Quinten Patterson

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

Heterozygous Mutation of Vegfr3 Reduces Renal Lymphatics without Renal Dysfunction

Journal of the American Society of Nephrology(2021)10.1681/asn.2021010061

N/A

0DataRank · unranked

30 citations

Chitkale Hiremath, Quinten Patterson, Saumya Vora, Zhiguo Shang, Andrew R. Jamieson +5 more

Heterozygous mutation of Vegfr3 decreases renal lymphatics but is dispensable for renal function

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.01.17.427041

N/A

0DataRank · unranked

1 citations

Chitkale Hiremath, Quinten Patterson, Saumya Vora, Zhiguo Shang, Andrew R. Jamieson +5 more

Rap1 regulates lumen continuity via Afadin in renal epithelia

Developmental Biology(2023)10.1016/j.ydbio.2023.05.003

N/A

0DataRank · unranked

12 citations

Lei Gao, Kenya Geshow, Quinten Patterson, Haley R. Barlow, Ondine Cleaver +2 more