Liat Ganon

Homozygous SLC2A9 Mutations Cause Severe Renal Hypouricemia

Dganit Dinour, Nicola K. Gray, Susan Campbell et al. · Journal of the American Society of Nephrology · 2009 · 232 citations

Genetics, Renal Pathology, Genetic Epidemiology +16

Loss-of-Function Mutations of <i>CYP24A1</i> , the Vitamin D 24-Hydroxylase Gene, Cause Long-standing Hypercalciuric Nephrolithiasis and Nephrocalcinosis

Dganit Dinour, Pazit Beckerman, Liat Ganon et al. · The Journal of Urology · 2013 · 137 citations

Maternal and infantile hypercalcemia caused by vitamin-D-hydroxylase mutations and vitamin D intake

Dganit Dinour, Miriam Davidovits, Shraga Aviner et al. · Pediatric Nephrology · 2014 · 78 citations

Nutrition, Metabolic Disorder, Inherited Metabolic Disease +8

Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failure

Giacomo Colussi, Liat Ganon, Silvana Penco et al. · Nephrology Dialysis Transplantation · 2013 · 60 citations

Two novel homozygous SLC2A9 mutations cause renal hypouricemia type 2

Dganit Dinour, Nicola K. Gray, Liat Ganon et al. · Nephrology Dialysis Transplantation · 2011 · 55 citations