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Results: 1 to 20 of 76

1.

Phenotypic characterization and genealogical tracing in an Afrikaner schizophrenia database.

Karayiorgou M, Torrington M, Abecasis GR, Pretorius H, Robertson B, Kaliski S, Lay S, Sobin C, Möller N, Lundy SL, Blundell ML, Gogos JA, Roos JL.

Am J Med Genet B Neuropsychiatr Genet. 2004 Jan 1;124B(1):20-8.

PMID:
14681908
[PubMed - indexed for MEDLINE]
2.

Multipoint and single point non-parametric linkage analysis with imperfect data.

Sullivan PF, Neale BM, Neale MC, van den Oord E, Kendler KS.

Am J Med Genet B Neuropsychiatr Genet. 2003 Aug 15;121B(1):89-94.

PMID:
12898581
[PubMed - indexed for MEDLINE]
3.

Genome-wide scan in a large complex pedigree with predominantly male schizophrenics from the island of Kosrae: evidence for linkage to chromosome 2q.

Wijsman EM, Rosenthal EA, Hall D, Blundell ML, Sobin C, Heath SC, Williams R, Brownstein MJ, Gogos JA, Karayiorgou M.

Mol Psychiatry. 2003 Jul;8(7):695-705, 643.

PMID:
12874606
[PubMed - indexed for MEDLINE]
4.

Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series.

Hattori E, Liu C, Badner JA, Bonner TI, Christian SL, Maheshwari M, Detera-Wadleigh SD, Gibbs RA, Gershon ES.

Am J Hum Genet. 2003 May;72(5):1131-40. Epub 2003 Mar 19.

PMID:
12647258
[PubMed - indexed for MEDLINE]
Free PMC Article
5.

Using haplotype blocks to map human complex trait loci.

Cardon LR, Abecasis GR.

Trends Genet. 2003 Mar;19(3):135-40. Review.

PMID:
12615007
[PubMed - indexed for MEDLINE]
6.

Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia.

Chumakov I, Blumenfeld M, Guerassimenko O, Cavarec L, Palicio M, Abderrahim H, Bougueleret L, Barry C, Tanaka H, La Rosa P, Puech A, Tahri N, Cohen-Akenine A, Delabrosse S, Lissarrague S, Picard FP, Maurice K, Essioux L, Millasseau P, Grel P, Debailleul V, Simon AM, Caterina D, Dufaure I, Malekzadeh K, Belova M, Luan JJ, Bouillot M, Sambucy JL, Primas G, Saumier M, Boubkiri N, Martin-Saumier S, Nasroune M, Peixoto H, Delaye A, Pinchot V, Bastucci M, Guillou S, Chevillon M, Sainz-Fuertes R, Meguenni S, Aurich-Costa J, Cherif D, Gimalac A, Van Duijn C, Gauvreau D, Ouellette G, Fortier I, Raelson J, Sherbatich T, Riazanskaia N, Rogaev E, Raeymaekers P, Aerssens J, Konings F, Luyten W, Macciardi F, Sham PC, Straub RE, Weinberger DR, Cohen N, Cohen D.

Proc Natl Acad Sci U S A. 2002 Oct 15;99(21):13675-80. Epub 2002 Oct 3. Erratum in: Proc Natl Acad Sci U S A 2002 Dec 24;99(26):17221. Ouelette, G [corrected to Ouellette, G]; Realson, J [corrected to Raelson, J].

PMID:
12364586
[PubMed - indexed for MEDLINE]
Free PMC Article
7.

GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L.

Visapää I, Fellman V, Vesa J, Dasvarma A, Hutton JL, Kumar V, Payne GS, Makarow M, Van Coster R, Taylor RW, Turnbull DM, Suomalainen A, Peltonen L.

Am J Hum Genet. 2002 Oct;71(4):863-76. Epub 2002 Sep 5.

PMID:
12215968
[PubMed - indexed for MEDLINE]
Free PMC Article
8.

Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau.

Devlin B, Bacanu SA, Roeder K, Reimherr F, Wender P, Galke B, Novasad D, Chu A, TCuenco K, Tiobek S, Otto C, Byerley W.

Mol Psychiatry. 2002;7(7):689-94.

PMID:
12192612
[PubMed - indexed for MEDLINE]
Free Article
9.

Neuregulin 1 and susceptibility to schizophrenia.

Stefansson H, Sigurdsson E, Steinthorsdottir V, Bjornsdottir S, Sigmundsson T, Ghosh S, Brynjolfsson J, Gunnarsdottir S, Ivarsson O, Chou TT, Hjaltason O, Birgisdottir B, Jonsson H, Gudnadottir VG, Gudmundsdottir E, Bjornsson A, Ingvarsson B, Ingason A, Sigfusson S, Hardardottir H, Harvey RP, Lai D, Zhou M, Brunner D, Mutel V, Gonzalo A, Lemke G, Sainz J, Johannesson G, Andresson T, Gudbjartsson D, Manolescu A, Frigge ML, Gurney ME, Kong A, Gulcher JR, Petursson H, Stefansson K.

