PubRank

M W Thompson

Author PubWeight™ 84.80‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy. Nature 1986 4.13
2 Cloning of the breakpoint of an X;21 translocation associated with Duchenne muscular dystrophy. Nature 1986 3.62
3 Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy. Science 1988 2.82
4 Duplicational mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotypegenotype correlation. Am J Hum Genet 1990 2.20
5 Molecular and phenotypic analysis of patients with deletions within the deletion-rich region of the Duchenne muscular dystrophy (DMD) gene. Am J Hum Genet 1989 2.12
6 Marked hypocalcemia and ventricular fibrillation in two pediatric patients exposed to a fluoride-containing wheel cleaner. Ann Emerg Med 1996 2.11
7 An assessment of the creatine kinase test in the detection of carriers of Duchenne muscular dystrophy. J Pediatr 1967 1.92
8 Endopeptidase Clp: ATP-dependent Clp protease from Escherichia coli. Methods Enzymol 1994 1.89
9 Genetics of Duchenne muscular dystrophy. Annu Rev Genet 1988 1.82
10 Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome. Hum Genet 1984 1.64
11 Two new proteases in the MHC class I processing pathway. Nat Immunol 2000 1.63
12 Chronic hypertension and altered baroreflex responses in transgenic mice containing the human renin and human angiotensinogen genes. J Clin Invest 1996 1.59
13 Transient surfactant protein B deficiency in a term infant with severe respiratory failure. J Pediatr 1998 1.53
14 Aerobic performance of female marathon and male ultramarathon athletes. Eur J Appl Physiol Occup Physiol 1979 1.53
15 Partial gene duplication in Duchenne and Becker muscular dystrophies. J Med Genet 1988 1.50
16 Genetics of childhood spinal muscular atrophy. J Med Genet 1971 1.39
17 Carbon monoxide mass exposure in a pediatric population. Acad Emerg Med 1998 1.39
18 Endocardial fibroelastosis: family studies with special reference to counseling. J Pediatr 1971 1.35
19 Molecular properties of ClpAP protease of Escherichia coli: ATP-dependent association of ClpA and clpP. Biochemistry 1998 1.34
20 Functional expression of the human angiotensinogen gene in transgenic mice. J Biol Chem 1994 1.22
21 Comparison of oral cephalexin, topical mupirocin and topical bacitracin for treatment of impetigo. Pediatr Infect Dis J 1997 1.22
22 Skeletal muscle metabolic and ionic adaptations during intense exercise following sprint training in humans. J Appl Physiol (1985) 2000 1.19
23 Intramyocellular triacylglycerol in prolonged cycling with high- and low-carbohydrate availability. J Appl Physiol (1985) 2002 1.16
24 Effect of training on eccentric exercise-induced muscle damage. J Appl Physiol (1985) 1993 1.13
25 Mackinder's hereditary brachydactyly: phenotypic, radiological, dermatoglyphic and genetic observations in an Ontario family. Ann Hum Genet 1973 1.10
26 Intelligence and the gene for Duchenne muscular dystrophy. Arch Dis Child 1969 1.10
27 Sarcoplasmic reticulum function and muscle contractile character following fatiguing exercise in humans. J Physiol 2001 1.09
28 Genetic aspects of immotile cilia syndrome. Am J Med Genet 1986 1.07
29 Analysis of effects of W and f genic substitutions on fetal mouse hematology. Genetics 1968 1.06
30 Familial atrial septal defect of the primum type: a report of four cases in one sibship. Can Med Assoc J 1968 1.03
31 The influence of menstrual cycle phase on skeletal muscle contractile characteristics in humans. J Physiol 2001 1.02
32 Analysis of erythroid homeostatic mechanisms in normal and genetically anaemic mice. Br J Haematol 1966 0.99
33 Genetic counseling in clinical pediatrics. What to do with inquiries about heritable disorders. Clin Pediatr (Phila) 1967 0.98
