| Year |
Citation |
Score |
| 2017 |
Sniekers S, Stringer S, Watanabe K, Jansen PR, Coleman JRI, Krapohl E, Taskesen E, Hammerschlag AR, Okbay A, Zabaneh D, Amin N, Breen G, Cesarini D, Chabris CF, Iacono WG, ... ... Miller MB, et al. Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence. Nature Genetics. PMID 28530673 DOI: 10.1038/Ng.3869 |
0.341 |
|
| 2017 |
Zabaneh D, Krapohl E, Simpson MA, Miller MB, Iacono WG, McGue M, Putallaz M, Lubinski D, Plomin R, Breen G. Fine mapping genetic associations between the HLA region and extremely high intelligence. Scientific Reports. 7: 41182. PMID 28117369 DOI: 10.1038/Srep41182 |
0.324 |
|
| 2017 |
Robinson MR, Kleinman A, Graff M, Vinkhuyzen AAE, Couper DJ, Miller MB, Peyrot WJ, Abdellaoui A, Zietsch BP, Nolte IM, Vliet-Ostaptchouk JVV, Snieder H, Medland SE, Martin NG, Magnusson PKE, et al. Genetic evidence of assortative mating in humans Nature Human Behaviour. 1: 16. DOI: 10.1038/S41562-016-0016 |
0.343 |
|
| 2016 |
Okbay A, Baselmans BM, De Neve JE, Turley P, Nivard MG, Fontana MA, Meddens SF, Linnér RK, Rietveld CA, Derringer J, Gratten J, Lee JJ, Liu JZ, de Vlaming R, Ahluwalia TS, ... ... Miller MB, et al. Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature Genetics. 48: 1591. PMID 27898078 DOI: 10.1038/Ng1216-1587B |
0.305 |
|
| 2016 |
Barban N, Jansen R, de Vlaming R, Vaez A, Mandemakers JJ, Tropf FC, Shen X, Wilson JF, Chasman DI, Nolte IM, Tragante V, van der Laan SW, Perry JR, Kong A, ... ... Miller M, et al. Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nature Genetics. PMID 27798627 DOI: 10.1038/Ng.3698 |
0.353 |
|
| 2016 |
Weiss A, Baselmans BM, Hofer E, Yang J, Okbay A, Lind PA, Miller MB, Nolte IM, Zhao W, Hagenaars SP, Hottenga JJ, Matteson LK, Snieder H, Faul JD, Hartman CA, et al. Personality Polygenes, Positive Affect, and Life Satisfaction. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 1-11. PMID 27546527 DOI: 10.1017/Thg.2016.65 |
0.322 |
|
| 2016 |
Okbay A, Beauchamp JP, Fontana MA, Lee JJ, Pers TH, Rietveld CA, Turley P, Chen GB, Emilsson V, Meddens SF, Oskarsson S, Pickrell JK, Thom K, Timshel P, de Vlaming R, ... ... Miller MB, et al. Genome-wide association study identifies 74 loci associated with educational attainment. Nature. 533: 539-42. PMID 27225129 DOI: 10.1038/Nature17671 |
0.34 |
|
| 2016 |
Mbarek H, Steinberg S, Nyholt DR, Gordon SD, Miller MB, McRae AF, Hottenga JJ, Day FR, Willemsen G, de Geus EJ, Davies GE, Martin HC, Penninx BW, Jansen R, McAloney K, et al. Identification of Common Genetic Variants Influencing Spontaneous Dizygotic Twinning and Female Fertility. American Journal of Human Genetics. PMID 27132594 DOI: 10.1016/J.Ajhg.2016.03.008 |
0.319 |
|
| 2016 |
Okbay A, Baselmans BM, De Neve JE, Turley P, Nivard MG, Fontana MA, Meddens SF, Linnér RK, Rietveld CA, Derringer J, Gratten J, Lee JJ, Liu JZ, de Vlaming R, Ahluwalia TS, ... ... Miller MB, et al. Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses. Nature Genetics. PMID 27089181 DOI: 10.1038/Ng.3552 |
0.32 |
|
| 2016 |
Stringer S, Minică CC, Verweij KJ, Mbarek H, Bernard M, Derringer J, van Eijk KR, Isen JD, Loukola A, Maciejewski DF, Mihailov E, van der Most PJ, Sánchez-Mora C, Roos L, Sherva R, ... ... Miller MB, et al. Genome-wide association study of lifetime cannabis use based on a large meta-analytic sample of 32 330 subjects from the International Cannabis Consortium. Translational Psychiatry. 6: e769. PMID 27023175 DOI: 10.1038/Tp.2016.36 |
