Sort by
Items per page

Send to

Choose Destination

Links from PubMed

Items: 1 to 20 of 101


Predisposition locus for major depression at chromosome 12q22-12q23.2.

Abkevich V, Camp NJ, Hensel CH, Neff CD, Russell DL, Hughes DC, Plenk AM, Lowry MR, Richards RL, Carter C, Frech GC, Stone S, Rowe K, Chau CA, Cortado K, Hunt A, Luce K, O'Neil G, Poarch J, Potter J, Poulsen GH, Saxton H, Bernat-Sestak M, Thompson V, Gutin A, Skolnick MH, Shattuck D, Cannon-Albright L.

Am J Hum Genet. 2003 Dec;73(6):1271-81. Epub 2003 Nov 5.


Genome-wide scan for hypertension linkage to chromosome 12q23.1 - q23.3 in a Chinese family.

Dong Y, Yang L, Fang F, Zhang J, Jiang G, Xu S.

Indian J Med Res. 2013 May;137(5):935-41.


Genome-wide multipoint parametric linkage analysis of pulse pressure in large, extended utah pedigrees.

Camp NJ, Hopkins PN, Hasstedt SJ, Coon H, Malhotra A, Cawthon RM, Hunt SC.

Hypertension. 2003 Sep;42(3):322-8. Epub 2003 Jul 21.


Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.

Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q.

Am J Hum Genet. 2004 May;74(5):876-85. Epub 2004 Apr 7.


A genomewide linkage study on suicidality in major depressive disorder confirms evidence for linkage to 2p12.

Butler AW, Breen G, Tozzi F, Craddock N, Gill M, Korszun A, Maier W, Middleton LT, Mors O, Owen MJ, Perry J, Preisig M, Rice JP, Rietschel M, Jones L, Farmer AE, Lewis CM, McGuffin P.

Am J Med Genet B Neuropsychiatr Genet. 2010 Dec 5;153B(8):1465-73. doi: 10.1002/ajmg.b.31127. Epub 2010 Sep 30.


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.


Restless legs syndrome: confirmation of linkage to chromosome 12q, genetic heterogeneity, and evidence of complexity.

Desautels A, Turecki G, Montplaisir J, Xiong L, Walters AS, Ehrenberg BL, Brisebois K, Desautels AK, Gingras Y, Johnson WG, Lugaresi E, Coccagna G, Picchietti DL, Lazzarini A, Rouleau GA.

Arch Neurol. 2005 Apr;62(4):591-6.


Genome-wide linkage analyses of extended Utah pedigrees identifies loci that influence recurrent, early-onset major depression and anxiety disorders.

Camp NJ, Lowry MR, Richards RL, Plenk AM, Carter C, Hensel CH, Abkevich V, Skolnick MH, Shattuck D, Rowe KG, Hughes DC, Cannon-Albright LA.

Am J Med Genet B Neuropsychiatr Genet. 2005 May 5;135B(1):85-93.


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.


Genomewide linkage analysis of stature in multiple populations reveals several regions with evidence of linkage to adult height.

Hirschhorn JN, Lindgren CM, Daly MJ, Kirby A, Schaffner SF, Burtt NP, Altshuler D, Parker A, Rioux JD, Platko J, Gaudet D, Hudson TJ, Groop LC, Lander ES.

Am J Hum Genet. 2001 Jul;69(1):106-16. Epub 2001 Jun 15.


A major predisposition locus for severe obesity, at 4p15-p14.

Stone S, Abkevich V, Hunt SC, Gutin A, Russell DL, Neff CD, Riley R, Frech GC, Hensel CH, Jammulapati S, Potter J, Sexton D, Tran T, Gibbs D, Iliev D, Gress R, Bloomquist B, Amatruda J, Rae PM, Adams TD, Skolnick MH, Shattuck D.

Am J Hum Genet. 2002 Jun;70(6):1459-68. Epub 2002 Apr 15.


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.


A genome-wide scan points to a susceptibility locus for bipolar disorder on chromosome 12.

Shink E, Morissette J, Sherrington R, Barden N.

Mol Psychiatry. 2005 Jun;10(6):545-52.


Genomewide linkage scan for myopia susceptibility loci among Ashkenazi Jewish families shows evidence of linkage on chromosome 22q12.

Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes T, Ciner E, Bailey-Wilson JE.

Am J Hum Genet. 2004 Sep;75(3):448-59. Epub 2004 Jul 23.


A high-density genome scan detects evidence for a bipolar-disorder susceptibility locus on 13q32 and other potential loci on 1q32 and 18p11.2.

Detera-Wadleigh SD, Badner JA, Berrettini WH, Yoshikawa T, Goldin LR, Turner G, Rollins DY, Moses T, Sanders AR, Karkera JD, Esterling LE, Zeng J, Ferraro TN, Guroff JJ, Kazuba D, Maxwell ME, Nurnberger JI Jr, Gershon ES.

Proc Natl Acad Sci U S A. 1999 May 11;96(10):5604-9.


Genomewide linkage analysis of quantitative spirometric phenotypes in severe early-onset chronic obstructive pulmonary disease.

Silverman EK, Palmer LJ, Mosley JD, Barth M, Senter JM, Brown A, Drazen JM, Kwiatkowski DJ, Chapman HA, Campbell EJ, Province MA, Rao DC, Reilly JJ, Ginns LC, Speizer FE, Weiss ST.

Am J Hum Genet. 2002 May;70(5):1229-39. Epub 2002 Mar 25.


Genome scan of pedigrees multiply affected with bipolar disorder provides further support for the presence of a susceptibility locus on chromosome 12q23-q24, and suggests the presence of additional loci on 1p and 1q.

Curtis D, Kalsi G, Brynjolfsson J, McInnis M, O'Neill J, Smyth C, Moloney E, Murphy P, McQuillin A, Petursson H, Gurling H.

Psychiatr Genet. 2003 Jun;13(2):77-84.


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.


Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.

Desautels A, Turecki G, Montplaisir J, Sequeira A, Verner A, Rouleau GA.

Am J Hum Genet. 2001 Dec;69(6):1266-70. Epub 2001 Nov 6.


Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter.

Bayer Y, Neumann S, Meyer B, Rüschendorf F, Reske A, Brix T, Hegedüs L, Langer P, Nürnberg P, Paschke R.

J Clin Endocrinol Metab. 2004 Aug;89(8):4044-52.


Supplemental Content

Support Center