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Workshop Oral List

Oral list at Tue Apr 18 12:54:56 2006

Oral List
Oral/Poster No. Session Presenting
Author		 Title Subm. No.
1. Twin Studies
1/7 1 A. Loukola Identification of nicotine dependence and smoking behavior susceptibility loci in a Finnish twin family sample 199
2/9 1 Olli P.H. Pietiläinen Genetic background of neurocognitive traits in schizophrenia and bipolar disorder - an association study in twins 206
3/4 1 Kaisu Keskitalo Genetic effects on sweet taste preference: a twin study 225
4/3 1 Andreas Dahlgren Fine mapping of a QTL for body height on the human X chromosome 231
5/5 1 Antti Knaapila Food neophobia and uncontrolled eating are modified by genetic factors 252
6/6 1 Tellervo Korhonen Cigarette Smoking and Depression among Finnish Twins 178
7/8 1 Nick Martin Linkage for melanoma risk factors in an adolescent twin study 159
2. Genomics and Identity (Ethics)
8/13 2 Kazuto Kato Genome analysis and how human populations should be labeled 263
9/14 2 Darryl R.J. Macer Interpretations on Identity in International Genomics Declarations in Asia and the Pacific 74
10/18 2 I. C. Verma Genomics Confers Identity But Has Far-Reaching Consequences 350
11/16 2 Elisa Pieri Citizenship, Responsibility and the Promise of Personalised Medicine 256
12/11 2 Minakshi Bhardwaj Trends in genetics and a non-reductionist approach to geneticisation 201
13/12 2 Anthony Mark Cutter The Sum of its Parts? Exploring the Governance of Genomics and Personalisation 41
14/15 2 Santiago March Educational and outreach component for the national platform in genomic medicine in Mexico 315
3. Genetic Epidemiology
15/40 3 Sampo Sammalisto Identification of a Quantitative Trait Locus influencing Human HDL-cholesterol Levels 82
16/24 3 R.M. Corbo Gender and disease predisposition: combined effect of Apolipoprotein E (APOE) genotype and past fertility on age of onset of Alzheimer's disease in women 28
17/44 3 Mei-Shu Xu A variant in the CD209 promoter is associated with severity of Severe Acute Respiratory Syndrome (SARS) 91
18/38 3 Se-Min Park Association of NFKBIA polymorphism with development of asthma 197
19/26 3 Ciara Dolan Damaging cSNPs affecting platelet function and their role in cardiovascular disease 255
20/28 3 Tero Hiekkalinna Powerful, conservative and robust family-based association test: PSEUDOMARKER 295
21/42 3 J. Tuimala Genetic Polymorphisms in Folate Metabolism and Their Association with Chromosomal Aberrations 98
4. Comparative Genomics
22/46 4 Giorgio Bernardi Mapping bands and isochores on human chromosomes 224
23/48 4 D.M. Church Analysis of the mouse reference (C57BL/6J) and non-reference assemblies 268
24/59 4 Ryuichi Sakate Partitioning the human genome into differently conserved regions obtained by whole genome comparison among human, chimpanzee, mouse and rat lineages 331
25/51 4 Pille Hallast Comparison of CGB1, CGB2 and LHB genes in human and great apes 61
26/57 4 Robert Querfurth Phylogenetic Shadowing in Primate Promoter Regions 257
27/49 4 Carol A. Edwards Comparative sequence analysis of imprinting evolution in the Dlk1/Dio3 domain in extant mammals 144
28/60 4 Johanna Sandling Polymorphisms in the Insulin-like Growth Factor II (IGF2) Gene are Associated with Heart Muscle Phenotypes 146
5. Bioinformatics
29/79 5 D.R. Maglott Representing Genomes, Genes, Expression, Variation and Phenotype at NCBI 274
30/83 5 Jüri Reimand GOST - a Gene Ontology STatistics mining tool 120
31/81 5 J. Mudge The Vega Web Browser: Demonstrating the Importance of Multi-Speices Manual Annotation 94
32/72 5 Outi Hallikas Genome-wide prediction of mammalian enhancer elements based on high-throughput analysis of transcription factor binding affinity 330
