| Year |
Citation |
Score |
| 2022 |
Fu JM, Satterstrom FK, Peng M, Brand H, Collins RL, Dong S, Wamsley B, Klei L, Wang L, Hao SP, Stevens CR, Cusick C, Babadi M, Banks E, Collins B, ... ... Roeder K, et al. Rare coding variation provides insight into the genetic architecture and phenotypic context of autism. Nature Genetics. PMID 35982160 DOI: 10.1038/s41588-022-01104-0 |
0.315 |
|
| 2021 |
Lin KZ, Liu H, Roeder K. Covariance-based sample selection for heterogeneous data: Applications to gene expression and autism risk gene detection. Journal of the American Statistical Association. 116: 54-67. PMID 33731968 DOI: 10.1080/01621459.2020.1738234 |
0.37 |
|
| 2020 |
Yurko R, G'Sell M, Roeder K, Devlin B. A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk. Proceedings of the National Academy of Sciences of the United States of America. PMID 32522875 DOI: 10.1073/Pnas.1918862117 |
0.418 |
|
| 2020 |
Werling DM, Pochareddy S, Choi J, An JY, Sheppard B, Peng M, Li Z, Dastmalchi C, Santpere G, Sousa AMM, Tebbenkamp ATN, Kaur N, Gulden FO, Breen MS, Liang L, ... ... Roeder K, et al. Whole-Genome and RNA Sequencing Reveal Variation and Transcriptomic Coordination in the Developing Human Prefrontal Cortex. Cell Reports. 31: 107489. PMID 32268104 DOI: 10.1016/J.Celrep.2020.03.053 |
0.373 |
|
| 2020 |
Satterstrom FK, Kosmicki JA, Wang J, Breen MS, De Rubeis S, An JY, Peng M, Collins R, Grove J, Klei L, Stevens C, Reichert J, Mulhern MS, Artomov M, Gerges S, ... ... Roeder K, et al. Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism. Cell. PMID 31981491 DOI: 10.1016/J.Cell.2019.12.036 |
0.393 |
|
| 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 |
0.455 |
|
| 2019 |
An J, Lin K, Zhu L, Werling D, Dong S, Brand H, Wang H, Zhao X, Sestan N, State M, Willsey J, Talkowski M, Devlin B, Roeder K, Sanders S. INSIGHTS INTO THE CONTRIBUTION OF RARE NONCODING VARIATION IN AUTISM SPECTRUM DISORDER THROUGH FAMILY-BASED WHOLE-GENOME SEQUENCING European Neuropsychopharmacology. 29: S36. DOI: 10.1016/J.Euroneuro.2019.07.073 |
0.361 |
|
| 2019 |
Satterstrom F, Kosmicki J, Wang J, Collins R, de Rubeis S, Breen M, Gerges S, Børglum A, Buxbaum J, Cutler D, Devlin B, Roeder K, Sanders S, Talkowski M, Daly M. 31DISCOVERY AND CHARACTERIZATION OF 102 GENES ASSOCIATED WITH AUTISM FROM EXOME SEQUENCING OF 37,269 INDIVIDUALS European Neuropsychopharmacology. 29: S1083-S1084. DOI: 10.1016/J.Euroneuro.2018.08.038 |
0.35 |
|
| 2019 |
Werling D, Brand H, An J, Stone M, Glessner J, Zhu L, Collins R, Daly M, State M, Quinlan A, Marth G, Roeder K, Devlin B, Sanders S, Talkowski M. LIMITED CONTRIBUTION OF RARE, NONCODING VARIATION TO AUTISM SPECTRUM DISORDER FROM SEQUENCING OF 2,076 GENOMES IN QUARTET FAMILIES European Neuropsychopharmacology. 29: S784-S785. DOI: 10.1016/J.Euroneuro.2017.08.010 |
0.463 |
|
| 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 |
0.367 |
|
| 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 |
0.314 |
|
| 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 |
0.306 |
|
| 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 |
0.345 |
|
| 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 |
0.422 |
|
| 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 |
0.361 |
|
| 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 |
0.33 |
|
| 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 |
0.441 |
|
| 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 |
0.415 |
|
| 2017 |
Buxbaum J, Cicek E, Devlin B, Klei L, Roeder K, De Rubeis S. Combining Autism And Intellectual Disability Exome Data Implicates Disruption Of Neocortical Development In Both Disorders European Neuropsychopharmacology. 27: S437. DOI: 10.1016/J.Euroneuro.2016.09.497 |
0.385 |
|
| 2017 |
Buxbaum J, Cicek E, Devlin B, Klei L, Roeder K, De Rubeis S. Integrative Analyses of Autism And Intellectual Disability Exome Data Reveal Similarities And Divergences And Identify Novel Risk Genes For Both Disorders European Neuropsychopharmacology. 27: S419-S420. DOI: 10.1016/J.Euroneuro.2016.09.469 |
0.35 |
|
| 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 |
0.331 |
|
| 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 |
0.421 |
|
| 2015 |
Liu L, Lei J, Roeder K. NETWORK ASSISTED ANALYSIS TO REVEAL THE GENETIC BASIS OF AUTISM. The Annals of Applied Statistics. 9: 1571-1600. PMID 27134692 DOI: 10.1214/15-Aoas844 |
0.409 |
|
| 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 |
0.394 |
|
| 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 |
0.328 |
|
| 2014 |
De Rubeis S, He X, Goldberg AP, Poultney CS, Samocha K, Cicek AE, Kou Y, Liu L, Fromer M, Walker S, Singh T, Klei L, Kosmicki J, Shih-Chen F, Aleksic B, ... ... Roeder K, et al. Synaptic, transcriptional and chromatin genes disrupted in autism. Nature. 515: 209-15. PMID 25363760 DOI: 10.1038/Nature13772 |
0.331 |
|
