Genome-wide scans using archived neonatal dried blood spot samples
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Published in BMC genomics (04.07.2009)
Published in BMC genomics (04.07.2009)
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Genetic Variation in NFKBIE Is Associated With Increased Risk of Pneumococcal Meningitis in Children
Lundbo, Lene F., Harboe, Zitta Barrella, Clausen, Louise N., Hollegaard, Mads V., Sørensen, Henrik T., Hougaard, David M., Konradsen, Helle B., Nørgaard, Mette, Benfield, Thomas
Published in EBioMedicine (01.01.2016)
Published in EBioMedicine (01.01.2016)
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RNA sequencing of archived neonatal dried blood spots
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Published in Molecular genetics and metabolism reports (01.03.2017)
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Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population
Robinson, Elise B, St Pourcain, Beate, Anttila, Verneri, Kosmicki, Jack A, Bulik-Sullivan, Brendan, Grove, Jakob, Maller, Julian, Samocha, Kaitlin E, Sanders, Stephan J, Ripke, Stephan, Martin, Joanna, Hollegaard, Mads V, Werge, Thomas, Hougaard, David M, Neale, Benjamin M, Evans, David M, Skuse, David, Mortensen, Preben Bo, Børglum, Anders D, Ronald, Angelica, Smith, George Davey, Daly, Mark J
Published in Nature genetics (01.05.2016)
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Evaluation of whole genome amplified DNA to decrease material expenditure and increase quality
Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Poulsen, Jesper B., Hansen, Christine S., Hougaard, David M., Hollegaard, Mads V.
Published in Molecular genetics and metabolism reports (01.06.2017)
Published in Molecular genetics and metabolism reports (01.06.2017)
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Polygenic Risk Score, Parental Socioeconomic Status, Family History of Psychiatric Disorders, and the Risk for Schizophrenia: A Danish Population-Based Study and Meta-analysis
Agerbo, Esben, Sullivan, Patrick F, Vilhjálmsson, Bjarni J, Pedersen, Carsten B, Mors, Ole, Børglum, Anders D, Hougaard, David M, Hollegaard, Mads V, Meier, Sandra, Mattheisen, Manuel, Ripke, Stephan, Wray, Naomi R, Mortensen, Preben B
Published in JAMA psychiatry (Chicago, Ill.) (01.07.2015)
Published in JAMA psychiatry (Chicago, Ill.) (01.07.2015)
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A genome-wide association study identifies CDHR3 as a susceptibility locus for early childhood asthma with severe exacerbations
Bønnelykke, Klaus, Sleiman, Patrick, Nielsen, Kasper, Kreiner-Møller, Eskil, Mercader, Josep M, Belgrave, Danielle, den Dekker, Herman T, Husby, Anders, Sevelsted, Astrid, Faura-Tellez, Grissel, Mortensen, Li Juel, Paternoster, Lavinia, Flaaten, Richard, Mølgaard, Anne, Smart, David E, Thomsen, Philip F, Rasmussen, Morten A, Bonàs-Guarch, Silvia, Holst, Claus, Nohr, Ellen A, Yadav, Rachita, March, Michael E, Blicher, Thomas, Lackie, Peter M, Jaddoe, Vincent W V, Simpson, Angela, Holloway, John W, Duijts, Liesbeth, Custovic, Adnan, Davies, Donna E, Torrents, David, Gupta, Ramneek, Hollegaard, Mads V, Hougaard, David M, Hakonarson, Hakon, Bisgaard, Hans
Published in Nature genetics (01.01.2014)
