Format
Sort by
Items per page

Send to

Choose Destination

Search results

Items: 39

1.

Genetic Variants of VEGFA and FLT4 Are Determinants of Survival in Renal Cell Carcinoma Patients Treated with Sorafenib.

Crona DJ, Skol AD, Leppänen VM, Glubb DM, Etheridge AS, Hilliard E, Peña CE, Peterson YK, Klauber-DeMore N, Alitalo KK, Innocenti F.

Cancer Res. 2019 Jan 1;79(1):231-241. doi: 10.1158/0008-5472.CAN-18-1089. Epub 2018 Nov 1.

PMID:
30385613
2.

Evaluation of Genetic Predisposition for MYCN-Amplified Neuroblastoma.

Hungate EA, Applebaum MA, Skol AD, Vaksman Z, Diamond M, McDaniel L, Volchenboum SL, Stranger BE, Maris JM, Diskin SJ, Onel K, Cohn SL.

J Natl Cancer Inst. 2017 Oct 1;109(10). doi: 10.1093/jnci/djx093.

3.

A p53-regulated apoptotic gene signature predicts treatment response and outcome in pediatric acute lymphoblastic leukemia.

Bainer RO, Trendowski MR, Cheng C, Pei D, Yang W, Paugh SW, Goss KH, Skol AD, Pavlidis P, Pui CH, Gilliam TC, Evans WE, Onel K.

Cancer Manag Res. 2017 Sep 13;9:397-410. doi: 10.2147/CMAR.S139864. eCollection 2017.

4.

Integrative genetic analysis suggests that skin color modifies the genetic architecture of melanoma.

Hulur I, Skol AD, Gamazon ER, Cox NJ, Onel K.

PLoS One. 2017 Oct 3;12(10):e0185730. doi: 10.1371/journal.pone.0185730. eCollection 2017.

5.

Does MAOA increase susceptibility to prenatal stress in young children?

Massey SH, Hatcher AE, Clark CAC, Burns JL, Pine DS, Skol AD, Mroczek DK, Espy KA, Goldman D, Cook E Jr, Wakschlag LS.

Neurotoxicol Teratol. 2017 May;61:82-91. doi: 10.1016/j.ntt.2017.01.005. Epub 2017 Feb 3.

6.
7.

A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.

Hungate EA, Vora SR, Gamazon ER, Moriyama T, Best T, Hulur I, Lee Y, Evans TJ, Ellinghaus E, Stanulla M, Rudant J, Orsi L, Clavel J, Milne E, Scott RJ, Pui CH, Cox NJ, Loh ML, Yang JJ, Skol AD, Onel K.

Nat Commun. 2016 Feb 12;7:10635. doi: 10.1038/ncomms10635.

8.

Whole-exome Sequence Analysis Implicates Rare Il17REL Variants in Familial and Sporadic Inflammatory Bowel Disease.

Sasaki MM, Skol AD, Hungate EA, Bao R, Huang L, Kahn SA, Allan JM, Brant SR, McGovern DP, Peter I, Silverberg MS, Cho JH, Kirschner BS, Onel K.

Inflamm Bowel Dis. 2016 Jan;22(1):20-7. doi: 10.1097/MIB.0000000000000610.

9.

Establishing a translational genomics infrastructure in pediatric cancer: the GREAT KIDS experience.

Pinto N, Volchenboum SL, Skol AD, Rhodes L, Doan A, Fein-Levy C, Lipton JM, Cunningham JM, Onel K.

Per Med. 2015 Jun;12(3):221-229. doi: 10.2217/pme.14.90.

PMID:
29771652
10.

Integrated genomic analysis suggests MLL3 is a novel candidate susceptibility gene for familial nasopharyngeal carcinoma.

Sasaki MM, Skol AD, Bao R, Rhodes LV, Chambers R, Vokes EE, Cohen EE, Onel K.

Cancer Epidemiol Biomarkers Prev. 2015 Aug;24(8):1222-8. doi: 10.1158/1055-9965.EPI-15-0275. Epub 2015 May 26.

11.

Enrichment of inflammatory bowel disease and colorectal cancer risk variants in colon expression quantitative trait loci.

