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HIGH-DIMENSIONAL VARIABLE SELECTIONWASSERMAN, Larry; ROEDER, Kathryn.Annals of statistics. 2009, Vol 37, Num 5, pp 2178-2201, issn 0090-5364, 24 p., aArticle

Searching for disease susceptibility variants in structured populations : DESIGN AND ANALYSIS ISSUES IN GENOMIC STUDIES IN POPULATION SCIENCESROEDER, Kathryn; LUCA, Diana.Genomics (San Diego, Calif.). 2009, Vol 93, Num 1, pp 1-4, issn 0888-7543, 4 p.Article

Analysis of multilocus models of associationDEVLIN, B; ROEDER, Kathryn; WASSERMAN, Larry et al.Genetic epidemiology. 2003, Vol 25, Num 1, pp 36-47, issn 0741-0395, 12 p.Article

Transmission/disequilibrium test meets measured haplotype analysis : Family-based association analysis guided by evolution of haplotypesSELTMAN, Howard; ROEDER, Kathryn; DEVLIN, B et al.American journal of human genetics. 2001, Vol 68, Num 5, pp 1250-1263, issn 0002-9297Article

False discovery control with p-value weightingGENOVESE, Christopher R; ROEDER, Kathryn; WASSERMAN, Larry et al.Biometrika. 2006, Vol 93, Num 3, pp 509-524, issn 0006-3444, 16 p.Article

Association studies for quantitative traits in structured populationsBACANU, Silviu-Alin; DEVLIN, B; ROEDER, Kathryn et al.Genetic epidemiology. 2002, Vol 22, Num 1, pp 78-93, issn 0741-0395Article

Unbiased methods for population-based association studiesDEVLIN, B; ROEDER, Kathryn; BACANU, Silviu-Alin et al.Genetic epidemiology. 2001, Vol 21, Num 4, pp 273-284, issn 0741-0395Article

STRUCTURED, SPARSE REGRESSION WITH APPLICATION TO HIV DRUG RESISTANCEPERCIVAL, Daniel; ROEDER, Kathryn; ROSENFELD, Roni et al.The Annals of applied statistics. 2011, Vol 5, Num 2, pp 628-644, issn 1932-6157, 17 p.Article

A SPECTRAL GRAPH APPROACH TO DISCOVERING GENETIC ANCESTRYLEE, Ann B; LUCA, Diana; ROEDER, Kathryn et al.The Annals of applied statistics. 2010, Vol 4, Num 1, pp 179-202, issn 1932-6157, 24 p.Article

Evolutionary-based association analysis using haplotype dataSELTMAN, Howard; ROEDER, Kathryn; DEVLIN, B et al.Genetic epidemiology. 2003, Vol 25, Num 1, pp 48-58, issn 0741-0395, 11 p.Article

A Bayesian hierarchical model for allele frequenciesLOCKWOOD, John R; ROEDER, Kathryn; DEVLIN, B et al.Genetic epidemiology. 2001, Vol 20, Num 1, pp 17-33, issn 0741-0395Article

Using linkage genome scans to improve power of association in genome scansROEDER, Kathryn; BACANU, Silvi-Alin; WASSERMAN, Larry et al.American journal of human genetics. 2006, Vol 78, Num 2, pp 243-252, issn 0002-9297, 10 p.Article

Mixture models for linkage analysis of affected sibling pairs and covariatesDEVLIN, B; JONES, Bobby L; BACANU, Silviu-Alin et al.Genetic epidemiology. 2002, Vol 22, Num 1, pp 52-65, issn 0741-0395Article

Genome-wide distribution of linkage disequilibrium in the population of Palau and its implications for gene flow in Remote OceaniaDEVLIN, B; ROEDER, Kathryn; OTTO, Caleb et al.Human genetics. 2001, Vol 108, Num 6, pp 521-528, issn 0340-6717Article

Unintentional overdose and suicide among substance users: A review of overlap and risk factorsBOHNERT, Amy S. B; ROEDER, Kathryn; ILGEN, Mark A et al.Drug and alcohol dependence. 2010, Vol 110, Num 3, pp 183-192, issn 0376-8716, 10 p.Article

Depression and mental health help-seeking behaviors in a predominantly African American population of children and adolescents with epilepsyROEDER, Ruth; ROEDER, Kathryn; ASANO, Eishi et al.Epilepsia (Copenhagen). 2009, Vol 50, Num 8, pp 1943-1952, issn 0013-9580, 10 p.Article

Suicide attempts and overdoses among adults entering addictions treatment: Comparing correlates in a U.S. national studyBOHNERT, Amy S. B; ROEDER, Kathryn M; ILGEN, Mark A et al.Drug and alcohol dependence. 2011, Vol 119, Num 1-2, pp 106-112, issn 0376-8716, 7 p.Article

On the identification of disease mutations by the analysis of haplotype similarity and goodness of fitTZENG, Jung-Ying; DEVLIN, B; WASSERMAN, Larry et al.American journal of human genetics. 2003, Vol 72, Num 4, pp 891-902, issn 0002-9297, 12 p.Article

Candidate Gene Analysis of Femoral Neck Trabecular and Cortical Volumetric Bone Mineral Density in Older MenYERGES, Laura M; KLEI, Lambertus; MOFFETT, Susan P et al.Journal of bone and mineral research (Print). 2010, Vol 25, Num 2, pp 330-338, issn 0884-0431, 9 p.Article

De novo mutations revealed by whole-exome sequencing are strongly associated with autismSANDERS, Stephan J; MURTHA, Michael T; WALKER, Michael F et al.Nature (London). 2012, Vol 485, Num 7397, pp 237-241, issn 0028-0836, 5 p.Article

Feasibility and acceptability of interventions to delay gun access in VA mental health settingsWALTERS, Heather; KULKARNI, Madhur; FORMAN, Jane et al.General hospital psychiatry. 2012, Vol 34, Num 6, pp 692-698, issn 0163-8343, 7 p.Article

Patterns and rates of exonic de novo mutations in autism spectrum disordersNEALE, Benjamin M; YAN KOU; POLAK, Paz et al.Nature (London). 2012, Vol 485, Num 7397, pp 242-245, issn 0028-0836, 4 p.Article

Do common variants play a role in risk for autism? Evidence and theoretical musingsDEVLIN, Bernie; MELHEM, Nadine; ROEDER, Kathryn et al.Brain research. 2011, Vol 1380, pp 78-84, issn 0006-8993, 7 p.Article

African ancestry and lung function in Puerto Rican childrenBREHM, John M; ACOSTA-PEREZ, Edna; PAUL, Kathryn et al.Journal of allergy and clinical immunology. 2012, Vol 129, Num 6, pp 1484-1490, issn 0091-6749, 7 p.Article

Vitamin D Insufficiency and Severe Asthma Exacerbations in Puerto Rican ChildrenBREHM, John M; ACOSTA-PEREZ, Edna; LITONJUA, Augusto A et al.American journal of respiratory and critical care medicine. 2012, Vol 186, Num 2, pp 140-146, issn 1073-449X, 7 p.Article

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