Year |
Citation |
Score |
2019 |
Hsu YH, Estrada K, Evangelou E, Ackert-Bicknell C, Akesson K, Beck T, Brown SJ, Capellini T, Carbone L, Cauley J, Cheung CL, Cummings SR, Czerwinski S, Demissie S, Econs M, ... ... Koller DL, et al. Meta-Analysis of Genomewide Association Studies Reveals Genetic Variants for Hip Bone Geometry. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. e3698. PMID 30888730 DOI: 10.1002/Jbmr.3698 |
0.363 |
|
2018 |
Budde M, Friedrichs S, Alliey-Rodriguez N, Ament S, Badner JA, Berrettini WH, Bloss CS, Byerley W, Cichon S, Comes AL, Coryell W, Craig DW, Degenhardt F, Edenberg HJ, Foroud T, ... ... Koller DL, et al. Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder. European Neuropsychopharmacology : the Journal of the European College of Neuropsychopharmacology. PMID 30503783 DOI: 10.1016/J.Euroneuro.2018.10.005 |
0.353 |
|
2018 |
Breuer R, Mattheisen M, Frank J, Krumm B, Treutlein J, Kassem L, Strohmaier J, Herms S, Mühleisen TW, Degenhardt F, Cichon S, Nöthen MM, Karypis G, Kelsoe J, Greenwood T, ... ... Koller D, et al. Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics. International Journal of Bipolar Disorders. 6: 24. PMID 30415424 DOI: 10.1186/S40345-018-0132-X |
0.397 |
|
2017 |
Zillikens MC, Demissie S, Hsu YH, Yerges-Armstrong LM, Chou WC, Stolk L, Livshits G, Broer L, Johnson T, Koller DL, Kutalik Z, Luan J, Malkin I, Ried JS, Smith AV, et al. Large meta-analysis of genome-wide association studies identifies five loci for lean body mass. Nature Communications. 8: 80. PMID 28724990 DOI: 10.1038/S41467-017-00031-7 |
0.328 |
|
2016 |
Hou L, Bergen SE, Akula N, Song J, Hultman CM, Landén M, Adli M, Alda M, Ardau R, Arias B, Aubry JM, Backlund L, Badner JA, Barrett TB, Bauer M, ... ... Koller DL, et al. Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. Human Molecular Genetics. PMID 27329760 DOI: 10.1093/Hmg/Ddw181 |
0.471 |
|
2015 |
Alam I, Koller DL, Cañete T, Blázquez G, Mont-Cardona C, López-Aumatell R, Martínez-Membrives E, Díaz-Morán S, Tobeña A, Fernández-Teruel A, Stridh P, Diez M, Olsson T, Johannesson M, Baud A, et al. Fine mapping of bone structure and strength QTLs in heterogeneous stock rat. Bone. 81: 417-26. PMID 26297441 DOI: 10.1016/J.Bone.2015.08.013 |
0.387 |
|
2015 |
Schneider BP, Li L, Radovich M, Shen F, Miller C, Flockhart DA, Jiang G, Vance GH, Gardner L, Vatta M, Bai C, Lai D, Koller D, Zhao F, O'Neill A, et al. Genome-wide association studies for taxane-induced peripheral neuropathy (TIPN) in ECOG-5103 and ECOG-1199. Clinical Cancer Research : An Official Journal of the American Association For Cancer Research. PMID 26138065 DOI: 10.1158/1078-0432.Ccr-15-0586 |
0.308 |
|
2015 |
Farlow JL, Lin H, Sauerbeck L, Lai D, Koller DL, Pugh E, Hetrick K, Ling H, Kleinloog R, van der Vlies P, Deelen P, Swertz MA, Verweij BH, Regli L, Rinkel GJ, et al. Lessons learned from whole exome sequencing in multiplex families affected by a complex genetic disorder, intracranial aneurysm. Plos One. 10: e0121104. PMID 25803036 DOI: 10.1371/Journal.Pone.0121104 |
0.403 |
|
2015 |
Wetherill L, Agrawal A, Kapoor M, Bertelsen S, Bierut LJ, Brooks A, Dick D, Hesselbrock M, Hesselbrock V, Koller DL, Le N, Nurnberger JI, Salvatore JE, Schuckit M, Tischfield JA, et al. Association of substance dependence phenotypes in the COGA sample. Addiction Biology. 20: 617-27. PMID 24832863 DOI: 10.1111/Adb.12153 |
0.352 |
|
2014 |
