Yudi Pawitan - Publications

Affiliations: 
Medical Epidemiology and Biostatistics Karolinska Institute, Stockholm, Sweden 

81 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
2020 Ning Z, Pawitan Y, Shen X. High-definition likelihood inference of genetic correlations across human complex traits. Nature Genetics. PMID 32601477 DOI: 10.1038/S41588-020-0653-Y  0.315
2019 Mou T, Deng W, Gu F, Pawitan Y, Vu TN. Reproducibility of Methods to Detect Differentially Expressed Genes from Single-Cell RNA Sequencing. Frontiers in Genetics. 10: 1331. PMID 32010190 DOI: 10.3389/Fgene.2019.01331  0.326
2019 Deng W, Mou T, Niu N, Wang L, Pawitan Y, Vu TN. Alternating EM algorithm for a bilinear model in isoform quantification from RNA-seq data. Bioinformatics (Oxford, England). PMID 31400221 DOI: 10.1093/Bioinformatics/Btz640  0.326
2019 Dahlqwist E, Pawitan Y, Sjölander A. Regression standardization and attributable fraction estimation with between-within frailty models for clustered survival data. Statistical Methods in Medical Research. 28: 462-485. PMID 28901198 DOI: 10.1177/0962280217727558  0.316
2018 Vu TN, Deng W, Trac QT, Calza S, Hwang W, Pawitan Y. A fast detection of fusion genes from paired-end RNA-seq data. Bmc Genomics. 19: 786. PMID 30382840 DOI: 10.1186/S12864-018-5156-1  0.315
2018 Lee W, Sjölander A, Larsson A, Pawitan Y. Likelihood-based inference for bounds of causal parameters. Statistics in Medicine. PMID 30155912 DOI: 10.1002/Sim.7949  0.304
2018 Wang M, Uebbing S, Pawitan Y, Scofield DG. RPASE: individual based allele-specific expression detection without prior knowledge of haplotype phase. Molecular Ecology Resources. PMID 29858523 DOI: 10.1111/1755-0998.12909  0.309
2018 Lee S, Lee Y, Pawitan Y. Sparse pathway-based prediction models for high-throughput molecular data Computational Statistics & Data Analysis. 126: 125-135. DOI: 10.1016/J.Csda.2018.04.012  0.316
2017 Ning Z, Lee Y, Joshi PK, Wilson JF, Pawitan Y, Shen X. A Selection Operator for Summary Association Statistics Reveals Allelic Heterogeneity of Complex Traits. American Journal of Human Genetics. 101: 903-912. PMID 29198721 DOI: 10.1016/J.Ajhg.2017.09.027  0.318
2017 Liu XR, Pawitan Y, Clements MS. Generalized survival models for correlated time-to-event data. Statistics in Medicine. PMID 28905409 DOI: 10.1002/Sim.7451  0.329
2017 Pettersson A, Gerke T, Fall K, Pawitan Y, Holmberg L, Giovannucci EL, Kantoff PW, Adami HO, Rider JR, Mucci LA. The ABC model of prostate cancer: A conceptual framework for the design and interpretation of prognostic studies. Cancer. PMID 28152172 DOI: 10.1002/Cncr.30582  0.313
2017 Lee S, Pawitan Y, Ingelsson E, Lee Y. Sparse estimation of gene-gene interactions in prediction models. Statistical Methods in Medical Research. 26: 2319-2332. PMID 26265764 DOI: 10.1177/0962280215597261  0.312
2016 Vu TN, Pramana S, Calza S, Suo C, Lee D, Pawitan Y. Comprehensive landscape of subtype-specific coding and non-coding RNA transcripts in breast cancer. Oncotarget. PMID 27634900 DOI: 10.18632/Oncotarget.11998  0.302
2016 Lee D, Ganna A, Pawitan Y, Lee W. Nonparametric estimation of the rediscovery rate. Statistics in Medicine. PMID 26910365 DOI: 10.1002/Sim.6915  0.327
