Lyn R. Griffiths

Q: What Schools Are Affiliated With Lyn R. Griffiths

Lyn R. Griffiths is affiliated with the following schools: Queensland University of Technology, University of New South Wales, University of Sydney, Griffith University

Lyn R. Griffiths's AcademicInfluence.com Rankings

Lyn R. Griffiths

Biology

#6328

World Rank

#9016

Historical Rank

Genetics

#811

World Rank

#903

Historical Rank

biology Degrees

Download Badge

Biology

Why Is Lyn R. Griffiths Influential?

(Suggest an Edit or Addition)

According to Wikipedia, Lyn Robyn Griffiths is an Australian academic who serves as Distinguished Professor of molecular genetics at Queensland University of Technology, where she is director of the Centre for Genomics and Personalised Health, the Genomics Research Centre and the BridgeTech Programs. Griffiths is internationally renowned for her work in the discovery of the genetics of migraine headaches.

(See a Problem?)

Lyn R. Griffiths's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Multiple sclerosis genomic map implicates peripheral immune cells and microglia in susceptibility (2019) (589)
Mitochondrial genome acquisition restores respiratory function and tumorigenic potential of cancer cells without mitochondrial DNA. (2015) (543)
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20 (2009) (540)
Genome-wide association study reveals three susceptibility loci for common migraine in the general population (2011) (361)
Beta-actin--an unsuitable internal control for RT-PCR. (2001) (354)
Mutations in cardiac T-box factor gene TBX20 are associated with diverse cardiac pathologies, including defects of septation and valvulogenesis and cardiomyopathy. (2007) (328)
A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura (2010) (315)
Association of a polymorphism of the angiotensin I-converting enzyme gene with essential hypertension. (1992) (287)
An analysis of DNA methylation in human adipose tissue reveals differential modification of obesity genes before and after gastric bypass and weight loss (2015) (199)
Association of a vitamin D receptor polymorphism with sporadic breast cancer development (1999) (182)
G-protein beta3 subunit gene (GNB3) variant in causation of essential hypertension. (1998) (179)
Locked nucleic acid (LNA) single nucleotide polymorphism (SNP) genotype analysis and validation using real-time PCR. (2004) (176)
Circulating microRNAs involved in multiple sclerosis (2012) (158)
Immunodeficiency-associated lymphomas. (2008) (150)
The methylenetetrahydrofolate reductase gene variant C677T influences susceptibility to migraine with aura (2004) (150)
Directional dominance on stature and cognition in diverse human populations (2015) (144)
Single-nucleotide polymorphism alleles in the insulin receptor gene are associated with typical migraine. (2001) (141)
VARIATION IN THE VITAMIN D RECEPTOR GENE IS ASSOCIATED WITH MULTIPLE SCLEROSIS IN AN AUSTRALIAN POPULATION (2005) (138)
Quantitative and qualitative changes in gene expression patterns characterize the activity of plaques in multiple sclerosis. (2003) (138)
The estrogen receptor 1 G594A polymorphism is associated with migraine susceptibility in two independent case/control groups (2004) (120)
Familial typical migraine (1998) (119)
Familial typical migraine: significant linkage and localization of a gene to Xq24–28 (2000) (116)
A molecular genetic approach for forensic animal species identification. (2003) (109)
Evidence for allelic association of the dopamine β-hydroxylase gene (DBH) with susceptibility to typical migraine (2000) (107)
The effects of vitamin supplementation and MTHFR (C677T) genotype on homocysteine-lowering and migraine disability (2009) (106)
Large-Scale Association Study Identifies ICAM Gene Region as Breast and Prostate Cancer Susceptibility Locus (2004) (106)
Evidence for an X-linked genetic component in familial typical migraine. (1998) (104)
The measurement of adenosine and estrogen receptor expression in rat brains following ovariectomy using quantitative PCR analysis. (2003) (103)
Methods for extracting genomic DNA from whole blood samples: current perspectives (2014) (103)
Genetic variants of angiotensin converting enzyme and methylenetetrahydrofolate reductase may act in combination to increase migraine susceptibility. (2005) (103)
Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine (2015) (98)
Polymorphisms of glutathione S-transferase genes (GSTM1, GSTP1 and GSTT1) and breast cancer susceptibility. (2000) (97)
Investigation of hormone receptor genes in migraine (2005) (92)
Functional analysis of missense variants in the TRESK (KCNK18) K+ channel (2012) (90)
Advances in genetics of migraine (2019) (89)
Frequency in hypertensives of alleles for a RFLP associated with the renin gene. (1988) (87)
Studies on the Pathophysiology and Genetic Basis of Migraine (2013) (86)
Next Generation Sequencing Methods for Diagnosis of Epilepsy Syndromes (2018) (86)
A typical migraine susceptibility region localizes to chromosome 1q31 (2002) (85)
Genetics of Migraine: Insights into the Molecular Basis of Migraine Disorders (2017) (83)
The association between time spent outdoors and myopia using a novel biomarker of outdoor light exposure. (2012) (80)
Review: Alternative Splicing (AS) of Genes As An Approach for Generating Protein Complexity (2013) (79)
Chromosomal aberrations in squamous cell carcinoma and solar keratoses revealed by comparative genomic hybridization. (2003) (78)
Polymorphic variants of NFKB1 and its inhibitory protein NFKBIA, and their involvement in sporadic breast cancer. (2002) (73)
Comparison of genomic DNA extraction techniques from whole blood samples: a time, cost and quality evaluation study (2012) (72)
Association between a 19 bp deletion polymorphism at the dopamine beta-hydroxylase (DBH) locus and migraine with aura (2006) (72)
A genetic variant located in miR-423 is associated with reduced breast cancer risk. (2012) (71)
Ratios of T-cell immune effectors and checkpoint molecules as prognostic biomarkers in diffuse large B-cell lymphoma: a population-based study. (2015) (70)
Associations of autozygosity with a broad range of human phenotypes (2019) (68)
The methylentetrahydrofolate reductase gene variant (C677T) as a risk factor for essential hypertension in Caucasians. (2004) (68)
Novel NOD2 haplotype strengthens the association between TLR4 Asp299gly and Crohn's disease in an Australian population (2008) (67)
Association of estrogen receptor and glucocorticoid receptor gene polymorphisms with sporadic breast cancer (2001) (66)
Epistatic effects of potassium channel variation on cardiac repolarization and atrial fibrillation risk. (2012) (66)
A saturated map of common genetic variants associated with human height (2022) (65)
Genotypes of the MTHFR C677T and MTRR A66G genes act independently to reduce migraine disability in response to vitamin supplementation (2012) (65)
Minor head trauma-induced sporadic hemiplegic migraine coma. (2006) (62)
Human Mesenchymal Stem Cells Retain Multilineage Differentiation Capacity Including Neural Marker Expression after Extended In Vitro Expansion (2015) (60)
