| 10 Years of GWAS Discovery: Biology, Function, and Translation | American Journal of Human Genetics | 2017 | 1.7K |
| Wnt signaling in cancer | Oncogene | 2017 | 1.2K |
| The Human Gene Mutation Database: towards a comprehensive repository of inherited mutation data for medical research, genetic diagnosis and next-generation sequencing studies | Human Genetics | 2017 | 775 |
| LncRNA-mediated regulation of cell signaling in cancer | Oncogene | 2017 | 742 |
| Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations | American Journal of Human Genetics | 2017 | 665 |
| Census and evaluation of p53 target genes | Oncogene | 2017 | 427 |
| InterVar: Clinical Interpretation of Genetic Variants by the 2015 ACMG-AMP Guidelines | American Journal of Human Genetics | 2017 | 426 |
| Cancer-associated fibroblast exosomes regulate survival and proliferation of pancreatic cancer cells | Oncogene | 2017 | 391 |
| Hypoxic lung cancer-secreted exosomal miR-23a increased angiogenesis and vascular permeability by targeting prolyl hydroxylase and tight junction protein ZO-1 | Oncogene | 2017 | 332 |
| circRNA_100290 plays a role in oral cancer by functioning as a sponge of the miR-29 family | Oncogene | 2017 | 321 |
| Autophagy in cancer metastasis | Oncogene | 2017 | 282 |
| Extracellular purines, purinergic receptors and tumor growth | Oncogene | 2017 | 272 |
| LncRNA HULC triggers autophagy via stabilizing Sirt1 and attenuates the chemosensitivity of HCC cells | Oncogene | 2017 | 244 |
| Evaluating the Clinical Validity of Gene-Disease Associations: An Evidence-Based Framework Developed by the Clinical Genome Resource | American Journal of Human Genetics | 2017 | 242 |
| Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease | American Journal of Human Genetics | 2017 | 235 |
| mTORC1 and mTORC2 in cancer and the tumor microenvironment | Oncogene | 2017 | 225 |
| High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies | American Journal of Human Genetics | 2017 | 214 |
| Clinical exome sequencing: results from 2819 samples reflecting 1000 families | European Journal of Human Genetics | 2017 | 201 |
| International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases | American Journal of Human Genetics | 2017 | 200 |
| Hypoxic stress: obstacles and opportunities for innovative immunotherapy of cancer | Oncogene | 2017 | 194 |
| Deep intronic mutations and human disease | Human Genetics | 2017 | 188 |
| The Microbiome and Human Biology | Annual Review of Genomics and Human Genetics | 2017 | 181 |
| Increased expression of programmed cell death protein 1 on NK cells inhibits NK-cell-mediated anti-tumor function and indicates poor prognosis in digestive cancers | Oncogene | 2017 | 181 |
| Acquired CDK6 amplification promotes breast cancer resistance to CDK4/6 inhibitors and loss of ER signaling and dependence | Oncogene | 2017 | 179 |
| Variant Interpretation: Functional Assays to the Rescue | American Journal of Human Genetics | 2017 | 171 |
