한범 (서울대학교 의과대학)님 | 한빛사연구자 > 한빛사

서울대학교 의과대학

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최종업데이트 2025.07.16.

Admixed and single-continental genome segments of the same ancestry have distinct linkage disequilibrium patterns
- Genome Biol., Jul 11 2025, 26 (1) 201 | https://doi.org/10.1186/s13059-025-03672-w
- 2025-07
- 의약학
- 한빛사논문
BIGFAM - variance components analysis from relatives without genotype
- Nat. Commun., Published: 01 July 2025 | https://doi.org/10.1038/s41467-025-60502-0
- 2025-07
- 생명과학
- 한빛사논문
FastRNA: An efficient solution for PCA of single-cell RNA-sequencing data based on a batch-accounting count model
- Am. J. Hum. Genet., Available online 6 October 2022 | https://doi.org/10.1016/j.ajhg.2022.09.008
- 2022-10
- 의약학
- 한빛사논문
A theory-based practical solution to correct for sex-differential participation bias
- Genome Biol., Published 27 June 2022 | https://doi.org/10.1186/s13059-022-02703-0
- 2022-06
- 의약학
- 한빛사논문
MarcoPolo: a method to discover differentially expressed genes in single-cell RNA-seq data without depending on prior clustering
- Nucleic Acids Res., Published: 14 April 2022 | https://doi.org/10.1093/nar/gkac216
- 2022-04
- 의약학
- 한빛사논문
Accurate imputation of human leukocyte antigens with CookHLA
- Nat. Commun., Published 24 February 2021, 12, 1264 | https://doi.org/10.1038/s41467-021-21541-5
- 2021-02
- 의약학
- 한빛사논문
PLEIO: a method to map and interpret pleiotropic loci with GWAS summary statistics
- Am. J. Hum. Genet., Available online 21 December 2020 | https://doi.org/10.1016/j.ajhg.2020.11.017
- 2020-12
- 의약학
- 한빛사논문
Genomic GPS: using genetic distance from individuals to public data for genomic analysis without disclosing personal genomes
- Genome Biol., Published: 27 August 2019, 20, Article number: 175 | https://doi.org/10.1186/s13059-019-1792-2
- 2019-08
- 의약학
- 한빛사논문
- 한범(서울아산병원, 울산의대)
Imputing Phenotypes for Genome-wide Association Studies
- Am. J. Hum. Genet., Available online 9 June 2016 | doi:10.1016/j.ajhg.2016.04.013
- 2016-06
- 의약학
- 한빛사논문
- 한범(서울아산병원, 울산의대, Brigham and Women's Hospital and Harvard Medical School, Broad Institute of MIT and Harvard, Partners Center for Personalized Genetic Medicine)
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A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases
- Nat. Genet., Published online 16 May 2016 | doi:10.1038/ng.3572
- 2016-05
- 의약학
- 한빛사논문

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