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HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum
Author / Creator:Clissold, Rhian L. ; Hamilton, Alexander J. ; Hattersley, Andrew T. ; Ellard, Sian ; Bingham, Coralie
Publisher:London: Nature Publishing Group UK
Journal title:Nature reviews. Nephrology, 2015-02, Vol.11 (2), p.102-112
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Comment on a recent article titled ‘Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia’
Author / Creator:Clissold, Rhian ; Bingham, Coralie ; Hattersley, Andrew
Publisher:Japan: John Wiley & Sons, Inc
Journal title:Journal of diabetes investigation, 2024-06, Vol.15 (6), p.790-790
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A case of acute tubulointerstitial nephritis following administration of the Oxford-AstraZeneca COVID-19 vaccine: a case report
Author / Creator:Williams, Samuel B M ; Holwill, Stephen D J ; Clissold, Rhian L ; Bingham, Coralie
Publisher:England: BioMed Central Ltd
Journal title:BMC nephrology, 2023-03, Vol.24 (1), p.52-4, Article 52
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Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion
Author / Creator:Clissold, Rhian L ; Ashfield, Beth ; Burrage, Joe ; Hannon, Eilis ; Bingham, Coralie ; Mill, Jonathan ; Hattersley, Andrew ; Dempster, Emma L
Publisher:Germany: BioMed Central Ltd
Journal title:Clinical epigenetics, 2018-07, Vol.10 (1), p.97-11, Article 97
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Remission of Membranous Nephropathy after Treatment of Localised Prostate Cancer
Author / Creator:Adlington, Daniel ; Moore, Jason ; Bingham, Coralie
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Case reports in nephrology and dialysis, 2019-05, Vol.9 (2), p.79-84
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Factors determining penetrance in familial atypical haemolytic uraemic syndrome
Author / Creator:Sansbury, Francis H ; Cordell, Heather J ; Bingham, Coralie ; Bromilow, Gilly ; Nicholls, Anthony ; Powell, Roy ; Shields, Bev ; Smyth, Lucy ; Warwicker, Paul ; Strain, Lisa ; Wilson, Valerie ; Goodship, Judith A ; Goodship, Timothy H J ; Turnpenny, Peter D
Publisher:England: BMJ Publishing Group LTD
Journal title:Journal of medical genetics, 2014-11, Vol.51 (11), p.756-764
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Discovery of a novel dominant mutation in the REN gene after forty years of renal disease: a case report
Author / Creator:Clissold, Rhian L ; Clarke, Helen C ; Spasic-Boskovic, Olivera ; Brugger, Kim ; Abbs, Stephen ; Bingham, Coralie ; Shaw-Smith, Charles
Publisher:England: BioMed Central Ltd
Journal title:BMC nephrology, 2017-07, Vol.18 (1), p.234-234, Article 234
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Contrasting Diabetes Phenotypes Associated With Hepatocyte Nuclear Factor-1α and -1β Mutations
Author / Creator:PEARSON, Ewan R ; BADMAN, Michael K ; LOCKWOOD, Christopher R ; CLARK, Penelope M ; ELLARD, Sian ; BINGHAM, Coralie ; HATTERSLEY, Andrew T
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2004-05, Vol.27 (5), p.1102-1107
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The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay
Author / Creator:HARRIES, L. W ; BINGHAM, Coralie ; BELLANNE-CHANTELOT, Christine ; HATTERSLEY, A. T ; ELLARD, Sian
Publisher:Heidelberg: Springer
Journal title:Human genetics, 2005-11, Vol.118 (2), p.214-224
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The Mutated Human Gene Encoding Hepatocyte Nuclear Factor 1β Inhibits Kidney Formation in Developing Xenopus Embryos
Author / Creator:Wild, Wiltrud ; von Strandmann, Elke Pogge ; Nastos, Aristotelis ; Senkel, Sabine ; Lingott-Frieg, Anja ; Bulman, Michael ; Bingham, Coralie ; Ellard, Sian ; Hattersley, Andrew T. ; Ryffel, Gerhart U.
Publisher:National Academy of Sciences of the United States of America
Journal title:Proceedings of the National Academy of Sciences - PNAS, 2000-04, Vol.97 (9), p.4695-4700
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The Generalized Aminoaciduria Seen in Patients With Hepatocyte Nuclear Factor-1α Mutations Is a Feature of All Patients With Diabetes and Is Associated With Glucosuria
Author / Creator:BINGHAM, Coralie ; ELLARD, Sian ; NICHOLLS, Anthony J ; PENNOCK, Charles A ; ALLEN, John ; JAMES, Alan J ; SATCHELL, Simon C ; SALZMANN, Maurice B ; HATTERSLEY, Andrew T
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes (New York, N.Y.), 2001-09, Vol.50 (9), p.2047-2052
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Prevention of recurrence of atypical hemolytic uremic syndrome post renal transplant with the use of higher-dose eculizumab
Author / Creator:Riddell, Amy ; Goodship, Tim ; Bingham, Coralie
Publisher:Germany: Dustri - Verlag Dr. Karl Feistle GmbH & Co. KG
Journal title:Clinical nephrology, 2016-10, Vol.86 (10), p.200-202
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The Common PKD1 p.(Ile3167Phe) Variant Is Hypomorphic and Associated with Very Early Onset, Biallelic Polycystic Kidney Disease
Author / Creator:Durkie, Miranda ; Watson, Christopher M. ; Winship, Peter ; Hogg, Anne-Cecile ; Nyanhete, Rodney ; Cooley, Sharon ; Valluru, Manoj K. ; Shaw-Smith, Charles ; Bingham, Coralie ; Gilchrist, Mark ; Kenny, Janna ; Consortium, Genomics England Research ; Ong, Albert C. M.
Publisher:Hoboken: Hindawi
Journal title:Human mutation, 2023-07, Vol.2023, p.1-8
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Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing
Author / Creator:Clissold, Rhian ; Shields, Beverley ; Ellard, Sian ; Hattersley, Andrew ; Bingham, Coralie
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Nephron, 2015-01, Vol.130 (2), p.134-140
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Familial interstitial nephritis: 42 years from case series to genetic diagnosis
Author / Creator:Clissold, Rhian L ; Bingham, Coralie ; Shaw-Smith, Charles
Publisher:Germany: Dustri - Verlag Dr. Karl Feistle GmbH & Co. KG
Journal title:Clinical nephrology, 2019-06, Vol.91 (6), p.386-388
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The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype
Author / Creator:Hamilton, Alexander J ; Bingham, Coralie ; McDonald, Timothy J ; Cook, Paul R ; Caswell, Richard C ; Weedon, Michael N ; Oram, Richard A ; Shields, Beverley M ; Shepherd, Maggie ; Inward, Carol D ; Hamilton-Shield, Julian P ; Kohlhase, Jürgen ; Ellard, Sian ; Hattersley, Andrew T
Publisher:England: BMJ Publishing Group
Journal title:Journal of medical genetics, 2014-03, Vol.51 (3), p.165-169
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The effects of a digital health intervention on patient activation in chronic kidney disease
Author / Creator:Lightfoot, Courtney J. ; Wilkinson, Thomas J. ; Sohansoha, Gurneet K. ; Gillies, Clare L. ; Vadaszy, Noemi ; Ford, Ella C. ; Davies, Melanie J. ; Yates, Thomas ; Smith, Alice C. ; Graham-Brown, Matthew P. M.
Publisher:London: Nature Publishing Group UK
Journal title:NPJ digital medicine, 2024-11, Vol.7 (1), p.318-13, Article 318
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Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1[beta]-associated renal disease and can be symptomatic
Author / Creator:Clissold, Rhian L ; Fulford, Jon ; Hudson, Michelle ; Shields, Beverley M ; Mcdonald, Timothy J ; Ellard, Sian ; Hattersley, Andrew T ; Bingham, Coralie
Publisher:Oxford University Press
Journal title:Clinical kidney journal, 2018-08, Vol.11 (4), p.453
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ArticlesPeer ReviewedFull Text
Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic
Author / Creator:Clissold, Rhian L ; Fulford, Jon ; Hudson, Michelle ; Shields, Beverley M ; McDonald, Timothy J ; Ellard, Sian ; Hattersley, Andrew T ; Bingham, Coralie
Publisher:England: Oxford University Press
Journal title:Clinical kidney journal, 2018-08, Vol.11 (4), p.453-458
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Transcription factor HNF1β and novel partners affect nephrogenesis
Author / Creator:Dudziak, Karin ; Mottalebi, Nima ; Senkel, Sabine ; Edghill, Emma L. ; Rosengarten, Stefan ; Roose, Magdalena ; Bingham, Coralie ; Ellard, Sian ; Ryffel, Gerhart U.
Publisher:Elsevier Inc
Journal title:Kidney international, 2008-07, Vol.74 (2), p.210-217
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HNF1B-associated renal and extra-renal disease—an expanding clinical spectrum

