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Items: 1 to 20 of 234

1.

A genomewide screen for autism-spectrum disorders: evidence for a major susceptibility locus on chromosome 3q25-27.

Auranen M, Vanhala R, Varilo T, Ayers K, Kempas E, Ylisaukko-Oja T, Sinsheimer JS, Peltonen L, Järvelä I.

Am J Hum Genet. 2002 Oct;71(4):777-90.

2.

Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland.

Auranen M, Varilo T, Alen R, Vanhala R, Ayers K, Kempas E, Ylisaukko-Oja T, Peltonen L, Järvelä I.

Mol Psychiatry. 2003 Oct;8(10):879-84.

PMID:
14515138
3.

A genomewide screen for autism susceptibility loci.

Liu J, Nyholt DR, Magnussen P, Parano E, Pavone P, Geschwind D, Lord C, Iversen P, Hoh J, Ott J, Gilliam TC; Autism Genetic Resource Exchange Consortium..

Am J Hum Genet. 2001 Aug;69(2):327-40.

4.

Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21.

Volders PG, Zhu Q, Timmermans C, Eurlings PM, Su X, Arens YH, Li L, Jongbloed RJ, Xia M, Rodriguez LM, Chen YH.

Heart Rhythm. 2007 Apr;4(4):469-75.

PMID:
17399636
5.

An analysis of candidate autism loci on chromosome 2q24-q33: evidence for association to the STK39 gene.

Ramoz N, Cai G, Reichert JG, Silverman JM, Buxbaum JD.

Am J Med Genet B Neuropsychiatr Genet. 2008 Oct 5;147B(7):1152-8. doi: 10.1002/ajmg.b.30739.

PMID:
18348195
6.

Examination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genes.

Hutcheson HB, Olson LM, Bradford Y, Folstein SE, Santangelo SL, Sutcliffe JS, Haines JL.

BMC Med Genet. 2004 May 5;5:12.

7.

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families.

Ylisaukko-oja T, Alarcón M, Cantor RM, Auranen M, Vanhala R, Kempas E, von Wendt L, Järvelä I, Geschwind DH, Peltonen L.

Ann Neurol. 2006 Jan;59(1):145-55.

PMID:
16288458
8.

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.

9.

Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families.

Venken T, Alaerts M, Souery D, Goossens D, Sluijs S, Navon R, Van Broeckhoven C, Mendlewicz J, Del-Favero J, Claes S.

Mol Psychiatry. 2008 Apr;13(4):442-50.

PMID:
17579605
10.

Genomewide linkage scan for schizophrenia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 10q22.

Fallin MD, Lasseter VK, Wolyniec PS, McGrath JA, Nestadt G, Valle D, Liang KY, Pulver AE.

Am J Hum Genet. 2003 Sep;73(3):601-11.

11.

Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree.

Panhuysen CI, Karban A, Knodle Manning A, Bayless TM, Duerr RH, Bailey-Wilson JE, Epstein EH Jr, Brant SR.

Hum Genet. 2006 Aug;120(1):31-41.

PMID:
16733713
12.

Genomewide scan identifies susceptibility locus for dyslexia on Xq27 in an extended Dutch family.

de Kovel CG, Hol FA, Heister JG, Willemen JJ, Sandkuijl LA, Franke B, Padberg GW.

J Med Genet. 2004 Sep;41(9):652-7.

13.

Evidence for asthma susceptibility genes on chromosome 11 in an African-American population.

Huang SK, Mathias RA, Ehrlich E, Plunkett B, Liu X, Cutting GR, Wang XJ, Li XD, Togias A, Barnes KC, Malveaux F, Rich S, Mellen B, Lange E, Beaty TH; Comparative Study on the Genetics of Asthma..

Hum Genet. 2003 Jul;113(1):71-5.

PMID:
12664305
14.

Evidence for two schizophrenia susceptibility genes on chromosome 22q13.

Condra JA, Neibergs H, Wei W, Brennan MD.

Psychiatr Genet. 2007 Oct;17(5):292-8.

PMID:
17728668
15.

A search for specific and common susceptibility loci for schizophrenia and bipolar disorder: a linkage study in 13 target chromosomes.

Maziade M, Roy MA, Rouillard E, Bissonnette L, Fournier JP, Roy A, Garneau Y, Montgrain N, Potvin A, Cliche D, Dion C, Wallot H, Fournier A, Nicole L, Lavallée JC, Mérette C.

Mol Psychiatry. 2001 Nov;6(6):684-93.

16.

Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.

Holliday EG, McLean DE, Nyholt DR, Mowry BJ.

Arch Gen Psychiatry. 2009 Oct;66(10):1058-67. doi: 10.1001/archgenpsychiatry.2009.136.

PMID:
19805696
17.

Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes.

Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA.

Neurosci Lett. 2004 Dec 6;372(3):209-14.

PMID:
15542242
18.

A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.

Pillai SG, Chiano MN, White NJ, Speer M, Barnes KC, Carlsen K, Gerritsen J, Helms P, Lenney W, Silverman M, Sly P, Sundy J, Tsanakas J, von Berg A, Whyte M, Varsani S, Skelding P, Hauser M, Vance J, Pericak-Vance M, Burns DK, Middleton LT, Brewster SR, Anderson WH, Riley JH.

Eur J Hum Genet. 2006 Mar;14(3):307-16. Erratum in: Eur J Hum Genet. 2007 Jun;15(6):714.

19.

Exclusion of linkage to the HLA region in ninety multiplex sibships with autism.

Rogers T, Kalaydjieva L, Hallmayer J, Petersen PB, Nicholas P, Pingree C, McMahon WM, Spiker D, Lotspeich L, Kraemer H, McCague P, Dimiceli S, Nouri N, Peachy T, Yang J, Hinds D, Risch N, Myers RM.

J Autism Dev Disord. 1999 Jun;29(3):195-201.

PMID:
10425582
20.

Evidence for an interaction of schizophrenia susceptibility loci on chromosome 6q23.3 and 10q24.33-q26.13 in Arab Israeli families.

Alkelai A, Kohn Y, Olender T, Sarner-Kanyas K, Rigbi A, Hamdan A, Ben-Asher E, Lancet D, Lerer B.

Am J Med Genet B Neuropsychiatr Genet. 2009 Oct 5;150B(7):914-25. doi: 10.1002/ajmg.b.30918.

PMID:
19152384
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