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Review Cycle Records

Molecular Genetics & Genomic Medicine

Wiley SCIE OA
2026新锐 4区2025中科院 4区2025 JCR Q3
206.1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

20 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

136 天

Clinical Utility of Trio Exome Sequencing in Rwandan Children With Autism Spectrum Disorder

作者Olivier Hakizimana; Janvier Hitayezu; Jeanne P. Uyisenga; Norbert Dukuze; Marie Viviane Akimana; Laurence Mizero; Claudine Bampire; Charles Mudenge; Xavier Kanyambari Butoto; Laura Helou; Benoit Charloteaux; Jean‐Hubert Caberg; Vinciane Dideberg; Leonor Palmeira; Abdullateef Isiaka Alagbonsi; Vincent Bours; Annette Uwineza

作者单位1. Postgraduate Studies, School of Health Sciences, College of Medicine and Health Sciences University of Rwanda Kigali Rwanda; 2. Department of Biochemistry, Molecular Biology and Genetics, School of Medicine and Pharmacy, College of Medicine and Health Sciences University of Rwanda Kigali Rwanda; 3. Center for Human Genetics, Centre Hospitalier Universitaire Sart‐Tilman University of Liege Liege Belgium; 4. Department of Pediatrics University Teaching Hospital of Kigali (CHUK) Kigali Rwanda; 5. Department of Biology, College of Science and Technology University of Rwanda Kigali Rwanda; 6. Department of Psychiatry Ndera Neuropsychiatric Teaching Hospital Kigali Rwanda; 7. Department of Psychiatry and Behavioral Sciences, School of Medicine and Pharmacy, College of Medicine and Health Sciences University of Rwanda Kigali Rwanda; 8. Department of Physiology, School of Medicine and Pharmacy, College of Medicine and Health Sciences University of Rwanda Kigali Rwanda

PDF源文件 DOI 网页
128 天

Novel TCOF1 Frameshift Variant and Phenotypic Heterogeneity in a Chinese Family With Treacher Collins Syndrome

作者Feiyang Fan; Ying Chen; Tianyu Zhang; Jing Ma

作者单位1. Department of Facial Plastic and Reconstructive Surgery, Eye & ENT Hospital, ENT Institute Fudan University Shanghai China; 2. NHC Key Laboratory of Hearing Medicine Fudan University Shanghai China; 3. Institute of Medical Genetics & Genomics Fudan University Shanghai China; 4. Shanghai Key Laboratory of Gene Editing and Cell Therapy for Rare Diseases Fudan University Shanghai China; 5. Surgery Laboratory, Institute of Medical Sciences General Hospital of Ningxia Medical University Yinchuan Ningxia China

PDF源文件 DOI 网页
264 天

Phenotypic and Genotypic Landscape of Sitosterolemia in China: Including a Rare Case With Nephronophthisis

作者Dan Ding; Hongmei Wu; Fei Zhao; Bixia Zheng; Qiuxia Chen

作者单位1. Department of Nephrology Children's Hospital of Nanjing Medical University Nanjing China; 2. Nanjing Key Laboratory of Pediatrics Children's Hospital of Nanjing Medical University Nanjing China

PDF源文件 DOI 网页
238 天

Compound Heterozygous PCDH15 Variants Associated With Cone‐Rod Dystrophy in a Chinese Pedigree

作者Lei Zhang; Qianfeng Wang; Haiyan Wang; Wei Jia; Bowen Zhang; Ru Wang; Wei Qiang; Shuwei Bai

作者单位1. Shaanxi Eye Hospital Xi'an People's Hospital (Xi'an Fourth Hospital), Affiliated People's Hospital of Northwest University Xi'an China; 2. Xi'an Key Laboratory of Digital Medical Technology of Ophthalmologic Imaging Xi'an China; 3. Medical College of Optometry and Ophthalmology Shandong University of Traditional Chinese Medicine Jinan Shandong China

PDF源文件 DOI 网页
188 天

Costello Syndrome Associated With Somatic Mosaicism of Rare p.Gly13Asp HRAS Variant: Expanding the Phenotypic Spectrum

作者Jovan Lalosevic; Katarina Djordjevic; Mirjana Gajic‐Veljic; Sonja Pavlovic; Vladimir Gasic; Marina Andjelkovic; Milos Nikolic

作者单位1. Clinic of Dermatology and Venereology University Clinical Center of Serbia Belgrade Serbia; 2. University of Belgrade, Faculty of Medicine Belgrade Serbia; 3. Institute of Molecular Genetics and Genetic Engineering (IMGGE) University of Belgrade Belgrade Serbia

PDF源文件 DOI 网页
188 天

Bioinformatics Analysis and Experimental Validation of Key Genes Associated With Hypoxia and Ischemia in Myocardial Infarction

作者Longsheng Zhang; Ning Liang

作者单位1. Ward 1, Department of Tuberculosis HIV/AIDS Clinical Treatment Center of Guangxi (Nanning) and The Fourth People's Hospital of Nanning Nanning Guangxi China; 2. The First Affiliated Hospital of Guangxi Medical University Nanning Guangxi China; 3. Ward 1, Department of Cardiovascular Medicine The Third People's Hospital of Nanning Nanning Guangxi China

PDF源文件 DOI 网页
212 天

Molecular Characterisation of Treacher Collins Syndrome in a South African Cohort: Novel Disease‐Causing Variants in TCOF1 and POLR1D

作者Patracia Nevondwe; Maria Mudau; Heather Seymour; Robyn Kerr; Zané Lombard; Amanda Krause; Nadia Carstens

作者单位1. Division of Human Genetics National Health Laboratory Service and School of Pathology, The University of the Witwatersrand Johannesburg South Africa; 2. Genomics Platform South African Medical Research Council Cape Town South Africa

PDF源文件 DOI 网页
164 天

Clinical Application of Long‐Read Sequencing for FMR1 Gene Mutation Detection in Populations From Shandong, China

作者Yan Li; Fei Hou; Shan Shan; Yingying Peng; Hua Jin

作者单位1. Department of Prenatal Diagnosis Jinan Maternity and Child Care Hospital Affiliated to Shandong First Medical University (Jinan Maternity and Child Care Hospital) Jinan China; 2. Medical Research Center Jinan Maternity and Child Care Hospital Affiliated to Shandong First Medical University (Jinan Maternity and Child Care Hospital) Jinan China

PDF源文件 DOI 网页
607 天

Analysis of Genetic Factors in a Family With Short Stature

作者Siqing Zhang; Tian Zuo; Youping Deng; Dongchi Zhao; Lihong Liao

作者单位1. Department of Pediatrics Zhongnan Hospital of Wuhan University Wuhan Hubei China; 2. Hubei Provincial Key Laboratory of Pediatric Genetic Metabolic and Endocrine Rare Diseases Wuhan China

PDF源文件 DOI 网页
133 天

Genomic Profiling of Anophthalmia/Microphthalmia‐Associated CNVs Reveals Complex Genotype–Phenotype Correlations and Incomplete Penetrance

作者Dong Wu; Mengting Zhang; Qian Zhang; Fengyang Wang; Qiaofang Hou; Hongyan Liu; Shixiu Liao; Hai Xiao

作者单位1. Medical Genetics Institute of Henan Provincial People's Hospital Zhengzhou China; 2. NHC Key Laboratory of Birth Defects Prevention, Institute of Reproductive Health, Henan Academy of Innovations in Medical Science Zhengzhou China; 3. Department of Medical Genetics The Affiliated People's Hospital, Zhengzhou University Zhengzhou China

PDF源文件 DOI 网页

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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?

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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96.4 天

中位数77 天

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