| Year |
Citation |
Score |
| 2023 |
Wang S, Chiu CY, Wilson AF, Bailey-Wilson JE, Agron E, Chew EY, Ahn J, Xiong M, Fan R. Gene-level association analysis of bivariate ordinal traits with functional regressions. Genetic Epidemiology. PMID 37101379 DOI: 10.1002/gepi.22524 |
0.419 |
|
| 2022 |
Chiu CY, Wang S, Zhang B, Luo Y, Simpson C, Zhang W, Wilson AF, Bailey-Wilson JE, Agron E, Chew EY, Zhang J, Xiong M, Fan R. Gene-level association analysis of ordinal traits with functional ordinal logistic regressions. Genetic Epidemiology. PMID 35438198 DOI: 10.1002/gepi.22451 |
0.436 |
|
| 2021 |
Jiang Y, Chiu CY, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, ... ... Fan R, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration. Journal of the American Statistical Association. 116: 531-545. PMID 34321704 DOI: 10.1080/01621459.2020.1799809 |
0.404 |
|
| 2021 |
Zhang B, Chiu CY, Yuan F, Sang T, Cook RJ, Wilson AF, Bailey-Wilson JE, Chew EY, Xiong M, Fan R. Gene-based analysis of bi-variate survival traits via functional regressions with applications to eye diseases. Genetic Epidemiology. PMID 33645812 DOI: 10.1002/gepi.22381 |
0.352 |
|
| 2020 |
Jiang Y, Chiu C, Yan Q, Chen W, Gorin MB, Conley YP, Lakhal-Chaieb ML, Cook RJ, Amos CI, Wilson AF, Bailey-Wilson JE, McMahon FJ, Vazquez AI, Yuan A, Zhong X, ... ... Fan R, et al. Gene-Based Association Testing of Dichotomous Traits With Generalized Functional Linear Mixed Models Using Extended Pedigrees: Applications to Age-Related Macular Degeneration Journal of the American Statistical Association. 1-15. DOI: 10.1080/01621459.2020.1799809 |
0.418 |
|
| 2019 |
Chiu CY, Zhang B, Wang S, Shao J, Lakhal-Chaieb ML, Cook RJ, Wilson AF, Bailey-Wilson JE, Xiong M, Fan R. Gene-based association analysis of survival traits via functional regression-based mixed effect cox models for related samples. Genetic Epidemiology. PMID 31502722 DOI: 10.1002/Gepi.22254 |
0.506 |
|
| 2018 |
Chiu CY, Yuan F, Zhang BS, Yuan A, Li X, Fang HB, Lange K, Weeks DE, Wilson AF, Bailey-Wilson JE, Musolf AM, Stambolian D, Lakhal-Chaieb ML, Cook RJ, McMahon FJ, ... ... Fan R, et al. Linear mixed models for association analysis of quantitative traits with next-generation sequencing data. Genetic Epidemiology. PMID 30537345 DOI: 10.1002/Gepi.22177 |
0.481 |
|
| 2018 |
Shane B, Pangilinan F, Mills JL, Fan R, Gong T, Cropp CD, Kim Y, Ueland PM, Bailey-Wilson JE, Wilson AF, Brody LC, Molloy AM. The 677C→T variant of MTHFR is the major genetic modifier of biomarkers of folate status in a young, healthy Irish population. The American Journal of Clinical Nutrition. PMID 30339177 DOI: 10.1093/Ajcn/Nqy209 |
0.387 |
|
| 2018 |
Yan Q, Ding Y, Liu Y, Sun T, Fritsche LG, Clemons T, Ratnapriya R, Klein ML, Cook RJ, Liu Y, Fan R, Wei L, Abecasis GR, Swaroop A, Chew EY, et al. Genome-wide Analysis of Disease Progression in Age-related Macular Degeneration. Human Molecular Genetics. PMID 29346644 DOI: 10.1093/Hmg/Ddy002 |
0.399 |
|
| 2017 |
Boghossian NS, Sicko RJ, Giannakou A, Dimopoulos A, Caggana M, Tsai MY, Yeung EH, Pankratz N, Cole BR, Romitti PA, Browne ML, Fan R, Liu A, Kay DM, Mills JL. Rare copy number variants identified in prune belly syndrome. European Journal of Medical Genetics. PMID 29174092 DOI: 10.1016/J.Ejmg.2017.11.008 |
0.382 |
|
| 2017 |
