Jiannis Ragoussis

发表

Algorithm implementation for CNV discovery using Affymetrix and Illumina SNP array data.

Laura Winchester, Jiannis Ragoussis, J. Ragoussis, 2012, Methods in molecular biology.

GenoSNP: a variational Bayes within-sample SNP genotyping algorithm that does not require a reference population

Eleni Giannoulatou, Christopher Yau, Christopher C. Holmes, 2008, Bioinform..

BeadArray-based genotyping.

Jiannis Ragoussis, Helen Butler, J. Ragoussis, 2008, Methods in molecular biology.

hsa-miR-210 Is Induced by Hypoxia and Is an Independent Prognostic Factor in Breast Cancer

Carme Camps, Jiannis Ragoussis, Francesca M. Buffa, 2008, Clinical Cancer Research.

microRNA-associated progression pathways and potential therapeutic targets identified by integrated mRNA and microRNA expression profiling in breast cancer.

Carme Camps, Jiannis Ragoussis, Marian Taylor, 2011, Cancer research.

Explorer CMIP and ATP 2 C 2 Modulate Phonological Short-Term Memory in Language Impairment

Dorothy V. M. Bishop, Gillian Baird, Dianne F. Newbury, 2009 .

Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease

John Broxholme, Jiannis Ragoussis, Mark W Hankins, 2013, European Journal of Human Genetics.

Next-generation sequencing (NGS) as a diagnostic tool for retinal degeneration reveals a much higher detection rate in early-onset disease

John Broxholme, Jiannis Ragoussis, Mark W Hankins, 2012, European Journal of Human Genetics.

SW-ARRAY: a dynamic programming solution for the identification of copy-number changes in genomic DNA using array comparative genome hybridization data

Åsa Hedman, John Broxholme, Jiannis Ragoussis, 2005, Nucleic acids research.

Integrated analysis of microRNA and mRNA expression and association with HIF binding reveals the complexity of microRNA expression regulation under hypoxia

Anton J. Enright, Martin Reczko, Carme Camps, 2014, Molecular Cancer.

Direct targeting of Sec23a by miR-200s influences cancer cell secretome and promotes metastatic colonization

Jiannis Ragoussis, Benjamin A. Garcia, Francesca M. Buffa, 2011, Nature Medicine.

MicroRNA-125a is over-expressed in insulin target tissues in a spontaneous rat model of Type 2 Diabetes

Carme Camps, Quin F. Wills, Jiannis Ragoussis, 2009, BMC Medical Genomics.

Recessive Mutations in SPTBN2 Implicate β-III Spectrin in Both Cognitive and Motor Development

Peter Donnelly, Gilean McVean, Jean-Baptiste Cazier, 2012, PLoS genetics.

Concordant Regulation of Gene Expression by Hypoxia and 2-Oxoglutarate-dependent Dioxygenase Inhibition

Jiannis Ragoussis, J. Ragoussis, P. Ratcliffe, 2006, Journal of Biological Chemistry.

The Use of Genome-Wide eQTL Associations in Lymphoblastoid Cell Lines to Identify Novel Genetic Pathways Involved in Complex Traits

Christian Gieger, Lon R. Cardon, Kourosh R. Ahmadi, 2011, PloS one.

Direct reprogramming of fibroblasts into endothelial cells capable of angiogenesis and reendothelialization in tissue-engineered vessels

Jiannis Ragoussis, Yanhua Hu, Jing-Dong J. Han, 2012, Proceedings of the National Academy of Sciences.

Comparing CNV detection methods for SNP arrays.

Christopher Yau, Jiannis Ragoussis, Laura Winchester, 2009, Briefings in functional genomics & proteomics.

Regenerant Arabidopsis Lineages Display a Distinct Genome-Wide Spectrum of Mutations Conferring Variant Phenotypes

Jiannis Ragoussis, Aziz Mithani, Caifu Jiang, 2011, Current Biology.

Genotyping technologies for all.

Jiannis Ragoussis, J. Ragoussis, 2006, Drug discovery today. Technologies.

A statistical approach for detecting genomic aberrations in heterogeneous tumor samples from single nucleotide polymorphism genotyping data

Oliver Sieber, Christopher Yau, Jiannis Ragoussis, 2010, Genome Biology.

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

Kay E. Davies, Jean-Baptiste Cazier, Jiannis Ragoussis, 2011, PLoS genetics.

