M
Michael Rutter
Researcher at King's College London
Publications - 684
Citations - 158378
Michael Rutter is an academic researcher from King's College London. The author has contributed to research in topics: Autism & Conduct disorder. The author has an hindex of 188, co-authored 676 publications receiving 151592 citations. Previous affiliations of Michael Rutter include VCU Medical Center & Center for Advanced Study in the Behavioral Sciences.
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Emanuel Miller Lecture: Attachment insecurity, disinhibited attachment, and attachment disorders: where do research findings leave the concepts?
TL;DR: It is seriously misleading to view all of these patterns through the lens of security/insecurity, and heterogeneity in social relationship features necessarily has implications for the assessment measures for social relationships that need to be used.
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Early Hospital Admissions and Later Disturbances of Behaviour: An Attempted Replication of Douglas' Findings
David Quinton,Michael Rutter +1 more
TL;DR: It is confirmed that single hospital admissions of children for up to a week carry no increased risk of later emotional or behavioural disturbance and the validity of the finding is strengthened by the fact that detailed psychiatric assessments gave rise to much the same findings as did teacher questionnaire scores.
Journal ArticleDOI
Psychological sequelae of brain damage in children.
TL;DR: The author reviews the empirical evidence on the psychological sequelae of brain damage in childhood, concluding that brain injury causes a markedly increased risk in both intellectual impairment and psychiatric disorder.
Stress, coping and development: some issues and some questions
TL;DR: The concept of psychosocial stress is reviewed in relation to empirical findings on the effects of different types of life, events in childhood and adult life and it is concluded that the concept is unhelpfully broad and that the events need to be subdivided according to their characteristics and meaning.
Journal ArticleDOI
A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder
Jillian P. Casey,Tiago R. Magalhaes,Tiago R. Magalhaes,Judith Conroy,Regina Regan,Naisha Shah,Richard Anney,Denis C. Shields,Brett S. Abrahams,Joana Almeida,Elena Bacchelli,Anthony J. Bailey,Gillian Baird,Agatino Battaglia,Tom Berney,Nadia Bolshakova,Patrick Bolton,Thomas Bourgeron,Sean Brennan,Phil Cali,Catarina Correia,Catarina Correia,Christina Corsello,Marc N. Coutanche,Geraldine Dawson,Geraldine Dawson,Maretha de Jonge,Richard Delorme,Eftichia Duketis,Frederico Duque,Annette Estes,Penny Farrar,Bridget A. Fernandez,Susan E. Folstein,Suzanne Foley,Eric Fombonne,Christine M. Freitag,John R. Gilbert,Christopher Gillberg,Joseph T. Glessner,Jonathan Green,Stephen J. Guter,Hakon Hakonarson,Richard Holt,Gillian Hughes,Vanessa Hus,Roberta Igliozzi,Cecilia Kim,Sabine M. Klauck,Alexander Kolevzon,Janine A. Lamb,Marion Leboyer,Ann Le Couteur,Bennett L. Leventhal,Bennett L. Leventhal,Catherine Lord,Sabata C. Lund,Elena Maestrini,Carine Mantoulan,Christian R. Marshall,Helen McConachie,Christopher J. McDougle,Jane McGrath,William M. McMahon,Alison K. Merikangas,Judith Miller,Fiorella Minopoli,Ghazala Mirza,Jeff Munson,Stanley F. Nelson,Gudrun Nygren,Guiomar Oliveira,Alistair T. Pagnamenta,Katerina Papanikolaou,Jeremy R. Parr,Barbara Parrini,Andrew Pickles,Dalila Pinto,Joseph Piven,David J. Posey,Annemarie Poustka,Fritz Poustka,Jiannis Ragoussis,Bernadette Rogé,Michael Rutter,Ana Filipa Sequeira,Ana Filipa Sequeira,Latha Soorya,Inês Sousa,Nuala Sykes,Vera Stoppioni,Raffaella Tancredi,Maïté Tauber,Ann P. Thompson,Susanne Thomson,John Tsiantis,Herman van Engeland,John B. Vincent,Fred R. Volkmar,Jacob A. S. Vorstman,Simon Wallace,Kai Wang,Thomas H. Wassink,Kathy White,Kirsty Wing,Kerstin Wittemeyer,Brian L. Yaspan,Lonnie Zwaigenbaum,Catalina Betancur,Joseph D. Buxbaum,Rita M. Cantor,Edwin H. Cook,Hilary Coon,Michael L. Cuccaro,Daniel H. Geschwind,Jonathan L. Haines,Joachim Hallmayer,Anthony P. Monaco,John I. Nurnberger,Margaret A. Pericak-Vance,Gerard D. Schellenberg,Stephen W. Scherer,James S. Sutcliffe,Peter Szatmari,Veronica J. Vieland,Ellen M. Wijsman,Andrew Green,Michael Gill,Louise Gallagher,Astrid M. Vicente,Astrid M. Vicente,Sean Ennis +131 more
TL;DR: A large scale analysis to identify candidate genes which may contain low-frequency recessive variation contributing to ASD while taking into account the potential contribution of population differences to the genetic heterogeneity of ASD highlights the applicability of HH mapping in complex disorders such as ASD and offers an alternative approach to the analysis of genome-wide association data.