Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 47

1.

Genotypic discrepancies arising from imputation.

Hinrichs AL, Culverhouse RC, Suarez BK.

BMC Proc. 2014 Jun 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S17. doi: 10.1186/1753-6561-8-S1-S17. eCollection 2014.

2.

Identifying cryptic population structure in multigenerational pedigrees in a Mexican American sample.

Culverhouse RC, Hinrichs AL, Suarez BK.

BMC Proc. 2014 Jun 17;8(Suppl 1):S4. doi: 10.1186/1753-6561-8-S1-S4. eCollection 2014.

3.

Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees.

Bickeböller H, Bailey JN, Beyene J, Cantor RM, Cordell HJ, Culverhouse RC, Engelman CD, Fardo DW, Ghosh S, König IR, Lorenzo Bermejo J, Melton PE, Santorico SA, Satten GA, Sun L, Tintle NL, Ziegler A, MacCluer JW, Almasy L.

BMC Proc. 2014 Jun 17;8(Suppl 1):S1. doi: 10.1186/1753-6561-8-S1-S1. eCollection 2014.

4.

Return of individual genetic results in a high-risk sample: enthusiasm and positive behavioral change.

Hartz SM, Olfson E, Culverhouse R, Cavazos-Rehg P, Chen LS, DuBois J, Fisher S, Kaphingst K, Kaufman D, Plunk A, Ramnarine S, Solomon S, Saccone NL, Bierut LJ.

Genet Med. 2014 Aug 28. doi: 10.1038/gim.2014.110. [Epub ahead of print]

PMID:
25166427
5.

Practical barriers and ethical challenges in genetic data sharing.

Simpson CL, Goldenberg AJ, Culverhouse R, Daley D, Igo RP, Jarvik GP, Mandal DM, Mascalzoni D, Montgomery CG, Pierce B, Plaetke R, Shete S, Goddard KA, Stein CM.

Int J Environ Res Public Health. 2014 Aug 15;11(8):8383-98. doi: 10.3390/ijerph110808383.

6.

Variants near CHRNB3-CHRNA6 are associated with DSM-5 cocaine use disorder: evidence for pleiotropy.

Sadler B, Haller G, Agrawal A, Culverhouse R, Bucholz K, Brooks A, Tischfield J, Johnson EO, Edenberg H, Schuckit M, Saccone N, Bierut L, Goate A.

Sci Rep. 2014 Mar 28;4:4497. doi: 10.1038/srep04497.

PMID:
24675634
7.

Multiple distinct CHRNB3-CHRNA6 variants are genetic risk factors for nicotine dependence in African Americans and European Americans.

Culverhouse RC, Johnson EO, Breslau N, Hatsukami DK, Sadler B, Brooks AI, Hesselbrock VM, Schuckit MA, Tischfield JA, Goate AM, Saccone NL, Bierut LJ.

Addiction. 2014 May;109(5):814-22. doi: 10.1111/add.12478. Epub 2014 Feb 18.

PMID:
24401102
8.

Protocol for a collaborative meta-analysis of 5-HTTLPR, stress, and depression.

Culverhouse RC, Bowes L, Breslau N, Nurnberger JI Jr, Burmeister M, Fergusson DM, Munafò M, Saccone NL, Bierut LJ; 5-HTTLPR, Stress, and Depression Consortium.

BMC Psychiatry. 2013 Nov 12;13:304. doi: 10.1186/1471-244X-13-304.

9.

Interpreting joint SNP analysis results: when are two distinct signals really two distinct signals?

Schwantes-An TH, Culverhouse R, Duan W, Ramnarine S, Rice JP, Saccone NL.

Genet Epidemiol. 2013 Apr;37(3):301-9. doi: 10.1002/gepi.21712. Epub 2013 Feb 12.

10.

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers.

