| Year |
Citation |
Score |
| 2024 |
Kim EE, Jang CS, Kim H, Han B. PASTRY: achieving balanced power for detecting risk and protective minor alleles in meta-analysis of association studies with overlapping subjects. Bmc Bioinformatics. 25: 24. PMID 38216869 DOI: 10.1186/s12859-023-05627-z |
0.304 |
|
| 2023 |
Jung S, Lee CH, Sul JH, Han B. Building an optimal predictive model for imputing tissue-specific gene expression by combining genotype and whole-blood transcriptome data. Hgg Advances. 4: 100223. PMID 37576186 DOI: 10.1016/j.xhgg.2023.100223 |
0.626 |
|
| 2023 |
Sakaue S, Gurajala S, Curtis M, Luo Y, Choi W, Ishigaki K, Kang JB, Rumker L, Deutsch AJ, Schönherr S, Forer L, LeFaive J, Fuchsberger C, Han B, Lenz TL, et al. Tutorial: a statistical genetics guide to identifying HLA alleles driving complex disease. Nature Protocols. PMID 37495751 DOI: 10.1038/s41596-023-00853-4 |
0.308 |
|
| 2022 |
Kim C, Kim YJ, Choi W, Jang HM, Hwang MY, Jung S, Lim H, Hong SB, Yoon K, Kim BJ, Park HY, Han B. Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signals. Human Molecular Genetics. PMID 35043955 DOI: 10.1093/hmg/ddac016 |
0.358 |
|
| 2021 |
Li J, Kong N, Han B, Sul JH. Rare variants regulate expression of nearby individual genes in multiple tissues. Plos Genetics. 17: e1009596. PMID 34061836 DOI: 10.1371/journal.pgen.1009596 |
0.706 |
|
| 2021 |
Moll M, Jackson VE, Yu B, Grove ML, London SJ, Gharib SA, Bartz TM, Sitlani CM, Dupuis J, O'Connor GT, Xu H, Cassano PA, Patchen BK, Kim WJ, Park J, ... ... Han B, et al. A Systematic Analysis of Protein-altering Exonic Variants in Chronic Obstructive Pulmonary Disease. American Journal of Physiology. Lung Cellular and Molecular Physiology. PMID 33909500 DOI: 10.1152/ajplung.00009.2021 |
0.327 |
|
| 2021 |
Jung S, Ye BD, Lee HS, Baek J, Kim G, Park D, Park SH, Yang SK, Han B, Liu J, Song K. Identification of three novel susceptibility loci for inflammatory bowel disease in Koreans in an extended genome-wide association study. Journal of Crohn's & Colitis. PMID 33853113 DOI: 10.1093/ecco-jcc/jjab060 |
0.35 |
|
| 2021 |
Cook S, Choi W, Lim H, Luo Y, Kim K, Jia X, Raychaudhuri S, Han B. Accurate imputation of human leukocyte antigens with CookHLA. Nature Communications. 12: 1264. PMID 33627654 DOI: 10.1038/s41467-021-21541-5 |
0.317 |
|
| 2020 |
Lee CH, Shi H, Pasaniuc B, Eskin E, Han B. PLEIO: a method to map and interpret pleiotropic loci with GWAS summary statistics. American Journal of Human Genetics. PMID 33352115 DOI: 10.1016/j.ajhg.2020.11.017 |
0.63 |
|
| 2020 |
Choi W, Luo Y, Raychaudhuri S, Han B. HATK: HLA Analysis Toolkit. Bioinformatics (Oxford, England). PMID 32735319 DOI: 10.1093/Bioinformatics/Btaa684 |
0.361 |
|
| 2020 |
Jung S, Liu W, Baek J, Moon JW, Ye BD, Lee HS, Park SH, Yang SK, Han B, Liu J, Song K. Expression Quantitative Trait Loci (eQTL) Mapping in Korean Patients With Crohn's Disease and Identification of Potential Causal Genes Through Integration With Disease Associations. Frontiers in Genetics. 11: 486. PMID 32477412 DOI: 10.3389/Fgene.2020.00486 |
0.48 |
|
| 2020 |