| 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 |
0.403 |
|
| 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 |
0.334 |
|
| 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 |
0.43 |
|
| 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 |
0.379 |
|
| 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 |
0.375 |
|
| 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 |
0.389 |
|
| 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 |
0.754 |
|
| 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 |
0.365 |
|
| 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 |
0.425 |
|
| 2013 |
Lee SH, Ripke S, Neale BM, Faraone SV, Purcell SM, Perlis RH, Mowry BJ, Thapar A, Goddard ME, Witte JS, Absher D, Agartz I, Akil H, Amin F, ... ... Roeder K, et al. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs. Nature Genetics. 45: 984-94. PMID 23933821 DOI: 10.1038/Ng.2711 |
0.58 |
|
| 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 |
0.304 |
|
| 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 |
0.438 |
|
| 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 |
0.337 |
|
| 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 |
0.395 |
|
| 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 |
0.359 |
|
| 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 |
0.361 |
|
| 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 |
0.446 |
|
| 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 |
0.444 |
|
| 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 |
0.389 |
|
| 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 |
0.381 |
|
| 2012 |
Achkar JP, Klei L, de Bakker PI, Bellone G, Rebert N, Scott R, Lu Y, Regueiro M, Brzezinski A, Kamboh MI, Fiocchi C, Devlin B, Trucco M, Ringquist S, Roeder K, et al. Amino acid position 11 of HLA-DRβ1 is a major determinant of chromosome 6p association with ulcerative colitis. Genes and Immunity. 13: 245-52. PMID 22170232 DOI: 10.1038/Gene.2011.79 |
0.311 |
|
| 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 |
0.403 |
|
| 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 |
0.366 |
|
| 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 |
0.401 |
|
| 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 |
0.373 |
|
| 2011 |
Zmuda JM, Yerges-Armstrong LM, Moffett SP, Klei L, Kammerer CM, Roeder K, Cauley JA, Kuipers A, Ensrud KE, Nestlerode CS, Hoffman AR, Lewis CE, Lang TF, Barrett-Connor E, Ferrell RE, et al. Genetic analysis of vertebral trabecular bone density and cross-sectional area in older men. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. 22: 1079-90. PMID 21153022 DOI: 10.1007/S00198-010-1296-0 |
0.342 |
|
| 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 |
0.412 |
|
| 2011 |
McGovern DPB, Gardet A, Törkvist L, Goyette P, Essers J, Taylor KD, Neale BM, Ong RTH, Lagace 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 (vol 42, pg 332, 2010) Nature Genetics. 43: 388-388. DOI: 10.1038/Ng0411-388C |
0.359 |
|
| 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 |
0.75 |
|
| 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 |
0.39 |
|
| 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 |
0.765 |
|
| 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 |
0.758 |
|
| 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 |
0.403 |
|
| 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 |
0.366 |
|
| 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 |
0.344 |
|
| 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 |
0.421 |
|
| 2010 |
Neale BM, Rivas MA, Voight BF, Altshuler D, Devlin B, Orho-Melander M, Katherisan S, Roeder K, Daly MJ. Testing for an unusual distribution of rare variation Behavior Genetics. 40: 807-807. DOI: 10.1007/S10519-010-9392-7 |
0.316 |
|
| 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 |
0.378 |
|
| 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 |
0.348 |
|
| 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 |
0.416 |
|
| 2009 |
Silverberg MS, Cho JH, Rioux JD, McGovern DPB, Wu J, Annese V, Achkar J, Goyette P, Scott R, Xu W, Barmada MM, Klei L, Daly MJ, Abraham C, Bayless TM, ... ... Roeder K, et al. Erratum: Corrigendum: Ulcerative colitis-risk loci on chromosomes 1p36 and 12q15 found by genome-wide association study Nature Genetics. 41: 762-762. DOI: 10.1038/Ng0609-762A |
0.309 |
|
| 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 |
0.432 |
|
| 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 |
0.421 |
|
| 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 |
0.401 |
|
| 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 |
0.323 |
|
| 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 |
0.431 |
|
| 2006 |
Sabatti C, Satten GA, Allen AS, Epstein MP, Chatterjee N, Spinka C, Chen J, Carroll RJ, Tzeng JY, Roeder K, Li H, Lin DY, Zeng D. Journal of the American Statistical Association: Comment Journal of the American Statistical Association. 101: 104-118. DOI: 10.1198/016214505000000817 |
