Sultana MH Faradz - Concepedia

Author

Sultana MH Faradz

Also Known As

BenC. J. Hamel, Faradz, S.M.H., Faradz, Sultana, Faradz, Sultana M.H., Faradz, Sultana Mh, S M H Faradz, S. M. H. Faradz, S.M.H. Faradz, SULTANA M. H. FARADZ, Sultana Faradz

221

Publications

2.6K

Citations

H-Index

133

Concepts

All Affiliations

Diponegoro University Radboud University Nijmegen Radboud University Medical Center The University of Melbourne Dr. Kariadi Hospital

About

Sultana MH Faradz is an author at Diponegoro University specializing in medicine, genetics, and public health.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	21	713
2	Education	2	2	49
3	Health Sciences	1	1	16
4	Language Studies	1	1	23
5	Natural Sciences	1	1	21

Sultana MH Faradz

Publications

2.3K

Citations

H-Index

Page 1

	Year	Citations
Disorders of sex development: insights from targeted gene sequencing of a large international patient cohort Stefanie Eggers, Simon Sadedin, Jocelyn A. van den Bergen, Genome biology	2016	382
Gonadoblastoma Arising in Undifferentiated Gonadal Tissue within Dysgenetic Gonads Martine Cools, Hans Stoop, Anne‐Marie F. Kersemaekers, The Journal of Clinical Endocrinology & Metabolism	2006	226
Side Effects of Minocycline Treatment in Patients With Fragile X Syndrome and Exploration of Outcome Measures Agustini Utari, Weerasak Chonchaiya, Susan M. Rivera, American Journal on Intellectual and Developmental Disabilities	2010	101
<i>SMAD2</i>Mutations Are Associated with Arterial Aneurysms and Dissections Dimitra Micha, Dongchuan Guo, Yvonne Hilhorst‐Hofstee, Human Mutation Vascular DiseaseMolecular PhysiologySystems BiologyUnaffected ParentsSmad2 Mutations	2015	95
Immune‐mediated disorders among women carriers of fragile X premutation alleles Tri Indah Winarni, Weerasak Chonchaiya, Tanjung Ayu Sumekar, American Journal of Medical Genetics Part A	2012	94
Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark Galuh Astuti, Mette Bertelsen, Markus N. Preising, European Journal of Human Genetics BiologyMendelian DisorderGenetic DisorderMedicineGenetics	2015	91
Imbalance of Angiopoietin-1 and Angiopoetin-2 in Severe Dengue and Relationship with Thrombocytopenia, Endothelial Activation, and Vascular Stability Meta Michels, Kis Djamiatun, Rob Fijnheer, American Journal of Tropical Medicine and Hygiene Vascular DiseaseImmunologyEndothelial ActivationVascular StabilityPlasma Leakage	2012	84
Severe Dengue Is Associated with Consumption of von Willebrand Factor and Its Cleaving Enzyme ADAMTS-13 Kis Djamiatun, André van der Ven, Philip G. de Groot, PLoS neglected tropical diseases	2012	74
Functional characterization of novel <i>NR5A1</i> variants reveals multiple complex roles in disorders of sex development Gorjana Robevska, Jocelyn A. van den Bergen, Thomas Ohnesorg, Human Mutation GeneticsMolecular GeneticsDisease Gene IdentificationSexual DisordersClinical Genetics	2017	48
Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches Brendan Backhouse, Chloe Hanna, Gorjana Robevska, Sexual Development GeneticsGenetic EpidemiologyPathologyGynecologyMolecular Genetics	2018	44

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