Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Results: 1 to 20 of 152

1.

Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.

Bakkaloglu B, O'Roak BJ, Louvi A, Gupta AR, Abelson JF, Morgan TM, Chawarska K, Klin A, Ercan-Sencicek AG, Stillman AA, Tanriover G, Abrahams BS, Duvall JA, Robbins EM, Geschwind DH, Biederer T, Gunel M, Lifton RP, State MW.

Am J Hum Genet. 2008 Jan;82(1):165-73. doi: 10.1016/j.ajhg.2007.09.017.

PMID:
18179895
[PubMed - indexed for MEDLINE]
Free PMC Article
2.

The genetics of autism.

Muhle R, Trentacoste SV, Rapin I.

Pediatrics. 2004 May;113(5):e472-86. Review.

PMID:
15121991
[PubMed - indexed for MEDLINE]
3.

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene.

Alarcón M, Abrahams BS, Stone JL, Duvall JA, Perederiy JV, Bomar JM, Sebat J, Wigler M, Martin CL, Ledbetter DH, Nelson SF, Cantor RM, Geschwind DH.

Am J Hum Genet. 2008 Jan;82(1):150-9. doi: 10.1016/j.ajhg.2007.09.005.

PMID:
18179893
[PubMed - indexed for MEDLINE]
Free PMC Article
4.

Copy number and sequence variants implicate APBA2 as an autism candidate gene.

Babatz TD, Kumar RA, Sudi J, Dobyns WB, Christian SL.

Autism Res. 2009 Dec;2(6):359-64. doi: 10.1002/aur.107.

PMID:
20029827
[PubMed - indexed for MEDLINE]
5.

Disruption of CNTNAP2 and additional structural genome changes in a boy with speech delay and autism spectrum disorder.

Poot M, Beyer V, Schwaab I, Damatova N, Van't Slot R, Prothero J, Holder SE, Haaf T.

Neurogenetics. 2010 Feb;11(1):81-9. doi: 10.1007/s10048-009-0205-1. Epub 2009 Jul 7.

PMID:
19582487
[PubMed - indexed for MEDLINE]
6.

A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism.

Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A.

Am J Hum Genet. 2008 Jan;82(1):160-4. doi: 10.1016/j.ajhg.2007.09.015.

PMID:
18179894
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population.

Li X, Hu Z, He Y, Xiong Z, Long Z, Peng Y, Bu F, Ling J, Xun G, Mo X, Pan Q, Zhao J, Xia K.

Psychiatr Genet. 2010 Jun;20(3):113-7. doi: 10.1097/YPG.0b013e32833a216f.

PMID:
20414140
[PubMed - indexed for MEDLINE]
8.

Altered functional connectivity in frontal lobe circuits is associated with variation in the autism risk gene CNTNAP2.

Scott-Van Zeeland AA, Abrahams BS, Alvarez-Retuerto AI, Sonnenblick LI, Rudie JD, Ghahremani D, Mumford JA, Poldrack RA, Dapretto M, Geschwind DH, Bookheimer SY.

Sci Transl Med. 2010 Nov 3;2(56):56ra80. doi: 10.1126/scitranslmed.3001344.

PMID:
21048216
[PubMed - indexed for MEDLINE]
Free PMC Article
9.

Contact in the genetics of autism and schizophrenia.

Burbach JP, van der Zwaag B.

Trends Neurosci. 2009 Feb;32(2):69-72. doi: 10.1016/j.tins.2008.11.002. Epub 2009 Jan 8.

PMID:
19135727
[PubMed - indexed for MEDLINE]
10.

Allelic heterogeneity at the serotonin transporter locus (SLC6A4) confers susceptibility to autism and rigid-compulsive behaviors.

Sutcliffe JS, Delahanty RJ, Prasad HC, McCauley JL, Han Q, Jiang L, Li C, Folstein SE, Blakely RD.

Am J Hum Genet. 2005 Aug;77(2):265-79. Epub 2005 Jul 1.

PMID:
15995945
[PubMed - indexed for MEDLINE]
Free PMC Article
11.

Genetic variation in CNTNAP2 alters brain function during linguistic processing in healthy individuals.

Whalley HC, O'Connell G, Sussmann JE, Peel A, Stanfield AC, Hayiou-Thomas ME, Johnstone EC, Lawrie SM, McIntosh AM, Hall J.

