Recruitment for Genetic Studies of Epilepsy

Bằng Misiewicz, Sylwia, Winawer, Melodie R.
Được phát hành 2012

Evidence for a Shared Genetic Susceptibility to Migraine and Epilepsy

Bằng Winawer, Melodie R., Connors, Robert
Được phát hành 2013

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

Bằng Tobochnik, Steven, Fahlstrom, Robyn, Shain, Catherine, Winawer, Melodie R.
Xuất bản năm Neurology (2017)

Autosomal dominant partial epilepsy with auditory features: Defining the phenotype

Bằng Winawer, Melodie R., Ottman, Ruth, Hauser, W. Allen, Pedley, Timothy A.
Được phát hành 2000

Mapping a mouse limbic seizure susceptibility locus on chromosome 10

Bằng Winawer, Melodie R., Gildersleeve, Sandra S., Phillips, Austin G., Rabinowitz, Daniel, Palmer, Abraham A.
Được phát hành 2011

Genetic effects on sleep/wake variation of seizures

Bằng Winawer, Melodie R., Shih, Jerry, Beck, Erin S., Hunter, Jessica E., Epstein, Michael P.
Xuất bản năm Epilepsia (2016)

Familial aggregation of status epilepticus in generalized and focal epilepsies

Bằng Weisenberg, Judith L.Z., Fitzgerald, Robert T., Constantino, John N., Winawer, Melodie R., Thio, Liu Lin
Xuất bản năm Neurology (2020)

Reproductive decision-making in families containing multiple individuals with epilepsy

Bằng Nakamura, Jacquelyn, Sorge, Shawn T., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth
Xuất bản năm Epilepsia (2021)

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

Bằng Winawer, Melodie R., Klassen, Tara L., Teed, Sarah, Shipman, Marissa, Leung, Emily H., Palmer, Abraham A.
Được phát hành 2014

Familial Clustering of Seizure Types within the Idiopathic Generalized Epilepsies

Bằng Winawer, Melodie R., Marini, Carla, Grinton, Bronwyn E, Rabinowitz, Daniel, Berkovic, Samuel F., Scheffer, Ingrid E., Ottman, Ruth
Được phát hành 2005

Genetic attribution and perceived impact of epilepsy in multiplex epilepsy families

Bằng Garofalo, Diana C., Sorge, Shawn T., Hesdorffer, Dale C., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth
Xuất bản năm Epilepsia (2019)

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

Bằng Winawer, Melodie R., Kuperman, Rachel, Niethammer, Martin, Sherman, Steven, Rabinowitz, Daniel, Guell, Irene Plana, Ponder, Christine A., Palmer, Abraham A.
Được phát hành 2007

Depression and Genetic Causal Attribution of Epilepsy in Multiplex Epilepsy Families

Bằng Sorge, Shawn T., Hesdorffer, Dale C., Phelan, Jo C., Winawer, Melodie R., Shostak, Sara, Goldsmith, Jeff, Chung, Wendy K., Ottman, Ruth
Xuất bản năm Epilepsia (2016)

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

Bằng Santoro, Bina, Lee, Janet Y., Englot, Dario J., Gildersleeve, Sandra, Piskorowski, Rebecca A., Siegelbaum, Steven A., Winawer, Melodie R., Blumenfeld, Hal
Được phát hành 2010

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

Bằng Distler, Margaret G., Gorfinkle, Naomi, Papale, Ligia A., Wuenschell, Gerald E., Termini, John, Escayg, Andrew, Winawer, Melodie R., Palmer, Abraham A.
Được phát hành 2013

Genetic Causal Attribution of Epilepsy and its Implications for Felt Stigma

Bằng Sabatello, Maya, Phelan, Jo C., Hesdorffer, Dale C., Shostak, Sara, Goldsmith, Jeff, Sorge, Shawn T., Winawer, Melodie R., Chung, Wendy K., Ottman, Ruth
Xuất bản năm Epilepsia (2015)

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

Bằng Caminiti, Courtney B., Hesdorffer, Dale C., Shostak, Sara, Goldsmith, Jeff, Sorge, Shawn T., Winawer, Melodie R., Phelan, Jo C., Chung, Wendy K., Ottman, Ruth
Xuất bản năm Epilepsia (2015)

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

Bằng 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
Được phát hành 2002

Genetic Testing Preferences in Families Containing Multiple Individuals with Epilepsy

Bằng 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
Xuất bản năm Epilepsia (2014)

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

Bằng 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.
Được phát hành 2013