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European Journal of Human Genetics : EJHG|June 4, 2015
Towards a European consensus for reporting incidental findings during clinical NGS testingJayne Y Hehir-Kwa, Mireille Claustres, Ros J Hastings, et al.European Journal of Human Genetics : EJHG|June 30, 2005
Molecular characterisation of patients with subtelomeric 22q abnormalities using chromosome specific array-based comparative genomic hybridisationDavid A Koolen, William Reardon, Elisabeth M Rosser, et al.Nature Reviews. Endocrinology|May 28, 2020
International consensus on the diagnosis and management of dumping syndromeEmidio Scarpellini, Joris Arts, George Karamanolis, et al.Nature Genetics|November 16, 2010
A de novo paradigm for mental retardationLisenka E L M Vissers, Joep de Ligt, Christian Gilissen, et al.Immunity, Inflammation and Disease|October 27, 2022
Exploratory analysis of interleukin-38 in hospitalized COVID-19 patientsDennis M de Graaf, Lisa U Teufel, Aline H de Nooijer, et al.American Journal of Medical Genetics. Part A|October 13, 2011
MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletionsServi J C Stevens, Conny M A van Ravenswaaij-Arts, Jannie W H Janssen, et al.Otology & Neurotology : Official Publication of the American Otological Society, American Neurotology Society [And] European Academy of Otology and Neurotology|May 12, 2001
Hearing rehabilitation using the BAHA bone-anchored hearing aid: results in 40 patientsL R Lustig, H A Arts, D E Brackmann, et al.Journal of Clinical Lipidology|December 4, 2019
High-density lipoprotein cholesterol efflux capacity is not associated with atherosclerosis and prevalence of cardiovascular outcome: The CODAM studyTatjana Josefs, Kristiaan Wouters, Uwe J F Tietge, et al.Communications Materials|July 21, 2025
Evaluation of in situ tissue-engineered arteriovenous grafts suitable for cannulation in a large animal modelPaul J Besseling, Wojciech Szymczyk, Martin Teraa, et al.American Journal of Human Genetics|May 13, 2003
Definition of a critical region on chromosome 18 for congenital aural atresia by arrayCGHJoris A Veltman, Yvonne Jonkers, Inge Nuijten, et al.Pageof 204