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Aaron Ziegler - Publications

Affiliations: 
Oregon Health and Science University, Portland, OR 
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49 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
2021 Belsky MA, Shelly S, Rothenberger SD, Ziegler A, Hoffman B, Hapner ER, Gartner-Schmidt JL, Gillespie AI. Phonation Resistance Training Exercises (PhoRTE) With and Without Expiratory Muscle Strength Training (EMST) For Patients With Presbyphonia: A Noninferiority Randomized Clinical Trial. Journal of Voice : Official Journal of the Voice Foundation. PMID 33741235 DOI: 10.1016/j.jvoice.2021.02.015  0.505
2021 Ziegler A, Korzun T, Leclerc AA, Gillespie AI. Cannabis Consumption Among Patients With a Voice Disorder: A Multicenter E-Survey Study. Journal of Voice : Official Journal of the Voice Foundation. PMID 33726939 DOI: 10.1016/j.jvoice.2021.02.012  0.503
2018 Ziegler A, Henke T, Wiedrick J, Helou LB. Effectiveness of testosterone therapy for masculinizing voice in transgender patients: A meta-analytic review International Journal of Transgenderism. 19: 25-45. DOI: 10.1080/15532739.2017.1411857  0.677
2015 Kunz M, König IR, Schillert A, Kruppa J, Ziegler A, Grallert H, Müller-Nurasyid M, Lieb W, Franke A, Ranki A, Panelius J, Koskenmies S, Hasan T, Kere J, Rönn AC, et al. Genome-wide association study identifies new susceptibility loci for cutaneous lupus erythematosus. Experimental Dermatology. 24: 510-5. PMID 25827949 DOI: 10.1111/Exd.12708  0.301
2014 Dering C, König IR, Ramsey LB, Relling MV, Yang W, Ziegler A. A comprehensive evaluation of collapsing methods using simulated and real data: excellent annotation of functionality and large sample sizes required. Frontiers in Genetics. 5: 323. PMID 25309579 DOI: 10.3389/Fgene.2014.00323  0.328
2014 Lohmann K, Schmidt A, Schillert A, Winkler S, Albanese A, Baas F, Bentivoglio AR, Borngräber F, Brüggemann N, Defazio G, Del Sorbo F, Deuschl G, Edwards MJ, Gasser T, Gómez-Garre P, ... ... Ziegler A, et al. Genome-wide association study in musician's dystonia: a risk variant at the arylsulfatase G locus? Movement Disorders : Official Journal of the Movement Disorder Society. 29: 921-7. PMID 24375517 DOI: 10.1002/Mds.25791  0.315
2013 Bottolo L, Chadeau-Hyam M, Hastie DI, Zeller T, Liquet B, Newcombe P, Yengo L, Wild PS, Schillert A, Ziegler A, Nielsen SF, Butterworth AS, Ho WK, Castagné R, Munzel T, et al. GUESS-ing polygenic associations with multiple phenotypes using a GPU-based evolutionary stochastic search algorithm. Plos Genetics. 9: e1003657. PMID 23950726 DOI: 10.1371/Journal.Pgen.1003657  0.325
2013 Loley C, König IR, Hothorn L, Ziegler A. A unifying framework for robust association testing, estimation, and genetic model selection using the generalized linear model. European Journal of Human Genetics : Ejhg. 21: 1442-8. PMID 23572026 DOI: 10.1038/Ejhg.2013.62  0.307
2013 Garnier S, Truong V, Brocheton J, Zeller T, Rovital M, Wild PS, Ziegler A, Munzel T, Tiret L, Blankenberg S, Deloukas P, Erdmann J, Hengstenberg C, Samani NJ, et al. Genome-wide haplotype analysis of cis expression quantitative trait loci in monocytes. Plos Genetics. 9: e1003240. PMID 23382694 DOI: 10.1371/Journal.Pgen.1003240  0.315
2013 Deloukas P, Kanoni S, Willenborg C, Farrall M, Assimes TL, Thompson JR, Ingelsson E, Saleheen D, Erdmann J, Goldstein BA, Stirrups K, König IR, Cazier JB, Johansson A, ... ... Ziegler A, et al. Large-scale association analysis identifies new risk loci for coronary artery disease. Nature Genetics. 45: 25-33. PMID 23202125 DOI: 10.1038/Ng.2480  0.302
2012 Franceschini N, van Rooij FJ, Prins BP, Feitosa MF, Karakas M, Eckfeldt JH, Folsom AR, Kopp J, Vaez A, Andrews JS, Baumert J, Boraska V, Broer L, Hayward C, Ngwa JS, ... ... Ziegler A, et al. Discovery and fine mapping of serum protein loci through transethnic meta-analysis. American Journal of Human Genetics. 91: 744-53. PMID 23022100 DOI: 10.1016/J.Ajhg.2012.08.021  0.304
