PubRank

Timothy C Cox

Author PubWeight™ 44.12‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Compensatory growth of healthy cardiac cells in the presence of diseased cells restores tissue homeostasis during heart development. Dev Cell 2008 2.15
2 Maternal ethanol consumption alters the epigenotype and the phenotype of offspring in a mouse model. PLoS Genet 2010 2.03
3 Subclassification of the RBCC/TRIM superfamily reveals a novel motif necessary for microtubule binding. J Biol Chem 2006 1.88
4 Mutation discovery in mice by whole exome sequencing. Genome Biol 2011 1.69
5 Microtia: epidemiology and genetics. Am J Med Genet A 2011 1.42
6 A genome-wide screen for modifiers of transgene variegation identifies genes with critical roles in development. Genome Biol 2008 1.35
7 Solution structure of the RBCC/TRIM B-box1 domain of human MID1: B-box with a RING. J Mol Biol 2006 1.34
8 Solution structure of the MID1 B-box2 CHC(D/C)C(2)H(2) zinc-binding domain: insights into an evolutionarily conserved RING fold. J Mol Biol 2007 1.16
9 Vascular remodeling of the vitelline artery initiates extravascular emergence of hematopoietic clusters. Blood 2010 1.13
10 Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice. PLoS Genet 2011 1.13
11 Evolution of cerebral arteriopathies in childhood arterial ischemic stroke. Ann Neurol 2006 1.12
12 Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1. J Med Genet 2011 1.11
13 MID1 and MID2 homo- and heterodimerise to tether the rapamycin-sensitive PP2A regulatory subunit, alpha 4, to microtubules: implications for the clinical variability of X-linked Opitz GBBB syndrome and other developmental disorders. BMC Cell Biol 2002 1.10
14 Efficacy of sonic and ultrasonic activation for removal of calcium hydroxide from mesial canals of mandibular molars: a microtomographic study. J Endod 2011 1.07
15 A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome. Am J Hum Genet 2012 1.07
16 Purifying natively folded proteins from inclusion bodies using sarkosyl, Triton X-100, and CHAPS. Biotechniques 2010 1.06
17 Structure of the MID1 tandem B-boxes reveals an interaction reminiscent of intermolecular ring heterodimers. Biochemistry 2008 1.03
18 A novel distinctive cerebrovascular phenotype is associated with heterozygous Arg179 ACTA2 mutations. Brain 2012 1.02
19 Facial suture synostosis of newborn Fgfr1(P250R/+) and Fgfr2(S252W/+) mouse models of Pfeiffer and Apert syndromes. Birth Defects Res A Clin Mol Teratol 2011 0.96
20 Effects of cell grafting on coronary remodeling after myocardial infarction. J Am Heart Assoc 2013 0.95
21 Deletion of a conserved regulatory element required for Hmx1 expression in craniofacial mesenchyme in the dumbo rat: a newly identified cause of congenital ear malformation. Dis Model Mech 2012 0.91
22 Expression profiles of cIRF6, cLHX6 and cLHX7 in the facial primordia suggest specific roles during primary palatogenesis. BMC Dev Biol 2006 0.91
23 Expression of three spalt (sal) gene homologues in zebrafish embryos. Dev Genes Evol 2002 0.91
24 Complementation of a yeast CYC3 deficiency identifies an X-linked mammalian activator of apocytochrome c. Genomics 2002 0.90
25 Perspectives and challenges in advancing research into craniofacial anomalies. Am J Med Genet C Semin Med Genet 2013 0.89
26 A micro-computed tomography-based comparison of the canal transportation and centering ability of ProTaper Universal rotary and WaveOne reciprocating files. Quintessence Int 2014 0.87
27 Hmx1 is required for the normal development of somatosensory neurons in the geniculate ganglion. Dev Biol 2012 0.87
28 Cyclin-dependent kinase-like 5 (CDKL5) mutation screening in Rett syndrome and related disorders. Twin Res Hum Genet 2010 0.86
29 Preferential associated anomalies in 818 cases of microtia in South America. Am J Med Genet A 2013 0.86
30 Lack of association between the A118G polymorphism of the mu opioid receptor gene (OPRM1) and opioid dependence: A meta-analysis. Pharmgenomics Pers Med 2009 0.85
31 The MID1 E3 ligase catalyzes the polyubiquitination of Alpha4 (α4), a regulatory subunit of protein phosphatase 2A (PP2A): novel insights into MID1-mediated regulation of PP2A. J Biol Chem 2013 0.84
32 A new X-linked syndrome with agenesis of the corpus callosum, mental retardation, coloboma, micrognathia, and a mutation in the Alpha 4 gene at Xq13. Am J Med Genet A 2003 0.82
33 Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development. Int J Dev Biol 2002 0.81
34 Respiratory tract lung geometry and dosimetry model for male Sprague-Dawley rats. Inhal Toxicol 2014 0.81
35 Subcortical and cerebellar volumetric deficits in paediatric sickle cell anaemia. Br J Haematol 2013 0.80
36 Somatic FGFR and TWIST mutations are not a common cause of isolated nonsyndromic single suture craniosynostosis. J Craniofac Surg 2007 0.80
37 In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci. Mamm Genome 2015 0.79
38 Comparing canal transportation and centering ability of endosequence and vortex rotary files by using micro-computed tomography. J Endod 2012 0.79
39 Branch-based model for the diameters of the pulmonary airways: accounting for departures from self-consistency and registration errors. Anat Rec (Hoboken) 2012 0.78
40 Oculoauriculofrontonasal syndrome: case series revealing new bony nasal anomalies in an old syndrome. Am J Med Genet A 2013 0.78
41 X-linked microtubule-associated protein, Mid1, regulates axon development. Proc Natl Acad Sci U S A 2013 0.78
42 Abnormalities of cervical arteries in children with arterial ischemic stroke. Neurology 2011 0.77
43 Microtomographic analysis of lower urinary tract obstruction. Pediatr Dev Pathol 2013 0.76
44 Convulsive status epilepticus in children with intractable epilepsy is frequently focal in origin. Can J Neurol Sci 2002 0.75