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Items: 1 to 20 of 144

1.

Genomewide scan in Ashkenazi Jewish families demonstrates evidence of linkage of ocular refraction to a QTL on chromosome 1p36.

Wojciechowski R, Moy C, Ciner E, Ibay G, Reider L, Bailey-Wilson JE, Stambolian D.

Hum Genet. 2006 May;119(4):389-99. Epub 2006 Feb 24.

2.
3.

Genomewide linkage scans for ocular refraction and meta-analysis of four populations in the Myopia Family Study.

Wojciechowski R, Stambolian D, Ciner E, Ibay G, Holmes TN, Bailey-Wilson JE.

Invest Ophthalmol Vis Sci. 2009 May;50(5):2024-32. doi: 10.1167/iovs.08-2848. Epub 2009 Jan 17.

4.

Genomewide scan of ocular refraction in African-American families shows significant linkage to chromosome 7p15.

Ciner E, Wojciechowski R, Ibay G, Bailey-Wilson JE, Stambolian D.

Genet Epidemiol. 2008 Jul;32(5):454-63. doi: 10.1002/gepi.20318.

5.

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.

6.

An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.

Shugart YY, Silverberg MS, Duerr RH, Taylor KD, Wang MH, Zarfas K, Schumm LP, Bromfield G, Steinhart AH, Griffiths AM, Kane SV, Barmada MM, Rotter JI, Mei L, Bernstein CN, Bayless TM, Langelier D, Cohen A, Bitton A, Rioux JD, Cho JH, Brant SR.

Genes Immun. 2008 Mar;9(2):161-7. doi: 10.1038/sj.gene.6364460. Epub 2008 Jan 31.

7.

An international collaborative family-based whole genome quantitative trait linkage scan for myopic refractive error.

Abbott D, Li YJ, Guggenheim JA, Metlapally R, Malecaze F, Calvas P, Rosenberg T, Paget S, Zayats T, Mackey DA, Feng S, Young TL.

Mol Vis. 2012;18:720-9. Epub 2012 Mar 26.

8.

Dissecting the genetic heterogeneity of myopia susceptibility in an Ashkenazi Jewish population using ordered subset analysis.

Simpson CL, Wojciechowski R, Ibay G, Stambolian D, Bailey-Wilson JE.

Mol Vis. 2011;17:1641-51. Epub 2011 Jun 17.

9.

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. Epub 2003 Aug 15.

10.

Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12.

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

Mol Vis. 2006 Dec 4;12:1499-505.

11.

Confirmation of linkage to ocular refraction on chromosome 22q and identification of a novel linkage region on 1q.

Klein AP, Duggal P, Lee KE, Klein R, Bailey-Wilson JE, Klein BE.

Arch Ophthalmol. 2007 Jan;125(1):80-5.

PMID:
17210856
12.

Identification of a prostate cancer susceptibility locus on chromosome 7q11-21 in Jewish families.

Friedrichsen DM, Stanford JL, Isaacs SD, Janer M, Chang BL, Deutsch K, Gillanders E, Kolb S, Wiley KE, Badzioch MD, Zheng SL, Walsh PC, Jarvik GP, Hood L, Trent JM, Isaacs WB, Ostrander EA, Xu J.

Proc Natl Acad Sci U S A. 2004 Feb 17;101(7):1939-44. Epub 2004 Feb 9.

13.

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.

14.

Comparison of genome screens for two independent cohorts provides replication of suggestive linkage of bone mineral density to 3p21 and 1p36.

Wilson SG, Reed PW, Bansal A, Chiano M, Lindersson M, Langdown M, Prince RL, Thompson D, Thompson E, Bailey M, Kleyn PW, Sambrook P, Shi MM, Spector TD.

Am J Hum Genet. 2003 Jan;72(1):144-55. Epub 2002 Dec 11.

15.

Genomewide linkage scan in schizoaffective disorder: significant evidence for linkage at 1q42 close to DISC1, and suggestive evidence at 22q11 and 19p13.

Hamshere ML, Bennett P, Williams N, Segurado R, Cardno A, Norton N, Lambert D, Williams H, Kirov G, Corvin A, Holmans P, Jones L, Jones I, Gill M, O'Donovan MC, Owen MJ, Craddock N.

Arch Gen Psychiatry. 2005 Oct;62(10):1081-8.

PMID:
16203953
16.

Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.

Holliday EG, Nyholt DR, Tirupati S, John S, Ramachandran P, Ramamurti M, Ramadoss AJ, Jeyagurunathan A, Kottiswaran S, Smith HJ, Filippich C, Nertney DA, Nancarrow DJ, Hayward NK, Watkins WS, Jorde LB, Thara R, Mowry BJ.

Am J Psychiatry. 2009 Feb;166(2):206-15. doi: 10.1176/appi.ajp.2008.08030442. Epub 2008 Oct 1. Erratum in: Am J Psychiatry. 2009 Feb;166(2):238.

PMID:
18829870
17.

Fine mapping of a region on chromosome 8p gives evidence for a QTL contributing to individual differences in an anxiety-related personality trait: TPQ harm avoidance.

Dina C, Nemanov L, Gritsenko I, Rosolio N, Osher Y, Heresco-Levy U, Sariashvilli E, Bachner-Melman R, Zohar AH, Benjamin J, Belmaker RH, Ebstein RP.

Am J Med Genet B Neuropsychiatr Genet. 2005 Jan 5;132B(1):104-8.

PMID:
15578609
18.

Quantitative trait loci for BMD identified by autosome-wide linkage scan to chromosomes 7q and 21q in men from the Amish Family Osteoporosis Study.

Streeten EA, McBride DJ, Pollin TI, Ryan K, Shapiro J, Ott S, Mitchell BD, Shuldiner AR, O'Connell JR.

J Bone Miner Res. 2006 Sep;21(9):1433-42.

19.

Linkage and association studies of prostate cancer susceptibility: evidence for linkage at 8p22-23.

Xu J, Zheng SL, Hawkins GA, Faith DA, Kelly B, Isaacs SD, Wiley KE, Chang B, Ewing CM, Bujnovszky P, Carpten JD, Bleecker ER, Walsh PC, Trent JM, Meyers DA, Isaacs WB.

Am J Hum Genet. 2001 Aug;69(2):341-50. Epub 2001 Jul 6.

20.

Candidate high myopia loci on chromosomes 18p and 12q do not play a major role in susceptibility to common myopia.

Ibay G, Doan B, Reider L, Dana D, Schlifka M, Hu H, Holmes T, O'Neill J, Owens R, Ciner E, Bailey-Wilson JE, Stambolian D.

BMC Med Genet. 2004 Aug 3;5:20.

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