Hulur I, Gamazon ER, Skol AD, Xicola RM, Llor X, Onel K, Ellis NA, Kupfer SS.

BMC Genomics. 2015 Feb 27;16:138. doi: 10.1186/s12864-015-1292-z.

12.

Genetic analysis of the pathogenic molecular sub-phenotype interferon-alpha identifies multiple novel loci involved in systemic lupus erythematosus.

Kariuki SN, Ghodke-Puranik Y, Dorschner JM, Chrabot BS, Kelly JA, Tsao BP, Kimberly RP, Alarcón-Riquelme ME, Jacob CO, Criswell LA, Sivils KL, Langefeld CD, Harley JB, Skol AD, Niewold TB.

Genes Immun. 2015 Jan-Feb;16(1):15-23. doi: 10.1038/gene.2014.57. Epub 2014 Oct 23.

13.

A meta-analysis of Hodgkin lymphoma reveals 19p13.3 TCF3 as a novel susceptibility locus.

Cozen W, Timofeeva MN, Li D, Diepstra A, Hazelett D, Delahaye-Sourdeix M, Edlund CK, Franke L, Rostgaard K, Van Den Berg DJ, Cortessis VK, Smedby KE, Glaser SL, Westra HJ, Robison LL, Mack TM, Ghesquieres H, Hwang AE, Nieters A, de Sanjose S, Lightfoot T, Becker N, Maynadie M, Foretova L, Roman E, Benavente Y, Rand KA, Nathwani BN, Glimelius B, Staines A, Boffetta P, Link BK, Kiemeney L, Ansell SM, Bhatia S, Strong LC, Galan P, Vatten L, Habermann TM, Duell EJ, Lake A, Veenstra RN, Visser L, Liu Y, Urayama KY, Montgomery D, Gaborieau V, Weiss LM, Byrnes G, Lathrop M, Cocco P, Best T, Skol AD, Adami HO, Melbye M, Cerhan JR, Gallagher A, Taylor GM, Slager SL, Brennan P, Coetzee GA, Conti DV, Onel K, Jarrett RF, Hjalgrim H, van den Berg A, McKay JD.

Nat Commun. 2014 Jun 12;5:3856. doi: 10.1038/ncomms4856.

14.

Radiation-induced apoptosis varies among individuals and is modified by sex and age.

Applebaum MA, Skol AD, Bond EE, Overholtzer M, Bond GL, Onel K.

Int J Radiat Biol. 2014 Oct;90(10):903-8. doi: 10.3109/09553002.2014.925603. Epub 2014 Jun 25.

15.

Shared and independent colorectal cancer risk alleles in TGFβ-related genes in African and European Americans.

Kupfer SS, Skol AD, Hong E, Ludvik A, Kittles RA, Keku TO, Sandler RS, Ellis NA.

Carcinogenesis. 2014 Sep;35(9):2025-30. doi: 10.1093/carcin/bgu088. Epub 2014 Apr 21.

16.

Discovery and functional assessment of gene variants in the vascular endothelial growth factor pathway.

Paré-Brunet L, Glubb D, Evans P, Berenguer-Llergo A, Etheridge AS, Skol AD, Di Rienzo A, Duan S, Gamazon ER, Innocenti F.

Hum Mutat. 2014 Feb;35(2):227-35. doi: 10.1002/humu.22475. Epub 2013 Nov 27.

17.

Gene-expression-guided selection of candidate loci and molecular phenotype analyses enhance genetic discovery in systemic lupus erythematosus.

Koldobskaya Y, Ko K, Kumar AA, Agik S, Arrington J, Kariuki SN, Franek BS, Kumabe M, Utset TO, Jolly M, Skol AD, Niewold TB.

Clin Dev Immunol. 2012;2012:682018. doi: 10.1155/2012/682018. Epub 2012 Jul 25.

18.

Improved minimum cost and maximum power two stage genome-wide association study designs.

Stanhope SA, Skol AD.

PLoS One. 2012;7(9):e42367. doi: 10.1371/journal.pone.0042367. Epub 2012 Sep 6.

19.

The limits of genome-wide methods for pharmacogenomic testing.

Gamazon ER, Skol AD, Perera MA.

Pharmacogenet Genomics. 2012 Apr;22(4):261-72. doi: 10.1097/FPC.0b013e328350ca5f.

