Stephen Viviano

ORCID: 0000-0003-2059-4531

Biochemistry, Genetics and Molecular Biology

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 6 papers. Top paper: “CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability”.

CFAP45, a heterotaxy and congenital heart disease gene, affects cilia stability

Developmental Biology(2023)10.1016/j.ydbio.2023.04.006

N/A

0.500DataRank · unranked

27 citations

Mehreen Pasha, María Elena Guerra, Stephen Viviano, Weidong Ji, Monica Konstantino +7 more

A novel SMARCC1 BAFopathy implicates neural progenitor epigenetic dysregulation in human hydrocephalus

Brain(2023)10.1093/brain/awad405

N/A

0.442DataRank · unranked

18 citations

Garrett Allington, Stephen Viviano, Stephen McGee, Emre Kiziltug, Shaojie Ma +25 more

A novel SMARCC1 -mutant BAFopathy implicates epigenetic dysregulation of neural progenitors in hydrocephalus

medRxiv(2023)10.1101/2023.03.19.23287455

N/A

0.104DataRank · unranked

1 citations

Stephen Viviano, Garrett Allington, Stephen McGee, Emre Kiziltug, Kedous Y. Mekbib +24 more

Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease

Proceedings of the National Academy of Sciences(2023)10.1073/pnas.2214997120

N/A

0DataRank · unranked

20 citations

Tanyeri Barak, Leon D. Kaulen, Octavian Henegariu, Sheng Chih Jin, Stephanie Marie Aguilera +25 more

CC2D1A causes ciliopathy, intellectual disability, heterotaxy, renal dysplasia, and abnormal CSF flow

Life Science Alliance(2024)10.26508/lsa.202402708

N/A

0DataRank · unranked

6 citations

Irmak Sakin, Stephen Viviano, Gülten Tuncel, Stephanie Marie Aguilera, Gizem Goles +15 more

Novel Variants in VARS2 Demonstrate the Phenotypic Variability of a Rare Mitochondriopathy That Responds to Valine Supplementation

Journal of Inherited Metabolic Disease(2025)10.1002/jimd.70053

N/A

0DataRank · unranked

5 citations

Stephen Viviano, Fazliny Abd Rahman, Samuel D. Strohbehn, Aimee Allworth, Norma Pérez +9 more