| Year |
Citation |
Score |
| 2021 |
Machado HE, Bergland A, Taylor RW, Tilk S, Behrman E, Dyer K, Fabian DK, Flatt T, González J, Karasov TL, Kim BY, Kozeretska I, Lazzaro BP, Merritt T, Pool JE, et al. Broad geographic sampling reveals the shared basis and environmental correlates of seasonal adaptation in Drosophila. Elife. 10. PMID 34155971 DOI: 10.7554/eLife.67577 |
0.726 |
|
| 2021 |
Armstrong EE, Khan A, Taylor RW, Gouy A, Greenbaum G, Thiéry A, Kang JTL, Redondo SA, Prost S, Barsh G, Kaelin C, Phalke S, Chugani A, Gilbert M, Miquelle D, et al. Recent evolutionary history of tigers highlights contrasting roles of genetic drift and selection. Molecular Biology and Evolution. PMID 33592092 DOI: 10.1093/molbev/msab032 |
0.76 |
|
| 2020 |
Armstrong EE, Taylor RW, Miller DE, Kaelin CB, Barsh GS, Hadly EA, Petrov D. Long live the king: chromosome-level assembly of the lion (Panthera leo) using linked-read, Hi-C, and long-read data. Bmc Biology. 18: 3. PMID 31915011 DOI: 10.1186/S12915-019-0734-5 |
0.736 |
|
| 2020 |
Haines JA, Nason SE, Skurdal AMM, Bourchier T, Boutin S, Taylor RW, McAdam AG, Lane JE, Kelley AD, Humphries MM, Gorrell JC, Dantzer B, Coltman DW, Hämäläinen A. Sex- and context-specific associations between personality and a measure of fitness but no link with life history traits Animal Behaviour. 167: 23-39. DOI: 10.1016/J.Anbehav.2020.06.013 |
0.738 |
|
| 2020 |
Westrick SE, Taylor RW, Boutin S, Lane JE, McAdam AG, Dantzer B. Attentive red squirrel mothers have faster growing pups and higher lifetime reproductive success Behavioral Ecology and Sociobiology. 74. DOI: 10.1007/S00265-020-02856-7 |
0.724 |
|
| 2019 |
Natesh M, Taylor RW, Truelove NK, Hadly EA, Palumbi SR, Petrov DA, Ramakrishnan U. Empowering conservation practice with efficient and economical genotyping from poor quality samples. Methods in Ecology and Evolution. 10: 853-859. PMID 31511786 DOI: 10.1111/2041-210X.13173 |
0.544 |
|
| 2018 |
Armstrong EE, Taylor RW, Prost S, Blinston P, van der Meer E, Madzikanda H, Mufute O, Mandisodza-Chikerema R, Stuelpnagel J, Sillero-Zubiri C, Petrov D. Cost-effective assembly of the African wild dog (Lycaon pictus) genome using linked reads. Gigascience. PMID 30346553 DOI: 10.1093/Gigascience/Giy124 |
0.74 |
|
| 2017 |
Cooper E, Taylor R, Kelley A, Martinig A, Boutin S, Humphries M, Dantzer B, Lane J, McAdam A. Personality is correlated with natal dispersal in North American red squirrels (Tamiasciurus hudsonicus) Behaviour. 154: 939-961. DOI: 10.1163/1568539X-00003450 |
0.743 |
|
| 2014 |
Taylor RW, Boutin S, Humphries MM, McAdam AG. Selection on female behaviour fluctuates with offspring environment. Journal of Evolutionary Biology. 27: 2308-21. PMID 25293495 DOI: 10.1111/Jeb.12495 |
0.712 |
|
| 2014 |
McCoy RC, Taylor RW, Blauwkamp TA, Kelley JL, Kertesz M, Pushkarev D, Petrov DA, Fiston-Lavier AS. Illumina TruSeq synthetic long-reads empower de novo assembly and resolve complex, highly-repetitive transposable elements. Plos One. 9: e106689. PMID 25188499 DOI: 10.1371/Journal.Pone.0106689 |
0.717 |
|
| 2012 |
Taylor RW, Boon AK, Dantzer B, Réale D, Humphries MM, Boutin S, Gorrell JC, Coltman DW, McAdam AG. Low heritabilities, but genetic and maternal correlations between red squirrel behaviours. Journal of Evolutionary Biology. 25: 614-24. PMID 22268892 DOI: 10.1111/J.1420-9101.2012.02456.X |
0.753 |
|
| 2012 |
Shonfield J, Taylor RW, Boutin S, Humphries MM, McAdam AG. Territorial defence behaviour in red squirrels is influenced by local density Behaviour. 149: 369-390. DOI: 10.1163/156853912X637842 |
0.695 |
|
| 2011 |
McFarlane SE, Lane JE, Taylor RW, Gorrell JC, Coltman DW, Humphries MM, Boutin S, McAdam AG. The heritability of multiple male mating in a promiscuous mammal. Biology Letters. 7: 368-71. PMID 21159688 DOI: 10.1098/Rsbl.2010.1003 |
0.699 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2016 |
Alston CL, Compton AG, Formosa LE, Strecker V, Oláhová M, Haack TB, Smet J, Stouffs K, Diakumis P, Ciara E, Cassiman D, Romain N, Yarham JW, He L, De Paepe B, ... ... Taylor RW, et al. Biallelic Mutations in TMEM126B Cause Severe Complex I Deficiency with a Variable Clinical Phenotype. American Journal of Human Genetics. PMID 27374774 DOI: 10.1016/J.Ajhg.2016.05.021 |
0.2 |
|
| 2023 |
Bradford YM, Van Slyke CE, Howe DG, Fashena D, Frazer K, Martin R, Paddock H, Pich C, Ramachandran S, Ruzicka L, Singer A, Taylor R, Tseng WC, Westerfield M. From Multi-Allele Fish to Non-Standard Environments, How ZFIN Assigns Phenotypes, Human Disease Models, and Gene Expression Annotations to Genes. Genetics. PMID 36864549 DOI: 10.1093/genetics/iyad032 |
0.175 |
|
| 2014 |
Smith PM, Elson JL, Greaves LC, Wortmann SB, Rodenburg RJ, Lightowlers RN, Chrzanowska-Lightowlers ZM, Taylor RW, Vila-Sanjurjo A. The role of the mitochondrial ribosome in human disease: searching for mutations in 12S mitochondrial rRNA with high disruptive potential. Human Molecular Genetics. 23: 949-67. PMID 24092330 DOI: 10.1093/hmg/ddt490 |
0.166 |
|
| 2014 |
Campbell G, Krishnan KJ, Deschauer M, Taylor RW, Turnbull DM. Dissecting the mechanisms underlying the accumulation of mitochondrial DNA deletions in human skeletal muscle. Human Molecular Genetics. 23: 4612-20. PMID 24740879 DOI: 10.1093/Hmg/Ddu176 |
0.16 |
|
| 2015 |
Huemer M, Karall D, Schossig A, Abdenur JE, Al Jasmi F, Biagosch C, Distelmaier F, Freisinger P, Graham BH, Haack TB, Hauser N, Hertecant J, Ebrahimi-Fakhari D, Konstantopoulou V, Leydiker K, ... ... Taylor RW, et al. Clinical, morphological, biochemical, imaging and outcome parameters in 21 individuals with mitochondrial maintenance defect related to FBXL4 mutations. Journal of Inherited Metabolic Disease. PMID 25868664 DOI: 10.1007/S10545-015-9836-6 |
0.153 |
|
| 2015 |
Gorman GS, Pfeffer G, Griffin H, Blakely EL, Kurzawa-Akanbi M, Gabriel J, Sitarz K, Roberts M, Schoser B, Pyle A, Schaefer AM, McFarland R, Turnbull DM, Horvath R, Chinnery PF, ... Taylor RW, et al. Clonal expansion of secondary mitochondrial DNA deletions associated with spinocerebellar ataxia type 28. Jama Neurology. 72: 106-11. PMID 25420100 DOI: 10.1001/Jamaneurol.2014.1753 |
0.148 |
|
| 2015 |
Spiegel R, Saada A, Flannery PJ, Burté F, Soiferman D, Khayat M, Sagüés VE, Vladovski E, Taylor RW, Bindoff LA, Shaag A, Mandel H, Furman O, Shalev SA, Elpeleg O, et al. Fatal infantile mitochondrial encephalomyopathy, hypertrophic cardiomyopathy and optic atrophy associated with a homozygous OPA1 mutation. Journal of Medical Genetics. PMID 26561570 DOI: 10.1136/Jmedgenet-2015-103361 |
0.145 |
|
| 2013 |
Reid SF, Narendra A, Taylor RW, Zeil J. Foraging ecology of the night-active bull ant Myrmecia pyriformis Australian Journal of Zoology. 61: 170-177. DOI: 10.1071/ZO13027 |
0.145 |
|
| 2012 |
Neeve VC, Samuels DC, Bindoff LA, van den Bosch B, Van Goethem G, Smeets H, Lombès A, Jardel C, Hirano M, Dimauro S, De Vries M, Smeitink J, Smits BW, de Coo IF, Saft C, ... ... Taylor RW, et al. What is influencing the phenotype of the common homozygous polymerase-γ mutation p.Ala467Thr? Brain : a Journal of Neurology. 135: 3614-26. PMID 23250882 DOI: 10.1093/Brain/Aws298 |
0.144 |
|
| 2016 |
Wilson IJ, Carling PJ, Alston CL, Floros VI, Pyle A, Hudson G, Sallevelt SC, Lamperti C, Carelli V, Bindoff LA, Samuels DC, Wonnapinij P, Zeviani M, Taylor RW, Smeets HJ, et al. Mitochondrial DNA Sequence Characteristics Modulate the Size of the Genetic Bottleneck. Human Molecular Genetics. PMID 26740552 DOI: 10.1093/Hmg/Ddv626 |
0.139 |
|
| 2014 |
Melchionda L, Haack TB, Hardy S, Abbink TE, Fernandez-Vizarra E, Lamantea E, Marchet S, Morandi L, Moggio M, Carrozzo R, Torraco A, Diodato D, Strom TM, Meitinger T, Tekturk P, ... ... Taylor RW, et al. Mutations in APOPT1, encoding a mitochondrial protein, cause cavitating leukoencephalopathy with cytochrome c oxidase deficiency. American Journal of Human Genetics. 95: 315-25. PMID 25175347 DOI: 10.1016/j.ajhg.2014.08.003 |
0.138 |
|
| 2014 |
Taylor RW, Pyle A, Griffin H, Blakely EL, Duff J, He L, Smertenko T, Alston CL, Neeve VC, Best A, Yarham JW, Kirschner J, Schara U, Talim B, Topaloglu H, et al. Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies. Jama. 312: 68-77. PMID 25058219 DOI: 10.1001/Jama.2014.7184 |
0.138 |
|
| 2016 |
