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M. Hollegaard · SciRah

Researcher profile · Semantic Scholar

M. Hollegaard

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M. Hollegaard — researcher profile on SciRah

h-index: 32
Works: 68
Citations: 19K

Most-cited papers

Biological Insights From 108 Schizophrenia-Associated Genetic Loci
S. Ripke, B. Neale, A. Corvin, J. Walters +296 more
2014Nature7,486 citations Open access
Semantic Scholar
Identification of common genetic risk variants for autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +272 more
2019Nature Genetics2,146 citations Open access
Semantic Scholar
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
F. Satterstrom, Jack A. Kosmicki, Jiebiao Wang, M. Breen +186 more
2019Cell2,103 citations Open access
Semantic Scholar
Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder
D. Demontis, R. Walters, Joanna Martin, M. Mattheisen +217 more
2018Nature Genetics1,852 citations Open access
Semantic Scholar
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium
C. Marshall, D. Howrigan, D. Merico, B. Thiruvahindrapuram +265 more
2016bioRxiv1,294 citations Open access
Semantic Scholar
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes
D. Ruderfer, S. Ripke, A. McQuillin, J. Boocock +496 more
2018Cell675 citations Open access
Semantic Scholar
Genome-wide associations for birth weight and correlations with adult disease
M. Horikoshi, R. Beaumont, F. Day, Nicole M. Warrington +159 more
2016Nature462 citations Open access
Semantic Scholar
Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
E. Robinson, B. St Pourcain, V. Anttila, Jack A. Kosmicki +18 more
2015Nature Genetics402 citations Open access
Semantic Scholar
New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism
M. Horikoshi, H. Yaghootkar, Dennis O. Mook-Kanamori, U. Sovio +144 more
2012Nature Genetics331 citations Open access
Semantic Scholar
Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis.
E. Agerbo, P. Sullivan, B. Vilhjálmsson, C. Pedersen +9 more
2015JAMA psychiatry273 citations Open access
Semantic Scholar
Cytokine gene polymorphism in human disease: on-line databases, Supplement 3
M. Hollegaard, J. L. Bidwell
2006Genes and Immunity259 citations Open access
Semantic Scholar
An epigenetic clock for gestational age at birth based on blood methylation data
A. Knight, J. Craig, C. Theda, M. Bækvad-Hansen +43 more
2016Genome Biology244 citations Open access
Semantic Scholar
Discovery of the first genome-wide significant risk loci for ADHD
D. Demontis, R. Walters, Joanna Martin, M. Mattheisen +67 more
2017bioRxiv231 citations Open access
Semantic Scholar
Common variants associated with general and MMR vaccine-related febrile seizures
B. Feenstra, B. Pasternak, F. Geller, L. Carstensen +11 more
2014Nature Genetics144 citations Open access
Semantic Scholar
ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social-communication difficulties
B. St Pourcain, E. Robinson, V. Anttila, Brendan Bulik Sullivan +19 more
2017Molecular Psychiatry133 citations Open access
Semantic Scholar
Common Variant at 16p11.2 Conferring Risk of Psychosis
S. Steinberg, S. de Jong, M. Mattheisen, J. Costas +127 more
2012Molecular Psychiatry111 citations Open access
Semantic Scholar
Genome-wide association analyses identify variants in developmental genes associated with hypospadias
F. Geller, B. Feenstra, L. Carstensen, T. Pers +15 more
2014Nature Genetics110 citations Open access
Semantic Scholar
Common risk variants identified in autism spectrum disorder
J. Grove, S. Ripke, T. Als, M. Mattheisen +71 more
2017bioRxiv105 citations Open access