34 Relationships among age-associated strength changes and physical activity level, limb dominance, and muscle group in women. J Gerontol A Biol Sci Med Sci 2000 0.97
35 Carrier detection and genetic counselling in Duchenne muscular dystrophy: a follow-up study. Can Med Assoc J 1976 0.95
36 Specific cellular defects in patients with Fanconi anemia. J Cell Physiol 1979 0.94
37 Physiological responses to prolonged exercise in ultramarathon athletes. J Appl Physiol (1985) 1986 0.93
38 Dermatophyphics in childhood leukemia. Can Med Assoc J 1971 0.93
39 Complex segregation analysis and computer-assisted genetic risk assessment for Duchenne muscular dystrophy. Am J Med Genet 1983 0.93
40 Serum creatine kinase and pyruvate kinase in Duchenne muscular dystrophy carrier detection. Muscle Nerve 1979 0.92
41 Linkage analysis of polymorphisms within the DNA fragment XJ cloned from the breakpoint of an X;21 translocation associated with X linked muscular dystrophy. J Med Genet 1986 0.92
42 Human skeletal sarcoplasmic reticulum Ca2+ uptake and muscle function with aging and strength training. J Appl Physiol (1985) 1999 0.92
43 Fasting for 72 h increases intramyocellular lipid content in nondiabetic, physically fit men. Am J Physiol Endocrinol Metab 2002 0.90
44 Nutritional and fluid intake in a 100-km ultramarathon. Int J Sport Nutr 1998 0.87
45 Effects of bacterial endotoxin on hemopoietic colony-forming cells in the spleens of normal mice and mice of genotype S1-S1 d . Cell Tissue Kinet 1970 0.87
46 Impaired calcium pump function does not slow relaxation in human skeletal muscle after prolonged exercise. J Appl Physiol (1985) 1997 0.86
47 Incidence of salt-losing form of congenital virilizing adrenal hyperplasia. Arch Dis Child 1972 0.86
48 Paternal inheritance of translocation chromosomes in a t(X;21) patient with X linked muscular dystrophy. J Med Genet 1986 0.85
49 Effect of 10-day cast immobilization on sarcoplasmic reticulum calcium regulation in humans. Acta Physiol Scand 2001 0.85
50 Estimated aerobic performance and energy cost of severe exercise of 24 h duration. Ergonomics 1979 0.84
51 Acetaminophen ingestion in childhood--cost and relative risk of alternative referral strategies. J Toxicol Clin Toxicol 1994 0.84
52 The cellular basis for the defect in haemopoiesis in flexed-tailed mice. I. The nature and persistance of the defect. Br J Haematol 1966 0.84
53 Biochemical and genetic studies in cystinuria: observations on double heterozygotes of genotype I-II. J Clin Invest 1971 0.84
54 A comparison of the absorption and metabolism of isopropyl alcohol by oral, dermal and inhalation routes. Vet Hum Toxicol 1986 0.83
55 Finger pattern combinations in normal individuals and in Down's syndrome. Hum Biol 1973 0.83
56 Malposition of pediatric gastric lavage tubes demonstrated radiographically. J Emerg Med 1992 0.83
57 Portable, inexpensive instruments to quantify stratum corneum hydration and skin erythema: applications to clothing science. Dermatol Online J 2001 0.82
58 Effect of prolonged exercise and pre-exercise dietary manipulation on hepatic triglycerides in trained men. Eur J Appl Physiol 2011 0.82
59 Serum creatine kinase in the detection of Duchenne muscular dystrophy carriers: effects of season and multiple testing. Muscle Nerve 1982 0.81
60 Effect of temperature and duration of hyperthermia on HSP72 induction in rat tissues. Mol Cell Biochem 2004 0.81
61 Acromesomelic dwarfism: description of a patient and comparison with previously reported cases. Hum Genet 1976 0.81
62 Plasma Hsp72 is higher in runners with more serious symptoms of exertional heat illness. Eur J Appl Physiol 2006 0.80
