Yoeri Sleyp

Also affiliated with KU Leuven

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 5 papers. Top paper: “Shared heritability of human face and brain shape”.

Shared heritability of human face and brain shape

Nature Genetics(2021)10.1038/s41588-021-00827-w

N/A

2.4DataRank · unranked

110 citations

Yoeri Sleyp, Hanne Hoskens, Karlijne Indencleef, Jeffrey P. Spence, Rose Bruffaerts +14 more

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Nature Communications(2020)10.1038/s41467-020-18723-y

N/A

0.808DataRank · unranked

218 citations

Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe +95 more

Shared heritability of face and brain shape distinct from cognitive traits

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.29.269258

N/A

0DataRank · unranked

1 citations

Yoeri Sleyp, Hanne Hoskens, Karlijne Indencleef, Jeffrey P. Spence, Rose Bruffaerts +14 more

De novo missense variants in the E3 ubiquitin ligase adaptor KLHL20 cause a developmental disorder with intellectual disability, epilepsy, and autism spectrum disorder

Genetics in Medicine(2022)10.1016/j.gim.2022.08.020

N/A

0DataRank · unranked

10 citations

Irene Valenzuela, Andrea Accogli, Katleen Ballon, Bruria Ben‐Zeev, Samuel F. Berkovic +39 more

Advancing Genotype-Phenotype Analysis through 3D Facial Morphometry: Insights from Cri-du-Chat Syndrome

medRxiv(2025)10.1101/2025.06.01.25327945

N/A

0DataRank · unranked

0 citations

Harold Matthews, Yoeri Sleyp, Peter Hammond, Mark D. Shriver, Seth M. Weinberg +9 more