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Journal Abstract Search

196 related items for PubMed ID: 10581476

  • 1. Testing for linkage of eye tracking dysfunction and schizophrenia to markers on chromosomes 6, 8, 9, 20, and 22 in families multiply affected with schizophrenia.
    Arolt V, Lencer R, Purmann S, Schürmann M, Müller-Myhsok B, Krecker K, Schwinger E.
    Am J Med Genet; 1999 Dec 15; 88(6):603-6. PubMed ID: 10581476
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  • 4. Eye tracking dysfunction is a putative phenotypic susceptibility marker of schizophrenia and maps to a locus on chromosome 6p in families with multiple occurrence of the disease.
    Arolt V, Lencer R, Nolte A, Müller-Myhsok B, Purmann S, Schürmann M, Leutelt J, Pinnow M, Schwinger E.
    Am J Med Genet; 1996 Nov 22; 67(6):564-79. PubMed ID: 8950416
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  • 6. Familial hemiplegic migraine: clinical features and probable linkage to chromosome 1 in an Italian family.
    Cevoli S, Pierangeli G, Monari L, Valentino ML, Bernardoni P, Mochi M, Cortelli P, Montagna P.
    Neurol Sci; 2002 Apr 22; 23(1):7-10. PubMed ID: 12111614
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  • 11. A schizophrenia gene locus on chromosome 17q21 in a new set of families of Mexican and central american ancestry: evidence from the NIMH Genetics of schizophrenia in latino populations study.
    Escamilla M, Hare E, Dassori AM, Peralta JM, Ontiveros A, Nicolini H, Raventós H, Medina R, Mendoza R, Jerez A, Muñoz R, Almasy L.
    Am J Psychiatry; 2009 Apr 22; 166(4):442-9. PubMed ID: 19188284
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  • 12. No evidence for association to the G72/G30 locus in an independent sample of schizophrenia families.
    Mulle JG, Chowdari KV, Nimgaonkar V, Chakravarti A.
    Mol Psychiatry; 2005 May 22; 10(5):431-3. PubMed ID: 15753958
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  • 14. Chromosome 9p-linked families with frontotemporal dementia associated with motor neuron disease.
    Le Ber I, Camuzat A, Berger E, Hannequin D, Laquerrière A, Golfier V, Seilhean D, Viennet G, Couratier P, Verpillat P, Heath S, Camu W, Martinaud O, Lacomblez L, Vercelletto M, Salachas F, Sellal F, Didic M, Thomas-Anterion C, Puel M, Michel BF, Besse C, Duyckaerts C, Meininger V, Campion D, Dubois B, Brice A, French Research Network on FTD/FTD-MND.
    Neurology; 2009 May 12; 72(19):1669-76. PubMed ID: 19433740
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  • 19. An allelic association study of two polymorphic markers in close proximity to a balanced translocation t(1:11) that co-segregates with mental illness.
    Wilson-Annan JC, Blackwood DH, Muir W, Millar JK, Porteous DJ.
    Psychiatr Genet; 1997 May 12; 7(4):171-4. PubMed ID: 9460802
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