Rodney J. Scott Medical Genetics Hunter Medical Research Institute Biography Publications Institution JoVE Articles Rodney J. Scott has not added a biography. If you are Rodney J. Scott and would like to personalize this page please email our Author Liaison for assistance. Publications Differing Contributions of Classical Risk Factors to Type 2 Diabetes in Multi-Ethnic Malaysian Populations International Journal of Environmental Research and Public Health. 12, 2018 | Pubmed ID: 30544761 Genetic Risk Score Mendelian Randomization Shows That Obesity Measured As Body Mass Index, but Not Waist:hip Ratio, is Causal for Endometrial Cancer Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology. Aug, 2016 | Pubmed ID: 27550749 Reevaluation of RINT1 As a Breast Cancer Predisposition Gene Breast Cancer Research and Treatment. Aug, 2016 | Pubmed ID: 27544226 Corrigendum: Genetic Variants Associated with Subjective Well-being, Depressive Symptoms, and Neuroticism Identified Through Genome-wide Analyses Nature Genetics. Jul, 2016 | Pubmed ID: 27463399 Transcriptome-wide Mega-analyses Reveal Joint Dysregulation of Immunologic Genes and Transcription Regulators in Brain and Blood in Schizophrenia Schizophrenia Research. Jul, 2016 | Pubmed ID: 27450777 A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 Through YY1 Binding American Journal of Human Genetics. Jun, 2016 | Pubmed ID: 27259051 A Novel Polymorphic Repeat in the Upstream Regulatory Region of the Estrogen-induced Gene EIG121 is Not Associated with the Risk of Developing Breast or Endometrial Cancer BMC Research Notes. 2016 | Pubmed ID: 27230222 Genome-wide Association Study Identifies 74 Loci Associated with Educational Attainment Nature. May, 2016 | Pubmed ID: 27225129 Five Endometrial Cancer Risk Loci Identified Through Genome-wide Association Analysis Nature Genetics. Jun, 2016 | Pubmed ID: 27135401 A Polymorphic Repeat in the IGF1 Promoter Influences the Risk of Endometrial Cancer Endocrine Connections. May, 2016 | Pubmed ID: 27090263 Genetic Variants Associated with Subjective Well-being, Depressive Symptoms, and Neuroticism Identified Through Genome-wide Analyses Nature Genetics. Jun, 2016 | Pubmed ID: 27089181 Renin-angiotensin System Gene Polymorphisms and Endometrial Cancer Endocrine Connections. May, 2016 | Pubmed ID: 27068935 Lynch Syndrome Mutation Spectrum in New South Wales, Australia, Including 55 Novel Mutations Molecular Genetics & Genomic Medicine. Mar, 2016 | Pubmed ID: 27064304 Do Founder Mutations Characteristic of Some Cancer Sites Also Predispose to Pancreatic Cancer? International Journal of Cancer. Aug, 2016 | Pubmed ID: 27038244 Genome-wide Significant Results Identified for Plasma Apolipoprotein H Levels in Middle-aged and Older Adults Scientific Reports. 2016 | Pubmed ID: 27030319 Early Changes of Endometrial Neoplasia Revealed by Loss of Mismatch Repair Gene Protein Expression in a Patient Diagnosed with Lynch Syndrome Pathology. Jan, 2016 | Pubmed ID: 27020214 GWAS Meta-analysis of 16 852 Women Identifies New Susceptibility Locus for Endometrial Cancer Human Molecular Genetics. Mar, 2016 | Pubmed ID: 27008869 Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women JAMA Psychiatry. May, 2016 | Pubmed ID: 27007234 Associations Between Methylenetetrahydrofolate Reductase Polymorphisms, Serum Homocysteine Levels, and Incident Cortical Cataract JAMA Ophthalmology. Mar, 2016 | Pubmed ID: 26986182 Thank You to All Our Manuscript Reviewers in 2015 Hereditary Cancer in Clinical Practice. 2016 | Pubmed ID: 26933466 No Evidence That Protein Truncating Variants in BRIP1 Are Associated with Breast Cancer Risk: Implications for Gene Panel Testing Journal of Medical Genetics. May, 2016 | Pubmed ID: 26921362 Copy Number Variants Associated with 18p11.32, DCC and the Promoter 1B Region of APC in Colorectal Polyposis Patients Meta Gene. Feb, 2016 | Pubmed ID: 26909336 When is a Mutation Not a Mutation: the Case of the C.594-2A>C Splice Variant in a Woman Harbouring Another BRCA1 Mutation in Trans Hereditary Cancer in Clinical Practice. 2016 | Pubmed ID: 26884819 A Variant at 9p21.3 Functionally Implicates CDKN2B in Paediatric B-cell Precursor Acute Lymphoblastic Leukaemia Aetiology Nature Communications. 