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Results 1-10 of 38 (Search time: 0.003 seconds).
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PreviewIssue DateTitleAuthor(s)
2012KCNQ2 encephalopathy: Emerging phenotype of a neonatal epileptic encephalopathyWeckhuysen, S.; Mandelstam, S.; Suls, A.; Audenaert, D.; Deconinck, T.; Claes, L.; Deprez, L.; Smets, K.; Hristova, D.; Yordanova, I.; Jordanova, A.; Ceulemans, B.; Jansen, A.; Hasaerts, D.; Roelens, F.; Lagae, L.; Yendle, S.; Stanley, T.; Heron, S.; Mulley, J.; et al.
2013Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposityCousminer, D.; Berry, D.; Timpson, N.; Ang, W.; Thiering, E.; Byrne, E.; Taal, H.; Huikari, V.; Bradfield, J.; Kerkhof, M.; Groen-Blokhuis, M.; Kreiner-Møller, E.; Marinelli, M.; Holst, C.; Leinonen, J.; Perry, J.; Surakka, I.; Kettunen, J.; Anttila, V.; Kaakinen, M.; et al.
2012Genome-wide association for abdominal subcutaneous and visceral adipose reveals a novel locus for visceral fat in womenPalmer, L.; Fox, C.S.; Liu, Y.; White, C.C.; Feitosa, M.; Smith, A.V.; Heard-Costa, N.; Lohman, K.; GIANT Consortium; MAGIC Consortium; GLGC Consortium; Johnson, A.D.; Foster, M.C.; Greenawalt, D.M.; Griffin, P.; Ding, J.; Newman, A.B.; Tylavsky, F.; Miljkovic, I.; Kritchevsky, S.B.; et al.; Bray, M.
2017Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biasesStessman, H.; Xiong, B.; Coe, B.; Wang, T.; Hoekzema, K.; Fenckova, M.; Kvarnung, M.; Gerdts, J.; Trinh, S.; Cosemans, N.; Vives, L.; Lin, J.; Turner, T.; Santen, G.; Ruivenkamp, C.; Kriek, M.; Van Haeringen, A.; Aten, E.; Friend, K.; Liebelt, J.; et al.
2013Feeding the futureMcCouch, S.; Baute, G.; Bradeen, J.; Bramel, P.; Bretting, P.; Buckler, E.; Burke, J.; Charest, D.; Cloutier, S.; Cole, G.; Dempewolf, H.; Dingkuhn, M.; Feuillet, C.; Gepts, P.; Grattapaglia, D.; Guarino, L.; Jackson, S.; Knapp, S.; Langridge, P.; Lawton-Rauh, A.; et al.
2016Characterization of leukemias with ETV6-ABL1 fusionZaliova, M.; Moorman, A.; Cazzaniga, G.; Stanulla, M.; Harvey, R.; Roberts, K.; Heatley, S.; Loh, M.; Konopleva, M.; Chen, I.; Zimmermannova, O.; Schwab, C.; Smith, O.; Mozziconacci, M.; Chabannon, C.; Kim, M.; Frederik Falkenburg, J.; Norton, A.; Marshall, K.; Haas, O.; et al.; Annual Meeting of the American-Society-of-Hematology (5 Dec 2015 - 8 Dec 2015 : Orlando, FL)
2015Association of the colorectal CpG island methylator phenotype with molecular features, risk factors, and family historyWeisenberger, D.; Levine, A.; Long, T.; Buchanan, D.; Walters, R.; Clendenning, M.; Rosty, C.; Joshi, A.; Stern, M.; Le Marchand, L.; Lindor, N.; Daftary, D.; Gallinger, S.; Selander, T.; Bapat, B.; Newcomb, P.; Campbell, P.; Casey, G.; Ahnen, D.; Baron, J.; et al.
2010Genome-wide pharmacogenetics of antidepressant response in the GENDEP projectUher, R.; Perroud, N.; Ng, M.; Hauser, J.; Henigsberg, N.; Maier, W.; Mors, O.; Placentino, A.; Rietschel, M.; Souery, D.; Zagar, T.; Czerski, P.; Jerman, B.; Larsen, E.; Schulze, T.; Zobel, A.; Cohen-Woods, S.; Pirlo, K.; Butler, A.; Muglia, P.; et al.
2008X-linked protocadherin 19 mutations cause female-limited epilepsy and cognitive impairmentDibbens, L.; Tarpey, P.; Hynes, K.; Bayly, M.; Scheffer, I.; Smith, R.; Bomar, J.; Sutton, E.; Vandeleur, L.; Shoubridge, C.; Edkins, S.; Turner, S.; Stevens, C.; O'Meara, S.; Tofts, C.; Barthorpe, S.; Buck, G.; Cole, J.; Halliday, K.; Jones, D.; et al.
2016Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and IDvan Bon, B.W.M.; Coe, B.P.; Bernier, R.; Green, C.; Gerdts, J.; Witherspoon, K.; Kleefstra, T.; Willemsen, M.H.; Kumar, R.; Bosco, P.; Fichera, M.; Li, D.; Amaral, D.; Cristofoli, F.; Peeters, H.; Haan, E.; Romano, C.; Mefford, H.C.; Scheffer, I.; Gecz, J.; et al.

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