Investigation of the CACNA1A gene as a candidate for typical migraine susceptibility. (2001) (59)
A possible role for mitochondrial dysfunction in migraine (2012) (59)
Polymorphisms of MTHFR, eNOS, ACE, AGT, ApoE, PON1, PDE4D, and Ischemic Stroke: Meta-Analysis. (2017) (58)
A genome-wide scan provides evidence for loci influencing a severe heritable form of common migraine (2005) (58)
Integrative genomic profiling reveals conserved genetic mechanisms for tumorigenesis in common entities of non‐Hodgkin's lymphoma (2011) (57)
Inhibition of platelet aggregation and 5-HT release by extracts of Australian plants used traditionally as headache treatments. (2000) (56)
Effect of coffee combining green coffee bean constituents with typical roasting products on the Nrf2/ARE pathway in vitro and in vivo. (2012) (56)
Cell surface heparan sulfate proteoglycans as novel markers of human neural stem cell fate determination. (2016) (54)
Association and linkage analyses of restriction fragment length polymorphisms for the human renin and antithrombin III genes in essential hypertension. (1991) (54)
Identification of molecular genetic factors that influence migraine (2011) (54)
Association of a RFLP for the insulin receptor gene, but not insulin, with essential hypertension. (1991) (53)
The impact of APOA5, APOB, APOC3 and ABCA1 gene polymorphisms on ischemic stroke: Evidence from a meta-analysis. (2017) (52)
The search for migraine genes: an overview of current knowledge (2007) (50)
Regulatory Mechanisms of Epigenetic miRNA Relationships in Human Cancer and Potential as Therapeutic Targets (2020) (50)
Association of the NuMA region on chromosome 11q13 with breast cancer susceptibility. (2005) (50)
Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (2018) (50)
Migraine association and linkage studies of an endothelial nitric oxide synthase (NOS3) gene polymorphism (1997) (48)
Eye movement disorders are an early manifestation of CACNA1A mutations in children (2016) (48)
Evaluation of a 7-Gene Genetic Profile for Athletic Endurance Phenotype in Ironman Championship Triathletes (2015) (47)
Mesenchymal stem cells, neural lineage potential, heparan sulfate proteoglycans and the matrix. (2014) (47)
Genetic and biochemical changes of the serotonergic system in migraine pathobiology (2017) (47)
Independent, marked associations of alleles of the insulin receptor and dipeptidyl carboxypeptidase-I genes with essential hypertension. (1993) (46)
A Potential Epigenetic Marker Mediating Serum Folate and Vitamin B12 Levels Contributes to the Risk of Ischemic Stroke (2015) (46)
The gene SMART study: method, study design, and preliminary findings (2017) (46)
Marked association of a RFLP for the low density lipoprotein receptor gene with obesity in essential hypertensives. (1992) (46)
Common variants in the regulative regions of GRIA1 and GRIA3 receptor genes are associated with migraine susceptibility (2010) (46)
An X Chromosome Association Scan of the Norfolk Island Genetic Isolate Provides Evidence for a Novel Migraine Susceptibility Locus at Xq12 (2012) (44)
The role of vascular and hormonal genes in migraine susceptibility. (2006) (44)
An epigenetic clock for human skeletal muscle (2019) (44)
No role for estrogen receptor 1 gene intron 1 Pvu II and exon 4 C325G polymorphisms in migraine susceptibility (2006) (44)
Heparan Sulfate Proteoglycans and Human Breast Cancer Epithelial Cell Tumorigenicity (2014) (44)
Single Nucleotide Polymorphism in hsa-mir-196a-2 and Breast Cancer Risk: A Case Control Study (2011) (44)
Selenium Status of the Australian Population: Effect of Age, Gender and Cardiovascular Disease (2008) (43)
Induction of antioxidative Nrf2 gene transcription by coffee in humans: depending on genotype? (2012) (42)
Environments for Healthy Living (EFHL) Griffith Birth Cohort Study: Background and Methods (2012) (42)
Molecular cytogenetic analysis of basal cell carcinoma DNA using comparative genomic hybridization. (2001) (42)
Phenotypical Characterisation of the Isolated Norfolk Island Population Focusing on Epidemiological Indicators of Cardiovascular Disease (2006) (40)
The Role of the MTHFR Gene in Migraine (2012) (39)
An investigation of the 5‐HT2C receptor gene as a migraine candidate gene (2003) (39)
A causal role for TRESK loss of function in migraine mechanisms (2019) (39)
Association of HincII RFLP of low density lipoprotein receptor gene with obesity in essential hypertensives (1995) (39)
The Influence of OLR1 and PCSK9 Gene Polymorphisms on Ischemic Stroke: Evidence from a Meta-Analysis (2015) (39)
Isolation of Bioactive Compounds That Relate to the Anti-Platelet Activity of Cymbopogon ambiguus (2011) (38)
Investigation of Homocysteine-Pathway-Related Variants in Essential Hypertension (2012) (37)
Shared Molecular Genetic Mechanisms Underlie Endometriosis and Migraine Comorbidity (2020) (37)
Analysis of the MTHFR C677T variant with migraine phenotypes (2010) (37)
Migrainomics — identifying brain and genetic markers of migraine (2017) (35)
Complete Mitochondrial Genome Sequencing Reveals Novel Haplotypes in a Polynesian Population (2012) (35)
A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility (2012) (34)
Cytogenetic alterations in nonmelanoma skin cancer: A review (2005) (34)
Exploiting Heparan Sulfate Proteoglycans in Human Neurogenesis—Controlling Lineage Specification and Fate (2017) (34)
Semaphorin-plexin signalling genes associated with human breast tumourigenesis. (2011) (34)
Mapping eQTLs in the Norfolk Island genetic isolate identifies candidate genes for CVD risk traits. (2013) (33)
Polymorphisms of the VDR gene are associated with presence of solar keratoses on the skin (2008) (33)
Genetic association analysis of miRNA SNPs implicates MIR145 in breast cancer susceptibility (2015) (32)
An examination of MS candidate genes identified as differentially regulated in multiple sclerosis plaque tissue, using absolute and comparative real-time Q-PCR analysis. (2005) (32)
Association between migraine and a functional polymorphism at the dopamine β-hydroxylase locus (2009) (32)
Clinical and genetic spectrum of SCN2A-associated episodic ataxia. (2019) (32)
Association study of calcitonin gene-related polypeptide-alpha (CALCA) gene polymorphism with migraine (2011) (31)
Gene expression studies in multiple sclerosis. (2007) (31)
No evidence for involvement of the human inducible nitric oxide synthase (iNOS) gene in susceptibility to typical migraine. (2001) (31)
Relative abundance of full-length and truncated FOXP1 isoforms is associated with differential NFkappaB activity in Follicular Lymphoma. (2009) (31)
The human μ-opioid receptor gene polymorphism (A118G) is associated with head pain severity in a clinical cohort of female migraine with aura patients (2012) (30)
Stimulation of MMP-11 (stromelysin-3) expression in mouse fibroblasts by cytokines, collagen and co-culture with human breast cancer cell lines (2004) (30)
Investigation of Gamma-aminobutyric acid (GABA) A receptors genes and migraine susceptibility (2008) (30)
Genetic investigation of methylenetetrahydrofolate reductase (MTHFR) and catechol-O-methyl transferase (COMT) in multiple sclerosis (2006) (30)
