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Results: 1 to 20 of 34

1.

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes.

Li Y, Willer CJ, Ding J, Scheet P, Abecasis GR.

Genet Epidemiol. 2010 Dec;34(8):816-34. doi: 10.1002/gepi.20533.

PMID:
21058334
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

Systematic removal of outliers to reduce heterogeneity in case-control association studies.

Shen Y, Liu Z, Ott J.

Hum Hered. 2010;70(4):227-31. doi: 10.1159/000320422. Epub 2010 Oct 6.

PMID:
20924194
[PubMed - indexed for MEDLINE]
Free PMC Article
3.

Excess of rare variants in genes identified by genome-wide association study of hypertriglyceridemia.

Johansen CT, Wang J, Lanktree MB, Cao H, McIntyre AD, Ban MR, Martins RA, Kennedy BA, Hassell RG, Visser ME, Schwartz SM, Voight BF, Elosua R, Salomaa V, O'Donnell CJ, Dallinga-Thie GM, Anand SS, Yusuf S, Huff MW, Kathiresan S, Hegele RA.

Nat Genet. 2010 Aug;42(8):684-7. doi: 10.1038/ng.628. Epub 2010 Jul 25.

PMID:
20657596
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Genomewide association studies and assessment of the risk of disease.

Manolio TA.

N Engl J Med. 2010 Jul 8;363(2):166-76. doi: 10.1056/NEJMra0905980. Review. No abstract available.

PMID:
20647212
[PubMed - indexed for MEDLINE]
Free Article
5.

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction.

Bezzina CR, Pazoki R, Bardai A, Marsman RF, de Jong JS, Blom MT, Scicluna BP, Jukema JW, Bindraban NR, Lichtner P, Pfeufer A, Bishopric NH, Roden DM, Meitinger T, Chugh SS, Myerburg RJ, Jouven X, Kääb S, Dekker LR, Tan HL, Tanck MW, Wilde AA.

Nat Genet. 2010 Aug;42(8):688-91. doi: 10.1038/ng.623. Epub 2010 Jul 11.

PMID:
20622880
[PubMed - indexed for MEDLINE]
Free PMC Article
6.

Risk factors for appropriate cardioverter-defibrillator shocks, inappropriate cardioverter-defibrillator shocks, and time to mortality in 549 patients with heart failure.

Desai H, Aronow WS, Ahn C, Gandhi K, Hussain S, Lai HM, Sharma M, Frishman WH, Cohen M, Sorbera C.

Am J Cardiol. 2010 May 1;105(9):1336-8. doi: 10.1016/j.amjcard.2009.12.057. Epub 2010 Mar 11.

PMID:
20403488
[PubMed - indexed for MEDLINE]
7.

Common variants in cardiac ion channel genes are associated with sudden cardiac death.

Albert CM, MacRae CA, Chasman DI, VanDenburgh M, Buring JE, Manson JE, Cook NR, Newton-Cheh C.

Circ Arrhythm Electrophysiol. 2010 Jun;3(3):222-9. doi: 10.1161/CIRCEP.110.944934. Epub 2010 Apr 17.

PMID:
20400777
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Common variants in KCNN3 are associated with lone atrial fibrillation.

Ellinor PT, Lunetta KL, Glazer NL, Pfeufer A, Alonso A, Chung MK, Sinner MF, de Bakker PI, Mueller M, Lubitz SA, Fox E, Darbar D, Smith NL, Smith JD, Schnabel RB, Soliman EZ, Rice KM, Van Wagoner DR, Beckmann BM, van Noord C, Wang K, Ehret GB, Rotter JI, Hazen SL, Steinbeck G, Smith AV, Launer LJ, Harris TB, Makino S, Nelis M, Milan DJ, Perz S, Esko T, Köttgen A, Moebus S, Newton-Cheh C, Li M, Möhlenkamp S, Wang TJ, Kao WH, Vasan RS, Nöthen MM, MacRae CA, Stricker BH, Hofman A, Uitterlinden AG, Levy D, Boerwinkle E, Metspalu A, Topol EJ, Chakravarti A, Gudnason V, Psaty BM, Roden DM, Meitinger T, Wichmann HE, Witteman JC, Barnard J, Arking DE, Benjamin EJ, Heckbert SR, Kääb S.

Nat Genet. 2010 Mar;42(3):240-4. doi: 10.1038/ng.537. Epub 2010 Feb 21.

