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Results: 1 to 20 of 3733

1.

Simple, rapid and accurate genotyping-by-sequencing from aligned whole genomes with ArrayMaker.

Willet CE, Haase B, Charleston MA, Wade CM.

Bioinformatics. 2014 Oct 21. pii: btu691. [Epub ahead of print]

PMID:
25336502
[PubMed - as supplied by publisher]
2.

Exploring the genetics of irritable bowel syndrome: a GWA study in the general population and replication in multinational case-control cohorts.

Ek WE, Reznichenko A, Ripke S, Niesler B, Zucchelli M, Rivera NV, Schmidt PT, Pedersen NL, Magnusson P, Talley NJ, Holliday EG, Houghton L, Gazouli M, Karamanolis G, Rappold G, Burwinkel B, Surowy H, Rafter J, Assadi G, Li L, Papadaki E, Gambaccini D, Marchi S, Colucci R, Blandizzi C, Barbaro R, Karling P, Walter S, Ohlsson B, Tornblom H, Bresso F, Andreasson A, Dlugosz A, Simren M, Agreus L, Lindberg G, Boeckxstaens G, Bellini M, Stanghellini V, Barbara G, Daly MJ, Camilleri M, Wouters MM, D'Amato M.

Gut. 2014 Sep 23. pii: gutjnl-2014-307997. doi: 10.1136/gutjnl-2014-307997. [Epub ahead of print]

PMID:
25248455
[PubMed - as supplied by publisher]
3.

Longitudinal data analysis in genome-wide association studies.

Beyene J, Hamid JS.

Genet Epidemiol. 2014 Sep;38 Suppl 1:S68-73. doi: 10.1002/gepi.21828.

PMID:
25112192
[PubMed - indexed for MEDLINE]
4.

Population-based association and gene by environment interactions in Genetic Analysis Workshop 18.

Satten GA, Biswas S, Papachristou C, Turkmen A, König IR.

Genet Epidemiol. 2014 Sep;38 Suppl 1:S49-56. doi: 10.1002/gepi.21825.

PMID:
25112188
[PubMed - indexed for MEDLINE]
5.

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.

PMID:
25112184
[PubMed - indexed for MEDLINE]
6.

Drinking from the Holy Grail: analysis of whole-genome sequencing from the Genetic Analysis Workshop 18.

Paterson AD.

Genet Epidemiol. 2014 Sep;38 Suppl 1:S1-4. doi: 10.1002/gepi.21818.

PMID:
25112182
[PubMed - indexed for MEDLINE]
7.

CHI3L1 polymorphisms associate with asthma in a Taiwanese population.

Tsai Y, Ko Y, Huang M, Lin M, Wu C, Wang C, Chen Y, Li J, Tseng Y, Wang T.

BMC Med Genet. 2014 Jul 23;15:86. doi: 10.1186/1471-2350-15-86.

PMID:
25056157
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Genome-wide association and network analysis of lung function in the Framingham Heart Study.

Liao SY, Lin X, Christiani DC.

Genet Epidemiol. 2014 Sep;38(6):572-8. doi: 10.1002/gepi.21841. Epub 2014 Jul 8.

PMID:
25044411
[PubMed - indexed for MEDLINE]
9.

The role of local ancestry adjustment in association studies using admixed populations.

Zhang J, Stram DO.

Genet Epidemiol. 2014 Sep;38(6):502-15. doi: 10.1002/gepi.21835. Epub 2014 Jul 15.

PMID:
25043967
[PubMed - indexed for MEDLINE]
Free Article
10.

Weighted Interaction SNP Hub (WISH) network method for building genetic networks for complex diseases and traits using whole genome genotype data.

Kogelman LJ, Kadarmideen HN.

BMC Syst Biol. 2014;8 Suppl 2:S5. doi: 10.1186/1752-0509-8-S2-S5. Epub 2014 Mar 13.

PMID:
25032480
[PubMed - in process]
Free PMC Article
11.

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease.

