1. Altered auto-phosphorylation of novel TNNI3K variants associated with AV-nodal re-entry tachycardia and conduction disease. (25th November 2020) Authors: Pham, C; Munoz-Martin, N; Podliesna, S; Milano, A; Beekman, L; Vermeer, A; Frantzen, C; Jansen, S; Van De Laar, I; Nieuwhof, K; Christiaans, I; Bezzina, C.R; Lodder, E.M Journal: European heart journal Issue: Volume 41:(2020)Supplement 2 Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Germline SMARCB1 mutation and somatic NF2 mutations in familial multiple meningiomas. Issue 2 (7th October 2010) Authors: Christiaans, I; Kenter, S B; Brink, H C; van Os, T A M; Baas, F; van den Munckhof, P; Kidd, A M J; Hulsebos, T J M Journal: Journal of medical genetics Issue: Volume 48:Issue 2(2011) Page Start: 93 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. P333HCN4 mutations in multiple families with bradycardia and left ventricular noncompaction cardiomyopathy. (15th July 2014) Authors: Milano, A; Vermeer, AMC; Lodder, ER; Barc, J; Verkerk, AO; Van Der Bilt, IAC; Pinto, Y; Christiaans, I; Wilde, AA; Bezzina, CR Journal: Cardiovascular research Issue: Volume 103(2014)Supplement 1 Page Start: S60 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Recurrent variant of unknown significance in KCNH2 classified through functional characterisation. (19th May 2022) Authors: Copier, JS; Bootsma, M; Wilde, AAM; Bertels, RA; Bikker, H; Christiaans, I; Koopmann, TT; Lommerse, AAJ; Bezzina, CR; Verkerk, AO; Barge-Schaapveld, DQCM; Lodder, EM Journal: Europace Issue: Volume 24:Supplement 1(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