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Items: 47

1.

Rare genetic variation implicated in non-Hispanic white families with Alzheimer disease.

Beecham GW, Vardarajan B, Blue E, Bush W, Jaworski J, Barral S, DeStefano A, Hamilton-Nelson K, Kunkle B, Martin ER, Naj A, Rajabli F, Reitz C, Thornton T, van Duijn C, Goate A, Seshadri S, Farrer LA, Boerwinkle E, Schellenberg G, Haines JL, Wijsman E, Mayeux R, Pericak-Vance MA; Alzheimer's Disease Sequencing Project.

Neurol Genet. 2018 Nov 21;4(6):e286. doi: 10.1212/NXG.0000000000000286. eCollection 2018 Dec.

2.

Replication of a rare risk haplotype on 1p36.33 for autism spectrum disorder.

Chapman NH, Bernier RA, Webb SJ, Munson J, Blue EM, Chen DH, Heigham E, Raskind WH, Wijsman EM.

Hum Genet. 2018 Oct;137(10):807-815. doi: 10.1007/s00439-018-1939-3. Epub 2018 Oct 1.

PMID:
30276537
3.

Transgelin induces dysfunction of fetal endothelial colony-forming cells from gestational diabetic pregnancies.

Varberg KM, Garretson RO, Blue EK, Chu C, Gohn CR, Tu W, Haneline LS.

Am J Physiol Cell Physiol. 2018 Oct 1;315(4):C502-C515. doi: 10.1152/ajpcell.00137.2018. Epub 2018 Jun 27.

PMID:
29949406
4.

Analysis of pedigree data in populations with multiple ancestries: Strategies for dealing with admixture in Caribbean Hispanic families from the ADSP.

Nafikov RA, Nato AQ Jr, Sohi H, Wang B, Brown L, Horimoto AR, Vardarajan BN, Barral SM, Tosto G, Mayeux RP, Thornton TA, Blue E, Wijsman EM.

Genet Epidemiol. 2018 Sep;42(6):500-515. doi: 10.1002/gepi.22133. Epub 2018 Jun 3.

PMID:
29862559
5.

Mutations in the Epithelial Cadherin-p120-Catenin Complex Cause Mendelian Non-Syndromic Cleft Lip with or without Cleft Palate.

Cox LL, Cox TC, Moreno Uribe LM, Zhu Y, Richter CT, Nidey N, Standley JM, Deng M, Blue E, Chong JX, Yang Y, Carstens RP, Anand D, Lachke SA, Smith JD, Dorschner MO, Bedell B, Kirk E, Hing AV, Venselaar H, Valencia-Ramirez LC, Bamshad MJ, Glass IA, Cooper JA, Haan E, Nickerson DA, van Bokhoven H, Zhou H, Krahn KN, Buckley MF, Murray JC, Lidral AC, Roscioli T.

Am J Hum Genet. 2018 Jun 7;102(6):1143-1157. doi: 10.1016/j.ajhg.2018.04.009. Epub 2018 May 24.

6.

Whole genome sequencing of Caribbean Hispanic families with late-onset Alzheimer's disease.

Vardarajan BN, Barral S, Jaworski J, Beecham GW, Blue E, Tosto G, Reyes-Dumeyer D, Medrano M, Lantigua R, Naj A, Thornton T, DeStefano A, Martin E, Wang LS, Brown L, Bush W, van Duijn C, Goate A, Farrer L, Haines JL, Boerwinkle E, Schellenberg G, Wijsman E, Pericak-Vance MA, Mayeux R; Alzheimer's Disease Sequencing Project, Wang LS.

Ann Clin Transl Neurol. 2018 Mar 13;5(4):406-417. doi: 10.1002/acn3.537. eCollection 2018 Apr.

7.

Functional annotation of genomic variants in studies of late-onset Alzheimer's disease.

Butkiewicz M, Blue EE, Leung YY, Jian X, Marcora E, Renton AE, Kuzma A, Wang LS, Koboldt DC, Haines JL, Bush WS.

Bioinformatics. 2018 Aug 15;34(16):2724-2731. doi: 10.1093/bioinformatics/bty177.

8.

Mycophenolic acid induces senescence of vascular precursor cells.

Go E, Tarnawsky SP, Shelley WC, Banno K, Lin Y, Gil CH, Blue EK, Haneline LS, O'Neil KM, Yoder MC.

PLoS One. 2018 Mar 14;13(3):e0193749. doi: 10.1371/journal.pone.0193749. eCollection 2018.

9.

Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project.

