| Year |
Citation |
Score |
| 2024 |
Wong KW, Hui KF, Lam KP, Kwong DL, Lung ML, Yang W, Chiang AKS. Meta-analysis of Epstein-Barr virus genomes in Southern Chinese identifies genetic variants and high risk viral lineage associated with nasopharyngeal carcinoma. Plos Pathogens. 20: e1012263. PMID 38805547 DOI: 10.1371/journal.ppat.1012263 |
0.317 |
|
| 2022 |
Yin X, Kim K, Suetsugu H, Bang SY, Wen L, Koido M, Ha E, Liu L, Sakamoto Y, Jo S, Leng RX, Otomo N, Kwon YC, Sheng Y, Sugano N, ... ... Yang W, et al. Biological insights into systemic lupus erythematosus through an immune cell-specific transcriptome-wide association study. Annals of the Rheumatic Diseases. PMID 35609976 DOI: 10.1136/annrheumdis-2022-222345 |
0.355 |
|
| 2021 |
Zhang YM, Zhou XJ, Wang YN, Liu XZ, Wang YF, Lau YL, Yang WL, Zhang H. Shared genetic study gives insights into the shared and distinct pathogenic immunity components of IgA nephropathy and SLE. Molecular Genetics and Genomics : Mgg. PMID 34076728 DOI: 10.1007/s00438-021-01798-7 |
0.376 |
|
| 2021 |
Wang YF, Zhang Y, Lin Z, Zhang H, Wang TY, Cao Y, Morris DL, Sheng Y, Yin X, Zhong SL, Gu X, Lei Y, He J, Wu Q, Shen JJ, ... ... Yang W, et al. Identification of 38 novel loci for systemic lupus erythematosus and genetic heterogeneity between ancestral groups. Nature Communications. 12: 772. PMID 33536424 DOI: 10.1038/s41467-021-21049-y |
0.31 |
|
| 2021 |
Song Q, Lei Y, Shao L, Li W, Kong Q, Lin Z, Qin X, Wei W, Hou F, Li J, Guo X, Mao Y, Cao Y, Liu Z, Zheng L, ... ... Yang W, et al. Genome-wide association study on Northern Chinese identifies KLF2, DOT1L and STAB2 associated with systemic lupus erythematosus. Rheumatology (Oxford, England). PMID 33493351 DOI: 10.1093/rheumatology/keab016 |
0.324 |
|
| 2020 |
Yin X, Kim K, Suetsugu H, Bang SY, Wen L, Koido M, Ha E, Liu L, Sakamoto Y, Jo S, Leng RX, Otomo N, Laurynenka V, Kwon YC, Sheng Y, ... ... Yang W, et al. Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus. Annals of the Rheumatic Diseases. PMID 33272962 DOI: 10.1136/annrheumdis-2020-219209 |
0.345 |
|
| 2020 |
Zhang F, Wang YF, Zhang Y, Lin Z, Cao Y, Zhang H, Liu ZY, Morris DL, Sheng Y, Cui Y, Zhang X, Vyse TJ, Lau YL, Yang W, Chen Y. Independent Replication on Genome-Wide Association Study Signals Identifies as a Novel Locus for Systemic Lupus Erythematosus. Frontiers in Genetics. 11: 600. PMID 32719713 DOI: 10.3389/Fgene.2020.00600 |
0.468 |
|
| 2019 |
Wang TY, Wang YF, Zhang Y, Shen JJ, Guo M, Yang J, Lau YL, Yang W. Identification of Regulatory Modules That Stratify Lupus Disease Mechanism through Integrating Multi-Omics Data. Molecular Therapy. Nucleic Acids. 19: 318-329. PMID 31877408 DOI: 10.1016/J.Omtn.2019.11.019 |
0.362 |
|
| 2019 |
Wang YF, Lau YL, Yang W. Genetic studies on systemic lupus erythematosus in East Asia point to population differences in disease susceptibility. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. PMID 30897304 DOI: 10.1002/Ajmg.C.31696 |
