All papers authored by Samuel Berkovic
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2024
Sindhu Viswanathan 
,
Karen L. Oliver ,
Brigid M. Regan,
Amy L. Schneider,
Candace T. Myers,
Michele G. Mehaffey,
Amy J. LaCroix,
Jayne Antony,
Richard Webster,
Michael Cardamone,
Gopinath M. Subramanian,
Annie T. G. Chiu ,
Eugenia Roza,
Raluca I. Teleanu,
Stephen Malone
and 12 other authors
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,
Karen L. Oliver ,
Brigid M. Regan,
Amy L. Schneider,
Candace T. Myers,
Michele G. Mehaffey,
Amy J. LaCroix,
Jayne Antony,
Richard Webster,
Michael Cardamone,
Gopinath M. Subramanian,
Annie T. G. Chiu ,
Eugenia Roza,
Raluca I. Teleanu,
Stephen Malone
and 12 other authors
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2023
Rebekah V. Harris ,
Karen L. Oliver ,
Piero Perucca ,
Pasquale Striano,
Angelo Labate ,
Antonella Riva ,
Bronwyn E. Grinton,
Joshua Reid,
Jessica Hutton,
Marian Todaro,
Terence J. O'Brien,
Patrick Kwan,
Lynette G. Sadleir,
Saul A. Mullen,
Emanuela Dazzo
and 6 other authors
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,
Karen L. Oliver ,
Piero Perucca ,
Pasquale Striano,
Angelo Labate ,
Antonella Riva ,
Bronwyn E. Grinton,
Joshua Reid,
Jessica Hutton,
Marian Todaro,
Terence J. O'Brien,
Patrick Kwan,
Lynette G. Sadleir,
Saul A. Mullen,
Emanuela Dazzo
and 6 other authors
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Thuong T. Ha,
Rosemary Burgess,
Morgan Newman,
Ching Moey,
Simone A. Mandelstam ,
Alison E. Gardner,
Atma M. Ivancevic ,
Duyen Pham,
Raman Kumar ,
Nicholas Smith,
Chirag Patel,
Stephen Malone,
Monique M. Ryan,
Sophie Calvert,
Clare L. van Eyk
and 7 other authors
,
Alison E. Gardner,
Atma M. Ivancevic ,
Duyen Pham,
Raman Kumar ,
Nicholas Smith,
Chirag Patel,
Stephen Malone,
Monique M. Ryan,
Sophie Calvert,
Clare L. van Eyk
and 7 other authors
Aicardi Syndrome Is a Genetically Heterogeneous Disorder
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Matthew J. Y. Kang ,
Dhamidhu Eratne ,
Hannah Dobson ,
Charles B. Malpas ,
Michael Keem,
Courtney Lewis,
Jasleen Grewal,
Vivian Tsoukra,
Christa Dang ,
Ramon Mocellin,
Tomas Kalincik ,
Alexander F. Santillo ,
Henrik Zetterberg ,
Kaj Blennow ,
Christiane Stehmann
and 11 other authors
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,
Dhamidhu Eratne ,
Hannah Dobson ,
Charles B. Malpas ,
Michael Keem,
Courtney Lewis,
Jasleen Grewal,
Vivian Tsoukra,
Christa Dang ,
Ramon Mocellin,
Tomas Kalincik ,
Alexander F. Santillo ,
Henrik Zetterberg ,
Kaj Blennow ,
Christiane Stehmann
and 11 other authors
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Karen L. Oliver ,
Ingrid E. Scheffer ,
Mark F. Bennett ,
Bronwyn E. Grinton ,
Melanie Bahlo ,
Samuel F. Berkovic
,
Ingrid E. Scheffer ,
Mark F. Bennett ,
Bronwyn E. Grinton ,
Melanie Bahlo ,
Samuel F. Berkovic
Genes4Epilepsy: An epilepsy gene resource
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Johanna Krueger,
Johanna Krüger,
Julian Schubert,
Josua Kegele,
Audrey Labalme,
Miaomiao Mao,
Jacqueline Heighway,
Guiscard Seebohm,
Pu Yan,
Mahmoud Koko,
Kezban Aslan-Kara,
Hande Caglayan,
Bernhard J. Steinhoff,
Yvonne G. Weber,
Pascale Keo-Kosal
and 8 other authors
Loss-of-function variants in the KCNQ5 gene are implicated in genetic generalized epilepsies
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Andrew Paul Fennell ,
Anne Elizabeth Baxter,
Samuel Frank Berkovic ,
Carolyn Jane Ellaway ,
Caitlin Forwood ,
Michael Stephen Hildebrand ,
Smitha Kumble ,
Colina McKeown,
David Mowat ,
Gemma Poke ,
Sulekha Rajagopalan ,
Brigid M. Regan,
Ingrid Eileen Scheffer ,
Zornitza Stark ,
Chloe Alice Stutterd
and 4 other authors
,
Anne Elizabeth Baxter,
Samuel Frank Berkovic ,
Carolyn Jane Ellaway ,
Caitlin Forwood ,
Michael Stephen Hildebrand ,
Smitha Kumble ,
Colina McKeown,
David Mowat ,
Gemma Poke ,
Sulekha Rajagopalan ,
Brigid M. Regan,
Ingrid Eileen Scheffer ,
Zornitza Stark ,
Chloe Alice Stutterd
and 4 other authors
The diverse pleiotropic effects of spliceosomal protein PUF60: A case series of Verheij syndrome
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Karen L. Oliver ,
Colin A. Ellis,
