Kathryn Roeder - Publications

Affiliations: 
Carnegie Mellon University, Pittsburgh, PA 
Area:
Statistics

119 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
2019 Jalbrzikowski M, Liu F, Foran W, Roeder K, Devlin B, Luna B. Resting-State Functional Network Organization Is Stable Across Adolescent Development for Typical and Psychosis Spectrum Youth. Schizophrenia Bulletin. PMID 31424081 DOI: 10.1093/schbul/sbz053  0.52
2019 Wang J, Devlin B, Roeder K. Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression. Bioinformatics (Oxford, England). PMID 31400192 DOI: 10.1093/bioinformatics/btz619  0.52
2019 Grove J, Ripke S, Als TD, Mattheisen M, Walters RK, Won H, Pallesen J, Agerbo E, Andreassen OA, Anney R, Awashti S, Belliveau R, Bettella F, Buxbaum JD, Bybjerg-Grauholm J, ... ... Roeder K, et al. Identification of common genetic risk variants for autism spectrum disorder. Nature Genetics. PMID 30804558 DOI: 10.1038/s41588-019-0344-8  0.52
2018 Zhu L, Lei J, Klei L, Devlin B, Roeder K. Semisoft clustering of single-cell data. Proceedings of the National Academy of Sciences of the United States of America. PMID 30587579 DOI: 10.1073/pnas.1817715116  0.52
2018 An JY, Lin K, Zhu L, Werling DM, Dong S, Brand H, Wang HZ, Zhao X, Schwartz GB, Collins RL, Currall BB, Dastmalchi C, Dea J, Duhn C, Gilson MC, ... ... Roeder K, et al. Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362. PMID 30545852 DOI: 10.1126/science.aat6576  0.52
2018 Zhu L, Lei J, Devlin B, Roeder K. A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA. The Annals of Applied Statistics. 12: 609-632. PMID 30174778 DOI: 10.1214/17-AOAS1110  0.52
2018 Chen S, Fragoza R, Klei L, Liu Y, Wang J, Roeder K, Devlin B, Yu H. An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders. Nature Genetics. PMID 29892012 DOI: 10.1038/s41588-018-0130-z  0.52
2018 Hauberg ME, Fullard JF, Zhu L, Cohain AT, Giambartolomei C, Misir R, Reach S, Johnson JS, Wang M, Mattheisen M, Børglum AD, Zhang B, Sieberts SK, Peters MA, Domenici E, ... ... Roeder K, et al. Differential activity of transcribed enhancers in the prefrontal cortex of 537 cases with schizophrenia and controls. Molecular Psychiatry. PMID 29740122 DOI: 10.1038/s41380-018-0059-8  0.52
2018 Werling DM, Brand H, An JY, Stone MR, Zhu L, Glessner JT, Collins RL, Dong S, Layer RM, Markenscoff-Papadimitriou E, Farrell A, Schwartz GB, Wang HZ, Currall BB, Zhao X, ... ... Roeder K, et al. An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics. PMID 29700473 DOI: 10.1038/s41588-018-0107-y  0.52
2017 Yip BHK, Bai D, Mahjani B, Klei L, Pawitan Y, Hultman CM, Grice DE, Roeder K, Buxbaum JD, Devlin B, Reichenberg A, Sandin S. Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden. Biological Psychiatry. PMID 29100626 DOI: 10.1016/j.biopsych.2017.09.007  0.52
2017 Zhu L, Lei J, Devlin B, Roeder K. TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES. The Annals of Applied Statistics. 11: 1810-1831. PMID 29081874 DOI: 10.1214/17-AOAS1062  0.52
2017 Chaste P, Roeder K, Devlin B. The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability. Annual Review of Genomics and Human Genetics. PMID 28426285 DOI: 10.1146/annurev-genom-083115-022647  0.52
2017 Bodea CA, Middleton FA, Melhem NM, Klei L, Song Y, Tiobech J, Marumoto P, Yano V, Faraone SV, Roeder K, Myles-Worsley M, Devlin B, Byerley W. Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31. Molecular Neuropsychiatry. 2: 173-184. PMID 28277564 DOI: 10.1159/000450726  0.52
2017 Kosmicki JA, Samocha KE, Howrigan DP, Sanders SJ, Slowikowski K, Lek M, Karczewski KJ, Cutler DJ, Devlin B, Roeder K, Buxbaum JD, Neale BM, MacArthur DG, Wall DP, Robinson EB, et al. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples. Nature Genetics. PMID 28191890 DOI: 10.1038/ng.3789  0.52
