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European Journal of Human Genetics : EJHG|May 2, 2023
Expanding the phenotypic spectrum of NAA10-related neurodevelopmental syndrome and NAA15-related neurodevelopmental syndromeGholson J Lyon, Marall Vedaie, Travis Beisheim, et al.
Clinical Genetics|July 2, 2021
CHEDDA syndrome is an underrecognized neurodevelopmental disorder with a highly restricted ATN1 mutation spectrumElizabeth E Palmer, Chloe Whitton, Mais O Hashem, et al.
ESMO Open|January 11, 2025
Nivolumab combination therapies in patients with advanced gastric and gastroesophageal junction cancer: the phase II FRACTION gastric cancer studyG Ku, G M Haag, H Park, et al.
Molecular Psychiatry|March 11, 2015
Common polygenic risk for autism spectrum disorder (ASD) is associated with cognitive ability in the general populationT-K Clarke, M K Lupton, A M Fernandez-Pujals, et al.
Drugs & Aging|February 12, 2019
EuGMS Task and Finish group on Fall-Risk-Increasing Drugs (FRIDs): Position on Knowledge Dissemination, Management, and Future ResearchL J Seppala, N van der Velde, T Masud, et al.
European Geriatric Medicine|October 15, 2021
EuGMS Task and Finish group on Fall-Risk-Increasing Drugs (FRIDs): Position on Knowledge Dissemination, Management, and Future ResearchL J Seppala, N van der Velde, T Masud, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 3, 2018
Correction: Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 8, 2018
Expanding the clinical phenotype of individuals with a 3-bp in-frame deletion of the NF1 gene (c.2970_2972del): an update of genotype-phenotype correlationMagdalena Koczkowska, Tom Callens, Alicia Gomes, et al.
Theoretical Medicine and Bioethics|October 12, 2012
Peer review versus editorial review and their role in innovative scienceGeorg Steinhauser, Wolfram Adlassnig, Jesaka Ahau Risch, et al.
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