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
93
天
Research Progress on the Pathogenesis and Diagnostic and Therapeutic Potential of Ciliopathies Regulated by IFT172
作者
Dandan Chen; Yuhan Wang; Pengyao Ren; Yangyang Zhou; Chun Zhang; Waner Wang; Jiayi Geng; Yitong Chai; Jiajia Xie; Shuangjie Li; Zhongyi Yan; Xiaoqing Wang; Lei Zhang展开收起
作者单位
1. Department of Pathogen Biology, School of Basic Medical Sciences Henan University Kaifeng China; 2. Henan Provincial Engineering Center for Tumor Molecular Medicine, Kaifeng Key Laboratory of Cell Signal Transduction Henan University Kaifeng China; 3. Kaifeng155 Hospital, China RongTong Medical Healthcare Group Co. Ltd. Kaifeng China; 4. Shanghai Yangzhi Rehabilitation Hospital (Shanghai Sunshine Rehabilitation Center) Tongji University School of Medicine Shanghai China; 5. Clinical Center for Brain and Spinal Cord Research Tongji University Shanghai China; 6. Affiliated Shanghai Blue Cross Brain Hospital, School of Medicine Tongji University Shanghai China展开收起
30
天
Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants
作者
Evan Burchfiel; Xiaonan Zhao; Nichole M. Owen; Tia Gordon; Mahshid S. Azamian; Eric C. Kao; Fan Xia; Xi Luo; Jill A. Rosenfeld; Seema R. Lalani; Allison P. Ortega; Steven B. Bleyl; Florence Petit; Sulekha Rajagopolan; Bénédicte Demeer; Meredith K. Gillespie; Lijia Huang; Matthew Osmond; Kym M. Boycott; Kyra E. Stuurman; Marjon A. van Slegtenhorst; Haley Soller; Céline Jost; Aurore Garde; Hana Safraou; Laurence Faivre; Victor Faundes; Daryl A. Scott展开收起
作者单位
1. Department of Molecular and Human Genetics Baylor College of Medicine Houston Texas USA; 2. Baylor Genetics Houston Texas USA; 3. Department of Cell and Gene Therapy Baylor College of Medicine Houston Texas USA; 4. Department of Pediatrics, Division of Medical Genetics University of Utah Salt Lake City Utah USA; 5. Clinical Genetics Department Univ. Lille, CHU Lille Lille France; 6. Department of Clinical Genetics Liverpool Hospital Liverpool New South Wales Australia; 7. Centre Hospitalier Universitaire de Amiens‐Picardie Amiens France; 8. Chimere INSERM UA21 University of Picardie‐Jules Verne Amiens France; 9. Department of Genetics Children's Hospital of Eastern Ontario Ottawa Ontario Canada; 10. Children's Hospital of Eastern Ontario Research Institute University of Ottawa Ottawa Ontario Canada; 11. Department of Clinical Genetics Erasmus MC University Medical Center Rotterdam the Netherlands; 12. Division of Genetics and Genomic Medicine UPMC Children's Hospital of Pittsburgh Pittsburgh Pennsylvania USA; 13. Université Bourgogne Europe, CHU Dijon Bourgogne, Inserm, CTM UMR1231 Dijon France; 14. Laboratoire de Génomique Médicale, Inserm, UMR1231, équipe GAD Université Bourgogne Europe, CHU Dijon Bourgogne Dijon France; 15. Laboratorio de Genética y Enfermedades Metabólicas, Instituto de Nutrición y Tecnología de los Alimentos Universidad de Chile Santiago Chile展开收起
28
天
USP34 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes
作者
Helena Wigoda; Amjad Khan; Bryce A. Mendelsohn; Noriko Miyake; Nobuhiko Okamoto; Naomichi Matsumoto; Patricia J. C. Knijnenburg; Johanna M. van Hagen; Jiddeke van de Kamp; Quinten Waisfisz; Bryn D. Webb展开收起
作者单位
1. Department of Pediatrics Center for Precision Medicine University of Wisconsin School of Medicine and Public Health Madison Wisconsin USA; 2. Department of Zoology Institute of Biological Sciences, University of Lakki Marwat Lakki Marwat Khyber Pakhtunkhwa Pakistan; 3. Department of Medical Genetics Kaiser Permanente Oakland Medical Center Oakland California USA; 4. Department of Pediatrics Nagasaki University Institute of Biomedical Sciences Nagasaki Japan; 5. Department of Medical Genetics Osaka Women's and Children's Hospital Izumi Osaka Japan; 6. Department of Human Genetics Graduate School of Medicine, Yokohama City University Yokohama Japan; 7. Department of Human Genetics Amsterdam UMC Amsterdam the Netherlands展开收起
