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Items: 1 to 20 of 52

1.

Identification of genetic variants influencing the human plasma proteome.

Johansson Å, Enroth S, Palmblad M, Deelder AM, Bergquist J, Gyllensten U.

Proc Natl Acad Sci U S A. 2013 Mar 19;110(12):4673-8. doi: 10.1073/pnas.1217238110. Epub 2013 Mar 4.

2.

Identification of cis-regulatory variation influencing protein abundance levels in human plasma.

Lourdusamy A, Newhouse S, Lunnon K, Proitsi P, Powell J, Hodges A, Nelson SK, Stewart A, Williams S, Kloszewska I, Mecocci P, Soininen H, Tsolaki M, Vellas B, Lovestone S; AddNeuroMed Consortium, Dobson R; Alzheimer's Disease Neuroimaging Initiative.

Hum Mol Genet. 2012 Aug 15;21(16):3719-26. Epub 2012 May 16.

3.

Identification of a late onset Alzheimer's disease candidate risk variant at 9q21.33 in Polish patients.

Gaj P, Paziewska A, Bik W, Dąbrowska M, Baranowska-Bik A, Styczynska M, Chodakowska-Żebrowska M, Pfeffer-Baczuk A, Barcikowska M, Baranowska B, Ostrowski J.

J Alzheimers Dis. 2012;32(1):157-68.

PMID:
22785395
4.

Genetic variation and human longevity.

Soerensen M.

Dan Med J. 2012 May;59(5):B4454.

PMID:
22549493
5.

Quantitative trait loci mapping of the mouse plasma proteome (pQTL).

Holdt LM, von Delft A, Nicolaou A, Baumann S, Kostrzewa M, Thiery J, Teupser D.

Genetics. 2013 Feb;193(2):601-8. doi: 10.1534/genetics.112.143354. Epub 2012 Nov 19.

6.
7.

Mining the LIPG allelic spectrum reveals the contribution of rare and common regulatory variants to HDL cholesterol.

Khetarpal SA, Edmondson AC, Raghavan A, Neeli H, Jin W, Badellino KO, Demissie S, Manning AK, DerOhannessian SL, Wolfe ML, Cupples LA, Li M, Kathiresan S, Rader DJ.

PLoS Genet. 2011 Dec;7(12):e1002393. doi: 10.1371/journal.pgen.1002393. Epub 2011 Dec 8.

8.

Targeted proteomics of low-level proteins in human plasma by LC/MSn: using human growth hormone as a model system.

Wu SL, Amato H, Biringer R, Choudhary G, Shieh P, Hancock WS.

J Proteome Res. 2002 Sep-Oct;1(5):459-65.

PMID:
12645918
9.

Proteome-wide analysis of disease-associated SNPs that show allele-specific transcription factor binding.

Butter F, Davison L, Viturawong T, Scheibe M, Vermeulen M, Todd JA, Mann M.

PLoS Genet. 2012 Sep;8(9):e1002982. doi: 10.1371/journal.pgen.1002982. Epub 2012 Sep 27.

10.

Next-generation DNA sequencing-based assay for measuring allelic expression imbalance (AEI) of candidate neuropsychiatric disorder genes in human brain.

Xu X, Wang H, Zhu M, Sun Y, Tao Y, He Q, Wang J, Chen L, Saffen D.

BMC Genomics. 2011 Oct 20;12:518. doi: 10.1186/1471-2164-12-518.

11.

Impact of SORL1 single nucleotide polymorphisms on Alzheimer's disease cerebrospinal fluid markers.

Alexopoulos P, Guo LH, Kratzer M, Westerteicher C, Kurz A, Perneczky R.

Dement Geriatr Cogn Disord. 2011;32(3):164-70. doi: 10.1159/000332017. Epub 2011 Oct 13.

12.

Genetic profiling using genome-wide significant coronary artery disease risk variants does not improve the prediction of subclinical atherosclerosis: the Cardiovascular Risk in Young Finns Study, the Bogalusa Heart Study and the Health 2000 Survey--a meta-analysis of three independent studies.

Hernesniemi JA, Seppälä I, Lyytikäinen LP, Mononen N, Oksala N, Hutri-Kähönen N, Juonala M, Taittonen L, Smith EN, Schork NJ, Chen W, Srinivasan SR, Berenson GS, Murray SS, Laitinen T, Jula A, Kettunen J, Ripatti S, Laaksonen R, Viikari J, Kähönen M, Raitakari OT, Lehtimäki T.