63 Cystic fibrosis in Ontario. Am J Med Genet 1985 0.80
64 Dermatoglyphics in congenital virilizing adrenal hyperplasia. Am J Dis Child 1971 0.80
65 Effect of altered pre-exercise carbohydrate availability on selection and perception of effort during prolonged cycling. Eur J Appl Physiol 2006 0.80
66 Influence of time until emesis on the efficacy of decontamination using acetaminophen as a marker in a pediatric population. Ann Emerg Med 1993 0.79
67 The utility of immature reticulocyte fraction as an indicator of erythropoietic response to altitude training in elite cyclists. Int J Lab Hematol 2009 0.78
68 Creatine kinase isozyme transition in chicks with hereditary muscular dystrophy. Muscle Nerve 1981 0.78
69 Clinical, pathological and genetic aspects of a form of cystic disease of the renal medulla: familial juvenile nephronophthisis (FJN). Clin Nephrol 1978 0.78
70 Skeletal muscle strength and endurance are maintained during moderate dehydration. Int J Sports Med 2012 0.77
71 Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase, hemopexin, pyruvate kinase, and lactate dehydrogenase in combination. Am J Med Genet 1982 0.77
72 The problem of Duchenne muscular dystrophy. Philos Trans R Soc Lond B Biol Sci 1988 0.77
73 Birthweight in congenital virilizing adrenal hyperplasia. Arch Dis Child 1971 0.75
74 Investigation of the secretion and metabolism of cortisol during a 100 km race using [4-14C] and [11 alpha-3H] cortisol. Acta Endocrinol (Copenh) 1980 0.75
75 Analysis of an X-autosome translocation responsible for X-linked muscular dystrophy. Cold Spring Harb Symp Quant Biol 1986 0.75
76 Genital changes in congenital virilizing adrenal hyperplasia. J Pediatr 1972 0.75
77 A report on a family with a (1;2) translocation: cytologic and linkage analysis. Cytogenet Cell Genet 1976 0.75
78 Sex-linked hereditary ataxic deplegia, the borderland between cerebral palsy and Pelizaeus-Merzbacher disease. Can J Neurol Sci 1974 0.75
79 The steroid II-oxygenation index by gas-liquid chromatography. Clin Chim Acta 1971 0.75
80 Norma Ford Walker 1893-1968. Can J Genet Cytol 1968 0.75
81 Creatine kinase- "no phospho-, please!". Muscle Nerve 1981 0.75
82 Clinical nurse specialist: making the shift from critical care to home care. Dimens Crit Care Nurs 1996 0.75
83 A report on a family with a (1;2) translocation: cytologic and linkage analysis. Birth Defects Orig Artic Ser 1976 0.75
84 Short-term suppression of plasma free fatty acids fails to improve insulin sensitivity when intramyocellular lipid is elevated. Diabet Med 2006 0.75
85 Systematic monitoring of generic standards of patient care. J Nurs Qual Assur 1988 0.75
86 Heat exposure does not alter eccentric exercise-induced increases in mitochondrial calcium and respiratory dysfunction. Eur J Appl Physiol 2011 0.75
87 Pseudomonas aeruginosa in hospital. Lancet 1973 0.75
88 The problem of intersex. J Am Med Womens Assoc 1967 0.75
89 Genetics and genetic counselling. Med Serv J Can 1967 0.75
90 Genetics society of Canada symposium. II. On methodology in genetics research. Winnipeg, Manitoba, May 17, 1968. Methodology in human genetics. Can J Genet Cytol 1968 0.75
91 Steroid studies in parents of patients with congenital virilizing adrenal hyperplasia. J Clin Endocrinol Metab 1971 0.75
92 Duchenne muscular dystrophy carrier detection using logistic discrimination: serum creatine kinase and hemopexin in combination. Am J Med Genet 1981 0.75
93 Extracorporeal membrane oxygenation for hydrocarbon aspiration. Am J Dis Child 1990 0.75
94 Expired air temperature during prolonged exercise in cool- and hot-humid environments. Eur J Appl Physiol Occup Physiol 1997 0.75