2016 | Pubmed ID: 26868379 Genetic Associations at 53 Loci Highlight Cell Types and Biological Pathways Relevant for Kidney Function Nature Communications. 2016 | Pubmed ID: 26831199 Targeted Next-generation Sequencing of 22 Mismatch Repair Genes Identifies Lynch Syndrome Families Cancer Medicine. May, 2016 | Pubmed ID: 26811195 Panel Testing for Familial Breast Cancer: Calibrating the Tension Between Research and Clinical Care Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. May, 2016 | Pubmed ID: 26786923 Serum Concentrations of Selenium and Copper in Patients Diagnosed with Pancreatic Cancer Cancer Research and Treatment : Official Journal of Korean Cancer Association. Jul, 2016 | Pubmed ID: 26727715 Altered Neural Signaling and Immune Pathways in Peripheral Blood Mononuclear Cells of Schizophrenia Patients with Cognitive Impairment: A Transcriptome Analysis Brain, Behavior, and Immunity. Mar, 2016 | Pubmed ID: 26697997 The Prevalence of Unique SNPs in the Renin-angiotensin System Highlights the Need for Pharmacogenetics in Indigenous Australians Clinical and Experimental Pharmacology & Physiology. Feb, 2016 | Pubmed ID: 26667052 The Presence of the Intron 3 16 Bp Duplication Polymorphism of P53 (rs17878362) in Breast Cancer is Associated with a Low Δ40p53:p53 Ratio and Better Outcome Carcinogenesis. Jan, 2016 | Pubmed ID: 26586794 CYP19A1 Fine-mapping and Mendelian Randomization: Estradiol is Causal for Endometrial Cancer Endocrine-related Cancer. Feb, 2016 | Pubmed ID: 26574572 A Meta-analysis of 120 246 Individuals Identifies 18 New Loci for Fibrinogen Concentration Human Molecular Genetics. Jan, 2016 | Pubmed ID: 26561523 VariantSpark: Population Scale Clustering of Genotype Information BMC Genomics. 2015 | Pubmed ID: 26651996 MiRNAs and Other Epigenetic Changes As Biomarkers in Triple Negative Breast Cancer International Journal of Molecular Sciences. 2015 | Pubmed ID: 26633365 Meta-analysis of Genome-wide Association Studies Identifies Common Susceptibility Polymorphisms for Colorectal and Endometrial Cancer Near SH2B3 and TSHZ1 Scientific Reports. 2015 | Pubmed ID: 26621817 Genome-wide DNA Methylation Profiling of CD8+ T Cells Shows a Distinct Epigenetic Signature to CD4+ T Cells in Multiple Sclerosis Patients Clinical Epigenetics. 2015 | Pubmed ID: 26550040 Novel Genes Associated with Lymph Node Metastasis in Triple Negative Breast Cancer Scientific Reports. 2015 | Pubmed ID: 26537449 Narrowing the Critical Region for Overgrowth Within 13q14.2-q14.3 Microdeletions European Journal of Medical Genetics. Nov, 2015 | Pubmed ID: 26475974 Methylation of the Corticotropin Releasing Hormone Gene Promoter in BeWo Cells: Relationship to Gene Activity International Journal of Endocrinology. 2015 | Pubmed ID: 26457081 Reevaluation of the BRCA2 Truncating Allele C.9976A > T (p.Lys3326Ter) in a Familial Breast Cancer Context Scientific Reports. 2015 | Pubmed ID: 26455428 Do Common Genotypes of FK506 Binding Protein 5 (FKBP5) Moderate the Effects of Childhood Maltreatment on Cognition in Schizophrenia and Healthy Controls? Journal of Psychiatric Research. Nov, 2015 | Pubmed ID: 26424418 Comprehensive Genetic Assessment of the ESR1 Locus Identifies a Risk Region for Endometrial Cancer Endocrine-related Cancer. Oct, 2015 | Pubmed ID: 26330482 CX3CR1 is Dysregulated in Blood and Brain from Schizophrenia Patients Schizophrenia Research. Oct, 2015 | Pubmed ID: 26285829 Genetic and Environmental Factors Affecting TNF-α Responses in Relation to Sudden Infant Death Syndrome Frontiers in Immunology. 2015 | Pubmed ID: 26284064 Prevalence of PALB2 Mutations in Australian Familial Breast Cancer Cases and Controls Breast Cancer Research : BCR. 2015 | Pubmed ID: 26283626 Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. Nov, 2015 | Pubmed ID: 26282643 Understanding Xeroderma Pigmentosum Complementation Groups Using Gene Expression Profiling After UV-Light Exposure International Journal of Molecular Sciences. 2015 | Pubmed ID: 26184184 Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis Journal of the National Cancer Institute. Sep, 2015 | Pubmed ID: 26134033 Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia Gastroenterology Research and Practice. 