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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1956 1
1957 1
1965 1
1968 2
1970 2
1971 2
1972 5
1973 1
1974 2
1975 1
1976 4
1977 1
1978 2
1979 1
1980 3
1981 4
1982 5
1983 7
1984 6
1985 2
1986 9
1987 3
1988 4
1989 2
1990 10
1991 9
1992 8
1993 12
1994 10
1995 11
1996 19
1997 10
1998 9
1999 16
2000 15
2001 12
2002 18
2003 18
2004 18
2005 19
2006 21
2007 17
2008 28
2009 22
2010 16
2011 22
2012 32
2013 39
2014 41
2015 44
2016 52
2017 66
2018 66
2019 61
2020 52
2021 64
2022 53
2023 51
2024 23

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Quoted phrase not found in phrase index: "Intellectual developmental disorder 61"
Page 1
Endocrine manifestations of Down syndrome.
Whooten R, Schmitt J, Schwartz A. Whooten R, et al. Curr Opin Endocrinol Diabetes Obes. 2018 Feb;25(1):61-66. doi: 10.1097/MED.0000000000000382. Curr Opin Endocrinol Diabetes Obes. 2018. PMID: 29135488 Free PMC article. Review.
Incidence Rates and Cumulative Incidences of the Full Spectrum of Diagnosed Mental Disorders in Childhood and Adolescence.
Dalsgaard S, Thorsteinsson E, Trabjerg BB, Schullehner J, Plana-Ripoll O, Brikell I, Wimberley T, Thygesen M, Madsen KB, Timmerman A, Schendel D, McGrath JJ, Mortensen PB, Pedersen CB. Dalsgaard S, et al. JAMA Psychiatry. 2020 Feb 1;77(2):155-164. doi: 10.1001/jamapsychiatry.2019.3523. JAMA Psychiatry. 2020. PMID: 31746968 Free PMC article.
Girls had a higher risk than boys of schizophrenia (0.76% [95% CI, 0.72%-0.80%] vs 0.48% [95% CI, 0.39%-0.59%]), obsessive-compulsive disorder (0.96% [95% CI, 0.92%-1.00%] vs 0.63% [95% CI, 0.56%-0.72%]), and mood disorders (2.54% [95% CI, 2.47%-2.61%] vs 1.10% [95% …
Girls had a higher risk than boys of schizophrenia (0.76% [95% CI, 0.72%-0.80%] vs 0.48% [95% CI, 0.39%-0.59%]), obsessive-compulsive dis …
Childhood disintegrative disorder and autism spectrum disorder: a systematic review.
Mehra C, Sil A, Hedderly T, Kyriakopoulos M, Lim M, Turnbull J, Happe F, Baird G, Absoud M. Mehra C, et al. Dev Med Child Neurol. 2019 May;61(5):523-534. doi: 10.1111/dmcn.14126. Epub 2018 Dec 13. Dev Med Child Neurol. 2019. PMID: 30548847 Free article. Review.
AIM: In an attempt to clarify the debate surrounding the diagnostic validity of childhood disintegrative disorder (CDD), we systematically reviewed its characteristics and compared it with autism spectrum disorder (ASD). ...The prevalence of CDD was 1.1 to 9.2 per 1 …
AIM: In an attempt to clarify the debate surrounding the diagnostic validity of childhood disintegrative disorder (CDD), we systemati …
Global developmental delay and intellectual disability in the era of genomics: Diagnosis and challenges in resource limited areas.
Masri AT, Oweis L, Ali M, Hamamy H. Masri AT, et al. Clin Neurol Neurosurg. 2023 Jul;230:107799. doi: 10.1016/j.clineuro.2023.107799. Epub 2023 May 22. Clin Neurol Neurosurg. 2023. PMID: 37236004
AIMS: To report the diagnostic yield of clinical singleton whole exome sequencing (WES) performed among a group of Jordanian children presenting with global developmental delay /intellectual disability (GDD/ID), discuss the underlying identified genetic disor …
AIMS: To report the diagnostic yield of clinical singleton whole exome sequencing (WES) performed among a group of Jordanian children presen …
Delineating the genotypic and phenotypic spectrum of HECW2-related neurodevelopmental disorders.
Acharya A, Kavus H, Dunn P, Nasir A, Folk L, Withrow K, Wentzensen IM, Ruzhnikov MRZ, Fallot C, Smol T, Rama M, Brown K, Whalen S, Ziegler A, Barth M, Chassevent A, Smith-Hicks C, Afenjar A, Courtin T, Heide S, Font-Montgomery E, Heid C, Hamm JA, Love DR, Thabet F, Misra VK, Cunningham M, Leal SM, Jarvela I, Normand EA, Zou F, Helal M, Keren B, Torti E, Chung WK, Schrauwen I. Acharya A, et al. J Med Genet. 2022 Jul;59(7):669-677. doi: 10.1136/jmedgenet-2021-107871. Epub 2021 Jul 28. J Med Genet. 2022. PMID: 34321324 Review.