2016 Peng Z, Andersson K, Lindholm J, Dethlefsen O, Pramana S, Pawitan Y, Nistér M, Nilsson S, Li C. Improving the Prediction of Prostate Cancer Overall Survival by Supplementing Readily Available Clinical Data with Gene Expression Levels of IGFBP3 and F3 in Formalin-Fixed Paraffin Embedded Core Needle Biopsy Material. Plos One. 11: e0145545. PMID 26731648 DOI: 10.1371/Journal.Pone.0145545  0.327
2016 Li C, Peng Z, Andersson K, Lindholm J, Dethlefsen O, Pawitan Y, Nistér M, Nilsson S. Validation of a 3-gene signature and development of an authentic cohort database to improve overall survival prediction and clinical treatment decision for patients with newly diagnosed prostate cancer. Journal of Clinical Oncology. 34: 5047-5047. DOI: 10.1200/Jco.2016.34.15_Suppl.5047  0.304
2016 Ganna A, Fall T, Salihovic S, Lee W, Broeckling CD, Kumar J, Hägg S, Stenemo M, Magnusson PKE, Prenni JE, Lind L, Pawitan Y, Ingelsson E. Large-scale non-targeted metabolomic profiling in three human population-based studies Metabolomics. 12: 1-13. DOI: 10.1007/S11306-015-0893-5  0.312
2015 Hägg S, Ganna A, van der Laan SW, Esko T, Pers TH, Locke AE, Berndt SI, Justice AE, Kahali B, Siemelink MA, Pasterkamp G, Strachan DP, Speliotes EK, North KE, ... ... Pawitan Y, et al. Gene-Based Meta-Analysis of Genome-Wide Association Studies Implicates New Loci Involved in Obesity. Human Molecular Genetics. PMID 26376864 DOI: 10.1093/Hmg/Ddv379  0.336
2015 Suo C, Hrydziuszko O, Lee D, Pramana S, Saputra D, Joshi H, Calza S, Pawitan Y. Integration of somatic mutation, expression and functional data reveals potential driver genes predictive of breast cancer survival. Bioinformatics (Oxford, England). PMID 25810432 DOI: 10.1093/Bioinformatics/Btv164  0.336
2015 Lee W, Alexeyenko A, Pernemalm M, Guegan J, Dessen P, Lazar V, Lehtiö J, Pawitan Y. Identifying and assessing interesting subgroups in a heterogeneous population Biomed Research International. 2015. DOI: 10.1155/2015/462549  0.324
2015 Gusnanto A, Pawitan Y. Sparse alternatives to ridge regression: a random effects approach Journal of Applied Statistics. 42: 12-26. DOI: 10.1080/02664763.2014.929640  0.309
2014 Peng Z, Andersson K, Lindholm J, Bodin I, Pramana S, Pawitan Y, Nistér M, Nilsson S, Li C. Operator dependent choice of prostate cancer biopsy has limited impact on a gene signature analysis for the highly expressed genes IGFBP3 and F3 in prostate cancer epithelial cells. Plos One. 9: e109610. PMID 25296164 DOI: 10.1371/Journal.Pone.0109610  0.321
2014 Ganna A, Lee D, Ingelsson E, Pawitan Y. Rediscovery rate estimation for assessing the validation of significant findings in high-throughput studies. Briefings in Bioinformatics. PMID 25256289 DOI: 10.1093/Bib/Bbu033  0.315
2014 Suo C, Calza S, Salim A, Pawitan Y. Joint estimation of isoform expression and isoform-specific read distribution using multisample RNA-Seq data. Bioinformatics (Oxford, England). 30: 506-13. PMID 24307704 DOI: 10.1093/Bioinformatics/Btt704  0.35
2013 Lee D, Lee Y, Pawitan Y, Lee W. Sparse partial least-squares regression for high-throughput survival data analysis. Statistics in Medicine. 32: 5340-52. PMID 24105836 DOI: 10.1002/Sim.5975  0.345
2013 Gusnanto A, Ploner A, Shuweihdi F, Pawitan Y. Partial least squares and logistic regression random-effects estimates for gene selection in supervised classification of gene expression data. Journal of Biomedical Informatics. 46: 697-709. PMID 23747842 DOI: 10.1016/J.Jbi.2013.05.008  0.322
