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

Sophie Saunier

Hôpital Necker-Enfants Malades

ORCID: 0000-0002-1069-0047

Also affiliated with Inserm, Université Paris Cité, Institut Necker Enfants Malades, Institut des Maladies Génétiques Imagine

Biochemistry, Genetics and Molecular BiologyMedicine

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 nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitment”.

Novel nephronophthisis-associated variants reveal functional importance of MAPKBP1 dimerization for centriolar recruitment

Kidney International(2020)10.1016/j.kint.2020.05.027

N/A

0DataRank · unranked

12 citations

Wenjun Jin, Anastasia Ertel, Melanie Nemitz‐Kliemchen, Nydia Panitz, Elena Hantmann +12 more

Mutation of Growth Arrest Specific 8 Reveals a Role in Motile Cilia Function and Human Disease

PMC(2020)10.17615/2swt-hn18

N/A

0DataRank · unranked

0 citations

Nicolas F. Berbari, Erik B. Malarkey, Raqual Bower, Sophie Saunier, Jonathan D. Porath +16 more

Implication of transcription factor FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

Kidney International(2023)10.1016/j.kint.2023.11.032

N/A

0DataRank · unranked

9 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Nurit Assia Batzir +55 more

Implication of FOXD2 dysfunction in syndromic congenital anomalies of the kidney and urinary tract (CAKUT)

medRxiv(2023)10.1101/2023.03.21.23287206

N/A

0DataRank · unranked

1 citations

Thanh-Minh T. Nguyen, Can Koşukçu, Julia Calzada‐Wack, Yong Li, Seha Saygılı +47 more