Published in Nature genetics (01.01.2014)
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Common variants associated with general and MMR vaccine–related febrile seizures
Feenstra, Bjarke, Pasternak, Björn, Geller, Frank, Carstensen, Lisbeth, Wang, Tongfei, Huang, Fen, Eitson, Jennifer L, Hollegaard, Mads V, Svanström, Henrik, Vestergaard, Mogens, Hougaard, David M, Schoggins, John W, Jan, Lily Yeh, Melbye, Mads, Hviid, Anders
Published in Nature genetics (01.12.2014)
Published in Nature genetics (01.12.2014)
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Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis
Winkel, Bo G, Hollegaard, Mads V, Olesen, Morten S, Svendsen, Jesper H, Haunsø, Stig, Hougaard, David M, Tfelt-Hansen, Jacob
Published in BMC medical genetics (09.02.2011)
Published in BMC medical genetics (09.02.2011)
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An epigenetic clock for gestational age at birth based on blood methylation data
Knight, Anna K, Craig, Jeffrey M, Theda, Christiane, Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Hansen, Christine S, Hollegaard, Mads V, Hougaard, David M, Mortensen, Preben B, Weinsheimer, Shantel M, Werge, Thomas M, Brennan, Patricia A, Cubells, Joseph F, Newport, D Jeffrey, Stowe, Zachary N, Cheong, Jeanie L Y, Dalach, Philippa, Doyle, Lex W, Loke, Yuk J, Baccarelli, Andrea A, Just, Allan C, Wright, Robert O, Téllez-Rojo, Mara M, Svensson, Katherine, Trevisi, Letizia, Kennedy, Elizabeth M, Binder, Elisabeth B, Iurato, Stella, Czamara, Darina, Räikkönen, Katri, Lahti, Jari M T, Pesonen, Anu-Katriina, Kajantie, Eero, Villa, Pia M, Laivuori, Hannele, Hämäläinen, Esa, Park, Hea Jin, Bailey, Lynn B, Parets, Sasha E, Kilaru, Varun, Menon, Ramkumar, Horvath, Steve, Bush, Nicole R, LeWinn, Kaja Z, Tylavsky, Frances A, Conneely, Karen N, Smith, Alicia K
Published in Genome Biology (07.10.2016)
Published in Genome Biology (07.10.2016)
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Genome-wide association analyses identify variants in developmental genes associated with hypospadias
Geller, Frank, Feenstra, Bjarke, Carstensen, Lisbeth, Pers, Tune H, van Rooij, Iris A L M, Körberg, Izabella Baranowska, Choudhry, Shweta, Karjalainen, Juha M, Schnack, Tine H, Hollegaard, Mads V, Feitz, Wout F J, Roeleveld, Nel, Hougaard, David M, Hirschhorn, Joel N, Franke, Lude, Baskin, Laurence S, Nordenskjöld, Agneta, van der Zanden, Loes F M, Melbye, Mads
Published in Nature genetics (01.09.2014)
Published in Nature genetics (01.09.2014)
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CCND2, CTNNB1, DDX3X, GLI2, SMARCA4, MYC, MYCN, PTCH1, TP53, and MLL2 gene variants and risk of childhood medulloblastoma
Dahlin, Anna M., Hollegaard, Mads V., Wibom, Carl, Andersson, Ulrika, Hougaard, David M., Deltour, Isabelle, Hjalmars, Ulf, Melin, Beatrice
Published in Journal of neuro-oncology (01.10.2015)
Published in Journal of neuro-oncology (01.10.2015)
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Gene expression profiling of archived dried blood spot samples from the Danish Neonatal Screening Biobank
Grauholm, Jonas, Khoo, Sok Kean, Nickolov, Radoslav Z., Poulsen, Jesper B., Bækvad-Hansen, Marie, Hansen, Christine S., Hougaard, David M., Hollegaard, Mads V.