PMID:
20173747
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

A new highly penetrant form of obesity due to deletions on chromosome 16p11.2.

Walters RG, Jacquemont S, Valsesia A, de Smith AJ, Martinet D, Andersson J, Falchi M, Chen F, Andrieux J, Lobbens S, Delobel B, Stutzmann F, El-Sayed Moustafa JS, Chèvre JC, Lecoeur C, Vatin V, Bouquillon S, Buxton JL, Boute O, Holder-Espinasse M, Cuisset JM, Lemaitre MP, Ambresin AE, Brioschi A, Gaillard M, Giusti V, Fellmann F, Ferrarini A, Hadjikhani N, Campion D, Guilmatre A, Goldenberg A, Calmels N, Mandel JL, Le Caignec C, David A, Isidor B, Cordier MP, Dupuis-Girod S, Labalme A, Sanlaville D, Béri-Dexheimer M, Jonveaux P, Leheup B, Ounap K, Bochukova EG, Henning E, Keogh J, Ellis RJ, Macdermot KD, van Haelst MM, Vincent-Delorme C, Plessis G, Touraine R, Philippe A, Malan V, Mathieu-Dramard M, Chiesa J, Blaumeiser B, Kooy RF, Caiazzo R, Pigeyre M, Balkau B, Sladek R, Bergmann S, Mooser V, Waterworth D, Reymond A, Vollenweider P, Waeber G, Kurg A, Palta P, Esko T, Metspalu A, Nelis M, Elliott P, Hartikainen AL, McCarthy MI, Peltonen L, Carlsson L, Jacobson P, Sjöström L, Huang N, Hurles ME, O'Rahilly S, Farooqi IS, Männik K, Jarvelin MR, Pattou F, Meyre D, Walley AJ, Coin LJ, Blakemore AI, Froguel P, Beckmann JS.

Nature. 2010 Feb 4;463(7281):671-5. doi: 10.1038/nature08727.

PMID:
20130649
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Several common variants modulate heart rate, PR interval and QRS duration.

Holm H, Gudbjartsson DF, Arnar DO, Thorleifsson G, Thorgeirsson G, Stefansdottir H, Gudjonsson SA, Jonasdottir A, Mathiesen EB, Njølstad I, Nyrnes A, Wilsgaard T, Hald EM, Hveem K, Stoltenberg C, Løchen ML, Kong A, Thorsteinsdottir U, Stefansson K.

Nat Genet. 2010 Feb;42(2):117-22. doi: 10.1038/ng.511. Epub 2010 Jan 10.

PMID:
20062063
[PubMed - indexed for MEDLINE]
11.

Genetic variation in SCN10A influences cardiac conduction.

Chambers JC, Zhao J, Terracciano CM, Bezzina CR, Zhang W, Kaba R, Navaratnarajah M, Lotlikar A, Sehmi JS, Kooner MK, Deng G, Siedlecka U, Parasramka S, El-Hamamsy I, Wass MN, Dekker LR, de Jong JS, Sternberg MJ, McKenna W, Severs NJ, de Silva R, Wilde AA, Anand P, Yacoub M, Scott J, Elliott P, Wood JN, Kooner JS.

Nat Genet. 2010 Feb;42(2):149-52. doi: 10.1038/ng.516. Epub 2010 Jan 10.

PMID:
20062061
[PubMed - indexed for MEDLINE]
12.

Genome-wide association study of PR interval.

Pfeufer A, van Noord C, Marciante KD, Arking DE, Larson MG, Smith AV, Tarasov KV, Müller M, Sotoodehnia N, Sinner MF, Verwoert GC, Li M, Kao WH, Köttgen A, Coresh J, Bis JC, Psaty BM, Rice K, Rotter JI, Rivadeneira F, Hofman A, Kors JA, Stricker BH, Uitterlinden AG, van Duijn CM, Beckmann BM, Sauter W, Gieger C, Lubitz SA, Newton-Cheh C, Wang TJ, Magnani JW, Schnabel RB, Chung MK, Barnard J, Smith JD, Van Wagoner DR, Vasan RS, Aspelund T, Eiriksdottir G, Harris TB, Launer LJ, Najjar SS, Lakatta E, Schlessinger D, Uda M, Abecasis GR, Müller-Myhsok B, Ehret GB, Boerwinkle E, Chakravarti A, Soliman EZ, Lunetta KL, Perz S, Wichmann HE, Meitinger T, Levy D, Gudnason V, Ellinor PT, Sanna S, Kääb S, Witteman JC, Alonso A, Benjamin EJ, Heckbert SR.

