| 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 |
0.532 |
|
| 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 |
0.516 |
|
| 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 |
0.637 |
|
| 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 |
0.355 |
|
| 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 |
0.688 |
|
| 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 |
0.352 |
|
| 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 |
0.624 |
|
| 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 |
0.592 |
|
| 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 |
0.608 |
|
| 2008 |
Veeramah KR, Zeitlyn D, Fanso VG, Mendell NR, Connell BA, Weale ME, Bradman N, Thomas MG. Sex-Specific Genetic Data Support One of Two Alternative Versions of the Foundation of the Ruling Dynasty of the Nso' in Cameroon. Current Anthropology. 49: 707-714. PMID 19081799 DOI: 10.1086/590119 |
0.324 |
|
| 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 |
0.334 |
|
| 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 |
0.673 |
|
| 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 |
0.582 |
|
| 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 |
0.518 |
|
| 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 |
0.68 |
|
| 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 |
0.344 |
|
| 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 |
0.726 |
|
| 2005 |
Bailey-Wilson JE, Almasy L, de Andrade M, Bailey J, Bickeböller H, Cordell HJ, Daw EW, Goldin L, Goode EL, Gray-McGuire C, Hening W, Jarvik G, Maher BS, Mendell N, Paterson AD, et al. Genetic Analysis Workshop 14: microsatellite and single-nucleotide polymorphism marker loci for genome-wide scans. Bmc Genetics. 6: S1. PMID 16451554 DOI: 10.1186/1471-2156-6-S1-S1 |
0.302 |
|
| 2005 |
de Andrade M, Mendell NR. Summary of contributions to GAW Group 12: multivariate methods. Genetic Epidemiology. 29: S91-5. PMID 16342176 DOI: 10.1002/Gepi.20115 |
0.333 |
|
| 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 |
0.365 |
|
| 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 |
0.341 |
|
| 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 |
0.659 |
|
| 2004 |
Johnson AH, Leke RG, Mendell NR, Shon D, Suh YJ, Bomba-Nkolo D, Tchinda V, Kouontchou S, Thuita LW, van der Wel AM, Thomas A, Stowers A, Saul A, Zhou A, Taylor DW, et al. Human leukocyte antigen class II alleles influence levels of antibodies to the Plasmodium falciparum asexual-stage apical membrane antigen 1 but not to merozoite surface antigen 2 and merozoite surface protein 1. Infection and Immunity. 72: 2762-71. PMID 15102786 DOI: 10.1128/Iai.72.5.2762-2771.2004 |
0.623 |
|
| 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 |
0.347 |
|
| 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 |
0.673 |
|
| 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 |
0.377 |
|
| 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 |
0.308 |
|
| 2003 |
Nemesure B, Jiao X, He Q, Leske MC, Wu SY, Hennis A, Mendell N, Redman J, Garchon HJ, Agarwala R, Schäffer AA, Hejtmancik F. A genome-wide scan for primary open-angle glaucoma (POAG): the Barbados Family Study of Open-Angle Glaucoma. Human Genetics. 112: 600-9. PMID 12616399 DOI: 10.1007/S00439-003-0910-Z |
0.345 |
|
| 2003 |
Levy D, Ji F, Ulgen A, Coleman M, Shon D, Matthysse S, Holzman P, Mendell N. Quantitative and qualitative phenotypes for thought disorder: Implications for linkage studies of schizophrenia Schizophrenia Research. 60: 84. DOI: 10.1016/S0920-9964(03)80637-0 |
0.546 |
|
| 2003 |
Mendell N, O'Driscoll G, Matthysse S, Holzman P, Levy D. A meta-analysis of studies of antisaccade performance in biological relatives of schizophrenia patients Schizophrenia Research. 60: 267. DOI: 10.1016/S0920-9964(03)80415-2 |
0.302 |
|
| 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 |
0.348 |
|
| 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 |
0.398 |
|
| 2001 |
Nemesure B, He Q, Mendell N, Wu SY, Hejtmancik JF, Hennis A, Leske MC. Inheritance of open-angle glaucoma in the Barbados family study. American Journal of Medical Genetics. 103: 36-43. PMID 11562932 DOI: 10.1002/Ajmg.1498 |
0.322 |
|
| 2001 |
Lo Y, Mendell NR, Rubin DB. Testing the number of components in a normal mixture Biometrika. 88: 767-778. DOI: 10.1093/Biomet/88.3.767 |
