Jakob Grove

发表

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

Clara Albiñana, Jakob Grove, John J. McGrath, 2020, bioRxiv.

Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

Jakob Grove, Esben Agerbo, Robert Plomin, 2018, Nature Genetics.

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

Jakob Grove, Stephan Ripke, Preben Bo Mortensen, 2015, Nature Genetics.

Novel variation and de novo mutation rates in population-wide de novo assembled Danish trios

Jakob Grove, Anders D. Børglum, Xun Xu, 2015, Nature Communications.

Discovery of the first genome-wide significant risk loci for ADHD

Jakob Grove, Esben Agerbo, Anders D. Børglum, 2017, bioRxiv.

Common risk variants identified in autism spectrum disorder

Jakob Grove, Esben Agerbo, Anders D. Børglum, 2017, bioRxiv.

Joint Analysis of SNPs and Proteins Identifies Regulatory IL18 Gene Variations Decreasing the Chance of Spastic Cerebral Palsy

Jakob Grove, David M. Hougaard, Kristin Skogstrand, 2013, Human mutation.

Genome-wide association study identifies 30 Loci Associated with Bipolar Disorder

Jakob Grove, Esben Agerbo, Andres Metspalu, 2017, bioRxiv.

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Jakob Grove, Anders D. Børglum, Aysu Okbay, 2016, Nature Genetics.

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Jakob Grove, Anders D. Børglum, Aysu Okbay, 2016 .

Autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) have a similar burden of rare protein-truncating variants

Jakob Grove, F Kyle Satterstrom, Raymond K Walters, 2019, Nature Neuroscience.