Howard DM, Folkersen L, Coleman JRI, Adams MJ, Glanville K, Werge T, Hagenaars SP, Han B, Porteous D, Campbell A, Clarke TK, Breen G, Sullivan PF, Wray NR, Lewis CM, et al. Genetic stratification of depression in UK Biobank. Translational Psychiatry. 10: 163. PMID 32448866 DOI: 10.1038/S41398-020-0848-0 |
0.31 |
|
| 2020 |
Lee KS, Kim KH, Oh YM, Han B, Kim WJ. A genome wide association study for lung function in the Korean population using an exome array. The Korean Journal of Internal Medicine. PMID 32336055 DOI: 10.3904/Kjim.2019.204 |
0.327 |
|
| 2019 |
Jang CS, Choi W, Cook S, Han B. Analysis of differences in human leukocyte antigen between the two Wellcome Trust Case Control Consortium control datasets. Genomics & Informatics. 17: e29. PMID 31610625 DOI: 10.5808/Gi.2019.17.3.E29 |
0.362 |
|
| 2019 |
Kim K, Baik H, Jang CS, Roh JK, Eskin E, Han B. Genomic GPS: using genetic distance from individuals to public data for genomic analysis without disclosing personal genomes. Genome Biology. 20: 175. PMID 31455387 DOI: 10.1186/S13059-019-1792-2 |
0.417 |
|
| 2019 |
Kim H, Kim Y, Han B, Jang JY, Kim Y. Clinically Applicable Deep Learning Algorithm Using Quantitative Proteomic Data. Journal of Proteome Research. PMID 31314536 DOI: 10.1021/Acs.Jproteome.9B00268 |
0.315 |
|
| 2019 |
Pouget JG, Han B, Wu Y, Mignot E, Ollila HM, Barker J, Spain S, Dand N, Trembath R, Martin J, Mayes MD, Bossini-Castillo L, López-Isac E, Jin Y, et al. Cross-disorder analysis of schizophrenia and 19 immune-mediated diseases identifies shared genetic risk. Human Molecular Genetics. PMID 31211845 DOI: 10.1093/Hmg/Ddz145 |
0.369 |
|
| 2018 |
Lee HS, Yang SK, Hong M, Jung S, Kim BM, Moon JW, Park SH, Ye BD, Oh SH, Kim KM, Yoon YS, Yu CS, Baek J, Lee CH, Han B, et al. An intergenic variant rs9268877 between HLA-DRA and HLA-DRB contributes to the clinical course and long-term outcome of ulcerative colitis. Journal of Crohn's & Colitis. PMID 29905830 DOI: 10.1093/Ecco-Jcc/Jjy080 |
0.433 |
|
| 2018 |
Kang EY, Lee CH, Furlotte NA, Joo JWJ, Kostem E, Zaitlen N, Eskin E, Han B. An Association Mapping Framework To Account for Potential Sex Difference in Genetic Architectures. Genetics. PMID 29752291 DOI: 10.1534/Genetics.117.300501 |
0.759 |
|
| 2018 |
Hong M, Ye BD, Yang SK, Jung S, Lee HS, Kim BM, Lee SB, Hong J, Baek J, Park SH, Han B, Li Y, Liu W, Haritunians T, Taylor KD, et al. Immunochip meta-analysis of inflammatory bowel disease identifies three novel loci and four novel associations in previously reported loci. Journal of Crohn's & Colitis. PMID 29584801 DOI: 10.1093/Ecco-Jcc/Jjy002 |
0.41 |
|
| 2017 |
Lee HS, Lee SB, Kim BM, Hong M, Jung S, Hong J, Baek J, Han B, Oh SH, Kim KM, Park SH, Yang SK, Ye BD, Song K. Association of CDKN2A/B with inflammatory bowel disease in Koreans. Journal of Gastroenterology and Hepatology. PMID 29063720 DOI: 10.1111/Jgh.14031 |
0.34 |
|
| 2017 |
Kim EE, Lee S, Lee CH, Oh H, Song K, Han B. FOLD: a method to optimize power in meta-analysis of genetic association studies with overlapping subjects. Bioinformatics (Oxford, England). PMID 29036405 DOI: 10.1093/Bioinformatics/Btx463 |
0.446 |
|
| 2017 |
