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Items: 1 to 20 of 91

1.

Localization of a susceptibility gene for common forms of stroke to 5q12.

Gretarsdottir S, Sveinbjörnsdottir S, Jonsson HH, Jakobsson F, Einarsdottir E, Agnarsson U, Shkolny D, Einarsson G, Gudjonsdottir HM, Valdimarsson EM, Einarsson OB, Thorgeirsson G, Hadzic R, Jonsdottir S, Reynisdottir ST, Bjarnadottir SM, Gudmundsdottir T, Gudlaugsdottir GJ, Gill R, Lindpaintner K, Sainz J, Hannesson HH, Sigurdsson GT, Frigge ML, Kong A, Gudnason V, Stefansson K, Gulcher JR.

Am J Hum Genet. 2002 Mar;70(3):593-603. Epub 2002 Feb 6.

2.

Linkage of ischemic stroke to the PDE4D region on 5q in a Swedish population.

Nilsson-Ardnor S, Wiklund PG, Lindgren P, Nilsson AK, Janunger T, Escher SA, Hallbeck B, Stegmayr B, Asplund K, Holmberg D.

Stroke. 2005 Aug;36(8):1666-71. Epub 2005 Jul 14.

3.

Localization of a gene for peripheral arterial occlusive disease to chromosome 1p31.

Gudmundsson G, Matthiasson SE, Arason H, Johannsson H, Runarsson F, Bjarnason H, Helgadottir K, Thorisdottir S, Ingadottir G, Lindpaintner K, Sainz J, Gudnason V, Frigge ML, Kong A, Gulcher JR, Stefansson K.

Am J Hum Genet. 2002 Mar;70(3):586-92. Epub 2002 Feb 6.

4.

Genome-wide linkage scan of common stroke in families from northern Sweden.

Nilsson-Ardnor S, Janunger T, Wiklund PG, Lackovic K, Nilsson AK, Lindgren P, Escher SA, Stegmayr B, Asplund K, Holmberg D.

Stroke. 2007 Jan;38(1):34-40. Epub 2006 Nov 22.

5.

Localization of a susceptibility gene for type 2 diabetes to chromosome 5q34-q35.2.

Reynisdottir I, Thorleifsson G, Benediktsson R, Sigurdsson G, Emilsson V, Einarsdottir AS, Hjorleifsdottir EE, Orlygsdottir GT, Bjornsdottir GT, Saemundsdottir J, Halldorsson S, Hrafnkelsdottir S, Sigurjonsdottir SB, Steinsdottir S, Martin M, Kochan JP, Rhees BK, Grant SF, Frigge ML, Kong A, Gudnason V, Stefansson K, Gulcher JR.

Am J Hum Genet. 2003 Aug;73(2):323-35. Epub 2003 Jul 8.

6.

PDE4D gene in the STRK1 region on 5q12: susceptibility gene for ischemic stroke.

Nakayama T, Asai S, Sato N, Soma M.

Curr Med Chem. 2007;14(30):3171-8. Review.

PMID:
18220751
7.

A major susceptibility gene for asthma maps to chromosome 14q24.

Hakonarson H, Bjornsdottir US, Halapi E, Palsson S, Adalsteinsdottir E, Gislason D, Finnbogason G, Gislason T, Kristjansson K, Arnason T, Birkisson I, Frigge ML, Kong A, Gulcher JR, Stefansson K.

Am J Hum Genet. 2002 Sep;71(3):483-91. Epub 2002 Jul 15.

8.

Genomewide scan and fine mapping of quantitative trait loci for intraocular pressure on 5q and 14q in West Africans.

Rotimi CN, Chen G, Adeyemo AA, Jones LS, Agyenim-Boateng K, Eghan BA Jr, Zhou J, Doumatey A, Lashley K, Huang H, Fasanmade O, Akinsola FB, Ezepue F, Amoah A, Akafo S, Chen Y, Oli J, Johnson T.

Invest Ophthalmol Vis Sci. 2006 Aug;47(8):3262-7.

PMID:
16877390
9.

Genomewide genetic linkage analysis confirms the presence of susceptibility loci for schizophrenia, on chromosomes 1q32.2, 5q33.2, and 8p21-22 and provides support for linkage to schizophrenia, on chromosomes 11q23.3-24 and 20q12.1-11.23.