2015 | Pubmed ID: 26101521 Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression American Journal of Human Genetics. Jul, 2015 | Pubmed ID: 26073781 Proteotranscriptomic Profiling of 231-BR Breast Cancer Cells: Identification of Potential Biomarkers and Therapeutic Targets for Brain Metastasis Molecular & Cellular Proteomics : MCP. Sep, 2015 | Pubmed ID: 26041846 Biobank Classification in an Australian Setting Biopreservation and Biobanking. Jun, 2015 | Pubmed ID: 26035012 Nerve Fibers Infiltrate the Tumor Microenvironment and Are Associated with Nerve Growth Factor Production and Lymph Node Invasion in Breast Cancer Molecular Oncology. Oct, 2015 | Pubmed ID: 26009480 Genetic Burden Associated with Varying Degrees of Disease Severity in Endometriosis Molecular Human Reproduction. Jul, 2015 | Pubmed ID: 25882541 Virus Infections and Sudden Death in Infancy: The Role of Interferon-γ Frontiers in Immunology. 2015 | Pubmed ID: 25814991 Folate Pathway Gene Polymorphisms and Risk of Childhood Brain Tumors: Results from an Australian Case-control Study Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology. Jun, 2015 | Pubmed ID: 25809864 Exploring the Risk Factors for Sudden Infant Deaths and Their Role in Inflammatory Responses to Infection Frontiers in Immunology. 2015 | Pubmed ID: 25798137 Thank You to All Our Manuscript Reviewers in 2014 Hereditary Cancer in Clinical Practice. 2015 | Pubmed ID: 25763118 Cis-Expression Quantitative Trait Loci Mapping Reveals Replicable Associations with Heroin Addiction in OPRM1 Biological Psychiatry. Oct, 2015 | Pubmed ID: 25744370 Selenium As a Marker of Cancer Risk and of Selection for Control Examinations in Surveillance Contemporary Oncology (Poznań, Poland). 2015 | Pubmed ID: 25691823 Prevalence of BRCA1 and BRCA2 Germline Mutations in Patients with Triple-negative Breast Cancer Breast Cancer Research and Treatment. Feb, 2015 | Pubmed ID: 25682074 Breastfeeding and Nutrition to 2 Years of Age and Risk of Childhood Acute Lymphoblastic Leukemia and Brain Tumors Nutrition and Cancer. 2015 | Pubmed ID: 25646650 Methylome Sequencing in Triple-negative Breast Cancer Reveals Distinct Methylation Clusters with Prognostic Value Nature Communications. 2015 | Pubmed ID: 25641231 Genetics of Hand Grip Strength in Mid to Late Life Age (Dordrecht, Netherlands). Feb, 2015 | Pubmed ID: 25637336 Paternal Dietary Folate, B6 and B12 Intake, and the Risk of Childhood Brain Tumors Nutrition and Cancer. 2015 | Pubmed ID: 25625505 Genetic Overlap Between Diagnostic Subtypes of Ischemic Stroke Stroke; a Journal of Cerebral Circulation. Mar, 2015 | Pubmed ID: 25613305 Management of Ovarian and Endometrial Cancers in Women Belonging to HNPCC Carrier Families: Review of the Literature and Results of Cancer Risk Assessment in Polish HNPCC Families Hereditary Cancer in Clinical Practice. 2015 | Pubmed ID: 25606063 Candidate Locus Analysis of the TERT-CLPTM1L Cancer Risk Region on Chromosome 5p15 Identifies Multiple Independent Variants Associated with Endometrial Cancer Risk Human Genetics. Feb, 2015 | Pubmed ID: 25487306 Effects of Gender, Cytokine Gene Polymorphisms and Environmental Factors on Inflammatory Responses Innate Immunity. Jul, 2015 | Pubmed ID: 25432967 Identification of Genome-wide SNP-SNP and SNP-clinical Boolean Interactions in Age-related Macular Degeneration Methods in Molecular Biology (Clifton, N.J.). 2015 | Pubmed ID: 25403535 Folate Pathway Gene Polymorphisms, Maternal Folic Acid Use, and Risk of Childhood Acute Lymphoblastic Leukemia Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology. Jan, 2015 | Pubmed ID: 25395472 Polymorphisms in Nucleotide Excision Repair Genes and Susceptibility to Colorectal Cancer in the Polish Population Molecular Biology Reports. Mar, 2015 | Pubmed ID: 25391773 Rare Germline Copy Number Deletions of Likely Functional Importance Are Implicated in Endometrial Cancer Predisposition Human Genetics. Mar, 2015 | Pubmed ID: 25381466 Fine-mapping of the HNF1B Multicancer Locus Identifies Candidate Variants That Mediate Endometrial Cancer Risk Human Molecular Genetics. Mar, 2015 | Pubmed ID: 25378557 Association Between Endometriosis and the Interleukin 1A (IL1A) Locus Human Reproduction (Oxford, England). Jan, 2015 | Pubmed ID: 25336714 Polygenic Overlap Between Kidney Function and Large Artery Atherosclerotic Stroke Stroke; a Journal of Cerebral Circulation. Dec, 2014 | Pubmed ID: 25352485 Confirmation of Childhood Acute Lymphoblastic Leukemia Variants, ARID5B and IKZF1, and Interaction with Parental Environmental Exposures PloS One. 2014 | Pubmed ID: 25310577 Vehicle Refuelling, Use of Domestic Wood Heaters and the Risk of Childhood Brain Tumours: Results from an Australian Case-control Study Pediatric Blood & Cancer. Oct, 2014 | Pubmed ID: 25283072 Expanding the Genetic Basis of Copy Number Variation in Familial Breast Cancer Hereditary Cancer in Clinical Practice. 