Paul J. Lockhart

11.9k citations

126 papers · 5.2k indexed · 2 hit papers · h-index 34

Nutrition and Dietetics top 0.5%
- Trace Elements in Health 13
Neurology top 1%
- Parkinson's Disease Mechanisms and Treatments 29
Cellular and Molecular Neuroscience top 1%
- Genetic Neurodegenerative Diseases 24
- Nuclear Receptors and Signaling 14
Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments 29
Health, Toxicology and Mutagenesis top 1%
Molecular Biology
- RNA regulation and disease 15
- Mitochondrial Function and Pathology 14
Genetics
- Genetics and Neurodevelopmental Disorders 15
- Genomics and Rare Diseases 12

Co-authors: Matthew J. Farrer Julian F. B. Mercer James Camakaris Michael J. Petris J. F. B. Mercer Martin B. Delatycki Janetta G. Culvenor Paul A. Gleeson
Cited by: Nutrition and Dietetics Neurology Cellular and Molecular Neuroscience
Journals: Journal of Biological Chemistry (2 papers)Neuron (1 paper)Nature Genetics (2 papers)
Partner nations: Australia United States United Kingdom

In The Last Decade

Paul J. Lockhart

123 papers receiving 5.1k citations

Hit Papers

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Peers

Countries citing papers authored by Paul J. Lockhart

Since Specialization

Citations

This map shows the geographic impact of Paul J. Lockhart's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Paul J. Lockhart with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul J. Lockhart more than expected).

Fields of papers citing papers by Paul J. Lockhart

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Paul J. Lockhart. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Paul J. Lockhart. The network helps show where Paul J. Lockhart may publish in the future.

