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2
The role of copy number variants in the genetic architecture of common familial epilepsies 미리보기

학술저널

issue
EPILEPSIA; JAN 20 2024, 13p.
Author
Almanza, Edith P.
Nguyen, John
Mehaffey, Michelle
Sulovari, Arvis
Wang, Tianyun
Galey, Miranda
Miller, Danny E.
Eichler, Evan E.
Mefford, Heather C.
Abou-Khalil, Bassel
Afawi, Zaid Afawi
Allen, Andrew S.
Amrom, Dina
Andermann, Eva
Bautista, Jocelyn F.
Bellows, Susannah T.
Berkovic, Samuel F.
Bluvstein, Judith
Boro, Alexis
Burgess, Rosemary
Cascino, Gregory D.
Chung, Seo-Kyung
Consalvo, Damian
Cossette, Patrick
Crompton, Douglas E.
Crumrine, Patricia
Curtis, Sarah W.
Delanty, Norman
Devinsky, Orrin
Dlugos, Dennis
Ellis, Colin A.
Epstein, Michael P.
Fiol, Miguel
Fountain, Nathan B.
Freyer, Catharine
Friedman, Dan
Geller, Eric B.
Glauser, Tracy
Glynn, Simon
Goldstein, David B.
Gravel, Micheline
Haas, Kevin
Harris, Rebekah, V
Haut, Sheryl
Heinzen, Erin L.
Helmers, Sandra
Henry, Olivia J.
Joshi, Sucheta
Kirsch, Heidi E.
Kivity, Sara
Knowlton, Robert C.
Kossoff, Eric
Kuzniecky, Ruben
Loeb, Rebecca
Lowenstein, Daniel H.
Marson, Anthony G.
McCormack, Mark
McGuire, Shannon M.
McKenna, Kevin
Motika, Paul, V
Mullen, Saul A.
Novotny, Edward J.
O'Brien, Terence J.
Oliver, Karen L.
Ottman, Ruth
Paolicchi, Juliann M.
Parent, Jack M.
Park, Kristen L.
Paterson, Sarah J.
Petrovski, Slave
Pickrell, William O.
Poduri, Annapurna
Rees, Mark, I
Sadleir, Lynette G.
Scheffer, Ingrid E.
Shellhaas, Renee A.
Sherr, Elliott H.
Shih, Jerry J.
Shinnar, Shlomo
Singh, Rani K.
Sirven, Joseph
Smith, Michael C.
Smith, Philip E. M.
Sperling, Michael R.
Sullivan, Joseph
Thio, Liu Lin
Thomas, Rhys H.
Venkat, Anu
Vining, Eileen P. G.
Von Allmen, Gretchen K.
Weisenberg, Judith
Widdess-Walsh, Peter
Winawer, Melodie R.
Epi4K Consortium
DB Label
Database : Science Citation Index Expanded
원문보기
Full Text (Wiley-DB)  등재 - Web of Science  등재 - SCOPUS  조회 - Impact Factor (JCR) 
8
De novo mutations in epileptic encephalopathies 미리보기

학술저널

issue
Nature. Sep 12, 2013 501(7466):217-221
Author
Allen, Andrew S.
Cossette, Patrick
Delanty, Norman
Eichler, Evan E.
Epstein, Michael P.
Glauser, Tracy
Goldstein, David B.
Han, Yujun
Heinzen, Erin L.
Hitomi, Yuki
Howell, Katherine B.
Johnson, Michael R.
Kuzniecky, Ruben
Lowenstein, Daniel H.
Lu, Yi-Fan
Madou, Maura R. Z.
Marson, Anthony G.
Mefford, Heather C.
Nieh, Sahar Esmaeeli
OʼBrien, Terence J.
Ottman, Ruth
Petrovski, Slavé
Poduri, Annapurna
Ruzzo, Elizabeth K.
Sherr, Elliott H.
Yuskaitis, Christopher J.
Abou-Khalil, Bassel
Alldredge, Brian K.
Bautista, Jocelyn F.
Berkovic, Samuel F.
Boro, Alex
Cascino, Gregory D.
Consalvo, Damian
Crumrine, Patricia
Devinsky, Orrin
Dlugos, Dennis
Fiol, Miguel
Fountain, Nathan B.
French, Jacqueline
Friedman, Daniel
Geller, Eric B.
Glynn, Simon
Haut, Sheryl R.
Hayward, Jean
Helmers, Sandra L.
Joshi, Sucheta
Kanner, Andres
Kirsch, Heidi E.
Knowlton, Robert C.
Kossoff, Eric H.
Kuperman, Rachel
McGuire, Shannon M.
Motika, Paul V.
Novotny, Edward J.
Paolicchi, Juliann M.
Parent, Jack M.
Park, Kristen
Scheffer, Ingrid E.
Shellhaas, Renée A.
Shih, Jerry J.
Singh, Rani
Sirven, Joseph
Smith, Michael C.
Sullivan, Joseph
Thio, Liu Lin
Venkat, Anu
Vining, Eileen P. G.
Von Allmen, Gretchen K.
Weisenberg, Judith L.
Widdess-Walsh, Peter
Winawer, Melodie R.
DB Label
Database : Journals@OVID
원문보기
Full Text Full Text (원문보기) Full Text (Nature)  등재 - Web of Science (SCIE)  등재 - SCOPUS  조회 - Impact Factor (JCR)  원문복사신청 - FRIC 
10
Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data 미리보기

