(Q38395767)

2 September 2017

title

Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing (English)

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2 September 2017

main subject

whole genome sequencing

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5

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2 September 2017

Jonas Bybjerg-Grauholm

object named as

Jonas Grauholm

2

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Mads Vilhelm Hollegaard

object named as

Mads Vilhelm Hollegaard

1

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Jakob Grove

object named as

Jakob Grove

4

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author name string

Ronni Nielsen

3

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2 September 2017

David Michael Hougaard

6

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2 September 2017

publication date

13 June 2013

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Molecular Genetics and Metabolism

2 September 2017

published in

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2 September 2017

volume

110

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2 September 2017

issue

1-2

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2 September 2017

page(s)

65-72

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

2 September 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.004

High-throughput genotyping on archived dried blood spot samples

7 January 2021

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Genotyping whole-genome-amplified DNA from 3- to 25-year-old neonatal dried blood spot samples with reference to fresh genomic DNA.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.004

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7 January 2021

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Phenylketonuria screening registry as a resource for population genetic studies

7 January 2021

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Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.004

Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YMGME.2013.06.004

Joint analysis of SNPs and proteins identifies regulatory IL18 gene variations decreasing the chance of spastic cerebral palsy

7 January 2021

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Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study

7 January 2021

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CACNA1C (rs1006737) is associated with schizophrenia

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Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe.

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Common variants conferring risk of schizophrenia

7 January 2021

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Common variants at VRK2 and TCF4 conferring risk of schizophrenia

7 January 2021

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New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism

7 January 2021

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Expanding the range of ZNF804A variants conferring risk of psychosis

7 January 2021

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Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis

7 January 2021

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Assessing the accuracy and power of population genetic inference from low-pass next-generation sequencing data

7 January 2021

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Simultaneous measurement of 25 inflammatory markers and neurotrophins in neonatal dried blood spots by immunoassay with xMAP technology

7 January 2021

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Acquiring genome-wide gene expression profiles in Guthrie card blood spots using microarrays

7 January 2021

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DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study

7 January 2021

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Archived Guthrie blood spots as a novel source for quantitative DNA methylation analysis.

7 January 2021

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7 January 2021

Identifiers

DOI

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2 September 2017

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