Mads Vilhelm Hollegaard · researcher · YYNN

Mads Vilhelm Hollegaard

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researcher

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Works
8

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

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

scientific article

Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight

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

scientific article published on 13 June 2013

The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome

Polymorphisms in the tumor necrosis factor alpha and interleukin 1-beta promoters with possible gene regulatory functions increase the risk of preterm birth

The Prevalence of Mutations inKCNQ1, KCNH2,andSCN5Ain an Unselected National Cohort of Young Sudden Unexplained Death Cases

article by BO GREGERS WINKEL et al published 6 August 2012 in Journal of Cardiovascular Electrophysiology

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

scientific article published on February 2013

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