Published in Molecular genetics and metabolism (01.11.2015)
Published in Molecular genetics and metabolism (01.11.2015)
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Common variants near MBNL1 and NKX2-5 are associated with infantile hypertrophic pyloric stenosis
Feenstra, Bjarke, Geller, Frank, Krogh, Camilla, Hollegaard, Mads V, Gørtz, Sanne, Boyd, Heather A, Murray, Jeffrey C, Hougaard, David M, Melbye, Mads
Published in Nature genetics (01.03.2012)
Published in Nature genetics (01.03.2012)
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Robustness of genome-wide scanning using archived dried blood spot samples as a DNA source
Hollegaard, Mads V, Grove, Jakob, Grauholm, Jonas, Kreiner-Møller, Eskil, Bønnelykke, Klaus, Nørgaard, Mette, Benfield, Thomas L, Nørgaard-Pedersen, Bent, Mortensen, Preben B, Mors, Ole, Sørensen, Henrik T, Harboe, Zitta B, Børglum, Anders D, Demontis, Ditte, Ørntoft, Torben F, Bisgaard, Hans, Hougaard, David M
Published in BMC genetics (04.07.2011)
Published in BMC genetics (04.07.2011)
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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
Agerbo, Esben, Mortensen, Preben B, Wiuf, Carsten, Pedersen, Michael S, McGrath, John, Hollegaard, Mads V, Nørgaard-Pedersen, Bent, Hougaard, David M, Mors, Ole, Pedersen, Carsten B
Published in Schizophrenia research (01.02.2012)
Published in Schizophrenia research (01.02.2012)
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UGT1A128 polymorphism and acute lymphoblastic leukemia in children: a Danish case–control study
Petersen, Jesper P., Overvad, Kim, Hollegaard, Mads V., Ebbesen, Finn, Henriksen, Tine B., Thorlacius-Ussing, Ole, Hougaard, David M., Schrøder, Henrik
Published in Pediatric research (01.11.2014)
Published in Pediatric research (01.11.2014)
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Replication Study and Meta-Analysis in European Samples Supports Association of the 3p21.1 Locus with Bipolar Disorder
Vassos, Evangelos, Steinberg, Stacy, Cichon, Sven, Breen, Gerome, Sigurdsson, Engilbert, Andreassen, Ole A, Djurovic, Srdjan, Morken, Gunnar, Grigoroiu-Serbanescu, Maria, Diaconu, Carmen C, Czerski, Piotr M, Hauser, Joanna, Babadjanova, Gulja, Abramova, Lilia I, Mühleisen, Thomas W, Nöthen, Markus M, Rietschel, Marcella, McGuffin, Peter, St. Clair, David, Gustafsson, Omar, Melle, Ingrid, Pietiläinen, Olli P.H, Ruggeri, Mirella, Tosato, Sarah, Werge, Thomas, Ophoff, Roel A, Rujescu, Dan, Børglum, Anders D, Mors, Ole, Mortensen, Preben B, Demontis, Ditte, Hollegaard, Mads V, van Winkel, Ruud, Kenis, Gunter, De Hert, Marc, Réthelyi, János M, Bitter, István, Rubino, I. Alex, Golimbet, Vera, Kiemeney, Lambertus A, van den Berg, Leonard H, Franke, Barbara, Jönsson, Erik G, Farmer, Anne, Stefansson, Hreinn, Stefansson, Kari, Collier, David A
Published in Biological psychiatry (1969) (15.10.2012)
Published in Biological psychiatry (1969) (15.10.2012)
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Mannose-Binding Lectin Gene, MBL2, Polymorphisms Do Not Increase Susceptibility to Invasive Meningococcal Disease in a Population of Danish Children
Lundbo, Lene F., Sørensen, Henrik T., Clausen, Louise N., Hollegaard, Mads V., Hougaard, David M., Konradsen, Helle B., Harboe, Zitta Barrella, Nørgaard, Mette, Benfield, Thomas
Published in Open forum infectious diseases (01.12.2015)
Published in Open forum infectious diseases (01.12.2015)
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High-throughput genotyping on archived dried blood spot samples
Hollegaard, Mads V, Grove, Jakob, Thorsen, Poul, Nørgaard-Pedersen, Bent, Hougaard, David M
Published in Genetic testing and molecular biomarkers (01.04.2009)
Published in Genetic testing and molecular biomarkers (01.04.2009)
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