Charlotte Hor

Publications | Mémoires et thèses

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11 publications

2018 | 2011 | 2010 | 2009 | 2007 | 2006 | 2001 |
A systems genetics resource and analysis of sleep regulation in the mouse.
Diessler S., Jan M., Emmenegger Y., Guex N., Middleton B., Skene D.J., Ibberson M., Burdet F., Götz L., Pagni M. et al., 2018/08. PLoS biology, 16 (8) pp. e2005750. Peer-reviewed.
A high-resolution anatomical atlas of the transcriptome in the mouse embryo.
Diez-Roux G., Banfi S., Sultan M., Geffers L., Anand S., Rozado D., Magen A., Canidio E., Pagani M., Peluso I. et al., 2011. PLoS Biology, 9 (1) pp. e1000582.
 
Copy number variation modifies expression time courses.
Chaignat E., Yahya-Graison E.A., Henrichsen C.N., Chrast J., Schütz F., Pradervand S., Reymond A., 2011. Genome Research, 21 (1) pp. 106-113.
Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome.
Henrichsen C.N., Csárdi G., Zabot M.T., Fusco C., Bergmann S., Merla G., Reymond A., 2011. PLoS Computational Biology, 7 (1) pp. e1001054. Peer-reviewed.
 
A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromes.
Gimelli S., Chrast J., Baban A., Henrichsen C.N., Lerone M., Zuffardi O., Gimelli G., Reymond A., 2010. American Journal of Medical Genetics. Part A, 152A (5) pp. 1285-1294. Peer-reviewed.
Copy number variants, diseases and gene expression.
Henrichsen C.N., Chaignat E., Reymond A., 2009. Human Molecular Genetics, 18 (R1) pp. R1-R8. Peer-reviewed.
 
Segmental copy number variation shapes tissue transcriptomes.
Henrichsen C.N., Vinckenbosch N., Zöllner S., Chaignat E., Pradervand S., Schütz F., Ruedi M., Kaessmann H., Reymond A., 2009. Nature Genetics, 41 (4) pp. 424-429. Peer-reviewed.
 
Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions.
Denoeud F., Kapranov P., Ucla C., Frankish A., Castelo R., Drenkow J., Lagarde J., Alioto T., Manzano C., Chrast J. et al., 2007. Genome Research, 17 (6) pp. 746-759. Peer-reviewed.
 
Side effects of genome structural changes.
Reymond A., Henrichsen C.N., Harewood L., Merla G., 2007. Current Opinion in Genetics and Development, 17 (5) pp. 381-386. Peer-reviewed.
 
Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes.
Merla G., Howald C., Henrichsen C.N., Lyle R., Wyss C., Zabot M.T., Antonarakis S.E., Reymond A., 2006. American Journal of Human Genetics, 79 (2) pp. 332-341. Peer-reviewed.
 
From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map.
Reymond A., Friedli M., Henrichsen C.N., Chapot F., Deutsch S., Ucla C., Rossier C., Lyle R., Guipponi M., Antonarakis S.E., 2001. Genomics, 78 (1-2) pp. 46-54.
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