0.379 |
|
| 2019 |
Yeung KS, Lee TL, Mok MY, Mak CCY, Yang W, Chong PCY, Lee PPW, Ho MHK, Choufani S, Lau CS, Lau YL, Weksberg R, Chung BHY. Cell Lineage-specific Genome-wide DNA Methylation Analysis of Patients with Paediatric-onset Systemic Lupus Erythematosus. Epigenetics. PMID 30806140 DOI: 10.1080/15592294.2019.1585176 |
0.35 |
|
| 2018 |
Hui KF, Chan TF, Yang W, Shen JJ, Lam KP, Kwok H, Sham PC, Tsao SW, Kwong DL, Lung ML, Chiang AKS. High risk Epstein-Barr virus variants characterized by distinct polymorphisms in the EBER locus are strongly associated with nasopharyngeal carcinoma. International Journal of Cancer. PMID 30536939 DOI: 10.1002/Ijc.32049 |
0.416 |
|
| 2018 |
Leung GKC, Mak CCY, Fung JLF, Wong WHS, Tsang MHY, Yu MHC, Pei SLC, Yeung KS, Mok GTK, Lee CP, Hui APW, Tang MHY, Chan KYK, Liu APY, Yang W, et al. Identifying the genetic causes for prenatally diagnosed structural congenital anomalies (SCAs) by whole-exome sequencing (WES). Bmc Medical Genomics. 11: 93. PMID 30359267 DOI: 10.1186/S12920-018-0409-Z |
0.315 |
|
| 2018 |
Tang CS, Li P, Lai FP, Fu AX, Lau ST, So MT, Lui KN, Li Z, Zhuang X, Yu M, Liu X, Ngo ND, Miao X, Zhang X, Yi B, ... ... Yang W, et al. Identification of Genes Associated with Hirschsprung Disease, Based on Whole-genome Sequence Analysis, and Potential Effects on Enteric Nervous System Development. Gastroenterology. PMID 30217742 DOI: 10.1053/J.Gastro.2018.09.012 |
0.413 |
|
| 2018 |
Mak CC, Leung GK, Mok GT, Yeung KS, Yang W, Fung CW, Chan SH, Lee SL, Lee NC, Pfundt R, Lau YL, Chung BH. Exome sequencing for paediatric-onset diseases: impact of the extensive involvement of medical geneticists in the diagnostic odyssey. Npj Genomic Medicine. 3: 19. PMID 30109123 DOI: 10.1038/S41525-018-0056-5 |
0.358 |
|
| 2018 |
Zhang H, Zhang Y, Wang YF, Morris D, Hirankarn N, Sheng Y, Shen J, Pan HF, Yang J, Yang S, Cui Y, Ye DQ, Vyse TJ, Zhang X, Lau YL, ... Yang W, et al. Meta-analysis of GWAS on both Chinese and European populations identifies GPR173 as a novel X chromosome susceptibility gene for SLE. Arthritis Research & Therapy. 20: 92. PMID 29724251 DOI: 10.1186/S13075-018-1590-3 |
0.421 |
|
| 2018 |
Sun J, Yang C, Fei W, Zhang X, Sheng Y, Zheng X, Tang H, Yang W, Yang S, Fan X, Zhang X. HLA-DQβ1 amino acid position 87 and DQB1*0301 are associated with Chinese Han SLE. Molecular Genetics & Genomic Medicine. PMID 29676044 DOI: 10.1002/Mgg3.403 |
0.374 |
|
| 2018 |
Wang B, Bao S, Zhang Z, Zhou X, Wang J, Fan Y, Zhang Y, Li Y, Chen L, Jia Y, Li J, Li M, Zheng W, Mu N, Wang L, ... ... Yang W, et al. A rare variant in MLKL confers susceptibility to ApoE ɛ4-negative Alzheimer's disease in Hong Kong Chinese population. Neurobiology of Aging. PMID 29656768 DOI: 10.1016/J.Neurobiolaging.2018.03.006 |
0.363 |
|
| 2018 |
