Rowan Digital Works

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals., Joshua E. Motelow, Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen-Chen Anne Feng, Daniel P. Howrigan, Liam E. Abbott, Katherine Tashman, Felecia Cerrato, Caroline Cusick, Tarjinder Singh, Henrike Heyne, Andrea E. Byrnes, Claire Churchhouse, Nick Watts, Matthew Solomonson, Dennis Lal, Namrata Gupta, Benjamin M. Neale, Gianpiero L. Cavalleri, Patrick Cossette, Chris Cotsapas, Peter De Jonghe, Tracy Dixon-Salazar, Renzo Guerrini, Hakon Hakonarson, Erin L. Heinzen, Ingo Helbig, Patrick Kwan, Anthony G. Marson, Slavé Petrovski, Sitharthan Kamalakaran, Sanjay M. Sisodiya, Randy Stewart, Sarah Weckhuysen, Chantal Depondt, Dennis J. Dlugos, Ingrid E. Scheffer, Pasquale Striano, Catharine Freyer, Roland Krause, Patrick May, Kevin McKenna, Brigid M. Regan, Caitlin A. Bennett, Costin Leu, Stephanie L. Leech, Terence J. O’Brien
Thomas Ferraro

Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals., Joshua E. Motelow, Gundula Povysil, Ryan S. Dhindsa, Kate E. Stanley, Andrew S. Allen, Yen-Chen Anne Feng, Daniel P. Howrigan, Liam E. Abbott, Katherine Tashman, Felecia Cerrato, Caroline Cusick, Tarjinder Singh, Henrike Heyne, Andrea E. Byrnes, Claire Churchhouse, Nick Watts, Matthew Solomonson, Dennis Lal, Namrata Gupta, Benjamin M. Neale, Gianpiero L. Cavalleri, Patrick Cossette, Chris Cotsapas, Peter De Jonghe, Tracy Dixon-Salazar, Renzo Guerrini, Hakon Hakonarson, Erin L. Heinzen, Ingo Helbig, Patrick Kwan, Anthony G. Marson, Slavé Petrovski, Sitharthan Kamalakaran, Sanjay M. Sisodiya, Randy Stewart, Sarah Weckhuysen, Chantal Depondt, Dennis J. Dlugos, Ingrid E. Scheffer, Pasquale Striano, Catharine Freyer, Roland Krause, Patrick May, Kevin McKenna, Brigid M. Regan, Caitlin A. Bennett, Costin Leu, Stephanie L. Leech, Terence J. O’Brien
Russell Buono

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals, Epi Collaborative, Yen-Chen Anne Feng, Daniel P. Howrigan, Liam E. Abbott, Katherine Tashman, Felecia Cerrato, Tarjinder Singh, Henrike Heyne, Andrea Byrnes, Claire Churchhouse, Dennis Lal, Erin L. Heinzen, Gianpiero L. Cavalleri, Hakon Hakonarson, Ingo Helbig, Roland Krause, Patrick May, Sarah Weckhuysen, Slavé Petrovski, Sitharthan Kamalakaran, Sanjay M. Sisodiya, Patrick Cossette, Chris Cotsapas, Peter De Jonghe, Tracy Dixon-Salazar, Renzo Guerrini, Patrick Kwan, Anthony G. Marson, Randy Stewart, Chantal Depondt, Dennis J. Dlugos, Ingrid E. Scheffer, Pasquale Striano, Catharine Freyer, Kevin McKenna, Brigid M. Regan, Susannah T. Bellows, Costin Leu, Caitlin A. Bennett, Esther M.C. Johns, Alexandra Macdonald, Hannah Shilling, Rosemary Burgess, Dorien Weckhuysen, Melanie Bahlo, Terence J. O’Brien, Marian Todaro, Hannah Stamberger, Danielle M. Andrade
Thomas Ferraro

Ultra-rare genetic variation in the epilepsies: a whole-exome sequencing study of 17,606 individuals, Epi Collaborative, Yen-Chen Anne Feng, Daniel P. Howrigan, Liam E. Abbott, Katherine Tashman, Felecia Cerrato, Tarjinder Singh, Henrike Heyne, Andrea Byrnes, Claire Churchhouse, Dennis Lal, Erin L. Heinzen, Gianpiero L. Cavalleri, Hakon Hakonarson, Ingo Helbig, Roland Krause, Patrick May, Sarah Weckhuysen, Slavé Petrovski, Sitharthan Kamalakaran, Sanjay M. Sisodiya, Patrick Cossette, Chris Cotsapas, Peter De Jonghe, Tracy Dixon-Salazar, Renzo Guerrini, Patrick Kwan, Anthony G. Marson, Randy Stewart, Chantal Depondt, Dennis J. Dlugos, Ingrid E. Scheffer, Pasquale Striano, Catharine Freyer, Kevin McKenna, Brigid M. Regan, Susannah T. Bellows, Costin Leu, Caitlin A. Bennett, Esther M.C. Johns, Alexandra Macdonald, Hannah Shilling, Rosemary Burgess, Dorien Weckhuysen, Melanie Bahlo, Terence J. O’Brien, Marian Todaro, Hannah Stamberger, Danielle M. Andrade
Russell Buono

Novel De Novo Mutation of a Conserved SCN1A Amino-Acid Residue (R1596), Dennis J. Dlugos, Thomas N. Ferraro, Russell J. Buono
Russell Buono

Novel De Novo Mutation of a Conserved SCN1A Amino-Acid Residue (R1596), Dennis J. Dlugos, Thomas N. Ferraro, Russell J. Buono
Thomas Ferraro

Challenges and opportunities in the application of pharmacogenetics to antiepileptic drug therapy, Thomas N. Ferraro, Dennis J. Dlugos, Russell J. Buono
Thomas Ferraro

Challenges and opportunities in the application of pharmacogenetics to antiepileptic drug therapy, Thomas N. Ferraro, Dennis J. Dlugos, Russell J. Buono
Russell Buono

Role of genetics in the diagnosis and treatment of epilepsy, Thomas N. Ferraro, Dennis J. Dlugos, Russell J. Buono
Thomas Ferraro

Role of genetics in the diagnosis and treatment of epilepsy, Thomas N. Ferraro, Dennis J. Dlugos, Russell J. Buono
Russell Buono

Lack of association between variations in the brain-derived neurotrophic factor (BDNF) gene and temporal lobe epilepsy, Falk W. Lohoff, Thomas N. Ferraro, John P. Dahl, Marie A. Hildebrandt, Theresa M. Scattergood, Michael J. O’Connor, Michael R. Sperling, Dennis J. Dlugos, Wade H. Berrettini, Russell J. Buono
Thomas Ferraro

Lack of association between variations in the brain-derived neurotrophic factor (BDNF) gene and temporal lobe epilepsy, Falk W. Lohoff, Thomas N. Ferraro, John P. Dahl, Marie A. Hildebrandt, Theresa M. Scattergood, Michael J. O’Connor, Michael R. Sperling, Dennis J. Dlugos, Wade H. Berrettini, Russell J. Buono
Russell Buono

Recruitment rates and fear of phlebotomy in pediatric patients in a genetic study of epilepsy., Dennis J. Dlugos, Theresa M. Scattergood, Thomas N. Ferraro, Wade H. Berrettinni, Russell J. Buono
Thomas Ferraro