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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

88 related items for PubMed ID: 11776268

  • 1. Towards the genetic basis of periodic catatonia: pedigree sample for genome scan I and II.
    Stöber G, Pfuhlmann B, Nürnberg G, Schmidtke A, Reis A, Franzek E, Wienker TF.
    Eur Arch Psychiatry Clin Neurosci; 2001; 251 Suppl 1():I25-30. PubMed ID: 11776268
    [Abstract] [Full Text] [Related]

  • 2. Splitting schizophrenia: periodic catatonia-susceptibility locus on chromosome 15q15.
    Stöber G, Saar K, Rüschendorf F, Meyer J, Nürnberg G, Jatzke S, Franzek E, Reis A, Lesch KP, Wienker TF, Beckmann H.
    Am J Hum Genet; 2000 Nov; 67(5):1201-7. PubMed ID: 11001582
    [Abstract] [Full Text] [Related]

  • 3. Periodic catatonia: confirmation of linkage to chromosome 15 and further evidence for genetic heterogeneity.
    Stöber G, Seelow D, Rüschendorf F, Ekici A, Beckmann H, Reis A.
    Hum Genet; 2002 Oct; 111(4-5):323-30. PubMed ID: 12384773
    [Abstract] [Full Text] [Related]

  • 4. hKCNN3 which maps to chromosome 1q21 is not the causative gene in periodic catatonia, a familial subtype of schizophrenia.
    Stöber G, Meyer J, Nanda I, Wienker TF, Saar K, Jatzke S, Schmid M, Lesch KP, Beckmann H.
    Eur Arch Psychiatry Clin Neurosci; 2000 Oct; 250(4):163-8. PubMed ID: 11009068
    [Abstract] [Full Text] [Related]

  • 5. Systematic mutation analysis of KIAA0767 and KIAA1646 in chromosome 22q-linked periodic catatonia.
    Stöber G, Kohlmann B, Iekiera M, Rubie C, Gawlik M, Möller-Ehrlich K, Meitinger T, Bettecken T.
    BMC Psychiatry; 2005 Oct 14; 5():36. PubMed ID: 16225677
    [Abstract] [Full Text] [Related]

  • 6. No causative DLL4 mutations in periodic catatonia patients from 15q15 linked families.
    McKeane DP, Meyer J, Dobrin SE, Melmed KM, Ekawardhani S, Tracy NA, Lesch KP, Stephan DA.
    Schizophr Res; 2005 Jun 01; 75(1):1-3. PubMed ID: 15820317
    [Abstract] [Full Text] [Related]

  • 7. Evaluation of conserved and ultra-conserved non-genic sequences in chromosome 15q15-linked periodic catatonia.
    Schanze D, Ekici AB, Pfuhlmann B, Reis A, Stöber G.
    Am J Med Genet B Neuropsychiatr Genet; 2012 Jan 01; 159B(1):77-86. PubMed ID: 22162401
    [Abstract] [Full Text] [Related]

  • 8. Genetic predisposition and environmental causes in periodic and systematic catatonia.
    Stöber G.
    Eur Arch Psychiatry Clin Neurosci; 2001 Jan 01; 251 Suppl 1():I21-4. PubMed ID: 11776267
    [Abstract] [Full Text] [Related]

  • 9. Exposure to prenatal infections, genetics and the risk of systematic and periodic catatonia.
    Stöber G, Franzek E, Beckmann H, Schmidtke A.
    J Neural Transm (Vienna); 2002 May 01; 109(5-6):921-9. PubMed ID: 12111478
    [Abstract] [Full Text] [Related]

  • 10. Irish study on high-density schizophrenia families: field methods and power to detect linkage.
    Kendler KS, O'Neill FA, Burke J, Murphy B, Duke F, Straub RE, Shinkwin R, Ni Nuallain M, MacLean CJ, Walsh D.
    Am J Med Genet; 1996 Apr 09; 67(2):179-90. PubMed ID: 8723045
    [Abstract] [Full Text] [Related]

  • 11. Linkage and family-based association study of schizophrenia and the synapsin III locus that maps to chromosome 22q13.
    Stöber G, Meyer J, Nanda I, Wienker TF, Saar K, Knapp M, Jatzke S, Schmid M, Lesch KP, Beckmann H.
    Am J Med Genet; 2000 Jun 12; 96(3):392-7. PubMed ID: 10898920
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13. Genome-wide linkage scan for prostate cancer susceptibility genes in men with aggressive disease: significant evidence for linkage at chromosome 15q12.
    Lange EM, Ho LA, Beebe-Dimmer JL, Wang Y, Gillanders EM, Trent JM, Lange LA, Wood DP, Cooney KA.
    Hum Genet; 2006 May 12; 119(4):400-7. PubMed ID: 16508751
    [Abstract] [Full Text] [Related]

  • 14. Genome-wide linkage scan of schizophrenia: a cross-isolate study.
    Bulayeva KB, Glatt SJ, Bulayev OA, Pavlova TA, Tsuang MT.
    Genomics; 2007 Feb 12; 89(2):167-77. PubMed ID: 17140763
    [Abstract] [Full Text] [Related]

  • 15. Genome-wide multipoint linkage analyses of multiplex schizophrenia pedigrees from the oceanic nation of Palau.
    Devlin B, Bacanu SA, Roeder K, Reimherr F, Wender P, Galke B, Novasad D, Chu A, TCuenco K, Tiobek S, Otto C, Byerley W.
    Mol Psychiatry; 2002 Feb 12; 7(7):689-94. PubMed ID: 12192612
    [Abstract] [Full Text] [Related]

  • 16. Linkage genome scan for loci predisposing to panic disorder or agoraphobia.
    Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.
    Am J Med Genet; 2001 Aug 08; 105(6):548-57. PubMed ID: 11496373
    [Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Age-related maculopathy: an expanded genome-wide scan with evidence of susceptibility loci within the 1q31 and 17q25 regions.
    Weeks DE, Conley YP, Tsai HJ, Mah TS, Rosenfeld PJ, Paul TO, Eller AW, Morse LS, Dailey JP, Ferrell RE, Gorin MB.
    Am J Ophthalmol; 2001 Nov 08; 132(5):682-92. PubMed ID: 11704029
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 5.