Researcher
Paul Lockhart
Murdoch Childrens Research Institute
Statistics
13 papers found
All papers authored by Paul Lockhart
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2023
Haloom Rafehi 
,
Justin Read,
David J. Szmulewicz,
Kayli C. Davies,
Penny Snell,
Liam G. Fearnley,
Liam Scott,
Mirja Thomsen,
Greta Gillies,
Kate Pope,
Mark F. Bennett,
Jacob E. Munro ,
Kathie J. Ngo,
Luke Chen,
Mathew J. Wallis
and 16 other authors
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,
Justin Read,
David J. Szmulewicz,
Kayli C. Davies,
Penny Snell,
Liam G. Fearnley,
Liam Scott,
Mirja Thomsen,
Greta Gillies,
Kate Pope,
Mark F. Bennett,
Jacob E. Munro ,
Kathie J. Ngo,
Luke Chen,
Mathew J. Wallis
and 16 other authors
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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
Download from onlinelibrary.wiley.com
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
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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Jacqueline M. Ogier ,
Yujing Gao ,
Eileen M. Dunne ,
Michael A. Wilson ,
Sarath C. Ranganathan ,
Gregory H. Tesch ,
David J. Nikolic Paterson ,
Alain Dabdoub ,
Rachel A. Burt ,
Bryony A. Nayagam ,
Paul J. Lockhart
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,
Yujing Gao ,
Eileen M. Dunne ,
Michael A. Wilson ,
Sarath C. Ranganathan ,
Gregory H. Tesch ,
David J. Nikolic Paterson ,
Alain Dabdoub ,
Rachel A. Burt ,
Bryony A. Nayagam ,
Paul J. Lockhart
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Jacqueline M. Ogier ,
Yujing Gao ,
Eileen M. Dunne ,
Michael A. Wilson ,
Sarath C. Ranganathan ,
Gregory H. Tesch ,
David J. Nikolic Paterson ,
Alain Dabdoub ,
Rachel A. Burt ,
Bryony A. Nayagam ,
Paul J. Lockhart
,
Yujing Gao ,
Eileen M. Dunne ,
Michael A. Wilson ,
Sarath C. Ranganathan ,
Gregory H. Tesch ,
David J. Nikolic Paterson ,
Alain Dabdoub ,
Rachel A. Burt ,
Bryony A. Nayagam ,
Paul J. Lockhart
ASK1 is a novel molecular target for preventing aminoglycoside-induced hair cell death
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2021
Miriam Fanjul‐Fernández,
Natasha J. Brown,
Peter Hickey,
Peter Diakumis,
Haloom Rafehi ,
Kiymet Bozaoglu,
Cherie C. Green,
Audrey Rattray,
Savannah Young,
Dana Alhuzaimi,
Hayley S. Mountford,
Greta Gillies,
Vesna Lukic,
Tanya Vick,
Keri Finlay
and 7 other authors
,
Kiymet Bozaoglu,
Cherie C. Green,
Audrey Rattray,
Savannah Young,
Dana Alhuzaimi,
Hayley S. Mountford,
Greta Gillies,
Vesna Lukic,
Tanya Vick,
Keri Finlay
and 7 other authors
A family study implicates GBE1 in the etiology of autism spectrum disorder
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2020
Haloom Rafehi ,
David J. Szmulewicz,
Kate Pope,
Mathew Wallis,
John Christodoulou,
Susan M. White,
Martin B. Delatycki,
Paul J. Lockhart ,
Melanie Bahlo
Download from api.wiley.com
,
David J. Szmulewicz,
Kate Pope,
Mathew Wallis,
John Christodoulou,
Susan M. White,
Martin B. Delatycki,
Paul J. Lockhart ,
Melanie Bahlo
Download from api.wiley.com
2017
Ashley P. L. Marsh ,
Delphine Heron,
Timothy J. Edwards,
Angélique Quartier ,
Charles Galea,
Caroline Nava,
Agnès Rastetter,
Marie-Laure Moutard,
Vicki Anderson,
Pierre Bitoun,
Jens Bunt ,
Anne Faudet,
Catherine Garel,
Greta Gillies,
Ilan Gobius
and 38 other authors
,
Delphine Heron,
Timothy J. Edwards,
Angélique Quartier ,
Charles Galea,
Caroline Nava,
Agnès Rastetter,
Marie-Laure Moutard,
Vicki Anderson,
Pierre Bitoun,
Jens Bunt ,
Anne Faudet,
Catherine Garel,
Greta Gillies,
Ilan Gobius
and 38 other authors
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
Download from hal-univ-rennes1.archives-ouvertes.fr
2014
Davor Lessel ,
Bruno Vaz,
Swagata Halder,
Paul J. Lockhart ,
Ivana Marinovic-Terzic,
Jaime Lopez-Mosqueda,
Melanie Philipp,
Joe C. H. Sim,
Katherine R. Smith ,
Judith Oehler,
Elisa Cabrera,
Raimundo Freire ,
Kate Pope,
Amsha Nahid,
Fiona Norris
and 22 other authors
Download from www.nature.com
,
Bruno Vaz,
Swagata Halder,
Paul J. Lockhart ,
Ivana Marinovic-Terzic,
Jaime Lopez-Mosqueda,
Melanie Philipp,
Joe C. H. Sim,
Katherine R. Smith ,
Judith Oehler,
Elisa Cabrera,
Raimundo Freire ,
Kate Pope,
Amsha Nahid,
Fiona Norris
and 22 other authors
Download from www.nature.com
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