Hollegaard MV - Search Results

1

Mannose-binding lectin gene, MBL2, polymorphisms are not associated with susceptibility to invasive pneumococcal disease in children.

Lundbo LF, Harboe ZB, Clausen LN, Hollegaard MV, Sørensen HT, Hougaard DM, Konradsen HB, Nørgaard M, Benfield T. Lundbo LF, et al. Among authors: hollegaard mv. Clin Infect Dis. 2014 Aug 15;59(4):e66-71. doi: 10.1093/cid/ciu276. Epub 2014 Apr 24. Clin Infect Dis. 2014. PMID: 24771334

2

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

Hollegaard MV, Skogstrand K, Thorsen P, Nørgaard-Pedersen B, Hougaard DM, Grove J. Hollegaard MV, et al. Hum Mutat. 2013 Jan;34(1):143-8. doi: 10.1002/humu.22173. Epub 2012 Sep 4. Hum Mutat. 2013. PMID: 22837141

3

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

Hollegaard MV, Grove J, Thorsen P, Wang X, Mandrup S, Christiansen M, Norgaard-Pedersen B, Wojdemann KR, Tabor A, Attermann J, Hougaard DM. Hollegaard MV, et al. Acta Obstet Gynecol Scand. 2008;87(12):1285-90. doi: 10.1080/00016340802468340. Acta Obstet Gynecol Scand. 2008. PMID: 18951205 Free article.

4

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

Hollegaard MV, Thorsen P, Norgaard-Pedersen B, Hougaard DM. Hollegaard MV, et al. Electrophoresis. 2009 Jul;30(14):2532-5. doi: 10.1002/elps.200800655. Electrophoresis. 2009. PMID: 19639574

5

Polymorphisms in the promoter region of relaxin-2 and preterm birth: involvement of relaxin in the etiology of preterm birth.

Vogel I, Hollegaard MV, Hougaard DM, Thorsen P, Grove J. Vogel I, et al. Among authors: hollegaard mv. In Vivo. 2009 Nov-Dec;23(6):1005-9. In Vivo. 2009. PMID: 20023247 Free article.

6

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

Hollegaard MV, Grauholm J, Nørgaard-Pedersen B, Hougaard DM. Hollegaard MV, et al. Mol Genet Metab. 2013 Apr;108(4):225-31. doi: 10.1016/j.ymgme.2013.01.016. Epub 2013 Feb 1. Mol Genet Metab. 2013. PMID: 23422032

7

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

Hollegaard MV, Grauholm J, Nielsen R, Grove J, Mandrup S, Hougaard DM. Hollegaard MV, et al. Mol Genet Metab. 2013 Sep-Oct;110(1-2):65-72. doi: 10.1016/j.ymgme.2013.06.004. Epub 2013 Jun 13. Mol Genet Metab. 2013. PMID: 23830478

8

Extreme neonatal hyperbilirubinemia and a specific genotype: a population-based case-control study.

Petersen JP, Henriksen TB, Hollegaard MV, Vandborg PK, Hougaard DM, Thorlacius-Ussing O, Ebbesen F. Petersen JP, et al. Among authors: hollegaard mv. Pediatrics. 2014 Sep;134(3):510-5. doi: 10.1542/peds.2014-0035. Epub 2014 Aug 4. Pediatrics. 2014. PMID: 25092941

9

UGT1A1*28 Genotypes and Respiratory Disease in Very Preterm Infants: A Cohort Study.

Petersen JP, Ebbesen F, Hollegaard MV, Andersson S, Hougaard DM, Thorlacius-Ussing O, Henriksen TB. Petersen JP, et al. Among authors: hollegaard mv. Neonatology. 2016;109(2):124-9. doi: 10.1159/000442042. Epub 2015 Dec 15. Neonatology. 2016. PMID: 26666247 Free article.

10

Elevated polygenic burden for autism is associated with differential DNA methylation at birth.

Hannon E, Schendel D, Ladd-Acosta C, Grove J; iPSYCH-Broad ASD Group; Hansen CS, Andrews SV, Hougaard DM, Bresnahan M, Mors O, Hollegaard MV, Bækvad-Hansen M, Hornig M, Mortensen PB, Børglum AD, Werge T, Pedersen MG, Nordentoft M, Buxbaum J, Daniele Fallin M, Bybjerg-Grauholm J, Reichenberg A, Mill J. Hannon E, et al. Among authors: hollegaard mv. Genome Med. 2018 Mar 28;10(1):19. doi: 10.1186/s13073-018-0527-4. Genome Med. 2018. PMID: 29587883 Free PMC article.

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