Rodney J Scott

发表

ONCOSTATIN M (OSM) IS INCREASED IN ASTHMA WITH INCOMPLETELY REVERSIBLE AIRFLOW OBSTRUCTION

Jodie L Simpson, Katherine J Baines, Michael J Boyle, 2009, Experimental lung research.

Deletion Mutations in an Australian Series of HNPCC Patients

Rodney J Scott, Mary McPhillips, Cliff J Meldrum, 2005, Hereditary cancer in clinical practice.

Modifier Genes and HNPCC: Variable phenotypic expression in HNPCC and the search for modifier genes

Rodney J Scott, R. Scott, R. Scott, 2008, European Journal of Human Genetics.

Phenotype-genotype correlations in a series of wolfram syndrome families.

Rodney J Scott, Cliff J Meldrum, Casey J A Smith, 2004, Diabetes care.

Identification of genome-wide SNP-SNP and SNP-clinical Boolean interactions in age-related macular degeneration.

Jie Jin Wang, Christopher Oldmeadow, Paul Mitchell, 2015, Methods in molecular biology.

TAPES: A tool for assessment and prioritisation in exome studies

Rodney J Scott, Alexandre Xavier, Bente A Talseth-Palmer, 2019, PLoS Comput. Biol..

The NOD2 3020insC Mutation and the Risk of Colorectal Cancer

Rodney J Scott, Anna Jakubowska, Grzegorz Kurzawski, 2004, Cancer Research.

A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2genes

Rodney J Scott, Alexander Dobrovic, Stephen B Fox, 2011 .

Application of a 5-tiered scheme for standardized classification of 2,360 unique mismatch repair gene variants in the InSiGHT locus-specific database

Rodney J Scott, John-Paul Plazzer, Finlay Macrae, 2013, Nature Genetics.

Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.

Christian Gieger, Thomas Meitinger, Paul Mitchell, 2013, Human molecular genetics.

Association between endometriosis and the interleukin 1A (IL1A) locus.

Yadav Sapkota, Mark McEvoy, Rodney J Scott, 2015, Human reproduction.

Capturing all disease-causing mutations for clinical and research use: Toward an effortless system for the Human Variome Project

Mauno Vihinen, George P Patrinos, Rodney J Scott, 2009, Genetics in Medicine.

Small Molecular Weight Variants of p53 Are Expressed in Human Melanoma Cells and Are Induced by the DNA-Damaging Agent Cisplatin

Borivoj Vojtesek, Rodney J Scott, David P Lane, 2008, Clinical Cancer Research.

How to use an article about genetic association: B: Are the results of the study valid?

Ammarin Thakkinstian, Mark McEvoy, Rodney J Scott, 2009, JAMA.

Planning the Human Variome Project: The Spain report

Toshio Kojima, John M. Hancock, Sue Povey, 2009, Human mutation.

Cortical Brain Abnormalities in 4474 Individuals With Schizophrenia and 5098 Control Subjects via the Enhancing Neuro Imaging Genetics Through Meta Analysis (ENIGMA) Consortium

Adrian Preda, Peter Kochunov, Elliot Hong, 2018, Biological Psychiatry.

Comparison of HapMap and 1000 Genomes Reference Panels in a Large-Scale Genome-Wide Association Study

Jie Huang, Uwe Völker, Ming-Huei Chen, 2017, PloS one.

Smad4 haploinsufficiency: a matter of dosage

Rodney J Scott, Patrick Franken, Riccardo Fodde, 2008, PathoGenetics.

Transcriptional phenotypes of asthma defined by gene expression profiling of induced sputum samples.

Jodie L Simpson, Katherine J Baines, Rodney J Scott, 2011, The Journal of allergy and clinical immunology.

Altered gene expression in the superior temporal gyrus in schizophrenia

Rodney J Scott, Paul A Tooney, R. Scott, 2008, BMC Genomics.

Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits

Christian Gieger, Gonçalo Abecasis, He Gao, 2018, Nature Genetics.

STaRRRT: a table of short tandem repeats in regulatory regions of the human genome

Rodney J Scott, Elizabeth G Holliday, R. Scott, 2013, BMC Genomics.

Five endometrial cancer risk loci identified through genome-wide association analysis

Hui Zhao, Mark McEvoy, Julian Peto, 2016, Nature Genetics.

PALB2,CHEK2 and ATM rare variants and cancer risk: Data from COGS

Dong Liang, Jane E. Carpenter, Peter Kraft, 2016 .

Genetic analysis of over one million people identifies 535 novel loci for blood pressure

Christian Gieger, Gonçalo Abecasis, He Gao, 2017, bioRxiv.

How to use an article about genetic association: A: Background concepts.

Ammarin Thakkinstian, Mark McEvoy, Rodney J Scott, 2009, JAMA.

Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk

Rodney J Scott, Grzegorz Kurzawski, Janina Suchy, 2008, BMC Cancer.

Methylome sequencing in triple-negative breast cancer reveals distinct methylation clusters with prognostic value

Rodney J Scott, Matt Trau, Mark D Robinson, 2015, Nature Communications.

GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.

Harvey Risch, Peter Kraft, Mark McEvoy, 2016, Human molecular genetics.

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

Rodney J Scott, Finlay Macrae, Annika Lindblom, 2011, The Lancet.

Combined analysis of exon splicing and genome wide polymorphism data predict schizophrenia risk loci.

Christopher Oldmeadow, Rodney J Scott, John R Attia, 2014, Journal of psychiatric research.

Identification of nine new susceptibility loci for endometrial cancer

Peter Kraft, Mark McEvoy, Julian Peto, 2018, Nature Communications.

P53 in human melanoma fails to regulate target genes associated with apoptosis and the cell cycle and may contribute to proliferation

Rodney J Scott, Bente A Talseth-Palmer, Peter Hersey, 2011, BMC Cancer.

Microarrays--identifying molecular portraits for prostate tumors with different Gleason patterns.

Pablo Moscato, Rodney J Scott, Alexandre Mendes, 2008, Methods in molecular medicine.