1.
Mutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features
by Johansen, Anide
American journal of human genetics, 2016-10-06, Vol.99 (4), p.912-916
2.
Recessive and Dominant De Novo ITPR1 Mutations Cause Gillespie Syndrome
by Gerber, Sylvie
American journal of human genetics, 2016-05-05, Vol.98 (5), p.971-980
3.
The Confidential Inquiry into premature deaths of people with intellectual disabilities in the UK: a population-based study
by Heslop, Pauline, Dr
The Lancet (British edition), 2014, Vol.383 (9920), p.889-895
4.
Brief Report: Service Use and Associated Expenditures Among Adolescents with Autism Spectrum Disorder Transitioning to Adulthood
by Shea, Lindsay L
Journal of autism and developmental disorders, 2018-04-07, Vol.48 (9), p.3223-3227
5.
The Choice between Formal and Informal Intellectual Property: A Review
by Hall, B.H
Journal of economic literature, 2014-06-01, Vol.52 (2), p.375-423
6.
Fifteen-Year Prospective Follow-Up Study of Adult Outcomes of Autism Spectrum Disorders Among Children Attending Centers in Five Regional Departments in France: The EpiTED Cohort
by Baghdadli, Amaria
Journal of Autism and Developmental Disorders, 2019-01-30, Vol.49 (6), p.2243-2256
7.
Anxiety Disorders in Williams Syndrome Contrasted with Intellectual Disability and the General Population: A Systematic Review and Meta-Analysis
by Royston, R
Journal of autism and developmental disorders, 2016-09-30, Vol.47 (12), p.3765-3777
8.
Genetics of early onset cognitive impairment
by Ropers, Hans Hilger
Annual review of genomics and human genetics, 2010, Vol.11 (1), p.161-187
9.
TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations
by O’Rawe, Jason A
American journal of human genetics, 2015-12-03, Vol.97 (6), p.922-932
10.
Epidemiology of gastrostomy insertion for children and adolescents with intellectual disability
by Wong, Kingsley
European journal of pediatrics, 2018-12-15, Vol.178 (3), p.351-361
11.
Psychopathology in children and adolescents with autism compared to young people with intellectual disability
by BRERETON, Avril V
Journal of autism and developmental disorders, 2006, Vol.36 (7), p.863-870
12.
Autosomal-Recessive Intellectual Disability with Cerebellar Atrophy Syndrome Caused by Mutation of the Manganese and Zinc Transporter Gene SLC39A8
by Boycott, Kym M
American journal of human genetics, 2015-12-03, Vol.97 (6), p.886-893
13.
Mutations in DYNC1H1 cause severe intellectual disability with neuronal migration defects
by Willemsen, Marjolein H
Journal of medical genetics, 2012-03, Vol.49 (3), p.179-183
14.
High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies
by Hamdan, Fadi F
American journal of human genetics, 2017-11-02, Vol.101 (5), p.664-685
15.
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study
by Rauch, Anita, Prof
The Lancet (British edition), 2012, Vol.380 (9854), p.1674-1682
16.
Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
by Davies, R.W
Nature Medicine, 2020-12-01, Vol.26 (12), p.1912-1918
17.
BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription
by Dias, Cristina
American journal of human genetics, 2016-08-04, Vol.99 (2), p.253-274
18.
Does Quality of Life Differ for Children With Autism Spectrum Disorder and Intellectual Disability Compared to Peers Without Autism?
by Arias, Víctor B
Journal of autism and developmental disorders, 2017-09-11, Vol.48 (1), p.123-136
19.
Comorbid Symptomology in Adults with Autism Spectrum Disorder and Intellectual Disability
by Cervantes, Paige E
Journal of autism and developmental disorders, 2015-08-09, Vol.45 (12), p.3961-3970
20.
Promoting Social Interactions and Job Independence for College Students with Autism or Intellectual Disability: A Pilot Study
by Gilson, Carly B
Journal of autism and developmental disorders, 2016-08-29, Vol.46 (11), p.3583-3596