Alston CL, Howard C, Oláhová M, Hardy SA, He L, Murray PG, O'Sullivan S, Doherty G, Shield JP, Hargreaves IP, Monavari AA, Knerr I, McCarthy P, Morris AA, Thorburn DR, ... ... Taylor RW, et al. A recurrent mitochondrial p.Trp22Arg NDUFB3 variant causes a distinctive facial appearance, short stature and a mild biochemical and clinical phenotype. Journal of Medical Genetics. PMID 27091925 DOI: 10.1136/jmedgenet-2015-103576 |
0.136 |
|
| 2013 |
Lax NZ, Gnanapavan S, Dowson SJ, Alston CL, He L, Polvikoski TM, Jaros E, O'Donovan DG, Yarham JW, Turnbull DM, Dean AF, Taylor RW. Early-onset cataracts, spastic paraparesis, and ataxia caused by a novel mitochondrial tRNAGlu (MT-TE) gene mutation causing severe complex I deficiency: a clinical, molecular, and neuropathologic study. Journal of Neuropathology and Experimental Neurology. 72: 164-75. PMID 23334599 DOI: 10.1097/Nen.0B013E31828129C5 |
0.136 |
|
| 2015 |
Oláhová M, Haack TB, Alston CL, Houghton JA, He L, Morris AA, Brown GK, McFarland R, Chrzanowska-Lightowlers ZM, Lightowlers RN, Prokisch H, Taylor RW. A truncating PET100 variant causing fatal infantile lactic acidosis and isolated cytochrome c oxidase deficiency. European Journal of Human Genetics : Ejhg. 23: 935-9. PMID 25293719 DOI: 10.1038/ejhg.2014.214 |
0.132 |
|
| 2015 |
Taylor RW. Ants with Attitude: Australian Jack-jumpers of the Myrmecia pilosula species complex, with descriptions of four new species (Hymenoptera: Formicidae: Myrmeciinae). Zootaxa. 3911: 493-520. PMID 25661627 |
0.132 |
|
| 2015 |
Taylor RW. Ants with Attitude: Australian Jack-jumpers of the Myrmecia pilosula specie complex, with descriptions of four new species (Hymenoptera: Formicidae: Myrmeciinae) Zootaxa. 3911: 493-520. DOI: 10.11646/zootaxa.3911.4.2 |
0.132 |
|
| 2013 |
Godde K, Taylor RW. Distinguishing body mass and activity level from the lower limb: can entheses diagnose obesity? Forensic Science International. 226: 303.e1-7. PMID 23422166 DOI: 10.1016/j.forsciint.2013.01.027 |
0.131 |
|
| 2020 |
Turnbull T, Taylor R, Sciarretta JD, Davis JM. Sporogenic Aspergillus Infections : A Geographical Influence in an Invariable Trauma Population. The American Surgeon. 3134820923324. PMID 32683931 DOI: 10.1177/0003134820923324 |
0.131 |
|
| 2022 |
Romero J, Islam MT, Taylor R, Grayson C, Schoenrock A, Wong A. High-throughput design of bacterial anti-sense RNAs using CAREng. Bioinformatics Advances. 2: vbac069. PMID 36699397 DOI: 10.1093/bioadv/vbac069 |
0.13 |
|
| 2013 |
Spyropoulos A, Manford M, Horvath R, Alston CL, Yu-Wai-Man P, He L, Taylor RW, Chinnery PF. Near-identical segregation of mtDNA heteroplasmy in blood, muscle, urinary epithelium, and hair follicles in twins with optic atrophy, ptosis, and intractable epilepsy. Jama Neurology. 70: 1552-5. PMID 24126373 DOI: 10.1001/jamaneurol.2013.4111 |
0.129 |
|
| 2015 |
Taylor RW. Australasian ants of the subfamily Heteroponerinae (Hymenoptera: Formicidae): (2) the species-group of Heteroponera relicta (Wheeler),with descriptions of nine new species and observations on morphology, biogeography and phylogeny of the genus. Zootaxa. 3947: 151-80. PMID 25947727 |
0.126 |
|
| 2015 |
Taylor RW. Australasian ants of the subfamily Heteroponerinae (Hymenoptera: Formicidae): (2) the species-group of Heteroponera relicta (Wheeler), with descriptions of nine new species and observations on morphology, biogeography and phylogeny of the genus Zootaxa. 3947: 151-180. DOI: 10.11646/zootaxa.3947.2.1 |
0.126 |
|
| 2015 |
Taylor RW, Roy M, Jospe MR, Osborne HR, Meredith-Jones KJ, Williams SM, Brown RC. Determining how best to support overweight adults to adhere to lifestyle change: protocol for the SWIFT study. Bmc Public Health. 15: 861. PMID 26341820 DOI: 10.1186/s12889-015-2205-4 |
0.125 |
|
| 2015 |
Ahting U, Mayr JA, Vanlander AV, Hardy SA, Santra S, Makowski C, Alston CL, Zimmermann FA, Abela L, Plecko B, Rohrbach M, Spranger S, Seneca S, Rolinski B, Hagendorff A, ... ... Taylor RW, et al. Clinical, biochemical, and genetic spectrum of seven patients with NFU1 deficiency. Frontiers in Genetics. 6: 123. PMID 25918518 DOI: 10.3389/fgene.2015.00123 |
0.124 |
|
| 2016 |
Rygiel KA, Tuppen HA, Grady JP, Vincent A, Blakely EL, Reeve AK, Taylor RW, Picard M, Miller J, Turnbull DM. Complex mitochondrial DNA rearrangements in individual cells from patients with sporadic inclusion body myositis. Nucleic Acids Research. PMID 27131788 DOI: 10.1093/Nar/Gkw382 |
0.124 |
|
| 2024 |
Atamian A, Birtele M, Hosseini N, Nguyen T, Seth A, Del Dosso A, Paul S, Tedeschi N, Taylor R, Coba MP, Samarasinghe R, Lois C, Quadrato G. Human cerebellar organoids with functional Purkinje cells. Cell Stem Cell. 31: 39-51.e6. PMID 38181749 DOI: 10.1016/j.stem.2023.11.013 |
0.12 |
|
| 2014 |
Grady JP, Campbell G, Ratnaike T, Blakely EL, Falkous G, Nesbitt V, Schaefer AM, McNally RJ, Gorman GS, Taylor RW, Turnbull DM, McFarland R. Disease progression in patients with single, large-scale mitochondrial DNA deletions. Brain : a Journal of Neurology. 137: 323-34. PMID 24277717 DOI: 10.1093/Brain/Awt321 |
0.119 |
|
| 2015 |
Powell CA, Kopajtich R, D'Souza AR, Rorbach J, Kremer LS, Husain RA, Dallabona C, Donnini C, Alston CL, Griffin H, Pyle A, Chinnery PF, Strom TM, Meitinger T, Rodenburg RJ, ... ... Taylor RW, et al. TRMT5 Mutations Cause a Defect in Post-transcriptional Modification of Mitochondrial tRNA Associated with Multiple Respiratory-Chain Deficiencies. American Journal of Human Genetics. 97: 319-28. PMID 26189817 DOI: 10.1016/J.Ajhg.2015.06.011 |
0.119 |
|
| 2013 |
Elson JL, Cadogan M, Apabhai S, Whittaker RG, Phillips A, Trennell MI, Horvath R, Taylor RW, McFarland R, McColl E, Turnbull DM, Gorman GS. Initial development and validation of a mitochondrial disease quality of life scale. Neuromuscular Disorders : Nmd. 23: 324-9. PMID 23433484 DOI: 10.1016/J.Nmd.2012.12.012 |
0.114 |
|
| 2015 |
Lightowlers RN, Taylor RW, Turnbull DM. Mutations causing mitochondrial disease: What is new and what challenges remain? Science (New York, N.Y.). 349: 1494-9. PMID 26404827 DOI: 10.1126/Science.Aac7516 |
0.112 |
|
| 2016 |
Martikainen MH, Ng YS, Gorman GS, Alston CL, Blakely EL, Schaefer AM, Chinnery PF, Burn DJ, Taylor RW, McFarland R, Turnbull DM. Clinical, Genetic, and Radiological Features of Extrapyramidal Movement Disorders in Mitochondrial Disease. Jama Neurology. PMID 27111573 DOI: 10.1001/Jamaneurol.2016.0355 |
0.111 |
|
| 2015 |
Rocha MC, Grady JP, Grünewald A, Vincent A, Dobson PF, Taylor RW, Turnbull DM, Rygiel KA. A novel immunofluorescent assay to investigate oxidative phosphorylation deficiency in mitochondrial myopathy: understanding mechanisms and improving diagnosis. Scientific Reports. 5: 15037. PMID 26469001 DOI: 10.1038/Srep15037 |
0.111 |
|
| 2024 |
Sneed L, Taylor R, Cook I, Befi M, Fitchett B, Samelson D, Bemmel V. Initial Psychometric Properties of the Catalight Family Wellbeing Scale. Journal of Autism and Developmental Disorders. PMID 38300503 DOI: 10.1007/s10803-024-06254-0 |
0.111 |
|
| 2013 |
Taylor RW, Williams SM, Farmer VL, Taylor BJ. Changes in physical activity over time in young children: a longitudinal study using accelerometers. Plos One. 8: e81567. PMID 24282607 DOI: 10.1371/journal.pone.0081567 |
0.111 |
|
| 2015 |
Haack TB, Jackson CB, Murayama K, Kremer LS, Schaller A, Kotzaeridou U, de Vries MC, Schottmann G, Santra S, Büchner B, Wieland T, Graf E, Freisinger P, Eggimann S, Ohtake A, ... ... Taylor RW, et al. Deficiency of ECHS1 causes mitochondrial encephalopathy with cardiac involvement. Annals of Clinical and Translational Neurology. 2: 492-509. PMID 26000322 DOI: 10.1002/Acn3.189 |
0.111 |
|
| 2013 |
Baruffini E, Dallabona C, Invernizzi F, Yarham JW, Melchionda L, Blakely EL, Lamantea E, Donnini C, Santra S, Vijayaraghavan S, Roper HP, Burlina A, Kopajtich R, Walther A, Strom TM, ... ... Taylor RW, et al. MTO1 mutations are associated with hypertrophic cardiomyopathy and lactic acidosis and cause respiratory chain deficiency in humans and yeast. Human Mutation. 34: 1501-9. PMID 23929671 DOI: 10.1002/humu.22393 |
0.108 |
|
| 2014 |
Grady JP, Murphy JL, Blakely EL, Haller RG, Taylor RW, Turnbull DM, Tuppen HA. Accurate measurement of mitochondrial DNA deletion level and copy number differences in human skeletal muscle. Plos One. 9: e114462. PMID 25474153 DOI: 10.1371/Journal.Pone.0114462 |
0.107 |
|
| 2021 |
Fan L, Lim Y, Wong GS, Taylor R. Factors affecting successful use of intranasal dexmedetomidine: a cohort study from a national paediatrics tertiary centre. Translational Pediatrics. 10: 765-772. PMID 34012826 DOI: 10.21037/tp-20-358 |
