🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Arnaud Bruneel

ORCID: 0000-0001-8411-3309

Also affiliated with Université Paris-Saclay, Assistance Publique – Hôpitaux de Paris, Hôpital Bichat-Claude-Bernard

Biochemistry, Genetics and Molecular BiologyImmunology and MicrobiologyChemistry

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: “Consensus guideline for the diagnosis and management of mannose phosphate isomerase‐congenital disorder of glycosylation”.

Consensus guideline for the diagnosis and management of mannose phosphate isomerase‐congenital disorder of glycosylation

Journal of Inherited Metabolic Disease(2020)10.1002/jimd.12241

N/A

0.628DataRank · unranked

65 citations

Ruqaiah Altassan, Delphine Borgel, Arnaud Bruneel, Joana Correia, M Girard +16 more

A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.04.013

N/A

0DataRank · unranked

22 citations

Paulina Sosicka, François Fenaille, Annie Harroche, Sandrine Vuillaumier‐Barrot, Mindy Porterfield +27 more

Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy

Brain(2022)10.1093/brain/awac110

N/A

0DataRank · unranked

20 citations

Johanne Dubail, Sergio Aguilera, Chiara Paganini, Catherine Vanhulle, Walid Haouari +12 more