Paper Review Records
All Paper Review Records
10 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.
88
days
Spectrum of inherited metabolic disorders diagnosed through newborn screening and symptomatic referrals in Eastern Türkiye
AuthorsSezai Arslan; Filiz Ekinci Uğan; Oğuzhan Yaralı; Hasan Kahveci
AffiliationsDepartment of Inherited Metabolic Diseases, Erzurum City Hospital, Erzurum, Turkey; Department of Nutrition and Dietetics, Erzurum City Hospital, Erzurum, Turkey; Department of Medical Genetics, Erzurum City Hospital, Erzurum, Turkey; Department of Neonatology, University of Health Sciences Erzurum Medical Faculty, Erzurum, Turkey
129
days
Clinical practice considerations for restarting pegvaliase in adults with phenylketonuria
AuthorsMarkey McNutt; Katherine J. Anderson; Ashley Andrews; Erin Cooney; Brittany M. Murray; Michelle Tharp; Erika Vucko; Leah Wessenberg; Kassi Wilson; Derek Wong; Joyanna Hansen; Sarah Rose; Bridget Wardley; Janet A. Thomas
AffiliationsUT Southwestern Medical Center, Dallas, TX, USA; University of Vermont Health, Burlington, VT, USA; University of Utah, Salt Lake City, UT, USA; University of Texas Medical Branch, Galveston, TX, USA; Boston Children's Hospital, Boston, MA, USA; University of Mississippi Medical Center, Jackson, MS, USA; Ann & Robert H. Lurie Children's Hospital, Chicago, IL, USA; Oregon Health and Science University, Portland, OR, USA; University of South Florida, Tampa, FL, USA; David Geffen School of Medicine at UCLA, Los Angeles, CA, USA; BioMarin Pharmaceutical Inc., Novato, CA, USA; University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, CO, USA
160
days
Severe mitochondrial cardiomyopathy with m.3303C > T variant in the mitochondrial tRNALeu(UUR) gene: A study of large family analysis
AuthorsShuichi Yatsuga
AffiliationsDepartment of Pediatrics, Fukuoka University, Fukuoka, Fukuoka, Japan; Department of Medical Genetics, Hakodate Goryoukaku Hospital, Hakodate, Hokkaido, Japan
76
days
DNAJC12 p.Asp44Gly associated with mild hyperphenylalaninemia and migraine-like headaches: Structural and deep learning analyses
AuthorsJie Zhang; Binghe Xiao; Zhiliang Wang; Xiang Li
AffiliationsDepartment of Rehabilitation, Huashan Hospital of Fudan University, Shanghai, China; Department of Ophthalmology, Huashan Hospital of Fudan University, Shanghai, China; Department of Neurology, Huashan Hospital of Fudan University, Shanghai, China
42
days
A blended phenotype of primary immunodeficiency and Temtamy syndrome: Dual homozygosity for STK4 and C12orf57 gene variants in a Tunisian infant
AuthorsM. Hsairi; A. Kammoun; H. Fendri; M. Guirat; H. Kammoun; Z. Mnif; L. Gargouri
AffiliationsDepartment of Pediatrics B, Hedi Chaker University Hospital, Tunisia; Department of Radiology, Hedi Chaker University Hospital, Tunisia; Department of Human Genetics, Hedi Chaker University Hospital, Tunisia; Faculty of Medicine, University of Sfax, Sfax 3000, Tunisia
26
days
Molecular and clinical heterogeneity in an Iranian case series of Joubert syndrome
AuthorsSheyda Khalilian; Mohadeseh Fathi; Zahra Farbood; Fatemeh Dehghanian; Marjan Masoudi; Soudeh Ghafouri-Fard; Seyed Alireza Dastgheib; Mohammad Miryounesi
AffiliationsDepartment of Medical Genetics, Shahid Beheshti University of Medical Sciences, Tehran, Iran; Department of Medical Genetics, Shiraz University of Medical Sciences, Shiraz, Iran
179
days
Plasma KL-6 reflects pulmonary severity and longitudinal response to enzyme replacement therapy in acid sphingomyelinase deficiency type B
AuthorsKarla Cifuentes-Uribe; Nathalie Guffon; Lucie Boulière; Ségolène Turquier; Cécile Acquaviva-Bourdain; Roseline Froissart; Magali Pettazzoni
AffiliationsNational Reference Centre for Hereditary Metabolic Diseases, Hospices Civils de Lyon, France; Department of Biochemistry and Molecular Biology, Lyon University Hospital, France; Department of Pulmonary Function Testing, Louis Pradel Hospital, Hospices Civils de Lyon, France
60
days
Mucopolysaccharidosis type IIIA and IIIC phenotypic progression: A case series
AuthorsPaola Naal-Chan; Ermilo Echeverria-Ortegon; Jary-Davis Couoh-Castañeda; Jose-Luis Millet-Herrera; Fabiola-Concepcion Solis-Baeza; Myrna-Edith Perez-Garcia; Jorge-Santiago Rivera-Lavalle; Addy-Manuela Castillo-Espinola; Olga-Berenice Reyes-Flores; Felix-Julian Campos-Garcia
AffiliationsDepartment of Pediatrics, General Hospital “Dr. Agustin O'Horan”, Servicios de Salud del Instituto Mexicano del Seguro Social para el Bienestar (IMSS-BIENESTAR), Yucatan, Mexico; Center for Evidence-Based Health Research, Marista University, Yucatan, Mexico; Pediatric Cardiology, Unidad Medica de Alta Especialidad, Instituto Mexicano del Seguro Social, Yucatan, Mexico; Department of Genetics, General Hospital “Dr. Agustin O'Horan”, Servicios de Salud del Instituto Mexicano del Seguro Social para el Bienestar (IMSS-BIENESTAR), Yucatan, Mexico
161
days
Proteomic alterations in patient bone-derived stromal cells and their secretomes in osteogenesis imperfecta
AuthorsKishore Garapati; Dong-Gi Mun; Rex Devasahayam Arokia Balaya; Mayank Saraswat; Santosh Renuse; Gregory Trahan; Richard K. Kandasamy; David R. Deyle; Akhilesh Pandey
AffiliationsManipal Academy of Higher Education (MAHE), Manipal, Karnataka, India; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA; Institute of Bioinformatics, International Technology Park, Bangalore, Karnataka, India; Department of Clinical Genomics, Mayo Clinic, Rochester, MN, USA; Department of Quantitative Health Sciences, Mayo Clinic, Rochester, MN, USA; Center for Individualized Medicine, Mayo Clinic, Rochester, MN, USA
61
days
Diagnostic yield and variant spectrum of whole-exome sequencing in Iranian probands with congenital and early-onset ocular disorders
AuthorsAli Asadi; Seyed Ataollah Sadat Shandiz; Amirhossein Ebrahimi; Zahra Sadat Hosseini; Niyousha Shirsalimi; Hossein Neamatzadeh; Ahmad Ebrahimi
AffiliationsDepartment of Biology, CT.C., Islamic Azad University, Tehran, Iran; Department of Computer Engineering, Shiraz University, Shiraz, Iran; Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran; Department of Art, Faculty of Shariati, National University of Skills, Tehran, Iran; Hematology and Oncology Research Center, Non-Communicable Diseases Research Institute, Shahid Sadoughi University of Medical Science, Yazd, Iran; Genia Medical Genetics Center, Tehran, Iran
Expert Matching · Case Demo
Turn Your Submission Goalsinto a Verifiable Journal Plan
Share your field, deadline, and author profile. CrushSCI uses real review records to suggest a title direction, shortlist journals, and estimate timelines.
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 review96.4 days
Median77 days