Wang YF, Zhang Y, Zhu Z, Wang TY, Morris DL, Shen JJ, Zhang H, Pan HF, Yang J, Yang S, Ye DQ, Vyse TJ, Cui Y, Zhang X, Sheng Y, ... ... Yang W, et al. Identification of,andas loci associated with systemic lupus erythematosus (SLE) and evaluation of SLE genetics in drug repositioning. Annals of the Rheumatic Diseases. PMID 29625966 DOI: 10.1136/Annrheumdis-2018-213093 |
0.414 |
|
| 2017 |
Mao H, Yang W, Latour S, Yang J, Winter S, Zheng J, Ni K, Lv M, Liu C, Huang H, Chan KW, Pui-Wah Lee P, Tu W, Fischer A, Lau YL. RASGRP1 mutation in autoimmune lymphoproliferative syndrome-like disease. The Journal of Allergy and Clinical Immunology. PMID 29155103 DOI: 10.1016/J.Jaci.2017.10.026 |
0.378 |
|
| 2017 |
Shen JJ, Wang TY, Yang W. Regulatory and evolutionary signatures of sex-biased genes on both the X chromosome and the autosomes. Biology of Sex Differences. 8: 35. PMID 29096703 DOI: 10.1186/S13293-017-0156-4 |
0.321 |
|
| 2017 |
Molineros JE, Yang W, Zhou XJ, Sun C, Okada Y, Zhang H, Chua KH, Lau YL, Kochi Y, Suzuki A, Yamamoto K, Ma J, Bang SY, Lee HS, Kim K, et al. Confirmation of five novel susceptibility loci for Systemic Lupus Erythematosus (SLE) and integrated network analysis of 82 SLE susceptibility loci. Human Molecular Genetics. PMID 28108556 DOI: 10.1093/Hmg/Ddx026 |
0.451 |
|
| 2017 |
Yeung KS, Chung BH, Choufani S, Mok MY, Wong WL, Mak CC, Yang W, Lee PP, Wong WH, Chen YA, Grafodatskaya D, Wong RW, Lau CS, Chan DT, Weksberg R, et al. Genome-Wide DNA Methylation Analysis of Chinese Patients with Systemic Lupus Erythematosus Identified Hypomethylation in Genes Related to the Type I Interferon Pathway. Plos One. 12: e0169553. PMID 28085900 DOI: 10.1371/Journal.Pone.0169553 |
0.334 |
|
| 2017 |
Nath S, Yang W, Zhou X, Sun C, Okada Y, Bae S, Shen N, Molineros J. 3 Confirmation of 5 novel susceptibility loci for systemic lupus erythematosus (sle) and integrated network analysis of 82 sle susceptibility loci Lupus Science & Medicine. 4. DOI: 10.1136/Lupus-2017-000215.3 |
0.463 |
|
| 2016 |
Zhou XJ, Nath SK, Qi YY, Sun C, Hou P, Zhang YM, Lv JC, Shi SF, Liu LJ, Chen R, Yang W, He KZ, Li Y, Zhang H. Novel identified associations of RGS1 and RASGRP1 variants in IgA Nephropathy. Scientific Reports. 6: 35781. PMID 27804980 DOI: 10.1038/Srep35781 |
0.488 |
|
| 2016 |
Chen R, Lau YL, Zhang Y, Yang W. SRinversion: a tool for detecting short inversions by splitting and re-aligning poorly mapped and unmapped sequencing reads. Bioinformatics (Oxford, England). PMID 27503227 DOI: 10.1093/Bioinformatics/Btw516 |
0.326 |
|
| 2016 |
Zhang F, Wu L, Qian J, Qu B, Xia S, La T, Wu Y, Ma J, Zeng J, Guo Q, Cui Y, Yang W, Huang J, Zhu W, Yao Y, et al. Identification of the long noncoding RNA NEAT1 as a novel inflammatory regulator acting through MAPK pathway in human lupus. Journal of Autoimmunity. PMID 27481557 DOI: 10.1016/J.Jaut.2016.07.012 |
0.319 |
|
| 2016 |
