| Year |
Citation |
Score |
| 2019 |
Ling YH, Chen SP, Fann CS, Wang SJ, Wang YF. TRPM8 genetic variant is associated with chronic migraine and allodynia. The Journal of Headache and Pain. 20: 115. PMID 31842742 DOI: 10.1186/S10194-019-1064-2 |
0.403 |
|
| 2019 |
Liu CM, Liu YL, Hwu HG, Fann CS, Yang UC, Hsu PC, Chang CC, Chen WJ, Hwang TJ, Hsieh MH, Liu CC, Chien YL, Lin YT, Tsuang MT. Genetic associations and expression of extra-short isoforms of disrupted-in-schizophrenia 1 in a neurocognitive subgroup of schizophrenia. Journal of Human Genetics. PMID 30976040 DOI: 10.1038/S10038-019-0597-1 |
0.422 |
|
| 2016 |
Liu YL, Wang SC, Hwu HG, Fann CS, Yang UC, Yang WC, Hsu PC, Chang CC, Wen CC, Tsai-Wu JJ, Hwang TJ, Hsieh MH, Liu CC, Chien YL, Fang CP, et al. Haplotypes of the D-Amino Acid Oxidase Gene Are Significantly Associated with Schizophrenia and Its Neurocognitive Deficits. Plos One. 11: e0150435. PMID 26986737 DOI: 10.1371/Journal.Pone.0150435 |
0.456 |
|
| 2015 |
Fuh JL, Chung MY, Yao SC, Chen PK, Liao YC, Hsu CL, Wang PJ, Wang YF, Chen SP, Fann CS, Kao LS, Wang SJ. Susceptible genes of restless legs syndrome in migraine. Cephalalgia : An International Journal of Headache. PMID 26643377 DOI: 10.1177/0333102415620907 |
0.31 |
|
| 2015 |
Chen PL, Shih SR, Wang PW, Lin YC, Chu CC, Lin JH, Chen SC, Chang CC, Huang TS, Tsai KS, Tseng FY, Wang CY, Lu JY, Chiu WY, Chang CC, ... ... Fann CS, et al. Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. Nature Communications. 6: 7633. PMID 26151496 DOI: 10.1038/Ncomms8633 |
0.325 |
|
| 2015 |
Leu HB, Chung CM, Lin SJ, Chiang KM, Yang HC, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Yin WH, Chiu TY, Chen CI, Fann CS, et al. Association of circadian genes with diurnal blood pressure changes and non-dipper essential hypertension: a genetic association with young-onset hypertension. Hypertension Research : Official Journal of the Japanese Society of Hypertension. 38: 155-62. PMID 25410879 DOI: 10.1038/Hr.2014.152 |
0.387 |
|
| 2014 |
Chang SW, Fann CS, Su WH, Wang YC, Weng CC, Yu CJ, Hsu CL, Hsieh AR, Chien RN, Chu CM, Tai DI. A genome-wide association study on chronic HBV infection and its clinical progression in male Han-Taiwanese. Plos One. 9: e99724. PMID 24940741 DOI: 10.1371/Journal.Pone.0099724 |
0.393 |
|
| 2013 |
Chien YL, Hwu HG, Fann CS, Chang CC, Tsuang MT, Liu CM. DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in Taiwan. Journal of Human Genetics. 58: 229-32. PMID 23364393 DOI: 10.1038/Jhg.2012.157 |
0.426 |
|
| 2011 |
Chen PL, Fann CS, Chu CC, Chang CC, Chang SW, Hsieh HY, Lin M, Yang WS, Chang TC. Comprehensive genotyping in two homogeneous Graves' disease samples reveals major and novel HLA association alleles. Plos One. 6: e16635. PMID 21307958 DOI: 10.1371/Journal.Pone.0016635 |
0.337 |
|
| 2011 |
Lee MT, Chen CH, Lee CS, Chen CC, Chong MY, Ouyang WC, Chiu NY, Chuo LJ, Chen CY, Tan HK, Lane HY, Chang TJ, Lin CH, Jou SH, Hou YM, ... ... Fann CS, et al. Genome-wide association study of bipolar I disorder in the Han Chinese population. Molecular Psychiatry. 16: 548-56. PMID 20386566 DOI: 10.1038/mp.2010.43 |
0.316 |
|
| 2010 |
Liu YL, Liu CM, Fann CS, Yang WC, Chen YH, Tseng LJ, Liu SK, Hsieh MH, Hwang TJ, Chan HY, Chen JJ, Chen WJ, Hwu HG. Genetic variants of IL-6 and its receptor are not associated with schizophrenia in Taiwan. Neuroscience Letters. 468: 330-3. PMID 19914334 DOI: 10.1016/J.Neulet.2009.11.026 |
0.306 |
|
| 2009 |
Yang HC, Liang YJ, Wu YL, Chung CM, Chiang KM, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Leu HB, Yin WH, Chiu TY, Chen CI, ... Fann CS, et al. Genome-wide association study of young-onset hypertension in the Han Chinese population of Taiwan. Plos One. 4: e5459. PMID 19421330 DOI: 10.1371/journal.pone.0005459 |
0.301 |
|
| 2009 |
Chien YL, Liu CM, Fann CS, Liu YL, Hwu HG. Association of the 3' region of COMT with schizophrenia in Taiwan. Journal of the Formosan Medical Association = Taiwan Yi Zhi. 108: 301-9. PMID 19369177 DOI: 10.1016/S0929-6646(09)60070-X |
0.448 |
|
| 2008 |
Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Chang CC, Yang WC, Lin JJ, Chou FH, et al. RASD2, MYH9, and CACNG2 genes at chromosome 22q12 associated with the subgroup of schizophrenia with non-deficit in sustained attention and executive function. Biological Psychiatry. 64: 789-96. PMID 18571626 DOI: 10.1016/J.Biopsych.2008.04.035 |
0.446 |
|
| 2007 |
