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New approaches to the study of behavioural phenotypes.
J Intellect Disabil Res. 2022 Aug;66(8-9):667-668. doi: 10.1111/jir.12961.
J Intellect Disabil Res. 2022.
PMID: 35981964
No abstract available.
Reversed gender ratio of autism spectrum disorder in Smith-Magenis syndrome.
Nag HE, Nordgren A, Anderlid BM, Nærland T.
Nag HE, et al.
Mol Autism. 2018 Jan 8;9:1. doi: 10.1186/s13229-017-0184-2. eCollection 2018.
Mol Autism. 2018.
PMID: 29321841
Free PMC article.
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Parental experiences with behavioural problems in Smith-Magenis syndrome: The need for syndrome-specific competence.
Nag HE, Hoxmark LB, Nærland T.
Nag HE, et al.
J Intellect Disabil. 2019 Sep;23(3):359-372. doi: 10.1177/1744629519847375. Epub 2019 May 2.
J Intellect Disabil. 2019.
PMID: 31046579
Free PMC article.
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Age-related changes in behavioural and emotional problems in Smith-Magenis syndrome measured with the Developmental Behavior Checklist.
Nag HE, Nærland T.
Nag HE, et al.
J Intellect Disabil. 2021 Dec;25(4):429-440. doi: 10.1177/1744629519901056. Epub 2020 Jan 26.
J Intellect Disabil. 2021.
PMID: 31984836
Free PMC article.
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Bidirectional genetic overlap between autism spectrum disorder and cognitive traits.
Hope S, Shadrin AA, Lin A, Bahrami S, Rødevand L, Frei O, Hübenette SJ, Cheng W, Hindley G, Nag H, Ulstein L, Efrim-Budisteanu M, O'Connell K, Dale AM, Djurovic S, Nærland T, Andreassen OA.
Hope S, et al.
Transl Psychiatry. 2023 Sep 14;13(1):295. doi: 10.1038/s41398-023-02563-7.
Transl Psychiatry. 2023.
PMID: 37709755
Free PMC article.
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A structured assessment of motor function, behavior, and communication in patients with Wolf-Hirschhorn syndrome.
Nag HE, Bergsaker DK, Hunn BS, Schmidt S, Hoxmark LB.
Nag HE, et al.
Eur J Med Genet. 2017 Nov;60(11):610-617. doi: 10.1016/j.ejmg.2017.08.013. Epub 2017 Aug 14.
Eur J Med Genet. 2017.
PMID: 28818479
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A structured assessment of motor function and behavior in patients with Kleefstra syndrome.
Schmidt S, Nag HE, Hunn BS, Houge G, Hoxmark LB.
Schmidt S, et al. Among authors: nag he.
Eur J Med Genet. 2016 Apr;59(4):240-8. doi: 10.1016/j.ejmg.2016.01.004. Epub 2016 Jan 22.
Eur J Med Genet. 2016.
PMID: 26808425
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