Emilie Falconnet

7.9k total citations
16 papers, 672 citations indexed

About

Emilie Falconnet is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Emilie Falconnet has authored 16 papers receiving a total of 672 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Cancer Research. Recurrent topics in Emilie Falconnet's work include Epigenetics and DNA Methylation (5 papers), Cystic Fibrosis Research Advances (3 papers) and Genetic Syndromes and Imprinting (2 papers). Emilie Falconnet is often cited by papers focused on Epigenetics and DNA Methylation (5 papers), Cystic Fibrosis Research Advances (3 papers) and Genetic Syndromes and Imprinting (2 papers). Emilie Falconnet collaborates with scholars based in Switzerland, Italy and United States. Emilie Falconnet's co-authors include Stylianos E. Antonarakis, Federico Santoni, Christelle Borel, Marco Garieri, Pascale Ribaux, Michel Guipponi, Georgios Stamoulis, Sergey I. Nikolaev, Audrey Letourneau and Emmanouil T. Dermitzakis and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Blood.

In The Last Decade

Emilie Falconnet

16 papers receiving 667 citations

Peers

Countries citing papers authored by Emilie Falconnet

Since Specialization

Citations

This map shows the geographic impact of Emilie Falconnet's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Emilie Falconnet with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Emilie Falconnet more than expected).

Fields of papers citing papers by Emilie Falconnet

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Emilie Falconnet. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Emilie Falconnet. The network helps show where Emilie Falconnet may publish in the future.

Co-authorship network of co-authors of Emilie Falconnet

This figure shows the co-authorship network connecting the top 25 collaborators of Emilie Falconnet. A scholar is included among the top collaborators of Emilie Falconnet based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Emilie Falconnet. Emilie Falconnet is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

