Browsing by Author Weksberg, R

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TitleAuthor(s)Issue DateViews
 
2011
247
 
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
60
 
Autism spectrum disorders and epigenetics
Journal:Journal of the American Academy of Child and Adolescent Psychiatry
2010
222
 
2013
195
 
2017
38
 
2017
46
 
2019
42
 
2013
84
 
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
121
 
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
123
 
2020
35
 
2009
38
 
2020
21
 
2021
1
 
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
148
 
2017
205
 
2013
67
 
2003
230
 
2013
86
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
89