PLoS One. 2012;7(1):e28931. doi: 10.1371/journal.pone.0028931. Epub 2012 Jan 25.

13.

Isotope coded protein label quantification of serum proteins--comparison with the label-free LC-MS and validation using the MRM approach.

Turtoi A, Mazzucchelli GD, De Pauw E.

Talanta. 2010 Feb 15;80(4):1487-95. doi: 10.1016/j.talanta.2009.07.035. Epub 2009 Jul 25.

PMID:
20082806
14.

Data mining of high density genomic variant data for prediction of Alzheimer's disease risk.

Briones N, Dinu V.

BMC Med Genet. 2012 Jan 25;13:7. doi: 10.1186/1471-2350-13-7.

15.

Clinical implications of old and new genes for open-angle glaucoma.

Ramdas WD, van Koolwijk LM, Cree AJ, Janssens AC, Amin N, de Jong PT, Wolfs RC, Gibson J, Kirwan JF, Hofman A, Rivadeneira F, Oostra BA, Uitterlinden AG, Ennis S, Lotery AJ, Lemij HG, Klaver CC, Vingerling JR, Jansonius NM, van Duijn CM.

Ophthalmology. 2011 Dec;118(12):2389-97. doi: 10.1016/j.ophtha.2011.05.040. Epub 2011 Aug 27.

PMID:
21872936
16.

Mapping of numerous disease-associated expression polymorphisms in primary peripheral blood CD4+ lymphocytes.

Murphy A, Chu JH, Xu M, Carey VJ, Lazarus R, Liu A, Szefler SJ, Strunk R, Demuth K, Castro M, Hansel NN, Diette GB, Vonakis BM, Adkinson NF Jr, Klanderman BJ, Senter-Sylvia J, Ziniti J, Lange C, Pastinen T, Raby BA.

Hum Mol Genet. 2010 Dec 1;19(23):4745-57. doi: 10.1093/hmg/ddq392. Epub 2010 Sep 10.

17.

Powerful identification of cis-regulatory SNPs in human primary monocytes using allele-specific gene expression.

Almlöf JC, Lundmark P, Lundmark A, Ge B, Maouche S, Göring HH, Liljedahl U, Enström C, Brocheton J, Proust C, Godefroy T, Sambrook JG, Jolley J, Crisp-Hihn A, Foad N, Lloyd-Jones H, Stephens J, Gwilliam R, Rice CM, Hengstenberg C, Samani NJ, Erdmann J, Schunkert H, Pastinen T, Deloukas P, Goodall AH, Ouwehand WH, Cambien F, Syvänen AC.

PLoS One. 2012;7(12):e52260. doi: 10.1371/journal.pone.0052260. Epub 2012 Dec 26.

18.

Genome-wide scan on total serum IgE levels identifies FCER1A as novel susceptibility locus.

Weidinger S, Gieger C, Rodriguez E, Baurecht H, Mempel M, Klopp N, Gohlke H, Wagenpfeil S, Ollert M, Ring J, Behrendt H, Heinrich J, Novak N, Bieber T, Krämer U, Berdel D, von Berg A, Bauer CP, Herbarth O, Koletzko S, Prokisch H, Mehta D, Meitinger T, Depner M, von Mutius E, Liang L, Moffatt M, Cookson W, Kabesch M, Wichmann HE, Illig T.

PLoS Genet. 2008 Aug;4(8):e1000166. doi: 10.1371/journal.pgen.1000166. Epub 2008 Aug 22.

19.

Targeted screening of cis-regulatory variation in human haplotypes.

Verlaan DJ, Ge B, Grundberg E, Hoberman R, Lam KC, Koka V, Dias J, Gurd S, Martin NW, Mallmin H, Nilsson O, Harmsen E, Dewar K, Kwan T, Pastinen T.

Genome Res. 2009 Jan;19(1):118-27. doi: 10.1101/gr.084798.108. Epub 2008 Oct 29.

20.

Investigating diversity in human plasma proteins.

Nedelkov D, Kiernan UA, Niederkofler EE, Tubbs KA, Nelson RW.

Proc Natl Acad Sci U S A. 2005 Aug 2;102(31):10852-7. Epub 2005 Jul 25.

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