All papers authored by Sarah Heron
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2021
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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2016
Nicholas J. Smith,
Jill Lipsett,
Leanne M. Dibbens,
Sarah E. Heron
BRAT1-associated neurodegeneration: Intra-familial phenotypic differences in siblings
Download from api.wiley.com
Elena Gardella,
Sándor Beniczky,
Rikke S. Møller,
Felicitas Becker,
Johannes R. Lemke,
Steffen Syrbe,
Hans Eiberg,
Thomas Bast,
Bernhard Steinhoff,
Peter Nürnberg,
Pia Gellert,
Hans Atli Dahl,
Sarah Weckhuysen,
Sarah E. Heron ,
Leanne M. Dibbens
and 3 other authors
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,
Leanne M. Dibbens
and 3 other authors
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Zaid Afawi,
Karen L. Oliver ,
Sara Kivity,
Aziz Mazarib,
Ilan Blatt,
Miriam Y. Neufeld,
Katherine L. Helbig,
Hadassa Goldberg-Stern,
Adel J. Misk,
Rachel Straussberg,
Simri Walid,
Muhammad Mahajnah,
Tally Lerman-Sagie,
Bruria Ben-Zeev,
Esther Kahana
and 19 other authors
,
Sara Kivity,
Aziz Mazarib,
Ilan Blatt,
Miriam Y. Neufeld,
Katherine L. Helbig,
Hadassa Goldberg-Stern,
Adel J. Misk,
Rachel Straussberg,
Simri Walid,
Muhammad Mahajnah,
Tally Lerman-Sagie,
Bruria Ben-Zeev,
Esther Kahana
and 19 other authors
Multiplex families with epilepsy
Download from www.ncbi.nlm.nih.gov
Michael G. Ricos,
Bree L. Hodgson,
Tommaso Pippucci,
Akzam Saidin,
Yeh Sze Ong,
Sarah E. Heron ,
Laura Licchetta,
Francesca Bisulli,
Marta A. Bayly,
James Hughes,
Sara Baldassari,
Flavia Palombo,
Epilepsy Electroclinical Study Group,
Margherita Santucci,
Stefano Meletti
and 9 other authors
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,
Laura Licchetta,
Francesca Bisulli,
Marta A. Bayly,
James Hughes,
Sara Baldassari,
Flavia Palombo,
Epilepsy Electroclinical Study Group,
Margherita Santucci,
Stefano Meletti
and 9 other authors
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Weber Yg,
Elena Gardella,
Felicitas Becker,
Rikke S. Møller,
Julian Schubert,
Johannes R. Lemke,
Line H. G. Larsen,
Møller Rs,
Hans Eiberg,
Lemke Jr,
Michael Nothnagel,
Holger Thiele,
Janine Altmueller,
Larsen Lh,
Janine Altmüller
and 20 other authors
and 20 other authors
Benign infantile seizures and paroxysmal dyskinesia caused by an SCN8A mutation
Download from dx.doi.org
2015
Bronwyn E. Grinton,
Sarah E. Heron ,
James T. Pelekanos,
Sameer M. Zuberi ,
Sara Kivity,
Zaid Afawi,
Tristiana C. Williams,
Dan M. Casalaz,
Simone Yendle,
Ilan Linder,
Dorit Lev,
Tally Lerman-Sagie,
Stephen Malone,
Haim Bassan,
Hadassa Goldberg-Stern
and 8 other authors
,
James T. Pelekanos,
Sameer M. Zuberi ,
Sara Kivity,
Zaid Afawi,
Tristiana C. Williams,
Dan M. Casalaz,
Simone Yendle,
Ilan Linder,
Dorit Lev,
Tally Lerman-Sagie,
Stephen Malone,
Haim Bassan,
Hadassa Goldberg-Stern
and 8 other authors
Familial neonatal seizures in 36 families: Clinical and genetic features correlate with outcome
Download from www.researchgate.net
Toshiyuki Yamamoto,
Keiko Shimojima,
Noriko Sangu,
Yuta Komoike,
Atsushi Ishii,
Shinpei Abe,
Shintaro Yamashita,
Katsumi Imai,
Tetsuo Kubota,
Tatsuya Fukasawa,
Tohru Okanishi ,
Hideo Enoki,
Takuya Tanabe,
Akira Saito,
Toru Furukawa
and 7 other authors
Download from doi.org
,
Hideo Enoki,
Takuya Tanabe,
Akira Saito,
Toru Furukawa
and 7 other authors
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Rikke S. Moller,
Sarah E. Heron ,
Line H. G. Larsen,
Chiao Xin Lim,
Michael G. Ricos,
Marta A. Bayly,
Marjan J. A. van Kempen,
Sylvia Klinkenberg,
Ian Andrews,
Kent Kelley,
Gabriel M. Ronen,
David Callen,
Jacinta M. McMahon,
Simone C. Yendle,
Gemma L. Carvill
and 16 other authors
,
Line H. G. Larsen,
Chiao Xin Lim,
Michael G. Ricos,
Marta A. Bayly,
Marjan J. A. van Kempen,
Sylvia Klinkenberg,
Ian Andrews,
Kent Kelley,
Gabriel M. Ronen,
David Callen,
Jacinta M. McMahon,
Simone C. Yendle,
Gemma L. Carvill
and 16 other authors
Mutations in KCNT1 cause a spectrum of focal epilepsies
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2014
Mikko Muona ,
Samuel F. Berkovic,
