Medical Genetics
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Smad4 haploinsufficiency: a matter of dosage.
PathoGenetics , 2008 | Pubmed ID: 19014666
Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome.
The New England journal of medicine Dec, 2008 | Pubmed ID: 19073976
Genetic epidemiology studies in hereditary non-polyposis colorectal cancer.
Methods in molecular biology (Clifton, N.J.) , 2009 | Pubmed ID: 19107430
How to use an article about genetic association: A: Background concepts.
JAMA Jan, 2009 | Pubmed ID: 19126812
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: C: What are the results and will they help me in caring for my patients?
JAMA Jan, 2009 | Pubmed ID: 19155457
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
Polymorphisms in TP53 and MDM2 combined are associated with high grade endometrial cancer.
Gynecologic oncology Apr, 2009 | Pubmed ID: 19193430
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
Planning the human variome project: the Spain report.
Human mutation Apr, 2009 | Pubmed ID: 19306394
Genetic variants in MUTYH are not associated with endometrial cancer risk.
Hereditary cancer in clinical practice , 2009 | Pubmed ID: 19338676
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
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
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
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
Immune responses of airway neutrophils are impaired in asthma.
Experimental lung research Sep, 2009 | Pubmed ID: 19842845
Oncostatin M (OSM) is increased in asthma with incompletely reversible airflow obstruction.
Experimental lung research Nov, 2009 | Pubmed ID: 19916861
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
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
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
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
Detecting genotyping error using measures of degree of Hardy-Weinberg disequilibrium.
Statistical applications in genetics and molecular biology , 2010 | Pubmed ID: 20196755
Polymorphisms in genes of the steroid hormone biosynthesis and metabolism pathways and endometrial cancer risk.
Cancer epidemiology Jun, 2010 | Pubmed ID: 20381444
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
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis.
Nature genetics Jun, 2010 | Pubmed ID: 20502484
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
Toll-like receptor (TLR) and nucleosome-binding oligomerization domain (NOD) gene polymorphisms and endometrial cancer risk.
BMC cancer , 2010 | Pubmed ID: 20646321
Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility.
BMC cancer , 2010 | Pubmed ID: 20701755
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
Leiden Open Variation Database of the MUTYH gene.
Human mutation Nov, 2010 | Pubmed ID: 20725929
Nucleotide excision repair gene expression after Cisplatin treatment in melanoma.
Cancer research Oct, 2010 | Pubmed ID: 20807809
Cytokine gene polymorphisms and risk for upper respiratory symptoms in highly-trained athletes.
Exercise immunology review , 2010 | Pubmed ID: 20839488
Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo.
PLoS genetics Oct, 2010 | Pubmed ID: 21060863
Exposure to professional pest control treatments and the risk of childhood acute lymphoblastic leukemia.
International journal of cancer Oct, 2011 | Pubmed ID: 21080443
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
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
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
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
An X-linked haplotype of Neandertal origin is present among all non-African populations.
Molecular biology and evolution Jul, 2011 | Pubmed ID: 21266489
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
Genome-wide association study identifies a common variant associated with risk of endometrial cancer.
Nature genetics May, 2011 | Pubmed ID: 21499250
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
A high-throughput protocol for mutation scanning of the BRCA1 and BRCA2 genes.
BMC cancer , 2011 | Pubmed ID: 21702907
Systemic upregulation of neutrophil α-defensins and serine proteases in neutrophilic asthma.
Thorax Nov, 2011 | Pubmed ID: 21785157
Potential association of vitamin D receptor polymorphism Taq1 with multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) Jan, 2012 | Pubmed ID: 21816760
Long term transcriptional reactivation of epigenetically silenced genes in colorectal cancer cells requires DNA hypomethylation and histone acetylation.
PloS one , 2011 | Pubmed ID: 21829702
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature Aug, 2011 | Pubmed ID: 21833088
Smoking related cancers and loci at chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish population.
PloS one , 2011 | Pubmed ID: 21966413
DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome.
Cancer epidemiology Apr, 2012 | Pubmed ID: 21974800
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
Parental prenatal smoking and risk of childhood acute lymphoblastic leukemia.
American journal of epidemiology Jan, 2012 | Pubmed ID: 22143821
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
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci.
Annals of neurology Dec, 2011 | Pubmed ID: 22190364
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
Are myocardial infarction--associated single-nucleotide polymorphisms associated with ischemic stroke?