Differential gene expression in breast cancer cell lines and stroma–tumor differences in microdissected breast cancer biopsies revealed by display array analysis (2002) (30)
Reliability and validity of conjunctival ultraviolet autofluorescence measurement (2012) (29)
Legacy of mutiny on the Bounty: founder effect and admixture on Norfolk Island (2010) (29)
The GSTM1 null genotype confers an increased risk for solar keratosis development in an Australian Caucasian population. (2002) (29)
Iloperidone: Preclinical Profile and Early Clinical Evaluation (1997) (29)
The effect of 1 mg folic acid supplementation on clinical outcomes in female migraine with aura patients (2016) (28)
Dopamine Receptor Genes and Migraine With and Without Aura: An Association Study (2002) (28)
Comparison of diagnostic tests in myasthenia gravis. (1983) (28)
Linkage disequilibrium analysis in the genetically isolated Norfolk Island population (2008) (27)
Effects of Dietary Folate Intake on Migraine Disability and Frequency (2015) (27)
No association between MTHFR A1298C and MTRR A66G polymorphisms, and MS in an Australian cohort (2007) (27)
Prospects for whole genome linkage disequilibrium mapping in domestic dog breeds (2003) (27)
Methylome-wide association study of whole blood DNA in the Norfolk Island isolate identifies robust loci associated with age (2017) (27)
Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients (2016) (27)
Distribution of conjunctival ultraviolet autoflourescence in a population-based study: the Norfolk Island Eye Study (2011) (26)
Investigation of Brain‐Derived Neurotrophic Factor (BDNF) Gene Variants in Migraine (2014) (26)
Association of the microRNA-Single Nucleotide Polymorphism rs2910164 in miR146a with sporadic breast cancer susceptibility: A case control study. (2016) (26)
Next‐generation sequencing identifies novel CACNA1A gene mutations in episodic ataxia type 2 (2016) (25)
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 gene. (2013) (25)
A genetic analysis of serotonergic biosynthetic and metabolic enzymes in migraine using a DNA pooling approach (2005) (25)
Association study of the calcitonin gene-related polypeptide-alpha (CALCA) and the receptor activity modifying 1 (RAMP1) genes with migraine. (2013) (25)
The Biology of the Glutamatergic System and Potential Role in Migraine (2013) (24)
BDNF and TNF-α polymorphisms in memory (2013) (24)
Chromosome I linkage studies in Charcot-Marie-Tooth neuropathy type I. (1988) (24)
Significant differences in gene expression of GABA receptors in peripheral blood leukocytes of migraineurs. (2011) (24)
Ion channelopathies and migraine pathogenesis (2017) (24)
Cardiomyopathy Classification: Ongoing Debate in the Genomics Era (2012) (24)
Association of microRNA 17–92 cluster host gene (MIR17HG) polymorphisms with breast cancer (2015) (23)
European and Polynesian admixture in the Norfolk Island population (2010) (23)
Linkage mapping of CVD risk traits in the isolated Norfolk Island population (2008) (23)
Cross-trait analyses with migraine reveal widespread pleiotropy and suggest a vascular component to migraine headache (2020) (23)
Influence of family history on frequency of glucagon receptor Gly40Ser mutation in hypertensive subjects. (1997) (23)
Principal Component and Linkage Analysis of Cardiovascular Risk Traits in the Norfolk Isolate (2009) (23)
CROSS‐SECTIONAL STUDY OF A MICROSATELLITE MARKER IN THE LOW DENSITY LIPOPROTEIN RECEPTOR GENE IN OBESE NORMOTENSIVES (1995) (22)
Analysis of chromosome 1 microsatellite markers and the FHM2-ATP1A2 gene mutations in migraine pedigrees (2005) (22)
Genetic polymorphisms in DPF3 associated with risk of breast cancer and lymph node metastases (2005) (22)
Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk Island. (2012) (22)
Expression of glucocorticoid and progesterone nuclear receptor genes in archival breast cancer tissue (2002) (22)
Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality (2020) (22)
Polyalanine Repeat Polymorphism in RUNX2 Is Associated with Site-Specific Fracture in Post-Menopausal Females (2013) (22)
Progesterone, glucocorticoid, but not estrogen receptor mRNA is altered in breast cancer stroma. (2007) (21)
Clinical Relevance of MTHFR, eNOS, ACE, and ApoE Gene Polymorphisms and Serum Vitamin Profile among Malay Patients with Ischemic Stroke. (2015) (21)
Association of oestrogen-receptor gene (ESR1) polymorphisms with migraine in the large Norfolk Island pedigree (2013) (21)
Association of a GRIA3 Gene Polymorphism With Migraine in an Australian Case‐Control Cohort (2013) (21)
High‐resolution loss of heterozygosity screening implicates PTPRJ as a potential tumor suppressor gene that affects susceptibility to non‐hodgkin's lymphoma (2013) (21)
Fluorescence detection of plant extracts that affect neuronal voltage-gated Ca2+ channels. (2002) (20)
Novel STAT binding elements mediate IL-6 regulation of MMP-1 and MMP-3 (2017) (19)
Genetic testing for exercise prescription and injury prevention: AIS-Athlome consortium-FIMS joint statement (2017) (19)
The genetics of endurance: frequency of the ACTN3 R577X variant in Ironman World Championship athletes. (2013) (19)
Epigenetics and migraine; complex mitochondrial interactions contributing to disease susceptibility. (2014) (19)
High performance liquid chromatography determined alkamide levels in Australian-grown Echinacea spp. (1998) (19)
Development of an eight gene expression profile implicating human breast tumours of all grade (2012) (19)
Modulation of in vitro platelet 5-HT release by species of Erythrina and Cymbopogon. (2001) (19)
Fully validated LC-MS/MS method for quantification of homocysteine concentrations in samples of human serum: a new approach. (2014) (19)
Molecular Mechanisms of Migraine (2003) (18)
The null allele of GSTM1 does not affect susceptibility to solar keratoses in the Australian white population. (1998) (18)
Polymorphisms of the SIPA1 gene and sporadic breast cancer susceptibility (2009) (18)
Exploring the Hereditary Nature of Migraine (2021) (18)
Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case (2018) (18)
In vitro and in vivo MMP gene expression localisation by In Situ-RT-PCR in cell culture and paraffin embedded human breast cancer cell line xenografts (2006) (18)
Genetics of Menstrual Migraine: The Molecular Evidence (2010) (17)
Two novel mutations and a previously unreported intronic polymorphism in the NOTCH3 gene. (2012) (17)
Pharmacogenetics of migraine: genetic variants and their potential role in migraine therapy. (2007) (17)
Dysregulated MicroRNA Expression Profiles and Potential Cellular, Circulating and Polymorphic Biomarkers in Non-Hodgkin Lymphoma (2016) (17)
Sibpair studies implicate chromosome 18 in essential hypertension (2004) (17)
Molecular genetic analyses of RFLPs for PCR-amplified growth hormone gene, renal kallikrein gene and atrial natriuretic factor gene in essential hypertension (1993) (16)
Blood gene expression studies in migraine: Potential and caveats (2016) (16)
Age-related changes in cardiac adenosine receptor expression (2004) (16)
