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Items: 5

1.

Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences.

Lebrun N, Mehler-Jacob C, Poirier K, Zordan C, Lacombe D, Carion N, Billuart P, Bienvenu T.

Gene. 2018 Dec 30;679:305-313. doi: 10.1016/j.gene.2018.09.016. Epub 2018 Sep 12.

PMID:
30217758
2.

Whole exome sequencing reveals inherited and de novo variants in autism spectrum disorder: a trio study from Saudi families.

Al-Mubarak B, Abouelhoda M, Omar A, AlDhalaan H, Aldosari M, Nester M, Alshamrani HA, El-Kalioby M, Goljan E, Albar R, Subhani S, Tahir A, Asfahani S, Eskandrani A, Almusaiab A, Magrashi A, Shinwari J, Monies D, Al Tassan N.

Sci Rep. 2017 Jul 18;7(1):5679. doi: 10.1038/s41598-017-06033-1.

3.

Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.

Chen R, Davis LK, Guter S, Wei Q, Jacob S, Potter MH, Cox NJ, Cook EH, Sutcliffe JS, Li B.

Mol Autism. 2017 Mar 21;8:14. doi: 10.1186/s13229-017-0130-3. eCollection 2017.

4.

Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders.

Vallianatos CN, Iwase S.

Epigenomics. 2015;7(3):503-19. doi: 10.2217/epi.15.1. Review.

5.

Role of H3K4 demethylases in complex neurodevelopmental diseases.

Wynder C, Stalker L, Doughty ML.

Epigenomics. 2010 Jun;2(3):407-18. doi: 10.2217/epi.10.12. Review.

PMID:
22121901

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