2016 Fromer M, Roussos P, Sieberts SK, Johnson JS, Kavanagh DH, Perumal TM, Ruderfer DM, Oh EC, Topol A, Shah HR, Klei LL, Kramer R, Pinto D, Gümüş ZH, Cicek AE, ... ... Roeder K, et al. Gene expression elucidates functional impact of polygenic risk for schizophrenia. Nature Neuroscience. PMID 27668389 DOI: 10.1038/nn.4399  0.52
2016 Bodea CA, Neale BM, Ripke S, Daly MJ, Devlin B, Roeder K. A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies. American Journal of Human Genetics. PMID 27087321 DOI: 10.1016/j.ajhg.2016.02.025  0.52
2016 Cole DA, Zelkowitz RL, Nick E, Martin NC, Roeder KM, Sinclair-McBride K, Spinelli T. Longitudinal and Incremental Relation of Cybervictimization to Negative Self-Cognitions and Depressive Symptoms in Young Adolescents. Journal of Abnormal Child Psychology. PMID 26747449 DOI: 10.1007/s10802-015-0123-7  0.52
2015 Sanders SJ, He X, Willsey AJ, Ercan-Sencicek AG, Samocha KE, Cicek AE, Murtha MT, Bal VH, Bishop SL, Dong S, Goldberg AP, Jinlu C, Keaney JF, Klei L, Mandell JD, ... ... Roeder K, et al. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci. Neuron. 87: 1215-1233. PMID 26402605 DOI: 10.1016/j.neuron.2015.09.016  0.52
2015 Cicek AE, Roeder K, Ozsoyoglu G. MIRA: mutual information-based reporter algorithm for metabolic networks. Bioinformatics (Oxford, England). 31: 1160. PMID 25762654 DOI: 10.1093/bioinformatics/btv081  0.52
2015 Cotney J, Muhle RA, Sanders SJ, Liu L, Willsey AJ, Niu W, Liu W, Klei L, Lei J, Yin J, Reilly SK, Tebbenkamp AT, Bichsel C, Pletikos M, Sestan N, ... Roeder K, et al. The autism-associated chromatin modifier CHD8 regulates other autism risk genes during human neurodevelopment. Nature Communications. 6: 6404. PMID 25752243 DOI: 10.1038/ncomms7404  0.52
2015 Cole DA, Sinclair-McBride KR, Zelkowitz R, Bilsk SA, Roeder K, Spinelli T. Peer Victimization and Harsh Parenting Predict Cognitive Diatheses for Depression in Children and Adolescents. Journal of Clinical Child and Adolescent Psychology : the Official Journal For the Society of Clinical Child and Adolescent Psychology, American Psychological Association, Division 53. 1-13. PMID 25751612 DOI: 10.1080/15374416.2015.1004679  0.52
2015 Liu L, Lei J, Roeder K. Network assisted analysis to reveal the genetic basis of autism Annals of Applied Statistics. 9: 1571-1600. DOI: 10.1214/15-AOAS844  0.52
2014 Zhao T, Roeder K, Liu H. Positive Semidefinite Rank-based Correlation Matrix Estimation with Application to Semiparametric Graph Estimation. Journal of Computational and Graphical Statistics : a Joint Publication of American Statistical Association, Institute of Mathematical Statistics, Interface Foundation of North America. 23: 895-922. PMID 25382957 DOI: 10.1080/10618600.2013.858633  0.52
2014 Dong S, Walker MF, Carriero NJ, DiCola M, Willsey AJ, Ye AY, Waqar Z, Gonzalez LE, Overton JD, Frahm S, Keaney JF, Teran NA, Dea J, Mandell JD, Hus Bal V, ... ... Roeder K, et al. De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder. Cell Reports. 9: 16-23. PMID 25284784 DOI: 10.1016/j.celrep.2014.08.068  0.52
2014 Samocha KE, Robinson EB, Sanders SJ, Stevens C, Sabo A, McGrath LM, Kosmicki JA, Rehnström K, Mallick S, Kirby A, Wall DP, MacArthur DG, Gabriel SB, DePristo M, Purcell SM, ... ... Roeder K, et al. A framework for the interpretation of de novo mutation in human disease. Nature Genetics. 46: 944-50. PMID 25086666 DOI: 10.1038/ng.3050  0.52
2014 Gaugler T, Klei L, Sanders SJ, Bodea CA, Goldberg AP, Lee AB, Mahajan M, Manaa D, Pawitan Y, Reichert J, Ripke S, Sandin S, Sklar P, Svantesson O, Reichenberg A, ... ... Roeder K, et al. Most genetic risk for autism resides with common variation. Nature Genetics. 46: 881-5. PMID 25038753 DOI: 10.1038/ng.3039  0.52
