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Zuurremmers: hoog inzetten, of juist laag? Het DIAMOND-onderzoek naar effectiviteit en kosten van de step-up en de step-downbenadering bij maagklachten in de eerste lijn.
Marrewijk, C.J. van ; Mujakovic, S. ; Fransen, G.A.J. ; Numans, M.E.; Wit, N.J. de; Muris, J.W.M.; Oijen, M.G.H. van ; Jansen, J.B.M.J. ; Grobbee, D.E.; Knottnerus, J.A.; Laheij, R.J.F. et al. sine al.
2009, Article / Letter to editor (Huisarts en Wetenschap, vol. 52, iss. 8, (2009), pp. 374-381)
ZNF674: A New Kruppel-Associated Box-Containing Zinc-Finger Gene Involved in Nonsyndromic X-Linked Mental Retardation
Lugtenberg, D. ; Yntema, H.G. ; Banning, M.J.G. ; Oudakker, A.R. ; Firth, H.; Willatt, L.; Raynaud, M.; Kleefstra, T. ; Fryns, J.P. ; Ropers, H.H.; Chelly, J. ; Moraine, C.; Gecz, J. ; Reeuwijk, J. van ; Nabuurs, S.B. ; Vries, L.B.A. de ; Hamel, B.C.J. ; Brouwer, A.P.M. de ; Bokhoven, J.H.L.M. van et al. sine al.
2006, Article / Letter to editor (American Journal of Human Genetics, vol. 78, iss. 2, (2006), pp. 265-278)
ZNF506-dependent positive feedback loop regulates H2AX signaling after DNA damage
Nowsheen, S.; Aziz, K.; Luo, K.; Deng, M.; Qin, B.; Yuan, J.; Jeganathan, K.B.; Yu, J. ; Zhang, H.; Ding, W.; Deursen, J.M.A. van ; Lou, Z. et al. sine al.
2018, Article / Letter to editor (Nature Communications, vol. 9, iss. 1, (2018), article 2736)
Zinc supplementation inhibits complement activation in age-related macular degeneration
Smailhodzic, D. ; Asten, F van; Blom, A.M.; Mohlin, F.C.; Hollander, A.I. den ; Ven, J.P.H. van de; Huet, R.A.C. van ; Groenewoud, J.M.M. ; Tian, Y.; Berendschot, T.T.; Lechanteur, Y.T.E. ; Fauser, S.; Bruijn, C. de; Daha, M.R.; Wilt, G.J. van der ; Hoyng, C.B. ; Klevering, B.J. et al. sine al.
2014, Article / Letter to editor (PLoS One, vol. 9, iss. 11, (2014), article e112682)
Zinc finger 81 (ZNF81) mutations associated with X-linked mental retardation.
Kleefstra, T. ; Yntema, H.G. ; Oudakker, A.R. ; Banning, M.J.G. ; Kalscheuer, V.M.M.; Chelly, J.; Moraine, C.; Ropers, H.H.; Fryns, J.P.; Janssen, I.M. ; Sistermans, E.A. ; Nillesen, W.M.; Vries, L.B.A. de ; Hamel, B.C.J. ; Bokhoven, J.H.L.M. van et al. sine al.
2004, Article / Letter to editor (Journal of Medical Genetics, vol. 41, iss. 5, (2004), pp. 394-399)
Zimmermann-Laband syndrome in a patient with severe mental retardation
Buggenhout, G.J.C.M. van; Brunner, H.G. ; Trommelen, J.C.M.; Hamel, B.C.J.
1995, Article / Letter to editor (Genetic Counseling, vol. 6, iss. 4, (1995), pp. 321)
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction
Gabriele, M.; Vulto-van Silfhout, A.T. ; Germain, P.L.; Vitriolo, A.; Kumar, R.; Douglas, E.; Haan, E.; Kosaki, K.; Takenouchi, T.; Rauch, A.; Steindl, K.; Frengen, E.; Misceo, D.; Pedurupillay, C.R.; Stromme, P.; Rosenfeld, J.A.; Shao, Y.; Craigen, W.J.; Schaaf, C.P.; Rodriguez-Buritica, D.; Farach, L.; Friedman, J.; Thulin, P.; McLean, S.D.; Nugent, K.M.; Morton, J.; Nicholl, J.; Andrieux, J.; Stray-Pedersen, A.; Chambon, P.; Patrier, S.; Lynch, S.A.; Kjaergaard, S.; Torring, P.M.; Brasch-Andersen, C.; Ronan, A.; Haeringen, A. van; Anderson, P.J.; Powis, Z.; Brunner, H.G. ; Pfundt, R.P. ; Schuurs-Hoeijmakers, J.H.M. ; Bon, B.W.M. van ; Lelieveld, S.H.; Gilissen, C.F. ; Nillesen, W.M.; Vissers, L.E.L.M. ; Gecz, J.; Koolen, D.A. ; Testa, G.; Vries, B.B. de et al. sine al.