2012 Yang J, Loos RJ, Powell JE, Medland SE, Speliotes EK, Chasman DI, Rose LM, Thorleifsson G, Steinthorsdottir V, Mägi R, Waite L, Smith AV, Yerges-Armstrong LM, Monda KL, Hadley D, ... ... Ziegler A, et al. FTO genotype is associated with phenotypic variability of body mass index. Nature. 490: 267-72. PMID 22982992 DOI: 10.1038/Nature11401  0.316
2012 Ziegler A, Sun YV. Study designs and methods post genome-wide association studies Human Genetics. 131: 1525-1531. PMID 22898893 DOI: 10.1007/S00439-012-1209-8  0.314
2012 Timmann C, Thye T, Vens M, Evans J, May J, Ehmen C, Sievertsen J, Muntau B, Ruge G, Loag W, Ansong D, Antwi S, Asafo-Adjei E, Nguah SB, Kwakye KO, ... ... Ziegler A, et al. Genome-wide association study indicates two novel resistance loci for severe malaria. Nature. 489: 443-6. PMID 22895189 DOI: 10.1038/Nature11334  0.31
2012 Murabito JM, White CC, Kavousi M, Sun YV, Feitosa MF, Nambi V, Lamina C, Schillert A, Coassin S, Bis JC, Broer L, Crawford DC, Franceschini N, Frikke-Schmidt R, Haun M, ... ... Ziegler A, et al. Association between chromosome 9p21 variants and the ankle-brachial index identified by a meta-analysis of 21 genome-wide association studies. Circulation. Cardiovascular Genetics. 5: 100-12. PMID 22199011 DOI: 10.1161/Circgenetics.111.961292  0.323
2011 Dering C, Ziegler A, König IR, Hemmelmann C. Comparison of collapsing methods for the statistical analysis of rare variants. Bmc Proceedings. 5: 1-4. PMID 22373249 DOI: 10.1186/1753-6561-5-S9-S115  0.316
2011 Rotival M, Zeller T, Wild PS, Maouche S, Szymczak S, Schillert A, Castagné R, Deiseroth A, Proust C, Brocheton J, Godefroy T, Perret C, Germain M, Eleftheriadis M, Sinning CR, ... ... Ziegler A, et al. Integrating genome-wide genetic variations and monocyte expression data reveals trans-regulated gene modules in humans. Plos Genetics. 7: e1002367. PMID 22144904 DOI: 10.1371/Journal.Pgen.1002367  0.325
2011 O'Donnell CJ, Kavousi M, Smith AV, Kardia SL, Feitosa MF, Hwang SJ, Sun YV, Province MA, Aspelund T, Dehghan A, Hoffmann U, Bielak LF, Zhang Q, Eiriksdottir G, van Duijn CM, ... ... Ziegler A, et al. Genome-wide association study for coronary artery calcification with follow-up in myocardial infarction. Circulation. 124: 2855-64. PMID 22144573 DOI: 10.1161/Circulationaha.110.974899  0.307
2011 Sun YV, Sung YJ, Tintle N, Ziegler A. Identification of genetic association of multiple rare variants using collapsing methods Genetic Epidemiology. 35. PMID 22128049 DOI: 10.1002/Gepi.20658  0.322
2011 Wild PS, Zeller T, Schillert A, Szymczak S, Sinning CR, Deiseroth A, Schnabel RB, Lubos E, Keller T, Eleftheriadis MS, Bickel C, Rupprecht HJ, Wilde S, Rossmann H, Diemert P, ... ... Ziegler A, et al. A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circulation. Cardiovascular Genetics. 4: 403-12. PMID 21606135 DOI: 10.1161/Circgenetics.110.958728  0.328
2011 Schunkert H, König IR, Kathiresan S, Reilly MP, Assimes TL, Holm H, Preuss M, Stewart AF, Barbalic M, Gieger C, Absher D, Aherrahrou Z, Allayee H, Altshuler D, Anand SS, ... ... Ziegler A, et al. Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease. Nature Genetics. 43: 333-8. PMID 21378990 DOI: 10.1038/Ng.784  0.305
2011 Erdmann J, Willenborg C, Nahrstaedt J, Preuss M, König I, Baumert J, Linsel-Nitschke P, Gieger C, Tennstedt S, Belcredi P, Aherrahrou Z, Klopp N, Loley C, Stark K, Hengstenberg C, ... ... Ziegler A, et al. Genome-wide association study identifies a new locus for coronary artery disease on chromosome 10p11.23 European Heart Journal. 32: 158-168. PMID 21088011 DOI: 10.1093/Eurheartj/Ehq405  0.308
