Top 20 of Intellectual Disability

Article title # Publications/# Citations

Autism Diagnostic Interview-Revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders.

1994: ALe Couteur; CLord; MRutter;

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Development of a rating scale for primary depressive illness.

1967: MHamilton;

492

Association between microdeletion and microduplication at 16p11.2 and autism.

2008: Autism Consortium; DAltshuler; DEArking; AChakravarti; MJDaly; MAFerreira; RFossdal; TGreen; ... JFGusella; JMKorn; DTMiller; OSPlatt; DMRuderfer; ESaemundsen; SLSantangelo; YShen; PSklar; HStefansson; KStefansson; RETanzi; CAWalsh; LAWeiss; BLWu;

368

Toward a functional analysis of self-injury.

1994: KEBauman; MFDorsey; BAIwata; GSRichman; KJSlifer;

307

Altered synaptic plasticity in a mouse model of fragile X mental retardation.

2002: MFBear; SMGallagher; KMHuber; STWarren;

265

A comparison of two approaches for identifying reinforcers for persons with severe and profound disabilities.

1992: LGBowman; WFisher; LPHagopian; JCOwens; CCPiazza; ISlevin;

225

Recurrent rearrangements of chromosome 1q21.1 and variable pediatric phenotypes.

2008: SEAntonarakis; LArmengol; CBaker; DBaralle; JCBarber; FBena; EMBongers; ABroomer; ... KBuysse; ICasuga; CChen; JClayton-Smith; ACollins; BConrad; ACoppola; JACrolla; ADe Coene; Nde Leeuw; TDe Ravel; BBde Vries; KDevriendt; EEEichler; XEstivill; MFichera; HVFirth; LGallagher; SGallati; LGaunt; MGill; GGimelli; SGimelli; LGoossens; SGribble; RCHennekam; RHochstenbach; SHuang; AItsara; ZJiang; MCKing; SJKnight; KELi; CLilley; MLo Giudice; AMale; VKMaloney; JMcClellan; HCMefford; SGMehta; BMenten; CMercer; GMortier; MRNelen; SNik-Zainal; KNorga; SMPark; GParkin; MPoot; LRäber; WReardon; RRegan; SReitano; CRomano; CESchwartz; SSchwartz; MSchwerzmann; JSebat; AJSharp; ISimonic; CSkinner; FSpeleman; YSpysschaert; REStevenson; PStriano; JSSutcliffe; MTassabehji; ESTobias; JLTolmie; Evan Binsbergen; JAVeltman; PVerloo; JRVermeesch; TWalsh; LWillatt; CGWoods;

165

ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry Syndrome.

2004: PBialek; SBrancorsini; AHanauer; SJacquot; GKarsenty; LLi; HCMasuoka; KMatsuda; ... PSassone-Corsi; TSchinke; TMTownes; XYang;

163

Discovery of previously unidentified genomic disorders from the duplication architecture of the human genome.

2006: DGAlbertson; EBlair; ZCheng; EEEichler; PSEis; CAFitzpatrick; CGuiver; SHansen; ... RCHennekam; JAHurst; SJKnight; DPinkel; SMPrice; RRegan; TARichmond; SSchwartz; RSegraves; RRSelzer; AJSharp; HStewart;

160

High rates of schizophrenia in adults with velo-cardio-facial syndrome.

1999: LAJones; KCMurphy; MJOwen;

154

Autism diagnostic observation schedule: a standardized observation of communicative and social behavior.

1989: SGoode; JHeemsbergen; HJordan; CLord; LMawhood; MRutter; ESchopler;

146

A practical clinical approach to diagnosis of fetal alcohol spectrum disorders: clarification of the 1996 institute of medicine criteria.

2005: ASAragón; DGBuckley; JPGossage; HEHoyme; KLJones; WOKalberg; NKhaole; PKodituwakku; ... PAMay; JHMiller; LKRobinson; PMTrujillo; DLViljoen;

145

Dendritic anomalies in disorders associated with mental retardation.

2000: WEKaufmann; HWMoser;

137

Evidence that fragile X mental retardation protein is a negative regulator of translation.

2001: UFischer; EMKeidel; BLaggerbauer; DOstareck; AOstareck-Lederer;

137

A recurrent 15q13.3 microdeletion syndrome associated with mental retardation and seizures.

2008: CBaker; CBarbacioru; BDBernardina; ABroomer; LCastiglia; ICasuga; CChen; RCiccone; ... GMCooper; MDe Gregori; EEEichler; PFailla; MFichera; GGimelli; RGiorda; ZJiang; SJKnight; KLi; SMansour; HCMefford; VMurday; FNovara; RRegan; CRomano; RJSchroer; CESchwartz; AJSharp; CSkinner; REStevenson; CTorniero; MVentura; YWang; CXiao; OZuffardi;

132

Abnormal dendritic spine characteristics in the temporal and visual cortices of patients with fragile-X syndrome: a quantitative examination.

2001: PCras; RACrisostomo; WTGreenough; JBHarris; MIdupulapati; SAIrwin; FKooy; PBKozlowski; ... BPLarsen; BPatel; RASwain; IJWeiler; PJWillems;

132

A de novo paradigm for mental retardation.

2010: PArts; HGBrunner; Jde Ligt; BBde Vries; Pde Vries; Mdel Rosario; CGilissen; AHoischen; ... IJanssen; MSteehouwer; BWvan Bon; Bvan Lier; JAVeltman; LEVissers; NWieskamp;

131

Enzyme defect associated with a sex-linked human neurological disorder and excessive purine synthesis.

1967: WNKelley; FMRosenbloom; JESeegmiller;

130

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

1993: DAtkinson; AKEwart; WJin; MTKeating; MLeppert; CAMorris; PSpallone; KSternes; ADStock;

129

Abnormal behavior associated with a point mutation in the structural gene for monoamine oxidase A.

1993: XOBreakefield; HGBrunner; MNelen; HHRopers; BAvan Oost;

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