1. Functional Variation
001 : Balam-Ortiz et al : Population Analysis of Functional SNPs in The Angiotensinogen (AGT) Gene in Mexican Mestizo Populations 002 : Beaulieu et al : An ENSEMBL/BIOMART - based environment for the analysis of regulatory regions functional assays 003 : Dionne et al : Functional impact of regulatory polymorphisms (rSNP) in G1/S cell cycle checkpoint genes 004 : Durán-González et al : Association of the A163G Osteoprotegerin Polymorphism with Osteoporosis in Mexican patients with Rheumatoid Arthritis 005 : Ghahramani Seno et al : PTCHD3 gene: a copy number variable gene in humans 006 : Girard et al : The UGT1A1 glucuronidation pathway is regulated by a new mechanism of alternative splicing in the UGT1A gene 007 : Grundberg et al : Population variability of induced gene expression: an approach for functional variant discovery in human primary cells 008 : Jankowski et al : Direct Sequencing Quality Control: a Novel Software Approach to Reducing Variant Review Time and Labor 009 : Koboldt et al : Identification of functional SNPs in noncoding regions of the human genome 010 : Lancet et al : Variability modes of human olfactory receptors: inactive alleles and prevalent copy number variation 011 : Mena-Ramírez et al : Polymorphisms C677T and A1298C in the methylenetetrahydrofolate reductase gene and osteoporosis in Mexican patients with rheumatoid arthritis 012 : Muiños-Gimeno et al : Variants in miRNA target sites of different isoforms of the NTRK3 candidate gene for psychiatric disorders 013 : Ruchat et al : Association between mu-opioid receptor-1 polymorphisms and obesity and insulin resistance indices: results from the Quebec family study (QFS) 014 : Saferali et al : Lack of correlation between DNA methylation of promoter regions and allelic imbalance in expression of non-imprinted genes in lymphoblastoid cell lines 015 : Samuel et al : Novel Regulatory Regions in the Interleukin 6 Gene and Implications for Disease/Gene Association Studies 016 : Stobdan et al : Variants of vascular homeostasis genes associate with High-altitude pulmonary edema 017 : Villarreal-Molina et al : ABCA1 Gene Variant is Associated with Early-Onset Type 2 Diabetes in the Mexican Population 018 : Wetmur et al : A common polymorphism in the CARD domain of RIG-I modifies the innate immune response of human dendritic cells 019 : Zuo et al : Mirn29 is upregulated during skeletal muscle differentiation2. Cancer Genomics
020 : Aburatani : Cancer genome and epigenome 021 : Akbari et al : Germline BRCA2 mutations and risk of esophageal squamous cell carcinoma: Is stop codon K3326X variant associated with the disease? 022 : Birch et al : Transcriptome Analysis of Serous Epithelial Ovarian Cancers Identifies Differentially Expressed Chromosome 3 Genes 023 : Birerdinc et al : Putative Tumor Suppressive Role of KCNRG in B-cell Chronic Lymphocytic Leukemia 024 : Buys et al : Identification of Genomic Changes Predicting Response to Chemotherapy for Non-small Cell Lung Cancer 025 : Cai et al : Mutations in the equilibrative nucleoside transporter 1 SLC29A1 are responsible for cytarabine resistance in CCRF-CEM cells 026 : Desjardins et al : ZNF350/ZBRK1 haplotypes in high-risk non-BRCA1/2 families of French Canadian origin 027 : Eis et al : Integrated Oncogenomics - Ultra-High Resolution Microarray Applications for Genome-Wide Cancer Research 028 : Espinosa-García et al : Gene Expression profiling in Cervical Cancer: differences between HPV 16 variants 029 : Evrard et al : Mutation scanning of the cytidine deaminase (CDA) and dihydropyrimidine dehydrogenase (DPYD) genes by high-resolution melting curve analysis in cancer patients treated with antimetabolites drugs 030 : Falk et al : Mapping of cancer regulatory pathways and identification of prognostic cancer biomarkers using ChIP-DSL promoter analysis 031 : Guardado et al : Identification of genes associated with cervical cancer with high resolution genome-wide analysis using the Affymetrix 500K SNP mapping array: A Case Control Study 032 : Guenard et al : Germline mutations in BRIP1/FANCJ are rare in non-BRCA1/BRCA2 French Canadian Breast Cancer Families 033 : Healy et al : Functional promoter SNPs in TGFβ1 and the susceptibility to childhood leukemia 034 : Joseph et al : Human splicing related genes localize within genomic regions frequently re-arranged in cancer 035 : Kovalenko et al : Evaluation of the Cepheid GeneXpert® system