2014 | Pubmed ID: 24955146 Common Variants of Xeroderma Pigmentosum Genes and Prostate Cancer Risk Gene. Aug, 2014 | Pubmed ID: 24933002 Genome-wide Association Analysis Identifies Six New Loci Associated with Forced Vital Capacity Nature Genetics. Jul, 2014 | Pubmed ID: 24929828 Maternal Dietary Intake of Folate and Vitamins B6 and B12 During Pregnancy and Risk of Childhood Brain Tumors Nutrition and Cancer. 2014 | Pubmed ID: 24897174 KRAS Mutation Testing of Metastatic Colorectal Cancer in Australia: Where Are We At? Asia-Pacific Journal of Clinical Oncology. Sep, 2014 | Pubmed ID: 24811330 Genome-wide Association Study Identifies Two Novel Genomic Regions in Irritable Bowel Syndrome The American Journal of Gastroenterology. May, 2014 | Pubmed ID: 24797007 Prevalence of the E318K and V320I MITF Germline Mutations in Polish Cancer Patients and Multiorgan Cancer Risk-a Population-based Study Cancer Genetics. Apr, 2014 | Pubmed ID: 24767713 The Architecture of Risk for Type 2 Diabetes: Understanding Asia in the Context of Global Findings International Journal of Endocrinology. 2014 | Pubmed ID: 24744783 The Expression of Dicer and Drosha in Matched Normal Tissues, Tumours and Lymph Node Metastases in Triple Negative Breast Cancer BMC Cancer. 2014 | Pubmed ID: 24725360 Epithelioid Trophoblastic Tumour Simulating a High Grade Carcinoma Pathology. Apr, 2014 | Pubmed ID: 24614716 Dupuytren's Disease and the Risk of Malignant Neoplasms Hereditary Cancer in Clinical Practice. 2014 | Pubmed ID: 24598251 Sputum Gene Expression Signature of 6 Biomarkers Discriminates Asthma Inflammatory Phenotypes The Journal of Allergy and Clinical Immunology. Apr, 2014 | Pubmed ID: 24582314 Combined Analysis of Exon Splicing and Genome Wide Polymorphism Data Predict Schizophrenia Risk Loci Journal of Psychiatric Research. May, 2014 | Pubmed ID: 24507884 Decreased Expression of Key Tumour Suppressor MicroRNAs is Associated with Lymph Node Metastases in Triple Negative Breast Cancer BMC Cancer. 2014 | Pubmed ID: 24479446 Childhood and Parental Diagnostic Radiological Procedures and Risk of Childhood Brain Tumors Cancer Causes & Control : CCC. Mar, 2014 | Pubmed ID: 24445596 Application of a 5-tiered Scheme for Standardized Classification of 2,360 Unique Mismatch Repair Gene Variants in the InSiGHT Locus-specific Database Nature Genetics. Feb, 2014 | Pubmed ID: 24362816 Preliminary Evidence of an Interaction Between the FOXP2 Gene and Childhood Emotional Abuse Predicting Likelihood of Auditory Verbal Hallucinations in Schizophrenia Journal of Psychiatric Research. Mar, 2014 | Pubmed ID: 24360035 Exposure to Household Painting and Floor Treatments, and Parental Occupational Paint Exposure and Risk of Childhood Brain Tumors: Results from an Australian Case-control Study Cancer Causes & Control : CCC. Mar, 2014 | Pubmed ID: 24337771 The Relative MRNA Expression of P53 Isoforms in Breast Cancer is Associated with Clinical Features and Outcome Carcinogenesis. Mar, 2014 | Pubmed ID: 24336193 Catechol-O-methyltransferase (COMT) Genotype Moderates the Effects of Childhood Trauma on Cognition and Symptoms in Schizophrenia Journal of Psychiatric Research. Feb, 2014 | Pubmed ID: 24252819 Progesterone Activates Multiple Innate Immune Pathways in Chlamydia Trachomatis-infected Endocervical Cells American Journal of Reproductive Immunology (New York, N.Y. : 1989). Feb, 2014 | Pubmed ID: 24206234 Genome-wide Association Study of Endometrial Cancer in E2C2 Human Genetics. Feb, 2014 | Pubmed ID: 24096698 Cytokine Gene Polymorphism Among Indigenous Australians Innate Immunity. May, 2014 | Pubmed ID: 23940076 Common Genetic Variants in the Plasminogen Activation Pathway Are Not Associated with Multiple Sclerosis Multiple Sclerosis (Houndmills, Basingstoke, England). Apr, 2014 | Pubmed ID: 23897640 Low Prevalence of Germline PALB2 Mutations in Australian Triple-negative Breast Cancer International Journal of Cancer. Jan, 2014 | Pubmed ID: 23824750 The Male Excess in Sudden Infant Deaths Innate Immunity. Jan, 2014 | Pubmed ID: 23608823 Intermediate Lobe Immunoreactivity in a Patient with Suspected Lymphocytic Hypophysitis Pituitary. Feb, 2014 | Pubmed ID: 23329361 Copy Number Variation in Hereditary Non-polyposis Colorectal Cancer Genes. 