BDNF Variants May Modulate Long-Term Visual Memory Performance in a Healthy Cohort (2017) (16)
Signaling pathway genes for blood pressure, folate and cholesterol levels among hypertensives: an epistasis analysis (2014) (16)
An investigation of the C77G and C772T variations within the human protein tyrosine phosphatase receptor type C gene for association with multiple sclerosis in an Australian population (2009) (16)
Randomised, Double Blind, Placebo-Controlled Trial of Echinacea Supplementation in Air Travellers (2011) (16)
Investigation of an inducible nitric oxide synthase gene (NOS2A) polymorphism in a multiple sclerosis population (2004) (16)
Genetic polymorphisms in miRNAs targeting the estrogen receptor and their effect on breast cancer risk (2014) (16)
Association analysis of a highly polymorphic CAG Repeat in the human potassium channel gene KCNN3 and migraine susceptibility (2005) (15)
Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine (2014) (15)
A pharmacogenomic evaluation of migraine therapy (2007) (15)
Analysis of 3 common polymorphisms in the KCNK18 gene in an Australian Migraine case-control cohort. (2013) (15)
Investigation of the low-density lipoprotein receptor gene and cholesterol as a risk factor for migraine (2004) (15)
Role of the apolipoprotein E and catechol-O-methyltransferase genes in prospective and retrospective memory traits. (2012) (15)
The Norfolk Island Eye Study (NIES): Rationale, Methodology and Distribution of Ocular Biometry (Biometry of the Bounty) (2011) (14)
The NRP1 migraine risk variant shows evidence of association with menstrual migraine (2018) (14)
Prevalence and predictors of refractive error in a genetically isolated population: the Norfolk Island Eye Study (2011) (14)
Cytogenetics of melanoma and nonmelanoma skin cancer. (2008) (14)
Perianal Disease Combined With NOD2 Genotype Predicts Need for IBD-related Surgery in Crohn’s Disease Patients From a Population-based Cohort (2013) (14)
No mutations detected in the INSR gene in a chromosome 19p13 linked migraine pedigree. (2004) (14)
Meta‐analysis of genome‐wide DNA methylation and integrative omics of age in human skeletal muscle (2021) (14)
Computational epigenetic profiling of CpG islets in MTHFR (2014) (14)
Investigation of polymorphisms in genes involved in estrogen metabolism in menstrual migraine. (2017) (13)
Cytogenetics of melanoma and nonmelanoma skin cancer. (2014) (13)
Investigation of glutathione S-transferase zeta and the development of sporadic breast cancer (2001) (13)
A population genomics overview of the neuronal nitric oxide synthase (nNOS) gene and its relationship to migraine susceptibility. (2005) (13)
An Assessment of MMP and TIMP Gene Expression in Cell Lines and Stroma – Tumour Differences in MicrodissectedBreast Cancer Biopsies (2003) (13)
Genetic insights into migraine and glutamate: a protagonist driving the headache (2016) (13)
Paradoxical effect of penicillin in-vivo. (1985) (13)
High levels of BACH2 associated with lower levels of BCL2 transcript abundance in t(14;18)(q21;q34) translocation positive non-Hodgkin's lymphoma. (2009) (13)
Simultaneous determination of aldrin, dieldrin, endrin, heptachlor, and p,p'-DDT in medicinal plant extracts using a novel high performance liquid chromatography method (1999) (13)
Data defining markers of human neural stem cell lineage potential (2016) (13)
Association of heparan sulfate proteoglycans SDC1 and SDC4 polymorphisms with breast cancer in an Australian Caucasian population (2015) (13)
Long-Term Consumption of Anthocyanin-Rich Fruit Juice: Impact on Gut Microbiota and Antioxidant Markers in Lymphocytes of Healthy Males (2020) (12)
A novel multiplex PCR-RFLP method for simultaneous detection of the MTHFR 677 C > T, eNOS +894 G > T and - eNOS -786 T > C variants among Malaysian Malays (2012) (12)
Investigation of Two Wnt Signalling Pathway Single Nucleotide Polymorphisms in a Breast Cancer-Affected Australian Population (2011) (12)
Targeted next generation sequencing identifies a genetic spectrum of DNA variants in patients with hemiplegic migraine (2019) (12)
The central nervous system in canine giant axonal neuropathy (1979) (12)
A genome-wide association study of essential hypertension in an Australian population using a DNA pooling approach (2017) (12)
Correction: Complete Mitochondrial Genome Sequencing Reveals Novel Haplotypes in a Polynesian Population (2012) (12)
Common polygenic variation contributes to risk of migraine in the Norfolk Island population (2015) (12)
Variants in the human potassium channel gene (KCNN3) are associated with migraine in a high risk genetic isolate (2011) (12)
Ion torrent high throughput mitochondrial genome sequencing (HTMGS) (2019) (11)
Isolation of two phenylethanoid glycosides from Eremophila gilesii. (2003) (11)
The B subunit of coagulation factor XIII is linked to renin and the Duffy blood group to alpha-spectrin on human chromosome 1. (1989) (11)
Association Study of MTHFD1 Coding Polymorphisms R134K and R653Q With Migraine Susceptibility (2014) (11)
Investigation of the role of the GABRG2 gene variant in migraine (2012) (11)
Chromosome 17 and the inducible nitric oxide synthase gene in human essential hypertension (2001) (11)
Association Analyses of RFLPs for the α2- and β1-Adrenoceptor Genes in Essential Hypertension (1992) (11)
Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants (2020) (11)
Whole-Exome Sequencing Implicates SCN2A in Episodic Ataxia, but Multiple Ion Channel Variants May Contribute to Phenotypic Complexity (2018) (10)
SCANNING THE GENOME FOR ESSENTIAL HYPERTENSION LOCI (1998) (10)
IS‐RT‐PCR assay detection of MT‐MMP in a human breast cancer cell line (1996) (10)
Meta-Analysis of Factor V, Factor VII, Factor XII, and Factor XIII-A Gene Polymorphisms and Ischemic Stroke (2019) (10)
Genes for essential hypertension : the first decade of research (1998) (10)
Investigation of lymphotoxin α genetic variants in migraine. (2013) (10)
Shorter Telomere Length in Peripheral Blood Cells Associated With Migraine in Women (2010) (10)
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort (2012) (10)
The role of adenosine-related genes variants in susceptibility to essential hypertension (2004) (10)
Prevalence of Chronic Ocular Diseases in a Genetic Isolate: The Norfolk Island Eye Study (NIES) (2011) (10)
Single Nucleotide Polymorphisms in MIR143 Contribute to Protection against Non-Hodgkin Lymphoma (NHL) in Caucasian Populations (2019) (10)
Serum bilirubin concentration is modified by UGT1A1 Haplotypes and influences risk of Type-2 diabetes in the Norfolk Island genetic isolate (2015) (10)
A new method to detect loss of heterozygosity using cohort heterozygosity comparisons (2010) (9)
Investigating diagnostic sequencing techniques for CADASIL diagnosis (2020) (9)
Matrix metalloproteinase localisation by in situ-RT-PCR in archival human breast biopsy material. (2008) (9)
Association analysis of chromosome 1 migraine candidate genes (2007) (9)
Identification of a novel mutation C144F in the notch3 gene in an Australian CADASIL pedigree (2000) (9)