2014 Melhem NM, Lu C, Dresbold C, Middleton FA, Klei L, Wood S, Faraone SV, Vinogradov S, Tiobech J, Yano V, Roeder K, Byerley W, Myles-Worsley M, Devlin B. Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 165: 521-30. PMID 24980794 DOI: 10.1002/ajmg.b.32255  0.52
2014 Roeder KM, Cole DA, Sinclair KR, Dukewich TL, Preacher KJ, Felton JW, Jacky A, Tilghman-Osborne C. Sensitive periods for the effect of peer victimization on self-cognition: moderation by age and gender. Development and Psychopathology. 26: 1035-48. PMID 24969338 DOI: 10.1017/S0954579414000601  0.52
2014 Cicek AE, Roeder K, Ozsoyoglu G. MIRA: mutual information-based reporter algorithm for metabolic networks. Bioinformatics (Oxford, England). 30: i175-84. PMID 24931981 DOI: 10.1093/bioinformatics/btu290  0.52
2014 Blumenthal I, Ragavendran A, Erdin S, Klei L, Sugathan A, Guide JR, Manavalan P, Zhou JQ, Wheeler VC, Levin JZ, Ernst C, Roeder K, Devlin B, Gusella JF, Talkowski ME. Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families. American Journal of Human Genetics. 94: 870-83. PMID 24906019 DOI: 10.1016/j.ajhg.2014.05.004  0.52
2014 Cole DA, Martin NC, Sterba SK, Sinclair-McBride K, Roeder KM, Zelkowitz R, Bilsky SA. Peer victimization (and harsh parenting) as developmental correlates of cognitive reactivity, a diathesis for depression. Journal of Abnormal Psychology. 123: 336-49. PMID 24886008 DOI: 10.1037/a0036489  0.52
2014 Liu L, Lei J, Sanders SJ, Willsey AJ, Kou Y, Cicek AE, Klei L, Lu C, He X, Li M, Muhle RA, Ma'ayan A, Noonan JP, Sestan N, McFadden KA, ... ... Roeder K, et al. DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics. Molecular Autism. 5: 22. PMID 24602502 DOI: 10.1186/2040-2392-5-22  0.52
2014 Cole DA, Dukewich TL, Roeder K, Sinclair KR, McMillan J, Will E, Bilsky SA, Martin NC, Felton JW. Linking peer victimization to the development of depressive self-schemas in children and adolescents. Journal of Abnormal Child Psychology. 42: 149-60. PMID 23824686 DOI: 10.1007/s10802-013-9769-1  0.52
2013 Crossett A, Lee AB, Klei L, Devlin B, Roeder K. REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING. The Annals of Applied Statistics. 7: 669-690. PMID 24587841 DOI: 10.1214/12-AOAS598  0.52
2013 Willsey AJ, Sanders SJ, Li M, Dong S, Tebbenkamp AT, Muhle RA, Reilly SK, Lin L, Fertuzinhos S, Miller JA, Murtha MT, Bichsel C, Niu W, Cotney J, Ercan-Sencicek AG, ... ... Roeder K, et al. Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism. Cell. 155: 997-1007. PMID 24267886 DOI: 10.1016/j.cell.2013.10.020  0.52
2013 He X, Sanders SJ, Liu L, De Rubeis S, Lim ET, Sutcliffe JS, Schellenberg GD, Gibbs RA, Daly MJ, Buxbaum JD, State MW, Devlin B, Roeder K. Integrated model of de novo and inherited genetic variants yields greater power to identify risk genes. Plos Genetics. 9: e1003671. PMID 23966865 DOI: 10.1371/journal.pgen.1003671  0.52
2013 Schafer CM, Campbell NG, Cai G, Yu F, Makarov V, Yoon S, Daly MJ, Gibbs RA, Schellenberg GD, Devlin B, Sutcliffe JS, Buxbaum JD, Roeder K. Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA. Genomics. 102: 270-7. PMID 23743231 DOI: 10.1016/j.ygeno.2013.05.005  0.52
2013 Bilsky SA, Cole DA, Dukewich TL, Martin NC, Sinclair KR, Tran CV, Roeder KM, Felton JW, Tilghman-Osborne C, Weitlauf AS, Maxwell MA. Does supportive parenting mitigate the longitudinal effects of peer victimization on depressive thoughts and symptoms in children? Journal of Abnormal Psychology. 122: 406-19. PMID 23713500 DOI: 10.1037/a0032501  0.52
2013 Liu L, Sabo A, Neale BM, Nagaswamy U, Stevens C, Lim E, Bodea CA, Muzny D, Reid JG, Banks E, Coon H, Depristo M, Dinh H, Fennel T, Flannick J, ... ... Roeder K, et al. Analysis of rare, exonic variation amongst subjects with autism spectrum disorders and population controls. Plos Genetics. 9: e1003443. PMID 23593035 DOI: 10.1371/journal.pgen.1003443  0.52
