Paper Review Records
全部论文审稿周期
10 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
205
天
Identification of novel HUWE1 variants in Turner-type X-linked intellectual disability
作者
Jingjing Zhang; Jing He; Hairui Pan; Dan Wang; Qinghua Zhang; Shengju Hao; Ling Hui; Chuan Zhang展开收起
作者单位
Medical Genetics Center, Gansu Provincial Maternity and Child-care Hospital (Gansu Provincial Central Hospital)/Gansu Clinical Research Center for Birth Defects and Rare Diseases, Lanzhou, Gansu, 730000, China; Gansu Key Laboratory of Maternal-Fetal Medicine and Reproductive Protection, Lanzhou, Gansu, 730000, China展开收起
104
天
Two new cases of fragile X syndrome without CGG triplet expansion. Clinical-molecular characterization and review of the literature
作者
Giulia Lauretti; Roberta Pietrobono; Benedetta Niccolini; Clarissa Modafferi; Maria Accadia; Ada Piepoli; Daniela Orteschi; Maria Grazia Pomponi; Pietro Chiurazzi; Maurizio Genuardi; Giovanni Neri; Elisabetta Tabolacci展开收起
作者单位
UOC Genetica Medica, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, 00168, Italy; Dept. of Life Sciences and Public Health, Section of Genomic Medicine, Catholic University of Sacred Heart, Rome, 00168, Italy; Medical Genetics Service, Hospital Cardinale G. Panico, Tricase, 73039, Italy; Division of Medical Genetics, Fondazione IRCCS Casa Sollievo della Sofferenza, San Giovanni Rotondo, 71013, Italy展开收起
97
天
Clinical and genetic spectrum of trichorhinophalangeal syndrome type I/III in 20 children of Korean origin
作者
Ayoung Park; Naye Choi; Tae-Joon Cho; Jung Min Ko展开收起
作者单位
Department of Pediatrics, Hallym University Sacred Heart Hospital, Hallym University College of Medicine, Anyang, South Korea; Department of Pediatrics, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, South Korea; Department of Orthopaedic Surgery, Seoul National University Children's Hospital, Seoul National University College of Medicine, Seoul, South Korea; Center for Rare Diseases, Seoul National University Hospital, Seoul, South Korea展开收起
204
天
Hearing outcomes after cochlear implantation in two patients with ATP6V1B2-related deafness and onychodystrophy
作者
Sarah Chamieh; Pauline Marzin; Sophie Achard; Pierre Blanc; Laurence Jonard; Saba Battelino; Katarina Trebusak; Margaux Serey-Gaut; Sandrine Marlin展开收起
作者单位
Service de Médecine Génomique des maladies rares, Hôpital Necker Enfants Malades, AP-HP Centre Université de Paris, Paris, 75015, France; CRMR Surdités Génétiques, Service de Médecine Génomique des maladies rares, Hôpital Necker Enfants Malades, AP-HP Centre Université de Paris, Paris, 75015, France; Service d'ORL Pédiatrique et de Chirurgie Cervico-Faciale, Hôpital Necker-Enfants Malades, AP-HP, Université de Paris Cité, Paris, 75015, France; Laboratoire de Biologie Médicale Multi-Sites SeqOIA, Paris, 75014, France; UF Développement et morphogénèse, Fédération de Génétique et médecine génomique, Service de Médecine génomique des maladies rares, Hôpital Necker-Enfants Malades, AP-HP, Paris, 75015, France; Department of Otorhinolaryngology and Cervicofacial Surgery, University Medical Centre Ljubljana, Ljubljana, 1000, Slovenia; Institute of Biochemistry and Molecular Genetics, Faculty of Medicine, University of Ljubljana, Ljubljana, 1000, Slovenia; Centre de recherche en Audiologie, Hôpital Necker Enfants Malades, AP-HP, Paris, 75015, France; Genetics of rare Ophthalmological, auditory and mitochondrial disorders, Institut Imagine, Inserm U1163, Université Paris Cité, Paris, France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