BRD2 (RING3) Is a Probable Major Susceptibility Gene for Common Juvenile Myoclonic Epilepsy

Deb K. Pal, Oleg V. Evgrafov, P Tabares, +3

The American Journal of Human Genetics

Neurobiology Of DiseaseGenetic DisorderGeneticsNeuroscienceNeurology +5

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

Martina Durner, Mehdi Keddache, Livia Tomasini, +16

Annals of Neurology

Reproducibility and Complications in Gene Searches: Linkage on Chromosome 6, Heterogeneity, Association, and Maternal Inheritance in Juvenile Myoclonic Epilepsy

David A. Greenberg, Martina Durner, Mehdi Keddache, +14

The American Journal of Human Genetics

Maternal InheritanceGenetic TestingDevelopmental BiologyGenetic DisorderGenetics +8

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

Steven P. Hamilton, Abby J. Fyer, Martina Durner, +5

Proceedings of the National Academy of Sciences

GeneticsGenetic EpidemiologyDisease Gene IdentificationGenetic ComponentClinical Genetics +14

Malic Enzyme 2 May Underlie Susceptibility to Adolescent-Onset Idiopathic Generalized Epilepsy

David A. Greenberg, Eftìhia Cayanis, Lisa J. Strug, +13

The American Journal of Human Genetics

PsychiatryMay Underlie SusceptibilityNeurologyNeuropathologyMedicine +1

Further Evidence for the Increased Power of LOD Scores Compared with Nonparametric Methods

Martina Durner, Veronica J. Vieland, David A. Greenberg

The American Journal of Human Genetics

Increased PowerBiostatisticsStatistical InferencePsychometricsNonparametric Methods +2

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

Abby J. Fyer, Steven P. Hamilton, Martina Durner, +11

Biological Psychiatry

PsychiatryGenetic DisorderGeneticsPsychiatric GeneticsThird-pass Genome Scan +5

Evidence for Linkage of Adolescent-Onset Idiopathic Generalized Epilepsies to Chromosome 8—and Genetic Heterogeneity

Martina Durner, Guillan Zhou, Ding‐Yi Fu, +14

The American Journal of Human Genetics

Linkage and mutational analysis of CLCN2 in childhood absence epilepsy

Kate V. Everett, Barry A. Chioza, Jean Aicardi, +20

Epilepsy Research

Molecular NeuroscienceGenetic DisorderGeneticsNeurologyNeuroscience +5

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

Deb K. Pal, Martina Durner, Irene Klotz, +9

Brain and Development

Neuropsychological FunctioningComplex InheritanceNeurologyNeuroscienceAbnormal Development +2