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GALUH DYAH NUR ASTUTI

Universitas Diponegoro S2 - Ilmu Biomedik SINTA ID : 6086873
690
SINTA Score Overall
166
SINTA Score 3Yr
1.313
Affil Score
258
Affil Score 3Yr
Latest number of publications
  Scopus Analysis  

Lipopeptide-mediated Cas9 RNP delivery: A promising broad therapeutic strategy for safely removing deep-intronic variants in ABCA4
Q1 Journal Molecular Therapy Nucleic Acids
Author Order : 7 of 16     Creator : Vázquez-Domínguez I.
2024 0 cited
Exome variant prioritization in a large cohort of hearing-impaired individuals indicates IKZF2 to be associated with non-syndromic hearing loss and guides future research of unsolved cases
Q1 Journal Human Genetics
Author Order : 7 of 47     Creator : Velde H.M.
2024 0 cited
Early detection of active Human CytomegaloVirus (hCMV) infection in pregnant women using data generated for noninvasive fetal aneuploidy testing
Q1 Journal eBioMedicine
Author Order : 2 of 13     Creator : Faas B.H.W.
2024 3 cited
Towards Uncovering the Role of Incomplete Penetrance in Maculopathies through Sequencing of 105 Disease-Associated Genes
Q1 Journal Biomolecules
Author Order : 5 of 60     Creator : Hitti-Malin R.J.
2024 0 cited
Whole genome sequencing identifies elusive variants in genetically unsolved Italian inherited retinal disease patients
Q3 Journal Human Genetics and Genomics Advances
Author Order : 7 of 15     Creator : Zeuli R.
2024 0 cited
Automatized detection of uniparental disomies in a large cohort
Q1 Journal Human Genetics
Author Order : 7 of 9     Creator : Moch J.
2024 1 cited
Clinical exome sequencing data from patients with inborn errors of immunity: Cohort level diagnostic yield and the benefit of systematic reanalysis
Q1 Journal Clinical Immunology
Author Order : 0 of 0     Creator : Vorsteveld E.E.
2024 0 cited
Patient-derived glioblastoma organoids reflect tumor heterogeneity and treatment sensitivity
Q1 Journal Neuro-Oncology Advances
Author Order : 6 of 23     Creator : Verduin M.
2023 1 cited
Exome sequencing identifies novel genes and variants in patients with Hirschsprung disease
Q1 Journal Journal of Pediatric Surgery
Author Order : 8 of 8     Creator : Gunadi
2023 4 cited
Whole genome sequencing for USH2A-associated disease reveals several pathogenic deep-intronic variants that are amenable to splice correction
Q3 Journal Human Genetics and Genomics Advances
Author Order : 34 of 50     Creator : Reurink J.
2023 11 cited
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Summary

Article Quartile
Research Output
  Scopus GScholar WOS
Article 32 51 0
Citation 1082 1539 0
Cited Document 25 27 0
H-Index 14 16
i10-Index 17 18
G-Index 1 1
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