Neveen A Soliman
Neveen A Soliman
Professor of Pediatrics, Cairo University
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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome
CE Sadowski, S Lovric, S Ashraf, WL Pabst, HY Gee, S Kohl, ...
Journal of the American Society of Nephrology 26 (6), 1279-1289, 2015
COQ6 mutations in human patients produce nephrotic syndrome with sensorineural deafness
SF Heeringa, G Chernin, M Chaki, W Zhou, AJ Sloan, Z Ji, LX Xie, ...
The Journal of clinical investigation 121 (5), 2013-2024, 2011
TTC21B contributes both causal and modifying alleles across the ciliopathy spectrum
EE Davis, Q Zhang, Q Liu, BH Diplas, LM Davey, J Hartley, C Stoetzel, ...
Nature genetics 43 (3), 189-196, 2011
Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery
CAG Scott EM, Halees A, Itan Y, Spencer EG, He Y, Azab MA, Gabriel SB ...
Nat Genet. 48 (9), 1071-6, 2016
ARHGDIA mutations cause nephrotic syndrome via defective RHO GTPase signaling
HY Gee, P Saisawat, S Ashraf, TW Hurd, V Vega-Warner, H Fang, ...
The Journal of clinical investigation 123 (8), 3243-3253, 2013
Mutations in 12 known dominant disease-causing genes clarify many congenital anomalies of the kidney and urinary tract
DY Hwang, GC Dworschak, S Kohl, P Saisawat, A Vivante, AC Hilger, ...
Kidney international 85 (6), 1429-1433, 2014
Identification of 99 novel mutations in a worldwide cohort of 1,056 patients with a nephronophthisis-related ciliopathy
J Halbritter, JD Porath, KA Diaz, DA Braun, S Kohl, M Chaki, SJ Allen, ...
Human genetics 132 (8), 865-884, 2013
ANKS6 is a central component of a nephronophthisis module linking NEK8 to INVS and NPHP3
S Hoff, J Halbritter, D Epting, V Frank, TMT Nguyen, J Van Reeuwijk, ...
Nature genetics 45 (8), 951-956, 2013
Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy
EA Otto, G Ramaswami, S Janssen, M Chaki, SJ Allen, W Zhou, R Airik, ...
Journal of medical genetics 48 (2), 105-116, 2011
Cystinosis: a review
MA Elmonem, KR Veys, NA Soliman, M van Dyck, LP van den Heuvel, ...
Orphanet journal of rare diseases 11 (1), 1-17, 2016
High-throughput mutation analysis in patients with a nephronophthisis-associated ciliopathy applying multiplexed barcoded array-based PCR amplification and next-generation …
J Halbritter, K Diaz, M Chaki, JD Porath, B Tarrier, C Fu, JL Innis, SJ Allen, ...
Journal of medical genetics 49 (12), 756-767, 2012
Whole exome sequencing of patients with steroid-resistant nephrotic syndrome
JK Warejko, W Tan, A Daga, D Schapiro, JA Lawson, S Shril, S Lovric, ...
Clinical Journal of the American Society of Nephrology 13 (1), 53-62, 2018
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly
DA Braun, J Rao, G Mollet, D Schapiro, MC Daugeron, W Tan, ...
Nature genetics 49 (10), 1529-1538, 2017
Whole-exome sequencing identifies causative mutations in families with congenital anomalies of the kidney and urinary tract
AT van der Ven, DM Connaughton, H Ityel, N Mann, M Nakayama, J Chen, ...
Journal of the American Society of Nephrology 29 (9), 2348-2361, 2018
Whole exome sequencing frequently detects a monogenic cause in early onset nephrolithiasis and nephrocalcinosis
A Daga, AJ Majmundar, DA Braun, HY Gee, JA Lawson, S Shril, ...
Kidney international 93 (1), 204-213, 2018
Rapid detection of monogenic causes of childhood-onset steroid-resistant nephrotic syndrome
S Lovric, H Fang, V Vega-Warner, CE Sadowski, HY Gee, J Halbritter, ...
Clinical Journal of the American Society of Nephrology 9 (6), 1109-1116, 2014
FAT1 mutations cause a glomerulotubular nephropathy
HY Gee, CE Sadowski, PK Aggarwal, JD Porath, TA Yakulov, M Schueler, ...
Nature communications 7 (1), 1-11, 2016
Mutations in TRAF3IP1/IFT54 reveal a new role for IFT proteins in microtubule stabilization
AA Bizet, A Becker-Heck, R Ryan, K Weber, E Filhol, P Krug, J Halbritter, ...
Nature communications 6 (1), 1-14, 2015
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment
S Ashraf, H Kudo, J Rao, A Kikuchi, E Widmeier, JA Lawson, W Tan, ...
Nature communications 9 (1), 1-14, 2018
Whole exome sequencing identifies causative mutations in the majority of consanguineous or familial cases with childhood-onset increased renal echogenicity
DA Braun, M Schueler, J Halbritter, HY Gee, JD Porath, JA Lawson, ...
Kidney international 89 (2), 468-475, 2016
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