BACKGROUND: Variants in HECW2 have recently been reported to cause a neurodevelopmental disorder with hypotonia, seizures and impaired language; however, only six variants have been reported and the clinical characteristics have only broadly been defined. ...Clinical chara …
BACKGROUND: Variants in HECW2 have recently been reported to cause a neurodevelopmental disorder with hypotonia, seizures and impaire …
Familial and genetic associations between autism spectrum disorder and other neurodevelopmental and psychiatric disorders.
Ghirardi L, Kuja-Halkola R, Butwicka A, Martin J, Larsson H, D'Onofrio BM, Lichtenstein P, Taylor MJ. Ghirardi L, et al. J Child Psychol Psychiatry. 2021 Nov;62(11):1274-1284. doi: 10.1111/jcpp.13508. Epub 2021 Aug 20. J Child Psychol Psychiatry. 2021. PMID: 34415058
We estimated familial and genetic associations between ASD and nine disorder groups, and explored differences in these associations for ASD in the context of intellectual disability, epilepsy, chromosomal abnormalities, and congenital malformations. ...Strong …
We estimated familial and genetic associations between ASD and nine disorder groups, and explored differences in these associations f …
Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement.
Lacombe D, Bloch-Zupan A, Bredrup C, Cooper EB, Houge SD, García-Miñaúr S, Kayserili H, Larizza L, Lopez Gonzalez V, Menke LA, Milani D, Saettini F, Stevens CA, Tooke L, Van der Zee JA, Van Genderen MM, Van-Gils J, Waite J, Adrien JL, Bartsch O, Bitoun P, Bouts AHM, Cueto-González AM, Dominguez-Garrido E, Duijkers FA, Fergelot P, Halstead E, Huisman SA, Meossi C, Mullins J, Nikkel SM, Oliver C, Prada E, Rei A, Riddle I, Rodriguez-Fonseca C, Rodríguez Pena R, Russell J, Saba A, Santos-Simarro F, Simpson BN, Smith DF, Stevens MF, Szakszon K, Taupiac E, Totaro N, Valenzuena Palafoll I, Van Der Kaay DCM, Van Wijk MP, Vyshka K, Wiley S, Hennekam RC. Lacombe D, et al. J Med Genet. 2024 May 21;61(6):503-519. doi: 10.1136/jmg-2023-109438. J Med Genet. 2024. PMID: 38471765 Free PMC article. Review.
Rubinstein-Taybi syndrome (RTS) is an archetypical genetic syndrome that is characterised by intellectual disability, well-defined facial features, distal limb anomalies and atypical growth, among numerous other signs and symptoms. ...
Rubinstein-Taybi syndrome (RTS) is an archetypical genetic syndrome that is characterised by intellectual disability, well-def …
Self-Harm Events and Suicide Deaths Among Autistic Individuals in Ontario, Canada.
Lai MC, Saunders NR, Huang A, Artani A, Wilton AS, Zaheer J, Ameis SH, Brown HK, Lunsky Y. Lai MC, et al. JAMA Netw Open. 2023 Aug 1;6(8):e2327415. doi: 10.1001/jamanetworkopen.2023.27415. JAMA Netw Open. 2023. PMID: 37552480 Free PMC article.
Neighborhood-level income and rurality indices, and individual-level broad diagnostic categories of intellectual disabilities, mood and anxiety disorders, schizophrenia spectrum disorders, substance use disorders, and personality disorders were covariates. RESULTS: For sel …
Neighborhood-level income and rurality indices, and individual-level broad diagnostic categories of intellectual disabilities, mood a …
Mental, Neurological, and Somatic Comorbidities and Their Treatment in Persons With Intellectual Disability.
Weih M, Köhler S, Schöll N, Schulz M, Hering R. Weih M, et al. Dtsch Arztebl Int. 2022 Jun 17;119(24):418-414. doi: 10.3238/arztebl.m2022.0193. Dtsch Arztebl Int. 2022. PMID: 35506265 Free PMC article.
BACKGROUND: Persons with intellectual disability (ID) often suffer from significant comorbidities. ...Future analyses should be devoted to the specific care of people with intellectual disability, who constitute an especially multimorbid and vulnerable …
BACKGROUND: Persons with intellectual disability (ID) often suffer from significant comorbidities. ...Future analyses should b …
Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.
Butler MG. Butler MG. J Intellect Disabil Res. 2017 Jun;61(6):568-579. doi: 10.1111/jir.12382. Epub 2017 Apr 7. J Intellect Disabil Res. 2017. PMID: 28387067 Free PMC article. Review.
METHODS: The literature was reviewed and clinical and cytogenetic findings summarised in 200 individuals with this microdeletion along with the role of deleted genes in diagnosis, medical care and counseling of those affected and their family members. RESULTS: Reported findings i …
METHODS: The literature was reviewed and clinical and cytogenetic findings summarised in 200 individuals with this microdeletion along with …
928 results