Paper Review Records
All Paper Review Records
25 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.
93
days
Research Progress on the Pathogenesis and Diagnostic and Therapeutic Potential of Ciliopathies Regulated by IFT172
Authors
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 ZhangShow moreShow less
Affiliations
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 ChinaShow moreShow less
30
days
Neurodevelopmental Phenotypes and Brain Anomalies in Individuals With Heterozygous SEMA6A Variants
Authors
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. ScottShow moreShow less
Affiliations
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 ChileShow moreShow less
28
days
USP34 Haploinsufficiency as a Cause of Neurodevelopmental Phenotypes
Authors
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. WebbShow moreShow less
Affiliations
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 NetherlandsShow moreShow less
88
days
An Ancient Founder GDF2 Variant Potentially Causes Semi‐Dominant Non‐Syndromic Pulmonary Arterial Hypertension
Authors
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. AlkurayaShow moreShow less
Affiliations
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 ArabiaShow moreShow less
167
days
The WHO Classification of Genetic Tumour Syndromes: Considerations for Genetics
Authors
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 LokuhettyShow moreShow less
Affiliations
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 CanadaShow moreShow less
54
days
Clinical Variability Including Non‐Dilated Left Ventricular and Dilated Cardiomyopathy in a Pedigree With an Intragenic CTNNA3 Copy Number Variation
Authors
Carmela Fusco; Sandra Mastroianno; Silvia Morlino; Riccardo Pracella; Federica Russo; Ester Maria Lucia Bevere; Orazio Palumbo; Giuseppe Di Stolfo; Marco CastoriShow moreShow less
Affiliations
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 ItalyShow moreShow less
Expert Matching · Case Demo
Turn Your Submission Goalsinto a Verifiable Journal Plan
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Client
I work in environmental engineering and need an SCI paper published within three months. I have no grant funding or prominent co-author. Which journals could I target?
CrushSCI
Yes. We will first screen for feasibility against the 90-day deadline, then identify comparable papers without grant support or prominent co-authors. The final shortlist will prioritize research quality and journal scope.
- Suggested title
- Machine Learning and Life-Cycle Assessment for Predicting and Optimizing Carbon Emissions in Urban Wastewater Treatment
- Database shortlist
- Environmental Technology & Innovation
SampleLatest 5 valid paper samples from 2026
Average review62 days
Median65 days