2013 Hong MG, Karlsson R, Magnusson PK, Lewis MR, Isaacs W, Zheng LS, Xu J, Grönberg H, Ingelsson E, Pawitan Y, Broeckling C, Prenni JE, Wiklund F, Prince JA. A genome-wide assessment of variability in human serum metabolism. Human Mutation. 34: 515-24. PMID 23281178 DOI: 10.1002/Humu.22267  0.341
2012 Eschrich SA, Fulp WJ, Pawitan Y, Foekens JA, Smid M, Martens JW, Echevarria M, Kamath V, Lee JH, Harris EE, Bergh J, Torres-Roca JF. Validation of a radiosensitivity molecular signature in breast cancer. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. 18: 5134-43. PMID 22832933 DOI: 10.1158/1078-0432.Ccr-12-0891  0.301
2012 Ku CS, Cooper DN, Wu M, Roukos DH, Pawitan Y, Soong R, Iacopetta B. Gene discovery in familial cancer syndromes by exome sequencing: prospects for the elucidation of familial colorectal cancer type X. Modern Pathology : An Official Journal of the United States and Canadian Academy of Pathology, Inc. 25: 1055-68. PMID 22522846 DOI: 10.1038/Modpathol.2012.62  0.319
2012 Lee W, Gusnanto A, Salim A, Magnusson P, Sim X, Tai ES, Pawitan Y. Estimating the number of true discoveries in genome-wide association studies. Statistics in Medicine. 31: 1177-89. PMID 21987428 DOI: 10.1002/Sim.4391  0.341
2012 Sjölander A, Johansson ALV, Lundholm C, Altman D, Almqvist C, Pawitan Y. Analysis of 1:1 matched cohort studies and twin studies, with binary exposures and binary outcomes Statistical Science. 27: 395-411. DOI: 10.1214/12-Sts390  0.302
2012 Li C, Peng Z, Skoog L, Hellborg H, Jonstam G, Wingmo I, Hjelm-Eriksson M, Harmenberg U, Ährlund-Richter L, Pramana S, Pawitan Y, Nistér M, Nilsson S. Gene expression biomarkers to predict overall survival of prostate cancer patients. Journal of Clinical Oncology. 30: 4561-4561. DOI: 10.1200/Jco.2012.30.15_Suppl.4561  0.343
2012 Torres-Roca JF, Fulp WJ, Pawitan Y, Foekens J, Smid M, Kamath V, Echevarria M, Lee J, Harris EE, Bergh J, Eschrich S. Abstract 678: Validation of a radiosensitivity molecular signature in breast cancer Cancer Research. 72: 678-678. DOI: 10.1158/1538-7445.Am2012-678  0.309
2012 Li C, Peng Z, Skoog L, Hjelm-Eriksson M, Ährlund-Richter L, Harmenberg U, Pawitan Y, Cedermark GC, Nistér M, Nilsson S. A Prostate Cancer Expression Signature to Predict Survival Benefit of Primary Hormone Therapy Annals of Oncology. 23. DOI: 10.1016/S0923-7534(20)33463-3  0.327
2012 Johansson CH, Azimi A, Pernemalm M, Pawitan Y, Stolt MF, Lazar V, Lundeberg J, Lehtio J, Egyhazi S, Hansson J. P2.17 Proteomics and Gene Expression Profiling of Melanoma Chemotherapy Response in Tumors Annals of Oncology. 23: 27-27. DOI: 10.1016/S0923-7534(20)31340-5  0.301
2011 Ku CS, Teo SM, Naidoo N, Sim X, Teo YY, Pawitan Y, Seielstad M, Chia KS, Salim A. Copy number polymorphisms in new HapMap III and Singapore populations. Journal of Human Genetics. 56: 552-60. PMID 21677662 DOI: 10.1038/Jhg.2011.54  0.316
2011 Teo SM, Ku CS, Naidoo N, Hall P, Chia KS, Salim A, Pawitan Y. A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals. Journal of Human Genetics. 56: 524-33. PMID 21633363 DOI: 10.1038/Jhg.2011.52  0.309
2011 Teo SM, Pawitan Y, Kumar V, Thalamuthu A, Seielstad M, Chia KS, Salim A. Multi-platform segmentation for joint detection of copy number variants. Bioinformatics (Oxford, England). 27: 1555-61. PMID 21471018 DOI: 10.1093/Bioinformatics/Btr162  0.324
2011 Ku CS, Naidoo N, Teo SM, Pawitan Y. Regions of homozygosity and their impact on complex diseases and traits. Human Genetics. 129: 1-15. PMID 21104274 DOI: 10.1007/S00439-010-0920-6  0.305