Gurling HM, Kalsi G, Brynjolfson J, Sigmundsson T, Sherrington R, Mankoo BS, Read T, Murphy P, Blaveri E, McQuillin A, Petursson H, Curtis D.

Am J Hum Genet. 2001 Mar;68(3):661-73.

10.

Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.

Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, Yang H.

Genet Med. 2005 Jul-Aug;7(6):397-405.

PMID:
16024971
11.

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.

12.

A genomewide scan for loci predisposing to type 2 diabetes in a U.K. population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication of a susceptibility locus on chromosome 1q.

Wiltshire S, Hattersley AT, Hitman GA, Walker M, Levy JC, Sampson M, O'Rahilly S, Frayling TM, Bell JI, Lathrop GM, Bennett A, Dhillon R, Fletcher C, Groves CJ, Jones E, Prestwich P, Simecek N, Rao PV, Wishart M, Bottazzo GF, Foxon R, Howell S, Smedley D, Cardon LR, Menzel S, McCarthy MI.

Am J Hum Genet. 2001 Sep;69(3):553-69. Epub 2001 Aug 1. Erratum in: Am J Hum Genet 2002 Apr;70(4):1075.

13.

Attention-deficit/hyperactivity disorder in a population isolate: linkage to loci at 4q13.2, 5q33.3, 11q22, and 17p11.

Arcos-Burgos M, Castellanos FX, Pineda D, Lopera F, Palacio JD, Palacio LG, Rapoport JL, Berg K, Bailey-Wilson JE, Muenke M.

Am J Hum Genet. 2004 Dec;75(6):998-1014. Epub 2004 Oct 20.

14.

Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.

Vionnet N, Hani EH, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Leprêtre F, Lecoeur C, Gallina P, Zekiri L, Dina C, Froguel P.

Am J Hum Genet. 2000 Dec;67(6):1470-80. Epub 2000 Nov 6.

15.

Genomewide search in familial Paget disease of bone shows evidence of genetic heterogeneity with candidate loci on chromosomes 2q36, 10p13, and 5q35.

Hocking LJ, Herbert CA, Nicholls RK, Williams F, Bennett ST, Cundy T, Nicholson GC, Wuyts W, Van Hul W, Ralston SH.

Am J Hum Genet. 2001 Nov;69(5):1055-61. Epub 2001 Sep 5.

16.

Genome-wide scan of Graves' disease: evidence for linkage on chromosome 5q31 in Chinese Han pedigrees.

Jin Y, Teng W, Ben S, Xiong X, Zhang J, Xu S, Shugart YY, Jin L, Chen J, Huang W.

J Clin Endocrinol Metab. 2003 Apr;88(4):1798-803.

PMID:
12679476
17.

Linkage of essential hypertension to chromosome 18q.

Kristjansson K, Manolescu A, Kristinsson A, Hardarson T, Knudsen H, Ingason S, Thorleifsson G, Frigge ML, Kong A, Gulcher JR, Stefansson K.

Hypertension. 2002 Jun;39(6):1044-9.

18.

Linkage genome scan for loci predisposing to panic disorder or agoraphobia.

Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.

Am J Med Genet. 2001 Aug 8;105(6):548-57.

PMID:
11496373
19.

A novel stroke locus identified in a northern Sweden pedigree: linkage to chromosome 9q31-33.

Janunger T, Nilsson-Ardnor S, Wiklund PG, Lindgren P, Escher SA, Lackovic K, Nilsson AK, Stegmayr B, Asplund K, Holmberg D.

Neurology. 2009 Nov 24;73(21):1767-73. doi: 10.1212/WNL.0b013e3181c34b1d.

PMID:
19933978
20.

A susceptibility gene for late-onset idiopathic Parkinson's disease.

Hicks AA, Pétursson H, Jónsson T, Stefánsson H, Jóhannsdóttir HS, Sainz J, Frigge ML, Kong A, Gulcher JR, Stefánsson K, Sveinbjörnsdóttir S.

Ann Neurol. 2002 Nov;52(5):549-55.

PMID:
12402251

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