Hartz SM, Short SE, Saccone NL, Culverhouse R, Chen L, Schwantes-An TH, Coon H, Han Y, Stephens SH, Sun J, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Geller F, Gubjartsson D, Hansel NN, Jiang C, Keskitalo-Vuokko K, Liu Z, Lyytikäinen LP, Michel M, Rawal R, Rosenberger A, Scheet P, Shaffer JR, Teumer A, Thompson JR, Vink JM, Vogelzangs N, Wenzlaff AS, Wheeler W, Xiao X, Yang BZ, Aggen SH, Balmforth AJ, Baumeister SE, Beaty T, Bennett S, Bergen AW, Boyd HA, Broms U, Campbell H, Chatterjee N, Chen J, Cheng YC, Cichon S, Couper D, Cucca F, Dick DM, Foroud T, Furberg H, Giegling I, Gu F, Hall AS, Hällfors J, Han S, Hartmann AM, Hayward C, Heikkilä K, Hewitt JK, Hottenga JJ, Jensen MK, Jousilahti P, Kaakinen M, Kittner SJ, Konte B, Korhonen T, Landi MT, Laatikainen T, Leppert M, Levy SM, Mathias RA, McNeil DW, Medland SE, Montgomery GW, Muley T, Murray T, Nauck M, North K, Pergadia M, Polasek O, Ramos EM, Ripatti S, Risch A, Ruczinski I, Rudan I, Salomaa V, Schlessinger D, Styrkársdóttir U, Terracciano A, Uda M, Willemsen G, Wu X, Abecasis G, Barnes K, Bickeböller H, Boerwinkle E, Boomsma DI, Caporaso N, Duan J, Edenberg HJ, Francks C, Gejman PV, Gelernter J, Grabe HJ, Hops H, Jarvelin MR, Viikari J, Kähönen M, Kendler KS, Lehtimäki T, Levinson DF, Marazita ML, Marchini J, Melbye M, Mitchell BD, Murray JC, Nöthen MM, Penninx BW, Raitakari O, Rietschel M, Rujescu D, Samani NJ, Sanders AR, Schwartz AG, Shete S, Shi J, Spitz M, Stefansson K, Swan GE, Thorgeirsson T, Völzke H, Wei Q, Wichmann HE, Amos CI, Breslau N, Cannon DS, Ehringer M, Grucza R, Hatsukami D, Heath A, Johnson EO, Kaprio J, Madden P, Martin NG, Stevens VL, Stitzel JA, Weiss RB, Kraft P, Bierut LJ.

Arch Gen Psychiatry. 2012 Aug;69(8):854-60. doi: 10.1001/archgenpsychiatry.2012.124.

11.

Smoking and genetic risk variation across populations of European, Asian, and African American ancestry--a meta-analysis of chromosome 15q25.

Chen LS, Saccone NL, Culverhouse RC, Bracci PM, Chen CH, Dueker N, Han Y, Huang H, Jin G, Kohno T, Ma JZ, Przybeck TR, Sanders AR, Smith JA, Sung YJ, Wenzlaff AS, Wu C, Yoon D, Chen YT, Cheng YC, Cho YS, David SP, Duan J, Eaton CB, Furberg H, Goate AM, Gu D, Hansen HM, Hartz S, Hu Z, Kim YJ, Kittner SJ, Levinson DF, Mosley TH, Payne TJ, Rao DC, Rice JP, Rice TK, Schwantes-An TH, Shete SS, Shi J, Spitz MR, Sun YV, Tsai FJ, Wang JC, Wrensch MR, Xian H, Gejman PV, He J, Hunt SC, Kardia SL, Li MD, Lin D, Mitchell BD, Park T, Schwartz AG, Shen H, Wiencke JK, Wu JY, Yokota J, Amos CI, Bierut LJ.

Genet Epidemiol. 2012 May;36(4):340-51. doi: 10.1002/gepi.21627. Erratum in: Genet Epidemiol. 2012 Jul;36(5):525-6.

12.

A comparison of methods sensitive to interactions with small main effects.

Culverhouse RC.

Genet Epidemiol. 2012 May;36(4):303-11. doi: 10.1002/gepi.21622. Epub 2012 Mar 28.

13.

Stratify or adjust? Dealing with multiple populations when evaluating rare variants.