for quantitative diagnostic assessment of BCR-ABL transcripts 036 : Lalonde et al : Functional impact of polymorphisms in the promoter region of the apoptosis gene MDM2 037 : Line et al : Autoantibody profiles in melanoma patients 038 : Liu et al : Up-regulation of vascular endothelial growth factor D in clear cell renal cell carcinoma (ccRCC) by CD74 039 : Lockwood et al : Novel Genetic and Epigenetic Features of Lung Tumor Genomes 040 : Mahmoud et al : Characterzation of the anti-cancer effect of novel synthetic nucleosides on the human promyelocytic cell line (HL-60) 041 : Manyam et al : Effects of the tumor-specific telomere elongation on the adjacent gene expressions 042 : Meunier et al : Detection of a novel locus on chromosome 3 responsible for susceptibility to colon cancer (CRC) in mice 043 : Milani et al : Allelic imbalance in gene expression as a guide to cis-acting regulatory single nucleotide polymorphisms 044 : Peng et al : PCGF1 (NSPc1) plays a role in promoting G2/M transition and cell proliferation rate by repressing CDKN1A (p21Waf1/Cip1) transcription via RARE 045 : Sinnett et al : Impact of regulatory genetics in the susceptibility to childhood leukemia 046 : Tang et al : The Upregulation of Nicotinamide N-methyltransferase Caused the Drug-resistance of Clear Cell Renal Cell Carcinoma 047 : Teng et al : Sensitive and Quantitative Detection of Somatic Tumor Mutations by Hi-Res MeltingTM on the LightScanner® 048 : Vazquez-Mena et al : High resolution genome-wide analysis of copy number alterations in cervical cancer using the Affymetrix 100K SNP mapping array 049 : Vucic et al : High Resolution Analysis of Copy Number Amplifications in Cancer Genomes 050 : Weibrecht et al : Detection of individual endogenous molecular interactions and post-translational modifications in situ 051 : Wojnarowicz et al : Construction of a chromosome 17 transcriptome in ovarian cancer identifies differentially expressed genes 052 : Xu et al : Sodium selenite induces apoptosis through activation of Endoplasmic Reticulum stress in human acute promyelocytic leukemia-derived NB4 cells3. Ethical Issues Related to Genome-Wide Scans
053 : Bhardwaj : From research to clinical practice: power of association studies and ethical susceptibility 054 : Boggio : Ownership and circulation of samples and data in genome-wide scans 055 : Bombard et al : Huntington disease and genetic discrimination: the experience in Canada 056 : Cousineau et al : Scientific integrity and information sharing 057 : Geransar et al : Fads in the virtual gene shop: Direct-to-consumer advertisements and access to genetic tests 058 : Lafrenière et al : Participating in Decision-Making Regarding Genetic Technologies: - A Matter of Self-Perceived Competence? 059 : Lara-Alvarez et al : Ethical, legal and social aspects of the Mexican Genomic Variability Project 060 : Lunshof : Telling the truth - Veracity and the language of consent 061 : Macer : Challenges to the Concept of the Right to Know (or Not to Know) in International Ethics Standards raised by Genome-Wide Scans 062 : Walmsley et al : What interests and values should guide biobanking in British Columbia? A deliberative public consultation4. Genes Chromosomes and Diseases
063 : Alhopuro et al : NOD2 variants and the risk of colorectal cancer 064 : Alter et al : Stepwise replication identifies a low-producing lymphotoxin-α allele as a major risk factor for early-onset leprosy 065 : Bosch et al : Generation and expansion of FAM90A, a novel primate specific gene family located within a copy number variant on human chromosome 8p23.1 066 : Burger et al : Unorthodox genome and gene structures in mitochondria of trypanosome pathogens and their relatives 067 : Choo et al : Reduced expression and promoter hypomethylation of the Period1 gene in cervical cancer 068 : Datta et al : Functional Characterization Of Hyaluronan Binding Protein (HABP1/gC1qR/SF2p32) As A Cell Cycle Regulatory Protein 069 : Davalos et al : Trichoepithelioma Multiple Familial 070 : Dhillon et al : HFE Genotypes in Controls and Patients with Primary Haemochromatosis and other Chronic Liver Diseases 071 : Dohey et al : A New Variant Database for Mismatch Repair Genes Associated with Lynch Syndrome 072 : Dávalos et al : Brachydactyly and Mental Retardation Syndrome in a male patient with a del(2)(q37) 073 : Gallant et al : Genetic study of anti-mycobacterial immune responses 074 : Grundberg