33/66 5 Christoph Bock Predicting CpG island methylation from DNA sequence and genomic location at 90% accuracy 24
34/85 5 Mikhail Skoblov In silico search for natural antisense transcripts in human genome and analysis of their expression patterns 117
6. Genomic Variation and Diversity
35/125 6 T. Varilo Extended LD intervals favor regional isolates in LD-based genome-wide mapping studies 68
36/98 6 David Comas The portability of tagSNPs across human populations 93
37/95 6 Nina Bosch Complexity and evolution of copy number variants and segmental duplications on human chromosome 8p23.1 140
38/126 6 S.J. White Frequency of common copy number variation in five different ethnic populations 292
39/108 6 Oscar Lao Proportioning whole-genome single-nucleotide-polymorphism diversity for identification of geographic population structure and genetic ancestry 70
40/94 6 Luis B. Barreiro Evolutionary neutrality of Mannose-Binding Lectin (MBL2) during human evolution supports its immunological redundancy 145
41/103 6 Michelle Gardner Extreme Population differences across Neuregulin 1, the gene associated with Schizophrenia, with suggestive evidence for selection 69
42/127 6 Bryndis Yngvadottir Evolution by gene loss? 200
7. New and Emerging Technologies
43/134 7 David R. Bentley Human genome re-sequencing with next-generation technology 211
44/135 7 Anthony J. Brookes A Molecular Counting Technology For Research Into Copy-Number Variation 89
45/151 7 Mats Nilsson Single-molecule genotyping 272
46/150 7 Lev Nikolaev Identification, genome mapping and CTCF binding of potential insulators within the FXYD5-COX7A1 locus of human chromosome 19q13.12 51
47/139 7 Osamu Gotoh Multiple cDNA quantification method based on DNA encoding technology 184
48/154 7 Uwe Radelof RZPD Protein Arrays - the currently most comprehensive collection of arrayed proteins 246
49/131 7 Silke Argo The MIACA Standard for High-Throughput Assays in Disease Research 214
8. Genetics of Immune System Disorders
50/165 8 Maritta Pykäläinen Genes and pathways involved in IL-4 induced human T helper 2 cell differentiation 298
51/167 8 Jana Weissfuss A Candidate Gene Association Study using the GenolinkTM Genotyping System revealed presumptive Genetic Associations concerning Rheumatoid Arthritis 293
52/159 8 Sara Bruce Gene expression analysis reveals novel downstream signaling pathways for GPR154 upon Neuropeptide S stimulation 177
53/162 8 V. Dideberg The TNF/ADAM17 system: implication of an ADAM17 haplotype in the clinical response to infliximab in Crohn's Disease 101
54/164 8 Lotta Koskinen Linkage and association study of MYO9B variants in Finnish and Hungarian populations supports the role of CELIAC4 locus (19p13) in celiac disease 264
55/163 8 Changwon Kang Ethnic differences in association of susceptibility to rheumatoid arthritis with single-nucleotide polymorphisms in PADI4, RUNX1 and SLC22A4 genes 73
56/166 8 Ann-Christine Syvänen Genetic variation in the Interferon Regulatory Factor 5 gene in autoimmune diseases 213
9. Transcriptome; expression profile; non-coding RNA
57/175 9 Jian Huang A transcriptome atlas of human hepatocytes 16
58/169 9 Pelin Akan Identification and characterization of core promoter elements using reporter assays and ChIP on CHIP 87
59/187 9 Yutaka Suzuki Identification and comparative studies of promoter regions of human and mouse genes 156
60/186 9 Marc Sultan Gene Expression Variation In Three Brain Tissues Of A Mouse Model Of Down Syndrome 227
61/171 9 Taro Fukao Genome-wide Screening of Primary miRNA Transcripts: Towards Regulatory Mechanisms for miRNA Expression 95
62/179 9 Daniel Klevebring A new microarray-based method to study sense and antisense transcripts 232
63/172 9 Chenna Reddy Galiveti RNomics – Analysis of novel in silico derived non-protein coding RNAs in the human genome 244
