Highlights
Gehrig, Corinne
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2021
Scientific Articles
2016
Scientific Articles
2015
Scientific Articles
unige:77402![]() ![]() | DNA-Methylation Patterns in Trisomy 21 Using Cells from Monozygotic Twins | Sailani, Mohammad Reza; Santoni, Federico; Letourneau, Audrey; Borel, Christelle; ... Antonarakis, Stylianos |
unige:77363![]() ![]() | Galanin pathogenic mutations in temporal lobe epilepsy | Guipponi, Michel; Chentouf, Amina; Webling, Kristin E B; Freimann, Krista; ... Antonarakis, Stylianos |
unige:77359![]() ![]() | Tissue-specific effects of genetic and epigenetic variation on gene regulation and splicing | Gutierrez Arcelus, Maria; Ongen, Halit; Lappalainen, Tuuli Emilia; Montgomery, Stephen; ... Dermitzakis, Emmanouil |
2014
Scientific Articles
2013
Scientific Articles
unige:33562![]() ![]() | Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications | Coppola, Antonietta; Romito, Antonio; Borel, Christelle; Gehrig, Corinne; ... Cobellis, Gilda |
unige:34514![]() ![]() | Passive and active DNA methylation and the interplay with genetic variation in gene regulation | Gutierrez Arcelus, Maria; Lappalainen, Tuuli Emilia; Montgomery, Stephen; Buil Demur, Alfonso Alberto; ... Dermitzakis, Emmanouil |
2012
Professional Articles
unige:34654![]() ![]() | Exome sequencing identifies recurrent somatic MAP2K1 and MAP2K2 mutations in melanoma | Nikolaev, Sergey Igorievich; Rimoldi, Donata; Iseli, Christian; Valsesia, Armand; ... Antonarakis, Stylianos |
2011
Scientific Articles
2009
Scientific Articles
unige:9231![]() ![]() | Detection of genomic variation by selection of a 9 mb DNA region and high throughput sequencing | Nikolaev, S. I.; Iseli, Christian; Sharp, A. J.; Robyr, Daniel; ... Antonarakis, Stylianos |
unige:5576![]() ![]() | Genotype-phenotype correlations in Down syndrome identified by array CGH in 30 cases of partial trisomy and partial monosomy chromosome 21 | Lyle, Robert; Bena, Frédérique; Gagos, Sarantis; Gehrig, Corinne; ... Antonarakis, Stylianos |
unige:8907![]() ![]() | Proliferation deficits and gene expression dysregulation in Down's syndrome (Ts1Cje) neural progenitor cells cultured from neurospheres | Moldrich, R. X.; Dauphinot, Luce; Laffaire, Julien; Vitalis, Tania; ... Potier, M. C. |
2008
Scientific Articles
2007
Scientific Articles
2006
Scientific Articles
2005
Scientific Articles
unige:8724![]() ![]() | Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes | Deutsch, Samuel; Lyle, Robert; Dermitzakis, Emmanouil; Attar, Homa; ... Antonarakis, Stylianos |
2004
Scientific Articles
unige:8870![]() ![]() | Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome | Lyle, Robert; Gehrig, Corinne; Neergaard-Henrichsen, Charlotte; Deutsch, Samuel; Antonarakis, Stylianos |
2002
Scientific Articles
2001
Scientific Articles
unige:8981![]() ![]() | An apparently dominant bipolar affective disorder (BPAD) locus on chromosome 20p11.2-q11.2 in a large Turkish pedigree | Radhakrishna, U.; Senol, S.; Herken, H.; Gucuyener, K.; ... Antonarakis, Stylianos |
unige:8625![]() ![]() | Axonemal beta heavy chain dynein DNAH9: cDNA sequence, genomic structure, and investigation of its role in primary ciliary dyskinesia | Bartoloni, Lucia; Blouin, Jean-Louis; Maiti, A. K.; Sainsbury, A.; ... Antonarakis, Stylianos |
unige:9029![]() ![]() | Insertion of beta-satellite repeats identifies a transmembrane protease causing both congenital and childhood onset autosomal recessive deafness | Scott, Hamish Steele; Kudoh, J.; Wattenhofer, M.; Shibuya, K.; ... Antonarakis, Stylianos |
2000
Scientific Articles
unige:8878![]() ![]() | No deleterious mutations in the FOXJ1 (alias HFH-4) gene in patients with primary ciliary dyskinesia (PCD) | Maiti, A. K.; Bartoloni, Lucia; Mitchison, H. M.; Meeks, M.; ... Antonarakis, Stylianos |
1999
Scientific Articles
unige:8605![]() ![]() | Lack of linkage or association between schizophrenia and the polymorphic trinucleotide repeat within the KCNN3 gene on chromosome 1q21 | Antonarakis, Stylianos; Blouin, Jean-Louis; Lasseter, V. K.; Gehrig, Corinne; ... Pulver, A. E. |
unige:8698![]() ![]() | No evidence for linkage between schizophrenia and markers at chromosome 15q13-14 | Curtis, L.; Blouin, Jean-Louis; Radhakrishna, U.; Gehrig, Corinne; ... Antonarakis, Stylianos |
1998
Scientific Articles
unige:8891![]() ![]() | Loss of LKB1 kinase activity in Peutz-Jeghers syndrome, and evidence for allelic and locus heterogeneity | Mehenni, H.; Gehrig, Corinne; Nezu, J.; Oku, A.; ... Antonarakis, Stylianos |
unige:8646![]() ![]() | Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 | Blouin, Jean-Louis; Dombroski, B. A.; Nath, S. K.; Lasseter, V. K.; ... Pulver, A. E. |
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