Diana Zelenika


Ontology type: schema:Person     


Person Info

NAME

Diana

SURNAME

Zelenika

Publications in SciGraph latest 50 shown

  • 2016-12 Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia in BMC GENETICS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 TCF12 is mutated in anaplastic oligodendroglioma in NATURE COMMUNICATIONS
  • 2015-10 Genetic association analyses highlight biological pathways underlying mitral valve prolapse in NATURE GENETICS
  • 2015-01 Common variation in PHACTR1 is associated with susceptibility to cervical artery dissection in NATURE GENETICS
  • 2014-11 Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma in NATURE GENETICS
  • 2014-03 AP1S2 is mutated in X-linked Dandy–Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome) in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2014-02 Association of Genetic Variants in CDK6 and XRCC1 with the Risk of Dysplastic Nevi in Melanoma-Prone Families in JOURNAL OF INVESTIGATIVE DERMATOLOGY
  • 2013-12 Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease in NATURE GENETICS
  • 2013-08 Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice in DIABETOLOGIA
  • 2013-07 Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16 in NATURE GENETICS
  • 2013-06 Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis in NATURE GENETICS
  • 2013-06 Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly in NATURE GENETICS
  • 2013-04 A variant in FTO shows association with melanoma risk not due to BMI in NATURE GENETICS
  • 2012-12 High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly in BMC GENOMICS
  • 2012-06 A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance in NATURE GENETICS
  • 2012-05 Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis in NATURE GENETICS
  • 2012-02-01 Serial translocation by means of circular intermediates underlies colour sidedness in cattle in NATURE
  • 2011-12 A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1 in BMC MEDICAL GENETICS
  • 2011-12 Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-12 Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis in ORPHANET JOURNAL OF RARE DISEASES
  • 2011-12 Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine in BMC GENOMICS
  • 2011-11 Genome-wide association study identifies three new melanoma susceptibility loci in NATURE GENETICS
  • 2011-10-19 A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma in NATURE
  • 2011-10 Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk in NATURE
  • 2011-06 Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2011-05 Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease in NATURE GENETICS
  • 2011-01 Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3 in NATURE GENETICS
  • 2011-01 Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease in NATURE GENETICS
  • 2011-01 CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs in NATURE GENETICS
  • 2010-10 A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum in NEUROGENETICS
  • 2009-10 Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease in NATURE GENETICS
  • 2008-12 Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans in BMC EVOLUTIONARY BIOLOGY
  • 2008-12 Lung cancer susceptibility locus at 5p15.33 in NATURE GENETICS
  • 2008-04 A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25 in NATURE
  • 2007-11 Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families in NEUROGENETICS
  • 2007-10 A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 in NATURE GENETICS
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