Michael Inouye
Genetics · 2007–2023
A researcher in the Science corpus: 21 papers; trusts 12 researchers and is trusted by 8 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 198 citations into it; #2,156 of 6,854 by trust here, #161 by citations
- Molecular Biology — 147 citations into it; #6,453 of 17,773 by trust here, #2,535 by citations
- Artificial Intelligence — 16 citations into it; #17,766 of 35,345 by trust here, #22,463 by citations
- Food Science — 7 citations into it
- Computer Vision and Pattern Recognition — 6 citations into it
- Natural Language Processing — 5 citations into it
Whom Michael Inouye trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Martin C. J. Maiden
- Nick Patterson
- Alkes L Price
- Iain M. Johnstone
- Hui Zou
- Christoph Lippert
- Heng Li
- A. Lu
- Trevor J. Hastie
Who trusts Michael Inouye overall
- Philip Thomas Lanken Conradsen Clausen
- Florian Privé
- Alfred Ferrer Florensa
- Longda Jiang
- Martin Hunt
- Frank Moller Aarestrup
Papers from Michael Inouye's perspective
Ordered by how strongly the researchers Michael Inouye trusts endorse each paper. Same corpus, a different order for every researcher.
- The Sequence Alignment/Map format and SAMtools (Bioinform.)
- UK Biobank: An Open Access Resource for Identifying the Causes of a Wide Range of Complex Diseases of Middle and Old Age
- 5分で分かる!? 有名論文ナナメ読み:Jacob Devlin et al. : BERT : Pre-training of Deep Bidirectional Transformers for Language Understanding
- Approximately independent linkage disequilibrium blocks in human populations (bioRxiv)
- Detection and interpretation of shared genetic influences on 42 human traits (Nature Genetics)
- 10 Years of GWAS Discovery: Biology, Function, and Translation. (American Journal of Human Genetics)
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
- The Ensembl Variant Effect Predictor
- SPAdes: A New Genome Assembly Algorithm and Its Applications to Single-Cell Sequencing (J. Comput. Biol.)
- Deep Learning
Their papers
- The diploid genome sequence of an Asian individual (2008) — 987 citations
- SRST2: Rapid genomic surveillance for public health and hospital microbiology labs (2014) — 996 citations
- Integrating common and rare genetic variation in diverse human populations (2010) — 3,033 citations
- Fast Principal Component Analysis of Large-Scale Genome-Wide Data (2014) — 321 citations
- Green Algorithms: Quantifying the Carbon Footprint of Computation (2020) — 522 citations
- Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study (2008) — 685 citations
- The Polygenic Score Catalog: an open database for reproducibility and systematic evaluation (2020) — 298 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- The NHGRI-EBI GWAS Catalog: knowledgebase and deposition resource (2022) — 1,303 citations
- Greengenes2 unifies microbial data in a single reference tree (2023) — 563 citations
- Improving reporting standards for polygenic scores in risk prediction studies (2020) — 381 citations
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) — 602 citations
- Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults Implications for Primary Prevention (2019)
- FastSpar: rapid and scalable correlation estimation for compositional data (2018) — 323 citations
- FlashPCA2: principal component analysis of biobank-scale genotype datasets (2016) — 380 citations
- The infant airway microbiome in health and disease impacts later asthma development (2015) — 849 citations
- The developmental pathway for CD103+CD8+ tissue-resident memory T cells of skin (2013) — 1,247 citations
- Common variants near MC4R are associated with fat mass, weight and risk of obesity (2008) — 1,371 citations
- Variants in MTNR1B influence fasting glucose levels (2008) — 723 citations
- A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21 (2007) — 704 citations