Athina Ververi

Biochemistry, Genetics and Molecular BiologyNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 4 papers. Top paper: “Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome”.

Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

Human Molecular Genetics(2020)10.1093/hmg/ddaa050

N/A

0DataRank · unranked

42 citations

Athina Ververi, Ana Beleza‐Meireles, Weizhen Ji, Emily K. Mis, Quinten Patterson +25 more

Restrictive dermopathy due to ZMPSTE24 deficiency

Clinical Dysmorphology(2023)10.1097/mcd.0000000000000453

N/A

0DataRank · unranked

0 citations

Evgeniya Babatseva, Georgıos Mitsiakos, Georgia Karagiannopoulou, Marina Malakozi, Aikaterini Patsatsi +3 more

Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.01.013

N/A

0DataRank · unranked

25 citations

Eva Jacobs, Lies Vantomme, Pontus LeBlanc, Elke Bogaert, Annelies Dheedene +95 more

A novel ABCC9 variant in a Greek family with Cantu syndrome affecting multiple generations highlights the functional role of the SUR2B NBD1

American Journal of Medical Genetics Part A(2024)10.1002/ajmg.a.63815

N/A

0DataRank · unranked

2 citations

Athina Ververi, Ellen J. Thompson, Rob Tryon, Alexandros Sotiriadis, Fotios Rouvalis +4 more