20.

A genome-wide meta-analysis of nodular sclerosing Hodgkin lymphoma identifies risk loci at 6p21.32.

Cozen W, Li D, Best T, Van Den Berg DJ, Gourraud PA, Cortessis VK, Skol AD, Mack TM, Glaser SL, Weiss LM, Nathwani BN, Bhatia S, Schumacher FR, Edlund CK, Hwang AE, Slager SL, Fredericksen ZS, Strong LC, Habermann TM, Link BK, Cerhan JR, Robison LL, Conti DV, Onel K.

Blood. 2012 Jan 12;119(2):469-75. doi: 10.1182/blood-2011-03-343921. Epub 2011 Nov 15.

21.

QTLRel: an R package for genome-wide association studies in which relatedness is a concern.

Cheng R, Abney M, Palmer AA, Skol AD.

BMC Genet. 2011 Jul 27;12:66. doi: 10.1186/1471-2156-12-66.

22.

Variants at 6q21 implicate PRDM1 in the etiology of therapy-induced second malignancies after Hodgkin's lymphoma.

Best T, Li D, Skol AD, Kirchhoff T, Jackson SA, Yasui Y, Bhatia S, Strong LC, Domchek SM, Nathanson KL, Olopade OI, Huang RS, Mack TM, Conti DV, Offit K, Cozen W, Robison LL, Onel K.

Nat Med. 2011 Jul 24;17(8):941-3. doi: 10.1038/nm.2407.

23.

Fine-mapping alleles for body weight in LG/J × SM/J F₂ and F(34) advanced intercross lines.

Parker CC, Cheng R, Sokoloff G, Lim JE, Skol AD, Abney M, Palmer AA.

Mamm Genome. 2011 Oct;22(9-10):563-71. doi: 10.1007/s00335-011-9349-z. Epub 2011 Jul 15.

24.

Promoter variant of PIK3C3 is associated with autoimmunity against Ro and Sm epitopes in African-American lupus patients.

Kariuki SN, Franek BS, Mikolaitis RA, Utset TO, Jolly M, Skol AD, Niewold TB.

J Biomed Biotechnol. 2010;2010:826434. doi: 10.1155/2010/826434. Epub 2010 Jul 4.

25.

Trait-stratified genome-wide association study identifies novel and diverse genetic associations with serologic and cytokine phenotypes in systemic lupus erythematosus.

Kariuki SN, Franek BS, Kumar AA, Arrington J, Mikolaitis RA, Utset TO, Jolly M, Crow MK, Skol AD, Niewold TB.

Arthritis Res Ther. 2010;12(4):R151. doi: 10.1186/ar3101. Epub 2010 Jul 26.

26.

Genome-wide association studies and the problem of relatedness among advanced intercross lines and other highly recombinant populations.

Cheng R, Lim JE, Samocha KE, Sokoloff G, Abney M, Skol AD, Palmer AA.

Genetics. 2010 Jul;185(3):1033-44. doi: 10.1534/genetics.110.116863. Epub 2010 May 3.

27.

Novel single nucleotide polymorphism associations with colorectal cancer on chromosome 8q24 in African and European Americans.

Kupfer SS, Torres JB, Hooker S, Anderson JR, Skol AD, Ellis NA, Kittles RA.

Carcinogenesis. 2009 Aug;30(8):1353-7. doi: 10.1093/carcin/bgp123. Epub 2009 Jun 11.

28.

Genome-wide association study to identify novel loci associated with therapy-related myeloid leukemia susceptibility.

Knight JA, Skol AD, Shinde A, Hastings D, Walgren RA, Shao J, Tennant TR, Banerjee M, Allan JM, Le Beau MM, Larson RA, Graubert TA, Cox NJ, Onel K.

Blood. 2009 May 28;113(22):5575-82. doi: 10.1182/blood-2008-10-183244. Epub 2009 Mar 18.

29.

Interaction of prenatal exposure to cigarettes and MAOA genotype in pathways to youth antisocial behavior.

Wakschlag LS, Kistner EO, Pine DS, Biesecker G, Pickett KE, Skol AD, Dukic V, Blair RJ, Leventhal BL, Cox NJ, Burns JL, Kasza KE, Wright RJ, Cook EH Jr.