Stroke; a journal of cerebral circulation Apr, 2012 | Pubmed ID: 22363065
Brain transcriptome perturbations in the Hfe(-/-) mouse model of genetic iron loading.
Brain research Apr, 2012 | Pubmed ID: 22370144
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
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
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
Transcriptome sequencing revealed significant alteration of cortical promoter usage and splicing in schizophrenia.
PloS one , 2012 | Pubmed ID: 22558445
Nodular prurigo of the vulva.
Pathology Oct, 2012 | Pubmed ID: 22643768
Common variants at 6p21.1 are associated with large artery atherosclerotic stroke.
Nature genetics Sep, 2012 | Pubmed ID: 22941190
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
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
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
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
Genome-wide association meta-analysis identifies new endometriosis risk loci.
Nature genetics Dec, 2012 | Pubmed ID: 23104006
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
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
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
DNA and RNA analyses in detection of genetic predisposition to cancer.
Hereditary cancer in clinical practice , 2012 | Pubmed ID: 23206658
Gene expression analysis reveals schizophrenia-associated dysregulation of immune pathways in peripheral blood mononuclear cells.
Journal of psychiatric research Apr, 2013 | Pubmed ID: 23218666
Parental alcohol consumption and risk of childhood acute lymphoblastic leukemia and brain tumors.
Cancer causes & control : CCC Feb, 2013 | Pubmed ID: 23247637
Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
Nature genetics Dec, 2012 | Pubmed ID: 23263486
Parental smoking and risk of childhood brain tumors.
International journal of cancer Jul, 2013 | Pubmed ID: 23280760
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
Intermediate lobe immunoreactivity in a patient with suspected lymphocytic hypophysitis.
Pituitary Feb, 2014 | Pubmed ID: 23329361
Comparison of cytokine gene polymorphisms among Greek patients with invasive meningococcal disease or viral meningitis.
Journal of medical microbiology May, 2013 | Pubmed ID: 23378564
Ischemic stroke is associated with the ABO locus: the EuroCLOT study.
Annals of neurology Jan, 2013 | Pubmed ID: 23381943
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
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
Genetic modifiers of cancer risk in Lynch syndrome: a review.
Familial cancer Jun, 2013 | Pubmed ID: 23471748
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
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
Reply to Win and Jenkins.
International journal of cancer Oct, 2013 | Pubmed ID: 23536415
Exposure to pesticides and the risk of childhood brain tumors.
Cancer causes & control : CCC Jul, 2013 | Pubmed ID: 23558445
The male excess in sudden infant deaths.
Innate immunity Jan, 2014 | Pubmed ID: 23608823
Can selenium levels act as a marker of colorectal cancer risk?
BMC cancer , 2013 | Pubmed ID: 23627542
Genetic variation and its role in malignancy.
International journal of biomedical science : IJBS Sep, 2011 | Pubmed ID: 23675233
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment.
Science (New York, N.Y.) Jun, 2013 | Pubmed ID: 23722424
Genetic loci for retinal arteriolar microcirculation.
PloS one , 2013 | Pubmed ID: 23776548
Low prevalence of germline PALB2 mutations in Australian triple-negative breast cancer.
International journal of cancer Jan, 2014 | Pubmed ID: 23824750
Common genetic variants in the plasminogen activation pathway are not associated with multiple sclerosis.
Multiple sclerosis (Houndmills, Basingstoke, England) Apr, 2014 | Pubmed ID: 23897640
Genome-wide analysis of blood pressure variability and ischemic stroke.
Stroke; a journal of cerebral circulation Oct, 2013 | Pubmed ID: 23929743
Cytokine gene polymorphism among Indigenous Australians.
Innate immunity May, 2014 | Pubmed ID: 23940076
Regulators of global genome repair do not respond to DNA damaging therapy but correlate with survival in melanoma.
PloS one , 2013 | Pubmed ID: 23940574
Meta-analysis of mismatch repair polymorphisms within the cogent consortium for colorectal cancer susceptibility.
PloS one , 2013 | Pubmed ID: 24039736
Genome-wide association study of endometrial cancer in E2C2.
Human genetics Feb, 2014 | Pubmed ID: 24096698
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
STaRRRT: a table of short tandem repeats in regulatory regions of the human genome.
BMC genomics , 2013 | Pubmed ID: 24228761
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
The relative mRNA expression of p53 isoforms in breast cancer is associated with clinical features and outcome.
Carcinogenesis Mar, 2014 | Pubmed ID: 24336193
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
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
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
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
Childhood and parental diagnostic radiological procedures and risk of childhood brain tumors.
