Author

A. Kuechler

Centre National de la Recherche Scientifique

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Ecology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:statistical model· 2 Research Focus:differential expression· 1 Research Focus:ecology & biodiversity· 1 Organism:human· 1 Organism:multiple species· 1

Frequent Co-Authors

A. Apostolakis· 1 shared A. L. Boesing· 1 shared A. M. Fiore-Donno· 1 shared A. Petersen· 1 shared A. S. Zaitsev· 1 shared A. Vaknin-Dembinsky· 1 shared A. Waheeb· 1 shared Adam JacksoniD· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperEcology

A. Apostolakis

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Author profile →

2 papers

Recent·Most cited

A fast-slow trait continuum at the level of entire communities

M. Neyret, G. Le Provost, A. L. Boesing, F. D. Schneider, D. Baulechner, J. Bergmann, F. de Vries, A. M. Fiore-Donno, S. Geisen, K. Goldmann, A. Kuechler, R. Saifutdinov, N. K. Simons, J. Tobias, A. S. Zaitsev, , Sch

The paper shows that slow and fast functional strategies manifest at the ecosystem level, driven by disturbance and resource availability in grassland communities.

bioRxiv · Jul 12, 2023Ecology

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Joery den Hoed, Elke de Boer, Norine Voisin, Alexander J.M. Dingemans, Nicolas Guex, Laurens Wiel, Christoffer Nellåker, Shivarajan Manickavasagam Amudhavalli, Siddarth Banka, Frederique Sloan Bena, Bruria Ben‐Zeev, Vincent Robert Bonagura, Ange‐Line Bruel, Theresa Brunet, Han G. Brunner, , Lisenka E.L.M. Vissers

The paper identifies mutation-specific pathophysiological mechanisms in SATB1 variants causing distinct neurodevelopmental disorders.

The American Journal of Human Genetics · Jan 28, 2021Peer-reviewedGenetics