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Items: 19

1.

Early-life stress impairs developmental programming in Cadherin 13 (CDH13)-deficient mice.

Kiser DP, Popp S, Schmitt-Böhrer AG, Strekalova T, van den Hove DL, Lesch KP, Rivero O.

Prog Neuropsychopharmacol Biol Psychiatry. 2018 Aug 28;89:158-168. doi: 10.1016/j.pnpbp.2018.08.010. [Epub ahead of print]

2.

Conditional deletion of Cadherin 13 perturbs Golgi cells and disrupts social and cognitive behaviors.

Tantra M, Guo L, Kim J, Zainolabidin N, Eulenburg V, Augustine GJ, Chen AI.

Genes Brain Behav. 2018 Jul;17(6):e12466. doi: 10.1111/gbb.12466. Epub 2018 Mar 15.

PMID:
29446202
3.

The role of cadherin genes in five major psychiatric disorders: A literature update.

Hawi Z, Tong J, Dark C, Yates H, Johnson B, Bellgrove MA.

Am J Med Genet B Neuropsychiatr Genet. 2018 Mar;177(2):168-180. doi: 10.1002/ajmg.b.32592. Epub 2017 Sep 18. Review.

PMID:
28921840
4.

Cdh13 and AdipoQ gene knockout alter instrumental and Pavlovian drug conditioning.

King CP, Militello L, Hart A, St Pierre CL, Leung E, Versaggi CL, Roberson N, Catlin J, Palmer AA, Richards JB, Meyer PJ.

Genes Brain Behav. 2017 Sep;16(7):686-698. doi: 10.1111/gbb.12382. Epub 2017 May 2.

5.

No genetic association between attention-deficit/hyperactivity disorder (ADHD) and Parkinson's disease in nine ADHD candidate SNPs.

Geissler JM; International Parkinson Disease Genomics Consortium members, Romanos M, Gerlach M, Berg D, Schulte C.

Atten Defic Hyperact Disord. 2017 Jun;9(2):121-127. doi: 10.1007/s12402-017-0219-8. Epub 2017 Feb 7.

PMID:
28176268
6.

Cadherin 13: human cis-regulation and selectively-altered addiction phenotypes and cerebral cortical dopamine in knockout mice.

Drgonova J, Walther D, Hartstein GL, Bukhari MO, Baumann MH, Katz J, Hall FS, Arnold ER, Flax S, Riley A, Rivero-Martin O, Lesch KP, Troncoso J, Ranscht B, Uhl GR.

Mol Med. 2016 Oct;22:537-547. doi: 10.2119/molmed.2015.00170. Epub 2016 Aug 18.

7.

Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition.

Rivero O, Selten MM, Sich S, Popp S, Bacmeister L, Amendola E, Negwer M, Schubert D, Proft F, Kiser D, Schmitt AG, Gross C, Kolk SM, Strekalova T, van den Hove D, Resink TJ, Nadif Kasri N, Lesch KP.

Transl Psychiatry. 2015 Oct 13;5:e655. doi: 10.1038/tp.2015.152.

8.

Cadherin-13 gene is associated with hyperactive/impulsive symptoms in attention/deficit hyperactivity disorder.

Salatino-Oliveira A, Genro JP, Polanczyk G, Zeni C, Schmitz M, Kieling C, Anselmi L, Menezes AM, Barros FC, Polina ER, Mota NR, Grevet EH, Bau CH, Rohde LA, Hutz MH.

Am J Med Genet B Neuropsychiatr Genet. 2015 Apr;168B(3):162-9. doi: 10.1002/ajmg.b.32293. Epub 2015 Mar 4.

PMID:
25739828
9.

Decreased serum levels of adiponectin in adult attention deficit hyperactivity disorder.

Mavroconstanti T, Halmøy A, Haavik J.

Psychiatry Res. 2014 Apr 30;216(1):123-30. doi: 10.1016/j.psychres.2014.01.025. Epub 2014 Feb 5.

PMID:
24559850
10.

Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients.

Mavroconstanti T, Johansson S, Winge I, Knappskog PM, Haavik J.

PLoS One. 2013 Aug 1;8(8):e71445. doi: 10.1371/journal.pone.0071445. Print 2013.

11.

Impact of the ADHD-susceptibility gene CDH13 on development and function of brain networks.

Rivero O, Sich S, Popp S, Schmitt A, Franke B, Lesch KP.

