Association between methylenetetrahydrofolate reductase (MTHFR) polymorphism and carotid intima medial thickness progression in post ischaemic stroke patient

Tekijä Pramukarso, Dodik T., Faradz, Sultana M.H., Sari, Stefani, Hadisaputro, Soeharyo
Julkaisussa Ann Transl Med (2015)

AB174. Genetic counseling in the couple with compound heterozygous carrier based on the result of mutation effect analysis on cystic fibrosis transmembrane conductance regulator (C...

Tekijä Permata Sari, Ariestya Indah, Farhat, Raed, Ladeveze, Véronique, Faradz, Sultana M. H., Kitzis, Alain
Julkaisussa Ann Transl Med (2015)

A Single Common Assay for Robust and Rapid Fragile X Mental Retardation Syndrome Screening From Dried Blood Spots

Tekijä Tan, Vivienne J., Lian, Mulias, Faradz, Sultana M.H., Winarni, Tri I., Chong, Samuel S.
Julkaisussa Front Genet (2018)

Methadone Use in a Male With the FMR1 Premutation and FXTAS

Tekijä Muzar, Zukhrofi, Lozano, Reymundo, Schneider, Andrea, Adams, Patrick E., Faradz, Sultana M.H., Tassone, Flora, Hagerman, Randi J.
Julkaisussa Am J Med Genet A (2015)

A Rare, Recurrent, De Novo 14q32.2q32.31 Microdeletion of 1.1 Mb in a 20-Year-Old Female Patient with a Maternal UPD(14)-Like Phenotype and Intellectual Disability

Tekijä Zada, Almira, Mundhofir, Farmaditya E. P., Pfundt, Rolph, Leijsten, Nico, Nillesen, Willy, Faradz, Sultana M. H., de Leeuw, Nicole
Julkaistu 2014

Social stigmatisation in late identified patients with disorders of sex development in Indonesia

Tekijä Ediati, Annastasia, Juniarto, A Zulfa, Birnie, Erwin, Okkerse, Jolanda, Wisniewski, Amy, Drop, Stenvert, Faradz, Sultana M H, Dessens, Arianne
Julkaisussa BMJ Paediatr Open (2017)

Quality of Life in Late-Treated Patients With Disorders of Sex Development: Insights for Patient-Centered Care

Tekijä Ediati, Annastasia, Verrips, Gijsbert H. W., Juniarto, Achmad Zulfa, Faradz, Sultana M. H., Drop, Stenvert L. S., Dessens, Arianne B.
Julkaisussa Front Pediatr (2019)

Identification of Expanded Alleles of the FMR1 Gene Among High-Risk Population in Indonesia by Using Blood Spot Screening

Tekijä Winarni, Tri Indah, Utari, Agustini, Mundhofir, Farmaditya E.P., Tong, Tzuhan, Durbin-Johnson, Blythe, Faradz, Sultana M.H., Tassone, Flora
Julkaistu 2012

Toll-Like Receptor 4 Polymorphisms in Dengue Virus–Infected Children

Tekijä Djamiatun, Kis, Ferwerda, Bart, Netea, Mihai G., van der Ven, André J. A. M., Dolmans, Wil M. V., Faradz, Sultana M. H.
Julkaistu 2011

Side Effects of Minocycline Treatment in Patients With Fragile X Syndrome and Exploration of Outcome Measures

Tekijä Utari, Agustini, Chonchaiya, Weerasak, Rivera, Susan M., Schneider, Andrea, Hagerman, Randi J., Faradz, Sultana M. H., Ethell, Iryna M., Nguyen, Danh V.
Julkaistu 2010

Mowat-Wilson Syndrome: The First Clinical and Molecular Report of an Indonesian Patient

Tekijä Mundhofir, Farmaditya E. P., Yntema, Helger G., van der Burgt, Ineke, Hamel, Ben C. J., Faradz, Sultana M. H., van Bon, Bregje W. M.
Julkaistu 2012