Liu YL, Fann CS, Liu CM, Chang CC, Yang WC, Wu JY, Hung SI, Chan HY, Chen JJ, Hsieh MH, Hwang TJ, Faraone SV, Tsuang MT, Chen WJ, Hwu HG. HTF9C gene of 22q11.21 region associates with schizophrenia having deficit-sustained attention. Psychiatric Genetics. 17: 333-8. PMID 18075473 DOI: 10.1097/Ypg.0B013E328133F321 |
0.414 |
|
| 2007 |
Chen PL, Fann CS, Chang CC, Wu IL, Chiu WY, Lin CY, Yang WS, Chang TC. Linkage of Graves' disease to the human leucocyte antigen region in the Chinese-Han population in Taiwan. Clinical Endocrinology. 66: 646-51. PMID 17492952 DOI: 10.1111/J.1365-2265.2007.02787.X |
0.317 |
|
| 2007 |
Liu CM, Liu YL, Fann CS, Yang WC, Wu JY, Hung SI, Chen WJ, Chueh CM, Liu WM, Liu CC, Hsieh MH, Hwang TJ, Faraone SV, Tsuang MT, Hwu HG. No association evidence between schizophrenia and dystrobrevin-binding protein 1 (DTNBP1) in Taiwanese families. Schizophrenia Research. 93: 391-8. PMID 17407805 DOI: 10.1016/J.Schres.2007.02.003 |
0.393 |
|
| 2007 |
Liu YL, Fann CS, Liu CM, Chang CC, Yang WC, Hung SI, Yu SL, Hwang TJ, Hsieh MH, Liu CC, Tsuang MM, Wu JY, Jou YS, Faraone SV, Tsuang MT, et al. More evidence supports the association of PPP3CC with schizophrenia. Molecular Psychiatry. 12: 966-74. PMID 17339875 DOI: 10.1038/Sj.Mp.4001977 |
0.355 |
|
| 2007 |
Liu CM, Liu YL, Fann CS, Chen WJ, Yang WC, Ouyang WC, Chen CY, Jou YS, Hsieh MH, Liu SK, Hwang TJ, Faraone SV, Tsuang MT, Hwu HG. Association evidence of schizophrenia with distal genomic region of NOTCH4 in Taiwanese families. Genes, Brain, and Behavior. 6: 497-502. PMID 17054719 DOI: 10.1111/J.1601-183X.2006.00276.X |
0.353 |
|
| 2006 |
Liu YL, Fann CS, Liu CM, Chen WJ, Wu JY, Hung SI, Chen CH, Jou YS, Liu SK, Hwang TJ, Hsieh MH, Ouyang WC, Chan HY, Chen JJ, Yang WC, et al. A single nucleotide polymorphism fine mapping study of chromosome 1q42.1 reveals the vulnerability genes for schizophrenia, GNPAT and DISC1: Association with impairment of sustained attention. Biological Psychiatry. 60: 554-62. PMID 16997000 DOI: 10.1016/J.Biopsych.2006.04.024 |
0.433 |
|
| 2006 |
Liu YL, Fann CS, Liu CM, Chang CC, Wu JY, Hung SI, Liu SK, Hsieh MH, Hwang TJ, Chan HY, Chen JJ, Faraone SV, Tsuang MT, Chen WJ, Hwu HG. No association of G72 and D-amino acid oxidase genes with schizophrenia. Schizophrenia Research. 87: 15-20. PMID 16842973 DOI: 10.1016/J.Schres.2006.06.020 |
0.424 |
|
| 2006 |
Liu YL, Fann CS, Liu CM, Wu JY, Hung SI, Chan HY, Chen JJ, Pan CC, Liu SK, Hsieh MH, Hwang TJ, Ouyang WC, Chen CY, Lin JJ, Chou FH, et al. Absence of significant associations between four AKT1 SNP markers and schizophrenia in the Taiwanese population. Psychiatric Genetics. 16: 39-41. PMID 16395129 DOI: 10.1097/01.Ypg.0000180681.80546.F3 |
0.428 |
|
| 2005 |
Sun HS, Fann CS, Lane HY, Chang YT, Chang CJ, Liu YL, Cheng AT. A functional polymorphism in the promoter region of the tryptophan hydroxylase gene is associated with alcohol dependence in one aboriginal group in Taiwan. Alcoholism, Clinical and Experimental Research. 29: 1-7. PMID 15654285 DOI: 10.1097/01.Alc.0000150635.51934.6D |
0.352 |
|
| 2001 |
Saito T, Guan F, Papolos DF, Rajouria N, Fann CS, Lachman HM. Polymorphism in SNAP29 gene promoter region associated with schizophrenia. Molecular Psychiatry. 6: 193-201. PMID 11317222 DOI: 10.1038/sj.mp.4000825 |
0.308 |
|
| 2000 |
Pan W, Chen J, Fann C, Jou Y, Wu S. Linkage analysis with candidate genes: the Taiwan young-onset hypertension genetic study. Human Genetics. 107: 210-215. PMID 11071381 DOI: 10.1007/S004390000365 |
0.32 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2016 |
Sengupta Chattopadhyay A, Lin YC, Hsieh AR, Chang CC, Lian IB, Fann CS. Using propensity score adjustment method in genetic association studies. Computational Biology and Chemistry. 62: 1-11. PMID 26991546 DOI: 10.1016/J.Compbiolchem.2016.02.017 |
0.293 |
|
| 2018 |
Tung YC, Fann CS, Chang CC, Chu CC, Yang WS, Hwu WL, Chen PL, Tsai WY. Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan. Pediatric Diabetes. PMID 29383806 DOI: 10.1111/Pedi.12645 |
0.287 |
|
| 2010 |
Chung CM, Wang RY, Chen JW, Fann CS, Leu HB, Ho HY, Ting CT, Lin TH, Sheu SH, Tsai WC, Chen JH, Jong YS, Lin SJ, Chen YT, Pan WH. A genome-wide association study identifies new loci for ACE activity: potential implications for response to ACE inhibitor. The Pharmacogenomics Journal. 10: 537-44. PMID 20066004 DOI: 10.1038/tpj.2009.70 |
0.281 |
|
| 2005 |
Chen P, Jou YS, Fann CS, Chen JW, Wu SY, Pan WH. Lipoprotein lipase gene is linked and associated with hypertension in Taiwan young-onset hypertension genetic study. Journal of Biomedical Science. 12: 651-8. PMID 16132104 DOI: 10.1007/s11373-005-7707-0 |
0.276 |
|
| 2011 |
