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Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

Science (American Association for the Advancement of Science), 2018-02, Vol.359 (6376), p.693-697

2018

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Fast and efficient QTL mapper for thousands of molecular phenotypes

Bioinformatics, 2016-05, Vol.32 (10), p.1479-1485

2016

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Mapping cis- and trans-regulatory effects across multiple tissues in twins

Nature genetics, 2012-10, Vol.44 (10), p.1084-1089

2012

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Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction

Nature communications, 2021-09, Vol.12 (1), p.5276-5276, Article 5276

2021

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Quantitative variability of 342 plasma proteins in a human twin population

Molecular systems biology, 2015-02, Vol.11 (2), p.786-n/a

2015

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Inference and quantification of peptidoforms in large sample cohorts by SWATH-MS

Nature biotechnology, 2017-08, Vol.35 (8), p.781-788

2017

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Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia

Nature communications, 2018-08, Vol.9 (1), p.3121-15, Article 3121

2018

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Changes in the gene expression profile during spontaneous migraine attacks

Scientific reports, 2021-04, Vol.11 (1), p.8294-10, Article 8294

2021

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Key pathways and genes that are altered during treatment with hyperbaric oxygen in patients with sepsis due to necrotizing soft tissue infection (HBOmic study)

European journal of medical research, 2023-11, Vol.28 (1), p.1-507, Article 507

2023

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Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements

American journal of human genetics, 2013-11, Vol.93 (5), p.876-890

2013

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Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing

PLoS genetics, 2015-01, Vol.11 (1), p.e1004958-e1004958

2015

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Copy Number Variants and Polygenic Risk Scores Predict Need of Care in Autism and/or ADHD Families

Journal of autism and developmental disorders, 2021, Vol.51 (1), p.276-285

2021

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Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort

Human molecular genetics, 2018-02, Vol.27 (4), p.732-741

2018

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Human Disease Variation in the Light of Population Genomics

Cell, 2019-03, Vol.177 (1), p.115-131

2019

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Parent-of-Origin inference for biobanks

Nature communications, 2022-11, Vol.13 (1), p.6668-15, Article 6668

2022

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Correction: Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants

Journal of neurodevelopmental disorders, 2023-09, Vol.15 (1), p.1-31, Article 31

2023

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Genetic interactions affecting human gene expression identified by variance association mapping

eLife, 2014-04, Vol.3, p.e01381-e01381

2014

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Cross-tissue eQTL enrichment of associations in schizophrenia

PloS one, 2018-09, Vol.13 (9), p.e0202812-e0202812

2018

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Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders

European journal of human genetics : EJHG, 2019-09, Vol.27 (9), p.1445-1455

2019

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Circulating Proteomic Signatures of Chronological Age

The journals of gerontology. Series A, Biological sciences and medical sciences, 2015-07, Vol.70 (7), p.809-816

2015

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Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants

Journal of neurodevelopmental disorders, 2021-12, Vol.13 (1), p.54-54, Article 54

2021

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Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study

Scientific reports, 2021-08, Vol.11 (1), p.17463-17463, Article 17463

2021

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Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

Fast and efficient QTL mapper for thousands of molecular phenotypes

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

Passive and active DNA methylation and the interplay with genetic variation in gene regulation

Mapping cis- and trans-regulatory effects across multiple tissues in twins

Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction

Regulatory variants at KLF14 influence type 2 diabetes risk via a female-specific effect on adipocyte size and body composition

Quantitative variability of 342 plasma proteins in a human twin population

Inference and quantification of peptidoforms in large sample cohorts by SWATH-MS

Evaluation of chromatin accessibility in prefrontal cortex of individuals with schizophrenia

Changes in the gene expression profile during spontaneous migraine attacks

Key pathways and genes that are altered during treatment with hyperbaric oxygen in patients with sepsis due to necrotizing soft tissue infection (HBOmic study)

Global Analysis of DNA Methylation Variation in Adipose Tissue from Twins Reveals Links to Disease-Associated Variants in Distal Regulatory Elements

Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing

Copy Number Variants and Polygenic Risk Scores Predict Need of Care in Autism and/or ADHD Families

Age-dependent changes in mean and variance of gene expression across tissues in a twin cohort

Human Disease Variation in the Light of Population Genomics

Parent-of-Origin inference for biobanks

Correction: Pleiotropy between language impairment and broader behavioral disorders—an investigation of both common and rare genetic variants

Genetic interactions affecting human gene expression identified by variance association mapping

Cross-tissue eQTL enrichment of associations in schizophrenia

Immunity and mental illness: findings from a Danish population-based immunogenetic study of seven psychiatric and neurodevelopmental disorders

Circulating Proteomic Signatures of Chronological Age

Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants

Genetic regulation of spermine oxidase activity and cancer risk: a Mendelian randomization study

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