2013 Ringquist S, Bellone G, Lu Y, Roeder K, Trucco M. Clustering and alignment of polymorphic sequences for HLA-DRB1 genotyping. Plos One. 8: e59835. PMID 23555798 DOI: 10.1371/journal.pone.0059835  0.52
2013 Lim ET, Raychaudhuri S, Sanders SJ, Stevens C, Sabo A, MacArthur DG, Neale BM, Kirby A, Ruderfer DM, Fromer M, Lek M, Liu L, Flannick J, Ripke S, Nagaswamy U, ... ... Roeder K, et al. Rare complete knockouts in humans: population distribution and significant role in autism spectrum disorders. Neuron. 77: 235-42. PMID 23352160 DOI: 10.1016/j.neuron.2012.12.029  0.52
2012 Zhao T, Liu H, Roeder K, Lafferty J, Wasserman L. The huge Package for High-dimensional Undirected Graph Estimation in R. Journal of Machine Learning Research : Jmlr. 13: 1059-1062. PMID 26834510  0.52
2012 Buxbaum JD, Daly MJ, Devlin B, Lehner T, Roeder K, State MW. The autism sequencing consortium: large-scale, high-throughput sequencing in autism spectrum disorders. Neuron. 76: 1052-6. PMID 23259942 DOI: 10.1016/j.neuron.2012.12.008  0.52
2012 Whitcomb DC, LaRusch J, Krasinskas AM, Klei L, Smith JP, Brand RE, Neoptolemos JP, Lerch MM, Tector M, Sandhu BS, Guda NM, Orlichenko L, Alkaade S, Amann ST, ... ... Roeder K, et al. Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis. Nature Genetics. 44: 1349-54. PMID 23143602 DOI: 10.1038/ng.2466  0.52
2012 Klei L, Sanders SJ, Murtha MT, Hus V, Lowe JK, Willsey AJ, Moreno-De-Luca D, Yu TW, Fombonne E, Geschwind D, Grice DE, Ledbetter DH, Lord C, Mane SM, Martin CL, ... ... Roeder K, et al. Common genetic variants, acting additively, are a major source of risk for autism. Molecular Autism. 3: 9. PMID 23067556 DOI: 10.1186/2040-2392-3-9  0.52
2012 Walters H, Kulkarni M, Forman J, Roeder K, Travis J, Valenstein M. Feasibility and acceptability of interventions to delay gun access in VA mental health settings. General Hospital Psychiatry. 34: 692-8. PMID 22959420 DOI: 10.1016/j.genhosppsych.2012.07.012  0.52
2012 Anney R, Klei L, Pinto D, Almeida J, Bacchelli E, Baird G, Bolshakova N, Bölte S, Bolton PF, Bourgeron T, Brennan S, Brian J, Casey J, Conroy J, Correia C, ... ... Roeder K, et al. Individual common variants exert weak effects on the risk for autism spectrum disorderspi. Human Molecular Genetics. 21: 4781-92. PMID 22843504 DOI: 10.1093/hmg/dds301  0.52
2012 Brehm JM, Acosta-Pérez E, Klei L, Roeder K, Barmada M, Boutaoui N, Forno E, Kelly R, Paul K, Sylvia J, Litonjua AA, Cabana M, Alvarez M, Colón-Semidey A, Canino G, et al. Vitamin D insufficiency and severe asthma exacerbations in Puerto Rican children. American Journal of Respiratory and Critical Care Medicine. 186: 140-6. PMID 22652028 DOI: 10.1164/rccm.201203-0431OC  0.52
2012 Brehm JM, Acosta-Pérez E, Klei L, Roeder K, Barmada MM, Boutaoui N, Forno E, Cloutier MM, Datta S, Kelly R, Paul K, Sylvia J, Calvert D, Thornton-Thompson S, Wakefield D, et al. African ancestry and lung function in Puerto Rican children. The Journal of Allergy and Clinical Immunology. 129: 1484-90.e6. PMID 22560959 DOI: 10.1016/j.jaci.2012.03.035  0.52
2012 Neale BM, Kou Y, Liu L, Ma'ayan A, Samocha KE, Sabo A, Lin CF, Stevens C, Wang LS, Makarov V, Polak P, Yoon S, Maguire J, Crawford EL, Campbell NG, ... ... Roeder K, et al. Patterns and rates of exonic de novo mutations in autism spectrum disorders. Nature. 485: 242-5. PMID 22495311 DOI: 10.1038/nature11011  0.52
2012 Sanders SJ, Murtha MT, Gupta AR, Murdoch JD, Raubeson MJ, Willsey AJ, Ercan-Sencicek AG, DiLullo NM, Parikshak NN, Stein JL, Walker MF, Ober GT, Teran NA, Song Y, El-Fishawy P, ... ... Roeder K, et al. De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature. 485: 237-41. PMID 22495306 DOI: 10.1038/nature10945  0.52