Nat Genet. 2010 Feb;42(2):153-9. doi: 10.1038/ng.517. Epub 2010 Jan 10.

PMID:
20062060
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Rates and predictors of appropriate implantable cardioverter-defibrillator therapy delivery: results from the EVADEF cohort study.

Otmani A, Trinquart L, Marijon E, Lavergne T, Waintraub X, Lepillier A, Chatellier G, Le Heuzey JY; EVADEF investigators.

Am Heart J. 2009 Aug;158(2):230-237.e1. doi: 10.1016/j.ahj.2009.05.019.

PMID:
19619699
[PubMed - indexed for MEDLINE]
14.

Prevalence of appropriate cardioverter-defibrillator shocks in 1038 consecutive patients with implantable cardioverter-defibrillators.

Kruger A, Aronow WS, Lai H, Desai H, Singla A, Frishman WH, Cohen M, Sorbera C.

Am J Ther. 2009 Jul-Aug;16(4):323-5. doi: 10.1097/MJT.0b013e3181727a59.

PMID:
19617719
[PubMed - indexed for MEDLINE]
15.

Common variants at ten loci modulate the QT interval duration in the QTSCD Study.

Pfeufer A, Sanna S, Arking DE, Müller M, Gateva V, Fuchsberger C, Ehret GB, Orrú M, Pattaro C, Köttgen A, Perz S, Usala G, Barbalic M, Li M, Pütz B, Scuteri A, Prineas RJ, Sinner MF, Gieger C, Najjar SS, Kao WH, Mühleisen TW, Dei M, Happle C, Möhlenkamp S, Crisponi L, Erbel R, Jöckel KH, Naitza S, Steinbeck G, Marroni F, Hicks AA, Lakatta E, Müller-Myhsok B, Pramstaller PP, Wichmann HE, Schlessinger D, Boerwinkle E, Meitinger T, Uda M, Coresh J, Kääb S, Abecasis GR, Chakravarti A.

Nat Genet. 2009 Apr;41(4):407-14. doi: 10.1038/ng.362. Epub 2009 Mar 22.

PMID:
19305409
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Common variants at ten loci influence QT interval duration in the QTGEN Study.

Newton-Cheh C, Eijgelsheim M, Rice KM, de Bakker PI, Yin X, Estrada K, Bis JC, Marciante K, Rivadeneira F, Noseworthy PA, Sotoodehnia N, Smith NL, Rotter JI, Kors JA, Witteman JC, Hofman A, Heckbert SR, O'Donnell CJ, Uitterlinden AG, Psaty BM, Lumley T, Larson MG, Stricker BH.

Nat Genet. 2009 Apr;41(4):399-406. doi: 10.1038/ng.364. Epub 2009 Mar 22.

PMID:
19305408
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes.

Nejentsev S, Walker N, Riches D, Egholm M, Todd JA.

Science. 2009 Apr 17;324(5925):387-9. doi: 10.1126/science.1167728. Epub 2009 Mar 5.

PMID:
19264985
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genetic variations in nitric oxide synthase 1 adaptor protein are associated with sudden cardiac death in US white community-based populations.

Kao WH, Arking DE, Post W, Rea TD, Sotoodehnia N, Prineas RJ, Bishe B, Doan BQ, Boerwinkle E, Psaty BM, Tomaselli GF, Coresh J, Siscovick DS, Marbán E, Spooner PM, Burke GL, Chakravarti A.

Circulation. 2009 Feb 24;119(7):940-51. doi: 10.1161/CIRCULATIONAHA.108.791723. Epub 2009 Feb 9.

PMID:
19204306
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Implantable cardioverter-defibrillators after myocardial infarction.

Myerburg RJ.

N Engl J Med. 2008 Nov 20;359(21):2245-53. doi: 10.1056/NEJMra0803409. Review. No abstract available.

PMID:
19020326
[PubMed - indexed for MEDLINE]
20.

Genetic determinants of sudden cardiac death.

Noseworthy PA, Newton-Cheh C.

Circulation. 2008 Oct 28;118(18):1854-63. doi: 10.1161/CIRCULATIONAHA.108.783654. Review. No abstract available.

PMID:
18955676
[PubMed - indexed for MEDLINE]
Free Article

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