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Poster List

Poster list at Fri May 19 13:22:47 2006

Poster List
Poster
No.		 Session Presenting
Author		 Title Subm. No.
1. Twin Studies
1 1 D.I. Boomsma Heritability of expression profiles in twin families 129
2 1 Ulla Broms The Nicotine Dependence Syndrome Scale in Finnish Smokers - Genetic architecture of nicotine dependence 34
3 1 Andreas Dahlgren Fine mapping of a QTL for body height on the human X chromosome 231
4 1 Kaisu Keskitalo Genetic effects on sweet taste preference: a twin study 225
5 1 Antti Knaapila Food neophobia and uncontrolled eating are modified by genetic factors 252
6 1 Tellervo Korhonen Cigarette Smoking and Depression among Finnish Twins 178
7 1 A. Loukola Identification of nicotine dependence and smoking behavior susceptibility loci in a Finnish twin family sample 199
8 1 Nick Martin Linkage for melanoma risk factors in an adolescent twin study 159
9 1 Olli P.H. Pietiläinen Genetic background of neurocognitive traits in schizophrenia and bipolar disorder - an association study in twins 206
10 1 Tatyana Y. Zaripova Studying the degree of heritability of mental abilities by twins method 84
2. Genomics and Identity (Ethics)
11 2 Minakshi Bhardwaj Trends in genetics and a non-reductionist approach to geneticisation 201
12 2 Anthony Mark Cutter The Sum of its Parts? Exploring the Governance of Genomics and Personalisation 41
13 2 Kazuto Kato Genome analysis and how human populations should be labeled 263
14 2 Darryl R.J. Macer Interpretations on Identity in International Genomics Declarations in Asia and the Pacific 74
15 2 Santiago March Educational and outreach component for the national platform in genomic medicine in Mexico 315
16 2 Elisa Pieri Citizenship, Responsibility and the Promise of Personalised Medicine 256
17 2 Patricia Sorokin Confidentiality and the Human Genome: Towards a much needed legislative proposal 323
18 2 I. C. Verma Genomics Confers Identity But Has Far-Reaching Consequences 350
3. Genetic Epidemiology
19 3 Mi-Hyun Ahn IL8 Gene Polymorphisms are Associated with Idiopathic Pulmonary Fibrosis 107
20 3 Mervi Alanne Selenoprotein S is associated to coronary heart disease in two prospectively followed Finnish cohorts 182
21 3 Khalid Alharbi Online Encyclopedia for Genetic Epidemiology studies (OEGE) 47
22 3 Andrei Anghel The Assessment of the Incidence and Prevalence of HFE-related Hemochromatosis in Romanian Subjects by means of Molecular Screening and Web-based Approach 195
23 3 S.A. Borinskaya ADH1B*47His allele frequency distribution in populations of Russia and neighboring countries 273
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
25 3 L. del Bosque-Plata Geographical distribution of genetic variants associated with Type 2 Diabetes in Mexico 318
26 3 Ciara Dolan Damaging cSNPs affecting platelet function and their role in cardiovascular disease 255
27 3 Lin He Population-based studies on the role of Apolipoprotein E in the metabolic disorders of T3, T4 and TSH 254
28 3 Tero Hiekkalinna Powerful, conservative and robust family-based association test: PSEUDOMARKER 295
29 3 Kerstin Imrell HLA associations to 'fringe phenotypes' in multiple sclerosis 90
30 3 Mari Kaunisto Association Testing of Eight Migraine with Aura Candidate Genes in 1798 Finnish Individuals 123
31 3 Ui-Soon Khoo The protective role of homozygous L-SIGN (CLEC4M) in SARS coronavirus infection 194
32 3 Kati Komulainen The LPIN1 gene is associated with obesity and cardiovascular risk factors at the population level 196
33 3 Sanna Korja ARL11/ARLTS1 germ line variants and the risk for breast, prostate and colorectal cancer 128
34 3 Timurs Maculins Estimation of the cystic fibrosis mutation dF508 frequency in Latvia 13
35 3 Mohamed Saifulaman Mohamed Said A Common Single Nucleotide Polymorphism Pattern in Mental Retardation Cases within the Malaysian Population - A Preliminary Case Study 166
36 3 Reedik Mägi Visualization tool for r2-bin based tagSNP selection 99
37 3 T.V. Nasedkina Association studies of biotransformation gene polymorphism and genetic susceptibility to lymphoproliferative diseases in Russian Population 349
38 3 Se-Min Park Association of NFKBIA polymorphism with development of asthma 197
39 3 Anna Rautanen Associations of body size at birth with late life cortisol concentrations and glucose tolerance are mediated by haplotypes of glucocorticoid receptor gene 39
