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198.3平均天数
188中位天数
62最短天数
607最长天数
1392025发文量

Paper Review Records

全部论文审稿周期

25 篇有效样本 · 按发表日期由新到旧排列
审稿天数=录用日期-收稿日期;保留 PDF/DOI/网页源链接

201 天

Rare Biallelic CTU2 Variants in an Individual With CAKUT : Clinical Characterization and Minigene Splicing Analysis

作者
Qian Liu; Xueqin Cheng; Bixia Zheng; Chunli Wang; Wei Zhou; Aihua Zhang展开收起
作者单位
1. Department of Nephrology Children's Hospital of Nanjing Medical University Nanjing Jiangsu China; 2. Nanjing Key Laboratory of Pediatrics Children's Hospital of Nanjing Medical University Nanjing Jiangsu China展开收起
PDF源文件 DOI 网页
313 天

A Synonymous DLG4 Variant (c. 771G >A) Causes Exon 9 Skipping via Paternal Germline Mosaicism in DLG4 ‐Related Synaptopathy

作者
Jing Chen; Qinfei Zhao; Xinyue Zhang; Nan Wu; Xuxiang Xi; Yin Zeng; Sa Wu; Kun Yuan; Zezhang Liu; Xiangsheng Wu; Shaoying Zeng展开收起
作者单位
1. Department of Laboratory Medicine First Affiliated Hospital of Gannan Medical University Ganzhou Jiangxi China; 2. Nanchang University Nanchang China; 3. The First School of Clinical Medicine Gannan Medical University Ganzhou Jiangxi China; 4. Department of Obstetrics and Gynecology First Affiliated Hospital of Gannan Medical University Ganzhou Jiangxi China; 5. BGI Genomics Shenzhen Guangdong China; 6. Clin Lab BGI Genomics Wuhan Hubei China展开收起
PDF源文件 DOI 网页
111 天

Knowledge Mapping of Alport Syndrome: A Bibliometric Analysis From 2000 to 2025

作者
Xiujuan Cao; Wei Zhou; Yong Wang; Lvxian Wu; Jianhua Mao展开收起
作者单位
1. Department of Nephrology, The Children's Hospital Zhejiang University School of Medicine, National Clinical Research Center for Child Health, National Children's Regional Medical Center Hangzhou Zhejiang China; 2. Department of Pediatrics Jinhua Municipal Central Hospital Jinhua China; 3. The Key Laboratory for Screening and Diagnosis of Maternal and Child Genetic Disease of Health Commission of Jiangxi Province Jiujiang Jiangxi China; 4. Department of Internal Medicine Yanbian University Hospital Yanji Jilin China展开收起
PDF源文件 DOI 网页
156 天

Identification of the MYH6 c. 804G >C Synonymous Variant Causing Exon Skipping in a Hypertrophic Cardiomyopathy Family

作者
Songlin Zhang; Xiaohua Tang; Leixiang Yang; Yang Wang; Yong Cui; Xiaopan Chen展开收起
作者单位
1. Laboratory Medicine Center, Department of Genetic and Genomic Medicine Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College Hangzhou Zhejiang China; 2. Key Laboratory of Birth Defects Wenzhou Central Hospital Wenzhou Zhejiang China; 3. Heart Center, Department of Cardiovascular Surgery Zhejiang Provincial People's Hospital, Affiliated People's Hospital, Hangzhou Medical College Hangzhou Zhejiang China展开收起
PDF源文件 DOI 网页
124 天

COQ2‐Associated Primary Coenzyme Q10 Deficiency Presenting With Proteinuria: A Case Report and Literature Review

作者
Yuqi Yue; Fei Zhao; Qiuxia Chen展开收起
作者单位
1. Department of Nephrology Children's Hospital of Nanjing Medical University Nanjing China展开收起
PDF源文件 DOI 网页
349 天

Body Region Dysmorphology Is Predictive of Genetic Diagnoses in Infants With Congenital Heart Disease

作者
Benjamin M. Helm; Leah Wetherill; Benjamin J. Landis; Stephanie M. Ware展开收起
作者单位
1. Department of Medical and Molecular Genetics Indiana University School of Medicine Indianapolis Indiana USA; 2. Department of Pediatrics Indiana University School of Medicine Indianapolis Indiana USA展开收起
PDF源文件 DOI 网页

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拟题建议
《融合机器学习与生命周期评价的城市污水处理碳排放预测与优化》

样本口径2026 年最近 5 篇有效论文样本

平均审稿62 天

中位数65 天

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