0.107 |
|
| 2021 |
Taylor R, McCrea A, Poldiak NP, Muertos K, Biswas S, Kaufmann C. Trauma Recidivism in an Aging Population: Who Is Most at Risk? Hca Healthcare Journal of Medicine. 2: 63-69. PMID 37424893 DOI: 10.36518/2689-0216.1121 |
0.104 |
|
| 2014 |
Nesbitt V, Alston CL, Blakely EL, Fratter C, Feeney CL, Poulton J, Brown GK, Turnbull DM, Taylor RW, McFarland R. A national perspective on prenatal testing for mitochondrial disease. European Journal of Human Genetics : Ejhg. 22: 1255-9. PMID 24642831 DOI: 10.1038/Ejhg.2014.35 |
0.102 |
|
| 2015 |
Haack TB, Staufner C, Köpke MG, Straub BK, Kölker S, Thiel C, Freisinger P, Baric I, McKiernan PJ, Dikow N, Harting I, Beisse F, Burgard P, Kotzaeridou U, Kühr J, ... ... Taylor RW, et al. Biallelic Mutations in NBAS Cause Recurrent Acute Liver Failure with Onset in Infancy. American Journal of Human Genetics. 97: 163-9. PMID 26073778 DOI: 10.1016/J.Ajhg.2015.05.009 |
0.101 |
|
| 2015 |
Oláhová M, Hardy SA, Hall J, Yarham JW, Haack TB, Wilson WC, Alston CL, He L, Aznauryan E, Brown RM, Brown GK, Morris AA, Mundy H, Broomfield A, Barbosa IA, ... ... Taylor RW, et al. LRPPRC mutations cause early-onset multisystem mitochondrial disease outside of the French-Canadian population. Brain : a Journal of Neurology. PMID 26510951 DOI: 10.1093/brain/awv291 |
0.101 |
|
| 2015 |
Gorman GS, Schaefer AM, Ng Y, Gomez N, Blakely EL, Alston CL, Feeney C, Horvath R, Yu-Wai-Man P, Chinnery PF, Taylor RW, Turnbull DM, McFarland R. Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease. Annals of Neurology. 77: 753-9. PMID 25652200 DOI: 10.1002/Ana.24362 |
0.1 |
|
| 2013 |
Cameron SL, Taylor RW, Heath AL. Parent-led or baby-led? Associations between complementary feeding practices and health-related behaviours in a survey of New Zealand families. Bmj Open. 3: e003946. PMID 24327363 DOI: 10.1136/bmjopen-2013-003946 |
0.1 |
|
| 2013 |
Bonnen PE, Yarham JW, Besse A, Wu P, Faqeih EA, Al-Asmari AM, Saleh MA, Eyaid W, Hadeel A, He L, Smith F, Yau S, Simcox EM, Miwa S, Donti T, ... ... Taylor RW, et al. Mutations in FBXL4 cause mitochondrial encephalopathy and a disorder of mitochondrial DNA maintenance. American Journal of Human Genetics. 93: 471-81. PMID 23993193 DOI: 10.1016/j.ajhg.2013.07.017 |
0.1 |
|
| 2013 |
Haack TB, Kopajtich R, Freisinger P, Wieland T, Rorbach J, Nicholls TJ, Baruffini E, Walther A, Danhauser K, Zimmermann FA, Husain RA, Schum J, Mundy H, Ferrero I, Strom TM, ... ... Taylor RW, et al. ELAC2 mutations cause a mitochondrial RNA processing defect associated with hypertrophic cardiomyopathy. American Journal of Human Genetics. 93: 211-23. PMID 23849775 DOI: 10.1016/J.Ajhg.2013.06.006 |
0.098 |
|
| 2014 |
Taylor RW, Benz F, Sigle DO, Bowman RW, Bao P, Roth JS, Heath GR, Evans SD, Baumberg JJ. Watching individual molecules flex within lipid membranes using SERS. Scientific Reports. 4: 5940. PMID 25113088 DOI: 10.1038/Srep05940 |
0.096 |
|
| 2018 |
Sutherland L, Ruhe M, Gattegno-Ho D, Mann K, Greaves J, Koscielniak M, Meek S, Lu Z, Waterfall M, Taylor R, Tsakiridis A, Brown H, Maciver SK, Joshi A, Clinton M, et al. LIF-dependent survival of embryonic stem cells is regulated by a novel palmitoylated Gab1 signalling protein. Journal of Cell Science. PMID 30154213 DOI: 10.1242/jcs.222257 |
0.094 |
|
| 2014 |
Griffin HR, Pyle A, Blakely EL, Alston CL, Duff J, Hudson G, Horvath R, Wilson IJ, Santibanez-Koref M, Taylor RW, Chinnery PF. Accurate mitochondrial DNA sequencing using off-target reads provides a single test to identify pathogenic point mutations. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 962-71. PMID 24901348 DOI: 10.1038/gim.2014.66 |
0.093 |
|
| 2015 |
Lehmann D, Schubert K, Joshi PR, Hardy SA, Tuppen HA, Baty K, Blakely EL, Bamberg C, Zierz S, Deschauer M, Taylor RW. Pathogenic mitochondrial mt-tRNA(Ala) variants are uniquely associated with isolated myopathy. European Journal of Human Genetics : Ejhg. PMID 25873012 DOI: 10.1038/ejhg.2015.73 |
0.093 |
|
| 2015 |
Daniels L, Heath AM, Williams SM, Cameron SL, Fleming EA, Taylor BJ, Wheeler BJ, Gibson RS, Taylor RW. Baby-Led Introduction to SolidS (BLISS) study: a randomised controlled trial of a baby-led approach to complementary feeding. Bmc Pediatrics. 15: 179. PMID 26563757 DOI: 10.1186/s12887-015-0491-8 |
0.092 |
|
| 2015 |
Gorman GS, Grady JP, Ng Y, Schaefer AM, McNally RJ, Chinnery PF, Yu-Wai-Man P, Herbert M, Taylor RW, McFarland R, Turnbull DM. Mitochondrial donation--how many women could benefit? The New England Journal of Medicine. 372: 885-7. PMID 25629662 DOI: 10.1056/Nejmc1500960 |
0.092 |
|
| 2016 |
Ng YS, Alston CL, Diodato D, Morris AA, Ulrick N, Kmoch S, Houštěk J, Martinelli D, Haghighi A, Atiq M, Gamero MA, Garcia-Martinez E, Kratochvílová H, Santra S, Brown RM, ... ... Taylor RW, et al. The clinical, biochemical and genetic features associated with RMND1-related mitochondrial disease. Journal of Medical Genetics. PMID 27412952 DOI: 10.1136/jmedgenet-2016-103910 |
0.092 |
|
| 2016 |
Metodiev MD, Thompson K, Alston CL, Morris AA, He L, Assouline Z, Rio M, Bahi-Buisson N, Pyle A, Griffin H, Siira S, Filipovska A, Munnich A, Chinnery PF, McFarland R, ... ... Taylor RW, et al. Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies. American Journal of Human Genetics. PMID 27132592 DOI: 10.1016/j.ajhg.2016.03.010 |
0.091 |
|
| 2015 |
Ferrer-Cortès X, Narbona J, Bujan N, Matalonga L, Del Toro M, Arranz JA, Riudor E, Garcia-Cazorla A, Jou C, O'Callaghan M, Pineda M, Montero R, Arias A, García-Villoria J, Alston CL, ... Taylor RW, et al. A leaky splicing mutation in NFU1 is associated with a particular biochemical phenotype. Consequences for the diagnosis. Mitochondrion. 26: 72-80. PMID 26688339 DOI: 10.1016/j.mito.2015.12.004 |
0.09 |
|
| 2013 |
Wedatilake Y, Brown RM, McFarland R, Yaplito-Lee J, Morris AA, Champion M, Jardine PE, Clarke A, Thorburn DR, Taylor RW, Land JM, Forrest K, Dobbie A, Simmons L, Aasheim ET, et al. SURF1 deficiency: a multi-centre natural history study. Orphanet Journal of Rare Diseases. 8: 96. PMID 23829769 DOI: 10.1186/1750-1172-8-96 |
0.09 |
|
| 2014 |
Greaves LC, Nooteboom M, Elson JL, Tuppen HA, Taylor GA, Commane DM, Arasaradnam RP, Khrapko K, Taylor RW, Kirkwood TB, Mathers JC, Turnbull DM. Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing. Plos Genetics. 10: e1004620. PMID 25232829 DOI: 10.1371/Journal.Pgen.1004620 |
0.09 |
|
| 2015 |
Nisar R, Hanson PS, He L, Taylor RW, Blain PG, Morris CM. Diquat causes caspase-independent cell death in SH-SY5Y cells by production of ROS independently of mitochondria. Archives of Toxicology. PMID 25693864 DOI: 10.1007/s00204-015-1453-5 |
0.089 |
|
| 2013 |
Yu-Wai-Man C, Smith FE, Firbank MJ, Guthrie G, Guthrie S, Gorman GS, Taylor RW, Turnbull DM, Griffiths PG, Blamire AM, Chinnery PF, Yu-Wai-Man P. Extraocular muscle atrophy and central nervous system involvement in chronic progressive external ophthalmoplegia. Plos One. 8: e75048. PMID 24086434 DOI: 10.1371/Journal.Pone.0075048 |
0.089 |
|
| 2015 |
Keogh MJ, Daud D, Pyle A, Duff J, Griffin H, He L, Alston CL, Steele H, Taggart S, Basu AP, Taylor RW, Horvath R, Ramesh V, Chinnery PF. A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism. Neurogenetics. 16: 65-7. PMID 25418441 DOI: 10.1007/s10048-014-0431-z |
0.087 |
|
| 2015 |
Ejaz A, Kim Y, Spolverato G, Taylor R, Hundt J, Pawlik TM. Understanding drivers of hospital charge variation for episodes of care among patients undergoing hepatopancreatobiliary surgery. Hpb : the Official Journal of the International Hepato Pancreato Biliary Association. 17: 955-63. PMID 26256003 DOI: 10.1111/Hpb.12452 |
0.087 |
|
| 2013 |
Zamzami MA, Duley JA, Price GR, Venter DJ, Yarham JW, Taylor RW, Catley LP, Florin TH, Marinaki AM, Bowling F. Inosine triphosphate pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects. Journal of Hematology & Oncology. 6: 24. PMID 23547827 DOI: 10.1186/1756-8722-6-24 |
0.087 |
|
| 2015 |
Mills VC, Skidmore PM, Watson EO, Taylor RW, Fleming EA, Heath AL. Relative validity and reproducibility of a food frequency questionnaire for identifying the dietary patterns of toddlers in New Zealand. Journal of the Academy of Nutrition and Dietetics. 115: 551-8. PMID 25441956 DOI: 10.1016/j.jand.2014.09.016 |
0.086 |
|
| 2016 |
Sallevelt SC, de Die-Smulders CE, Hendrickx AT, Hellebrekers DM, de Coo IF, Alston CL, Knowles C, Taylor RW, McFarland R, Smeets HJ. De novo mtDNA point mutations are common and have a low recurrence risk. Journal of Medical Genetics. PMID 27450679 DOI: 10.1136/jmedgenet-2016-103876 |