Blue EE, Bis JC, Dorschner MO, Tsuang DW, Barral SM, Beecham G, Below JE, Bush WS, Butkiewicz M, Cruchaga C, DeStefano A, Farrer LA, Goate A, Haines J, Jaworski J, Jun G, Kunkle B, Kuzma A, Lee JJ, Lunetta KL, Ma Y, Martin E, Naj A, Nato AQ, Navas P, Nguyen H, Reitz C, Reyes D, Salerno W, Schellenberg GD, Seshadri S, Sohi H, Thornton TA, Valadares O, van Duijn C, Vardarajan BN, Wang LS, Boerwinkle E, Dupuis J, Pericak-Vance MA, Mayeux R, Wijsman EM; on behalf of the Alzheimer’s Disease Sequencing Project.

Dement Geriatr Cogn Disord. 2018;45(1-2):1-17. doi: 10.1159/000485503. Epub 2018 Feb 27.

PMID:
29486463
10.

Variation in Cilia Protein Genes and Progression of Lung Disease in Cystic Fibrosis.

Blue E, Louie TL, Chong JX, Hebbring SJ, Barnes KC, Rafaels NM, Knowles MR, Gibson RL, Bamshad MJ, Emond MJ; U.S. National Heart, Lung, and Blood Institute “Grand Opportunity” Exome Sequencing Project (LungGO).

Ann Am Thorac Soc. 2018 Apr;15(4):440-448. doi: 10.1513/AnnalsATS.201706-451OC.

PMID:
29323929
11.

An 8-generation family with X-linked Charcot-Marie-Tooth: Confirmation Of the pathogenicity Of a 3' untranslated region mutation in GJB1 and its clinical features.

Chen DH, Ma M, Scavina M, Blue E, Wolff J, Karna P, Dorschner MO, Raskind WH, Bird TD.

Muscle Nerve. 2018 May;57(5):859-862. doi: 10.1002/mus.26037. Epub 2017 Dec 28.

PMID:
29236290
12.

Variants regulating ZBTB4 are associated with age-at-onset of Alzheimer's disease.

Blue EE, Yu CE, Thornton TA, Chapman NH, Kernfeld E, Jiang N, Shively KM, Buckingham KJ, Marvin CT, Bamshad MJ, Bird TD, Wijsman EM.

Genes Brain Behav. 2018 Jul;17(6):e12429. doi: 10.1111/gbb.12429. Epub 2017 Nov 20.

PMID:
29045054
13.

Copy Number Changes Identified Using Whole Exome Sequencing in Nonsyndromic Cleft Lip and Palate in a Honduran Population.

Cai Y, Patterson KE, Reinier F, Keesecker SE, Blue E, Bamshad M, Haddad J Jr.

Birth Defects Res. 2017 Oct 2;109(16):1257-1267. doi: 10.1002/bdr2.1063. Epub 2017 Jul 27.

14.

Kinetic analyses of vasculogenesis inform mechanistic studies.

Varberg KM, Winfree S, Chu C, Tu W, Blue EK, Gohn CR, Dunn KW, Haneline LS.

Am J Physiol Cell Physiol. 2017 Apr 1;312(4):C446-C458. doi: 10.1152/ajpcell.00367.2016. Epub 2017 Jan 18.

15.

Estimating relationships between phenotypes and subjects drawn from admixed families.

Blue EM, Brown LA, Conomos MP, Kirk JL, Nato AQ Jr, Popejoy AB, Raffa J, Ranola J, Wijsman EM, Thornton T.

BMC Proc. 2016 Oct 18;10(Suppl 7):357-362. eCollection 2016.

16.

Identity-by-descent estimation with population- and pedigree-based imputation in admixed family data.

Saad M, Nato AQ Jr, Grimson FL, Lewis SM, Brown LA, Blue EM, Thornton TA, Thompson EA, Wijsman EM.

BMC Proc. 2016 Oct 18;10(Suppl 7):295-301. eCollection 2016.

17.

Mesenchyme Homeobox 2 Enhances Migration of Endothelial Colony Forming Cells Exposed to Intrauterine Diabetes Mellitus.

Gohn CR, Blue EK, Sheehan BM, Varberg KM, Haneline LS.

J Cell Physiol. 2017 Jul;232(7):1885-1892. doi: 10.1002/jcp.25734. Epub 2017 Feb 16.

18.

Using Whole Exome Sequencing to Identify Candidate Genes With Rare Variants In Nonsyndromic Cleft Lip and Palate.

Aylward A, Cai Y, Lee A, Blue E, Rabinowitz D, Haddad J Jr; University of Washington Center for Mendelian Genomics.

Genet Epidemiol. 2016 Jul;40(5):432-41. doi: 10.1002/gepi.21972. Epub 2016 May 27.

19.

Becoming a Nurse and Army Officer Through the ROTC Program.

Blue E.

Medsurg Nurs. 2015 May-Jun;24(3):Suppl 9. No abstract available.

PMID:
26285375
20.