Lin N, Zhu Y, Fan R, Xiong M. A quadratically regularized functional canonical correlation analysis for identifying the global structure of pleiotropy with NGS data. Plos Computational Biology. 13: e1005788. PMID 29040274 DOI: 10.1371/Journal.Pcbi.1005788 |
0.488 |
|
| 2017 |
Carter TC, Sicko RJ, Kay DM, Browne ML, Romitti PA, Edmunds ZL, Liu A, Fan R, Druschel CM, Caggana M, Brody LC, Mills JL. Copy-number variants and candidate gene mutations in isolated split hand/foot malformation. Journal of Human Genetics. PMID 28539665 DOI: 10.1038/Jhg.2017.56 |
0.35 |
|
| 2016 |
Chiu CY, Jung J, Chen W, Weeks DE, Ren H, Boehnke M, Amos CI, Liu A, Mills JL, Ting Lee ML, Xiong M, Fan R. Meta-analysis of quantitative pleiotropic traits for next-generation sequencing with multivariate functional linear models. European Journal of Human Genetics : Ejhg. PMID 28000696 DOI: 10.1038/Ejhg.2016.170 |
0.648 |
|
| 2016 |
Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R. A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing. Genetic Epidemiology. PMID 27917525 DOI: 10.1002/Gepi.22014 |
0.654 |
|
| 2016 |
Dimopoulos A, Sicko RJ, Kay DM, Rigler SL, Fan R, Romitti PA, Browne ML, Druschel CM, Caggana M, Brody LC, Mills JL. Copy number variants in a population-based investigation of Klippel-Trenaunay syndrome. American Journal of Medical Genetics. Part A. PMID 27901321 DOI: 10.1002/Ajmg.A.37868 |
0.362 |
|
| 2016 |
Sicko RJ, Browne ML, Rigler SL, Druschel CM, Liu G, Fan R, Romitti PA, Caggana M, Kay DM, Brody LC, Mills JL. Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development Pathways. Plos One. 11: e0165174. PMID 27788187 DOI: 10.1371/Journal.Pone.0165174 |
0.374 |
|
| 2016 |
Hagen EM, Sicko RJ, Kay DM, Rigler SL, Dimopoulos A, Ahmad S, Doleman MH, Fan R, Romitti PA, Browne ML, Caggana M, Brody LC, Shaw GM, Jelliffe-Pawlowski LL, Mills JL. Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways. Human Genetics. PMID 27637763 DOI: 10.1007/S00439-016-1727-X |
0.339 |
|
| 2016 |
Fan R, Chiu CY, Jung J, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Chen Z, Mills JL, Xiong M. A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits. Genetic Epidemiology. PMID 27374056 DOI: 10.1002/Gepi.21984 |
0.634 |
|
| 2016 |
Fan R, Wang Y, Yan Q, Ding Y, Weeks DE, Lu Z, Ren H, Cook RJ, Xiong M, Swaroop A, Chew EY, Chen W. Gene-Based Association Analysis for Censored Traits Via Fixed Effect Functional Regressions. Genetic Epidemiology. PMID 26782979 DOI: 10.1002/Gepi.21947 |
0.526 |
|
| 2015 |
Fan R, Wang Y, Chiu CY, Chen W, Ren H, Li Y, Boehnke M, Amos CI, Moore JH, Xiong M. Meta-analysis of Complex Diseases at Gene Level by Generalized Functional Linear Models. Genetics. PMID 26715663 DOI: 10.1534/Genetics.115.180869 |
0.529 |
|
| 2015 |
Boghossian NS, Sicko RJ, Kay DM, Rigler SL, Caggana M, Tsai MY, Yeung EH, Pankratz N, Cole BR, Druschel CM, Romitti PA, Browne ML, Fan R, Liu A, Brody LC, et al. Rare copy number variants implicated in posterior urethral valves. American Journal of Medical Genetics. Part A. PMID 26663319 DOI: 10.1002/Ajmg.A.37493 |
0.395 |
|
| 2015 |
Ozaki M, Molloy AM, Mills JL, Fan R, Wang Y, Gibney ER, Shane B, Brody LC, Parle-McDermott A. The Dihydrofolate Reductase 19 bp Polymorphism Is Not Associated with Biomarkers of Folate Status in Healthy Young Adults, Irrespective of Folic Acid Intake. The Journal of Nutrition. PMID 26269242 DOI: 10.3945/Jn.115.216101 |
0.346 |
|
| 2015 |
