Genetics in medicine Genetics in Medicine, 24(10), 2112-2122. Lippincott Williams and Wilkins Genetics in Medicine, 24, 2112-2122 Genetics in Medicine, 24(10), 2112-2122. Nature Publishing Group Genetics in Medicine, 24(10), 2112-2122. ELSEVIER SCIENCE INC Genetics in Medicine, 24(10), 2112-2122. Lippincott Williams & Wilkins Genetics in Medicine, 24, 10, pp. 2112-2122 van den Bersselaar, L M, Verhagen, J M A, Bekkers, J A, Kempers, M, Houweling, A C, Baars, M, Overwater, E, Hilhorst-Hofstee, Y, Barge-Schaapveld, D Q C M, Rompen, E, Krapels, I P C, Dulfer, E, Wessels, M W, Loeys, B L, Verhagen, H J M, Maugeri, A, Roos-Hesselink, J W, Brüggenwirth, H T & van de Laar, I M B H 2022, ' Expanding the genetic and phenotypic spectrum of ACTA2-related vasculopathies in a Dutch cohort ', Genetics in Medicine, vol. 24, no. 10, pp. 2112-2122 . https://doi.org/10.1016/j.gim.2022.07.009 Genetics in medicine, 24(10), 2112-2122. Lippincott Williams and Wilkins
Circulation. Genomic and Precision Medicine, 15, 5, pp. 375-385 van der Meulen, M H, Herkert, J C, den Boer, S L, du Marchie Sarvaas, G J, Blom, N A, ten Harkel, A D J, Breur, H M P J, Rammeloo, L A J, Tanke, R B, Marcelis, C, van de Laar, I M B H, Verhagen, J M A, Lekanne Dit Deprez, R H, Barge-Schaapveld, D Q C M, Baas, A F, Sammani, A, Christiaans, I, van Tintelen, J P & Dalinghaus, M 2022, ' Genetic Evaluation of A Nation-Wide Dutch Pediatric DCM Cohort : The Use of Genetic Testing in Risk Stratification ', Circulation: Genomic and Precision Medicine, vol. 15, no. 5, pp. 375-385 . https://doi.org/10.1161/CIRCGEN.120.002981 Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd. Circulation. Genomic and precision medicine, 15(5), 375-385. Lippincott Williams & Wilkins Circulation. Genomic and precision medicine, 15(5):e002981. LIPPINCOTT WILLIAMS & WILKINS Circulation: Genomic and Precision Medicine, 15(5), 375-385. Lippincott Williams and Wilkins Ltd. Circulation. Genomic and Precision Medicine, 15, 375-385 Circulation: Genomic and Precision Medicine, 15(5), 375-385. LIPPINCOTT WILLIAMS & WILKINS
Neurology, 92, 11, pp. e1225-e1237 Circulation. Genomic and Precision Medicine Neurology Neurology, American Academy of Neurology, 2019, 92 (11), pp.e1225. ⟨10.1212/WNL.0000000000007098⟩ Circ Genom Precis Med Circulation-Genomic and Precision Medicine, 12(9), 397-406. Lippincott Williams & Wilkins Neurology, 92(11), E1225-E1237. Lippincott Williams and Wilkins van der Knaap, M S, Bugiani, M, Mendes, M I, Riley, L G, Smith, D E C, Rudinger-Thirion, J, Frugier, M, Breur, M, Crawford, J, van Gaalen, J, Schouten, M, Willems, M, Waisfisz, Q, Mau-Them, F T, Rodenburg, R J, Taft, R J, Keren, B, Christodoulou, J, Depienne, C, Simons, C, Salomons, G S & Mochel, F 2019, ' Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy ', Neurology, vol. 92, no. 11, pp. E1225-E1237 . https://doi.org/10.1212/WNL.0000000000007098 Neurology, 92, e1225-e1237 Neurology, 92(11), E1225-E1237. American Academy of Neurology Circulation. Genomic and precision medicine, 12(9), 397. Lippincott Williams and Wilkins Ltd. Circulation. Genomic and precision medicine, 12(9), 397-406. LIPPINCOTT WILLIAMS & WILKINS Van Der Knaap, M S, Bugiani, M, Mendes, M I, Riley, L G, Smith, D E C, Rudinger-Thirion, J, Frugier, M, Breur, M, Crawford, J, Van Gaalen, J, Schouten, M, Willems, M, Waisfisz, Q, Mau-Them, F T, Rodenburg, R J, Taft, R J, Keren, B, Christodoulou, J, Depienne, C, Simons, C, Salomons, G S & Mochel, F 2019, ' Biallelic variants in LARS2 and KARS cause deafness and (ovario)leukodystrophy ', Neurology, vol. 92, no. 11, pp. E1225-E1237 . https://doi.org/10.1212/WNL.0000000000007098
Human Mutation Human Mutation, 39(9), 1173-1192. Wiley Human Mutation, 39(9), 1173-1192. Wiley-Liss Inc. Human Mutation, 39, 9, pp. 1173-1192 Human Mutation, 39(9), 1173-1192 Overwater, E, Marsili, L, Baars, M J H, Baas, A F, van de Beek, I, Dulfer, E, van Hagen, J M, Hilhorst-Hofstee, Y, Kempers, M, Krapels, I P, Menke, L A, Verhagen, J M A, Yeung, K K, Zwijnenburg, P J G, Groenink, M, van Rijn, P, Weiss, M M, Voorhoeve, E, van Tintelen, J P, Houweling, A C & Maugeri, A 2018, ' Results of next-generation sequencing gene panel diagnostics including copy-number variation analysis in 810 patients suspected of heritable thoracic aortic disorders ', Human Mutation, vol. 39, no. 9, pp. 1173-1192 . https://doi.org/10.1002/humu.23565 Human Mutation, 39, 1173-1192 Human mutation, 39(9), 1173-1192. Wiley-Liss Inc.