2012 Ilgen MA, Conner KR, Roeder KM, Blow FC, Austin K, Valenstein M. Patterns of treatment utilization before suicide among male veterans with substance use disorders. American Journal of Public Health. 102: S88-92. PMID 22390610 DOI: 10.2105/AJPH.2011.300392  0.52
2012 Mechanic LE, Chen HS, Amos CI, Chatterjee N, Cox NJ, Divi RL, Fan R, Harris EL, Jacobs K, Kraft P, Leal SM, McAllister K, Moore JH, Paltoo DN, Province MA, ... ... Roeder K, et al. Next generation analytic tools for large scale genetic epidemiology studies of complex diseases. Genetic Epidemiology. 36: 22-35. PMID 22147673 DOI: 10.1002/gepi.20652  0.52
2012 Zhao T, Roeder K, Liu H. Smooth-projected neighborhood pursuit for high-dimensional nonparanormal graph estimation Advances in Neural Information Processing Systems. 1: 162-170.  0.52
2011 Melhem N, Middleton F, McFadden K, Klei L, Faraone SV, Vinogradov S, Tiobech J, Yano V, Kuartei S, Roeder K, Byerley W, Devlin B, Myles-Worsley M. Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees. Biological Psychiatry. 70: 1115-21. PMID 21982423 DOI: 10.1016/j.biopsych.2011.08.009  0.52
2011 Eisenberg D, Nicklett EJ, Roeder K, Kirz NE. Eating disorder symptoms among college students: prevalence, persistence, correlates, and treatment-seeking. Journal of American College Health : J of Ach. 59: 700-7. PMID 21950250 DOI: 10.1080/07448481.2010.546461  0.52
2011 Percival D, Roeder K, Rosenfeld R, Wasserman L. STRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCE. The Annals of Applied Statistics. 5: 628-644. PMID 21892380 DOI: 10.1214/10-AOAS428  0.52
2011 Chu SH, Roeder K, Ferrell RE, Devlin B, DeMichele-Sweet MA, Kamboh MI, Lopez OL, Sweet RA. TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease. Neurobiology of Aging. 32: 2328.e1-9. PMID 21820212 DOI: 10.1016/j.neurobiolaging.2011.06.016  0.52
2011 Bohnert AS, Roeder KM, Ilgen MA. Suicide attempts and overdoses among adults entering addictions treatment: comparing correlates in a U.S. National Study. Drug and Alcohol Dependence. 119: 106-12. PMID 21715108 DOI: 10.1016/j.drugalcdep.2011.05.032  0.52
2011 Sanders SJ, Ercan-Sencicek AG, Hus V, Luo R, Murtha MT, Moreno-De-Luca D, Chu SH, Moreau MP, Gupta AR, Thomson SA, Mason CE, Bilguvar K, Celestino-Soper PB, Choi M, Crawford EL, ... ... Roeder K, et al. Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron. 70: 863-85. PMID 21658581 DOI: 10.1016/j.neuron.2011.05.002  0.52
2011 Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Kathiresan S, Purcell SM, Roeder K, Daly MJ. Testing for an unusual distribution of rare variants. Plos Genetics. 7: e1001322. PMID 21408211 DOI: 10.1371/journal.pgen.1001322  0.52
2011 Ilgen MA, Roeder KM, Webster L, Mowbray OP, Perron BE, Chermack ST, Bohnert AS. Measuring pain medication expectancies in adults treated for substance use disorders. Drug and Alcohol Dependence. 115: 51-6. PMID 21111540 DOI: 10.1016/j.drugalcdep.2010.10.007  0.52
2011 Devlin B, Melhem N, Roeder K. Do common variants play a role in risk for autism? Evidence and theoretical musings. Brain Research. 1380: 78-84. PMID 21078308 DOI: 10.1016/j.brainres.2010.11.026  0.52
2010 Liu H, Roeder K, Wasserman L. Stability Approach to Regularization Selection (StARS) for High Dimensional Graphical Models. Advances in Neural Information Processing Systems. 24: 1432-1440. PMID 25152607  0.52
2010 Crossett A, Kent BP, Klei L, Ringquist S, Trucco M, Roeder K, Devlin B. Using ancestry matching to combine family-based and unrelated samples for genome-wide association studies. Statistics in Medicine. 29: 2932-45. PMID 20862653 DOI: 10.1002/sim.4057  0.52
