These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
47 related articles for article (PubMed ID: 9754632)
1. Linkage and association analysis of chromosomal regions containing genes related to neuroendocrine or serotonin function in families with early-onset, recurrent major depression. Neiswanger K; Zubenko GS; Giles DE; Frank E; Kupfer DJ; Kaplan BB Am J Med Genet; 1998 Sep; 81(5):443-9. PubMed ID: 9754632 [TBL] [Abstract][Full Text] [Related]
2. Genetic linkage of region containing the CREB1 gene to depressive disorders in women from families with recurrent, early-onset, major depression. Zubenko GS; Hughes HB; Maher BS; Stiffler JS; Zubenko WN; Marazita ML Am J Med Genet; 2002 Dec; 114(8):980-7. PubMed ID: 12457397 [TBL] [Abstract][Full Text] [Related]
3. Genome survey for susceptibility loci for recurrent, early-onset major depression: results at 10cM resolution. Zubenko GS; Hughes HB; Stiffler JS; Zubenko WN; Kaplan BB Am J Med Genet; 2002 May; 114(4):413-22. PubMed ID: 11992563 [TBL] [Abstract][Full Text] [Related]
4. A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q. Badenhop RF; Moses MJ; Scimone A; Mitchell PB; Ewen KR; Rosso A; Donald JA; Adams LJ; Schofield PR Mol Psychiatry; 2001 Jul; 6(4):396-403. PubMed ID: 11443523 [TBL] [Abstract][Full Text] [Related]
5. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study. Sutton BS; Langefeld CD; Campbell JK; Haffner SM; Norris JM; Scherzinger AL; Wagenknecht LE; Bowden DW Int J Obes (Lond); 2006 Sep; 30(9):1433-41. PubMed ID: 16520807 [TBL] [Abstract][Full Text] [Related]
6. Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands. Hanna GL; Veenstra-VanderWeele J; Cox NJ; Boehnke M; Himle JA; Curtis GC; Leventhal BL; Cook EH Am J Med Genet; 2002 Jul; 114(5):541-52. PubMed ID: 12116192 [TBL] [Abstract][Full Text] [Related]
7. Genome-wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families. Xu J; Gillanders EM; Isaacs SD; Chang BL; Wiley KE; Zheng SL; Jones M; Gildea D; Riedesel E; Albertus J; Freas-Lutz D; Markey C; Meyers DA; Walsh PC; Trent JM; Isaacs WB Prostate; 2003 Dec; 57(4):320-5. PubMed ID: 14601028 [TBL] [Abstract][Full Text] [Related]
8. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease. Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828 [TBL] [Abstract][Full Text] [Related]
9. Linkage analysis in a large family from Pakistan with depression and a high incidence of consanguineous marriages. Ayub M; Irfan M; Maclean A; Naeem F; MacGregor S; Visscher PM; Muir W; Blackwood D Hum Hered; 2008; 66(3):190-8. PubMed ID: 18506107 [TBL] [Abstract][Full Text] [Related]
10. Genome linkage screen for prostate cancer susceptibility loci: results from the Mayo Clinic Familial Prostate Cancer Study. Cunningham JM; McDonnell SK; Marks A; Hebbring S; Anderson SA; Peterson BJ; Slager S; French A; Blute ML; Schaid DJ; Thibodeau SN; Prostate; 2003 Dec; 57(4):335-46. PubMed ID: 14601030 [TBL] [Abstract][Full Text] [Related]
11. Whole genome linkage scan of recurrent depressive disorder from the depression network study. McGuffin P; Knight J; Breen G; Brewster S; Boyd PR; Craddock N; Gill M; Korszun A; Maier W; Middleton L; Mors O; Owen MJ; Perry J; Preisig M; Reich T; Rice J; Rietschel M; Jones L; Sham P; Farmer AE Hum Mol Genet; 2005 Nov; 14(22):3337-45. PubMed ID: 16203746 [TBL] [Abstract][Full Text] [Related]
12. 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. PubMed ID: 12782963 [TBL] [Abstract][Full Text] [Related]
13. Autosomal dominant infantile gastroesophageal reflux disease: exclusion of a 13q14 locus in five well characterized families. Orenstein SR; Shalaby TM; Finch R; Pfuetzer RH; DeVandry S; Chensny LJ; Bannada MM; Whitcomb DC Am J Gastroenterol; 2002 Nov; 97(11):2725-32. PubMed ID: 12425539 [TBL] [Abstract][Full Text] [Related]
14. Genomewide survey of panic disorder. Crowe RR; Goedken R; Samuelson S; Wilson R; Nelson J; Noyes R Am J Med Genet; 2001 Jan; 105(1):105-9. PubMed ID: 11424978 [TBL] [Abstract][Full Text] [Related]
15. Linkage analysis of 153 prostate cancer families over a 30-cM region containing the putative susceptibility locus HPCX. Lange EM; Chen H; Brierley K; Perrone EE; Bock CH; Gillanders E; Ray ME; Cooney KA Clin Cancer Res; 1999 Dec; 5(12):4013-20. PubMed ID: 10632333 [TBL] [Abstract][Full Text] [Related]
16. A genome-wide linkage scan of familial benign recurrent vertigo: linkage to 22q12 with evidence of heterogeneity. Lee H; Jen JC; Wang H; Chen Z; Mamsa H; Sabatti C; Baloh RW; Nelson SF Hum Mol Genet; 2006 Jan; 15(2):251-8. PubMed ID: 16330481 [TBL] [Abstract][Full Text] [Related]
17. 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 [TBL] [Abstract][Full Text] [Related]
18. No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1. Sander T; Windemuth C; Schulz H; Saar K; Gennaro E; Bianchi A; Zara F; Bulteau C; Kaminska A; Ville D; Cieuta C; Prud'homme JF; Dulac O; Bate L; Gardiner RM; de Haan GJ; Janssen GA; Witte J; Halley DJ; Lindhout D; Wienker TF; Janz D; Am J Med Genet; 2002 Aug; 114(6):673-8. PubMed ID: 12210286 [TBL] [Abstract][Full Text] [Related]
19. Primary ciliary dyskinesia: a genome-wide linkage analysis reveals extensive locus heterogeneity. Blouin JL; Meeks M; Radhakrishna U; Sainsbury A; Gehring C; Saïl GD; Bartoloni L; Dombi V; O'Rawe A; Walne A; Chung E; Afzelius BA; Armengot M; Jorissen M; Schidlow DV; van Maldergem L; Walt H; Gardiner RM; Probst D; Guerne PA; Delozier-Blanchet CD; Antonarakis SE Eur J Hum Genet; 2000 Feb; 8(2):109-18. PubMed ID: 10757642 [TBL] [Abstract][Full Text] [Related]