Mol Psychiatry. 2010 Sep;15(9):928-37. doi: 10.1038/mp.2009.22. Epub 2009 Mar 3.

30.

Optimal designs for two-stage genome-wide association studies.

Skol AD, Scott LJ, Abecasis GR, Boehnke M.

Genet Epidemiol. 2007 Nov;31(7):776-88.

31.

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies.

Skol AD, Scott LJ, Abecasis GR, Boehnke M.

Nat Genet. 2006 Feb;38(2):209-13. Epub 2006 Jan 15. Erratum in: Nat Genet. 2006 Mar;38(3):390.

PMID:
16415888
32.

Genome scan of schizophrenia families in a large Veterans Affairs Cooperative Study sample: evidence for linkage to 18p11.32 and for racial heterogeneity on chromosomes 6 and 14.

Faraone SV, Skol AD, Tsuang DW, Young KA, Haverstock SL, Prabhudesai S, Mena F, Menon AS, Leong L, Sautter F, Baldwin C, Bingham S, Weiss D, Collins J, Keith T, Vanden Eng JL, Boehnke M, Tsuang MT, Schellenberg GD.

Am J Med Genet B Neuropsychiatr Genet. 2005 Nov 5;139B(1):91-100.

PMID:
16152571
33.

An algorithm to construct genetically similar subsets of families with the use of self-reported ethnicity information.

Skol AD, Xiao R, Boehnke M; Veterans Affairs Cooperative Study 366 Investigators.

Am J Hum Genet. 2005 Sep;77(3):346-54. Epub 2005 Jul 14.

34.

Evaluation of SLC2A10 (GLUT10) as a candidate gene for type 2 diabetes and related traits in Finns.

Mohlke KL, Skol AD, Scott LJ, Valle TT, Bergman RN, Tuomilehto J, Boehnke M, Collins FS; FUSION Study Group.

Mol Genet Metab. 2005 Aug;85(4):323-7.

PMID:
15936967
35.

Genetic variation near the hepatocyte nuclear factor-4 alpha gene predicts susceptibility to type 2 diabetes.

Silander K, Mohlke KL, Scott LJ, Peck EC, Hollstein P, Skol AD, Jackson AU, Deloukas P, Hunt S, Stavrides G, Chines PS, Erdos MR, Narisu N, Conneely KN, Li C, Fingerlin TE, Dhanjal SK, Valle TT, Bergman RN, Tuomilehto J, Watanabe RM, Boehnke M, Collins FS.

Diabetes. 2004 Apr;53(4):1141-9.

36.

Modest evidence for linkage and possible confirmation of association between NOTCH4 and schizophrenia in a large Veterans Affairs Cooperative Study sample.

Skol AD, Young KA, Tsuang DW, Faraone SV, Haverstock SL, Bingham S, Prabhudesai S, Mena F, Menon AS, Yu CE, Rundell P, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, Keith T, Boehnke M, Schellenberg GD, Tsuang MT.

Am J Med Genet B Neuropsychiatr Genet. 2003 Apr 1;118B(1):8-15.

PMID:
12627457
37.

Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample.

Faraone SV, Skol AD, Tsuang DW, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sautter F, Baldwin C, Weiss D, Collins J, Keith T, Boehnke M, Tsuang MT, Schellenberg GD.

Am J Med Genet. 2002 Aug 8;114(6):598-604.

PMID:
12210272
38.

Examination of genetic linkage of chromosome 15 to schizophrenia in a large Veterans Affairs Cooperative Study sample.

Tsuang DW, Skol AD, Faraone SV, Bingham S, Young KA, Prabhudesai S, Haverstock SL, Mena F, Menon AS, Bisset D, Pepple J, Sauter F, Baldwin C, Weiss D, Collins J, Boehnke M, Schellenberg GD, Tsuang MT; Veterans Affairs Cooperative Study.

Am J Med Genet. 2001 Dec 8;105(8):662-8.

PMID:
11803512
39.

Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data.

Douglas JA, Skol AD, Boehnke M.

Am J Hum Genet. 2002 Feb;70(2):487-95. Epub 2002 Jan 8.

Supplemental Content

Support Center