Liu CM, Fann CS, Chen CY, Liu YL, Oyang YJ, Yang WC, Chang CC, Wen CC, Chen WJ, Hwang TJ, Hsieh MH, Liu CC, Faraone SV, Tsuang MT, Hwu HG. ANXA7, PPP3CB, DNAJC9, and ZMYND17 genes at chromosome 10q22 associated with the subgroup of schizophrenia with deficits in attention and executive function. Biological Psychiatry. 70: 51-8. PMID 21531385 DOI: 10.1016/J.Biopsych.2011.02.033 |
0.275 |
|
| 2014 |
Hsieh AR, Chang SW, Chen PL, Chu CC, Hsiao CL, Yang WS, Chang CC, Wu JY, Chen YT, Chang TC, Fann CS. Predicting HLA genotypes using unphased and flanking single-nucleotide polymorphisms in Han Chinese population. Bmc Genomics. 15: 81. PMID 24476119 DOI: 10.1186/1471-2164-15-81 |
0.274 |
|
| 2013 |
Yang HC, Liu CM, Liu YL, Chen CW, Chang CC, Fann CS, Chiou JJ, Yang UC, Chen CH, Faraone SV, Tsuang MT, Hwu HG. The DAO gene is associated with schizophrenia and interacts with other genes in the Taiwan Han Chinese population. Plos One. 8: e60099. PMID 23555897 DOI: 10.1371/Journal.Pone.0060099 |
0.268 |
|
| 2006 |
Yang HC, Lin CH, Hsu CL, Hung SI, Wu JY, Pan WH, Chen YT, Fann CS. A comparison of major histocompatibility complex SNPs in Han Chinese residing in Taiwan and Caucasians. Journal of Biomedical Science. 13: 489-98. PMID 16544196 DOI: 10.1007/s11373-006-9077-7 |
0.264 |
|
| 2013 |
Chung CM, Wang RY, Fann CS, Chen JW, Jong YS, Jou YS, Yang HC, Kang CS, Chen CC, Chang HC, Pan WH. Fine-mapping angiotensin-converting enzyme gene: separate QTLs identified for hypertension and for ACE activity. Plos One. 8: e56119. PMID 23469169 DOI: 10.1371/journal.pone.0056119 |
0.263 |
|
| 2005 |
Hung SI, Chung WH, Liou LB, Chu CC, Lin M, Huang HP, Lin YL, Lan JL, Yang LC, Hong HS, Chen MJ, Lai PC, Wu MS, Chu CY, Wang KH, ... ... Fann CS, et al. HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol. Proceedings of the National Academy of Sciences of the United States of America. 102: 4134-9. PMID 15743917 DOI: 10.1073/pnas.0409500102 |
0.261 |
|
| 2021 |
Wu LS, Huang MC, Fann CS, Lane HY, Kuo CJ, Chiu WC, Kwok PY, Cheng AT. Genome-wide association study of early-onset bipolar I disorder in the Han Taiwanese population. Translational Psychiatry. 11: 301. PMID 34016946 DOI: 10.1038/s41398-021-01407-6 |
0.256 |
|
| 2005 |
Liu CM, Hwu HG, Fann CS, Lin CY, Liu YL, Ou-Yang WC, Lee SF. Linkage evidence of schizophrenia to loci near neuregulin 1 gene on chromosome 8p21 in Taiwanese families. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 134: 79-83. PMID 15704228 DOI: 10.1002/ajmg.b.20161 |
0.249 |
|
| 2010 |
Tsai FJ, Yang CF, Chen CC, Chuang LM, Lu CH, Chang CT, Wang TY, Chen RH, Shiu CF, Liu YM, Chang CC, Chen P, Chen CH, Fann CS, Chen YT, et al. A genome-wide association study identifies susceptibility variants for type 2 diabetes in Han Chinese. Plos Genetics. 6: e1000847. PMID 20174558 DOI: 10.1371/journal.pgen.1000847 |
0.247 |
|
| 2002 |
Chang YT, Sun HS, Fann CS, Chang CJ, Liao ZH, Huang JL, Loh EW, Yu WY, Cheng AT. Association of the gamma-aminobutyric acid A receptor gene cluster with alcohol dependence in Taiwanese Han. Molecular Psychiatry. 7: 828-9. PMID 12232773 DOI: 10.1038/Sj.Mp.4001110 |
0.244 |
|
| 2018 |
Chang LC, Chang CC, Chen PL, Wang SH, Chen YH, Tsai YH, Shih SR, Chiu WY, Fann CS, Yang WS, Chang TC. Thyrotropin receptor antibodies and a genetic hint in antithyroid drug-induced adverse drug reactions. Expert Opinion On Drug Safety. 1-10. PMID 30067105 DOI: 10.1080/14740338.2018.1502747 |
0.241 |
|
| 2009 |
Chen P, Jou YS, Fann CS, Chen JW, Chung CM, Lin CY, Wu SY, Kang MJ, Chen YC, Jong YS, Lo HM, Kang CS, Chen CC, Chang HC, Huang NK, et al. Lipoprotein lipase variants associated with an endophenotype of hypertension: hypertension combined with elevated triglycerides. Human Mutation. 30: 49-55. PMID 18649389 DOI: 10.1002/humu.20812 |
0.241 |
|
| 2008 |
Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CS. Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling. Human Mutation. 29: 1055-62. PMID 18470944 DOI: 10.1002/humu.20760 |
0.235 |
|
| 2012 |
Wu DB, Chang CJ, Huang YC, Wen YW, Wu CL, Fann CS. Cost-effectiveness analysis of pneumococcal conjugate vaccine in Taiwan: a transmission dynamic modeling approach. Value in Health : the Journal of the International Society For Pharmacoeconomics and Outcomes Research. 15: S15-9. PMID 22265061 DOI: 10.1016/J.Jval.2011.11.013 |
0.233 |
|
| 2008 |
Fann C, Wu D, Huang Y, Chang C. Pin23 Cost-Effectiveness Analysis Of 7-Valent Pneumococcal Conjugate Vaccine In Taiwan: Transmission Dynamic Model-Based Evaluations Value in Health. 11. DOI: 10.1016/S1098-3015(10)66467-4 |
