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Papers共 13 篇Author StatisticsCo-AuthorSimilar Experts

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The Role of Copy Number Variants in the Genetic Architecture of Common Familial Epilepsies
Edith P. Almanza Fuerte,John Nguyen, Michelle Mehaffey,Arvis Sulovari,Tianyun Wang,Miranda Galey,Danny E. Miller,Evan E. Eichler,Heather C. Mefford,Bassel Abou-Khalil, Afawi,Andrew S. Allen,Dina Amrom,Eva Andermann,Jocelyn F. Bautista,Susannah T. Bellows,Samuel F. Berkovic,Judith Bluvstein,Alexis Boro,Rosemary Burgess,Gregory D. Cascino,Seo-Kyung Chung,Damian Consalvo,Patrick Cossette,Douglas E. Crompton,Patricia Crumrine,Sarah W. Curtis,Norman Delanty,Orrin Devinsky,Dennis Dlugos,Colin A. Ellis,Michael P. Epstein,Miguel Fiol,Nathan B. Fountain,Catharine Freyer, Dan Friedman,Eric B. Geller,Tracy Glauser,Simon Glynn,David B. Goldstein,Micheline Gravel,Kevin Haas,Rebekah V. Harris,Sheryl Haut,Erin L. Heinzen,Sandra Helmers,Olivia J. Henry,Sucheta Joshi,Heidi E. Kirsch,Sara Kivity,Robert C. Knowlton,Eric Kossoff,Ruben Kuzniecky,Rebecca Loeb,Daniel H. Lowenstein,Anthony G. Marson,Mark McCormack, Shannon M. McGuire,Kevin McKenna,Paul V. Motika,Saul A. Mullen,Edward J. Novotny,Terence J. O'Brien,Karen L. Oliver,Ruth Ottman,Juliann M. Paolicchi,Jack M. Parent,Kristen L. Park,Sarah J. Paterson,Slave Petrovski,William O. Pickrell,Annapurna Poduri,Mark I. Rees,Lynette G. Sadleir,Ingrid E. Scheffer,Renee A. Shellhaas,Elliott H. Sherr,Jerry J. Shih,Shlomo Shinnar,Rani K. Singh,Joseph Sirven,Michael C. Smith,Philip E. M. Smith,Michael R. Sperling,Joseph Sullivan,Liu Lin Thio,Rhys H. Thomas,Anu Venkat,Eileen P. G. Vining,Gretchen K. Von Allmen,Judith Weisenberg,Peter Widdess-Walsh,Melodie R. Winawer
EPILEPSIAno. 3 (2024): 792-804
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Ultra-rare Genetic Variation in the Common Epilepsies: a Case- 1 Control Sequencing Study
EpiK Consortium, Epilepsy Phenome, Genome Project,Joseph Sirven, Liu Lin,Anu Venkat, E. P. Vining, G. V. Allmen, Judith L. Z. Weisenberg, M. Winawer
semanticscholar
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Ultra-rare Genetic Variation in Common Epilepsies: a Case-Control Sequencing Study
Andrew S. Allen,Susannah T. Bellows,Samuel F. Berkovic,Joshua Bridgers,Rosemary Burgess,Gianpiero Cavalleri,Seo-Kyung Chung,Patrick Cossette,Norman Delanty,Dennis Dlugos,Michael P. Epstein,Catharine Freyer,David B. Goldstein,Erin L. Heinzen,Michael S. Hildebrand,Michael R. Johnson,Ruben Kuzniecky,Daniel H. Lowenstein,Anthony G. Marson,Richard Mayeux,Caroline Mebane,Heather C. Mefford,Terence J. O'Brien,Ruth Ottman,Steven Petrou,Slave Petrovski,William O. Pickrell,Annapurna Poduri,Rodney A. Radtke,Mark I. Rees,Brigid M. Regan,Zhong Ren,Ingrid E. Scheffer,Graeme J. Sills,Rhys H. Thomas,Quanli Wang,Bassel Abou-Khalil,Brian K. Alldredge,Dina Amrom,Eva Andermann,Frederick Andermann,Jocelyn F. Bautista,Judith Bluvstein,Alex Boro,Gregory D. Cascino,Damian Consalvo,Patricia Crumrine,Orrin Devinsky,Miguel Fiol,Nathan B. Fountain,Jacqueline French,Daniel Friedman,Eric B. Geller,Tracy Glauser,Simon Glynn,Kevin Haas,Sheryl R. Haut,Jean Hayward,Sandra L. Helmers,Sucheta Joshi,Andres Kanner,Heidi E. Kirsch,Robert C. Knowlton,Eric H. Kossoff,Rachel Kuperman,Paul V. Motika,Edward J. Novotny,Juliann M. Paolicchi,Jack M. Parent,Kristen Park,Lynette G. Sadleir,Renee A. Shellhaas,Elliott H. Sherr,Jerry J. Shih,Shlomo Shinnar,Rani K. Singh,Joseph Sirven,Michael C. Smith,Joseph Sullivan,Liu Lin Thio,Anu Venkat,Eileen P. G. Vining,Gretchen K. Von Allmen,Judith L. Weisenberg,Peter Widdess-Walsh,Melodie R. Winawer
Lancet neurologyno. 2 (2017): 135-143
