Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: heritabilities von Souren, N. Y, Paulussen, A. D. C, Loos, R. J. F, Gielen, M, Beunen, G, Fagard, R, Derom, C, Vlietinck, R, Zeegers, M. P

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Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq von Koster, R., Brandão, R. D., Tserpelis, D., van Roozendaal, C. E. P., van Oosterhoud, C. N., Claes, K. B. M., Paulussen, A. D. C., Sinnema, M., Vreeburg, M., van der Schoot, V., Stumpel, C. T. R. M., Broen, M. P. G., Spruijt, L., Jongmans, M. C. J., Lesnik Oberstein, S. A. J., Plomp, A. S., Misra-Isrie, M., Duijkers, F. A., Louwers, M. J., Szklarczyk, R., Derks, K. W. J., Brunner, H. G., van den Wijngaard, A., van Geel, M., Blok, M. J.

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Modeling Genetic and Environmental Factors to Increase Heritability and Ease the Identification of Candidate Genes for Birth Weight: A Twin Study von Gielen, M., Lindsey, P. J., Derom, C., Smeets, H. J. M., Souren, N. Y., Paulussen, A. D. C., Derom, R., Nijhuis, J. G.

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Preimplantation genetic testing for more than one genetic condition: clinical and ethical considerations and dilemmas von van der Schoot, V, Dondorp, W, Dreesen, J C F M, Coonen, E, Paulussen, A D C, de Wert, G, de Die-Smulders, C E M

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Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012 von Mersy, E, Smits, L J M, van Winden, L A A P, de Die-Smulders, C E M, Paulussen, A D C, Macville, M V E, Coumans, A B C, Frints, S G M

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BRCA1 mutation carriers have a lower number of mature oocytes after ovarian stimulation for IVF/PGD von Derks-Smeets, I. A. P., van Tilborg, T. C., van Montfoort, A., Smits, L., Torrance, H. L., Meijer-Hoogeveen, M., Broekmans, F., Dreesen, J. C. F. M., Paulussen, A. D. C., Tjan-Heijnen, V. C. G., Homminga, I., van den Berg, M. M. J., Ausems, M. G. E. M., de Rycke, M., de Die-Smulders, C. E. M., Verpoest, W., van Golde, R.

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Postzygotic mosaicism in basal cell naevus syndrome von Reinders, M.G.H.C., Boersma, H.J., Leter, E.M., Vreeburg, M., Paulussen, A.D.C., Arits, A.H.M.M., Roemen, G.M.J.M., Speel, E.J.M., Steijlen, P.M., Geel, M., Mosterd, K.

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Refining the phenotypical and mutational spectrum of Taybi-Linder syndrome von Putoux, A., Alqahtani, A., Pinson, L., Paulussen, A.D.C., Michel, J., Besson, A., Mazoyer, S., Borg, I., Nampoothiri, S., Vasiljevic, A., Uwineza, A., Boggio, D., Champion, F., de Die-Smulders, C.E., Gardeitchik, T., van Putten, W.K., Perez, M.J., Musizzano, Y., Razavi, F., Drunat, S., Verloes, A., Hennekam, R., Guibaud, L., Alix, E., Sanlaville, D., Lesca, G., Edery, P.

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Efficiency of BRCAPRO and Myriad II mutation probability thresholds versus cancer history criteria alone for BRCA1/2 mutation detection von van Harssel, J. J. T., van Roozendaal, C. E. P., Detisch, Y., Brandão, R. D., Paulussen, A. D. C., Zeegers, M., Blok, M. J., Gómez García, E. B.