0.086 |
|
| 2013 |
Yarham JW, Blakely EL, Alston CL, Roberts ME, Ealing J, Pal P, Turnbull DM, McFarland R, Taylor RW. The m.3291T>C mt-tRNA(Leu(UUR)) mutation is definitely pathogenic and causes multisystem mitochondrial disease. Journal of the Neurological Sciences. 325: 165-9. PMID 23273904 DOI: 10.1016/J.Jns.2012.12.003 |
0.084 |
|
| 2014 |
Blakely EL, Alston CL, Lecky B, Chakrabarti B, Falkous G, Turnbull DM, Taylor RW, Gorman GS. Distal weakness with respiratory insufficiency caused by the m.8344A > G "MERRF" mutation. Neuromuscular Disorders : Nmd. 24: 533-6. PMID 24792523 DOI: 10.1016/J.Nmd.2014.03.011 |
0.084 |
|
| 2015 |
Elson JL, Smith PM, Greaves LC, Lightowlers RN, Chrzanowska-Lightowlers ZM, Taylor RW, Vila-Sanjurjo A. The presence of highly disruptive 16S rRNA mutations in clinical samples indicates a wider role for mutations of the mitochondrial ribosome in human disease. Mitochondrion. 25: 17-27. PMID 26349026 DOI: 10.1016/j.mito.2015.08.004 |
0.083 |
|
| 2014 |
Balreira A, Boczonadi V, Barca E, Pyle A, Bansagi B, Appleton M, Graham C, Hargreaves IP, Rasic VM, Lochmüller H, Griffin H, Taylor RW, Naini A, Chinnery PF, Hirano M, et al. ANO10 mutations cause ataxia and coenzyme Q₁₀ deficiency. Journal of Neurology. 261: 2192-8. PMID 25182700 DOI: 10.1007/s00415-014-7476-7 |
0.083 |
|
| 2014 |
Saunders H, Taylor RW. The Art and Environment of Embedded Librarianship College and Undergraduate Libraries. 21: 145-154. DOI: 10.1080/10691316.2014.906775 |
0.082 |
|
| 2015 |
Gorman GS, Blakely EL, Hornig-Do HT, Tuppen HA, Greaves LC, He L, Baker A, Falkous G, Newman J, Trenell MI, Lecky B, Petty RK, Turnbull DM, McFarland R, Taylor RW. Novel MTND1 mutations cause isolated exercise intolerance, complex I deficiency and increased assembly factor expression. Clinical Science (London, England : 1979). 128: 895-904. PMID 25626417 DOI: 10.1042/Cs20140705 |
0.081 |
|
| 2017 |
Tikhanovich I, Zhao J, Olson J, Adams A, Taylor R, Bridges B, Marshall L, Roberts B, Weinman SA. Protein Arginine Methyltransferase 1 modulates innate immune responses through regulation of peroxisome proliferator-activated receptor gamma-dependent macrophage differentiation. The Journal of Biological Chemistry. PMID 28330868 DOI: 10.1074/Jbc.M117.778761 |
0.081 |
|
| 2015 |
Euro L, Konovalova S, Asin-Cayuela J, Tulinius M, Griffin H, Horvath R, Taylor RW, Chinnery PF, Schara U, Thorburn DR, Suomalainen A, Chihade J, Tyynismaa H. Structural modeling of tissue-specific mitochondrial alanyl-tRNA synthetase (AARS2) defects predicts differential effects on aminoacylation. Frontiers in Genetics. 6: 21. PMID 25705216 DOI: 10.3389/Fgene.2015.00021 |
0.081 |
|
| 2015 |
Rygiel KA, Grady JP, Taylor RW, Tuppen HA, Turnbull DM. Triplex real-time PCR--an improved method to detect a wide spectrum of mitochondrial DNA deletions in single cells. Scientific Reports. 5: 9906. PMID 25989140 DOI: 10.1038/Srep09906 |
0.081 |
|
| 2013 |
Schaefer AM, Walker M, Turnbull DM, Taylor RW. Endocrine disorders in mitochondrial disease. Molecular and Cellular Endocrinology. 379: 2-11. PMID 23769710 DOI: 10.1016/J.Mce.2013.06.004 |
0.08 |
|
| 2013 |
Al-Owain M, Colak D, Albakheet A, Al-Younes B, Al-Humaidi Z, Al-Sayed M, Al-Hindi H, Al-Sugair A, Al-Muhaideb A, Rahbeeni Z, Al-Sehli A, Al-Fadhli F, Ozand PT, Taylor RW, Kaya N. Clinical and biochemical features associated with BCS1L mutation. Journal of Inherited Metabolic Disease. 36: 813-20. PMID 22991165 DOI: 10.1007/S10545-012-9536-4 |
0.079 |
|
| 2015 |
Chrysostomou A, Grady JP, Laude A, Taylor RW, Turnbull DM, Lax NZ. Investigating complex I deficiency in Purkinje cells and synapses in patients with mitochondrial disease. Neuropathology and Applied Neurobiology. PMID 26337858 DOI: 10.1111/Nan.12282 |
0.079 |
|
| 2013 |
Nesbitt V, Pitceathly RD, Turnbull DM, Taylor RW, Sweeney MG, Mudanohwo EE, Rahman S, Hanna MG, McFarland R. The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management. Journal of Neurology, Neurosurgery, and Psychiatry. 84: 936-8. PMID 23355809 DOI: 10.1136/Jnnp-2012-303528 |
0.078 |
|
| 2014 |
Pyle A, Ramesh V, Bartsakoulia M, Boczonadi V, Gomez-Duran A, Herczegfalvi A, Blakely EL, Smertenko T, Duff J, Eglon G, Moore D, Man PY, Douroudis K, Santibanez-Koref M, Griffin H, ... ... Taylor RW, et al. Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene. Journal of Neuromuscular Diseases. 1: 55-63. PMID 26380172 DOI: 10.3233/Jnd-140003 |
0.078 |
|
| 2015 |
Ng YS, Grady JP, Lax NZ, Bourke JP, Alston CL, Hardy SA, Falkous G, Schaefer AG, Radunovic A, Mohiddin SA, Ralph M, Alhakim A, Taylor RW, McFarland R, Turnbull DM, et al. Sudden adult death syndrome in m.3243A>G-related mitochondrial disease: an unrecognized clinical entity in young, asymptomatic adults. European Heart Journal. PMID 26188002 DOI: 10.1093/Eurheartj/Ehv306 |
0.078 |
|
| 2022 |
Meek S, Watson T, Eory L, McFarlane G, Wynne FJ, McCleary S, Dunn LEM, Charlton EM, Craig C, Shih B, Regan T, Taylor R, Sutherland L, Gossner A, Chintoan-Uta C, et al. Stem cell-derived porcine macrophages as a new platform for studying host-pathogen interactions. Bmc Biology. 20: 14. PMID 35027054 DOI: 10.1186/s12915-021-01217-8 |
0.077 |
|
| 2014 |
Kopajtich R, Nicholls TJ, Rorbach J, Metodiev MD, Freisinger P, Mandel H, Vanlander A, Ghezzi D, Carrozzo R, Taylor RW, Marquard K, Murayama K, Wieland T, Schwarzmayr T, Mayr JA, et al. Mutations in GTPBP3 cause a mitochondrial translation defect associated with hypertrophic cardiomyopathy, lactic acidosis, and encephalopathy. American Journal of Human Genetics. 95: 708-20. PMID 25434004 DOI: 10.1016/J.Ajhg.2014.10.017 |
0.077 |
|
| 2013 |
Whittaker RG, Hall E, Mansoor MK, Taylor RW, Turnbull DM. Incidence of carpal tunnel syndrome in adult patients with mitochondrial disease. Journal of the Peripheral Nervous System : Jpns. 18: 59-61. PMID 23521646 DOI: 10.1111/Jns5.12009 |
0.076 |
|
| 2014 |
Almalki A, Alston CL, Parker A, Simonic I, Mehta SG, He L, Reza M, Oliveira JM, Lightowlers RN, McFarland R, Taylor RW, Chrzanowska-Lightowlers ZM. Mutation of the human mitochondrial phenylalanine-tRNA synthetase causes infantile-onset epilepsy and cytochrome c oxidase deficiency. Biochimica Et Biophysica Acta. 1842: 56-64. PMID 24161539 DOI: 10.1016/j.bbadis.2013.10.008 |
0.076 |
|
| 2015 |
Haszard JJ, Skidmore PM, Williams SM, Taylor RW. Associations between parental feeding practices, problem food behaviours and dietary intake in New Zealand overweight children aged 4-8 years. Public Health Nutrition. 18: 1036-43. PMID 24955942 DOI: 10.1017/S1368980014001256 |
0.075 |
|
| 2014 |
Pfeffer G, Gorman GS, Griffin H, Kurzawa-Akanbi M, Blakely EL, Wilson I, Sitarz K, Moore D, Murphy JL, Alston CL, Pyle A, Coxhead J, Payne B, Gorrie GH, Longman C, ... ... Taylor RW, et al. Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance. Brain : a Journal of Neurology. 137: 1323-36. PMID 24727571 DOI: 10.1093/Brain/Awu060 |
0.075 |
|
| 2014 |
Uusimaa J, Evans J, Smith C, Butterworth A, Craig K, Ashley N, Liao C, Carver J, Diot A, Macleod L, Hargreaves I, Al-Hussaini A, Faqeih E, Asery A, Al Balwi M, ... ... Taylor RW, et al. Clinical, biochemical, cellular and molecular characterization of mitochondrial DNA depletion syndrome due to novel mutations in the MPV17 gene. European Journal of Human Genetics : Ejhg. 22: 184-91. PMID 23714749 DOI: 10.1038/ejhg.2013.112 |
0.074 |
|
| 2014 |
Yarham JW, Lamichhane TN, Pyle A, Mattijssen S, Baruffini E, Bruni F, Donnini C, Vassilev A, He L, Blakely EL, Griffin H, Santibanez-Koref M, Bindoff LA, Ferrero I, Chinnery PF, ... ... Taylor RW, et al. Defective i6A37 modification of mitochondrial and cytosolic tRNAs results from pathogenic mutations in TRIT1 and its substrate tRNA. Plos Genetics. 10: e1004424. PMID 24901367 DOI: 10.1371/Journal.Pgen.1004424 |
0.074 |
|
| 2015 |
Alston CL, Ceccatelli Berti C, Blakely EL, Oláhová M, He L, McMahon CJ, Olpin SE, Hargreaves IP, Nolli C, McFarland R, Goffrini P, O'Sullivan MJ, Taylor RW. A recessive homozygous p.Asp92Gly SDHD mutation causes prenatal cardiomyopathy and a severe mitochondrial complex II deficiency. Human Genetics. 134: 869-79. PMID 26008905 DOI: 10.1007/s00439-015-1568-z |
0.074 |
|
| 2015 |
