Browsing by Author Weksberg, R

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TitleAuthor(s)Issue DateViews
 
2011
135
 
2q23.1 microdeletion involving the MBD5 gene - large deletion associated with a relatively mild phenotype
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2009
2009
56
 
Autism spectrum disorders and epigenetics
Journal:Journal of the American Academy of Child and Adolescent Psychiatry
2010
118
 
2013
75
 
2017
16
 
2017
30
 
2013
54
 
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations
Proceeding/Conference:Annual Scientific Meeting of the Canadian College of Medical Geneticists, CCMG 2010
2010
45
 
Crosstalk between histone modifications and DNA methylation in patients with intellectual disability due to JARID1C mutations
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2010
2010
54
 
2009
19
 
Pinto, DPagnamenta, ATKlei, LAnney, RMerico, DRegan, RConroy, JMagalhaes, TRCorreia, CAbrahams, BSAlmeida, JBacchelli, EBader, GDBailey, AJBaird, GBattaglia, ABerney, TBolshakova, NBölte, SBolton, PFBourgeron, TBrennan, SBrian, JBryson, SECarson, ARCasallo, GCasey, JChung, BHYCochrane, LCorsello, CCrawford, ELCrossett, ACytrynbaum, CDawson, GDe Jonge, MDelorme, RDrmic, IDuketis, EDuque, FEstes, AFarrar, PFernandez, BAFolstein, SEFombonne, EFreitag, CMGilbert, JGillberg, CGlessner, JTGoldberg, JGreen, AGreen, JGuter, SJHakonarson, HHeron, EAHill, MHolt, RHowe, JLHughes, GHus, VIgliozzi, RKim, CKlauck, SMKolevzon, AKorvatska, OKustanovich, VLajonchere, CMLamb, JALaskawiec, MLeboyer, MLe Couteur, ALeventhal, BLLionel, ACLiu, XQLord, CLotspeich, LLund, SCMaestrini, EMahoney, WMantoulan, CMarshall, CRMcconachie, HMcdougle, CJMcgrath, JMcmahon, WMMerikangas, AMigita, OMinshew, NJMirza, GKMunson, JNelson, SFNoakes, CNoor, ANygren, GOliveira, GPapanikolaou, KParr, JRParrini, BPaton, TPickles, APilorge, MPiven, JPonting, CPPosey, DJPoustka, APoustka, FPrasad, ARagoussis, JRenshaw, KRickaby, JRoberts, WRoeder, KRoge, BRutter, MLBierut, LJRice, JPSalt, JSansom, KSato, DSegurado, RSequeira, AFSenman, LShah, NSheffield, VCSoorya, LSousa, IStein, OSykes, NStoppioni, VStrawbridge, CTancredi, RTansey, KThiruvahindrapduram, BThompson, APThomson, STryfon, ATsiantis, JVan Engeland, HVincent, JBVolkmar, FWallace, SWang, KWang, ZWassink, THWebber, CWeksberg, RWing, KWittemeyer, KWood, SWu, JYaspan, BLZurawiecki, DZwaigenbaum, LBuxbaum, JDCantor, RMCook, EHCoon, HCuccaro, MLDevlin, BEnnis, SGallagher, LGeschwind, DHGill, MHaines, JLHallmayer, JMiller, JMonaco, APNurnberger Jr, JIPaterson, ADPericakVance, MASchellenberg, GDSzatmari, PVicente, AMVieland, VJWijsman, EMScherer, SWSutcliffe, JSBetancur, C
2010
110
 
2017
90
 
2013
72
 
2003
100
 
2013
48
NSD1+/- DNA methylation (DNAm) signature: A novel functional diagnostic tool for Sotos syndrome
Proceeding/Conference:Annual Meeting of the American Society of Human Genetics, ASHG 2014
2014
101
 
2012
71
 
2011
49
 
2018
24
 
2010
120