2017, Article / Letter to editor (American Journal of Human Genetics, vol. 100, iss. 6, (2017), pp. 907-925)
Young age and a positive family history of colorectal cancer are complementary selection criteria for the identification of Lynch syndrome
Manders, P. ; Spruijt, L. ; Kets, C.M. ; Willems, H.W. ; Bodmer, D. ; Hebeda, K.M. ; Nagtegaal, I.D. ; Krieken, J.H. van ; Ligtenberg, M.J.L. ; Hoogerbrugge, N.
2011, Article / Letter to editor (European Journal of Cancer, vol. 47, iss. 9, (2011), pp. 1407-1413)
Yeast artificial chromosome cloning of the Xq13.3-q21.31 region and fine mapping of a deletion associated with choroideremia and nonspecific mental retardation
Maarel, S.M. van der; Scholten, I.H.J.M.; Maat-Kievit, J.A.; Huber, I.; Kok, Y.J.M. de; Wijs, I.J. de; Pol, T.J.R. van de; Bokhoven, H. van ; Dunnen, J.T. den ; Ommen, G.J.B. van; Philippe, C.; Monaco, A.P.; Smeets, H.J.M. ; Ropers, H.-H.; Cremers, F.P.M. et al. sine al.
1995, Article / Letter to editor (European Journal of Human Genetics, vol. 3, iss. 4, (1995), pp. 207-218)
Y chromosome mosaicism is associated with age-related macular degeneration
Grassmann, F.; Kiel, C.; Hollander, A.I. den ; Weeks, D.E.; Lotery, A.; Cipriani, V.; Weber, B.H.
2019, Article / Letter to editor (European Journal of Human Genetics, vol. 27, iss. 1, (2019), pp. 36-41)
XRCC1 and XPD DNA repair gene polymorphisms: a potential risk factor for glaucoma in the Pakistani population
Yousaf, S.; Khan, M.I. ; Micheal, S.; Akhtar, F.; Ali, S.H.; Riaz, M.; Ali, M.; Lall, P.; Waheed, N.K.; Hollander, A.I. den ; Ahmed, A.; Qamar, R. et al. sine al.
2011, Article / Letter to editor (Molecular Vision, vol. 17, (2011), pp. 1153-1163)
Xq13.2q21.1 duplication encompassing the ATRX gene in a man with mental retardation, minor facial and genital anomalies, short stature and broad thorax.
Lugtenberg, D. ; Brouwer, A.P.M. de ; Oudakker, A.R. ; Pfundt, R.P. ; Hamel, B.C.J. ; Bokhoven, H. van ; Bongers, E.M.H.F.
2009, Article / Letter to editor (American Journal of Medical Genetics. Part A, vol. 149A, iss. 4, (2009), pp. 760-766)
Xeroderma pigmentosum-Cockayne syndrome complex : a further case
Hamel, B.C.J. ; Raams, A.; Schuitema-Dijkstra, A.R.; Simons, P.J.; Burgt, C.J.A. van der; Jaspers, N.G.J.; Kleijer, W.J.
1996, Article / Letter to editor (Journal of Medical Genetics, vol. 33, iss. 7, (1996), pp. 607-610)
X-linked sideroblastic anemia due to ALAS2 intron 1 enhancer element GATA-binding site mutations
Campagna, D.R.; Bie, C.I. De; Schmitz-Abe, K.; Sweeney, M.; Sendamarai, A.K.; Schmidt, P.J.; Heeney, M.M.; Yntema, H.G. ; Kannengiesser, C.; Grandchamp, B.; Niemeyer, C.M.; Knoers, N.V.A.M. ; Swart, S.; Marron, G.; Wijk, R. van; Raymakers, R.A.P. ; May, A.; Markianos, K.; Bottomley, S.S.; Swinkels, D.W. ; Fleming, M.D. et al. sine al.
