Pierce KD - Search Results

1

Mutations in SLC20A2 are a major cause of familial idiopathic basal ganglia calcification.

Hsu SC, Sears RL, Lemos RR, Quintáns B, Huang A, Spiteri E, Nevarez L, Mamah C, Zatz M, Pierce KD, Fullerton JM, Adair JC, Berner JE, Bower M, Brodaty H, Carmona O, Dobricić V, Fogel BL, García-Estevez D, Goldman J, Goudreau JL, Hopfer S, Janković M, Jaumà S, Jen JC, Kirdlarp S, Klepper J, Kostić V, Lang AE, Linglart A, Maisenbacher MK, Manyam BV, Mazzoni P, Miedzybrodzka Z, Mitarnun W, Mitchell PB, Mueller J, Novaković I, Paucar M, Paulson H, Simpson SA, Svenningsson P, Tuite P, Vitek J, Wetchaphanphesat S, Williams C, Yang M, Schofield PR, de Oliveira JR, Sobrido MJ, Geschwind DH, Coppola G. Hsu SC, et al. Among authors: pierce kd. Neurogenetics. 2013 Feb;14(1):11-22. doi: 10.1007/s10048-012-0349-2. Epub 2013 Jan 20. Neurogenetics. 2013. PMID: 23334463 Free PMC article.

2

Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders.

Toma C, Pierce KD, Shaw AD, Heath A, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. Among authors: pierce kd. PLoS Genet. 2018 Dec 26;14(12):e1007535. doi: 10.1371/journal.pgen.1007535. eCollection 2018 Dec. PLoS Genet. 2018. PMID: 30586385 Free PMC article.

3

An examination of multiple classes of rare variants in extended families with bipolar disorder.

Toma C, Shaw AD, Allcock RJN, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. Among authors: pierce kd. Transl Psychiatry. 2018 Mar 13;8(1):65. doi: 10.1038/s41398-018-0113-y. Transl Psychiatry. 2018. PMID: 29531218 Free PMC article.

4

A linkage and exome study of multiplex families with bipolar disorder implicates rare coding variants of ANK3 and additional rare alleles at 10q11-q21.

Toma C, Shaw AD, Heath A, Pierce KD, Mitchell PB, Schofield PR, Fullerton JM. Toma C, et al. Among authors: pierce kd. J Psychiatry Neurosci. 2021 Mar 17;46(2):E247-E257. doi: 10.1503/jpn.200083. J Psychiatry Neurosci. 2021. PMID: 33729739 Free PMC article.

5

Cortical mediation of relationships between dopamine receptor D2 and cognition is absent in youth at risk of bipolar disorder.

Overs BJ, Lenroot RK, Roberts G, Green MJ, Toma C, Hadzi-Pavlovic D, Pierce KD, Schofield PR, Mitchell PB, Fullerton JM. Overs BJ, et al. Among authors: pierce kd. Psychiatry Res Neuroimaging. 2021 Mar 30;309:111258. doi: 10.1016/j.pscychresns.2021.111258. Epub 2021 Jan 28. Psychiatry Res Neuroimaging. 2021. PMID: 33529975

6

Role of charged residues in coupling ligand binding and channel activation in the extracellular domain of the glycine receptor.

Absalom NL, Lewis TM, Kaplan W, Pierce KD, Schofield PR. Absalom NL, et al. Among authors: pierce kd. J Biol Chem. 2003 Dec 12;278(50):50151-7. doi: 10.1074/jbc.M305357200. Epub 2003 Oct 2. J Biol Chem. 2003. PMID: 14525990 Free article.

7

Vulnerability of white matter tracts and cognition to the SOD2 polymorphism: A preliminary study of antioxidant defense genes in brain aging.

Salminen LE, Schofield PR, Pierce KD, Bruce SE, Griffin MG, Tate DF, Cabeen RP, Laidlaw DH, Conturo TE, Bolzenius JD, Paul RH. Salminen LE, et al. Among authors: pierce kd. Behav Brain Res. 2017 Jun 30;329:111-119. doi: 10.1016/j.bbr.2017.04.041. Epub 2017 Apr 27. Behav Brain Res. 2017. PMID: 28457881 Free PMC article.

8

Cation-selective mutations in the M2 domain of the inhibitory glycine receptor channel reveal determinants of ion-charge selectivity.

Keramidas A, Moorhouse AJ, Pierce KD, Schofield PR, Barry PH. Keramidas A, et al. Among authors: pierce kd. J Gen Physiol. 2002 May;119(5):393-410. doi: 10.1085/jgp.20028552. J Gen Physiol. 2002. PMID: 11981020 Free PMC article.

9

BDNF Genotype Interacts with Motor Function to Influence Rehabilitation Responsiveness Poststroke.

Shiner CT, Pierce KD, Thompson-Butel AG, Trinh T, Schofield PR, McNulty PA. Shiner CT, et al. Among authors: pierce kd. Front Neurol. 2016 May 17;7:69. doi: 10.3389/fneur.2016.00069. eCollection 2016. Front Neurol. 2016. PMID: 27242654 Free PMC article.

10

Epigenetic signatures relating to disease-associated genotypic burden in familial risk of bipolar disorder.

Hesam-Shariati S, Overs BJ, Roberts G, Toma C, Watkeys OJ, Green MJ, Pierce KD, Edenberg HJ, Wilcox HC, Stapp EK, McInnis MG, Hulvershorn LA, Nurnberger JI, Schofield PR, Mitchell PB, Fullerton JM. Hesam-Shariati S, et al. Among authors: pierce kd. Transl Psychiatry. 2022 Aug 3;12(1):310. doi: 10.1038/s41398-022-02079-6. Transl Psychiatry. 2022. PMID: 35922419 Free PMC article.

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