Semantic Scholar
Elevated polygenic burden for autism is associated with differential DNA methylation at birth
E. Hannon, D. Schendel, C. Ladd-Acosta, J. Grove +18 more
2018Genome Medicine100 citations Open access
Semantic Scholar
Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source
M. Hollegaard, J. Grove, Jonas Grauholm, E. Kreiner-Møller +13 more
2011BMC Genetics83 citations Open access
Semantic Scholar
The Prevalence of Mutations in KCNQ1, KCNH2, and SCN5A in an Unselected National Cohort of Young Sudden Unexplained Death Cases
B. Winkel, M. K. Larsen, K. Berge, T. Leren +13 more
2012Cardiovascular Electrophysiology80 citations
Semantic Scholar
High loading of polygenic risk in cases with chronic schizophrenia
S. Meier, E. Agerbo, R. Maier, C. Pedersen +20 more
2016Molecular Psychiatry72 citations
Semantic Scholar
Archived neonatal dried blood spot samples can be used for accurate whole genome and exome-targeted next-generation sequencing.
M. Hollegaard, Jonas Grauholm, R. Nielsen, J. Grove +2 more
2013Molecular Genetics and Metabolism69 citations
Semantic Scholar
Synopsis of Preterm Birth Genetic Association Studies: The Preterm Birth Genetics Knowledge Base (PTBGene)
S. Dolan, M. Hollegaard, M. Merialdi, A. Betrán +12 more
2010Public Health Genomics64 citations Open access
Semantic Scholar
DNA methylome profiling using neonatal dried blood spot samples: a proof-of-principle study.
M. Hollegaard, Jonas Grauholm, B. Nørgaard-Pedersen, D. Hougaard
2013Molecular Genetics and Metabolism57 citations
Semantic Scholar
Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight
E. Hannon, D. Schendel, C. Ladd-Acosta, J. Grove +17 more
2019Philosophical Transactions of the Royal Society of London. Biological Sciences56 citations Open access
Semantic Scholar
DNA Methylation at the Neonatal State and at the Time of Diagnosis: Preliminary Support for an Association with the Estrogen Receptor 1, Gamma-Aminobutyric Acid B Receptor 1, and Myelin Oligodendrocyte Glycoprotein in Female Adolescent Patients with OCD
J. Nissen, C. Hansen, A. Starnawska, M. Mattheisen +3 more
2016Frontiers in Psychiatry45 citations Open access
Semantic Scholar
Genotyping whole‐genome‐amplified DNA from 3‐ to 25‐year‐old neonatal dried blood spot samples with reference to fresh genomic DNA
M. Hollegaard, P. Thorsen, B. Nørgaard-Pedersen, D. Hougaard
2009Electrophoresis43 citations
Semantic Scholar
High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA
J. Poulsen, F. Lescai, J. Grove, M. Bækvad-Hansen +16 more
2016PLoS ONE41 citations Open access
Semantic Scholar
High-Throughput Genotyping on Archived Dried Blood Spot Samples
M. Hollegaard, J. Grove, P. Thorsen, B. Nørgaard-Pedersen +1 more
2009Genetic Testing and Molecular Biomarkers41 citations
Semantic Scholar
Common Variants near MBNL1 and NKX2-5 are Associated with Infantile Hypertrophic Pyloric Stenosis
B. Feenstra, F. Geller, C. Krogh, M. Hollegaard +5 more
2012Nature Genetics40 citations Open access
Semantic Scholar
Polymorphisms in the tumor necrosis factor alpha and interleukin 1‐beta promoters with possible gene regulatory functions increase the risk of preterm birth
M. Hollegaard, J. Grove, P. Thorsen, Xiao-Bin Wang +7 more
2008Acta Obstetricia et Gynecologica Scandinavica39 citations
Semantic Scholar
Modelling the contribution of family history and variation in single nucleotide polymorphisms to risk of schizophrenia: a Danish national birth cohort-based study.
E. Agerbo, P. Mortensen, C. Wiuf, M. S. Pedersen +6 more
2012Schizophrenia Research36 citations
Semantic Scholar
