1.
The Roles of Specific Genes Implicated as Circulating Factors Involved in Normal and Disordered Phosphate Homeostasis: Frizzled Related Protein-4, Matrix Extracellular Phosphoglyco...
by White, Kenneth E
Endocrine reviews, 2006, Vol.27 (3), p.221-241
2.
A signature of circulating inflammatory proteins and development of end-stage renal disease in diabetes
by Niewczas, Monika A
Nature medicine, 2019, Vol.25 (5), p.805-813
3.
Identification of a mutation in complement factor H-related protein 5 in patients of Cypriot origin with glomerulonephritis
by Gale, Daniel P, MRCP
The Lancet (British edition), 2010, Vol.376 (9743), p.794-801
4.
Mutations in the Tight-Junction Gene Claudin 19 ( CLDN19) Are Associated with Renal Magnesium Wasting, Renal Failure, and Severe Ocular Involvement
by Konrad, Martin
American journal of human genetics, 2006, Vol.79 (5), p.949-957
5.
Mutations in EMP2 Cause Childhood-Onset Nephrotic Syndrome
by Gee, Heon Yung
American journal of human genetics, 2014, Vol.94 (6), p.884-890
6.
Defects of CRB2 Cause Steroid-Resistant Nephrotic Syndrome
by Ebarasi, Lwaki
American journal of human genetics, 2015, Vol.96 (1), p.153-161
7.
Follow-up results of patients with ADCK4 mutations and the efficacy of CoQ10 treatment
by Atmaca, Mustafa
Pediatric nephrology (Berlin, West), 2017, Vol.32 (8), p.1369-1375
8.
Mutations in MAPKBP1 Cause Juvenile or Late-Onset Cilia-Independent Nephronophthisis
by Macia, Maxence S
American journal of human genetics, 2017, Vol.100 (2), p.323-333
9.
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort
by Thomas, Rosemary
Pediatric nephrology (Berlin, West), 2011, Vol.26 (6), p.897-903
10.
Dominant Renin Gene Mutations Associated with Early-Onset Hyperuricemia, Anemia, and Chronic Kidney Failure
by Živná, Martina
American journal of human genetics, 2009, Vol.85 (2), p.204-213
11.
Protection against Loss of Innate Defenses in Adulthood by Low Advanced Glycation End Products (AGE) Intake: Role of the Antiinflammatory AGE Receptor-1
by Vlassara, Helen
The journal of clinical endocrinology and metabolism, 2009, Vol.94 (11), p.4483-4491
12.
HNF1B nephropathy has a slow-progressive phenotype in childhood—with the exception of very early onset cases: results of the German Multicenter HNF1B Childhood Registry
by Okorn, Christine
Pediatric nephrology (Berlin, West), 2019, Vol.34 (6), p.1065-1075
13.
Association of CREBRF variants with obesity and diabetes in Pacific Islanders from Guam and Saipan
by Hanson, Robert L
Diabetologia, 2019, Vol.62 (9), p.1647-1652
14.
Mutations in INF2 may be associated with renal histology other than focal segmental glomerulosclerosis
by Büscher, Anja K
Pediatric nephrology (Berlin, West), 2017, Vol.33 (3), p.433-437
15.
Nephronophthisis
by Salomon, Rémi
Pediatric nephrology (Berlin, West), 2008, Vol.24 (12), p.2333-2344
16.
Focal segmental glomerulosclerosis and medullary nephrocalcinosis in children with ADCK4 mutations
by Park, Eujin
Pediatric nephrology (Berlin, West), 2017, Vol.32 (9), p.1547-1554
17.
MEIS1 and BTBD9: genetic association with restless leg syndrome in end stage renal disease
by Schormair, Barbara
Journal of medical genetics, 2011, Vol.48 (7), p.462-466
18.
The Haptoglobin genotype predicts cardio-renal mortality in type 1 diabetes
by Costacou, Tina
Journal of diabetes and its complications, 2016, Vol.30 (2), p.221-226
19.
Klotho G-395A gene polymorphism: impact on progression of end-stage renal disease and development of cardiovascular complications in children on dialysis
by Elghoroury, Eman A
Pediatric nephrology (Berlin, West), 2018, Vol.33 (6), p.1019-1027
20.
Inherited glomerular diseases in the gilded age of genomic advancements
by Gulati, Ashima
Pediatric nephrology (Berlin, West), 2019, Vol.35 (6), p.959-968
