Alexandre Reymond

69.1k total citations · 1 hit paper
122 papers, 8.6k citations indexed

About

Alexandre Reymond is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Alexandre Reymond has authored 122 papers receiving a total of 8.6k indexed citations (citations by other indexed papers that have themselves been cited), including 91 papers in Molecular Biology, 51 papers in Genetics and 24 papers in Plant Science. Recurrent topics in Alexandre Reymond's work include Genomic variations and chromosomal abnormalities (37 papers), Genomics and Chromatin Dynamics (22 papers) and Chromosomal and Genetic Variations (22 papers). Alexandre Reymond is often cited by papers focused on Genomic variations and chromosomal abnormalities (37 papers), Genomics and Chromatin Dynamics (22 papers) and Chromosomal and Genetic Variations (22 papers). Alexandre Reymond collaborates with scholars based in Switzerland, United States and United Kingdom. Alexandre Reymond's co-authors include Stylianos E. Antonarakis, Emmanouil T. Dermitzakis, Charlotte N. Henrichsen, Robert Lyle, Samuel Deutsch, Giuseppe Merla, Catherine Ucla, Viesturs Simanis, Roderic Guigó and Jennifer Harrow and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Alexandre Reymond

121 papers receiving 8.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

The tripartite motif family identifies cell compartments

2001 1.1k citations Alexandre Reymond profile →

Peers

Countries citing papers authored by Alexandre Reymond

Since Specialization

Citations

This map shows the geographic impact of Alexandre Reymond'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 Alexandre Reymond with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Alexandre Reymond more than expected).

Fields of papers citing papers by Alexandre Reymond

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexandre Reymond. 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 Alexandre Reymond. The network helps show where Alexandre Reymond may publish in the future.

