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Last Name
Institution

Martina Durner

TitleASSOCIATE PROFESSOR
InstitutionMount Sinai
DepartmentPsychiatry
Address

     Bibliographic 
     selected publications
    Publications listed below are automatically derived from MEDLINE/PubMed and other sources, which might result in incorrect or missing publications. Faculty can login to make corrections and additions.
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    1. Wittkowski KM, Sonakya V, Song T, Seybold MP, Keddache M, Durner M. From single-SNP to wide-locus: genome-wide association studies identifying functionally related genes and intragenic regions in small sample studies. Pharmacogenomics. 2013 Mar; 14(4):391-401.
      View in: PubMed
    2. Ritter BP, Angelo GW, Durner M, Rossy-Fullana E, Carrion-Baralt J, Silverman JM, Bespalova IN. Mutation screening of PDZD2, GOLPH3, and MTMR12 genes in patients with schizophrenia. Psychiatr Genet. 2012 Feb; 22(1):51-2.
      View in: PubMed
    3. Bespalova IN, Durner M, Ritter BP, Angelo GW, Rossy-Fullana E, Carrion-Baralt J, Schmeidler J, Silverman JM. Non-synonymous variants in the AMACR gene are associated with schizophrenia. Schizophr Res. 2010 Dec; 124(1-3):208-15.
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    4. Bespalova I, Angelo G, Ritter B, Rossy-Fullana E, Carrion-Baralt J, Durner M, Silverman J. Mutation analysis of the C1QTNF3 gene in patients with schizophrenia. Psychiatry Res. 2010 Sep 30; 179(2):235-7.
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    5. Vierck E, Cauley R, Kugler SL, Mandelbaum DE, Pal DK, Durner M. Polyspike and waves do not predict generalized tonic-clonic seizures in childhood absence epilepsy. J Child Neurol. 2010 Apr; 25(4):475-81.
      View in: PubMed
    6. Logue MW, Durner M, Heiman GA, Hodge SE, Hamilton SP, Knowles JA, Fyer AJ, Weissman MM. A linkage search for joint panic disorder/bipolar genes. Am J Med Genet B Neuropsychiatr Genet. 2009 Dec 5; 150B(8):1139-46.
      View in: PubMed
    7. Chioza BA, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley JM, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis ML, Guerrini R, Kjeldsen MJ, Nabbout R, Nashef L, Sander T, Sirén A, Wirrell E, McKeigue P, Robinson R, Gardiner RM, Everett KV. Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14. Epilepsy Res. 2009 Dec; 87(2-3):247-55.
      View in: PubMed
    8. Everett K, Chioza B, Aicardi J, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dooley J, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Guerrini R, Heils A, Kjeldsen M, Nabbout R, Sander T, Wirrell E, McKeigue P, Robinson R, Taske N, Gardiner M. Linkage and mutational analysis of CLCN2 in childhood absence epilepsy. Epilepsy Res. 2007 Jul; 75(2-3):145-53.
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    9. Gorroochurn P, Hodge SE, Heiman GA, Durner M, Greenberg DA. Non-replication of association studies: "pseudo-failures" to replicate? Genet Med. 2007 Jun; 9(6):325-31.
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    10. Durner M, Gorroochurn P, Marini C, Guerrini R. Can we increase the likelihood of success for future association studies in epilepsy? Epilepsia. 2006 Oct; 47(10):1617-21; author reply 1757-8.
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    11. Fyer AJ, Hamilton SP, Durner M, Haghighi F, Heiman GA, Costa R, Evgrafov O, Adams P, de Leon AB, Taveras N, Klein DF, Hodge SE, Weissman MM, Knowles JA. A third-pass genome scan in panic disorder: evidence for multiple susceptibility loci. Biol Psychiatry. 2006 Aug 15; 60(4):388-401.
