Published in Mutat Res on June 02, 2007
Macrophage activation by endogenous danger signals. J Pathol (2008) 2.38
Why interleukin-10 supplementation does not work in Crohn's disease patients. World J Gastroenterol (2013) 1.02
The challenges for molecular nutrition research 1: linking genotype to healthy nutrition. Genes Nutr (2008) 0.96
Lack of evidence for association of primary sclerosing cholangitis and primary biliary cirrhosis with risk alleles for Crohn's disease in Polish patients. BMC Med Genet (2008) 0.92
Role of dietary polyphenols in the management of peptic ulcer. World J Gastroenterol (2015) 0.90
Viruses, autophagy genes, and Crohn's disease. Viruses (2011) 0.86
Interactions between dietary n-3 fatty acids and genetic variants and risk of disease. Br J Nutr (2012) 0.84
Epidemiology and gene markers of ulcerative colitis in the Chinese. World J Gastroenterol (2009) 0.82
IGR2096a_1 T and IGR2198a_1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn's disease in Hungarian patients. Int J Colorectal Dis (2009) 0.80
Tumor necrosis factor receptor superfamily, member 1B haplotypes increase or decrease the risk of inflammatory bowel diseases in a New Zealand caucasian population. Gastroenterol Res Pract (2009) 0.80
Atherogenic diets exacerbate colitis in mice deficient in glutathione peroxidase. Inflamm Bowel Dis (2010) 0.79
Use of complementary and alternative medicine in Swedish patients with inflammatory bowel disease: a controlled study. Eur J Gastroenterol Hepatol (2016) 0.77
Zinc proteome interaction network as a model to identify nutrient-affected pathways in human pathologies. Genes Nutr (2014) 0.76
Genetic update on inflammatory factors in ulcerative colitis: Review of the current literature. World J Gastrointest Pathophysiol (2014) 0.76
Anti-inflammatory Effects of Herbal Preparations STW5 and STW5-II in Cytokine-Challenged Normal Human Colon Cells. Front Pharmacol (2016) 0.75
Rapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clustering. Am J Hum Genet (2007) 24.68
A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay. Nat Genet (2010) 6.62
Haplotype phasing: existing methods and new developments. Nat Rev Genet (2011) 4.66
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Ann Neurol (2011) 3.52
High-resolution detection of identity by descent in unrelated individuals. Am J Hum Genet (2010) 3.41
Evaluation of Nyholt's procedure for multiple testing correction. Hum Hered (2005) 2.50
Genetic loci associated with plasma phospholipid n-3 fatty acids: a meta-analysis of genome-wide association studies from the CHARGE Consortium. PLoS Genet (2011) 2.33
Cathepsin L in secretory vesicles functions as a prohormone-processing enzyme for production of the enkephalin peptide neurotransmitter. Proc Natl Acad Sci U S A (2003) 1.83
Performance of genotype imputation for rare variants identified in exons and flanking regions of genes. PLoS One (2011) 1.72
Population structure can inflate SNP-based heritability estimates. Am J Hum Genet (2011) 1.54
Identity by descent between distant relatives: detection and applications. Annu Rev Genet (2012) 1.39
Dilated cardiomyopathy in mice deficient for the lysosomal cysteine peptidase cathepsin L. Proc Natl Acad Sci U S A (2002) 1.37
Identification of large gene deletions and duplications in KCNQ1 and KCNH2 in patients with long QT syndrome. Heart Rhythm (2008) 1.33
The genetic basis of premature ovarian failure. Aust N Z J Obstet Gynaecol (2006) 1.29
The case for strategic international alliances to harness nutritional genomics for public and personal health. Br J Nutr (2005) 1.24
Interactions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophrenia. Behav Brain Funct (2007) 1.19
Genetic factors in chronic inflammation: single nucleotide polymorphisms in the STAT-JAK pathway, susceptibility to DNA damage and Crohn's disease in a New Zealand population. Mutat Res (2010) 1.18
