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Results: 1 to 20 of 215

1.

Exome sequencing of extended families with autism reveals genes shared across neurodevelopmental and neuropsychiatric disorders.

Cukier HN, Dueker ND, Slifer SH, Lee JM, Whitehead PL, Lalanne E, Leyva N, Konidari I, Gentry RC, Hulme WF, Booven DV, Mayo V, Hofmann NK, Schmidt MA, Martin ER, Haines JL, Cuccaro ML, Gilbert JR, Pericak-Vance MA.

Mol Autism. 2014 Jan 10;5(1):1. doi: 10.1186/2040-2392-5-1.

PMID:
24410847
[PubMed]
Free PMC Article
2.

KIAA1462, a coronary artery disease associated gene, is a candidate gene for late onset Alzheimer disease in APOE carriers.

Murdock DG, Bradford Y, Schnetz-Boutaud N, Mayo P, Allen MJ, D'Aoust LN, Liang X, Mitchell SL, Zuchner S, Small GW, Gilbert JR, Pericak-Vance MA, Haines JL.

PLoS One. 2013 Dec 12;8(12):e82194. doi: 10.1371/journal.pone.0082194. eCollection 2013.

PMID:
24349219
[PubMed - in process]
Free PMC Article
3.

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease.

Lambert JC, Ibrahim-Verbaas CA, Harold D, Naj AC, Sims R, Bellenguez C, DeStafano AL, Bis JC, Beecham GW, Grenier-Boley B, Russo G, Thorton-Wells TA, Jones N, Smith AV, Chouraki V, Thomas C, Ikram MA, Zelenika D, Vardarajan BN, Kamatani Y, Lin CF, Gerrish A, Schmidt H, Kunkle B, Dunstan ML, Ruiz A, Bihoreau MT, Choi SH, Reitz C, Pasquier F, Cruchaga C, Craig D, Amin N, Berr C, Lopez OL, De Jager PL, Deramecourt V, Johnston JA, Evans D, Lovestone S, Letenneur L, Morón FJ, Rubinsztein DC, Eiriksdottir G, Sleegers K, Goate AM, Fiévet N, Huentelman MW, Gill M, Brown K, Kamboh MI, Keller L, Barberger-Gateau P, McGuiness B, Larson EB, Green R, Myers AJ, Dufouil C, Todd S, Wallon D, Love S, Rogaeva E, Gallacher J, St George-Hyslop P, Clarimon J, Lleo A, Bayer A, Tsuang DW, Yu L, Tsolaki M, Bossù P, Spalletta G, Proitsi P, Collinge J, Sorbi S, Sanchez-Garcia F, Fox NC, Hardy J, Deniz Naranjo MC, Bosco P, Clarke R, Brayne C, Galimberti D, Mancuso M, Matthews F; European Alzheimer's Disease Initiative (EADI); Genetic and Environmental Risk in Alzheimer's Disease; Alzheimer's Disease Genetic Consortium; Cohorts for Heart and Aging Research in Genomic Epidemiology, Moebus S, Mecocci P, Del Zompo M, Maier W, Hampel H, Pilotto A, Bullido M, Panza F, Caffarra P, Nacmias B, Gilbert JR, Mayhaus M, Lannefelt L, Hakonarson H, Pichler S, Carrasquillo MM, Ingelsson M, Beekly D, Alvarez V, Zou F, Valladares O, Younkin SG, Coto E, Hamilton-Nelson KL, Gu W, Razquin C, Pastor P, Mateo I, Owen MJ, Faber KM, Jonsson PV, Combarros O, O'Donovan MC, Cantwell LB, Soininen H, Blacker D, Mead S, Mosley TH Jr, Bennett DA, Harris TB, Fratiglioni L, Holmes C, de Bruijn RF, Passmore P, Montine TJ, Bettens K, Rotter JI, Brice A, Morgan K, Foroud TM, Kukull WA, Hannequin D, Powell JF, Nalls MA, Ritchie K, Lunetta KL, Kauwe JS, Boerwinkle E, Riemenschneider M, Boada M, Hiltuenen M, Martin ER, Schmidt R, Rujescu D, Wang LS, Dartigues JF, Mayeux R, Tzourio C, Hofman A, Nöthen MM, Graff C, Psaty BM, Jones L, Haines JL, Holmans PA, Lathrop M, Pericak-Vance MA, Launer LJ, Farrer LA, van Duijn CM, Van Broeckhoven C, Moskvina V, Seshadri S, Williams J, Schellenberg GD, Amouyel P.