0.63 |
|
| 2015 |
Oetting WS, Schladt DP, Guan W, Miller MB, Remmel RP, Dorr C, Sanghavi K, Mannon RB, Herrera B, Matas AJ, Salomon DR, Kwok PY, Keating BJ, Israni AK, Jacobson PA, et al. Genomewide Association Study of Tacrolimus Concentrations in African American Kidney Transplant Recipients Identifies Multiple CYP3A5 Alleles. American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons. PMID 26485092 DOI: 10.1111/Ajt.13495 |
0.303 |
|
| 2015 |
Li YR, van Setten J, Verma SS, Lu Y, Holmes MV, Gao H, Lek M, Nair N, Chandrupatla H, Chang B, Karczewski KJ, Wong C, Mohebnasab M, Mukhtar E, Phillips R, ... ... Miller MB, et al. Concept and design of a genome-wide association genotyping array tailored for transplantation-specific studies. Genome Medicine. 7: 90. PMID 26423053 DOI: 10.1186/S13073-015-0211-X |
0.323 |
|
| 2015 |
van den Berg SM, de Moor MH, Verweij KJ, Krueger RF, Luciano M, Arias Vasquez A, Matteson LK, Derringer J, Esko T, Amin N, Gordon SD, Hansell NK, Hart AB, Seppälä I, Huffman JE, ... ... Miller M, et al. Meta-analysis of Genome-Wide Association Studies for Extraversion: Findings from the Genetics of Personality Consortium. Behavior Genetics. PMID 26362575 DOI: 10.1007/S10519-015-9735-5 |
0.369 |
|
| 2015 |
Spain SL, Pedroso I, Kadeva N, Miller MB, Iacono WG, McGue M, Stergiakouli E, Smith GD, Putallaz M, Lubinski D, Meaburn EL, Plomin R, Simpson MA. A genome-wide analysis of putative functional and exonic variation associated with extremely high intelligence. Molecular Psychiatry. PMID 26239293 DOI: 10.1038/Mp.2015.108 |
0.358 |
|
| 2015 |
de Moor MH, van den Berg SM, Verweij KJ, Krueger RF, Luciano M, Arias Vasquez A, Matteson LK, Derringer J, Esko T, Amin N, Gordon SD, Hansell NK, Hart AB, Seppälä I, ... ... Miller M, et al. Meta-analysis of Genome-wide Association Studies for Neuroticism, and the Polygenic Association With Major Depressive Disorder. Jama Psychiatry. 72: 642-50. PMID 25993607 DOI: 10.1001/Jamapsychiatry.2015.0554 |
0.326 |
|
| 2015 |
Conomos MP, Miller MB, Thornton TA. Robust inference of population structure for ancestry prediction and correction of stratification in the presence of relatedness. Genetic Epidemiology. 39: 276-93. PMID 25810074 DOI: 10.1002/Gepi.21896 |
0.301 |
|
| 2015 |
Pistis G, Porcu E, Vrieze SI, Sidore C, Steri M, Danjou F, Busonero F, Mulas A, Zoledziewska M, Maschio A, Brennan C, Lai S, Miller MB, Marcelli M, Urru MF, et al. Rare variant genotype imputation with thousands of study-specific whole-genome sequences: implications for cost-effective study designs. European Journal of Human Genetics : Ejhg. 23: 975-83. PMID 25293720 DOI: 10.1038/Ejhg.2014.216 |
0.338 |
|
| 2014 |
Vrieze SI, Malone SM, Pankratz N, Vaidyanathan U, Miller MB, Kang HM, McGue M, Abecasis G, Iacono WG. Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes. Psychophysiology. 51: 1300-8. PMID 25387709 DOI: 10.1111/Psyp.12349 |
0.323 |
|
| 2014 |
Vaidyanathan U, Malone SM, Miller MB, McGue M, Iacono WG. Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: a genome-wide association study. Psychophysiology. 51: 1285-99. PMID 25387708 DOI: 10.1111/Psyp.12348 |
