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Page 1
Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A.
J Exp Med. 2021 Oct 4;218(10):e20201560. doi: 10.1084/jem.20201560. Epub 2021 Aug 13.
J Exp Med. 2021.
PMID: 34387651
Free PMC article.
Diagnosing Autism Spectrum Disorder in Toddlers Born Very Preterm: Estimated Prevalence and Usefulness of Screeners and the Autism Diagnostic Observation Schedule (ADOS).
Vermeirsch J, Verhaeghe L, Casaer A, Faes F, Oostra A, Roeyers H.
Vermeirsch J, et al. Among authors: faes f.
J Autism Dev Disord. 2021 May;51(5):1508-1527. doi: 10.1007/s10803-020-04573-6.
J Autism Dev Disord. 2021.
PMID: 32757085
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Genomic aberrations of the CACNA2D1 gene in three patients with epilepsy and intellectual disability.
Vergult S, Dheedene A, Meurs A, Faes F, Isidor B, Janssens S, Gautier A, Le Caignec C, Menten B.
Vergult S, et al. Among authors: faes f.
Eur J Hum Genet. 2015 May;23(5):628-32. doi: 10.1038/ejhg.2014.141. Epub 2014 Jul 30.
Eur J Hum Genet. 2015.
PMID: 25074461
Free PMC article.
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Congenital fixed dilated pupils due to ACTA2- multisystemic smooth muscle dysfunction syndrome.
Roulez FM, Faes F, Delbeke P, Van Bogaert P, Rodesch G, De Zaeytijd J, Depasse F, Coucke PJ, Meire FM.
Roulez FM, et al. Among authors: faes f.
J Neuroophthalmol. 2014 Jun;34(2):137-43. doi: 10.1097/WNO.0000000000000090.
J Neuroophthalmol. 2014.
PMID: 24621862
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New RAB3GAP1 mutations in patients with Warburg Micro Syndrome from different ethnic backgrounds and a possible founder effect in the Danish.
Morris-Rosendahl DJ, Segel R, Born AP, Conrad C, Loeys B, Brooks SS, Müller L, Zeschnigk C, Botti C, Rabinowitz R, Uyanik G, Crocq MA, Kraus U, Degen I, Faes F.
Morris-Rosendahl DJ, et al. Among authors: faes f.
Eur J Hum Genet. 2010 Oct;18(10):1100-6. doi: 10.1038/ejhg.2010.79. Epub 2010 May 26.
Eur J Hum Genet. 2010.
PMID: 20512159
Free PMC article.
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