Author

Vardiella Meiner

Hadassah Medical CenterORCID 0000-0001-6284-9657Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:gene regulatory network inference· 1 Research Focus:variant effect prediction· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Tamar HareliD· 2 shared Alana R. CowelliD· 1 shared Avital Eilat· 1 shared Ayelet ShaueriD· 1 shared Benjamin T GoultiD· 1 shared Christina Arapatzi· 1 shared Danit Oz-Levi· 1 shared Donna R. ZwasiD· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Tamar HarelORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Reconsidering Silent Variant Unveils SGCA's Role in Atypical Cardiomyopathy

Smadar Horowitz Cederboim, Ronit Hoffman-Lipschuetz, Ronen Y. Durst, Tamar Harel, Shoshi Shpitzen, Ayelet Shauer, Donna R. Zwas, Avital Eilat, Orr Tomer, Vardiella Meiner

The paper identifies a synonymous variant in SGCA causing atypical cardiomyopathy in LGMDR3 patients, highlighting the need for thorough variant interpretation in consanguineous populations.

medRxiv · Feb 10, 2025 · PreprintGenetic & Genomic Medicine

Talin1 dysfunction is genetically linked to systemic capillary leak syndrome.

Naama Elefant, Pinelopi Nikolopoulou, V Vassiliki Papadaki, Danit Oz-Levi, Georgia Rouni, Racheli Sion‐Sarid, William JS Edwards, Christina Arapatzi, Shira Yanovsky‐Dagan, Alana R. Cowell, Vardiella Meiner, Vladimir Vainstein, Sofia Grammenoudi, Doron Lancet, Benjamin T Goult, , Vassiliki Kostourou

The paper identifies a rare TLN1 splice-site variant in a familial SCLS case, linking Talin1 dysfunction to systemic capillary leak syndrome through disrupted endothelial barrier integrity.

JCI Insight · Dec 19, 2024Peer-reviewedGenetic & Genomic Medicine