Cook S, Han B. MergeReference: A Tool for Merging Reference Panels for HLA Imputation. Genomics & Informatics. 15: 108-111. PMID 29020726 DOI: 10.5808/Gi.2017.15.3.108 |
0.393 |
|
| 2017 |
Lee CH, Eskin E, Han B. Increasing the power of meta-analysis of genome-wide association studies to detect heterogeneous effects. Bioinformatics (Oxford, England). 33: i379-i388. PMID 28881976 DOI: 10.1093/Bioinformatics/Btx242 |
0.634 |
|
| 2017 |
Duong D, Gai L, Snir S, Kang EY, Han B, Sul JH, Eskin E. Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes. Bioinformatics (Oxford, England). 33: i67-i74. PMID 28881962 DOI: 10.1093/Bioinformatics/Btx227 |
0.798 |
|
| 2017 |
Lee HS, Oh H, Baek J, Jung S, Hong M, Kim KM, Shin HD, Kim KJ, Park SH, Ye BD, Han B, Yang SK, Song K. X chromosome-wide association study identifies a susceptibility locus for inflammatory bowel disease in Koreans. Journal of Crohn's & Colitis. PMID 28333213 DOI: 10.1093/Ecco-Jcc/Jjx023 |
0.352 |
|
| 2016 |
Lee CH, Cook S, Lee JS, Han B. Comparison of Two Meta-Analysis Methods: Inverse-Variance-Weighted Average and Weighted Sum of Z-Scores. Genomics & Informatics. 14: 173-180. PMID 28154508 DOI: 10.5808/Gi.2016.14.4.173 |
0.354 |
|
| 2016 |
Hinks A, Bowes J, Cobb J, Ainsworth HC, Marion MC, Comeau ME, Sudman M, Han B, Becker ML, Bohnsack JF, de Bakker PI, Haas JP, Hazen M, Lovell DJ, et al. Fine-mapping the MHC locus in juvenile idiopathic arthritis (JIA) reveals genetic heterogeneity corresponding to distinct adult inflammatory arthritic diseases. Annals of the Rheumatic Diseases. PMID 27998952 DOI: 10.1136/Annrheumdis-2016-210025 |
0.393 |
|
| 2016 |
Kang EY, Martin L, Mangul S, Isvilanonda W, Zou J, Ben-David E, Han B, Lusis AJ, Shifman S, Eskin E. Discovering SNPs Regulating Human Gene Expression Using Allele Specific Expression from RNA-Seq Data. Genetics. PMID 27765809 DOI: 10.1534/Genetics.115.177246 |
0.774 |
|
| 2016 |
Jung J, Lee HC, Seol HS, Choi YS, Kim E, Lee EJ, Rhee JK, Singh SR, Jun ES, Han B, Hong SM, Kim SC, Chang S. Generation and molecular characterization of pancreatic cancer patient-derived xenografts reveals their heterologous nature. Oncotarget. PMID 27613834 DOI: 10.18632/Oncotarget.11530 |
0.303 |
|
| 2016 |
Yang SK, Hong M, Oh H, Low HQ, Jung S, Ahn S, Kim Y, Baek J, Lee CH, Kim E, Kim KM, Ye BD, Kim KJ, Park SH, Lee HS, ... ... Han B, et al. Identification of Loci at 1q21 and 16q23 That Affect Susceptibility to Inflammatory Bowel Disease in Koreans. Gastroenterology. PMID 27569725 DOI: 10.1053/J.Gastro.2016.08.025 |
0.42 |
|
| 2016 |
Duong D, Zou J, Hormozdiari F, Sul JH, Ernst J, Han B, Eskin E. Using genomic annotations increases statistical power to detect eGenes. Bioinformatics (Oxford, England). 32: i156-i163. PMID 27307612 DOI: 10.1093/Bioinformatics/Btw272 |
0.768 |
|
| 2016 |
Hormozdiari F, Kang EY, Bilow M, Ben-David E, Vulpe C, McLachlan S, Lusis AJ, Han B, Eskin E. Imputing Phenotypes for Genome-wide Association Studies. American Journal of Human Genetics. PMID 27292110 DOI: 10.1016/J.Ajhg.2016.04.013 |
0.76 |
|
| 2016 |
Kang EY, Park Y, Li X, Segrè AV, Han B, Eskin E. ForestPMPlot: A Flexible Tool for Visualizing Heterogeneity between Studies in Meta-analysis. G3 (Bethesda, Md.). PMID 27194809 DOI: 10.1534/G3.116.029439 |
