日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Does surgical approach affect Hirschsprung-associated enterocolitis risk? A comparison between transanal Swenson-like and endorectal pull-throughs

手术入路是否会影响先天性巨结肠相关性肠炎的风险？经肛门Swenson样手术与直肠内拖出术的比较

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0340813
Putri, Azzahra Fatinnuha Azmi Prayogi; Afandy, Dwiki; Habibiy, Ahmad Zakiy; Nurhidayah, Setiani Silvy; Vujira, Khanza Adzkia; Adhityo, Pramana; Candy, Gilang Vigorous Akbar Eka; Iskandar, Kristy; Purnomo, Eko; Gunadi
肠炎
发表日期：2026
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Exome sequencing facilitates personalized treatment in developmental and epileptic encephalopathy patients: transforming current clinical practice in Indonesia

外显子组测序助力发育性和癫痫性脑病患者实现个性化治疗：正在改变印度尼西亚目前的临床实践。

期刊:Lancet Regional Health - Southeast Asia
影响因子:6.2
doi:10.1016/j.lansea.2025.100638
Triono, Agung; Iskandar, Kristy; Sumpono, Auliya S B; Hikmawan, Tyas I; Gunadi; Herini, Elisabeth S
发育与干细胞
癫痫
神经科学
发表日期：2025
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Aberrant SOX10 and RET expressions in patients with Hirschsprung disease

先天性巨结肠患者的SOX10和RET表达异常

期刊:BMC Pediatrics
影响因子:2
doi:10.1186/s12887-024-04682-6
Gunadi; Amadeus, Verrell Christopher; Utami, Fadila Dyah Trie; Halim, Fiqih Vidiantoro; Novebri, Nabilah Anisa; Hanggoro, Rahaditya Alrasyidi; Lestari, Avinindita Nura; Iskandar, Kristy; Dwihantoro, Andi; Purnomo, Eko
SOX
RET
发表日期：2024
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Coinfection of severe acute respiratory syndrome coronavirus 2 and polyomavirus in a patient with coronavirus disease 2019 detected by enrichment next-generation sequencing: a case report

通过富集二代测序检测到一名2019冠状病毒病患者合并严重急性呼吸综合征冠状病毒2和多瘤病毒感染：病例报告

期刊:Journal of Medical Case Reports
影响因子:0.8
doi:10.1186/s13256-024-05005-0
Gunadi; Geometri, Esensi Tarian; Adhityo, Pramana; Abidin, Ali Zainal; Marcellus; Puspitarani, Dyah Ayu; Utami, Fadila Dyah Trie; Iskandar, Kristy; Wibawa, Hendra; Hakim, Mohamad Saifudin
微生物学
炎症/感染
发表日期：2024
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The importance of prenatal diagnosis for the surgical strategy of giant cystic meconium peritonitis: A case report

产前诊断对巨大囊性胎粪性腹膜炎手术策略的重要性：病例报告

期刊:Heliyon
影响因子:3.6
doi:10.1016/j.heliyon.2023.e12960
Gunadi; Prathana, Saskia; Amadeus, Verrell Christopher; Ramadhita; Iskandar, Kristy; Anggraini, Alifah
发表日期：2023
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Identification of the genetic basis of pediatric neurogenetic disorders at a tertiary referral hospital in Indonesia: Contribution of whole exome sequencing

在印度尼西亚一家三级转诊医院中，通过全外显子组测序鉴定儿童神经遗传疾病的遗传基础：

期刊:PLoS One
影响因子:2.6
doi:10.1371/journal.pone.0293113
Triono, Agung; Iskandar, Kristy; Hadiyanto, Marissa Leviani; Nugrahanto, Andika Priamas; Diantika, Kania; Wijayanti, Veronica Wulan; Herini, Elisabeth Siti
发表日期：2023
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Prognostic factors for the outcomes of COVID-19 patients infected with SARS-CoV-2 Omicron and Delta variants

SARS-CoV-2 Omicron 和 Delta 变异株感染 COVID-19 患者预后的预后因素

期刊:BMC Medical Genomics
影响因子:2
doi:10.1186/s12920-023-01637-1
Gunadi; Hakim, Mohamad Saifudin; Wibawa, Hendra; Vujira, Khanza Adzkia; Puspitarani, Dyah Ayu; Supriyati, Endah; Trisnawati, Ika; Iskandar, Kristy; Khair, Riat El; Afiahayati; Siswanto; Puspadewi, Yunika; Irianingsih, Sri Handayani; Nugrahaningsih, Dwi Aris Agung; Eryvinka, Laudria Stella; Utami, Fadila Dyah Trie; Devana, Edita Mayda; Aditama, Lanang; Kinasih, Nathania Christi Putri; Hediningsih, Yekti; Ananda, Nur Rahmi; Marcellus; Arguni, Eggi; Nuryastuti, Titik; Wibawa, Tri
炎症/感染
SARS-CoV-2
发表日期：2023
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Collagen gene cluster expression and liver fibrogenesis in patients with biliary atresia: a preliminary study

胆道闭锁患者胶原基因簇表达与肝纤维化：一项初步研究

期刊:BMC Research Notes
影响因子:1.7
doi:10.1186/s13104-023-06636-0
Gunadi; Puspitarani, Dyah Ayu; Vujira, Khanza Adzkia; Utami, Fadila Dyah Trie; Devana, Edita Mayda; Halim, Fiqih Vidiantoro; Iskandar, Kristy; Makhmudi, Akhmad
发表日期：2023
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Phenotypes of a female patient with novel de novo frameshift ARX variant identified by whole-exome sequencing: a case report

通过全外显子组测序鉴定出一种新的从头发生的ARX移码变异的女性患者的表型：病例报告

期刊:Annals of Medicine and Surgery
影响因子:1.6
doi:10.1097/MS9.0000000000000197
Iskandar, Kristy; Herini, Elisabeth S; Triono, Agung; Hadiyanto, Marissa L; Nugrahanto, Andika P; Gunadi
发表日期：2023
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De novo mutation of the TSC2 gene in patient with Tuberous Sclerosis Complex-Associated Neuropsychiatric Disorders (TAND) Phenotype: a case report

结节性硬化症相关神经精神障碍（TAND）表型患者TSC2基因新生突变：病例报告

期刊:Annals of Medicine and Surgery
影响因子:1.6
doi:10.1097/MS9.0000000000000489
Triono, Agung; Herini, Elisabeth S; Iskandar, Kristy; Hadiyanto, Marissa L; Diantika, Kania; Wijayanti, Veronica W; Gunadi
发表日期：2023
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