Morris DL, Sheng Y, Zhang Y, Wang YF, Zhu Z, Tombleson P, Chen L, Cunninghame Graham DS, Bentham J, Roberts AL, Chen R, Zuo X, Wang T, Wen L, Yang C, ... ... Yang W, et al. Genome-wide association meta-analysis in Chinese and European individuals identifies ten new loci associated with systemic lupus erythematosus. Nature Genetics. PMID 27399966 DOI: 10.1038/Ng.3603 |
0.453 |
|
| 2016 |
Leng RX, Pan HF, Liu J, Yang XK, Zhang C, Tao SS, Wang DG, Li XM, Li XP, Yang W, Ye DQ. Evidence for genetic association of TBX21 and IFNG with systemic lupus erythematosus in a Chinese Han population. Scientific Reports. 6: 22081. PMID 26916970 DOI: 10.1038/Srep22081 |
0.4 |
|
| 2015 |
Zhu Z, Liang Z, Liany H, Yang C, Wen L, Lin Z, Sheng Y, Lin Y, Ye L, Cheng Y, Chang Y, Liu L, Yang L, Shi Y, Shen C, ... ... Yang W, et al. Discovery of a novel genetic susceptibility locus on X chromosome for systemic lupus erythematosus. Arthritis Research & Therapy. 17: 349. PMID 26635088 DOI: 10.1186/S13075-015-0857-1 |
0.441 |
|
| 2015 |
Zhang J, Zhang L, Zhang Y, Yang J, Guo M, Sun L, Pan HF, Hirankarn N, Ying D, Zeng S, Lee TL, Lau CS, Chan TM, Leung AM, Mok CC, ... ... Yang W, et al. Gene-based meta-analysis of GWAS data identifies independent SNPs in ANXA6 as associated with SLE in Asian populations. Arthritis & Rheumatology (Hoboken, N.J.). PMID 26202167 DOI: 10.1002/Art.39275 |
0.469 |
|
| 2015 |
Tam RC, Lee AL, Yang W, Lau CS, Chan VS. Systemic Lupus Erythematosus Patients Exhibit Reduced Expression of CLEC16A Isoforms in Peripheral Leukocytes. International Journal of Molecular Sciences. 16: 14428-40. PMID 26121298 DOI: 10.3390/Ijms160714428 |
0.35 |
|
| 2015 |
Ying D, Sham PC, Smith DK, Zhang L, Lau YL, Yang W. HaploShare: identification of extended haplotypes shared by cases and evaluation against controls. Genome Biology. 16: 92. PMID 25956955 DOI: 10.1186/S13059-015-0662-9 |
0.313 |
|
| 2015 |
Huang Y, Yang J, Ying D, Zhang Y, Shotelersuk V, Hirankarn N, Sham PC, Lau YL, Yang W. HLAreporter: a tool for HLA typing from next generation sequencing data. Genome Medicine. 7: 25. PMID 25908942 DOI: 10.1186/S13073-015-0145-3 |
0.309 |
|
| 2015 |
Zhang Y, Wang Y, Yang J, Zhang J, Sun L, Hirankarn N, Pan HF, Lau CS, Chan TM, Lee TL, Leung AM, Mok CC, Zhang L, Shen JJ, Wong SN, ... ... Yang W, et al. Meta-analysis of two Chinese populations identifies an autoimmune disease risk allele in 22q11.21 as associated with systemic lupus erythematosus. Arthritis Research & Therapy. 17: 67. PMID 25880549 DOI: 10.1186/S13075-015-0577-6 |
0.448 |
|
| 2015 |
Zhang Y, Yang J, Zhang J, Sun L, Hirankarn N, Pan HF, Lau CS, Chan TM, Lee TL, Leung AM, Mok CC, Zhang L, Wang Y, Shen JJ, Wong SN, ... ... Yang W, et al. Genome-wide search followed by replication reveals genetic interaction of CD80 and ALOX5AP associated with systemic lupus erythematosus in Asian populations. Annals of the Rheumatic Diseases. PMID 25862617 DOI: 10.1136/Annrheumdis-2014-206367 |