0.717 |
|
| 2016 |
Han B, Pouget JG, Slowikowski K, Stahl E, Lee CH, Diogo D, Hu X, Park YR, Kim E, Gregersen PK, Dahlqvist SR, Worthington J, Martin J, Eyre S, Klareskog L, et al. A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases. Nature Genetics. PMID 27182969 DOI: 10.1038/Ng.3572 |
0.377 |
|
| 2016 |
Joo JW, Hormozdiari F, Han B, Eskin E. Multiple testing correction in linear mixed models. Genome Biology. 17: 62. PMID 27039378 DOI: 10.1186/S13059-016-0903-6 |
0.589 |
|
| 2016 |
Ellinghaus D, Jostins L, Spain SL, Cortes A, Bethune J, Han B, Park YR, Raychaudhuri S, Pouget JG, Hübenthal M, Folseraas T, Wang Y, Esko T, Metspalu A, Westra HJ, et al. Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci. Nature Genetics. PMID 26974007 DOI: 10.1038/Ng.3528 |
0.4 |
|
| 2016 |
Han B, Duong D, Sul JH, de Bakker PI, Eskin E, Raychaudhuri S. A general framework for meta-analyzing dependent studies with overlapping subjects in association mapping. Human Molecular Genetics. PMID 26908615 DOI: 10.1093/Hmg/Ddw049 |
0.769 |
|
| 2015 |
Kwak SH, Kim YJ, Chae J, Lee CH, Han B, Kim JI, Jung HS, Cho YM, Park KS. Association of HLA Genotype and Fulminant Type 1 Diabetes in Koreans. Genomics & Informatics. 13: 126-31. PMID 26865843 DOI: 10.5808/Gi.2015.13.4.126 |
0.379 |
|
| 2015 |
Ombrello MJ, Remmers EF, Tachmazidou I, Grom A, Foell D, Haas JP, Martini A, Gattorno M, Özen S, Prahalad S, Zeft AS, Bohnsack JF, Mellins ED, Ilowite NT, Russo R, ... ... Han B, et al. HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis. Proceedings of the National Academy of Sciences of the United States of America. PMID 26598658 DOI: 10.1073/Pnas.1520779112 |
0.378 |
|
| 2015 |
Lenz TL, Deutsch AJ, Han B, Hu X, Okada Y, Eyre S, Knapp M, Zhernakova A, Huizinga TW, Abecasis G, Becker J, Boeckxstaens GE, Chen WM, Franke A, Gladman DD, et al. Widespread non-additive and interaction effects within HLA loci modulate the risk of autoimmune diseases. Nature Genetics. PMID 26258845 DOI: 10.1038/Ng.3379 |
0.324 |
|
| 2015 |
Trynka G, Westra HJ, Slowikowski K, Hu X, Xu H, Stranger BE, Klein RJ, Han B, Raychaudhuri S. Disentangling the Effects of Colocalizing Genomic Annotations to Functionally Prioritize Non-coding Variants within Complex-Trait Loci. American Journal of Human Genetics. 97: 139-52. PMID 26140449 DOI: 10.1016/J.Ajhg.2015.05.016 |
0.521 |
|
| 2015 |
Sul JH, Raj T, de Jong S, de Bakker PI, Raychaudhuri S, Ophoff RA, Stranger BE, Eskin E, Han B. Accurate and fast multiple-testing correction in eQTL studies. American Journal of Human Genetics. 96: 857-68. PMID 26027500 DOI: 10.1016/J.Ajhg.2015.04.012 |
0.762 |
|
| 2015 |
Viatte S, Plant D, Han B, Fu B, Yarwood A, Thomson W, Symmons DP, Worthington J, Young A, Hyrich KL, Morgan AW, Wilson AG, Isaacs JD, Raychaudhuri S, Barton A. Association of HLA-DRB1 haplotypes with rheumatoid arthritis severity, mortality, and treatment response. Jama. 313: 1645-56. PMID 25919528 DOI: 10.1001/Jama.2015.3435 |
0.37 |
|
| 2015 |