40 3 Sampo Sammalisto Identification of a Quantitative Trait Locus influencing Human HDL-cholesterol Levels 82
41 3 Kaisa Silander Assessment of the impact of allelic variants of the klotho gene for the risk of coronary heart disease and mortality in two prospective case-cohort samples 189
42 3 J. Tuimala Genetic Polymorphisms in Folate Metabolism and Their Association with Chromosomal Aberrations 98
43 3 A.S. Whitehead Loss of function polymorphisms in NAT1 protect against spina bifida 164
44 3 Mei-Shu Xu A variant in the CD209 promoter is associated with severity of Severe Acute Respiratory Syndrome (SARS) 91
45 3 Tero Ylisaukko-oja Genome-wide Scan for Autism in an Extended Pedigree from a Regional Subisolate in Finland 299
4. Comparative Genomics
46 4 Giorgio Bernardi Mapping bands and isochores on human chromosomes 224
47 4 Jianguo Chen Analysis of Placenta and Testis ESTs from Peromyscus 11
48 4 D.M. Church Analysis of the mouse reference (C57BL/6J) and non-reference assemblies 268
49 4 Carol A. Edwards Comparative sequence analysis of imprinting evolution in the Dlk1/Dio3 domain in extant mammals 144
50 4 Ekaterina Ermakova Evolutionary patterns in alternatively spliced coding regions of mammalian and Drosophila genes 92
51 4 Pille Hallast Comparison of CGB1, CGB2 and LHB genes in human and great apes 61
52 4 Elizabeth Kuczek Sequencing the genome of the model marsupial, the Tammar wallaby 77
53 4 Ruth C. Lovering Gene Nomenclature and Gene Ontology - the perfect partnership? 80
54 4 Sofia Mikko Linkage mapping of the silver coat color locus in the horse 242
55 4 Kazuhiro Nakayama Variation of the melanocortin 1 receptor gene and the agouti signaling protein gene in the macaques: implication for the coat color phenotypes 66
56 4 H. Noguchi Comparative genome analysis of False Killer Whale 204
57 4 Robert Querfurth Phylogenetic Shadowing in Primate Promoter Regions 257
58 4 Ann-Charlotte Rönn A microarray-system for forensic identification of primate species subject to bush meat trade 216
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
60 4 Johanna Sandling Polymorphisms in the Insulin-like Growth Factor II (IGF2) Gene are Associated with Heart Muscle Phenotypes 146
61 4 Justyna M. Szamalek Precise characterization of the macro- and micro-chromosomal differences that distinguish human and chimpanzee genomes 193
62 4 Kunihiko Takamatsu Comparative analysis of primate-specific gene DSCR9 317
63 4 Tadayuki Takeda Analysis for Human Gene Promoters by Comparative Genomics 168
64 4 M.W. Wright HCOP: The HGNC Comparison of Orthology Predictions Search Tool 20
5. Bioinformatics
65 5 Marc Aubry Functional annotation of gene clusters: beyond the canonical approach 251
66 5 Christoph Bock Predicting CpG island methylation from DNA sequence and genomic location at 90% accuracy 24
67 5 Gerome Breen Evidence of an Association of Tandem Repeats with Gene and Gene Function 281
68 5 Emily Dimmer The Gene Ontology Annotation (GOA) Database 137
69 5 W. Fu Bioinformatic Pipeline for the Identification of Transcription Factor Binding Sites in Mouse and Human 147
70 5 Tom R. Gaunt MIDAS: a graphical linkage disequilibrium analysis tool 53
71 5 Marcus Gry Björklund A global tissue-based heatmap of protein expression and distribution 233
72 5 Outi Hallikas Genome-wide prediction of mammalian enhancer elements based on high-throughput analysis of transcription factor binding affinity 330
73 5 Gennaro Iaccarino Spline Functions to Disclose the Genomic Signature 287
74 5 Sigeo Ihara Extraction of biological meaning from gene expression data using literature 157
75 5 Jongsun Jung Genes for Ligand-interacting Proteins in Human Genome 365
76 5 Anna-Kaarina Järvinen Bioinformatic Analysis of Gene Copy Number Alterations in Head and Neck Cancer Using Different Microarray Platforms 205
77 5 Maria Krestyaninova Open source customisable Patient and Sample System for Information Management for biomedical studies 303
78 5 Hoi Yee Li Genome-Wide Study Of The Anti-Tumor Effect Of Gold-1a, A Novel Chemo-Cytotoxic Agent For Hepatocellular Carcinoma (HCC) 18
79 5 D.R. Maglott Representing Genomes, Genes, Expression, Variation and Phenotype at NCBI 274
80 5 Lois J. Maltais Mouse Genome Informatics (MGI): The ever expanding resource 7
81 5 J. Mudge The Vega Web Browser: Demonstrating the Importance of Multi-Speices Manual Annotation 94