et al : In situ detection of single nucleic acid molecules using padlock probes and target-primed RCA 075 : Hamel et al : Characterizing the role of the major BRCA2 partner, PALB2/FANCN, in hereditary breast cancer 076 : Han et al : Family-Based Association Analysis of Paired Box 6 (PAX6) Gene Polymorphisms in High Myopia 077 : Hui et al : Genome wide association study for asthma and atopy in a general Australian population 078 : Iles et al : Chromatin architecture in human spermatozoa probed by comparative genome hybridization microarrays reveals region specific and highly conserved retention of acetylated nucleosomes along chromosomes 079 : Jiménez-Morales et al : CHRM2 polymorphisms are associated with childhood-onset asthma 080 : Khusnutdinova et al : Analysis of mitochondrial DNA haplogroups in Parkinson's disease patients of Tatar ethnic origin from the Volga-Ural region of Russia 081 : Klovins et al : Full gene sequence analysis of somatostatin receptor 5 in patients with acromegaly 082 : Kubo et al : Nonsynonymous SNP in PRKCH encoding protein kinase c-η increases the risk of cerebral infarction 083 : Labbé et al : Association Mapping of Inflammatory Bowel Disease Susceptibility Genes on Chromosome 19p 084 : Lam : Standardization of molecular investigations of genetic diseases due to consanguinity: DNA-based diagnosis of genetic diseases by whole-genome scan using a single-nucleotide polymorphism microarray 085 : Lam et al : Processes of copy number change in human DNA : The dynamics of α-globin gene deletion 086 : Lawson et al : Ectopic recombination and de novo deletions in the human HBB (β-globin) gene cluster 087 : Lee et al : Identification and characterization of IVD gene mutations in Korean patients with isovaleric acidemia 088 : Libioulle et al : A novel susceptibility locus for Crohn's disease identified by whole genome association maps to a gene desert on chromosome 5p13.1 and modulates the expression level of neighbouring genes 089 : Liu et al : Peroxisome proliferator-activated receptor gamma coactivator 1 alpha gene variations are not strongly associated with type 2 Diabetes in Chinese population 090 : Lopez-Cardona et al : Melnick-needles: case report 091 : Maglott et al : RefSeqGene, dbSNP, and Genome Workbench: data and tools for gene-specific information at NCBI 092 : Mong et al : Association of growth hormone-releasing hormone receptor (GHRHR) with adiposity in Hong Kong Chinese adolescents 093 : Montgomery et al : High resolution melting analysis of the CFTR gene: an alternative to traditional scanning methods 094 : Møller et al : Whole genome array CGH of epilepsy patients with congenital brain malformations 095 : Ng et al : Association of Complement Factor H Polymorphisms with Exudative Age-related Macular Degeneration in Ethnic Chinese 096 : Noor et al : A novel locus for autosomal recessive non-syndromic mental retardation (NSMR) maps to chromosome 4p15.33-p15.2 097 : Paquin et al : Genome-Wide Association Study in the Quebec Founder Population Generates Map of Interacting Genes Associated with Schizophrenia 098 : Park et al : Effects of Adiponectin Genotypes on Susceptibility of Obesity in Healthy Koreans 099 : Pathan et al : The PLA2G2A gene shows no major influence in the genetic susceptibility of IBD 100 : Piehler et al : ABC transporter pseudogenes: Evidence for transcription and function 101 : Piton et al : Systematic screening of synaptic X chromosome genes as candidates for autism and schizophrenia 102 : Raelson et al : A Genome-Wide Association Study of Crohn's Disease Identifies Multiple Risk Loci and Genes 103 : Rafiq et al : A novel locus for autosomal recessive mental retardation maps to 2p25.3-25.2 in a consanguineous Pakistani family 104 : Ramirez et al : Association Study of TAPBP, NFKBIL1, and MIF Polymorphisms in Childhood with Juvenile Rheumatoid Arthritis in Mexican Population 105 : Ranque et al : The granulomatous Mitsuda reaction is linked to chromosomes 2q35 and 17q21-25 in Vietnamese families of leprosy patients 106 : Ray et al : Genomic variation in the pigmentation genes among Indians with special reference to oculocutaneous albinism 107 : Rogaev et al : Positional Cloning of Genes for Human Diseases Using Populations with Founder effect 108 : Roychoudhury et al : IL1B Promoter Polymorphism Regulates The Expression Of Gastric Acid Stimulating Hormone Gastrin 109 : Samuels et al : The Atlantic Medical