Foroud T, Lai D, Koller D, Van't Hof F, Kurki MI, Anderson CS, Brown RD, Connolly ES, Eriksson JG, Flaherty M, Fornage M, von Und Zu Fraunberg M, Gaál EI, Laakso A, Hernesniemi J, et al. Genome-wide association study of intracranial aneurysm identifies a new association on chromosome 7. Stroke; a Journal of Cerebral Circulation. 45: 3194-9. PMID 25256182 DOI: 10.1161/Strokeaha.114.006096 |
0.32 |
|
2014 |
Perry JR, Day F, Elks CE, Sulem P, Thompson DJ, Ferreira T, He C, Chasman DI, Esko T, Thorleifsson G, Albrecht E, Ang WQ, Corre T, Cousminer DL, Feenstra B, ... ... Koller DL, et al. Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche. Nature. 514: 92-7. PMID 25231870 DOI: 10.1038/Nature13545 |
0.408 |
|
2014 |
Kemp JP, Medina-Gomez C, Estrada K, St Pourcain B, Heppe DH, Warrington NM, Oei L, Ring SM, Kruithof CJ, Timpson NJ, Wolber LE, Reppe S, Gautvik K, Grundberg E, Ge B, ... ... Koller DL, et al. Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment. Plos Genetics. 10: e1004423. PMID 24945404 DOI: 10.1371/Journal.Pgen.1004423 |
0.428 |
|
2014 |
Alam I, Padgett LR, Ichikawa S, Alkhouli M, Koller DL, Lai D, Peacock M, Xuei X, Foroud T, Edenberg HJ, Econs MJ. SIBLING family genes and bone mineral density: Association and allele-specific expression in humans Bone. 64: 166-172. PMID 24747200 DOI: 10.1016/J.Bone.2014.04.013 |
0.381 |
|
2014 |
Alam I, Koller DL, Cañete T, Blázquez G, López-Aumatell R, Martínez-Membrives E, Díaz-Morán S, Tobeña A, Fernández-Teruel A, Stridh P, Diez M, Olsson T, Johannesson M, Baud A, Econs MJ, et al. High-resolution genome screen for bone mineral density in heterogeneous stock rat. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 29: 1619-26. PMID 24643965 DOI: 10.1002/Jbmr.2195 |
0.468 |
|
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, ... ... Koller DL, 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 |
0.302 |
|
2013 |
Chen C, Cheng L, Grennan K, Pibiri F, Zhang C, Badner JA, Kelsoe JR, Greenwood TA, Nievergelt CM, Barrett TB, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, ... ... Koller DL, et al. Two gene co-expression modules differentiate psychotics and controls Molecular Psychiatry. 18: 1308-1314. PMID 23147385 DOI: 10.1038/Mp.2012.146 |
0.337 |
|
2013 |
Wang JC, Foroud T, Hinrichs AL, Le NX, Bertelsen S, Budde JP, Harari O, Koller DL, Wetherill L, Agrawal A, Almasy L, Brooks AI, Bucholz K, Dick D, Hesselbrock V, et al. A genome-wide association study of alcohol-dependence symptom counts in extended pedigrees identifies C15orf53. Molecular Psychiatry. 18: 1218-24. PMID 23089632 DOI: 10.1038/Mp.2012.143 |
0.432 |
|
2013 |
Koller DL, Zheng HF, Karasik D, Yerges-Armstrong L, Liu CT, McGuigan F, Kemp JP, Giroux S, Lai D, Edenberg HJ, Peacock M, Czerwinski SA, Choh AC, McMahon G, St Pourcain B, et al. Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 28: 547-58. PMID 23074152 DOI: 10.1002/Jbmr.1796 |
0.464 |
|
2013 |
Gamazon ER, Badner JA, Cheng L, Zhang C, Zhang D, Cox NJ, Gershon ES, Kelsoe JR, Greenwood TA, Nievergelt CM, Chen C, McKinney R, Shilling PD, Schork NJ, Smith EN, ... ... Koller DL, et al. Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants. Molecular Psychiatry. 18: 340-6. PMID 22212596 DOI: 10.1038/Mp.2011.174 |
0.415 |
|
2013 |
White KE, Koller DL, Corbin T. Skeletal Genetics: From Gene Identification to Murine Models of Disease Basic and Applied Bone Biology. 149-171. DOI: 10.1016/B978-0-12-416015-6.00008-3 |
0.343 |
|
2012 |
Nissen S, Liang S, Shehktman T, Kelsoe JR, Greenwood TA, Nievergelt CM, McKinney R, Shilling PD, Smith EN, Schork NJ, Bloss CS, Nurnberger JI, Edenberg HJ, Foroud T, ... Koller DL, et al. Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 159: 941-50. PMID 23038240 DOI: 10.1002/Ajmg.B.32099 |
0.348 |
|
2012 |