0.231 |
|
| 2021 |
Wu LS, Huang MC, Chen CK, Shen CY, Fann CS, Lin CY, Lin CC, Cheng AT. Genome-Wide Association Study of Lithium-Induced Dry Mouth in Bipolar I Disorder. Journal of Personalized Medicine. 11. PMID 34945737 DOI: 10.3390/jpm11121265 |
0.23 |
|
| 2014 |
Sengupta Chattopadhyay A, Hsiao CL, Chang CC, Lian IeB, Fann CS. Summarizing techniques that combine three non-parametric scores to detect disease-associated 2-way SNP-SNP interactions. Gene. 533: 304-12. PMID 24076437 DOI: 10.1016/J.Gene.2013.09.041 |
0.229 |
|
| 2012 |
Wen W, Cho YS, Zheng W, Dorajoo R, Kato N, Qi L, Chen CH, Delahanty RJ, Okada Y, Tabara Y, Gu D, Zhu D, Haiman CA, Mo Z, Gao YT, ... ... Fann CS, et al. Meta-analysis identifies common variants associated with body mass index in east Asians. Nature Genetics. 44: 307-11. PMID 22344219 DOI: 10.1038/Ng.1087 |
0.228 |
|
| 2016 |
Li C, Chou P, Chang C, Fann C. The Comparisons of Biologics with Methotrexate for Treating Rheumatoid Arthritis Patients in Taiwan: The use of Cost-Utility Analysis and Budget Impact Analysis Value in Health. 19. DOI: 10.1016/J.Jval.2016.08.106 |
0.227 |
|
| 2001 |
Wu CN, Lin YC, Fann C, Liao NS, Shih SR, Ho MS. Protection against lethal enterovirus 71 infection in newborn mice by passive immunization with subunit VP1 vaccines and inactivated virus. Vaccine. 20: 895-904. PMID 11738755 DOI: 10.1016/S0264-410X(01)00385-1 |
0.226 |
|
| 2009 |
Chang C, Wu D, Lin Y, Fann C. Pmc3 Using Frontier Analysis To Optimize The Overall Life Years Gained In Vaccination Policy Of Infectious Diseases Value in Health. 12. DOI: 10.1016/S1098-3015(10)73156-9 |
0.222 |
|
| 2008 |
Lin CH, Li LH, Ho SF, Chuang TP, Wu JY, Chen YT, Fann CS. A large-scale survey of genetic copy number variations among Han Chinese residing in Taiwan. Bmc Genetics. 9: 92. PMID 19108714 DOI: 10.1186/1471-2156-9-92 |
0.22 |
|
| 2009 |
Chang C, Wu D, Lin Y, Wang P, Fann C. Pmc48 A Dynamic Model To Maximize The Helath Benefits In Mutually Exclusive Susceptible Infectious Population Value in Health. 12. DOI: 10.1016/S1098-3015(10)74950-0 |
0.218 |
|
| 2006 |
Yang HC, Lin CH, Hung SI, Fann CS. A comparison of individual genotyping and pooled DNA analysis for polymorphism validation prior to large-scale genetic studies. Annals of Human Genetics. 70: 350-9. PMID 16674557 DOI: 10.1111/j.1529-8817.2005.00232.x |
0.216 |
|
| 2006 |
Lin CC, Yang WC, Lin SJ, Chen TW, Lee WS, Chang CF, Lee PC, Lee SD, Su TS, Fann CS, Chung MY. Length polymorphism in heme oxygenase-1 is associated with arteriovenous fistula patency in hemodialysis patients. Kidney International. 69: 165-72. PMID 16374439 DOI: 10.1038/sj.ki.5000019 |
0.215 |
|
| 2021 |
Chang ML, Lin YS, Chang MY, Hsu CL, Chien RN, Fann CS. Accelerated cardiovascular risk after viral clearance in hepatitis C patients with the NAMPT-rs61330082 TT genotype: An 8-year prospective cohort study. Virulence. 12: 270-280. PMID 33446046 DOI: 10.1080/21505594.2020.1870080 |
0.215 |
|
| 2014 |
Lin YC, Hsieh AR, Hsiao CL, Wu SJ, Wang HM, Lian IeB, Fann CS. Identifying rare and common disease associated variants in genomic data using Parkinson's disease as a model. Journal of Biomedical Science. 21: 88. PMID 25175702 DOI: 10.1186/s12929-014-0088-9 |
0.212 |
|
| 2000 |
Wassertheil-Smoller S, Fann C, Allman RM, Black HR, Camel GH, Davis B, Masaki K, Pressel S, Prineas RJ, Stamler J, Vogt TM. Relation of low body mass to death and stroke in the systolic hypertension in the elderly program Archives of Internal Medicine. 160: 494-500. PMID 10695689 DOI: 10.1001/Archinte.160.4.494 |
0.211 |
|
| 2009 |
Lin CH, Lin YC, Wu JY, Pan WH, Chen YT, Fann CS. A genome-wide survey of copy number variations in Han Chinese residing in Taiwan. Genomics. 94: 241-6. PMID 19559783 DOI: 10.1016/j.ygeno.2009.06.004 |
0.211 |
|
| 2006 |
Yang HC, Pan CC, Lin CY, Fann CS. PDA: Pooled DNA analyzer. Bmc Bioinformatics. 7: 233. PMID 16643673 DOI: 10.1186/1471-2105-7-233 |
0.206 |
|
| 2005 |
Yang HC, Chang CC, Lin CY, Chen CL, Lin CY, Fann CS. A genome-wide scanning and fine mapping study of COGA data. Bmc Genetics. 6: S30. PMID 16451640 DOI: 10.1186/1471-2156-6-S1-S30 |
0.202 |
|
| 2017 |
Spracklen CN, Chen P, Kim YJ, Wang X, Cai H, Li S, Long J, Wu Y, Wang YX, Takeuchi F, Wu JY, Jung KJ, Hu C, Akiyama K, Zhang Y, ... ... Fann CS, et al. Association analyses of East Asian individuals and trans-ancestry analyses with European individuals reveal new loci associated with cholesterol and triglyceride levels. Human Molecular Genetics. PMID 28334899 DOI: 10.1093/Hmg/Ddx062 |