2014, Article / Letter to editor (American Journal of Hematology, vol. 89, iss. 3, (2014), pp. 315-319)
X-linked primary ciliary dyskinesia due to mutations in the cytoplasmic axonemal dynein assembly factor PIH1D3.
Olcese, C.; Patel, M.P.; Shoemark, A.; Kiviluoto, S.; Legendre, M.; Williams, H.J.; Vaughan, C.K.; Hayward, J.; Goldenberg, A.; Emes, R.D.; Munye, M.M.; Dyer, L.; Cahill, T.; Bevillard, J.; Gehrig, C.; Guipponi, M.; Chantot, S.; Duquesnoy, P.; Thomas, L.; Jeanson, L.; Copin, B.; Tamalet, A.; Thauvin-Robinet, C.; Papon, J.F.; Garin, A.; Pin, I.; Vera, G.; Aurora, P.; Fassad, M.R.; Jenkins, L.; Boustred, C.; Cullup, T.; Dixon, M.; Onoufriadis, A.; Bush, A.; Chung, E.M.; Antonarakis, S.E.; Loebinger, M.R.; Wilson, R.; Armengot, M.; Escudier, E.; Hogg, C.; Amselem, S.; Sun, Z.; Bartoloni, L.; Blouin, J.L.; Mitchison, H.M.; Schmidts, M. ; et al. et al. sine al.
2017, Article / Letter to editor (Nature Communications, vol. 8, (2017), pp. 14279)
X-linked mental retardation: further lumping, splitting and emerging phenotypes.
Kleefstra, T. ; Hamel, B.C.J.
2005, Article / Letter to editor (Clinical Genetics, vol. 67, iss. 6, (2005), pp. 451-467)
X-linked mental retardation: a comprehensive molecular screen of 47 candidate genes from a 7.4 Mb interval in Xp11.
Jensen, L.R.; Lenzner, S.; Moser, B.; Freude, K.; Tzschach, A.; Wei, C.; Fryns, J.P.; Chelly, J.; Turner, G.; Moraine, C.; Hamel, B.C.J. ; Ropers, H.H.; Kuss, A.W. et al. sine al.
2007, Article / Letter to editor (European Journal of Human Genetics, vol. 15, iss. 1, (2007), pp. 68-75)
X-linked mental retardation.
Ropers, H.H.; Hamel, B.C.J.
2005, Article / Letter to editor (Nature Reviews. Genetics, vol. 6, iss. 1, (2005), pp. 46-57)
X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family.
Laumonnier, F.; Bonnet-Brilhault, F.; Gomot, M.; Blanc, R.; David, A.; Moizard, M.P.; Raynaud, M.; Ronce, N.; Lemonnier, E.; Calvas, P.; Laudier, B.; Chelly, J.; Fryns, J.P.; Ropers, H.H.; Hamel, B.C.J. ; Andres, C.; Barthelemy, C.; Moraine, C.; Briault, S. et al. sine al.
2004, Article / Letter to editor (American Journal of Human Genetics, vol. 74, iss. 3, (2004), pp. 552-557)
X-linked mental retardation : a clinical and molecular study
Hamel, Bernardus Carolus Josephus
1999, Dissertation
X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation
Synofzik, M.; Muller vom Hagen, M.; Haack, T.B.; Wilhelm, C.; Lindig, T.; Beck-Wodl, S.; Nabuurs, S.B. ; Kuilenburg, A.B.P. van; Brouwer, A.P. de ; Schols, L.
2014, Article / Letter to editor (Orphanet Journal of Rare Diseases, vol. 9, iss. 1, (2014), pp. 24)
X chromosome inactivation does not define the development of premature ovarian failure in fragile X premutation carriers.
Spath, M.A. ; Nillesen, W.M.; Smits, A.P.T. ; Feuth, A.B. ; Braat, D.D.M. ; Geurts van Kessel, A.H.M. ; Yntema, H.G.
