Diana Zelenika

发表

Implication of the immune system in Alzheimer's disease: evidence from genome-wide pathway analysis.

Simon Heath, Christophe Tzourio, Philippe Amouyel, 2010, Journal of Alzheimer's disease : JAD.

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

Albert David, Jean Weissenbach, José-Alain Sahel, 2011, Orphanet journal of rare diseases.

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

Melissa Bondy, Andre Franke, Anthony Swerdlow, 2011, Human molecular genetics.

Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis

Jean-Baptiste Cazier, Dominique Gauguier, Daniel E. Platt, 2012, PloS one.

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

Marko Hočevar, Florence Demenais, Kari Stefansson, 2013, Nature Genetics.

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

Michael R Knowles, Pierre-Yves Boëlle, Fred A Wright, 2012, Nature Genetics.

Genome-Wide Population-Based Association Study of Extremely Overweight Young Adults – The GOYA Study

Torben Hansen, Niels Grarup, Allan Linneberg, 2011, PloS one.

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

Elodie Ey, Thomas Bourgeron, Roberto Toro, 2012, PLoS genetics.

Genome-wide association study identifies five susceptibility loci for glioma

Melissa Bondy, Anthony Swerdlow, Maria Feychting, 2009, Nature Genetics.

Using Prior Information from the Medical Literature in GWAS of Oral Cancer Identifies Novel Susceptibility Variant on Chromosome 4 - the AdAPT Method

Angus Roberts, Jon Wakefield, Hamish Cunningham, 2012, PloS one.

Lung cancer susceptibility locus at 5p15.33

Simon Heath, Tomas Axelsson, Jolanta Lissowska, 2008, Nature Genetics.

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

Renzo Guerrini, Patrick Nitschke, Elena Fontana, 2013, Nature Genetics.

Fine Mapping of Quantitative Trait Loci Affecting Female Fertility in Dairy Cattle on BTA03 Using a Dense Single-Nucleotide Polymorphism Map

Mathieu Gautier, Didier Boichard, Ivo G. Gut, 2008, Genetics.

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

Paolo Vineis, Theodore R Holford, Peter Kraft, 2014, Nature Genetics.

Genetic Variants in Novel Pathways Influence Blood Pressure and Cardiovascular Disease Risk

Christian Gieger, Xiaofeng Zhu, Paolo Vineis, 2011, Nature.

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

Paolo Vineis, Salvatore Panico, Vittorio Krogh, 2011, Nature Genetics.

Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions

Jean-Baptiste Poline, Thomas Bourgeron, Philippe Pinel, 2012, The Journal of Neuroscience.

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

Marc Gewillig, Rachel Soemedi, Koenraad Devriendt, 2012, American journal of human genetics.

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

Christian Gieger, Alex Doney, Inês Barroso, 2010, Nature Genetics.

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

Paolo Vineis, Wolfgang Ahrens, Antonio Agudo, 2008, Nature.

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

Brent S. Pedersen, Naftali Kaminski, James D. Crapo, 2013, Nature Genetics.

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

Anne Boland, Maria Martinez, J. Kaufman, 2011, European Journal of Human Genetics.

Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4

Simon Heath, Michel Georges, Liming Liang, 2007, PLoS genetics.

Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

Elodie Ey, Thomas Bourgeron, Roberto Toro, 2014, PLoS genetics.

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

Johan T den Dunnen, Simon Heath, Fernando Rivadeneira, 2008, American journal of human genetics.

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

Claude Bouchard, Beverley Balkau, Bengt Sennblad, 2012, Nature Genetics.

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

Hilkka Soininen, Sandro Sorbi, Philippe Amouyel, 2011, Neurobiology of Aging.

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

Michael Jones, Julian Peto, Simon Heath, 2011, Journal of the National Cancer Institute.

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

Simon Heath, Steve Best, Martin Farrall, 2007, Nature Genetics.

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

Mohamad Saad, Alexandra Durr, Christophe Tzourio, 2011, Human molecular genetics.

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

Isabelle Cleynen, Michel Georges, Paul Rutgeerts, 2011, Nature Genetics.