0.389 |
|
| 2015 |
Tu X, Chong WP, Zhai Y, Zhang H, Zhang F, Wang S, Liu W, Wei M, Siu NH, Yang H, Yang W, Cao W, Lau YL, He F, Zhou G. Functional polymorphisms of the CCL2 and MBL genes cumulatively increase susceptibility to severe acute respiratory syndrome coronavirus infection. The Journal of Infection. 71: 101-9. PMID 25818534 DOI: 10.1016/J.Jinf.2015.03.006 |
0.328 |
|
| 2015 |
Li MJ, Deng J, Wang P, Yang W, Ho SL, Sham PC, Wang J, Li M. wKGGSeq: A Comprehensive Strategy-Based and Disease-Targeted Online Framework to Facilitate Exome Sequencing Studies of Inherited Disorders. Human Mutation. 36: 496-503. PMID 25676918 DOI: 10.1002/Humu.22766 |
0.337 |
|
| 2015 |
Yang W, Lau YL. Solving the genetic puzzle of systemic lupus erythematosus. Pediatric Nephrology (Berlin, Germany). 30: 1735-48. PMID 25239301 DOI: 10.1007/S00467-014-2947-8 |
0.381 |
|
| 2015 |
Zhang Y, Zhang J, Yang J, Wang Y, Zhang L, Zuo X, Sun L, Pan HF, Hirankarn N, Wang T, Chen R, Ying D, Zeng S, Shen JJ, Lee TL, ... ... Yang W, et al. Meta-analysis of GWAS on two Chinese populations followed by replication identifies novel genetic variants on the X chromosome associated with systemic lupus erythematosus. Human Molecular Genetics. 24: 274-84. PMID 25149475 DOI: 10.1093/Hmg/Ddu429 |
0.452 |
|
| 2014 |
Yang W, Lee PP, Thong MK, Ramanujam TM, Shanmugam A, Koh MT, Chan KW, Ying D, Wang Y, Shen JJ, Yang J, Lau YL. Compound heterozygous mutations in TTC7A cause familial multiple intestinal atresias and severe combined immunodeficiency. Clinical Genetics. PMID 25534311 DOI: 10.1111/Cge.12553 |
0.347 |
|
| 2014 |
Zhou XJ, Nath SK, Qi YY, Cheng FJ, Yang HZ, Zhang Y, Yang W, Ma JY, Zhao MH, Shen N, Zhang H. Brief Report: identification of MTMR3 as a novel susceptibility gene for lupus nephritis in northern Han Chinese by shared-gene analysis with IgA nephropathy. Arthritis & Rheumatology (Hoboken, N.J.). 66: 2842-8. PMID 24943867 DOI: 10.1002/Art.38749 |
0.459 |
|
| 2014 |
Zeng S, Yang J, Chung BH, Lau YL, Yang W. EFIN: predicting the functional impact of nonsynonymous single nucleotide polymorphisms in human genome. Bmc Genomics. 15: 455. PMID 24916671 DOI: 10.1186/1471-2164-15-455 |
0.344 |
|
| 2014 |
Zhang J, Zhang Y, Yang J, Zhang L, Sun L, Pan HF, Hirankarn N, Ying D, Zeng S, Lee TL, Lau CS, Chan TM, Leung AM, Mok CC, Wong SN, ... ... Yang W, et al. Three SNPs in chromosome 11q23.3 are independently associated with systemic lupus erythematosus in Asians. Human Molecular Genetics. 23: 524-33. PMID 24001599 DOI: 10.1093/Hmg/Ddt424 |
0.469 |
|
| 2013 |
Zhang J, Zhang Y, Zhang L, Yang J, Ying D, Zeng S, Lee TL, Lau CS, Chan TM, Leung AM, Mok CC, Wong SN, Lee KW, Ho MH, Lee PP, ... ... Yang W, et al. Epistatic interaction between genetic variants in susceptibility gene ETS1 correlates with IL-17 levels in SLE patients. Annals of Human Genetics. 77: 344-50. PMID 23614478 DOI: 10.1111/Ahg.12018 |
