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Author Details

Johanna Schleutker
Institute of Biomedicine, University of Turku
1991
179
46
PMIDPaper TitleJournal TitlePublished Year
36674564Transcripts of the Prostate Cancer-Associated Gene <i>ANO7</i> Are Retained in the Nuclei of Prostatic Epithelial Cells.Int J Mol Sci2023
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36586737TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients.Neurobiol Aging2023
37311464Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.Am J Hum Genet2023
36674564Transcripts of the Prostate Cancer-Associated Gene <i>ANO7</i> Are Retained in the Nuclei of Prostatic Epithelial Cells.Int J Mol Sci2023
37292833Evaluating Approaches for Constructing Polygenic Risk Scores for Prostate Cancer in Men of African and European Ancestry.medRxiv2023
37945903Characterizing prostate cancer risk through multi-ancestry genome-wide discovery of 187 novel risk variants.Nat Genet2023
37292833Evaluating Approaches for Constructing Polygenic Risk Scores for Prostate Cancer in Men of African and European Ancestry.medRxiv2023
37311464Evaluating approaches for constructing polygenic risk scores for prostate cancer in men of African and European ancestry.Am J Hum Genet2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36586737TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patients.Neurobiol Aging2023
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
35307828Genetic analysis reveals novel variants for vascular cognitive impairment.Acta Neurol Scand2022
36086804Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).Acta Neurol Scand2022
35043958The variant rs77559646 associated with aggressive prostate cancer disrupts ANO7 mRNA splicing and protein expression.Hum Mol Genet2022
35307828Genetic analysis reveals novel variants for vascular cognitive impairment.Acta Neurol Scand2022
35152271Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score.Prostate Cancer Prostatic Dis2022
36086804Clinical features and spectrum of NOTCH3 variants in Finnish patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL).Acta Neurol Scand2022
35043958The variant rs77559646 associated with aggressive prostate cancer disrupts ANO7 mRNA splicing and protein expression.Hum Mol Genet2022
35152271Prostate cancer risk stratification improvement across multiple ancestries with new polygenic hazard score.Prostate Cancer Prostatic Dis2022
32800727Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer.Eur Urol2021
33798739Multisite Evaluation and Validation of a Sensitive Diagnostic and Screening System for Spinal Muscular Atrophy that Reports SMN1 and SMN2 Copy Number, along with Disease Modifier and Gene Duplication Variants.J Mol Diagn2021
34063511A Rare Variant in <i>ERF</i> (rs144812092) Predisposes to Prostate and Bladder Cancers in an Extended Pedigree.Cancers (Basel)2021
34012061Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease.Prostate Cancer Prostatic Dis2021
33473200Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33623038Polygenic hazard score is associated with prostate cancer in multi-ethnic populations.Nat Commun2021
33727568PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice.Sci Rep2021
32800727Two-stage Study of Familial Prostate Cancer by Whole-exome Sequencing and Custom Capture Identifies 10 Novel Genes Associated with the Risk of Prostate Cancer.Eur Urol2021
33420416Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer.Prostate Cancer Prostatic Dis2021
33398198Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33436325Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.Eur Urol Oncol2021
33268848Whole-exome sequencing of Finnish patients with vascular cognitive impairment.Eur J Hum Genet2021
34470488<i>COL4A1</i> and <i>COL4A2</i> Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes.Stroke2021
33623038Polygenic hazard score is associated with prostate cancer in multi-ethnic populations.Nat Commun2021
33727568PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J mice.Sci Rep2021
33798739Multisite Evaluation and Validation of a Sensitive Diagnostic and Screening System for Spinal Muscular Atrophy that Reports SMN1 and SMN2 Copy Number, along with Disease Modifier and Gene Duplication Variants.J Mol Diagn2021
34470488<i>COL4A1</i> and <i>COL4A2</i> Duplication Causes Cerebral Small Vessel Disease With Recurrent Early Onset Ischemic Strokes.Stroke2021
34063511A Rare Variant in <i>ERF</i> (rs144812092) Predisposes to Prostate and Bladder Cancers in an Extended Pedigree.Cancers (Basel)2021
34012061Novel prostate cancer susceptibility gene SP6 predisposes patients to aggressive disease.Prostate Cancer Prostatic Dis2021
33436325Rare Germline Variants in ATM Predispose to Prostate Cancer: A PRACTICAL Consortium Study.Eur Urol Oncol2021
33398198Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33420416Additional SNPs improve risk stratification of a polygenic hazard score for prostate cancer.Prostate Cancer Prostatic Dis2021
33473200Publisher Correction: Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction.Nat Genet2021
33268848Whole-exome sequencing of Finnish patients with vascular cognitive impairment.Eur J Hum Genet2021
32514134The effect of sample size on polygenic hazard models for prostate cancer.Eur J Hum Genet2020
32183364Inherited DNA Repair Gene Mutations in Men with Lethal Prostate Cancer.Genes (Basel)2020
32176628The interactome of the prostate-specific protein Anoctamin 7.Cancer Biomark2020
32634151ShAn: An easy-to-use tool for interactive and integrated variant annotation.PLoS One2020
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Francesca Demichelis
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Collaborators

Fredrik Wiklund
Co-authored papers 60
Janet L Stanford
Fred Hutchinson Cancer Research Center
Co-authored papers 57
Stephen N Thibodeau
Mayo Clinic
Co-authored papers 56
Henrik Gr??nberg
Karolinska Institute
Co-authored papers 55
Zsofia Kote-Jarai
The Institute of Cancer Research
Co-authored papers 53
Douglas F Easton
University of Cambridge
Co-authored papers 53
Rosalind A Eeles
The Institute of Cancer Research
Co-authored papers 52
Graham G Giles
Co-authored papers 51
David E Neal
University of Oxford, John Radcliffe Hospital
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Børge G Nordestgaard
Co-authored papers 41
Cezary Cybulski
International Hereditary Cancer Center, Pomeranian Medical University
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Daniel J Schaid
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Christopher A Haiman
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Co-authored papers 39
Ruth C Travis
Co-authored papers 39
Shannon K McDonnell
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Kay-Tee Khaw
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Jianfeng Xu
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William B Isaacs
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Freddie C Hamdy
University of Oxford
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Elaine A Ostrander
National Cancer Institute
Co-authored papers 30
John D Carpten
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Olli Kallioniemi
Karolinska Institute
Co-authored papers 26
Judith A Clements
Co-authored papers 25
Sue A Ingles
Co-authored papers 24
William J Blot
Vanderbilt University Medical Center
Co-authored papers 23
Sonja I Berndt
Co-authored papers 23
Demetrius Albanes
Co-authored papers 22
Kathleen A Cooney
Duke University School of Medicine, and the Duke Cancer Institute
Co-authored papers 22
Esther M John
Co-authored papers 21
Tokhir Dadaev
The Institute of Cancer Research
Co-authored papers 20
Release 1.2