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Adrian Lungu
Adrian Lungu
Fundeni clinical institute
Verified email at mediakompass.ro
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Cited by
Year
Functional rare and low frequency variants in BLK and BANK1 contribute to human lupus
SH Jiang, V Athanasopoulos, JI Ellyard, A Chuah, J Cappello, A Cook, ...
Nature communications 10 (1), 2201, 2019
862019
Prevalence of hypertension in children with early-stage ADPKD
L Massella, D Mekahli, D Paripović, L Prikhodina, N Godefroid, ...
Clinical Journal of the American Society of Nephrology 13 (6), 874-883, 2018
842018
Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria
J Savige, H Storey, E Watson, JM Hertz, C Deltas, A Renieri, F Mari, ...
European journal of human genetics 29 (8), 1186-1197, 2021
782021
Guidelines for genetic testing and management of Alport syndrome
J Savige, BS Lipska-Zietkiewicz, E Watson, JM Hertz, C Deltas, F Mari, ...
Clinical Journal of the American Society of Nephrology 17 (1), 143-154, 2022
742022
ADPedKD: a global online platform on the management of children with ADPKD
S De Rechter, D Bockenhauer, LM Guay-Woodford, I Liu, AJ Mallett, ...
Kidney international reports 4 (9), 1271-1284, 2019
232019
FHR-5 Serum Levels and CFHR5 Genetic Variations in Patients With Immune Complex-Mediated Membranoproliferative Glomerulonephritis and C3-Glomerulopathy
N Garam, M Cserhalmi, Z Prohaszka, A Szilagyi, N Veszeli, E Szabo, ...
Frontiers in immunology 12, 720183, 2021
162021
C4 nephritic factor in patients with immune-complex-mediated membranoproliferative glomerulonephritis and C3-glomerulopathy
N Garam, Z Prohászka, Á Szilágyi, C Aigner, A Schmidt, M Gaggl, ...
Orphanet journal of rare diseases 14, 1-14, 2019
142019
Identification of disease-causing variants by comprehensive genetic testing with exome sequencing in adults with suspicion of hereditary FSGS
MC Braunisch, KM Riedhammer, PM Herr, S Draut, R Günthner, ...
European Journal of Human Genetics 29 (2), 262-270, 2021
122021
Validation of distinct pathogenic patterns in a cohort of membranoproliferative glomerulonephritis patients by cluster analysis
N Garam, Z Prohaszka, A Szilagyi, C Aigner, A Schmidt, M Gaggl, ...
Clinical kidney journal 13 (2), 225-234, 2020
122020
Recovery of kidney function in children treated with maintenance dialysis
M Bonthuis, J Harambat, E Bérard, K Cransberg, A Duzova, L Garneata, ...
Clinical journal of the American Society of Nephrology 13 (10), 1510-1516, 2018
102018
Clinical factors and adverse kidney outcomes in children with antineutrophil cytoplasmic antibody–associated glomerulonephritis
M Marlais, T Wlodkowski, N Printza, D Kronsteiner, R Krisam, L Sauer, ...
American Journal of Kidney Diseases 81 (1), 119-122, 2023
82023
De Novo PACSIN1 Gene Variant Found in Childhood Lupus and a Role for PACSIN1/TRAF4 Complex in Toll‐like Receptor 7 Activation
C Xie, H Zhou, V Athanasopoulos, Q Shen, Y Zhang, X Meng, G Burgio, ...
Arthritis & Rheumatology 75 (6), 1058-1071, 2023
42023
Review of the Pathologic Characteristics in Myhre Syndrome: Gain-of-Function Pathogenic Variants in SMAD4 cause a Multisystem Fibroproliferative Response
LJ Starr, ME Lindsay, D Perry, G Gheewalla, PA VanderLaan, A Majid, ...
Pediatric and Developmental Pathology 25 (6), 611-623, 2022
32022
Renal X-inactivation in female individuals with X-linked Alport syndrome primarily determined by age
R Günthner, L Knipping, S Jeruschke, R Satanoskij, B Lorenz-Depiereux, ...
Frontiers in Medicine 9, 953643, 2022
32022
Correction: Consensus statement on standards and guidelines for the molecular diagnostics of Alport syndrome: refining the ACMG criteria
J Savige, H Storey, E Watson, JM Hertz, C Deltas, A Renieri, F Mari, ...
European Journal of Human Genetics 32 (1), 132-132, 2024
22024
High prevalence of hypertension in a European cohort of children with ADPKD: results of the ADPKiDs study
L Massella, D Mekahli, D Paripovic, L Prikhodina, N Godefroid, ...
Pediatric Nephrology 31 (10), 1728-1728, 2016
22016
Is there a dominant‐negative effect in individuals with heterozygous disease‐causing variants in COL4A3/COL4A4?
KM Riedhammer, H Simmendinger, V Tasic, J Putnik, N Abazi‐Emini, ...
Clinical Genetics, 2024
12024
Steroid-Resistant Nephrotic Syndrome due to NPHS2 Variants Is Not Associated With Posttransplant Recurrence
J Kachmar, O Boyer, B Lipska-Ziętkiewicz, V Morinière, O Gribouval, ...
Kidney International Reports, 2024
12024
The multifaceted phenotypic and genotypic spectrum of type-IV-collagen-related nephropathy—A human genetics department experience
J Ćomić, KM Riedhammer, R Günthner, CW Schaaf, P Richthammer, ...
Frontiers in Medicine 9, 957733, 2022
12022
Validation of pathogenic patterns in a novel cohort of patients with membranoproliferative glomerulonephritis by cluster analysis
N Garam, Z Prohászka, M Rudniczki, C Aigner, AC Lungu, J Reiterova, ...
Molecular Immunology 102, 153, 2018
12018
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