82 5 Katsuhiko Murakami Identification of regulatory motif pairs with positional preferences in human pol-II promoter sequences 364
83 5 Jüri Reimand GOST - a Gene Ontology STatistics mining tool 120
84 5 Risto Renkonen Data integration in bioinformatics 187
85 5 Mikhail Skoblov In silico search for natural antisense transcripts in human genome and analysis of their expression patterns 117
86 5 Martti Tolvanen Primate pseudogenes for carbonic anhydrase XV 220
87 5 Mauno Vihinen From genes to diseases. Exploring disease-causing mutations by analysing amino acid substitutions at the sequence and structural level 222
88 5 H. Vuorikoski Transcriptional regulation in development of human osteoclast: the use of DNA microarray data with in silico binding site predictions and transcription factor information 358
89 5 Chisato Yamasaki TACT: Transcriptome Auto-annotation Conducting Tool of H-InvDB 342
6. Genomic Variation and Diversity
90 6 Barbara Arredi Confronting Y chromosome variability to linguistic classification in East Asia 150
91 6 Guenter Assum Differences in the variability patterns of two genomic regions result from a population bottleneck in the history of the European population 261
92 6 P. Astolfi Preliminary investigation to single out reproductive longevity in Sardinian mothers 85
93 6 Eros Balam Initial analysis of cardiovascular-related genetic polymorphisms in Mexican Mestizo Populations 316
94 6 Luis B. Barreiro Evolutionary neutrality of Mannose-Binding Lectin (MBL2) during human evolution supports its immunological redundancy 145
95 6 Nina Bosch Complexity and evolution of copy number variants and segmental duplications on human chromosome 8p23.1 140
96 6 D.R. Carvalho-Silva A Shared Y-chromosomal Heritage between Muslims and Hindus in India 149
97 6 Jiayou Chu HLA-A, B and DRB1 alleles and haplotypes in Naxi and Han populations in southwestern China (Yunnan province) 43
98 6 David Comas The portability of tagSNPs across human populations 93
99 6 Peggy Eis Analysis of DNA Copy Number Variation in the Human Genome Using Sub-Kb Resolution Array CGH 321
100 6 L.P. Fernandez Melanocortin-1 receptor, MC1R, gene variants and melanoma risk in a Spanish population 366
101 6 Anna Ferrer-Admetlla Population heterogeneity in genes related to the host-pathogen interactions: a worldwide perspective 30
102 6 L.S.H. Gan Confounding of mtDNA Analysis in Differentially Lysed Samples by Nuclear Mitochondrial (NUMT) Pseudogene 158
103 6 Michelle Gardner Extreme Population differences across Neuregulin 1, the gene associated with Schizophrenia, with suggestive evidence for selection 69
104 6 Ellen Gunnarsdottir Investigating candidate obesity associated genes in Polynesians 360
105 6 Alfredo Hidalgo-Miranda Constuction of a Haplotype Map of the Mexican Population 314
106 6 Elza Khusnutdinova Patterns of genetic diversity of populations living in four Eurasian regions 23
107 6 Damian Labuda Heuristic Approach for Analysis of the Recombination Density along DNA sequence 276
108 6 Oscar Lao Proportioning whole-genome single-nucleotide-polymorphism diversity for identification of geographic population structure and genetic ancestry 70
109 6 Tuuli Lappalainen Genetic variation in the Volga-Ural region 138
110 6 Ping Liang Retrotransposons, a Major Contributor of Human Genome Diversity 279
111 6 Ulrika Liljedahl Providing access to genetic variation: The SNP technology platform at Uppsala University 266
112 6 Per Lundmark Utility of HapMap data in European populations 236
113 6 Andres Moreno-Estrada Exploring human genetic variation through SNPs in genes with accelerated evolution in the human lineage 38
114 6 N. Niikawa A single-nucleotide polymorphism in the ABCC11 gene is the determinant of human earwax type 340
115 6 Lluis Quintana-Murci Sub-Saharan African sequence diversity at the NAT2 gene: new insights into hunter-gatherers and agriculturalists variation in drug response 125
116 6 Anna Ramirez-Soriano Power analysis of neutrality tests under demographic expansions and recombination 29
117 6 Zsolt Ronai Quantification of C4A and C4B complement genes by real time PCR 122
118 6 Claudia Schmegner The mutation rate but not the mutation pattern changes at a GC-content transition in the human NF1 gene region: Implications for the evolution of the mammalian genome structure 270
119 6 T.P. Sneddon Variable copy number gene nomenclature 57