Validation of a commercially available test that enables the quantification of the numbers of CGG trinucleotide repeat expansion in FMR1 gene

Tekijä Lim, Grace X. Y., Yeo, Minli, Koh, Yvonne Y., Winarni, Tri Indah, Rajan-Babu, Indhu-Shree, Chong, Samuel S., Faradz, Sultana M. H., Guan, Ming
Julkaisussa PLoS One (2017)

Identification of a novel nonsense mutation in RP1 that causes autosomal recessive retinitis pigmentosa in an Indonesian family

Tekijä Siemiatkowska, Anna M., Astuti, Galuh D.N., Arimadyo, Kentar, den Hollander, Anneke I., Faradz, Sultana M.H., Cremers, Frans P.M., Collin, Rob W.J.
Julkaistu 2012

Variants in congenital hypogonadotrophic hypogonadism genes identified in an Indonesian cohort of 46,XY under-virilised boys

Tekijä Ayers, Katie L., Bouty, Aurore, Robevska, Gorjana, van den Bergen, Jocelyn A., Juniarto, Achmad Zulfa, Listyasari, Nurin Aisyiyah, Sinclair, Andrew H., Faradz, Sultana M. H.
Julkaisussa Hum Genomics (2017)

Functional analysis of novel desert hedgehog gene variants improves the clinical interpretation of genomic data and provides a more accurate diagnosis for patients with 46, XY diff...

Tekijä Ayers, Katie, van den Bergen, Jocelyn, Robevska, Gorjana, Listyasari, Nurin, Raza, Jamal, Atta, Irum, Riedl, Stefan, Rothacker, Karen, Choong, Catherine, Faradz, Sultana M H, Sinclair, Andrew
Julkaisussa J Med Genet (2019)

Functional Characterization of Two New Variants in the Bone Morphogenetic Protein 7 Prodomain in Two Pairs of Monozygotic Twins With Hypospadias

Tekijä Bouty, Aurore, Walton, Kelly, Listyasari, Nurin Aisyiyah, Robevska, Gorjana, Van den Bergen, Jocelyn, Santosa, Ardy, Faradz, Sultana M H, Harrison, Craig, Ayers, Katie L, Sinclair, Andrew H
Julkaisussa J Endocr Soc (2019)

Missense mutations at homologous positions in the fourth and fifth laminin A G-like domains of eyes shut homolog cause autosomal recessive retinitis pigmentosa

Tekijä Khan, Muhammad Imran, Collin, Rob W.J., Arimadyo, Kentar, Micheal, Shazia, Azam, Maleeha, Qureshi, Nadeem, Faradz, Sultana M.H., den Hollander, Anneke I., Qamar, Raheel, Cremers, Frans P.M.
Julkaistu 2010

Imbalance of Angiopoietin-1 and Angiopoetin-2 in Severe Dengue and Relationship with Thrombocytopenia, Endothelial Activation, and Vascular Stability

Tekijä Michels, Meta, van der Ven, André J. A. M., Djamiatun, Kis, Fijnheer, Rob, de Groot, Philip G., Griffioen, Arjan W., Sebastian, Silvie, Faradz, Sultana M. H., de Mast, Quirijn
Julkaistu 2012

Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark

Tekijä Astuti, Galuh D N, Bertelsen, Mette, Preising, Markus N, Ajmal, Muhammad, Lorenz, Birgit, Faradz, Sultana M H, Qamar, Raheel, Collin, Rob W J, Rosenberg, Thomas, Cremers, Frans P M
Julkaisussa Eur J Hum Genet (2016)

Severe Dengue Is Associated with Consumption of von Willebrand Factor and Its Cleaving Enzyme ADAMTS-13

Tekijä Djamiatun, Kis, van der Ven, Andre J. A. M., de Groot, Philip G., Faradz, Sultana M. H., Hapsari, D., Dolmans, Wil M. V., Sebastian, Silvie, Fijnheer, Rob, de Mast, Quirijn
Julkaistu 2012