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Grant A. Mitchell - Publications

Affiliations: 
Biochemistry Université de Montréal, Montréal, Canada 
Area:
Biochemistry, Genetics
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Year Citation  Score
2020 Otsuka H, Kimura T, Ago Y, Nakama M, Aoyama Y, Abdelkreem E, Matsumoto H, Ohnishi H, Sasai H, Osawa M, Yamaguchi S, Mitchell GA, Fukao T. Deficiency of 3-hydroxybutyrate dehydrogenase (BDH1) in mice causes low ketone body levels and fatty liver during fasting. Journal of Inherited Metabolic Disease. PMID 32279332 DOI: 10.1002/Jimd.12243  0.334
2020 Xia B, Shi XC, Xie BC, Zhu MQ, Chen Y, Chu XY, Cai GH, Liu M, Yang SZ, Mitchell GA, Pang WJ, Wu JW. Urolithin A exerts antiobesity effects through enhancing adipose tissue thermogenesis in mice. Plos Biology. 18: e3000688. PMID 32218572 DOI: 10.1371/Journal.Pbio.3000688  0.313
2020 Nardi N, Proulx F, Brunel-Guiton C, Oligny LL, Piché N, Mitchell GA, Joyal JS. Fulminant Necrotizing Enterocolitis and Multiple Organ Dysfunction in a Toddler with Mitochondrial DNA Depletion Syndrome-13. Journal of Pediatric Intensive Care. 9: 54-59. PMID 31984159 DOI: 10.1055/S-0039-1697620  0.303
2019 Beauregard-Lacroix E, Salian S, Kim H, Ehresmann S, DʹAmours G, Gauthier J, Saillour V, Bernard G, Mitchell GA, Soucy JF, Michaud JL, Campeau PM. A variant of neonatal progeroid syndrome, or Wiedemann-Rautenstrauch syndrome, is associated with a nonsense variant in POLR3GL. European Journal of Human Genetics : Ejhg. PMID 31695177 DOI: 10.1038/S41431-019-0539-6  0.311
2019 Yang H, Zhao C, Tang MC, Wang Y, Wang SP, Allard P, Furtos A, Mitchell GA. Inborn errors of mitochondrial acyl-coenzyme a metabolism: acyl-CoA biology meets the clinic. Molecular Genetics and Metabolism. PMID 31186158 DOI: 10.1016/J.Ymgme.2019.05.002  0.363
2019 Zhang X, Zhang CC, Yang H, Soni KG, Wang SP, Mitchell GA, Wu JW. An Epistatic Interaction between and Reveals New Pathways of Adipose Tissue Lipolysis. Cells. 8. PMID 31035700 DOI: 10.3390/Cells8050395  0.337
2019 Levtova A, Waters PJ, Buhas D, Lévesque S, Auray-Blais C, Clarke JTR, Laframboise R, Maranda B, Mitchell GA, Brunel-Guitton C, Braverman NE. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohort. Journal of Inherited Metabolic Disease. 42: 107-116. PMID 30740739 DOI: 10.1002/Jimd.12032  0.313
2019 Yang H, Zhao C, Wang Y, Wang SP, Mitchell GA. Hereditary diseases of coenzyme A thioester metabolism. Biochemical Society Transactions. PMID 30626707 DOI: 10.1042/Bst20180423  0.319
2017 Xia B, Cai GH, Yang H, Wang SP, Mitchell GA, Wu JW. Adipose Tissue Deficiency of Hormone-Sensitive Lipase Causes Fatty Liver in Mice. Plos Genetics. 13: e1007110. PMID 29232702 DOI: 10.1371/Journal.Pgen.1007110  0.337
2017 Alvarez F, Atkinson S, Bouchard M, Brunel-Guitton C, Buhas D, Bussières JF, Dubois J, Fenyves D, Goodyer P, Gosselin M, Halac U, Labbé P, Laframboise R, Maranda B, ... ... Mitchell GA, et al. The Québec NTBC Study. Advances in Experimental Medicine and Biology. 959: 187-195. PMID 28755196 DOI: 10.1007/978-3-319-55780-9_17  0.31
2017 Halac U, Dubois J, Mitchell GA. The Liver in Tyrosinemia Type I: Clinical Management and Course in Quebec. Advances in Experimental Medicine and Biology. 959: 75-83. PMID 28755185 DOI: 10.1007/978-3-319-55780-9_6  0.306
2017 Grünert SC, Schlatter SM, Schmitt RN, Gemperle-Britschgi C, Mrázová L, Balcı MC, Bischof F, Çoker M, Das AM, Demirkol M, de Vries M, Gökçay G, Häberle J, Uçar SK, Lotz-Havla AS, ... ... Mitchell GA, et al. 3-Hydroxy-3-methylglutaryl-coenzyme A lyase deficiency: Clinical presentation and outcome in a series of 37 patients. Molecular Genetics and Metabolism. PMID 28583327 DOI: 10.1016/J.Ymgme.2017.05.014  0.367
2017 Wu JW, Preuss C, Wang SP, Yang H, Ji B, Carter GW, Gladdy R, Andelfinger G, Mitchell GA. Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice. Plos Genetics. 13: e1006716. PMID 28459858 DOI: 10.1371/Journal.Pgen.1006716  0.334
2017 Martins C, Brunel-Guitton C, Lortie A, Gauvin F, Morales CR, Mitchell GA, Pshezhetsky AV. Atypical juvenile presentation of GM2 gangliosidosis AB in a patient compound-heterozygote for c.259G > T and c.164C > T mutations in the GM2A gene. Molecular Genetics and Metabolism Reports. 11: 24-29. PMID 28417072 DOI: 10.1016/J.Ymgmr.2017.01.017  0.352
2017 Peña-Quintana L, Scherer G, Curbelo-Estévez ML, Jiménez-Acosta F, Hartmann B, Roche F, Meavilla-Olivas S, Pérez-Cerdá C, García Segarra N, Giguère Y, Huppke P, Mitchell GA, Mönch E, Trump D, Vianey-Saban C, et al. TYROSINEMIA TYPE II: Mutation update, eleven novel mutations and description of five independent subjects with a novel founder mutation. Clinical Genetics. PMID 28255985 DOI: 10.1111/Cge.13003  0.349
2016 Yang H, Al-Hertani W, Cyr D, Laframboise R, Parizeault G, Wang SP, Rossignol F, Berthier MT, Giguère Y, Waters PJ, Mitchell GA. Hypersuccinylacetonaemia and normal liver function in maleylacetoacetate isomerase deficiency. Journal of Medical Genetics. PMID 27876694 DOI: 10.1136/Jmedgenet-2016-104289  0.326
2016 Yang H, Wu JW, Wang SP, Severi I, Sartini L, Frizzell N, Cinti S, Yang G, Mitchell GA. Adipose-Specific Deficiency of Fumarate Hydratase in Mice Protects Against Obesity, Hepatic Steatosis and Insulin Resistance. Diabetes. PMID 27554470 DOI: 10.2337/Db16-0136  0.326
2016 Montaño AM, Lock-Hock N, Steiner RD, Graham BH, Szlago M, Greenstein R, Pineda M, Gonzalez-Meneses A, Çoker M, Bartholomew D, Sands MS, Wang R, Giugliani R, Macaya A, Pastores G, ... ... Mitchell GA, et al. Clinical course of sly syndrome (mucopolysaccharidosis type VII). Journal of Medical Genetics. PMID 26908836 DOI: 10.1136/Jmedgenet-2015-103322  0.327
2016 Sasarman F, Maftei C, Campeau PM, Brunel-Guitton C, Mitchell GA, Allard P. Biosynthesis of glycosaminoglycans: associated disorders and biochemical tests. Journal of Inherited Metabolic Disease. 39: 173-88. PMID 26689402 DOI: 10.1007/S10545-015-9903-Z  0.322
2015 Meijer IA, Sasarman F, Maftei C, Rossignol E, Vanasse M, Major P, Mitchell GA, Brunel-Guitton C. LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy. Molecular Genetics and Metabolism Reports. 5: 85-88. PMID 28649549 DOI: 10.1016/J.Ymgmr.2015.10.010  0.361
2015 Wünnemann F, Kokta V, Leclerc S, Thibeault M, McCuaig C, Hatami A, Stheneur C, Grenier JC, Awadalla P, Mitchell GA, Andelfinger G, Preuss C. Aortic Dilatation Associated With a De Novo Mutation in the SOX18 Gene: Expanding the Clinical Spectrum of Hypotrichosis-Lymphedema-Telangiectasia Syndrome. The Canadian Journal of Cardiology. PMID 26148450 DOI: 10.1016/J.Cjca.2015.04.004  0.325
2015 Tetreault M, Fahiminiya S, Antonicka H, Mitchell GA, Geraghty MT, Lines M, Boycott KM, Shoubridge EA, Mitchell JJ, Michaud JL, Majewski J. Whole-exome sequencing identifies novel ECHS1 mutations in Leigh syndrome. Human Genetics. 134: 981-91. PMID 26099313 DOI: 10.1007/S00439-015-1577-Y  0.377
2015 Sasarman F, Thiffault I, Weraarpachai W, Salomon S, Maftei C, Gauthier J, Ellazam B, Webb N, Antonicka H, Janer A, Brunel-Guitton C, Elpeleg O, Mitchell G, Shoubridge EA. The 3' addition of CCA to mitochondrial tRNASer(AGY) is specifically impaired in patients with mutations in the tRNA nucleotidyl transferase TRNT1. Human Molecular Genetics. 24: 2841-7. PMID 25652405 DOI: 10.1093/Hmg/Ddv044  0.336
2015 Wu JW, Yang H, Wang SP, Soni KG, Brunel-Guitton C, Mitchell GA. Inborn errors of cytoplasmic triglyceride metabolism. Journal of Inherited Metabolic Disease. 38: 85-98. PMID 25300978 DOI: 10.1007/S10545-014-9767-7  0.355
2014 Wang SP, Yang H, Wu JW, Gauthier N, Fukao T, Mitchell GA. Metabolism as a tool for understanding human brain evolution: lipid energy metabolism as an example. Journal of Human Evolution. 77: 41-9. PMID 25488255 DOI: 10.1016/J.Jhevol.2014.06.013  0.539
2014 Wang SP, Wu JW, Bourdages H, Lefebvre JF, Casavant S, Leavitt BR, Labuda D, Trasler J, Smith CE, Hermo L, Mitchell GA. The catalytic function of hormone-sensitive lipase is essential for fertility in male mice. Endocrinology. 155: 3047-53. PMID 24797631 DOI: 10.1210/En.2014-1031  0.323
2014 Fukao T, Mitchell G, Sass JO, Hori T, Orii K, Aoyama Y. Ketone body metabolism and its defects. Journal of Inherited Metabolic Disease. 37: 541-51. PMID 24706027 DOI: 10.1007/S10545-014-9704-9  0.374
2014 Stockler-Ipsiroglu S, van Karnebeek C, Longo N, Korenke GC, Mercimek-Mahmutoglu S, Marquart I, Barshop B, Grolik C, Schlune A, Angle B, Araújo HC, Coskun T, Diogo L, Geraghty M, Haliloglu G, ... ... Mitchell G, et al. Guanidinoacetate methyltransferase (GAMT) deficiency: outcomes in 48 individuals and recommendations for diagnosis, treatment and monitoring. Molecular Genetics and Metabolism. 111: 16-25. PMID 24268530 DOI: 10.1016/J.Ymgme.2013.10.018  0.308
2013 Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, ... ... Mitchell GA, et al. Deficiency of asparagine synthetase causes congenital microcephaly and a progressive form of encephalopathy. Neuron. 80: 429-41. PMID 24139043 DOI: 10.1016/J.Neuron.2013.08.013  0.347
2013 Dũng VC, Tomatsu S, Montaño AM, Gottesman G, Bober MB, Mackenzie W, Maeda M, Mitchell GA, Suzuki Y, Orii T. Mucopolysaccharidosis IVA: correlation between genotype, phenotype and keratan sulfate levels. Molecular Genetics and Metabolism. 110: 129-38. PMID 23876334 DOI: 10.1016/J.Ymgme.2013.06.008  0.356
2013 Gauthier N, Wu JW, Wang SP, Allard P, Mamer OA, Sweetman L, Moser AB, Kratz L, Alvarez F, Robitaille Y, Lépine F, Mitchell GA. A liver-specific defect of Acyl-CoA degradation produces hyperammonemia, hypoglycemia and a distinct hepatic Acyl-CoA pattern. Plos One. 8: e60581. PMID 23861731 DOI: 10.1371/Journal.Pone.0060581  0.584
2013 Thiffault I, Dicaire MJ, Tetreault M, Huang KN, Demers-Lamarche J, Bernard G, Duquette A, Larivière R, Gehring K, Montpetit A, McPherson PS, Richter A, Montermini L, Mercier J, Mitchell GA, et al. Diversity of ARSACS mutations in French-Canadians. The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques. 40: 61-6. PMID 23250129 DOI: 10.1017/S0317167100012968  0.314
2012 Lian J, Wei E, Wang SP, Quiroga AD, Li L, Di Pardo A, van der Veen J, Sipione S, Mitchell GA, Lehner R. Liver specific inactivation of carboxylesterase 3/triacylglycerol hydrolase decreases blood lipids without causing severe steatosis in mice. Hepatology (Baltimore, Md.). 56: 2154-62. PMID 22707181 DOI: 10.1002/Hep.25881  0.331
