The power of genetic diversity in genome-wide association studies of lipids SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ... Nature 600 (7890), 675-679, 2021 | 631 | 2021 |
A saturated map of common genetic variants associated with human height L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ... Nature 610 (7933), 704-712, 2022 | 555 | 2022 |
Ccr4-Not complex: the control freak of eukaryotic cells JE Miller, JC Reese Critical reviews in biochemistry and molecular biology 47 (4), 315-333, 2012 | 215 | 2012 |
Effect of a fluid bolus on cardiovascular collapse among critically ill adults undergoing tracheal intubation (PrePARE): a randomised controlled trial DR Janz, JD Casey, MW Semler, DW Russell, J Dargin, DJ Vonderhaar, ... The Lancet Respiratory Medicine 7 (12), 1039-1047, 2019 | 107 | 2019 |
Genetic risk factors associated with preeclampsia and hypertensive disorders of pregnancy JS Tyrmi, T Kaartokallio, AI Lokki, T Jääskeläinen, E Kortelainen, ... JAMA cardiology 8 (7), 674-683, 2023 | 68 | 2023 |
Human-disease phenotype map derived from PheWAS across 38,682 individuals A Verma, L Bang, JE Miller, Y Zhang, MTM Lee, Y Zhang, ... The American Journal of Human Genetics 104 (1), 55-64, 2019 | 63 | 2019 |
Genome-wide mapping of decay factor–mrna interactions in yeast identifies nutrient-responsive transcripts as targets of the deadenylase ccr4 JE Miller, L Zhang, H Jiang, Y Li, BF Pugh, JC Reese G3: Genes, Genomes, Genetics 8 (1), 315-330, 2018 | 41 | 2018 |
Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis S Kanoni, SE Graham, Y Wang, I Surakka, S Ramdas, X Zhu, SL Clarke, ... Genome biology 23 (1), 268, 2022 | 39 | 2022 |
A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids S Ramdas, J Judd, SE Graham, S Kanoni, Y Wang, I Surakka, B Wenz, ... The American Journal of Human Genetics 109 (8), 1366-1387, 2022 | 32 | 2022 |
Identification of exon skipping events associated with Alzheimer’s disease in the human hippocampus S Han, JE Miller, S Byun, D Kim, SL Risacher, AJ Saykin, Y Lee, K Nho, ... BMC Medical Genomics 12, 51-61, 2019 | 27 | 2019 |
A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts Y Veturi, A Lucas, Y Bradford, D Hui, S Dudek, E Theusch, A Verma, ... Nature genetics 53 (7), 972-981, 2021 | 24 | 2021 |
The effects of alternative splicing on miRNA binding sites in bladder cancer S Han, D Kim, M Shivakumar, YJ Lee, T Garg, JE Miller, JH Kim, D Kim, ... PloS one 13 (1), e0190708, 2018 | 24 | 2018 |
Exome-wide rare variant analysis from the DiscovEHR study identifies novel candidate predisposition genes for endometrial cancer M Shivakumar, JE Miller, VR Dasari, R Gogoi, D Kim Frontiers in Oncology 9, 574, 2019 | 22 | 2019 |
Comprehensive inherited risk estimation for risk-based breast cancer screening in women N Mars, S Kerminen, M Tamlander, M Pirinen, E Jakkula, K Aaltonen, ... Journal of Clinical Oncology 42 (13), 1477-1487, 2024 | 17 | 2024 |
Codon bias among synonymous rare variants is associated with Alzheimer’s disease imaging biomarker JE Miller, MK Shivakumar, SL Risacher, AJ Saykin, S Lee, K Nho, D Kim, ... PACIFIC SYMPOSIUM ON BIOCOMPUTING 2018: Proceedings of the Pacific Symposium …, 2018 | 16 | 2018 |
The public health impact of poor sleep on severe COVID-19, influenza and upper respiratory infections SE Jones, FI Maisha, SJ Strausz, V Lammi, BE Cade, A Tervi, ... Ebiomedicine 93, 2023 | 15 | 2023 |
Rare variants in the splicing regulatory elements of EXOC3L4 are associated with brain glucose metabolism in Alzheimer’s disease JE Miller, MK Shivakumar, Y Lee, S Han, E Horgousluoglu, SL Risacher, ... BMC medical genomics 11, 45-52, 2018 | 15 | 2018 |
Innovative strategies for annotating the “relationSNP” between variants and molecular phenotypes JE Miller, Y Veturi, MD Ritchie BioData mining 12, 1-22, 2019 | 13 | 2019 |
Evidence of a causal effect of genetic tendency to gain muscle mass on uterine leiomyomata E Sliz, JS Tyrmi, N Rahmioglu, KT Zondervan, CM Becker, O Uimari, ... Nature Communications 14 (1), 542, 2023 | 12 | 2023 |
CAS-viewer: web-based tool for splicing-guided integrative analysis of multi-omics cancer data S Han, D Kim, Y Kim, K Choi, JE Miller, D Kim, Y Lee BMC Medical Genomics 11, 105-116, 2018 | 12 | 2018 |