Statistical Genetics Group

Website of the Statistical Genetics Group

SGG joins SIB

The group has become member of the Swiss Institute of Bioinformatics (SIB) after the voting of the SIB Foundation Council on 26 June. Further details are here.

Zoltán nominated as Assistant Professor

In April 2013 Zoltán Kutalik was nominated as Assistant Professor of the Faculty of Biology and Medicine of the University of Lausanne. He will be working in the Statistics Unit of the Institute of Social and Preventive Medicine (IUMSP) of the Lausanne University Hospital (CHUV).

Leenaards prize 2013

The team of Pierre-Yves Bochud (CHUV-UNIL), Zoltán Kutalik (UNIL-SIB), Oscar Marchetti (CHUV-UNIL) and Christian van Delden (HUG & UNIGE) received the Leenaards Prize 2013 for their project “Host genome and transcriptome: new diagnostic and treatment strategies for fungal infections“.

More details can be found: UNIL News, CHUV News, SIB News, UNIGE News, HUG News, Leenaards Foundation, 24 heures, Le Temps, L’Agefi, La Liberté

Multi-SNP association method reveals allelic heterogeneity

There are many known examples of the allelic heterogeneity and imperfect tagging phenomena. The former one is of great importance in monogenic traits but has not yet been systematically investigated and quantified in complex-trait genome-wide association studies (GWASs). We devised a multi-SNP association method that estimates the effect of loci harboring multiple association signals by using GWAS summary statistics.

Read More

Two novel SNPs associated with HCV-induced fibrosis progression

Only a fraction of patients with chronic HCV infection develop liver fibrosis, a process that might also be affected by genetic factors. We studied well-characterized HCV-infected patients of European descent who underwent liver biopsies before treatment.

Read More

Hypergenes eNOS discovery

The HYPERGENES Project investigated associations between genetic variants and essential hypertension pursuing a 2-stage study by recruiting cases and controls from extensively characterized cohorts recruited over many years in different European regions.

Read More

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Underweight and obese phenotypes can both pose health risks. But whereas obesity has been associated with a number of genetic variants, little is known about the genetic basis of underweight. A large-scale screen of data from 28 cytogenetic centres in Europe and North America now shows that being underweight is frequently associated with duplication of a short region on chromosome 16.

Read More

Novel method to estimate explained variance of GWAS hits reveals large fraction of the missing heritability

Genome-wide association studies (GWAS) are conducted with the promise to discover novel genetic variants associated with diverse traits. For most traits, associated markers individually explain just a modest fraction of the phenotypic variation, but their number can well be in the hundreds. We developed a maximum likelihood method that allows us to infer the distribution of associated variants even when many of them were missed by chance.

Read More

Hundreds of genomic variants are associated with human anthropometric traits

Via the CoLaus and Hypergenes cohorts our group contributed to the meta-analysis of the GIANT consortium that revealed hundreds of genetic variants associated with human height; 18 new loci for body mass index; and 13 new loci for waist-hip-ratio.

Read More

Genome-wide Association Study reveals new HLA-haplotype strongly protective against narcolepsy

We are involved in a Genome-wide Association Study on narcolepsy conducted by Mehdi Tafti’s Group at the University of Lausanne. In brief, we identified a haplotype in the HLA-region that is strongly protective against narcolepsy. More than 10% of HLA-positive controls carry this DRB1*1301-DQB1*0603 haplotype, which was found in virtually no narcoleptic cases. The research findings were published in Nature Genetics.

Page 2 of 2

Powered by WordPress & Theme by Anders Norén