2012 Wu JW, Wang SP, Casavant S, Moreau A, Yang GS, Mitchell GA. Fasting energy homeostasis in mice with adipose deficiency of desnutrin/adipose triglyceride lipase. Endocrinology. 153: 2198-207. PMID 22374972 DOI: 10.1210/En.2011-1518  0.336
2011 Wu JW, Wang SP, Alvarez F, Casavant S, Gauthier N, Abed L, Soni KG, Yang G, Mitchell GA. Deficiency of liver adipose triglyceride lipase in mice causes progressive hepatic steatosis. Hepatology (Baltimore, Md.). 54: 122-32. PMID 21465509 DOI: 10.1002/Hep.24338  0.568
2011 Hamdan FF, Gauthier J, Araki Y, Lin DT, Yoshizawa Y, Higashi K, Park AR, Spiegelman D, Dobrzeniecka S, Piton A, Tomitori H, Daoud H, Massicotte C, Henrion E, Diallo O, ... ... Mitchell G, et al. Excess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disability. American Journal of Human Genetics. 88: 306-16. PMID 21376300 DOI: 10.1016/J.Ajhg.2011.03.011  0.321
2011 Deveault C, Billingsley G, Duncan JL, Bin J, Theal R, Vincent A, Fieggen KJ, Gerth C, Noordeh N, Traboulsi EI, Fishman GA, Chitayat D, Knueppel T, Millán JM, Munier FL, ... ... Mitchell GA, et al. BBS genotype-phenotype assessment of a multiethnic patient cohort calls for a revision of the disease definition. Human Mutation. 32: 610-9. PMID 21344540 DOI: 10.1002/Humu.21480  0.341
2011 Debray FG, Morin C, Janvier A, Villeneuve J, Maranda B, Laframboise R, Lacroix J, Decarie JC, Robitaille Y, Lambert M, Robinson BH, Mitchell GA. LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiency. Journal of Medical Genetics. 48: 183-9. PMID 21266382 DOI: 10.1136/Jmg.2010.081976  0.351
2010 Debray FG, Lambert M, Allard P, Mitchell GA. Low citrulline in Leigh disease: still a biomarker of maternally inherited Leigh syndrome. Journal of Child Neurology. 25: 1000-2. PMID 20472868 DOI: 10.1177/0883073809351983  0.348
2010 Billingsley G, Bin J, Fieggen KJ, Duncan JL, Gerth C, Ogata K, Wodak SS, Traboulsi EI, Fishman GA, Paterson A, Chitayat D, Knueppel T, Millán JM, Mitchell GA, Deveault C, et al. Mutations in chaperonin-like BBS genes are a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Journal of Medical Genetics. 47: 453-63. PMID 20472660 DOI: 10.1136/Jmg.2009.073205  0.333
2010 Wei E, Ben Ali Y, Lyon J, Wang H, Nelson R, Dolinsky VW, Dyck JR, Mitchell G, Korbutt GS, Lehner R. Loss of TGH/Ces3 in mice decreases blood lipids, improves glucose tolerance, and increases energy expenditure. Cell Metabolism. 11: 183-93. PMID 20197051 DOI: 10.1016/J.Cmet.2010.02.005  0.314
2008 Orii KE, Fukao T, Song XQ, Mitchell GA, Kondo N. Liver-specific silencing of the human gene encoding succinyl-CoA: 3-ketoacid CoA transferase. The Tohoku Journal of Experimental Medicine. 215: 227-36. PMID 18648183 DOI: 10.1620/Tjem.215.227  0.331
2008 Randall DR, Colobong KE, Hemmelgarn H, Sinclair GB, Hetty E, Thomas A, Bodamer OA, Volkmar B, Fernhoff PM, Casey R, Chan AK, Mitchell G, Stockler S, Melancon S, Rupar T, et al. Heparin cofactor II-thrombin complex: a biomarker of MPS disease. Molecular Genetics and Metabolism. 94: 456-61. PMID 18511319 DOI: 10.1016/J.Ymgme.2008.05.001  0.313
2008 Debray FG, Lambert M, Gagne R, Maranda B, Laframboise R, MacKay N, Robinson BH, Mitchell GA. Pyruvate dehydrogenase deficiency presenting as intermittent isolated acute ataxia. Neuropediatrics. 39: 20-3. PMID 18504677 DOI: 10.1055/S-2008-1077084  0.368
2008 Mitchell GA, Gauthier N, Lesimple A, Wang SP, Mamer O, Qureshi I. Hereditary and acquired diseases of acyl-coenzyme A metabolism. Molecular Genetics and Metabolism. 94: 4-15. PMID 18337138 DOI: 10.1016/J.Ymgme.2007.12.005  0.569
2008 Hermo L, Chung S, Gregory M, Smith CE, Wang SP, El-Alfy M, Cyr DG, Mitchell GA, Trasler J. Alterations in the testis of hormone sensitive lipase-deficient mice is associated with decreased sperm counts, sperm motility, and fertility. Molecular Reproduction and Development. 75: 565-77. PMID 17886267 DOI: 10.1002/Mrd.20800  0.311
2007 Richter A, Mitchell GA, Rasquin A. [North American Indian childhood cirrhosis (NAIC)]. MéDecine Sciences : M/S. 23: 1002-7. PMID 18021715 DOI: 10.1051/Medsci/200723111002  0.337
2007 Debray FG, Lambert M, Lortie A, Vanasse M, Mitchell GA. Long-term outcome of Leigh syndrome caused by the NARP-T8993C mtDNA mutation. American Journal of Medical Genetics. Part A. 143: 2046-51. PMID 17663470 DOI: 10.1002/Ajmg.A.31880  0.351
2007 Sakurai S, Fukao T, Haapalainen AM, Zhang G, Yamada K, Lilliu F, Yano S, Robinson P, Gibson MK, Wanders RJ, Mitchell GA, Wierenga RK, Kondo N. Kinetic and expression analyses of seven novel mutations in mitochondrial acetoacetyl-CoA thiolase (T2): identification of a Km mutant and an analysis of the mutational sites in the structure. Molecular Genetics and Metabolism. 90: 370-8. PMID 17236799 DOI: 10.1016/J.Ymgme.2006.12.002  0.314
2006 Debray FG, Lambert M, Vanasse M, Decarie JC, Cameron J, Levandovskiy V, Robinson BH, Mitchell GA. Intermittent peripheral weakness as the presenting feature of pyruvate dehydrogenase deficiency. European Journal of Pediatrics. 165: 462-6. PMID 16552546 DOI: 10.1007/S00431-006-0104-5  0.346
2005 Fortier M, Soni K, Laurin N, Wang SP, Mauriège P, Jirik FR, Mitchell GA. Human hormone-sensitive lipase (HSL): expression in white fat corrects the white adipose phenotype of HSL-deficient mice. Journal of Lipid Research. 46: 1860-7. PMID 15961788 DOI: 10.1194/Jlr.M500081-Jlr200  0.328
2005 Park SY, Kim HJ, Wang S, Higashimori T, Dong J, Kim YJ, Cline G, Li H, Prentki M, Shulman GI, Mitchell GA, Kim JK. Hormone-sensitive lipase knockout mice have increased hepatic insulin sensitivity and are protected from short-term diet-induced insulin resistance in skeletal muscle and heart American Journal of Physiology - Endocrinology and Metabolism. 289: E30-E39. PMID 15701680 DOI: 10.1152/Ajpendo.00251.2004  0.308
2004 Wang SP, Chung S, Soni K, Bourdages H, Hermo L, Trasler J, Mitchell GA. Expression of human hormone-sensitive lipase (HSL) in postmeiotic germ cells confers normal fertility to HSL-deficient mice. Endocrinology. 145: 5688-93. PMID 15345679 DOI: 10.1210/En.2004-0919  0.307
2004 Soni KG, Lehner R, Metalnikov P, O'Donnell P, Semache M, Gao W, Ashman K, Pshezhetsky AV, Mitchell GA. Carboxylesterase 3 (EC 3.1.1.1) is a major adipocyte lipase. The Journal of Biological Chemistry. 279: 40683-9. PMID 15220344 DOI: 10.1074/Jbc.M400541200  0.307
2004 Peyot ML, Nolan CJ, Soni K, Joly E, Lussier R, Corkey BE, Wang SP, Mitchell GA, Prentki M. Hormone-sensitive lipase has a role in lipid signaling for insulin secretion but is nonessential for the incretin action of glucagon-like peptide 1. Diabetes. 53: 1733-42. PMID 15220197 DOI: 10.2337/Diabetes.53.7.1733  0.319
2004 Xu F, Morin C, Mitchell G, Ackerley C, Robinson BH. The role of the LRPPRC (leucine-rich pentatricopeptide repeat cassette) gene in cytochrome oxidase assembly: mutation causes lowered levels of COX (cytochrome c oxidase) I and COX III mRNA. The Biochemical Journal. 382: 331-6. PMID 15139850 DOI: 10.1042/Bj20040469  0.361
2004 Gallione CJ, Repetto GM, Legius E, Rustgi AK, Schelley SL, Tejpar S, Mitchell G, Drouin E, Westermann CJ, Marchuk DA. A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 (SMAD4). Lancet (London, England). 363: 852-9. PMID 15031030 DOI: 10.1016/S0140-6736(04)15732-2  0.326
2004 Simard LR, Viel J, Lambert M, Paradis G, Levy E, Delvin EE, Mitchell GA. The Δ > 15 Kb deletion French Canadian founder mutation in familial hypercholesterolemia: Rapid polymerase chain reaction-based diagnostic assay and prevalence in Quebec Clinical Genetics. 65: 202-208. PMID 14756670 DOI: 10.1111/J.0009-9163.2004.00223.X  0.306
2003 Laberge AM, Mitchell GA, van de Werve G, Lambert M. Long-term follow-up of a new case of liver glycogen synthase deficiency. American Journal of Medical Genetics. Part A. 120: 19-22. PMID 12794686 DOI: 10.1002/Ajmg.A.20110  0.351
2003 Mootha VK, Lepage P, Miller K, Bunkenborg J, Reich M, Hjerrild M, Delmonte T, Villeneuve A, Sladek R, Xu F, Mitchell GA, Morin C, Mann M, Hudson TJ, Robinson B, et al. Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proceedings of the National Academy of Sciences of the United States of America. 100: 605-10. PMID 12529507 DOI: 10.1073/Pnas.242716699  0.305
2002 Chagnon P, Michaud J, Mitchell G, Mercier J, Marion JF, Drouin E, Rasquin-Weber A, Hudson TJ, Richter A. A missense mutation (R565W) in cirhin (FLJ14728) in North American Indian childhood cirrhosis. American Journal of Human Genetics. 71: 1443-9. PMID 12417987 DOI: 10.1086/344580  0.356
2002 Vuillaumier-Barrot S, Bizec CL, Lonlay Pd, Barnier A, Mitchell G, Pelletier V, Prevost C, Saudubray JM, Durand G, Seta N. Protein losing enteropathy-hepatic fibrosis syndrome in Saguenay-Lac St-Jean, Quebec is a congenital disorder of glycosylation type Ib Journal of Medical Genetics. 39: 849-851. PMID 12414827 DOI: 10.1136/Jmg.39.11.849  0.356
2002 Li H, Brochu M, Wang SP, Rochdi L, Côté M, Mitchell G, Gallo-Payet N. Hormone-sensitive lipase deficiency in mice causes lipid storage in the adrenal cortex and impaired corticosterone response to corticotropin stimulation. Endocrinology. 143: 3333-40. PMID 12193545 DOI: 10.1210/En.2002-220341  0.333
2002 Lahjouji K, Elimrani I, Wu J, Mitchell GA, Qureshi IA. A heterozygote phenotype is present in the jvs +/- mutant mouse livers. Molecular Genetics and Metabolism. 76: 76-80. PMID 12175785 DOI: 10.1016/S1096-7192(02)00017-3  0.357
2002 Corzo D, Gibson W, Johnson K, Mitchell G, LePage G, Cox GF, Casey R, Zeiss C, Tyson H, Cutting GR, Raymond GV, Smith KD, Watkins PA, Moser AB, Moser HW, et al. Contiguous deletion of the X-linked adrenoleukodystrophy gene (ABCD1) and DXS1357E: a novel neonatal phenotype similar to peroxisomal biogenesis disorders. American Journal of Human Genetics. 70: 1520-31. PMID 11992258 DOI: 10.1086/340849  0.373
2001 Berry GT, Fukao T, Mitchell GA, Mazur A, Ciafre M, Gibson J, Kondo N, Palmieri MJ. Neonatal hypoglycaemia in severe succinyl-CoA: 3-oxoacid CoA-transferase deficiency Journal of Inherited Metabolic Disease. 24: 587-595. PMID 11757586 DOI: 10.1023/A:1012419911789  0.348
