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Cover Image, Volume 173A, Number 11, November 2017.

Justice CM, Kim J, Kim SD, Kim K, Yagnik G, Cuellar A, Carrington B, Lu CL, Sood R, Boyadjiev SA, Wilson AF.

Am J Med Genet A. 2017 Nov;173(11):i. doi: 10.1002/ajmg.a.38511.


The FUT2 secretor variant p.Trp154Ter influences serum vitamin B12 concentration via holo-haptocorrin, but not holo-transcobalamin, and is associated with haptocorrin glycosylation.

Velkova A, Diaz JEL, Pangilinan F, Molloy AM, Mills JL, Shane B, Sanchez E, Cunningham C, McNulty H, Cropp CD, Bailey-Wilson JE, Wilson AF, Brody LC.

Hum Mol Genet. 2017 Oct 12. doi: 10.1093/hmg/ddx369. [Epub ahead of print]


A variant associated with sagittal nonsyndromic craniosynostosis alters the regulatory function of a non-coding element.

Justice CM, Kim J, Kim SD, Kim K, Yagnik G, Cuellar A, Carrington B, Lu CL, Sood R, Boyadjiev SA, Wilson AF.

Am J Med Genet A. 2017 Nov;173(11):2893-2897. doi: 10.1002/ajmg.a.38392. Epub 2017 Oct 6.


Persistent response of Fanconi anemia haematopoietic stem and progenitor cells to oxidative stress.

Li Y, Amarachintha S, Wilson AF, Li X, Du W.

Cell Cycle. 2017 Jun 18;16(12):1201-1209. doi: 10.1080/15384101.2017.1320627. Epub 2017 May 5.


Fancd2 in vivo interaction network reveals a non-canonical role in mitochondrial function.

Zhang T, Du W, Wilson AF, Namekawa SH, Andreassen PR, Meetei AR, Pang Q.

Sci Rep. 2017 Apr 5;7:45626. doi: 10.1038/srep45626.


Type I error rates of rare single nucleotide variants are inflated in tests of association with non-normally distributed traits using simple linear regression methods.

Schwantes-An TH, Sung H, Sabourin JA, Justice CM, Sorant AJM, Wilson AF.

BMC Proc. 2016 Oct 18;10(Suppl 7):385-388. doi: 10.1186/s12919-016-0060-7. eCollection 2016.


A comparison study of multivariate fixed models and Gene Association with Multiple Traits (GAMuT) for next-generation sequencing.

Chiu CY, Jung J, Wang Y, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Mills JL, Boehnke M, Xiong M, Fan R.

Genet Epidemiol. 2017 Jan;41(1):18-34. doi: 10.1002/gepi.22014. Epub 2016 Dec 5.


A Comparison Study of Fixed and Mixed Effect Models for Gene Level Association Studies of Complex Traits.

Fan R, Chiu CY, Jung J, Weeks DE, Wilson AF, Bailey-Wilson JE, Amos CI, Chen Z, Mills JL, Xiong M.

Genet Epidemiol. 2016 Dec;40(8):702-721. doi: 10.1002/gepi.21984. Epub 2016 Jul 4.


Evaluation of IRX Genes and Conserved Noncoding Elements in a Region on 5p13.3 Linked to Families with Familial Idiopathic Scoliosis and Kyphosis.

Justice CM, Bishop K, Carrington B, Mullikin JC, Swindle K, Marosy B, Sood R, Miller NH, Wilson AF.

G3 (Bethesda). 2016 Jun 1;6(6):1707-12. doi: 10.1534/g3.116.029975.


A Common Polymorphism in HIBCH Influences Methylmalonic Acid Concentrations in Blood Independently of Cobalamin.

Molloy AM, Pangilinan F, Mills JL, Shane B, O'Neill MB, McGaughey DM, Velkova A, Abaan HO, Ueland PM, McNulty H, Ward M, Strain JJ, Cunningham C, Casey M, Cropp CD, Kim Y, Bailey-Wilson JE, Wilson AF, Brody LC.

Am J Hum Genet. 2016 May 5;98(5):869-882. doi: 10.1016/j.ajhg.2016.03.005. Epub 2016 Apr 28.


SCO2 Mediates Oxidative Stress-Induced Glycolysis to Oxidative Phosphorylation Switch in Hematopoietic Stem Cells.

Du W, Amarachintha S, Wilson AF, Pang Q.

Stem Cells. 2016 Apr;34(4):960-71. doi: 10.1002/stem.2260. Epub 2015 Dec 31.


Common Variants at Putative Regulatory Sites of the Tissue Nonspecific Alkaline Phosphatase Gene Influence Circulating Pyridoxal 5'-Phosphate Concentration in Healthy Adults.

Carter TC, Pangilinan F, Molloy AM, Fan R, Wang Y, Shane B, Gibney ER, Midttun Ø, Ueland PM, Cropp CD, Kim Y, Wilson AF, Bailey-Wilson JE, Brody LC, Mills JL.

J Nutr. 2015 Jul;145(7):1386-93. doi: 10.3945/jn.114.208769. Epub 2015 May 13.


Loss of Faap20 Causes Hematopoietic Stem and Progenitor Cell Depletion in Mice Under Genotoxic Stress.

Zhang T, Wilson AF, Mahmood Ali A, Namekawa SH, Andreassen PR, Ruhikanta Meetei A, Pang Q.

Stem Cells. 2015 Jul;33(7):2320-30. doi: 10.1002/stem.2048. Epub 2015 May 25.


Pleiotropy analysis of quantitative traits at gene level by multivariate functional linear models.

Wang Y, Liu A, Mills JL, Boehnke M, Wilson AF, Bailey-Wilson JE, Xiong M, Wu CO, Fan R.

Genet Epidemiol. 2015 May;39(4):259-75. doi: 10.1002/gepi.21895. Epub 2015 Mar 23.


Genetic modifiers of neurofibromatosis type 1-associated café-au-lait macule count identified using multi-platform analysis.

Pemov A, Sung H, Hyland PL, Sloan JL, Ruppert SL, Baldwin AM, Boland JF, Bass SE, Lee HJ, Jones KM, Zhang X; NISC Comparative Sequencing Program, Mullikin JC, Widemann BC, Wilson AF, Stewart DR.

PLoS Genet. 2014 Oct 16;10(10):e1004575. doi: 10.1371/journal.pgen.1004575. eCollection 2014 Oct.


Generalized functional linear models for gene-based case-control association studies.

Fan R, Wang Y, Mills JL, Carter TC, Lobach I, Wilson AF, Bailey-Wilson JE, Weeks DE, Xiong M.

Genet Epidemiol. 2014 Nov;38(7):622-637. doi: 10.1002/gepi.21840. Epub 2014 Sep 9.


Survey and Systematic Literature Review of Probiotics Stocked in Academic Medical Centers within the United States.

Abe AM, Gregory PJ, Hein DJ, Cochrane ZR, Wilson AF.

Hosp Pharm. 2013 Nov;48(10):834-47. doi: 10.1310/hpj4810-834.


Informatics and genetic epidemiology.

Ziegler A, Wilson AF, Gagnon F.

Methods Inf Med. 2014;53(1):1-2. No abstract available.


Functional linear models for association analysis of quantitative traits.

Fan R, Wang Y, Mills JL, Wilson AF, Bailey-Wilson JE, Xiong M.

Genet Epidemiol. 2013 Nov;37(7):726-42. doi: 10.1002/gepi.21757.

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