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Journal Abstract Search

517 related items for PubMed ID: 15292347

  • 1. 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
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  • 2. Further indications for genetic heterogeneity of euthyroid familial goiter.
    Neumann S, Bayer Y, Reske A, Tajtáková M, Langer P, Paschke R.
    J Mol Med (Berl); 2003 Nov; 81(11):736-45. PubMed ID: 14564411
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  • 5. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families.
    Arason A, Gunnarsson H, Johannesdottir G, Jonasson K, Bendahl PO, Gillanders EM, Agnarsson BA, Jönsson G, Pylkäs K, Mustonen A, Heikkinen T, Aittomäki K, Blomqvist C, Melin B, Johannsson OT, Møller P, Winqvist R, Nevanlinna H, Borg A, Barkardottir RB.
    Breast Cancer Res; 2010 Nov; 12(4):R50. PubMed ID: 20637093
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  • 7. Genome-wide linkage meta-analysis identifies susceptibility loci at 2q34 and 13q31.3 for genetic generalized epilepsies.
    EPICURE Consortium, 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
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  • 10. 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
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  • 16. An autosomal genome-wide screen for celiac disease in Bedouin families.
    Ding YC, Weizman Z, Yerushalmi B, Elbedour K, Garner CP, Neuhausen SL.
    Genes Immun; 2008 Jan; 9(1):81-6. PubMed ID: 17943142
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  • 18. 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
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  • 19. A locus for generalized tonic-clonic seizure susceptibility maps to chromosome 10q25-q26.
    Puranam RS, Jain S, Kleindienst AM, Saxena S, Kim MK, Kelly Changizi B, Padma MV, Andrews I, Elston RC, Tiwari HK, McNamara JO.
    Ann Neurol; 2005 Sep 22; 58(3):449-58. PubMed ID: 16130088
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