| Year |
Citation |
Score |
| 2019 |
Lee JY, Kim W, Brook JS, Finch SJ, Brook DW. Adolescent Risk and Protective Factors Predicting Triple Trajectories of Substance Use from Adolescence into Adulthood Journal of Child and Family Studies. 29: 403-412. DOI: 10.1007/S10826-019-01629-9 |
0.305 |
|
| 2017 |
Gordon D, Londono D, Patel P, Kim W, Finch SJ, Heiman GA. An Analytic Solution to the Computation of Power and Sample Size for Genetic Association Studies under a Pleiotropic Mode of Inheritance. Human Heredity. 81: 194-209. PMID 28315880 DOI: 10.1159/000457135 |
0.46 |
|
| 2013 |
Londono D, Chen KM, Musolf A, Wang R, Shen T, Brandon J, Herring JA, Wise CA, Zou H, Jin M, Yu L, Finch SJ, Matise TC, Gordon D. A novel method for analyzing genetic association with longitudinal phenotypes. Statistical Applications in Genetics and Molecular Biology. 12: 241-61. PMID 23502345 DOI: 10.1515/Sagmb-2012-0070 |
0.665 |
|
| 2012 |
Kim W, Londono D, Zhou L, Xing J, Nato AQ, Musolf A, Matise TC, Finch SJ, Gordon D. Single-variant and multi-variant trend tests for genetic association with next-generation sequencing that are robust to sequencing error. Human Heredity. 74: 172-83. PMID 23594495 DOI: 10.1159/000346824 |
0.43 |
|
| 2012 |
Londono D, Buyske S, Finch SJ, Sharma S, Wise CA, Gordon D. TDT-HET: a new transmission disequilibrium test that incorporates locus heterogeneity into the analysis of family-based association data. Bmc Bioinformatics. 13: 13. PMID 22264315 DOI: 10.1186/1471-2105-13-13 |
0.449 |
|
| 2011 |
Jin J, Cerise JE, Kang SJ, Yoon EJ, Yoon S, Mendell NR, Finch SJ. Principal components ancestry adjustment for Genetic Analysis Workshop 17 data. Bmc Proceedings. 5: S66. PMID 22373457 DOI: 10.1186/1753-6561-5-S9-S66 |
0.663 |
|
| 2011 |
Gordon D, Finch SJ, De La Vega FM, De La Vega F. A new expectation-maximization statistical test for case-control association studies considering rare variants obtained by high-throughput sequencing. Human Heredity. 71: 113-25. PMID 21734402 DOI: 10.1159/000325590 |
0.413 |
|
| 2010 |
Londono D, Haynes C, De La Vega FM, Finch SJ, Gordon D. A cost-effective statistical method to correct for differential genotype misclassification when performing case-control genetic association. Human Heredity. 70: 102-8. PMID 20606457 DOI: 10.1159/000314470 |
0.452 |
|
| 2010 |
Gadow KD, DeVincent CJ, Pisarevskaya V, Olvet DM, Xu W, Mendell NR, Finch SJ, Hatchwell E. Parent-child DRD4 genotype as a potential biomarker for oppositional, anxiety, and repetitive behaviors in children with autism spectrum disorder. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 34: 1208-14. PMID 20600463 DOI: 10.1016/J.Pnpbp.2010.06.019 |
0.482 |
|
| 2009 |
Huang C, Li K, Fleur RS, Chang SW, Choi SH, Shen T, Shin SY, Finch SJ, Mendell NR. Family-based analysis of a myocardial infarction endophenotype: comparison of sampling designs. Bmc Proceedings. 3: S120. PMID 20017986 DOI: 10.1186/1753-6561-3-S7-S120 |
0.736 |
|
| 2009 |
Chang SW, Choi SH, Li K, Fleur RS, Huang C, Shen T, Ahn K, Gordon D, Kim W, Wu R, Mendell NR, Finch SJ. Growth mixture modeling as an exploratory analysis tool in longitudinal quantitative trait loci analysis. Bmc Proceedings. 3: S112. PMID 20017977 DOI: 10.1186/1753-6561-3-S7-S112 |
0.769 |
|
| 2009 |
Ahn K, Gordon D, Finch SJ. Increase of rejection rate in case-control studies with the differential genotyping error rates. Statistical Applications in Genetics and Molecular Biology. 8: Article25. PMID 19492983 DOI: 10.2202/1544-6115.1429 |
0.741 |
|
| 2009 |
Tintle N, Gordon D, Van Bruggen D, Finch S. The cost effectiveness of duplicate genotyping for testing genetic association. Annals of Human Genetics. 73: 370-8. PMID 19344449 DOI: 10.1111/J.1469-1809.2009.00516.X |
0.605 |
|
| 2008 |