Co-authorship network of co-authors of Alexandre Reymond

This figure shows the co-authorship network connecting the top 25 collaborators of Alexandre Reymond. A scholar is included among the top collaborators of Alexandre Reymond 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 Alexandre Reymond. Alexandre Reymond is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Disentangling mechanisms behind the pleiotropic effects of proximal 16p11.2 BP4-5 CNVs 2024 ·The American Journal of Human Genetics ·Chiara Auwerx, (unknown), Zoltán Kutalik, Alexandre Reymond	1
2	Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease 2023 ·Cell Reports Medicine ·Ruth Hanßen, Chiara Auwerx, (unknown), Marie C. Sadler, Elana Henning, Julia M. Keogh, Rebecca Bounds, (unknown), Helen V. Firth, Zoltán Kutalik, I. Sadaf Farooqi, Alexandre Reymond, Katherine Lawler	14
3	Contribution of schizophrenia polygenic burden to longitudinal phenotypic variance in 22q11.2 deletion syndrome 2022 ·Molecular Psychiatry ·Maris Alver, Valentina Mancini, Kristi Läll, Maude Schneider, Luciana Romano, Lili Milani, Mari Nelis, Reedik Mägi, Tōnu Esko, Andres Metspalu, Emmanouil T. Dermitzakis, Stéphan Eliez, Alexandre Reymond	7
4	From pharmacogenetics to pharmaco-omics: Milestones and future directions 2022 ·Human Genetics and Genomics Advances ·Chiara Auwerx, Marie C. Sadler, Alexandre Reymond, Zoltán Kutalik	25
5	Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome 2021 ·Nature Communications ·Eleonora Porcu, Marie C. Sadler, Kaido Lepik, Chiara Auwerx, Andrew R. Wood, Antoine Weihs, Maroun Bou Sleiman, Diogo M. Ribeiro, Stefania Bandinelli, Toshiko Tanaka, Matthias Nauck, Uwe Völker, Olivier Delaneau, Andres Metspalu, Alexander Teumer, Timothy M. Frayling, Federico Santoni, Alexandre Reymond, Zoltán Kutalik	63
6	Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder 2021 ·npj Genomic Medicine ·Francesca Mattioli, Hossein Darvish, (unknown), Abbas Tafakhori, Saghar Ghasemi Firouzabadi, (unknown), (unknown), Alexandre Reymond, Stylianos E. Antonarakis, Muhammad Ansar	12
7	Pathogenic homozygous variant in POMK gene is the cause of prenatally detected severe ventriculomegaly in two Lithuanian families 2019 ·American Journal of Medical Genetics Part A ·Eglė Preikšaitienė, Norine Voisin, Lucie Gueneau, (unknown), (unknown), (unknown), Laima Ambrozaitytė, (unknown), Alexandre Reymond, Vaidutis Kučinskas	6
8	Bayesian association scan reveals loci associated with human lifespan and linked biomarkers 2017 ·Nature Communications ·Aaron F. McDaid, Peter K. Joshi, Eleonora Porcu, (unknown), Hao Li, Vincenzo Sorrentino, Maria Litovchenko, R. Bevers, Sina Rüeger, Alexandre Reymond, Murielle Bochud, Bart Deplancke, Robert W. Williams, Marc Robinson‐Rechavi, Fred Paccaud, Valentin Rousson, Johan Auwerx, James F. Wilson, Zoltán Kutalik	47
9	Novel H3K4me3 marks are enriched at human- and chimpanzee-specific cytogenetic structures 2014 ·Genome Research ·Giuliana Giannuzzi, Eugenia Migliavacca, Alexandre Reymond	5
10	A Fish-Specific Transposable Element Shapes the Repertoire of p53 Target Genes in Zebrafish 2012 ·PLoS ONE ·Lucia Micale, Maria Nicla Loviglio, Marta Manzoni, Carmela Fusco, Bartolomeo Augello, Eugenia Migliavacca, (unknown), Eugenio Monti, Giuseppe Borsani, Alexandre Reymond, Giuseppe Merla	16
11	Detecting Long-Range Chromatin Interactions Using the Chromosome Conformation Capture Sequencing (4C-seq) Method 2011 ·Methods in molecular biology ·Nele Gheldof, Marion Leleu, Daan Noordermeer, Jacques Rougemont, Alexandre Reymond	38
12	Copy number variation modifies expression time courses 2010 ·Genome Research ·(unknown), Emilie Ait‐Yahya, Charlotte N. Henrichsen, Jacqueline Chrast, Frédéric Schütz, Sylvain Pradervand, Alexandre Reymond	48
13	The effect of translocation-induced nuclear reorganization on gene expression 2010 ·Genome Research ·Louise Harewood, Frédéric Schütz, Shelagh Boyle, Paul Perry, Mauro Delorenzi, Wendy A. Bickmore, Alexandre Reymond	80
14	Assaying the regulatory potential of mammalian conserved non-coding sequences in human cells 2008 ·Genome biology ·Catia Attanasio, Alexandre Reymond, Richard Humbert, Robert Lyle, Michael S. Kuehn, Shane Neph, Peter J. Sabo, Jeff Goldy, Molly Weaver, Andrew Haydock, Kristin Lee, Michael O. Dorschner, Emmanouil T. Dermitzakis, Stylianos E. Antonarakis, J Stamatoyannopoulos	16
15	A novel TMPRSS3 missense mutation in a DFNB8/10 family prevents proteolytic activation of the protein 2005 ·Human Genetics ·Marie Wattenhofer‐Donzé, (unknown), Ditte Andreasen, Ersan Kalay, Refik Çaylan, (unknown), Nicole Fowler‐Jaeger, Alexandre Reymond, Bernard C. Rossier, Ahmet Karagüzel, Stylianos E. Antonarakis	38
16	Comparison of Human Chromosome 21 Conserved Nongenic Sequences (CNGs) With the Mouse and Dog Genomes Shows That Their Selective Constraint Is Independent of Their Genic Environment 2004 ·Genome Research ·Emmanouil T. Dermitzakis, Ewen F. Kirkness, (unknown), Ewan Birney, Alexandre Reymond, Stylianos E. Antonarakis	56
17	Evolutionary Discrimination of Mammalian Conserved Non-Genic Sequences (CNGs) 2003 ·Science ·Emmanouil T. Dermitzakis, Alexandre Reymond, Nathalie Scamuffa, Catherine Ucla, Ewen F. Kirkness, Colette Rossier, Stylianos E. Antonarakis	148
18	Functional genomics of the B-box gene family reveals a possible role in subcellular compartmentalization 1999 ·The American Journal of Human Genetics ·Germana Meroni, Alexandre Reymond, (unknown), Stefano Cairo, Daniela Riganelli, Giuseppe Merla, Elena Zanaria, Silvia Messali, Lucilla Luzi, Alessandro Guffanti, Pier Giuseppe Pelicci, Andrea Ballabio	1
19	Domains of p85^cdc10required for function of the fission yeast DSC-1 factor 1993 ·Nucleic Acids Research ·Alexandre Reymond, Viesturs Simanis	10
20	Mutations in the cdc10 start gene of Schizosaccbaromyces pombe implicate the region of homology between cdc10 and SWl6 as important for p85cdc10 function 1992 ·Molecular and General Genetics MGG ·Alexandre Reymond, Susanne Schmidt, Viesturs Simanis	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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