Genetics and Genomics Initiative: Molecular Characterization of Monogenic Disorders in Atlantic Canada 110 : Sengupta et al : Hyperhomocysteinemia in Indian population: Causes and Effects 111 : Sham et al : Mapping the locus for a novel cataract mouse mutant with microphthalmia and closed eyelid 112 : Silva-Zolezzi et al : Association of Complement Factor H (CFH) and ARMS2 with advanced age-related macular degeneration in the Mexican population 113 : Taylor et al : A comparison of the incidence of deleterious and unclassified variants of the BRCA1 and BRCA2 genes in control and at risk populations for familial breast and ovarian cancer in Ontario, Canada 114 : Taylor et al : Co-transcription of genes into single transcripts: another regulatory mechanism for gene expression in vertebrates 115 : Thiffault et al : A selection of different analysis tools to uncover the cause of an autosomal recessive spastic ataxia associated with frequent white matter changes (ARSAL) in the French-Canadian population 116 : Valdmanis et al : Evaluation of linkage to chromosome 9p for families with ALS and FTD 117 : Vandepoele et al : A Constitutional Translocation t(1;17)(p36.2;q11.2) in a Neuroblastoma Patient Disrupts NBPF1, a Member of a Recently Expanded Gene Family 118 : Velázquez-Cruz et al : Association of TYK2 with childhood-onset Systemic Lupus Erythematosus in Mexican population 119 : Walker et al : The IL23R gene is not associated with Rheumatoid Arthritis in the Canadian population 120 : Waye et al : Association of leptin receptor (LEPR) with adiposity in Hong Kong Chinese adolescents 121 : Xu et al : Study of the susceptibility SNPs pattern within three metabolic pathways of neurotransmitters in paranoid schizophrenia 122 : Yip et al : Association of SLC11A1 polymorphisms with tuberculosis in Chinese: the effect of sex and age 123 : Zhang et al : Ultra-Deep Digital Analysis of the Transcriptome5. Bioinformatics and Biostatistics
124 : 't Hoen et al : Literature-aided interpretation of microarray data: a generic compendium approach, applied to muscle development and disease 125 : Akiva et al : Non-SNP Sequence Variations In The Human Genome 126 : Allard et al : From Genome-Wide Association Studies to GeneMaps and BioMarkers: Overview of a Disease Gene Identification Process 127 : Anwar : Application of a novel structured network pattern database technology towards accelerating personalised medicine research 128 : Becker et al : GAD and GADview: a genomic view of common human disease 129 : Bei et al : SNP Extractor: a web-based Tool to extract specific SNP information from NCBI SNP database 130 : Bharadwaj et al : Disease gene prediction based on domain interaction and network motif analysis in Type 2 Diabetes Mellitus 131 : Brahmachari et al : MicroRNA mediated regulatory networks: an in-silico approach 132 : Campbell et al : Worldwide Distribution of Haplotype Variation at the SORT1 Locus: Implications for Human Demographic History 133 : Chari et al : A system for integrative multi-dimensional analysis of genomes 134 : Davidovich et al : Tag SNPs Selected According to Prediction Accuracy Provide Higher Power to Association Studies 135 : den Dunnen et al : Comparison of gene expression data in different commercial and home-spotted platforms: a biological question driven study 136 : Estrada-Gil et al : Ancestry block analysis corrects for stratification in genome-wide association studies in Mexican admixed populations 137 : Kho et al : InforSense GenSense - a software suite for the analysis and interpretation of GWA Studies 138 : Kimmel et al : GEVALT - An integrated software tool for genotype analysis 139 : Kojima et al : A method for identifying genome-wide copy number variations from signal intensity distribution of high-density oligonucleotide genotyping arrays 140 : Kouduka et al : A measure of genome distance obtained by Genome profiling used for versatile purposes 141 : Kovac : Integrative teaching/learning of problem based medical pathophysiology in the postgenomic era 142 : Laulederkind et al : Disease Portals: A Platform for Genetic and Genomic Research 143 : Morozova et al : From pottery styles to mouse development: a method for delineating mammalian transcriptional regulatory networks 144 : Rivera et al : Gene Analysis in Phase Space 145 : Sandoval et al : Comparison of data reduction methods for family based association analysis of blood pressure intermediate