2011 Lee D, Lee W, Lee Y, Pawitan Y. Sparse partial least-squares regression and its applications to high-throughput data analysis Chemometrics and Intelligent Laboratory Systems. 109: 1-8. DOI: 10.1016/J.Chemolab.2011.07.002  0.319
2010 Yip BH, Moger TA, Pawitan Y. Genetic analysis of age-at-onset traits based on case-control family data. Statistics in Medicine. 29: 3258-66. PMID 21170919 DOI: 10.1002/Sim.3907  0.334
2010 Lee D, Lee W, Lee Y, Pawitan Y. Super-sparse principal component analyses for high-throughput genomic data. Bmc Bioinformatics. 11: 296. PMID 20525176 DOI: 10.1186/1471-2105-11-296  0.33
2010 Mei TS, Salim A, Calza S, Seng KC, Seng CK, Pawitan Y. Identification of recurrent regions of Copy-Number Variants across multiple individuals. Bmc Bioinformatics. 11: 147. PMID 20307285 DOI: 10.1186/1471-2105-11-147  0.302
2010 Ku CS, Loy EY, Pawitan Y, Chia KS. The pursuit of genome-wide association studies: where are we now? Journal of Human Genetics. 55: 195-206. PMID 20300123 DOI: 10.1038/Jhg.2010.19  0.302
2010 Sboner A, Demichelis F, Calza S, Pawitan Y, Setlur SR, Hoshida Y, Perner S, Adami HO, Fall K, Mucci LA, Kantoff PW, Stampfer M, Andersson SO, Varenhorst E, Johansson JE, et al. Molecular sampling of prostate cancer: a dilemma for predicting disease progression. Bmc Medical Genomics. 3: 8. PMID 20233430 DOI: 10.1186/1755-8794-3-8  0.316
2010 Yip BH, Reilly M, Cnattingius S, Pawitan Y. Matched ascertainment of informative families for complex genetic modelling. Behavior Genetics. 40: 404-14. PMID 20033275 DOI: 10.1007/S10519-009-9322-8  0.331
2009 Pawitan Y, Seng KC, Magnusson PK. How many genetic variants remain to be discovered? Plos One. 4: e7969. PMID 19956539 DOI: 10.1371/Journal.Pone.0007969  0.318
2009 Huang J, Salim A, Lei K, O'Sullivan K, Pawitan Y. Classification of array CGH data using smoothed logistic regression model. Statistics in Medicine. 28: 3798-810. PMID 19856275 DOI: 10.1002/Sim.3753  0.323
2009 Tan CS, Salim A, Ploner A, Lehtiö J, Chia KS, Pawitan Y. Correlating gene and protein expression data using Correlated Factor Analysis. Bmc Bioinformatics. 10: 272. PMID 19723309 DOI: 10.1186/1471-2105-10-272  0.306
2009 Hong MG, Pawitan Y, Magnusson PK, Prince JA. Strategies and issues in the detection of pathway enrichment in genome-wide association studies. Human Genetics. 126: 289-301. PMID 19408013 DOI: 10.1007/S00439-009-0676-Z  0.341
2008 Weichselbaum RR, Ishwaran H, Yoon T, Nuyten DS, Baker SW, Khodarev N, Su AW, Shaikh AY, Roach P, Kreike B, Roizman B, Bergh J, Pawitan Y, van de Vijver MJ, Minn AJ. An interferon-related gene signature for DNA damage resistance is a predictive marker for chemotherapy and radiation for breast cancer. Proceedings of the National Academy of Sciences of the United States of America. 105: 18490-5. PMID 19001271 DOI: 10.1073/Pnas.0809242105  0.305
2008 Mucci LA, Pawitan Y, Demichelis F, Fall K, Stark JR, Adami HO, Andersson SO, Andrén O, Eisenstein A, Holmberg L, Huang W, Kantoff PW, Kim R, Perner S, Stampfer MJ, et al. Testing a multigene signature of prostate cancer death in the Swedish Watchful Waiting Cohort. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 17: 1682-8. PMID 18583469 DOI: 10.1158/1055-9965.Epi-08-0044  0.321
