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Rick M. Tankard

Murdoch University AU

ORCID 0000-0002-8847-9401
31
Publications
1,364
Citations
14
H-Index
18
i10-Index
9.0
2yr Mean Cite
True
Cite/Paper
Data combined from OpenAlex + Semantic Scholar. OA = OpenAlex S2 = Semantic Scholar
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Publication & Citation Trends

Publications

28 total

Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry OA

A. Cortese, Sarah J Beecroft, S. Facchini, R. Curró, M. Cabrera-Serrano - Nature Communications, 2024
Cited by 0 Semantic Scholar

Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease PDF

Marie‐Gabrielle Duperron, Maria J. Knol, Quentin Le Grand, Tavia E. Evans, Aniket Mishra et al. - Nature Medicine, 2023
Cited by 114 OpenAlex

A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry OA

A. Cortese, S. Beecroft, S. Facchini, R. Curró, M. Cabrera-Serrano - Nature Communications, 2023
Cited by 21 Semantic Scholar

Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores OA

I. de Rojas, S. Moreno-Grau, N. Tesi, B. Grenier‐Boley, V. Andrade - Nature Communications, 2023
Cited by 0 Semantic Scholar

variants in Alzheimer's disease and risk stratification by polygenic risk

I. de Rojas, Tesi Sonia, Grenier-Boley Niccolo, A. Benjamin, N. Stringa - Unknown Venue, 2023
Cited by 1 Semantic Scholar

Comprehensive analysis of epigenetic clocks reveals associations between disproportionate biological ageing and hippocampal volume OA

Lidija Milicic, M. Vacher, T. Porter, V. Doré, S. Burnham - GeroScience, 2022
Cited by 27 Semantic Scholar

Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25 OA

M. Barbier, M. Bahlo, Alessandra Pennisi, Maxime Jacoupy, Rick M. Tankard - Annals of Neurology, 2022
Cited by 22 Semantic Scholar

Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores PDF

Itziar de Rojas, Sonia Moreno–Grau, Niccoló Tesi, Benjamin Grenier‐Boley, Víctor Andrade et al. - Nature Communications, 2021
Cited by 329 OpenAlex

Genetic variants associated with longitudinal changes in brain structure across the lifespan OA

R. Brouwer, M. Klein, K. Grasby, H. Schnack, N. Jahanshad - Nature Neuroscience, 2021
Cited by 166 Semantic Scholar

Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing Data PDF

Rick M. Tankard, Mark F. Bennett, Peter Degorski, Martin B. Delatycki, Paul J. Lockhart et al. - The American Journal of Human Genetics, 2018
Cited by 150 OpenAlex

Research Topics

Genetic Associations and Epidemiology (7) Genetic Neurodegenerative Diseases (7) Epigenetics and DNA Methylation (4) RNA modifications and cancer (4) Fetal and Pediatric Neurological Disorders (4)

Affiliations

Royal Children's Hospital
AU 2015 - 2015
University of Melbourne
AU 2022 - 2014
Murdoch University
AU 2025 - 2017
Walter and Eliza Hall Institute of Medical Research
AU 2022 - 2013
Curtin University
AU 2024 - 2022

External Profiles

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