phenotypes during physiological testing 146 : Scaria et al : Computational design and validation of artificial anti-viral microRNAs 147 : Shao et al : Insight into intra-molecular signaling events in post-translational modifications (PTMs) exploiting structural modelling 148 : Sneddon et al : Accounting for variation: A hierarchical database structure 149 : St-Onge et al : Feature selection methods in the detection of gene-gene interactions in the susceptibility to childhood leukemia 150 : Stojkovic et al : Streamlining Genetic Analysis - IT Methodology and Computational Platform for Genome-Wide Association Studies 151 : Tang et al : Structural modeling of the Saccharomyces cerevisiae and Candida albicans PEPCKs: models for the antifungal drug design 152 : Wojcik et al : Exact p-value computation and exact False Discovery Rate estimation for genome-wide association studies 153 : Wright et al : If We Could Talk to the Animals6. Neurological Disease Genetics
154 : Bolduc et al : Defining the candidate-interval of a new form of limb-girdle muscular dystrophy using microsatellite- and SNP-based genotyping 155 : Gijselinck et al : Genomic Progranulin deletions in frontotemporal dementia patients 156 : Huang et al : Mutation Screening of AP3M2 in Japanese Epilepsy Patients 157 : Kunita et al : The Rab5 activator ALS2/alsin acts as a novel Rac1 effector through Rac1-activated macropinocytosis 158 : Lai et al : Translational readthroughs of stop codons in dystrophin 159 : Nuñez-Reveles et al : Further clinical and neuroimaging delineation in a patient with Joubert syndrome 160 : Otomo et al : ALS2/alsin is localized to endosomes in primary cultured hippocampal neurons and implicated in axon elongation 161 : Park et al : Identification of PSEN1 and APP gene mutations in Korean patients with early-onset Alzheimer's disease 162 : Poulin et al : Ion Channel Genes and Episodic Neurological Disorders: What we can learn from a large-scale mutation screen 163 : Qiang et al : Dok5 is involved in neurotrophin-induced MAPK activation via interaction with TrkB and TrkC 164 : Reardon et al : X-linked infantile spinal muscular atrophy (XL-SMA): new insights into gene discovery and pathogenesis 165 : Riviere et al : HSN2 is a tissue-specific alternative exon of the WNK1 gene 166 : Smith et al : DNA Changes at Multiple Fragile Sites are Linked to Schizophrenia 167 : Suzuki-Utsunomiya et al : ALS2CL, a novel ALS2-interactor, modulates ALS2-mediated endosome dynamics7. Unique Population Resources
168 : Bahl et al : Determinants of population substructure and scope for LD-based association studies: Analysis of the Phase 1 data of the Indian Genome Variation (IGV) Consortium 169 : Beaulieu et al : A decision-model assessing cost-effectiveness of pharmacogenomic-based tests for everyday medical practice 170 : Bherer et al : Differential genetic contribution of founders to the regional gene pools of Quebec 171 : Chu et al : HLA polymorphisms in five populations in southwestern China 172 : Coppock et al : NHGRI Sample Repository for Human Genetic Research: a Resource for Human Genetic Variation Studies 173 : Fortin : Human Genomic Databases are Global Public Goods? 174 : Gerbault et al : Regionalization of the Founder Effect in Quebec 175 : Hidalgo-Miranda et al : Haplotype-sharing between the Mexican Mestizos and European, Asian and African populations 176 : Kravtsova et al : Reconstruction of genetic history of Tatars by anthropological and molecular-genetic methods 177 : Mukerji et al : The Indian Genome Variation (IGV) Initiative: Overview and analysis of Phase 1 data 178 : Parra et al : A genome-wide admixture mapping panel for Hispanic/Latino populations 179 : Sandoval-Ramírez et al : The distribution of mtDNA haplotypes differs among Tarahumara, Huichol, Purépecha, and Mestizo Mexican Populations 180 : Thavanati et al : Recessive alleles and Longevity among Kurichians: a tribal population of Kerala, India 181 : Tonin et al : Heterogeneity of BRCA1/2 mutations in hereditary breast and/or ovarian cancer French Canadian families from Quebec Canada 182 : Uribe-Figueroa et al : Analysis of Copy Number Variation polymorphisms in the Mexican Mestizo population 183 : Yong et al : Molecular Characterization of a polymorphic 3Mb deletion at Chromosome Yp11.2 containing the AMELY locus in Singapore and Malaysia populations8. Animal Models
