CrushSCI.com
提供学术论文选刊润色服务
EUROPEAN JOURNAL OF HUMAN GENETICS 期刊封面 生物学
返回期刊列表

Review Cycle Records

EUROPEAN JOURNAL OF HUMAN GENETICS

Springer SCIE 非OA
2026新锐 2区2025中科院 2区2025 JCR Q1
179.1平均天数
158.5中位天数
14最短天数
315最长天数
2212025发文量

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

14 天

Clinical implementation of polygenic risk scores—updates on ancestry-adjusted PRS and their use in practice

作者Eleanor Roberts; Nicola Flaum; D. Gareth Evans

作者单位1. Division of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK; 2. Manchester Breast Centre, The Christie, Manchester, UK; 3. Manchester Centre for Genomic Medicine, St Mary’s Hospital, Manchester Academic Health Centre (MAHSC), Division of Evolution, Infection and Genomic Sciences, University of Manchester, Manchester, UK; 4. Prevent Breast Cancer Prevention Centre, University Hospital of South Manchester NHS Trust, Manchester, UK; 5. Manchester Centre for Genomic Medicine, St Mary’s Hospital, Central Manchester University Hospitals NHS Foundation Trust, Manchester, UK

PDF源文件 DOI 网页
99 天

Re: Clinical implementation of polygenic risk scores — equity metrics are needed before clinical translation

作者Laura Piñero-Roig

作者单位1. MD Student, Faculty of Medicine, Universitat de Barcelona, Barcelona, Spain

PDF源文件 DOI 网页
257 天

Bridging the gap: integrating hereditary cancer into precision oncology

作者Alejandra Rezqallah; Mara Cruellas; Judith Balmaña

作者单位1. Hereditary Cancer Genetics Group, Medical Oncology Department, University Hospital Vall d’Hebron and Vall d’Hebron Institute of Oncology, Barcelona, Spain; 2. Hereditary Cancer Unit, Medical Oncology Department, University Hospital Lozano Blesa / Instituto de Investigación Sanitaria de Aragón, Zaragoza, Spain

PDF源文件 DOI 网页
189 天

CMIP as a novel candidate gene for neurodevelopmental and neuropsychiatric disorders

作者Matthias De Wachter; Mathijs B. van der Lei; Amber Decleve; Kevin De Man; Ellen Elinck; An-Sofie Schoonjans; Evan Gouy; Louis Januel; Pauline Monin; Audrey Labalme; Amelle Shillington; Himanshu Goel; Juliet P. Taylor; Katherine Neas; David A. Koolen; Francois Lecoquierre; Alice Goldenberg; Theresa Brunet; Melanie Brugger; Minjie Luo; Magdalena Krygier; Maria Mazurkiewicz-Bełdzińska; Manon Degoutin; Claire Beneteau; Cyril Goizet; David D. Weaver; Emily G. Farrow; Angela Lee; Randi N. Gadea; Berten Ceulemans; Peter A. M. de Witte; Daniëlle Copmans; Anna C. Jansen; R. Frank Kooy