2010, Article / Letter to editor (American Journal of Medical Genetics. Part A, vol. 152A, iss. 2, (2010), pp. 387-393)
Women's Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results
Schendel, R.V. van; Page-Christiaens, G.; Beulen, L. ; Bilardo, C.M.; Boer, M.A. de; Coumans, A.B.C.; Faas, B.H.W. ; Langen, I.M. van; Lichtenbelt, K.D.; Maarle, M.C. van; Macville, M.V.E.; Oepkes, D.; Pajkrt, E.; Henneman, L. et al. sine al.
2017, Article / Letter to editor (Journal of Genetic Counseling, vol. 26, iss. 6, (2017), pp. 1348-1356)
Women's Attitudes towards the Option to Choose between Karyotyping and Rapid Targeted Testing during Pregnancy
Kooper, A.J.A. ; Smeets, D.F.C.M. ; Feenstra, I. ; Wijnberger, L.D.; Rijnders, R.J.; Quartero, R.W.; Boekkooi, P.F.; Vugt, J.M.G. van; Smits, A.P.T.
2013, Article / Letter to editor (Obstetrics and Gynecology International, vol. 2013, (2013), pp. 636459)
Women's and healthcare professionals' preferences for prenatal testing: a discrete choice experiment
Beulen, L. ; Grutters, J.P.C. ; Faas, B.H.W. ; Feenstra, I. ; Groenewoud, H. ; Vugt, J.M.G. van; Bekker, M.N.
2015, Article / Letter to editor (Prenatal Diagnosis, vol. 35, iss. 6, (2015), pp. 549-557)
WNT5A mutations in patients with autosomal dominant Robinow syndrome.
Person, A.D.; Beiraghi, S.; Sieben, C.M.; Hermanson, S.; Neumann, A.N.; Robu, M.E.; Schleiffarth, J.R.; Billington, C.J.; Bokhoven, J.H.L.M. van ; Hoogeboom, J.M.; Mazzeu, J.F.; Petryk, A.; Schimmenti, L.A.; Brunner, H.G. ; Ekker, S.C.; Lohr, J.L. et al. sine al.
2010, Article / Letter to editor (Developmental Dynamics, vol. 239, iss. 1, (2010), pp. 327-337)
Wnt5a Deficiency Leads to Anomalies in Ureteric Tree Development, Tubular Epithelial Cell Organization and Basement Membrane Integrity Pointing to a Role in Kidney Collecting Duct Patterning
Pietila, I.; Prunskaite-Hyyrylainen, R.; Kaisto, S.; Tika, E.; Eerde, A.M. van; Salo, A.M.; Garma, L.; Miinalainen, I.; Feitz, W.F.J. ; Bongers, E.M.H.F. ; Juffer, A.; Knoers, N.V.; Renkema, K.Y.; Myllyharju, J.; Vainio, S.J. et al. sine al.
2016, Article / Letter to editor (PLoS One, vol. 11, iss. 1, (2016), article e0147171)
WNT Signaling Perturbations Underlie the Genetic Heterogeneity of Robinow Syndrome
White, J.J.; Mazzeu, J.F.; Coban-Akdemir, Z.; Bayram, Y.; Bahrambeigi, Vahid; Hoischen, A. ; Bon, B.W. van ; Brunner, H.G. ; Lupski, J.R.; Carvalho, C.M.
2018, Article / Letter to editor (American Journal of Human Genetics, vol. 102, iss. 1, (2018), pp. 27-43)
Whole-genome sequencing reveals important role for TBK1 and OPTN mutations in frontotemporal lobar degeneration without motor neuron disease
Pottier, C.; Bieniek, K.F.; Finch, N.; Vorst, M. van de; Baker, M.; Perkersen, R.; Brown, P.; Ravenscroft, T.; Blitterswijk, M. van; Nicholson, A.M.; DeTure, M.; Knopman, D.S.; Josephs, K.A.; Parisi, J.E.; Petersen, R.C.; Boylan, K.B.; Boeve, B.F.; Graff-Radford, N.R.; Veltman, J.A. ; Gilissen, C.; Murray, M.E.; Dickson, D.W.; Rademakers, R. et al. sine al.