Ramirez A, van der Flier WM, Herold C, Ramonet D, Heilmann S, Lewczuk P, Popp J, Lacour A, Drichel D, Louwersheimer E, Kummer MP, Cruchaga C, Hoffmann P, Teunissen C, Holstege H, Kornhuber J, Peters O, Naj AC, Chouraki V, Bellenguez C, Gerrish A; International Genomics of Alzheimer's Project (IGAP); Alzheimer's Disease Neuroimaging Initiative (ADNI), Heun R, Frölich L, Hüll M, Buscemi L, Herms S, Kölsch H, Scheltens P, Breteler MM, Rüther E, Wiltfang J, Goate A, Jessen F, Maier W, Heneka MT, Becker T, Nöthen MM.

Hum Mol Genet. 2014 Jul 15. pii: ddu372. [Epub ahead of print]

PMID:
25027320
[PubMed - as supplied by publisher]
12.

Genome-wide association identifies regulatory Loci associated with distinct local histogram emphysema patterns.

Castaldi PJ, Cho MH, San José Estépar R, McDonald ML, Laird N, Beaty TH, Washko G, Crapo JD, Silverman EK; COPDGene Investigators.

Am J Respir Crit Care Med. 2014 Aug 15;190(4):399-409. doi: 10.1164/rccm.201403-0569OC.

PMID:
25006744
[PubMed - indexed for MEDLINE]
13.

Genetic loci associated with changes in lipid levels leading to constitution-based discrepancy in Koreans.

Chung SK, Yu H, Park AY, Kim JY, Cha S.

BMC Complement Altern Med. 2014 Jul 9;14:230. doi: 10.1186/1472-6882-14-230.

PMID:
25005712
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Epigenomic analysis of primary human T cells reveals enhancers associated with TH2 memory cell differentiation and asthma susceptibility.

Seumois G, Chavez L, Gerasimova A, Lienhard M, Omran N, Kalinke L, Vedanayagam M, Ganesan AP, Chawla A, Djukanović R, Ansel KM, Peters B, Rao A, Vijayanand P.

Nat Immunol. 2014 Aug;15(8):777-88. doi: 10.1038/ni.2937. Epub 2014 Jul 6.

PMID:
24997565
[PubMed - indexed for MEDLINE]
15.

Utility of large consanguineous family-based model for investigating the genetics of type 2 diabetes mellitus.

Al-Sinani S, Hassan MO, Zadjali F, Al-Yahyaee S, Albarwani S, Rizvi S, Jaju D, Comuzzie A, Voruganti VS, Bayoumi R.

Gene. 2014 Sep 10;548(1):22-8. doi: 10.1016/j.gene.2014.06.053. Epub 2014 Jun 30.

PMID:
24993573
[PubMed - indexed for MEDLINE]
16.

Identification of a melanoma susceptibility locus and somatic mutation in TET2.

Song F, Amos CI, Lee JE, Lian CG, Fang S, Liu H, MacGregor S, Iles MM, Law MH, Lindeman NI, Montgomery GW, Duffy DL, Cust AE, Jenkins MA, Whiteman DC, Kefford RF, Giles GG, Armstrong BK, Aitken JF, Hopper JL, Brown KM, Martin NG, Mann GJ, Bishop DT, Bishop JA; GenoMEL consortium, Kraft P, Qureshi AA, Kanetsky PA, Hayward NK, Hunter DJ, Wei Q, Han J.

Carcinogenesis. 2014 Sep;35(9):2097-101. doi: 10.1093/carcin/bgu140. Epub 2014 Jun 30.

PMID:
24980573
[PubMed - indexed for MEDLINE]
17.

Polymorphism of the cystatin C gene in patients with acute coronary syndromes: Results from the PLATelet inhibition and patient Outcomes study.

Akerblom A, Eriksson N, Wallentin L, Siegbahn A, Barratt BJ, Becker RC, Budaj A, Himmelmann A, Husted S, Storey RF, Johansson A, James SK; PLATO Investigators.

Am Heart J. 2014 Jul;168(1):96-102.e2. doi: 10.1016/j.ahj.2014.03.010. Epub 2014 Apr 4.

PMID:
24952865
[PubMed - indexed for MEDLINE]
18.

C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysis.

