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337 results

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Page 1
Common genetic variants influence human subcortical brain structures.
Hibar DP, Stein JL, Renteria ME, Arias-Vasquez A, Desrivières S, Jahanshad N, Toro R, Wittfeld K, Abramovic L, Andersson M, Aribisala BS, Armstrong NJ, Bernard M, Bohlken MM, Boks MP, Bralten J, Brown AA, Chakravarty MM, Chen Q, Ching CR, Cuellar-Partida G, den Braber A, Giddaluru S, Goldman AL, Grimm O, Guadalupe T, Hass J, Woldehawariat G, Holmes AJ, Hoogman M, Janowitz D, Jia T, Kim S, Klein M, Kraemer B, Lee PH, Olde Loohuis LM, Luciano M, Macare C, Mather KA, Mattheisen M, Milaneschi Y, Nho K, Papmeyer M, Ramasamy A, Risacher SL, Roiz-Santiañez R, Rose EJ, Salami A, Sämann PG, Schmaal L, Schork AJ, Shin J, Strike LT, Teumer A, van Donkelaar MM, van Eijk KR, Walters RK, Westlye LT, Whelan CD, Winkler AM, Zwiers MP, Alhusaini S, Athanasiu L, Ehrlich S, Hakobjan MM, Hartberg CB, Haukvik UK, Heister AJ, Hoehn D, Kasperaviciute D, Liewald DC, Lopez LM, Makkinje RR, Matarin M, Naber MA, McKay DR, Needham M, Nugent AC, Pütz B, Royle NA, Shen L, Sprooten E, Trabzuni D, van der Marel SS, van Hulzen KJ, Walton E, Wolf C, Almasy L, Ames D, Arepalli S, Assareh AA, Bastin ME, Brodaty H, Bulayeva KB, Carless MA, Cichon S, Corvin A, Curran JE, Czisch M, de Zubica… See abstract for full author list ➔ Hibar DP, et al. Among authors: van eijk kr, van duijn cm, van der marel ss, van haren ne, van der lee sj, van der wee nj, van donkelaar mm, van tol mj, van t ent d, van der brug m, van bokhoven h, van hulzen kj. Nature. 2015 Apr 9;520(7546):224-9. doi: 10.1038/nature14101. Epub 2015 Jan 21. Nature. 2015. PMID: 25607358 Free PMC article.
Splitting p63.
van Bokhoven H, Brunner HG. van Bokhoven H, et al. Am J Hum Genet. 2002 Jul;71(1):1-13. doi: 10.1086/341450. Epub 2002 May 30. Am J Hum Genet. 2002. PMID: 12037717 Free PMC article. Review.
The p63 gene in EEC and other syndromes.
Brunner HG, Hamel BC, Van Bokhoven H. Brunner HG, et al. Among authors: van bokhoven h. J Med Genet. 2002 Jun;39(6):377-81. doi: 10.1136/jmg.39.6.377. J Med Genet. 2002. PMID: 12070241 Free PMC article. Review.
Expanding phenotype of XNP mutations: mild to moderate mental retardation.
Yntema HG, Poppelaars FA, Derksen E, Oudakker AR, van Roosmalen T, Jacobs A, Obbema H, Brunner HG, Hamel BC, van Bokhoven H. Yntema HG, et al. Among authors: van roosmalen t, van bokhoven h. Am J Med Genet. 2002 Jul 1;110(3):243-7. doi: 10.1002/ajmg.10446. Am J Med Genet. 2002. PMID: 12116232
Pathogenesis of split-hand/split-foot malformation.
Duijf PH, van Bokhoven H, Brunner HG. Duijf PH, et al. Among authors: van bokhoven h. Hum Mol Genet. 2003 Apr 1;12 Spec No 1:R51-60. doi: 10.1093/hmg/ddg090. Hum Mol Genet. 2003. PMID: 12668597 Review.
Feingold syndrome: clinical review and genetic mapping.
Celli J, van Bokhoven H, Brunner HG. Celli J, et al. Among authors: van bokhoven h. Am J Med Genet A. 2003 Nov 1;122A(4):294-300. doi: 10.1002/ajmg.a.20471. Am J Med Genet A. 2003. PMID: 14518066 Review.
Sequence analysis of the PLEXIN-D1 gene in Möbius syndrome patients.
van der Zwaag B, Verzijl HT, Wichers KH, Beltran-Valero de Bernabe D, Brunner HG, van Bokhoven H, Padberg GW. van der Zwaag B, et al. Among authors: van bokhoven h. Pediatr Neurol. 2004 Aug;31(2):114-8. doi: 10.1016/j.pediatrneurol.2004.02.004. Pediatr Neurol. 2004. PMID: 15301830
337 results