88
天
An Ancient Founder GDF2 Variant Potentially Causes Semi‐Dominant Non‐Syndromic Pulmonary Arterial Hypertension
作者
Abdullah Aldalaan; Seba Nadeef; Ebtissal Khouj; Fayez Alahmadi; Bayan Aljamal; Noura Alturaif; Nadeen Alharbi; Firdous Abdulwahab; Mashael Alqahtani; Fatima Alzubi; Omar Abuyousef; Mais O. Hashem; Hamdiah Zaytoun; Hanadi Alhamoud; Tarfa Alshidi; Amal Jaafar; Lama Alabdi; Fowzan S. Alkuraya展开收起
作者单位
1. Pulmonary Hypertension Program, Lung Health Center, King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia; 2. Department of Translational Genomics Center for Genomic Medicine, King Faisal Specialist Hospital, and Research Center Riyadh Saudi Arabia; 3. Innovation and Research, King Faisal Specialist Hospital and Research Centre Riyadh Saudi Arabia; 4. Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Center Riyadh Saudi Arabia; 5. Lifera Omics Riyadh Kingdom of Saudi Arabia展开收起
167
天
The WHO Classification of Genetic Tumour Syndromes: Considerations for Genetics
作者
Ian A. Cree; Mark J. Arends; Joseph D. Khoury; Erika R. E. Denton; Anthony J. Gill; Alexander J. Lazar; Ian M. Frayling; Stefan M. Pfister; Mark A. Rubin; Katia R. M. Leite; Raymond Dalgleish; Elspeth A. Bruford; Sharon E. Plon; Ada Hamosh; Michael Francis Walsh; Gabrielle Goldman‐Lévy; Harshima Wijesinghe; William D. Foulkes; Dilani Lokuhetty展开收起
作者单位
1. International Agency for Research on Cancer Lyon France; 2. Cancer Research UK Scotland Centre, Institute of Genetics and Cancer University of Edinburgh Edinburgh UK; 3. Department of Pathology, Microbiology, and Immunology University of Nebraska Medical Center Omaha Nebraska USA; 4. Norfolk and Norwich University Hospitals NHS Foundation Trust Norwich UK; 5. NSW Health Pathology, Department of Anatomical Pathology Royal North Shore Hospital St Leonards New South Wales Australia; 6. Departments of Pathology and Genomic Medicine The University of Texas MD Anderson Cancer Center Houston Texas USA; 7. Inherited Tumour Syndromes Research Group, School of Medicine Cardiff University Cardiff UK; 8. Hopp Children's Cancer Center Heidelberg (KiTZ) Heidelberg Germany; 9. Universität Bern Bern Switzerland; 10. University of São Paulo Medical School São Paulo São Paulo Brazil; 11. Division of Genetics and Genome Biology University of Leicester Leicester UK; 12. School of Clinical Medicine University of Cambridge Cambridge UK; 13. Baylor College of Medicine Houston Texas USA; 14. Department of Genetic Medicine (DGM), McKusick‐Nathans Institute Johns Hopkins University Baltimore Maryland USA; 15. Memorial Sloan Kettering Cancer Center New York New York USA; 16. Department of Human Genetics McGill University Montreal Quebec Canada展开收起
54
天
Clinical Variability Including Non‐Dilated Left Ventricular and Dilated Cardiomyopathy in a Pedigree With an Intragenic CTNNA3 Copy Number Variation
作者
Carmela Fusco; Sandra Mastroianno; Silvia Morlino; Riccardo Pracella; Federica Russo; Ester Maria Lucia Bevere; Orazio Palumbo; Giuseppe Di Stolfo; Marco Castori展开收起
作者单位
1. Inborn Errors of Morphogenesis Research Unit and Division of Medical Genetics Fondazione IRCCS‐Casa Sollievo Della Sofferenza San Giovanni Rotondo Italy; 2. Division of Electrophysiology Fondazione IRCCS‐Casa Sollievo Della Sofferenza San Giovanni Rotondo Italy展开收起
Expert Matching · Case Demo
把投稿要求，转成可验证的期刊方案
说清专业、时限和作者背景，CrushSCI 结合真实审稿样本，给出拟题方向、期刊初筛与周期判断。
客户询问
我是环境工程专业，需要一篇 SCI，希望 3 个月内见刊。没有基金，也没有大牛挂名，可以投哪些期刊？
CrushSCI回复
可以。先按 90 天时限做可行性筛选，同步查找无基金、无知名作者挂靠的典型论文案例，作为选刊依据。重点核对研究质量与期刊 scope。
- 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