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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies
Silke Appenzeller,Rudi Balling,Nina Barišić,Stéphanie Baulac,Hande Çağlayan,Dana Craiu,Peter De Jonghe,Christel Depienne,Petia Dimova,Tania Djémié,Padhraig Gormley,Renzo Guerrini,Ingo Helbig,Helle Hjalgrim,Dorota Hoffman‐Zacharska,Johanna Jähn,Karl Martin Klein,Bobby Koeleman,Vladimı́r Komárek,Roland Krause,Gregor Kuhlenbäumer,Éric Leguern,Anna‐Elina Lehesjoki,Johannes R. Lemke,Holger Lerche,Tarja Linnankivi,Carla Marini,Patrick May,Rikke S. Møller,Hiltrud Muhle,Deb K. Pal,Aarno Palotie,Manuela Pendziwiat,Angela Robbiano,Filip Roelens,Felix Rosenow,Kaja Kristine Selmer,Joan Serratosa,Sanjay M. Sisodiya,Ulrich Stephani,Katalin Štěrbová,Pasquale Striano,Arvid Suls,Tiina Talvik,Sarah von Spiczak,Yvonne Weber,Sarah Weckhuysen,Federico Zara,Bassel Abou‐Khalil,Brian K. Alldredge,Eva Andermann,Frédérick Andermann,Dina Amrom,Jocelyn F. Bautista,Samuel F. Berkovic,Judith Bluvstein,Alex Boro,Gregory D. Cascino,D. Consalvo,Patricia K. Crumrine,Orrin Devinsky,Dennis Dlugos, Michael P. Epstein,Miguel Fiol,Nathan B. Fountain,Jacqueline French,Daniel J. Friedman,Eric B. Geller,Tracy A. Glauser,Simon Glynn, Kevin R. Haas,Sheryl R. Haut,Jean Hayward,Sandra L. Helmers,Sucheta M. Joshi,Andrés M. Kanner,Heidi E. Kirsch,Robert C. Knowlton,Eric H. Kossoff,Rachel Kuperman,Ruben Kuzniecky,Daniel H. Lowenstein, Shannon M. McGuire,Paul Motika,Edward J. Novotny,Ruth Ottman,Juliann Paolicchi,Jack M. Parent,Kristen Park,Annapurna Poduri,Lynette G. Sadleir,Ingrid E. Scheffer,Renée A. Shellhaas,Elliott H. Sherr,Jerry J. Shih,Rani K. Singh,Joseph Sirven,Michael C. Smith, Joe Sullivan,Liu Lin Thio,Anu Venkat,Eileen P.G. Vining,Gretchen K. Von Allmen,Judith Weisenberg,Peter Widdess‐Walsh,Melodie R. Winawer,Andrew S. Allen,Patrick Cossette,Norman Delanty,Evan E. Eichler,David B. Goldstein,Yujun Han,Erin L. Heinzen,Michael R. Johnson,Anthony G Marson,Heather C. Mefford,Sahar Esmaeeli Nieh,Terence J. O’Brien,Stephen Petrou,Slavé Petrovski,Elizabeth K. Ruzzo
American journal of human genetics（2017）
Cited24Views0Bibtex
24
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Copy Number Variant Analysis from Exome Data in 349 Patients with Epileptic Encephalopathy
Bassel Abou-Khalil, Brian K. Alldredge, Andrew S. Allen, Eva Andermann, Frederick Andermann,Dina Amrom,Jocelyn F. Bautista, Samuel F. Berkovic,Alex Boro,Gregory Cascino, Bradley P. Coe,Damian Consalvo, Joseph Cook, Patrick Cossette,Patricia Crumrine, Norman Delanty, Orrin Devinsky, Dennis Dlugos, Evan E. Eichler, Michael P. Epstein,Miguel Fiol, Nathan B. Fountain, Jacqueline French, Daniel Friedman,Eric B. Geller,Tracy Glauser,Simon Glynn, David B. Goldstein,Sheryl R. Haut,Jean Hayward, Erin L. Heinzen,Sandra L. Helmers, Michael R. Johnson,Sucheta Joshi,Andres Kanner, Heidi E. Kirsch, Robert C. Knowlton, Eric H. Kossoff, Nik Krumm,Rachel Kuperman, Ruben Kuzniecky, Daniel H. Lowenstein, Anthony G. Marson, Shannon M. McGuire, Heather C. Mefford,Paul V. Motika, Ben Nelson,Sahar Esmaeeli Nieh,Edward J. Novotny, Terence J. O'Brien,Ruth Ottman,Juliann M. Paolicchi,Jack Parent,Kristen Park,Stephen Petrou,Slave Petrovski, Annapurna Poduri,Archana Raja,Elizabeth K. Ruzzo,Ingrid E. Scheffer, Renee A. Shellhaas,Elliott Sherr, Jerry J. Shih, Rani Singh,Joseph Sirven, Michael C. Smith, Joe Sullivan,Liu Lin Thio,Anu Venkat,Eileen P. G. Vining,Gretchen K. Von Allmen,Judith L. Weisenberg,Peter Widdess-Walsh,Melodie R. Winawer
ANNALS OF NEUROLOGY（2015）
Cited52Views0Bibtex
52
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Author Statistics

#Papers: 13

#Citation: 812

H-Index: 8

G-Index: 13

Sociability: 6

Diversity: 0

Activity: 0

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