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Rick M. Tankard

Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
2021 · Itziar de Rojas, Sonia Moreno-Grau, et al. · Nature Communications · 322
Genetic variants associated with longitudinal changes in brain structure across the lifespan
2022 · Rachel M. Brouwer, Marieke Klein, et al. · Nature Neuroscience · 227
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Detecting Expansions of Tandem Repeats in Cohorts Sequenced with Short-Read Sequencing Data
2018 · Rick M. Tankard, Mark F. Bennett, et al. · The American Journal of Human Genetics · 139
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Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
2023 · Marie-Gabrielle Duperron, Maria J. Knol, et al. · Nature Medicine · 129
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Recent advances in the detection of repeat expansions with short-read next-generation sequencing
2018 · Melanie Bahlo, Mark F Bennett, et al. · F1000Research · 117
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Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
2017 · Ashley P L Marsh, Delphine Heron, et al. · Nature Genetics · 101
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Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss
2015 · Ashley P.L. Marsh, Vesna Lukic, et al. · Neurology Genetics · 39
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Pathogenic Variants in GPC4 Cause Keipert Syndrome
2019 · David J. Amor, Sarah E.M. Stephenson, et al. · The American Journal of Human Genetics · 34
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Comprehensive analysis of epigenetic clocks reveals associations between disproportionate biological ageing and hippocampal volume
2022 · Lidija Milicic, Michael Vacher, et al. · GeroScience · 32
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A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
2024 · Andrea Cortese, Sarah J. Beecroft, et al. · Nature Communications · 30
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Common variants in Alzheimer’s disease: Novel association of six genetic variants with AD and risk stratification by polygenic risk scores
2019 · Itziar de Rojas, Sonia Moreno-Grau, et al. · medRxiv · 28
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PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
2015 · Michael S. Hildebrand, Rick Tankard, et al. · Annals of Clinical and Translational Neurology · 28
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Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
2022 · Mathieu Barbier, Melanie Bahlo, et al. · Annals of Neurology · 26
Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency
2016 · David J. Amor, Ashley P.L. Marsh, et al. · Neurology Genetics · 22
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Challenges of diagnostic exome sequencing in an inbred founder population
2013 · Dimitar N. Azmanov, Teodora Chamova, et al. · Molecular Genetics & Genomic Medicine · 15
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Using familial information for variant filtering in high-throughput sequencing studies
2014 · Melanie Bahlo, Rick Tankard, et al. · Human Genetics · 13
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Age-dependent genetic variants associated with longitudinal changes in brain structure across the lifespan
2020 · Rachel M. Brouwer, Marieke Klein, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 11
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Dynamics of Brain Structure and its Genetic Architecture over the Lifespan
2020 · Brouwer, Rachel M., Klein, Marieke, et al. · Zenodo (CERN European Organization for Nuclear Research) · 11
Genetic investigation into an increased susceptibility to biliary atresia in an extended New Zealand Māori family
2018 · Sophia R. Cameron-Christie, Justin Wilde, et al. · BMC Medical Genomics · 8
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A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
2023 · Andrea Cortese, Sarah J Beecroft, et al. · medRxiv · 7
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Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
2022 · Marie‐Gabrielle Duperron, Maria J. Knol, et al. · Alzheimer s & Dementia · 4
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Identifying disease-causing short tandem repeat expansions in massively parallel sequencing data, with a focus on ataxias
2017 · Rick M. Tankard · Murdoch University Research Portal · 1
Genomics of diffusion-imaging integrating GWAS, exome data and single-cell sequencing unravels lifespan determinants of cerebral small vessel disease
2025 · Stephanie Debette, Yasaman Saba, et al. · Research Square
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Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
2024 · Andrea Cortese, Sarah J. Beecroft, et al. · Nature Communications
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Author Correction: Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
2023 · Itziar de Rojas, Sonia Moreno-Grau, et al. · Nature Communications
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Works count: 33
Citation count: 1,343
H-index: 15
I10-index: 18
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