Erratum: Common Variant Burden Contributes to the Familial Aggregation of Migraine in 1,589 Families (Neuron (2018) 98(4) (743–753.e4), (S0896627318303222) (10.1016/j.neuron.2018.04.014)) (2018) (9)
Heterogeneity evidence and linkage studies on Charcot‐Marie‐Tooth disease (1989) (9)
A novel fully validated LC-MS/MS method for quantification of pyridoxal-5'-phosphate concentrations in samples of human whole blood. (2015) (9)
Tiered analysis of whole-exome sequencing for epilepsy diagnosis (2020) (9)
Genetic and epigenetic variants in the MTHFR gene are not associated with non-Hodgkin lymphoma (2015) (9)
Accounting for cell lineage and sex effects in the identification of cell-specific DNA methylation using a Bayesian model selection algorithm (2017) (9)
Heparan Sulfate Proteoglycans as Drivers of Neural Progenitors Derived From Human Mesenchymal Stem Cells (2018) (9)
Association of the SNP rs2623047 in the HSPG modification enzyme SULF1 with an Australian Caucasian breast cancer cohort. (2014) (9)
Genome-wide allele-specific methylation is enriched at gene regulatory regions in a multi-generation pedigree from the Norfolk Island isolate (2019) (9)
An emerging role for epigenetic factors in relation to executive function (2018) (9)
Exploring Neuronal Vulnerability to Head Trauma Using a Whole Exome Approach (2020) (8)
The current state of play in human neural stem cell models: what we have learnt from the rodent (2014) (8)
Syndecan-1 Facilitates the Human Mesenchymal Stem Cell Osteo-Adipogenic Balance (2020) (8)
Genetic Analysis of GRIA2 and GRIA4 Genes in Migraine (2014) (8)
Genetic variants associated with exercise performance in both moderately trained and highly trained individuals (2020) (8)
Investigation of a neuronal nitric oxide synthase gene (NOS1) polymorphism in a multiple sclerosis population (2004) (8)
Investigation of the 1758G>C and 2880A>G variants within the NCOA3 gene in a breast cancer affected Australian population. (2011) (8)
Genetic Variation in Cytokine-Related Genes and Migraine Susceptibility (2013) (8)
Investigation of the NOTCH3 and TNFSF7 Genes on C19p13 as Candidates for Migraine (2008) (8)
Detection of mRNA levels for the estrogen alpha, estrogen beta and androgen nuclear receptor genes in archival breast cancer tissue. (2006) (8)
Increase in bronchopulmonary infection due to Branhamella catarrhalis. (1986) (8)
Skeletal muscle methylome and transcriptome integration reveals profound sex differences related to muscle function and substrate metabolism (2021) (7)
A CREB1 Gene Polymorphism (rs2253206) Is Associated with Prospective Memory in a Healthy Cohort (2017) (7)
An Envirogenomic Signature Is Associated with Risk of IBD-Related Surgery in a Population-Based Crohn’s Disease Cohort (2013) (7)
Allelic variation investigation of the estrogen receptor within an Australian multiple sclerosis population (2007) (7)
Gene Expression Profiling in Human Breast Cancer - Toward Personalised Therapeutics? (2010) (7)
In silico analyses reveal common cellular pathways affected by loss of heterozygosity (LOH) events in the lymphomagenesis of Non-Hodgkin’s lymphoma (NHL) (2014) (7)
A novel immunodeficiency disorder characterized by genetic amplification of interleukin 25 (2011) (7)
Comprehensive Exonic Sequencing of Known Ataxia Genes in Episodic Ataxia (2020) (6)
Gene‐centric analysis implicates nuclear encoded mitochondrial protein gene variants in migraine susceptibility (2017) (6)
Genome wide association study of response to interval and continuous exercise training: the Predict-HIIT study (2021) (6)
HSPGs glypican‐1 and glypican‐4 are human neuronal proteins characteristic of different neural phenotypes (2020) (6)
Investigating the influence of mtDNA and nuclear encoded mitochondrial variants on high intensity interval training outcomes (2020) (6)
Critical evaluation of linear regression models for cell-subtype specific methylation signal from mixed blood cell DNA (2018) (6)
Association analysis of somatostatin receptor (SSTR1 and SSTR2) polymorphisms in breast cancer and solar keratosis. (2001) (6)
Methylenetetrahydrofolate Reductase CpG Islands: Epigenotyping (2016) (6)
A Phenomic Scan of the Norfolk Island Genetic Isolate Identifies a Major Pleiotropic Effect Locus Associated with Metabolic and Renal Disorder Markers (2015) (5)
Regional chromosomal assignment of human renin gene to 1q12----qter and use in linkage studies in Charcot-Marie-Tooth disease. (1987) (5)
Detection of a Novel Mutation in the CACNA1A gene (2012) (5)
PTEN and NDUFB8 aberrations in cervical cancer tissue. (2007) (5)
Investigation of the [−/A]8 and C1236T genetic variations within the human toll-like receptor 3 gene for association with multiple sclerosis (2010) (5)
Potential antioxidant response to coffee — A matter of genotype? (2014) (5)
Single Nucleotide Polymorphism in hsa-mir-196 a-2 and Breast Cancer Risk : A Case Control Study (2011) (5)
Case-control study of ADARB1 and ADARB2 gene variants in migraine (2015) (5)
Exploring new avenues for modifying course of progression of Alzheimer's disease: The rise of natural medicine (2021) (5)
Heparan Sulfate Proteoglycans, Tumour Progression and the Cancer Stem Cell Niche (2009) (5)
EHMTI-0047. Genetic association and gene expression studies suggest that genetic variants in the SYNE1 and TNF genes are related to menstrual migraine (2014) (5)
Using Monozygotic Twins to Dissect Common Genes in Posttraumatic Stress Disorder and Migraine (2021) (5)
Biochemical studies of the neurotransmitter glutamate: A key player in migraine (2015) (5)
Investigation of APOE isoforms and the association between APOE E3 and E4 with migraine in the Australian Caucasian population (2013) (5)
Current understanding of DNA methylation and age-related disease (2018) (5)
Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked Glycosylation (2017) (5)
Towards a translational medical research ecosystem (2011) (5)
Meta-analysis of genome-wide DNA methylation and integrative OMICs in human skeletal muscle (2020) (4)
Investigation of Association between PFO Complicated by Cryptogenic Stroke and a Common Variant of the Cardiac Transcription Factor GATA4 (2011) (4)
Saliva as a comparable-quality source of DNA for Whole Exome Sequencing on Ion platforms. (2020) (4)
Non-linkage of insulin receptor locus with essential hypertension in an affected pedigree (1993) (4)
Microarray gene expression analysis in MS (2000) (4)
Differential stability of variant OPN1LW gene transcripts in myopic patients (2019) (4)
Moraxella urethritis mimicking gonorrhoea. (1991) (3)
Genetic Association Analysis Implicates Six MicroRNA-Related SNPs With Increased Risk of Breast Cancer in Australian Caucasian Women. (2021) (3)
Variant Call Format–Diagnostic Annotation and Reporting Tool (2019) (3)
Erratum to: ‘Mutiny on the Bounty’: the genetic history of Norfolk Island reveals extreme gender-biased admixture (2015) (3)
Variation H452Y in HTR2A Gene Affects Immediate Visual Memory (2014) (3)
Evaluating the suitability of current mitochondrial DNA interpretation guidelines for multigenerational whole mitochondrial genome comparisons (2022) (3)
Detection of mRNA for nuclear receptor co-activators 1 and 3 in archival breast cancer tissue and surrounding stroma: a tissue expression study (2010) (3)
