Hilde Peeters

Also affiliated with Center for Human Genetics, 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 17 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

3D facial phenotyping by biometric sibling matching used in contemporary genomic methodologies

PLoS Genetics(2021)10.1371/journal.pgen.1009528

N/A

0.830DataRank · unranked

32 citations

Dongjing Liu, Sahin Naqvi, Myoung Keun Lee, Ryan J. Eller, Karlijne Indencleef +13 more

Insights into the genetic architecture of the human face

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.05.12.090555

N/A

0DataRank · unranked

10 citations

Karlijne Indencleef, Sahin Naqvi, Ryan J. Eller, Jasmien Roosenboom, Myoung Keun Lee +17 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

Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Genome Medicine(2021)10.1186/s13073-021-00870-6

N/A

0DataRank · unranked

117 citations

Tianyun Wang, Kendra Hoekzema, Jill A. Rosenfeld, Pengfei Liu, Hui Guo +95 more

Large-scale open-source three-dimensional growth curves for clinical facial assessment and objective description of facial dysmorphism

Scientific Reports(2021)10.1038/s41598-021-91465-z

N/A

0DataRank · unranked

42 citations

R. Palmer, Gareth Baynam, Oliver Quarrell, Ophir D. Klein, Richard A. Spritz +10 more

Multi-Scale Part-Based Syndrome Classification of 3D Facial Images

IEEE Access(2022)10.1109/access.2022.3153357

N/A

0DataRank · unranked

12 citations

Harold Matthews, Nele Nauwelaers, Michiel Vanneste, Shunwang Gong, Giorgos Bouritsas +9 more

Refining nosology by modelling variation among facial phenotypes: the RASopathies

Journal of Medical Genetics(2022)10.1136/jmedgenet-2021-108366

N/A

0DataRank · unranked

10 citations

Michiel Vanneste, Kaitlin Katsura, David Aponte, Michael A. Patton, Peter Hammond +7 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

A 3D Clinical Face Phenotype Space of Genetic Syndromes using a Triplet-Based Singular Geometric Autoencoder

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.12.27.521999

N/A

0DataRank · unranked

5 citations

Eduarda Caldeira, Harold Matthews, Michiel Vanneste, Nele Nauwelaers, Meng Yuan +11 more

Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.12.07.570544

N/A

0DataRank · unranked

3 citations

Hanne Hoskens, Seppe Goovaerts, Harold Matthews, J. David Aponte, Joanne B. Cole +11 more

Syndrome-informed phenotyping identifies a polygenic background for achondroplasia-like facial variation in the general population

Nature Communications(2024)10.1038/s41467-024-54839-1

N/A

0DataRank · unranked

9 citations

Hanne Hoskens, Seppe Goovaerts, Harold Matthews, Jay Devine, J. David Aponte +12 more

A 3D Clinical Face Phenotype Space of Genetic Syndromes Using a Triplet-Based Singular Geometric Autoencoder

IEEE Access(2024)10.1109/access.2024.3524428

N/A

0DataRank · unranked

1 citations

Eduarda Caldeira, Harold Matthews, Michiel Vanneste, Nele Nauwelaers, Meng Yuan +10 more

Optimized phenotyping of complex morphological traits: enhancing discovery of common and rare genetic variants

Briefings in Bioinformatics(2025)10.1093/bib/bbaf090

N/A

0DataRank · unranked

2 citations

Seppe Goovaerts, M. K. Lee, Jay Devine, Stephen Richmond, Susan Walsh +7 more

Biallelic MADD variants cause a phenotypic spectrum ranging from developmental delay to a multisystem disorder

Brain(2020)10.1093/brain/awaa204

N/A

0DataRank · unranked

59 citations

Fanny Kortüm, Georg Christoph Korenke, Malik Alawi, René Santer, Mathias Woidy +95 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

NCKAP1 Disruptive Variants Lead to a Neurodevelopmental Disorder with Core Features of Autism

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.10.002

N/A

0DataRank · unranked

42 citations

Qiumeng Zhang, Rujia Dai, Bin Yu, Kendra Hoekzema, Jieqiong Tan +53 more