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Parent-of-origin specific linkage and association of the IGF2 gene region with birth weight and adult metabolic risk factors von Souren, N.Y, Paulussen, A.D.C, Steyls, A, Loos, R.J.F, Brandao, R.D, Gielen, M, Smeets, H.J.M, Beunen, G, Fagard, R, Derom, C, Vlietinck, R, Geraedts, J.P, Zeegers, M.P

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Association between the IL6-174G/C SNP and maximally attained lung function von van den Borst, B, Souren, N Y, Gielen, M, Loos, R J F, Paulussen, A D C, Derom, C, Schols, A M W J, Zeegers, M P A

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A single hERG mutation underlying a spectrum of acquired and congenital long QT syndrome phenotypes von Saenen, J.B, Paulussen, A.D.C, Jongbloed, R.J, Marcelis, C.L, Gilissen, R.A.H.J, Aerssens, J, Snyders, D.J, Raes, A.L

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Pathogenic neurofibromatosis type 1 (NF1) RNA splicing resolved by targeted RNAseq von Koster, R, Brandao, R. D, Tserpelis, D, van Roozendaal, C. E. P, van Oosterhoud, C. N, Claes, Kathleen, Paulussen, A. D. C, Sinnema, M, Vreeburg, M, van der Schoot, V, Stumpel, C. T. R. M, Broen, M. P. G, Spruijt, L, Jongmans, M. C. J, Oberstein, S. A. J. Lesnik, Plomp, A. S, Misra-Isrie, M, Duijkers, F. A, Louwers, M. J, Szklarczyk, R, Derks, K. W. J, Brunner, H. G, van den Wijngaard, A, van Geel, M, Blok, M. J

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Risk factors for drug-induced long-QT syndrome von Paulussen, A D C, Aerssens, J

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Postzygotic mosaicism in basal cell naevus syndrome von Reinders, M G H C, Boersma, H J, Leter, E M, Vreeburg, M, Paulussen, A D C, Arits, A H M M, Roemen, G M J M, Speel, E J M, Steijlen, P M, van Geel, M, Mosterd, K

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Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification von Kamps, Rick, Brandão, Rita D, Bosch, Bianca J van den, Paulussen, Aimee D C, Xanthoulea, Sofia, Blok, Marinus J, Romano, Andrea

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Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro von Natesan, Senthilkumar A., Bladon, Alex J., Coskun, Serdar, Qubbaj, Wafa, Prates, Renata, Munne, Santiago, Coonen, Edith, Dreesen, Joseph C.F.M., Stevens, Servi J.C., Paulussen, Aimee D.C., Stock-Myer, Sharyn E., Wilton, Leeanda J., Jaroudi, Souraya, Wells, Dagan, Brown, Anthony P.C., Handyside, Alan H.

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Diagnostic exome-based preconception carrier testing in consanguineous couples: results from the first 100 couples in clinical practice von Sallevelt, Suzanne C.E.H., Stegmann, Alexander P.A., de Koning, Bart, Velter, Crool, Steyls, Anja, van Esch, Melanie, Lakeman, Phillis, Yntema, Helger, Esteki, Masoud Zamani, de Die-Smulders, Christine E.M., Gilissen, Christian, van den Wijngaard, Arthur, Brunner, Han G., Paulussen, Aimée D.C.

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Preimplantation genetic testing for Neurofibromatosis type 1: more than 20 years of clinical experience von Vernimmen, Vivian, Paulussen, Aimée D C, Dreesen, Jos C F M, van Golde, Ron J, Zamani Esteki, Masoud, Coonen, Edith, van Buul-van Zwet, Marianne L, Homminga, Irene, Derijck, Alwin A H A, Brandts, Lloyd, Stumpel, Constance T R M, de Die-Smulders, Christine E M

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Erythrocyte Inosine triphosphatase activity: A potential biomarker for adverse events during combination antiretroviral therapy for HIV von Peltenburg, N Chantal, Bierau, Jörgen, Bakker, Jaap A, Schippers, Jolanda A, Lowe, Selwyn H, Paulussen, Aimée D C, van den Bosch, Bianca J C, Leers, Mathie P G, Hansen, Bettina E, Verbon, Annelies

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