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.
24. Quantitative trait loci on chromosomes 2p, 4p, and 13q influence bone mineral density of the forearm and hip in Mexican Americans. Kammerer CM; Schneider JL; Cole SA; Hixson JE; Samollow PB; O'Connell JR; Perez R; Dyer TD; Almasy L; Blangero J; Bauer RL; Mitchell BD J Bone Miner Res; 2003 Dec; 18(12):2245-52. PubMed ID: 14672361 [TBL] [Abstract][Full Text] [Related]
25. Suggestive linkage to chromosomal regions 13q31 and 22q12 in families with psychotic bipolar disorder. Potash JB; Zandi PP; Willour VL; Lan TH; Huo Y; Avramopoulos D; Shugart YY; MacKinnon DF; Simpson SG; McMahon FJ; DePaulo JR; McInnis MG Am J Psychiatry; 2003 Apr; 160(4):680-6. PubMed ID: 12668356 [TBL] [Abstract][Full Text] [Related]
26. 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. PubMed ID: 15824258 [TBL] [Abstract][Full Text] [Related]
27. Genome scan of Arab Israeli families maps a schizophrenia susceptibility gene to chromosome 6q23 and supports a locus at chromosome 10q24. Lerer B; Segman RH; Hamdan A; Kanyas K; Karni O; Kohn Y; Korner M; Lanktree M; Kaadan M; Turetsky N; Yakir A; Kerem B; Macciardi F Mol Psychiatry; 2003 May; 8(5):488-98. PubMed ID: 12808429 [TBL] [Abstract][Full Text] [Related]
28. Ordered subset linkage analysis supports a susceptibility locus for age-related macular degeneration on chromosome 16p12. Schmidt S; Scott WK; Postel EA; Agarwal A; Hauser ER; De La Paz MA; Gilbert JR; Weeks DE; Gorin MB; Haines JL; Pericak-Vance MA BMC Genet; 2004 Jul; 5():18. PubMed ID: 15238159 [TBL] [Abstract][Full Text] [Related]
29. 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; Hum Mol Genet; 2003 Oct; 12(20):2599-608. PubMed ID: 12925570 [TBL] [Abstract][Full Text] [Related]
30. Bipolar disorder and panic disorder in families: an analysis of chromosome 18 data. MacKinnon DF; Xu J; McMahon FJ; Simpson SG; Stine OC; McInnis MG; DePaulo JR Am J Psychiatry; 1998 Jun; 155(6):829-31. PubMed ID: 9619158 [TBL] [Abstract][Full Text] [Related]
31. Mood-incongruent psychotic features in bipolar disorder: familial aggregation and suggestive linkage to 2p11-q14 and 13q21-33. Goes FS; Zandi PP; Miao K; McMahon FJ; Steele J; Willour VL; Mackinnon DF; Mondimore FM; Schweizer B; Nurnberger JI; Rice JP; Scheftner W; Coryell W; Berrettini WH; Kelsoe JR; Byerley W; Murphy DL; Gershon ES; Bipolar Disorder Phenome Group ; Depaulo JR; McInnis MG; Potash JB Am J Psychiatry; 2007 Feb; 164(2):236-47. PubMed ID: 17267786 [TBL] [Abstract][Full Text] [Related]
32. 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; 21(1):28-33. PubMed ID: 16124010 [TBL] [Abstract][Full Text] [Related]
33. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter. Detera-Wadleigh SD; Hsieh WT; Berrettini WH; Goldin LR; Rollins DY; Muniec D; Grewal R; Guroff JJ; Turner G; Coffman D Am J Med Genet; 1994 Sep; 54(3):206-18. PubMed ID: 7810578 [TBL] [Abstract][Full Text] [Related]
34. Genome-wide linkage scan in a large bipolar disorder sample from the National Institute of Mental Health genetics initiative suggests putative loci for bipolar disorder, psychosis, suicide, and panic disorder. Cheng R; Juo SH; Loth JE; Nee J; Iossifov I; Blumenthal R; Sharpe L; Kanyas K; Lerer B; Lilliston B; Smith M; Trautman K; Gilliam TC; Endicott J; Baron M Mol Psychiatry; 2006 Mar; 11(3):252-60. PubMed ID: 16402137 [TBL] [Abstract][Full Text] [Related]
35. Complete genomic screen in Parkinson disease: evidence for multiple genes. Scott WK; Nance MA; Watts RL; Hubble JP; Koller WC; Lyons K; Pahwa R; Stern MB; Colcher A; Hiner BC; Jankovic J; Ondo WG; Allen FH; Goetz CG; Small GW; Masterman D; Mastaglia F; Laing NG; Stajich JM; Slotterbeck B; Booze MW; Ribble RC; Rampersaud E; West SG; Gibson RA; Middleton LT; Roses AD; Haines JL; Scott BL; Vance JM; Pericak-Vance MA JAMA; 2001 Nov; 286(18):2239-44. PubMed ID: 11710888 [TBL] [Abstract][Full Text] [Related]
36. Evidence for genetic linkage between a polymorphism in the adenosine 2A receptor and panic disorder. Hamilton SP; Slager SL; De Leon AB; Heiman GA; Klein DF; Hodge SE; Weissman MM; Fyer AJ; Knowles JA Neuropsychopharmacology; 2004 Mar; 29(3):558-65. PubMed ID: 14666117 [TBL] [Abstract][Full Text] [Related]
37. Investigation of polymorphisms in the CREM gene in panic disorder. Hamilton SP; Slager SL; Mayo D; Heiman GA; Klein DF; Hodge SE; Fyer AJ; Weissman MM; Knowles JA Am J Med Genet B Neuropsychiatr Genet; 2004 Apr; 126B(1):111-5. PubMed ID: 15048659 [TBL] [Abstract][Full Text] [Related]
38. Linkage analysis of candidate genes in autoimmune thyroid disease. III. Detailed analysis of chromosome 14 localizes Graves' disease-1 (GD-1) close to multinodular goiter-1 (MNG-1). International Consortium for the Genetics of Autoimmune Thyroid Disease. Tomer Y; Barbesino G; Greenberg DA; Concepcion E; Davies TF J Clin Endocrinol Metab; 1998 Dec; 83(12):4321-7. PubMed ID: 9851771 [TBL] [Abstract][Full Text] [Related]
39. Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome. International Consortium for the Genetics of Autoimmune Thyroid Disease. Barbesino G; Tomer Y; Concepcion ES; Davies TF; Greenberg DA J Clin Endocrinol Metab; 1998 Sep; 83(9):3290-5. PubMed ID: 9745443 [TBL] [Abstract][Full Text] [Related]
40. 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] [Previous] [Next] [New Search]