Kim W, Gordon D, Sebat J, Ye KQ, Finch SJ. Computing power and sample size for case-control association studies with copy number polymorphism: application of mixture-based likelihood ratio test. Plos One. 3: e3475. PMID 18941524 DOI: 10.1371/Journal.Pone.0003475 |
0.43 |
|
| 2008 |
Yang Y, Wise CA, Gordon D, Finch SJ. A family-based likelihood ratio test for general pedigree structures that allows for genotyping error and missing data. Human Heredity. 66: 99-110. PMID 18382089 DOI: 10.1159/000119109 |
0.446 |
|
| 2007 |
Yang Y, Tashman AP, Lee JY, Yoon S, Mao W, Ahn K, Kim W, Mendell NR, Gordon D, Finch SJ. Mixture modeling of microarray gene expression data. Bmc Proceedings. 1: S50. PMID 18466550 DOI: 10.1186/1753-6561-1-S1-S50 |
0.701 |
|
| 2007 |
Falk CT, Finch SJ, Kim W, Mukhopadhyay ND, Gong B, Hinrichs A, Li X, Liu X, Malhotra A, Mehta T, Page G, Rao S, Saccone N, Shete S, Yang Y, et al. Data mining of RNA expression and DNA genotype data: presentation group 5 contributions to Genetic Analysis Workshop 15. Genetic Epidemiology. 31: S43-50. PMID 18046764 DOI: 10.1002/Gepi.20279 |
0.324 |
|
| 2007 |
Ji F, Finch SJ, Haynes C, Mendell NR, Gordon D. Incorporation of genetic model parameters for cost-effective designs of genetic association studies using DNA pooling. Bmc Genomics. 8: 238. PMID 17634103 DOI: 10.1186/1471-2164-8-238 |
0.436 |
|
| 2007 |
Gordon D, Haynes C, Yang Y, Kramer PL, Finch SJ. Linear trend tests for case-control genetic association that incorporate random phenotype and genotype misclassification error. Genetic Epidemiology. 31: 853-70. PMID 17565750 DOI: 10.1002/Gepi.20246 |
0.467 |
|
| 2007 |
Tintle NL, Gordon D, McMahon FJ, Finch SJ. Using duplicate genotyped data in genetic analyses: testing association and estimating error rates. Statistical Applications in Genetics and Molecular Biology. 6: Article4. PMID 17402919 DOI: 10.2202/1544-6115.1251 |
0.664 |
|
| 2007 |
Tung L, Gordon D, Finch SJ. The impact of genotype misclassification errors on the power to detect a gene-environment interaction using cox proportional hazards modeling. Human Heredity. 63: 101-10. PMID 17283439 DOI: 10.1159/000099182 |
0.394 |
|
| 2007 |
Ahn K, Haynes C, Kim W, Fleur RS, Gordon D, Finch SJ. The effects of SNP genotyping errors on the power of the Cochran-Armitage linear trend test for case/control association studies. Annals of Human Genetics. 71: 249-61. PMID 17096677 DOI: 10.1111/J.1469-1809.2006.00318.X |
0.759 |
|
| 2006 |
Gordon D, Haynes C, Finch SJ, Brown AM. Increase in linkage information by stratification of pedigree data into gold-standard and standard diagnoses: application to the NIMH Alzheimer Disease Genetics Initiative Dataset. Human Heredity. 61: 97-103. PMID 16707902 DOI: 10.1159/000093303 |
0.405 |
|
| 2005 |
Ji F, Yang Y, Haynes C, Finch SJ, Gordon D. Computing asymptotic power and sample size for case-control genetic association studies in the presence of phenotype and/or genotype misclassification errors. Statistical Applications in Genetics and Molecular Biology. 4: Article37. PMID 16646856 DOI: 10.2202/1544-6115.1184 |
0.419 |
|
| 2005 |
Duan T, Finch SJ, Ye KQ, Chase GA, Mendell NR. Using mixture models to characterize disease-related traits. Bmc Genetics. 6: S99. PMID 16451715 DOI: 10.1186/1471-2156-6-S1-S99 |
0.325 |
|
| 2005 |
Sung H, Finch SJ, Ye KQ, Mendell NR. A gene-model-free method for linkage analysis of a disease-related-trait based on analysis of proband/sibling pairs. Bmc Genetics. 6: S47. PMID 16451658 DOI: 10.1186/1471-2156-6-S1-S47 |
0.382 |
|
| 2005 |
Tintle NL, Ahn K, Mendell NR, Gordon D, Finch SJ. Characteristics of replicated single-nucleotide polymorphism genotypes from COGA: Affymetrix and Center for Inherited Disease Research. Bmc Genetics. 6: S154. PMID 16451615 DOI: 10.1186/1471-2156-6-S1-S154 |