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    12. Chioza B, Everett K, Aschauer H, Brouwer O, Callenbach P, Covanis A, Dulac O, Durner M, Eeg-Olofsson O, Feucht M, Friis M, Heils A, Kjeldsen M, Larsson K, Lehesjoki AE, Nabbout R, Olsson I, Sander T, Sirén A, Robinson R, Rees M, Gardiner RM. Evaluation of CACNA1H in European patients with childhood absence epilepsy. Epilepsy Res. 2006 May; 69(2):177-81.
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    13. Pal DK, Durner M, Klotz I, Dicker E, Shinnar S, Resor S, Cohen J, Harden C, Moshé SL, Ballaban-Gill K, Bromfield EB, Greenberg DA. Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsy. Brain Dev. 2006 Mar; 28(2):92-8.
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    14. Bespalova IN, Angelo GW, Durner M, Smith CJ, Siever LJ, Buxbaum JD, Silverman JM. Fine mapping of the 5p13 locus linked to schizophrenia and schizotypal personality disorder in a Puerto Rican family. Psychiatr Genet. 2005 Sep; 15(3):205-10.
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    15. Durner M, Pal D, Greenberg D. Genetics of juvenile myoclonic epilepsy: faulty components and faulty wiring? Adv Neurol. 2005; 95:245-54.
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    16. Greenberg DA, Cayanis E, Strug L, Marathe S, Durner M, Pal DK, Alvin GB, Klotz I, Dicker E, Shinnar S, Bromfield EB, Resor S, Cohen J, Moshe SL, Harden C, Kang H. Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy. Am J Hum Genet. 2005 Jan; 76(1):139-46.
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    17. Pal DK, Evgrafov OV, Tabares P, Zhang F, Durner M, Greenberg DA. BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy. Am J Hum Genet. 2003 Aug; 73(2):261-70.
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    18. Hamilton SP, Fyer AJ, Durner M, Heiman GA, Baisre de Leon A, Hodge SE, Knowles JA, Weissman MM. Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q. Proc Natl Acad Sci U S A. 2003 Mar 4; 100(5):2550-5.
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    19. Pal DK, Kugler SL, Mandelbaum DE, Durner M. Phenotypic features of familial febrile seizures: case-control study. Neurology. 2003 Feb 11; 60(3):410-4.
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    20. Pal DK, Durner M, Greenberg DA. Effect of misspecification of gene frequency on the two-point LOD score. Eur J Hum Genet. 2001 Nov; 9(11):855-9.
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    21. 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. Genome scan of idiopathic generalized epilepsy: evidence for major susceptibility gene and modifying genes influencing the seizure type. Ann Neurol. 2001 Mar; 49(3):328-35.
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    22. Slager SL, Juo SH, Durner M, Hodge SE. Markov chain Monte Carlo linkage analysis: effect of bin width on the probability of linkage. Genet Epidemiol. 2001; 21 Suppl 1:S700-5.
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    23. Durner M, Shinnar S, Resor SR, Moshe SL, Rosenbaum D, Cohen J, Harden C, Kang H, Hertz S, Wallace S, Luciano D, Ballaban-Gil K, Greenberg DA. No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q. Am J Med Genet. 2000 Feb 7; 96(1):49-52.
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    24. Hallmann K, Durner M, Sander T, Steinlein OK. Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy. Am J Med Genet. 2000 Feb 7; 96(1):8-11.
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    25. Greenberg DA, Durner M, Keddache M, Shinnar S, Resor SR, Moshe SL, Rosenbaum D, Cohen J, Harden C, Kang H, Wallace S, Luciano D, Ballaban-Gil K, Tomasini L, Zhou G, Klotz I, Dicker E. Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy. Am J Hum Genet. 2000 Feb; 66(2):508-16.
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    26. Durner M, Zhou G, Fu D, Abreu P, Shinnar S, Resor SR, Moshe SL, Rosenbaum D, Cohen J, Harden C, Kang H, Wallace S, Luciano D, Ballaban-Gil K, Klotz I, Dicker E, Greenberg DA. Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity. Am J Hum Genet. 1999 May; 64(5):1411-9.