2013 | Pubmed ID: 24705261 The Importance of a Large Sample Cohort for Studies on Modifier Genes Influencing Disease Severity in FAP Patients Hereditary Cancer in Clinical Practice. 2013 | Pubmed ID: 24373140 STaRRRT: a Table of Short Tandem Repeats in Regulatory Regions of the Human Genome BMC Genomics. 2013 | Pubmed ID: 24228761 Meta-analysis of Mismatch Repair Polymorphisms Within the Cogent Consortium for Colorectal Cancer Susceptibility PloS One. 2013 | Pubmed ID: 24039736 Regulators of Global Genome Repair Do Not Respond to DNA Damaging Therapy but Correlate with Survival in Melanoma PloS One. 2013 | Pubmed ID: 23940574 Genome-wide Analysis of Blood Pressure Variability and Ischemic Stroke Stroke; a Journal of Cerebral Circulation. Oct, 2013 | Pubmed ID: 23929743 Genetic Loci for Retinal Arteriolar Microcirculation PloS One. 2013 | Pubmed ID: 23776548 GWAS of 126,559 Individuals Identifies Genetic Variants Associated with Educational Attainment Science (New York, N.Y.). Jun, 2013 | Pubmed ID: 23722424 Can Selenium Levels Act As a Marker of Colorectal Cancer Risk? BMC Cancer. 2013 | Pubmed ID: 23627542 Exposure to Pesticides and the Risk of Childhood Brain Tumors Cancer Causes & Control : CCC. Jul, 2013 | Pubmed ID: 23558445 Reply to Win and Jenkins International Journal of Cancer. Oct, 2013 | Pubmed ID: 23536415 Continuing Difficulties in Interpreting CNV Data: Lessons from a Genome-wide CNV Association Study of Australian HNPCC/lynch Syndrome Patients BMC Medical Genomics. 2013 | Pubmed ID: 23531357 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 Human Molecular Genetics. Jul, 2013 | Pubmed ID: 23474815 Genetic Modifiers of Cancer Risk in Lynch Syndrome: a Review Familial Cancer. Jun, 2013 | Pubmed ID: 23471748 Gene Expression Profiling in Treatment-naive Schizophrenia Patients Identifies Abnormalities in Biological Pathways Involving AKT1 That Are Corrected by Antipsychotic Medication The International Journal of Neuropsychopharmacology / Official Scientific Journal of the Collegium Internationale Neuropsychopharmacologicum (CINP). Aug, 2013 | Pubmed ID: 23442539 Altered Expression of the Plasminogen Activation Pathway in Peripheral Blood Mononuclear Cells in Multiple Sclerosis: Possible Pathomechanism of Matrix Metalloproteinase Activation Multiple Sclerosis (Houndmills, Basingstoke, England). Sep, 2013 | Pubmed ID: 23401127 Ischemic Stroke is Associated with the ABO Locus: the EuroCLOT Study Annals of Neurology. Jan, 2013 | Pubmed ID: 23381943 Comparison of Cytokine Gene Polymorphisms Among Greek Patients with Invasive Meningococcal Disease or Viral Meningitis Journal of Medical Microbiology. May, 2013 | Pubmed ID: 23378564 Insights into the Genetic Architecture of Early Stage Age-related Macular Degeneration: a Genome-wide Association Study Meta-analysis PloS One. 2013 | Pubmed ID: 23326517 Parental Smoking and Risk of Childhood Brain Tumors International Journal of Cancer. Jul, 2013 | Pubmed ID: 23280760 Parental Alcohol Consumption and Risk of Childhood Acute Lymphoblastic Leukemia and Brain Tumors Cancer Causes & Control : CCC. Feb, 2013 | Pubmed ID: 23247637 Gene Expression Analysis Reveals Schizophrenia-associated Dysregulation of Immune Pathways in Peripheral Blood Mononuclear Cells Journal of Psychiatric Research. Apr, 2013 | Pubmed ID: 23218666 Genetic Association of Refractive Error and Axial Length with 15q14 but Not 15q25 in the Blue Mountains Eye Study Cohort Ophthalmology. Feb, 2013 | Pubmed ID: 23131718 Cell Cycle-related Genes As Modifiers of Age of Onset of Colorectal Cancer in Lynch Syndrome: a Large-scale Study in Non-Hispanic White Patients Carcinogenesis. Feb, 2013 | Pubmed ID: 23125224 Combined Analysis of Three Lynch Syndrome Cohorts Confirms the Modifying Effects of 8q23.3 and 11q23.1 in MLH1 Mutation Carriers International Journal of Cancer. Apr, 2013 | Pubmed ID: 22987364 Genomweiten Verband Analysen Identifizieren 18 Neue Loci Urat-Serumkonzentration Zugeordnet Nature Genetics. Dec, 2012 | Pubmed ID: 23263486 DNA and RNA Analyses in Detection of Genetic Predisposition to Cancer Hereditary Cancer in Clinical Practice. 