Nat Genet. 2013 Dec;45(12):1452-8. doi: 10.1038/ng.2802. Epub 2013 Oct 27.

PMID:
24162737
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Leptin signaling in the medial nucleus tractus solitarius reduces food seeking and willingness to work for food.

Kanoski SE, Alhadeff AL, Fortin SM, Gilbert JR, Grill HJ.

Neuropsychopharmacology. 2014 Feb;39(3):605-13. doi: 10.1038/npp.2013.235. Epub 2013 Sep 4.

PMID:
24002186
[PubMed - in process]
5.

C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease.

Nuytemans K, Bademci G, Kohli MM, Beecham GW, Wang L, Young JI, Nahab F, Martin ER, Gilbert JR, Benatar M, Haines JL, Scott WK, Züchner S, Pericak-Vance MA, Vance JM.

Ann Hum Genet. 2013 Sep;77(5):351-63. doi: 10.1111/ahg.12033. Epub 2013 Jul 12.

PMID:
23845100
[PubMed - in process]
Free PMC Article
6.

Parkinsonism and distinct dementia patterns in a family with the MAPT R406W mutation.

Carney RM, Kohli MA, Kunkle BW, Naj AC, Gilbert JR, Züchner S, Pericak-Vance MA.

Alzheimers Dement. 2014 May;10(3):360-5. doi: 10.1016/j.jalz.2013.02.011. Epub 2013 May 30.

PMID:
23727082
[PubMed - in process]
7.

Assessing crossmodal matching of abstract auditory and visual stimuli in posterior superior temporal sulcus with MEG.

Gilbert JR, Pillai AS, Horwitz B.

Brain Cogn. 2013 Jul;82(2):161-70. doi: 10.1016/j.bandc.2013.03.004. Epub 2013 May 11.

PMID:
23665947
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Evaluating mitochondrial DNA variation in autism spectrum disorders.

Hadjixenofontos A, Schmidt MA, Whitehead PL, Konidari I, Hedges DJ, Wright HH, Abramson RK, Menon R, Williams SM, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA, Martin ER, McCauley JL.

Ann Hum Genet. 2013 Jan;77(1):9-21. doi: 10.1111/j.1469-1809.2012.00736.x. Epub 2012 Nov 6.

PMID:
23130936
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Early sensory cortex is activated in the absence of explicit input during crossmodal item retrieval: evidence from MEG.

Pillai AS, Gilbert JR, Horwitz B.

Behav Brain Res. 2013 Feb 1;238:265-72. doi: 10.1016/j.bbr.2012.10.011. Epub 2012 Oct 18.

PMID:
23084971
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Accelerated calvarial healing in mice lacking Toll-like receptor 4.

Wang D, Gilbert JR, Cray JJ Jr, Kubala AA, Shaw MA, Billiar TR, Cooper GM.

PLoS One. 2012;7(10):e46945. doi: 10.1371/journal.pone.0046945. Epub 2012 Oct 10.

PMID:
23071670
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.

Cukier HN, Lee JM, Ma D, Young JI, Mayo V, Butler BL, Ramsook SS, Rantus JA, Abrams AJ, Whitehead PL, Wright HH, Abramson RK, Haines JL, Cuccaro ML, Pericak-Vance MA, Gilbert JR.

Autism Res. 2012 Dec;5(6):385-97. doi: 10.1002/aur.1251. Epub 2012 Oct 10.

PMID:
23055267
[PubMed - indexed for MEDLINE]
Free PMC Article
12.

A peak-clustering method for MEG group analysis to minimise artefacts due to smoothness.

Gilbert JR, Shapiro LR, Barnes GR.

PLoS One. 2012;7(9):e45084. Epub 2012 Sep 14.

PMID:
23024795
[PubMed - indexed for MEDLINE]
Free PMC Article
13.

Genome-wide association and linkage study in the Amish detects a novel candidate late-onset Alzheimer disease gene.