Fan R, Wang Y, Boehnke M, Chen W, Li Y, Ren H, Lobach I, Xiong M. Gene Level Meta-Analysis of Quantitative Traits by Functional Linear Models. Genetics. PMID 26058849 DOI: 10.1534/Genetics.115.178343 |
0.529 |
|
| 2015 |
Wang Y, Liu A, Mills JL, Boehnke M, Wilson AF, Bailey-Wilson JE, Xiong M, Wu CO, Fan R. Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models. Genetic Epidemiology. 39: 259-75. PMID 25809955 DOI: 10.1002/Gepi.21895 |
0.486 |
|
| 2015 |
Rigler SL, Kay DM, Sicko RJ, Fan R, Liu A, Caggana M, Browne ML, Druschel CM, Romitti PA, Brody LC, Mills JL. Novel copy-number variants in a population-based investigation of classic heterotaxy. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 348-57. PMID 25232849 DOI: 10.1038/Gim.2014.112 |
0.378 |
|
| 2014 |
Lobach I, Fan R, Manga P. Genotype-based association models of complex diseases to detect gene-gene and gene-environment interactions. Statistics and Its Interface. 7: 51-60. PMID 26191336 DOI: 10.4310/Sii.2014.V7.N1.A6 |
0.473 |
|
| 2014 |
Fan R, Wang Y, Mills JL, Carter TC, Lobach I, Wilson AF, Bailey-Wilson JE, Weeks DE, Xiong M. Generalized functional linear models for gene-based case-control association studies. Genetic Epidemiology. 38: 622-37. PMID 25203683 DOI: 10.1002/Gepi.21840 |
0.49 |
|
| 2013 |
Fan R, Lo SH. A robust model-free approach for rare variants association studies incorporating gene-gene and gene-environmental interactions. Plos One. 8: e83057. PMID 24358248 DOI: 10.1371/Journal.Pone.0083057 |
0.351 |
|
| 2013 |
Fan R, Wang Y, Mills JL, Wilson AF, Bailey-Wilson JE, Xiong M. Functional linear models for association analysis of quantitative traits. Genetic Epidemiology. 37: 726-42. PMID 24130119 DOI: 10.1002/Gepi.21757 |
0.52 |
|
| 2013 |
Fan R, Lee A, Lu Z, Liu A, Troendle JF, Mills JL. Association analysis of complex diseases using triads, parent-child dyads and singleton monads. Bmc Genetics. 14: 78. PMID 24007308 DOI: 10.1186/1471-2156-14-78 |
0.445 |
|
| 2013 |
Feenstra B, Geller F, Carstensen L, Romitti PA, Körberg IB, Bedell B, Krogh C, Fan R, Svenningsson A, Caggana M, Nordenskjöld A, Mills JL, Murray JC, Melbye M. Plasma lipids, genetic variants near APOA1, and the risk of infantile hypertrophic pyloric stenosis. Jama. 310: 714-21. PMID 23989729 DOI: 10.1001/Jama.2013.242978 |
0.324 |
|
| 2012 |
Lobach I, Fan R. Genotype-Based Bayesian Analysis of Gene-Environment Interactions with Multiple Genetic Markers and Misclassification in Environmental Factors. Journal of Probability and Statistics. 2012. PMID 26180529 DOI: 10.1155/2012/151259 |
0.432 |
|
| 2012 |
Fan R, Albert PS, Schisterman EF. A discussion of gene-gene and gene-environment interactions and longitudinal genetic analysis of complex traits. Statistics in Medicine. 31: 2565-8. PMID 22969024 DOI: 10.1002/Sim.5495 |
0.345 |
|
| 2012 |
Fan R, Zhang Y, Albert PS, Liu A, Wang Y, Xiong M. Longitudinal association analysis of quantitative traits. Genetic Epidemiology. 36: 856-69. PMID 22965819 DOI: 10.1002/Gepi.21673 |
0.502 |
|
| 2012 |
Mechanic LE, Chen HS, Amos CI, Chatterjee N, Cox NJ, Divi RL, Fan R, Harris EL, Jacobs K, Kraft P, Leal SM, McAllister K, Moore JH, Paltoo DN, Province MA, et al. Next generation analytic tools for large scale genetic epidemiology studies of complex diseases. Genetic Epidemiology. 36: 22-35. PMID 22147673 DOI: 10.1002/Gepi.20652 |
0.424 |
|
| 2012 |