2015, Article / Letter to editor (Acta Neuropathologica, vol. 130, iss. 1, (2015), pp. 77-92)
Whole-genome sequencing of spermatocytic tumors provides insights into the mutational processes operating in the male germline
Giannoulatou, E.; Maher, G.J.; Ding, Z.; Gillis, A.J.; Dorssers, L.C.J.; Hoischen, A. ; Rajpert-De Meyts, E.; McVean, G.; Wilkie, A.O.M.; Looijenga, L.H.J.; Goriely, A. et al. sine al.
2017, Article / Letter to editor (PLoS One, vol. 12, iss. 5, (2017), article e0178169)
Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics
El, C.G. van; Cornel, M.C.; Borry, P.; Hastings, R.J.; Fellmann, F.; Hodgson, S.; Howard, H.C.; Cambon-Thomsen, A.; Knoppers, B.M.; Meijers-Heijboer, H.; Scheffer, H. ; Tranebjaerg, L.; Dondorp, W.; Wert, G.M.W.R. de ; Committee, E.P.a.P.P. et al. sine al.
2013, Article / Letter to editor (European Journal of Human Genetics, vol. 21, iss. 6, (2013), pp. 580-584)
Whole-genome sequence variation, population structure and demographic history of the Dutch population
Francioli, L.C.; Menelaou, A.; Pulit, S.L.; Dijk, F. van; Palamara, P.F.; Elbers, C.C. ; Neerincx, P.B.; Ye, K.; Guryev, V.; Kloosterman, W.P.; Deelen, P.; Abdellaoui, A.; Leeuwen, E.M. van; Oven, M. van; Vermaat, M.; Li, M.; Laros, J.F.; Karssen, L.C.; Kanterakis, A.; Amin, N.; Hottenga, J.J.; Lameijer, E.W.; Kattenberg, M.; Dijkstra, M.; Byelas, H.; Setten, J. van; Schaik, B.D. van; Bot, J.; Nijman, I.J.; Renkens, I.; Marschall, T.; Schönhuth, A.; Hehir-Kwa, J.Y. ; Handsaker, R.E.; Polak, P.; Sohail, M.; Vuzman, D.; Hormozdiari, F.; Enckevort, D. van; Mei, H.; Koval, V.; Moed, M.H.; Velde, K.J. van der; Rivadeneira, F.; Estrada, K.; Medina-Gomez, C.; Isaacs, A.; McCarroll, S.A.; Beekman, M.; Craen, A.J. de; Suchiman, H.E.; Hofman, A.; Oostra, B.; Uitterlinden, A.G.; Willemsen, G.; Platteel, M.; Veldink, J.H.; Berg, L.H. van den ; Pitts, S.J.; Potluri, S.; Sundar, P.; Cox, D.R.; Sunyaev, S.R.; Dunnen, J.T. den; Stoneking, M.; Knijff, P. de ; Kayser, M.; Li, Q.; Li, Y.; Du, Y.; Chen, R.; Cao, H.; Li, N.; Cao, S.; Wang, J; Bovenberg, J.A.; Pe'er, I.; Slagboom, P.E.; Duijn, C.M. van; Boomsma, D.I. ; Ommen, G.J. van; Bakker, P.I. de; Swertz, M.A.; Wijmenga, C. et al. sine al.
2014, Article / Letter to editor (Nature Genetics, vol. 46, iss. 8, (2014), pp. 818-825)
Whole-genome methylation profiling of the retinal pigment epithelium of individuals with age-related macular degeneration reveals differential methylation of the SKI, GTF2H4, and TNXB genes
Porter, L.F.; Saptarshi, Neil; Fang, Yongxiang; Rathi, Sonika; Hollander, A.I. den ; Jong, E.K. de ; Chavali, Venkata R.M.; Paraoan, Luminita
2019, Article / Letter to editor (Clinical Epigenetics, vol. 11, (2019), article 6)
Whole-genome array comparative genome hybridization: the preferred diagnostic choice in postnatal clinical cytogenetics.
Veltman, J.A. ; Vries, B.B. van
2007, Article / Letter to editor (Journal of Molecular Diagnostics, vol. 9, iss. 2, (2007), pp. 277)
Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis
Cnossen, W.R.; Morsche, R.H.M. te ; Hoischen, A. ; Gilissen, C.F. ; Chrispijn, M. ; Venselaar, H. ; Mehdi, S.; Bergmann, C.; Veltman, J.A. ; Drenth, J.P.H.