Focusing on genomic and phenomic correlations in respiration of non-melanotic skin cancers. (2005) (3)
Mini review: genome and transcriptome editing using CRISPR-cas systems for haematological malignancy gene therapy (2021) (3)
Epigenetic Regulation of miR-92a and TET2 and Their Association in Non-Hodgkin Lymphoma (2021) (3)
SLC17A3 rs9379800 and Ischemic Stroke Susceptibility at the Northern Region of Malaysia. (2021) (3)
Variant Call Format (VCF)-Diagnostic Annotation and Reporting Tool (VCF-DART) A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data. (2019) (2)
Three-Dimensional Human Neural Stem Cell Models to Mimic Heparan Sulfate Proteoglycans and the Neural Niche (2021) (2)
Acetylcholine receptor antibodies in the diagnosis and management of myasthenia gravis. (1981) (2)
Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size (2017) (2)
Analysis of SDHD and MMP12 in an affected solar keratosis and control cohort. (2007) (2)
Investigation of Association between PFO Complicated by Cryptogenic Stroke and a Common Variant of the Cardiac Transcription Factor GATA 4 (2011) (2)
Current Status of Pharmacogenomics Testing for Anti-Tumor Drug Therapies (2012) (2)
Syndecan-1 and -4 influence Wnt signaling and cell migration in human breast cancers. (2022) (2)
Common PPARγ variants C161T and Pro12Ala are not associated with inflammatory bowel disease in an Australian cohort. (2012) (2)
Genome-wide DNA methylation and transcriptome integration reveal distinct sex differences in skeletal muscle (2021) (2)
A Sensitive Assay for Creatine Kinase in Serum Samples Dried on Paper: Enhanced Thermal Stability of the Dried Enzyme (1983) (2)
Genetic polymorphisms in DPF 3 associated with risk of breast cancer and lymph node metastases (2005) (2)
Gene expression patterning in breast cancer biopsies, by real time quantitative RT-PCR analysis (2001) (2)
Two novel mutations and a previously unreported intronic polymorphism in the NOTCH 3 gene (2012) (2)
Investigation of CACNA1I Cav3.3 Dysfunction in Hemiplegic Migraine (2022) (2)
Authors response to: Critique of "Chromosome 17 and inducible nitric oxide synthase gene in human essential hypertension" by Rutherford et al. in Human Genetics published on-line September 2001 (2001) (2)
Investigation of the CADM2 polymorphism rs17518584 in memory and executive functions measures in a cohort of young healthy individuals (2018) (1)
Comparison of genomic DNA extraction techniques from whole blood samples: a time, cost and quality evaluation study (2012) (1)
The MTHFR gene variant ( C 677 T ) influences susceptibility to migraine with aura (2003) (1)
Identification of a novel mutation C144F in the notch3 gene in an Australian CADASIL pedigree Communicated by: Mark H. Paalman Online Citation: Human Mutation, Mutation and Polymorphism Report #176 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr176.pdf Acknowledgments: We would li (2000) (1)
Investigation of the NOTCH 3 and TNFSF 7 Genes on C 19 p 13 as Candidates for Migraine (2017) (1)
Refractive Error Is Associated With Degree Of Conjunctival UV Autofluorescence (2011) (1)
Closing the case of APOE in multiple sclerosis : no association with disease risk in over 29,000 subjects (2012) (1)
An investigation of genetic polymorphisms in heparan sulfate proteoglycan core proteins and key modification enzymes in an Australian Caucasian multiple sclerosis population (2020) (1)
Cerebrovascular Function in Hormonal Migraine: An Exploratory Study (2021) (1)
Association of polymorphisms in ARRB2 and clinical response to methadone for pain in advanced cancer. (2022) (1)
Confirmation that Xq27 and Xq28 are susceptibility loci for migraine in independent pedigrees and a case-control cohort (2012) (1)
Genome-wide linkage and association analysis of primary open-angle glaucoma endophenotypes in the Norfolk Island isolate (2017) (1)
Development of an accurate genomic ancestry prediction strategy to enable the accounting of Australian and Japanese historical military remains (2020) (1)
Techniques for RNA extraction from cells cultured in starPEG–heparin hydrogels (2021) (1)
A combinatorial in silico approach for microRNA-target identification: Order out of chaos. (2021) (1)
Pedigree derived mutation rate across the entire mitochondrial genome of the Norfolk Island population (2021) (1)
Study of leukemia inhibitory factor polymorphism within an Australian multiple sclerosis population (2009) (1)
Syndecan-4 regulates the HER2-positive breast cancer cell proliferation cells via CK19/AKT signalling. (2022) (1)
Global reported impacts of COVID‐19 on lymphoma patients and the emerging clinical management approaches in response to the ongoing pandemic (2023) (1)
Mapping the Genes Involved in Migraine Susceptibility (2005) (1)
A genome-wide methylation study of body fat traits in the Norfolk Island isolate. (2021) (1)
DNA probes in Charcot-Marie-Tooth neuropathy. (1988) (1)
Nutraceuticals in migraine treatment (2013) (1)
A chromosome 1 BglI RFLP for the LR67 anonymous DNA segment [D1S26]. (1988) (1)
A chromosome 1 Bgll RFLP for the LR67 anonymous DNA segment [DIS26] (1988) (1)
SDC4-rs1981429 and ATM-rs228590 may provide early biomarkers of breast cancer risk. (2022) (1)
The MinION as a cost-effective technology for diagnostic screening of the SCN1A gene in epilepsy patients (2021) (1)
Multi-phenotype genome-wide association studies of the Norfolk Island isolate implicate pleiotropic loci involved in chronic kidney disease (2021) (1)
RE: Six novel rare non-synonymous mutations for migraine without aura identified by exome sequencing (2017) (1)
A LOCUS ON THE LONG ARM OF CHROMOSOME 1 AS A POSSIBLE CAUSE OF ESSENTIAL HYPERTENSION (1991) (1)
Endophenotype profiles of MTHFR and ACE gene polymorphisms in migraine susceptibility (2017) (1)
FOXP1 truncated isoforms differentially regulate target genes in diffuse large B cell lymphoma. (2013) (0)
Lack of association of the gene GATA-4 mutation in migraine. (2006) (0)
The Norfolk Island Genetic Isolate: A tool for complex disease gene mapping. (2005) (0)
Saliva-derived DNA performs well in large-scale, high-density SNP microarray studies (2011) (0)
The effectiveness of a standardised Echinacea preparation in preventing colds, flus and other respiratory disorders for air- travellers (2010) (0)
Association of breast cancer pathology with the expression of nuclear receptors and their coactivators (2009) (0)
Genetic legacy of the mutiny on the Bounty: Use of the Norfolk Island population for CVD and migraine gene mapping (2009) (0)
Next Generation Sequencing Identifies Novel CACNA1A 1 Gene Mutations in Episodic Ataxia Type 2 (2017) (0)
Molecular Genetic Studies on Breast and Skin Cancer (2005) (0)
Single Nucleotide Polymorphism in hsa mir 196 a 2 and Breast Cancer Risk : A Case Control (2017) (0)
Detection and estimation of the levels of specific environmental contaminants in medicinal plants (2000) (0)
A genome-wide linkage analysis of migraine in the descendents of the Bounty Mutineers implicates the 13q chromosomal region (2009) (0)