2010 Lango Allen H, Estrada K, Lettre G, Berndt SI, Weedon MN, Rivadeneira F, Willer CJ, Jackson AU, Vedantam S, Raychaudhuri S, Ferreira T, Wood AR, Weyant RJ, Segrè AV, Speliotes EK, ... ... Ziegler A, et al. Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature. 467: 832-8. PMID 20881960 DOI: 10.1038/Nature09410  0.331
2010 Heinig M, Petretto E, Wallace C, Bottolo L, Rotival M, Lu H, Li Y, Sarwar R, Langley SR, Bauerfeind A, Hummel O, Lee YA, Paskas S, Rintisch C, Saar K, ... ... Ziegler A, et al. A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk. Nature. 467: 460-4. PMID 20827270 DOI: 10.1038/Nature09386  0.309
2010 Schwarz DF, König IR, Ziegler A. On safari to Random Jungle: a fast implementation of Random Forests for high-dimensional data. Bioinformatics (Oxford, England). 26: 1752-8. PMID 20505004 DOI: 10.1093/Bioinformatics/Btq257  0.318
2010 Ziegler A, Gillespie AI, Abbott KV. Behavioral treatment of voice disorders in teachers. Folia Phoniatrica Et Logopaedica : Official Organ of the International Association of Logopedics and Phoniatrics (Ialp). 62: 9-23. PMID 20093840 DOI: 10.1159/000239059  0.728
2009 Schwarz DF, Szymczak S, Ziegler A, König IR. Evaluation of single-nucleotide polymorphism imputation using random forests. Bmc Proceedings. 3: S65. PMID 20018059 DOI: 10.1186/1753-6561-3-S7-S65  0.307
2009 Ziegler A. Genome-wide association studies: quality control and population-based measures. Genetic Epidemiology. 33. PMID 19924716 DOI: 10.1002/Gepi.20472  0.304
2009 Szymczak S, Igl BW, Ziegler A. Detecting SNP-expression associations: a comparison of mutual information and median test with standard statistical approaches. Statistics in Medicine. 28: 3581-96. PMID 19691035 DOI: 10.1002/Sim.3695  0.32
2009 Santos PS, Höhne J, Schlattmann P, König IR, Ziegler A, Uchanska-Ziegler B, Ziegler A. Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs. European Journal of Human Genetics : Ejhg. 17: 1182-9. PMID 19259136 DOI: 10.1038/Ejhg.2009.16  0.301
2009 Kathiresan S, Voight BF, Purcell S, Musunuru K, Ardissino D, Mannucci PM, Anand S, Engert JC, Samani NJ, Schunkert H, Erdmann J, Reilly MP, Rader DJ, Morgan T, ... ... Ziegler A, ... ... Ziegler A, et al. Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nature Genetics. 41: 334-41. PMID 19198609 DOI: 10.1038/Ng.327  0.303
2009 Serra A, Görgens H, Alhadad K, Ziegler A, Fitze G, Schackert HK. Analysis of RET, ZEB2, EDN3 and GDNF genomic rearrangements in 80 patients with Hirschsprung disease (using multiplex ligation-dependent probe amplification). Annals of Human Genetics. 73: 147-151. PMID 19183406 DOI: 10.1111/J.1469-1809.2008.00503.X  0.303
2009 Ziegler A, Ewhida A, Brendel M, Kleensang A. More powerful haplotype sharing by accounting for the mode of inheritance. Genetic Epidemiology. 33: 228-36. PMID 18839399 DOI: 10.1002/Gepi.20373  0.306
2008 Ludwig KU, Schumacher J, Schulte-Körne G, König IR, Warnke A, Plume E, Anthoni H, Peyrard-Janvid M, Meng H, Ziegler A, Remschmidt H, Kere J, Gruen JR, Müller-Myhsok B, Nöthen MM, et al. Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample. Psychiatric Genetics. 18: 310-2. PMID 19018237 DOI: 10.1097/Ypg.0B013E3283063A78  0.313
2008 Noack B, Görgens H, Hempel U, Fanghänel J, Hoffmann T, Ziegler A, Schackert HK. Cathepsin C Gene Variants in Aggressive Periodontitis Journal of Dental Research. 87: 958-963. PMID 18809751 DOI: 10.1177/154405910808701017  0.316
2008 Linsel-Nitschke P, Götz A, Erdmann J, Braenne I, Braund P, Hengstenberg C, Stark K, Fischer M, Schreiber S, El Mokhtari NE, Schaefer A, Schrezenmeir J, Schrezenmeier J, Rubin D, Hinney A, ... ... Ziegler A, et al. Lifelong reduction of LDL-cholesterol related to a common variant in the LDL-receptor gene decreases the risk of coronary artery disease--a Mendelian Randomisation study. Plos One. 3: e2986. PMID 18714375 DOI: 10.1371/Journal.Pone.0002986  0.308
