david thorburn

Citado por

	Total	Desde 2020
Citas	27013	10731
Índice h	79	51
Índice i10	211	153

2400

1200

600

1800

199920002001200220032004200520062007200820092010201120122013201420152016201720182019202020212022202320242025126 107 168 224 202 293 301 376 382 485 654 733 825 1161 1262 1192 1222 1355 1483 1610 1604 1938 2334 2107 1951 2075 311

Acceso público

Ver todo

122 artículos

11 artículos

disponibles

no disponibles

Basado en requisitos de financiación

Coautores

John ChristodoulouMurdoch Children's Research InstituteDirección de correo verificada de mcri.edu.au
Alison G ComptonPhD, Murdoch Childrens Research InstituteDirección de correo verificada de mcri.edu.au
Michael T RyanMonash University, MelbourneDirección de correo verificada de monash.edu
Ann FrazierMurdoch Children's Research Institute, AustraliaDirección de correo verificada de mcri.edu.au
Robert W TaylorNewcastle UniversityDirección de correo verificada de ncl.ac.uk
Vamsi MoothaMassachusetts General Hospital, Harvard Medical School, HHMIDirección de correo verificada de hms.harvard.edu
Robert McFarlandNewcastle UniversityDirección de correo verificada de ncl.ac.uk
Akira OhtakeDepartment of Pediatrics & Clinical Genomics, Faculty of Medicine, Saitama Medical UniversityDirección de correo verificada de saitama-med.ac.jp
Sarah E CalvoBroad Institute, Massachusetts General Hospital, Harvard Medical SchoolDirección de correo verificada de broadinstitute.org
Shamima RahmanProfessor of Paediatric Metabolic Medicine, UCLDirección de correo verificada de ucl.ac.uk
Elena TuckerMurdoch Childrens Research InstituteDirección de correo verificada de mcri.edu.au
David A. StroudDepartment of Biochemistry and Pharmacology, The University of MelbourneDirección de correo verificada de unimelb.edu.au
Patrick F ChinneryUniversity of CambridgeDirección de correo verificada de medschl.cam.ac.uk
Michael LazarouWalter and Eliza Hall Institute of Medical Research, co-affiliated with Monash UniversityDirección de correo verificada de wehi.edu.au
Josephine M ForbesMater Research Institute - The University of QueenslandDirección de correo verificada de mater.uq.edu.au
Philip KuchelEmeritus Professor of Biochemistry, University of SydneyDirección de correo verificada de sydney.edu.au
Melanie BahloTheme Leader, Healthy Development and Ageing, The Walter and Eliza Hall Institute ofDirección de correo verificada de wehi.edu.au
Doug TurnbullProfessor of Neurology, Newcastle UniversityDirección de correo verificada de newcastle.ac.uk
David J. PagliariniHHMI/Washington University School of Medicine in St. LouisDirección de correo verificada de wustl.edu
Prof. dr. Jan A.M. SmeitinkProfessor in Mitochondrial MedicineDirección de correo verificada de radboudumc.nl