Co-authorship network

The 25 scholars most cited alongside Paul J. Lockhart, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Paul J. Lockhart Line = papers co-authored together Paul J. Lockhart links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Ectopic HCN4 Provides a Target Biomarker for the Genetic Spectrum of mTORopathies Neurology Genetics ·Matthew Coleman,Paulo Pinares-Garcia,Sarah Stephenson,Wei Shern Lee,Daniz Kooshavar,Catriona McLean,Katherine B. Howell,Richard J. Leventer,Christopher A. Reid,Paul J. Lockhart	2024	2
2	Brain volumes in genetic syndromes associated with mTOR dysregulation: a systematic review and meta-analysis Molecular Psychiatry ·Jonathan M. Payne,Kristina M. Haebich,Rebecca A Mitchell,Kiymet Bozaoglu,Emma Giliberto,Paul J. Lockhart,Alice Maier,Silvia Velasco,Gareth Ball,Kathryn N. North,Darren R. Hocking	2024	0
3	The clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasia Brain ·Emma Macdonald‐Laurs,Aaron E. L. Warren,Peter Francis,Simone Mandelstam,Wei Shern Lee,Matthew Coleman,Sarah Stephenson,Sarah Barton,Colleen D’Arcy,Paul J. Lockhart,Richard J. Leventer,A. Simon Harvey	2023	11
4	Expanding the clinical and radiological phenotypes of leukoencephalopathy due to biallelic HMBS mutations American Journal of Medical Genetics Part A ·Chloe Stutterd,Alexa Kidd,Chris Florkowski,Edward Janus,Miriam Fanjul,Anthony Raizis,Teddy Y. Wu,John S. Archer,Richard J. Leventer,David J. Amor,Vesna Lukić,Melanie Bahlo,Paul Gow,Paul J. Lockhart,Marjo S. van der Knaap,Martin B. Delatycki	2021	2
5	Prevalence of RFC1 -mediated spinocerebellar ataxia in a North American ataxia cohort Neurology Genetics ·Dona Aboud Syriani,Darice Y. Wong,Sameer Andani,Claudio M. de Gusmão,Yuanming Mao,May Sanyoura,Giacomo L Glotzer,Paul J. Lockhart,Sharon Hassin‐Baer,Vikram Khurana,Christopher M. Gómez,Susan Perlman,Soma Das,Brent L. Fogel	2020	32
6	Distribution of Parkinson’s disease associated RAB39B in mouse brain tissue Molecular Brain ·Yujing Gao,Gabrielle R. Wilson,Sarah Stephenson,Mustapha Oulad‐Abdelghani,Nicolas Charlet‐Berguerand,Kiymet Bozaoglu,Catriona McLean,Paul Q. Thomas,David I. Finkelstein,Paul J. Lockhart	2020	7
7	Prevalence of RFC1-Mediated Spinocerebellar Ataxia in a North American Ataxia Cohort Annals of Neurology ·Dona Aboud Syriani,Darice Y. Wong,Sameer Andani,Claudio M. de Gusmão,Yuanming Mao,May Sanyoura,Giacomo L Glotzer,Paul J. Lockhart,Sharon Hassin‐Baer,Vikram Khurana,Christopher M. Gómez,Susan Perlman,Soma Das,Brent L. Fogel	2020	3
8	Generation of four iPSC lines from Neurofibromatosis Type 1 patients Stem Cell Research ·Kiymet Bozaoglu,Wei Shern Lee,Kristina M. Haebich,Kathryn N. North,Jonathan M. Payne,Paul J. Lockhart	2020	2
9	Second‐hit DEPDC5 mutation is limited to dysmorphic neurons in cortical dysplasia type IIA Annals of Clinical and Translational Neurology ·Wei Shern Lee,Sarah Stephenson,Katherine B. Howell,Kate Pope,Greta Gillies,Alison Wray,Wirginia Maixner,Simone Mandelstam,Samuel F. Berkovic,Ingrid E. Scheffer,Duncan MacGregor,A. Simon Harvey,Paul J. Lockhart,Richard J. Leventer	2019	55
10	Genetic Analysis of Patients Who Experienced Awareness with Recall while under General Anesthesia Anesthesiology ·Jamie Sleigh,Kate Leslie,Andrew Davidson,David J. Amor,Peter Diakumis,Vesna Lukić,Paul J. Lockhart,Melanie Bahlo	2019	5
11	Familial early onset Parkinson's disease caused by a homozygous frameshift variant in PARK7: Clinical features and literature update Parkinsonism & Related Disorders ·Sarah Stephenson,Ruth Djaldetti,Haloom Rafehi,Gabrielle R. Wilson,Greta Gillies,Melanie Bahlo,Paul J. Lockhart	2019	7
12	An Open Label Clinical Pilot Study of Resveratrol as a Treatment for Friedreich Ataxia (S43.006) Neurology ·Eppie M. Yiu,Geneieve Tai,Roger E. Peverill,Katherine J. Lee,Kevin D. Croft,Trevor A. Mori,Sarah Stephenson,Paul J. Lockhart,Joseph P. Sarsero,Andrew Churchyard,Marguerite V. Evans‐Galea,Monique M. Ryan,Louise A. Corben,Martin Delatycki	2013	2
13	ironXS: high-school screening for hereditary haemochromatosis is acceptable and feasible European Journal of Human Genetics ·Martin B. Delatycki,Michelle Wolthuizen,Veronica Collins,Elizabeth Varley,Joanna Craven,Katrina J. Allen,Lyle C. Gurrin,MaryAnne Aitken,M. Kaye Trembath,Lyndal Bond,Gabrielle R. Wilson,Sarah Stephenson,Ivan Macciocca,Chriselle Hickerton,Paul J. Lockhart,Sylvia A. Metcalfe	2012	8
14	Mutant torsinA interacts with tyrosine hydroxylase in cultured cells Neuroscience ·Casey O’Farrell,Karen L. M. Martin,M. Hutton,Martin B. Delatycki,Mark Cookson,Paul J. Lockhart	2009	15
15	Multiplication of the α-Synuclein Gene Is Not a Common Disease Mechanism in Lewy Body Disease Journal of Molecular Neuroscience ·Paul J. Lockhart,Jennifer M. Kachergus,Sarah Lincoln,Mary Hulihan,Gina Bisceglio,Natalie Thomas,Dennis W. Dickson,Matthew J. Farrer	2004	8
16	It's a double knock‐out! The quaking mouse is a spontaneous deletion of parkin and parkin co‐regulated gene (PACRG) Movement Disorders ·Paul J. Lockhart,Casey O’Farrell,Matthew J. Farrer	2004	48
17	Lack of mutations in DJ‐1 in a cohort of Taiwanese ethnic Chinese with early‐onset parkinsonism Movement Disorders ·Paul J. Lockhart,Rebecca Bounds,Mary Hulihan,Jennifer M. Kachergus,Sarah Lincoln,Chin‐Hsien Lin,Ruey‐Meei Wu,Matthew J. Farrer	2004	19
18	Accurate Determination of Ataxin-2 Polyglutamine Expansion in Patients with Intermediate-Range Repeats Genetic Testing ·Jennifer Hussey,Paul J. Lockhart,William Seltzer,Zbigniew K. Wszołek,Haydeh Payami,Melissa Hanson,Katrina Gwinn,Matthew J. Farrer	2002	14
19	Parkin Protects against the Toxicity Associated with Mutant α-Synuclein Neuron ·Leonard Petrucelli,Casey O’Farrell,Paul J. Lockhart,Melisa J. Baptista,Kathryn Kehoe,Liselot Vink,Peter S. Choi,Benjamin Wolozin,Matthew J. Farrer,John Hardy,Mark Cookson	2002	457
20	Isolation of a partial candidate gene for Menkes disease by positional cloningbreakdown → Nature Genetics ·Julian F. B. Mercer,Janie Livingston,Bryan Hall,Jennifer A. Paynter,Catherine R. Begy,Settara C. Chandrasekharappa,Paul J. Lockhart,Andrew Grimes,Mrinal Bhave,David Siemieniak,Thomas W. Glover	1993	545

About Paul J. Lockhart

Paul J. Lockhart is a scholar working on Cellular and Molecular Neuroscience, Neurology and Neurology, having authored 126 papers that have together received 5.2k indexed citations. Recurring topics across this work include Parkinson's Disease Mechanisms and Treatments (29 papers), Genetic Neurodegenerative Diseases (24 papers), RNA regulation and disease (15 papers), Genetics and Neurodevelopmental Disorders (15 papers), Nuclear Receptors and Signaling (14 papers), Mitochondrial Function and Pathology (14 papers), Trace Elements in Health (13 papers) and Genomics and Rare Diseases (12 papers). The work is most often cited by research in Nutrition and Dietetics (1.5k citations), Neurology (1.2k citations) and Cellular and Molecular Neuroscience (1.2k citations). Paul J. Lockhart has collaborated with scholars based in Australia, United States and United Kingdom. Frequent co-authors include Matthew J. Farrer, Julian F. B. Mercer, James Camakaris, Michael J. Petris, J. F. B. Mercer, Martin B. Delatycki, Janetta G. Culvenor, Paul A. Gleeson, Thomas W. Glover and Jennifer A. Paynter. Their work appears in journals such as Journal of Biological Chemistry, Neuron and Nature Genetics.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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