Meier S, Mattheisen M, Vassos E, Strohmaier J, Treutlein J, Josef F, Breuer R, Degenhardt F, Mühleisen TW, Müller-Myhsok B, Steffens M, Schmael C, McMahon FJ, Nöthen MM, ... ... Koller DL, et al. Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1. Translational Psychiatry. 2: e165. PMID 23010768 DOI: 10.1038/Tp.2012.81 |
0.42 |
|
2012 |
Teng M, Ichikawa S, Padgett LR, Wang Y, Mort M, Cooper DN, Koller DL, Foroud T, Edenberg HJ, Econs MJ, Liu Y. regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions. Bioinformatics (Oxford, England). 28: 1879-86. PMID 22611130 DOI: 10.1093/Bioinformatics/Bts275 |
0.396 |
|
2012 |
Ayalew M, Le-Niculescu H, Levey DF, Jain N, Changala B, Patel SD, Winiger E, Breier A, Shekhar A, Amdur R, Koller D, Nurnberger JI, Corvin A, Geyer M, Tsuang MT, et al. Convergent functional genomics of schizophrenia: from comprehensive understanding to genetic risk prediction. Molecular Psychiatry. 17: 887-905. PMID 22584867 DOI: 10.1038/Mp.2012.37 |
0.383 |
|
2012 |
Estrada K, Styrkarsdottir U, Evangelou E, Hsu YH, Duncan EL, Ntzani EE, Oei L, Albagha OM, Amin N, Kemp JP, Koller DL, Li G, Liu CT, Minster RL, Moayyeri A, et al. Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture. Nature Genetics. 44: 491-501. PMID 22504420 DOI: 10.1038/Ng.2249 |
0.445 |
|
2012 |
Badner JA, Koller D, Foroud T, Edenberg H, Nurnberger JI, Zandi PP, Willour VL, McMahon FJ, Potash JB, Hamshere M, Grozeva D, Green E, Kirov G, Jones I, Jones L, et al. Genome-wide linkage analysis of 972 bipolar pedigrees using single-nucleotide polymorphisms. Molecular Psychiatry. 17: 818-26. PMID 21769101 DOI: 10.1038/Mp.2011.89 |
0.448 |
|
2011 |
Sklar P, Ripke S, Scott LJ, Andreassen OA, Cichon S, Craddock N, Edenberg HJ, Nurnberger JI, Rietschel M, Blackwood D, Corvin A, Flickinger M, Guan W, Mattingsdal M, McQuillin A, ... ... Koller DL, et al. Large-scale genome-wide association analysis of bipolar disorder identifies a new susceptibility locus near ODZ4 Nature Genetics. 43: 977-985. PMID 21926972 DOI: 10.1038/Ng.943 |
0.367 |
|
2011 |
Smith EN, Koller DL, Panganiban C, Szelinger S, Zhang P, Badner JA, Barrett TB, Berrettini WH, Bloss CS, Byerley W, Coryell W, Edenberg HJ, Foroud T, Gershon ES, Greenwood TA, et al. Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes. Plos Genetics. 7: e1002134. PMID 21738484 DOI: 10.1371/Journal.Pgen.1002134 |
0.461 |
|
2011 |
Alam I, Koller DL, Sun Q, Roeder RK, Cañete T, Blázquez G, López-Aumatell R, MartÃnez-Membrives E, Vicens-Costa E, Mont C, DÃaz S, Tobeña A, Fernández-Teruel A, Whitley A, Strid P, et al. Heterogeneous stock rat: a unique animal model for mapping genes influencing bone fragility. Bone. 48: 1169-77. PMID 21334473 DOI: 10.1016/J.Bone.2011.02.009 |
0.392 |
|
2011 |
Zlojutro M, Manz N, Rangaswamy M, Xuei X, Flury-Wetherill L, Koller D, Bierut LJ, Goate A, Hesselbrock V, Kuperman S, Nurnberger J, Rice JP, Schuckit MA, Foroud T, Edenberg HJ, et al. Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 156: 44-58. PMID 21184583 DOI: 10.1002/Ajmg.B.31136 |
0.473 |
|
2011 |
Wang TJ, Zhang F, Richards JB, Kestenbaum B, Van Meurs JB, Berry D, Kiel DP, Streeten EA, Ohlsson C, Koller DL, Peltonen L, Cooper JD, O'Reilly PF, Houston DK, Glazer NL, et al. Common genetic determinants of vitamin D insufficiency: A genome-wide association study Obstetrical and Gynecological Survey. 66: 91-93. DOI: 10.1097/Ogx.0B013E318216B03D |
0.342 |
|
2011 |