2010 Lee AB, Luca D, Roeder K. A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRY. The Annals of Applied Statistics. 4: 179-202. PMID 20689656 DOI: 10.1214/09-AOAS281  0.52
2010 Anney R, Klei L, Pinto D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Sykes N, Pagnamenta AT, Almeida J, Bacchelli E, Bailey AJ, Baird G, Battaglia A, ... ... Roeder K, et al. A genome-wide scan for common alleles affecting risk for autism. Human Molecular Genetics. 19: 4072-82. PMID 20663923 DOI: 10.1093/hmg/ddq307  0.52
2010 Travis J, Roeder K, Walters H, Piette J, Heisler M, Ganoczy D, Valenstein M, Pfeiffer P. Telephone-based mutual peer support for depression: a pilot study. Chronic Illness. 6: 183-91. PMID 20634226 DOI: 10.1177/1742395310369570  0.52
2010 Pinto D, Pagnamenta AT, Klei L, Anney R, Merico D, Regan R, Conroy J, Magalhaes TR, Correia C, Abrahams BS, Almeida J, Bacchelli E, Bader GD, Bailey AJ, Baird G, ... ... Roeder K, et al. Functional impact of global rare copy number variation in autism spectrum disorders. Nature. 466: 368-72. PMID 20531469 DOI: 10.1038/nature09146  0.52
2010 Bohnert AS, Roeder K, Ilgen MA. Unintentional overdose and suicide among substance users: a review of overlap and risk factors. Drug and Alcohol Dependence. 110: 183-92. PMID 20430536 DOI: 10.1016/j.drugalcdep.2010.03.010  0.52
2010 McGovern DP, Gardet A, Törkvist L, Goyette P, Essers J, Taylor KD, Neale BM, Ong RT, Lagacé C, Li C, Green T, Stevens CR, Beauchamp C, Fleshner PR, Carlson M, ... ... Roeder K, et al. Genome-wide association identifies multiple ulcerative colitis susceptibility loci. Nature Genetics. 42: 332-7. PMID 20228799 DOI: 10.1038/ng.549  0.52
2010 Wu J, Devlin B, Ringquist S, Trucco M, Roeder K. Screen and clean: a tool for identifying interactions in genome-wide association studies. Genetic Epidemiology. 34: 275-85. PMID 20088021 DOI: 10.1002/gepi.20459  0.52
2010 Yerges LM, Klei L, Cauley JA, Roeder K, Kammerer CM, Ensrud KE, Nestlerode CS, Lewis C, Lang TF, Barrett-Connor E, Moffett SP, Hoffman AR, Ferrell RE, Orwoll ES, Zmuda JM, et al. Candidate gene analysis of femoral neck trabecular and cortical volumetric bone mineral density in older men. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 330-8. PMID 19619005 DOI: 10.1359/jbmr.090729  0.52
2010 Lee AB, Luca D, Klei L, Devlin B, Roeder K. Discovering genetic ancestry using spectral graph theory. Genetic Epidemiology. 34: 51-9. PMID 19455578 DOI: 10.1002/gepi.20434  0.52
2009 Roeder K, Wasserman L. Genome-Wide Significance Levels and Weighted Hypothesis Testing. Statistical Science : a Review Journal of the Institute of Mathematical Statistics. 24: 398-413. PMID 20711421 DOI: 10.1214/09-STS289  0.52
2009 Wasserman L, Roeder K. HIGH DIMENSIONAL VARIABLE SELECTION. Annals of Statistics. 37: 2178-2201. PMID 19784398  0.32
2009 Yerges LM, Klei L, Cauley JA, Roeder K, Kammerer CM, Moffett SP, Ensrud KE, Nestlerode CS, Marshall LM, Hoffman AR, Lewis C, Lang TF, Barrett-Connor E, Ferrell RE, Orwoll ES, et al. High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 24: 2039-49. PMID 19453261 DOI: 10.1359/jbmr.090524  0.52
2009 Roeder R, Roeder K, Asano E, Chugani HT. Depression and mental health help-seeking behaviors in a predominantly African American population of children and adolescents with epilepsy. Epilepsia. 50: 1943-52. PMID 19260941 DOI: 10.1111/j.1528-1167.2009.02046.x  0.52
2009 Silverberg MS, Cho JH, Rioux JD, McGovern DP, Wu J, Annese V, Achkar JP, Goyette P, Scott R, Xu W, Barmada MM, Klei L, Daly MJ, Abraham C, Bayless TM, ... ... Roeder K, et al. Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study. Nature Genetics. 41: 216-20. PMID 19122664 DOI: 10.1038/ng.275  0.52
2009 Roeder K, Luca D. Searching for disease susceptibility variants in structured populations. Genomics. 93: 1-4. PMID 18519160 DOI: 10.1016/j.ygeno.2008.04.004  0.52
