Recruitment for Genetic Studies of Epilepsy

Por Misiewicz, Sylwia, Winawer, Melodie R.
Publicado em 2012

Evidence for a Shared Genetic Susceptibility to Migraine and Epilepsy

Por Winawer, Melodie R., Connors, Robert
Publicado em 2013

Familial aggregation of focal seizure semiology in the Epilepsy Phenome/Genome Project

Por Tobochnik, Steven, Fahlstrom, Robyn, Shain, Catherine, Winawer, Melodie R.
Publicado no Neurology (2017)

Autosomal dominant partial epilepsy with auditory features: Defining the phenotype

Por Winawer, Melodie R., Ottman, Ruth, Hauser, W. Allen, Pedley, Timothy A.
Publicado em 2000

Mapping a mouse limbic seizure susceptibility locus on chromosome 10

Por Winawer, Melodie R., Gildersleeve, Sandra S., Phillips, Austin G., Rabinowitz, Daniel, Palmer, Abraham A.
Publicado em 2011

Genetic effects on sleep/wake variation of seizures

Por Winawer, Melodie R., Shih, Jerry, Beck, Erin S., Hunter, Jessica E., Epstein, Michael P.
Publicado no Epilepsia (2016)

Familial aggregation of status epilepticus in generalized and focal epilepsies

Por Weisenberg, Judith L.Z., Fitzgerald, Robert T., Constantino, John N., Winawer, Melodie R., Thio, Liu Lin
Publicado no Neurology (2020)

A locus on mouse Ch10 influences susceptibility to limbic seizure severity: fine mapping and in silico candidate gene analysis

Por Winawer, Melodie R., Klassen, Tara L., Teed, Sarah, Shipman, Marissa, Leung, Emily H., Palmer, Abraham A.
Publicado em 2014

Familial Clustering of Seizure Types within the Idiopathic Generalized Epilepsies

Por Winawer, Melodie R., Marini, Carla, Grinton, Bronwyn E, Rabinowitz, Daniel, Berkovic, Samuel F., Scheffer, Ingrid E., Ottman, Ruth
Publicado em 2005

Genetic attribution and perceived impact of epilepsy in multiplex epilepsy families

Por Garofalo, Diana C., Sorge, Shawn T., Hesdorffer, Dale C., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth
Publicado no Epilepsia (2019)

Use of chromosome substitution strains to identify seizure susceptibility loci in mice

Por Winawer, Melodie R., Kuperman, Rachel, Niethammer, Martin, Sherman, Steven, Rabinowitz, Daniel, Guell, Irene Plana, Ponder, Christine A., Palmer, Abraham A.
Publicado em 2007

Depression and Genetic Causal Attribution of Epilepsy in Multiplex Epilepsy Families

Por Sorge, Shawn T., Hesdorffer, Dale C., Phelan, Jo C., Winawer, Melodie R., Shostak, Sara, Goldsmith, Jeff, Chung, Wendy K., Ottman, Ruth
Publicado no Epilepsia (2016)

Increased seizure severity and seizure-related death in mice lacking HCN1 channels

Por Santoro, Bina, Lee, Janet Y., Englot, Dario J., Gildersleeve, Sandra, Piskorowski, Rebecca A., Siegelbaum, Steven A., Winawer, Melodie R., Blumenfeld, Hal
Publicado em 2010

Glyoxalase 1 and its substrate methylglyoxal are novel regulators of seizure susceptibility

Por Distler, Margaret G., Gorfinkle, Naomi, Papale, Ligia A., Wuenschell, Gerald E., Termini, John, Escayg, Andrew, Winawer, Melodie R., Palmer, Abraham A.
Publicado em 2013

Genetic Causal Attribution of Epilepsy and its Implications for Felt Stigma

Por Sabatello, Maya, Phelan, Jo C., Hesdorffer, Dale C., Shostak, Sara, Goldsmith, Jeff, Sorge, Shawn T., Winawer, Melodie R., Chung, Wendy K., Ottman, Ruth
Publicado no Epilepsia (2015)

Parents’ interest in genetic testing of their offspring in multiplex epilepsy families

Por Caminiti, Courtney B., Hesdorffer, Dale C., Shostak, Sara, Goldsmith, Jeff, Sorge, Shawn T., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth
Publicado no Epilepsia (2015)

Four New Families with Autosomal Dominant Partial Epilepsy with Auditory Features: Clinical Description and Linkage to Chromosome 10q24

Por Winawer, Melodie R., Boneschi, Filippo Martinelli, Barker-Cummings, Christie, Lee, Joseph H., Liu, Jianjun, Mekios, Constantine, Gilliam, T. Conrad, Pedley, Timothy A., Hauser, W. Allen, Ottman, Ruth
Publicado em 2002

Genetic Testing Preferences in Families Containing Multiple Individuals with Epilepsy

Por Okeke, Janice O., Tangel, Virginia E., Sorge, Shawn T., Hesdorffer, Dale C., Winawer, Melodie R., Goldsmith, Jeff, Phelan, Jo C., Chung, Wendy K., Shostak, Sara, Ottman, Ruth
Publicado no Epilepsia (2014)

Issues related to symptomatic and disease-modifying treatments affecting cognitive and neuropsychiatric comorbidities of epilepsy

Por Brooks-Kayal, Amy R., Bath, Kevin G., Berg, Anne T., Galanopoulou, Aristea S., Holmes, Gregory L., Jensen, Frances E., Kanner, Andres M., O’Brien, Terence J., Whittemore, Vicky H., Winawer, Melodie R., Patel, Manisha, Scharfman, Helen E.
Publicado em 2013

Somatic SLC35A2 variants in the brain are associated with intractable neocortical epilepsy

Por Winawer, Melodie R., Griffin, Nicole G., Samanamud, Jorge, Baugh, Evan H., Rathakrishnan, Dinesh, Ramalingam, Senthilmurugan, Zagzag, David, Schevon, Catherine A., Dugan, Patricia, Hegde, Manu, Sheth, Sameer A., McKhann, Guy M., Doyle, Werner K., Grant, Gerald A., Porter, Brenda E., Mikati, Mohamad A., Muh, Carrie R., Malone, Colin D., Bergin, Ann Marie R., Peters, Jurriaan M., McBrian, Danielle K., Pack, Alison M., Akman, Cigdem I., LaCoursiere, Christopher M., Keever, Katherine M., Madsen, Joseph R., Yang, Edward, Lidov, Hart G.W., Shain, Catherine, Allen, Andrew S., Canoll, Peter, Crino, Peter B., Poduri, Annapurna H., Heinzen, Erin L.
Publicado no Ann Neurol (2018)