2012 | Pubmed ID: 23206658 Long-term Effect of Resistant Starch on Cancer Risk in Carriers of Hereditary Colorectal Cancer: an Analysis from the CAPP2 Randomised Controlled Trial The Lancet. Oncology. Dec, 2012 | Pubmed ID: 23140761 Genome-wide Association Meta-analysis Identifies New Endometriosis Risk Loci Nature Genetics. Dec, 2012 | Pubmed ID: 23104006 MicroRNA-16 is Down-regulated in Mutated FLT3 Expressing Murine Myeloid FDC-P1 Cells and Interacts with Pim-1 PloS One. 2012 | Pubmed ID: 22970245 Maternal Dietary Intake of Folate and Vitamins B6 and B12 During Pregnancy and the Risk of Childhood Acute Lymphoblastic Leukemia Nutrition and Cancer. 2012 | Pubmed ID: 22966944 Maternal Use of Folic Acid and Other Supplements and Risk of Childhood Brain Tumors Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology. Nov, 2012 | Pubmed ID: 22941336 Gemeinsame Varianten Bei 6p21.1 Sind Große Arterie Atherosklerotischen Strich Zugeordnet Nature Genetics. Sep, 2012 | Pubmed ID: 22941190 Nodular Prurigo of the Vulva Pathology. Oct, 2012 | Pubmed ID: 22643768 Transcriptome Sequencing Revealed Significant Alteration of Cortical Promoter Usage and Splicing in Schizophrenia PloS One. 2012 | Pubmed ID: 22558445 Changes in Brain Transcripts Related to Alzheimer's Disease in a Model of HFE Hemochromatosis Are Not Consistent with Increased Alzheimer's Disease Risk Journal of Alzheimer's Disease : JAD. 2012 | Pubmed ID: 22466002 Bilateral Dysgerminoma Associated with Gonadoblastoma and Sex-cord Stromal Tumour with Annular Tubules in a 28-year-old Fertile Woman with Normal Karyotype Pathology. Apr, 2012 | Pubmed ID: 22437743 Genome-wide Association Study Identifies a Possible Susceptibility Locus for Endometrial Cancer Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology. Jun, 2012 | Pubmed ID: 22426144 Brain Transcriptome Perturbations in the Hfe(-/-) Mouse Model of Genetic Iron Loading Brain Research. Apr, 2012 | Pubmed ID: 22370144 Are Myocardial Infarction--associated Single-nucleotide Polymorphisms Associated with Ischemic Stroke? Stroke; a Journal of Cerebral Circulation. Apr, 2012 | Pubmed ID: 22363065 Identification of TPIT and Other Novel Autoantigens in Lymphocytic Hypophysitis: Immunoscreening of a Pituitary CDNA Library and Development of Immunoprecipitation Assays European Journal of Endocrinology / European Federation of Endocrine Societies. Mar, 2012 | Pubmed ID: 22193973 8q23.3 and 11q23.1 As Modifying Loci Influencing the Risk for CRC in Lynch Syndrome European Journal of Human Genetics : EJHG. May, 2012 | Pubmed ID: 22166948 Parental Prenatal Smoking and Risk of Childhood Acute Lymphoblastic Leukemia American Journal of Epidemiology. Jan, 2012 | Pubmed ID: 22143821 DNA Repair Gene Polymorphisms and Risk of Early Onset Colorectal Cancer in Lynch Syndrome Cancer Epidemiology. Apr, 2012 | Pubmed ID: 21974800 Potential Association of Vitamin D Receptor Polymorphism Taq1 with Multiple Sclerosis Multiple Sclerosis (Houndmills, Basingstoke, England). Jan, 2012 | Pubmed ID: 21816760 Genetic Variation and Its Role in Malignancy International Journal of Biomedical Science : IJBS. Sep, 2011 | Pubmed ID: 23675233 Genomweiten Meta-Analyse Identifiziert Die Neuartige Multiple Sklerose Anfälligkeit Loci Annals of Neurology. Dec, 2011 | Pubmed ID: 22190364 Long-term Effect of Aspirin on Cancer Risk in Carriers of Hereditary Colorectal Cancer: an Analysis from the CAPP2 Randomised Controlled Trial Lancet (London, England). Dec, 2011 | Pubmed ID: 22036019 Smoking Related Cancers and Loci at Chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish Population PloS One. 2011 | Pubmed ID: 21966413 Genetische Risiko Und Eine Primäre Rolle Für Die Zellvermittelte Immune Mechanismen Bei Multipler Sklerose Nature. Aug, 2011 | Pubmed ID: 21833088 Long Term Transcriptional Reactivation of Epigenetically Silenced Genes in Colorectal Cancer Cells Requires DNA Hypomethylation and Histone Acetylation PloS One. 2011 | Pubmed ID: 21829702 Systemic Upregulation of Neutrophil α-defensins and Serine Proteases in Neutrophilic Asthma Thorax. Nov, 2011 | Pubmed ID: 21785157 A High-throughput Protocol for Mutation Scanning of the BRCA1 and BRCA2 Genes BMC Cancer. 