2008 Linsel-Nitschke P, Götz A, Medack A, König IR, Bruse P, Lieb W, Mayer B, Stark K, Hengstenberg C, Fischer M, Baessler A, Ziegler A, Schunkert H, Erdmann J. Genetic variation in the arachidonate 5-lipoxygenase-activating protein (ALOX5AP) is associated with myocardial infarction in the German population. Clinical Science (London, England : 1979). 115: 309-15. PMID 18318662 DOI: 10.1042/Cs20070468  0.303
2008 Ziegler A, König IR, Thompson JR. Biostatistical aspects of genome-wide association studies. Biometrical Journal. Biometrische Zeitschrift. 50: 8-28. PMID 18217698 DOI: 10.1002/Bimj.200710398  0.321
2008 Schwarz DF, Hädicke O, Erdmann J, Ziegler A, Bayer D, Möller S. SNPtoGO: characterizing SNPs by enriched GO terms. Bioinformatics (Oxford, England). 24: 146-8. PMID 18024970 DOI: 10.1093/Bioinformatics/Btm551  0.301
2007 Szymczak S, Nuzzo A, Fuchsberger C, Schwarz DF, Ziegler A, Bellazzi R, Igl BW. Genetic association studies for gene expressions: permutation-based mutual information in a comparison with standard ANOVA and as a novel approach for feature selection. Bmc Proceedings. 1: S9. PMID 18466593 DOI: 10.1186/1753-6561-1-S1-S9  0.304
2007 Ziegler A, DeStefano AL, König IR, Bardel C, Brinza D, Bull S, Cai Z, Glaser B, Jiang W, Lee KE, Li CX, Li J, Li X, Majoram P, Meng Y, et al. Data mining, neural nets, trees--problems 2 and 3 of Genetic Analysis Workshop 15. Genetic Epidemiology. 31: S51-60. PMID 18046765 DOI: 10.1002/Gepi.20280  0.326
2006 Schumacher J, Anthoni H, Dahdouh F, König IR, Hillmer AM, Kluck N, Manthey M, Plume E, Warnke A, Remschmidt H, Hülsmann J, Cichon S, Lindgren CM, Propping P, Zucchelli M, ... Ziegler A, et al. Strong genetic evidence of DCDC2 as a susceptibility gene for dyslexia. American Journal of Human Genetics. 78: 52-62. PMID 16385449 DOI: 10.1086/498992  0.314
2005 Kleensang A, Franke D, König IR, Ziegler A. Haplotype-sharing analysis for alcohol dependence based on quantitative traits and the Mantel statistic Bmc Genetics. 6: 1-5. PMID 16451689 DOI: 10.1186/1471-2156-6-S1-S75  0.305
2005 Beckmann L, Ziegler A, Duggal P, Bailey-Wilson JE. Haplotypes and haplotype-tagging single-nucleotide polymorphism: presentation Group 8 of Genetic Analysis Workshop 14. Genetic Epidemiology. 29: S59-71. PMID 16342175 DOI: 10.1002/Gepi.20111  0.325
2003 Hauser ER, Hsu FC, Daley D, Olson JM, Rampersaud E, Lin JP, Paterson AD, Poisson LM, Chase GA, Dahmen G, Ziegler A. Effects of covariates: a summary of Group 5 contributions. Genetic Epidemiology. 25: S43-9. PMID 14635168 DOI: 10.1002/Gepi.10283  0.303
2003 Fitze G, Appelt H, König IR, Stein U, Walther W, Gossen M, Schreiber M, Ziegler A, Roesner D, Schackert HK. Functional haplotypes of the RET proto-oncogene promoter are associated with Hirschsprung disease (HSCR) Human Molecular Genetics. 12: 3207-3214. PMID 14600022 DOI: 10.1093/Hmg/Ddg354  0.303
2001 Böddeker IR, Ziegler A. Sequential Designs for Genetic Epidemiological Linkage or Association Studies A Review of the Literature Biometrical Journal. 43: 501-525. DOI: 10.1002/1521-4036(200108)43:4<501::Aid-Bimj501>3.0.Co;2-I  0.307
2000 Oeffner F, Bornholdt D, Ziegler A, Hinney A, Görg T, Gerber G, Goldschmidt HP, Siegfried W, Wright A, Hebebrand J, Grzeschik KH. Significant association between a silent polymorphism in the neuromedin B gene and body weight in German children and adolescents. Acta Diabetologica. 37: 93-101. PMID 11194934 DOI: 10.1007/S005920070026  0.31
1999 Stegmann K, Ziegler A, Ngo ETKM, Kohlschmidt N, Schröter B, Ermert A, Koch MC. Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD). American Journal of Medical Genetics. 87: 23-29. PMID 10528242 DOI: 10.1002/(Sici)1096-8628(19991105)87:1<23::Aid-Ajmg5>3.0.Co;2-E  0.317
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