作者单位1. Department of Pediatric Neurology, Antwerp University Hospital, University of Antwerp, Edegem, Belgium; 2. Department of Medical Genetics, University of Antwerp, Antwerp, Belgium; 3. Laboratory for Molecular Biodiscovery, Department of Pharmaceutical and Pharmacological Sciences, KU Leuven, Leuven, Belgium; 4. Leuven Childhood Epilepsy Center, Leuven Brain Institute, KU Leuven, UZ Leuven, Leuven, Belgium; 5. Research on Healthcare Performance Reshape, INSERM U1290, Université Claude Bernard Lyon 1, Lyon, France; 6. Hospices Civils de Lyon, Service de Génétique, Lyon, France; 7. Cincinnati Children’s Medical Center, Cincinnati, USA; 8. School of Medicine and Public Health, University of Newcastle, Callaghan, Australia; 9. Genetic Health Service NZ (North), Auckland, New Zealand; 10. Genetic Health Service NZ, Wellington South, New Zealand; 11. Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, The Netherlands, Donders Institute for Brain, Cognition and Behaviour, Nijmegen, The Netherlands; 12. Hospitalo-Universitaire, CHU de Rouen, Rouen, France; 13. Institute of Human Genetics, School of Medicine and Health, Technical University of Munich, Munich, Germany; 14. Division of Genomic Diagnostics, Department of Pathology and Laboratory Medicine, Children’s Hospital of Philadelphia, Philadelphia, USA; 15. Department of Pathology and Laboratory Medicine, The Perelman School of Medicine at the University of Pennsylvania, Philadelphia, USA; 16. Department of Developmental Neurology, Medical University of Gdańsk, Gdańsk, Poland; 17. CHU Bordeaux, Service de Génétique Médicale, Bordeaux, France; 18. Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, USA; 19. Clinical Genetics and Genomics Laboratory, Pathology and Laboratory Medicine, Children’s Mercy Kansas City, Kansas City, USA; 20. Department of Translational Neurosciences, University of Antwerp, Antwerp, Belgium

PDF源文件 DOI 网页
118 天

Parent and professional experiences of a clinical trial of prenatal and postnatal stem cell therapy for severe osteogenesis imperfecta

作者Bikiran Behera; Charlotta Ingvoldstad Malmgren; Eva Åström; Lyn S. Chitty; Belinda Crowe; Anna L. David; Catherine DeVile; Oliver Semler; Magnus Westgren; Cecilia Götherström; Melissa Hill

作者单位1. BSc Paediatrics and Child Health, UCL Great Ormond Street Institute of Child Health, London, UK; 2. Center for Research Ethics and Bioethics, Uppsala University, Uppsala, Sweden; 3. Center for Fetal Medicine, Karolinska University Hospital, Stockholm, Sweden; 4. Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden; 5. Department of Women’s and Children’s Health, Karolinska Institutet, Stockholm, Sweden; 6. Astrid Lindgren Children’s Hospital, Karolinska University Hospital, Stockholm, Sweden; 7. North Thames Genomic Laboratory Hub, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK; 8. Genetics and Genomic Medicine, UCL Great Ormond Street Institute of Child Health, London, UK; 9. Department of Neurosciences, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK; 10. Elizabeth Garrett Anderson Institute for Women’s Health, University College London, London, UK; 11. NIHR University College London Hospitals Biomedical Research Centre, London, UK; 12. Department of Pediatrics, University Hospital Cologne, Koln, Germany; 13. Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden; 14. Department of Gynecology and Reproductive Medicine, Karolinska University Hospital, Stockholm, Sweden

PDF源文件 DOI 网页
127 天

Systematic analysis of homozygous autosomal copy number losses in exomes improves diagnostic yield and uncovers ultra-rare recessive disorders

作者Ankur Chaurasia; Anju Shukla; Shruti Pande; Greeshma Purushothama; Akhil Kanathay Ashokan; Purvi Majethia; Namanpreet Kaur; Priyanka Upadhyai; Neha Quadri; Gandham SriLakshmi Bhavani; Dhanya Lakshmi Narayanan; Shalini S. Nayak; Sheela Nampoothiri; Ataf H. Sabir; Alaa A. Mohammed; Sophie Shaw; Verity L. Hartill; Christopher M. Watson; Colin A. Johnson; Afrah Alshammari; Andrew E. Fry; James A. Poulter; William G. Newman; Paul R. Kasher; Siddharth Banka; Katta M. Girisha