2009 Wasserman L, Roeder K. High-dimensional variable selection Annals of Statistics. 37: 2178-2201. DOI: 10.1214/08-AOS646  0.52
2008 Luca D, Ringquist S, Klei L, Lee AB, Gieger C, Wichmann HE, Schreiber S, Krawczak M, Lu Y, Styche A, Devlin B, Roeder K, Trucco M. On the use of general control samples for genome-wide association studies: genetic matching highlights causal variants. American Journal of Human Genetics. 82: 453-63. PMID 18252225 DOI: 10.1016/j.ajhg.2007.11.003  0.52
2008 Klei L, Luca D, Devlin B, Roeder K. Pleiotropy and principal components of heritability combine to increase power for association analysis. Genetic Epidemiology. 32: 9-19. PMID 17922480 DOI: 10.1002/gepi.20257  0.52
2007 Roeder K, Devlin B, Wasserman L. Improving power in genome-wide association studies: weights tip the scale. Genetic Epidemiology. 31: 741-7. PMID 17549760 DOI: 10.1002/gepi.20237  0.52
2007 Devlin B, Klei L, Myles-Worsley M, Tiobech J, Otto C, Byerley W, Roeder K. Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation. Human Genetics. 121: 675-84. PMID 17436020 DOI: 10.1007/s00439-007-0358-7  0.52
2007 Klei L, Roeder K. Testing for association based on excess allele sharing in a sample of related cases and controls. Human Genetics. 121: 549-57. PMID 17342507 DOI: 10.1007/s00439-007-0345-z  0.52
2006 Steffens M, Lamina C, Illig T, Bettecken T, Vogler R, Entz P, Suk EK, Toliat MR, Klopp N, Caliebe A, König IR, Köhler K, Ludemann J, Diaz Lacava A, Fimmers R, ... ... Roeder K, et al. SNP-based analysis of genetic substructure in the German population. Human Heredity. 62: 20-9. PMID 17003564 DOI: 10.1159/000095850  0.52
2006 Roeder K, Bacanu SA, Wasserman L, Devlin B. Using linkage genome scans to improve power of association in genome scans. American Journal of Human Genetics. 78: 243-52. PMID 16400608 DOI: 10.1086/500026  0.52
2005 Rinaldo A, Bacanu SA, Devlin B, Sonpar V, Wasserman L, Roeder K. Characterization of multilocus linkage disequilibrium. Genetic Epidemiology. 28: 193-206. PMID 15637716 DOI: 10.1002/gepi.20056  0.52
2005 Roeder K, Bacanu SA, Sonpar V, Zhang X, Devlin B. Analysis of single-locus tests to detect gene/disease associations. Genetic Epidemiology. 28: 207-19. PMID 15637715 DOI: 10.1002/gepi.20050  0.52
2004 Devlin B, Bacanu SA, Roeder K. Genomic Control to the extreme. Nature Genetics. 36: 1129-30; author repl. PMID 15514657 DOI: 10.1038/ng1104-1129  0.52
2003 Zhang X, Roeder K, Wallstrom G, Devlin B. Integration of association statistics over genomic regions using Bayesian adaptive regression splines. Human Genomics. 1: 20-9. PMID 15601530  0.52
2003 Seltman H, Roeder K, Devlin B. Evolutionary-based association analysis using haplotype data. Genetic Epidemiology. 25: 48-58. PMID 12813726 DOI: 10.1002/gepi.10246  0.52
2003 Devlin B, Roeder K, Wasserman L. Analysis of multilocus models of association. Genetic Epidemiology. 25: 36-47. PMID 12813725 DOI: 10.1002/gepi.10237  0.52
2003 Tzeng JY, Devlin B, Wasserman L, Roeder K. On the identification of disease mutations by the analysis of haplotype similarity and goodness of fit. American Journal of Human Genetics. 72: 891-902. PMID 12610778 DOI: 10.1086/373881  0.52
2002 Bacanu SA, Devlin B, Roeder K. Association studies for quantitative traits in structured populations. Genetic Epidemiology. 22: 78-93. PMID 11754475 DOI: 10.1002/gepi.1045  0.52
2002 Devlin B, Jones BL, Bacanu SA, Roeder K. Mixture models for linkage analysis of affected sibling pairs and covariates. Genetic Epidemiology. 22: 52-65. PMID 11754473 DOI: 10.1002/gepi.1043  0.52
2001 Devlin B, Roeder K, Wasserman L. Genomic control, a new approach to genetic-based association studies. Theoretical Population Biology. 60: 155-66. PMID 11855950 DOI: 10.1006/tpbi.2001.1542  0.52