0.771 |
|
| 2005 |
Gordon D, Haynes C, Blumenfeld J, Finch SJ. PAWE-3D: visualizing power for association with error in case-control genetic studies of complex traits. Bioinformatics (Oxford, England). 21: 3935-7. PMID 16123114 DOI: 10.1093/Bioinformatics/Bti643 |
0.429 |
|
| 2005 |
Gordon D, Finch SJ. Factors affecting statistical power in the detection of genetic association. The Journal of Clinical Investigation. 115: 1408-18. PMID 15931375 DOI: 10.1172/Jci24756 |
0.364 |
|
| 2005 |
Edwards BJ, Haynes C, Levenstien MA, Finch SJ, Gordon D. Power and sample size calculations in the presence of phenotype errors for case/control genetic association studies. Bmc Genetics. 6: 18. PMID 15819990 DOI: 10.1186/1471-2156-6-18 |
0.425 |
|
| 2005 |
Bromet EJ, Finch SJ, Carlson GA, Fochtmann L, Mojtabai R, Craig TJ, Kang S, Ye Q. Time to remission and relapse after the first hospital admission in severe bipolar disorder. Social Psychiatry and Psychiatric Epidemiology. 40: 106-13. PMID 15685401 DOI: 10.1007/S00127-005-0864-7 |
0.549 |
|
| 2005 |
Gordon D, De La Vega FM, Finch SJ, Ye KQ. Power for complex trait genetic association Clinical Neuroscience Research. 5: 31-35. DOI: 10.1016/J.Cnr.2005.07.004 |
0.36 |
|
| 2004 |
Gordon D, Yang Y, Haynes C, Finch SJ, Mendell NR, Brown AM, Haroutunian V. Increasing power for tests of genetic association in the presence of phenotype and/or genotype error by use of double-sampling. Statistical Applications in Genetics and Molecular Biology. 3: Article26. PMID 16646805 DOI: 10.2202/1544-6115.1085 |
0.457 |
|
| 2004 |
Kang SJ, Finch SJ, Haynes C, Gordon D. Quantifying the percent increase in minimum sample size for SNP genotyping errors in genetic model-based association studies. Human Heredity. 58: 139-44. PMID 15812170 DOI: 10.1159/000083540 |
0.669 |
|
| 2004 |
Ulgen A, Yoo YJ, Gordon D, Finch SJ, Mendell NR. Percentiles of the null distribution of 2 maximum lod score tests. Human Heredity. 57: 39-48. PMID 15133311 DOI: 10.1159/000077388 |
0.332 |
|
| 2004 |
Kang SJ, Gordon D, Brown AM, Ott J, Finch SJ. Tradeoff between no-call reduction in genotyping error rate and loss of sample size for genetic case/control association studies. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 116-27. PMID 14992497 |
0.644 |
|
| 2004 |
Kang SJ, Gordon D, Finch SJ. What SNP genotyping errors are most costly for genetic association studies? Genetic Epidemiology. 26: 132-41. PMID 14748013 DOI: 10.1002/Gepi.10301 |
0.654 |
|
| 2004 |
Nöthen MM, Hao K, Schulze TG, Ott J, Granath RO, Rietschel M, Lindholm E, Shmulewitz D, Zhang J, Greenberg DA, Hodge SE, Halldórsson BV, Istrail S, Vega FMDL, McMahon FJ, ... ... Finch SJ, et al. Contents Vol. 58, 2004 Human Heredity. 58: 207-208. DOI: 10.1159/000085013 |
0.519 |
|
| 2004 |
Nöthen MM, Hao K, Schulze TG, Ott J, Granath RO, Rietschel M, Lindholm E, Shmulewitz D, Zhang J, Greenberg DA, Hodge SE, Halldórsson BV, Istrail S, Vega FMDL, McMahon FJ, ... ... Finch SJ, et al. Subject Index Vol. 58, 2004 Human Heredity. 58: 206. DOI: 10.1159/000085012 |
0.534 |
|
| 2004 |
Ning Y, Finch SJ. The Likelihood ratio test with the box-cox transformation for the normal mixture problem: Power and sample size study Communications in Statistics Part B: Simulation and Computation. 33: 553-565. DOI: 10.1081/Sac-200033328 |
0.355 |
|
| 2003 |
Yoo YJ, Huo Y, Ning Y, Gordon D, Finch S, Mendell NR. Power of maximum HLOD tests to detect linkage to obesity genes. Bmc Genetics. 4: S16. PMID 14975084 DOI: 10.1186/1471-2156-4-S1-S16 |
0.367 |
|
| 2003 |
Gordon D, Levenstien MA, Finch SJ, Ott J. Errors and linkage disequilibrium interact multiplicatively when computing sample sizes for genetic case-control association studies Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 490-501. PMID 12603052 |
