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Items: 12

1.

Governing the research-care divide in clinical biobanking: Dutch perspectives.

Boeckhout M, Douglas CM.

Life Sci Soc Policy. 2015;11:7. doi: 10.1186/s40504-015-0025-z. Epub 2015 Aug 6. Review.

2.

Superparamagnetic-bead Based Method: An Effective DNA Extraction from Dried Blood Spots (DBS) for Diagnostic PCR.

Sirdah MM.

J Clin Diagn Res. 2014 Apr;8(4):FC01-4. doi: 10.7860/JCDR/2014/8171.4226. Epub 2014 Apr 15.

3.

High quality genome-wide genotyping from archived dried blood spots without DNA amplification.

St Julien KR, Jelliffe-Pawlowski LL, Shaw GM, Stevenson DK, O'Brodovich HM, Krasnow MA; Stanford BPD Study Group.

PLoS One. 2013 May 30;8(5):e64710. doi: 10.1371/journal.pone.0064710. Print 2013.

4.

Visual automated fluorescence electrophoresis provides simultaneous quality, quantity, and molecular weight spectra for genomic DNA from archived neonatal blood spots.

Klassen TL, Drabek J, Tomson T, Sveinsson O, von Döbeln U, Noebels JL, Goldman AM.

J Mol Diagn. 2013 May;15(3):283-90. doi: 10.1016/j.jmoldx.2013.01.003. Epub 2013 Mar 19.

5.

A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).

Enciso-Mora V, Broderick P, Ma Y, Jarrett RF, Hjalgrim H, Hemminki K, van den Berg A, Olver B, Lloyd A, Dobbins SE, Lightfoot T, van Leeuwen FE, Försti A, Diepstra A, Broeks A, Vijayakrishnan J, Shield L, Lake A, Montgomery D, Roman E, Engert A, von Strandmann EP, Reiners KS, Nolte IM, Smedby KE, Adami HO, Russell NS, Glimelius B, Hamilton-Dutoit S, de Bruin M, Ryder LP, Molin D, Sorensen KM, Chang ET, Taylor M, Cooke R, Hofstra R, Westers H, van Wezel T, van Eijk R, Ashworth A, Rostgaard K, Melbye M, Swerdlow AJ, Houlston RS.

Nat Genet. 2010 Dec;42(12):1126-1130. doi: 10.1038/ng.696. Epub 2010 Oct 31.

6.

Assessing the utility of whole-genome amplified serum DNA for array-based high throughput genotyping.

Bucasas KL, Pandya GA, Pradhan S, Fleischmann RD, Peterson SN, Belmont JW.

BMC Genet. 2009 Dec 18;10:85. doi: 10.1186/1471-2156-10-85.

7.

Whole genome microarray analysis, from neonatal blood cards.

Hardin J, Finnell RH, Wong D, Hogan ME, Horovitz J, Shu J, Shaw GM.

BMC Genet. 2009 Jul 22;10:38. doi: 10.1186/1471-2156-10-38.

8.

Genome-wide scans using archived neonatal dried blood spot samples.

Hollegaard MV, Grauholm J, Børglum A, Nyegaard M, Nørgaard-Pedersen B, Ørntoft T, Mortensen PB, Wiuf C, Mors O, Didriksen M, Thorsen P, Hougaard DM.

BMC Genomics. 2009 Jul 4;10:297. doi: 10.1186/1471-2164-10-297.

9.

The Spanish HIV BioBank: a model of cooperative HIV research.

García-Merino I, de Las Cuevas N, Jiménez JL, Gallego J, Gómez C, Prieto C, Serramía MJ, Lorente R, Muñoz-Fernández MA; Spanish HIV BioBank.

Retrovirology. 2009 Mar 9;6:27. doi: 10.1186/1742-4690-6-27.

10.

Archived unfrozen neonatal blood spots are amenable to quantitative gene expression analysis.

Haak PT, Busik JV, Kort EJ, Tikhonenko M, Paneth N, Resau JH.

Neonatology. 2009;95(3):210-6. doi: 10.1159/000155652. Epub 2008 Sep 18.

11.

Multiple strand displacement amplification of mitochondrial DNA from clinical samples.

Maragh S, Jakupciak JP, Wagner PD, Rom WN, Sidransky D, Srivastava S, O'Connell CD.

BMC Med Genet. 2008 Feb 7;9:7. doi: 10.1186/1471-2350-9-7.

12.

Production of in vitro amplified DNA pseudolibraries and high-throughput cDNA target amplification.

Frey D, Kambach C, Steinmetz MO, Jaussi R.

BMC Biotechnol. 2007 Jun 12;7:31.

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