Anders Rosengren
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View article: Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology
Analysis of exonic deletions in a large population study provides novel insights into NRXN1 pathology Open
The NRXN1 locus is a hotspot for non-recurrent copy number variants and exon-disrupting NRXN1 deletions have been associated with increased risk of neurodevelopmental disorders in case-control studies. However, corresponding population-bas…
View article: Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants
Population-Based Risk of Psychiatric Disorders Associated With Recurrent Copy Number Variants Open
Importance Recurrent copy number variants (rCNVs) have been associated with increased risk of psychiatric disorders in case-control studies, but their population-level impact is unknown. Objective To provide unbiased population-based estim…
View article: Phenotypic and ancestry-related assortative mating in autism
Phenotypic and ancestry-related assortative mating in autism Open
View article: Steppe Ancestry in Western Eurasia and the Spread of the Germanic Languages
Steppe Ancestry in Western Eurasia and the Spread of the Germanic Languages Open
Summary Today, Germanic languages, including German, English, Frisian, Dutch and the Nordic languages, are widely spoken in northwest Europe. However, key aspects of the assumed arrival and diversification of this linguistic group remain c…
View article: Publisher Correction: Population genomics of post-glacial western Eurasia
Publisher Correction: Population genomics of post-glacial western Eurasia Open
View article: The selection landscape and genetic legacy of ancient Eurasians
The selection landscape and genetic legacy of ancient Eurasians Open
The Holocene (beginning around 12,000 years ago) encompassed some of the most significant changes in human evolution, with far-reaching consequences for the dietary, physical and mental health of present-day populations. Using a dataset of…
View article: Population genomics of post-glacial western Eurasia
Population genomics of post-glacial western Eurasia Open
View article: 100 ancient genomes show repeated population turnovers in Neolithic Denmark
100 ancient genomes show repeated population turnovers in Neolithic Denmark Open
View article: Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses
Depression pathophysiology, risk prediction of recurrence and comorbid psychiatric disorders using genome-wide analyses Open
View article: DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals
DanMAC5: a browser of aggregated sequence variants from 8,671 whole genome sequenced Danish individuals Open
Objectives Allele counts of sequence variants obtained by whole genome sequencing (WGS) often play a central role in interpreting the results of genetic and genomic research. However, such variant counts are not readily available for indiv…
View article: Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks
Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks Open
View article: Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p
Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p Open
View article: Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups
Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups Open
View article: The Selection Landscape and Genetic Legacy of Ancient Eurasians
The Selection Landscape and Genetic Legacy of Ancient Eurasians Open
Summary The Eurasian Holocene (beginning c. 12 thousand years ago) encompassed some of the most significant changes in human evolution, with far-reaching consequences for the dietary, physical and mental health of present-day populations. …
View article: Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities
Identification of 64 new risk loci for major depression, refinement of the genetic architecture and risk prediction of recurrence and comorbidities Open
Major depression (MD) is a common mental disorder and a leading cause of disability worldwide. We conducted a GWAS meta-analysis of more than 1.3 million individuals, including 371,184 with MD, identifying 243 risk loci. Sixty-four loci ar…
View article: Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder
Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention-deficit hyperactivity disorder Open
View article: Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks
Accuracy of haplotype estimation and whole genome imputation affects complex trait analyses in complex biobanks Open
Sample recruitment for research consortia, hospitals, biobanks, and personal genomics companies span years, necessitating genotyping in batches, using different technologies. As marker content on genotyping arrays varies systematically, in…
View article: Genetic correlates of phenotypic heterogeneity in autism
Genetic correlates of phenotypic heterogeneity in autism Open
View article: The female protective effect against autism spectrum disorder
The female protective effect against autism spectrum disorder Open
Autism spectrum disorder (ASD) is diagnosed three to four times more frequently in males than in females. Genetic studies of rare variants support a female protective effect (FPE) against ASD. However, sex differences in common inherited g…
View article: Population genomics of postglacial western eurasia
Population genomics of postglacial western eurasia Open
Summary Western Eurasia witnessed several large-scale human migrations during the Holocene 1–5 . To investigate the cross-continental impacts we shotgun-sequenced 317 primarily Mesolithic and Neolithic genomes from across Northern and West…
View article: Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention deficit hyperactivity disorder
Differences in the genetic architecture of common and rare variants in childhood, persistent and late-diagnosed attention deficit hyperactivity disorder Open
Attention deficit hyperactivity disorder (ADHD) is a neurodevelopmental disorder, with onset in childhood (“childhood ADHD”), and around two thirds of affected individuals will continue to have ADHD symptoms in adulthood (“persistent ADHD”…
View article: Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups
Identification of shared and differentiating genetic risk for autism spectrum disorder, attention deficit hyperactivity disorder and case subgroups Open
Attention deficit hyperactivity disorder (ADHD) and autism spectrum disorder (ASD) are highly heritable neurodevelopmental disorders with a considerable overlap in their genetic etiology. We dissected their shared and distinct genetic arch…
View article: The female protective effect against autism spectrum disorder
The female protective effect against autism spectrum disorder Open
Autism spectrum disorder (ASD) is diagnosed 3-4 times more frequently in males than in females. Genetic studies of rare variants support a female protective effect (FPE) against ASD. However, sex differences in common, inherited genetic ri…
View article: Genetic correlates of phenotypic heterogeneity in autism
Genetic correlates of phenotypic heterogeneity in autism Open
The substantial phenotypic heterogeneity in autism limits our understanding of its genetic aetiology. To address this gap, we investigated genetic differences between autistic individuals (N max = 12,893) based on core (i.e., social commun…
View article: Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study
Prevalence of rearrangements in the 22q11.2 region and population-based risk of neuropsychiatric and developmental disorders in a Danish population: a case-cohort study Open
View article: CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits
CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits Open
View article: Synthesis of heavy hydrocarbons at the core-mantle boundary
Synthesis of heavy hydrocarbons at the core-mantle boundary Open
View article: 座談会 2型糖尿病の病態生理の解明に向けた,バイオインフォマティクスと膵島研究の組み合わせ
座談会 2型糖尿病の病態生理の解明に向けた,バイオインフォマティクスと膵島研究の組み合わせ Open