0.334 |
|
| 2014 |
Vaidyanathan U, Malone SM, Donnelly JM, Hammer MA, Miller MB, McGue M, Iacono WG. Heritability and molecular genetic basis of antisaccade eye tracking error rate: a genome-wide association study. Psychophysiology. 51: 1272-84. PMID 25387707 DOI: 10.1111/Psyp.12347 |
0.356 |
|
| 2014 |
Vaidyanathan U, Isen JD, Malone SM, Miller MB, McGue M, Iacono WG. Heritability and molecular genetic basis of electrodermal activity: a genome-wide association study. Psychophysiology. 51: 1259-71. PMID 25387706 DOI: 10.1111/Psyp.12346 |
0.376 |
|
| 2014 |
Malone SM, Vaidyanathan U, Basu S, Miller MB, McGue M, Iacono WG. Heritability and molecular-genetic basis of the P3 event-related brain potential: a genome-wide association study. Psychophysiology. 51: 1246-58. PMID 25387705 DOI: 10.1111/Psyp.12345 |
0.364 |
|
| 2014 |
Malone SM, Burwell SJ, Vaidyanathan U, Miller MB, McGue M, Iacono WG. Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study. Psychophysiology. 51: 1225-45. PMID 25387704 DOI: 10.1111/Psyp.12344 |
0.343 |
|
| 2014 |
Kirkpatrick RM, McGue M, Iacono WG, Miller MB, Basu S. Results of a "GWAS plus:" general cognitive ability is substantially heritable and massively polygenic. Plos One. 9: e112390. PMID 25383866 DOI: 10.1371/Journal.Pone.0112390 |
0.345 |
|
| 2014 |
Rietveld CA, Esko T, Davies G, Pers TH, Turley P, Benyamin B, Chabris CF, Emilsson V, Johnson AD, Lee JJ, de Leeuw C, Marioni RE, Medland SE, Miller MB, Rostapshova O, et al. Common genetic variants associated with cognitive performance identified using the proxy-phenotype method. Proceedings of the National Academy of Sciences of the United States of America. 111: 13790-4. PMID 25201988 DOI: 10.1073/Pnas.1404623111 |
0.316 |
|
| 2014 |
Kirkpatrick RM, McGue M, Iacono WG, Miller MB, Basu S, Pankratz N. Low-Frequency Copy-Number Variants and General Cognitive Ability: No Evidence of Association. Intelligence. 42: 98-106. PMID 24497650 DOI: 10.1016/J.Intell.2013.11.005 |
0.366 |
|
| 2014 |
Benyamin B, Pourcain B, Davis OS, Davies G, Hansell NK, Brion MJ, Kirkpatrick RM, Cents RA, Franić S, Miller MB, Haworth CM, Meaburn E, Price TS, Evans DM, Timpson N, et al. Childhood intelligence is heritable, highly polygenic and associated with FNBP1L. Molecular Psychiatry. 19: 253-8. PMID 23358156 DOI: 10.1038/Mp.2012.184 |
0.361 |
|
| 2013 |
Basu S, Zhang Y, Ray D, Miller MB, Iacono WG, McGue M. A rapid gene-based genome-wide association test with multivariate traits. Human Heredity. 76: 53-63. PMID 24247328 DOI: 10.1159/000356016 |
0.321 |
|
| 2013 |
McGue M, Zhang Y, Miller MB, Basu S, Vrieze S, Hicks B, Malone S, Oetting WS, Iacono WG. A genome-wide association study of behavioral disinhibition. Behavior Genetics. 43: 363-73. PMID 23942779 DOI: 10.1007/S10519-013-9606-X |
0.346 |
|
| 2013 |
Rietveld CA, Medland SE, Derringer J, Yang J, Esko T, Martin NW, Westra HJ, Shakhbazov K, Abdellaoui A, Agrawal A, Albrecht E, Alizadeh BZ, Amin N, Barnard J, Baumeister SE, ... ... Miller MB, et al. GWAS of 126,559 individuals identifies genetic variants associated with educational attainment. Science (New York, N.Y.). 340: 1467-71. PMID 23722424 DOI: 10.1126/Science.1235488 |
0.331 |
|
| 2013 |