0.202 |
|
| 2015 |
Chang CJ, Chou T, Fann CS. The Metabolic co-Morbidities Prevalence and Related Treatment Costs Between Haart Treated and not Treated Hiv Infected Patients In Taiwan Value in Health. 18. DOI: 10.1016/J.Jval.2015.03.1332 |
0.202 |
|
| 2016 |
Chang C, Wang Y, Huang Y, Fann C, Chang C. Muscular-Skeletal Disorders - Clinical Outcomes StudiesPMS1 - Acute Cardiovascular Adverse Reaction of Cox-2 Inhibitors Among Osteroarthritis Patients in Taiwan Value in Health. 19. DOI: 10.1016/J.Jval.2016.08.115 |
0.201 |
|
| 2012 |
Lin YC, Hsiao CL, Hsieh AR, Lian IeB, Fann CS. Using maximal segmental score in genome-wide association studies. Genetic Epidemiology. 36: 594-601. PMID 22807216 DOI: 10.1002/gepi.21652 |
0.193 |
|
| 2011 |
Hsieh AR, Hsiao CL, Chang SW, Wang HM, Fann CS. On the use of multifactor dimensionality reduction (MDR) and classification and regression tree (CART) to identify haplotype-haplotype interactions in genetic studies. Genomics. 97: 77-85. PMID 21111805 DOI: 10.1016/J.Ygeno.2010.11.003 |
0.193 |
|
| 2001 |
Saito T, Guan F, Papolos DF, Lau S, Klein M, Fann CS, Lachman HM. Mutation analysis of SYNJ1: a possible candidate gene for chromosome 21q22-linked bipolar disorder. Molecular Psychiatry. 6: 387-95. PMID 11443522 DOI: 10.1038/Sj.Mp.4000871 |
0.192 |
|
| 2008 |
Lian IeB, Lin YH, Lin YC, Yang HC, Chang CJ, Fann CS. Using the longest significance run to estimate region-specific p-values in genetic association mapping studies. Bmc Bioinformatics. 9: 246. PMID 18503718 DOI: 10.1186/1471-2105-9-246 |
0.19 |
|
| 2016 |
Chen PL, Fann CS, Shih SR, Yang WS, Chang TC. First step towards precision medicine for antithyroid drug-induced agranulocytosis. The Lancet. Diabetes & Endocrinology. PMID 27157821 DOI: 10.1016/S2213-8587(16)30013-4 |
0.189 |
|
| 2015 |
Chang CJ, Chou T, Fann CS. Clinical, Mediciation and Economical Outcome Research of Advanced Colorectal Cancer Relapse Using Reimbursement and Cancer Registry Databases. Value in Health : the Journal of the International Society For Pharmacoeconomics and Outcomes Research. 18: A451. PMID 26532536 DOI: 10.1016/J.Jval.2015.09.1137 |
0.187 |
|
| 2010 |
Ding SL, Yu JC, Chen ST, Hsu GC, Hsu HM, Ho JY, Lin YH, Chang CC, Fann CS, Cheng CW, Wu PE, Shen CY. Diverse associations between ESR1 polymorphism and breast cancer development and progression. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 16: 3473-84. PMID 20570923 DOI: 10.1158/1078-0432.CCR-09-3092 |
0.185 |
|
| 2015 |
Chang CJ, Chou T, Chang S, Chien L, Fann CS. Impact on Time Gap Between Approval and Reimbursement of Target Therapy to Advanced Colorectal Cancer. Value in Health : the Journal of the International Society For Pharmacoeconomics and Outcomes Research. 18: A486-7. PMID 26532731 DOI: 10.1016/J.Jval.2015.09.1337 |
0.184 |
|
| 2003 |
Stopkova P, Saito T, Fann CS, Papolos DF, Vevera J, Paclt I, Zukov I, Stryjer R, Strous RD, Lachman HM. Polymorphism screening of PIP5K2A: a candidate gene for chromosome 10p-linked psychiatric disorders. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 123: 50-8. PMID 14582145 DOI: 10.1002/ajmg.b.20012 |
0.183 |
|
| 2007 |
Lachman HM, Fann CS, Bartzis M, Evgrafov OV, Rosenthal RN, Nunes EV, Miner C, Santana M, Gaffney J, Riddick A, Hsu CL, Knowles JA. Genomewide suggestive linkage of opioid dependence to chromosome 14q. Human Molecular Genetics. 16: 1327-34. PMID 17409192 DOI: 10.1093/hmg/ddm081 |
0.18 |
|
| 2005 |
Lo YL, Yu JC, Chen ST, Yang HC, Fann CS, Mau YC, Shen CY. Breast cancer risk associated with genotypic polymorphism of the mitosis-regulating gene Aurora-A/STK15/BTAK. International Journal of Cancer. Journal International Du Cancer. 115: 276-83. PMID 15688402 DOI: 10.1002/ijc.20855 |
0.18 |
|
| 2003 |
Hwu HG, Liu CM, Fann CS, Ou-Yang WC, Lee SF. Linkage of schizophrenia with chromosome 1q loci in Taiwanese families. Molecular Psychiatry. 8: 445-52. PMID 12740602 DOI: 10.1038/sj.mp.4001235 |
0.177 |
|
| 2014 |
Liao F, Hsu YC, Kuo SH, Yang YC, Chen JP, Hsu PN, Lin CW, Chen LT, Cheng AL, Fann CS, Lin JT, Wu MS. Genetic polymorphisms and tissue expression of interleukin-22 associated with risk and therapeutic response of gastric mucosa-associated lymphoid tissue lymphoma. Blood Cancer Journal. 4: eXX. PMID 25303370 DOI: 10.1038/bcj.2014.70 |
0.174 |
|
| 2001 |
Liu CM, Hwu HG, Lin MW, Ou-Yang WC, Lee SF, Fann CS, Wong SH, Hsieh SH. Suggestive evidence for linkage of schizophrenia to markers at chromosome 15q13-14 in Taiwanese families. American Journal of Medical Genetics. 105: 658-61. PMID 11803511 DOI: 10.1002/ajmg.1547 |