0.31 |
|
| 2001 |
Neus JL, Mendell NR. A lilliefors test of fit to the two-component homoscedastic normal mixture Communications in Statistics Part B: Simulation and Computation. 30: 277-289. DOI: 10.1081/Sac-100002367 |
0.327 |
|
| 1999 |
Nemesure BB, He Q, Mendell NR. A normalized identity-by-state statistic for linkage analysis of sib pairs Genetic Epidemiology. 17. PMID 10597512 DOI: 10.1002/Gepi.13701707110 |
0.375 |
|
| 1999 |
He Q, Nemesure BB, Mendell NR. Performance of the nonparametric linkage analysis using GENEHUNTER for a complicated genetic disease Genetic Epidemiology. 17. PMID 10597501 DOI: 10.1002/Gepi.1370170799 |
0.384 |
|
| 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 |
0.347 |
|
| 1998 |
Levy D, Lo Y, Matthysse S, Holzman P, Mendell N. 217. Quantitative characterization of thought disorder in linkage studies of schizophrenia Biological Psychiatry. 43: S64. DOI: 10.1016/S0006-3223(98)90665-5 |
0.318 |
|
| 1997 |
He Q, Nemesure BB, Mendell NR. The power of iterated generalized least squares (GLS) method to detect direct relationships in the analysis of correlated quantitative traits Genetic Epidemiology. 14: 797-801. PMID 9433580 DOI: 10.1002/(Sici)1098-2272(1997)14:6<797::Aid-Gepi39>3.0.Co;2-J |
0.362 |
|
| 1997 |
Chuang RJ, Mendell NR. The approximate null distribution of the likelihood ratio test for a mixture of two bivariate normal distributions with equal covariance Communications in Statistics Part B: Simulation and Computation. 26: 631-648. DOI: 10.1080/03610919708813402 |
0.304 |
|
| 1996 |
Nemesure BB, He Q, Mendell N. Integration of linkage analyses and disease association studies. Genetic Epidemiology. 12: 653-8. PMID 8787989 DOI: 10.1002/Gepi.1370120622 |
0.346 |
|
| 1996 |
Aitkin M, Finch S, Mendell N, Thode H. A new test for the presence of a normal mixture distribution based on the posterior Bayes factor Statistics and Computing. 6: 121-125. DOI: 10.1007/Bf00162522 |
0.303 |
|
| 1995 |
Nemesure BB, Greenberg DA, Mendell NR. Simulation study comparing interval estimates for the recombination fraction Genetic Epidemiology. 12: 351-359. PMID 8536952 DOI: 10.1002/Gepi.1370120403 |
0.323 |
|
| 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 |
0.303 |
|
| 1993 |
Levy DL, Holzman PS, Matthysse S, Mendell NR. Eye tracking dysfunction and schizophrenia: a critical perspective. Schizophrenia Bulletin. 19: 461-536. PMID 8235455 DOI: 10.1093/Schbul/19.3.461 |
0.336 |
|
| 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 |
0.341 |
|
| 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 |
0.306 |
|
| 1988 |
Enelow JM, Mendell NR, Ramesh S. A Comparison of Two Distance Metrics Through Regression Diagnostics of a Model of Relative Candidate Evaluation The Journal of Politics. 50: 1057-1071. DOI: 10.2307/2131392 |
0.302 |
|
| 1983 |
Falk CT, Mendell NR, Rubinstein P. Effect of population associations and reduced penetrance on observed and expected genotype frequencies in a simple genetic model: Application to HLA and insulin dependent diabetes mellitus Annals of Human Genetics. 47: 161-165. PMID 6410972 DOI: 10.1111/J.1469-1809.1983.Tb00983.X |
0.333 |
|
| 1982 |
Blumenthal MN, Namboodiri K, Mendell N, Gleich G, Elston RC, Yunis E. Genetic transmission of serum IgE Levels. American Journal of Medical Genetics. 10: 219-28. PMID 7304670 DOI: 10.1002/Ajmg.1320100304 |
0.383 |
|
| 1978 |
Blumenthal MN, Dalmasso AP, Roitman B, Kelly J, Noreen H, Emmy L, Mendell NR, Yunis EJ. Lack of linkage between hereditary angioedema and the A and B loci of the HLA system Vox Sanguinis. 35: 132-136. PMID 676240 DOI: 10.1111/J.1423-0410.1978.Tb02911.X |
0.35 |
|
| 1975 |
Roberts RC, Mendell NR. A case of polydactyly with multiple thresholds in the mouse. Proceedings of the Royal Society of London. Series B, Biological Sciences. 191: 427-44. PMID 2925 DOI: 10.1098/Rspb.1975.0137 |
0.311 |
|
| 1974 |
Mendell NR, Elston RC. Multifactorial qualitative traits: genetic analysis and prediction of recurrence risks Biometrics. 30: 41-57. PMID 4813384 DOI: 10.2307/2529616 |
0.329 |
|
| 1974 |
Smith C, Mendell NR. Recurrence risks from family history and metric traits Annals of Human Genetics. 37: 275-286. PMID 4812949 DOI: 10.1111/J.1469-1809.1974.Tb01835.X |
0.315 |
|
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