Brito S, Thompson K, Campistol J, Colomer J, Hardy SA, He L, Fernández-Marmiesse A, Palacios L, Jou C, Jiménez-Mallebrera C, Armstrong J, Montero R, Artuch R, Tischner C, Wenz T, ... ... Taylor RW, et al. Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations. Frontiers in Genetics. 6: 102. PMID 25852744 DOI: 10.3389/fgene.2015.00102 |
0.073 |
|
| 2015 |
Bargiela D, Shanmugarajah P, Lo C, Blakely EL, Taylor RW, Horvath R, Wharton S, Chinnery PF, Hadjivassiliou M. Mitochondrial pathology in progressive cerebellar ataxia. Cerebellum & Ataxias. 2: 16. PMID 26640698 DOI: 10.1186/s40673-015-0035-x |
0.073 |
|
| 2016 |
Floyd BJ, Wilkerson EM, Veling MT, Minogue CE, Xia C, Beebe ET, Wrobel RL, Cho H, Kremer LS, Alston CL, Gromek KA, Dolan BK, Ulbrich A, Stefely JA, Bohl SL, ... ... Taylor RW, et al. Mitochondrial Protein Interaction Mapping Identifies Regulators of Respiratory Chain Function. Molecular Cell. PMID 27499296 DOI: 10.1016/J.Molcel.2016.06.033 |
0.073 |
|
| 2016 |
Dalla Rosa I, Cámara Y, Durigon R, Moss CF, Vidoni S, Akman G, Hunt L, Johnson MA, Grocott S, Wang L, Thorburn DR, Hirano M, Poulton J, Taylor RW, Elgar G, et al. MPV17 Loss Causes Deoxynucleotide Insufficiency and Slow DNA Replication in Mitochondria. Plos Genetics. 12: e1005779. PMID 26760297 DOI: 10.1371/Journal.Pgen.1005779 |
0.072 |
|
| 2015 |
Lax NZ, Alston CL, Schon K, Park SM, Krishnakumar D, He L, Falkous G, Ogilvy-Stuart A, Lees C, King RH, Hargreaves IP, Brown GK, McFarland R, Dean AF, Taylor RW. Neuropathologic Characterization of Pontocerebellar Hypoplasia Type 6 Associated With Cardiomyopathy and Hydrops Fetalis and Severe Multisystem Respiratory Chain Deficiency due to Novel RARS2 Mutations. Journal of Neuropathology and Experimental Neurology. 74: 688-703. PMID 26083569 DOI: 10.1097/NEN.0000000000000209 |
0.072 |
|
| 2013 |
Spendiff S, Reza M, Murphy JL, Gorman G, Blakely EL, Taylor RW, Horvath R, Campbell G, Newman J, Lochmüller H, Turnbull DM. Mitochondrial DNA deletions in muscle satellite cells: implications for therapies. Human Molecular Genetics. 22: 4739-47. PMID 23847047 DOI: 10.1093/Hmg/Ddt327 |
0.071 |
|
| 2016 |
Salmon AR, Esteban R, Taylor RW, Hugall JT, Smith CA, Whyte G, Scherman OA, Aizpurua J, Abell C, Baumberg JJ. Monitoring Early-Stage Nanoparticle Assembly in Microdroplets by Optical Spectroscopy and SERS. Small (Weinheim An Der Bergstrasse, Germany). PMID 26865562 DOI: 10.1002/Smll.201503513 |
0.071 |
|
| 2016 |
Gupta A, Colmenero I, Ragge NK, Blakely EL, He L, McFarland R, Taylor RW, Vogt J, Milford DV. Compound heterozygous RMND1 gene variants associated with chronic kidney disease, dilated cardiomyopathy and neurological involvement: a case report. Bmc Research Notes. 9: 325. PMID 27350610 DOI: 10.1186/s13104-016-2131-2 |
0.07 |
|
| 2016 |
Moir C, Meredith-Jones K, Taylor BJ, Gray A, Heath AM, Dale K, Galland B, Lawrence J, Sayers RM, Taylor RW. Early Intervention to Encourage Physical Activity in Infants and Toddlers: An RCT. Medicine and Science in Sports and Exercise. PMID 27471782 DOI: 10.1249/MSS.0000000000001055 |
0.07 |
|
| 2014 |
Tserkezis C, Taylor RW, Beitner J, Esteban R, Baumberg JJ, Aizpurua J. Optical response of metallic nanoparticle heteroaggregates with subnanometric gaps Particle and Particle Systems Characterization. 31: 152-160. DOI: 10.1002/Ppsc.201300287 |
0.068 |
|
| 2013 |
Alston CL, Schaefer AM, Raman P, Solaroli N, Krishnan KJ, Blakely EL, He L, Craig K, Roberts M, Vyas A, Nixon J, Horvath R, Turnbull DM, Karlsson A, Gorman GS, ... Taylor RW, et al. Late-onset respiratory failure due to TK2 mutations causing multiple mtDNA deletions. Neurology. 81: 2051-3. PMID 24198295 DOI: 10.1212/01.Wnl.0000436931.94291.E6 |
0.068 |
|
| 2015 |
Puranik CP, Hill A, Henderson Jeffries K, Harrell SN, Taylor RW, Frazier-Bowers SA. Characterization of short root anomaly in a Mexican cohort--hereditary idiopathic root malformation. Orthodontics & Craniofacial Research. 18: 62-70. PMID 25865534 DOI: 10.1111/ocr.12073 |
0.068 |
|
| 2014 |
Kraus CD, Campbell PM, Spears R, Taylor RW, Buschang PH. Bony adaptation after expansion with light-to-moderate continuous forces. American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics. 145: 655-66. PMID 24785930 DOI: 10.1016/j.ajodo.2014.01.017 |
0.068 |
|
| 2015 |
Cameron SL, Taylor RW, Heath AL. Development and pilot testing of Baby-Led Introduction to SolidS--a version of Baby-Led Weaning modified to address concerns about iron deficiency, growth faltering and choking. Bmc Pediatrics. 15: 99. PMID 26306667 DOI: 10.1186/s12887-015-0422-8 |
0.067 |
|
| 2016 |
Mathieu L, Costa AL, le Bachelier C, Slama A, Lebre AS, Taylor RW, Bastin J, Djouadi F. Resveratrol attenuates oxidative stress in mitochondrial Complex I deficiency: involvement of SIRT3. Free Radical Biology & Medicine. PMID 27126960 DOI: 10.1016/j.freeradbiomed.2016.04.027 |
0.067 |
|
| 2014 |
Haghighi A, Haack TB, Atiq M, Mottaghi H, Haghighi-Kakhki H, Bashir RA, Ahting U, Feichtinger RG, Mayr JA, Rötig A, Lebre AS, Klopstock T, Dworschak A, Pulido N, Saeed MA, ... ... Taylor RW, et al. Sengers syndrome: six novel AGK mutations in seven new families and review of the phenotypic and mutational spectrum of 29 patients. Orphanet Journal of Rare Diseases. 9: 119. PMID 25208612 DOI: 10.1186/S13023-014-0119-3 |
0.066 |
|
| 2015 |
Taylor R, Miller RH, Miller RD, Porter M, Dalgleish J, Prince JT. Automated structural classification of lipids by machine learning. Bioinformatics (Oxford, England). 31: 621-5. PMID 25359887 DOI: 10.1093/bioinformatics/btu723 |
0.064 |
|
| 2015 |
Rygiel KA, Miller J, Grady JP, Rocha MC, Taylor RW, Turnbull DM. Mitochondrial and inflammatory changes in sporadic inclusion body myositis. Neuropathology and Applied Neurobiology. 41: 288-303. PMID 24750247 DOI: 10.1111/Nan.12149 |
0.062 |
|
| 2015 |
Schiff M, Haberberger B, Xia C, Mohsen AW, Goetzman ES, Wang Y, Uppala R, Zhang Y, Karunanidhi A, Prabhu D, Alharbi H, Prochownik EV, Haack T, Häberle J, Munnich A, ... ... Taylor RW, et al. Complex I assembly function and fatty acid oxidation enzyme activity of ACAD9 both contribute to disease severity in ACAD9 deficiency. Human Molecular Genetics. 24: 3238-47. PMID 25721401 DOI: 10.1093/Hmg/Ddv074 |
0.062 |
|
| 2013 |
Giordano C, Perli E, Orlandi M, Pisano A, Tuppen HA, He L, Ierinò R, Petruzziello L, Terzi A, Autore C, Petrozza V, Gallo P, Taylor RW, d'Amati G. Cardiomyopathies due to homoplasmic mitochondrial tRNA mutations: morphologic and molecular features. Human Pathology. 44: 1262-70. PMID 23332932 DOI: 10.1016/j.humpath.2012.10.011 |
0.061 |
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| 2014 |
Perli E, Giordano C, Pisano A, Montanari A, Campese AF, Reyes A, Ghezzi D, Nasca A, Tuppen HA, Orlandi M, Di Micco P, Poser E, Taylor RW, Colotti G, Francisci S, et al. The isolated carboxy-terminal domain of human mitochondrial leucyl-tRNA synthetase rescues the pathological phenotype of mitochondrial tRNA mutations in human cells. Embo Molecular Medicine. 6: 169-82. PMID 24413190 DOI: 10.1002/emmm.201303198 |
0.061 |
|
| 2014 |
Di Foggia V, Zhang X, Licastro D, Gerli MF, Phadke R, Muntoni F, Mourikis P, Tajbakhsh S, Ellis M, Greaves LC, Taylor RW, Cossu G, Robson LG, Marino S. Bmi1 enhances skeletal muscle regeneration through MT1-mediated oxidative stress protection in a mouse model of dystrophinopathy. The Journal of Experimental Medicine. 211: 2617-33. PMID 25452464 DOI: 10.1084/jem.20140317 |
0.06 |
|
| 2013 |
Blakely EL, Yarham JW, Alston CL, Craig K, Poulton J, Brierley C, Park SM, Dean A, Xuereb JH, Anderson KN, Compston A, Allen C, Sharif S, Enevoldson P, Wilson M, ... ... Taylor RW, et al. Pathogenic mitochondrial tRNA point mutations: nine novel mutations affirm their importance as a cause of mitochondrial disease. Human Mutation. 34: 1260-8. PMID 23696415 DOI: 10.1002/Humu.22358 |
0.06 |
|
| 2020 |
Melmer PD, Taylor R, Muertos K, Sciarretta JD. Stats and ladders: Injury risk and outcomes following falls from ladders. American Journal of Surgery. PMID 32172926 DOI: 10.1016/j.amjsurg.2020.02.051 |
0.059 |
|
| 2014 |
Taylor RW, Martens WL. Hyper-compression in music production: Listener preferences on dynamic range reduction 136th Audio Engineering Society Convention 2014. 94-103. |
0.058 |
|
| 2014 |
Dawson AM, Taylor RW, Williams SM, Taylor BJ, Brown DA. Do parents recall and understand children's weight status information after BMI screening? A randomised controlled trial. Bmj Open. 4: e004481. PMID 25079920 DOI: 10.1136/bmjopen-2013-004481 |