2014, Article / Letter to editor (Proceedings of the National Academy of Sciences USA, vol. 111, iss. 14, (2014), pp. 5343-5348)
Whole-exome sequencing points to considerable genetic heterogeneity of cerebral palsy
McMichael, G.; Bainbridge, M.N.; Haan, E.; Corbett, M.; Gardner, A.; Thompson, S.; Bon, B.W.M. van ; Eyk, C.L. van; Broadbent, J.; Reynolds, C.; O'Callaghan, M.E.; Nguyen, L.S.; Adelson, D.L.; Russo, R.; Jhangiani, S.; Doddapaneni, H.; Muzny, D.M.; Gibbs, R.A.; Gecz, J.; MacLennan, A.H. et al. sine al.
2015, Article / Letter to editor (Molecular Psychiatry, vol. 20, iss. 2, (2015), pp. 176-182)
Whole exome sequencing of suspected mitochondrial patients in clinical practice
Wortmann, S.B.; Koolen, D.A. ; Smeitink, J.A.M. ; Heuvel, L.P.W.J. van den ; Rodenburg, R.J.T.
2015, Article / Letter to editor (Journal of Inherited Metabolic Disease, vol. 38, iss. 3, (2015), pp. 437-443)
Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis
Saes, J.L. ; Simons, A. ; Munnik, S.A. de ; Nijziel, M.R.; Blijlevens, N.M.A. ; Jongmans, M.C. ; Reijden, B.A. van der ; Brons, P.P. ; Heerde, W.L. van ; Schols, S.E.M.
2019, Article / Letter to editor (Haemophilia, vol. 25, iss. 1, (2019), pp. 127-135)
Whole Exome Sequencing in Patients with the Cuticular Drusen Subtype of Age-Related Macular Degeneration
Duvvari, M.R.; Ven, J.P.H. van de; Geerlings, M.J. ; Saksens, N.T.M. ; Bakker, B. ; Henkes, A.; Neveling, K. ; Rosario, M. del ; Westra, D. ; Heuvel, B. van den ; Schick, T.; Fauser, S.; Boon, C.J.F. ; Hoyng, C.B. ; Jong, E.K. de ; Hollander, A.I. den et al. sine al.
2016, Article / Letter to editor (PLoS One, vol. 11, iss. 3, (2016), article e0152047)
Whole exome sequencing identifies a heterozygous missense variant in the PRDM5 gene in a family with Axenfeld-Rieger syndrome
Micheal, S.; Siddiqui, S.N.; Zafar, S.N.; Venselaar, H. ; Qamar, R.; Khan, M.I. ; Hollander, A.I. den
2016, Article / Letter to editor (Neurogenetics, vol. 17, iss. 1, (2016), pp. 17-23)
Whole exome sequencing and array-based molecular karyotyping as aids to prenatal diagnosis in fetuses with suspected Simpson-Golabi-Behmel syndrome
Kehrer, C.; Hoischen, A. ; Menkhaus, R.; Schwab, E.; Muller, A.; Kim, S.; Kreiss, M.; Weitensteiner, V.; Hilger, A.; Berg, C. van den; Geipel, A.; Reutter, H.; Gembruch, U. et al. sine al.
2016, Article / Letter to editor (Prenatal Diagnosis, vol. 36, iss. 10, (2016), pp. 961-965)
Who is prone to high levels of distress after prophylactic mastectomy and/or salpingo-ovariectomy?
Bresser, P.J.; Gool, A.R. van; Seynaeve, C.; Duivenvoorden, H.J.; Niermeijer, M.F. ; Geel, A.N. van; Menke, M.; Klijn, J.G.M.; Tibben, A.
2007, Article / Letter to editor (Annals of Oncology, vol. 18, iss. 10, (2007), pp. 1641-1645)
White matter microstructure and developmental improvement of hyperactive/impulsive symptoms in Attention-Deficit/Hyperactivity Disorder
Francx, W.C.L. ; Zwiers, M.P. ; Mennes, M.J.J. ; Oosterlaan, J.; Heslenfeld, D.J.; Hoekstra, P.J.; Hartman, C.A.; Franke, B. ; Faraone, S.V; O'Dwyer, L.G. ; Buitelaar, J.K. et al. sine al.
