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Marta Lapsley

Researcher at St Helier Hospital

Publications -  21
Citations -  1743

Marta Lapsley is an academic researcher from St Helier Hospital. The author has contributed to research in topics: Tubular proteinuria & Dent's disease. The author has an hindex of 16, co-authored 21 publications receiving 1605 citations. Previous affiliations of Marta Lapsley include National Health Service.

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Meta-analysis identifies multiple loci associated with kidney function–related traits in east Asian populations

Yukinori Okada, +414 more
- 01 Aug 2012 - 
TL;DR: A meta-analysis of genome-wide association studies for kidney function–related traits, including 71,149 east Asian individuals from 18 studies in 11 population-, hospital- or family-based cohorts, conducted as part of the Asian Genetic Epidemiology Network (AGEN), identified 17 loci newly associated with kidney function-related traits.
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Genetic loci influencing kidney function and chronic kidney disease

John C. Chambers, +102 more
- 01 May 2010 - 
TL;DR: Using genome-wide association, common variants at 2p12–p13, 6q26, 17q23 and 19q13 associated with serum creatinine associated with chronic kidney disease are identified.
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Glomerular protein sieving and implications for renal failure in Fanconi syndrome

TL;DR: This model explains why tubular proteinuria of Fanconi syndrome includes proteins of mass of albumin and above as well as low-molecular-weight proteins, and further characterizes the endocytic pathway(s) believed defective in these syndromes.
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Urinary Megalin Deficiency Implicates Abnormal Tubular Endocytic Function in Fanconi Syndrome

TL;DR: A striking deficiency of urinary megalin was observed for eight of nine families with Dent's disease and for the two families with Lowe's syndrome and the measured levels of cubilin were normal for all patients, consistent with defective recycling ofmegalin to the apical cell surface of the proximal tubule epithelium.