Leanne M. Dibbens,
Karen L. Oliver ,
Snezana Maljevic ,
Marta A. Bayly,
Tarja Joensuu,
Laura Canafoglia ,
Silvana Franceschetti,
Roberto Michelucci,
Salla Markkinen,
Sarah E. Heron ,
Michael S. Hildebrand ,
Eva Andermann,
Frederick Andermann
and 37 other authors
,
Samuel F. Berkovic,
Leanne M. Dibbens,
Karen L. Oliver ,
Snezana Maljevic ,
Marta A. Bayly,
Tarja Joensuu,
Laura Canafoglia ,
Silvana Franceschetti,
Roberto Michelucci,
Salla Markkinen,
Sarah E. Heron ,
Michael S. Hildebrand ,
Eva Andermann,
Frederick Andermann
and 37 other authors
A recurrent de novo mutation in KCNC1 causes progressive myoclonus epilepsy
Download from www.nature.com
Lata Vadlamudi,
Roger L. Milne,
Kate Lawrence,
Sarah E. Heron ,
Jazmin Eckhaus,
Deborah Keay,
Mary Connellan,
Yvonne Torn-Broers,
R. Anne Howell,
John C. Mulley,
Ingrid E. Scheffer,
Leanne M. Dibbens,
John L. Hopper,
Samuel F. Berkovic
Download from espace.library.uq.edu.au
,
Jazmin Eckhaus,
Deborah Keay,
Mary Connellan,
Yvonne Torn-Broers,
R. Anne Howell,
John C. Mulley,
Ingrid E. Scheffer,
Leanne M. Dibbens,
John L. Hopper,
Samuel F. Berkovic
Download from espace.library.uq.edu.au
Ingrid E. Scheffer,
Sarah E. Heron ,
Brigid M. Regan,
Simone Mandelstam ,
Douglas E. Crompton,
Bree L. Hodgson,
Laura Licchetta,
Federica Provini,
Francesca Bisulli,
Lata Vadlamudi,
Jozef Gecz,
Alan Connelly,
Paolo Tinuper,
Michael G. Ricos,
Samuel F. Berkovic
and 1 other authors
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,
Brigid M. Regan,
Simone Mandelstam ,
Douglas E. Crompton,
Bree L. Hodgson,
Laura Licchetta,
Federica Provini,
Francesca Bisulli,
Lata Vadlamudi,
Jozef Gecz,
Alan Connelly,
Paolo Tinuper,
Michael G. Ricos,
Samuel F. Berkovic
and 1 other authors
Download from www.researchgate.net
Martin Puskarjov ,
Patricia Seja,
Sarah E. Heron ,
Tristiana C. Williams,
Faraz Ahmad,
Xenia Iona,
Karen L. Oliver ,
Bronwyn E. Grinton,
Laszlo Vutskits,
Ingrid E. Scheffer,
Steven Petrou,
Peter Blaesse,
Leanne M. Dibbens,
Samuel F. Berkovic,
Kai Kaila
Download from onlinelibrary.wiley.com
,
Patricia Seja,
Sarah E. Heron ,
Tristiana C. Williams,
Faraz Ahmad,
Xenia Iona,
Karen L. Oliver ,
Bronwyn E. Grinton,
Laszlo Vutskits,
Ingrid E. Scheffer,
Steven Petrou,
Peter Blaesse,
Leanne M. Dibbens,
Samuel F. Berkovic,
Kai Kaila
Download from onlinelibrary.wiley.com
Carol J. Milligan,
Melody Li,
Elena V. Gazina,
Sarah E. Heron ,
Umesh Nair,
Chantel Trager,
Christopher A. Reid,
Anu Venkat,
Donald P. Younkin,
Dennis J. Dlugos,
Slave Petrovski,
David B. Goldstein,
Leanne M. Dibbens,
Ingrid E. Scheffer,
Samuel F. Berkovic
and 1 other authors
,
Umesh Nair,
Chantel Trager,
Christopher A. Reid,
Anu Venkat,
Donald P. Younkin,
Dennis J. Dlugos,
Slave Petrovski,
David B. Goldstein,
Leanne M. Dibbens,
Ingrid E. Scheffer,
Samuel F. Berkovic
and 1 other authors
KCNT1 Gain of Function in 2 Epilepsy Phenotypes is Reversed by Quinidine
Download from www.ncbi.nlm.nih.gov
2013
Karl Martin Klein,
Catherine J. Bromhead,
Katherine R. Smith,
Christopher J. O'Callaghan,
Susan J. Corcoran,
Sarah E. Heron ,
Xenia Iona,
Bree L. Hodgson,
Jacinta M. McMahon,
Kate M. Lawrence,
Ingrid E. Scheffer,
Leanne M. Dibbens,
Melanie Bahlo,
Samuel F. Berkovic
,
Xenia Iona,
Bree L. Hodgson,
Jacinta M. McMahon,
Kate M. Lawrence,
Ingrid E. Scheffer,
Leanne M. Dibbens,
Melanie Bahlo,
Samuel F. Berkovic
Autosomal dominant vasovagal syncope
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Leanne M. Dibbens,
Boukje de Vries,
Simona Donatello,
Sarah E. Heron ,
Bree L. Hodgson,
Satyan Chintawar,
Douglas E. Crompton,
Susannah T. Bellows,
James N. Hughes,
Karl Martin Klein,
Petra M. C. Callenbach,
Mark A. Corbett,
Alison E. Gardner,
Sara Kivity,
Xenia Iona
and 20 other authors
,
Bree L. Hodgson,
Satyan Chintawar,
Douglas E. Crompton,
Susannah T. Bellows,
James N. Hughes,
Karl Martin Klein,
Petra M. C. Callenbach,
Mark A. Corbett,
Alison E. Gardner,
Sara Kivity,
Xenia Iona
and 20 other authors
Mutations in DEPDC5 cause familial focal epilepsy with variable foci
Download from www.researchgate.net
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