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The Clinical Neuropsychologist|September 3, 2010
Developmental profile and trajectory of neuropsychological skills in a child with Kabuki syndrome: implications for assessment of syndromes associated with intellectual disabilityJacqueline H Sanz, Paul Lipkin, Kenneth Rosenbaum, et al.
The Lancet. Digital Health|September 5, 2021
Development and evaluation of a machine learning-based point-of-care screening tool for genetic syndromes in children: a multinational retrospective studyAntonio R Porras, Kenneth Rosenbaum, Carlos Tor-Diez, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|January 9, 2015
Ensemble learning for the detection of facial dysmorphologyQian Zhao, Naoufel Werghi, Kazunori Okada, et al.
Medical Image Computing and Computer-Assisted Intervention : MICCAI ... International Conference on Medical Image Computing and Computer-Assisted Intervention|March 1, 2014
Hierarchical constrained local model using ICA and its application to Down syndrome detectionQian Zhao, Kazunori Okada, Kenneth Rosenbaum, et al.
Annual International Conference of the IEEE Engineering in Medicine and Biology Society. IEEE Engineering in Medicine and Biology Society. Annual International Conference|October 11, 2013
Automated Down syndrome detection using facial photographsQian Zhao, Kenneth Rosenbaum, Kazunori Okada, et al.
Medical Image Analysis|May 20, 2014
Digital facial dysmorphology for genetic screening: Hierarchical constrained local model using ICAQian Zhao, Kazunori Okada, Kenneth Rosenbaum, et al.
Frontiers in Pediatrics|April 4, 2022
Case Report: A Case Study on the Neurodevelopmental Profile of a Child With Pallister-Killian Syndrome and His Unaffected TwinCarole A Samango-Sprouse, Mary P Hamzik, Kenneth Rosenbaum, et al.
American Journal of Human Genetics|March 3, 2015
Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic featuresEmma Tham, Anna Lindstrand, Avni Santani, et al.
American Journal of Medical Genetics. Part A|March 19, 2008
Clinical and molecular analysis of arylsulfatase E in patients with brachytelephalangic chondrodysplasia punctataMichelle Nino, Claudia Matos-Miranda, Momoe Maeda, et al.
American Journal of Medical Genetics. Part A|November 16, 2007
Muenke syndrome (FGFR3-related craniosynostosis): expansion of the phenotype and review of the literatureEmily S Doherty, Felicitas Lacbawan, Donald W Hadley, et al.
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