PubRank

Matthew Edwards

Author PubWeight™ 39.47‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 An integrated semiconductor device enabling non-optical genome sequencing. Nature 2011 20.85
2 Meta-analysis of 13 genome scans reveals multiple cleft lip/palate genes with novel loci on 9q21 and 2q32-35. Am J Hum Genet 2004 2.65
3 Premature arthritis is a distinct type II collagen phenotype. Arthritis Rheum 2010 1.66
4 Treg depletion inhibits efficacy of cancer immunotherapy: implications for clinical trials. PLoS One 2008 1.49
5 The sphingosine 1-phosphate receptor agonist FTY720 differentially affects the sequestration of CD4+/CD25+ T-regulatory cells and enhances their functional activity. J Immunol 2005 1.30
6 GDF5 is a second locus for multiple-synostosis syndrome. Am J Hum Genet 2006 1.24
7 Molecular consequences of dominant Bethlem myopathy collagen VI mutations. Ann Neurol 2007 1.15
8 Restoration of LDL receptor function in cells from patients with autosomal recessive hypercholesterolemia by retroviral expression of ARH1. J Clin Invest 2002 0.99
9 Atrx deficiency induces telomere dysfunction, endocrine defects, and reduced life span. J Clin Invest 2013 0.98
10 The natural history and osteodystrophy of mucolipidosis types II and III. J Paediatr Child Health 2010 0.95
11 Differential expression of pyloric atresia in junctional epidermolysis bullosa with ITGB4 mutations suggests that pyloric atresia is due to factors other than the mutations and not predictive of a poor outcome: three novel mutations and a review of the literature. Acta Derm Venereol 2008 0.89
12 Evaluation of satisfaction of parents with the use of videoconferencing for a pediatric genetic consultation. Twin Res Hum Genet 2011 0.89
13 Treatment with anti-gremlin 1 antibody ameliorates chronic hypoxia/SU5416-induced pulmonary arterial hypertension in mice. Am J Pathol 2013 0.85
14 Paternal uniparental isodisomy for chromosome 14 with mosaicism for a supernumerary marker chromosome 14. Am J Med Genet A 2007 0.82
15 A novel genetic syndrome characterized by pediatric cataract, dysmorphism, ectodermal features, and developmental delay in an indigenous Australian family. Am J Med Genet A 2009 0.79
16 Primary corneal myxoma. Cornea 2008 0.77
17 Optimization aspects of comprehensive two-dimensional gas chromatography. J Chromatogr A 2012 0.77
18 Diverse phenotypic consequences of mutations affecting the C-terminus of FLNA. J Mol Med (Berl) 2015 0.77
19 Surgery in patients with Fuchs'. Ophthalmology 2006 0.75
20 Ten-year review of Henoch-Schonlein purpura in Campbelltown Hospital, south-western Sydney. J Paediatr Child Health 2014 0.75
21 Case 32. Eosinophilia: reactive or neoplastic? Leuk Lymphoma 2007 0.75
22 Preparing residents in training to become health-care leaders: a pilot project. Acad Psychiatry 2014 0.75
23 Contact Lens-Related "Keratoschisis"-An Unusual Case of Corneal Stroma Lamellar Trauma. Cornea 2016 0.75