2001 Chung S, Wang SP, Pan L, Mitchell G, Trasler J, Hermo L. Infertility and testicular defects in hormone-sensitive lipase-deficient mice. Endocrinology. 142: 4272-81. PMID 11564684 DOI: 10.1210/Endo.142.10.8424  0.327
2001 Lahjouji K, Mitchell GA, Qureshi IA. Carnitine transport by organic cation transporters and systemic carnitine deficiency Molecular Genetics and Metabolism. 73: 287-297. PMID 11509010 DOI: 10.1006/Mgme.2001.3207  0.311
2001 Russo PA, Mitchell GA, Tanguay RM. Tyrosinemia: A review Pediatric and Developmental Pathology. 4: 212-221. PMID 11370259 DOI: 10.1007/S100240010146  0.335
2001 Bouchard L, Robert MF, Vinarov D, Stanley CA, Thompson GN, Morris A, Leonard JV, Quant P, Hsu BY, Boneh A, Boukaftane Y, Ashmarina L, Wang S, Miziorko H, Mitchell GA. Mitochondrial 3-hydroxy-3-methylglutaryl-CoA synthase deficiency: clinical course and description of causal mutations in two patients. Pediatric Research. 49: 326-31. PMID 11228257 DOI: 10.1203/00006450-200103000-00005  0.394
2001 Lee N, Daly MJ, Delmonte T, Lander ES, Xu F, Hudson TJ, Mitchell GA, Morin CC, Robinson BH, Rioux JD. A genomewide linkage-disequilibrium scan localizes the Saguenay-Lac-Saint-Jean cytochrome oxidase deficiency to 2p16. American Journal of Human Genetics. 68: 397-409. PMID 11156535 DOI: 10.1086/318197  0.346
2000 Drouin E, Russo P, Tuchweber B, Mitchell G, Rasquin-Weber A. North American Indian Cirrhosis in Children: A Review of 30 Cases Journal of Pediatric Gastroenterology and Nutrition. 31: 395-404. PMID 11045837 DOI: 10.1097/00005176-200010000-00013  0.346
2000 Fukao T, Mitchell GA, Song XQ, Nakamura H, Kassovska-Bratinova S, Orii KE, Wraith JE, Besley G, Wanders RJA, Niezen-Koning KE, Berry GT, Palmieri M, Kondo N. Succinyl-CoA:3-ketoacid CoA transferase (SCOT): Cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutations Genomics. 68: 144-151. PMID 10964512 DOI: 10.1006/Geno.2000.6282  0.339
2000 Laberge AM, Mitchell G, Werve GVd, Lambert M. A new caw of hepatic glycogen snthase deficiency. biochemical findings and comparison with reported cases Genetics in Medicine. 2: 80-80. DOI: 10.1097/00125817-200001000-00105  0.36
1999 Camacho JA, Obie C, Biery B, Goodman BK, Hu CA, Almashanu S, Steel G, Casey R, Lambert M, Mitchell GA, Valle D. Hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome is caused by mutations in a gene encoding a mitochondrial ornithine transporter. Nature Genetics. 22: 151-8. PMID 10369256 DOI: 10.1038/9658  0.312
1998 Wang SP, Marth JD, Oligny LL, Vachon M, Robert MF, Ashmarina L, Mitchell GA. 3-Hydroxy-3-methylglutaryl-CoA lyase (HL): Gene targeting causes prenatal lethality in HL-deficient mice Human Molecular Genetics. 7: 2057-2062. PMID 9817922 DOI: 10.1093/Hmg/7.13.2057  0.364
1998 Song XQ, Fukao T, Watanabe H, Shintaku H, Hirayama K, Kassovska-Bratinova S, Kondo N, Mitchell GA. Succinyl-CoA:3-ketoacid CoA transferase (SCOT) deficiency: Two pathogenic mutations, V133E and C456F, in Japanese siblings Human Mutation. 12: 83-88. PMID 9671268 DOI: 10.1002/(Sici)1098-1004(1998)12:2<83::Aid-Humu2>3.0.Co;2-P  0.345
1998 Richard C, Tranchemontagne J, Elsliger MA, Mitchell GA, Potier M, Pshezhetsky AV. Molecular pathology of galactosialidosis in a patient affected with two new frameshift mutations in the cathepsin A/protective protein gene Human Mutation. 11: 461-469. PMID 9603439 DOI: 10.1002/(Sici)1098-1004(1998)11:6<461::Aid-Humu7>3.0.Co;2-F  0.354
1998 Mitchell GA, Ozand PT, Robert MF, Ashmarina L, Roberts J, Gibson KM, Wanders RJ, Wang S, Chevalier I, Plöchl E, Miziorko H. HMG CoA lyase deficiency: Identification of five causal point mutations in codons 41 and 42, including a frequent Saudi Arabian mutation, R41Q American Journal of Human Genetics. 62: 295-300. PMID 9463337 DOI: 10.1086/301730  0.328
1997 Sztrolovics R, Wang SP, Lapierre P, Chen HS, Robert MF, Mitchell GA. Hormone-sensitive lipase (Lipe): sequence analysis of the 129Sv mouse Lipe gene. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 8: 86-9. PMID 9060404 DOI: 10.1007/S003359900363  0.304
1996 Roberts JR, Mitchell GA, Miziorko HM. Modeling of a mutation responsible for human 3-hydroxy-3- methylglutaryl-CoA lyase deficiency implicates histidine 233 as an active site residue Journal of Biological Chemistry. 271: 24604-24609. PMID 8798725 DOI: 10.1074/Jbc.271.40.24604  0.307
1996 Wang SP, Robert MF, Gibson KM, Wanders RJA, Mitchell GA. 3-Hydroxy-3-methylglutaryl CoA lyase (HL): Mouse and human HL gene (HMGCL) cloning and detection of large gene deletions in two unrelated HL-deficient patients Genomics. 33: 99-104. PMID 8617516 DOI: 10.1006/Geno.1996.0164  0.309
1995 Wakazono A, Fukao T, Yamaguchi S, Hori T, Orii T, Lambert M, Mitchell GA, Lee GW, Hashimoto T. Molecular, biochemical, and clinical characterization of mitochondrial acetoacetyl‐coenzyme A thiolase deficiency in two further patients Human Mutation. 5: 34-42. PMID 7728148 DOI: 10.1002/Humu.1380050105  0.32
1994 Boukaftane Y, Duncan A, Wang S, Labuda D, Robert MF, Sarrazin J, Schappert K, Mitchell GA. Human Mitochondrial HMG CoA Synthase: Liver cDNA and Partial Genomic Cloning, Chromosome Mapping to 1p12-p13, and Possible Role in Vertebrate Evolution Genomics. 23: 552-559. PMID 7851882 DOI: 10.1006/Geno.1994.1542  0.309
1992 Lemay JF, Lambert MA, Mitchell GA, Vanasse M, Valle D, Arbour JF, Dubé J, Flessas J, Laberge M, Lafleur L, Orquin J, Qureshi IA, Dery R. Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: Neurologic, ophthalmologic, and neuropsychologic examination of six patients The Journal of Pediatrics. 121: 725-730. PMID 1432421 DOI: 10.1016/S0022-3476(05)81900-6  0.303
1992 Phaneuf D, Lambert M, Laframboise R, Mitchell G, Lettre F, Tanguay RM. Type 1 hereditary tyrosinemia. Evidence for molecular heterogeneity and identification of a causal mutation in a French Canadian patient. The Journal of Clinical Investigation. 90: 1185-92. PMID 1401056 DOI: 10.1172/Jci115979  0.351
1988 Bonnefont JP, Mitchell G, Nguyen-Hoang N, Pelet A, Rimoldi M, Donato SD, Saudubray JM. Hepatic and muscular presentations of carnitine palmitoyl transferase deficiency: two distinct entities. Pediatric Research. 24: 308-311. PMID 3211616 DOI: 10.1203/00006450-198809000-00006  0.365
1986 Mitchell GA, Watkins D, Melançon SB, Rosenblatt DS, Geoffroy G, Orquin J, Homsy MB, Dallaire L. Clinical heterogeneity in cobalamin C variant of combined homocystinuria and methylmalonic aciduria. The Journal of Pediatrics. 108: 410-5. PMID 3950820 DOI: 10.1016/S0022-3476(86)80882-4  0.318
1985 Duran M, Mitchell G, Klerk JBCd, Jager JPd, Hofkamp M, Bruinvis L, Ketting D, Saudubray J, Wadman SK. Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids The Journal of Pediatrics. 107: 397-404. PMID 4032135 DOI: 10.1016/S0022-3476(85)80514-X  0.319
1983 Gaudry M, Munnich A, Ogier H, Marsac C, Marquet A, Saudubray JM, Mitchell G, Causse M, Frezal J. Deficient Liver Biotinidase Activity In Multiple Carboxylase Deficiency The Lancet. 322: 397. PMID 6135889 DOI: 10.1016/S0140-6736(83)90363-X  0.304
Low-probability matches (unlikely to be authored by this person)
2005 Yu B, Mitchell GA, Richter A. Nucleolar localization of cirhin, the protein mutated in North American Indian childhood cirrhosis. Experimental Cell Research. 311: 218-28. PMID 16225863 DOI: 10.1016/J.Yexcr.2005.08.012  0.3
2008 Wang S, Soni KG, Semache M, Casavant S, Fortier M, Pan L, Mitchell GA. Lipolysis and the integrated physiology of lipid energy metabolism. Molecular Genetics and Metabolism. 95: 117-26. PMID 18762440 DOI: 10.1016/J.Ymgme.2008.06.012  0.299
1992 Michaud J, Brody LC, Steel G, Fontaine G, Martin LS, Valle D, Mitchell G. Strand-separating conformational polymorphism analysis: Efficacy of detection of point mutations in the human ornithine δ-aminotransferase gene Genomics. 13: 389-394. PMID 1612597 DOI: 10.1016/0888-7543(92)90258-T  0.299
2014 Gizicki R, Robert MC, Gómez-López L, Orquin J, Decarie JC, Mitchell GA, Roy MS, Ospina LH. Long-term visual outcome of methylmalonic aciduria and homocystinuria, cobalamin C type. Ophthalmology. 121: 381-6. PMID 24126030 DOI: 10.1016/J.Ophtha.2013.08.034  0.299
2017 Mitchell GA, Yang H. Remaining Challenges in the Treatment of Tyrosinemia from the Clinician's Viewpoint. Advances in Experimental Medicine and Biology. 959: 205-213. PMID 28755198 DOI: 10.1007/978-3-319-55780-9_19  0.298
2016 Janer A, Prudent J, Paupe V, Fahiminiya S, Majewski J, Sgarioto N, Des Rosiers C, Forest A, Lin ZY, Gingras AC, Mitchell G, McBride HM, Shoubridge EA. SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome. Embo Molecular Medicine. PMID 27390132 DOI: 10.15252/Emmm.201506159  0.298
1997 Boukaftane Y, Mitchell GA. Cloning and characterization of the human mitochondrial 3-hydroxy-3-methylglutaryl CoA synthase gene Gene. 195: 121-126. PMID 9305755 DOI: 10.1016/S0378-1119(97)00067-X  0.296
1999 Brun N, Robitaille Y, Grignon A, Robinson BH, Mitchell GA, Lambert M. Pyruvate carboxylase deficiency: prenatal onset of ischemia-like brain lesions in two sibs with the acute neonatal form. American Journal of Medical Genetics. 84: 94-101. PMID 10323732 DOI: 10.1002/(Sici)1096-8628(19990521)84:2<94::Aid-Ajmg3>3.0.Co;2-1  0.294
2018 Yang H, Rossignol F, Cyr D, Laframboise R, Wang SP, Soucy JF, Berthier MT, Giguère Y, Waters PJ, Mitchell GA. Mildly elevated succinylacetone and normal liver function in compound heterozygotes with pathogenic and pseudodeficient FAH alleles. Molecular Genetics and Metabolism Reports. 14: 55-58. PMID 29326876 DOI: 10.1016/J.Ymgmr.2017.12.002  0.293
2004 Fukao T, Lopaschuk GD, Mitchell GA. Pathways and control of ketone body metabolism: on the fringe of lipid biochemistry. Prostaglandins, Leukotrienes, and Essential Fatty Acids. 70: 243-51. PMID 14769483 DOI: 10.1016/J.Plefa.2003.11.001  0.293
2004 Tuinstra RL, Wang CZ, Mitchell GA, Miziorko HM. Evaluation of 3-hydroxy-3-methylglutaryl-coenzyme A lyase arginine-41 as a catalytic residue: use of acetyldithio-coenzyme A to monitor product enolization. Biochemistry. 43: 5287-95. PMID 15122894 DOI: 10.1021/Bi0499765  0.292
1995 Mitchell GA, Jakobs C, Gibson KM, Robert MF, Burlina A, Dionisi-Vici C, Dallaire L. Molecular prenatal diagnosis of 3-hydroxy-3-methylglutaryl CoA lyase deficiency Prenatal Diagnosis. 15: 725-729. PMID 7479590 DOI: 10.1002/Pd.1970150807  0.291