0.382 |
|
| 2013 |
Li MX, Kwan JS, Bao SY, Yang W, Ho SL, Song YQ, Sham PC. Predicting mendelian disease-causing non-synonymous single nucleotide variants in exome sequencing studies. Plos Genetics. 9: e1003143. PMID 23341771 DOI: 10.1371/Journal.Pgen.1003143 |
0.33 |
|
| 2013 |
Yang W, Tang H, Zhang Y, Tang X, Zhang J, Sun L, Yang J, Cui Y, Zhang L, Hirankarn N, Cheng H, Pan HF, Gao J, Lee TL, Sheng Y, et al. Meta-analysis followed by replication identifies loci in or near CDKN1B, TET3, CD80, DRAM1, and ARID5B as associated with systemic lupus erythematosus in Asians. American Journal of Human Genetics. 92: 41-51. PMID 23273568 DOI: 10.1016/J.Ajhg.2012.11.018 |
0.468 |
|
| 2013 |
Kaiser R, Taylor KE, Deng Y, Zhao J, Li Y, Nititham J, Chang M, Catanese J, Begovich AB, Brown EE, Edberg JC, McGwin G, Alarcón GS, Ramsey-Goldman R, Reveille JD, ... ... Yang W, et al. Brief Report: Single-nucleotide polymorphisms in VKORC1 are risk factors for systemic lupus erythematosus in Asians. Arthritis and Rheumatism. 65: 211-5. PMID 23124848 DOI: 10.1002/Art.37751 |
0.436 |
|
| 2013 |
Wong EH, Cui L, Ng CL, Tang CS, Liu XL, So MT, Yip BH, Cheng G, Zhang R, Tang WK, Yang W, Lau YL, Baum L, Kwan P, Sun LD, et al. Genome-wide copy number variation study in anorectal malformations. Human Molecular Genetics. 22: 621-31. PMID 23108157 DOI: 10.1093/Hmg/Dds451 |
0.388 |
|
| 2013 |
Zhang L, Zhang J, Yang J, Ying D, Lau YL, Yang W. PriVar: a toolkit for prioritizing SNVs and indels from next-generation sequencing data. Bioinformatics (Oxford, England). 29: 124-5. PMID 23104884 DOI: 10.1093/Bioinformatics/Bts627 |
0.385 |
|
| 2012 |
Zhao H, Yang W, Qiu R, Li J, Xin Q, Wang X, Feng Y, Shan S, Liu Y, Gong Y, Liu Q. An intronic variant associated with systemic lupus erythematosus changes the binding affinity of Yinyang1 to downregulate WDFY4 Genes and Immunity. 13: 536-542. PMID 22972472 DOI: 10.1038/Gene.2012.33 |
0.314 |
|
| 2012 |
Guo Y, Baum LW, Sham PC, Wong V, Ng PW, Lui CH, Sin NC, Tsoi TH, Tang CS, Kwan JS, Yip BH, Xiao SM, Thomas GN, Lau YL, Yang W, et al. Two-stage genome-wide association study identifies variants in CAMSAP1L1 as susceptibility loci for epilepsy in Chinese. Human Molecular Genetics. 21: 1184-9. PMID 22116939 DOI: 10.1093/Hmg/Ddr550 |
0.438 |
|
| 2012 |
Li R, Yang W, Zhang J, Hirankarn N, Pan HF, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Li XP, Avihingsanon Y, Lee TL, et al. Association of CD247 with systemic lupus erythematosus in Asian populations. Lupus. 21: 75-83. PMID 22004975 DOI: 10.1177/0961203311422724 |
0.437 |
|
| 2011 |
Khor CC, Davila S, Breunis WB, Lee YC, Shimizu C, Wright VJ, Yeung RS, Tan DE, Sim KS, Wang JJ, Wong TY, Pang J, Mitchell P, Cimaz R, Dahdah N, ... ... Yang W, et al. Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki disease. Nature Genetics. 43: 1241-6. PMID 22081228 DOI: 10.1038/Ng.981 |
