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Lista de obras de Diana Zelenika

A Follow-Up Study of a Genome-wide Association Scan Identifies a Susceptibility Locus for Venous Thrombosis on Chromosome 6p24.1

scholarly article by Pierre-Emmanuel Morange et al published April 2010 in American Journal of Human Genetics

A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15.

artículo científico publicado en 2007

A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

artículo científico publicado en 2011

A family-based genome-wide association study reveals an association of spondyloarthritis with MAPK14.

artículo científico publicado en 2016

A follow-up study of a genome-wide association scan identifies a susceptibility locus for venous thrombosis on chromosome 6p24.1.

artículo científico publicado en 2010

A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance

artículo científico publicado en 2012

A genome-wide association search for type 2 diabetes genes in African Americans

artículo científico publicado en 2012

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

artículo científico publicado en 2011

A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium

artículo científico publicado en 2011

A multi-stage multi-design strategy provides strong evidence that the BAI3 locus is associated with early-onset venous thromboembolism

artículo científico publicado en 2010

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

artículo científico publicado en 2010

A novel locus (CORD12) for autosomal dominant cone-rod dystrophy on chromosome 2q24.2-2q33.1.

artículo científico publicado en 2011

A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25

artículo científico publicado en 2008

A variant in FTO shows association with melanoma risk not due to BMI

artículo científico publicado en 2013

AP1S2 is mutated in X-linked Dandy-Walker malformation with intellectual disability, basal ganglia disease and seizures (Pettigrew syndrome).

artículo científico publicado en 2013

Alpha-synuclein gene rearrangements in dominantly inherited parkinsonism: frequency, phenotype, and mechanisms

artículo científico publicado en 2009

Antiviral agent cidofovir decreases Epstein-Barr virus (EBV) oncoproteins and enhances the radiosensitivity in EBV-related malignancies

artículo científico publicado en 2003

Association analysis indicates that a variant GATA-binding site in the PIK3CB promoter is a Cis-acting expression quantitative trait locus for this gene and attenuates insulin resistance in obese children

artículo científico publicado en 2007

Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls

scientific article published on 22 July 2013

Association between circadian genes, bipolar disorders and chronotypes.

artículo científico publicado en 2014

Association of genetic variants in CDK6 and XRCC1 with the risk of dysplastic nevi in melanoma-prone families

artículo científico publicado en 2013

Association of the CpG methylation pattern of the proximal insulin gene promoter with type 1 diabetes

artículo científico publicado en 2012

Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD.

artículo científico publicado en 2011

CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogs

artículo científico publicado en 2011

Caution in interpreting results from imputation analysis when linkage disequilibrium extends over a large distance: a case study on venous thrombosis

artículo científico publicado en 2012

Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms

artículo científico publicado en 2013

Chromosome 7p11.2 (EGFR) variation influences glioma risk

scientific journal article

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats

artículo científico publicado en 2013

Combining gene mapping and phenotype assessment for fast mutation finding in non-consanguineous autosomal recessive retinitis pigmentosa families

artículo científico publicado en 2011

Common and rare variant analysis in early-onset bipolar disorder vulnerability

artículo científico publicado en 2014

Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.

artículo científico publicado en 2009

Common variants at 30 loci contribute to polygenic dyslipidemia

artículo científico publicado en 2009

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Common variants at five new loci associated with early-onset inflammatory bowel disease

artículo científico publicado en 2009

Complete exon sequencing of all known Usher syndrome genes greatly improves molecular diagnosis

artículo científico publicado en 2011

Complex signatures of selection for the melanogenic loci TYR, TYRP1 and DCT in humans

artículo científico publicado en 2008

Comprehensive linkage and association analyses identify haplotype, near to the TNFSF15 gene, significantly associated with spondyloarthritis

artículo científico publicado en 2009

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease

artículo científico publicado en 2012

Deciphering the 8q24.21 association for glioma

artículo científico publicado en 2013

Development and implementation of a highly-multiplexed SNP array for genetic mapping in maritime pine and comparative mapping with loblolly pine

artículo científico publicado en 2011

Effect of 17q21 variants and smoking exposure in early-onset asthma

artículo científico publicado en 2008

Erratum to: Childhood acute leukemia, maternal beverage intake during pregnancy, and metabolic polymorphisms

scholarly article published in Cancer Causes & Control

Erratum: Corrigendum: A SUMOylation-defective MITF germline mutation predisposes to melanoma and renal carcinoma

artículo científico publicado en 2015

Erratum: Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

article

Erratum: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Evidence of the association of BIN1 and PICALM with the AD risk in contrasting European populations.