120 6 Maria Sokolova DNA diagnostics of adult-type hypolactasia in populations of Russia and neighboring countries 135
121 6 Clara S.M. Tang Correlation of intron length with 5'-to-3' decline of transcription-coupled DNA repair and rise of methylation-dependent mutation 44
122 6 Hua Tang Delineating Genetic Ancestry in Admixed Individuals: a High Density Genotype Approach 311
123 6 Kun Tang A new approach for using genome scans to detect recent positive selection in the human genome 357
124 6 Maria Torres hiHgh-throughput gene dosage diagnosis by SNP typing-dependant allele asymmetry (STAA) analysis using MALDI-TOF mass spectrometry 228
125 6 T. Varilo Extended LD intervals favor regional isolates in LD-based genome-wide mapping studies 68
126 6 S.J. White Frequency of common copy number variation in five different ethnic populations 292
127 6 Bryndis Yngvadottir Evolution by gene loss? 200
128 6 R.Y.Y. Yong Association of Y chromosome variation with paternal ancestry origin of three ethnic populations in Singapore 249
129 6 Tatiana Zerjal Y-chromosomal insights into the genetic impact of the Indian caste system 202
7. New and Emerging Technologies
130 7 A. Ahlford A microarray system for genome-wide SNP mapping in Drosophila melanogaster 65
131 7 Silke Argo The MIACA Standard for High-Throughput Assays in Disease Research 214
132 7 Tatyana Azhikina RIDGES - a new technique for construction of high density map of unmethylated CpG sites within preselected genomic loci 52
133 7 David Barker Multiplexed DNA Methylation Profiling Reveals Distinct Methylation Signatures for Human Cancer Cells, Normal Adult Cells, Somatic Stem Cells and Embryonic Stem Cells 302
134 7 David R. Bentley Human genome re-sequencing with next-generation technology 211
135 7 Anthony J. Brookes A Molecular Counting Technology For Research Into Copy-Number Variation 89
136 7 Philip Chambers Addition of a short GC clamp improves the quality of the data generated by the LightScanner for some PCR fragments 49
137 7 Trena A. Cormier SNP Genotyping of Saliva DNA using Affymetrix® GeneChip® Scanner 3000 System 76
138 7 Thomas Froehlich The LightCycler 480 System: High-Throughput Analysis of Nucleic Acids Using Fluorescent-based Real-Time PCR 277
139 7 Osamu Gotoh Multiple cDNA quantification method based on DNA encoding technology 184
140 7 Marco Groth Method for preparing single-stranded DNA templates for Pyrosequencing using vector ligation and universal biotinylated primers 359
141 7 Jenny Göransson High-resolution digital quantification of single DNA molecules 278
142 7 Michael A. Harvey Genotyping of DNA from dried clinical samples collected on chemically modified matrices 151
143 7 Sara Henriksson In situ genotyping SNPs in single copy genes using padlock probes and target primed rolling circle amplification 271
144 7 Emilie Hultin A Signal Amplification Assay for Multiplex Genotyping by Allele-Specific Primer Extension 343
145 7 Magnus Isaksson Selector probes for verification of array-based data in multiplex assays suitable for diagnostics 325
146 7 Poh-San Lai A simple method for rapid screening of known and unknown mutations in G6PD gene using melt curve analysis 130
147 7 Jorma Lampinen Efficient Characterization of DNA Using Photometric, Fluorometric and Luminometric Test Battery 223
148 7 Christian Maercker Development of life cell chips to monitor cell differentiation processes for drug lead validation 258
149 7 Yuichi Michikawa On-chip optical detection system for allele-specific extension of 3’-LNA modified oligonucleotides 345
150 7 Lev Nikolaev Identification, genome mapping and CTCF binding of potential insulators within the FXYD5-COX7A1 locus of human chromosome 19q13.12 51
151 7 Mats Nilsson Single-molecule genotyping 272
152 7 Maija Partanen Rapid magnetic particle based method to obtain high quality DNA from variable sample types 131
153 7 Erik Pettersson Tri-nucleotide threading for parallel amplification of minute amounts of genomic DNA 238
154 7 Uwe Radelof RZPD Protein Arrays - the currently most comprehensive collection of arrayed proteins 246
155 7 D.A. Vouyiouklis Design study 4 within GeneExpress: The nuts and bolts 25
156 7 Shea Ping Yip Multiplex minisequencing coupled with denaturing high performance liquid chromatography as a general platform for genotyping multiple mutations 188
157 7 Pawel Zajac Tri-nucleotide threading for multiplex gene expression analysis 247