Vrieze SI, McGue M, Miller MB, Hicks BM, Iacono WG. Three mutually informative ways to understand the genetic relationships among behavioral disinhibition, alcohol use, drug use, nicotine use/dependence, and their co-occurrence: twin biometry, GCTA, and genome-wide scoring. Behavior Genetics. 43: 97-107. PMID 23362009 DOI: 10.1007/S10519-013-9584-Z |
0.35 |
|
| 2012 |
Miller MB, Basu S, Cunningham J, Eskin E, Malone SM, Oetting WS, Schork N, Sul JH, Iacono WG, McGue M. The Minnesota Center for Twin and Family Research genome-wide association study. Twin Research and Human Genetics : the Official Journal of the International Society For Twin Studies. 15: 767-74. PMID 23363460 DOI: 10.1017/Thg.2012.62 |
0.325 |
|
| 2012 |
Miller MB, Deyoung CG, McGue M. Assumptions in studies of heritability and genotype-phenotype association. The Behavioral and Brain Sciences. 35: 372-3. PMID 23095394 DOI: 10.1017/S0140525X12001380 |
0.313 |
|
| 2011 |
Vrieze SI, McGue M, Miller MB, Legrand LN, Schork NJ, Iacono WG. An assessment of the individual and collective effects of variants on height using twins and a developmentally informative study design. Plos Genetics. 7: e1002413. PMID 22174699 DOI: 10.1371/Journal.Pgen.1002413 |
0.353 |
|
| 2011 |
Li X, Basu S, Miller MB, Iacono WG, McGue M. A rapid generalized least squares model for a genome-wide quantitative trait association analysis in families. Human Heredity. 71: 67-82. PMID 21474944 DOI: 10.1159/000324839 |
0.349 |
|
| 2009 |
Krueger KA, Tsuji S, Fukuda Y, Takahashi Y, Goto J, Mitsui J, Ishiura H, Dalton JC, Miller MB, Day JW, Ranum LP. SNP haplotype mapping in a small ALS family. Plos One. 4: e5687. PMID 19479031 DOI: 10.1371/Journal.Pone.0005687 |
0.348 |
|
| 2008 |
Sherva R, Miller MB, Pankow JS, Hunt SC, Boerwinkle E, Mosley TH, Weder AB, Curb JD, Luke A, Morrison AC, Fornage M, Arnett DK. A whole-genome scan for stroke or myocardial infarction in family blood pressure program families. Stroke; a Journal of Cerebral Circulation. 39: 1115-20. PMID 18323513 DOI: 10.1161/Strokeaha.107.490433 |
0.59 |
|
| 2008 |
Bielinski SJ, Pankow JS, Foster CL, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating soluble ICAM-1 levels shows linkage to ICAM gene cluster region on chromosome 19: the NHLBI Family Heart Study follow-up examination. Atherosclerosis. 199: 172-8. PMID 18045607 DOI: 10.1016/J.Atherosclerosis.2007.10.006 |
0.349 |
|
| 2007 |
Miller MB, Lind GR, Li N, Jang SY. Genetic Analysis Workshop 15: simulation of a complex genetic model for rheumatoid arthritis in nuclear families including a dense SNP map with linkage disequilibrium between marker loci and trait loci. Bmc Proceedings. 1: S4. PMID 18466538 DOI: 10.1186/1753-6561-1-S1-S4 |
0.335 |
|
| 2007 |
Witte JS, Schnell AH, Cordell HJ, Spielman RS, Amos CI, Miller MB, Almasy L, MacCluer JW. Introduction to Genetic Analysis Workshop 15 summaries. Genetic Epidemiology. 31: S1-6. PMID 18046756 DOI: 10.1002/Gepi.20274 |
0.316 |
|
| 2007 |
Jackola DR, Miller MB, Liebeler CL, Blumenthal MN. Search for quantitative trait loci of atopy-associated immune responses using allergen-specific IgG1 as an "endophenotype". Human Immunology. 68: 839-43. PMID 17961772 DOI: 10.1016/J.Humimm.2007.07.006 |
0.302 |
|
| 2007 |