2001 Seltman H, Roeder K, Devlin B. Transmission/disequilibrium test meets measured haplotype analysis: family-based association analysis guided by evolution of haplotypes. American Journal of Human Genetics. 68: 1250-63. PMID 11309689 DOI: 10.1086/320110  0.52
1999 Devlin B, Roeder K. Genomic control for association studies. Biometrics. 55: 997-1004. PMID 11315092  0.52
1997 Crowley EM, Roeder K, Bina M. A statistical model for locating regulatory regions in genomic DNA. Journal of Molecular Biology. 268: 8-14. PMID 9149136 DOI: 10.1006/jmbi.1997.0965  0.52
1997 Roeder K, Wasserman L. Practical Bayesian density estimation using mixtures of normals Journal of the American Statistical Association. 92: 894-902.  0.52
1997 Lindsay B, Roeder K. Moment-based oscillation properties of mixture models Annals of Statistics. 25: 378-386.  0.52
1997 Müller P, Roeder K. A Bayesian semiparametric model for case-control studies with errors in variables Biometrika. 84: 523-537.  0.52
1996 Devlin B, Risch N, Roeder K. Disequilibrium mapping: composite likelihood for pairwise disequilibrium. Genomics. 36: 1-16. PMID 8812410 DOI: 10.1006/geno.1996.0419  0.52
1995 Lambert D, Roeder K. Overdispersion diagnostics for generalized linear models Journal of the American Statistical Association. 90: 1225-1236. DOI: 10.1080/01621459.1995.10476627  0.52
1994 Devlin B, Risch N, Roeder K. Comments on the statistical aspects of the NRC's report on DNA typing. Journal of Forensic Sciences. 39: 28-40. PMID 8113709  0.52
1994 Roeder K. A graphical technique for determining the number of components in a mixture of normals Journal of the American Statistical Association. 89: 487-495. DOI: 10.1080/01621459.1994.10476772  0.52
1993 Devlin B, Risch N, Roeder K. NRC report on DNA typing. Science (New York, N.Y.). 260: 1057-9. PMID 8493540  0.52
1993 Devlin B, Risch N, Roeder K. Statistical evaluation of DNA fingerprinting: a critique of the NRC's report. Science (New York, N.Y.). 259: 748-9, 837. PMID 8430323  0.52
1992 Lindsay BG, Roeder K. Residual diagnostics for mixture models Journal of the American Statistical Association. 87: 785-794. DOI: 10.1080/01621459.1992.10475280  0.52
1992 Devlin B, Risch N, Roeder K. Forensic inference from dna fingerprints Journal of the American Statistical Association. 87: 337-350. DOI: 10.1080/01621459.1992.10475213  0.52
1991 Devlin B, Risch N, Roeder K. Estimation of allele frequencies for VNTR loci. American Journal of Human Genetics. 48: 662-76. PMID 2014794  0.52
1990 Devlin B, Risch N, Roeder K. No excess of homozygosity at loci used for DNA fingerprinting. Science (New York, N.Y.). 249: 1416-20. PMID 2205919  0.52
1990 Roeder K. Density estimation with confidence sets exemplified by superclusters and voids in the galaxies Journal of the American Statistical Association. 85: 617-624. DOI: 10.1080/01621459.1990.10474918  0.52
1989 Roeder K, Devlin B, Lindsay BG. Application of maximum likelihood methods to population genetic data for the estimation of individual fertilities Biometrics. 45: 363-379.  0.52
1988 Devlin B, Roeder K, Ellstrand NC. Fractional paternity assignment: theoretical development and comparison to other methods. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. 76: 369-80. PMID 24232200 DOI: 10.1007/BF00265336  0.52
1987 Lindsay BG, Roeder K. A unified treatment of integer parameter models Journal of the American Statistical Association. 82: 758-764. DOI: 10.1080/01621459.1987.10478496  0.52
1987 Roeder K, Dennis B, Garton EO. Estimating density from variable circular plot censuses Journal of Wildlife Management. 51: 224-230.  0.52
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