Eur Neuropsychopharmacol. 2013 Jun;23(6):492-507. doi: 10.1016/j.euroneuro.2012.06.009. Epub 2012 Jul 12. Review.

PMID:
22795700
12.

The genetics of attention deficit/hyperactivity disorder in adults, a review.

Franke B, Faraone SV, Asherson P, Buitelaar J, Bau CH, Ramos-Quiroga JA, Mick E, Grevet EH, Johansson S, Haavik J, Lesch KP, Cormand B, Reif A; International Multicentre persistent ADHD CollaboraTion.

Mol Psychiatry. 2012 Oct;17(10):960-87. doi: 10.1038/mp.2011.138. Epub 2011 Nov 22. Review.

13.

CDH13 is associated with working memory performance in attention deficit/hyperactivity disorder.

Arias-Vásquez A, Altink ME, Rommelse NN, Slaats-Willemse DI, Buschgens CJ, Fliers EA, Faraone SV, Sergeant JA, Oosterlaan J, Franke B, Buitelaar JK.

Genes Brain Behav. 2011 Nov;10(8):844-51. doi: 10.1111/j.1601-183X.2011.00724.x. Epub 2011 Sep 23.

14.

Genome-scan for IQ discrepancy in autism: evidence for loci on chromosomes 10 and 16.

Chapman NH, Estes A, Munson J, Bernier R, Webb SJ, Rothstein JH, Minshew NJ, Dawson G, Schellenberg GD, Wijsman EM.

Hum Genet. 2011 Jan;129(1):59-70. doi: 10.1007/s00439-010-0899-z. Epub 2010 Oct 21.

15.

Case-control genome-wide association study of attention-deficit/hyperactivity disorder.

Neale BM, Medland S, Ripke S, Anney RJ, Asherson P, Buitelaar J, Franke B, Gill M, Kent L, Holmans P, Middleton F, Thapar A, Lesch KP, Faraone SV, Daly M, Nguyen TT, Schäfer H, Steinhausen HC, Reif A, Renner TJ, Romanos M, Romanos J, Warnke A, Walitza S, Freitag C, Meyer J, Palmason H, Rothenberger A, Hawi Z, Sergeant J, Roeyers H, Mick E, Biederman J; IMAGE II Consortium Group.

J Am Acad Child Adolesc Psychiatry. 2010 Sep;49(9):906-20. doi: 10.1016/j.jaac.2010.06.007. Epub 2010 Aug 5.

16.

Do candidate genes discriminate patients with an autism spectrum disorder from those with attention deficit/hyperactivity disorder and is there an effect of lifetime substance use disorders?

Sizoo B, van den Brink W, Franke B, Vasquez AA, van Wijngaarden-Cremers P, van der Gaag RJ.

World J Biol Psychiatry. 2010 Aug;11(5):699-708. doi: 10.3109/15622975.2010.480985.

PMID:
20446882
17.

Genome-wide association studies in ADHD.

Franke B, Neale BM, Faraone SV.

Hum Genet. 2009 Jul;126(1):13-50. doi: 10.1007/s00439-009-0663-4. Epub 2009 Apr 22. Review.

18.

Molecular genetics of adult ADHD: converging evidence from genome-wide association and extended pedigree linkage studies.

Lesch KP, Timmesfeld N, Renner TJ, Halperin R, Röser C, Nguyen TT, Craig DW, Romanos J, Heine M, Meyer J, Freitag C, Warnke A, Romanos M, Schäfer H, Walitza S, Reif A, Stephan DA, Jacob C.

J Neural Transm (Vienna). 2008 Nov;115(11):1573-85. doi: 10.1007/s00702-008-0119-3. Epub 2008 Oct 7.

PMID:
18839057
19.

Genome-wide association scan of quantitative traits for attention deficit hyperactivity disorder identifies novel associations and confirms candidate gene associations.

Lasky-Su J, Neale BM, Franke B, Anney RJ, Zhou K, Maller JB, Vasquez AA, Chen W, Asherson P, Buitelaar J, Banaschewski T, Ebstein R, Gill M, Miranda A, Mulas F, Oades RD, Roeyers H, Rothenberger A, Sergeant J, Sonuga-Barke E, Steinhausen HC, Taylor E, Daly M, Laird N, Lange C, Faraone SV.

Am J Med Genet B Neuropsychiatr Genet. 2008 Dec 5;147B(8):1345-54. doi: 10.1002/ajmg.b.30867.

PMID:
18821565

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