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes.

Chapman NH, Nato AQ Jr, Bernier R, Ankenman K, Sohi H, Munson J, Patowary A, Archer M, Blue EM, Webb SJ, Coon H, Raskind WH, Brkanac Z, Wijsman EM.

Hum Genet. 2015 Oct;134(10):1055-68. doi: 10.1007/s00439-015-1585-y. Epub 2015 Jul 24.

21.

Identification and functional characterization of natural human melanocortin 1 receptor mutant alleles in Pakistani population.

Shahzad M, Sires Campos J, Tariq N, Herraiz Serrano C, Yousaf R, Jiménez-Cervantes C, Yousaf S, Waryah YM, Dad HA, Blue EM, Sobreira N, López-Giráldez F; University of Washington Center for Mendelian Genomics, Kausar T, Ali M, Waryah AM, Riazuddin S, Shaikh RS, García-Borrón JC, Ahmed ZM.

Pigment Cell Melanoma Res. 2015 Nov;28(6):730-5. doi: 10.1111/pcmr.12400. Epub 2015 Sep 22.

22.

The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities.

Chong JX, Buckingham KJ, Jhangiani SN, Boehm C, Sobreira N, Smith JD, Harrell TM, McMillin MJ, Wiszniewski W, Gambin T, Coban Akdemir ZH, Doheny K, Scott AF, Avramopoulos D, Chakravarti A, Hoover-Fong J, Mathews D, Witmer PD, Ling H, Hetrick K, Watkins L, Patterson KE, Reinier F, Blue E, Muzny D, Kircher M, Bilguvar K, López-Giráldez F, Sutton VR, Tabor HK, Leal SM, Gunel M, Mane S, Gibbs RA, Boerwinkle E, Hamosh A, Shendure J, Lupski JR, Lifton RP, Valle D, Nickerson DA; Centers for Mendelian Genomics, Bamshad MJ.

Am J Hum Genet. 2015 Aug 6;97(2):199-215. doi: 10.1016/j.ajhg.2015.06.009. Epub 2015 Jul 9. Review.

23.

Epigenetic Regulation of Placenta-Specific 8 Contributes to Altered Function of Endothelial Colony-Forming Cells Exposed to Intrauterine Gestational Diabetes Mellitus.

Blue EK, Sheehan BM, Nuss ZV, Boyle FA, Hocutt CM, Gohn CR, Varberg KM, McClintick JN, Haneline LS.

Diabetes. 2015 Jul;64(7):2664-75. doi: 10.2337/db14-1709. Epub 2015 Feb 26.

24.

Next-generation gene discovery for variants of large impact on lipid traits.

Rosenthal E, Blue E, Jarvik GP.

Curr Opin Lipidol. 2015 Apr;26(2):114-9. doi: 10.1097/MOL.0000000000000156. Review.

25.

Rare variants in RTEL1 are associated with familial interstitial pneumonia.

Cogan JD, Kropski JA, Zhao M, Mitchell DB, Rives L, Markin C, Garnett ET, Montgomery KH, Mason WR, McKean DF, Powers J, Murphy E, Olson LM, Choi L, Cheng DS, Blue EM, Young LR, Lancaster LH, Steele MP, Brown KK, Schwarz MI, Fingerlin TE, Schwartz DA, Lawson WE, Loyd JE, Zhao Z, Phillips JA 3rd, Blackwell TS.

Am J Respir Crit Care Med. 2015 Mar 15;191(6):646-55. doi: 10.1164/rccm.201408-1510OC.

26.

Identity-by-descent graphs offer a flexible framework for imputation and both linkage and association analyses.

Blue EM, Cheung CY, Glazner CG, Conomos MP, Lewis SM, Sverdlov S, Thornton T, Wijsman EM.

BMC Proc. 2014 Jun 17;8(Suppl 1 Genetic Analysis Workshop 18Vanessa Olmo):S19. doi: 10.1186/1753-6561-8-S1-S19. eCollection 2014.

27.

Estimating and adjusting for ancestry admixture in statistical methods for relatedness inference, heritability estimation, and association testing.

Thornton T, Conomos MP, Sverdlov S, Blue EM, Cheung CY, Glazner CG, Lewis SM, Wijsman EM.

BMC Proc. 2014 Jun 17;8(Suppl 1):S5. doi: 10.1186/1753-6561-8-S1-S5. eCollection 2014.

28.

Fetal hyperglycemia and a high-fat diet contribute to aberrant glucose tolerance and hematopoiesis in adult rats.

Blue EK, Ballman K, Boyle F, Oh E, Kono T, Quinney SK, Thurmond DC, Evans-Molina C, Haneline LS.

Pediatr Res. 2015 Feb;77(2):316-25. doi: 10.1038/pr.2014.185. Epub 2014 Nov 20.