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    27. Durner M, Vieland VJ, Greenberg DA. Further evidence for the increased power of LOD scores compared with nonparametric methods. Am J Hum Genet. 1999 Jan; 64(1):281-9.
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    28. Aisen PS, Luddy A, Durner M, Reinhard JF, Pasinetti GM. HLA-DR4 influences glial activity in Alzheimer's disease hippocampus. J Neurol Sci. 1998 Nov 26; 161(1):66-9.
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    29. Durner M, Abreu P. Exploring linkage of chromosome 18 markers and bipolar disease. Genet Epidemiol. 1997; 14(6):623-7.
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    30. Greenberg DA, Durner M, Shinnar S, Resor S, Rosenbaum D, Klotz I, Dicker E, Keddache M, Zhou G, Yang X, Altstiel L. Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsy. Neurology. 1996 Sep; 47(3):750-5.
      View in: PubMed
    31. Durner M, Greenberg DA, Hodge SE. Phenocopies versus genetic heterogeneity: can we use phenocopy frequencies in linkage analysis to compensate for heterogeneity? Hum Hered. 1996 Sep-Oct; 46(5):265-73.
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    32. Sander T, Hildmann T, Wienker TF, Ramel C, Beck-Mannagetta G, Bianchi A, Sailer U, Berek K, Bauer G, Neitzel H, Schmitz B, Durner M, Johnson KJ, Janz D. Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20. Am J Med Genet. 1996 Feb 16; 67(1):31-9.
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    33. Greenberg DA, Durner M, Resor S, Rosenbaum D, Shinnar S. The genetics of idiopathic generalized epilepsies of adolescent onset: differences between juvenile myoclonic epilepsy and epilepsy with random grand mal and with awakening grand mal. Neurology. 1995 May; 45(5):942-6.
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    34. Knapp M, Durner M, Baur MP. Screening for linkage and association in nuclear families. Genet Epidemiol. 1995; 12(6):619-23.
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    35. Hodge SE, Durner M, Vieland VJ, Greenberg DA. Better data analysis through data exploration. Am J Hum Genet. 1993 Sep; 53(3):775-7.
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    36. Durner M, Greenberg DA, Hodge SE. Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods. Am J Hum Genet. 1992 Oct; 51(4):859-70.
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    37. Durner M, Janz D, Zingsem J, Greenberg DA. Possible association of juvenile myoclonic epilepsy with HLA-DRw6. Epilepsia. 1992 Sep-Oct; 33(5):814-6.
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    38. Durner M, Greenberg DA, Delgado-Escueta AV. Is there a genetic relationship between epilepsy and birth defects? Neurology. 1992 Apr; 42(4 Suppl 5):63-7.
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    39. Greenberg DA, Durner M, Delgado-Escueta AV. Evidence for multiple gene loci in the expression of the common generalized epilepsies. Neurology. 1992 Apr; 42(4 Suppl 5):56-62.
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    40. Durner M, Greenberg DA. Effect of heterogeneity and assumed mode of inheritance on lod scores. Am J Med Genet. 1992 Feb 1; 42(3):271-5.
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    41. Durner M, Sander T, Greenberg DA, Johnson K, Beck-Mannagetta G, Janz D. Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients. Neurology. 1991 Oct; 41(10):1651-5.
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    42. Weissbecker KA, Durner M, Janz D, Scaramelli A, Sparkes RS, Spence MA. Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6. Am J Med Genet. 1991 Jan; 38(1):32-6.
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    43. Greenberg DA, Durner M, Delgado-Escueta AV, Janz D. Is juvenile myoclonic epilepsy an autosomal recessive disease? Ann Neurol. 1990 Jul; 28(1):110-1.
      View in: PubMed
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    Mount Sinai Profiles is managed by Conduits - The Institutes for Translational Sciences at Icahn School of Medicine, supported by the National Center for Research Resources and the National Center for Advancing Translational Sciences of the National Institutes of Health through Grant Number UL1TR000067