Cummings AC, Jiang L, Velez Edwards DR, McCauley JL, Laux R, McFarland LL, Fuzzell D, Knebusch C, Caywood L, Reinhart-Mercer L, Nations L, Gilbert JR, Konidari I, Tramontana M, Cuccaro ML, Scott WK, Pericak-Vance MA, Haines JL.

Ann Hum Genet. 2012 Sep;76(5):342-51. doi: 10.1111/j.1469-1809.2012.00721.x.

PMID:
22881374
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE).

Krupp DR, Xu PT, Thomas S, Dellinger A, Etchevers HC, Vekemans M, Gilbert JR, Speer MC, Ashley-Koch AE, Gregory SG; National Birth Defects Prevention Study.

Birth Defects Res A Clin Mol Teratol. 2012 Sep;94(9):683-92. doi: 10.1002/bdra.23040. Epub 2012 Jul 18.

PMID:
22806986
[PubMed - indexed for MEDLINE]
Free PMC Article
15.

Linkage and association of successful aging to the 6q25 region in large Amish kindreds.

Edwards DR, Gilbert JR, Hicks JE, Myers JL, Jiang L, Cummings AC, Guo S, Gallins PJ, Konidari I, Caywood L, Reinhart-Mercer L, Fuzzell D, Knebusch C, Laux R, Jackson CE, Pericak-Vance MA, Haines JL, Scott WK.

Age (Dordr). 2013 Aug;35(4):1467-77. doi: 10.1007/s11357-012-9447-1. Epub 2012 Jul 7.

PMID:
22773346
[PubMed - indexed for MEDLINE]
16.

Evaluation of copy number variations reveals novel candidate genes in autism spectrum disorder-associated pathways.

Griswold AJ, Ma D, Cukier HN, Nations LD, Schmidt MA, Chung RH, Jaworski JM, Salyakina D, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Martin ER, Haines JL, Gilbert JR, Cuccaro ML, Pericak-Vance MA.

Hum Mol Genet. 2012 Aug 1;21(15):3513-23. doi: 10.1093/hmg/dds164. Epub 2012 Apr 27.

PMID:
22543975
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Evidence of novel fine-scale structural variation at autism spectrum disorder candidate loci.

Hedges DJ, Hamilton-Nelson KL, Sacharow SJ, Nations L, Beecham GW, Kozhekbaeva ZM, Butler BL, Cukier HN, Whitehead PL, Ma D, Jaworski JM, Nathanson L, Lee JM, Hauser SL, Oksenberg JR, Cuccaro ML, Haines JL, Gilbert JR, Pericak-Vance MA.

Mol Autism. 2012 Apr 2;3:2. doi: 10.1186/2040-2392-3-2.

PMID:
22472195
[PubMed]
Free PMC Article
18.

MCP1 SNPs and pulmonary tuberculosis in cohorts from West Africa, the USA and Argentina: lack of association or epistasis with IL12B polymorphisms.

Velez Edwards DR, Tacconelli A, Wejse C, Hill PC, Morris GA, Edwards TL, Gilbert JR, Myers JL, Park YS, Stryjewski ME, Abbate E, Estevan R, Rabna P, Novelli G, Hamilton CD, Adegbola R, Østergaar L, Williams SM, Scott WK, Sirugo G.

PLoS One. 2012;7(2):e32275. doi: 10.1371/journal.pone.0032275. Epub 2012 Feb 27.

PMID:
22384203
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Vitamin D receptor and Alzheimer's disease: a genetic and functional study.

Wang L, Hara K, Van Baaren JM, Price JC, Beecham GW, Gallins PJ, Whitehead PL, Wang G, Lu C, Slifer MA, Züchner S, Martin ER, Mash D, Haines JL, Pericak-Vance MA, Gilbert JR.

Neurobiol Aging. 2012 Aug;33(8):1844.e1-9. doi: 10.1016/j.neurobiolaging.2011.12.038. Epub 2012 Feb 4.

PMID:
22306846
[PubMed - indexed for MEDLINE]
20.

Exploring the relationship between autism spectrum disorder and epilepsy using latent class cluster analysis.

Cuccaro ML, Tuchman RF, Hamilton KL, Wright HH, Abramson RK, Haines JL, Gilbert JR, Pericak-Vance M.

J Autism Dev Disord. 2012 Aug;42(8):1630-41. doi: 10.1007/s10803-011-1402-y.

PMID:
22105141
[PubMed - indexed for MEDLINE]

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