184 : Bodzioch et al : Comparative Analysis of Nuclearly-Encoded Humanin Orthologs in Mammals 185 : Brahmachari et al : A putative cis-acting element promoting CGG repeat instability in a transgenic mouse model 186 : Brockmann et al : Crosstalk between muscle and fat tissues? 187 : Cabrera et al : Texas Institute for Genomic Medicine (TIGM): Knocking Out All Murine Genes in Embryonic Stem Cells 188 : Di Pietrantonio et al : The genetic dissection of host responsiveness to different strains of BCG 189 : Fang et al : Protein kinase C-ζ regulation of GLUT4 translocation through actin remodeling in CHO cells 190 : Finnell et al : Characterization of a new Fkbp8 gt(neo) allele of the Fkbp8 Gene 191 : Fodil-Cornu et al : Analysis of Resistance and Susceptibility to MCMV infection in different mouse strains models 192 : Jee et al : Gene Expression profile in the hippocampus of early- and middle-stage Alzheimer's disease transgenic mice using oligonucleotide microarray 193 : Karar et al : Srebf1 mediated transcriptional regulation of sterol metabolism in murine liver exposed to acute hypobaric hypoxia 194 : Maltais et al : Comprehensive functional annotation of mouse orthologs of human disease genes: MGI and the GO Reference Genome Project 195 : Mercader et al : Differentially expressed miRNAs regulate levels of predicted mRNA targets in the hypothalamus of an anorexia mouse model 196 : Min-Oo et al : Genetic mapping reveals a role for pantetheinase in the host response to blood-stage malaria 197 : Nagase et al : Analysis of DNA methylation in tissue development and carcinogenesis in C57BL/6J mice 198 : Ngai et al : Histone post translational modifications (PTMs) in the senescence-accelerated prone mouse (SAMP8) 199 : Nyberg et al : Intra-allelic Genetic Heterogeneity of Hypertrophic Cardiomyopathy in the Maine Coon Cat 200 : Pasha et al : Cloning, genomic organization and expression analysis of yak HIF1A 201 : Pyzik et al : Immunogenetics of infection: MHC class I molecules and NK cell receptors interplay in the recognition of MCMV infected cells in mice 202 : Richards-Smith et al : Mouse Mutant Phenotypes as Models for Human Disease 203 : Richer et al : ENU Facing the Infectious Diseases Global Threat 204 : Savitsky et al : Comparative Analysis of the Ciliome of Tetrahymena thermophila: A Tool for Analysis of Potential Ciliopathies 205 : Seda et al : New recombinant inbred rat strain panel for integrative genomics of metabolic syndrome 206 : Sedova et al : Nutrigenomic, metabolic and transcriptomic aspects of fetal origins of metabolic syndrome 207 : Smiljakovic et al : Reproductive Tract - from Protein to Animal - Variome Approach 208 : Szantai et al : Comparison of Human and Canine Dopamine D4 Receptor Genes 209 : Toyoda et al : MusBanks: an artificial intelligence integrating world-wide mouse mutant resources via biomolecular networks 210 : Tuo et al : Progressive Retinal Degeneration in CCL2/CX3CR1 Deficient Mice, a Novel Animal Model of Age-Related Macular Degeneration 211 : Wiltshire : Mouse Genetic Model of Cardiovirulent Coxsackievirus B3 Infection9. Disease Modifiers
212 : Alcaraz et al : Zfp423 marks a pathway in control of neural precursor proliferation and renewal 213 : Belleau et al : Evidence For Modifier Gene(s) Altering Glaucoma Severity In A Huge French-Canadian Myocilin Family 214 : Bossé et al : Genetic variants at the IL-33 locus are associated with asthma 215 : Chowdhury et al : Systems Biology Approaches Identify G-Quadruplex DNA (Telomere-Like Motifs) in a Genome-Wide Regulatory Role 216 : Córdova et al : the NFE2L2 -650C>A variant: A possible modifier gene in systemic lupus erythematosus 217 : Dorfman et al : Modulatory effect of MBL2 on the onset of Pseudomonas aeruginosa infection is influenced by TGFB1 variants in pediatric Cysctic Fibrosis patients 218 : Heaney et al : Transgenerational epistasis between Dnd1Ter and other modifier genes controls susceptibility to testicular germ cell tumors 219 : Howell et al : The disease modifier SCNM1 interacts with spliceosome protein U1-70K and the novel factor LUC7L2 220 : Lebel et al : Genotype/phenotype correlation studies in French-Canadian glaucoma families co-segregating myocilin and WDR36 mutations/variations 221 : Omoyinmi et al : Role of CAPN10 in insulin secretion 222 : Villani et al : The Familial Mediterranean Fever (MEFV) Gene as a New Susceptibility and Modifier Gene for Ulcerative Colitis10. Genetics of the Heart
