Laurence Legeai‐Mallet

Also affiliated with Université Paris Cité, 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 5 papers. Top paper: “Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy”.

Mutations in the Kinesin-2 Motor KIF3B Cause an Autosomal-Dominant Ciliopathy

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.005

N/A

1.3DataRank · unranked

55 citations

Xénia Latypova, Lokuliyanage Dona Samudita Senaratne, Ludovic Martin, Daniel C. Koboldt, Georgios Kellaris +72 more

Prevention of guanylyl cyclase–B dephosphorylation rescues achondroplastic dwarfism

JCI Insight(2021)10.1172/jci.insight.147832

N/A

0DataRank · unranked

18 citations

Jerid W. Robinson, Yun-Wen Lin, Yi‐Ching Lee, Nabil Kaci, Laurence Legeai‐Mallet +2 more

Phosphatase inhibition by LB-100 enhances BMN-111 stimulation of bone growth

JCI Insight(2021)10.1172/jci.insight.141426

N/A

0DataRank · unranked

13 citations

Nabil Kaci, Jeremy R. Egbert, Thibault Horville, Léa Loisay, Giulia Vigone +8 more

FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse model.

PubMed(2022)10.1084/jem.20201879

N/A

0DataRank · unranked

22 citations

Stéphanie Moriceau, Roman Hossein Khonsari, Yann Heuzé, Léa Loisay, Valérie Boitez +14 more

Embryonic cranial cartilage defects in the Fgfr3Y367C/+ mouse model of achondroplasia

The Anatomical Record(2023)10.1002/ar.25327

N/A

0DataRank · unranked

5 citations

Nishchal Sapkota, Kazuhiko Kawasaki, Yejia Zhang, Danny Z. Chen, Mizuho Kawasaki +5 more