Yarwood A, Han B, Raychaudhuri S, Bowes J, Lunt M, Pappas DA, Kremer J, Greenberg JD, Plenge R, Worthington J, Barton A, Eyre S. A weighted genetic risk score using all known susceptibility variants to estimate rheumatoid arthritis risk. Annals of the Rheumatic Diseases. 74: 170-6. PMID 24092415 DOI: 10.1136/Annrheumdis-2013-204133 |
0.356 |
|
| 2015 |
Hinks A, Cobb J, Bowes J, Han B, Ainsworth H, Marion M, Sudman M, Bohnsack J, Wedderburn L, Haas J, Videm V, Rygg M, Nordal E, Brown M, Yeung R, et al. OP0121 Analysis of the MHC Region in a Large Cohort of Juvenile Idiopathic Arthritis Cases Identifies Independent Effects at HLA-DRB1 for the Most Common Subtypes of JIA Annals of the Rheumatic Diseases. 74: 114.1-114. DOI: 10.1136/Annrheumdis-2015-Eular.3887 |
0.398 |
|
| 2014 |
Kim K, Bang SY, Lee HS, Okada Y, Han B, Saw WY, Teo YY, Bae SC. The HLA-DRβ1 amino acid positions 11-13-26 explain the majority of SLE-MHC associations. Nature Communications. 5: 5902. PMID 25533202 DOI: 10.1038/Ncomms6902 |
0.349 |
|
| 2014 |
Dunstan SJ, Hue NT, Han B, Li Z, Tram TT, Sim KS, Parry CM, Chinh NT, Vinh H, Lan NP, Thieu NT, Vinh PV, Koirala S, Dongol S, Arjyal A, et al. Variation at HLA-DRB1 is associated with resistance to enteric fever. Nature Genetics. 46: 1333-6. PMID 25383971 DOI: 10.1038/Ng.3143 |
0.379 |
|
| 2014 |
Okada Y, Han B, Tsoi LC, Stuart PE, Ellinghaus E, Tejasvi T, Chandran V, Pellett F, Pollock R, Bowcock AM, Krueger GG, Weichenthal M, Voorhees JJ, Rahman P, Gregersen PK, et al. Fine mapping major histocompatibility complex associations in psoriasis and its clinical subtypes. American Journal of Human Genetics. 95: 162-72. PMID 25087609 DOI: 10.1016/J.Ajhg.2014.07.002 |
0.367 |
|
| 2014 |
Okada Y, Kim K, Han B, Pillai NE, Ong RT, Saw WY, Luo M, Jiang L, Yin J, Bang SY, Lee HS, Brown MA, Bae SC, Xu H, Teo YY, et al. Risk for ACPA-positive rheumatoid arthritis is driven by shared HLA amino acid polymorphisms in Asian and European populations. Human Molecular Genetics. 23: 6916-26. PMID 25070946 DOI: 10.1093/Hmg/Ddu387 |
0.351 |
|
| 2014 |
Joo JW, Sul JH, Han B, Ye C, Eskin E. Effectively identifying regulatory hotspots while capturing expression heterogeneity in gene expression studies. Genome Biology. 15: r61. PMID 24708878 DOI: 10.1186/Gb-2014-15-4-R61 |
0.781 |
|
| 2014 |
Han B, Diogo D, Eyre S, Kallberg H, Zhernakova A, Bowes J, Padyukov L, Okada Y, González-Gay MA, Rantapää-Dahlqvist S, Martin J, Huizinga TW, Plenge RM, Worthington J, Gregersen PK, et al. Fine mapping seronegative and seropositive rheumatoid arthritis to shared and distinct HLA alleles by adjusting for the effects of heterogeneity. American Journal of Human Genetics. 94: 522-32. PMID 24656864 DOI: 10.1016/J.Ajhg.2014.02.013 |
0.321 |
|
| 2014 |
Kang EY, Han B, Furlotte N, Joo JW, Shih D, Davis RC, Lusis AJ, Eskin E. Meta-analysis identifies gene-by-environment interactions as demonstrated in a study of 4,965 mice. Plos Genetics. 10: e1004022. PMID 24415945 DOI: 10.1371/Journal.Pgen.1004022 |
0.795 |
|
| 2014 |
Han B, Kang EY, Raychaudhuri S, de Bakker PI, Eskin E. Fast pairwise IBD association testing in genome-wide association studies. Bioinformatics (Oxford, England). 30: 206-13. PMID 24158599 DOI: 10.1093/Bioinformatics/Btt609 |
0.769 |
|
| 2014 |