223 : Arenas et al : Effect of physiological stress on genetic linkage of blood pressure phenotypes in hypertensive families 224 : Awan et al : Vascular Calcifications in Homozygote Familial Hypercholesterolemia: the Quebec Experience 225 : Bailey et al : Common Polymorphisms in the Promoter of the Visfatin Gene (PBEF1) Influence Plasma Insulin Levels in a French Canadian Population 226 : Burgner et al : Common ancestral haplotypes of the major histocompatibility complex are strongly associated with susceptibility to Kawasaki disease in Australian Caucasians 227 : Canizales-Quinteros et al : INSIG2 polymorphism is associated with lower BMI and cholesterol/Apo B plasma levels in the Mexican population 228 : Chasman et al : Polymorphism in the apolipoprotein(a) gene, plasma levels of Lp(a), ancestry, and interaction with aspirin treatment in cardiovascular disease prevention 229 : Dastani et al : SNP analysis of positional candidates at a low HDL susceptibility locus on chromosome 16 in two French Canadian Studies 230 : Do et al : The Missense Mutation K45R in the Squalene Synthase Gene Influences Total Cholesterol Levels in Two Study Samples from a French Canadian Founder Population 231 : Douville et al : Identification and characterization of Meox target genes in the vasculature 232 : Duan et al : Genetic risk factors for depression in patients with coronary artery disease 233 : Eklund et al : C-reactive protein genetics is associated with carotid artery compliance in men in the cardiovascular risk in young Finns study 234 : Hamet et al : Systematic search for sex-specific genomic determinants of 608 cardiovascular traits in French Canadians reveals novel loci/haplotypes 235 : Joly et al : Informed Consent in Pharmacogenomic Research: A Natural Evolution? 236 : Kumar et al : Coronary artery disease in India: the interplay of diet and genetic polymorphisms 237 : Michaud et al : CYP2C9 and VKORC1 polymorphisms combined to phenotypic assessments: 238 : Nejatizadeh et al : Positive association of NOS3 gene polymorphisms and haplotypes in human essential hypertension in Indian population 239 : Noel et al : Search for X-linked genomic determinants underlying the phenotypes related to hypertension among French Canadian families 240 : Raitala et al : The PTPN22 C1858T polymorphism is associated with the risk factors for atherosclerosis. The Cardiovascular Risk in Young Finns Study 241 : Schnabel et al : Heritability, Environmental and Genetic Correlations and Linkage of Circulating Inflammatory Biomarker Concentrations 242 : Símová et al : Mutation Analysis of the FBN1 Gene in Czech Patients with Aortic Dilatation 243 : Yahi-Kerbane et al : P-glycoprotein and HERG closely interact in cardiac ventricular myocytes 244 : Yap et al : EMILIN1 gene is associated with human essential hypertension 245 : Yap et al : Genetics of Obesity Phenotypes: Preliminary Study of Obesity-Related Phenotypes and Association with Uncoupling Protein 2 and 3 246 : Yuan et al : Proteomic analysis of cardiomyocytes differentiation in mouse embryonic carcinoma P19CL6 cells 247 : Zakrzewski-Jakubiak et al : Genotype distribution of ten polymorphisms associated with the renin-angiotensin-aldosterone system in healthy volunteers and a population of maximally treated heart failure patients11. Large-Scale Genomics
248 : Aitman et al : FCGR3B copy number variation is associated with systemic but not organ-specific autoimmunity 249 : Argo et al : The German National Genome Research Network (NGFN) - Disease-Oriented and Systematic Genome Research 250 : Bauser et al : Analysis of the genomic insertion sites of viral gene therapy vectors using next generation sequencing technologies 251 : Bronnikov : Geneus: flexible open informatics platform for high throughput genomics laboratories 252 : Carvalho Santos et al : A Map of Transmission Ratio Distortion on Human Chromosome 6p 253 : Cha et al : Association study of SNPs in eight candidate genes with warfarin dosage in Japanese patients 254 : Donaldson et al : Producing Consistent Gene Sets across Multiple Genomes 255 : Frazer : A genome-wide map of eight million SNPs in the laboratory mouse genome 256 : Gauthier et al : Large-scale identification and characterization of developmental brain disease genes 257 : Gurd et al : Pooled heteronuclear RNA (hnRNA) sequencing: a new tool for large-scale cis-acting regulatory haplotype (rHaplotype) discovery 258 : Hamdan et al : Large scale sequencing