Seguir

david thorburn

murdoch children's research institute

Dirección de correo verificada de mcri.edu.au - Página principal

genetics biochemistry pathology


Título Ordenar por citas Ordenar por año Ordenar por título	Citado por Citado por	Año
A mitochondrial protein compendium elucidates complex I disease biology DJ Pagliarini, SE Calvo, B Chang, SA Sheth, SB Vafai, SE Ong, ... Cell 134 (1), 112-123, 2008	2314	2008
Mitochondrial diseases GS Gorman, PF Chinnery, S DiMauro, M Hirano, Y Koga, R McFarland, ... Nature reviews Disease primers 2 (1), 1-22, 2016	1580	2016
Leigh syndrome: clinical features and biochemical and DNA abnormalities S Rahman, RB Blok, HHM Dahl, DM Danks, DM Kirby, CW Chow, ... Annals of Neurology: Official Journal of the American Neurological …, 1996	951	1996
Diagnostic criteria for respiratory chain disorders in adults and children FP Bernier, A Boneh, X Dennett, CW Chow, MA Cleary, DR Thorburn Neurology 59 (9), 1406-1411, 2002	700	2002
Minimum birth prevalence of mitochondrial respiratory chain disorders in children D Skladal, J Halliday, DR Thorburn Brain 126 (8), 1905-1912, 2003	606	2003
Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing SE Calvo, AG Compton, SG Hershman, SC Lim, DS Lieber, EJ Tucker, ... Science translational medicine 4 (118), 118ra10-118ra10, 2012	570	2012
Leigh syndrome: one disorder, more than 75 monogenic causes NJ Lake, AG Compton, S Rahman, DR Thorburn Annals of neurology 79 (2), 190-203, 2016	564	2016
Accessory subunits are integral for assembly and function of human mitochondrial complex I DA Stroud, EE Surgenor, LE Formosa, B Reljic, AE Frazier, MG Dibley, ... Nature 538 (7623), 123-126, 2016	557	2016
RAGE-induced cytosolic ROS promote mitochondrial superoxide generation in diabetes MT Coughlan, DR Thorburn, SA Penfold, A Laskowski, BE Harcourt, ... Journal of the American Society of Nephrology 20 (4), 742-752, 2009	531	2009
Understanding mitochondrial complex I assembly in health and disease M Mimaki, X Wang, M McKenzie, DR Thorburn, MT Ryan Biochimica et Biophysica Acta (BBA)-Bioenergetics 1817 (6), 851-862, 2012	515	2012
Mitochondrial respiratory chain supercomplexes are destabilized in Barth Syndrome patients M McKenzie, M Lazarou, DR Thorburn, MT Ryan Journal of molecular biology 361 (3), 462-469, 2006	501	2006
Mitochondrial dysfunction in diabetic kidney disease JM Forbes, DR Thorburn Nature Reviews Nephrology 14 (5), 291-312, 2018	497	2018
Treatment for mitochondrial disorders G Pfeffer, K Majamaa, DM Turnbull, D Thorburn, PF Chinnery Cochrane Database of Systematic Reviews, 2012	472	2012
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency SE Calvo, EJ Tucker, AG Compton, DM Kirby, G Crawford, NP Burtt, ... Nature genetics 42 (10), 851-858, 2010	430	2010
Biochemical assays of respiratory chain complex activity DM Kirby, DR Thorburn, DM Turnbull, RW Taylor Methods in cell biology 80, 93-119, 2007	427	2007
The inheritance of mitochondrial DNA heteroplasmy: random drift, selection or both? PF Chinnery, DR Thorburn, DC Samuels, SL White, HHM Dahl, ... Trends in Genetics 16 (11), 500-505, 2000	335	2000
Mitochondrial disorders: prevalence, myths and advances DR Thorburn Journal of inherited metabolic disease 27, 349-362, 2004	323	2004
Respiratory chain complex I deficiency: an underdiagnosed energy generation disorder DM Kirby, M Crawford, MA Cleary, HHM Dahl, X Dennett, DR Thorburn Neurology 52 (6), 1255-1255, 1999	313	1999
Analysis of the assembly profiles for mitochondrial-and nuclear-DNA-encoded subunits into complex I M Lazarou, M McKenzie, A Ohtake, DR Thorburn, MT Ryan Molecular and cellular biology, 2007	291	2007
Mutation of the mitochondrial tyrosyl-tRNA synthetase gene, YARS2, causes myopathy, lactic acidosis, and sideroblastic anemia—MLASA syndrome LG Riley, S Cooper, P Hickey, J Rudinger-Thirion, M McKenzie, ... The American Journal of Human Genetics 87 (1), 52-59, 2010	290	2010

El sistema no puede realizar la operación en estos momentos. Inténtalo de nuevo más tarde.

Artículos 1–20

Citas por año

Citas duplicadas

Citas combinadas

Añadir coautoresCoautores

Seguir

Citado por

Coautores