0.171 |
|
| 2006 |
Chen WJ, Yang JY, Lin JH, Fann CS, Osyetrov V, King CC, Chen YM, Chang HL, Kuo HW, Liao F, Ho MS. Nasopharyngeal shedding of severe acute respiratory syndrome-associated coronavirus is associated with genetic polymorphisms. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 42: 1561-9. PMID 16652313 DOI: 10.1086/503843 |
0.171 |
|
| 1996 |
Ginns EI, Ott J, Egeland JA, Allen CR, Fann CS, Pauls DL, Weissenbachoff J, Carulli JP, Falls KM, Keith TP, Paul SM. A genome-wide search for chromosomal loci linked to bipolar affective disorder in the Old Order Amish. Nature Genetics. 12: 431-5. PMID 8630500 DOI: 10.1038/Ng0496-431 |
0.17 |
|
| 2003 |
Chen CH, Chang CJ, Yang WS, Chen CL, Fann CS. A genome-wide scan using tree-based association analysis for candidate loci related to fasting plasma glucose levels. Bmc Genetics. 4: S65. PMID 14975133 DOI: 10.1186/1471-2156-4-S1-S65 |
0.166 |
|
| 2023 |
Winsvold BS, Harder AVE, Ran C, Chalmer MA, Dalmasso MC, Ferkingstad E, Tripathi KP, Bacchelli E, Børte S, Fourier C, Petersen AS, Vijfhuizen LS, Magnusson SH, O'Connor E, Bjornsdottir G, ... ... Fann CS, et al. Cluster headache genome-wide association study and meta-analysis identifies eight loci and implicates smoking as causal risk factor. Annals of Neurology. PMID 37486023 DOI: 10.1002/ana.26743 |
0.164 |
|
| 2008 |
Wang RY, Chung CM, Fann CS, Yang HC, Chen JW, Jong YS, Jou YS, Lo HM, Ho FM, Kang CS, Chen CC, Chang HC, Shyue SK, Pan WH. Genome-wide scan for quantitative ACE activity in Taiwan young-onset hypertension study. Human Heredity. 65: 85-90. PMID 17898539 DOI: 10.1159/000108940 |
0.163 |
|
| 2022 |
Jiang YJ, Fann CS, Fuh JL, Chung MY, Huang HY, Chu KC, Wang YF, Hsu CL, Kao LS, Chen SP, Wang SJ. Genome-wide analysis identified novel susceptible genes of restless legs syndrome in migraineurs. The Journal of Headache and Pain. 23: 39. PMID 35350973 DOI: 10.1186/s10194-022-01409-9 |
0.16 |
|
| 2008 |
Chen PL, Fann CS, Chang CC, Wu IL, Chiu WY, Lin CY, Yang WS, Chang TC. Family-based association study of cytotoxic T-lymphocyte antigen-4 with susceptibility to Graves' disease in Han population of Taiwan. Genes and Immunity. 9: 87-92. PMID 18059468 DOI: 10.1038/sj.gene.6364445 |
0.16 |
|
| 2002 |
Sun HF, Chang YT, Fann CS, Chang CJ, Chen YH, Hsu YP, Yu WY, Cheng AT. Association study of novel human serotonin 5-HT(1B) polymorphisms with alcohol dependence in Taiwanese Han. Biological Psychiatry. 51: 896-901. PMID 12022963 |
0.158 |
|
| 2022 |
Chen SP, Hsu CL, Wang YF, Yang FC, Chen TH, Huang JH, Pan LH, Fuh JL, Chang HC, Lee YL, Chang HC, Lee KH, Chang YC, Fann CS, Wang SJ. Genome-wide analyses identify novel risk loci for cluster headache in Han Chinese residing in Taiwan. The Journal of Headache and Pain. 23: 147. PMID 36404298 DOI: 10.1186/s10194-022-01517-6 |
0.157 |
|
| 1998 |
Ginns EI, St Jean P, Philibert RA, Galdzicka M, Damschroder-Williams P, Thiel B, Long RT, Ingraham LJ, Dalwaldi H, Murray MA, Ehlert M, Paul S, Remortel BG, Patel AP, Anderson MC, ... ... Fann CS, et al. A genome-wide search for chromosomal loci linked to mental health wellness in relatives at high risk for bipolar affective disorder among the Old Order Amish. Proceedings of the National Academy of Sciences of the United States of America. 95: 15531-6. PMID 9861003 DOI: 10.1073/Pnas.95.26.15531 |
0.156 |
|
| 2021 |
Tsao YC, Wang SJ, Hsu CL, Wang YF, Fuh JL, Chen SP, Fann CS. Genome-wide association study reveals susceptibility loci for self-reported headache in a large community-based Asian population. Cephalalgia : An International Journal of Headache. 3331024211037269. PMID 34404248 DOI: 10.1177/03331024211037269 |
0.155 |
|
| 2008 |
Yang CF, Hwu WL, Yang LC, Chung WH, Chien YH, Hung CF, Chen HC, Tsai PJ, Fann CS, Liao F, Chen YT. A promoter sequence variant of ZNF750 is linked with familial psoriasis. The Journal of Investigative Dermatology. 128: 1662-8. PMID 18256691 DOI: 10.1038/jid.2008.1 |
0.147 |
|
| 2023 |
Lee CT, Tsai WH, Chang CC, Chen PC, Fann CS, Chang HK, Liu SY, Wu MZ, Chiu PC, Hsu WM, Yang WS, Lai LP, Tsai WY, Yang SB, Chen PL. Genotype-phenotype correlation in Taiwanese children with diazoxide-unresponsive congenital hyperinsulinism. Frontiers in Endocrinology. 14: 1283907. PMID 38033998 DOI: 10.3389/fendo.2023.1283907 |
0.145 |
|
| 2009 |
Chen HH, Lee WJ, Fann CS, Bouchard C, Pan WH. Severe obesity is associated with novel single nucleotide polymorphisms of the ESR1 and PPARgamma locus in Han Chinese. The American Journal of Clinical Nutrition. 90: 255-62. PMID 19491387 DOI: 10.3945/ajcn.2009.25914 |
