A review of software for microarray genotyping

por Lamy, Philippe, Grove, Jakob, Wiuf, Carsten
Publicado 2011

Congenital Cerebral Palsy, Child Sex and Parent Cardiovascular Risk

por Streja, Elani, Wu, Chunsen, Uldall, Peter, Grove, Jakob, Arah, Onyebuchi, Olsen, Jørn
Publicado 2013

Genome-wide analyses of self-reported empathy: correlations with autism, schizophrenia, and anorexia nervosa

por Warrier, Varun, Toro, Roberto, Chakrabarti, Bhismadev, Børglum, Anders D, Grove, Jakob, Hinds, David A., Bourgeron, Thomas, Baron-Cohen, Simon
Publicado 2018

Discordant associations of educational attainment with ASD and ADHD implicate a polygenic form of pleiotropy

por Verhoef, Ellen, Grove, Jakob, Shapland, Chin Yang, Demontis, Ditte, Burgess, Stephen, Rai, Dheeraj, Børglum, Anders D., St Pourcain, Beate
Publicado 2021

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 2012

Maternal caffeine intake during pregnancy is associated with birth weight but not with gestational length: results from a large prospective observational cohort study

por Sengpiel, Verena, Elind, Elisabeth, Bacelis, Jonas, Nilsson, Staffan, Grove, Jakob, Myhre, Ronny, Haugen, Margaretha, Meltzer, Helle Margrete, Alexander, Jan, Jacobsson, Bo, Brantsæter, Anne-Lise
Publicado 2013

Low to Moderate Average Alcohol Consumption and Binge Drinking in Early Pregnancy: Effects on Choice Reaction Time and Information Processing Time in Five-Year-Old Children

por Kilburn, Tina R., Eriksen, Hanne-Lise Falgreen, Underbjerg, Mette, Thorsen, Poul, Mortensen, Erik Lykke, Landrø, Nils Inge, Bakketeig, Leiv S., Grove, Jakob, Sværke, Claus, Kesmodel, Ulrik Schiøler
Publicado 2015

Social and non-social autism symptoms and trait domains are genetically dissociable

por Warrier, Varun, Toro, Roberto, Won, Hyejung, Leblond, Claire S., Cliquet, Freddy, Delorme, Richard, De Witte, Ward, Bralten, Janita, Chakrabarti, Bhismadev, Børglum, Anders D., Grove, Jakob, Poelmans, Geert, Hinds, David A., Bourgeron, Thomas, Baron-Cohen, Simon
Publicado 2019

Leveraging both individual-level genetic data and GWAS summary statistics increases polygenic prediction

por Albiñana, Clara, Grove, Jakob, McGrath, John J., Agerbo, Esben, Wray, Naomi R., Bulik, Cynthia M., Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Mortensen, Preben Bo, Privé, Florian, Vilhjálmsson, Bjarni J.
Publicado 2021

DNA methylation of the KLK8 gene in depression symptomatology

por Starnawska, Anna, Bukowski, Lina, Chernomorchenko, Ana, Elfving, Betina, Müller, Heidi Kaastrup, van den Oord, Edwin, Aberg, Karolina, Guintivano, Jerry, Grove, Jakob, Mors, Ole, Børglum, Anders D., Nielsen, Anders L., Qvist, Per, Staunstrup, Nicklas Heine
Publicado 2021

Co-occurring hydrocephalus in autism spectrum disorder: a Danish population-based cohort study

por Munch, Tina Nørgaard, Hedley, Paula Louise, Hagen, Christian Munch, Bækvad-Hansen, Marie, Bybjerg-Grauholm, Jonas, Grove, Jakob, Nordentoft, Merete, Børglum, Anders Dupont, Mortensen, Preben Bo, Werge, Thomas Mears, Melbye, Mads, Hougaard, David Michael, Christiansen, Michael
Publicado 2021

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 2011

Identification of the BRD1 interaction network and its impact on mental disorder risk

por Fryland, Tue, Christensen, Jane H., Pallesen, Jonatan, Mattheisen, Manuel, Palmfeldt, Johan, Bak, Mads, Grove, Jakob, Demontis, Ditte, Blechingberg, Jenny, Ooi, Hong Sain, Nyegaard, Mette, Hauberg, Mads E., Tommerup, Niels, Gregersen, Niels, Mors, Ole, Corydon, Thomas J., Nielsen, Anders L., Børglum, Anders D.
Publicado 2016