Fan R, Zhong M, Wang S, Zhang Y, Andrew A, Karagas M, Chen H, Amos CI, Xiong M, Moore JH. Entropy-based information gain approaches to detect and to characterize gene-gene and gene-environment interactions/correlations of complex diseases. Genetic Epidemiology. 35: 706-21. PMID 22009792 DOI: 10.1002/Gepi.20621 |
0.382 |
|
| 2011 |
Zhong M, Zhang Y, Lange K, Fan R. A cross-population extended haplotype-based homozygosity score test to detect positive selection in genome-wide scans. Statistics and Its Interface. 4: 51-63. PMID 26097641 DOI: 10.4310/Sii.2011.V4.N1.A6 |
0.416 |
|
| 2010 |
Lobach I, Fan R, Carroll RJ. Genotype-based association mapping of complex diseases: Gene-environment interactions with multiple genetic markers and measurement error in environmental exposures Genetic Epidemiology. 34: 792-802. PMID 21031455 DOI: 10.1002/Gepi.20523 |
0.498 |
|
| 2010 |
Zhong M, Lange K, Papp JC, Fan R. A powerful score test to detect positive selection in genome-wide scans. European Journal of Human Genetics : Ejhg. 18: 1148-59. PMID 20461112 DOI: 10.1038/Ejhg.2010.60 |
0.382 |
|
| 2009 |
Chen L, Zhong M, Chen WV, Amos CI, Fan R. A genome-wide association scan for rheumatoid arthritis data by Hotelling's T2 tests. Bmc Proceedings. 3: S6. PMID 20018053 DOI: 10.1186/1753-6561-3-S7-S6 |
0.372 |
|
| 2009 |
Massett MP, Fan R, Berk BC. Quantitative trait loci for exercise training responses in FVB/NJ and C57BL/6J mice. Physiological Genomics. 40: 15-22. PMID 19789284 DOI: 10.1152/Physiolgenomics.00116.2009 |
0.311 |
|
| 2009 |
Thomas NJ, DiAngelo S, Hess JC, Fan R, Ball MW, Geskey JM, Willson DF, Floros J. Transmission of surfactant protein variants and haplotypes in children hospitalized with respiratory syncytial virus. Pediatric Research. 66: 70-3. PMID 19287351 DOI: 10.1203/Pdr.0B013E3181A1D768 |
0.317 |
|
| 2008 |
Fan R, Liu L, Jung J, Zhong M. Combined linkage and association mapping of quantitative trait Loci with missing completely at random genotype data. Behavior Genetics. 38: 316-36. PMID 18306033 DOI: 10.1007/S10519-008-9194-3 |
0.653 |
|
| 2008 |
Jung J, Zhong M, Liu L, Fan R. Bivariate combined linkage and association mapping of quantitative trait loci. Genetic Epidemiology. 32: 396-412. PMID 18278817 DOI: 10.1002/Gepi.20313 |
0.66 |
|
| 2007 |
Yang Q, Biernacka JM, Chen MH, Houwing-Duistermaat JJ, Bergemann TL, Basu S, Fan R, Liu L, Bourgey M, Clerget-Darpoux F, Lin WY, Elston RC, Cupples LA, Apprey V, Cui J, et al. Using linkage and association to identify and model genetic effects: summary of GAW15 Group 4. Genetic Epidemiology. 31: S34-42. PMID 18046758 DOI: 10.1002/Gepi.20278 |
0.479 |
|
| 2007 |
Thomas NJ, Fan R, Diangelo S, Hess JC, Floros J. Haplotypes of the surfactant protein genes A and D as susceptibility factors for the development of respiratory distress syndrome. Acta Paediatrica (Oslo, Norway : 1992). 96: 985-9. PMID 17524024 DOI: 10.1111/J.1651-2227.2007.00319.X |
0.349 |
|
| 2007 |
Pavlovic J, Papagaroufalis C, Xanthou M, Liu W, Fan R, Thomas NJ, Apostolidou I, Papathoma E, Megaloyianni E, DiAngelo S, Floros J. Genetic variants of surfactant proteins A, B, C, and D in bronchopulmonary dysplasia. Disease Markers. 22: 277-91. PMID 17264398 DOI: 10.1155/2006/817805 |
0.36 |
|
| 2006 |
Floros J, Thomas NJ, Liu W, Papagaroufalis C, Xanthou M, Pereira S, Fan R, Guo X, Diangelo S, Pavlovic J. Family-based association tests suggest linkage between surfactant protein B (SP-B) (and flanking region) and respiratory distress syndrome (RDS): SP-B haplotypes and alleles from SP-B-linked loci are risk factors for RDS. Pediatric Research. 59: 616-21. PMID 16549540 DOI: 10.1203/01.Pdr.0000203145.48585.2C |