0.454 |
|
| 2011 |
Luo X, Yang W, Ye DQ, Cui H, Zhang Y, Hirankarn N, Qian X, Tang Y, Lau YL, de Vries N, Tak PP, Tsao BP, Shen N. A functional variant in microRNA-146a promoter modulates its expression and confers disease risk for systemic lupus erythematosus. Plos Genetics. 7: e1002128. PMID 21738483 DOI: 10.1371/Journal.Pgen.1002128 |
0.309 |
|
| 2011 |
Zhang Y, Yang W, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Lee TL, Ho MH, Lee PP, Wong WH, Yang J, Zhang J, et al. Two missense variants in UHRF1BP1 are independently associated with systemic lupus erythematosus in Hong Kong Chinese. Genes and Immunity. 12: 231-4. PMID 21326321 DOI: 10.1038/Gene.2010.66 |
0.458 |
|
| 2011 |
Zhang L, Yang W, Ying D, Cherny SS, Hildebrandt F, Sham PC, Lau YL. Homozygosity mapping on a single patient: identification of homozygous regions of recent common ancestry by using population data. Human Mutation. 32: 345-53. PMID 21309031 DOI: 10.1002/Humu.21432 |
0.369 |
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| 2011 |
Yang J, Yang W, Hirankarn N, Ye DQ, Zhang Y, Pan HF, Mok CC, Chan TM, Wong RW, Mok MY, Lee KW, Wong SN, Leung AM, Li XP, Avihingsanon Y, et al. ELF1 is associated with systemic lupus erythematosus in Asian populations. Human Molecular Genetics. 20: 601-7. PMID 21044949 DOI: 10.1093/Hmg/Ddq474 |
0.467 |
|
| 2010 |
Lin P, Mao F, Liu Q, Yang W, Shao C, Yan C, Gong Y. A novel deletion mutation in GJB1 causes X-linked Charcot-Marie-Tooth disease in a Han Chinese family. Muscle & Nerve. 42: 922-6. PMID 21104867 DOI: 10.1002/Mus.21790 |
0.377 |
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| 2010 |
Shen N, Fu Q, Deng Y, Qian X, Zhao J, Kaufman KM, Wu YL, Yu CY, Tang Y, Chen JY, Yang W, Wong M, Kawasaki A, Tsuchiya N, Sumida T, et al. Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus. Proceedings of the National Academy of Sciences of the United States of America. 107: 15838-43. PMID 20733074 DOI: 10.1073/Pnas.1001337107 |
0.379 |
|
| 2010 |
Niederer HA, Willcocks LC, Rayner TF, Yang W, Lau YL, Williams TN, Scott JA, Urban BC, Peshu N, Dunstan SJ, Hien TT, Phu NH, Padyukov L, Gunnarsson I, Svenungsson E, et al. Copy number, linkage disequilibrium and disease association in the FCGR locus. Human Molecular Genetics. 19: 3282-94. PMID 20508037 DOI: 10.1093/Hmg/Ddq216 |
0.442 |
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| 2010 |
Willcocks LC, Carr EJ, Niederer HA, Rayner TF, Williams TN, Yang W, Scott JA, Urban BC, Peshu N, Vyse TJ, Lau YL, Lyons PA, Smith KG. A defunctioning polymorphism in FCGR2B is associated with protection against malaria but susceptibility to systemic lupus erythematosus. Proceedings of the National Academy of Sciences of the United States of America. 107: 7881-5. PMID 20385827 DOI: 10.1073/Pnas.0915133107 |
0.413 |
|
| 2010 |