0.33 |
|
| 2002 |
Gordon D, Finch SJ, Nothnagel M, Ott J. Power and sample size calculations for case-control genetic association tests when errors are present: application to single nucleotide polymorphisms. Human Heredity. 54: 22-33. PMID 12446984 DOI: 10.1159/000066696 |
0.434 |
|
| 2002 |
Perrotta PL, Ozcan C, Whitbread JA, Finch SJ. Applying a novel statistical process control model to platelet quality monitoring. Transfusion. 42: 1059-66. PMID 12385419 |
0.518 |
|
| 2001 |
Young Ju Suh, Finch SJ, Mendell NR. Application of a Bayesian method for optimal subset regression to linkage analysis of Q1 and Q2 Genetic Epidemiology. 21: S706-S711. PMID 11793765 DOI: 10.1002/Gepi.2001.21.S1.S706 |
0.355 |
|
| 2001 |
Gordon D, Hoh J, Finch SJ, Levenstien MA, Edington J, Li W, Majewski J, Ott J. Two approaches for consolidating results from genome scans of complex traits: Selection methods and scan statistics Genetic Epidemiology. 21: S396-S402. PMID 11793706 DOI: 10.1002/Gepi.2001.21.S1.S396 |
0.406 |
|
| 2001 |
Finch SJ, Chen CH, Gordon D, Mendell NR. A study comparing precision of the maximum multipoint heterogeneity LOD statistic to three model-free multipoint linkage methods Genetic Epidemiology. 21: 315-325. PMID 11754467 DOI: 10.1002/Gepi.1037 |
0.389 |
|
| 1999 |
Chen CH, Finch SJ, Mendell NR, Gordon D. Comparison of empirical strategies to maximize GENEHUNTER lod scores Genetic Epidemiology. 17: S103-S108. PMID 10597420 DOI: 10.1002/Gepi.1370170718 |
0.326 |
|
| 1999 |
Ning Y, Finch SJ. The null distribution of the Likelihood Ratio Test for a mixture of two normals after a restricted Box-Cox transformation Communications in Statistics - Theory and Methods. 29: 449-461. DOI: 10.1080/03610910008813621 |
0.308 |
|
| 1997 |
Gordon D, Finch SJ, Jacobs AL, Mendell NR, Single RM, Marr TG. Association of posterior p-values of S.A.G.E. SIBPAL proportion-IBD and Haseman-Elston statistics for ACTHR112. Genetic Epidemiology. 14: 629-34. PMID 9433554 DOI: 10.1002/(Sici)1098-2272(1997)14:6<629::Aid-Gepi13>3.0.Co;2-S |
0.318 |
|
| 1995 |
Single RM, Finch SJ. Gain in efficiency from using generalized least squares in the Haseman- Elston test Genetic Epidemiology. 12: 889-894. PMID 8788027 DOI: 10.1002/Gepi.1370120660 |
0.317 |
|
| 1993 |
Mendell NR, Finch SJ, Thode HC. Where is the likelihood ratio test powerful for detecting two component normal mixtures? Biometrics. 49: 907-915. PMID 8241377 DOI: 10.2307/2532212 |
0.353 |
|
| 1991 |
Mendell NR, Thode HC, Finch SJ. The likelihood ratio test for the two-component normal mixture problem: Power and sample size analysis Biometrics. 47: 1143-1148. PMID 1835889 DOI: 10.2307/2532666 |
0.385 |
|
| 1988 |
Thode HC, Finch SJ, Mendell NR. Simulated percentage points for the null distribution of the likelihood ratio test for a mixture of two normals Biometrics. 44: 1195-1201. PMID 3233255 DOI: 10.2307/2531747 |
0.337 |
|
| 1988 |
Thode HC, Liu HK, Finch SJ. Large sample power of absolute moment tests Communications in Statistics - Simulation and Computation. 17: 1453-1458. DOI: 10.1080/03610918808812735 |
0.367 |
|
| 1986 |
Irwin C, Finch SJ. Use of weighted least squares regression in simulation studies Communications in Statistics - Simulation and Computation. 15: 291-300. DOI: 10.1080/03610918608812509 |
0.351 |
|
| 1983 |
Thode HC, Smith LA, Finch SJ. Power of Tests of Normality for Detecting Scale Contaminated Normal Samples Communications in Statistics - Simulation and Computation. 12: 675-695. DOI: 10.1080/03610918308812352 |
0.358 |
|
| 1977 |
Finch SJ. Robust univariate test of symmetry Journal of the American Statistical Association. 72: 387-392. DOI: 10.1080/01621459.1977.10481006 |
0.32 |
|
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