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Rick Tankard
Rick Tankard
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Year
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
I De Rojas, S Moreno-Grau, N Tesi, B Grenier-Boley, V Andrade, ...
Nature communications 12 (1), 3417, 2021
185*2021
Recent advances in the detection of repeat expansions with short-read next-generation sequencing
M Bahlo, MF Bennett, P Degorski, RM Tankard, MB Delatycki, PJ Lockhart
F1000Research 7, 2018
1172018
Detecting expansions of tandem repeats in cohorts sequenced with short-read sequencing data
RM Tankard, MF Bennett, P Degorski, MB Delatycki, PJ Lockhart, M Bahlo
The American Journal of Human Genetics 103 (6), 858-873, 2018
1092018
Mutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
APL Marsh, D Heron, TJ Edwards, A Quartier, C Galea, C Nava, ...
Nature genetics 49 (4), 511-514, 2017
912017
Genetic variants associated with longitudinal changes in brain structure across the lifespan
RM Brouwer, M Klein, KL Grasby, HG Schnack, N Jahanshad, J Teeuw, ...
Nature neuroscience 25 (4), 421-432, 2022
882022
PRIMA1 mutation: a new cause of nocturnal frontal lobe epilepsy
MS Hildebrand, R Tankard, EV Gazina, JA Damiano, KM Lawrence, ...
Annals of clinical and translational neurology 2 (8), 821-830, 2015
342015
Complete callosal agenesis, pontocerebellar hypoplasia, and axonal neuropathy due to AMPD2 loss
APL Marsh, V Lukic, K Pope, C Bromhead, R Tankard, MM Ryan, EM Yiu, ...
Neurology: Genetics 1 (2), e16, 2015
342015
Pathogenic variants in GPC4 cause Keipert syndrome
DJ Amor, SEM Stephenson, M Mustapha, MA Mensah, CW Ockeloen, ...
The American Journal of Human Genetics 104 (5), 914-924, 2019
272019
Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency
DJ Amor, APL Marsh, E Storey, R Tankard, G Gillies, MB Delatycki, ...
Neurology: Genetics 2 (6), e114, 2016
222016
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
MG Duperron, MJ Knol, Q Le Grand, TE Evans, A Mishra, A Tsuchida, ...
Nature medicine 29 (4), 950-962, 2023
192023
Dynamics of brain structure and its genetic architecture over the lifespan
RM Brouwer, NEM van Haren, MD Forti, LH van den Berg, BWJH Penninx, ...
Strukturelle und funktionelle Organisation des Gehirns, 2020
182020
Challenges of diagnostic exome sequencing in an inbred founder population
DN Azmanov, T Chamova, R Tankard, V Gelev, M Bynevelt, L Florez, ...
Molecular genetics & genomic medicine 1 (2), 71-76, 2013
182013
Using familial information for variant filtering in high-throughput sequencing studies
M Bahlo, R Tankard, V Lukic, KL Oliver, KR Smith
Human Genetics 133, 1331-1341, 2014
162014
Comprehensive analysis of epigenetic clocks reveals associations between disproportionate biological ageing and hippocampal volume
L Milicic, M Vacher, T Porter, V Doré, SC Burnham, P Bourgeat, ...
Geroscience 44 (3), 1807-1823, 2022
152022
Heterozygous PNPT1 Variants Cause Spinocerebellar Ataxia Type 25
M Barbier, M Bahlo, A Pennisi, M Jacoupy, RM Tankard, C Ewenczyk, ...
Annals of neurology 92 (1), 122-137, 2022
82022
Genetic investigation into an increased susceptibility to biliary atresia in an extended New Zealand Māori family
SR Cameron-Christie, J Wilde, A Gray, R Tankard, M Bahlo, D Markie, ...
BMC Medical Genomics 11, 1-13, 2018
82018
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry
A Cortese, SJ Beecroft, S Facchini, R Curro, M Cabrera-Serrano, ...
medRxiv, 2023.10. 09.23296582, 2023
32023
Genomics of perivascular space burden unravels early mechanisms of cerebral small vessel disease
S Debette, MG Duperron, M Knol, Q Le Grand, T Evans, A Mishra, ...
22021
Identifying disease-causing short tandem repeat expansions in massively parallel sequencing data, with a focus on ataxias
RM Tankard
PhD thesis, The University of Melbourne, 2017
22017
Detecting tandem repeat expansions in cohorts sequenced with short-read sequencing data
RM Tankard, MF Bennett, P Degorski, MB Delatycki, PJ Lockhart, M Bahlo
BioRxiv, 2017
12017
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