2017 Alvarez F, Mitchell GA. Tyrosinemia and Liver Transplantation: Experience at CHU Sainte-Justine. Advances in Experimental Medicine and Biology. 959: 67-73. PMID 28755184 DOI: 10.1007/978-3-319-55780-9_5  0.29
2006 Debray FG, Drouin E, Herzog D, Lortie A, Lambert M, Garel L, Mitchell GA, Michaud JL. Recurrent pancreatitis in mitochondrial cytopathy. American Journal of Medical Genetics. Part A. 140: 2330-5. PMID 17022070 DOI: 10.1002/Ajmg.A.31457  0.29
2013 Dridi L, Seyrantepe V, Fougerat A, Pan X, Bonneil E, Thibault P, Moreau A, Mitchell GA, Heveker N, Cairo CW, Issad T, Hinek A, Pshezhetsky AV. Positive regulation of insulin signaling by neuraminidase 1. Diabetes. 62: 2338-46. PMID 23520133 DOI: 10.2337/Db12-1825  0.289
1991 Mitchell GA, Labuda D, Fontaine G, Saudubray JM, Bonnefont EP, Lyonne S, Brody LC, Steel G, Obie C, Valle D. Splice-mediated insertion of an Alu sequence inactivates ornithine aminotransferase: A role for Alu elements in human mutation Proceedings of the National Academy of Sciences of the United States of America. 88: 815-819. PMID 1992472 DOI: 10.1073/Pnas.88.3.815  0.289
2001 Michaud JL, Boucher F, Melnyk A, Gauthier F, Goshu E, Lévy E, Mitchell GA, Himms-Hagen J, Fan CM. Sim1 haploinsufficiency causes hyperphagia, obesity and reduction of the paraventricular nucleus of the hypothalamus. Human Molecular Genetics. 10: 1465-73. PMID 11448938 DOI: 10.1093/Hmg/10.14.1465  0.289
1994 Gibson KM, Cassidy SB, Seaver LH, Wanders RJA, Kennaway NG, Mitchell GA, Spark RP. Fatal cardiomyopathy associated with 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Journal of Inherited Metabolic Disease. 17: 291-294. PMID 7807935 DOI: 10.1007/Bf00711810  0.288
1996 Feoli-Fonseca JC, Lambert M, Mitchell G, Melançon SB, Dallaire L, Millington DS, Qureshi IA. Chronic sodium benzoate therapy in children with inborn errors of urea synthesis: effect on carnitine metabolism and ammonia nitrogen removal. Biochemical and Molecular Medicine. 57: 31-6. PMID 8812724 DOI: 10.1006/Bmme.1996.0006  0.288
1997 Song XQ, Fukao T, Mitchell GA, Kassovska-Bratinova S, Ugarte M, Wanders RJA, Hirayama K, Shintaku H, Churchill P, Watanabe H, Orii T, Kondo N. Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): Development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency Biochimica Et Biophysica Acta - Molecular Basis of Disease. 1360: 151-156. PMID 9128180 DOI: 10.1016/S0925-4439(96)00074-9  0.288
2000 Laurin NN, Wang SP, Mitchell GA. The hormone-sensitive lipase gene is transcribed from at least five alternative first exons in mouse adipose tissue. Mammalian Genome : Official Journal of the International Mammalian Genome Society. 11: 972-8. PMID 11063252 DOI: 10.1007/S003350010185  0.286
2004 Fortier M, Wang SP, Mauriège P, Semache M, Mfuma L, Li H, Levy E, Richard D, Mitchell GA. Hormone-sensitive lipase-independent adipocyte lipolysis during beta-adrenergic stimulation, fasting, and dietary fat loading. American Journal of Physiology. Endocrinology and Metabolism. 287: E282-8. PMID 15271647 DOI: 10.1152/Ajpendo.00203.2003  0.286
1997 Merante F, Duncan AM, Mitchell G, Duff C, Rommens J, Robinson BH. Chromosomal localization of the human liver form cytochrome c oxidase subunit VIIa gene. Genome / National Research Council Canada = GéNome / Conseil National De Recherches Canada. 40: 318-24. PMID 9202412 DOI: 10.1139/G97-044  0.286
2001 Roduit R, Masiello P, Wang SP, Li H, Mitchell GA, Prentki M. A Role for Hormone-Sensitive Lipase in Glucose-Stimulated Insulin Secretion: A Study in Hormone-Sensitive Lipase-Deficient Mice Diabetes. 50: 1970-1975. PMID 11522661 DOI: 10.2337/Diabetes.50.9.1970  0.285
2015 Lee JR, Srour M, Kim D, Hamdan FF, Lim SH, Brunel-Guitton C, Décarie JC, Rossignol E, Mitchell GA, Schreiber A, Moran R, Van Haren K, Richardson R, Nicolai J, Oberndorff KM, et al. De novo mutations in the motor domain of KIF1A cause cognitive impairment, spastic paraparesis, axonal neuropathy, and cerebellar atrophy. Human Mutation. 36: 69-78. PMID 25265257 DOI: 10.1002/Humu.22709  0.285
1993 Luks FI, St-Vil D, Hancock BJ, Laberge JM, Bensoussan AL, Russo P, Mitchell G, Lambert M, Blanchard H. Surgical and metabolic aspects of liver transplantation for tyrosinemia. Transplantation. 56: 1376-80. PMID 8279006 DOI: 10.1097/00007890-199312000-00019  0.283
1999 Morin C, Dubé J, Robinson BH, Lacroix J, Michaud J, De Braekeleer M, Geoffroy G, Lortie A, Blanchette C, Lambert MA, Mitchell GA. Stroke-like episodes in autosomal recessive cytochrome oxidase deficiency. Annals of Neurology. 45: 389-92. PMID 10072055 DOI: 10.1002/1531-8249(199903)45:3<389::Aid-Ana16>3.0.Co;2-B  0.283
1993 Wang S, Nadeau JH, Duncan A, Robert MF, Fontaine G, Schappert K, Johnson KR, Zietkiewicz E, Hruz P, Miziorko H, Mitchell GA. 3-Hydroxy-3-methylglutaryl coenzyme A lyase (HL): cloning and characterization of a mouse liver HL cDNA and subchromosomal mapping of the human and mouse HL genes Mammalian Genome. 4: 382-387. PMID 8102917 DOI: 10.1007/Bf00360589  0.283
2014 Gauthier J, Ouled Amar Bencheikh B, Hamdan FF, Harrison SM, Baker LA, Couture F, Thiffault I, Ouazzani R, Samuels ME, Mitchell GA, Rouleau GA, Michaud JL, Soucy JF. A homozygous loss-of-function variant in MYH11 in a case with megacystis-microcolon-intestinal hypoperistalsis syndrome. European Journal of Human Genetics : Ejhg. PMID 25407000 DOI: 10.1038/Ejhg.2014.256  0.282
2017 Ghaddhab C, Morin C, Brunel-Guitton C, Mitchell GA, Van Vliet G, Huot C. Premature Ovarian Failure in French Canadian Leigh Syndrome. The Journal of Pediatrics. PMID 28284481 DOI: 10.1016/J.Jpeds.2017.02.008  0.279
1999 Merouani A, Genest J, Rozen R, Lambert M, Mitchell GA, Dubois J, Robitaille P. Cerebral vascular complication and hyperhomocysteinemia in a cystinotic uremic child Pediatric Nephrology. 13: 73-76. PMID 10100295 DOI: 10.1007/S004670050567  0.279
1998 Lee N, Morin C, Mitchell G, Robinson BH. Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc. Biochimica Et Biophysica Acta. 1406: 1-4. PMID 9545512 DOI: 10.1016/S0925-4439(98)00003-9  0.278
2017 Chinsky JM, Singh R, Ficicioglu C, van Karnebeek CDM, Grompe M, Mitchell G, Waisbren SE, Gucsavas-Calikoglu M, Wasserstein MP, Coakley K, Scott CR. Diagnosis and treatment of tyrosinemia type I: a US and Canadian consensus group review and recommendations. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28771246 DOI: 10.1038/Gim.2017.101  0.277
2016 Attané C, Peyot ML, Lussier R, Poursharifi P, Zhao S, Zhang D, Morin J, Pineda M, Wang S, Dumortier O, Ruderman NB, Mitchell GA, Simons B, Madiraju SR, Joly E, et al. A beta cell ATGL-lipolysis/adipose tissue axis controls energy homeostasis and body weight via insulin secretion in mice. Diabetologia. PMID 27677764 DOI: 10.1007/S00125-016-4105-2  0.276
2017 Wagner GR, Bhatt DP, O'Connell TM, Thompson JW, Dubois LG, Backos DS, Yang H, Mitchell GA, Ilkayeva OR, Stevens RD, Grimsrud PA, Hirschey MD. A Class of Reactive Acyl-CoA Species Reveals the Non-enzymatic Origins of Protein Acylation. Cell Metabolism. 25: 823-837.e8. PMID 28380375 DOI: 10.1016/J.Cmet.2017.03.006  0.275
2005 Cinti S, Mitchell G, Barbatelli G, Murano I, Ceresi E, Faloia E, Wang S, Fortier M, Greenberg AS, Obin MS. Adipocyte death defines macrophage localization and function in adipose tissue of obese mice and humans. Journal of Lipid Research. 46: 2347-55. PMID 16150820 DOI: 10.1194/Jlr.M500294-Jlr200  0.275
1995 Dallaire L, Mitchell G, Giguère R, Lefebvre F, Melançon SB, Lambert M. Prenatal diagnosis of Smith-Lemli-Opitz syndrome is possible by measurement of 7-dehydrocholesterol in amniotic fluid. Prenatal Diagnosis. 15: 855-8. PMID 8559757 DOI: 10.1002/Pd.1970150911  0.274
2006 Phan V, Clermont M, Merouani A, Litalien C, Tucci M, Lambert M, Mitchell G, Jouvet P. Duration of extracorporeal therapy in acute maple syrup urine disease: a kinetic model. Pediatric Nephrology. 21: 698-704. PMID 16518628 DOI: 10.1007/S00467-006-0044-3  0.274
2014 Kronick JB, Hernandez M, Tingley K, Potter BK, Chan AKJ, Coyle D, Dodds L, Dyack S, Feigenbaum A, Geraghty MT, Gillis J, Rockman-Greenberg C, Khan A, Little J, MacKenzie J, ... ... Mitchell G, et al. Metabolic clinic atlas: Organization of care for pediatric metabolic patients in Canada Clinical Biochemistry. 47: 152. DOI: 10.1016/J.Clinbiochem.2014.07.082  0.273
2015 Maftei C, Laberge A, Maranda B, Mitchell G, Nizard S, Tihy F, Lemyre E. MG-121 Five new patients with pure distal 1q trisomy, review of the literature and phenotype redefinition Journal of Medical Genetics. 52: A5.2-A5. DOI: 10.1136/Jmedgenet-2015-103577.13  0.273
1987 Sinnett D, Mitchell G, Lavergne L, Melanqon SB, Dallaire L, Pocicr M, Labuda D. INCONTINENTIA PIGMENTI (IP): LINKAGE ANALYSIS OF A KINDRED USING MULTIPLE Xp CENOMIC MARKERS Pediatric Research. 21. DOI: 10.1203/00006450-198704010-00385  0.272
1991 Martin LS, Mitchell GA, Michaud J, Brody LC, Valle D. A polymorphic synonymous mutation in human ornithine-δ-aminotransferase (N378N) Nucleic Acids Research. 19: 1962. PMID 2030983 DOI: 10.1093/Nar/19.8.1962  0.272
1996 Ashmarina LI, Robert MF, Elsliger MA, Mitchell GA. Characterization of the hydroxymethylglutaryl-CoA lyase precursor, a protein targeted to peroxisomes and mitochondria Biochemical Journal. 315: 71-75. PMID 8670134 DOI: 10.1042/Bj3150071  0.271
2007 Debray FG, Lambert M, Chevalier I, Robitaille Y, Decarie JC, Shoubridge EA, Robinson BH, Mitchell GA. Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseases. Pediatrics. 119: 722-33. PMID 17403843 DOI: 10.1542/Peds.2006-1866  0.271
2020 Tingley K, Lamoureux M, Pugliese M, Geraghty MT, Kronick JB, Potter BK, Coyle D, Wilson K, Kowalski M, Austin V, Brunel-Guitton C, Buhas D, Chan AKJ, Dyack S, Feigenbaum A, ... ... Mitchell G, et al. Evaluation of the quality of clinical data collection for a pan-Canadian cohort of children affected by inherited metabolic diseases: lessons learned from the Canadian Inherited Metabolic Diseases Research Network. Orphanet Journal of Rare Diseases. 15: 89. PMID 32276663 DOI: 10.1186/S13023-020-01358-Z  0.27
2007 Debray FG, Mitchell GA, Allard P, Robinson BH, Hanley JA, Lambert M. Diagnostic accuracy of blood lactate-to-pyruvate molar ratio in the differential diagnosis of congenital lactic acidosis. Clinical Chemistry. 53: 916-21. PMID 17384007 DOI: 10.1373/Clinchem.2006.081166  0.27