2008 Forshed J, Pernemalm M, Tan CS, Lindberg M, Kanter L, Pawitan Y, Lewensohn R, Stenke L, Lehtiö J. Proteomic data analysis workflow for discovery of candidate biomarker peaks predictive of clinical outcome for patients with acute myeloid leukemia. Journal of Proteome Research. 7: 2332-41. PMID 18452325 DOI: 10.1021/Pr070482E  0.326
2008 Demissie M, Mascialino B, Calza S, Pawitan Y. Unequal group variances in microarray data analyses. Bioinformatics (Oxford, England). 24: 1168-74. PMID 18344518 DOI: 10.1093/Bioinformatics/Btn100  0.308
2008 Calza S, Valentini D, Pawitan Y. Normalization of oligonucleotide arrays based on the least-variant set of genes. Bmc Bioinformatics. 9: 140. PMID 18318917 DOI: 10.1186/1471-2105-9-140  0.31
2008 Mucci LA, Pawitan Y, Demichelis F, Fall K, Stark JR, Adami HO, Andersson SO, Andrén O, Eisenstein AS, Holmberg L, Huang W, Kantoff PW, Perner S, Stampfer MJ, Johansson JE, et al. Nine-gene molecular signature is not associated with prostate cancer death in a watchful waiting cohort. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 17: 249-51. PMID 18199732 DOI: 10.1158/1055-9965.Epi-07-0722  0.311
2008 Moger TA, Pawitan Y, Borgan O. Case-cohort methods for survival data on families from routine registers. Statistics in Medicine. 27: 1062-74. PMID 17639506 DOI: 10.1002/Sim.3004  0.314
2008 Yip BH, Björk C, Lichtenstein P, Hultman CM, Pawitan Y. Covariance component models for multivariate binary traits in family data analysis. Statistics in Medicine. 27: 1086-105. PMID 17634971 DOI: 10.1002/Sim.2996  0.305
2007 Lindström LS, Yip B, Lichtenstein P, Pawitan Y, Czene K. Etiology of familial aggregation in melanoma and squamous cell carcinoma of the skin. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 16: 1639-43. PMID 17684139 DOI: 10.1158/1055-9965.Epi-07-0047  0.303
2007 Huang J, Gusnanto A, O'Sullivan K, Staaf J, Borg A, Pawitan Y. Robust smooth segmentation approach for array CGH data analysis. Bioinformatics (Oxford, England). 23: 2463-9. PMID 17660206 DOI: 10.1093/Bioinformatics/Btm359  0.31
2007 Ha ID, Lee Y, Pawitan Y. Genetic mixed linear models for twin survival data. Behavior Genetics. 37: 621-30. PMID 17401640 DOI: 10.1007/S10519-007-9150-7  0.347
2007 Perelman E, Ploner A, Calza S, Pawitan Y. Detecting differential expression in microarray data: comparison of optimal procedures. Bmc Bioinformatics. 8: 28. PMID 17257426 DOI: 10.1186/1471-2105-8-28  0.308
2007 Demichelis F, Fall K, Perner S, Andrén O, Schmidt F, Setlur SR, Hoshida Y, Mosquera JM, Pawitan Y, Lee C, Adami HO, Mucci LA, Kantoff PW, Andersson SO, Chinnaiyan AM, et al. TMPRSS2:ERG gene fusion associated with lethal prostate cancer in a watchful waiting cohort. Oncogene. 26: 4596-9. PMID 17237811 DOI: 10.1038/Sj.Onc.1210237  0.312
2007 Wennmalm K, Calza S, Ploner A, Hall P, Bjöhle J, Klaar S, Smeds J, Pawitan Y, Bergh J. Gene expression in 16q is associated with survival and differs between Sørlie breast cancer subtypes. Genes, Chromosomes & Cancer. 46: 87-97. PMID 17044045 DOI: 10.1002/Gcc.20392  0.325
2007 Salim A, Pawitan Y. Model-based maximum covariance analysis for irregularly observed climatological data Journal of Agricultural, Biological, and Environmental Statistics. 12: 1-24. DOI: 10.1198/108571107X177078  0.307
2006 Ivshina AV, George J, Senko O, Mow B, Putti TC, Smeds J, Lindahl T, Pawitan Y, Hall P, Nordgren H, Wong JE, Liu ET, Bergh J, Kuznetsov VA, Miller LD. Genetic reclassification of histologic grade delineates new clinical subtypes of breast cancer. Cancer Research. 66: 10292-301. PMID 17079448 DOI: 10.1158/0008-5472.Can-05-4414  0.304
