Loeys, Bart

Inborn errors of type I IFN immunity in patients with life-threatening COVID-19

Zhang, Q., Bastard, P., Liu, Z., Le Pen, J., Moncada-Velez, M., Chen, J., Ogishi, M., Sabli, I. K. D., Hodeib, S., Korol, C., et al. (2020) · Science

interferon and immune responsesSARS-CoV-2 and COVID-19 Research

Cited by 2,229

Losartan, an AT1 Antagonist, Prevents Aortic Aneurysm in a Mouse Model of Marfan Syndrome

Habashi, J. P., Judge, D. P., Holm, T. M., Cohn, R. D., Loeys, B. L., Cooper, T. K., Myers, L., Klein, E. C., Liu, G., Calvi, C., et al. (2006) · Science

Connective tissue disorders researchAortic aneurysm repair treatments

Cited by 1,794

Extending the phenotype of recurrent rearrangements of 16p11.2: deletions in mentally retarded patients without autism and in normal individuals

Bijlsma, E. K., Gijsbers, A. C. J., Schuurs-Hoeijmakers, J. H. M., van Haeringen, A., Fransen van de Putte, D. E., Anderlid, B.-M., Lundin, J., Lapunzina, P., Pérez Jurado, L. A., Delle Chiaie, B., et al. (2009) · European Journal of Medical Genetics

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 282

Ehlers-Danlos syndromes and Marfan syndrome

Callewaert, B., Malfait, F., Loeys, B., & De Paepe, A. (2008) · Best Practice & Research Clinical Rheumatology

Connective tissue disorders researchDermatological and Skeletal Disorders

Cited by 257

Biallelic loss of proprioception-related PIEZO2 causes muscular atrophy with perinatal respiratory distress, arthrogryposis, and scoliosis

Delle Vedove, A., Storbeck, M., Heller, R., Hölker, I., Hebbar, M., Shukla, A., Magnusson, O., Cirak, S., Girisha, K. M., O’Driscoll, M., et al. (2016) · The American Journal of Human Genetics

Hereditary Neurological DisordersMuscle Physiology and Disorders

Cited by 97

Recognizing the tenascin‐X deficient type of Ehlers–Danlos syndrome: a cross‐sectional study in 17 patients

Demirdas, S., Dulfer, E., Robert, L., Kempers, M., van Beek, D., Micha, D., van Engelen, B. G., Hamel, B., Schalkwijk, J., Loeys, B., et al. (2017) · Clinical Genetics

Connective tissue disorders researchGenomics and Rare Diseases

Cited by 60

Renal insufficiency, a frequent complication with age in oral‐facial‐digital syndrome type I

Saal, S., Faivre, L., Aral, B., Gigot, N., Toutain, A., Van Maldergem, L., Destree, A., Maystadt, I., Cosyns, J., Jouk, P., et al. (2010) · Clinical Genetics

Genetic and Kidney Cyst DiseasesGenomics and Rare Diseases

Cited by 36

Partial anomalous pulmonary venous return in Turner syndrome

van den Hoven, A. T., Chelu, R. G., Duijnhouwer, A. L., Demulier, L., Devos, D., Nieman, K., Witsenburg, M., van den Bosch, A. E., loeys, B. L., van Hagen, I. M., et al. (2017) · European Journal of Radiology

Congenital Heart Disease StudiesVascular anomalies and interventions

Cited by 32