#	Work	Indexed citations
1	Single cell transcriptome in aneuploidies reveals mechanisms of gene dosage imbalance 2019 ·Nature Communications ·Georgios Stamoulis, Marco Garieri, Periklis Makrythanasis, Audrey Letourneau, Michel Guipponi, Nikolaos I. Panousis, Frédérique Sloan‐Béna, Emilie Falconnet, Pascale Ribaux, Christelle Borel, Federico Santoni, Stylianos E. Antonarakis	28
2	Extensive cellular heterogeneity of X inactivation revealed by single-cell allele-specific expression in human fibroblasts 2018 ·Proceedings of the National Academy of Sciences ·Marco Garieri, Georgios Stamoulis, (unknown), Emilie Falconnet, Pascale Ribaux, Christelle Borel, Federico Santoni, Stylianos E. Antonarakis	56
3	Biallelic variants in FBXL3 cause intellectual disability, delayed motor development and short stature 2018 ·Human Molecular Genetics ·Muhammad Ansar, (unknown), Alessandro Serretti, Muhammad Tahir Sarwar, (unknown), Emmanuelle Ranza, Emilie Falconnet, Justyna Iwaszkiewicz, (unknown), (unknown), Federico Santoni, Vincent Zoete, André Mégarbané, Jawad Ahmed, (unknown), Periklis Makrythanasis, Stylianos E. Antonarakis	16
4	Visual impairment and progressive phthisis bulbi caused by recessive pathogenic variant in MARK3 2018 ·Human Molecular Genetics ·Muhammad Ansar, Hyung-Lok Chung, (unknown), Periklis Makrythanasis, Emilie Falconnet, (unknown), Michel Guipponi, (unknown), Ralph Fingerhut, Federico Santoni, Emmanuelle Ranza, Ali Muhammad Waryah, Hugo J. Bellen, Stylianos E. Antonarakis	16
5	The genomic landscape of human cellular circadian variation points to a novel role for the signalosome 2017 ·eLife ·(unknown), Cédric Howald, Konstantin Popadin, Bert Maier, Daniel Mauvoisin, Ermanno Moriggi, María Gutiérrez‐Arcelus, Emilie Falconnet, Christelle Borel, Dieter Kunz, Achim Kramer, Frédéric Gachon, Emmanouil T. Dermitzakis, Stylianos E. Antonarakis, Steven A. Brown	16
6	Detection of Imprinted Genes by Single-Cell Allele-Specific Gene Expression 2017 ·The American Journal of Human Genetics ·Federico Santoni, Georgios Stamoulis, Marco Garieri, Emilie Falconnet, Pascale Ribaux, Christelle Borel, Stylianos E. Antonarakis	50
7	HSA21 Single-Minded 2 (Sim2) Binding Sites Co-Localize with Super-Enhancers and Pioneer Transcription Factors in Pluripotent Mouse ES Cells 2015 ·PLoS ONE ·Audrey Letourneau, Gilda Cobellis, Alexandre Fort, Federico Santoni, Marco Garieri, Emilie Falconnet, Pascale Ribaux, Anne Vannier, Michel Guipponi, Piero Carninci, Christelle Borel, Stylianos E. Antonarakis	9
8	Biased Allelic Expression in Human Primary Fibroblast Single Cells 2014 ·The American Journal of Human Genetics ·Christelle Borel, Pedro G. Ferreira, Federico Santoni, Olivier Delaneau, Alexandre Fort, Konstantin Popadin, Marco Garieri, Emilie Falconnet, Pascale Ribaux, Michel Guipponi, Ismaël Padioleau, Piero Carninci, Emmanouil T. Dermitzakis, Stylianos E. Antonarakis	89
9	Extrachromosomal driver mutations in glioblastoma and low-grade glioma 2014 ·Nature Communications ·Sergey I. Nikolaev, Federico Santoni, Marco Garieri, Periklis Makrythanasis, Emilie Falconnet, Michel Guipponi, Anne Vannier, Ivan Radovanovic, Frédérique Béna, F Forestier, Karl Schaller, Valérie Dutoit, Virginie Clément‐Schatlo, Pierre‐Yves Dietrich, Stylianos E. Antonarakis	52
10	Frequent cases of RAS-mutated Down syndrome acute lymphoblastic leukaemia lack JAK2 mutations 2014 ·Nature Communications ·Sergey I. Nikolaev, Marco Garieri, Federico Santoni, Emilie Falconnet, Pascale Ribaux, Michel Guipponi, Aoife Murray, Jürgen Groet, Emanuela Giarin, Giuseppe Basso, Dean Nižetić, Stylianos E. Antonarakis	38
11	Cardiomyogenesis is controlled by the miR-99a/let-7c cluster and epigenetic modifications 2013 ·Stem Cell Research ·Antonietta Coppola, Antonio Romito, Christelle Borel, Corinne Gehrig, Maryline Gagnebin, Emilie Falconnet, Antonella Izzo, Lucia Altucci, Sandro Banfi, Stylianos E. Antonarakis, Gabriella Minchiotti, Gilda Cobellis	59
12	Exome sequencing identifies putative drivers of progression of transient myeloproliferative disorder to AMKL in infants with Down syndrome 2013 ·Blood ·Sergey I. Nikolaev, Federico Santoni, Anne Vannier, Emilie Falconnet, Emanuela Giarin, Giuseppe Basso, Alexander Hoischen, Joris A. Veltman, Jürgen Groet, Dean Nižetić, Stylianos E. Antonarakis	54
13	Static respiratory cilia associated with mutations in Dnahc11/DNAH11: A mouse model of PCD 2011 ·Human Mutation ·Jane S. Lucas, Elizabeth Adam, Patricia Goggin, Claire Jackson, Nicola Powles‐Glover, (unknown), (unknown), Martin Fray, Emilie Falconnet, Jean‐Louis Blouin, Michael Cheeseman, Lucia Bartoloni, Dominic P. Norris, Peter M. Lackie	48
14	Identification of cis- and trans-regulatory variation modulating microRNA expression levels in human fibroblasts 2010 ·Genome Research ·Christelle Borel, Samuel Deutsch, Audrey Letourneau, Eugenia Migliavacca, Stephen B. Montgomery, Antigone S. Dimas, Charles E. Vejnar, Homa Attar, Maryline Gagnebin, Corinne Gehrig, Emilie Falconnet, (unknown), Emmanouil T. Dermitzakis, Stylianos E. Antonarakis	52
15	Mutations in DNAH5 account for only 15% of a non-preselected cohort of patients with primary ciliary dyskinesia 2009 ·Journal of Medical Genetics ·Mike Failly, Lucia Bartoloni, Audrey Letourneau, (unknown), Emilie Falconnet, Colette Rossier, M. M. De Santi, Francesca Santamaria, Oliviero Sacco, C.D. DeLozier-Blanchet, Romain Lazor, (unknown)	55
16	<i>DNAI1</i> Mutations Explain Only 2% of Primary Ciliary Dykinesia 2008 ·Respiration ·Mike Failly, (unknown), (unknown), Emilie Falconnet, Colette Rossier, Francesca Santamaria, Maria Margherita De Santi, Romain Lazor, C.D. DeLozier-Blanchet, Lucia Bartoloni, Jean‐Louis Blouin	34

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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