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Maryline Gagnebin

Observed names: Gagnebin, Maryline, M Gagnebin, Marilyne Gagnebin
OpenAlex ID: A5083493166
Common Regulatory Variation Impacts Gene Expression in a Cell Type–Dependent Manner
2009 · Antigone S. Dimas, Samuel Deutsch, et al. · Science · 747
Passive and active DNA methylation and the interplay with genetic variation in gene regulation
2013 · Maria Gutierrez-Arcelus, Tuuli Lappalainen, et al. · eLife · 441
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Genetic Structure of Europeans: A View from the North–East
2009 · Mari Nelis, Tõnu Esko, et al. · PLoS ONE · 427
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Human microRNA-155 on Chromosome 21 Differentially Interacts with Its Polymorphic Target in the AGTR1 3′ Untranslated Region: A Mechanism for Functional Single-Nucleotide Polymorphisms Related to Phenotypes
2007 · Praveen Sethupathy, Christelle Borel, et al. · The American Journal of Human Genetics · 361
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Domains of genome-wide gene expression dysregulation in Down’s syndrome
2014 · Audrey Letourneau, Federico A. Santoni, et al. · Nature · 319
Tissue-Specific Effects of Genetic and Epigenetic Variation on Gene Regulation and Splicing
2015 · Maria Gutierrez-Arcelus, Halit Ongen, et al. · PLoS Genetics · 199
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Natural Gene-Expression Variation in Down Syndrome Modulates the Outcome of Gene-Dosage Imbalance
2007 · Paola Prandini, Samuel Deutsch, et al. · The American Journal of Human Genetics · 196
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Molecular and clinical characterization of 25 individuals with exonic deletions of NRXN1 and comprehensive review of the literature
2013 · Frédérique Béna, Damien L. Bruno, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 109
Gene expression variation and expression quantitative trait mapping of human chromosome 21 genes
2005 · Samuel Deutsch, Robert Lyle, et al. · Human Molecular Genetics · 106
Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts
2010 · Christelle Borel, Samuel Deutsch, et al. · Genome Research · 72
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Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications
2013 · Antonietta Coppola, Antonio Romito, et al. · Stem Cell Research · 67
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Monozygotic twins discordant for trisomy 21 and maternal 21q inheritance: A complex series of events
2008 · Sophie Dahoun, Sarantis Gagos, et al. · American Journal of Medical Genetics Part A · 41
Correction: Passive and active DNA methylation and the interplay with genetic variation in gene regulation
2013 · Maria Gutierrez-Arcelus, Tuuli Lappalainen, et al. · eLife · 33
Tandem repeat sequence variation as causative Cis-eQTLs for protein-coding gene expression variation: The case of CSTB
2012 · Christelle Borel, Eugenia Migliavacca, et al. · Human Mutation · 30
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Mapping of Small RNAs in the Human ENCODE Regions
2008 · Christelle Borel, Maryline Gagnebin, et al. · The American Journal of Human Genetics · 27
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Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele
2012 · Uppala Radhakrishna, Swapan K Nath, et al. · Journal of Medical Genetics · 14
No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients
2017 · M Guipponi, F Santoni, et al. · Translational Psychiatry · 9
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Author response: Passive and active DNA methylation and the interplay with genetic variation in gene regulation
2013 · Maria Gutierrez-Arcelus, Tuuli Lappalainen, et al. · eLife · 7
Extensive Natural Variation for Cellular Hydrogen Peroxide Release Is Genetically Controlled
2012 · Homa Attar, Karen Bedard, et al. · PLoS ONE · 5
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Correction: Genetic Structure of Europeans: A View from the North–East
2010 · Mari Nelis, Tõnu Esko, et al. · PLoS ONE · 4
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Correction: Corrigendum: Domains of genome-wide gene expression dysregulation in Down’s syndrome
2015 · Audrey Letourneau, Federico A. Santoni, et al. · Nature · 2
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Journal of Medical Genetics
2012 · Radhakrishna, Uppala, Nath, Swapan K., et al. · Creighton Digital Repository (CDR)
Works count: 25
Citation count: 3,216
H-index: 15
I10-index: 16
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