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Author Details

Yudi Pawitan
Karolinska Institute
1988
194
49
Timothy Clark (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36938752Comprehensive transcriptomic analysis to identify biological and clinical differences in cholangiocarcinoma.Cancer Med2023
37325708Hidden Genetic Regulation of Human Complex Traits via Brain Isoforms.Phenomics2023
37425374Psychiatric disorders and subsequent risk of cardiovascular disease: a longitudinal matched cohort study across three countries.EClinicalMedicine2023
37006328Infections among individuals with multiple sclerosis, Alzheimer's disease and Parkinson's disease.Brain Commun2023
36964195Prediction model for drug response of acute myeloid leukemia patients.NPJ Precis Oncol2023
36447380Gastrointestinal biopsy of normal mucosa or nonspecific inflammation and risk of neurodegenerative disease: Nationwide matched cohort study.Eur J Neurol2023
34288189The frequency of misattributed paternity in Sweden is low and decreasing: A nationwide cohort study.J Intern Med2022
35444688Integration of Distinct Analysis Strategies Improves Tissue-Trait Association Identification.Front Genet2022
35578620Biomarkers and Disease Trajectories Influencing Women's Health: Results from the UK Biobank Cohort.Phenomics2022
35855322Quantification of mutant-allele expression at isoform level in cancer from RNA-seq data.NAR Genom Bioinform2022
35387486Genetic Landscape of the ACE2 Coronavirus Receptor.Circulation2022
35357430Genetic and phenotypic links between obesity and extracellular vesicles.Hum Mol Genet2022
36173247Discovery of druggable cancer-specific pathways with application in acute myeloid leukemia.Gigascience2022
36270585Overall assessment for selected markers from high-throughput data.Stat Med2022
36347843T cell responses at diagnosis of amyotrophic lateral sclerosis predict disease progression.Nat Commun2022
35287794Correlation between leukocyte phenotypes and prognosis of amyotrophic lateral sclerosis.Elife2022
35251131Fusion Gene Detection Using Whole-Exome Sequencing Data in Cancer Patients.Front Genet2022
34864849Isoform-level quantification for single-cell RNA sequencing.Bioinformatics2022
33331190Associations between autoimmune diseases and amyotrophic lateral sclerosis: a register-based study.Amyotroph Lateral Scler Frontotemporal Degener2021
33625756The transcriptome-wide landscape of molecular subtype-specific mRNA expression profiles in acute myeloid leukemia.Am J Hematol2021
33619999Gastrointestinal biopsies and amyotrophic lateral sclerosis - results from a cohort study of 1.1 million individuals.Amyotroph Lateral Scler Frontotemporal Degener2021
33613642Nontrivial Replication of Loci Detected by Multi-Trait Methods.Front Genet2021
34645386Circall: fast and accurate methodology for discovery of circular RNAs from paired-end RNA-sequencing data.BMC Bioinformatics2021
31400221Alternating EM algorithm for a bilinear model in isoform quantification from RNA-seq data.Bioinformatics2020
33543134Creatinine and C-reactive protein in amyotrophic lateral sclerosis, multiple sclerosis and Parkinson's disease.Brain Commun2020
32010190Reproducibility of Methods to Detect Differentially Expressed Genes from Single-Cell RNA Sequencing.Front Genet2020
33110144A systems genomics approach to uncover the molecular properties of cancer genes.Sci Rep2020
32601477High-definition likelihood inference of genetic correlations across human complex traits.Nat Genet2020
32737166Profiles of histidine-rich glycoprotein associate with age and risk of all-cause mortality.Life Sci Alliance2020
32557963Blood biomarkers and prognosis of amyotrophic lateral sclerosis.Eur J Neurol2020
28901198Regression standardization and attributable fraction estimation with between-within frailty models for clustered survival data.Stat Methods Med Res2019
31420051Disease trajectories and mortality among women diagnosed with breast cancer.Breast Cancer Res2019
30941497On the relationship between the heritability and the attributable fraction.Hum Genet2019
31087715Antibiotics use and risk of amyotrophic lateral sclerosis in Sweden.Eur J Neurol2019
30911020CREDO: Highly confident disease-relevant A-to-I RNA-editing discovery in breast cancer.Sci Rep2019
31028395Cell-level somatic mutation detection from single-cell RNA sequencing.Bioinformatics2019
27587596Parametric and penalized generalized survival models.Stat Methods Med Res2018
30155912Likelihood-based inference for bounds of causal parameters.Stat Med2018
29858523RPASE: Individual-based allele-specific expression detection without prior knowledge of haplotype phase.Mol Ecol Resour2018
30012197Accumulation of potential driver genes with genomic alterations predicts survival of high-risk neuroblastoma patients.Biol Direct2018
30382840A fast detection of fusion genes from paired-end RNA-seq data.BMC Genomics2018
29490015Isoform-level gene expression patterns in single-cell RNA-sequencing data.Bioinformatics2018
29100626Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden.Biol Psychiatry2018
26265764Sparse estimation of gene-gene interactions in prediction models.Stat Methods Med Res2017
28250427Patterns of acute inflammatory symptoms prior to cancer diagnosis.Sci Rep2017
28152172The ABC model of prostate cancer: A conceptual framework for the design and interpretation of prognostic studies.Cancer2017
28288659A clinical model for identifying the short-term risk of breast cancer.Breast Cancer Res2017
29198721A Selection Operator for Summary Association Statistics Reveals Allelic Heterogeneity of Complex Traits.Am J Hum Genet2017
28905409Generalized survival models for correlated time-to-event data.Stat Med2017
26899349One CNV Discordance in NRXN1 Observed Upon Genome-wide Screening in 38 Pairs of Adult Healthy Monozygotic Twins.Twin Res Hum Genet2016
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Collaborators

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Co-authored papers 16
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Karolinska Institutet
Co-authored papers 10
Patrik K E Magnusson
Co-authored papers 9
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Co-authored papers 8
Lorelei A Mucci
Co-authored papers 8
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Co-authored papers 8
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Co-authored papers 6
Chen Suo
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KTH Royal Institute of Technology
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Andrea Ganna
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Liewei Wang
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Todd R Golub
Broad Institute of MIT and Harvard
Co-authored papers 3
Patrick F Sullivan
University of North Carolina at Chapel Hill
Co-authored papers 3
Peter Nilsson
Linkoping University
Co-authored papers 3
Tõnu Esko
Co-authored papers 3
Mark Seielstad
Co-authored papers 3
Release 1.2