Ingrid E. Scheffer,
Shiva Ganesan,
Costin Leu,
Lynette G. Sadleir,
Erin L. Heinzen,
Heather C. Mefford,
Andrew J. Bass,
Sarah W. Curtis,
Rebekah V. Harris ,
David C. Whiteman,
Ingo Helbig,
Ruth Ottman ,
Michael P. Epstein
and 2 other authors
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,
Colin A. Ellis,
Ingrid E. Scheffer,
Shiva Ganesan,
Costin Leu,
Lynette G. Sadleir,
Erin L. Heinzen,
Heather C. Mefford,
Andrew J. Bass,
Sarah W. Curtis,
Rebekah V. Harris ,
David C. Whiteman,
Ingo Helbig,
Ruth Ottman ,
Michael P. Epstein
and 2 other authors
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Juliet K. Knowles ,
Ingo Helbig ,
Cameron S. Metcalf ,
Laura S. Lubbers ,
Lori L. Isom ,
Scott Demarest ,
Ethan M. Goldberg ,
Alfred L. George ,
Holger Lerche ,
Sarah Weckhuysen ,
Vicky Whittemore,
Samuel F. Berkovic ,
Daniel H. Lowenstein
Download from onlinelibrary.wiley.com
,
Ingo Helbig ,
Cameron S. Metcalf ,
Laura S. Lubbers ,
Lori L. Isom ,
Scott Demarest ,
Ethan M. Goldberg ,
Alfred L. George ,
Holger Lerche ,
Sarah Weckhuysen ,
Vicky Whittemore,
Samuel F. Berkovic ,
Daniel H. Lowenstein
Download from onlinelibrary.wiley.com
Benjamin Sinclair ,
Varduhi Cahill,
Jarrel Seah,
Andy Kitchen,
Lucy E. Vivash ,
Zhibin Chen,
Charles B. Malpas ,
Marie F. O’Shea,
Patricia M. Desmond,
Rodney J. Hicks,
Andrew P. Morokoff,
James A. King,
Gavin C. Fabinyi,
Andrew H. Kaye,
Patrick Kwan
and 3 other authors
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,
Varduhi Cahill,
Jarrel Seah,
Andy Kitchen,
Lucy E. Vivash ,
Zhibin Chen,
Charles B. Malpas ,
Marie F. O’Shea,
Patricia M. Desmond,
Rodney J. Hicks,
Andrew P. Morokoff,
James A. King,
Gavin C. Fabinyi,
Andrew H. Kaye,
Patrick Kwan
and 3 other authors
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Mark F. Bennett ,
Michael S. Hildebrand,
Sayaka Kayumi ,
Mark A. Corbett ,
Sachin Gupta,
Zimeng Ye,
Michael Krivanek,
Rosemary Burgess,
Olivia J. Henry,
John A. Damiano,
Amber Boys,
Jozef Gécz ,
Melanie Bahlo ,
Ingrid E. Scheffer ,
Samuel F. Berkovic
,
Michael S. Hildebrand,
Sayaka Kayumi ,
Mark A. Corbett ,
Sachin Gupta,
Zimeng Ye,
Michael Krivanek,
Rosemary Burgess,
Olivia J. Henry,
John A. Damiano,
Amber Boys,
Jozef Gécz ,
Melanie Bahlo ,
Ingrid E. Scheffer ,
Samuel F. Berkovic
Evidence for a Dual-Pathway, 2-Hit Genetic Model for Focal Cortical Dysplasia and Epilepsy
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2021
Laura Canafoglia ,
Silvana Franceschetti ,
Antonio Gambardella ,
Pasquale Striano ,
Anna Teresa Giallonardo,
Paolo Tinuper,
Carlo Di Bonaventura,
Roberto Michelucci,
Edoardo Ferlazzo,
Tiziana Granata,
Adriana Magaudda,
Laura Licchetta,
Alessandro Filla,
Angela La Neve,
Patrizia Riguzzi
and 10 other authors
,
Silvana Franceschetti ,
Antonio Gambardella ,
Pasquale Striano ,
Anna Teresa Giallonardo,
Paolo Tinuper,
Carlo Di Bonaventura,
Roberto Michelucci,
Edoardo Ferlazzo,
Tiziana Granata,
Adriana Magaudda,
Laura Licchetta,
Alessandro Filla,
Angela La Neve,
Patrizia Riguzzi
and 10 other authors
Progressive Myoclonus Epilepsies
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Timothy E. Green,
Duncan MacGregor,
Susan M. Carden,
Rebekah V. Harris ,
Chelsee A. Hewitt,
Samuel F. Berkovic ,
Anthony J. Penington,
Ingrid E. Scheffer ,
Michael S. Hildebrand
Download from doi.org
,
Chelsee A. Hewitt,
Samuel F. Berkovic ,
Anthony J. Penington,
Ingrid E. Scheffer ,
Michael S. Hildebrand
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Sarah E. Heron ,
Brigid M. Regan,
Rebekah V. Harris ,
Alison E. Gardner,
Matthew J. Coleman ,
Mark F. Bennett ,
Bronwyn E. Grinton,
Katherine L. Helbig ,
Michael R. Sperling,
Sheryl Haut,
Eric B. Geller,
Peter Widdess-Walsh,
James T. Pelekanos,
Melanie Bahlo ,
Slavé Petrovski
and 7 other authors
,
Brigid M. Regan,
Rebekah V. Harris ,
Alison E. Gardner,
Matthew J. Coleman ,
Mark F. Bennett ,
Bronwyn E. Grinton,
Katherine L. Helbig ,
Michael R. Sperling,
Sheryl Haut,
Eric B. Geller,
Peter Widdess-Walsh,
James T. Pelekanos,
Melanie Bahlo ,
Slavé Petrovski
and 7 other authors
Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus
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