Nancy R. Mendell - Publications

Applied Mathematics and Statistics Stony Brook University, Stony Brook, NY, United States 
Statistics, Genetics, Epidemiology

31 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2012 Docherty AR, Coleman MJ, Tu X, Deutsch CK, Mendell NR, Levy DL. Comparison of putative intermediate phenotypes in schizophrenia patients with and without obsessive-compulsive disorder: examining evidence for the schizo-obsessive subtype. Schizophrenia Research. 140: 83-6. PMID 22796151 DOI: 10.1016/j.schres.2012.06.033  0.36
2012 Coleman MJ, Krastoshevsky O, Tu X, Mendell NR, Levy DL. The effects of perceptual encoding on the magnitude of object working memory impairment in schizophrenia. Schizophrenia Research. 139: 60-5. PMID 22640637 DOI: 10.1016/j.schres.2012.05.003  0.36
2012 Sung H, Mendell NR. Necessary and sufficient conditions for equality of sibling and parent-offspring risk of a disease endophenotype in case families. Annals of Human Genetics. 76: 86-91. PMID 22091704 DOI: 10.1111/j.1469-1809.2011.00685.x  1
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  0.48
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  0.48
2010 Levy DL, Coleman MJ, Sung H, Ji F, Matthysse S, Mendell NR, Titone D. The Genetic Basis of Thought Disorder and Language and Communication Disturbances in Schizophrenia. Journal of Neurolinguistics. 23: 176. PMID 20161689 DOI: 10.1016/j.jneuroling.2009.08.003  1
2010 Krause V, Krastoshevsky O, Coleman MJ, Bodkin JA, Lerbinger J, Boling L, Johnson F, Gibbs A, Cole JO, Huang Z, Mendell NR, Levy DL. Tailoring the definition of the clinical schizophrenia phenotype in linkage studies. Schizophrenia Research. 116: 133-42. PMID 19944571 DOI: 10.1016/j.schres.2009.10.023  0.36
2010 Coleman MJ, Titone D, Krastoshevsky O, Krause V, Huang Z, Mendell NR, Eichenbaum H, Levy DL. Reinforcement ambiguity and novelty do not account for transitive inference deficits in schizophrenia. Schizophrenia Bulletin. 36: 1187-200. PMID 19460878 DOI: 10.1093/schbul/sbp039  0.36
2009 Sunga H, Ji F, Levy DL, Matthysse S, Mendell NR. The power of linkage analysis of a disease-related endophenotype using asymmetrically ascertained sib pairs. Computational Statistics & Data Analysis. 53: 1829-1842. PMID 20160849 DOI: 10.1016/j.csda.2008.08.030  0.96
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  0.48
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  0.48
2009 McCarthy SE, Makarov V, Kirov G, Addington AM, McClellan J, Yoon S, Perkins DO, Dickel DE, Kusenda M, Krastoshevsky O, Krause V, Kumar RA, Grozeva D, Malhotra D, Walsh T, ... ... Mendell NR, et al. Microduplications of 16p11.2 are associated with schizophrenia. Nature Genetics. 41: 1223-7. PMID 19855392 DOI: 10.1038/ng.474  0.36
2009 Coleman MJ, Cestnick L, Krastoshevsky O, Krause V, Huang Z, Mendell NR, Levy DL. Schizophrenia patients show deficits in shifts of attention to different levels of global-local stimuli: evidence for magnocellular dysfunction. Schizophrenia Bulletin. 35: 1108-16. PMID 19737806 DOI: 10.1093/schbul/sbp090  0.36
2008 Levy DL, Bowman EA, Abel L, Krastoshevsky O, Krause V, Mendell NR. Does performance on the standard antisaccade task meet the co-familiality criterion for an endophenotype? Brain and Cognition. 68: 462-75. PMID 18842329 DOI: 10.1016/j.bandc.2008.08.027  0.36
2008 Yoo YJ, Mendell NR. The power and robustness of maximum LOD score statistics. Annals of Human Genetics. 72: 566-74. PMID 18410472 DOI: 10.1111/j.1469-1809.2008.00442.x  0.84
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  0.48
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  0.96
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  0.48
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  1
2005 Yoon S, Suh YJ, Mendell NR, Ye KQ. A Bayesian approach for applying Haseman-Elston methods. Bmc Genetics. 6: S39. PMID 16451649 DOI: 10.1186/1471-2156-6-S1-S39  0.52
2005 Ji F, Lee D, Mendell NR. A power study of bivariate LOD score analysis of a complex trait and fear/discomfort with strangers. Bmc Genetics. 6: S113. PMID 16451570 DOI: 10.1186/1471-2156-6-S1-S113  0.96
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  0.48
2004 Levy DL, Mendell NR, Holzman PS. The antisaccade task and neuropsychological tests of prefrontal cortical integrity in schizophrenia: empirical findings and interpretative considerations. World Psychiatry : Official Journal of the World Psychiatric Association (Wpa). 3: 32-40. PMID 16633452  0.36
2004 Levy DL, O'Driscoll G, Matthysse S, Cook SR, Holzman PS, Mendell NR. Antisaccade performance in biological relatives of schizophrenia patients: a meta-analysis. Schizophrenia Research. 71: 113-25. PMID 15374579 DOI: 10.1016/j.schres.2003.11.006  0.36
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  0.84
2003 Oh C, Ye KQ, He Q, Mendell NR. Locating disease genes using Bayesian variable selection with the Haseman-Elston method. Bmc Genetics. 4: S69. PMID 14975137 DOI: 10.1186/1471-2156-4-S1-S69  0.48
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  0.84
2003 Suh YJ, Ye KQ, Mendell NR. A method for evaluating the results of Bayesian model selection: application to linkage analyses of attributes determined by two or more genes. Human Heredity. 55: 147-52. PMID 12931054 DOI: 10.1159/000072320  0.48
2003 Brownstein J, Krastoshevsky O, McCollum C, Kundamal S, Matthysse S, Holzman PS, Mendell NR, Levy DL. Antisaccade performance is abnormal in schizophrenia patients but not in their biological relatives. Schizophrenia Research. 63: 13-25. PMID 12892854 DOI: 10.1016/S0920-9964(02)00438-3  0.36
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  0.32
1992 Mendell NR, Yuan H. Multivariate analysis of nevus counts in twins Cytogenetic and Genome Research. 59: 211-213. PMID 1737504 DOI: 10.1159/000133250  0.4
Show low-probability matches.