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci | NOVA. The University of Newcastle's Digital Repository (2011) (0)
Title : Relative Abundance of Full-Length and Truncated FOXP 1 Isoforms are Associated with NFκB Activity in Follicular Lymphoma (2010) (0)
Net antitumoral immunity and the predictive power of conventional prognosticators in diffuse large B-cell lymphoma. (2014) (0)
Migraine and glutamate: modulators of glutamatergic signalling as potential treatments of neuropsychiatric disorders (2015) (0)
Novel AlphasynucleinPAN in human Mesenchymal Stem Cells-derived neurons masks SNCA140 and creates dissociation of deleterious SNCA98 in astrocytoma stem cells (2022) (0)
Genetic risk profiling in migraine: hormonal and vascular genotypes and susceptibility to migraine. (2005) (0)
Implication of Vascular and Hormonal Gene Variants in Migraine Susceptibility (2004) (0)
Development and validation of an lc-ms/ms bioanalytical method for quantification of homocysteine (hcy) in samples of human serum (2014) (0)
Vascular and Hormonal Variants are Implicated in Migraine Susceptibility (2004) (0)
Causal relationships between migraine and microstructural white matter: a Mendelian randomization study (2023) (0)
Discriminating head trauma outcomes using machine learning and genomics (2021) (0)
Migraine linkage and association study of two polymorphisms in the human serotonergic receptor (5-HT 2c) (2000) (0)
SCANNING THB GENOME FOR ESSENTIALHYPERTENSION LOCI (1998) (0)
Authors' response—Approach to evaluating the reliability and validity of conjunctival ultraviolet autofluorescence measurement (2012) (0)
Identification and simultaneous analysis of harmane, harmol, isovitexin and vitexin in Passiflora incarnata extracts with a novel HLPC method (2001) (0)
Characterisation of migraine prevalence, heritability and symptom phenotypes in the Norfolk Island population (2009) (0)
GeneHunting: the search for genes involved in complex human disorders (2004) (0)
Abstract 561: A natural copy number variant in the GAEC1 oncogene is associated with breast cancer susceptibility (2014) (0)
BDNF and TNF-α polymorphisms in memory (2013) (0)
Investigating diagnostic sequencing techniques for CADASIL diagnosis (2020) (0)
Common polygenic variation contributes to risk of migraine in the Norfolk Island population (2015) (0)
Abstracts for the 44th Human Genetics Society of Australasia Annual Scientific Meeting, 14–17 August 2021 (2021) (0)
Investigating the influence of mtDNA and nuclear encoded mitochondrial variants on high intensity interval training outcomes (2020) (0)
The Maori Population is a Candidate for Admixture Gene Mapping. (2006) (0)
Investigation of Mitochondrial Related Variants in a Cerebral Small Vessel Disease Cohort (2022) (0)
The genetics of migraine (2007) (0)
The Norfolk Island Eye Study:Ocular Biometry of the Bounty Mutineers (2011) (0)
Identification of novel mitochondrial and mitochondrial related genetic loci associated with exercise response in the Gene SMART study (2020) (0)
Genetic variants associated with exercise performance in both moderately trained and highly trained individuals (2020) (0)
Development of an eight gene expression profile implicating human breast tumours of all grade (2011) (0)
glucocorticoid and progesterone nuclear receptor genes in archival breast cancer tissue (2017) (0)
Serum bilirubin concentration is modified by UGT1A1 Haplotypes and influences risk of Type-2 diabetes in the Norfolk Island genetic isolate (2015) (0)
Use of the Norfolk Island Genetic Isolate for Migraine Gene Mapping. (2005) (0)
Evaluation of an ancestry prediction strategy for historical military remains using a World War II-era sample and pedigrees with family-level admixture (2021) (0)
Ion channelopathies and migraine pathogenesis (2017) (0)
MicroRNA-Target Identification: A Combinatorial In Silico Approach. (2023) (0)
Association of KCNJ6 rs2070995 and methadone response for pain management in advanced cancer at end-of-life (2022) (0)
Genetic testing for exercise prescription and injury prevention: AIS-Athlome consortium-FIMS joint statement (2017) (0)
Genome-wide allele-specific methylation is enriched at gene regulatory regions in a multi-generation pedigree from the Norfolk Island isolate (2019) (0)
Exercise is associated with younger methylome and transcriptome profiles in human skeletal muscle (2023) (0)
GSTM1 and GSTT1 polymorphisms associated with pain in a chemotherapy-induced peripheral neuropathy cohort. (2023) (0)
The gene SMART study: method, study design, and preliminary findings (2017) (0)
Induction of antioxidative Nrf2 gene transcription by coffee in humans: depending on genotype? (2012) (0)
Computational epigenetic profiling of CpG islets in MTHFR (2014) (0)
Linkage and association study for the 2831T-G polymorphism in 5.ht 2c (2000) (0)
Journal Pre-proof A Customizable Analysis Pipeline for Identification of Clinically Relevant Genetic Variants in Next-Generation Sequencing Data (2020) (0)
Novel compound heterozygous missense mutations in GDAP1 cause Charcot–Marie–Tooth type 4A (2021) (0)
Tiered analysis of whole-exome sequencing for epilepsy diagnosis (2020) (0)
Whole Exome Sequencing of Hemiplegic Migraine Patients Shows an Increased Burden of Missense Variants in CACNA1H and CACNA1I Genes (2023) (0)
Migraine Linkage Mapping using the Norfolk Island Genetic Isolate. (2006) (0)
It's All About the Timing: Circadian Factors in Cluster Headache and Migraine. (2023) (0)
Genome wide association study of response to interval and continuous exercise training: the Predict-HIIT study (2021) (0)
In silico analyses reveal common cellular pathways affected by loss of heterozygosity (LOH) events in the lymphomagenesis of Non-Hodgkin’s lymphoma (NHL) (2014) (0)
Genetic analysis of endometriosis and depression identifies shared loci and implicates causal links with gastric mucosa abnormality (2020) (0)
Diagnosing sepsis in the ICU: Comparison of a gene expression signature to pre-existing biomarkers. (2023) (0)
Expression QTL analysis of glaucoma endophenotypes in the Norfolk Island isolate provides evidence that immune-related genes are associated with optic disc size (2017) (0)
Role of the Androgen Receptor Gene in Sporadic Breast Cancer (2004) (0)
Investigating a Genetic Link Between Alzheimer’s Disease and CADASIL-Related Cerebral Small Vessel Disease (2022) (0)
Skeletal muscle methylome and transcriptome integration reveals profound sex differences related to muscle function and substrate metabolism (2021) (0)
A genome-wide association study of essential hypertension in an Australian population using a DNA pooling approach (2016) (0)
Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients (2016) (0)
An investigation of genetic polymorphisms in heparan sulfate proteoglycan core proteins and key modification enzymes in an Australian Caucasian multiple sclerosis population (2020) (0)
Discriminating head trauma outcomes using machine learning and genomics (2021) (0)
Critique of "Sibpair studies implicate chromosome 18 in essential hypertension" by S. Rutherford, M.P. Johnson, and L.R. Griffiths. 2004. Am J Med Genet 126A:241-247. (2005) (0)
