Past Winners of the
- Young Investigator Awards for Outstanding Science,
- Isabelle Oberlé Award for Research on Genetics of Mental Retardation
- Lodewijk Sandkuijl Award for the best talk in Statistical Genetics
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European Human Genetics
Conference 2007 Nice, France; June 16-19, 2007 |
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| Young Investigator Awards for Outstanding Science | ||
| Julie Mollet (Paris) |
Prenyldiphosphate synthase PDSS1 and OH-benzoate prenyltransferase COQ2 mutations in ubiquinin deficiency and oxidative phosphorylation disorders | |
| Zrinka Biloglav (Zagreb) |
Epidemics of viral hemorrhagic fever in Medieval times as a possible selection pressure for CCR5del32 in Europe; new insights from Croatian island isolates | |
| Liat Linde (Jerusalem) |
Nonsense-mediated mRNA decay regulates response of cystic fibrosis patients to gentamycin | |
| Emma N. Hilton (Manchester) |
Left-sided embryonic expression of the BCL-6 corepressor BCOR, is required for vertebrate laterality determination | |
| Dagan Jenkins (Oxford) |
RAB23 mutations in Carpenter syndrome imply an unexpected role for the Hedgehog signalling in cranial suture development and obesity | |
| Isabelle Oberlé Award | ||
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Frank J. Kaiser (Lübeck) |
The cohesion protein NIPBL recruits histone deacetylases to mediate chromatin remodelling | |
| Lodewijk Sandkuijl Award | ||
| Vincent Plagnol (Cambridge) |
A genome-wide assessment of the genetic basis of type 1 diabetes | |
| Picture gallery of the awarding ceremony
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European Human Genetics
Conference 2006 Amsterdam, The Netherlands; May 6-9, 2006 |
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| Young Investigator Awards for Outstanding Science | ||
| Carmine Settembre (Naples) |
Life without sulfatases: exploiting a mouse model of multiple sulfatase deficiency | |
| Vladimir V. Strelnikov (Moscow) |
Identification of methylation and expression abnormalities associated with breast cancer | |
| Anne Fechter (Heidelberg) |
Targeted cloning of fragile sites - based on a previous tagging of fragile regions in a breast cancer cell line | |
| Ursula M. Smith (Birmingham) |
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome | |
| Isabelle Oberlé Award | ||
| Tjitske Kleefstra (Nijmegen) |
Haploinsufficiency of the Euchromatin Histone Methyl Transferase1 (Eu-HMTase1) gene causes the 9q subtelomeric deletion syndrome. | |
| Lodewijk Sandkuijl Award | ||
| Samuel Deutsch (Geneva) |
Quantitative mapping of loci influencing susceptibility to lentiviral infection | |
| Christoph Lange (Boston, MA) |
Screening and replication using the same data set: A testing strategy for case/control studies | |
| Picture gallery of the awarding ceremony
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European Human Genetics
Conference 2005 Prague, Czech Republic; May 7-10, 2005 |
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| Young Investigator Awards for Outstanding Science | ||
| Silvia Paracchini (Oxford) |
Chromosome 6p22 risk haplotype for dyslexia is associated with a reduced expression of KIAA0319 gene | |
| William J. Tapper (Southampton) |
The first genome wide linkage disequilibrium map | |
| Aida I. Al-Aqeel (Riyadh) |
Ethics and Genetics: An Islamic Perspective | |
| Isabelle Oberlé Award | ||
| Bartlomiej Budny (Berlin/Poznan) |
A new XLMR syndrome characterized by mental retardation, primary ciliary dyskinesia and macrocephaly, caused by a novel mutation in OFD1 | |
| Lodewijk Sandkuijl Award | ||
| Aaron Isaacs (Rotterdam) |
Plasma lipids: heritabilities, apoE, and effects of inbreeding in a genetically isolated population | |
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European Human Genetics
Conference 2004 Munich, Germany; June 12-15, 2004 |
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| Young Investigator Awards for Outstanding Science | ||
| Ernie
Bongers (Nijmegen) |
Mutations in the human TBX4 gene cause small patella syndrome | |
| Hilde
Peeters (Leuven) |
PA26 is a candidate gene for human heterotaxia | |
| Aurora Pujol
(Strasbourg) |
Functional overlap between ABCD1 (ALD) and ABCD2 (ALDR) transporters: a therapeutic target for X-linked adrenoleukodystrophy | |
| Nitin Sabherwal (Heidelberg) | Novel point mutations R173C and A170P in the SHOX homeodomain defines impaired nuclear translocation as a molecular cause for Léri-Weill dyschondrosteosis and Langer dysplasia | |
| Birgit
Zirn (Giessen) |
Expression profiling of Wilms tumors reveals novel prognostic markers | |
| Isabelle Oberlé Award | ||
| Gajja Salomons (Amsterdam) | High prevalence of SLC6A8 deficiency, a novel X-linked mental retardation syndrome | |
| Lodewijk Sandkuijl Award | ||
| Manuel A. R. Ferreira (Brisbane) | Accounting for strong age-specific sex-limitation in IgE QTL linkage analysis | |
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European Human Genetics
Conference 2003 Birmingham, England; May 3-6, 2003 |
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| Young Investigator Awards for outstanding science | ||
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Slawomir Wisniewski
(Poznan) |
Mutations of EDA, EDARADD and TRAF6 genes in anhidrotic ectodermal dysplasia genotype/phenotype correlation. | |
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Michel De Vos (Leeds) |
PMS2 mutation as a cause of primitive neuroectodermal tumours of childhood | |
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Martine J. van Belzen
(Utrecht) |
A major non-HLA locus in coeliac disease maps to chromosome 19 | |
| Isabelle Oberlé Award | ||
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Joris A. Veltman (Nijmegen) |
High resolution whole genome microdeletion screening by array CGH | |
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European Human Genetics Conference 2002 Strasbourg, France; May 25-28, 2002 |
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| Young Investigator Awards for outstanding science | ||
| John
Common (London) |
Genetic and functional analysis of connexins in skin disease and deafness | |
| Heymut
Omran (Freiburg) |
Mutations in DNAH5 cause primary ciliary dyskinesia and randomization of left-right asymmetry | |
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Richard Redon (Illkirch) |
Cyclin L/Ania-6a, a gene located at 3q25, is amplified and overexpressed in a head and neck cancer cell line | |
| Isabelle Oberlé Award | ||
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Florence Molinari (Paris) |
Mutation in Neurotrypsin is responsible for autosomal recessive non-specific mental retardation | |