Viatte S, Plant D, Han B, Fu B, Yarwood A, Thomson W, Symmons D, Worthington J, Young A, Hyrich K, Morgan A, Wilson A, Isaacs J, Raychaudhuri S, Barton A. OP0190 Personalized Genetic Medicine: Amino Acid Positions 11, 71 and 74 in HLA-DRB1 PREDICT Disease Severity, Treatment Response and Mortality in Rheumatoid Arthritis; Multi-Centre Prospective Cohort Studies Annals of the Rheumatic Diseases. 73: 134.2-134. DOI: 10.1136/Annrheumdis-2014-Eular.3155 |
0.314 |
|
| 2013 |
Hu X, Kim H, Brennan PJ, Han B, Baecher-Allan CM, De Jager PL, Brenner MB, Raychaudhuri S. Application of user-guided automated cytometric data analysis to large-scale immunoprofiling of invariant natural killer T cells. Proceedings of the National Academy of Sciences of the United States of America. 110: 19030-5. PMID 24191009 DOI: 10.1073/Pnas.1318322110 |
0.318 |
|
| 2013 |
He D, Wang Z, Han B, Parida L, Eskin E. IPED: inheritance path-based pedigree reconstruction algorithm using genotype data. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 20: 780-91. PMID 24093229 DOI: 10.1089/Cmb.2013.0080 |
0.615 |
|
| 2013 |
Sul JH, Han B, Ye C, Choi T, Eskin E. Effectively identifying eQTLs from multiple tissues by combining mixed model and meta-analytic approaches. Plos Genetics. 9: e1003491. PMID 23785294 DOI: 10.1371/Journal.Pgen.1003491 |
0.769 |
|
| 2013 |
Jia X, Han B, Onengut-Gumuscu S, Chen WM, Concannon PJ, Rich SS, Raychaudhuri S, de Bakker PI. Imputing amino acid polymorphisms in human leukocyte antigens. Plos One. 8: e64683. PMID 23762245 DOI: 10.1371/Journal.Pone.0064683 |
0.425 |
|
| 2013 |
Navon O, Sul JH, Han B, Conde L, Bracci PM, Riby J, Skibola CF, Eskin E, Halperin E. Rare variant association testing under low-coverage sequencing. Genetics. 194: 769-79. PMID 23636738 DOI: 10.1534/Genetics.113.150169 |
0.743 |
|
| 2013 |
He D, Han B, Eskin E. Hap-seq: an optimal algorithm for haplotype phasing with imputation using sequencing data. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 20: 80-92. PMID 23383995 DOI: 10.1089/Cmb.2012.0091 |
0.67 |
|
| 2013 |
Trynka G, Sandor C, Han B, Xu H, Stranger BE, Liu XS, Raychaudhuri S. Chromatin marks identify critical cell types for fine mapping complex trait variants Nature Genetics. 45: 124-130. PMID 23263488 DOI: 10.1038/Ng.2504 |
0.386 |
|
| 2013 |
Scharf JM, Yu D, Mathews CA, Neale BM, Stewart SE, Fagerness JA, Evans P, Gamazon E, Edlund CK, Service SK, Tikhomirov A, Osiecki L, Illmann C, Pluzhnikov A, Konkashbaev A, ... ... Han B, et al. Genome-wide association study of Tourette's syndrome. Molecular Psychiatry. 18: 721-8. PMID 22889924 DOI: 10.1038/Mp.2012.69 |
0.615 |
|
| 2013 |
Hinks A, Cobb J, Han B, Marion M, Sudman M, Martin P, Bohnsack J, Wedderburn L, Haas J, De Bakker P, Langefeld C, Raychaudhuri S, Prahalad S, Thompson S, Thomson W. PReS-FINAL-2135: Analysis of the HLA region in a large cohort of juvenile idiopathic arthritis cases identifies independent effects at HLA-DRB1 Pediatric Rheumatology. 11. DOI: 10.1186/1546-0096-11-S2-P148 |
0.424 |
|
| 2013 |
Yarwood A, Lunt M, Han B, Raychaudhuri S, Bowes J, Barton A, Eyre S, Raci. THU0010 A Weighted Genetic Risk Score Using 46 Loci to Predict Rheumatoid Arthritis Risk Annals of the Rheumatic Diseases. 72. DOI: 10.1136/Annrheumdis-2013-Eular.538 |