158 7 Luming Zhou High Resolution DNA Melting Analysis to Establish HLA Identity between Siblings 296
8. Genetics of Immune System Disorders
159 8 Sara Bruce Gene expression analysis reveals novel downstream signaling pathways for GPR154 upon Neuropeptide S stimulation 177
160 8 Soo-Cheon Chae The association of human Tim-4 gene SNPs in immune disorders and the haplotype of TIM gene family 161
161 8 Hun Soo Chang Genetic effect of CCR3 and IL-5 Receptor alpha Gene Polymorphisms on Eosinophilia in asthmatics 219
162 8 V. Dideberg The TNF/ADAM17 system: implication of an ADAM17 haplotype in the clinical response to infliximab in Crohn's Disease 101
163 8 Changwon Kang Ethnic differences in association of susceptibility to rheumatoid arthritis with single-nucleotide polymorphisms in PADI4, RUNX1 and SLC22A4 genes 73
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
165 8 Maritta Pykäläinen Genes and pathways involved in IL-4 induced human T helper 2 cell differentiation 298
166 8 Ann-Christine Syvänen Genetic variation in the Interferon Regulatory Factor 5 gene in autoimmune diseases 213
167 8 Jana Weissfuss A Candidate Gene Association Study using the GenolinkTM Genotyping System revealed presumptive Genetic Associations concerning Rheumatoid Arthritis 293
168 8 Wen K. Yang Effects of Abnormal SMN2 RNA Splicing on in vitro Growth of T lymphocytes of type II Spinal Muscular Atrophy Patients 119
9. Transcriptome; expression profile; non-coding RNA
169 9 Pelin Akan Identification and characterization of core promoter elements using reporter assays and ChIP on CHIP 87
170 9 Espen Enerly Organization of human miRNA genes 241
171 9 Taro Fukao Genome-wide Screening of Primary miRNA Transcripts: Towards Regulatory Mechanisms for miRNA Expression 95
172 9 Chenna Reddy Galiveti RNomics – Analysis of novel in silico derived non-protein coding RNAs in the human genome 244
173 9 Heidi Hemmoranta Gene expression of cord blood-derived CD34+ and CD133+ cells 132
174 9 Steffen Hennig A world of novel non-protein-coding RNAs: Candidate prediction and chip-design for experimental validation 288
175 9 Jian Huang A transcriptome atlas of human hepatocytes 16
176 9 Tadashi Imanishi Recent Advancement of H-Invitational Database, An Integrated Database of the Human Transcriptome 329
177 9 V.M. Kavsan Comparison of microarray and SAGE techniques in gene expression analysis of human glioblastoma 2
178 9 Anna Kiialainen Pathways of immune response and actin bundling stand out in transcript profiles of TYROBP(DAP12)/TREM2 deficient dendritic cells of PLOSL patients 186
179 9 Daniel Klevebring A new microarray-based method to study sense and antisense transcripts 232
180 9 Johan Lindberg Synovial joint variability and effect of blocking TNF-alpha in rheumatoid arthritis patients investigated by microarray technology 235
181 9 Riikka Lund Genome wide identification of novel genes involved in early Th1 and Th2 cell differentiation 250
182 9 Jean Mosser Iron-related transcriptomic variations in CaCo-2 cells, an in vitro model of intestinal absorptive cells 172
183 9 J. Ollila Correlation of Expression of Activation Induced Genes in Ramos B Cells to KEGG Pathways 284
184 9 Naoki Osada Divergence between human and macaque beyond the protein evolution 58
185 9 A. Rynditch Effect of alternative splicing on regulation of intersectin 1 functions 35
186 9 Marc Sultan Gene Expression Variation In Three Brain Tissues Of A Mouse Model Of Down Syndrome 227
187 9 Yutaka Suzuki Identification and comparative studies of promoter regions of human and mouse genes 156
188 9 Valtteri Wirta Gene discovery in adult neural stem cells 229
189 9 Chunlin Xiao Genome-Wide Identification and Validation of Inter-Species Conserved Probes on Applied Biosystems Human Microarray for Non-Human Primate Gene Expression Studies 100
190 9 Dahai Zhu Erk1/2 mitogen-activated protein kinase pathway involved in myostatin-regulated differentiation repression 104
10. Cancer Genomics
191 10 Jaime Berumen Mitochondrial DNA polymorphism associated with cervical cancer 313
192 10 Sergi Castellvi-Bel Biallelic and monoallelic MUTYH mutations and colorectal cancer 96
193 10 Jan-Gowth Chang Aberrant circadian gene expression in hepatocellular carcinoma 14
194 10 Peh Yean Cheah Mapping of hereditary mixed polyposis syndrome (HMPS) to chromosome 10q23 by genomewide single nucleotide polymorphism (SNP) scan and identification of HMPS mutation 72
