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Items: 1 to 20 of 152

1.

Genetic Approaches to Understanding Psychiatric Disease.

Michaelson JJ.

Neurotherapeutics. 2017 Jul;14(3):564-581. doi: 10.1007/s13311-017-0551-x. Review.

PMID:
28608171
2.

Intragenic CNTNAP2 Deletions: A Bridge Too Far?

Poot M.

Mol Syndromol. 2017 May;8(3):118-130. doi: 10.1159/000456021. Epub 2017 Feb 10. Review.

3.

How French media have portrayed ADHD to the lay public and to social workers.

Ponnou S, Gonon F.

Int J Qual Stud Health Well-being. 2017 Jun;12(sup1):1298244. doi: 10.1080/17482631.2017.1298244.

4.

Study books on ADHD genetics: balanced or biased?

Te Meerman S, Batstra L, Hoekstra R, Grietens H.

Int J Qual Stud Health Well-being. 2017 Jun;12(sup1):1305590. doi: 10.1080/17482631.2017.1305590.

5.

Neuronal Migration and AUTS2 Syndrome.

Hori K, Hoshino M.

Brain Sci. 2017 May 14;7(5). pii: E54. doi: 10.3390/brainsci7050054. Review.

6.

Analysis of shared homozygosity regions in Saudi siblings with attention deficit hyperactivity disorder.

Shinwari JMA, Al Yemni EAA, Alnaemi FM, Abebe D, Al-Abdulaziz BS, Al Mubarak BR, Ghaziuddin M, Al Tassan NA.

Psychiatr Genet. 2017 Aug;27(4):131-138. doi: 10.1097/YPG.0000000000000173.

7.

Next-generation DNA sequencing identifies novel gene variants and pathways involved in specific language impairment.

Chen XS, Reader RH, Hoischen A, Veltman JA, Simpson NH, Francks C, Newbury DF, Fisher SE.

Sci Rep. 2017 Apr 25;7:46105. doi: 10.1038/srep46105.

8.

Genome Wide Association Study (GWAS) between Attention Deficit Hyperactivity Disorder (ADHD) and Obsessive Compulsive Disorder (OCD).

Ritter ML, Guo W, Samuels JF, Wang Y, Nestadt PS, Krasnow J, Greenberg BD, Fyer AJ, McCracken JT, Geller DA, Murphy DL, Knowles JA, Grados MA, Riddle MA, Rasmussen SA, McLaughlin NC, Nurmi EL, Askland KD, Cullen B, Piacentini J, Pauls DL, Bienvenu J, Stewart E, Goes FS, Maher B, Pulver AE, Mattheisen M, Qian J, Nestadt G, Shugart YY.

Front Mol Neurosci. 2017 Mar 23;10:83. doi: 10.3389/fnmol.2017.00083. eCollection 2017.

9.

Attention-Deficit/Hyperactivity Disorder.

Banaschewski T, Becker K, Döpfner M, Holtmann M, Rösler M, Romanos M.

Dtsch Arztebl Int. 2017 Mar 3;114(9):149-159. doi: 10.3238/arztebl.2017.0149.

10.

Sequencing of sporadic Attention-Deficit Hyperactivity Disorder (ADHD) identifies novel and potentially pathogenic de novo variants and excludes overlap with genes associated with autism spectrum disorder.

Kim DS, Burt AA, Ranchalis JE, Wilmot B, Smith JD, Patterson KE, Coe BP, Li YK, Bamshad MJ, Nikolas M, Eichler EE, Swanson JM, Nigg JT, Nickerson DA, Jarvik GP; University of Washington Center for Mendelian Genomics.

Am J Med Genet B Neuropsychiatr Genet. 2017 Jun;174(4):381-389. doi: 10.1002/ajmg.b.32527. Epub 2017 Mar 22.

PMID:
28332277
11.

The Correlation-Base-Selection Algorithm for Diagnostic Schizophrenia Based on Blood-Based Gene Expression Signatures.

Zhang H, Xie Z, Yang Y, Zhao Y, Zhang B, Fang J.

Biomed Res Int. 2017;2017:7860506. doi: 10.1155/2017/7860506. Epub 2017 Feb 9.

12.

Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.

Rosenfeld JA, Patel A.

J Pediatr Genet. 2017 Mar;6(1):42-50. doi: 10.1055/s-0036-1584306. Epub 2016 May 30. Review.

PMID:
28180026
13.

Common and specific genes and peripheral biomarkers in children and adults with attention-deficit/hyperactivity disorder.

Bonvicini C, Faraone SV, Scassellati C.

World J Biol Psychiatry. 2017 Feb 24:1-21. doi: 10.1080/15622975.2017.1282175. [Epub ahead of print]

PMID:
28097908
14.

An endophenotype approach to the genetics of alcohol dependence: a genome wide association study of fast beta EEG in families of African ancestry.

Meyers JL, Zhang J, Wang JC, Su J, Kuo SI, Kapoor M, Wetherill L, Bertelsen S, Lai D, Salvatore JE, Kamarajan C, Chorlian D, Agrawal A, Almasy L, Bauer L, Bucholz KK, Chan G, Hesselbrock V, Koganti L, Kramer J, Kuperman S, Manz N, Pandey A, Seay M, Scott D, Taylor RE, Dick DM, Edenberg HJ, Goate A, Foroud T, Porjesz B.

Mol Psychiatry. 2017 Jan 10. doi: 10.1038/mp.2016.239. [Epub ahead of print]

PMID:
28070124
15.

The Genetic Etiology of Tourette Syndrome: Large-Scale Collaborative Efforts on the Precipice of Discovery.

Georgitsi M, Willsey AJ, Mathews CA, State M, Scharf JM, Paschou P.

Front Neurosci. 2016 Aug 3;10:351. doi: 10.3389/fnins.2016.00351. eCollection 2016.

16.

Essential role of the nuclear isoform of RBFOX1, a candidate gene for autism spectrum disorders, in the brain development.

Hamada N, Ito H, Nishijo T, Iwamoto I, Morishita R, Tabata H, Momiyama T, Nagata K.

Sci Rep. 2016 Aug 2;6:30805. doi: 10.1038/srep30805.

17.

From Genetics to Epigenetics: New Perspectives in Tourette Syndrome Research.

Pagliaroli L, Vető B, Arányi T, Barta C.

Front Neurosci. 2016 Jul 12;10:277. doi: 10.3389/fnins.2016.00277. eCollection 2016. Review.

18.

Collection of developmental history in the evaluation of schizophrenia spectrum disorders.

Reiersen AM.

Scand J Child Adolesc Psychiatr Psychol. 2016;4(1):36-43.

19.

SALM5 trans-synaptically interacts with LAR-RPTPs in a splicing-dependent manner to regulate synapse development.

Choi Y, Nam J, Whitcomb DJ, Song YS, Kim D, Jeon S, Um JW, Lee SG, Woo J, Kwon SK, Li Y, Mah W, Kim HM, Ko J, Cho K, Kim E.

Sci Rep. 2016 May 26;6:26676. doi: 10.1038/srep26676.

20.

Moving towards causality in attention-deficit hyperactivity disorder: overview of neural and genetic mechanisms.

Gallo EF, Posner J.

Lancet Psychiatry. 2016 Jun;3(6):555-67. doi: 10.1016/S2215-0366(16)00096-1. Epub 2016 May 13. Review.

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