10. Cancer Genomics
64/208 10 Lili Milani Imbalanced allelic expression as a tool for identifying functional regulatory polymorphisms 56
65/206 10 Vessela N. Kristensen Genetic variation in putative regulatory loci controlling gene expression in breast cancer 215
66/215 10 Eugene R. Zabarovsky Epigenetic analysis of cancer cells using NotI microarrays 248
67/214 10 Edith Y.T. Tse Estrogen Receptor α Gene Polymorphisms and Breast Cancer Risk in Chinese 163
68/209 10 M.C. Moran Moguel Insertion/Deletion (I/D) polymorphism in Angiotensin Converting Enzyme (ACE) in mexican women with breast cancer 8
69/196 10 Hannele Erkko Identification of a common polymorphism in the TOPBP1 gene associated with hereditary susceptibility to breast and ovarian cancer 67
70/203 10 Liesbeth Hameetman Homozygous deletion of EXT1 in non-hereditary osteochondromas 174
71/200 10 Brenda L. Gallie Genomic Changes in Human Retinoblastoma (RB) 152
11. Genomics of Complex Disorders
72/220 11 Joanne E. Curran Genetic analysis of transcriptional profiles for the identification of genes influencing common complex diseases 301
73/226 11 I. Hovatta Glyoxalase 1 and glutathione reductase 1 regulate anxiety in mice 12
74/242 11 T. Paunio Genes Behind A Complex Disease In A Simple Population: Schizophrenia Susceptibility Genes In Finland 267
75/244 11 Ludmila Prokunina-Olsson Genetic and functional studies on Type 2 diabetes-associated variants of the TCF7L2 gene in Finns 136
76/237 11 Jussi Naukkarinen USF1 and Common Cardiovascular disease: Evidence from adipose tissue transcript profiles and two independent autopsy studies 234
77/245 11 V. Pulkkinen G protein-coupled receptor for asthma susceptibility associates with respiratory distress syndrome 354
78/228 11 S.P. Kallio PRKCA shows association to multiple sclerosis in two populations 327
12. RNAi
79/257 12 Brian Harfe microRNA Regulation of murine limb development 328
80/262 12 Xavier Tordoir PATROCLES: The database of polymorphic miRNA-target interactions 253
81/260 12 Ilaria Piccini RNAi of human transcription factors for analysing regulatory networks 297
82/255 12 Tariq Alsheddi Whole-genome approach to highly specific siRNA design by CRM (Comprehensive Redundancy Minimizer) Algorithm 334
83/261 12 Omid Rasool Modification of an RNAi plasmid construct suitable for enriching transiently transfected cells 352
84/256 12 Mikael Björklund Genome-wide RNAi analysis of cell cycle and cell size regulation in Drosophila cells 356
85/258 12 Olli Kallioniemi High-throughput RNAi screening in cancer 363
13. Genes Chromosomes and Diseases
86/286 13 Miguel Angel Moreno-Pelayo Identification of the DFNA44 hearing-loss gene 48
87/266 13 Udy Bar-Yosef Characterization of the molecular defect underlying autosomal recessive congenital nuclear cataract in two inbred Bedouin Israeli families 134
88/292 13 Yan Shen Mutation Analysis of BMP4, BMP7, HOXA4 and HOXB6 Genes in Chinese Patients with Hypospadias 33
89/274 13 Heli Honkala From gene to function: Molecular genetics and biology of hydrolethalus syndrome 141
90/289 13 Gloria Queipo SOX9 duplications: an alternative etiology in XX sex reversal 103
91/295 13 Irma Silva-Zolezzi Expression profiling supports peroxisome proliferator-activated receptor alpha (PPARα) activation in livers of 70kDa Peroxisomal Membrane Protein (PMP70) deficient (Abcd3-/-) mice 310
92/270 13 J.T. Den Dunnen Cost-effective screening of deletions and duplications of up to 1500 loci in one assay: a bead-based approach 320
93/298 13 Tetsuro Toyoda Intelligent inferences in the omic space: toward high-throughput positional cloning in mouse models of human diseases 183
Created Sunday, 01-May-2005 20:15:35 BST
Updated Thursday, 20-Apr-2006 11:37:38 BST