disorder |
| Q52560096 | Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression. |
| Q37138548 | Genome-wide association of multiple complex traits in outbred mice by ultra-low-coverage sequencing. |
| Q115020741 | Leveraging eQTLs to identify individual-level tissue of interest for a complex trait |
| Q90776484 | Minimal phenotyping yields genome-wide association signals of low specificity for major depression |
| Q52370506 | Molecular Genetic Analysis Subdivided by Adversity Exposure Suggests Etiologic Heterogeneity in Major Depression. |
| Q30412070 | Molecular signatures of major depression |
| Q90640114 | No Evidence of Persistence or Inheritance of Mitochondrial DNA Copy Number in Holocaust Survivors and Their Descendants |
| Q38771561 | Reevaluation of SNP heritability in complex human traits |
| Q38779701 | The Genetic Architecture of Major Depressive Disorder in Han Chinese Women |
| Q98953154 | The Polygenic and Monogenic Basis of Blood Traits and Diseases |
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