0.395 |
|
| 2013 |
He D, Wang Z, Han B, Parida L, Eskin E. IPED: Inheritance path based pedigree reconstruction algorithm using genotype data Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 7821: 75-87. DOI: 10.1007/978-3-642-37195-0_7 |
0.581 |
|
| 2012 |
Darnell G, Duong D, Han B, Eskin E. Incorporating prior information into association studies. Bioinformatics (Oxford, England). 28: i147-53. PMID 22689754 DOI: 10.1093/Bioinformatics/Bts235 |
0.646 |
|
| 2012 |
Han B, Eskin E. Interpreting meta-analyses of genome-wide association studies. Plos Genetics. 8: e1002555. PMID 22396665 DOI: 10.1371/Journal.Pgen.1002555 |
0.632 |
|
| 2011 |
Sul JH, Han B, Eskin E. Increasing power of groupwise association test with likelihood ratio test. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 18: 1611-24. PMID 21919745 DOI: 10.1089/Cmb.2011.0161 |
0.774 |
|
| 2011 |
Han B, Eskin E. Random-effects model aimed at discovering associations in meta-analysis of genome-wide association studies. American Journal of Human Genetics. 88: 586-98. PMID 21565292 DOI: 10.1016/J.Ajhg.2011.04.014 |
0.611 |
|
| 2011 |
Sul JH, Han B, He D, Eskin E. An optimal weighted aggregated association test for identification of rare variants involved in common diseases. Genetics. 188: 181-8. PMID 21368279 DOI: 10.1534/Genetics.110.125070 |
0.781 |
|
| 2011 |
Han B, Hackel BM, Eskin E. Postassociation cleaning using linkage disequilibrium information. Genetic Epidemiology. 35: 1-10. PMID 21181893 DOI: 10.1002/Gepi.20544 |
0.639 |
|
| 2010 |
Kirby A, Kang HM, Wade CM, Cotsapas C, Kostem E, Han B, Furlotte N, Kang EY, Rivas M, Bogue MA, Frazer KA, Johnson FM, Beilharz EJ, Cox DR, Eskin E, et al. Fine mapping in 94 inbred mouse strains using a high-density haplotype resource. Genetics. 185: 1081-95. PMID 20439770 DOI: 10.1534/Genetics.110.115014 |
0.754 |
|
| 2009 |
Han B, Kang HM, Eskin E. Rapid and accurate multiple testing correction and power estimation for millions of correlated markers. Plos Genetics. 5: e1000456. PMID 19381255 DOI: 10.1371/Journal.Pgen.1000456 |
0.621 |
|
| 2009 |
Kang HM, Zaitlen NA, Han B, Eskin E. An adaptive and memory efficient algorithm for genotype imputation Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 5541: 482-495. DOI: 10.1007/978-3-642-02008-7_34 |
0.614 |
|
| 2008 |
Han B, Kang HM, Seo MS, Zaitlen N, Eskin E. Efficient association study design via power-optimized tag SNP selection Annals of Human Genetics. 72: 834-847. PMID 18702637 DOI: 10.1111/J.1469-1809.2008.00469.X |
0.732 |
|
| 2008 |
Han B, Dost B, Bafna V, Zhang S. Structural alignment of pseudoknotted RNA. Journal of Computational Biology : a Journal of Computational Molecular Cell Biology. 15: 489-504. PMID 18549303 DOI: 10.1089/Cmb.2007.0214 |
0.315 |
|
| 2008 |
Choi A, Zaitlen N, Han B, Pipatsrisawat K, Darwiche A, Eskin E. Efficient genome wide tagging by reduction to SAT Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 5251: 135-147. DOI: 10.1007/978-3-540-87361-7_12 |
0.667 |
|
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