195 10 Hege Edvardsen SNPs predictors of Docetaxel clearance 324
196 10 Hannele Erkko Identification of a common polymorphism in the TOPBP1 gene associated with hereditary susceptibility to breast and ovarian cancer 67
197 10 O. E. Fedorova Analysis of BRCA1/2 and CHEK2 mutations in breast cancer patients from Russia using oligonucleotide biochips 322
198 10 Henna Fredriksson Characterization of the Finnish prostate cancer susceptibility locus HPCX 127
199 10 M.D. Galibert Gene expression profiles of TEL/AML1 positive pediatric leukemia: new insights in leukemia molecular processes 218
200 10 Brenda L. Gallie Genomic Changes in Human Retinoblastoma (RB) 152
201 10 Carolin Graebsch Heterogenicity of CytochromeP450 1A1 mRNA transcripts in human tissue 259
202 10 S.A. Gutierrez Rubio EcoR 1 and Bgl II polymorphisms in NME1 gene associates with metastasis protection in Mexican patients with breast cancer 9
203 10 Liesbeth Hameetman Homozygous deletion of EXT1 in non-hereditary osteochondromas 174
204 10 Siina Junnila Integrated gene copy number and expression microarray analysis of primary gastric tumors highlights potential gastric cancer target genes 198
205 10 Duk-Hwan Kim Cis-acting polymorphism of Cyclin A2 gene and its different susceptibility to human cancers 176
206 10 Vessela N. Kristensen Genetic variation in putative regulatory loci controlling gene expression in breast cancer 215
207 10 Ann Lee Overexpression of RB1 transcript is significantly correlated with 13q14 allelic imbalance in colorectal carcinomas 118
208 10 Lili Milani Imbalanced allelic expression as a tool for identifying functional regulatory polymorphisms 56
209 10 M.C. Moran Moguel Insertion/Deletion (I/D) polymorphism in Angiotensin Converting Enzyme (ACE) in mexican women with breast cancer 8
210 10 Samuel Myllykangas Amplification profiling of human neoplasms 208
211 10 Silje H. Nordgard Electronic genotyping of SNPs with relevance for treatment in breast cancer 347
212 10 Sirkku Pollari RNA interference profiles, gene expression and copy number changes in bone metastatic breast cancer cells: an integrated molecular and functional screening 179
213 10 K. Rapakko Mutation analysis of the TP53BP1 gene in families with hereditary susceptibility to breast and/or ovarian cancer 37
214 10 Edith Y.T. Tse Estrogen Receptor α Gene Polymorphisms and Breast Cancer Risk in Chinese 163
215 10 Eugene R. Zabarovsky Epigenetic analysis of cancer cells using NotI microarrays 248
11. Genomics of Complex Disorders
216 11 Heidi Anthoni Characterization of the 2p12 dyslexia candidate region 19
217 11 V. Anttila Trait component analysis offers new tools to dissect the genetics of migraine and identifies new loci 230
218 11 P.T. Cheung ABCG5 and ABCG8 gene haplotypes are novel determinants of HDL levels in Chinese Females 124
219 11 S. Cohen Genetic variation in the Brain Derived Neurotrophic Factor (BDNF) gene and recurrent Major Depression 280
220 11 Joanne E. Curran Genetic analysis of transcriptional profiles for the identification of genes influencing common complex diseases 301
221 11 Ian N.M. Day IDDM2 locus: 5'-noncoding intron I splicing and translational efficiency effects of INS -23HphI – more than a tag for the INS promoter VNTR 54
222 11 Jianjun Gao Studies on the ACE gene insertion/deletion (I/D) polymorphism and psychometric IQ and psychomotor ability in Chinese children 260
223 11 Ilse Gijselinck Direct evidence for a large inversion of the MAPT genomic region using FISH of mechanically stretched chromosomes 97
224 11 William Hennah Families with the Risk Allele of DISC1 Reveal a Link Between Schizophrenia and Another Component of the Same Molecular Pathway, NDE1 121
225 11 Daniel W.H. Ho Linkage Analysis on Familial Early-onset Degenerative Disc Disease (DDD) 62
226 11 I. Hovatta Glyoxalase 1 and glutathione reductase 1 regulate anxiety in mice 12
227 11 Silvia Jiménez-Morales Association analysis of candidates genes with asthma in Mexican pediatric patients 308
228 11 S.P. Kallio PRKCA shows association to multiple sclerosis in two populations 327
229 11 A. Kemppinen Testing association between Myosin IXB and multiple sclerosis 326
230 11 Helena Kilpinen Identification of Genetic Variants Behind Infantile Autism and Asperger Syndrome on Chromosome 1 86
231 11 J.H. Lee Fine Mapping of 12p for Memory Traits in Familial Alzheimer Disease 309
232 11 Susanna Lemmelä Genome-Wide Scan of Exfoliation syndrome in a large Finnish family 143