0.058 |
|
| 2015 |
Hanisch F, Kornhuber M, Alston CL, Taylor RW, Deschauer M, Zierz S. SANDO syndrome in a cohort of 107 patients with CPEO and mitochondrial DNA deletions. Journal of Neurology, Neurosurgery, and Psychiatry. 86: 630-4. PMID 25143630 DOI: 10.1136/jnnp-2013-306748 |
0.058 |
|
| 2019 |
Melmer PD, Chaconas C, Taylor R, Verrico E, Cockcroft A, Pinnola A, Holmes S, Sciarretta JD, Davis JM. Impact of Laparoscopy on Training: Are Open Appendectomy and Cholecystectomy on the Brink of Extinction? The American Surgeon. 85: 761-763. PMID 31405424 |
0.057 |
|
| 2016 |
Taylor RW. Gut Motility Issues in Critical Illness. Critical Care Clinics. 32: 191-201. PMID 27016161 DOI: 10.1016/j.ccc.2015.11.003 |
0.056 |
|
| 2016 |
Taylor RW. Gut Motility Issues in Critical Illness Critical Care Clinics. DOI: 10.1016/j.ccc.2015.11.003 |
0.056 |
|
| 2015 |
Staufner C, Haack TB, Köpke MG, Straub BK, Kölker S, Thiel C, Freisinger P, Baric I, McKiernan PJ, Dikow N, Harting I, Beisse F, Burgard P, Kotzaeridou U, Lenz D, ... ... Taylor RW, et al. Recurrent acute liver failure due to NBAS deficiency: phenotypic spectrum, disease mechanisms, and therapeutic concepts. Journal of Inherited Metabolic Disease. PMID 26541327 DOI: 10.1007/S10545-015-9896-7 |
0.056 |
|
| 2016 |
Morison BJ, Taylor RW, Haszard JJ, Schramm CJ, Williams Erickson L, Fangupo LJ, Fleming EA, Luciano A, Heath AL. How different are baby-led weaning and conventional complementary feeding? A cross-sectional study of infants aged 6-8 months. Bmj Open. 6: e010665. PMID 27154478 DOI: 10.1136/bmjopen-2015-010665 |
0.056 |
|
| 2015 |
Brito S, Thompson K, Campistol J, Colomer J, Hardy SA, He L, Fernández-Marmiesse A, Palacios L, Jou C, Jiménez-Mallebrera C, Armstrong J, Montero R, Artuch R, Tischner C, Wenz T, ... ... Taylor RW, et al. Corrigendum: Long-term survival in a child with severe encephalopathy, multiple respiratory chain deficiency and GFM1 mutations. Frontiers in Genetics. 6: 254. PMID 26284110 DOI: 10.3389/fgene.2015.00254 |
0.055 |
|
| 2015 |
Pisano A, Cerbelli B, Perli E, Pelullo M, Bargelli V, Preziuso C, Mancini M, He L, Bates MG, Lucena JR, Della Monica PL, Familiari G, Petrozza V, Nediani C, Taylor RW, et al. Impaired mitochondrial biogenesis is a common feature to myocardial hypertrophy and end-stage ischemic heart failure. Cardiovascular Pathology : the Official Journal of the Society For Cardiovascular Pathology. 25: 103-112. PMID 26764143 DOI: 10.1016/j.carpath.2015.09.009 |
0.055 |
|
| 2016 |
Ehinger JK, Piel S, Ford R, Karlsson M, Sjövall F, Frostner EÅ, Morota S, Taylor RW, Turnbull DM, Cornell C, Moss SJ, Metzsch C, Hansson MJ, Fliri H, Elmér E. Cell-permeable succinate prodrugs bypass mitochondrial complex I deficiency. Nature Communications. 7: 12317. PMID 27502960 DOI: 10.1038/Ncomms12317 |
0.054 |
|
| 2014 |
Grünewald A, Lax NZ, Rocha MC, Reeve AK, Hepplewhite PD, Rygiel KA, Taylor RW, Turnbull DM. Quantitative quadruple-label immunofluorescence of mitochondrial and cytoplasmic proteins in single neurons from human midbrain tissue. Journal of Neuroscience Methods. 232: 143-9. PMID 24880043 DOI: 10.1016/J.Jneumeth.2014.05.026 |
0.054 |
|
| 2013 |
Jalil A, Usmani HA, Khan MI, Blakely EL, Taylor RW, Vassallo G, Ashworth J. Bilateral paediatric optic neuropathy precipitated by vitamin B12 deficiency and a novel mitochondrial DNA mutation. International Ophthalmology. 33: 687-90. PMID 23572439 DOI: 10.1007/s10792-013-9773-z |
0.054 |
|
| 2020 |
Melmer P, Taylor R, Muertos K, Sciarretta JD. Managing Craniomaxillofacial Injury Without Inpatient Consult: Outcomes and Patient Cost Savings. The American Surgeon. 3134820923329. PMID 32683930 DOI: 10.1177/0003134820923329 |
0.053 |
|
| 2014 |
Taylor RW. Evidence for the absence of worker behavioral subcastes in the sociobiologically primitive australian ant Nothomyrmecia macrops clark (Hymenoptera: Formicidae: myrmeciinae) Psyche (New York). 2014. DOI: 10.1155/2014/232057 |
0.052 |
|
| 2013 |
Taylor RW, Coulston RJ, Biedermann F, Mahajan S, Baumberg JJ, Scherman OA. In situ SERS monitoring of photochemistry within a nanojunction reactor. Nano Letters. 13: 5985-90. PMID 24188432 DOI: 10.1021/Nl403164C |
0.052 |
|
| 2016 |
de Laat P, Janssen MC, Alston CL, Taylor RW, Rodenburg RJ, Smeitink JA. Three families with 'de novo' m.3243A > G mutation. Bba Clinical. 6: 19-24. PMID 27331024 DOI: 10.1016/j.bbacli.2016.04.007 |
0.051 |
|
| 2013 |
Bates MG, Newman JH, Jakovljevic DG, Hollingsworth KG, Alston CL, Zalewski P, Klawe JJ, Blamire AM, MacGowan GA, Keavney BD, Bourke JP, Schaefer A, McFarland R, Newton JL, Turnbull DM, ... Taylor RW, et al. Defining cardiac adaptations and safety of endurance training in patients with m.3243A>G-related mitochondrial disease. International Journal of Cardiology. 168: 3599-608. PMID 23742928 DOI: 10.1016/J.Ijcard.2013.05.062 |
0.051 |
|
| 2015 |
Perli E, Fiorillo A, Giordano C, Pisano A, Montanari A, Grazioli P, Campese AF, Di Micco P, Tuppen HA, Genovese I, Poser E, Preziuso C, Taylor RW, Morea V, Colotti G, et al. Short peptides from leucyl-tRNA synthetase rescue disease-causing mitochondrial tRNA point mutations. Human Molecular Genetics. PMID 26721932 DOI: 10.1093/hmg/ddv619 |
0.051 |
|
| 2014 |
Dunn W, O'Neil M, Zhao J, Wu CH, Roberts B, Chakraborty S, Sherman C, Weaver B, Taylor R, Olson J, Olyaee M, Gilroy R, Schmitt T, Wan YJ, Weinman SA. Donor PNPLA3 rs738409 genotype affects fibrosis progression in liver transplantation for hepatitis C. Hepatology (Baltimore, Md.). 59: 453-60. PMID 24123231 DOI: 10.1002/Hep.26758 |
0.05 |
|
| 2015 |
Peterson S, Taylor R, Sawyer M, Nagy P, Paine L, Berenholtz S, Miller R, Petty B. The Power of Involving House Staff in Quality Improvement: An Interdisciplinary House Staff-Driven Vaccination Initiative. American Journal of Medical Quality : the Official Journal of the American College of Medical Quality. 30: 323-7. PMID 24814939 DOI: 10.1177/1062860614532682 |
0.05 |
|
| 2014 |
Dawson AM, Brown DA, Cox A, Williams SM, Treacy L, Haszard J, Meredith-Jones K, Hargreaves E, Taylor BJ, Ross J, Taylor RW. Using motivational interviewing for weight feedback to parents of young children. Journal of Paediatrics and Child Health. 50: 461-70. PMID 24617494 DOI: 10.1111/jpc.12518 |
0.049 |
|
| 2020 |
Yu EY, Hancock ML, Aronson W, Flaig T, Belkoff L, Tutrone R, Taylor R, Hardigan PC, Getzenberg RH. Phase 2 Trial of GTx-758, an Estrogen Receptor Alpha Agonist, in Men With Castration-Resistant Prostate Cancer. Clinical Genitourinary Cancer. PMID 32321673 DOI: 10.1016/j.clgc.2020.03.012 |
0.049 |
|
| 2015 |
Lehmann D, Schubert K, Joshi PR, Baty K, Blakely EL, Zierz S, Taylor RW, Deschauer M. A novel m.7539C>T point mutation in the mt-tRNA(Asp) gene associated with multisystemic mitochondrial disease. Neuromuscular Disorders : Nmd. 25: 81-4. PMID 25447692 DOI: 10.1016/j.nmd.2014.09.008 |
0.049 |
|
| 2015 |
Cameron SL, Heath AL, Gray AR, Churcher B, Davies RS, Newlands A, Galland BC, Sayers RM, Lawrence JA, Taylor BJ, Taylor RW. Lactation Consultant Support from Late Pregnancy with an Educational Intervention at 4 Months of Age Delays the Introduction of Complementary Foods in a Randomized Controlled Trial. The Journal of Nutrition. 145: 1481-90. PMID 25995280 DOI: 10.3945/jn.114.202689 |
0.049 |
|
| 2015 |
Hall AM, Vilasi A, Garcia-Perez I, Lapsley M, Alston CL, Pitceathly RD, McFarland R, Schaefer AM, Turnbull DM, Beaumont NJ, Hsuan JJ, Cutillas PR, Lindon JC, Holmes E, Unwin RJ, ... Taylor RW, et al. The urinary proteome and metabonome differ from normal in adults with mitochondrial disease. Kidney International. 87: 610-22. PMID 25207879 DOI: 10.1038/Ki.2014.297 |
0.048 |
|
| 2014 |
Cuairán C, Campbell PM, Kontogiorgos E, Taylor RW, Melo AC, Buschang PH. Local application of zoledronate enhances miniscrew implant stability in dogs. American Journal of Orthodontics and Dentofacial Orthopedics : Official Publication of the American Association of Orthodontists, Its Constituent Societies, and the American Board of Orthodontics. 145: 737-49. PMID 24880844 DOI: 10.1016/J.Ajodo.2014.01.020 |
0.048 |
|
| 2013 |
Kumar BN, Taylor RW, Pask GM, Zwiebel LJ, Newcomb RD, Christie DL. A conserved aspartic acid is important for agonist (VUAA1) and odorant/tuning receptor-dependent activation of the insect odorant co-receptor (Orco). Plos One. 8: e70218. PMID 23894621 DOI: 10.1371/Journal.Pone.0070218 |
0.047 |
|