Am J Hum Genet. 2002 Oct;71(4):877-92. Epub 2002 Jul 23.

PMID:
12145742
[PubMed - indexed for MEDLINE]
Free PMC Article
10.

Genome-wide scans of three independent sets of 90 Irish multiplex schizophrenia families and follow-up of selected regions in all families provides evidence for multiple susceptibility genes.

Straub RE, MacLean CJ, Ma Y, Webb BT, Myakishev MV, Harris-Kerr C, Wormley B, Sadek H, Kadambi B, O'Neill FA, Walsh D, Kendler KS.

Mol Psychiatry. 2002;7(6):542-59.

PMID:
12140777
[PubMed - indexed for MEDLINE]
Free Article
11.

Genome-wide scan for linkage to schizophrenia in a Spanish-origin cohort from Costa Rica.

DeLisi LE, Mesen A, Rodriguez C, Bertheau A, LaPrade B, Llach M, Riondet S, Razi K, Relja M, Byerley W, Sherrington R.

Am J Med Genet. 2002 Jul 8;114(5):497-508.

PMID:
12116183
[PubMed - indexed for MEDLINE]
12.

A genome-wide scan for linkage to chromosomal regions in 382 sibling pairs with schizophrenia or schizoaffective disorder.

DeLisi LE, Shaw SH, Crow TJ, Shields G, Smith AB, Larach VW, Wellman N, Loftus J, Nanthakumar B, Razi K, Stewart J, Comazzi M, Vita A, Heffner T, Sherrington R.

Am J Psychiatry. 2002 May;159(5):803-12.

PMID:
11986135
[PubMed - indexed for MEDLINE]
13.

Chromosome 1q12-q22 linkage results in eastern Québec families affected by schizophrenia.

Maziade M, Fournier A, Phaneuf D, Cliche D, Fournier JP, Roy MA, Mérette C.

Am J Med Genet. 2002 Jan 8;114(1):51-5.

PMID:
11840506
[PubMed - indexed for MEDLINE]
14.

The effect of pedigree complexity on quantitative trait linkage analysis.

Dyer TD, Blangero J, Williams JT, Göring HH, Mahaney MC.

Genet Epidemiol. 2001;21 Suppl 1:S236-43.

PMID:
11793675
[PubMed - indexed for MEDLINE]
15.

Genome-wide scan in a nationwide study sample of schizophrenia families in Finland reveals susceptibility loci on chromosomes 2q and 5q.

Paunio T, Ekelund J, Varilo T, Parker A, Hovatta I, Turunen JA, Rinard K, Foti A, Terwilliger JD, Juvonen H, Suvisaari J, Arajärvi R, Suokas J, Partonen T, Lönnqvist J, Meyer J, Peltonen L.

Hum Mol Genet. 2001 Dec 15;10(26):3037-48.

PMID:
11751686
[PubMed - indexed for MEDLINE]
Free Article
16.

Merlin--rapid analysis of dense genetic maps using sparse gene flow trees.

Abecasis GR, Cherny SS, Cookson WO, Cardon LR.

Nat Genet. 2002 Jan;30(1):97-101. Epub 2001 Dec 3.

PMID:
11731797
[PubMed - indexed for MEDLINE]
17.

Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively.

Thompson DA, McHenry CL, Li Y, Richards JE, Othman MI, Schwinger E, Vollrath D, Jacobson SG, Gal A.

Am J Hum Genet. 2002 Jan;70(1):224-9. Epub 2001 Nov 27.

PMID:
11727200
[PubMed - indexed for MEDLINE]
Free PMC Article
18.

Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method.

Camp NJ, Neuhausen SL, Tiobech J, Polloi A, Coon H, Myles-Worsley M.

Am J Hum Genet. 2001 Dec;69(6):1278-89. Epub 2001 Oct 19.

PMID:
11668428
[PubMed - indexed for MEDLINE]
Free PMC Article
19.

GRR: graphical representation of relationship errors.

Abecasis GR, Cherny SS, Cookson WO, Cardon LR.

Bioinformatics. 2001 Aug;17(8):742-3.

PMID:
11524377
[PubMed - indexed for MEDLINE]
Free Article
20.

A survey of affected-sibship statistics for nonparametric linkage analysis.

Sengul H, Weeks DE, Feingold E.

Am J Hum Genet. 2001 Jul;69(1):179-90. Epub 2001 Jun 11.

PMID:
11404816
[PubMed - indexed for MEDLINE]
Free PMC Article

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