학술저널

issue
EUROPEAN JOURNAL OF HUMAN GENETICS; JUN 2017, 25 7, p894-p899, 6p.
Author
Allen, Andrew S.
Berkovic, Samuel F.
Bridgers, Joshua
Cossette, Patrick
Dlugos, Dennis
Epstein, Michael P.
Glauser, Tracy
Goldstein, David B.
Heinzen, Erin L.
Jiang, Yu
Johnson, Michael R.
Kuzniecky, Ruben
Lowenstein, Daniel H.
Marson, Anthony G.
Mefford, Heather C.
O'Brien, Terence J.
Ottman, Ruth
Petrou, Steven
Petrovski, Slave
Poduri, Annapurna
Ren, Zhong
Scheffer, Ingrid E.
Sherr, Elliott
Wang, Quanli
Balling, Rudi
Barisic, Nina
Baulac, Stephanie
Caglayan, Hande
Craiu, Dana
De Jonghe, Peter
Depienne, Christel
Guerrini, Renzo
Helbig, Ingo
Hjalgrim, Helle
Hoffman-Zacharska, Dorota
Jaehn, Johanna
Klein, Karl Martin
Koeleman, Bobby
Komarek, Vladimir
Krause, Roland
Leguern, Eric
Lehesjoki, Anna-Elina
Lemke, Johannes R.
Lerche, Holger
Linnankivi, Tarja
Marini, Carla
May, Patrick
Moller, Rikke S.
Muhle, Hiltrud
Pal, Deb
Palotie, Aarno
Rosenow, Felix
Selmer, Kaja
Serratosa, Jose M.
Sisodiya, Sanjay
Stephani, Ulrich
Sterbova, Katalin
Striano, Pasquale
Suls, Arvid
Talvik, Tiina
von Spiczak, Sarah
Weber, Yvonne
Weckhuysen, Sarah
Zara, Federico
Abou-Khalil, Bassel
Alldredge, Brian K.
Amrom, Dina
Andermann, Eva
Andermann, Frederick
Bautista, Jocelyn F.
Bluvstein, Judith
Cascino, Gregory D.
Consalvo, Damian
Crumrine, Patricia
Devinsky, Orrin
Fiol, Miguel E.
Fountain, Nathan B.
French, Jacqueline
Friedman, Daniel
Haas, Kevin
Haut, Sheryl R.
Hayward, Jean
Joshi, Sucheta
Kanner, Andres
Kirsch, Heidi E.
Kossoff, Eric H.
Kuperman, Rachel
McGuire, Shannon M.
Motika, Paul V.
Novotny, Edward J.
Paolicchi, Juliann M.
Parent, Jack
Park, Kristen
Shellhaas, Renee A.
Sirven, Joseph
Smith, Michael C.
Sullivan, Joseph
Thio, Liu Lin
Venkat, Anu
Vining, Eileen P. G.
Von Allmen, Gretchen K.
Weisenberg, Judith L.
Widdess-Walsh, Peter
Winawer, Melodie R.
Epi4K Consortium
EuroEPINOMICS- RES Consortium
Epilepsy Phenome Genome Project
DB Label
Database : Science Citation Index Expanded
원문보기
등재 - Web of Science  등재 - SCOPUS  조회 - Impact Factor (JCR)  원문복사신청 - FRIC 
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