All papers authored by Richard Leventer
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2023
Emma Macdonald-Laurs 
,
Aaron E. L. Warren ,
Peter Francis,
Simone A. Mandelstam ,
Wei Shern Lee ,
Matthew Coleman ,
Sarah E. M. Stephenson ,
Sarah Barton ,
Colleen D’Arcy ,
Paul J. Lockhart ,
Richard J. Leventer ,
A. Simon Harvey
,
Aaron E. L. Warren ,
Peter Francis,
Simone A. Mandelstam ,
Wei Shern Lee ,
Matthew Coleman ,
Sarah E. M. Stephenson ,
Sarah Barton ,
Colleen D’Arcy ,
Paul J. Lockhart ,
Richard J. Leventer ,
A. Simon Harvey
The clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasia
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2022
Emma Macdonald‐Laurs ,
Aaron E. L. Warren ,
Wei Shern Lee ,
Joseph Yuan‐Mou Yang ,
Duncan MacGregor,
Paul J. Lockhart ,
Richard J. Leventer ,
Andrew Neal ,
A. Simon Harvey
,
Aaron E. L. Warren ,
Wei Shern Lee ,
Joseph Yuan‐Mou Yang ,
Duncan MacGregor,
Paul J. Lockhart ,
Richard J. Leventer ,
Andrew Neal ,
A. Simon Harvey
Intrinsic and secondary epileptogenicity in focal cortical dysplasia type II
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Wei Shern Lee ,
Richard J. Leventer ,
Paul J. Lockhart
,
Richard J. Leventer ,
Paul J. Lockhart
Droplet digital PCR as a first-tier molecular diagnostic tool for focal cortical dysplasia type II
Download from academic.oup.com
Nataliya Di Donato,
Renzo Guerrini ,
Charles J. Billington,
A. James Barkovich,
Philine Dinkel,
Elena Freri,
Michael Heide,
Elliot S. Gershon,
Tracy S. Gertler,
Robert J. Hopkin,
Suma Jacob,
Sarah K. Keedy,
Daniz Kooshavar,
Paul J. Lockhart,
Dietmar R. Lohmann
and 11 other authors
,
Charles J. Billington,
A. James Barkovich,
Philine Dinkel,
Elena Freri,
Michael Heide,
Elliot S. Gershon,
Tracy S. Gertler,
Robert J. Hopkin,
Suma Jacob,
Sarah K. Keedy,
Daniz Kooshavar,
Paul J. Lockhart,
Dietmar R. Lohmann
and 11 other authors
Monoallelic and biallelic mutations in RELN underlie a graded series of neurodevelopmental disorders
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Mathieu Barbier ,
Melanie Bahlo ,
Alessandra Pennisi ,
Maxime Jacoupy ,
Rick M. Tankard ,
Claire Ewenczyk,
Kayli C. Davies,
Patricia Lino‐Coulon ,
Claire Colace ,
Haloom Rafehi ,
Nicolas Auger,
Brendan R. E. Ansell ,
Ivo van der Stelt,
Katherine B. Howell ,
Marie Coutelier
and 15 other authors
,
Melanie Bahlo ,
Alessandra Pennisi ,
Maxime Jacoupy ,
Rick M. Tankard ,
Claire Ewenczyk,
Kayli C. Davies,
Patricia Lino‐Coulon ,
Claire Colace ,
Haloom Rafehi ,
Nicolas Auger,
Brendan R. E. Ansell ,
Ivo van der Stelt,
Katherine B. Howell ,
Marie Coutelier
and 15 other authors
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
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Wei Shern Lee,
Sara Baldassari,
Mathilde Chipaux,
Homa Adle‐Biassette,
Sarah E. M. Stephenson,
Wirginia Maixner,
A. Simon Harvey,
Paul J. Lockhart,
Stéphanie Baulac ,
Richard J. Leventer
,
Richard J. Leventer
Gradient of brain mosaic RHEB variants causes a continuum of cortical dysplasia
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Renske Oegema ,
Tahsin Stefan Barakat ,
Martina Wilke,
Katrien Stouffs ,
Dina Amrom ,
Eleonora Aronica,
Nadia Bahi-Buisson,
Valerio Conti ,
Andrew E. Fry ,
Tobias Geis,
David Gomez Andres ,
Elena Parrini ,
Ivana Pogledic ,
Edith Said,
Doriette Soler
and 12 other authors
Download from www.nature.com
,
Tahsin Stefan Barakat ,
Martina Wilke,
Katrien Stouffs ,
Dina Amrom ,
Eleonora Aronica,
Nadia Bahi-Buisson,
Valerio Conti ,
Andrew E. Fry ,
Tobias Geis,
David Gomez Andres ,
Elena Parrini ,
Ivana Pogledic ,
Edith Said,
Doriette Soler
and 12 other authors
Download from www.nature.com
2019
Wei Shern Lee,
Sarah E. M. Stephenson,
Katherine B. Howell,
Kate Pope,
Greta Gillies,
Alison Wray,
Wirginia Maixner,
Simone A. Mandelstam,
Samuel F. Berkovic ,
Ingrid E. Scheffer,
Duncan MacGregor,
Anthony Simon Harvey,
Paul J. Lockhart ,
Richard J. Leventer
,
Ingrid E. Scheffer,
Duncan MacGregor,
Anthony Simon Harvey,
Paul J. Lockhart ,
Richard J. Leventer
Second‐hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA
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