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1.
Genetic Analysis of 400 Patients Refines Understanding and Implicates a New Gene in Atypical Hemolytic Uremic Syndrome.
J Am Soc Nephrol
; 29(12): 2809-2819, 2018 12.
Article
in English
| MEDLINE | ID: mdl-30377230
2.
C3 glomerulonephritis secondary to mutations in factors H and I: rapid recurrence in deceased donor kidney transplant effectively treated with eculizumab.
Nephrol Dial Transplant
; 33(12): 2260-2265, 2018 12 01.
Article
in English
| MEDLINE | ID: mdl-29370420
3.
C4 Nephritic Factors in C3 Glomerulopathy: A Case Series.
Am J Kidney Dis
; 70(6): 834-843, 2017 Dec.
Article
in English
| MEDLINE | ID: mdl-28838767
4.
High-Throughput Genetic Testing for Thrombotic Microangiopathies and C3 Glomerulopathies.
J Am Soc Nephrol
; 27(4): 1245-53, 2016 Apr.
Article
in English
| MEDLINE | ID: mdl-26283675
5.
Characterising the spectrum of autosomal recessive hereditary hearing loss in Iran.
J Med Genet
; 52(12): 823-9, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26445815
6.
PDZD7 and hearing loss: More than just a modifier.
Am J Med Genet A
; 167A(12): 2957-65, 2015 Dec.
Article
in English
| MEDLINE | ID: mdl-26416264
7.
Comprehensive genetic analysis of complement and coagulation genes in atypical hemolytic uremic syndrome.
J Am Soc Nephrol
; 25(1): 55-64, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24029428
8.
Loss-of-function mutations of ILDR1 cause autosomal-recessive hearing impairment DFNB42.
Am J Hum Genet
; 88(2): 127-37, 2011 Feb 11.
Article
in English
| MEDLINE | ID: mdl-21255762
9.
Soluble CR1 therapy improves complement regulation in C3 glomerulopathy.
J Am Soc Nephrol
; 24(11): 1820-9, 2013 Nov.
Article
in English
| MEDLINE | ID: mdl-23907509
10.
Defining Nephritic Factors as Diverse Drivers of Systemic Complement Dysregulation in C3 Glomerulopathy.
Kidney Int Rep
; 9(2): 464-477, 2024 Feb.
Article
in English
| MEDLINE | ID: mdl-38344720
11.
Atypical postinfectious glomerulonephritis is associated with abnormalities in the alternative pathway of complement.
Kidney Int
; 83(2): 293-9, 2013 Feb.
Article
in English
| MEDLINE | ID: mdl-23235567
12.
A novel hybrid CFHR1/CFH gene causes atypical hemolytic uremic syndrome.
Pediatr Nephrol
; 28(11): 2221-5, 2013 Nov.
Article
in English
| MEDLINE | ID: mdl-23880784
13.
Human male infertility caused by mutations in the CATSPER1 channel protein.
Am J Hum Genet
; 84(4): 505-10, 2009 Apr.
Article
in English
| MEDLINE | ID: mdl-19344877
14.
Modeling C3 glomerulopathies: C3 convertase regulation on an extracellular matrix surface.
Front Immunol
; 13: 1073802, 2022.
Article
in English
| MEDLINE | ID: mdl-36846022
15.
Complement Factor I Variants in Complement-Mediated Renal Diseases.
Front Immunol
; 13: 866330, 2022.
Article
in English
| MEDLINE | ID: mdl-35619721
16.
DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.
Hum Mutat
; 32(7): 825-34, 2011 Jul.
Article
in English
| MEDLINE | ID: mdl-21520338
17.
Two Iranian families with a novel mutation in GJB2 causing autosomal dominant nonsyndromic hearing loss.
Am J Med Genet A
; 155A(5): 1202-11, 2011 May.
Article
in English
| MEDLINE | ID: mdl-21484990
18.
A novel deletion in the RCA gene cluster causes atypical hemolytic uremic syndrome.
Nephrol Dial Transplant
; 26(2): 739-41, 2011 Feb.
Article
in English
| MEDLINE | ID: mdl-20974643
19.
Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations.
Hum Genet
; 127(2): 155-62, 2010 Feb.
Article
in English
| MEDLINE | ID: mdl-19847460
20.
Soluble c5b-9 as a biomarker for complement activation in atypical hemolytic uremic syndrome.
Am J Kidney Dis
; 65(6): 968-9, 2015 Jun.
Article
in English
| MEDLINE | ID: mdl-25818678