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Journal Abstract Search
936 related items for PubMed ID: 17179998
1. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14. Ma DQ, Cuccaro ML, Jaworski JM, Haynes CS, Stephan DA, Parod J, Abramson RK, Wright HH, Gilbert JR, Haines JL, Pericak-Vance MA. Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998 [Abstract] [Full Text] [Related]
2. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23. Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF. Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797 [Abstract] [Full Text] [Related]
3. An autosomal genomic screen for autism. Collaborative Linkage Study of Autism. Am J Med Genet; 2001 Dec 08; 105(8):609-15. PubMed ID: 11811142 [Abstract] [Full Text] [Related]
4. Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19. Buxbaum JD, Silverman J, Keddache M, Smith CJ, Hollander E, Ramoz N, Reichert JG. Mol Psychiatry; 2004 Feb 08; 9(2):144-50. PubMed ID: 14699429 [Abstract] [Full Text] [Related]
5. Chromosome 10q harbors a susceptibility locus for bipolar disorder in Ashkenazi Jewish families. Venken T, Alaerts M, Souery D, Goossens D, Sluijs S, Navon R, Van Broeckhoven C, Mendlewicz J, Del-Favero J, Claes S. Mol Psychiatry; 2008 Apr 08; 13(4):442-50. PubMed ID: 17579605 [Abstract] [Full Text] [Related]
6. Evidence for further genetic locus heterogeneity and confirmation of RLS-1 in restless legs syndrome. Winkelmann J, Lichtner P, Pütz B, Trenkwalder C, Hauk S, Meitinger T, Strom T, Muller-Myhsok B. Mov Disord; 2006 Jan 08; 21(1):28-33. PubMed ID: 16124010 [Abstract] [Full Text] [Related]
7. Localization of a susceptibility locus for hepatocellular carcinoma to chromosome 4q in a hepatitis B hyperendemic area. Shih WL, Yu MW, Chen PJ, Yeh SH, Lo MT, Chang HC, Liaw YF, Lin SM, Liu CJ, Lee SD, Lin CL, Hsiao CK, Yang SY, Chen CJ. Oncogene; 2006 May 25; 25(22):3219-24. PubMed ID: 16407824 [Abstract] [Full Text] [Related]
8. Genome-wide linkage analysis for aggressive prostate cancer in Utah high-risk pedigrees. Christensen GB, Camp NJ, Farnham JM, Cannon-Albright LA. Prostate; 2007 May 01; 67(6):605-13. PubMed ID: 17299800 [Abstract] [Full Text] [Related]
9. Analysis of the autism chromosome 2 linkage region: GAD1 and other candidate genes. Rabionet R, Jaworski JM, Ashley-Koch AE, Martin ER, Sutcliffe JS, Haines JL, Delong GR, Abramson RK, Wright HH, Cuccaro ML, Gilbert JR, Pericak-Vance MA. Neurosci Lett; 2004 Dec 06; 372(3):209-14. PubMed ID: 15542242 [Abstract] [Full Text] [Related]
10. Genome-wide linkage analysis and evidence of gene-by-gene interactions in a sample of 362 multiplex Parkinson disease families. Pankratz N, Nichols WC, Uniacke SK, Halter C, Murrell J, Rudolph A, Shults CW, Conneally PM, Foroud T, Parkinson Study Group. Hum Mol Genet; 2003 Oct 15; 12(20):2599-608. PubMed ID: 12925570 [Abstract] [Full Text] [Related]
11. Finer linkage mapping of a primary hip osteoarthritis susceptibility locus on chromosome 6. Loughlin J, Mustafa Z, Dowling B, Southam L, Marcelline L, Räinä SS, Ala-Kokko L, Chapman K. Eur J Hum Genet; 2002 Sep 15; 10(9):562-8. PubMed ID: 12173034 [Abstract] [Full Text] [Related]
12. A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p. Pillai SG, Chiano MN, White NJ, Speer M, Barnes KC, Carlsen K, Gerritsen J, Helms P, Lenney W, Silverman M, Sly P, Sundy J, Tsanakas J, von Berg A, Whyte M, Varsani S, Skelding P, Hauser M, Vance J, Pericak-Vance M, Burns DK, Middleton LT, Brewster SR, Anderson WH, Riley JH. Eur J Hum Genet; 2006 Mar 15; 14(3):307-16. PubMed ID: 16391567 [Abstract] [Full Text] [Related]
13. Genome-wide linkage analysis for celiac disease in North American families. Neuhausen SL, Feolo M, Camp NJ, Farnham J, Book L, Zone JJ. Am J Med Genet; 2002 Jul 22; 111(1):1-9. PubMed ID: 12124726 [Abstract] [Full Text] [Related]
14. 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 22; 14(5):492-500. PubMed ID: 18227837 [Abstract] [Full Text] [Related]
15. High density SNP association study of a major autism linkage region on chromosome 17. Stone JL, Merriman B, Cantor RM, Geschwind DH, Nelson SF. Hum Mol Genet; 2007 Mar 15; 16(6):704-15. PubMed ID: 17376794 [Abstract] [Full Text] [Related]
16. Dense linkage disequilibrium mapping in the 15q11-q13 maternal expression domain yields evidence for association in autism. Nurmi EL, Amin T, Olson LM, Jacobs MM, McCauley JL, Lam AY, Organ EL, Folstein SE, Haines JL, Sutcliffe JS. Mol Psychiatry; 2003 Jun 15; 8(6):624-34, 570. PubMed ID: 12851639 [Abstract] [Full Text] [Related]
17. Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan. Kemp Z, Carvajal-Carmona L, Spain S, Barclay E, Gorman M, Martin L, Jaeger E, Brooks N, Bishop DT, Thomas H, Tomlinson I, Papaemmanuil E, Webb E, Sellick GS, Wood W, Evans G, Lucassen A, Maher ER, Houlston RS, ColoRectal tumour Gene Identification (CoRGI) Study Consortium. Hum Mol Genet; 2006 Oct 01; 15(19):2903-10. PubMed ID: 16923799 [Abstract] [Full Text] [Related]
18. Genome-wide linkage in three Dutch families maps a locus for abdominal aortic aneurysms to chromosome 19q13.3. Van Vlijmen-Van Keulen CJ, Rauwerda JA, Pals G. Eur J Vasc Endovasc Surg; 2005 Jul 01; 30(1):29-35. PubMed ID: 15933979 [Abstract] [Full Text] [Related]
19. PCAP is the major known prostate cancer predisposing locus in families from south and west Europe. Cancel-Tassin G, Latil A, Valéri A, Mangin P, Fournier G, Berthon P, Cussenot O. Eur J Hum Genet; 2001 Feb 01; 9(2):135-42. PubMed ID: 11313747 [Abstract] [Full Text] [Related]
20. 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 01; 13(2):77-84. PubMed ID: 12782963 [Abstract] [Full Text] [Related] Page: [Next] [New Search]