0.301 |
|
| 2006 |
Fan R, Jung J, Jin L. High-resolution association mapping of quantitative trait loci: a population-based approach. Genetics. 172: 663-86. PMID 16172503 DOI: 10.1534/Genetics.105.046417 |
0.648 |
|
| 2005 |
Fan R, Knapp M. Sibship T2 association tests of complex diseases for tightly linked markers. Human Genomics. 2: 90-112. PMID 16004725 DOI: 10.1186/1479-7364-2-2-90 |
0.478 |
|
| 2005 |
Jung J, Fan R, Jin L. Combined linkage and association mapping of quantitative trait loci by multiple markers. Genetics. 170: 881-98. PMID 15802526 DOI: 10.1534/Genetics.104.035147 |
0.66 |
|
| 2005 |
Fan R, Knapp M, Wjst M, Zhao C, Xiong M. High resolution T association tests of complex diseases based on family data. Annals of Human Genetics. 69: 187-208. PMID 15720300 DOI: 10.1046/J.1529-8817.2004.00151.X |
0.451 |
|
| 2005 |
Fan R, Spinka C, Jin L, Jung J. Pedigree linkage disequilibrium mapping of quantitative trait loci. European Journal of Human Genetics : Ejhg. 13: 216-31. PMID 15483647 DOI: 10.1038/Sj.Ejhg.5201301 |
0.661 |
|
| 2005 |
Fan R, Knapp M, Wjst M, Zhao C, Xiong M. High Resolution T2 Association Tests of Complex Diseases Based on Family Data: T2 Association Tests of Complex Diseases Annals of Human Genetics. 69: 187-208. DOI: 10.1046/J.1469-1809.2004.00151.X |
0.317 |
|
| 2003 |
Fan R, Jung J. High-resolution joint linkage disequilibrium and linkage mapping of quantitative trait loci based on sibship data. Human Heredity. 56: 166-87. PMID 15031619 DOI: 10.1159/000076392 |
0.599 |
|
| 2003 |
Fan R, Xiong M. Linkage and association studies of QTL for nuclear families by mixed models. Biostatistics (Oxford, England). 4: 75-95. PMID 12925331 DOI: 10.1093/Biostatistics/4.1.75 |
0.317 |
|
| 2003 |
Fan R, Knapp M. Genome association studies of complex diseases by case-control designs. American Journal of Human Genetics. 72: 850-68. PMID 12647259 DOI: 10.1086/373966 |
0.445 |
|
| 2003 |
Fan R, Xiong M. Combined high resolution linkage and association mapping of quantitative trait loci. European Journal of Human Genetics : Ejhg. 11: 125-37. PMID 12634860 DOI: 10.1038/Sj.Ejhg.5200941 |
0.452 |
|
| 2002 |
Fan R, Jung J. Association studies of QTL for multi-allele markers by mixed models. Human Heredity. 54: 132-50. PMID 12626846 DOI: 10.1159/000068839 |
0.631 |
|
| 2002 |
Fan R, Xiong M. High resolution mapping of quantitative trait loci by linkage disequilibrium analysis. European Journal of Human Genetics : Ejhg. 10: 607-15. PMID 12357331 DOI: 10.1038/Sj.Ejhg.5200843 |
0.399 |
|
| 2002 |
Xiong M, Fan R, Jin L. Linkage disequilibrium mapping of quantitative trait loci under truncation selection Human Heredity. 53: 158-172. PMID 12145552 DOI: 10.1159/000064978 |
0.337 |
|
| 2002 |
Fan R, Floros J, Xiong M. Models and tests of linkage and association studies of quantitative trait locus for multi-allele marker Loci Human Heredity. 53: 130-145. PMID 12145549 DOI: 10.1159/000064975 |
0.396 |
|
| 2001 |
Floros J, Fan R. Surfactant protein A and B genetic variants and respiratory distress syndrome: Allele interactions Biology of the Neonate. 80: 22-25. PMID 11359041 DOI: 10.1159/000047173 |
0.415 |
|
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