Davor Lessel


Ontology type: schema:Person     


Person Info

NAME

Davor

SURNAME

Lessel

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
  • 2018-12 Analyses of LMNA-negative juvenile progeroid cases confirms biallelic POLR3A mutations in Wiedemann–Rautenstrauch-like syndrome and expands the phenotypic spectrum of PYCR1 mutations in HUMAN GENETICS
  • 2018-10-03 Genome-wide association analysis suggests novel loci for Hashimoto’s thyroiditis in JOURNAL OF ENDOCRINOLOGICAL INVESTIGATION
  • 2018-07 Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci in NATURE GENETICS
  • 2017-12 Lessons learned from additional research analyses of unsolved clinical exome cases in GENOME MEDICINE
  • 2017-03 Compound heterozygous GATA5 mutations in a girl with hydrops fetalis, congenital heart defects and genital anomalies in HUMAN GENETICS
  • 2016-12 Phenotype and genotype in patients with Larsen syndrome: clinical homogeneity and allelic heterogeneity in seven patients in BMC MEDICAL GENETICS
  • 2016-12 The analysis of heterotaxy patients reveals new loss-of-function variants of GRK5 in SCIENTIFIC REPORTS
  • 2014-12 Chromatin retention of DNA damage sensors DDB2 and XPC through loss of p97 segregase causes genotoxicity in NATURE COMMUNICATIONS
  • 2014-11 Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features in NATURE GENETICS
  • 2014-08 KIT mutations in primary mediastinal B-cell lymphoma in BLOOD CANCER JOURNAL
  • 2013-01 Erstmanifestation einer fulminanten Malignen-Hyperthermie-Krise in DER ANAESTHESIST
  • 2012-12 Werner-Syndrom in MEDIZINISCHE GENETIK
  • 2010-07 WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations in HUMAN GENETICS
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