2015, Article / Letter to editor (Journal of Child Psychology and Psychiatry and Allied Disciplines, vol. 56, iss. 12, (2015), pp. 1289-1297)
White matter microstructural alterations in children with adhd: Categorical and dimensional perspectives
Wu, Z.; BraIten, J.; Cao, Q.J.; Hoogman, M. ; Zwiers, M.P. ; An, L.; Sun, L.; Yang, L.; Zang, Y.F.; Franke, B. ; Wang, Y.F. et al. sine al.
2017, Article / Letter to editor (Neuropsychopharmacology (New York), vol. 42, iss. 2, (2017), pp. 572-580)
Whipple's disease in mentally retarded patients: Report of two cases.
Pettersson, A.; Winsen, L.M.L. van; Oosten, B. van; Kramers, C. ; Ven, A.J.A.M. van der ; Savelkoul, P.J.M. ; Agtmael, M.A. van
2007, Article / Letter to editor (Scandinavian Journal of Infectious Diseases, vol. 39, iss. 11, (2007), pp. 1071-1073)
Weight status of persons with intellectual disabilities
Maaskant, M.A.; Knijff-Raeven, A.G.M. van; Schrojenstein Lantman, H.M.J. van ; Veenstra, M.
2009, Article / Letter to editor (Journal of Applied Research in Intellectual Disabilities, vol. 22, iss. 5, (2009), pp. 426-432)
WDR26 Haploinsufficiency Causes a Recognizable Syndrome of Intellectual Disability, Seizures, Abnormal Gait, and Distinctive Facial Features
Skraban, C.M.; Wells, C.F.; Markose, P.; Cho, M.T.; Nesbitt, A.I.; Au, P.Y.; Begtrup, A.; Bernat, J.A.; Bird, L.M.; Cao, K.; Brouwer, A.P.M. de ; Denenberg, E.H.; Douglas, G.; Gibson, K.M.; Grand, K.; Goldenberg, A.; Innes, A.M.; Juusola, J.; Kempers, M.J.E. ; Kinning, E.; Markie, D.M.; Owens, M.M.; Payne, K.; Person, R.; Pfundt, R.P. ; Stocco, A.; Turner, C.L.; Verbeek, N.E.; Walsh, L.E.; Warner, T.C.; Wheeler, P.G.; Wieczorek, D.; Wilkens, A.B.; Zonneveld-Huijssoon, E.; Kleefstra, T. ; Robertson, S.P.; Santani, A.; Gassen, K.L. van; Deardorff, M.A. et al. sine al.
2017, Article / Letter to editor (American Journal of Human Genetics, vol. 101, iss. 1, (2017), pp. 139-148)
Wafer reuse for repeated growth of iii-v solar cells
Bauhuis, G.J. ; Mulder, P. ; Haverkamp, E.J.; Schermer, J.J. ; Bongers, M.H.F. ; Oomen, G.; Koestler, W.; Strobl, G.
2010, Article / Letter to editor (Progress in Photovoltaics. Research and Applications, vol. 17, iss. 5, (2010), pp. 155-159)
Voxel-based morphometry analysis reveals frontal brain differences in participants with ADHD and their unaffected siblings
Bralten, J.; Greven, C.U. ; Franke, B. ; Mennes, M.J.J. ; Zwiers, M.P. ; Rommelse, N.N.J. ; Hartman, C.A.; Meer, D. van der ; O'Dwyer, L.G. ; Oosterlaan, J.; Hoekstra, P.J.; Heslenfeld, D.; Arias-Vasquez, A. ; Buitelaar, J.K. et al. sine al.
2016, Article / Letter to editor (Journal of Psychiatry & Neuroscience, vol. 41, iss. 4, (2016), pp. 272-279)
Vitamin A and clefting: putative biological mechanisms
Ackermans, M.M.; Zhou, Huiqing ; Carels, C.E.L. ; Wagener, F.A.D.T.G. ; Hoff, J.W. Von den
2011, Article / Letter to editor (Nutrition Reviews . New York, vol. 69, iss. 10, (2011), pp. 613-624)

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