Skuse, David

Strong association of de novo copy number mutations with autism

Sebat, J., Lakshmi, B., Malhotra, D., Troge, J., Lese-Martin, C., Walsh, T., Yamrom, B., Yoon, S., Krasnitz, A., Kendall, J., et al. (2007) · Science

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 2,795

Synaptic, transcriptional and chromatin genes disrupted in autism

Study, T. D., De Rubeis, S., Autism, H. M. C. F., UK10K Consortium, The Autism Sequencing Consortium, He, X., Goldberg, A. P., Poultney, C. S., Samocha, K., Ercument Cicek, A., et al. (2014) · Nature

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 2,746

The UK10K project identifies rare variants in health and disease

The UK10K Consortium, Writing group, Walter, K., Min, J. L., Huang, J., Crooks, L., Memari, Y., McCarthy, S., Perry, J. R. B., Xu, C., et al. (2015) · Nature

Genetic Associations and EpidemiologyGenomics and Rare Diseases

Cited by 1,040

Evidence from Turner's syndrome of an imprinted X-linked locus affecting cognitive function

Skuse, D. H., James, R. S., Bishop, D. V. M., Coppin, B., Dalton, P., Aamodt-Leeper, G., Bacarese-Hamilton, M., Creswell, C., McGurk, R., & Jacobs, P. A. (1997) · Nature

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesGenetic Syndromes and Imprinting

Cited by 747

Sex Differences in Autism Spectrum Disorder: Evidence from a Large Sample of Children and Adolescents

Mandy, W., Chilvers, R., Chowdhury, U., Salter, G., Seigal, A., & Skuse, D. (2012) · Journal of Autism and Developmental Disorders

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 715

Microduplications of 16p11.2 are associated with schizophrenia

Wellcome Trust Case Control Consortium, McCarthy, S. E., Makarov, V., Kirov, G., Addington, A. M., McClellan, J., Yoon, S., Perkins, D. O., Dickel, D. E., Kusenda, M., et al. (2009) · Nature Genetics

Genomic variations and chromosomal abnormalitiesSchizophrenia research and treatment

Cited by 711

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

iPSYCH-Broad Autism Group, Weiner, D. J., Psychiatric Genomics Consortium Autism Group, Wigdor, E. M., Ripke, S., Walters, R. K., Kosmicki, J. A., Grove, J., Samocha, K. E., Goldstein, J. I., et al. (2017) · Nature Genetics

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 516

Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

Leblond, C. S., Heinrich, J., Delorme, R., Proepper, C., Betancur, C., Huguet, G., Konyukh, M., Chaste, P., Ey, E., Rastam, M., et al. (2012) · PLoS Genetics

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 429

Genetic risk for autism spectrum disorders and neuropsychiatric variation in the general population

iPSYCH-SSI-Broad Autism Group, Robinson, E. B., St Pourcain, B., Anttila, V., Kosmicki, J. A., Bulik-Sullivan, B., Grove, J., Maller, J., Samocha, K. E., Sanders, S. J., et al. (2016) · Nature Genetics

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 367

The Developmental, Dimensional and Diagnostic Interview (3di): a novel computerized assessment for autism spectrum disorders

Skuse, D., Warrington, R., Bishop, D., Chowdhury, U., Lau, J., Mandy, W., & Place, M. (2004) · Journal of the American Academy of Child & Adolescent Psychiatry

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 342

Dopaminergic-neuropeptide interactions in the social brain

Skuse, D. H., & Gallagher, L. (2009) · Trends in Cognitive Sciences

Neuroendocrine regulation and behaviorNeurotransmitter Receptor Influence on Behavior

Cited by 340

Measuring autistic traits: heritability, reliability and validity of the Social and Communication Disorders Checklist

Skuse, D. H., Mandy, W. P. L., & Scourfield, J. (2005) · British Journal of Psychiatry

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 322

Imprinting, the X-chromosome, and the male brain: explaining sex differences in the liability to autism

Skuse, D. H. (2000) · Pediatric Research

Genetics and Neurodevelopmental DisordersAutism Spectrum Disorder Research

Cited by 285

An organization‐ and category‐level comparison of diagnostic requirements for mental disorders in ICD ‐11 and DSM ‐5

