Johanna Schleutker


Ontology type: schema:Person     


Person Info

NAME

Johanna

SURNAME

Schleutker

Publications in SciGraph latest 50 shown

  • 2019-12 Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry in NATURE COMMUNICATIONS
  • 2019-12 Shared heritability and functional enrichment across six solid cancers in NATURE COMMUNICATIONS
  • 2019-02 Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2018-12 Germline variation at 8q24 and prostate cancer risk in men of European ancestry in NATURE COMMUNICATIONS
  • 2018-12 Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants in NATURE COMMUNICATIONS
  • 2018-07 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2018-06 Germline variants in IL4, MGMT and AKT1 are associated with prostate cancer-specific mortality: An analysis of 12,082 prostate cancer cases in PROSTATE CANCER AND PROSTATIC DISEASES
  • 2017-12 Genetic association analysis of the RTK/ERK pathway with aggressive prostate cancer highlights the potential role of CCND2 in disease progression in SCIENTIFIC REPORTS
  • 2017-12 Germline EMSY sequence alterations in hereditary breast cancer and ovarian cancer families in BMC CANCER
  • 2017-12 Case-control analysis of truncating mutations in DNA damage response genes connects TEX15 and FANCD2 with hereditary breast cancer susceptibility in SCIENTIFIC REPORTS
  • 2017-11 FANCM mutation c.5791C>T is a risk factor for triple-negative breast cancer in the Finnish population in BREAST CANCER RESEARCH AND TREATMENT
  • 2017-01 Whole-exome sequencing of Finnish hereditary breast cancer families in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2016-12 Pubertal development and prostate cancer risk: Mendelian randomization study in a population-based cohort in BMC MEDICINE
  • 2016-08 Polyunsaturated fatty acids and prostate cancer risk: a Mendelian randomisation analysis from the PRACTICAL consortium in BRITISH JOURNAL OF CANCER
  • 2016-08 Genome-wide association of familial prostate cancer cases identifies evidence for a rare segregating haplotype at 8q24.21 in HUMAN GENETICS
  • 2016-04-07 Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation in NATURE COMMUNICATIONS
  • 2016-04 Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array in BRITISH JOURNAL OF CANCER
  • 2015-11 The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium in CANCER CAUSES & CONTROL
  • 2015-09 Reducing overdiagnosis by polygenic risk-stratified screening: findings from the Finnish section of the ERSPC in BRITISH JOURNAL OF CANCER
  • 2014-10 A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer in NATURE GENETICS
  • 2014-04 Evaluation of the RHINO gene for breast cancer predisposition in Finnish breast cancer families in BREAST CANCER RESEARCH AND TREATMENT
  • 2014-03 Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease in HUMAN GENETICS
  • 2013-04 Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array in NATURE GENETICS
  • 2013-04 Genetic heterogeneity in Finnish hereditary prostate cancer using ordered subset analysis in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-01 HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG) in HUMAN GENETICS
  • 2012-12 Screening of Finnish RAD51Cfounder mutations in prostate and colorectal cancer patients in BMC CANCER
  • 2012-12 Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families in BMC MEDICAL GENETICS
  • 2012-07 Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG) in HUMAN GENETICS
  • 2011-12 NMD and microRNA expression profiling of the HPCX1 locus reveal MAGEC1 as a candidate prostate cancer predisposition gene in BMC CANCER
  • 2011-08 Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study in NATURE GENETICS
  • 2011-02 Screening for BRCA1, BRCA2, CHEK2, PALB2, BRIP1, RAD50, and CDH1 mutations in high-risk Finnish BRCA1/2-founder mutation-negative breast and/or ovarian cancer individuals in BREAST CANCER RESEARCH
  • 2009-12 PALB2 variants in hereditary and unselected Finnish Prostate cancer cases in JOURNAL OF NEGATIVE RESULTS IN BIOMEDICINE
  • 2009-10 Identification of seven new prostate cancer susceptibility loci through a genome-wide association study in NATURE GENETICS
  • 2009-10 Genome-wide association and replication studies identify four variants associated with prostate cancer susceptibility in NATURE GENETICS
  • 2009-06 C-reactive protein haplotype is associated with high PSA as a marker of metastatic prostate cancer but not with overall cancer risk in BRITISH JOURNAL OF CANCER
  • 2008-08 ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2007-04 Segregation analysis of 1,546 prostate cancer families in Finland shows recessive inheritance in HUMAN GENETICS
  • 2007-03 A recurrent mutation in PALB2 in Finnish cancer families in NATURE
  • 2006-12 EPHB2 germline variants in patients with colorectal cancer or hyperplastic polyposis in BMC CANCER
  • 2006-02 Two-locus genome-wide linkage scan for prostate cancer susceptibility genes with an interaction effect in HUMAN GENETICS
  • 2005-11 A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region in HUMAN GENETICS
  • 2005-08 CHEK2 mutations in primary glioblastomas in JOURNAL OF NEURO-ONCOLOGY
  • 2005-08 A major locus for hereditary prostate cancer in Finland: localization by linkage disequilibrium of a haplotype in the HPCX region in HUMAN GENETICS
  • 2005-01 Hereditary prostate cancer in Finland: fine-mapping validates 3p26 as a major predisposition locus in HUMAN GENETICS
  • 2004-09 Nonsense-mediated decay microarray analysis identifies mutations of EPHB2 in human prostate cancer in NATURE GENETICS
  • 2003-11 CHEK2 variants associate with hereditary prostate cancer in BRITISH JOURNAL OF CANCER
  • 2002-08 Androgen receptor CAG polymorphism and prostate cancer risk in HUMAN GENETICS
  • 2002-02 Germline mutations in the ribonuclease L gene in families showing linkage with HPC1 in NATURE GENETICS
  • 2001-04 Relatives of Prostate Cancer Patients have an Increased Risk of Prostate and Stomach Cancers: A Population-Based, Cancer Registry study in Finland in CANCER CAUSES & CONTROL
  • 2001 A missense substitution A49T in the steroid 5-alpha-reductase gene (SRD5A2) is not associated with prostate cancer in Finland in BRITISH JOURNAL OF CANCER
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