Author

Дадали Елена Леонидовна

Research Centre for Medical GeneticsORCID 0000-0001-5602-2805Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:database / resource· 1 Approach:experimental assay· 1 Organism:mouse· 1 Approach:statistical model· 1 Organism:zebrafish· 1

Frequent Co-Authors

Akemi J. Tanaka· 1 shared Alexandre ReymondiD· 1 shared Alfredo BruscoiD· 1 shared Anna HurstiD· 1 shared Anna KuchinaiD· 1 shared Anna Mikhaleva· 1 shared Artem O. BorovikoviD· 1 shared Aysylu F. MurtazinaiD· 1 shared

Activity by Year

2019-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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1 shared paperGenetics

Akemi J. Tanaka

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2 papers

Recent·Most cited

Genetic & Genomic MedicineHuman GeneticsPeer-reviewedAug 8, 2026

The Russian FSHD registry: a first look at the cohort

Anna Kuchina, Darya Sherstyukova, Artem O. Borovikov…·Aysylu F. Murtazina

The paper describes the Russian FSHD registry, analyzing clinical and genetic data to identify disease trajectories and demographic patterns in a national cohort.

1 citation

humanstatistical model

𝕏 PostBluesky

GeneticsbioRxivPreprintJul 17, 2019

Variants in the degron of AFF3 cause a multi-system disorder with mesomelic dysplasia, horseshoe kidney and developmental and epileptic encephalopathy

Norine Voisin, Rhonda E. Schnur, Sofia Douzgou…·Alexandre Reymond

The paper identifies degron variants in AFF3 causing a multi-system disorder with specific clinical features and demonstrates phenotypic overlap with AFF4-related syndromes.

DOI 10.1101/693937

humanzebrafish

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