Cancer causes & control : CCC Mar, 2014 | Pubmed ID: 24445596
Decreased expression of key tumour suppressor microRNAs is associated with lymph node metastases in triple negative breast cancer.
BMC cancer , 2014 | Pubmed ID: 24479446
Combined analysis of exon splicing and genome wide polymorphism data predict schizophrenia risk loci.
Journal of psychiatric research May, 2014 | Pubmed ID: 24507884
Sputum gene expression signature of 6 biomarkers discriminates asthma inflammatory phenotypes.
The Journal of allergy and clinical immunology Apr, 2014 | Pubmed ID: 24582314
Dupuytren's disease and the risk of malignant neoplasms.
Hereditary cancer in clinical practice , 2014 | Pubmed ID: 24598251
Epithelioid trophoblastic tumour simulating a high grade carcinoma.
Pathology Apr, 2014 | Pubmed ID: 24614716
Copy number variation in hereditary non-polyposis colorectal cancer.
Genes , 2013 | Pubmed ID: 24705261
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
The architecture of risk for type 2 diabetes: understanding Asia in the context of global findings.
International journal of endocrinology , 2014 | Pubmed ID: 24744783
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
Genome-wide association study identifies two novel genomic regions in irritable bowel syndrome.
The American journal of gastroenterology May, 2014 | Pubmed ID: 24797007
KRAS mutation testing of metastatic colorectal cancer in Australia: where are we at?
Asia-Pacific journal of clinical oncology Sep, 2014 | Pubmed ID: 24811330
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
Genome-wide association analysis identifies six new loci associated with forced vital capacity.
Nature genetics Jul, 2014 | Pubmed ID: 24929828
Common variants of xeroderma pigmentosum genes and prostate cancer risk.
Gene Aug, 2014 | Pubmed ID: 24933002
Expanding the genetic basis of copy number variation in familial breast cancer.
Hereditary cancer in clinical practice , 2014 | Pubmed ID: 24955146
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
Confirmation of childhood acute lymphoblastic leukemia variants, ARID5B and IKZF1, and interaction with parental environmental exposures.
PloS one , 2014 | Pubmed ID: 25310577
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
Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk.
Human molecular genetics Mar, 2015 | Pubmed ID: 25378557
Rare germline copy number deletions of likely functional importance are implicated in endometrial cancer predisposition.
Human genetics Mar, 2015 | Pubmed ID: 25381466
Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population.
Molecular biology reports Mar, 2015 | Pubmed ID: 25391773
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
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
Effects of gender, cytokine gene polymorphisms and environmental factors on inflammatory responses.
Innate immunity Jul, 2015 | Pubmed ID: 25432967
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
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
Genetic overlap between diagnostic subtypes of ischemic stroke.
Stroke; a journal of cerebral circulation Mar, 2015 | Pubmed ID: 25613305
Paternal dietary folate, B6 and B12 intake, and the risk of childhood brain tumors.
Nutrition and cancer , 2015 | Pubmed ID: 25625505
Genetics of hand grip strength in mid to late life.
Age (Dordrecht, Netherlands) Feb, 2015 | Pubmed ID: 25637336
Methylome sequencing in triple-negative breast cancer reveals distinct methylation clusters with prognostic value.
Nature communications , 2015 | Pubmed ID: 25641231
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
Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer.
Breast cancer research and treatment Feb, 2015 | Pubmed ID: 25682074
Selenium as a marker of cancer risk and of selection for control examinations in surveillance.
Contemporary oncology (Poznań, Poland) , 2015 | Pubmed ID: 25691823
Cis-Expression Quantitative Trait Loci Mapping Reveals Replicable Associations with Heroin Addiction in OPRM1.
Biological psychiatry Oct, 2015 | Pubmed ID: 25744370
Thank you to all our manuscript reviewers in 2014.
Hereditary cancer in clinical practice , 2015 | Pubmed ID: 25763118
Exploring the risk factors for sudden infant deaths and their role in inflammatory responses to infection.
Frontiers in immunology , 2015 | Pubmed ID: 25798137
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
Virus Infections and Sudden Death in Infancy: The Role of Interferon-γ.
Frontiers in immunology , 2015 | Pubmed ID: 25814991
Genetic burden associated with varying degrees of disease severity in endometriosis.
Molecular human reproduction Jul, 2015 | Pubmed ID: 25882541
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
Biobank classification in an Australian setting.
