Paper Review Records
全部论文审稿周期
19 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
86
天
Transfer RNA-derived small RNAs: from biogenesis to regulatory roles in male reproductive system
作者
Xiaodan Jiang; Xinliang Gu; Yang Li; Xiaojue Chen; Shaoqing Ju展开收起
作者单位
1. Department of Laboratory Medicine, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China; 2. Research Center of Clinical Medicine, Affiliated Hospital of Nantong University, Nantong, China; 3. General Clinical Research Center, Nanjing First Hospital, Nanjing Medical University, Nanjing, China; 4. Department of Radiation Oncology, Affiliated Hospital of Nantong University, Nantong, China展开收起
217
天
Nanopore third-generation sequencing for the diagnosis of rare hemoglobinopathies in Southern China
作者
Fen Lin; Shi-Xiong Yang; Yi-Yuan Ge; Ying Yang; Long-Xu Xie; Li-Ye Yang展开收起
作者单位
1. Precision Medical Lab Center, Chaozhou Central Hospital, Chaozhou, China; 2. Central Research Laboratory, the Central Hospital of Xiaogan, Xiaogan, China; 3. Guangzhou Hybribio Medicine Technology Ltd., Guangzhou, China; 4. Precision Medical Lab Center, People’s Hospital of Yangjiang, Yangjiang, China展开收起
182
天
Further delineation of KIDAR syndrome: Two new cases with novel variants, functional analysis of the variants and a comprehensive review
作者
Şule Altıner; Ezgi Gökpınar İli; Ahmet Karer Yurtdaş; Okan Kurtçu; Neslihan Doğulu; Ayşe Öktem; Engin Köse; Fatma Tuba Eminoğlu; Behiye Tuğçe Yıldırım; Ayça Dilruba Aslanger; Gözde Yeşil Sayın; Halil Gürhan Karabulut展开收起
作者单位
1. Ankara University, School of Medicine, Department of Medical Genetics, Ankara, Turkey; 2. Başakşehir Çam and Sakura City Hospital, Genetics Diseases Center, İstanbul, Turkey; 3. Ankara University, School of Medicine, Department of Pediatric Metabolism, Ankara, Turkey; 4. Ankara University, School of Medicine, Department of Dermatology, Ankara, Turkey; 5. İstanbul University, İstanbul Faculty of Medicine, Department of Medical Genetics, İstanbul, Turkey展开收起
102
天
Associations of polygenic risk scores for type 2 diabetes with metabolic measures in Pacific Islanders from Guam and Saipan
作者
Maria J. Ramirez-Luzuriaga; Saied Safabakhsh; Rasol Salehi; Sayuko Kobes; Tanisha F. Aflague; Jenny Duenas Sarmiento; Joanne E. Curran; Robert G. Nelson; Jeffrey M. Curtis; Carol D. Moffett; Wen-Chi Hsueh; Robert L. Hanson展开收起
作者单位
1. Phoenix Epidemiology and Clinical Research Branch National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, USA; 2. Micronesian Institute for Disease Prevention and Research, Sinajana, Guam; 3. Pediatric Inherited Disease Research Center, Isfahan University of Medical Sciences, Isfahan, Iran; 4. South Texas Diabetes and Obesity Institute, University of Texas Rio Grande Valley, Brownsville, USA; 5. Research Division, Joslin Diabetes Center, Boston, USA; 6. Division of Metabolism, Endocrinology and Nutrition, University of Washington, Seattle, USA展开收起
196
天
SMN1 mutation spectrum and functional analysis of novel SMN1 variants in a Chinese spinal muscular atrophy cohort
作者
Gui-He Li; Li-Wen Wu; Jing Li; Sen-Wei Dong; Jing-Mei Hong; Ying-Xuan Xie; Yu-Hao Sun; Jin He; Ning Wang; Wan-Jin Chen; Hai-Zhu Chen展开收起
作者单位
1. Department of Neurology, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China; 2. Department of Neurology, Hunan Children’s Hospital, Changsha, China; 3. Department of Neurology, National Key Clinical Department and Key Discipline of Neurology, the First Affiliated Hospital of Sun Yat-sen University; Guangdong Provincial Key Laboratory of Diagnosis and Treatment of Major Neurological Diseases;, Guangzhou, China; 4. Department of Neurology, National Regional Medical Center, Binhai Campus of the First Affiliated Hospital, Fujian Medical University, Fuzhou, China; 5. Fujian Institute of Neurology, the First Affiliated Hospital, Fujian Medical University, Fuzhou, China展开收起
247
天
Identification and structural characterisation of a novel mutation in the CNKSR2 gene associated with Houge-Type X-Linked Intellectual Developmental Disorder
作者
Anil Kumar; Ajay Kumar; Chandraniv Dey; Arvinder Wander; Sudip Chakraborty; Anjana Munshi展开收起
作者单位
1. Department of Human Genetics and Molecular Medicine, Central University of Punjab, Bathinda, India; 2. Department of Computational Sciences, Central University of Punjab, Bathinda, India; 3. Department of Pediatrics, All India Institute of Medical Sciences, Bathinda, India展开收起
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