M. Durner

发表

Linkage and mutational analysis of CLCN2 in childhood absence epilepsy

E. Wirrell, P. McKeigue, J. Aicardi, 2007, Epilepsy Research.

Mutation analysis of the inwardly rectifying K(+) channels KCNJ6 (GIRK2) and KCNJ3 (GIRK1) in juvenile myoclonic epilepsy.

O. Steinlein, T. Sander, M. Durner, 2000, American journal of medical genetics.

A Third-Pass Genome Scan in Panic Disorder: Evidence for Multiple Susceptibility Loci

S. Hodge, M. Weissman, D. Klein, 2006, Biological Psychiatry.

Further genetic evidence for a panic disorder syndrome mapping to chromosome 13q

S. Hodge, M. Weissman, A. Fyer, 2003, Proceedings of the National Academy of Sciences of the United States of America.

Complex inheritance and parent-of-origin effect in juvenile myoclonic epilepsy

S. Moshé, S. Shinnar, E. Bromfield, 2006, Brain and Development.

Is Juvenile Myoclonic Epilepsy Polygenic

A. Delgado-Escueta, D. Janz, D. Greenberg, 1989 .

Evidence for multiple gene loci in the expression of the common generalized epilepsies.

A. Delgado-Escueta, D. Greenberg, M. Durner, 1992, Neurology.

HLA and Epilepsy

T. Sander, D. Janz, D. Greenberg, 1989 .

Is juvenile myoclonic epilepsy an autosomal recessive disease?

A. Delgado-Escueta, D. Janz, D. Greenberg, 1990, Annals of neurology.

Mutation screening of PDZD2, GOLPH3, and MTMR12 genes in patients with schizophrenia.

J. Silverman, M. Durner, J. Carrión-Baralt, 2012, Psychiatric genetics.

Exploring linkage of chromosome 18 markers and bipolar disease

P. Abreu, M. Durner, Martina Durner, 1997, Genetic epidemiology.

Fine mapping of the 5p13 locus linked to schizophrenia and schizotypal personality disorder in a Puerto Rican family

L. Siever, J. Buxbaum, J. Silverman, 2005, Psychiatric genetics.

Markov Chain Monte Carlo Linkage Analysis: Effect of Bin Width on the Probability of Linkage

S. Hodge, S. Slager, M. Durner, 2001, Genetic epidemiology.

Effect of heterogeneity and assumed mode of inheritance on lod scores.

D. Greenberg, M. Durner, 1992, American journal of medical genetics.

Non-replication of association studies: “pseudo-failures” to replicate?

Susan E Hodge, Prakash Gorroochurn, S. Hodge, 2007, Genetics in Medicine.

HLA-DR4 influences glial activity in Alzheimer's disease hippocampus

P. Aisen, G. Pasinetti, J. Reinhard, 1998, Journal of the Neurological Sciences.

Association of HLA class II alleles in patients with juvenile myoclonic epilepsy compared with patients with other forms of adolescent-onset generalized epilepsy

S. Shinnar, M. Keddache, D. Greenberg, 1996, Neurology.

BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy.

O. Evgrafov, P. Tabares, D. Pal, 2003, American journal of human genetics.

Better data analysis through data exploration.

V. Vieland, S. Hodge, D. Greenberg, 1993, American journal of human genetics.

Inter- and intrafamilial heterogeneity: effective sampling strategies and comparison of analysis methods.

S. Hodge, D. Greenberg, M. Durner, 1992, American journal of human genetics.

Non-synonymous variants in the AMACR gene are associated with schizophrenia

J. Schmeidler, J. Silverman, M. Durner, 2010, Schizophrenia Research.

Reproducibility and complications in gene searches: linkage on chromosome 6, heterogeneity, association, and maternal inheritance in juvenile myoclonic epilepsy.

S Shinnar, S. Moshé, S. Shinnar, 2000, American journal of human genetics.

The genetics of idiopathic generalized epilepsies of adolescent onset

S. Shinnar, D. Greenberg, S. Resor, 1995, Neurology.

Malic enzyme 2 may underlie susceptibility to adolescent-onset idiopathic generalized epilepsy.

S. Moshé, S. Shinnar, E. Bromfield, 2005, American journal of human genetics.

Phenotypic features of familial febrile seizures

D. Mandelbaum, D. Pal, S. Kugler, 2003, Neurology.

From single-SNP to wide-locus: genome-wide association studies identifying functionally related genes and intragenic regions in small sample studies.

Martin P. Seybold, K. Wittkowski, Tingting Song, 2013, Pharmacogenomics.

Further evidence for the increased power of LOD scores compared with nonparametric methods.

V. Vieland, D. Greenberg, M. Durner, 1999, American journal of human genetics.

Evaluation of CACNA1H in European patients with childhood absence epilepsy

A. Heils, O. Dulac, R. Nabbout, 2006, Epilepsy Research.

Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14

E. Wirrell, P. McKeigue, J. Aicardi, 2009, Epilepsy Research.

A linkage search for joint panic disorder/bipolar genes

S. Hodge, A. Fyer, M. Weissman, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mutation analysis of the C1QTNF3 gene in patients with schizophrenia

J. Silverman, M. Durner, J. Carrión-Baralt, 2010, Psychiatry Research.

Phenocopies versus genetic heterogeneity: can we use phenocopy frequencies in linkage analysis to compensate for heterogeneity?

S. Hodge, D. Greenberg, M. Durner, 1996, Human Heredity.

Evidence for linkage of adolescent-onset idiopathic generalized epilepsies to chromosome 8-and genetic heterogeneity.

S. Moshé, S. Shinnar, C. Harden, 1999, American journal of human genetics.

Confirmation of linkage between juvenile myoclonic epilepsy locus and the HLA region of chromosome 6.

M. Spence, D. Janz, R. Sparkes, 1991, American journal of medical genetics.

Can We Increase the Likelihood of Success for Future Association Studies in Epilepsy?

R. Guerrini, P. Gorroochurn, C. Marini, 2006, Epilepsia.

Polyspike and Waves Do Not Predict Generalized Tonic-Clonic Seizures in Childhood Absence Epilepsy

D. Mandelbaum, D. Pal, Esther Vierck, 2010, Journal of child neurology.

Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients

T. Sander, D. Janz, D. Greenberg, 1991, Neurology.

Genome scan of idiopathic generalized epilepsy: Evidence for major susceptibility gene and modifying genes influencing the seizure type

S Shinnar, S. Moshé, D. Labar, 2001, Annals of neurology.

Is there a genetic relationship between epilepsy and birth defects?

A. Delgado-Escueta, D. Greenberg, D A Greenberg, 1992, Neurology.

Common subtypes of idiopathic generalized epilepsies: lack of linkage to D20S19 close to candidate loci (EBN1, EEGV1) on chromosome 20.

T. Wienker, B. Schmitz, T. Sander, 1996, American journal of medical genetics.

Effect of misspecification of gene frequency on the two-point LOD score

D. Pal, D. Greenberg, Deb K Pal, 2001, European Journal of Human Genetics.

No evidence for a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q.

S. Moshé, S. Shinnar, C. Harden, 2000, American journal of medical genetics.

EVALUATION OF CACNA 1 H IN EUROPEAN PATIENTS WITH CHILDHOOD ABSENCE EPILEPSY

A. Heils, O. Dulac, R. Nabbout, 2008 .

Genetics of juvenile myoclonic epilepsy

D. Pal, D. Greenberg, M. Durner, 2005 .

Mutation analysis of the C1QTNF3 gene in patients with schizophrenia

J. Silverman, M. Durner, J. Carrión-Baralt, 2010, Psychiatry Research.