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Items: 1 to 20 of 10391

1.

Genetic association of DNMT variants can play a critical role in defining the methylation patterns in autism.

Alex AM, Saradalekshmi KR, Shilen N, Suresh PA, Banerjee M.

IUBMB Life. 2019 Feb 20. doi: 10.1002/iub.2021. [Epub ahead of print]

PMID:
30786140
2.

Autism and Schizophrenia-Associated CYFIP1 Regulates the Balance of Synaptic Excitation and Inhibition.

Davenport EC, Szulc BR, Drew J, Taylor J, Morgan T, Higgs NF, López-Doménech G, Kittler JT.

Cell Rep. 2019 Feb 19;26(8):2037-2051.e6. doi: 10.1016/j.celrep.2019.01.092.

PMID:
30784587
3.

A Novel Approach to Dysmorphology to Enhance the Phenotypic Classification of Autism Spectrum Disorder in the Study to Explore Early Development.

Shapira SK, Tian LH, Aylsworth AS, Elias ER, Hoover-Fong JE, Meeks NJL, Souders MC, Tsai AC, Zackai EH, Alexander AA, Yeargin-Allsopp M, Schieve LA.

J Autism Dev Disord. 2019 Feb 19. doi: 10.1007/s10803-019-03899-0. [Epub ahead of print]

PMID:
30783897
4.

The CNTNAP2-CASK complex modulates GluA1 subcellular distribution in interneurons.

Gao R, Zaccard CR, Shapiro LP, Dionisio LE, Martin-de-Saavedra MD, Piguel NH, Pratt CP, Horan KE, Penzes P.

Neurosci Lett. 2019 Feb 16. pii: S0304-3940(19)30117-X. doi: 10.1016/j.neulet.2019.02.025. [Epub ahead of print]

PMID:
30779956
5.

Beyond protein-coding genes.

Lozano-Ureña A, Ferrón SR.

Elife. 2019 Feb 19;8. pii: e45123. doi: 10.7554/eLife.45123.

6.

Molecular Mechanisms of Transcription Factor 4 in Pitt Hopkins Syndrome.

Rannals MD, Maher BJ.

Curr Genet Med Rep. 2017 Mar;5(1):1-7. doi: 10.1007/s40142-017-0110-0. Epub 2017 Feb 11.

7.

[Neurobiological bases of autism and cellular models for its experimental study].

Martínez-Morga M, Paz Quesada M, Bueno C, Martinez S.

Medicina (B Aires). 2019;79 Suppl 1:27-32. Spanish.

8.

[Autism. Genetic and biological aspects].

Arberas C, Ruggieri V.

Medicina (B Aires). 2019;79 Suppl 1:16-21. Spanish.

9.

Hyperinsulinaemic hypoglycaemia: A new presentation of 16p11.2 deletion syndrome.

Kostopoulou E, Dastamani A, Caiulo S, Antell H, Flanagan SE, Shah P.

Clin Endocrinol (Oxf). 2019 Feb 18. doi: 10.1111/cen.13951. [Epub ahead of print]

PMID:
30776145
10.

Chromosomal Microarray Analysis in Children with Unexplained Developmental Delay/Intellectual Disability.

Arican P, Olgac Dundar N, Ozyilmaz B, Cavusoglu D, Gencpinar P, Erdogan KM, Saka Guvenc M.

J Pediatr Genet. 2019 Mar;8(1):1-9. doi: 10.1055/s-0038-1676583. Epub 2018 Dec 14.

PMID:
30775046
11.

An eight-case 1q21 region series: novel aberrations and clinical variability with new features.

Ceylan AC, Sahin I, Erdem HB, Kayhan G, Simsek-Kiper PO, Utine GE, Percin F, Boduroglu K, Alikasifoglu M.

J Intellect Disabil Res. 2019 Feb 18. doi: 10.1111/jir.12592. [Epub ahead of print]

PMID:
30773728
12.

Clinical and genetic analysis of children with a dual diagnosis of Tourette syndrome and autism spectrum disorder.

Carias KV, Wevrick R.

J Psychiatr Res. 2019 Feb 7;111:145-153. doi: 10.1016/j.jpsychires.2019.01.023. [Epub ahead of print]

PMID:
30771620
13.

Fragile X mental retardation protein positively regulates PKA anchor Rugose and PKA activity to control actin assembly in learning/memory circuitry.

Sears JC, Choi WJ, Broadie K.

Neurobiol Dis. 2019 Feb 13. pii: S0969-9961(19)30035-X. doi: 10.1016/j.nbd.2019.02.004. [Epub ahead of print]

PMID:
30771457
14.

Behavioural and psychiatric phenotypes in female carriers of genetic mutations associated with X-linked ichthyosis.

Cavenagh A, Chatterjee S, Davies W.

PLoS One. 2019 Feb 15;14(2):e0212330. doi: 10.1371/journal.pone.0212330. eCollection 2019.

15.

Common Polygenic Variations for Psychiatric Disorders and Cognition in Relation to Brain Morphology in the General Pediatric Population.

Alemany S, Jansen PR, Muetzel RL, Marques N, El Marroun H, Jaddoe VWV, Polderman TJC, Tiemeier H, Posthuma D, White T.

J Am Acad Child Adolesc Psychiatry. 2019 Jan 9. pii: S0890-8567(19)30007-3. doi: 10.1016/j.jaac.2018.09.443. [Epub ahead of print]

PMID:
30768412
16.

Cognitive performance and functional outcomes of carriers of pathogenic copy number variants: analysis of the UK Biobank.

Kendall KM, Bracher-Smith M, Fitzpatrick H, Lynham A, Rees E, Escott-Price V, Owen MJ, O'Donovan MC, Walters JTR, Kirov G.

Br J Psychiatry. 2019 Feb 15:1-8. doi: 10.1192/bjp.2018.301. [Epub ahead of print]

PMID:
30767844
17.

Autism, spectrum or clusters? An EEG coherence study.

Duffy FH, Als H.

BMC Neurol. 2019 Feb 14;19(1):27. doi: 10.1186/s12883-019-1254-1.

18.

A Third Linear Association Between Olduvai (DUF1220) Copy Number and Severity of the Classic Symptoms of Inherited Autism.

Davis JM, Heft I, Scherer SW, Sikela JM.

Am J Psychiatry. 2019 Feb 15:appiajp201818080993. doi: 10.1176/appi.ajp.2018.18080993. [Epub ahead of print]

PMID:
30764650
19.

HLA-G allelic distribution in Sardinian children with Autism spectrum disorders: A replication study.

Guerini FR, Bolognesi E, Sotgiu S, Carta A, Clerici C, Chiappedi M, Ghezzo A, Zanette M, Mensi MM, Canevini MP, Zanzottera M, Agliardi C, Costa AS, Balottin U, Clerici M.

Brain Behav Immun. 2019 Feb 11. pii: S0889-1591(18)30614-7. doi: 10.1016/j.bbi.2019.02.003. [Epub ahead of print]

PMID:
30763769
20.

Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations.

Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L.

Hum Mutat. 2019 Feb 14. doi: 10.1002/humu.23724. [Epub ahead of print]

PMID:
30763456

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