| 2015 |
Casey JP, Crushell E, Thompson K, Twomey E, He L, Ennis S, Philip RK, Taylor RW, King MD, Lynch SA. Periventricular Calcification, Abnormal Pterins and Dry Thickened Skin: Expanding the Clinical Spectrum of RMND1? Jimd Reports. PMID 26238252 DOI: 10.1007/8904_2015_479 |
0.047 |
|
| 2015 |
Fangupo LJ, Heath AM, Williams SM, Somerville MR, Lawrence JA, Gray AR, Taylor BJ, Mills VC, Watson EO, Galland BC, Sayers RM, Hanna MB, Taylor RW. Impact of an early-life intervention on the nutrition behaviors of 2-y-old children: a randomized controlled trial. The American Journal of Clinical Nutrition. PMID 26224299 DOI: 10.3945/ajcn.115.111823 |
0.047 |
|
| 2016 |
Kullar P, Alston CL, Ball S, Blakely EL, Differ AM, Fratter C, Sweeney MG, Taylor RW, Chinnery PF. The frequency of the m.1555A>G (MTRNR1) variant in UK patients with suspected mitochondrial deafness. Hearing, Balance and Communication. 14: 101-102. PMID 27257558 DOI: 10.3109/21695717.2016.1151124 |
0.047 |
|
| 2017 |
Nawabi A, Garcia J, Jimenez A, Turner S, Olyaee M, Cui W, Schmitt T, Kumer S, Reintjes M, Taylor R, Olson J, Nawabi N, Nawabi P. The presence of donor liver granuloma requiring further workup to rule out parasitic disease. Journal of Surgical Case Reports. 2017: rjx042. PMID 28458868 DOI: 10.1093/jscr/rjx042 |
0.047 |
|
| 2015 |
Whittaker RG, Devine HE, Gorman GS, Schaefer AM, Horvath R, Ng Y, Nesbitt V, Lax NZ, McFarland R, Cunningham MO, Taylor RW, Turnbull DM. Epilepsy in adults with mitochondrial disease: A cohort study. Annals of Neurology. PMID 26381753 DOI: 10.1002/Ana.24525 |
0.046 |
|
| 2017 |
Pandya P, Pant C, Taylor R, Oni O. Impact of sustained virological response to chronic hepatitic C antiviral therapy on new onset diabetes mellitus type 2 after controlling for metabolic syndrome. Journal of Investigative Medicine : the Official Publication of the American Federation For Clinical Research. PMID 28232517 DOI: 10.1136/jim-2016-000343 |
0.045 |
|
| 2015 |
Watson EO, Heath AL, Taylor RW, Mills VC, Barris AC, Skidmore PM. Relative validity and reproducibility of an FFQ to determine nutrient intakes of New Zealand toddlers aged 12-24 months. Public Health Nutrition. 1-7. PMID 25824599 DOI: 10.1017/S1368980015000841 |
0.044 |
|
| 2015 |
Taylor RW, Cox A, Knight L, Brown DA, Meredith-Jones K, Haszard JJ, Dawson AM, Taylor BJ, Williams SM. A Tailored Family-Based Obesity Intervention: A Randomized Trial. Pediatrics. 136: 281-9. PMID 26195541 DOI: 10.1542/peds.2015-0595 |
0.044 |
|
| 2023 |
Melmer PD, Taylor R, Vera L, Wong D, Santos AP, Chung T, Sola JR, Castater CA, Nguyen J, Nottingham JM, Berg AF, Sleeman D, Namias N, Daley BJ, Procter L, et al. Optimizing Transitions of Care and Enhancing Surgical Education on Acute Care Surgery: A Multi-Institutional Survey Study. Journal of Surgical Education. PMID 37442698 DOI: 10.1016/j.jsurg.2023.06.025 |
0.043 |
|
| 2016 |
Cook DJ, Johnstone J, Marshall JC, Lauzier F, Thabane L, Mehta S, Dodek PM, McIntyre L, Pagliarello J, Henderson W, Taylor RW, Cartin-Ceba R, Golan E, Herridge M, Wood G, et al. Probiotics: Prevention of Severe Pneumonia and Endotracheal Colonization Trial-PROSPECT: a pilot trial. Trials. 17: 377. PMID 27480757 DOI: 10.1186/S13063-016-1495-X |
0.043 |
|
| 2022 |
Zain A, Lin JB, Thong WY, Taylor R. Super-refractory status epilepticus following acute Epstein-Barr virus myocarditis. Journal of Paediatrics and Child Health. PMID 35791665 DOI: 10.1111/jpc.16112 |
0.042 |
|
| 2015 |
Taylor RW, Williams SM, Dawson AM, Haszard JJ, Brown DA. Parental motivation to change body weight in young overweight children. Public Health Nutrition. 18: 1807-14. PMID 25287723 DOI: 10.1017/S1368980014002171 |
0.041 |
|
| 2016 |
Pant C, Jani BS, Desai M, Deshpande A, Pandya P, Taylor R, Gilroy R, Olyaee M. Hepatorenal syndrome in hospitalized patients with chronic liver disease: results from the Nationwide Inpatient Sample 2002-2012. Journal of Investigative Medicine : the Official Publication of the American Federation For Clinical Research. 64: 33-8. PMID 26755811 DOI: 10.1136/jim-d-15-00181 |
0.041 |
|
| 2015 |
McCann BJ, Tuppen HA, Küsters B, Lammens M, Smeitink JA, Taylor RW, Rodenburg RJ, Wortmann SB. A novel mitochondrial DNA m.7507A>G mutation is only pathogenic at high levels of heteroplasmy. Neuromuscular Disorders : Nmd. 25: 262-7. PMID 25497401 DOI: 10.1016/j.nmd.2014.11.002 |
0.041 |
|
| 2014 |
Williams SM, Farmer VL, Taylor BJ, Taylor RW. Do more active children sleep more? A repeated cross-sectional analysis using accelerometry. Plos One. 9: e93117. PMID 24695112 DOI: 10.1371/journal.pone.0093117 |
0.041 |
|
| 2014 |
Romaine IM, Taylor RW, Saidu SP, Kim K, Sulikowski GA, Zwiebel LJ, Waterson AG. Narrow SAR in odorant sensing Orco receptor agonists. Bioorganic & Medicinal Chemistry Letters. 24: 2613-6. PMID 24813736 DOI: 10.1016/J.Bmcl.2014.04.081 |
0.041 |
|
| 2015 |
Meredith-Jones KA, Williams SM, Taylor RW. Bioelectrical impedance as a measure of change in body composition in young children. Pediatric Obesity. 10: 252-9. PMID 25291012 DOI: 10.1111/ijpo.263 |
0.041 |
|
| 2014 |
Al-Hussaini A, Faqeih E, El-Hattab AW, Alfadhel M, Asery A, Alsaleem B, Bakhsh E, Ali A, Alasmari A, Lone K, Nahari A, Eyaid W, Al Balwi M, Craig K, Butterworth A, ... ... Taylor RW, et al. Clinical and molecular characteristics of mitochondrial DNA depletion syndrome associated with neonatal cholestasis and liver failure. The Journal of Pediatrics. 164: 553-9.e1-2. PMID 24321534 DOI: 10.1016/j.jpeds.2013.10.082 |
0.04 |
|
| 2014 |
Ruso S, Campbell PM, Rossmann J, Opperman LA, Taylor RW, Buschang PH. Bone response to buccal tooth movements-with and without flapless alveolar decortication. European Journal of Orthodontics. 36: 613-23. PMID 23965291 DOI: 10.1093/Ejo/Cjt057 |
0.039 |
|
| 2015 |
Carrozzo R, Verrigni D, Rasmussen M, de Coo R, Amartino H, Bianchi M, Buhas D, Mesli S, Naess K, Born AP, Woldseth B, Prontera P, Batbayli M, Ravn K, Joensen F, ... ... Taylor RW, et al. Succinate-CoA ligase deficiency due to mutations in SUCLA2 and SUCLG1: phenotype and genotype correlations in 71 patients. Journal of Inherited Metabolic Disease. PMID 26475597 DOI: 10.1007/s10545-015-9894-9 |
0.039 |
|
| 2021 |
Williams MJ, Grissett G, Beam J, Taylor R, Cunningham H, Williams ML. What is your diagnosis? Blood smear from a bull. Veterinary Clinical Pathology. PMID 33860961 DOI: 10.1111/vcp.12970 |
0.039 |
|
| 2014 |
Chau C, Campbell PM, Deljavan N, Taylor RW, Buschang PH. Retention of sealants during orthodontic treatment: An in vitro comparison of two etching protocols. The Angle Orthodontist. PMID 25469669 DOI: 10.2319/060614.1 |
0.038 |
|
| 2013 |
Henderson M, De Waele L, Hudson J, Eagle M, Sewry C, Marsh J, Charlton R, He L, Blakely EL, Horrocks I, Stewart W, Taylor RW, Longman C, Bushby K, Barresi R. Recessive desmin-null muscular dystrophy with central nuclei and mitochondrial abnormalities. Acta Neuropathologica. 125: 917-9. PMID 23575897 DOI: 10.1007/s00401-013-1113-x |
0.038 |
|
| 2016 |
Ng YS, Feeney C, Schaefer AM, Holmes CE, Hynd P, Alston CL, Grady JP, Roberts M, Maguire M, Bright A, Taylor RW, Yiannakou Y, McFarland R, Turnbull DM, Gorman GS. Pseudo-obstruction, stroke and mitochondrial dysfunction: A lethal combination. Annals of Neurology. PMID 27453452 DOI: 10.1002/Ana.24736 |
0.037 |
|
| 2016 |
Dombi E, Diot A, Morten K, Carver J, Lodge T, Fratter C, Ng YS, Liao C, Muir R, Blakely EL, Hargreaves I, Al-Dosary M, Sarkar G, Hickman SJ, Downes SM, ... ... Taylor RW, et al. The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy. Neurology. PMID 27164671 DOI: 10.1212/WNL.0000000000002688 |
0.037 |
|
| 2022 |
Wong JJM, Ong JSM, Ong C, Allen JC, Gandhi M, Fan L, Taylor R, Lim JKB, Poh PF, Chiou FK, Lee JH. Protein supplementation versus standard feeds in underweight critically ill children: a pilot dual-centre randomised controlled trial protocol. Bmj Open. 12: e047907. PMID 34983751 DOI: 10.1136/bmjopen-2020-047907 |
0.037 |
|
| 2013 |
Hüsken N, Taylor RW, Zigah D, Taveau JC, Lambert O, Scherman OA, Baumberg JJ, Kuhn A. Electrokinetic assembly of one-dimensional nanoparticle chains with cucurbit[7]uril controlled subnanometer junctions. Nano Letters. 13: 6016-22. PMID 24180422 DOI: 10.1021/Nl403224Q |
0.037 |
|
| 2015 |
Pant C, Desai M, Deshpande A, Taylor R, Olyaee M, Gilroy R. Esophageal variceal bleeding in hospitalized patients with cirrhosis. Journal of Hospital Medicine. 10: 453-6. PMID 25976490 DOI: 10.1002/jhm.2360 |