A 15q13.3 microdeletion segregating with autism

Jiannis Ragoussis, Annemarie Poustka, Sven Bölte, 2009, European Journal of Human Genetics.

A Targetable EGFR-Dependent Tumor-Initiating Program in Breast Cancer.

Kevin Petrecca, Jiannis Ragoussis, Dongmei Zuo, 2017, Cell reports.

Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

Jiannis Ragoussis, Ernesto Lowy, Alistair T. Pagnamenta, 2010, Biological Psychiatry.

Preparation of high-quality next-generation sequencing libraries from picogram quantities of target DNA.

Jiannis Ragoussis, David Buck, Siarhei Maslau, 2012, Genome research.

Affymetrix GeneChip® system: moving from research to the clinic

Jiannis Ragoussis, Gareth Elvidge, J. Ragoussis, 2006, Expert review of molecular diagnostics.

Genome-wide Association of Hypoxia-inducible Factor (HIF)-1α and HIF-2α DNA Binding with Expression Profiling of Hypoxia-inducible Transcripts

Jiannis Ragoussis, Richard R. Copley, J. Ragoussis, 2009, The Journal of Biological Chemistry.

A global network for investigating the genomic epidemiology of malaria

Taane G. Clark, Tom Oluoch, Giorgio Sirugo, 2008, Nature.

Genome-wide and fine-resolution association analysis of malaria in West Africa

Peter Donnelly, Michael Inouye, Giorgio Sirugo, 2009, Nature Genetics.

Single-cell RNA-seq reveals that glioblastoma recapitulates a normal neurodevelopmental hierarchy

Kevin Petrecca, Bratislav Misic, Jiannis Ragoussis, 2020, Nature Communications.

Extensive characterization of NF-κB binding uncovers non-canonical motifs and advances the interpretation of genetic functional traits

Martha Bulyk, Jiannis Ragoussis, Peter Humburg, 2011, Genome Biology.

MicroRNA-210 Regulates Mitochondrial Free Radical Response to Hypoxia and Krebs Cycle in Cancer Cells by Targeting Iron Sulfur Cluster Protein ISCU

Borivoj Vojnovic, Mircea Ivan, Jiannis Ragoussis, 2010, PloS one.

Quantitative high-throughput analysis of transcription factor binding specificities.

Jiannis Ragoussis, Richard Mott, Jane Linnell, 2004, Nucleic acids research.

MicroRNA-10b and breast cancer metastasis

Carme Camps, Jiannis Ragoussis, Stefano Colella, 2008, Nature.

Next generation sequencing for molecular diagnosis of neurological disorders using ataxias as a model

Jiannis Ragoussis, Andrea H. Németh, David Buck, 2013, Brain : a journal of neurology.

Comparative analysis of methods for gene transcription profiling data derived from different microarray technologies in rat and mouse models of diabetes

Jiannis Ragoussis, Dominique Gauguier, J. Ragoussis, 2009, BMC Genomics.

Association of the KIAA0319 dyslexia susceptibility gene with reading skills in the general population.

Jiannis Ragoussis, Andrew P Morris, Jean Golding, 2008, The American journal of psychiatry.

Genetically indistinguishable SNPs and their influence on inferring the location of disease-associated variants.

Jiannis Ragoussis, Andrew P Morris, Xiayi Ke, 2005, Genome research.

Quantitative profiling of protein-DNA binding on microarrays.

Jiannis Ragoussis, J. Ragoussis, Simon Field, 2006, Methods in molecular biology.

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

Dorothy V.M. Bishop, Gillian Baird, Dianne F. Newbury, 2009, American journal of human genetics.

Maleness-on-the-Y (MoY) orchestrates male sex determination in major agricultural fruit fly pests

Mark D. Robinson, Jiannis Ragoussis, Marco Salvemini, 2019, Science.

High-resolution genome-wide mapping of HIF-binding sites by ChIP-seq.

Jiannis Ragoussis, J. Ragoussis, P. Ratcliffe, 2011, Blood.

Benchmarking of the Oxford Nanopore MinION sequencing for quantitative and qualitative assessment of cDNA populations

Jiannis Ragoussis, Haig Djambazian, Dunarel Badescu, 2016, Scientific Reports.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

Metagenomic analysis of planktonic riverine microbial consortia using nanopore sequencing reveals insight into river microbe taxonomy and function

Dino Jolic, Richard M Leggett, Jiannis Ragoussis, 2020, GigaScience.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.