Urinary stone disease: closing the heritability gap by challenging conventional Mendelian inheritance-Reference-Cited by-同舟云学术

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Urinary stone disease: closing the heritability gap by challenging conventional Mendelian inheritance

Published:2023-11 Issue:5 Volume:104 Page:882-885
ISSN:0085-2538
Container-title:Kidney International
language:en
Short-container-title:Kidney International

Author:

Halbritter Jan^ORCID

Publisher

Elsevier BV

Subject

Nephrology

Reference15 articles.

1. Maternal family history of urolithiasis is associated with earlier age of onset of stone disease;Unno;World J Urol,2023

2. A twin study of genetic influences on nephrolithiasis in women and men;Goldfarb;Kidney Int Rep,2019

3. Genetic variants of calcium and vitamin D metabolism in kidney stone disease;Howles;Nat Commun,2019

4. Fourteen monogenic genes account for 15% of nephrolithiasis/nephrocalcinosis;Halbritter;J Am Soc Nephrol,2015

5. Systematic assessment of monogenic etiology in adult-onset kidney stone formers undergoing urological intervention-evidence for genetic pretest probability;Schonauer;Am J Med Genet C Semin Med Genet,2022

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Genetic causes of hypophosphatemia;Minerva Medica;2024-06

2. Prevalence and characteristics of genetic disease in adult kidney stone formers;Nephrology Dialysis Transplantation;2024-03-27

3. Prevalence and characteristics of genetic disease in adult kidney stone formers;2023-07-27

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