PubRank

Coralie Bingham

Author PubWeight™ 28.30‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Renal cysts and diabetes syndrome resulting from mutations in hepatocyte nuclear factor-1beta. Nephrol Dial Transplant 2004 2.20
2 Irreversible renal damage from accidental mushroom poisoning. BMJ 2012 1.97
3 Transcription factor HNF1beta and novel partners affect nephrogenesis. Kidney Int 2008 1.73
4 Mesangiocapillary glomerulonephritis type 2 associated with familial partial lipodystrophy (Dunnigan-Kobberling syndrome). Nephron Clin Pract 2004 1.51
5 HNF1B mutations associate with hypomagnesemia and renal magnesium wasting. J Am Soc Nephrol 2009 1.29
6 The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay. Hum Genet 2005 1.13
7 Distinct molecular and morphogenetic properties of mutations in the human HNF1beta gene that lead to defective kidney development. J Am Soc Nephrol 2003 1.02
8 Hepatocyte nuclear factor-1beta gene deletions--a common cause of renal disease. Nephrol Dial Transplant 2007 1.01
9 Contrasting diabetes phenotypes associated with hepatocyte nuclear factor-1alpha and -1beta mutations. Diabetes Care 2004 1.00
10 Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations. Am J Obstet Gynecol 2010 0.99
11 Whole gene deletion of the hepatocyte nuclear factor-1beta gene in a patient with the prune-belly syndrome. Nephrol Dial Transplant 2008 0.98
12 Sirolimus-induced remission of posttransplantation lymphoproliferative disorder. Am J Kidney Dis 2006 0.96
13 Severe hyperglycemia after renal transplantation in a pediatric patient with a mutation of the hepatocyte nuclear factor-1beta gene. Am J Kidney Dis 2002 0.90
14 Recent insights into kidney diseases associated with glomerular cysts. Pediatr Nephrol 2002 0.90
15 Conditional expression of hepatocyte nuclear factor-1beta, the maturity-onset diabetes of the young-5 gene product, influences the viability and functional competence of pancreatic beta-cells. J Endocrinol 2006 0.88
16 The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype. J Med Genet 2013 0.87
17 Renal failure complicating myeloma in pregnancy. Nephrol Dial Transplant 2007 0.86
18 Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations. J Pediatr Urol 2007 0.84
19 Acute tubulointerstitial nephritis, treatment with steroid and impact on renal outcomes. Nephrology (Carlton) 2012 0.82
20 Hypogammaglobulinemia and bronchiectasis in mycophenolate mofetil-treated renal transplant recipients: an emerging clinical phenomenon? Clin Transplant 2010 0.82
21 Mutation analyses of Uroplakin II in children with renal tract malformations. Nephrol Dial Transplant 2006 0.81
22 Urine C-peptide creatinine ratio can be used to assess insulin resistance and insulin production in people without diabetes: an observational study. BMJ Open 2013 0.80
23 Autosomal dominant inheritance of non-syndromic renal hypoplasia and dysplasia: dramatic variation in clinical severity in a single kindred. Nephrol Dial Transplant 2006 0.78
24 Right atrial thrombus as a complication of a temporary haemodialysis catheter--a potentially avoidable complication. Nephrol Dial Transplant 2005 0.78
25 In silico searching of human and mouse genome data identifies known and unknown HNF1 binding sites upstream of beta-cell genes. Mol Genet Metab 2003 0.78
26 The renal cysts and diabetes (RCAD) syndrome in a child with deletion of the hepatocyte nuclear factor-1β gene. Indian J Pediatr 2010 0.76
27 Prevention of recurrence of atypical hemolytic uremic syndrome post renal transplant with the use of higher-dose eculizumab
. Clin Nephrol 2016 0.75
28 Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing. Nephron 2015 0.75
29 Prevalence in the General Population of a CFH Sequence Variant Associated with Atypical Haemolytic Uraemic Syndrome in an Extensive Family from Southwest England. Nephron Extra 2013 0.75