Age at first birth in women is genetically associated with increased risk of schizophrenia
G. Ni, J. Gratten, N. Wray, Sang-Hong Lee +297 more
2017Scientific Reports25 citations Open access
Semantic Scholar
The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome.
B. Winkel, L. Yuan, M. Olesen, G. Sadjadieh +8 more
2015Heart Rhythm24 citations
Semantic Scholar
Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia.
A. Forstner, F. Basmanav, M. Mattheisen, A. Böhmer +22 more
2014Journal of Psychiatry & Neuroscience23 citations Open access
Semantic Scholar
CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma
A. Dahlin, M. Hollegaard, C. Wibom, U. Andersson +4 more
2015Journal of Neuro-Oncology22 citations Open access
Semantic Scholar
Genetic Variation in NFKBIE Is Associated With Increased Risk of Pneumococcal Meningitis in Children
L. F. Lundbo, Z. Harboe, L. Clausen, M. Hollegaard +5 more
2015EBioMedicine20 citations Open access
Semantic Scholar
Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank.
Jonas Grauholm, S. Khoo, R. Nickolov, J. Poulsen +4 more
2015Molecular Genetics and Metabolism20 citations
Semantic Scholar
Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis
B. Winkel, M. Hollegaard, M. Olesen, J. Svendsen +3 more
2011BMC Medical Genetics20 citations Open access
Semantic Scholar
RNA sequencing of archived neonatal dried blood spots
J. Bybjerg-Grauholm, C. Hagen, S. Khoo, Maria Louise Johannesen +5 more
2016Molecular Genetics and Metabolism Reports17 citations Open access
Semantic Scholar
Replication study and meta-analysis in European samples supports association of the 3p21.1 locus with bipolar disorder.
E. Vassos, S. Steinberg, S. Cichon, G. Breen +43 more
2012Biological Psychiatry17 citations Open access
Semantic Scholar
Joint Analysis of SNPs and Proteins Identifies Regulatory IL18 Gene Variations Decreasing the Chance of Spastic Cerebral Palsy
M. Hollegaard, K. Skogstrand, P. Thorsen, B. Nørgaard-Pedersen +2 more
2013Human Mutation16 citations Open access
Semantic Scholar
A population-based association study of glutamate decarboxylase 1 as a candidate gene for autism
H. Buttenschøn, M. B. Lauritsen, Agata El Daoud, M. Hollegaard +6 more
2009Journal of neural transmission16 citations
Semantic Scholar
Mannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish Children
L. F. Lundbo, H. Sørensen, L. Clausen, M. Hollegaard +5 more
2015Open Forum Infectious Diseases15 citations Open access
Semantic Scholar
Mannose-binding lectin gene, MBL2, polymorphisms are not associated with susceptibility to invasive pneumococcal disease in children.
L. F. Lundbo, Z. Harboe, L. Clausen, M. Hollegaard +5 more
2014Clinical Infectious Diseases15 citations
Semantic Scholar
Whole genome amplification and genetic analysis after extraction of proteins from dried blood spots.
M. Hollegaard, K. Sorensen, H. Petersen, Maria B Arnardottir +3 more
2007Clinical Chemistry14 citations
Semantic Scholar
Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality
M. Bækvad-Hansen, J. Bybjerg-Grauholm, J. Poulsen, Christine S. Hansen +2 more
2017Molecular Genetics and Metabolism Reports13 citations Open access
Semantic Scholar
Risk of schizophrenia in relation to parental origin and genome-wide divergence
C. Pedersen, D. Demontis, M. S. Pedersen, E. Agerbo +6 more
2011Psychological Medicine13 citations Open access
Semantic Scholar
Polymorphisms in the promoter region of relaxin-2 and preterm birth: involvement of relaxin in the etiology of preterm birth.
I. Vogel, M. Hollegaard, D. Hougaard, P. Thorsen +1 more
2009In Vivo13 citations
Semantic Scholar

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