Luke Mansard

Also affiliated with Université de Montpellier, Centre Hospitalier Universitaire de Montpellier, Institut de Génétique Moléculaire de Montpellier, Institute for Neurosciences of Montpellier, Institut Universitaire de Recherche Clinique

Biochemistry, Genetics and Molecular BiologyNeuroscience

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: “CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis”.

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

Journal of Clinical Investigation(2023)10.1172/jci161156

N/A

0.385DataRank · unranked

12 citations

Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg +28 more

SLC12A2 variants cause a neurodevelopmental disorder or cochleovestibular defect

Brain(2020)10.1093/brain/awaa176

N/A

0DataRank · unranked

49 citations

Emanuela Iovino, Luke Mansard, Christel Vaché, David Baux, Emma Bedoukian +15 more

CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.23.469779

N/A

0DataRank · unranked

0 citations

Kristof Van Schil, Sandra Liakopoulos, Miriam Bauwens, Alfredo Dueñas Rey, Stephan Käseberg +28 more

CEP76 impairment at the centrosome-cilium interface contributes to a spectrum of ciliopathies

Science Advances(2025)10.1126/sciadv.adw3717

N/A

0DataRank · unranked

1 citations

Erika Tavares, Katherine Bishara, Ayşegül Ozantürk, Leila Qebibo, Stephan Frangakis +25 more