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

Ultrarare Variants in DNA Damage Repair and Mitochondrial Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome and Acute Behavioral Regression in Neurodevelopmental Disorders

儿童急性起病神经精神综合征和神经发育障碍急性行为倒退中DNA损伤修复和线粒体基因的超罕见变异

期刊:Developmental Neuroscience
影响因子:2
doi:10.1159/000550301
Vettiatil, Dhanya; Soorajkumar, Anjana; Dubin, Robert A; Pedrosa, Erika M; Schornagel, Allan; Lambert, John S; Costa, Isadora Pinheiro; McDonald, Joseph; Swagemakers, Sigrid M A; van der Spek, Peter J; Frankovich, Jennifer; Cunningham, Janet L; Lachman, Herbert M
线粒体
发育与干细胞
毒理研究
神经科学
发表日期：2026
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Mapping human brain cell type origin and diseases through single-cell transcriptomics

通过单细胞转录组学绘制人类脑细胞类型起源和疾病图谱

期刊:Translational Psychiatry
影响因子:6.2
doi:10.1038/s41398-025-03562-6
Soorajkumar, Anjana; Balan, Bipin; Nassir, Nasna; Akter, Hosneara; Shahin, Zaha; Berdiev, Bakhrom K; Woodbury-Smith, Marc; Khalil, Reem; Cisse, Babacar; Benamer, Hani T S; Uddin, Mohammed
细胞生物学
神经科学
单细胞
发表日期：2025
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Absence of the LRRK2 mutation in Emirati Parkinson's disease patients in contrast to other Arab populations

与其他阿拉伯人群相比，阿联酋帕金森病患者中未发现LRRK2基因突变。

期刊:Frontiers in Aging Neuroscience
影响因子:4.5
doi:10.3389/fnagi.2025.1676115
Metta, Vinod; Soorajkumar, Anjana; Loney, Tom; Nassir, Nasna; Chaudhuri, K Ray; Uddin, Mohammed Jashim; Benamer, Hani T S
LRRK2
帕金森
神经科学
发表日期：2025
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Ultrarare Variants in DNA Damage Repair and Mitochondrial Genes in Pediatric Acute-Onset Neuropsychiatric Syndrome and Acute Behavioral Regression in Neurodevelopmental Disorders

儿童急性起病神经精神综合征和神经发育障碍急性行为倒退中DNA损伤修复和线粒体基因的超罕见变异

期刊:
影响因子:
doi:10.1101/2025.08.27.25333852
Vettiatil, Dhanya; Soorajkumar, Anjana; Dubin, Robert A; Pedrosa, Erika; Schornagel, Allan; Lambert, John S; Costa, Isadora Pinheiro; McDonald, Joseph; Swagemakers, Sigrid M A; van der Spek, Peter J; Frankovich, Jennifer; Cunningham, Janet L; Lachman, Herbert M
线粒体
发育与干细胞
毒理研究
神经科学
发表日期：2025
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Expanding deep phenotypic spectrum associated with atypical pathogenic structural variations overlapping 15q11-q13 imprinting region

与15q11-q13印记区域重叠的非典型致病结构变异相关的表型谱不断扩展

期刊:Brain and Behavior
影响因子:2.7
doi:10.1002/brb3.3437
Mim, Rabeya Akter; Soorajkumar, Anjana; Kosaji, Noor; Rahman, Muhammad Mizanur; Sarker, Shaoli; Karuvantevida, Noushad; Eshaque, Tamannyat Binte; Rahaman, Md Atikur; Islam, Amirul; Chowdhury, Mohammod Shah Jahan; Shams, Nusrat; Uddin, K M Furkan; Akter, Hosneara; Uddin, Mohammed
发表日期：2024
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Mutational spectrum and phenotypic variability of Duchenne muscular dystrophy and related disorders in a Bangladeshi population

孟加拉国人群中杜氏肌营养不良症及相关疾病的突变谱和表型变异性

期刊:Scientific Reports
影响因子:3.9
doi:10.1038/s41598-023-48982-w
Sarker, Shaoli; Eshaque, Tamannyat Binte; Soorajkumar, Anjana; Nassir, Nasna; Zehra, Binte; Kanta, Shayla Imam; Rahaman, Md Atikur; Islam, Amirul; Akter, Shimu; Ali, Mohammad Kawsar; Mim, Rabeya Akter; Uddin, K M Furkan; Chowdhury, Mohammod Shah Jahan; Shams, Nusrat; Baqui, Md Abdul; Lim, Elaine T; Akter, Hosneara; Woodbury-Smith, Marc; Uddin, Mohammed
发表日期：2023
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Computational Analysis of Short Linear Motifs in the Spike Protein of SARS-CoV-2 Variants Provides Possible Clues into the Immune Hijack and Evasion Mechanisms of Omicron Variant

对SARS-CoV-2变异株刺突蛋白中短线性基序的计算分析为揭示Omicron变异株的免疫劫持和逃避机制提供了可能的线索

期刊:International Journal of Molecular Sciences
影响因子:4.9
doi:10.3390/ijms23158822
Soorajkumar, Anjana; Alakraf, Ebrahim; Uddin, Mohammed; Du Plessis, Stefan S; Alsheikh-Ali, Alawi; Kandasamy, Richard K
SARS-CoV-2
免疫/内分泌
发表日期：2022
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