Biopreservation and biobanking Jun, 2015 | Pubmed ID: 26035012
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
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
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
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
Understanding Xeroderma Pigmentosum Complementation Groups Using Gene Expression Profiling after UV-Light Exposure.
International journal of molecular sciences , 2015 | Pubmed ID: 26184184
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
Prevalence of PALB2 mutations in Australian familial breast cancer cases and controls.
Breast cancer research : BCR , 2015 | Pubmed ID: 26283626
Genetic and Environmental Factors Affecting TNF-α Responses in Relation to Sudden Infant Death Syndrome.
Frontiers in immunology , 2015 | Pubmed ID: 26284064
CX3CR1 is dysregulated in blood and brain from schizophrenia patients.
Schizophrenia research Oct, 2015 | Pubmed ID: 26285829
Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer.
Endocrine-related cancer Oct, 2015 | Pubmed ID: 26330482
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
Reevaluation of the BRCA2 truncating allele c.9976A > T (p.Lys3326Ter) in a familial breast cancer context.
Scientific reports , 2015 | Pubmed ID: 26455428
Methylation of the Corticotropin Releasing Hormone Gene Promoter in BeWo Cells: Relationship to Gene Activity.
International journal of endocrinology , 2015 | Pubmed ID: 26457081
Narrowing the critical region for overgrowth within 13q14.2-q14.3 microdeletions.
European journal of medical genetics Nov, 2015 | Pubmed ID: 26475974
Novel genes associated with lymph node metastasis in triple negative breast cancer.
Scientific reports , 2015 | Pubmed ID: 26537449
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
A meta-analysis of 120 246 individuals identifies 18 new loci for fibrinogen concentration.
Human molecular genetics Jan, 2016 | Pubmed ID: 26561523
CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer.
Endocrine-related cancer Feb, 2016 | Pubmed ID: 26574572
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
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
MiRNAs and Other Epigenetic Changes as Biomarkers in Triple Negative Breast Cancer.
International journal of molecular sciences , 2015 | Pubmed ID: 26633365
VariantSpark: population scale clustering of genotype information.
BMC genomics , 2015 | Pubmed ID: 26651996
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
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
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
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
Targeted next-generation sequencing of 22 mismatch repair genes identifies Lynch syndrome families.
Cancer medicine May, 2016 | Pubmed ID: 26811195
Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function.
Nature communications , 2016 | Pubmed ID: 26831199
A variant at 9p21.3 functionally implicates CDKN2B in paediatric B-cell precursor acute lymphoblastic leukaemia aetiology.
Nature communications , 2016 | Pubmed ID: 26868379
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
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
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
Thank you to all our manuscript reviewers in 2015.
Hereditary cancer in clinical practice , 2016 | Pubmed ID: 26933466
Associations Between Methylenetetrahydrofolate Reductase Polymorphisms, Serum Homocysteine Levels, and Incident Cortical Cataract.
JAMA ophthalmology Mar, 2016 | Pubmed ID: 26986182
Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.
JAMA psychiatry May, 2016 | Pubmed ID: 27007234
GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer.
Human molecular genetics Mar, 2016 | Pubmed ID: 27008869
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
Genome-wide significant results identified for plasma apolipoprotein H levels in middle-aged and older adults.
Scientific reports , 2016 | Pubmed ID: 27030319
Do founder mutations characteristic of some cancer sites also predispose to pancreatic cancer?
International journal of cancer Aug, 2016 | Pubmed ID: 27038244
Lynch syndrome mutation spectrum in New South Wales, Australia, including 55 novel mutations.
Molecular genetics & genomic medicine Mar, 2016 | Pubmed ID: 27064304
Renin-angiotensin system gene polymorphisms and endometrial cancer.
Endocrine connections May, 2016 | Pubmed ID: 27068935
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Nature genetics Jun, 2016 | Pubmed ID: 27089181
A polymorphic repeat in the IGF1 promoter influences the risk of endometrial cancer.
Endocrine connections May, 2016 | Pubmed ID: 27090263
Five endometrial cancer risk loci identified through genome-wide association analysis.
Nature genetics Jun, 2016 | Pubmed ID: 27135401
Genome-wide association study identifies 74 loci associated with educational attainment.
Nature May, 2016 | Pubmed ID: 27225129
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
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
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
Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses.
Nature genetics Jul, 2016 | Pubmed ID: 27463399
Reevaluation of RINT1 as a breast cancer predisposition gene.
Breast cancer research and treatment Aug, 2016 | Pubmed ID: 27544226
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
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
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