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Prof. Sultana MH Faradz, MD, PhD
Prof. Sultana MH Faradz, MD, PhD
Center for Biomedical Research, Faculty of Medicine, Diponegoro University, Indonesia
Verified email at fk.undip.ac.id
Title
Cited by
Cited by
Year
Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort
S Eggers, S Sadedin, JA Van Den Bergen, G Robevska, T Ohnesorg, ...
Genome biology 17, 1-21, 2016
3182016
Gonadoblastoma arising in undifferentiated gonadal tissue within dysgenetic gonads
M Cools, H Stoop, AMF Kersemaekers, SLS Drop, KP Wolffenbuttel, ...
The Journal of Clinical Endocrinology & Metabolism 91 (6), 2404-2413, 2006
2152006
Tumor risk in disorders of sex development
J Pleskacova, R Hersmus, JW Oosterhuis, BA Setyawati, SM Faradz, ...
Sexual Development 4 (4-5), 259-269, 2010
1892010
Side effects of minocycline treatment in patients with fragile X syndrome and exploration of outcome measures
A Utari, W Chonchaiya, SM Rivera, A Schneider, RJ Hagerman, ...
American journal on intellectual and developmental disabilities 115 (5), 433-443, 2010
1232010
Immune‐mediated disorders among women carriers of fragile X premutation alleles
TI Winarni, W Chonchaiya, TA Sumekar, P Ashwood, GM Morales, ...
American journal of medical genetics Part A 158 (10), 2473-2481, 2012
1062012
Imbalance of angiopoietin-1 and angiopoetin-2 in severe dengue and relationship with thrombocytopenia, endothelial activation, and vascular stability
M Michels, AJAM van der Ven, K Djamiatun, R Fijnheer, PG de Groot, ...
The American journal of tropical medicine and hygiene 87 (5), 943, 2012
962012
SMAD2 Mutations Are Associated with Arterial Aneurysms and Dissections
D Micha, D Guo, Y Hilhorst‐Hofstee, F van Kooten, D Atmaja, E Overwater, ...
Human mutation 36 (12), 1145-1149, 2015
942015
Severe dengue is associated with consumption of von Willebrand factor and its cleaving enzyme ADAMTS-13
K Djamiatun, AJAM Van der Ven, PG de Groot, SMH Faradz, D Hapsari, ...
PLoS neglected tropical diseases 6 (5), e1628, 2012
832012
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark
GDN Astuti, M Bertelsen, MN Preising, M Ajmal, B Lorenz, SMH Faradz, ...
European Journal of Human Genetics 24 (7), 1071-1079, 2016
822016
Emotional and behavioral problems in late-identified Indonesian patients with disorders of sex development
A Ediati, SMH Faradz, AZ Juniarto, J van der Ende, SLS Drop, ...
Journal of Psychosomatic Research 79 (1), 76-84, 2015
522015
Social stigmatisation in late identified patients with disorders of sex development in Indonesia
A Ediati, AZ Juniarto, E Birnie, J Okkerse, A Wisniewski, S Drop, ...
BMJ Paediatrics Open 1 (1), 2017
512017
Gender development in Indonesian children, adolescents, and adults with disorders of sex development
A Ediati, AZ Juniarto, E Birnie, SLS Drop, SMH Faradz, AB Dessens
Archives of Sexual Behavior 44, 1339-1361, 2015
512015
Molecular genetic analysis of retinitis pigmentosa in Indonesia using genome-wide homozygosity mapping
AM Siemiatkowska, K Arimadyo, LM Moruz, GDN Astuti, M de Castro-Miro, ...
Molecular vision 17, 3013, 2011
512011
Functional characterization of novel NR5A1 variants reveals multiple complex roles in disorders of sex development
G Robevska, JA Van Den Bergen, T Ohnesorg, S Eggers, C Hanna, ...
Human mutation 39 (1), 124-139, 2018
472018
Hormonal evaluation in relation to phenotype and genotype in 286 patients with a disorder of sex development from Indonesia
AZ Juniarto, YG van der Zwan, A Santosa, MD Ariani, S Eggers, ...
Clinical Endocrinology 85 (2), 247-257, 2016
472016
Body image and sexuality in Indonesian adults with a disorder of sex development (DSD)
A Ediati, AZ Juniarto, E Birnie, SLS Drop, SMH Faradz, AB Dessens
The Journal of Sex Research 52 (1), 15-29, 2015
412015
Increased PAI-1 plasma levels and risk of death from dengue: no association with the 4G/5G promoter polymorphism
ATA Mairuhu, TE Setiati, P Koraka, CE Hack, A Leyte, SMH Faradz, ...
Thrombosis Journal 3, 1-8, 2005
402005
Whole exome sequencing combined with linkage analysis identifies a novel 3 bp deletion in NR5A1
S Eggers, KR Smith, M Bahlo, LHJ Looijenga, SLS Drop, ZA Juniarto, ...
European Journal of Human Genetics 23 (4), 486-493, 2015
392015
A novel homozygous 5 bp deletion in FKBP10 causes clinically Bruck syndrome in an Indonesian patient
ED Setijowati, FS Van Dijk, JM Cobben, RR Van Rijn, EA Sistermans, ...
European journal of medical genetics 55 (1), 17-21, 2012
342012
High plasma mid-regional pro-adrenomedullin levels in children with severe dengue virus infections
M Michels, K Djamiatun, SMH Faradz, MMJF Koenders, Q de Mast, ...
Journal of clinical virology 50 (1), 8-12, 2011
342011
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