0.141 |
|
| 2004 |
Chen WM, Liu YF, Lin MW, Chen IC, Lin PY, Lin GL, Jou YS, Lin YT, Fann CS, Wu JY, Hsiao KJ, Tsai SF. Autosomal dominant avascular necrosis of femoral head in two Taiwanese pedigrees and linkage to chromosome 12q13. American Journal of Human Genetics. 75: 310-7. PMID 15179599 DOI: 10.1086/422702 |
0.138 |
|
| 2002 |
Wu SY, Fann CS, Jou YS, Chen JW, Pan WH. Association between markers in chromosomal region 17q23 and young onset hypertension: a TDT study. Journal of Medical Genetics. 39: 42-4. PMID 11826023 DOI: 10.1136/jmg.39.1.42 |
0.138 |
|
| 1995 |
Pauls DL, Ott J, Paul SM, Allen CR, Fann CS, Carulli JP, Falls KM, Bouthillier CA, Gravius TC, Keith TP. Linkage analyses of chromosome 18 markers do not identify a major susceptibility locus for bipolar affective disorder in the Old Order Amish. American Journal of Human Genetics. 57: 636-43. PMID 7668292 |
0.134 |
|
| 2013 |
Lin MT, Hsu CL, Chen PL, Yang WS, Wang JK, Fann CS, Wu MH. A genome-wide association analysis identifies novel susceptibility loci for coronary arterial lesions in patients with Kawasaki disease. Translational Research : the Journal of Laboratory and Clinical Medicine. 161: 513-5. PMID 23454411 DOI: 10.1016/J.Trsl.2013.02.002 |
0.131 |
|
| 2005 |
Liu YF, Chen WM, Lin YF, Yang RC, Lin MW, Li LH, Chang YH, Jou YS, Lin PY, Su JS, Huang SF, Hsiao KJ, Fann CS, Hwang HW, Chen YT, et al. Type II collagen gene variants and inherited osteonecrosis of the femoral head. The New England Journal of Medicine. 352: 2294-301. PMID 15930420 DOI: 10.1056/NEJMoa042480 |
0.131 |
|
| 1997 |
Haghighi F, Li W, Fann CS. Affected-sib-pair analyses of bipolar disorder using data on chromosome 18. Genetic Epidemiology. 14: 641-6. PMID 9433556 DOI: 10.1002/(Sici)1098-2272(1997)14:6<641::Aid-Gepi15>3.0.Co;2-Q |
0.124 |
|
| 2012 |
Wang HM, Hsiao CL, Hsieh AR, Lin YC, Fann CS. Constructing endophenotypes of complex diseases using non-negative matrix factorization and adjusted rand index. Plos One. 7: e40996. PMID 22815890 DOI: 10.1371/journal.pone.0040996 |
0.124 |
|
| 1999 |
Fann CS, Shugart YY, Lachman H, Collins A, Chang CJ. The impact of redefining affection status for alcoholism on affected-sib-pair analysis. Genetic Epidemiology. 17: S151-6. PMID 10597428 DOI: 10.1002/Gepi.1370170726 |
0.115 |
|
| 2008 |
Yang HC, Hsieh HY, Fann CS. Kernel-based association test. Genetics. 179: 1057-68. PMID 18558654 DOI: 10.1534/genetics.107.084616 |
0.114 |
|
| 2010 |
Hsiao CL, Lian IeB, Hsieh AR, Fann CS. Modeling expression quantitative trait loci in data combining ethnic populations. Bmc Bioinformatics. 11: 111. PMID 20187971 DOI: 10.1186/1471-2105-11-111 |
0.11 |
|
| 2006 |
Yang HC, Lin CY, Fann CS. A sliding-window weighted linkage disequilibrium test. Genetic Epidemiology. 30: 531-45. PMID 16830340 DOI: 10.1002/gepi.20165 |
0.1 |
|
| 2008 |
Yang HC, Huang MC, Li LH, Lin CH, Yu AL, Diccianni MB, Wu JY, Chen YT, Fann CS. MPDA: microarray pooled DNA analyzer. Bmc Bioinformatics. 9: 196. PMID 18412951 DOI: 10.1186/1471-2105-9-196 |
0.099 |
|
| 2009 |
Lin CP, Fann CS. A novel tool for individual haplotype inference using mixed data. Journal of Biomedical Science. 16: 52. PMID 19486537 DOI: 10.1186/1423-0127-16-52 |
0.095 |
|
| 2006 |
Pan WH, Fann CS, Wu JY, Hung YT, Ho MS, Tai TH, Chen YJ, Liao CJ, Yang ML, Cheng AT, Chen YT. Han Chinese cell and genome bank in Taiwan: purpose, design and ethical considerations. Human Heredity. 61: 27-30. PMID 16534213 DOI: 10.1159/000091834 |
0.093 |
|
| 2016 |
Chen DP, Lin YC, Fann CS. Methods for identifying differentially methylated regions for sequence- and array-based data. Briefings in Functional Genomics. PMID 27323952 DOI: 10.1093/bfgp/elw018 |
0.092 |
|
| 2010 |
Shiao YM, Lee CC, Hsu YH, Huang SF, Lin CY, Li LH, Fann CS, Tsai CY, Tsai SF, Chiu HC. Ectopic and high CXCL13 chemokine expression in myasthenia gravis with thymic lymphoid hyperplasia. Journal of Neuroimmunology. 221: 101-6. PMID 20223524 DOI: 10.1016/j.jneuroim.2010.02.013 |
0.09 |
|
| 2021 |
Ip PP, Li Q, Lin WH, Chang CC, Fann CS, Chen HY, Liu FT, Lebrilla CB, Yang CC, Liao F. Analysis of site-specific glycan profiles of serum proteins in patients with multiple sclerosis or neuromyelitis optica spectrum disorder - a pilot study. Glycobiology. PMID 34132764 DOI: 10.1093/glycob/cwab053 |
0.089 |
|
| 2007 |
Yang HC, Fann CS. Association mapping using pooled DNA. Methods in Molecular Biology (Clifton, N.J.). 376: 161-75. PMID 17984545 DOI: 10.1007/978-1-59745-389-9_12 |