Bielinski SJ, Pankow JS, Miller MB, Hopkins PN, Eckfeldt JH, Hixson J, Liu Y, Register T, Myers RH, Arnett DK. Circulating MCP-1 levels shows linkage to chemokine receptor gene cluster on chromosome 3: the NHLBI family heart study follow-up examination. Genes and Immunity. 8: 684-90. PMID 17917677 DOI: 10.1038/Sj.Gene.6364434 |
0.31 |
|
| 2007 |
Lynch AI, Arnett DK, Pankow JS, Miller MB, North KE, Eckfeldt JH, Hunt SC, Rao DC, Djoussé L. Sex-specific effects of ACE I/D and AGT-M235T on pulse pressure: the HyperGEN Study. Human Genetics. 122: 33-40. PMID 17492314 DOI: 10.1007/S00439-007-0370-Y |
0.306 |
|
| 2007 |
Reilly C, Miller MB, Liu Y, Oetting WS, King R, Blumenthal M. Linkage analysis of a cluster-based quantitative phenotype constructed from pulmonary function test data in 27 multigenerational families with multiple asthmatic members. Human Heredity. 64: 136-45. PMID 17476113 DOI: 10.1159/000101992 |
0.317 |
|
| 2007 |
Sherva R, Miller MB, Lynch AI, Devereux RB, Rao DC, Oberman A, Hopkins PN, Kitzman DW, Atwood LD, Arnett DK. A whole genome scan for pulse pressure/stroke volume ratio in African Americans: the HyperGEN study. American Journal of Hypertension. 20: 398-402. PMID 17386346 DOI: 10.1016/J.Amjhyper.2006.10.001 |
0.603 |
|
| 2006 |
Redden DT, Divers J, Vaughan LK, Tiwari HK, Beasley TM, Fernández JR, Kimberly RP, Feng R, Padilla MA, Liu N, Miller MB, Allison DB. Regional admixture mapping and structured association testing: conceptual unification and an extensible general linear model. Plos Genetics. 2: e137. PMID 16934005 DOI: 10.1371/Journal.Pgen.0020137 |
0.313 |
|
| 2006 |
Bielinski SJ, Tang W, Pankow JS, Miller MB, Mosley TH, Boerwinkle E, Olshen RA, Curb JD, Jaquish CE, Rao DC, Weder A, Arnett DK. Genome-wide linkage scans for loci affecting total cholesterol, HDL-C, and triglycerides: the Family Blood Pressure Program. Human Genetics. 120: 371-80. PMID 16868761 DOI: 10.1007/S00439-006-0223-0 |
0.305 |
|
| 2006 |
Chang YP, Kim JD, Schwander K, Rao DC, Miller MB, Weder AB, Cooper RS, Schork NJ, Province MA, Morrison AC, Kardia SL, Quertermous T, Chakravarti A. The impact of data quality on the identification of complex disease genes: experience from the Family Blood Pressure Program. European Journal of Human Genetics : Ejhg. 14: 469-77. PMID 16493446 DOI: 10.1038/Sj.Ejhg.5201582 |
0.314 |
|
| 2005 |
Rasmussen-Torvik LJ, North KE, Gu CC, Lewis CE, Wilk JB, Chakravarti A, Chang YP, Miller MB, Li N, Devereux RB, Arnett DK. A population association study of angiotensinogen polymorphisms and haplotypes with left ventricular phenotypes. Hypertension. 46: 1294-9. PMID 16286570 DOI: 10.1161/01.Hyp.0000192653.17209.84 |
0.319 |
|
| 2005 |
Lewis CE, North KE, Arnett D, Borecki IB, Coon H, Ellison RC, Hunt SC, Oberman A, Rich SS, Province MA, Miller MB. Sex-specific findings from a genome-wide linkage analysis of human fatness in non-Hispanic whites and African Americans: the HyperGEN study. International Journal of Obesity (2005). 29: 639-49. PMID 15809668 DOI: 10.1038/Sj.Ijo.0802916 |
0.302 |
|
| 2004 |
Arnett DK, Miller MB, Coon H, Ellison RC, North KE, Province M, Leppert M, Eckfeldt JH. Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study. Human Genetics. 115: 468-74. PMID 15375693 DOI: 10.1007/S00439-004-1182-Y |
0.313 |
|
| 2004 |