29.

Differential effects of type and quantity of leaf damage on growth, reproduction and defence of lima bean (Phaseolus lunatus L.).

Blue E, Kay J, Younginger BS, Ballhorn DJ.

Plant Biol (Stuttg). 2015 May;17(3):712-9. doi: 10.1111/plb.12285. Epub 2014 Dec 30.

PMID:
25377879
30.

Value of Mendelian laws of segregation in families: data quality control, imputation, and beyond.

Blue EM, Sun L, Tintle NL, Wijsman EM.

Genet Epidemiol. 2014 Sep;38 Suppl 1:S21-8. doi: 10.1002/gepi.21821.

31.

Gestational diabetes induces alterations in the function of neonatal endothelial colony-forming cells.

Blue EK, DiGiuseppe R, Derr-Yellin E, Acosta JC, Pay SL, Hanenberg H, Schellinger MM, Quinney SK, Mund JA, Case J, Haneline LS.

Pediatr Res. 2014 Feb;75(2):266-72. doi: 10.1038/pr.2013.224. Epub 2013 Nov 14.

32.

Post-translational regulation of the cellular levels of DAPK.

Gallagher PJ, Blue EK.

Apoptosis. 2014 Feb;19(2):306-15. doi: 10.1007/s10495-013-0936-1. Review.

PMID:
24185832
33.

Fat-induced membrane cholesterol accrual provokes cortical filamentous actin destabilisation and glucose transport dysfunction in skeletal muscle.

Habegger KM, Penque BA, Sealls W, Tackett L, Bell LN, Blue EK, Gallagher PJ, Sturek M, Alloosh MA, Steinberg HO, Considine RV, Elmendorf JS.

Diabetologia. 2012 Feb;55(2):457-67. doi: 10.1007/s00125-011-2334-y. Epub 2011 Oct 15.

34.

Thymine DNA glycosylase represses myocardin-induced smooth muscle cell differentiation by competing with serum response factor for myocardin binding.

Zhou J, Blue EK, Hu G, Herring BP.

J Biol Chem. 2008 Dec 19;283(51):35383-92. doi: 10.1074/jbc.M805489200. Epub 2008 Oct 21.

35.
36.

Control of death-associated protein kinase (DAPK) activity by phosphorylation and proteasomal degradation.

Jin Y, Blue EK, Gallagher PJ.

J Biol Chem. 2006 Dec 22;281(51):39033-40. Epub 2006 Oct 20.

37.
38.
39.

Cleavage of X-H bonds (X = N, o, or C) by copper(I) alkyl complexes to form monomeric two-coordinate copper(I) systems.

Goj LA, Blue ED, Munro-Leighton C, Gunnoe TB, Petersen JL.

Inorg Chem. 2005 Nov 28;44(24):8647-9.

PMID:
16296815
40.

Synthesis, solid-state crystal structure, and reactivity of a monomeric copper(I) anilido complex.

Blue ED, Davis A, Conner D, Gunnoe TB, Boyle PD, White PS.

J Am Chem Soc. 2003 Aug 6;125(31):9435-41.

PMID:
12889974
42.

Synthesis, spectroscopy, and solid-state structural characterization of the hexanuclear copper macrocycle [Cu6Cl6(mu-PCHP)6].

Blue ED, Gunnoe TB, Brooks NR.

Angew Chem Int Ed Engl. 2002 Jul 15;41(14):2571-3. No abstract available.

PMID:
12203537
43.

220- and 130-kDa MLCKs have distinct tissue distributions and intracellular localization patterns.

Blue EK, Goeckeler ZM, Jin Y, Hou L, Dixon SA, Herring BP, Wysolmerski RB, Gallagher PJ.

Am J Physiol Cell Physiol. 2002 Mar;282(3):C451-60.

44.

Identification of a new form of death-associated protein kinase that promotes cell survival.

Jin Y, Blue EK, Dixon S, Hou L, Wysolmerski RB, Gallagher PJ.

J Biol Chem. 2001 Oct 26;276(43):39667-78. Epub 2001 Aug 2.

45.

Alterations in expression of myosin and myosin light chain kinases in response to vascular injury.

Gallagher PJ, Jin Y, Killough G, Blue EK, Lindner V.

Am J Physiol Cell Physiol. 2000 Oct;279(4):C1078-87.

46.

Letting go of Ben.

Blue E.

Nurs Spectr (Wash D C). 1999 Mar 8;9(5):20. No abstract available.

PMID:
10562177
47.

Activation of RNase L by 2',5'-oligoadenylates. Biophysical characterization.

Cole JL, Carroll SS, Blue ES, Viscount T, Kuo LC.

J Biol Chem. 1997 Aug 1;272(31):19187-92.

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