Estrada K, Evangelou E, Hsu Y, Styrkarsdottir U, Liu C, Moayyeri A, Kaptoge S, Duncan E, Amin N, Kiel D, Karasik D, Albagha O, Brown M, Spector T, Zillikens M, ... ... Koller D, et al. Association analyses of 47,500 individuals identifies six fracture loci and 82 BMD loci clustering in biological pathways that regulate osteoblast and osteoclast activity Bone. 48: S69. DOI: 10.1016/J.Bone.2011.03.070 |
0.348 |
|
2010 |
Elks CE, Perry JR, Sulem P, Chasman DI, Franceschini N, He C, Lunetta KL, Visser JA, Byrne EM, Cousminer DL, Gudbjartsson DF, Esko T, Feenstra B, Hottenga JJ, Koller DL, et al. Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies. Nature Genetics. 42: 1077-85. PMID 21102462 DOI: 10.1038/Ng.714 |
0.419 |
|
2010 |
Patel SD, Le-Niculescu H, Koller DL, Green SD, Lahiri DK, McMahon FJ, Nurnberger JI, Niculescu AB. Coming to grips with complex disorders: genetic risk prediction in bipolar disorder using panels of genes identified through convergent functional genomics. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 153: 850-77. PMID 20468069 DOI: 10.1002/Ajmg.B.31087 |
0.442 |
|
2010 |
Edenberg HJ, Koller DL, Xuei X, Wetherill L, McClintick JN, Almasy L, Bierut LJ, Bucholz KK, Goate A, Aliev F, Dick D, Hesselbrock V, Hinrichs A, Kramer J, Kuperman S, et al. Genome-wide association study of alcohol dependence implicates a region on chromosome 11. Alcoholism, Clinical and Experimental Research. 34: 840-52. PMID 20201924 DOI: 10.1111/J.1530-0277.2010.01156.X |
0.43 |
|
2010 |
Ichikawa S, Koller DL, Padgett LR, Lai D, Hui SL, Peacock M, Foroud T, Econs MJ. Replication of previous genome-wide association studies of bone mineral density in premenopausal American women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 25: 1821-9. PMID 20200978 DOI: 10.1002/Jbmr.62 |
0.445 |
|
2010 |
Koller DL, Ichikawa S, Lai D, Padgett LR, Doheny KF, Pugh E, Paschall J, Hui SL, Edenberg HJ, Xuei X, Peacock M, Econs MJ, Foroud T. Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women. The Journal of Clinical Endocrinology and Metabolism. 95: 1802-9. PMID 20164292 DOI: 10.1210/Jc.2009-1903 |
0.389 |
|
2009 |
Smith EN, Bloss CS, Badner JA, Barrett T, Belmonte PL, Berrettini W, Byerley W, Coryell W, Craig D, Edenberg HJ, Eskin E, Foroud T, Gershon E, Greenwood TA, Hipolito M, ... Koller DL, et al. Genome-wide association study of bipolar disorder in European American and African American individuals. Molecular Psychiatry. 14: 755-63. PMID 19488044 DOI: 10.1038/Mp.2009.43 |
0.427 |
|
2009 |
Peacock M, Koller DL, Lai D, Hui S, Foroud T, Econs MJ. Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci. Bone. 45: 443-8. PMID 19427925 DOI: 10.1016/J.Bone.2009.05.002 |
0.456 |
|
2009 |
Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Epistasis between QTLs for bone density variation in Copenhagen x dark agouti F2 rats. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 20: 180-6. PMID 19153792 DOI: 10.1007/S00335-008-9161-6 |
0.499 |
|
2009 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Langefeld C, Rouleau G, Connolly ES, Lai D, ... Koller DL, et al. Genome screen in familial intracranial aneurysm. Bmc Medical Genetics. 10: 3. PMID 19144135 DOI: 10.1186/1471-2350-10-3 |
0.331 |
|
2009 |
Zhang D, Cheng L, Qian Y, Alliey-Rodriguez N, Kelsoe JR, Greenwood T, Nievergelt C, Barrett TB, McKinney R, Schork N, Smith EN, Bloss C, Nurnberger J, Edenberg HJ, Foroud T, ... ... Koller D, et al. Singleton deletions throughout the genome increase risk of bipolar disorder. Molecular Psychiatry. 14: 376-80. PMID 19114987 DOI: 10.1038/Mp.2008.144 |
0.374 |
|
2009 |
Ichikawa S, Koller DL, Curry LR, Lai D, Xuei X, Edenberg HJ, Hui SL, Peacock M, Foroud T, Econs MJ. Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults. Calcified Tissue International. 84: 97-102. PMID 19093065 DOI: 10.1007/S00223-008-9200-Z |
