Sang Hong Lee
Genetics · 2011–2017
A researcher in the Science corpus: 8 papers; trusts 7 researchers and is trusted by 8 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 145 citations into it; #1,726 of 6,854 by trust here, #559 by citations
- Plant Science — 8 citations into it
Whom Sang Hong Lee trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Jian Yang
- Michael E. Goddard
- Peter M. Visscher
- Hans D. Daetwyler
- Teri Manolio
- Alkes L Price
- Paul M. Vanraden
- Frank Dudbridge
- Naomi R. Wray
- Suzanne M. Leal
Who trusts Sang Hong Lee overall
- Xiaoping Zhou
- Frank Dudbridge
- Naomi R. Wray
- Bogdan Pasaniuc
- Robert Plomin
- Alkes L Price
- Johanna S. Hardin
- Matthew Stephens
- Jian Yang
- Joseph K. Pickrell
Papers from Sang Hong Lee's perspective
Ordered by how strongly the researchers Sang Hong Lee trusts endorse each paper. Same corpus, a different order for every researcher.
- Accuracy of Predicting the Genetic Risk of Disease Using a Genome-Wide Approach (PLoS ONE)
- Efficient methods to compute genomic predictions. (Journal of Dairy Science)
- Genomewide association studies and assessment of the risk of disease. (New England Journal of Medicine)
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
- Data and Theory Point to Mainly Additive Genetic Variance for Complex Traits (PLoS Genetics)
- Pitfalls of predicting complex traits from SNPs
- Genomic selection: prediction of accuracy and maximisation of long term response (Genetica)
- Complement Factor H Polymorphism in Age-Related Macular Degeneration (Science)
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
- Heritability in the genomics era — concepts and misconceptions (Nature reviews genetics)
Their papers
- A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium (2016) — 1,284 citations
- Genetic evidence of assortative mating in humans (2017) — 288 citations
- Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index (2015) — 781 citations
- Dominance genetic variation contributes little to the missing heritability for human complex traits. (2015) — 200 citations
- Research review: Polygenic methods and their application to psychiatric traits. (2014) — 677 citations
- GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment (2013) — 874 citations
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (2012) — 647 citations
- Estimating missing heritability for disease from genome-wide association studies. (2011) — 1,100 citations