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

Caroline Michot

Hôpital Necker-Enfants Malades

ORCID: 0000-0002-8749-5899

Also affiliated with Inserm, Université Paris Cité, Institut Necker Enfants Malades

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 3 papers. Top paper: “A mutation in SLC37A4 causes a dominantly inherited congenital disorder of glycosylation characterized by liver dysfunction”.

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

A novel COL1A1 variant in a family with clinical features of hypermobile Ehlers‐Danlos syndrome that proved to be a COL1‐related overlap disorder

Clinical Case Reports(2021)10.1002/ccr3.4128

N/A

0DataRank · unranked

8 citations

Philippe de Mazancourt, Corinne Métay, Robert Carlier, Valérie Allamand, Corine Gartioux +8 more

Loss of function variants in ADAMTS6 : Connective tissue, Heart defect, thoracic Aortic aneurysm and Neuro developmental Syndrome (CHANS)

medRxiv(2025)10.1101/2025.05.02.25326573

N/A

0DataRank · unranked

1 citations

Pauline Arnaud, Angélique Bibimbou, Deborah E. Seifert, Zakaria Mougin, Louise Benarroch +18 more