233 11 Yan Li Association of the cholesterol 24S-hydroxylase polymorphism with Alzheimer's disease in Chinese 63
234 11 Ming-Wei Lin Genome-Wide Scan Identifies a Susceptibility Locus for Familial Primary Cutaneous Amyloidosis on Chromosome 5q11.2-q12 319
235 11 O.A. Makeeva Study of genetic component structure for cardiac remodeling in Russian patients with arterial hypertension 304
236 11 Hideichi Makino Relevance of Resistin Promoter SNP-420 in Human Type 2 Diabetes 26
237 11 Jussi Naukkarinen USF1 and Common Cardiovascular disease: Evidence from adipose tissue transcript profiles and two independent autopsy studies 234
238 11 Akira Oka A whole genome-wide association study of psoriasis within the Japanese population using 26,065 microsatellite markers 185
239 11 Outi M. Palo Evidence of linkage and association between psychosis and locus 4q32 in Finnish bipolar disorder families 207
240 11 Bruno Paquin Whole genome association study for psoriasis using the Quebec LD map 289
241 11 Alireza Pasdar Study of CETP gene polymorphisms and ischaemic stroke in a Scottish population, using pooled DNA samples 300
242 11 T. Paunio Genes Behind A Complex Disease In A Simple Population: Schizophrenia Susceptibility Genes In Finland 267
243 11 Juho O. Peltonen Replication of Linkage and Suggestive Association on Chromosome 7q22 in Finnish Schizophrenia Families 209
244 11 Ludmila Prokunina-Olsson Genetic and functional studies on Type 2 diabetes-associated variants of the TCF7L2 gene in Finns 136
245 11 V. Pulkkinen G protein-coupled receptor for asthma susceptibility associates with respiratory distress syndrome 354
246 11 R. Pylkkänen LDL receptor is associated with Alzheimer disease, CSF total tau, hyperphosphorylated tau and ABeta42 levels 355
247 11 Eva-Maria Pylkkö Association and haplotype analysis on linked region 1q32 in Finnish schizophrenia families 191
248 11 K. Rehnström Candidate gene analysis of five genes at 3q25-27 in Finnish autism families 175
249 11 Santiago Rodriguez Pleiotropic effects of a common IGF2-INS-TH haplotype on obesity, response to glucose, plasma triglycerides and smoking initiation 55
250 11 Jukka T. Salonen Genetic discovery platform in complex traits using a founder population 50
251 11 P. Soronen Functional candidate gene study of Finnish bipolar family sample 210
252 11 Joni A. Turunen Association of GABRG2 gene polymorphisms with schizophrenia and visual working memory 294
253 11 R. Velazquez-Cruz Association of a PDCD1 Polymorphism with Susceptibility to Childhood-onset Systemic Lupus Erythematosus in Mexican Population 239
254 11 Karoliina Wehkalampi Familial aggregation of constitutional delay of growth and puberty (CDGP) 60
12. RNAi
255 12 Tariq Alsheddi Whole-genome approach to highly specific siRNA design by CRM (Comprehensive Redundancy Minimizer) Algorithm 334
256 12 Mikael Björklund Genome-wide RNAi analysis of cell cycle and cell size regulation in Drosophila cells 356
257 12 Brian Harfe microRNA Regulation of murine limb development 328
258 12 Olli Kallioniemi High-throughput RNAi screening in cancer 363
259 12 Xiangning Meng Role of Focal Adhesion Kinase in migration and invasion of lung cancer 344
260 12 Ilaria Piccini RNAi of human transcription factors for analysing regulatory networks 297
261 12 Omid Rasool Modification of an RNAi plasmid construct suitable for enriching transiently transfected cells 352
262 12 Xavier Tordoir PATROCLES: The database of polymorphic miRNA-target interactions 253
13. Genes Chromosomes and Diseases
263 13 K. Alakurtti Developmental expression of cystatin B in mouse 243
264 13 A.-K. Anttonen Mutation analysis of SCN1A and SCN2A2 in Finnish patients with infantile onset intractable epilepsy 109
265 13 Ester Ballana Random inheritance of heteroplasmic mtDNA contributes to phenotypic variability in hearing impairment due to mutation A1555G 142
266 13 Udy Bar-Yosef Characterization of the molecular defect underlying autosomal recessive congenital nuclear cataract in two inbred Bedouin Israeli families 134
267 13 Hande Caglayan Identification of mutations in the F8 gene of hemophilia A patients with inhibitors 36
268 13 Kathryn S.E. Cheah Procollagen IIA facilitates BMP signaling in heart development 335
269 13 David Cockburn Complex dystrophin gene rearrangments - an increased frequency is detected by higher resolution techniques 286