0.423 |
|
2009 |
Jung J, Sun B, Kwon D, Koller DL, Foroud TM. Allelic-based gene-gene interaction associated with quantitative traits. Genetic Epidemiology. 33: 332-43. PMID 19058262 DOI: 10.1002/Gepi.20385 |
0.414 |
|
2008 |
Chu K, Koller DL, Ichikawa S, Snyder R, Curry L, Lai D, Austin A, Xuei X, Edenberg HJ, Hui SL, Foroud TM, Peacock M, Econs MJ. CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men. Bone. 43: 995-8. PMID 18755304 DOI: 10.1016/J.Bone.2008.07.249 |
0.4 |
|
2008 |
Alam I, Sun Q, Liu L, Koller DL, Liu Y, Edenberg HJ, Econs MJ, Foroud T, Turner CH. Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck. Physiological Genomics. 35: 191-6. PMID 18728226 DOI: 10.1152/Physiolgenomics.90237.2008 |
0.365 |
|
2008 |
Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Linkage screen for BMD phenotypes in male and female COP and DA rat strains. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 1382-8. PMID 18707222 DOI: 10.1359/Jbmr.080401 |
0.321 |
|
2008 |
Ichikawa S, Koller DL, Curry LR, Lai D, Xuei X, Pugh EW, Tsai YY, Doheny KF, Edenberg HJ, Hui SL, Foroud T, Peacock M, Econs MJ. Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 1680-8. PMID 18505370 DOI: 10.1359/Jbmr.080509 |
0.477 |
|
2008 |
Foroud T, Sauerbeck L, Brown R, Anderson C, Woo D, Kleindorfer D, Flaherty ML, Deka R, Hornung R, Meissner I, Bailey-Wilson JE, Rouleau G, Connolly ES, Lai D, Koller DL, et al. Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study. Stroke; a Journal of Cerebral Circulation. 39: 1434-40. PMID 18323491 DOI: 10.1161/Strokeaha.107.502930 |
0.411 |
|
2008 |
Alam I, Sun Q, Liu L, Koller DL, Carr LG, Econs MJ, Foroud T, Turner CH. Sex-specific genetic loci for femoral neck bone mass and strength identified in inbred COP and DA rats. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 850-9. PMID 18282130 DOI: 10.1359/Jbmr.080221 |
0.416 |
|
2008 |
Sun Q, Alam I, Liu L, Koller DL, Carr LG, Econs MJ, Foroud T, Turner CH. Genetic loci affecting bone structure and strength in inbred COP and DA rats. Bone. 42: 547-53. PMID 18158281 DOI: 10.1016/J.Bone.2007.11.004 |
0.421 |
|
2008 |
Foroud T, Ichikawa S, Koller D, Lai D, Curry L, Xuei X, Edenberg HJ, Hui S, Peacock M, Econs MJ. Association studies of ALOX5 and bone mineral density in healthy adults Osteoporosis International. 19: 637-643. PMID 17909879 DOI: 10.1007/S00198-007-0484-Z |
0.472 |
|
2008 |
Koller DL, Liu L, Alam I, Sun Q, Econs MJ, Foroud T, Turner CH. Epistatic effects contribute to variation in BMD in Fischer 344 x Lewis F2 rats. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 23: 41-7. PMID 17907919 DOI: 10.1359/Jbmr.071001 |
0.376 |
|
2007 |
Ioannidis JP, Ng MY, Sham PC, Zintzaras E, Lewis CM, Deng HW, Econs MJ, Karasik D, Devoto M, Kammerer CM, Spector T, Andrew T, Cupples LA, Duncan EL, Foroud T, ... ... Koller D, et al. Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 22: 173-83. PMID 17228994 DOI: 10.1359/Jbmr.060806 |
0.431 |
|
2006 |
Hui SL, Koller DL, Foroud TM, Econs MJ, Johnston CC, Peacock M. Heritability of changes in bone size and bone mass with age in premenopausal white sisters. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 21: 1121-5. PMID 16813533 DOI: 10.1359/Jbmr.060412 |
0.303 |
|
2006 |
Ichikawa S, Koller DL, Johnson ML, Lai D, Xuei X, Edenberg HJ, Klein RF, Orwoll ES, Hui SL, Foroud TM, Peacock M, Econs MJ. Human ALOX12, but not ALOX15, is associated with BMD in white men and women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 21: 556-64. PMID 16598376 DOI: 10.1359/Jbmr.051212 |