artículo científico publicado en 2011

Gene-environment interactions in 7610 women with breast cancer: prospective evidence from the Million Women Study

artículo científico publicado en 2010

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders

artículo científico publicado en 2012

Genetic association analyses highlight biological pathways underlying mitral valve prolapse

artículo científico publicado en 2015

Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk

artículo científico publicado en 2011

Genetics of venous thrombosis: insights from a new genome wide association study

artículo científico publicado en 2011

Genome wide association study for plasma levels of natural anticoagulant inhibitors and protein C anticoagulant pathway: the MARTHA project

article

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

artículo científico publicado en 2008

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population

artículo científico publicado en 2010

Genome-wide association study identifies eight loci associated with blood pressure

artículo científico publicado en 2009

Genome-wide association study identifies five susceptibility loci for glioma

artículo científico publicado en 2009

Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot

scientific journal article

Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma

artículo científico publicado en 2014

Genome-wide association study identifies multiple susceptibility loci for pulmonary fibrosis

scientific journal article

Genome-wide association study identifies three loci associated with melanoma risk

scientific article published on 05 July 2009

Genome-wide association study identifies three new melanoma susceptibility loci

artículo científico publicado en 2011

Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study in a Lebanese cohort confirms PHACTR1 as a major determinant of coronary artery stenosis

artículo científico publicado en 2012

Genome-wide association study of HPV seropositivity

artículo científico publicado en 2011

Genome-wide association study of age-related macular degeneration identifies associated variants in the TNXB-FKBPL-NOTCH4 region of chromosome 6p21.3

artículo científico publicado en 2012

Genome-wide association study of classical Hodgkin lymphoma and Epstein-Barr virus status-defined subgroups

scientific journal article

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

artículo científico publicado en 2013

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

scientific journal article

Genome-wide haplotype association study identifies the FRMD4A gene as a risk locus for Alzheimer's disease

artículo científico publicado en 2012

Genome-wide imputation study identifies novel HLA locus for pulmonary fibrosis and potential role for auto-immunity in fibrotic idiopathic interstitial pneumonia

artículo científico publicado en 2016

Genome-wide population-based association study of extremely overweight young adults--the GOYA study

artículo científico publicado en 2011

Global genetic architecture of an erythroid quantitative trait locus, HMIP-2

artículo científico publicado en 2014

High-resolution autosomal radiation hybrid maps of the pig genome and their contribution to the genome sequence assembly

artículo científico publicado en 2012

Implication of the Immune System in Alzheimer's Disease: Evidence from Genome-Wide Pathway Analysis

article

Incidence of Breast Cancer and Its Subtypes in Relation to Individual and Multiple Low-Penetrance Genetic Susceptibility Loci ⬇️

artículo científico publicado el 28 de julio de 2010

Increased expression of BIN1 mediates Alzheimer genetic risk by modulating tau pathology

artículo científico publicado en 2013

Induction of foxP3+ regulatory T cells in the periphery of T cell receptor transgenic mice tolerized to transplants

artículo científico publicado en 2004

Low penetrance susceptibility to glioma is caused by the TP53 variant rs78378222.

artículo científico publicado en 2013

Lung cancer susceptibility locus at 5p15.33

artículo científico publicado en 2008

Maternal smoking during pregnancy, genetic polymorphisms of metabolic enzymes, and childhood acute leukemia: the ESCALE Study (SFCE)

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: a gradient of severity in cognitive impairments

artículo científico publicado en 2014

Multiple apical plasma membrane constituents are associated with susceptibility to meconium ileus in individuals with cystic fibrosis

artículo científico publicado en 2012

Mutations in TUBG1, DYNC1H1, KIF5C and KIF2A cause malformations of cortical development and microcephaly

scientific article published on 21 April 2013

Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy

artículo científico publicado en 2009

Neuropeptide Y genotype, central obesity, and abdominal fat distribution: the POUNDS LOST trial

artículo científico publicado en 2015

New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk

artículo científico publicado en 2010

Newly identified loci that influence lipid concentrations and risk of coronary artery disease

artículo científico publicado en 2008

Novel Crohn disease locus identified by genome-wide association maps to a gene desert on 5p13.1 and modulates expression of PTGER4

artículo científico publicado en 2007

Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study

artículo científico publicado en 2011

Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals

artículo científico publicado en 2012

Prevalence and risk factors of the rheumatoid arthritis in Herzegovina region in 2003-2005.

artículo científico publicado en 2009

Quantitative variation in plasma angiotensin-I converting enzyme activity shows allelic heterogeneity in the ABO blood group locus

artículo científico publicado en 2013

Refinement of the SPG15 candidate interval and phenotypic heterogeneity in three large Arab families

artículo científico publicado en 2007

Regulatory T cells and dendritic cells in transplantation tolerance: molecular markers and mechanisms

artículo científico publicado en 2003

Regulatory T cells overexpress a subset of Th2 gene transcripts

artículo científico publicado en 2002

Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

artículo científico publicado en 2011

Serial translocation by means of circular intermediates underlies colour sidedness in cattle

artículo científico publicado en 2012

Seven new loci associated with age-related macular degeneration

artículo científico publicado en 2013

Sex-specific role for adenylyl cyclase type 7 in alcohol dependence

artículo científico publicado en 2011

Systematic Analysis of Candidate Genes for Alzheimer's Disease in a French, Genome-Wide Association Study

article

TCF12 is mutated in anaplastic oligodendroglioma

artículo científico publicado en 2015

The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study

artículo científico publicado en 2010

Thiazolidinediones partially reverse the metabolic disturbances observed in Bscl2/seipin-deficient mice

artículo científico publicado en 2013

Three genome-wide association studies and a linkage analysis identify HERC2 as a human iris color gene

artículo científico publicado en 2008

Using prior information from the medical literature in GWAS of oral cancer identifies novel susceptibility variant on chromosome 4--the AdAPT method

artículo científico publicado en 2012

Variations of SOST mRNA expression in human bone are associated with DNA polymorphism and DNA methylation in the SOST gene

artículo científico publicado en 2016

Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13.

artículo científico publicado en 2015

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