Recent published articles

Authors in bold are Jackson Laboratory faculty

Baker E, Culpepper C, Philips C, Bubier J, Langston M, Chesler E. Identifying common components across biological network graphs using a bipartite data model. BMC Proc 2014 Oct 13; 8(Suppl 6):S4.

Banchereau R, Baldwin N, Cepika AM, Athale S, Xue Y, Yu CI, Metang P, Cheruku A, Berthier I, Gayet I, Wang Y, Ohouo M, Snipes L, Xu H, Obermoser G, Blankenship D, Oh S, Ramilo O, Chaussabel D, Banchereau J, Palucka K, Pascual V. Transcriptional specialization of human dendritic cell subsets in response to microbial vaccines. Nat Commun 2014 Oct 22; 5:5283.

Brand H, Pillalamarri V, Collins RL, Eggert S, O'Dushlaine C, Braaten EB, Stone MR, Chambert K, Doty ND, Hanscom C, Rosenfeld JA, Ditmars H, Blais J, Mills R, Lee C, Gusella JF, McCarroll S, Smoller JW, Talkowski ME, Doyle AE. Cryptic and complex chromosomal aberrations in early-onset neuropsychiatric disorders. Am J Hum Genet 2014 Oct 2; 95(4):454-61.

DiTommaso T, Jones LK, Cottle DL; WTSI Mouse Genetics Program, Gerdin AK, Vancollie VE, Watt FM, Ramirez-Solis R, Bradley A, Steel KP, Sundberg JP, White JK, Smyth IM. Identification of genes important for cutaneous function revealed by a large scale reverse genetic screen in the mouse. PLoS Genet 2014 Oct 23; 10(10):e1004705.

Favaretto F, Milan G, Collin GB, Marshall JD, Stasi F, Maffei P, Vettor R, Naggert JK. GLUT4 defects in adipose tissue are early signs of metabolic alterations in Alms1GT/GT, a mouse model for obesity and insulin resistance. PLoS One 2014 Oct 9;9(10):e109540.

Noordmans GA, Huang Y, Savage H, van Dijk MC, Schaart G, Bergh Weerman MA, Heeringa P, Hillebrands JL, Korstanje R, van Goor H. Genetic analysis of intracapillary glomerular lipoprotein deposits in aging mice. PLoS One 2014 Oct 29;9(10):e111308.

Soundararajan R, Won J, Stearns TM, Charette JR, Hicks WL, Collin GB, Naggert JK, Krebs MP, Nishina PM. Gene profiling of postnatal Mfrprd6 mutant eyes reveals differential accumulation of Prss56, visual cycle and phototransduction mRNAs. PLoS One 2014 Oct 30; 9(10):e110299.

Sullivan LS, Koboldt DC, Bowne SJ, Lang S, Blanton SH, Cadena E, Avery CE, Lewis RA, Webb-Jones K, Wheaton DH, Birch DG, Coussa R, Ren H, Lopez I, Chakarova C, Koenekoop RK, Garcia CA, Fulton RS, Wilson RK, Weinstock GM, Daiger SP. A dominant mutation in hexokinase 1 (HK1) causes retinitis pigmentosa. Invest Ophthalmol Vis Sci 2014 Sep 4; 55(11):7147-58.

West PR, Amaral DG, Bais P, Smith AM, Egnash LA, Ross ME, Palmer JA, Fontaine BR, Conard KR, Corbett BA, Cezar GG, Donley EL, Burrier RE. Metabolomics as a tool for discovery of biomarkers of autism spectrum disorder in the blood plasma of children. PLoS One 2014 Nov 7; 9(11):e112445.

Wylie KM, Mihindukulasuriya KA, Zhou Y, Sodergren E, Storch GA, Weinstock GM. Metagenomic analysis of double-stranded DNA viruses in healthy adults. BMC Biol 2014 Sep 10; 12(1):71.