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YOGIK ONKY SILVANA WIJAYA

Universitas Gadjah Mada S2 - Magister Kebidanan SINTA ID : 6782946
562
SINTA Score Overall
149
SINTA Score 3Yr
562
Affil Score
149
Affil Score 3Yr
Latest number of publications
  Scopus Analysis  

Performance of cellulose-based card for direct genetic testing of spinal muscular atrophy
Q2 as Journal BMC Biotechnology
Author Order : 1 of 4     Creator : Wijaya Y.O.S.
2025 0 cited
Correction to: PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan (Genes, (2022), 13, 11, (2110), 10.3390/genes13112110)
Q2 as Journal Genes
Author Order : 9 of 21     Creator : Noguchi Y.
2023 0 cited
PCR-Based Screening of Spinal Muscular Atrophy for Newborn Infants in Hyogo Prefecture, Japan
Q2 as Journal Genes
Author Order : 9 of 21     Creator : Noguchi Y.
2022 18 cited
Stability and Oligomerization of Mutated SMN Protein Determine Clinical Severity of Spinal Muscular Atrophy
Q2 as Journal Genes
Author Order : 3 of 12     Creator : Niba E.T.E.
2022 9 cited
High Concentration or Combined Treatment of Antisense Oligonucleotides for Spinal Muscular Atrophy Perturbed SMN2 Splicing in Patient Fibroblasts
Q2 as Journal Genes
Author Order : 1 of 8     Creator : Wijaya Y.O.S.
2022 3 cited
Spinal muscular atrophy: Diagnosis, incidence, and newborn screening in Japan
Q2 as Journal International Journal of Neonatal Screening
Author Order : 6 of 21     Creator : Kimizu T.
2021 27 cited
Glycogen storage disease type ia screening using dried blood spots on filter paper: Application of cop-pcr for detection of the c.648g>t g6pc gene mutation
Q2 as Journal Kobe Journal of Medical Sciences
Author Order : 1 of 6     Creator : Wijaya Y.O.S.
2021 4 cited
Detection of spinal muscular atrophy patients using dried saliva spots
Q2 as Journal Genes
Author Order : 1 of 9     Creator : Wijaya Y.O.S.
2021 5 cited
Clinical phenotypes of spinal muscular atrophy patients with hybrid SMN gene
Q2 as Journal Brain and Development
Author Order : 3 of 12     Creator : Niba E.T.E.
2021 36 cited
Dbs screening for glycogen storage disease type 1a: Detection of c.648g>t mutation in g6pc by combination of modified competitive oligonucleotide priming-pcr and melting curve analysis
Q2 as Journal International Journal of Neonatal Screening
Author Order : 2 of 7     Creator : Niba E.T.E.
2021 4 cited
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Summary

Article Quartile
Research Output
  Scopus GScholar WOS
Article 19 31 0
Citation 190 294 0
Cited Document 16 21 0
H-Index 7 9
i10-Index 6 8
G-Index 1 1
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