The role of glutathione S-transferase M1, T1, P1 and Z1 in the development of solar keratosis with specific implication of GSTM1 and GSTT1. (2000) (0)
Novel STAT binding elements mediate IL-6 regulation of MMP-1 and MMP-3 (2017) (0)
Data on 2D culture characterisation of potential markers in human HER2-positive breast cancer cell lines (2023) (0)
Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease (2020) (0)
An analysis of DNA methylation in human adipose tissue reveals differential modification of obesity genes before and after gastric bypass and weight loss (2015) (0)
High levels of BACH 2 associated with lower levels of BCL 2 transcript abundance in t ( 14 ; 18 ) ( q 21 ; q 34 ) translocation positive non-Hodgkin ’ s lymphoma (2017) (0)
Use of the Norfolk Island Genetic Isolate to Identify Genetic Risk Factors for CVD. (2005) (0)
Emerging genomic biomarkers in migraine (2013) (0)
Investigating migraine in the descendents of the Bounty Mutineers (2009) (0)
Migraine susceptibility genotypes and B vitamins as a prophylactic treatment. (2006) (0)
Utilisation of a Whole-Genome Approach to Characterize a Novel Immunodeficiency Disorder and Implicate IL25 (2009) (0)
Critique on: Sibpair studies implicate chromosome 18 in essential hypertension. Author's reply (2005) (0)
Molecular Genetics of Migraine (2013) (0)
Natural products affecting the human serotonergic system (2000) (0)
Altered Monoamine Oxidase Gene Expression in Response to Ethanol Exposure. (2006) (0)
Ratios of T-cell immune-effectors with tumour associated macrophages and PD-1/PD-L1 axis immune-checkpoint molecules, add to the predictive power of conventional prognosticators in diffuse large B cell lymphoma (2015) (0)
Current status of pharmacogenomics testing for anti-tumor drug therapies: approaches to non-melanoma skin cancer. (2009) (0)
The Role of Vascular and Hormonal Gene Variants in Migraine Susceptibility (2005) (0)
Association and linkage analyses implicates glucocorticoid interacting gene variants in essential hypertension and obesity. (2000) (0)
A potential migraine susceptibility lucus refined to Xq28. (2006) (0)
An investigation of gene expression in human breast cancer using tissue microarray (2008) (0)
Use of the Susceptibility Markers for Genetic Risk Profiling in Migraine. (2006) (0)
Supplementary Material for: Dysregulation of the Expression of Asparagine-Linked Glycosylation 13 Short Isoform 2 Affects Nephrin Function by Altering Its N-Linked Glycosylation (2017) (0)
The effects of ovariectomy on the expression of estrogen and adenosine receptors in the rat bladder. (2002) (0)
High performance liquid chromatography determined alkamide levels in Australian-grown (1998) (0)
Novel genotypes associated with sporadic breast cancer susceptibility. (2000) (0)
Evidence for a typical migraine gene on chromosome 1 (2000) (0)
New compounds from the Australian native plants Eremophilia gileslii (2000) (0)
Blood samples for gene studies in familial hypertension (1990) (0)
An investigation of an ATP-binding cassette gene variant and susceptibility to essential hypertension (2008) (0)
EBV-positive DLBCL of the elderly expresses EBNA3A with conserved CD8+ T-cell epitopes. (2011) (0)
Identification of FOXP1 Transcriptional Targets in Diffuse Large B Cell Lymphoma (2012) (0)
Genomic and Phenomic Correlations in the Respiration of Cancers (2002) (0)
Circulating microRNAs involved in multiple sclerosis (2012) (0)
Focusing on genomic and phenomic aberrations in non-melanotic skin cancers. (2006) (0)
Linkage disequilibrium in an isolated population from Norfolk Island. (2006) (0)
Differential expression of novel breast tumour associated factors from microdissected formalin fixed paraffin embedded archival material (2001) (0)
Migraine Susceptibility: Role for Vascular and Hormonal Gene Variants (2004) (0)
Heparan sulfate proteoglycans and human breast cancerepithelial cell tumorigenicity (2014) (0)
' s response to reviews No role for Estrogen Receptor 1 Gene Intron 1 Pvu II and Exon 4 C 325 G Polymorphisms in Migraine Title : Susceptibility (2006) (0)
A potential epigenetic marker mediating serum folate and vitamin B12 levels contributes to ischemic stroke risk (2015) (0)
Genetics of Migraine: Implications for novel treatments (2009) (0)
Genetic susceptibility to complex traits: moving towards informed analysis of whole-genome screens (2009) (0)
Polymorphic investigation within the region of several sex hormone genes for association with multiple sclerosis within an Australian case-control population (2009) (0)
Isolation and use of chromosome 1 probes for linkage studies on Charcot‐Marie‐Tooth disease (1990) (0)
A natural copy number variant in the GAEC1 oncogene is associated with breast cancer susceptibility (2014) (0)
A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibility (2012) (0)
Cytogenetics of Basal Cell Carcinoma and Squamous Cell Carcinomas (2006) (0)
Ethanol exposure alters monoamine oxidase gene-expression in neuronal SH-SY5Y cells (2017) (0)
Association of the Vitamin D Receptor Gene with Multiple Sclerosis (2006) (0)
Genetic Risk Profiling in Migraine: Development of Gene Based Diagnostics (2006) (0)
Microarray in Multiple Sclerosis (2000) (0)
Title: Ethanol Exposure Alters Monoamine Oxidase Gene-Expression in Neuronal SH-SY5Y Cells (2017) (0)
Expression of the Nuclear Receptor Co-Activators 1 and 3 in Archival IDC Breast Cancer: Loss of ESRa Points the Way (2008) (0)
Coffee and chemoprevention – the genotype decides (2019) (0)
A sweet promise among Malaysians [Letter to the Editor] (2014) (0)
Norfolk Island Population Origin Analysis (2004) (0)
Cytogenetics of Primary Skin Tumors (2011) (0)
Polymorphisms of the SIPA 1 gene and sporadic breast cancer susceptibility (2017) (0)
Novel compound heterozygous missense mutations in GDAP1 cause Charcot–Marie–Tooth type 4A (2021) (0)
association of glucocorticoid and estrogen receptor gene polymorphisms and sporadic breast cancer susceptibility. (2000) (0)
Investigation of GRIA3 Receptor Gene and Migraine Susceptibility (2008) (0)
A possible role for mitochondrial dysfunction in migraine (2012) (0)
Whole exome sequencing diagnosis of X-linked moesin-associated immunodeficiency and development of a CRISPR/Cas9 rescue phenotype strategy (2018) (0)
of Age, Gender and Cardiovascular Disease (2008) (0)
Critique of “sibpair studies implicate chromosome 18 in essential hypertension” by S. Rutherford, M.P. Johnson, and L.R. Griffiths. Am J Med Genet 126A:241–247 (2004) (2005) (0)
Linkage studies on hypertrophic motor and sensory neuropathy type 1 (1990) (0)
Mapping the genes involved in migraine (2000) (0)
Association of a glucocorticoid receptor gene marker with human essential hypertension. (1999) (0)
Molecular genetic studies on migraine (2005) (0)
Tissue specific regulation of breast cancer associated factors, and tissue remodelling enzymes (2001) (0)
Loss of Heterozygosity (LOH) of PTPRJ in Non-Hodgkin`s Lymphoma (NHL) (2011) (0)

This paper list is powered by the following services:

Other Resources About Lyn R. Griffiths

en.wikipedia.org

What Schools Are Affiliated With Lyn R. Griffiths?

Lyn R. Griffiths is affiliated with the following schools: