Elisa De Franco

MedicineBiochemistry, 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 8 papers. Top paper: “Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylation”.

Bi-allelic variants in the ER quality-control mannosidase gene EDEM3 cause a congenital disorder of glycosylation

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.05.010

N/A

0.785DataRank · unranked

21 citations

Andrew C. Edmondson, Sandrine Duvet, Michael March, Ana Berta Sousa, Anna Lehman +23 more

Human inherited PD-L1 deficiency is clinically and immunologically less severe than PD-1 deficiency.

PubMed(2024)10.1084/jem.20231704

N/A

0.452DataRank · unranked

11 citations

Masato Ogishi, Clara Domingo‐Vila, Elisa De Franco, Matthew N. Wakeling, Zineb Imane +22 more

A Non-Coding Disease Modifier of Pancreatic Agenesis Identified by Genetic Correction in a Patient-Derived iPSC Line

Cell stem cell(2020)10.1016/j.stem.2020.05.001

N/A

0DataRank · unranked

26 citations

Elisa De Franco, Fabian L. Cardenas‐Diaz, Lisa R. Letourneau, May Sanyoura, Catherine Osorio-Quintero +5 more

In celebration of a century with insulin – Update of insulin gene mutations in diabetes

Molecular Metabolism(2021)10.1016/j.molmet.2021.101280

N/A

0DataRank · unranked

52 citations

Elisa De Franco, Honggang Ye, Soo-Young Park, Graeme I. Bell, Andrew T. Hattersley +1 more

Update of variants identified in the pancreatic β‐cell K ATP channel genes KCNJ11 and ABCC8 in individuals with congenital hyperinsulinism and diabetes

Human Mutation(2020)10.1002/humu.23995

N/A

0DataRank · unranked

175 citations

Cécile Saint‐Martin, Klaus Brusgaard, Amy E. Knight Johnson, Lydia Aguilar‐Bryan, Pamela Bowman +15 more

Congenital beta cell defects are not associated with markers of islet autoimmunity, even in the context of high genetic risk for type 1 diabetes

Diabetologia(2022)10.1007/s00125-022-05697-3

N/A

0DataRank · unranked

3 citations

William Hagopian, Bart O. Roep, Kashyap A. Patel, Brittany Resnick, Rebecca Dobbs +8 more

Primate-specific ZNF808 is essential for pancreatic development in humans

Nature Genetics(2023)10.1038/s41588-023-01565-x

N/A

0DataRank · unranked

49 citations

Nick Owens, Hossam Montaser, Matthew N. Wakeling, Jonna Saarimäki‐Vire, Athina Triantou +34 more

Loss of function variants in the primate-specific gene ZNF808 cause neonatal, transient and adult-onset diabetes

eBioMedicine(2026)10.1016/j.ebiom.2025.106113

N/A

0DataRank · unranked

0 citations

Kevin Colclough, Matthew B. Johnson, Matthew N Wakeling, Nick D.L. Owens, Shenali Anne Amaratunga +37 more