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
271 13 Alberto Ferlin Polymorphisms of the FSH receptor in infertile men: implications for a pharmacogenetic approach for male infertility 81
272 13 L.G. Goldfarb A disorder with phenotypic features of both Charcot-Marie-Tooth disease type 2D (CMT-2D) and distal spinal muscular atrophy type V (dSMA-V) is associated with glycyl-tRNA synthetase (GARS) mutations 40
273 13 M.S. Hildebrand DFNA17 Non-syndromic Sensorineural Hearing Loss in an Australian Family 32
274 13 Heli Honkala From gene to function: Molecular genetics and biology of hydrolethalus syndrome 141
275 13 T. Joensuu Expression analysis of the alternatively spliced cystatin B gene (CSTB) 269
276 13 Sabrina Joseph Higher genomic instability in young Asian radio-sensitive patients 181
277 13 Susana Kofman-Alfaro New dosage sensitive regions associated with abnormal gonadal development in XX -SRY negative sex reversal syndromes using high resolution CHG 102
278 13 Toshio Kojima Determination of Genomic Breakpoints in an Epileptic Patient Using Genotyping Array 346
279 13 M. Kriek Copy number variation in regions flanked (or unflanked) by duplicons among patients with developmental delay and/or congenital malformations; detection of reciprocal and partial Williams Beuren duplications 332
280 13 Mira Kyttälä The genetics of Meckel syndrome uncovers a novel embryonic ciliopathy 240
281 13 Jong-Young Lee Korean BAC Library Construction and Chromosomal Information of 1,144 BAC Clones 353
282 13 A.T. Liza-Sharmini The possible association of -20C and Gln 27 of beta-2 receptor adrenoreceptor polymorphisms in glaucoma patients and responsiveness of topical timolol 282
283 13 Esra Manguoglu Molecular Analysis of MEFV Gene in Turkish FMF Patients in Antalya Province 275
284 13 Shehnaaz S.M. Manji Identification, mapping and molecular characterisation of recessively inherited deafness 167
285 13 Josep Maria Mercader Neurotrophin signalling pathway genotyping in eating disorders 139
286 13 Miguel Angel Moreno-Pelayo Identification of the DFNA44 hearing-loss gene 48
287 13 Magdalena Nawara A novel mutation of IL1RAPL1 in a Polish nonspecific mental retardation (MRX) family 262
288 13 Chipui Pang Interaction of the RHO and RP1 genes in retinitis pigmentosa 113
289 13 Gloria Queipo SOX9 duplications: an alternative etiology in XX sex reversal 103
290 13 Andreas Rump Towards understanding the Pathomechanism of Stüve-Wiedemann Syndrome 339
291 13 Anne Saarinen Genotype-phenotype effect in patients with LRP5 mutations 88
292 13 Yan Shen Mutation Analysis of BMP4, BMP7, HOXA4 and HOXB6 Genes in Chinese Patients with Hypospadias 33
293 13 Yu-fei Shen Chromatin remodeling of myogenin gene in the early stage of differentiation of rhabdomyosarcoma derived cells 105
294 13 H. Annika Siitonen RECQL4: The gene behind three syndromes 126
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
296 13 Isabel Tapia-Páez Molecular studies on DYX1C1 a candidate gene for dyslexia 226
297 13 Todd D. Taylor Co-transcription in the human genome: new genes or alternative transcripts? 75
298 13 Tetsuro Toyoda Intelligent inferences in the omic space: toward high-throughput positional cloning in mouse models of human diseases 183
299 13 Fuu-Jen Tsai Wilson disease protein produced by alternative splicing localized in human liver cell and evaluated the effect in copper-induced toxicity 27
300 13 Li Ping Tsai Molecular diagnosis of EDA gene from patients with hypohidrotic ectodermal dysplasia in Taiwan 312
301 13 C.A. Venegas-Vega GTF2IRD1 Hemizygosity Implicated in Facial Dysmorphism and Development delay in Williams Syndrome 306
302 13 Sonja C. Vernes Mutation screening of FOXP1 in a cohort of Verbal Dyspraxia patients 337
303 13 Chun Mei Wang Compared protein expression in the difference brain area of the senescence accelerated prone mouse strain 8 using proteomic approach 160
304 13 Hans-Jörg Warnatz Generation and Analysis of a Comprehensive Protein Interactome of Human Chromosome 21 283
305 13 E. Katherine Zhang Aberrant splicing events causing retinoblastoma and hereditary hemorrhagic telangiectasia 290
306 13 Liyun Zhang Linkage analysis by SNP markers in autosomal dominant congenital cataract families 108
307 13 B.A. Zilfalil Identification of a novel SNP in the PTGFR gene among glaucomatous patients 285
Created Sunday, 01-May-2005 20:15:35 BST
Updated Fri 19 May 2006 13:22:47 BST