North KE, Rose KM, Borecki IB, Oberman A, Hunt SC, Miller MB, Blangero J, Almasy L, Pankow JS. Evidence for a gene on chromosome 13 influencing postural systolic blood pressure change and body mass index. Hypertension. 43: 780-4. PMID 14967843 DOI: 10.1161/01.Hyp.0000118921.66329.Da |
0.327 |
|
| 2003 |
Tang W, Miller MB, Rich SS, North KE, Pankow JS, Borecki IB, Myers RH, Hopkins PN, Leppert M, Arnett DK. Linkage analysis of a composite factor for the multiple metabolic syndrome: the National Heart, Lung, and Blood Institute Family Heart Study. Diabetes. 52: 2840-7. PMID 14578304 DOI: 10.2337/Diabetes.52.11.2840 |
0.322 |
|
| 2002 |
DeWan AT, Arnett DK, Miller MB, Peacock JM, Atwood LD, Province MA, Lewis CE, Hunt SC, Eckfeldt JH. Refined mapping of suggestive linkage to renal function in African Americans: the HyperGEN study. American Journal of Human Genetics. 71: 204-5. PMID 12068377 DOI: 10.1086/340730 |
0.331 |
|
| 2000 |
Kwapil TR, Miller MB, Zinser MC, Chapman LJ, Chapman J, Eckblad M. A longitudinal study of high scorers on the hypomanic personality scale. Journal of Abnormal Psychology. 109: 222-6. PMID 10895560 DOI: 10.1037/0021-843X.109.2.222 |
0.622 |
|
| 1997 |
Miller MB. Genomic scanning and the transmission/disequilibrium test: analysis of error rates. Genetic Epidemiology. 14: 851-6. PMID 9433589 DOI: 10.1002/(Sici)1098-2272(1997)14:6<854::Aid-Gepi48>3.0.Co;2-M |
0.304 |
|
| 1997 |
Kwapil TR, Miller MB, Zinser MC, Chapman J, Chapman LJ. Magical ideation and social anhedonia as predictors of psychosis proneness: a partial replication. Journal of Abnormal Psychology. 106: 491-5. PMID 9241953 DOI: 10.1037/0021-843X.106.3.491 |
0.619 |
|
| 1996 |
Kwapil TR, Chapman JP, Chapman LJ, Miller MB. Deviant olfactory experiences as indicators of risk for psychosis. Schizophrenia Bulletin. 22: 371-82. PMID 8782292 DOI: 10.1093/Schbul/22.2.371 |
0.615 |
|
| 1995 |
Miller MB, Chapman JP, Chapman LJ, Collins J. Task difficulty and cognitive deficits in schizophrenia. Journal of Abnormal Psychology. 104: 251-8. PMID 7790627 DOI: 10.1037//0021-843X.104.2.251 |
0.497 |
|
| 1994 |
Chapman LJ, Chapman JP, Curran TE, Miller MB. Do Children and the Elderly Show Heightened Semantic Priming? How to Answer the Question Developmental Review. 14: 159-185. DOI: 10.1006/Drev.1994.1007 |
0.493 |
|
| 1993 |
Miller MB, Chapman LJ, Chapman JP, Kwapil TR. Slowness and the preceding preparatory interval effect in schizophrenia. Journal of Abnormal Psychology. 102: 145-51. PMID 8436690 DOI: 10.1037/0021-843X.102.1.145 |
0.63 |
|
| 1993 |
Miller MB, Chapman LJ, Chapman JP, Kwapil TR. "Slowness and the preceding preparatory interval effect in schizophrenia": Correction. Journal of Abnormal Psychology. 102: 237-237. DOI: 10.1037/0021-843X.102.2.237 |
0.611 |
|
| 1993 |
Miller MB, Chapman LJ, Chapman JP, Kwapil TR. Correction: Slowness and the preceding preparatory interval effect in schizophrenia (Journal of Abnormal Psychology (1993) 102 (145-151)) Journal of Abnormal Psychology. 102: 237. DOI: 10.1037//0021-843X.102.2.237 |
0.614 |
|
| 1990 |
Miller MB, Chapman LJ, Chapman JP, Barnett EM. Schizophrenic deficit in span of apprehension. Journal of Abnormal Psychology. 99: 313-6. PMID 2212282 DOI: 10.1037//0021-843X.99.3.313 |
0.506 |
|
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