作者单位1. Department of Medical Genetics, Kasturba Medical College, Manipal, Manipal Academy of Higher Education, Manipal, India; 2. Division of Evolution, Infection and Genomics, School of Biological Sciences, Faculty of Biology, Medicine and Health, The University of Manchester, Manchester, UK; 3. Department of Paediatric Genetics, Amrita Institute of Medical Sciences & Research Centre, Cochin, India; 4. West Midlands Clinical Genetics Unit, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK; 5. Department of Cancer and Genomic Sciences, College of Medicine and Health, University of Birmingham, Birmingham, UK; 6. West Midlands Genomics Laboratory, Birmingham Women’s and Children’s NHS Foundation Trust, Birmingham, UK; 7. All Wales Medical Genomics Service, Wales Genomic Health Centre, Cardiff, UK; 8. Division of Molecular Medicine, Leeds Institute of Medical Research, University of Leeds, Leeds, UK; 9. Leeds Clinical Genomics Service, Chapel Allerton Hospital, Leeds, UK; 10. Yorkshire and North East Genomic Laboratory Hub, Central Lab, St. James’s University Hospital, Leeds, UK; 11. Department of Biology, College of Science, University of Hafr Al-Batin, Hafr Al-Batin, Saudi Arabia; 12. Division of Cancer and Genetics, Cardiff University, Cardiff, UK; 13. Manchester Centre for Genomic Medicine, St Mary’s Hospital, Health Innovation Manchester, Manchester University NHS Foundation Trust, Manchester, UK; 14. Division of Neuroscience, School of Biological Sciences, Faculty of Biology, Medicine and Health, Manchester Academic Health Science Centre, The University of Manchester, Manchester, UK; 15. Geoffrey Jefferson Brain Research Centre, Manchester Academic Health Science Centre, Northern Care Alliance NHS Foundation Trust and University of Manchester, Manchester, UK; 16. Department of Genetics, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Oman

PDF源文件 DOI 网页
128 天

Decoding splicing variants in high-throughput sequencing: a functional validation approach integrating deep learning tools

作者Clément Hersent; Lise Larrieu; Patricia Fergelot; Julie Miro; Mehdi Benkirane; Chloé Angelini; Francis Ramond; Cecilia Marelli; Isabelle Sabatier; Gaëtan Lesca; Christel Vaché; Mireille Cossée; Anne Bergougnoux; Klaus Dieterich; Christine Tranchant; Isabelle Marey; Anna Castrioto; Christel Thauvin-Robinet; Lydia Abou Haidar; François Rivier; Sylvie Tuffery-Giraud; Michel Koenig

作者单位1. Laboratoire de Génétique Moléculaire de Maladies Rares, Site Unique de Biologie, CHU de Montpellier, Montpellier, France; 2. PhyMedExp, Univ Montpellier, CNRS, INSERM, Montpellier, France; 3. Neurogenetics Reference Centre, Department of Medical Genetics, Bordeaux University Hospital, Bordeaux, France; 4. Department of Medical Genetics, Laboratory of Genomics Medicine, Sorbonne University, Hôpital de la Pitié-Salpêtrière, Assistance Publique- Hôpitaux de Paris (AP-HP), Paris, France; 5. Department of Medical Genetics, CHU of Saint-Etienne, Saint-Etienne, France; 6. MMDN, Université de Montpellier, EPHE, INSERM, Montpellier, France; 7. Expert Center for Neurogenetic Diseases, CHU de Montpellier, Montpellier, France; 8. Department of Pediatric Neurology, University Hospitals of Lyon, Lyon, France; 9. Department of Medical Genetics, University Hospitals of Lyon and Université Claude Bernard Lyon1, Lyon, France; 10. Department of Medical Genetics, CHU de Grenoble, Grenoble, Université Grenoble Alpes, INSERM U 1209, CNRS UMR 5309, Institut for Advanced Biosciences, Grenoble, France; 11. Department of Neurology, Hôpitaux Universitaires de Strasbourg, Strasbourg; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM-U964/CNRS-UMR7104/Université de Strasbourg, Illkirch, France; 12. Grenoble Institute of Neurosciences, Grenoble Alpes University Hospital Center, Inserm, U1216, Grenoble Alpes University, Grenoble, France; 13. Université de Bourgogne Europe, CHU Dijon Bourgogne, Centre de Génétique, Centre de Référence Maladies Rares Neurogène, INSERM, CTM UMR 1231, GAD, Dijon, France; 14. Department of Pediatric Neurology and Reference Center for Neuromuscular Diseases AOC, Gui de Chauliac Hospital, CHU de Montpellier, Montpellier, France