0.08 |
|
| 2003 |
Lin YM, Yang HC, Lai TJ, Fann CS, Sun HS. Receptor mediated effect of serotonergic transmission in patients with bipolar affective disorder. Journal of Medical Genetics. 40: 781-6. PMID 14569129 |
0.077 |
|
| 2014 |
Hsiao CL, Hsieh AR, Lian IeB, Lin YC, Wang HM, Fann CS. A novel method for identification and quantification of consistently differentially methylated regions. Plos One. 9: e97513. PMID 24818602 DOI: 10.1371/journal.pone.0097513 |
0.076 |
|
| 2004 |
Loh el W, Fann CS, Chang YT, Chang CJ, Cheng AT. Endogenous opioid receptor genes and alcohol dependence among Taiwanese Han. Alcoholism, Clinical and Experimental Research. 28: 15-9. PMID 14745298 DOI: 10.1097/01.ALC.0000106303.41755.B8 |
0.068 |
|
| 2017 |
Hsieh AR, Fann CS, Yeh CT, Lin HC, Wan SY, Chen YC, Hsu CL, Tai J, Lin SM, Tai DI. Effects of sex and generation on hepatitis B viral load in families with hepatocellular carcinoma. World Journal of Gastroenterology. 23: 876-884. PMID 28223732 DOI: 10.3748/wjg.v23.i5.876 |
0.068 |
|
| 2006 |
Yang HC, Liang YJ, Huang MC, Li LH, Lin CH, Wu JY, Chen YT, Fann CS. A genome-wide study of preferential amplification/hybridization in microarray-based pooled DNA experiments. Nucleic Acids Research. 34: e106. PMID 16931491 DOI: 10.1093/nar/gkl446 |
0.067 |
|
| 2013 |
Liao HC, Huang YH, Chen YJ, Kao SM, Lin HY, Huang CK, Liu HC, Hsu TR, Lin SP, Yang CF, Fann CS, Chiu PC, Hsieh KS, Fu YC, Ke YY, et al. Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A). Clinica Chimica Acta; International Journal of Clinical Chemistry. 426: 114-20. PMID 24055776 DOI: 10.1016/j.cca.2013.09.008 |
0.066 |
|
| 1998 |
Li W, Fann CS, Ott J. Low-order polynomial trends of female-to-male map distance ratios along human chromosomes. Human Heredity. 48: 266-70. PMID 9748696 DOI: 10.1159/000022814 |
0.064 |
|
| 1995 |
Fann CS, Ott J. Parsimonious estimation of sex-specific map distances by stepwise maximum likelihood regression. Genomics. 29: 571-5. PMID 8575747 DOI: 10.1006/Geno.1995.9964 |
0.061 |
|
| 2005 |
Hwu WL, Yang CF, Fann CS, Chen CL, Tsai TF, Chien YH, Chiang SC, Chen CH, Hung SI, Wu JY, Chen YT. Mapping of psoriasis to 17q terminus. Journal of Medical Genetics. 42: 152-8. PMID 15689454 DOI: 10.1136/jmg.2004.018564 |
0.058 |
|
| 2005 |
Chen CH, Kuo CL, Lin MC, Liang YJ, Fann CS. Construction of endophenotypes for complex diseases in the presence of heterogeneity. Bmc Genetics. 6: S139. PMID 16451598 DOI: 10.1186/1471-2156-6-S1-S139 |
0.055 |
|
| 2000 |
Brown DL, Fann CS, Chang CJ. Effect of glycoprotein IIb/IIIa inhibitors on the individual components of composite endpoints used in clinical trials of unstable angina and non-Q-wave myocardial infarction. Cardiovascular Drugs and Therapy / Sponsored by the International Society of Cardiovascular Pharmacotherapy. 14: 253-8. PMID 10935147 DOI: 10.1023/A:1007874422754 |
0.05 |
|
| 2018 |
Ip PP, Chung CY, Chang CC, Lee YF, Wang HM, Lian IB, Fann CS, Yang CC, Liao F. Differentiation of remitting neuromyelitis optica spectrum disorders from multiple sclerosis by integrating parameters from serum proteins and lymphocyte subsets. Journal of Neuroimmunology. PMID 29455925 DOI: 10.1016/j.jneuroim.2018.02.002 |
0.043 |
|
| 2002 |
Wu CW, Chen GD, Fann CS, Lee AF, Chi CW, Liu JM, Weier U, Chen JY. Clinical implications of chromosomal abnormalities in gastric adenocarcinomas. Genes, Chromosomes & Cancer. 35: 219-31. PMID 12353264 DOI: 10.1002/gcc.10106 |
0.04 |
|
| 2005 |
Yang HC, Pan CC, Lu RC, Fann CS. New adjustment factors and sample size calculation in a DNA-pooling experiment with preferential amplification. Genetics. 169: 399-410. PMID 15677751 DOI: 10.1534/genetics.104.032052 |
0.033 |
|
| 2001 |
Brown DL, Fann CS, Chang CJ. Meta-analysis of effectiveness and safety of abciximab versus eptifibatide or tirofiban in percutaneous coronary intervention. The American Journal of Cardiology. 87: 537-41. PMID 11230835 |
0.022 |
|
| 2001 |
Chang CJ, Fann CS. Using data mining to address heterogeneity in the Southampton data. Genetic Epidemiology. 21: S180-5. PMID 11793666 |
0.012 |
|
| 2001 |
Harish Z, Bregante AC, Morgan C, Fann CS, Callaghan CM, Witt MA, Levinson KA, Caspe WB. A comprehensive inner-city asthma program reduces hospital and emergency room utilization. Annals of Allergy, Asthma & Immunology : Official Publication of the American College of Allergy, Asthma, & Immunology. 86: 185-9. PMID 11258688 DOI: 10.1016/S1081-1206(10)62689-0 |
0.01 |
|
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