Diekstra FP, Van Deerlin VM, van Swieten JC, Al-Chalabi A, Ludolph AC, Weishaupt JH, Hardiman O, Landers JE, Brown RH Jr, van Es MA, Pasterkamp RJ, Koppers M, Andersen PM, Estrada K, Rivadeneira F, Hofman A, Uitterlinden AG, van Damme P, Melki J, Meininger V, Shatunov A, Shaw CE, Leigh PN, Shaw PJ, Morrison KE, Fogh I, Chiò A, Traynor BJ, Czell D, Weber M, Heutink P, de Bakker PI, Silani V, Robberecht W, van den Berg LH, Veldink JH.

Ann Neurol. 2014 Jul;76(1):120-33. doi: 10.1002/ana.24198. Epub 2014 Jun 27.

PMID:
24931836
[PubMed - indexed for MEDLINE]
19.

Genome-wide SNP analysis reveals a genetic basis for sea-age variation in a wild population of Atlantic salmon (Salmo salar).

Johnston SE, Orell P, Pritchard VL, Kent MP, Lien S, Niemelä E, Erkinaro J, Primmer CR.

Mol Ecol. 2014 Jul;23(14):3452-68. doi: 10.1111/mec.12832.

PMID:
24931807
[PubMed - indexed for MEDLINE]
20.

Genome-wide association analysis identifies six new loci associated with forced vital capacity.

Loth DW, Artigas MS, Gharib SA, Wain LV, Franceschini N, Koch B, Pottinger TD, Smith AV, Duan Q, Oldmeadow C, Lee MK, Strachan DP, James AL, Huffman JE, Vitart V, Ramasamy A, Wareham NJ, Kaprio J, Wang XQ, Trochet H, Kähönen M, Flexeder C, Albrecht E, Lopez LM, de Jong K, Thyagarajan B, Alves AC, Enroth S, Omenaas E, Joshi PK, Fall T, Viñuela A, Launer LJ, Loehr LR, Fornage M, Li G, Wilk JB, Tang W, Manichaikul A, Lahousse L, Harris TB, North KE, Rudnicka AR, Hui J, Gu X, Lumley T, Wright AF, Hastie ND, Campbell S, Kumar R, Pin I, Scott RA, Pietiläinen KH, Surakka I, Liu Y, Holliday EG, Schulz H, Heinrich J, Davies G, Vonk JM, Wojczynski M, Pouta A, Johansson A, Wild SH, Ingelsson E, Rivadeneira F, Völzke H, Hysi PG, Eiriksdottir G, Morrison AC, Rotter JI, Gao W, Postma DS, White WB, Rich SS, Hofman A, Aspelund T, Couper D, Smith LJ, Psaty BM, Lohman K, Burchard EG, Uitterlinden AG, Garcia M, Joubert BR, McArdle WL, Musk AB, Hansel N, Heckbert SR, Zgaga L, van Meurs JB, Navarro P, Rudan I, Oh YM, Redline S, Jarvis DL, Zhao JH, Rantanen T, O'Connor GT, Ripatti S, Scott RJ, Karrasch S, Grallert H, Gaddis NC, Starr JM, Wijmenga C, Minster RL, Lederer DJ, Pekkanen J, Gyllensten U, Campbell H, Morris AP, Gläser S, Hammond CJ, Burkart KM, Beilby J, Kritchevsky SB, Gudnason V, Hancock DB, Williams OD, Polasek O, Zemunik T, Kolcic I, Petrini MF, Wjst M, Kim WJ, Porteous DJ, Scotland G, Smith BH, Viljanen A, Heliövaara M, Attia JR, Sayers I, Hampel R, Gieger C, Deary IJ, Boezen HM, Newman A, Jarvelin MR, Wilson JF, Lind L, Stricker BH, Teumer A, Spector TD, Melén E, Peters MJ, Lange LA, Barr RG, Bracke KR, Verhamme FM, Sung J, Hiemstra PS, Cassano PA, Sood A, Hayward C, Dupuis J, Hall IP, Brusselle GG, Tobin MD, London SJ.

Nat Genet. 2014 Jul;46(7):669-77. doi: 10.1038/ng.3011. Epub 2014 Jun 15.

PMID:
24929828
[PubMed - indexed for MEDLINE]
Free PMC Article

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