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Is a standardized severity index needed in unicoronal craniosynostosis? Challenges in developing an objective metric.
van der Straeten R, Lif H, Geoffroy M, Taverne M, Paternoster G, Laporte S, Khonsari RH. 2026. Child's Nervous System.
Evaluation of a New Inclusive Next-Generation Synthetic Face Tool for Dysmorphology.
Benichou L, Breton L, Garcelon N, et al., Khonsari RH. 2026. American Journal of Medical Genetics.
Differential impact of Crouzon and Apert syndromes on upper airways morphology: implications for obstructive sleep apnea.
Remy F, Taverne M, Khonsari RH, Fauroux B, Khirani S, Martinez-Abadias N, Heuzé Y. 2025. Journal of Cranio-Maxillo-Facial Surgery.
The influence of closed sutures on cranial morphology in Apert and Crouzon syndromes: a quantitative analysis.
Delassus O, Ben Bouazza L, Rohée Traoré A, Uguen M, Boddaert N, Germanaud D, Mangin JF, Paternoster G, Taverne M, Khonsari RH. 2025. Journal of Anatomy.
Objective evaluation of 3D modeling or geometric morphometrics enabling patient-specific treatment in craniosynostosis — a systematic review.
Lif H, Taverne M, Paternoster G, Khonsari RH, Nowinski D. 2025. The Journal of Craniofacial Surgery.
Understanding the heterogenicity of unicoronal synostosis — a morphometric analysis of cases compared to controls.
Lif H, Nysjö J, Geoffroy M, Paternoster G, Taverne M, Khonsari RH, Nowinski D. 2024. Journal of Plastic, Reconstructive & Aesthetic Surgery.
Anatomy and mobility in the adult cadaveric craniocervical junction.
Taverne M, Laliève L, Persohn S, Khonsari RH, Paternoster G, James S, Blauwblomme T, Benichi S, Laporte S. 2024. Journal of Morphology.
Geometric growth of the normal human craniocervical junction from 0 to 18 years old.
Raoul-Duval J, Ganet A, Benichi S, et al., Khonsari RH, Taverne M. 2024. Journal of Anatomy.
New diagnostic criteria for metopic ridges and trigonocephaly: a 3D geometric approach.
Bloch K, Geoffroy M, Taverne M, van de Lande L, O'Sullivan E, Liang C, Paternoster G, Moazen M, Laporte S, Khonsari RH. 2024. Orphanet Journal of Rare Diseases.
Next Generation Phenotyping and Synthetic Faces in Coffin Siris Syndrome.
Hennocq Q, Lienhard O, Rao D, et al., Khonsari RH. 2024. Clinical Genetics.
Humanitarian Facial Recognition for Rare Craniofacial Malformations.
Hennocq Q, Bongibault T, Garcelon N, Khonsari RH. 2024. Plastic & Reconstructive Surgery – Global Open.
AI-based diagnosis and phenotype–genotype correlations in syndromic craniosynostoses.
Hennocq Q, Paternoster G, Collet C, et al., Khonsari RH. 2024. Journal of Cranio-Maxillofacial Surgery.
Next generation phenotyping for diagnosis and phenotype–genotype correlations in Kabuki syndrome.
Hennocq Q, Willems M, Amiel J, et al., Khonsari RH, Garcelon N. 2024. Scientific Reports (Nature).
Craniofacial growth and function in achondroplasia: a multimodal 3D study on 15 patients.
Morice A, Taverne M, Eché S, Griffon L, Fauroux B, Leboulanger N, Couloigner V, Baujat G, Picard A, Legeai-Mallet L, Kadlub N, Khonsari RH. 2023. Orphanet Journal of Rare Diseases.
Assessing craniofacial growth and form without landmarks: a new automatic approach based on spectral methods.
Magnet K, Bloch K, Taverne M, Melzi S, Geoffroy M, Khonsari RH, Ovsjanikov M. 2023. Journal of Morphology.