0.348 |
|
2006 |
Alam I, Sun Q, Liu L, Koller DL, Fishburn T, Carr LG, Econs MJ, Foroud T, Turner CH. Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength Bone. 39: 93-99. PMID 16461031 DOI: 10.1016/J.Bone.2005.12.009 |
0.468 |
|
2006 |
Ichikawa S, Johnson ML, Koller DL, Lai D, Xuei X, Edenberg HJ, Hui SL, Foroud TM, Peacock M, Econs MJ. Polymorphisms in the bone morphogenetic protein 2 (BMP2) gene do not affect bone mineral density in white men or women Osteoporosis International. 17: 587-592. PMID 16432645 DOI: 10.1007/S00198-005-0018-5 |
0.464 |
|
2005 |
Koller DL, Alam I, Sun Q, Liu L, Fishburn T, Carr LG, Econs MJ, Foroud T, Turner CH. Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 16: 578-86. PMID 16180139 DOI: 10.1007/S00335-004-2459-0 |
0.44 |
|
2005 |
Chu K, Koller DL, Snyder R, Fishburn T, Lai D, Waguespack SG, Foroud T, Econs MJ. Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes. Bone. 37: 655-61. PMID 16120485 DOI: 10.1016/J.Bone.2005.06.003 |
0.458 |
|
2005 |
Ichikawa S, Koller DL, Peacock M, Johnson ML, Lai D, Hui SL, Johnston CC, Foroud TM, Econs MJ. Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women. The Journal of Clinical Endocrinology and Metabolism. 90: 5921-7. PMID 16118344 DOI: 10.1210/Jc.2004-2253 |
0.463 |
|
2005 |
Alam I, Sun Q, Liu L, Koller DL, Fishburn T, Carr LG, Econs MJ, Foroud T, Turner CH. Whole-genome scan for linkage to bone strength and structure in inbred Fischer 344 and Lewis rats. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 20: 1589-96. PMID 16059631 DOI: 10.1359/Jbmr.050512 |
0.423 |
|
2005 |
Peacock M, Koller DL, Lai D, Hui S, Foroud T, Econs MJ. Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men. Bone. 37: 467-73. PMID 16046210 DOI: 10.1016/J.Bone.2005.05.005 |
0.465 |
|
2005 |
Peacock M, Koller DL, Fishburn T, Krishnan S, Lai D, Hui S, Johnston CC, Foroud T, Econs MJ. Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men. The Journal of Clinical Endocrinology and Metabolism. 90: 3060-6. PMID 15741260 DOI: 10.1210/Jc.2004-2143 |
0.411 |
|
2005 |
Koller DL, Ichikawa S, Johnson ML, Lai D, Xuei X, Edenberg HJ, Conneally PM, Hui SL, Johnston CC, Peacock M, Foroud T, Econs MJ. Contribution of the LRP5 gene to normal variation in peak BMD in women. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 20: 75-80. PMID 15619672 DOI: 10.1359/Jbmr.041019 |
0.64 |
|
2004 |
Koller DL, Peacock M, Lai D, Foroud T, Econs MJ. False positive rates in association studies as a function of degree of stratification. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 19: 1291-5. PMID 15231016 DOI: 10.1359/Jbmr.040409 |
0.435 |
|
2004 |
Peacock M, Koller DL, Hui S, Johnston CC, Foroud T, Econs MJ. Peak bone mineral density at the hip is linked to chromosomes 14q and 15q. Osteoporosis International : a Journal Established as Result of Cooperation Between the European Foundation For Osteoporosis and the National Osteoporosis Foundation of the Usa. 15: 489-96. PMID 15205721 DOI: 10.1007/S00198-003-1560-7 |
0.444 |
|
2004 |
Econs MJ, Koller DL, Hui SL, Fishburn T, Conneally PM, Johnston CC, Peacock M, Foroud TM. Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women. American Journal of Human Genetics. 74: 223-8. PMID 14730478 DOI: 10.1086/381401 |
0.648 |
|
2003 |
Liu Y, Xu F, Recker RR, Deng HW, Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Interpretation of Genetic Linkage Findings (multiple letters) Journal of Bone and Mineral Research. 18: 2077-2080. PMID 14606522 DOI: 10.1359/Jbmr.2003.18.11.2077 |
0.579 |
|
2003 |