2019 Madaan A, Chaudhari P, Nadeau-Vallée M, Hamel D, Zhu T, Mitchell G, Samuels M, Pundir S, Dabouz R, Howe Cheng CW, Mohammad Nezhady MA, Joyal JS, Rivera JC, Chemtob S. Müller Cell-Localized GPR81 (HCA) Regulates Inner Retinal Vasculature via Norrin/Wnt Pathways. The American Journal of Pathology. PMID 31220454 DOI: 10.1016/J.Ajpath.2019.05.016  0.269
2014 Hernandez M, Chakraborty P, Kronick JB, Potter BK, Chan AKJ, Coyle D, Dyack S, Feigenbaum A, Geraghty MT, Karaceper M, Khan A, Little J, MacKenzie J, Maranda B, Mhanni A, ... Mitchell G, et al. A REDCap database to support longitudinal follow-up of pediatric patients with inborn errors of metabolism Clinical Biochemistry. 47: 138. DOI: 10.1016/J.Clinbiochem.2014.07.040  0.268
2014 Rodrigue-Way A, Caron V, Bilodeau S, Keil S, Hassan M, Lévy E, Mitchell GA, Tremblay A. Scavenger receptor CD36 mediates inhibition of cholesterol synthesis via activation of the PPARγ/PGC-1α pathway and Insig1/2 expression in hepatocytes. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 28: 1910-23. PMID 24371122 DOI: 10.1096/Fj.13-240168  0.267
2008 Debray FG, Lambert M, Mitchell GA. Disorders of mitochondrial function. Current Opinion in Pediatrics. 20: 471-82. PMID 18622207 DOI: 10.1097/Mop.0B013E328306Ebb6  0.266
2009 De Bie I, Nizard SD, Mitchell GA. Fetal dilated cardiomyopathy: an unsuspected presentation of methylmalonic aciduria and hyperhomocystinuria, cblC type. Prenatal Diagnosis. 29: 266-70. PMID 19248038 DOI: 10.1002/Pd.2218  0.264
2000 Bétard C, Rasquin-Weber A, Brewer C, Drouin E, Clark S, Verner A, Darmond-Zwaig C, Fortin J, Mercier J, Chagnon P, Fujiwara TM, Morgan K, Richter A, Hudson TJ, Mitchell GA. Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22 - And identification of a shared haplotype American Journal of Human Genetics. 67: 222-228. PMID 10820129 DOI: 10.1086/302993  0.263
2009 Yu B, Mitchell GA, Richter A. Cirhin up-regulates a canonical NF-kappaB element through strong interaction with Cirip/HIVEP1. Experimental Cell Research. 315: 3086-98. PMID 19732766 DOI: 10.1016/J.Yexcr.2009.08.017  0.262
1985 Frézal J, Amédée-Manesme O, Mitchell G, Heuertz S, Rey F, Rey J, Saudubray JM. Maple syrup urine disease: two different forms within a single family. Human Genetics. 71: 89-91. PMID 4029957 DOI: 10.1007/Bf00295676  0.261
2007 Zafeiriou DI, Vargiami E, Mayapetek E, Augoustidou-Savvopoulou P, Mitchell GA. 3-Hydroxy-3-methylglutaryl coenzyme a lyase deficiency with reversible white matter changes after treatment. Pediatric Neurology. 37: 47-50. PMID 17628222 DOI: 10.1016/J.Pediatrneurol.2007.02.007  0.261
2009 Brunel-Guitton C, Rivard GE, Galipeau J, Alos N, Miron MC, Therrien R, Mitchell G, Lapierre G, Lambert M. Enzyme replacement therapy in pediatric patients with Gaucher disease: what should we use as maintenance dosage? Molecular Genetics and Metabolism. 96: 73-6. PMID 19083253 DOI: 10.1016/J.Ymgme.2008.11.158  0.261
1994 Makałowski W, Mitchell GA, Labuda D. Alu sequences in the coding regions of mRNA: a source of protein variability Trends in Genetics. 10: 188-193. PMID 8073532 DOI: 10.1016/0168-9525(94)90254-2  0.259
2013 Attané C, Peyot ML, Wang S, Mitchell GA, Lussier R, Pineda M, Madiraju MS, Joly E, Prentki M. Role of Adipose Triglyceride Lipase and Lipolysis in the Regulation of Insulin Secretion: Study in β-Cell-Specific ATGL-Deficient Mice Canadian Journal of Diabetes. 37: S58. DOI: 10.1016/J.Jcjd.2013.08.172  0.259
2003 Liet JM, Pelletier V, Robinson BH, Laryea MD, Wendel U, Morneau S, Morin C, Mitchell G, Lacroix J. The effect of short-term dimethylglycine treatment on oxygen consumption in cytochrome oxidase deficiency: a double-blind randomized crossover clinical trial. The Journal of Pediatrics. 142: 62-6. PMID 12520257 DOI: 10.1067/Mpd.2003.Mpd0333  0.258
2012 Ozanne B, Nelson J, Cousineau J, Lambert M, Phan V, Mitchell G, Alvarez F, Ducruet T, Jouvet P. Threshold for toxicity from hyperammonemia in critically ill children. Journal of Hepatology. 56: 123-8. PMID 21703182 DOI: 10.1016/J.Jhep.2011.03.021  0.256
2009 Kanshin E, Wang S, Ashmarina L, Fedjaev M, Nifant'ev I, Mitchell GA, Pshezhetsky AV. The stoichiometry of protein phosphorylation in adipocyte lipid droplets: analysis by N-terminal isotope tagging and enzymatic dephosphorylation. Proteomics. 9: 5067-77. PMID 19921680 DOI: 10.1002/Pmic.200800861  0.252
2014 Hamel D, Sanchez M, Duhamel F, Roy O, Honoré JC, Noueihed B, Zhou T, Nadeau-Vallée M, Hou X, Lavoie JC, Mitchell G, Mamer OA, Chemtob S. G-protein-coupled receptor 91 and succinate are key contributors in neonatal postcerebral hypoxia-ischemia recovery. Arteriosclerosis, Thrombosis, and Vascular Biology. 34: 285-93. PMID 24285580 DOI: 10.1161/Atvbaha.113.302131  0.251
1992 Dallaire L, Michaud J, Melancon SB, Potier M, Lambert M, Mitchell G, Boisvert J. Prenatal diagnosis of fetal anomalies during the second trimester of pregnancy: their characterization and delineation of defects in pregnancies at risk. Prenatal Diagnosis. 11: 629-35. PMID 1837356 DOI: 10.1002/Pd.1970110821  0.25
2010 Rousseau F, Lindsay C, Charland M, Labelle Y, Bergeron J, Blancquaert I, Delage R, Gilfix B, Miron M, Mitchell GA, Oligny L, Pazzagli M, Mamotte C, Payne D. Development and description of GETT: a genetic testing evidence tracking tool. Clinical Chemistry and Laboratory Medicine : Cclm / Fescc. 48: 1397-407. PMID 20658948 DOI: 10.1515/Cclm.2010.291  0.247
1994 Wang S, Lapierre P, Robert MF, Nadeau JH, Mitchell GA. Hormone-sensitive lipase maps to proximal chromosome 7 in mice and is genetically distinct from the Ad and Tub loci. Genomics. 24: 416-7. PMID 7698777 DOI: 10.1006/Geno.1994.1646  0.246
2003 Suc I, Brunet S, Mitchell G, Rivard GE, Levy E. Oxidative tyrosylation of high density lipoproteins impairs cholesterol efflux from mouse J774 macrophages: role of scavenger receptors, classes A and B. Journal of Cell Science. 116: 89-99. PMID 12456719 DOI: 10.1242/Jcs.00126  0.245
2006 Nolan CJ, Leahy JL, Delghingaro-Augusto V, Moibi J, Soni K, Peyot ML, Fortier M, Guay C, Lamontagne J, Barbeau A, Przybytkowski E, Joly E, Masiello P, Wang S, Mitchell GA, et al. Beta cell compensation for insulin resistance in Zucker fatty rats: increased lipolysis and fatty acid signalling. Diabetologia. 49: 2120-30. PMID 16868750 DOI: 10.1007/S00125-006-0305-5  0.244
1992 Zietkiewicz E, Sinnett D, Richer C, Mitchell G, Vanasse M, Labuda D. Single-strand conformational polymorphisms (SSCP): detection of useful polymorphisms at the dystrophin locus. Human Genetics. 89: 453-6. PMID 1618495 DOI: 10.1007/Bf00194322  0.243
2004 Lahjouji K, Elimrani I, Lafond J, Leduc L, Qureshi IA, Mitchell GA. L-Carnitine transport in human placental brush-border membranes is mediated by the sodium-dependent organic cation transporter OCTN2. American Journal of Physiology. Cell Physiology. 287: C263-9. PMID 15238359 DOI: 10.1152/Ajpcell.00333.2003  0.242
2008 Debray FG, Boulanger Y, Khiat A, Decarie JC, Orquin J, Roy MS, Lortie A, Ramos F, Verhoeven NM, Struys E, Blom HJ, Jakobs C, Levy E, Mitchell GA, Lambert M. Reduced brain choline in homocystinuria due to remethylation defects. Neurology. 71: 44-9. PMID 18591504 DOI: 10.1212/01.Wnl.0000316391.40236.C3  0.242
2014 Potter BK, Chakraborty P, Coyle D, Kronick JB, Wilson K, Brownell M, Chan A, Dodd L, Dyack S, Feigenbaum A, Fell D, Geraghty MT, Gillis J, Rockman-Greenberg C, Guttmann A, ... ... Mitchell G, et al. Building a pan-Canadian practice-based research network for inherited metabolic diseases: The first two years of the Canadian Inherited Metabolic Diseases Research Network (CIMDRN) Clinical Biochemistry. 47: 137-138. DOI: 10.1016/J.Clinbiochem.2014.07.039  0.241
2006 Magera MJ, Gunawardena ND, Hahn SH, Tortorelli S, Mitchell GA, Goodman SI, Rinaldo P, Matern D. Quantitative determination of succinylacetone in dried blood spots for newborn screening of tyrosinemia type I. Molecular Genetics and Metabolism. 88: 16-21. PMID 16448836 DOI: 10.1016/J.Ymgme.2005.12.005  0.24
2010 Brunel-Guitton C, Costa T, Mitchell GA, Lambert M. Treatment of cobalamin C (cblC) deficiency during pregnancy. Journal of Inherited Metabolic Disease. 33: S409-12. PMID 20830523 DOI: 10.1007/S10545-010-9202-7  0.239
2015 Meijer IA, Sasarman F, Maftei C, Rossignol E, Vanasse M, Major P, Mitchell GA, Brunel-Guitton C. LPIN1 deficiency with severe recurrent rhabdomyolysis and persistent elevation of creatine kinase levels due to chromosome 2 maternal isodisomy Molecular Genetics and Metabolism Reports. 5: 85-88. DOI: 10.1016/j.ymgmr.2015.10.010  0.239
2012 Larochelle J, Alvarez F, Bussières JF, Chevalier I, Dallaire L, Dubois J, Faucher F, Fenyves D, Goodyer P, Grenier A, Holme E, Laframboise R, Lambert M, Lindstedt S, Maranda B, ... ... Mitchell GA, et al. Effect of nitisinone (NTBC) treatment on the clinical course of hepatorenal tyrosinemia in Québec. Molecular Genetics and Metabolism. 107: 49-54. PMID 22885033 DOI: 10.1016/J.Ymgme.2012.05.022  0.238
2003 Elimrani I, Lahjouji K, Seidman E, Roy MJ, Mitchell GA, Qureshi I. Expression and localization of organic cation/carnitine transporter OCTN2 in Caco-2 cells. American Journal of Physiology. Gastrointestinal and Liver Physiology. 284: G863-71. PMID 12684216 DOI: 10.1152/Ajpgi.00220.2002  0.238
1984 Mitchell G, Saudubray JM, Gubler MC, Habib R, Ogier H, Frezal J, Boue J. Congenital anomalies in glutaric aciduria type 2. The Journal of Pediatrics. 104: 961. PMID 6726538 DOI: 10.1016/S0022-3476(84)80520-X  0.234
1983 Frézal J, Munnich A, Mitchell G. One gene, several messages. From multifunctional proteins to endogenous opiates. Human Genetics. 64: 311-314. PMID 6311726 DOI: 10.1007/Bf00292362  0.234
2019 Brossier D, Goyer I, Ziani L, Marquis C, Mitchell G, Ozanne B, Jouvet P. Influence of implementing a protocol for an intravenously administered ammonia scavenger on the management of acute hyperammonemia in a pediatric intensive care unit. Journal of Inherited Metabolic Disease. 42: 77-85. PMID 30740742 DOI: 10.1002/Jimd.12029  0.234
2013 Buha? D, Bernard G, Fukao T, Décarie JC, Chouinard S, Mitchell GA. A treatable new cause of chorea: beta-ketothiolase deficiency. Movement Disorders : Official Journal of the Movement Disorder Society. 28: 1054-6. PMID 23818432 DOI: 10.1002/Mds.25538  0.228