PDF源文件 DOI 网页
301 天

Hemizygous loss-of-function variants of EIF1AX are associated with a syndromic neurodevelopmental disorder

作者Kazuyuki Komatsu; Atsushi Sugie; Yohei Nitta; Jiro Osaka; Ummul Halilunnisa Mansoor Hussain; Mitsuru Kubota; Nobuyuki Shimozawa; Melissa T. Carter; Petra J. G. Zwijnenburg; Quinten Waisfisz; Felix Boschann; Denise Horn; Mitsuko Nakashima; Hirotomo Saitsu

作者单位1. Department of Biochemistry, Hamamatsu University School of Medicine, Hamamatsu, Japan; 2. Brain Research Institute, Niigata University, Niigata, Japan; 3. Department of General Pediatrics and Interdisciplinary Medicine, National Center for Child Health and Development, Tokyo, Japan; 4. Division of Genomics Research, Life Science Research Center, Gifu University, Gifu, Japan; 5. Department of Genetics, Children’s Hospital of Eastern Ontario, University of Ottawa, Ottawa, Canada; 6. Department of Clinical Genetics, Emma Children’s Hospital, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands; 7. Institute of Medical Genetics and Human Genetics, Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany; 8. Berlin Institute of Health at Charité – Universitätsmedizin Berlin, Berlin, Germany; 9. Berlin Institute of Health at Charité - Universitätsmedizin Berlin, BIH Biomedical Innovation Academy, BIH Charité Clinician Scientist Program, Berlin, Germany

PDF源文件 DOI 网页
243 天

Identifying genetic causes and establishing a diagnostic approach for WES-negative pediatric population with neurodevelopmental disorder

作者Yeseul Kim; Joowon Jang; Kyeong Seon Ryu; Jong-Hee Chae; Jung Min Ko; Man Jin Kim; Seungbok Lee; Jangsup Moon; Jin Sook Lee; Hoyeon Lee; Sung Im Cho; Seung Won Chae; Hansol Lim; Hara Lim; Hobin Sung; Seonhoo Youn; Hyesu Lee; Jee-Soo Lee; Moon-Woo Seong

作者单位1. Department of Laboratory Medicine, Seoul National University Hospital, Seoul National University College of Medicine, Seoul, Korea; 2. Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea; 3. Department of Pediatrics, Seoul National University Children’s Hospital, Seoul, Korea; 4. Department of Neurology, Seoul National University Hospital, Seoul, Korea; 5. Cancer Research Institute, Seoul National University College of Medicine, Seoul, Korea

PDF源文件 DOI 网页
315 天

Transcriptome-wide association studies implicate RCC1 and PHACTR4 in prostate cancer survival

作者Weijia Fu; Joseph H. Rothstein; Olle Melander; Hans Lilja; Weiva Sieh; Xiaoyu Song; Robert J. Klein

作者单位1. Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, USA; 2. Department of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, USA; 3. Department of Epidemiology, MD Anderson Cancer Center, Houston, USA; 4. Department of Clinical Sciences, Lund University, Malmö, Sweden; 5. Department of Internal Medicine, Skåne University Hospital, Malmö, Sweden; 6. Departments of Pathology and Laboratory Medicine, Surgery (Urology Service), and Medicine (GU-Oncology Service), Memorial Sloan Kettering Cancer Center, New York, USA; 7. Department of Translational Medicine, Lund University, Malmö, Sweden; 8. Centre for Biomedical Data Science, Duke-NUS Medical School, National University of, Singapore, Singapore

PDF源文件 DOI 网页

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。

CrushSCI 在线

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96.4 天

中位数77 天

Contact CrushSCI

联系 CrushSCI

扫码添加微信,或留下手机号/微信号,我们将与你确认稿件阶段、编辑需求和投稿计划。

当前选择:论文编辑服务

也可以预留联系方式

手机号和微信号至少填写一项,仅用于本次咨询联系,不会公开。