Triallelic single nucleotide polymorphisms and genotyping error in genetic epidemiology studies: MDR1 (ABCB1) G2677/T/A as an example. Cancer Epidemiol Biomarkers Prev (2007) 1.15
Comparison of responses of human melanoma cell lines to MEK and BRAF inhibitors. Front Genet (2013) 1.13
Genome-wide association study identifies novel loci associated with concentrations of four plasma phospholipid fatty acids in the de novo lipogenesis pathway: results from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) consortium. Circ Cardiovasc Genet (2013) 1.12
Additive genetic variation in schizophrenia risk is shared by populations of African and European descent. Am J Hum Genet (2013) 1.07
Has toll-like receptor 4 been prematurely dismissed as an inflammatory bowel disease gene? Association study combined with meta-analysis shows strong evidence for association. Am J Gastroenterol (2007) 1.07
Single nucleotide polymorphism in the tumor necrosis factor-alpha gene affects inflammatory bowel diseases risk. World J Gastroenterol (2008) 1.06
Exome sequencing reveals novel rare variants in the ryanodine receptor and calcium channel genes in malignant hyperthermia families. Anesthesiology (2013) 1.06
Mutational screening of FOXO3A and FOXO1A in women with premature ovarian failure. Fertil Steril (2006) 1.05
Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort. Hum Genet (2012) 1.05
YB-1, the E2F pathway, and regulation of tumor cell growth. J Natl Cancer Inst (2011) 1.04
Mutational analysis of BMP15 and GDF9 as candidate genes for premature ovarian failure. Fertil Steril (2006) 0.99
Interactions among genes influencing bacterial recognition increase IBD risk in a population-based New Zealand cohort. Hum Immunol (2009) 0.97
The transcriptional targets of mutant FOXL2 in granulosa cell tumours. PLoS One (2012) 0.97
Elevated serum gastrin levels in Jervell and Lange-Nielsen syndrome: a marker of severe KCNQ1 dysfunction? Heart Rhythm (2010) 0.96
Biophysical properties of 9 KCNQ1 mutations associated with long-QT syndrome. Circ Arrhythm Electrophysiol (2009) 0.95
Physical and transcript map of the region between D6S264 and D6S149 on chromosome 6q27, the minimal region of allele loss in sporadic epithelial ovarian cancer. Oncogene (2002) 0.95
Comparison of growth factor signalling pathway utilisation in cultured normal melanocytes and melanoma cell lines. BMC Cancer (2012) 0.93
A novel 30 bp deletion in the FOXL2 gene in a phenotypically normal woman with primary amenorrhoea: case report. Hum Reprod (2004) 0.93
On reducing the statespace of hidden Markov models for the identity by descent process. Theor Popul Biol (2002) 0.93
Long QT and Brugada syndrome gene mutations in New Zealand. Heart Rhythm (2007) 0.91
Centrosomal dysregulation in human metastatic melanoma cell lines. Cancer Genet (2011) 0.91
Expression of the meningococcal adhesin NadA is controlled by a transcriptional regulator of the MarR family. Mol Microbiol (2009) 0.88
First complete genome sequence of infectious laryngotracheitis virus. BMC Genomics (2011) 0.88
Cell type-specific functions of the lysosomal protease cathepsin L in the heart. J Biol Chem (2007) 0.87
INHA promoter polymorphisms are associated with premature ovarian failure. Mol Hum Reprod (2006) 0.87
Identification and expression analysis of kcnh2 genes in the zebrafish. Biochem Biophys Res Commun (2010) 0.87
IL23R and IL12B SNPs and Haplotypes Strongly Associate with Crohn's Disease Risk in a New Zealand Population. Gastroenterol Res Pract (2010) 0.85
Misdiagnosis of long QT syndrome as epilepsy at first presentation. Ann Emerg Med (2009) 0.84
Adult granulosa cell tumours (GCT): clinicopathological outcomes including FOXL2 mutational status and expression. Gynecol Oncol (2013) 0.83
Activin is a potent growth suppressor of epithelial ovarian cancer cells. Cancer Lett (2009) 0.83