1981 Lacroix J, Delage G, Mitchell G. Erysipeloid in an infant The Journal of Pediatrics. 99: 745-746. PMID 7299551 DOI: 10.1016/S0022-3476(81)80400-3  0.228
2008 Sapieha P, Sirinyan M, Hamel D, Zaniolo K, Joyal JS, Cho JH, Honoré JC, Kermorvant-Duchemin E, Varma DR, Tremblay S, Leduc M, Rihakova L, Hardy P, Klein WH, Mu X, ... ... Mitchell G, et al. The succinate receptor GPR91 in neurons has a major role in retinal angiogenesis. Nature Medicine. 14: 1067-76. PMID 18836459 DOI: 10.1038/Nm.1873  0.226
2013 Rodrigue-Way A, Keil S, Caron V, Bilodeau S, Levy E, Mitchell GA, Tremblay A. Scavenger Receptor CD36 Mediates Inhibition of Cholesterol Synthesis via Activation of the LKB1-AMPK Pathway and Insig1/Insig2 Expression in Hepatocytes Canadian Journal of Diabetes. 37. DOI: 10.1016/J.Jcjd.2013.08.196  0.226
2012 Maranda B, Fan L, Soucy JF, Simard L, Mitchell GA. Spinal muscular atrophy: clinical validation of a single-tube multiplex real time PCR assay for determination of SMN1 and SMN2 copy numbers. Clinical Biochemistry. 45: 88-91. PMID 22085534 DOI: 10.1016/J.Clinbiochem.2011.10.019  0.225
2015 Wu JW, Mitchell GA. Potential mechanism underlying the PNPLA3(I148M) - hepatic steatosis connection. Hepatology (Baltimore, Md.). PMID 26096616 DOI: 10.1002/Hep.27943  0.224
2002 Lahjouji K, Malo C, Mitchell GA, Qureshi IA. L-Carnitine transport in mouse renal and intestinal brush-border and basolateral membrane vesicles. Biochimica Et Biophysica Acta. 1558: 82-93. PMID 11750267 DOI: 10.1016/S0005-2736(01)00433-3  0.223
1992 Brody LC, Mitchell GA, Obie C, Michaud J, Steel G, Fontaine G, Robert MF, Sipila I, Kaiser-Kupfer M, Valle D. Ornithine δ-aminotransferase mutations in gyrate atrophy: Allelic heterogeneity and functional consequences Journal of Biological Chemistry. 267: 3302-3307. PMID 1737786  0.223
2013 de Laet C, Dionisi-Vici C, Leonard JV, McKiernan P, Mitchell G, Monti L, de Baulny HO, Pintos-Morell G, Spiekerkötter U. Recommendations for the management of tyrosinaemia type 1. Orphanet Journal of Rare Diseases. 8: 8. PMID 23311542 DOI: 10.1186/1750-1172-8-8  0.22
1990 Deragon JM, Sinnett D, Mitchell G, Potier M, Labuda D. Use of gamma irradiation to eliminate DNA contamination for PCR. Nucleic Acids Research. 18: 6149. PMID 2235513 DOI: 10.1093/Nar/18.20.6149  0.218
2021 Zhao C, Wang Y, Yang H, Wang S, Tang MC, Cyr D, Parente F, Allard P, Waters P, Furtos A, Yang G, Mitchell GA. Propionic acidemia in mice: Liver acyl-CoA levels and clinical course. Molecular Genetics and Metabolism. PMID 34896004 DOI: 10.1016/j.ymgme.2021.11.011  0.214
2008 Debray FG, Lambert M, Lemieux B, Soucy JF, Drouin R, Fenyves D, Dubé J, Maranda B, Laframboise R, Mitchell GA. Phenotypic variability among patients with hyperornithinaemia-hyperammonaemia-homocitrullinuria syndrome homozygous for the delF188 mutation in SLC25A15. Journal of Medical Genetics. 45: 759-64. PMID 18978333 DOI: 10.1136/jmg.2008.059097  0.209
1983 Mitchell G, Saudubray JM, Benoit Y, Rocchiccioli F, Charpentier C, Ogier H, Boue J. Antenatal Diagnosis Of Glutaricaciduria Type Ii The Lancet. 321: 1099-1099. PMID 6133123 DOI: 10.1016/S0140-6736(83)91929-3  0.205
2015 Rypens F, El‐Jalbout R, Garel L, Hudon L, Beaudin M, Mitchell G, Grignon A. P17.06: Fetal rectal prolapse secondary to distal colic atresia: P17.06: Fetal rectal prolapse secondary to distal colic atresia Ultrasound in Obstetrics & Gynecology. 46: 176-176. DOI: 10.1002/Uog.15480  0.205
1994 Ziȩtkiewicz E, Makałowski W, Mitchell GA, Labuda D, Sharma S, Maizel A, Jackson JR. Phylogenetic analysis of a reported complementary DNA sequence Science. 265: 1110-1111. PMID 8066452 DOI: 10.1126/Science.8066452  0.205
1994 Ashmarina LI, Rusnak N, Miziorko HM, Mitchell GA. 3-hydroxy-3-methylglutaryl-CoA lyase is present in mouse and human liver peroxisomes Journal of Biological Chemistry. 269: 31929-31932. PMID 7527399  0.201
1996 Kassovska-Bratinova S, Fukao T, Song XQ, Duncan AMV, Chen HS, Robert MF, Pérez-Cerdá C, Ugarte M, Chartrand C, Vobecky S, Kondo N, Mitchell GA. Succinyl CoA: 3-oxoacid CoA transferase (SCOT): Human cDNA cloning, human chromosomal mapping to 5p13, and mutation detection in a SCOT-deficient patient American Journal of Human Genetics. 59: 519-528. PMID 8751852  0.198
2010 Siles A, Mitchell GA, Dahdah NS. An infant with mucolipidosis-II and an atretic orifice of the left coronary artery. Cardiology in the Young. 20: 97-9. PMID 19825254 DOI: 10.1017/S1047951109991843  0.197
1989 Mitchell GA, Brody LC, Sipila I, Looney JE, Wong C, Engelhardt JF, Patel AS, Steel G, Obie C, Kaiser-Kupfer M, Valle D. At least two mutant alleles of ornithine δ-aminotransferase cause gyrate atrophy of the choroid and retina in Finns Proceedings of the National Academy of Sciences of the United States of America. 86: 197-201. PMID 2492100 DOI: 10.1073/pnas.86.1.197  0.187
2022 Wang Y, Yang H, Geerts C, Furtos A, Waters P, Cyr D, Wang S, Mitchell GA. The multiple facets of acetyl-CoA metabolism: Energetics, biosynthesis, regulation, acylation and inborn errors. Molecular Genetics and Metabolism. 138: 106966. PMID 36528988 DOI: 10.1016/j.ymgme.2022.106966  0.185
2021 Xie B, Shi X, Li Y, Xia B, Zhou J, Du M, Xing X, Bai L, Liu E, Alvarez F, Jin L, Deng S, Mitchell GA, Pan D, Li M, et al. Deficiency of ASGR1 in pigs recapitulates reduced risk factor for cardiovascular disease in humans. Plos Genetics. 17: e1009891. PMID 34762653 DOI: 10.1371/journal.pgen.1009891  0.185
1998 Mitchell GA, Wang SP, Ashmarina L, Robert MF, Bouchard G, Laurin N, Kassovska-Bratinova S, Boukaftane Y. Inborn errors of ketogenesis. Biochemical Society Transactions. 26: 136-40. PMID 9649735 DOI: 10.1042/Bst0260136  0.184
2022 Champagne M, Horvath GA, Perreault S, Gauthier J, Hyland K, Soucy JF, Mitchell GA. Intermittent neurologic decompensation: An underrecognized presentation of tyrosine hydroxylase deficiency. Jimd Reports. 63: 400-406. PMID 36101825 DOI: 10.1002/jmd2.12306  0.182
1988 Mitchell GA, Brody LC, Looney J, Steel G, Suchanek M, Dowling C, Der Kaloustian V, Kaiser-Kupfer M, Valle D. An initiator codon mutation in ornithine-δ-aminotransferase causing gyrate atrophy of the choroid and retina Journal of Clinical Investigation. 81: 630-633. PMID 3339136 DOI: 10.1172/JCI113365  0.182
2018 Levtova A, Waters PJ, Buhas D, Lévesque S, Auray-Blais C, Clarke JTR, Laframboise R, Maranda B, Mitchell GA, Brunel-Guitton C, Braverman NE. Combined malonic and methylmalonic aciduria due to ACSF3 mutations: benign clinical course in an unselected cohort. Journal of Inherited Metabolic Disease. PMID 29858964 DOI: 10.1007/s10545-018-0197-9  0.181
1988 Mitchell GA, Looney JE, Brody LC, Steel G, Suchanek M, Engelhardt JF, Willard HF, Valle D. Human ornithine-δ-aminotransferase. cDNA cloning and analysis of the structural gene Journal of Biological Chemistry. 263: 14288-14295. PMID 3170546  0.179
1995 Michaud J, Thompson GN, Brody LC, Steel G, Obie C, Fontaine G, Schappert K, Keith CG, Valle D, Mitchell GA. Pyridoxine-responsive gyrate atrophy of the choroid and retina: Clinical and biochemical correlates of the mutation A226V American Journal of Human Genetics. 56: 616-622. PMID 7887415  0.177
1993 Mitchell GA, Robert MF, Hruz PW, Wang S, Fontaine G, Behnke CE, Mende-Mueller LM, Schappert K, Lee C, Gibson KM, Miziorko HM. 3-Hydroxy-3-methylglutaryl coenzyme a lyase (HL):Cloning of human and chicken liver HL cDNAs and characterization of a mutation causing human HL deficiency Journal of Biological Chemistry. 268: 4376-4381. PMID 8440722  0.175
2022 Heckel E, Cagnone G, Agnihotri T, Cakir B, Das A, Kim JS, Kim N, Lavoie G, Situ A, Pundir S, Sun Y, Wünnemann F, Pierce KA, Dennis C, Mitchell GA, et al. Triglyceride-derived fatty acids reduce autophagy in a model of retinal angiomatous proliferation. Jci Insight. PMID 35167498 DOI: 10.1172/jci.insight.154174  0.17
2022 Yang H, Wang Y, Tang MC, Waters P, Wang S, Allard P, Ryan RO, Nuyt AM, Paradis P, Schiffrin EL, Furtos A, Mitchell GA. Cardiac-specific deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase in mice causes cardiomyopathy and a distinct pattern of acyl-coenzyme A-related biomarkers. Molecular Genetics and Metabolism. 137: 257-264. PMID 36228350 DOI: 10.1016/j.ymgme.2022.09.008  0.169
2001 Wang SP, Laurin N, Himms-Hagen J, Rudnicki MA, Levy E, Robert MF, Pan L, Oligny L, Mitchell GA. The adipose tissue phenotype of hormone-sensitive lipase deficiency in mice. Obesity Research. 9: 119-28. PMID 11316346 DOI: 10.1038/oby.2001.15  0.16
2022 Thibault LP, Mitchell GA, Parisien B, Hamel P, Blanchard AC. An Infant with Bilateral Keratitis: From Infectious to Genetic Diagnosis. The American Journal of Case Reports. 23: e937967. PMID 36447403 DOI: 10.12659/AJCR.937967  0.16
2023 Chen S, Mitchell GA, Soucy JF, Gauthier J, Brais B, La Piana R. TUFM-variants lead to white matter abnormalities mimicking multiple sclerosis. European Journal of Neurology. PMID 37433570 DOI: 10.1111/ene.15982  0.158
2024 Demaret T, Bédard K, Soucy JF, Watkins D, Allard P, Levtova A, O'Brien A, Brunel-Guitton C, Rosenblatt DS, Mitchell GA. The MMACHC variant c.158T>C: Mild clinical and biochemical phenotypes and marked hydroxocobalamin response in cblC patients. Molecular Genetics and Metabolism. 142: 108345. PMID 38387306 DOI: 10.1016/j.ymgme.2024.108345  0.153
1997 Fukao T, Song XQ, Mitchell GA, Yamaguchi S, Sukegawa K, Orii T, Kondo N. Enzymes of ketone body utilization in human tissues: Protein and messenger RNA levels of succinyl-coenzyme A (CoA):3-ketoacid CoA transferase and mitochondrial and cytosolic acetoacetyl-CoA thiolases Pediatric Research. 42: 498-502. PMID 9380443  0.153
1994 Roberts JR, Narasimhan C, Hruz PW, Mitchell GA, Miziorko HM. 3-Hydroxy-3-methylglutaryl-CoA lyase: Expression and isolation of the recombinant human enzyme and investigation of a mechanism for regulation of enzyme activity Journal of Biological Chemistry. 269: 17841-17846. PMID 8027038  0.146
1999 Ashmarina LI, Pshezhetsky AV, Branda SS, Isaya G, Mitchell GA. 3-Hydroxy-3-methylglutaryl coenzyme A lyase: Targeting and processing in peroxisomes and mitochondria Journal of Lipid Research. 40: 70-75. PMID 9869651  0.143
