User profiles for "author:P B Mortensen"

Peter B. Mortensen

Professor, Political Science, Aarhus University
Verified email at ps.au.dk
Cited by 4744

Punctuated equilibrium theory: Explaining stability and change in public policymaking

FR Baumgartner, BD Jones… - Theories of the policy …, 2018 - taylorfrancis.com
This chapter reviews Punctuated Equilibrium Theory (PET), and discusses new empirical
studies in the United States and elsewhere. It deals with an assessment of the strengths and …

Excess early mortality in schizophrenia

TM Laursen, M Nordentoft… - Annual review of clinical …, 2014 - annualreviews.org
Schizophrenia is often referred to as one of the most severe mental disorders, primarily
because of the very high mortality rates of those with the disorder. This article reviews the …

Short-chain fatty acids in the human colon: relation to gastrointestinal health and disease

PB Mortensen, MR Clausen - Scandinavian Journal of …, 1996 - Taylor & Francis
Fermentation, the process whereby anaerobic bacteria break down carbohydrates to short-
chain (C2-C6) fatty acids (SCFAs), is an important function of the large bowel. SCFAs …

Biological insights from 108 schizophrenia-associated genetic loci

C Pantelis, GN Papadimitriou, S Papiol… - Nature, 2014 - nature.com
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of
alleles, including common alleles of small effect that might be detected by genome-wide …

Common variants conferring risk of schizophrenia

H Stefansson, RA Ophoff, S Steinberg, OA Andreassen… - Nature, 2009 - nature.com
Schizophrenia is a complex disorder, caused by both genetic and environmental factors and
their interactions. Research on pathogenesis has traditionally focused on neurotransmitter …

Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

D Demontis, RK Walters, J Martin, M Mattheisen… - Nature …, 2019 - nature.com
Attention deficit/hyperactivity disorder (ADHD) is a highly heritable childhood behavioral
disorder affecting 5% of children and 2.5% of adults. Common genetic variants contribute …

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

S Ripke, C O'dushlaine, K Chambert, JL Moran… - Nature …, 2013 - nature.com
Schizophrenia is an idiopathic mental disorder with a heritable component and a substantial
public health impact. We conducted a multi-stage genome-wide association study (GWAS) …

Identification of common genetic risk variants for autism spectrum disorder

J Grove, S Ripke, TD Als, M Mattheisen, RK Walters… - Nature …, 2019 - nature.com
Autism spectrum disorder (ASD) is a highly heritable and heterogeneous group of
neurodevelopmental phenotypes diagnosed in more than 1% of children. Common genetic …

[PDF][PDF] Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism

FK Satterstrom, JA Kosmicki, J Wang, MS Breen… - Cell, 2020 - cell.com
We present the largest exome sequencing study of autism spectrum disorder (ASD) to date
(n= 35,584 total samples, 11,986 with ASD). Using an enhanced analytical framework to …

Rare coding variants in ten genes confer substantial risk for schizophrenia

T Singh, T Poterba, D Curtis, H Akil, M Al Eissa… - Nature, 2022 - nature.com
Rare coding variation has historically provided the most direct connections between gene
function and disease pathogenesis. By meta-analysing the whole exomes of 24,248 …