Browsing by Author Weksberg, R

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TitleAuthor(s)Issue DateViews
 
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
116
 
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
124
 
2020
48
 
2009
32
 
2020
46
 
2021
21
 
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
98
 
2017
137
 
2013
33
 
2003
217
 
2013
71
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
62
 
2012
195
 
2011
121
 
2018
79
 
2010
195
 
2011
139
 
2015
61
 
Rare SUZ12 variants commonly cause an overgrowth phenotype
Journal:American Journal of Medical Genetics Part C: Seminars in Medical Genetics
2019
24
2011
109