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2. Genome-wide linkage scan of epilepsy-related photoparoxysmal electroencephalographic response: evidence for linkage on chromosomes 7q32 and 16p13. Pinto D; Westland B; de Haan GJ; Rudolf G; da Silva BM; Hirsch E; Lindhout D; Trenité DG; Koeleman BP Hum Mol Genet; 2005 Jan; 14(1):171-8. PubMed ID: 15548544 [TBL] [Abstract][Full Text] [Related]
3. Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci. Pinto D; Kasteleijn-Nolst Trenité DG; Cordell HJ; Mattheisen M; Strauch K; Lindhout D; Koeleman BP Genet Epidemiol; 2007 Jan; 31(1):42-50. PubMed ID: 17123300 [TBL] [Abstract][Full Text] [Related]
4. Genetic dissection of photosensitivity and its relation to idiopathic generalized epilepsy. Tauer U; Lorenz S; Lenzen KP; Heils A; Muhle H; Gresch M; Neubauer BA; Waltz S; Rudolf G; Mattheisen M; Strauch K; Nürnberg P; Schmitz B; Stephani U; Sander T Ann Neurol; 2005 Jun; 57(6):866-73. PubMed ID: 15929039 [TBL] [Abstract][Full Text] [Related]
5. Genome scan of idiopathic generalized epilepsy: evidence for major susceptibility gene and modifying genes influencing the seizure type. Durner M; Keddache MA; Tomasini L; Shinnar S; Resor SR; Cohen J; Harden C; Moshe SL; Rosenbaum D; Kang H; Ballaban-Gil K; Hertz S; Labar DR; Luciano D; Wallace S; Yohai D; Klotz I; Dicker E; Greenberg DA Ann Neurol; 2001 Mar; 49(3):328-35. PubMed ID: 11261507 [TBL] [Abstract][Full Text] [Related]
6. Genome-wide scan of Swedish families with hereditary prostate cancer: suggestive evidence of linkage at 5q11.2 and 19p13.3. Wiklund F; Gillanders EM; Albertus JA; Bergh A; Damber JE; Emanuelsson M; Freas-Lutz DL; Gildea DE; Göransson I; Jones MS; Jonsson BA; Lindmark F; Markey CJ; Riedesel EL; Stenman E; Trent JM; Grönberg H Prostate; 2003 Dec; 57(4):290-7. PubMed ID: 14601025 [TBL] [Abstract][Full Text] [Related]
7. 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; 30(1):29-35. PubMed ID: 15933979 [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. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent. Lucas GJ; Riches PL; Hocking LJ; Cundy T; Nicholson GC; Walsh JP; Ralston SH J Bone Miner Res; 2008 Jan; 23(1):58-63. PubMed ID: 17907922 [TBL] [Abstract][Full Text] [Related]
10. Linkage and interaction of loci on 1q23 and 16q12 may contribute to susceptibility to systemic lupus erythematosus. Tsao BP; Cantor RM; Grossman JM; Kim SK; Strong N; Lau CS; Chen CJ; Shen N; Ginzler EM; Goldstein R; Kalunian KC; Arnett FC; Wallace DJ; Hahn BH Arthritis Rheum; 2002 Nov; 46(11):2928-36. PubMed ID: 12428234 [TBL] [Abstract][Full Text] [Related]
11. A genome-wide scan shows significant linkage between bipolar disorder and chromosome 12q24.3 and suggestive linkage to chromosomes 1p22-21, 4p16, 6q14-22, 10q26 and 16p13.3. Ewald H; Flint T; Kruse TA; Mors O Mol Psychiatry; 2002; 7(7):734-44. PubMed ID: 12192618 [TBL] [Abstract][Full Text] [Related]
12. Suggestive genetic linkage to chromosome 11p11.2-q12.2 in hereditary prostate cancer families with primary kidney cancer. Johanneson B; Deutsch K; McIntosh L; Friedrichsen-Karyadi DM; Janer M; Kwon EM; Iwasaki L; Hood L; Ostrander EA; Stanford JL Prostate; 2007 May; 67(7):732-42. PubMed ID: 17372923 [TBL] [Abstract][Full Text] [Related]
13. Genome-wide scan of brothers: replication and fine mapping of prostate cancer susceptibility and aggressiveness loci. Witte JS; Suarez BK; Thiel B; Lin J; Yu A; Banerjee TK; Burmester JK; Casey G; Catalona WJ Prostate; 2003 Dec; 57(4):298-308. PubMed ID: 14601026 [TBL] [Abstract][Full Text] [Related]
14. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis. Holliday EG; McLean DE; Nyholt DR; Mowry BJ Arch Gen Psychiatry; 2009 Oct; 66(10):1058-67. PubMed ID: 19805696 [TBL] [Abstract][Full Text] [Related]
15. 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]