0.527 |
|
| 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 |
0.392 |
|
| 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 |
0.349 |
|
| 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 DOI: 10.1186/1479-7364-1-1-20 |
0.417 |
|
| 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 |
0.411 |
|
| 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 |
0.407 |
|
| 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 |
0.597 |
|
| 2003 |
Tzeng J, Byerley W, Devlin B, Roeder K, Wasserman L. Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching Journal of the American Statistical Association. 98: 236-246. DOI: 10.1198/016214503388619256 |
0.607 |
|
| 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 |
0.445 |
|
| 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 |
0.565 |
|
| 2002 |
Devlin B, Bacanu S, Jones BL, Roeder K. ?Reply to Olson? Genetic Epidemiology. 23: 449-455. DOI: 10.1002/Gepi.10179 |
0.44 |
|
| 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 |
0.435 |
|
| 2001 |
Devlin B, Roeder K, Bacanu SA. Unbiased methods for population-based association studies. Genetic Epidemiology. 21: 273-84. PMID 11754464 DOI: 10.1002/Gepi.1034 |
0.393 |
|
| 2001 |
Devlin B, Roeder K, Otto C, Tiobech S, Byerley W. Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote Oceania. Human Genetics. 108: 521-8. PMID 11499679 DOI: 10.1007/S004390100511 |
0.357 |
|
| 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 |
0.374 |
|
| 2001 |
Lockwood JR, Roeder K, Devlin B. A Bayesian hierarchical model for allele frequencies. Genetic Epidemiology. 20: 17-33. PMID 11119294 DOI: 10.1002/1098-2272(200101)20:1<17::Aid-Gepi3>3.0.Co;2-Q |
0.349 |
|
| 2001 |
JONES BL, NAGIN DS, ROEDER K. A SAS Procedure Based on Mixture Models for Estimating Developmental Trajectories Sociological Methods & Research. 29: 374-393. DOI: 10.1177/0049124101029003005 |
0.523 |
|
| 2000 |
Devlin B, Roeder K, Wasserman L. Genomic control for association studies: a semiparametric test to detect excess-haplotype sharing. Biostatistics (Oxford, England). 1: 369-87. PMID 12933562 DOI: 10.1093/Biostatistics/1.4.369 |
0.415 |
|
| 2000 |
Bacanu SA, Devlin B, Roeder K. The power of genomic control. American Journal of Human Genetics. 66: 1933-44. PMID 10801388 DOI: 10.1086/302929 |
0.367 |
|
| 2000 |
Lam JC, Roeder K, Devlin B. Haplotype fine mapping by evolutionary trees. American Journal of Human Genetics. 66: 659-73. PMID 10677324 DOI: 10.1086/302756 |
0.346 |
|
| 1999 |
Devlin B, Roeder K. Genomic control for association studies. Biometrics. 55: 997-1004. PMID 11315092 DOI: 10.1111/J.0006-341X.1999.00997.X |
0.45 |
|
| 1999 |
Roeder K, Lynch KG, Nagin DS. Modeling Uncertainty in Latent Class Membership: A Case Study in Criminology Journal of the American Statistical Association. 94: 766-776. DOI: 10.1080/01621459.1999.10474179 |
0.311 |
|
| 1998 |
Roeder K. Measuring heterogeneity in forensic databases using hierarchical Bayes models Biometrika. 85: 269-287. DOI: 10.1093/Biomet/85.2.269 |
0.347 |
|
| 1997 |
Devlin B, Daniels M, Roeder K. The heritability of IQ. Nature. 388: 468-71. PMID 9242404 DOI: 10.1038/41319 |
0.334 |
|
| 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 |
0.322 |
|
| 1997 |
Andrews C, Devlin B, Perlin M, Roeder K. Binning clones by hybridization with complex probes: statistical refinement of an inner product mapping method. Genomics. 41: 141-54. PMID 9143488 DOI: 10.1006/Geno.1997.4652 |
0.308 |
|
| 1997 |
Müller P, Roeder K. A Bayesian semiparametric model for case-control studies with errors in variables Biometrika. 84: 523-537. DOI: 10.1093/Biomet/84.3.523 |
0.304 |
|
| 1997 |
Roeder K, Wasserman L. Practical Bayesian Density Estimation Using Mixtures of Normals Journal of the American Statistical Association. 92: 894-902. DOI: 10.1080/01621459.1997.10474044 |
0.302 |
|
| 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 |
0.352 |
|
| 1996 |
Roeder K, Carroll RJ, Lindsay BG. A Semiparametric Mixture Approach to Case-Control Studies with Errors in Covariables Journal of the American Statistical Association. 91: 722-732. DOI: 10.1080/01621459.1996.10476940 |
0.322 |
|
| 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 DOI: 10.1520/Jfs13568J |
0.356 |
|
| 1994 |
Roeder K. DNA Fingerprinting: A Review of the Controversy Statistical Science. 9: 222-247. DOI: 10.1214/Ss/1177010488 |
0.356 |
|
| 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 |
0.311 |
|
| 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 DOI: 10.1126/Science.2205919 |
0.341 |
|
| 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. DOI: 10.2307/2531483 |
0.313 |
|
| 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 |
0.319 |
|
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