Yang W, Shen N, Ye DQ, Liu Q, Zhang Y, Qian XX, Hirankarn N, Ying D, Pan HF, Mok CC, Chan TM, Wong RW, Lee KW, Mok MY, Wong SN, et al. Genome-wide association study in Asian populations identifies variants in ETS1 and WDFY4 associated with systemic lupus erythematosus. Plos Genetics. 6: e1000841. PMID 20169177 DOI: 10.1371/Journal.Pgen.1000841 |
0.48 |
|
| 2010 |
Lee PP, Chen TX, Jiang LP, Chan KW, Yang W, Lee BW, Chiang WC, Chen XY, Fok SF, Lee TL, Ho MH, Yang XQ, Lau YL. Clinical characteristics and genotype-phenotype correlation in 62 patients with X-linked agammaglobulinemia. Journal of Clinical Immunology. 30: 121-31. PMID 19904586 DOI: 10.1007/S10875-009-9341-5 |
0.351 |
|
| 2009 |
Wang L, Wang Z, Yang W. Linked region detection using high-density SNP genotype data via the minimum recombinant model of pedigree haplotype inference. Bmc Bioinformatics. 10: 216. PMID 19604391 DOI: 10.1186/1471-2105-10-216 |
0.328 |
|
| 2009 |
Yang W, Ying D, Lau YL. In-depth cDNA library sequencing provides quantitative gene expression profiling in cancer biomarker discovery. Genomics, Proteomics & Bioinformatics. 7: 1-12. PMID 19591787 DOI: 10.1016/S1672-0229(08)60028-5 |
0.339 |
|
| 2009 |
Chang YK, Yang W, Zhao M, Mok CC, Chan TM, Wong RW, Lee KW, Mok MY, Wong SN, Ng IO, Lee TL, Ho MH, Lee PP, Wong WH, Lau CS, et al. Association of BANK1 and TNFSF4 with systemic lupus erythematosus in Hong Kong Chinese. Genes and Immunity. 10: 414-20. PMID 19357697 DOI: 10.1038/Gene.2009.16 |
0.415 |
|
| 2009 |
Yang W, Zhao M, Hirankarn N, Lau CS, Mok CC, Chan TM, Wong RW, Lee KW, Mok MY, Wong SN, Avihingsanon Y, Lin IO, Lee TL, Ho MH, Lee PP, et al. ITGAM is associated with disease susceptibility and renal nephritis of systemic lupus erythematosus in Hong Kong Chinese and Thai. Human Molecular Genetics. 18: 2063-70. PMID 19286673 DOI: 10.1093/Hmg/Ddp118 |
0.455 |
|
| 2009 |
Yang W, Ng P, Zhao M, Hirankarn N, Lau CS, Mok CC, Chan TM, Wong RW, Lee KW, Mok MY, Wong SN, Avihingsanon Y, Lee TL, Ho MH, Lee PP, et al. Population differences in SLE susceptibility genes: STAT4 and BLK, but not PXK, are associated with systemic lupus erythematosus in Hong Kong Chinese. Genes and Immunity. 10: 219-26. PMID 19225526 DOI: 10.1038/Gene.2009.1 |
0.436 |
|
| 2008 |
Lin P, Li J, Liu Q, Mao F, Li J, Qiu R, Hu H, Song Y, Yang Y, Gao G, Yan C, Yang W, Shao C, Gong Y. A missense mutation in SLC33A1, which encodes the acetyl-CoA transporter, causes autosomal-dominant spastic paraplegia (SPG42). American Journal of Human Genetics. 83: 752-9. PMID 19061983 DOI: 10.1016/J.Ajhg.2008.11.003 |
0.314 |
|
| 2008 |
Yang W, Ng P, Zhao M, Wong TK, Yiu SM, Lau YL. Promoter-sharing by different genes in human genome--CPNE1 and RBM12 gene pair as an example. Bmc Genomics. 9: 456. PMID 18831769 DOI: 10.1186/1471-2164-9-456 |
0.35 |
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| 2008 |
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