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Items: 1 to 20 of 361

1.

A genome-wide screen and linkage mapping for a large pedigree with episodic ataxia.

Cader MZ, Steckley JL, Dyment DA, McLachlan RS, Ebers GC.

Neurology. 2005 Jul 12;65(1):156-8.

PMID:
16009908
2.

An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?

Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM.

Neurology. 2005 Oct 11;65(7):1111-3. Epub 2005 Aug 31.

PMID:
16135769
3.

A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23.

Chung MY, Lu YC, Cheng NC, Soong BW.

Brain. 2003 Jun;126(Pt 6):1293-9.

PMID:
12764052
4.

Localization of a gene (MCUL1) for multiple cutaneous leiomyomata and uterine fibroids to chromosome 1q42.3-q43.

Alam NA, Bevan S, Churchman M, Barclay E, Barker K, Jaeger EE, Nelson HM, Healy E, Pembroke AC, Friedmann PS, Dalziel K, Calonje E, Anderson J, August PJ, Davies MG, Felix R, Munro CS, Murdoch M, Rendall J, Kennedy S, Leigh IM, Kelsell DP, Tomlinson IP, Houlston RS.

Am J Hum Genet. 2001 May;68(5):1264-9. Epub 2001 Mar 14.

5.

Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3.

Hedera P, Blair MA, Andermann E, Andermann F, D'Agostino D, Taylor KA, Chahine L, Pandolfo M, Bradford Y, Haines JL, Abou-Khalil B.

Neurology. 2007 Jun 12;68(24):2107-12. Epub 2007 Mar 21.

PMID:
17377072
6.

A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.

McAuley EZ, Blair IP, Liu Z, Fullerton JM, Scimone A, Van Herten M, Evans MR, Kirkby KC, Donald JA, Mitchell PB, Schofield PR.

Mol Psychiatry. 2009 May;14(5):492-500. doi: 10.1038/sj.mp.4002146. Epub 2008 Jan 29.

PMID:
18227837
7.

Linkage of Paget disease of bone to a novel region on human chromosome 18q23.

Good DA, Busfield F, Fletcher BH, Duffy DL, Kesting JB, Andersen J, Shaw JT.

Am J Hum Genet. 2002 Feb;70(2):517-25. Epub 2001 Dec 7.

8.

Posterior column ataxia with retinitis pigmentosa (AXPC1) maps to chromosome 1q31-q32.

Higgins JJ, Morton DH, Loveless JM.

Neurology. 1999 Jan 1;52(1):146-50.

PMID:
9921862
9.

Genome-wide linkage scan, fine mapping, and haplotype analysis in a large, inbred, Arab Israeli pedigree suggest a schizophrenia susceptibility locus on chromosome 20p13.

Teltsh O, Kanyas K, Karni O, Levi A, Korner M, Ben-Asher E, Lancet D, Hamdan A, Lerer B, Kohn Y.

Am J Med Genet B Neuropsychiatr Genet. 2008 Mar 5;147B(2):209-15.

PMID:
17823922
10.

Familial occipitotemporal lobe epilepsy and migraine with visual aura: linkage to chromosome 9q.

Deprez L, Peeters K, Van Paesschen W, Claeys KG, Claes LR, Suls A, Audenaert D, Van Dyck T, Goossens D, Del-Favero J, De Jonghe P.

Neurology. 2007 Jun 5;68(23):1995-2002. Epub 2007 Apr 25.

PMID:
17460155
11.

Autosomal dominant spastic paraplegia with peripheral neuropathy maps to chr12q23-24.

Schüle R, Bonin M, Dürr A, Forlani S, Sperfeld AD, Klimpe S, Mueller JC, Seibel A, van de Warrenburg BP, Bauer P, Schöls L.

Neurology. 2009 Jun 2;72(22):1893-8. doi: 10.1212/WNL.0b013e3181a6086c. Epub 2009 Apr 8.

PMID:
19357379
12.

A schizophrenia-susceptibility locus at 6q25, in one of the world's largest reported pedigrees.

Lindholm E, Ekholm B, Shaw S, Jalonen P, Johansson G, Pettersson U, Sherrington R, Adolfsson R, Jazin E.

Am J Hum Genet. 2001 Jul;69(1):96-105. Epub 2001 May 25.

13.

Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.

Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A; French Research Network on FTD/FTD-MND.

Neurology. 2009 May 12;72(19):1669-76. doi: 10.1212/WNL.0b013e3181a55f1c.

PMID:
19433740
14.

Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.

Cevoli S, Pierangeli G, Monari L, Valentino ML, Bernardoni P, Mochi M, Cortelli P, Montagna P.

Neurol Sci. 2002 Apr;23(1):7-10.

PMID:
12111614
15.

A mutation in myotilin causes spheroid body myopathy.

Foroud T, Pankratz N, Batchman AP, Pauciulo MW, Vidal R, Miravalle L, Goebel HH, Cushman LJ, Azzarelli B, Horak H, Farlow M, Nichols WC.

Neurology. 2005 Dec 27;65(12):1936-40.

PMID:
16380616
16.

Genome-wide scan identifies a susceptibility locus for familial primary cutaneous amyloidosis on chromosome 5p13.1-q11.2.

Lee DD, Lin MW, Chen IC, Huang CY, Liu MT, Wang CR, Chang YT, Liu HN, Liu TT, Wong CK, Tsai SF.

Br J Dermatol. 2006 Dec;155(6):1201-8.

PMID:
17107390
17.

An autosomal dominant disorder with episodic ataxia, vertigo, and tinnitus.

Steckley JL, Ebers GC, Cader MZ, McLachlan RS.

Neurology. 2001 Oct 23;57(8):1499-502.

PMID:
11673600
18.

The autosomal recessive Kenny-Caffey syndrome locus maps to chromosome 1q42-q43.

Diaz GA, Khan KT, Gelb BD.

Genomics. 1998 Nov 15;54(1):13-8.

PMID:
9806825
19.

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
20.

A novel locus for an autosomal recessive hereditary spastic paraplegia (SPG35) maps to 16q21-q23.

Dick KJ, Al-Mjeni R, Baskir W, Koul R, Simpson MA, Patton MA, Raeburn S, Crosby AH.

Neurology. 2008 Jul 22;71(4):248-52. doi: 10.1212/01.wnl.0000319610.29522.8a. Epub 2008 May 7.

PMID:
18463364

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