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Comment on a recent article titled ‘Hepatocyte nuclear factor 1B deletion, but not intragenic mutation, might be more susceptible to hypomagnesemia’

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A case of acute tubulointerstitial nephritis following administration of the Oxford-AstraZeneca COVID-19 vaccine: a case report

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Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion

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Remission of Membranous Nephropathy after Treatment of Localised Prostate Cancer

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Factors determining penetrance in familial atypical haemolytic uraemic syndrome

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Discovery of a novel dominant mutation in the REN gene after forty years of renal disease: a case report

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Contrasting Diabetes Phenotypes Associated With Hepatocyte Nuclear Factor-1α and -1β Mutations

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The position of premature termination codons in the hepatocyte nuclear factor -1 beta gene determines susceptibility to nonsense-mediated decay

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The Mutated Human Gene Encoding Hepatocyte Nuclear Factor 1β Inhibits Kidney Formation in Developing Xenopus Embryos

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The Generalized Aminoaciduria Seen in Patients With Hepatocyte Nuclear Factor-1α Mutations Is a Feature of All Patients With Diabetes and Is Associated With Glucosuria

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Prevention of recurrence of atypical hemolytic uremic syndrome post renal transplant with the use of higher-dose eculizumab

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The Common PKD1 p.(Ile3167Phe) Variant Is Hypomorphic and Associated with Very Early Onset, Biallelic Polycystic Kidney Disease

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Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing

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Familial interstitial nephritis: 42 years from case series to genetic diagnosis

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The HNF4A R76W mutation causes atypical dominant Fanconi syndrome in addition to a β cell phenotype

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The effects of a digital health intervention on patient activation in chronic kidney disease

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Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1[beta]-associated renal disease and can be symptomatic

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Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic

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Transcription factor HNF1β and novel partners affect nephrogenesis

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