GWAS, cytomegalovirus infection, and schizophrenia

Por Grove, Jakob, Børglum, Anders D., Pearce, Brad D.
Publicado no Curr Behav Neurosci Rep (2014)

Covariance Association Test (CVAT) Identifies Genetic Markers Associated with Schizophrenia in Functionally Associated Biological Processes

Por Rohde, Palle Duun, Demontis, Ditte, Cuyabano, Beatriz Castro Dias, Børglum, Anders D., Sørensen, Peter
Publicado no Genetics (2016)

No association of polymorphisms in the serotonin transporter gene with thermal pain sensation in healthy individuals

Por Schaldemose, Ellen Lund, Horjales-Araujo, Emilia, Demontis, Ditte, Børglum, Anders D, Svensson, Peter, Finnerup, Nanna Brix
Publicado no Mol Pain (2014)

DNA Methylation Analysis of BRD1 Promoter Regions and the Schizophrenia rs138880 Risk Allele

Por Dyrvig, Mads, Qvist, Per, Lichota, Jacek, Larsen, Knud, Nyegaard, Mette, Børglum, Anders D., Christensen, Jane H.
Publicado no PLoS One (2017)

CtIP Mutations Cause Seckel and Jawad Syndromes

Por Qvist, Per, Huertas, Pablo, Jimeno, Sonia, Nyegaard, Mette, Hassan, Muhammad J., Jackson, Stephen P., Børglum, Anders D.
Publicado em 2011

Epigenome-Wide Association Study of Cognitive Functioning in Middle-Aged Monozygotic Twins

Por Starnawska, Anna, Tan, Qihua, McGue, Matt, Mors, Ole, Børglum, Anders D., Christensen, Kaare, Nyegaard, Mette, Christiansen, Lene
Publicado no Front Aging Neurosci (2017)

EWS and FUS bind a subset of transcribed genes encoding proteins enriched in RNA regulatory functions

Por Luo, Yonglun, Blechingberg, Jenny, Fernandes, Ana Miguel, Li, Shengting, Fryland, Tue, Børglum, Anders D., Bolund, Lars, Nielsen, Anders Lade
Publicado no BMC Genomics (2015)

Polymorphism in Serotonin Receptor 3B Is Associated with Pain Catastrophizing

Por Horjales-Araujo, Emilia, Demontis, Ditte, Lund, Ellen Kielland, Finnerup, Nanna Brix, Børglum, Anders D., Jensen, Troels Staehelin, Svensson, Peter, Vase, Lene
Publicado em 2013

Methylenetetrahydrofolate Reductase (MTHFR) C677T Polymorphism and Age at Onset of Schizophrenia: No Consistent Evidence for an Association in the Nordic Population

Por Saetre, Peter, Grove, Jakob, Børglum, Anders D, Mors, Ole, Werge, Thomas, Andreassen, Ole A, Vares, Maria, Agartz, Ingrid, Terenius, Lars, Jönsson, Erik G
Publicado em 2012

Aberrant recombination and repair during immunoglobulin class switching in BRCA1-deficient human B cells

Por Björkman, Andrea, Qvist, Per, Du, Likun, Bartish, Margarita, Zaravinos, Apostolos, Georgiou, Konstantinos, Børglum, Anders D., Gatti, Richard A., Törngren, Therese, Pan-Hammarström, Qiang
Publicado no Proc Natl Acad Sci U S A (2015)

Experimental validation of methods for differential gene expression analysis and sample pooling in RNA-seq

Por Rajkumar, Anto P., Qvist, Per, Lazarus, Ross, Lescai, Francesco, Ju, Jia, Nyegaard, Mette, Mors, Ole, Børglum, Anders D., Li, Qibin, Christensen, Jane H.
Publicado no BMC Genomics (2015)

Lung function discordance in monozygotic twins and associated differences in blood DNA methylation

Por Bolund, Anneli C. S., Starnawska, Anna, Miller, Martin R., Schlünssen, Vivi, Backer, Vibeke, Børglum, Anders D., Christensen, Kaare, Tan, Qihua, Christiansen, Lene, Sigsgaard, Torben
Publicado no Clin Epigenetics (2017)

α-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

Por Mogensen, Jens, Klausen, Ib C., Pedersen, Anders K., Egeblad, Henrik, Bross, Peter, Kruse, Torben A., Gregersen, Niels, Hansen, Peter S., Baandrup, Ulrik, Børglum, Anders D.
Publicado em 1999

Hypomethylation of FAM63B in bipolar disorder patients

Por Starnawska, Anna, Demontis, Ditte, McQuillin, Andrew, O’Brien, Niamh L., Staunstrup, Nicklas H., Mors, Ole, Nielsen, Anders L., Børglum, Anders D., Nyegaard, Mette
Publicado no Clin Epigenetics (2016)

Association of beta-adrenergic receptor polymorphisms and mortality in carvedilol-treated chronic heart-failure patients

Por Petersen, Morten, Andersen, Jon T, Hjelvang, Brian R, Broedbaek, Kasper, Afzal, Shoaib, Nyegaard, Mette, Børglum, Anders D, Stender, Steen, Køber, Lars, Torp-Pedersen, Christian, Poulsen, Henrik E
Publicado em 2011

Mutations in Calmodulin Cause Ventricular Tachycardia and Sudden Cardiac Death

Por Nyegaard, Mette, Overgaard, Michael T., Søndergaard, Mads T., Vranas, Marta, Behr, Elijah R., Hildebrandt, Lasse L., Lund, Jacob, Hedley, Paula L., Camm, A. John, Wettrell, Göran, Fosdal, Inger, Christiansen, Michael, Børglum, Anders D.
Publicado em 2012

A genome-wide study of panic disorder suggests the amiloride-sensitive cation channel 1 as a candidate gene

Por Gregersen, Noomi, Dahl, Hans A, Buttenschøn, Henriette N, Nyegaard, Mette, Hedemand, Anne, Als, Thomas D, Wang, August G, Joensen, Sofus, Woldbye, David PD, Koefoed, Pernille, Kristensen, Ann S, Kruse, Torben A, Børglum, Anders D, Mors, Ole
Publicado em 2012

Psychiatric Genomics: An Update and an Agenda

Por Sullivan, Patrick F, Agrawal, Arpana, Bulik, Cynthia M, Andreassen, Ole A, Børglum, Anders D, Breen, Gerome, Cichon, Sven, Edenberg, Howard J, Faraone, Stephen V, Gelernter, Joel, Mathews, Carol A, Nievergelt, Caroline M, Smoller, Jordan W, O’Donovan, Michael C
Publicado no Am J Psychiatry (2017)

Linkage disequilibrium mapping of a breast cancer susceptibility locus near RAI/PPP1R13L/iASPP

Por Nexø, Bjørn A, Vogel, Ulla, Olsen, Anja, Nyegaard, Mette, Bukowy, Zuzanna, Rockenbauer, Eszter, Zhang, Xiuqing, Koca, Cemile, Mains, Mette, Hansen, Bettina, Hedemand, Anne, Kjeldgaard, Anette, Laska, Magdalena J, Raaschou-Nielsen, Ole, Cold, Søren, Overvad, Kim, Tjønneland, Anne, Bolund, Lars, Børglum, Anders D
Publicado em 2008

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

Por 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
Publicado em 2011