2011 | Pubmed ID: 21702907 P53 in Human Melanoma Fails to Regulate Target Genes Associated with Apoptosis and the Cell Cycle and May Contribute to Proliferation BMC Cancer. 2011 | Pubmed ID: 21615965 Genome-wide Association Study Identifies a Common Variant Associated with Risk of Endometrial Cancer Nature Genetics. May, 2011 | Pubmed ID: 21499250 BRIP1, PALB2, and RAD51C Mutation Analysis Reveals Their Relative Importance As Genetic Susceptibility Factors for Breast Cancer Breast Cancer Research and Treatment. Jun, 2011 | Pubmed ID: 21409391 An X-linked Haplotype of Neandertal Origin is Present Among All Non-African Populations Molecular Biology and Evolution. Jul, 2011 | Pubmed ID: 21266489 Transcriptional Phenotypes of Asthma Defined by Gene Expression Profiling of Induced Sputum Samples The Journal of Allergy and Clinical Immunology. Jan, 2011 | Pubmed ID: 21211650 Maternal Consumption of Coffee and Tea During Pregnancy and Risk of Childhood ALL: Results from an Australian Case-control Study Cancer Causes & Control : CCC. Feb, 2011 | Pubmed ID: 21113653 Colorectal Cancer Susceptibility Loci on Chromosome 8q23.3 and 11q23.1 As Modifiers for Disease Expression in Lynch Syndrome Journal of Medical Genetics. Apr, 2011 | Pubmed ID: 21097774 Exposure to Professional Pest Control Treatments and the Risk of Childhood Acute Lymphoblastic Leukemia International Journal of Cancer. Oct, 2011 | Pubmed ID: 21080443 A Transcription Factor Map As Revealed by a Genome-wide Gene Expression Analysis of Whole-blood MRNA Transcriptome in Multiple Sclerosis PloS One. 2010 | Pubmed ID: 21152067 Vier Neuartige Loci (19q13, 6q24 12q24 Und 5q14) Beeinflussen Die Mikrozirkulation In-vivo PLoS Genetics. Oct, 2010 | Pubmed ID: 21060863 Cytokine Gene Polymorphisms and Risk for Upper Respiratory Symptoms in Highly-trained Athletes Exercise Immunology Review. 2010 | Pubmed ID: 20839488 Nucleotide Excision Repair Gene Expression After Cisplatin Treatment in Melanoma Cancer Research. Oct, 2010 | Pubmed ID: 20807809 Leiden Open Variation Database of the MUTYH Gene Human Mutation. Nov, 2010 | Pubmed ID: 20725929 MicroRNAs MiR-17 and MiR-20a Inhibit T Cell Activation Genes and Are Under-expressed in MS Whole Blood PloS One. 2010 | Pubmed ID: 20711463 Variant Alleles of the CYP1B1 Gene Are Associated with Colorectal Cancer Susceptibility BMC Cancer. 2010 | Pubmed ID: 20701755 Toll-like Receptor (TLR) and Nucleosome-binding Oligomerization Domain (NOD) Gene Polymorphisms and Endometrial Cancer Risk BMC Cancer. 2010 | Pubmed ID: 20646321 Demethylation by 5-aza-2'-deoxycytidine in Colorectal Cancer Cells Targets Genomic DNA Whilst Promoter CpG Island Methylation Persists BMC Cancer. 2010 | Pubmed ID: 20618997 Lack of Support for Association Between the KIF1B Rs10492972[C] Variant and Multiple Sclerosis Nature Genetics. Jun, 2010 | Pubmed ID: 20502484 MSH6 and PMS2 Mutation Positive Australian Lynch Syndrome Families: Novel Mutations, Cancer Risk and Age of Diagnosis of Colorectal Cancer Hereditary Cancer in Clinical Practice. 2010 | Pubmed ID: 20487569 Polymorphisms in Genes of the Steroid Hormone Biosynthesis and Metabolism Pathways and Endometrial Cancer Risk Cancer Epidemiology. Jun, 2010 | Pubmed ID: 20381444 Detecting Genotyping Error Using Measures of Degree of Hardy-Weinberg Disequilibrium Statistical Applications in Genetics and Molecular Biology. 2010 | Pubmed ID: 20196755 The Multiple Sclerosis Whole Blood MRNA Transcriptome and Genetic Associations Indicate Dysregulation of Specific T Cell Pathways in Pathogenesis Human Molecular Genetics. Jun, 2010 | Pubmed ID: 20190274 Have the Roles of Two Functional Polymorphisms in Breast Cancer, R72P in P53 and MDM2-309 in MDM2, Become Clearer? Breast Cancer Research : BCR. 2010 | Pubmed ID: 20156327 Combined IPLEX and TaqMan Assays to Screen for 45 Common Mutations in Lynch Syndrome and FAP Patients The Journal of Molecular Diagnostics : JMD. Jan, 2010 | Pubmed ID: 20007843 Maternal Folate and Other Vitamin Supplementation During Pregnancy and Risk of Acute Lymphoblastic Leukemia in the Offspring International Journal of Cancer. Jun, 2010 | Pubmed ID: 19839053 BRCA1-associated Breast and Ovarian Cancer Risks in Poland: No Association with Commonly Studied Polymorphisms Breast Cancer Research and Treatment. Jan, 2010 | Pubmed ID: 19360465 Capturing All Disease-causing Mutations for Clinical and Research Use: Toward an Effortless System for the Human Variome Project Genetics in Medicine : Official Journal of the American College of Medical Genetics. Dec, 2009 | Pubmed ID: 20010362 Oncostatin M (OSM) is Increased in Asthma with Incompletely Reversible Airflow Obstruction Experimental Lung Research. Nov, 2009 | Pubmed ID: 19916861 Immune Responses of Airway Neutrophils Are Impaired in Asthma Experimental Lung Research. Sep, 2009 | Pubmed ID: 19842845 A Multicenter Blinded Study to Evaluate KRAS Mutation Testing Methodologies in the Clinical Setting The Journal of Molecular Diagnostics : JMD. Nov, 2009 | Pubmed ID: 19815694 Clinical Characteristics of Tumors Derived from Colorectal Cancer Patients Who Harbor the Tumor Necrosis Factor Alpha-1031T/T and NOD2 3020insC Polymorphism Cancer Epidemiology. Aug, 2009 | Pubmed ID: 19679065 Genetic Variants in MUTYH Are Not Associated with Endometrial Cancer Risk Hereditary Cancer in Clinical Practice. 2009 | Pubmed ID: 19338676 Planning the Human Variome Project: the Spain Report Human Mutation. Apr, 2009 | Pubmed ID: 19306394 Haemochromatosis HFE Gene Polymorphisms As Potential Modifiers of Hereditary Nonpolyposis Colorectal Cancer Risk and Onset Age International Journal of Cancer. Jul, 2009 | Pubmed ID: 19291797 Polymorphisms in TP53 and MDM2 Combined Are Associated with High Grade Endometrial Cancer Gynecologic Oncology. Apr, 2009 | Pubmed ID: 19193430 MTHFR 677 C>T and 1298 A>C Polymorphisms and the Age of Onset of Colorectal Cancer in Hereditary Nonpolyposis Colorectal Cancer European Journal of Human Genetics : EJHG. May, 2009 | Pubmed ID: 19156174 How to Use an Article About Genetic Association: C: What Are the Results and Will They Help Me in Caring for My Patients? JAMA. Jan, 2009 | Pubmed ID: 19155457 How to Use an Article About Genetic Association: B: Are the Results of the Study Valid? JAMA. Jan, 2009 | Pubmed ID: 19141767 How to Use an Article About Genetic Association: A: Background Concepts JAMA. Jan, 2009 | Pubmed ID: 19126812 Genetic Epidemiology Studies in Hereditary Non-polyposis Colorectal Cancer Methods in Molecular Biology (Clifton, N.J.). 2009 | Pubmed ID: 19107430 Effect of Aspirin or Resistant Starch on Colorectal Neoplasia in the Lynch Syndrome The New England Journal of Medicine. Dec, 2008 | Pubmed ID: 19073976 Smad4 Haploinsufficiency: a Matter of Dosage PathoGenetics. 2008 | Pubmed ID: 19014666 Eine einfache Migration/Invasion Workflow mit einer automatisierten Leben-Zelle-Imager Xiajie Zhang1,2, Brianna C. Morten1,2, Rodney J. Scott1,2,3, Kelly A. Avery-Kiejda1,2 1Medical Genetics, Hunter Medical Research Institute, 2Priority Research Centre for Cancer Research, Innovation and Translation, School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, 3Pathology North, John Hunter Hospital JoVE 59042 Cancer Research Vergleich von drei verschiedenen Methoden zur Bestimmung Zellproliferation in Brustkrebs-Zelllinien Brianna C. Morten1,2, Rodney J. Scott1,2,3, Kelly A. Avery-Kiejda1,2 1Medical Genetics, Hunter Medical Research Institute, 2Priority Research Centre for Cancer, School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, 3Pathology North, John Hunter Hospital Biology
Eine einfache Migration/Invasion Workflow mit einer automatisierten Leben-Zelle-Imager Xiajie Zhang1,2, Brianna C. Morten1,2, Rodney J. Scott1,2,3, Kelly A. Avery-Kiejda1,2 1Medical Genetics, Hunter Medical Research Institute, 2Priority Research Centre for Cancer Research, Innovation and Translation, School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, 3Pathology North, John Hunter Hospital JoVE 59042 Cancer Research
Vergleich von drei verschiedenen Methoden zur Bestimmung Zellproliferation in Brustkrebs-Zelllinien Brianna C. Morten1,2, Rodney J. Scott1,2,3, Kelly A. Avery-Kiejda1,2 1Medical Genetics, Hunter Medical Research Institute, 2Priority Research Centre for Cancer, School of Biomedical Sciences and Pharmacy, Faculty of Health and Medicine, University of Newcastle, 3Pathology North, John Hunter Hospital Biology