Polygenic Heterogeneity Across Obsessive-Compulsive Disorder Subgroups Defined by a Comorbid Diagnosis

por Strom, Nora I., Grove, Jakob, Meier, Sandra M., Bækvad-Hansen, Marie, Becker Nissen, Judith, Damm Als, Thomas, Halvorsen, Matthew, Nordentoft, Merete, Mortensen, Preben B., Hougaard, David M., Werge, Thomas, Mors, Ole, Børglum, Anders D., Crowley, James J., Bybjerg-Grauholm, Jonas, Mattheisen, Manuel
Publicado 2021

The Eating Disorders Genetics Initiative (EDGI): study protocol

por Bulik, Cynthia M., Thornton, Laura M., Parker, Richard, Kennedy, Hannah, Baker, Jessica H., MacDermod, Casey, Guintivano, Jerry, Cleland, Lana, Miller, Allison L., Harper, Lauren, Larsen, Janne T., Yilmaz, Zeynep, Grove, Jakob, Sullivan, Patrick F., Petersen, Liselotte V., Jordan, Jennifer, Kennedy, Martin A., Martin, Nicholas G.
Publicado 2021

Genetic correlates of phenotypic heterogeneity in autism

por Warrier, Varun, Zhang, Xinhe, Reed, Patrick, Havdahl, Alexandra, Moore, Tyler M., Cliquet, Freddy, Leblond, Claire S., Rolland, Thomas, Rosengren, Anders, Rowitch, David H., Hurles, Matthew E., Geschwind, Daniel H., Børglum, Anders D., Robinson, Elise B., Grove, Jakob, Martin, Hilary C., Bourgeron, Thomas, Baron-Cohen, Simon
Publicado 2022

Multi-PGS enhances polygenic prediction by combining 937 polygenic scores

por Albiñana, Clara, Zhu, Zhihong, Schork, Andrew J., Ingason, Andrés, Aschard, Hugues, Brikell, Isabell, Bulik, Cynthia M., Petersen, Liselotte V., Agerbo, Esben, Grove, Jakob, Nordentoft, Merete, Hougaard, David M., Werge, Thomas, Børglum, Anders D., Mortensen, Preben Bo, McGrath, John J., Neale, Benjamin M., Privé, Florian, Vilhjálmsson, Bjarni J.
Publicado 2023

High-Quality Exome Sequencing of Whole-Genome Amplified Neonatal Dried Blood Spot DNA

por Poulsen, Jesper Buchhave, Lescai, Francesco, Grove, Jakob, Bækvad-Hansen, Marie, Christiansen, Michael, Hagen, Christian Munch, Maller, Julian, Stevens, Christine, Li, Shenting, Li, Qibin, Sun, Jihua, Wang, Jun, Nordentoft, Merete, Werge, Thomas Mears, Mortensen, Preben Bo, Børglum, Anders Dupont, Daly, Mark, Hougaard, David Michael, Bybjerg-Grauholm, Jonas, Hollegaard, Mads Vilhelm
Publicado 2016

A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

por Antaki, Danny, Guevara, James, Maihofer, Adam X., Klein, Marieke, Gujral, Madhusudan, Grove, Jakob, Carey, Caitlin E., Hong, Oanh, Arranz, Maria J., Hervas, Amaia, Corsello, Christina, Vaux, Keith K., Muotri, Alysson R., Iakoucheva, Lilia M., Courchesne, Eric, Pierce, Karen, Gleeson, Joseph G., Robinson, Elise, Nievergelt, Caroline M., Sebat, Jonathan
Publicado 2022

Risk variants and polygenic architecture of disruptive behavior disorders in the context of attention-deficit/hyperactivity disorder

por Demontis, Ditte, Walters, Raymond K., Rajagopal, Veera M., Waldman, Irwin D., Grove, Jakob, Als, Thomas D., Dalsgaard, Søren, Ribasas, Marta, Bybjerg-Grauholm, Jonas, Bækvad-Hansen, Maria, Werge, Thomas, Nordentoft, Merete, Mors, Ole, Mortensen, Preben Bo, Cormand, Bru, Hougaard, David M., Neale, Benjamin M., Franke, Barbara, Faraone, Stephen V., Børglum, Anders D.
Publicado 2021