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Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

The Lancet (British edition), 2009, Vol.373 (9659), p.234-239

2009

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The pursuit of genome-wide association studies: where are we now?

Journal of human genetics, 2010-04, Vol.55 (4), p.195-206

2010

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A systems genomics approach to uncover the molecular properties of cancer genes

Scientific reports, 2020-10, Vol.10 (1), p.18392-18392, Article 18392

2020

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Correlation between leukocyte phenotypes and prognosis of amyotrophic lateral sclerosis

eLife, 2022-03, Vol.11

2022

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Reproducibility of Methods to Detect Differentially Expressed Genes from Single-Cell RNA Sequencing

Frontiers in genetics, 2020-01, Vol.10, p.1331-1331

2020

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Model-based estimation of the attributable fraction for cross-sectional, case-control and cohort studies using the R package AF

European journal of epidemiology, 2016-06, Vol.31 (6), p.575-582

2016

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Cell-level somatic mutation detection from single-cell RNA sequencing

Bioinformatics, 2019-11, Vol.35 (22), p.4679-4687

2019

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Parametric and penalized generalized survival models

Statistical methods in medical research, 2018-05, Vol.27 (5), p.1531-1546

2018

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Correction to: Resolving Zeckhauser’s paradox

Theory and decision, 2020-11, Vol.89 (4), p.527-528

2020

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T cell responses at diagnosis of amyotrophic lateral sclerosis predict disease progression

Nature communications, 2022-11, Vol.13 (1), p.6733-6733, Article 6733

2022

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Between-within models for survival analysis

Statistics in medicine, 2013-08, Vol.32 (18), p.3067-3076

2013

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Validation of a Radiosensitivity Molecular Signature in Breast Cancer

Clinical cancer research, 2012-09, Vol.18 (18), p.5134-5143

2012

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interferon-related gene signature for DNA damage resistance is a predictive marker for chemotherapy and radiation for breast cancer

Proceedings of the National Academy of Sciences - PNAS, 2008-11, Vol.105 (47), p.18490-18495

2008

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An Expression Signature for p53 Status in Human Breast Cancer Predicts Mutation Status, Transcriptional Effects, and Patient Survival

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (38), p.13550-13555

2005

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Is the association between general cognitive ability and violent crime caused by family-level confounders?

PloS one, 2012-07, Vol.7 (7), p.e41783-e41783

2012

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Regression standardization and attributable fraction estimation with between-within frailty models for clustered survival data

Statistical methods in medical research, 2019-02, Vol.28 (2), p.462-485

2019

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Circall: fast and accurate methodology for discovery of circular RNAs from paired-end RNA-sequencing data

BMC bioinformatics, 2021-10, Vol.22 (1), p.495-495, Article 495

2021

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Network enrichment analysis: extension of gene-set enrichment analysis to gene networks

BMC bioinformatics, 2012-09, Vol.13 (1), p.226-226, Article 226

2012

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Integration of somatic mutation, expression and functional data reveals potential driver genes predictive of breast cancer survival

Bioinformatics, 2015-08, Vol.31 (16), p.2607-2613

2015

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Disease trajectories and mortality among women diagnosed with breast cancer

Breast cancer research : BCR, 2019-08, Vol.21 (1), p.95-95, Article 95

2019

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Genetic reclassification of histologic grade delineates new clinical subtypes of breast cancer

Cancer research (Chicago, Ill.), 2006-11, Vol.66 (21), p.10292-10301

2006

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CREDO: Highly confident disease-relevant A-to-I RNA-editing discovery in breast cancer

Scientific reports, 2019-03, Vol.9 (1), p.5064-5064, Article 5064

2019

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Resolving Zeckhauser’s paradox

Theory and decision, 2020-05, Vol.88 (4), p.595-607

2020

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A fast detection of fusion genes from paired-end RNA-seq data

BMC genomics, 2018-11, Vol.19 (1), p.786-786, Article 786

2018

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Isoform-level gene expression patterns in single-cell RNA-sequencing data

Bioinformatics, 2018-07, Vol.34 (14), p.2392-2400

2018

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Common genetic determinants of schizophrenia and bipolar disorder in Swedish families: a population-based study

The pursuit of genome-wide association studies: where are we now?

A systems genomics approach to uncover the molecular properties of cancer genes

Correlation between leukocyte phenotypes and prognosis of amyotrophic lateral sclerosis

Reproducibility of Methods to Detect Differentially Expressed Genes from Single-Cell RNA Sequencing

Model-based estimation of the attributable fraction for cross-sectional, case-control and cohort studies using the R package AF

Cell-level somatic mutation detection from single-cell RNA sequencing

Parametric and penalized generalized survival models

Correction to: Resolving Zeckhauser’s paradox

T cell responses at diagnosis of amyotrophic lateral sclerosis predict disease progression

Between-within models for survival analysis

Validation of a Radiosensitivity Molecular Signature in Breast Cancer

interferon-related gene signature for DNA damage resistance is a predictive marker for chemotherapy and radiation for breast cancer

An Expression Signature for p53 Status in Human Breast Cancer Predicts Mutation Status, Transcriptional Effects, and Patient Survival

Is the association between general cognitive ability and violent crime caused by family-level confounders?

Regression standardization and attributable fraction estimation with between-within frailty models for clustered survival data

Circall: fast and accurate methodology for discovery of circular RNAs from paired-end RNA-sequencing data

Network enrichment analysis: extension of gene-set enrichment analysis to gene networks

Integration of somatic mutation, expression and functional data reveals potential driver genes predictive of breast cancer survival

Disease trajectories and mortality among women diagnosed with breast cancer

Genetic reclassification of histologic grade delineates new clinical subtypes of breast cancer

CREDO: Highly confident disease-relevant A-to-I RNA-editing discovery in breast cancer

Resolving Zeckhauser’s paradox

A fast detection of fusion genes from paired-end RNA-seq data

Isoform-level gene expression patterns in single-cell RNA-sequencing data

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