Culverhouse RC, Hinrichs AL, Suarez BK.

BMC Proc. 2011 Nov 29;5 Suppl 9:S101. doi: 10.1186/1753-6561-5-S9-S101.

14.

Linkage analysis merging replicate phenotypes: an application to three quantitative phenotypes in two African samples.

Hinrichs AL, Culverhouse RC, Suarez BK.

BMC Proc. 2011 Nov 29;5 Suppl 9:S81. doi: 10.1186/1753-6561-5-S9-S81.

15.

Identifying rare variants from exome scans: the GAW17 experience.

Ghosh S, Bickeböller H, Bailey J, Bailey-Wilson JE, Cantor R, Culverhouse R, Daw W, Destefano AL, Engelman CD, Hinrichs A, Houwing-Duistermaat J, König IR, Kent J Jr, Laird N, Pankratz N, Paterson A, Pugh E, Suarez B, Sun Y, Thomas A, Tintle N, Zhu X, Ziegler A, Maccluer JW, Almasy L.

BMC Proc. 2011 Nov 29;5 Suppl 9:S1. doi: 10.1186/1753-6561-5-S9-S1.

16.

Regression and data mining methods for analyses of multiple rare variants in the Genetic Analysis Workshop 17 mini-exome data.

Bailey-Wilson JE, Brennan JS, Bull SB, Culverhouse R, Kim Y, Jiang Y, Jung J, Li Q, Lamina C, Liu Y, Mägi R, Niu YS, Simpson CL, Wang L, Yilmaz YE, Zhang H, Zhang Z.

Genet Epidemiol. 2011;35 Suppl 1:S92-100. doi: 10.1002/gepi.20657.

17.

The age of necrotizing enterocolitis onset: an application of Sartwell's incubation period model.

González-Rivera R, Culverhouse RC, Hamvas A, Tarr PI, Warner BB.

J Perinatol. 2011 Aug;31(8):519-23. doi: 10.1038/jp.2010.193. Epub 2011 Jan 27.

18.

Uncovering hidden variance: pair-wise SNP analysis accounts for additional variance in nicotine dependence.

Culverhouse RC, Saccone NL, Stitzel JA, Wang JC, Steinbach JH, Goate AM, Schwantes-An TH, Grucza RA, Stevens VL, Bierut LJ.

Hum Genet. 2011 Feb;129(2):177-88. doi: 10.1007/s00439-010-0911-7. Epub 2010 Nov 16.

19.

The restricted partition method.

Culverhouse R.

Adv Genet. 2010;72:117-39. doi: 10.1016/B978-0-12-380862-2.00006-0.

PMID:
21029851
20.

Multiple independent loci at chromosome 15q25.1 affect smoking quantity: a meta-analysis and comparison with lung cancer and COPD.

Saccone NL, Culverhouse RC, Schwantes-An TH, Cannon DS, Chen X, Cichon S, Giegling I, Han S, Han Y, Keskitalo-Vuokko K, Kong X, Landi MT, Ma JZ, Short SE, Stephens SH, Stevens VL, Sun L, Wang Y, Wenzlaff AS, Aggen SH, Breslau N, Broderick P, Chatterjee N, Chen J, Heath AC, Heliövaara M, Hoft NR, Hunter DJ, Jensen MK, Martin NG, Montgomery GW, Niu T, Payne TJ, Peltonen L, Pergadia ML, Rice JP, Sherva R, Spitz MR, Sun J, Wang JC, Weiss RB, Wheeler W, Witt SH, Yang BZ, Caporaso NE, Ehringer MA, Eisen T, Gapstur SM, Gelernter J, Houlston R, Kaprio J, Kendler KS, Kraft P, Leppert MF, Li MD, Madden PA, Nöthen MM, Pillai S, Rietschel M, Rujescu D, Schwartz A, Amos CI, Bierut LJ.

PLoS Genet. 2010 Aug 5;6(8). pii: e1001053. doi: 10.1371/journal.pgen.1001053.

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Loading ...
Write to the Help Desk