0.037 |
|
| 2013 |
Taylor RW, Williams SM, Dawson AM, Taylor BJ, Meredith-Jones K, Brown D. What factors influence uptake into family-based obesity treatment after weight screening? The Journal of Pediatrics. 163: 1657-1662.e1. PMID 24075623 DOI: 10.1016/j.jpeds.2013.08.033 |
0.037 |
|
| 2022 |
Gunsalus K, Taylor R, Croix N. Calcification and osseous metaplasia of the meibomian glands of a horse. Veterinary Ophthalmology. PMID 35861137 DOI: 10.1111/vop.13011 |
0.036 |
|
| 2015 |
Besse A, Wu P, Bruni F, Donti T, Graham BH, Craigen WJ, McFarland R, Moretti P, Lalani S, Scott KL, Taylor RW, Bonnen PE. The GABA transaminase, ABAT, is essential for mitochondrial nucleoside metabolism. Cell Metabolism. 21: 417-27. PMID 25738457 DOI: 10.1016/J.Cmet.2015.02.008 |
0.036 |
|
| 2016 |
McKiernan P, Ball S, Santra S, Foster K, Fratter C, Poulton J, Craig K, McFarland R, Rahman S, Hargreaves I, Gupte G, Sharif K, Taylor RW. Incidence of Primary Mitochondrial Disease in Children Presenting With Acute Liver Failure Under 2 Years of Age. Journal of Pediatric Gastroenterology and Nutrition. PMID 27482763 DOI: 10.1097/MPG.0000000000001345 |
0.036 |
|
| 2016 |
Lewis-Smith D, Kamer KJ, Griffin H, Childs AM, Pysden K, Titov D, Duff J, Pyle A, Taylor RW, Yu-Wai-Man P, Ramesh V, Horvath R, Mootha VK, Chinnery PF. Homozygous deletion in MICU1 presenting with fatigue and lethargy in childhood. Neurology. Genetics. 2: e59. PMID 27123478 DOI: 10.1212/Nxg.0000000000000059 |
0.035 |
|
| 2015 |
Payne BA, Gardner K, Blakely EL, Maddison P, Horvath R, Taylor RW, Chinnery PF. Clinical and pathological features of mitochondrial DNA deletion disease following antiretroviral treatment. Jama Neurology. 72: 603-5. PMID 25961175 DOI: 10.1001/jamaneurol.2015.0150 |
0.035 |
|
| 2012 |
Banerjee R, Chao JC, Taylor R, Siddiqui A. Management of calcaneal tuberosity fractures. The Journal of the American Academy of Orthopaedic Surgeons. 20: 253-8. PMID 22474095 DOI: 10.5435/JAAOS-20-04-253 |
0.035 |
|
| 2011 |
Dykhne T, Taylor R, Florence A, Billinge SJ. Data requirements for the reliable use of atomic pair distribution functions in amorphous pharmaceutical fingerprinting. Pharmaceutical Research. 28: 1041-8. PMID 21222019 DOI: 10.1007/s11095-010-0350-0 |
0.035 |
|
| 2014 |
Jones ST, Taylor RW, Esteban R, Abo-Hamed EK, Bomans PH, Sommerdijk NA, Aizpurua J, Baumberg JJ, Scherman OA. Gold nanorods with sub-nanometer separation using cucurbit[n]uril for SERS applications. Small (Weinheim An Der Bergstrasse, Germany). 10: 4298-303. PMID 25070698 DOI: 10.1002/Smll.201401063 |
0.034 |
|
| 2022 |
Dunn W, Song X, Koestler D, Grdinovac K, Al-Hihi E, Chen J, Taylor R, Wilson J, Weinman SA. Patients with type 2 diabetes and elevated fibrosis-4 are under-referred to hepatology and have unrecognized hepatic decompensation. Journal of Gastroenterology and Hepatology. PMID 35613944 DOI: 10.1111/jgh.15900 |
0.034 |
|
| 2014 |
Glebova NO, Hicks CW, Taylor R, Tosoian JJ, Orion KC, Arnaoutakis KD, Arnaoutakis GJ, Black JH. Readmissions after complex aneurysm repair are frequent, costly, and primarily at nonindex hospitals. Journal of Vascular Surgery. 60: 1429-37. PMID 25316154 DOI: 10.1016/j.jvs.2014.08.092 |
0.033 |
|
| 2013 |
Pockros PJ, Jensen D, Tsai N, Taylor R, Ramji A, Cooper C, Dickson R, Tice A, Kulkarni R, Vierling JM, Lou Munson M, Chen YC, Najera I, Thommes J. JUMP-C: a randomized trial of mericitabine plus pegylated interferon alpha-2a/ribavirin for 24 weeks in treatment-naïve HCV genotype 1/4 patients. Hepatology (Baltimore, Md.). 58: 514-23. PMID 23359491 DOI: 10.1002/hep.26275 |
0.032 |
|
| 2018 |
Razzano S, Taylor R, Schonauer F, Figus A. How to assess the volume of a DIEP flap using a free online calculator: The DIEP V (volume) method. Journal of Plastic, Reconstructive & Aesthetic Surgery : Jpras. PMID 30104142 DOI: 10.1016/j.bjps.2018.04.018 |
0.031 |
|
| 2015 |
Taylor RW, Williams SM, Farmer VL, Taylor BJ. The stability of sleep patterns in children 3 to 7 years of age. The Journal of Pediatrics. 166: 697-702.e1. PMID 25524316 DOI: 10.1016/j.jpeds.2014.11.014 |
0.031 |
|
| 2015 |
Jospe MR, Brown RC, Roy M, Taylor RW. Adherence to hunger training using blood glucose monitoring: a feasibility study. Nutrition & Metabolism. 12: 22. PMID 26075007 DOI: 10.1186/s12986-015-0017-2 |
0.031 |
|
| 2015 |
Olpin SE, Murphy E, Kirk RJ, Taylor RW, Quinlivan R. The investigation and management of metabolic myopathies. Journal of Clinical Pathology. 68: 410-7. PMID 25878327 DOI: 10.1136/jclinpath-2014-202808 |
0.03 |
|
| 2013 |
Taylor RW, Robinson A, Espinel PT, Baur LA, Wake M, Sabin MA. Research priorities in 2012 for the effective management of childhood obesity. Clinical Obesity. 3: 3-6. PMID 25586386 DOI: 10.1111/cob.12014 |
0.03 |
|
| 2016 |
Metodiev MD, Thompson K, Alston CL, Morris AA, He L, Assouline Z, Rio M, Bahi-Buisson N, Pyle A, Griffin H, Siira S, Filipovska A, Munnich A, Chinnery PF, McFarland R, ... ... Taylor RW, et al. Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies. American Journal of Human Genetics. 99: 246. PMID 27392079 DOI: 10.1016/j.ajhg.2016.06.013 |
0.029 |
|
| 2016 |
Taylor RW, Alpert GD. The myrmicine ant genus Metapone Forel (Hymenoptera: Formicidae): a global taxonomic review with descriptions of twelve new species. Zootaxa. 4105: 501-545. PMID 27394796 |
0.026 |
|
| 2015 |
Nisar R, Hanson PS, He L, Taylor RW, Blain PG, Morris CM. Erratum to: Diquat causes caspase-independent cell death in SH-SY5Y cells by production of ROS independently of mitochondria. Archives of Toxicology. PMID 26084419 DOI: 10.1007/s00204-015-1542-5 |
0.024 |
|
| 2011 |
Wu C, Gilroy R, Taylor R, Olyaee M, Abdulkarim B, Forster J, O'Neil M, Damjanov I, Wan YJ. Alteration of hepatic nuclear receptor-mediated signaling pathways in hepatitis C virus patients with and without a history of alcohol drinking. Hepatology (Baltimore, Md.). 54: 1966-74. PMID 21898497 DOI: 10.1002/hep.24645 |
0.023 |
|
| 2015 |
Katyal A, Dmello D, Taylor RW. Thrombolytic therapy for cardiac arrest secondary to acute pulmonary embolism: an oft overlooked strategy. The American Journal of Emergency Medicine. 33: 850-1. PMID 25843791 DOI: 10.1016/j.ajem.2015.03.053 |
0.021 |
|
| 2014 |
Courtney PM, Taylor R, Scolaro J, Donegan D, Mehta S. Displaced inferior ramus fractures as a marker of posterior pelvic injury. Archives of Orthopaedic and Trauma Surgery. 134: 935-9. PMID 24740699 DOI: 10.1007/s00402-014-1993-9 |
0.02 |
|
| 2011 |
Banerjee R, Chao J, Sadeghi C, Taylor R, Nickisch F. Fractures of the calcaneal tuberosity treated with suture fixation through bone tunnels. Journal of Orthopaedic Trauma. 25: 685-90. PMID 21654526 DOI: 10.1097/BOT.0b013e3181ffe61e |
0.018 |
|
| 2024 |
Taylor R, Madion M, Kleppe K, Mancini M, Mancini G, Hutson M, Yates J, Daigle H. Increasing Enoxaparin Dosing from 30 mg to 40 mg Does Not Affect Bleeding or VTE Risk in Bariatric Surgery Patients. The American Surgeon. 31348241241696. PMID 38531833 DOI: 10.1177/00031348241241696 |
0.01 |
|
| 2023 |
Crise AA, Taylor R, Zimmerman KL. Bilateral ocular opacification and weight loss in a cat. Journal of the American Veterinary Medical Association. 261: 1895-1897. PMID 38016285 DOI: 10.2460/javma.23.08.0470 |
0.01 |
|
| 2020 |
Wentzel J, Taylor R, Zino C, Avery M, Muertos K, Sciarretta JD. Moped and Motorcycle Trauma: Injury Prevention and an Opportunity to Intervene. The American Surgeon. 86: e113-e115. PMID 32223813 |
0.01 |
|
| 2015 |
Rennick LA, Campbell PM, Naidu A, Taylor RW, Buschang PH. Effectiveness of a novel topical powder on the treatment of traumatic oral ulcers in orthodontic patients: A randomized controlled trial. The Angle Orthodontist. PMID 26401826 DOI: 10.2319/050415-303.1 |
0.01 |
|
| 2014 |
Taylor RW, Zargarpour H. Interactive games The Ves Handbook of Visual Effects: Industry Standard Vfx Practices and Procedures. 847-880. |
0.01 |
|
| 2013 |
Bansal V, Taylor RW, Maly P, Johnson M, Yetter B. Enhanced capture of mercury in baghouse by using novel filtration media and filter design Aistech - Iron and Steel Technology Conference Proceedings. 1: 175-184. |
0.01 |
|
| 2010 |
Botek G, Anderson MA, Taylor R. Charcot neuroarthropathy: An often overlooked complication of diabetes. Cleveland Clinic Journal of Medicine. 77: 593-9. PMID 20810870 DOI: 10.3949/ccjm.77a.09163 |
0.01 |
|
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