of autosomal synaptic genes in patients with non-syndromic mental retardation 259 : Hyland et al : Next generation sequencing - opportunities and constraints in pooling and quantitative sequencing 260 : Ko et al : Study on the safety and efficacy biomarkers of anorectic agents 261 : Kwan et al : Genome-Wide Association of Human DNA Sequence Variation with Differential pre-mRNA Processing and Transcription Initiation 262 : Lee et al : ChargeSwitchTM-coated plates to streamline multi-step purification workflows 263 : Lettre et al : Genome-wide Association Study of Adult Height in 3,026 Scandinavian Individuals 264 : Mailman et al : Database of Genotype and Phenotype (dbGaP): a repository for genome-wide association studies 265 : Montpetit et al : Copy-number variant detection using Illumina whole genome arrays 266 : Morin et al : Identification of small RNAs important in embryonic stem cells and their differentiation 267 : Mägi et al : Minor alleles of SNPs are common in the human genome sequence 268 : Nutter et al : High Throughput Genomics using Applied Biosystem's SOLiDTM System 269 : Sugano : Identification and comparative studies of promoter regions of human and mouse genes 270 : Takeda et al : H-DBAS: Alternative Splicing Database of Completely Sequenced and Manually Annotated Full-length cDNAs Based on H-Invitational 271 : Wiemann et al : The MIACA minimum information guideline for cellular assays and systems biology 272 : Yamasaki et al : Extended annotation for the integrated database of human transcriptome, H-InvDB12. High Throughput Genetic Screens
273 : Boissinot et al : Improved microarray hybridization by using single-stranded DNA targets produced by Lambda exonuclease digestion 274 : Brown et al : Development of Broad-based ADME Panels for Use in Pharmacogenomic Studies 275 : Crocker et al : Development and comparison of two bead-based array assays for the detection of hemoglobinopathies 276 : Dahl et al : SNP fine mapping on a miniaturized platform using TaqMan® assays on a nanoliter scale 277 : de Silva et al : Algorithm for Conversion of TaqMan® Genotyping Assays to Unlabeled Probe Assays 278 : Erho et al : The Development of a Low Cost, High Accuracy Method for Computational Electrophoresis Gel Image Analysis 279 : Fournier et al : High-Quality, High-Throughput Genotyping and Genetic Analysis: A Platform for Gene Discovery and Pharmacogenomics Studies 280 : Futakami et al : Genomic DNA alterations induced by seconds-period UV-irradiation 281 : Geraghty et al : Comparison of DNA microextraction techniques from dried blood spots for multiplexing PCR: potential application for newborn screening and pharmacogenomics 282 : Ghimire Gautam et al : Novel Mutation Assay Based on Direct Measurement of Genomic DNA Alterations 283 : Hayes et al : Novel PlexorTM SNP Genotyping Technology: Comparisons with TaqMan® and Homogenous MassEXTENDTM MALDI-TOF Mass Spectrometry 284 : Le Calvez-Kelm et al : A Laboratory Information Management System (LIMS) for a high throughput candidate gene mutation screening workflow 285 : Maercker et al : Mesenchymal stem cells in live cell chips for high-content screenings in functional genomics 286 : McRae et al : Power and SNP Tagging in Whole Mitochondrial Genome Association Studies 287 : Mongrain et al : Development of clinical pharmacogenomics panels for CVD risk assessment using high throughput technologies 288 : Najera et al : Single Nucleotide Polymorphism (SNP) analysis in XX and XY sex reversal 289 : Nikpay et al : Genome-wide search for genomic determinants of tobacco, alcohol and coffee use in French Canadian Families 290 : Paquin et al : Genome-Wide Association Studies for Complex Diseases Using Samples from the Quebec Founder Population: Examples with Psoriasis and ADHD 291 : Qu et al : High resolution genome-wide association by a DNA pooling strategy 292 : Rocheleau et al : A genome-wide association study identifies novel risk loci for type 2 diabetes : assessment of population stratification effects 293 : Rogers : High-Throughput Targeted Re-Sequencing for SNP Discovery and Mutation Detection 294 : Samuël et al : Pediatric Research and Predisposition Genetic Testing 295 : Serre et al : Design and analysis methods for multi-ethnic association studies: the case of the INTERHEART study 296 : Sundararajan et al : Real-time Single-Cell Analysis of Gene Expression
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