Paul J. Lockhart

Also affiliated with The University of Melbourne, Murdoch Children's Research Institute

MedicineBiochemistry, Genetics and Molecular Biology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 5%percentile

0.461Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Population-scale variability at short tandem repeat loci reveals pathogenicity signature

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.06.631535

Top 41%

0.461DataRank

Top 41%11 citations

Isaac Xu, Sarah Fazal, Egor Dolzhenko, David Pellerin, Ben Weisburd +30 more

Papers

Driven by 20 papers — median percentile 59. Top paper: “Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders”.

Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders

Nature Communications(2020)10.1038/s41467-020-18723-y

N/A

0.808DataRank · unranked

218 citations

Kendra Hoekzema, Davide Vecchio, Huidan Wu, Arvis Sulovari, Bradley P. Coe +95 more

Clinical and genetic keys to cerebellar ataxia due to FGF14 GAA expansions

EBioMedicine(2023)10.1016/j.ebiom.2023.104931

N/A

0.612DataRank · unranked

58 citations

Claire-Sophie Davoine, David Pellerin, Giulia Coarelli, Marie Coutelier, Claire Ewenczyk +42 more

The clinical, imaging, pathological and genetic landscape of bottom-of-sulcus dysplasia

Brain(2024)10.1093/brain/awad379

N/A

0.520DataRank · unranked

31 citations

Aaron E. L. Warren, Peter Francis, Simone Mandelstam, Wei Shern Lee, Matthew Coleman +7 more

Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B)

Annals of Neurology(2024)10.1002/ana.27060

N/A

0.520DataRank · unranked

31 citations

Anirudh N. Eranki, Hannah A. Stevens, Sonya Watson, Darice Y. Wong, Veronica S. Avila +28 more

Population-scale variability at short tandem repeat loci reveals pathogenicity signature

bioRxiv (Cold Spring Harbor Laboratory)(2025)10.1101/2025.01.06.631535

Top 41%

0.461DataRank

Top 41%11 citations

Isaac Xu, Sarah Fazal, Egor Dolzhenko, David Pellerin, Ben Weisburd +30 more

Variants in ZFX are associated with an X-linked neurodevelopmental disorder with recurrent facial gestalt

The American Journal of Human Genetics(2024)10.1016/j.ajhg.2024.01.007

N/A

0.442DataRank · unranked

18 citations

Katie Hutchison, Dilan Wellalage Don, George McGillivray, Tae‐Ik Choi, Carolyn A Allan +51 more

DCC regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation

eLife(2021)10.7554/elife.61769

N/A

0.406DataRank · unranked

14 citations

Ilan Gobius, Ashley P.L. Marsh, Rodrigo Suárez, Jonathan W. C. Lim, Caitlin R. Bridges +16 more

De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders

medRxiv(2024)10.1101/2024.04.07.24305438

N/A

0.360DataRank · unranked

10 citations

Ruebena Dawes, Hyung Chul Kim, Sarah L. Stenton, Susan Walker, Alicia Ljungdahl +92 more

Genetic modifiers and ascertainment drive variable expressivity of complex disorders

medRxiv(2024)10.1101/2024.08.27.24312158

N/A

0.269DataRank · unranked

5 citations

Corrine Smolen, Anastasia Tyryshkina, Lucilla Pizzo, Deepro Banerjee, Matthew T. Oetjens +65 more

Monoallelic and biallelic mutations inRELNunderlie a graded series of neurodevelopmental disorders

Brain(2022)10.1093/brain/awac164

N/A

0DataRank · unranked

22 citations

Renzo Guerrini, Charles J. Billington, A. James Barkovich, Philine Dinkel, Elena Freri +21 more

Clinical and Neuropathological Features Associated With Loss of RAB39B

Movement Disorders(2020)10.1002/mds.27951

N/A

0DataRank · unranked

22 citations

Verónica Martínez‐Cerdeño, Kirk J. Hogan, Catriona McLean, Paul J. Lockhart, Yujing Gao

Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.015

N/A

0DataRank · unranked

40 citations

Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Deepro Banerjee +38 more

Assortative mating and parental genetic relatedness drive the pathogenicity of variably expressive variants

medRxiv(2023)10.1101/2023.05.18.23290169

N/A

0DataRank · unranked

5 citations

Matthew Jensen, Lisa Dyer, Lucilla Pizzo, Anastasia Tyryshkina, Deepro Banerjee +38 more

Expanding the clinical and genetic spectrum of ALPK3 variants: Phenotypes identified in pediatric cardiomyopathy patients and adults with heterozygous variants

American Heart Journal(2020)10.1016/j.ahj.2020.03.023

N/A

0DataRank · unranked

50 citations

Judith M.A. Verhagen, Raquel Yotti, Alireza Haghighi, Dean Phelan, Paul A. James +27 more

Pathogenic Variants in CEP85L Cause Sporadic and Familial Posterior Predominant Lissencephaly

Neuron(2020)10.1016/j.neuron.2020.01.027

N/A

0DataRank · unranked

35 citations

Alison M. Muir, Won‐Jing Wang, Yi-Ning Kang, Kun-Chuan Yang, Nian-Hsin Chao +26 more

Rapid Diagnosis of Spinocerebellar Ataxia 36 in a Three‐Generation Family Using Short‐Read Whole‐Genome Sequencing Data

Movement Disorders(2020)10.1002/mds.28105

N/A

0DataRank · unranked

21 citations

David J. Szmulewicz, Kate Pope, Mathew Wallis, John Christodoulou, Susan M. White +4 more

The DCC receptor regulates astroglial development essential for telencephalic morphogenesis and corpus callosum formation

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.08.03.233593

N/A

0DataRank · unranked

0 citations

Ilan Gobius, Ashley P.L. Marsh, Rodrigo Suárez, Caitlin R. Bridges, Yunan Ye +15 more

Sporadic hypothalamic hamartoma is a ciliopathy with somatic and bi-allelic contributions

Human Molecular Genetics(2021)10.1093/hmg/ddab366

N/A

0DataRank · unranked

20 citations

Joshua E. Motelow, Mark F. Bennett, Zimeng Ye, Caitlin A. Bennett, Nicole G. Griffin +17 more

Clonally Focused Public and Private T Cells in Resected Brain Tissue From Surgeries to Treat Children With Intractable Seizures

Frontiers in Immunology(2021)10.3389/fimmu.2021.664344

N/A

0DataRank · unranked

14 citations

Samuel D. Reyes, Emmanuelle Faure-Kumar, Sandi Lam, Michael W. Lawlor, Richard J. Leventer +10 more

A family study implicates GBE1 in the etiology of autism spectrum disorder

Human Mutation(2021)10.1002/humu.24289

N/A

0DataRank · unranked

3 citations

Natasha J. Brown, Peter F. Hickey, Peter Diakumis, Haloom Rafehi, Kiymet Bozaoglu +17 more

Paul J. Lockhart

Indexed papers

Top data-sharing exemplar

Papers