Am J Med Genet B Neuropsychiatr Genet. 2011 Dec;156B(8):941-8. doi: 10.1002/ajmg.b.31241. Epub 2011 Oct 10.

PMID:
21987501
[PubMed - indexed for MEDLINE]
12.

Analysis of two language-related genes in autism: a case-control association study of FOXP2 and CNTNAP2.

Toma C, Hervás A, Torrico B, Balmaña N, Salgado M, Maristany M, Vilella E, Martínez-Leal R, Planelles MI, Cuscó I, del Campo M, Pérez-Jurado LA, Caballero-Andaluz R, de Diego-Otero Y, Pérez-Costillas L, Ramos-Quiroga JA, Ribasés M, Bayés M, Cormand B.

Psychiatr Genet. 2013 Apr;23(2):82-5. doi: 10.1097/YPG.0b013e32835d6fc6.

PMID:
23277129
[PubMed - indexed for MEDLINE]
13.

A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.

Kumar RA, Sudi J, Babatz TD, Brune CW, Oswald D, Yen M, Nowak NJ, Cook EH, Christian SL, Dobyns WB.

J Med Genet. 2010 Feb;47(2):81-90. doi: 10.1136/jmg.2008.065821. Epub 2009 Jun 21.

PMID:
19546099
[PubMed - indexed for MEDLINE]
Free PMC Article
14.

Gene associated with seizures, autism, and hepatomegaly in an Amish girl.

Jackman C, Horn ND, Molleston JP, Sokol DK.

Pediatr Neurol. 2009 Apr;40(4):310-3. doi: 10.1016/j.pediatrneurol.2008.10.013.

PMID:
19302947
[PubMed - indexed for MEDLINE]
15.

Defining the contribution of CNTNAP2 to autism susceptibility.

Sampath S, Bhat S, Gupta S, O'Connor A, West AB, Arking DE, Chakravarti A.

PLoS One. 2013 Oct 17;8(10):e77906. doi: 10.1371/journal.pone.0077906. eCollection 2013.

PMID:
24147096
[PubMed - indexed for MEDLINE]
Free PMC Article
16.

Absence of CNTNAP2 leads to epilepsy, neuronal migration abnormalities, and core autism-related deficits.

Peñagarikano O, Abrahams BS, Herman EI, Winden KD, Gdalyahu A, Dong H, Sonnenblick LI, Gruver R, Almajano J, Bragin A, Golshani P, Trachtenberg JT, Peles E, Geschwind DH.

Cell. 2011 Sep 30;147(1):235-46. doi: 10.1016/j.cell.2011.08.040.

PMID:
21962519
[PubMed - indexed for MEDLINE]
Free PMC Article
17.

Mutations in the SHANK2 synaptic scaffolding gene in autism spectrum disorder and mental retardation.

Berkel S, Marshall CR, Weiss B, Howe J, Roeth R, Moog U, Endris V, Roberts W, Szatmari P, Pinto D, Bonin M, Riess A, Engels H, Sprengel R, Scherer SW, Rappold GA.

Nat Genet. 2010 Jun;42(6):489-91. doi: 10.1038/ng.589. Epub 2010 May 16.

PMID:
20473310
[PubMed - indexed for MEDLINE]
18.

Unraveling autism.

Stephan DA.

Am J Hum Genet. 2008 Jan;82(1):7-9. doi: 10.1016/j.ajhg.2007.12.003.

PMID:
18179879
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

Contactin 4 as an autism susceptibility locus.

Cottrell CE, Bir N, Varga E, Alvarez CE, Bouyain S, Zernzach R, Thrush DL, Evans J, Trimarchi M, Butter EM, Cunningham D, Gastier-Foster JM, McBride KL, Herman GE.

Autism Res. 2011 Jun;4(3):189-99. doi: 10.1002/aur.184. Epub 2011 Feb 9.

PMID:
21308999
[PubMed - indexed for MEDLINE]
Free PMC Article
20.

Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locus.

Benayed R, Gharani N, Rossman I, Mancuso V, Lazar G, Kamdar S, Bruse SE, Tischfield S, Smith BJ, Zimmerman RA, Dicicco-Bloom E, Brzustowicz LM, Millonig JH.

Am J Hum Genet. 2005 Nov;77(5):851-68. Epub 2005 Oct 5.

PMID:
16252243
[PubMed - indexed for MEDLINE]
Free PMC Article

Display Settings:

Format
Items per page
Sort by

Send to:

Choose Destination

Supplemental Content

Write to the Help Desk