Koller DL, Schriefer J, Sun Q, Shultz KL, Donahue LR, Rosen CJ, Foroud T, Beamer WG, Turner CH. Genetic effects for femoral biomechanics, structure, and density in C57BL/6J and C3H/HeJ inbred mouse strains. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1758-65. PMID 14584885 DOI: 10.1359/Jbmr.2003.18.10.1758 |
0.36 |
|
2003 |
Waguespack SG, Koller DL, White KE, Fishburn T, Carn G, Buckwalter KA, Johnson M, Kocisko M, Evans WE, Foroud T, Econs MJ. Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1513-8. PMID 12929941 DOI: 10.1359/Jbmr.2003.18.8.1513 |
0.375 |
|
2003 |
Koller DL, White KE, Liu G, Hui SL, Conneally PM, Johnston CC, Econs MJ, Foroud T, Peacock M. Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 18: 1057-65. PMID 12817759 DOI: 10.1359/Jbmr.2003.18.6.1057 |
0.63 |
|
2003 |
Song J, Koller DL, Foroud T, Carr K, Zhao J, Rice J, Nurnberger JI, Begleiter H, Porjesz B, Smith TL, Schuckit MA, Edenberg HJ. Association of GABA(A) receptors and alcohol dependence and the effects of genetic imprinting. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 117: 39-45. PMID 12555233 DOI: 10.1002/Ajmg.B.10022 |
0.382 |
|
2002 |
Dowsett SA, Archila L, Foroud T, Koller D, Eckert GJ, Kowolik MJ. The effect of shared genetic and environmental factors on periodontal disease parameters in untreated adult siblings in Guatemala. Journal of Periodontology. 73: 1160-8. PMID 12416774 DOI: 10.1902/Jop.2002.73.10.1160 |
0.372 |
|
2002 |
Carn G, Koller DL, Peacock M, Hui SL, Evans WE, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13. The Journal of Clinical Endocrinology and Metabolism. 87: 3819-24. PMID 12161516 DOI: 10.1210/Jcem.87.8.8740 |
0.674 |
|
2001 |
Pankratz N, Kirkwood SC, Flury L, Koller DL, Foroud T. Use of variable marker density, principal components, and neural networks in the dissection of disease etiology Genetic Epidemiology. 21: S732-737. PMID 11793770 DOI: 10.1002/Gepi.2001.21.S1.S732 |
0.729 |
|
2001 |
McClintick J, Koller DL, Pankratz N, Kirkwood SC, Naughton B, Foroud T. Parametric linkage analysis and disequilibrium methods to identify loci for complex disease Genetic Epidemiology. 21: S528-S533. PMID 11793731 DOI: 10.1002/Gepi.2001.21.S1.S528 |
0.741 |
|
2001 |
Koller DL, Liu G, Econs MJ, Hui SL, Morin PA, Joslyn G, Rodriguez LA, Conneally PM, Christian JC, Johnston CC, Foroud T, Peacock M. Genome screen for quantitative trait loci underlying normal variation in femoral structure. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 16: 985-91. PMID 11393795 DOI: 10.1359/Jbmr.2001.16.6.985 |
0.644 |
|
2000 |
Koller DL, Econs MJ, Morin PA, Christian JC, Hui SL, Parry P, Curran ME, Rodriguez LA, Conneally PM, Joslyn G, Peacock M, Johnston CC, Foroud T. Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis. The Journal of Clinical Endocrinology and Metabolism. 85: 3116-20. PMID 10999795 DOI: 10.1210/Jcem.85.9.6778 |
0.654 |
|
2000 |
Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li TK, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, et al. Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping. Alcoholism, Clinical and Experimental Research. 24: 933-45. PMID 10923994 |
0.588 |
|
2000 |
Takacs I, Koller DL, Peacock M, Christian JC, Evans WE, Hui SL, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sib pair linkage and association studies between bone mineral density and the interleukin-6 gene locus. Bone. 27: 169-73. PMID 10865225 DOI: 10.1016/S8756-3282(00)00296-9 |
0.597 |
|
2000 |