2015 Lamoureux MF, Tingley K, Kronick JB, Potter BK, Chan AK, Coyle D, Dodds L, Dyack S, Feigenbaum A, Geraghty M, Gillis J, Rockman-Greenberg C, Khan A, Little J, MacKenzie J, ... ... Mitchell G, et al. Metabolic Clinic Atlas: Organization of Care for Children with Inherited Metabolic Disease in Canada. Jimd Reports. 21: 15-22. PMID 25716610 DOI: 10.1007/8904_2014_347  0.143
2015 Levtova A, Camuzeaux S, Laberge AM, Allard P, Brunel-Guitton C, Diadori P, Rossignol E, Hyland K, Clayton PT, Mills PB, Mitchell GA. Normal Cerebrospinal Fluid Pyridoxal 5'-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic Encephalopathy. Jimd Reports. 22: 67-75. PMID 25762494 DOI: 10.1007/8904_2015_413  0.141
2000 Gibson KM, Ugarte M, Fukao T, Mitchell GA. Molecular and enzymatic methods for detection of genetic defects in distal pathways of branched-chain amino acid metabolism Methods in Enzymology. 324: 432-453. PMID 10989451  0.137
2022 Shelihan I, Rossignol E, Décarie JC, Bonnefont JP, Brivet M, Brunel-Guitton C, Mitchell GA. Infantile onset carnitine palmitoyltransferase 2 deficiency: Cortical polymicrogyria, schizencephaly, and gray matter heterotopias in an adolescent with normal development. Jimd Reports. 63: 3-10. PMID 35028265 DOI: 10.1002/jmd2.12243  0.135
1990 Mitchell GA, Lambert M, Paradis K. Metabolic diseases and liver failure in children Pediatrie. 45.  0.134
1989 Migeon BR, Axelman J, De Beur SJ, Valle D, Mitchell GA, Rosenbaum KN. Selection against lethal alleles in females heterozygous for incontinentia pigmenti American Journal of Human Genetics. 44: 100-106. PMID 2562819  0.134
1982 Mitchell GA, Meher‐Homji KM, Baker RSU. Sister chromatid exchange induction in two cell lines Environmental Mutagenesis. 4: 267-270. PMID 6284500 DOI: 10.1002/em.2860040309  0.132
1994 George AL, Sloan-Brown K, Fenichel GM, Mitchell GA, Spiegel R, Pascuzzi RM. Nonsense and missense mutations of the muscle chloride channel gene in patients with myotonia congenita Human Molecular Genetics. 3: 2071-2072. PMID 7874130  0.131
2008 Debray FG, Merouani A, Lambert M, Brochu P, Bernard C, Robinson BH, Mitchell GA. Acute tubular dysfunction with Fanconi syndrome: a new manifestation of mitochondrial cytopathies. American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation. 51: 691-6. PMID 18371545 DOI: 10.1053/j.ajkd.2007.11.024  0.125
1988 Colevas AD, Edwards JL, Hruban RH, Mitchell GA, Valle D, Hutchins GM. Glutaric acidemia type II. Comparison of pathologic features in two infants Archives of Pathology and Laboratory Medicine. 112: 1133-1139. PMID 3178428  0.124
2024 Demaret T, Joyal JS, Karalis A, Parente F, Delrue MA, Mitchell GA. Insulin therapy in acute decompensation of holocarboxylase synthetase deficiency with hyperglycemia and ketoacidosis. Molecular Genetics and Metabolism Reports. 39: 101073. PMID 38550975 DOI: 10.1016/j.ymgmr.2024.101073  0.122
2020 Mitchell GA, Sasai H, Bastin J, Sass JO, Wanders RJ, Yamaguchi S. Toshiyuki Fukao. Journal of Inherited Metabolic Disease. PMID 32989766 DOI: 10.1002/jimd.12308  0.12
2005 Laberge AM, Michaud J, Richter A, Lemyre E, Lambert M, Brais B, Mitchell GA. Population history and its impact on medical genetics in Quebec. Clinical Genetics. 68: 287-301. PMID 16143014 DOI: 10.1111/j.1399-0004.2005.00497.x  0.117
1978 Pochron SP, Mitchell GA, Albareda I, Huseby RM, Gargiulo RJ. A fluorescent substrate assay for plasminogen Thrombosis Research. 13: 733-739. PMID 105421 DOI: 10.1016/0049-3848(78)90179-2  0.109
2010 Urban TM, Mitchell GA, Wellborn-Kim JJ, Terneus WF, Callahan CM, Mendes J, Webber SL. Clinical response to unintentionally rapid infusion of drotrecogin alfa (activated). American Journal of Health-System Pharmacy : Ajhp : Official Journal of the American Society of Health-System Pharmacists. 67: 1174-7. PMID 20592322 DOI: 10.2146/ajhp090399  0.109
1994 Sipilä I, Valle D, Mitchell GA, Brody LC. Hyperornithinemia and gyrate atrophy: ornithine aminotransferase gene error causing a Finnish disease Duodecim; LääKetieteellinen Aikakauskirja. 110: 681-686. PMID 8542823  0.105
2010 Wellborn-Kim JJ, Mitchell GA, Terneus WF, Stowe CL, Malias MA, Sparkman GM, Hanson GW. Fondaparinux therapy in a hemodialysis patient with heparin-induced thrombocytopenia type II American Journal of Health-System Pharmacy. 67: 1075-1079. DOI: 10.2146/ajhp090394  0.104
2022 Sanchez M, Hamel D, Bajon E, Duhamel F, Bhosle VK, Zhu T, Rivera JC, Dabouz R, Nadeau-Vallée M, Sitaras N, Tremblay DÉ, Omri S, Habelrih T, Rouget R, Hou X, ... ... Mitchell G, et al. The Succinate Receptor SUCNR1 Resides at the Endoplasmic Reticulum and Relocates to the Plasma Membrane in Hypoxic Conditions. Cells. 11. PMID 35883628 DOI: 10.3390/cells11142185  0.102
2015 Bellerose J, Neugnot-Cerioli M, Bédard K, Brunel-Guitton C, Mitchell GA, Ospina LH, Beauchamp MH. A Highly Diverse Portrait: Heterogeneity of Neuropsychological Profiles in cblC Defect. Jimd Reports. PMID 26608391 DOI: 10.1007/8904_2015_517  0.101
1979 Lawson DE, Mitchell GA, Huseby RM. A sensitive fluorescent assay for determining α2-plasmin inhibitor using a synthetic substrate Thrombosis Research. 14: 323-332. PMID 155894 DOI: 10.1016/0049-3848(79)90241-X  0.1
1983 Baker RSU, Mitchell GA, Meher-Homji KM, Podobna E. Sensitivity of two Chinese hamster cell lines to SCE induction by a variety of chemical mutagens Mutation Research/Genetic Toxicology. 118: 103-116. PMID 6306456 DOI: 10.1016/0165-1218(83)90120-9  0.1
1978 Mitchell GA, Garguilo RJ, Huseby RM, Lawson DE, Pochron SP, Sehuanes JA. Assay for plasma heparin using a synthetic peptide substrate for thrombin: introduction of the fluorophore aminoisophthalic acid, dimethyl ester Thrombosis Research. 13: 47-52. PMID 694832 DOI: 10.1016/0006-2952(78)90185-5  0.092
1998 Mitchell GA, Dunnavan G. Illegal Use of β-Adrenergic Agonists in the United States Journal of Animal Science. 76: 208-211. PMID 9464900  0.091
1988 Valle DL, Mitchell GA. Inborn errors of metabolism in the molecular age Progress in Medical Genetics. 7: 100-129. PMID 3277250  0.088
2009 Mitchell GA. Genetics, physiology and perinatal influences in childhood obesity: View from the Chair International Journal of Obesity. 33. PMID 19363507 DOI: 10.1038/ijo.2009.16  0.08
1978 Mitchell GA, Hudson PM, Huseby RM, Pochron SP, Gargiulo RJ. Fluorescent substrate assay for antithrombin III Thrombosis Research. 12: 219-225. PMID 416516 DOI: 10.1016/0049-3848(78)90293-1  0.079
1985 Mitchell GA, Solorzano MM, Riesgo MI, Jaffe GE, Carter JH. Novel rhodamine tripeptide substrate for manual and automated colorimetric prothrombin time test Thrombosis Research. 40: 339-349. PMID 4082112 DOI: 10.1016/0049-3848(85)90269-5  0.079
1976 Mitchell GA, Pochron SP, Smutny PV, Guity R. Decreased radioassay values for folate after serum extraction when pteroylglutamic acid standards are used Clinical Chemistry. 22: 647-649. PMID 1261014  0.074
1995 Mitchell GA, Kassovska-Bratinova S, Boukaftane Y, Robert MF, Wang SP, Ashmarina L, Lambert M, Lapierre P, Potier E. Medical aspects of ketone body metabolism. Clinical and Investigative Medicine. MéDecine Clinique Et Experimentale. 18: 193-216. PMID 7554586  0.074
1983 Mitchell GA. Development and clinical use of automated synthetic substrate methods for the evaluation of coagulation and fibrinolysis Seminars in Thrombosis and Hemostasis. 9: 262-274.  0.069
1997 Brunt K, Mitchell GA. Statistical evaluation of an international collaborative study concerning the improved gas chromatographic determination of adipate in starch Starch/Staerke. 49: 296-301.  0.068
1982 Mitchell GA, Vanderbist MJ, Meert FF. Gas-liquid chromatographic determination of adipate content of acetylated di-starch adipate Journal of the Association of Official Analytical Chemists. 65: 238-240. PMID 7085540  0.067
2006 Hwang MY, Yum SY, Losonczy MF, Mitchell G, Kwon JS. Schizophrenia with obsessive compulsive features. Psychiatry (Edgmont (Pa. : Township)). 3: 34-41. PMID 20975826  0.066
1990 Mitchell GA. Methods of Starch Analysis Starch ‐ StäRke. 42: 131-134. DOI: 10.1002/star.19900420403  0.066
2011 Branch WT, Mitchell GA. Wisdom in medicine The Pharos of Alpha Omega Alpha-Honor Medical Society. Alpha Omega Alpha. 74: 12-17. PMID 21877511  0.061
2021 Chorfi S, Mitchell GA, Qian CX. Retinopathy of transcobalamin II deficiency: long-term stability with treatment. Ophthalmology. PMID 33476645 DOI: 10.1016/j.ophtha.2021.01.015  0.061
1993 Harrap SB, Mitchell GA, Casley DJ, Mirakian C, Doyle AE. Angiotensin II, sodium, and cardiovascular hypertrophy in spontaneously hypertensive rats Hypertension. 21: 50-55. PMID 8418023  0.06
1978 Chapman RF, Cook AG, Mitchell GA, Page WW. Wing dimorphism and flight in Zonocerus variegatus (L.) (Orthoptera: Pyrgomorphidae) Bulletin of Entomological Research. 68: 229-242. DOI: 10.1017/S0007485300007318  0.058
2011 Mitchell GA, Montési LGJ, Zhu W, Smith DK, Schouten H. Transient rifting north of the Galápagos Triple Junction Earth and Planetary Science Letters. 307: 461-469. DOI: 10.1016/J.Epsl.2011.05.027  0.058
1994 Lea PJ, Temkin RJ, Freeman KB, Mitchell GA, Robinson BH. Variations in mitochondrial ultrastructure and dynamics observed by high resolution scanning electron microscopy (HRSEM). Microscopy Research and Technique. 27: 269-77. PMID 8186445 DOI: 10.1002/jemt.1070270402  0.055
1989 Mitchell GA. Current status and recent trends of palustrine wetlands in the Tualatin Valley, Oregon. M.Sc. thesis .  0.054
2013 Arbuckle TE, Fraser WD, Fisher M, Davis K, Liang CL, Lupien N, Bastien S, Velez MP, von Dadelszen P, Hemmings DG, Wang J, Helewa M, Taback S, Sermer M, Foster W, ... ... Mitchell G, et al. Cohort profile: the maternal-infant research on environmental chemicals research platform. Paediatric and Perinatal Epidemiology. 27: 415-25. PMID 23772943 DOI: 10.1111/Ppe.12061  0.054
1981 Mitchell GA, Abdullahad CM, Ruiz JA, Huseby RM, Alvarez DE, Geiger TM, Black FM, Heller ZH. Fluorogenic substrate assays for factors VIII and IX: Introduction of a new solid phase fluorescent detection method Thrombosis Research. 21: 573-584. PMID 6791298 DOI: 10.1016/0049-3848(81)90258-9  0.054
1981 Mitchell GA, Meher-Homji KM, Baker RSU. Sister chromatid exchange assays: Pre-screening of chemicals for subtoxic levels Medical Laboratory Sciences. 38: 117-119. PMID 7339412  0.051
