191 related articles for article (PubMed ID: 15173224)
21. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
Wong FK; Hagberg C; Karsten A; Larson O; Gustavsson M; Huggare J; Larsson C; Teh BT; Linder-Aronson S
Cleft Palate Craniofac J; 2000 Jul; 37(4):357-62. PubMed ID: 10912714
[TBL] [Abstract][Full Text] [Related]
22. At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family.
McKay JD; Williamson J; Lesueur F; Stark M; Duffield A; Canzian F; Romeo G; Hoffman L
Eur J Endocrinol; 1999 Aug; 141(2):122-5. PubMed ID: 10427154
[TBL] [Abstract][Full Text] [Related]
23. Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter.
Bayer Y; Neumann S; Meyer B; Rüschendorf F; Reske A; Brix T; Hegedüs L; Langer P; Nürnberg P; Paschke R
J Clin Endocrinol Metab; 2004 Aug; 89(8):4044-52. PubMed ID: 15292347
[TBL] [Abstract][Full Text] [Related]
24. Model-based linkage analyses confirm chromosome 19q13.3 as a susceptibility locus for intracranial aneurysm.
Mineharu Y; Inoue K; Inoue S; Yamada S; Nozaki K; Hashimoto N; Koizumi A
Stroke; 2007 Apr; 38(4):1174-8. PubMed ID: 17322081
[TBL] [Abstract][Full Text] [Related]
25. DFNB68, a novel autosomal recessive non-syndromic hearing impairment locus at chromosomal region 19p13.2.
Santos RL; Hassan MJ; Sikandar S; Lee K; Ali G; Martin PE; Wambangco MA; Ahmad W; Leal SM
Hum Genet; 2006 Aug; 120(1):85-92. PubMed ID: 16703383
[TBL] [Abstract][Full Text] [Related]
26. Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC).
Pereira JS; da Silva JG; Tomaz RA; Pinto AE; Bugalho MJ; Leite V; Cavaco BM
Endocrine; 2015 May; 49(1):204-14. PubMed ID: 25381600
[TBL] [Abstract][Full Text] [Related]
27. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
; Leu C; de Kovel CG; Zara F; Striano P; Pezzella M; Robbiano A; Bianchi A; Bisulli F; Coppola A; Giallonardo AT; Beccaria F; Trenité DK; Lindhout D; Gaus V; Schmitz B; Janz D; Weber YG; Becker F; Lerche H; Kleefuss-Lie AA; Hallman K; Kunz WS; Elger CE; Muhle H; Stephani U; Møller RS; Hjalgrim H; Mullen S; Scheffer IE; Berkovic SF; Everett KV; Gardiner MR; Marini C; Guerrini R; Lehesjoki AE; Siren A; Nabbout R; Baulac S; Leguern E; Serratosa JM; Rosenow F; Feucht M; Unterberger I; Covanis A; Suls A; Weckhuysen S; Kaneva R; Caglayan H; Turkdogan D; Baykan B; Bebek N; Ozbek U; Hempelmann A; Schulz H; Rüschendorf F; Trucks H; Nürnberg P; Avanzini G; Koeleman BP; Sander T
Epilepsia; 2012 Feb; 53(2):308-18. PubMed ID: 22242659
[TBL] [Abstract][Full Text] [Related]
28. Familial nonmedullary thyroid carcinoma.
Malchoff CD; Malchoff DM
Cancer Control; 2006 Apr; 13(2):106-10. PubMed ID: 16735984
[TBL] [Abstract][Full Text] [Related]
29. In patients with thyroid cancer of follicular cell origin, a family history of nonmedullary thyroid cancer in one first-degree relative is associated with more aggressive disease.
Mazeh H; Benavidez J; Poehls JL; Youngwirth L; Chen H; Sippel RS
Thyroid; 2012 Jan; 22(1):3-8. PubMed ID: 22136209
[TBL] [Abstract][Full Text] [Related]
30. Diagnosis and Management of Hereditary Thyroid Cancer.
Bano G; Hodgson S
Recent Results Cancer Res; 2016; 205():29-44. PubMed ID: 27075347
[TBL] [Abstract][Full Text] [Related]
31. Familial nonmedullary thyroid carcinoma.
Mazeh H; Sippel RS
Thyroid; 2013 Sep; 23(9):1049-56. PubMed ID: 23734600
[TBL] [Abstract][Full Text] [Related]
32. 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]
33. Whole exome and target sequencing identifies MAP2K5 as novel susceptibility gene for familial non-medullary thyroid carcinoma.
Ye F; Gao H; Xiao L; Zuo Z; Liu Y; Zhao Q; Chen H; Feng W; Fu B; Sun L; Jiang X; He D; Jiang H; Yang M; Li L; Chen F; Liu X; Li S; Li Z; Jiang Y; Cheng L; Bu H
Int J Cancer; 2019 Mar; 144(6):1321-1330. PubMed ID: 30132833
[TBL] [Abstract][Full Text] [Related]
34. 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]
35. Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13.
Lee YA; Rüschendorf F; Windemuth C; Schmitt-Egenolf M; Stadelmann A; Nürnberg G; Ständer M; Wienker TF; Reis A; Traupe H
Am J Hum Genet; 2000 Oct; 67(4):1020-4. PubMed ID: 10986047
[TBL] [Abstract][Full Text] [Related]
36. A novel locus for restless legs syndrome maps to chromosome 19p in an Irish pedigree.
Skehan EB; Abdulrahim MM; Parfrey NA; Hand CK
Neurogenetics; 2012 May; 13(2):125-32. PubMed ID: 22411506
[TBL] [Abstract][Full Text] [Related]
37. Chromosome 19p13 loci in Finnish migraine with aura families.
Kaunisto MA; Tikka PJ; Kallela M; Leal SM; Papp JC; Korhonen A; Hämäläinen E; Harno H; Havanka H; Nissilä M; Säkö E; Ilmavirta M; Kaprio J; Färkkilä M; Ophoff RA; Palotie A; Wessman M
Am J Med Genet B Neuropsychiatr Genet; 2005 Jan; 132B(1):85-9. PubMed ID: 15449251
[TBL] [Abstract][Full Text] [Related]
38. Evidence for a putative bipolar disorder locus on 2p13-16 and other potential loci on 4q31, 7q34, 8q13, 9q31, 10q21-24, 13q32, 14q21 and 17q11-12.
Liu J; Juo SH; Dewan A; Grunn A; Tong X; Brito M; Park N; Loth JE; Kanyas K; Lerer B; Endicott J; Penchaszadeh G; Knowles JA; Ott J; Gilliam TC; Baron M
Mol Psychiatry; 2003 Mar; 8(3):333-42. PubMed ID: 12660806
[TBL] [Abstract][Full Text] [Related]
39. [Familial febrile convulsions is supposed to link to human chromosome 19p13.3].
Qi Y; Lü J; Wu X
Zhonghua Yi Xue Za Zhi; 2001 Jan; 81(1):27-9. PubMed ID: 11798847
[TBL] [Abstract][Full Text] [Related]
40. Localization and replication of the systemic lupus erythematosus linkage signal at 4p16: interaction with 2p11, 12q24 and 19q13 in European Americans.
Xing C; Sestak AL; Kelly JA; Nguyen KL; Bruner GR; Harley JB; Gray-McGuire C
Hum Genet; 2007 Jan; 120(5):623-31. PubMed ID: 16983533
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