First, M. B., Gaebel, W., Maj, M., Stein, D. J., Kogan, C. S., Saunders, J. B., Poznyak, V. B., Gureje, O., Lewis‐Fernández, R., Maercker, A., et al. (2021) · World Psychiatry

Mental Health and PsychiatryPersonality Disorders and Psychopathology

Cited by 236

Common polymorphism in the oxytocin receptor gene ( OXTR ) is associated with human social recognition skills

Skuse, D. H., Lori, A., Cubells, J. F., Lee, I., Conneely, K. N., Puura, K., Lehtimäki, T., Binder, E. B., & Young, L. J. (2014) · Proceedings of the National Academy of Sciences

Neuroendocrine regulation and behaviorFace Recognition and Perception

Cited by 207

Social Communication Competence and Functional Adaptation in a General Population of Children: Preliminary Evidence for Sex-by-Verbal IQ Differential Risk

Skuse, D. H., Mandy, W., Steer, C., Miller, L. L., Goodman, R., Lawrence, K., Emond, A., & Golding, J. (2009) · Journal of the American Academy of Child & Adolescent Psychiatry

Autism Spectrum Disorder ResearchChild and Adolescent Psychosocial and Emotional Development

Cited by 205

Testing the construct validity of proposed criteria for DSM-5 autism spectrum disorder

Mandy, W. P. L., Charman, T., & Skuse, D. H. (2012) · Journal of the American Academy of Child & Adolescent Psychiatry

Autism Spectrum Disorder ResearchChild Nutrition and Feeding Issues

Cited by 191

Research review: what is the association between the social-communication element of autism and repetitive interests, behaviours and activities?

Mandy, W. P. L., & Skuse, D. H. (2008) · Journal of Child Psychology and Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 169

Psychiatric disorders in children with 16p11.2 deletion and duplication

Niarchou, M., Chawner, S. J. R. A., Doherty, J. L., Maillard, A. M., Jacquemont, S., Chung, W. K., Green-Snyder, L., Bernier, R. A., Goin-Kochel, R. P., Hanson, E., et al. (2019) · Translational Psychiatry

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

Cited by 156

Rethinking the nature of genetic vulnerability to autistic spectrum disorders

Skuse, D. H. (2007) · Trends in Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 147

ASD and schizophrenia show distinct developmental profiles in common genetic overlap with population-based social communication difficulties

iPSYCH-SSI-Broad Autism Group, St Pourcain, B., Robinson, E. B., Anttila, V, Sullivan, B. B., Maller, J., Golding, J., Skuse, D., Ring, S., Evans, D. M., et al. (2018) · Molecular Psychiatry

Autism Spectrum Disorder ResearchSchizophrenia research and treatment

Cited by 125

The development of autistic social traits across childhood and adolescence in males and females

Mandy, W., Pellicano, L., St Pourcain, B., Skuse, D., & Heron, J. (2018) · Journal of Child Psychology and Psychiatry

Autism Spectrum Disorder ResearchChild and Adolescent Psychosocial and Emotional Development

Cited by 117

Autism Spectrum Disorders in Africa: Current Challenges in Identification, Assessment, and Treatment: A Report on the International Child Neurology Association Meeting on ASD in Africa, Ghana, April 3-5, 2014

Ruparelia, K., Abubakar, A., Badoe, E., Bakare, M., Visser, K., Chugani, D. C., Chugani, H. T., Donald, K. A., Wilmshurst, J. M., Shih, A., et al. (2016) · Journal of Child Neurology

Autism Spectrum Disorder ResearchFamily and Disability Support Research

Cited by 110

Whole-genome sequence-based analysis of thyroid function

Taylor, P. N., Porcu, E., Chew, S., Campbell, P. J., Traglia, M., Brown, S. J., Mullin, B. H., Shihab, H. A., Min, J., Walter, K., et al. (2015) · Nature Communications

Genetic Associations and EpidemiologyThyroid Disorders and Treatments

Cited by 104