Foroud T, Castelluccio PF, Koller DL, Edenberg HJ, Miller M, Bowman E, Rau NL, Smiley C, Rice JP, Goate A, Armstrong C, Bierut LJ, Reich T, Detera-Wadleigh SD, Goldin LR, et al. Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees. American Journal of Medical Genetics. 96: 18-23. PMID 10686547 DOI: 10.1002/(Sici)1096-8628(20000207)96:1<18::Aid-Ajmg6>3.0.Co;2-G |
0.422 |
|
2000 |
Foroud T, Edenberg HJ, Goate A, Rice J, Flury L, Koller DL, Bierut LJ, Conneally PM, Nurnberger JI, Bucholz KK, Li T, Hesselbrock V, Crowe R, Schuckit M, Porjesz B, et al. Alcoholism Susceptibility Loci: Confirmation Studies in a Replicate Sample and Further Mapping Alcoholism: Clinical and Experimental Research. 24: 933-945. DOI: 10.1111/J.1530-0277.2000.Tb04634.X |
0.625 |
|
1999 |
Takacs I, Koller DL, Peacock M, Christian JC, Hui SL, Conneally PM, Johnston CC, Foroud T, Econs MJ. Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus. The Journal of Clinical Endocrinology and Metabolism. 84: 4467-71. PMID 10599704 DOI: 10.1210/Jcem.84.12.6179 |
0.617 |
|
1999 |
Koller DL, Balding J, Foroud T. Nonparametric linkage and family-based association studies of a simulated complex disorder Genetic Epidemiology. 17: S627-S632. PMID 10597504 DOI: 10.1002/Gepi.13701707102 |
0.48 |
|
1999 |
White KE, Koller DL, Takacs I, Buckwalter KA, Foroud T, Econs MJ. Locus heterogeneity of autosomal dominant osteopetrosis (ADO) Journal of Clinical Endocrinology and Metabolism. 84: 1047-1051. PMID 10084593 DOI: 10.1210/Jcem.84.3.5578 |
0.44 |
|
1998 |
Foroud T, Bucholz KK, Edenberg HJ, Goate A, Neuman RJ, Porjesz B, Koller DL, Rice J, Reich T, Bierut LJ, Cloninger CR, Nurnberger JI, Li TK, Conneally PM, Tischfield JA, et al. Linkage of an alcoholism-related severity phenotype to chromosome 16. Alcoholism, Clinical and Experimental Research. 22: 2035-42. PMID 9884148 DOI: 10.1097/00000374-199812000-00020 |
0.546 |
|
1998 |
Koller DL, Rodriguez LA, Christian JC, Slemenda CW, Econs MJ, Hui SL, Morin P, Conneally PM, Joslyn G, Curran ME, Peacock M, Johnston CC, Foroud T. Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. 13: 1903-8. PMID 9844108 DOI: 10.1359/Jbmr.1998.13.12.1903 |
0.661 |
|
1998 |
Edenberg HJ, Reynolds J, Koller DL, Begleiter H, Bucholz KK, Conneally PM, Crowe R, Goate A, Hesselbrock V, Li TK, Nurnberger JI, Porjesz B, Reich T, Rice JP, Schuckit M, et al. A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence. Alcoholism, Clinical and Experimental Research. 22: 1080-5. PMID 9726278 |
0.516 |
|
1998 |
Edenberg HJ, Foroud T, Koller DL, Goate A, Rice J, Van Eerdewegh P, Reich T, Cloninger CR, Nurnberger JI, Kowalczuk M, Wu B, Li TK, Conneally PM, Tischfield JA, Wu W, et al. A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism. Alcoholism, Clinical and Experimental Research. 22: 505-12. PMID 9581660 |
0.513 |
|
1997 |
Murrell JR, Koller D, Foroud T, Goedert M, Spillantini MG, Edenberg HJ, Farlow MR, Ghetti B. Familial multiple-system tauopathy with presenile dementia is localized to chromosome 17. American Journal of Human Genetics. 61: 1131-8. PMID 9345089 DOI: 10.1086/301594 |
0.367 |
|
1997 |
Nichols WC, Koller DL, Slovis B, Foroud T, Terry VH, Arnold ND, Siemieniak DR, Wheeler L, Phillips JA, Newman JH, Conneally PM, Ginsburg D, Loyd JE. Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31-32. Nature Genetics. 15: 277-80. PMID 9054941 DOI: 10.1038/Ng0397-277 |
0.584 |
|
1997 |
Murrell L, Koller D, Foroud T, Goedert M, Spillantini MG, Farlow MR, Ghetti B. GENE MAP OF THE MSTD (MULTIPLE SYSTEM TAUOPATHY WITH PRESENILE DEMENTIA) REGION ON HUMAN CHROMOSOME 17q21–22 Journal of Neuropathology and Experimental Neurology. 56: 610. DOI: 10.1097/00005072-199705000-00171 |
0.37 |
|
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