Isolation of genes differentially expressed in dominant and subordinate bovine follicles. Endocrinology (2003) 0.83
Characterization of single-nucleotide polymorphisms relevant to inflammatory bowel disease in commonly used gastrointestinal cell lines. Inflamm Bowel Dis (2010) 0.83
Genetic analysis of MDR1 and inflammatory bowel disease reveals protective effect of heterozygous variants for ulcerative colitis. Inflamm Bowel Dis (2009) 0.82
Absence of 566C>T mutation in exon 7 of the FSHR gene in Indian women with premature ovarian failure. Int J Gynaecol Obstet (2009) 0.82
Association of DLG5 variants with inflammatory bowel disease in the New Zealand Caucasian population and meta-analysis of the DLG5 R30Q variant. Inflamm Bowel Dis (2007) 0.82
Modeling inflammatory bowel disease: the zebrafish as a way forward. Expert Rev Mol Diagn (2007) 0.81
Ontogeny of AMPA and NMDA receptor gene expression in the developing sheep white matter and cerebral cortex. Brain Res Mol Brain Res (2005) 0.81
The probiotic Escherichia coli Nissle 1917 reduces pathogen invasion and modulates cytokine expression in Caco-2 cells infected with Crohn's disease-associated E. coli LF82. Appl Environ Microbiol (2011) 0.80
Tumor necrosis factor receptor superfamily, member 1B haplotypes increase or decrease the risk of inflammatory bowel diseases in a New Zealand caucasian population. Gastroenterol Res Pract (2009) 0.80
Efficient clustering of identity-by-descent between multiple individuals. Bioinformatics (2013) 0.79
Nucleotide-binding oligomerization domain containing 1 (NOD1) haplotypes and single nucleotide polymorphisms modify susceptibility to inflammatory bowel diseases in a New Zealand caucasian population: a case-control study. BMC Res Notes (2009) 0.79
Mutational analysis of betaglycan/TGF-betaRIII in premature ovarian failure. Fertil Steril (2006) 0.79
An investigation into FOXE1 polyalanine tract length in premature ovarian failure. Mol Hum Reprod (2006) 0.78
Food-derived bioactives as potential regulators of the IL-12/IL-23 pathway implicated in inflammatory bowel diseases. Mutat Res (2010) 0.78
Functional analysis of the human inhibin alpha subunit variant A257T and its potential role in premature ovarian failure. Hum Reprod (2007) 0.77
FSH receptor gene variants are rarely associated with premature ovarian failure. Reprod Biomed Online (2013) 0.77
In vivo testing of microRNA-mediated gene knockdown in zebrafish. J Biomed Biotechnol (2012) 0.77
Nanocarrier systems for delivery of siRNA to ovarian cancer tissues. Expert Opin Drug Deliv (2012) 0.77
Nutrigenomics and gut health: meeting report from an international conference in Auckland, New Zealand, April 30, May 1-3, 2006. Genes Nutr (2007) 0.77
Nutrigenomics and gut health. Mutat Res (2007) 0.77
Mushroom intolerance: a novel diet-gene interaction in Crohn's disease. Br J Nutr (2009) 0.77
Investigating the association between inhibin alpha gene promoter polymorphisms and premature ovarian failure. Fertil Steril (2008) 0.77
Mutational analysis of inhibin alpha gene revealed three novel variations in Indian women with premature ovarian failure. Fertil Steril (2009) 0.76
Symptoms and signs associated with syncope in young people with primary cardiac arrhythmias. Heart Lung Circ (2011) 0.76
Altered placental lactogen and leptin expression in placentomes from bovine nuclear transfer pregnancies. Biol Reprod (2004) 0.75
SPACA3 gene variants in a New Zealand cohort of infertile and fertile couples. Hum Fertil (Camb) (2014) 0.75
Ethnic differences in disease presentation of uterine cancer in New Zealand women. J Fam Plann Reprod Health Care (2012) 0.75
Microarrays--analysis of signaling pathways. Methods Mol Med (2008) 0.75
Nanoparticulate carriers: an emerging tool for breast cancer therapy. J Drug Target (2014) 0.75
Costs and revenues of MRSA eradication in outpatients with chronic wounds--reimbursement of MRSA eradication. J Dtsch Dermatol Ges (2015) 0.75