Céline Schulz

Centre National de la Recherche Scientifique

Also affiliated with Université de Lille, University Hospital Regensburg, Unité de Glycobiologie Structurale et Fonctionnelle, University of Regensburg

Biochemistry, Genetics and Molecular BiologyChemistryImmunology and MicrobiologyMedicine

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 3 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

Absence of the dolichol synthesis gene DHRSX leads to N-glycosylation defects in Lec5 and Lec9 Chinese hamster ovary cells

Journal of Biological Chemistry(2024)10.1016/j.jbc.2024.107875

N/A

0.274DataRank · unranked

5 citations

Charlotte R. Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie N. Graff +9 more

The N-glycosylation defect in Lec5 and Lec9 CHO cells is caused by absence of the DHRSX gene

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.06.18.599300

N/A

0DataRank · unranked

0 citations

Charlotte R. Althoff, Francesco Caligiore, Erika Souche, Céline Schulz, Julie N. Graff +9 more