2006 Pawitan Y, Calza S, Ploner A. Estimation of false discovery proportion under general dependence. Bioinformatics (Oxford, England). 22: 3025-31. PMID 17046978 DOI: 10.1093/Bioinformatics/Btl527  0.374
2006 Calza S, Hall P, Auer G, Bjöhle J, Klaar S, Kronenwett U, Liu ET, Miller L, Ploner A, Smeds J, Bergh J, Pawitan Y. Intrinsic molecular signature of breast cancer in a population-based cohort of 412 patients. Breast Cancer Research : Bcr. 8: R34. PMID 16846532 DOI: 10.1186/Bcr1517  0.311
2006 Tan CS, Ploner A, Quandt A, Lehtiö J, Pawitan Y. Finding regions of significance in SELDI measurements for identifying protein biomarkers. Bioinformatics (Oxford, England). 22: 1515-23. PMID 16567365 DOI: 10.1093/Bioinformatics/Btl106  0.316
2006 Lindström L, Pawitan Y, Reilly M, Hemminki K, Lichtenstein P, Czene K. Estimation of genetic and environmental factors for melanoma onset using population-based family data. Statistics in Medicine. 25: 3110-23. PMID 16372390 DOI: 10.1002/Sim.2266  0.357
2006 Ploner A, Calza S, Gusnanto A, Pawitan Y. Multidimensional local false discovery rate for microarray studies. Bioinformatics (Oxford, England). 22: 556-65. PMID 16368770 DOI: 10.1093/Bioinformatics/Btk013  0.356
2006 Noh M, Yip B, Lee Y, Pawitan Y. Multicomponent variance estimation for binary traits in family-based studies. Genetic Epidemiology. 30: 37-47. PMID 16265627 DOI: 10.1002/Gepi.20099  0.337
2005 Gusnanto A, Ploner A, Pawitan Y. Fold-change estimation of differentially expressed genes using mixture mixed-model. Statistical Applications in Genetics and Molecular Biology. 4: Article26. PMID 16646844 DOI: 10.2202/1544-6115.1145  0.356
2005 Pawitan Y, Murthy KRK, Michiels S, Ploner A. Bias in the estimation of false discovery rate in microarray studies Bioinformatics. 21: 3865-3872. PMID 16105901 DOI: 10.1093/Bioinformatics/Bti626  0.379
2005 Noh M, Lee Y, Pawitan Y. Robust ascertainment-adjusted parameter estimation Genetic Epidemiology. 29: 68-75. PMID 15892092 DOI: 10.1002/Gepi.20078  0.317
2005 Pawitan Y, Michiels S, Koscielny S, Gusnanto A, Ploner A. False discovery rate, sensitivity and sample size for microarray studies Bioinformatics. 21: 3017-3024. PMID 15840707 DOI: 10.1093/Bioinformatics/Bti448  0.32
2004 Pawitan Y, Bjöhle J, Wedren S, Humphreys K, Skoog L, Huang F, Amler L, Shaw P, Hall P, Bergh J. Gene expression profiling for prognosis using Cox regression. Statistics in Medicine. 23: 1767-80. PMID 15160407 DOI: 10.1002/Sim.1769  0.364
2004 Pawitan Y, Griffin JM, Collins JD. Analysis and prediction of the BSE incidence in Ireland. Preventive Veterinary Medicine. 62: 267-83. PMID 15068891 DOI: 10.1016/J.Prevetmed.2003.12.001  0.317
2004 Pawitan Y, Reilly M, Nilsson E, Cnattingius S, Lichtenstein P. Estimation of genetic and environmental factors for binary traits using family data. Statistics in Medicine. 23: 449-465. PMID 14748038 DOI: 10.1002/Sim.1603  0.335
2002 Pawitan Y. In all likelihood : statistical modelling and inference using likelihood The Mathematical Gazette. 86: 375-376. DOI: 10.2307/3621915  0.309
2001 Pawitan Y. Two-staged estimation of variance components in generalized linear mixed models Journal of Statistical Computation and Simulation. 69: 1-17. DOI: 10.1080/00949650108812079  0.318
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