The genetics of kidney stone disease and nephrocalcinosis

P Singh, PC Harris, DJ Sas, JC Lieske - Nature Reviews Nephrology, 2022 - nature.com
Kidney stones (also known as urinary stones or nephrolithiasis) are highly prevalent,
affecting approximately 10% of adults worldwide, and the incidence of stone disease is …

Kidney stones

SR Khan, MS Pearle, WG Robertson… - Nature reviews Disease …, 2016 - nature.com
Kidney stones are mineral deposits in the renal calyces and pelvis that are found free or
attached to the renal papillae. They contain crystalline and organic components and are …

Genetic associations of protein-coding variants in human disease

BB Sun, MI Kurki, CN Foley, A Mechakra, CY Chen… - Nature, 2022 - nature.com
Genome-wide association studies (GWAS) have identified thousands of genetic variants
linked to the risk of human disease. However, GWAS have so far remained largely …

Exploring the genetic basis of early-onset chronic kidney disease

A Vivante, F Hildebrandt - Nature Reviews Nephrology, 2016 - nature.com
The primary causes of chronic kidney disease (CKD) in children differ from those of CKD in
adults. In the USA the most common diagnostic groups of renal disease that manifest before …

Genetics of kidney stone disease

SA Howles, RV Thakker - Nature Reviews Urology, 2020 - nature.com
Kidney stone disease (nephrolithiasis) is a common problem that can be associated with
alterations in urinary solute composition including hypercalciuria. Studies suggest that the …

Autosomal-recessive mutations in SLC34A1 encoding sodium-phosphate cotransporter 2A cause idiopathic infantile hypercalcemia

KP Schlingmann, J Ruminska… - Journal of the …, 2016 - journals.lww.com
Idiopathic infantile hypercalcemia (IIH) is characterized by severe hypercalcemia with failure
to thrive, vomiting, dehydration, and nephrocalcinosis. Recently, mutations in the vitamin D …

Genetic testing in steroid-resistant nephrotic syndrome: when and how?

S Lovric, S Ashraf, W Tan… - Nephrology Dialysis …, 2016 - academic.oup.com
Steroid-resistant nephrotic syndrome (SRNS) represents the second most frequent cause of
chronic kidney disease in the first three decades of life. It manifests histologically as focal …

[HTML][HTML] Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis

A Daga, AJ Majmundar, DA Braun, HY Gee… - Kidney international, 2018 - Elsevier
The incidence of nephrolithiasis continues to rise. Previously, we showed that a monogenic
cause could be detected in 11.4% of individuals with adult-onset nephrolithiasis or …

Genetics of Chronic Kidney Disease

A Vivante - New England Journal of Medicine, 2024 - Mass Medical Soc
Key Points Genetics of Chronic Kidney Disease Genetic causes of chronic kidney disease
(CKD) are not uncommon. Patients with CKD should be referred for genetic consultation and …

Whole-exome sequencing enables a precision medicine approach for kidney transplant recipients

N Mann, DA Braun, K Amann, W Tan… - Journal of the …, 2019 - journals.lww.com
Background Whole-exome sequencing (WES) finds a CKD-related mutation in
approximately 20% of patients presenting with CKD before 25 years of age. Although …