1995 Brocklehurst TF, Mitchell GA, Pleass W, Smith AC. The effect of step changes in sucrose concentration on the growth of Salmonella typhimurium LT2 Journal of Applied Bacteriology. 78: 495-500. PMID 7759382 DOI: 10.1111/j.1365-2672.1995.tb03091.x  0.05
1977 Chapman RF, Cook AG, Mitchell GA, Page WW. Descriptions and morphometrics of the nymphs of Zonocerus variegatus (L.) (Orthoptera: Acridoidea) Bulletin of Entomological Research. 67: 427-437. DOI: 10.1017/S0007485300011226  0.05
2023 Fahiminiya S, Oikonomopoulos S, Rivard GE, Gandhi M, Scott P, Montpetit A, Chen SH, Park K, Vezina C, Ragoussis J, Carvalho CMB, Mitchell GA, Soucy JF, Gauthier J. Deciphering a novel complex inversion affecting F8 in a family with severe haemophilia A by optical genome mapping. Haemophilia : the Official Journal of the World Federation of Hemophilia. PMID 36897533 DOI: 10.1111/hae.14771  0.05
2018 Turpin S, Patey N, Beaudin M, Mitchell G, Lambert R. H Syndrome: A Rare Genodermatosis Imaged With 18F-FDG PET/CT. Clinical Nuclear Medicine. 43: 36-37. PMID 29189375 DOI: 10.1097/RLU.0000000000001896  0.049
2014 Whittaker A, Moon M, Mitchell G, McBride B, Rossleigh MA, Rosenberg AR. The relative function of damaged kidneys in children does not deteriorate further at 3-year follow-up. Clinical Nuclear Medicine. 39: 1019-21. PMID 25384158 DOI: 10.1097/RLU.0000000000000591  0.047
1996 Kapuscinski M, Charchar F, Innes B, Mitchell GA, Norman TL, Harrap SB. Nerve growth factor gene and hypertension in spontaneously hypertensive rats. Journal of Hypertension. 14: 191-7. PMID 8728296 DOI: 10.1097/00004872-199602000-00007  0.045
1979 Gaines TP, Mitchell GA. Boron determination in plant tissue by the azomethine h method Communications in Soil Science and Plant Analysis. 10: 1099-1108. DOI: 10.1080/00103627909366965  0.045
2009 Branch WT, Frankel R, Gracey CF, Haidet PM, Weissmann PF, Cantey P, Mitchell GA, Inui TS. A good clinician and a caring person: Longitudinal faculty development and the enhancement of the human dimensions of care Academic Medicine. 84: 117-125. PMID 19116489 DOI: 10.1097/Acm.0B013E3181900F8A  0.042
1981 Bishop RC, Hudson PM, Mitchell GA, Pochron SP. USE OF FLUOROGENIC SUBSTRATES FOR THE ASSAY OF ANTITHROMBIN III AND HEPARIN Annals of the New York Academy of Sciences. 370: 720-730. PMID 6943977 DOI: 10.1111/j.1749-6632.1981.tb29780.x  0.041
1974 Mitchell GA, Smutny PV, Chambliss KW, Levin BD. Method for the determination of tracer antigen specific activity by radioimmunoassay. Immunochemistry. 11: 611-13. PMID 4477554 DOI: 10.1016/0019-2791(74)90254-7  0.041
1992 Mitchell GA. Research parks: Instrument, or harbinger of a new university paradigm? Interchange. 23: 99-104. DOI: 10.1007/BF01435226  0.04
1998 Mitchell GA, Wang SP, Ashmarina L, Robert MF, Bouchard G, Laurin N, Kassovska-Bratinova S, Boukaftane Y. Correction: Inborn errors of ketogenesis (Biochemical Society Transactions (1998) 26, 2 (136)) Biochemical Society Transactions. 26: 771.  0.04
1981 Jeracki RJ, Mitchell GA. Low and high speed propellers for general aviation performance potential and recent wind tunnel test results Sae Technical Papers. DOI: 10.4271/811090  0.04
1983 Mitchell GA, Simmons GL, Banning S. CONCENTRATOR FLOWSHEET DEVELOPMENT FOR BLACKBIRD COBALT-COPPER ORE .  0.038
1993 Mitchell GA. Future trends of welfare benefits in the '90s Employee Benefits Journal. 18: 29-33. PMID 10124133  0.037
2021 Bostan C, Mitchell G, Ellezam B, Soucy JF, Harissi-Dagher M, Hamel P. Corneal imaging with optical coherence tomography assisting the diagnosis of mucolipidosis type IV. Canadian Journal of Ophthalmology. Journal Canadien D'Ophtalmologie. PMID 33741364 DOI: 10.1016/j.jcjo.2021.02.018  0.037
1984 Mitchell GA. DEVELOPMENT OF ORAL SKILLS FOR THE PRESENTATION OF TECHNICAL INFORMATION Journal of Technical Writing and Communication. 14: 109-112.  0.037
1983 Mitchell GA. fibrinolysis=fibronolysis Seminars in Thrombosis and Hemostasis. 9: 268-280. PMID 6362010  0.035
2010 Mitchell GA, Harrison DW. Neuropsychological effects of hostility and pain on emotion perception. Journal of Clinical and Experimental Neuropsychology. 32: 174-89. PMID 19484642 DOI: 10.1080/13803390902889614  0.035
1970 Blackburn CR, Green WF, Mitchell GA. Studies of chronic nontuberculous lung disease in New Guinea Populations. The prevalence of Hemophilus influenzae precipitins. The American Review of Respiratory Disease. 102: 567-74. PMID 5456421 DOI: 10.1164/arrd.1970.102.4.567  0.035
2005 Mitchell GA. Distinctive expertise: Multimedia, the library, and the term paper of the future Information Technology and Libraries. 24: 32-36.  0.034
1995 Mitchell GA, Brocklehurst TF, Parker R, Smith AC. The effect of transient temperatures on the growth of Salmonella typhimurium LT2. II: excursions outside the growth region Journal of Applied Bacteriology. 79: 128-134. PMID 7592107 DOI: 10.1111/j.1365-2672.1995.tb00925.x  0.034
1987 Latimer JG, Mitchell CA, Mitchell GA. UV-B radiation and photosynthetic irradiance acclimate eggplant for outdoor exposure Hortscience : a Publication of the American Society For Horticultural Science. 22: 426-429. PMID 11538251  0.034
1997 Brocklehurst TF, Mitchell GA, Smith AC. A model experimental gel surface for the growth of bacteria on foods Food Microbiology. 14: 303-311. DOI: 10.1006/fmic.1997.0098  0.033
1971 Mitchell GA, Guerin LF, Pasieka AE. Antibody production in milk serum after virus instillation of goat mammary gland. IV. Experiments with protective properties of specific influenza antibody associated with lactogammaglobulin. Canadian Journal of Comparative Medicine. 35: 52-59. PMID 4251415  0.032
1995 Brocklehurst TF, Mitchell GA, Ridge YP, Seale R, Smith AC. The effect of transient temperatures on the growth of Salmonella typhimurium LT2 in gelatin gel International Journal of Food Microbiology. 27: 45-60. PMID 8527328 DOI: 10.1016/0168-1605(94)00152-V  0.032
1980 Bober LJ, Mitchell GA. SUMMARY OF ADVANCED METHODS FOR PREDICTING HIGH SPEED PROPELLER PERFORMANCE Aiaa Paper.  0.03
1994 Mitchell GA, Brocklehurst TF, Parker R, Smith AC. The effect of transient temperatures on the growth of Salmonella typhimurium LT2. I: cycling within the growth region Journal of Applied Bacteriology. 77: 113-119. PMID 7928777 DOI: 10.1111/j.1365-2672.1994.tb03052.x  0.03
2021 Fahiminiya S, Rivard GE, Scott P, Montpetit A, Bacot F, St-Louis J, Mitchell GA, Foulkes WD, Soucy JF, Gauthier J. A full molecular picture of F8 intron 1 inversion created with optical genome mapping. Haemophilia : the Official Journal of the World Federation of Hemophilia. PMID 34232555 DOI: 10.1111/hae.14375  0.027
1978 Mitchell GA, Bingham FT, Page AL. Yield and metal composition of lettuce and wheat grown on soils amended with sewage sludge enriched with cadmium, copper, nickel, and zinc Journal of Environmental Quality. 7: 165-171.  0.026
1988 McConnell JS, Wilkerson MH, Mitchell GA. Influences of nitrogen treatments and irrigation methods on soil chemical properties Communications in Soil Science and Plant Analysis. 19: 1925-1943. DOI: 10.1080/00103628809368061  0.026
1987 Michaelson GJ, Ping CL, Mitchell GA. Correlation of Mehlich 3, Bray 1, and ammonium acetate extractable P, K, Ca, and Mg for alaska agricultural soils Communications in Soil Science and Plant Analysis. 18: 1003-1015. DOI: 10.1080/00103628709367877  0.023
1979 Bingham FT, Page AL, Mitchell GA, Strong JE. Effects of liming an acid soil amended with sewage sludge enriched with Cd, Cu, Ni and Zn on yield and Cd content of wheat grain Journal of Environmental Quality. 8: 202-207.  0.022
2016 Mitchell GA, Wasylkiwskyj W. Theoretical anisotropic transverse resonance technique for the design of low-profile wideband antennas Iet Microwaves, Antennas and Propagation. 10: 487-493. DOI: 10.1049/Iet-Map.2015.0470  0.022
1989 Mitchell GA, Felthousen KA. Hypertensive left ventricular hypertrophy Southern Medical Journal. 82: 404-405. PMID 2522240  0.02
2004 Mitchell GA, Logie NJ, Handley RS. Observations on casualties from the Western Desert and Libya arriving at a base hospital. 1941 Journal of the Royal Army Medical Corps. 150. PMID 15624415  0.019
1977 Bingham FT, Mitchell GA, Mahler RJ, Page AL. YIELD AND HEAVY METAL CONTENT OF FOOD CROPS GROWN ON SOILS AMENDED WITH SEWAGE SLUDGE . 2.  0.018
1972 Mitchell GA. In memoriam. Geoffrey Thomas Ashley, B.Sc., M.D Journal of Anatomy. 112: 305-307. PMID 4562025  0.017
1972 Mitchell GA. Obituary--Geoffrey Thomas Ashley, B.Sc., M.D The Manchester Medical Gazette. 51: 106-108. PMID 4560956  0.017
1973 Mitchell GA. Anatomy in Manchester before 1871 The Manchester Medical Gazette. 53: 14-16. PMID 4608782  0.016
1991 Mitchell GA. Compliance issues and proper animal drug use in aquaculture Veterinary and Human Toxicology. 33: 9-10. PMID 1926755  0.014
2010 Allen B, Mitchell GA. Further consideration for noninvasive positive pressure ventilation in cardiogenic pulmonary edema Annals of Emergency Medicine. 56: 587-588. PMID 21036305 DOI: 10.1016/j.annemergmed.2010.05.019  0.014
1996 Mitchell GA. Inhibition of 4-hydroxyphenylpyruvate dioxygenase by 2-(2-nitro-4-trifluoromethylbenzoyl)-cyclohexane-1,3-dione and 2-(2-chloro-4-methanesulfonylbenzoyl)-cyclohexane-1,3-dione Human &Amp; Experimental Toxicology. 15: 179-181. PMID 8645506  0.014
1988 Mitchell GA. Administering sulfamethazine to food-producing animals Canadian Veterinary Journal. 29: 327-329.  0.013
2006 Fuller H, Mitchell GA. A culture of complaint Education Next. 6: 18-22.  0.012
1971 Mitchell GA. Prognathism corrected by surgery and minor tooth movement Journal - California Dental Association. 47: 32-35. PMID 5282038  0.012
1995 Mitchell GA. Strategies for health care cost containment Employee Benefits Journal. 20: 18-22. PMID 10142520  0.011
1998 Mitchell GA. Compliance issues and drug use in aquaculture production Veterinary and Human Toxicology. 40: 31-34. PMID 9823580  0.01
2017 Ghaddhab C, Morin C, Brunel-Guitton C, Mitchell GA, Van Vliet G, Huot C. Reply. The Journal of Pediatrics. PMID 28550952 DOI: 10.1016/j.jpeds.2017.04.067  0.01
1973 Mitchell GA. Around the departments. V. Anatomy The Manchester Medical Gazette. 52: 66-67. PMID 4802918  0.01
1892 Mitchell G. Crown and Bridge Work. The Dental Register. 46: 439-449. PMID 33700432  0.01
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