Paper Review Records
All Paper Review Records
15 valid samples · Newest publication first
Review days = acceptance date − received date. PDF, DOI, and publisher-page sources are retained.
140
days
Genotype-phenotype relationships in phenylalanine hydroxylase deficiency: Functional annotation-enhanced analysis of 23,427 individuals
Authors
Nenad Blau; Nastassja HimmelreichShow moreShow less
Affiliations
Division of Metabolism, University Children’s Hospital Zürich, Zürich, Switzerland; Dietmar-Hopp Metabolic Center and Centre for Pediatrics and Adolescent Medicine, Department I, University Children’s Hospital, Heidelberg, BW, Germany; Zentrum für Humangenetik Tübingen, Tübingen, BW, GermanyShow moreShow less
336
days
Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infants
Authors
David E. Godler; Ling Ling; Dinusha Gamage; Minh Bui; Michael J. Field; David J. AmorShow moreShow less
Affiliations
Department of Paediatrics, University of Melbourne, Parkville, VIC, Australia; Murdoch Children’s Research Institute, Royal Children’s Hospital, Parkville, VIC, Australia; Department of Pediatrics, Monash University, Clayton, VIC, Australia; E.D.G. Innovations and Consulting, St Kilda, VIC, Australia; Centre for Epidemiology & Biostatistics, Melbourne School of Population & Global Health, University of Melbourne, Carlton, VIC, Australia; Genetics of Learning Disability Service, Hunter Genetics, Waratah, NSW, AustraliaShow moreShow less
324
days
Evaluation of electrical impedance myography as a noninvasive musculoskeletal biomarker in infantile- and late-onset Pompe disease
Authors
Raquel van Gool; Nehal Shah; Amanda Cao; Lise Vrolix; Buket Sonbas Cobb; Benjamin Goodlett; Georgina Johnson; Hanne van der Heijden; Merve Koç Yekedüz; Carlos Camelo; Julie Shulman; Adam P. Vogel; M. Valerie Stein; Hawa Sakho; David Kronn; Nick Todd; Olaf Bodamer; Seward Rutkove; Walla Al-Hertani; Jaymin UpadhyayShow moreShow less
Affiliations
Department of Anesthesiology, Critical Care and Pain Medicine, Boston Children’s Hospital, Harvard Medical School, Boston, MA; Department of Neurology, Mental Health and Neuroscience Research Institute, Maastricht University, Maastricht, Limburg, The Netherlands; Department of Radiology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA; Department of Neurology, Beth Israel Deaconess Medical Center, Boston, MA; Department of Electrical and Electronic Engineering, Harran University, Şanlıurfa, Turkey; Division of Genetics and Genomics, Boston Children’s Hospital, Harvard Medical School, Boston, MA; Department of Audiology and Speech Pathology, The University of Melbourne, Parkville, Victoria, Australia; Department of Pediatric Metabolism, Ankara University, Faculty of Medicine, Ankara, Turkey; Department of Physical and Occupational Therapy, Boston Children’s Hospital, Boston, MA; Redenlab Pty Ltd, Melbourne, Victoria, Australia; Department of Pathology and Pediatrics, New York Medical College, Valhalla, NY; Division of Metabolic Disorders, Children's Hospital of Orange County, Rady Children's Health, Orange, CAShow moreShow less
181
days
Delineating the clinical and molecular spectrum of the neurodevelopmental disorder associated with SET
Authors
Yuwei Shi; Ananilia Silva; Christophe Debuy; Sourav Ghosh; Haley McConkey; Rachel Schot; Ruizhi Deng; Anita Nikoncuk; Marjon van Slegtenhorst; Lies H. Hoefsloot; Tjakko J. van Ham; Brittany N. Simpson; Dana Miller; Nishitha R. Pillai; Muriel Holder-Espinasse; Berta Almoguera; Fiona Blanco-Kelly; Virginia Clowes; Grace Yoon; Berrin Monteleone; Jaime Vasquez; Rubén Pérez de la Fuente; Sara Bellido-Cuéllar; Ursino Barrios-Machain; Yolanda Moreno-Sáez; Katharina Steindl; Anais Begemann; Anita Rauch; Tiffany Busa; Svetlana Gorokhova; Shenela Lakhani; Zachary Grinspan; Aurore Garde; Frederic Tran Mau Them; Ange-Line Bruel; Julian Delanne; Hana Safraou; Estelle Colin; Aditi Shah Parikh; Anne Slavotinek; Patrick Devine; Amelle Shillington; Arthur Sorlin; Didier Menzies; Lakshmi Mehta; Charlotte Close; Caleb Heid; Syed Ajaz Ahmed; Adriana Gomes; Lynne M. Bird; Erfan Aref-Eshghi; Kelly J. Cardona-Londoño; Stefan T. Arold; Jing-Mei Li; Tzung-Chien Hsieh; Tjitske Kleefstra; Kristina Lanko; Bekim Sadikovic; Tahsin Stefan BarakatShow moreShow less
Affiliations
Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands; Department of Pathology and Laboratory Medicine, Western University, London, ON, Canada; Verspeeten Clinical Genome Centre, London Health Sciences Centre, London, ON, Canada; Center for Experimental Neurotherapeutics, St. Jude Children’s Research Hospital, Department of Pediatrics, University of Tennessee Health Science Center, Le Bonheur Children’s Hospital, Memphis, TN; Division of Genetics and Metabolism, Department of Pediatrics, University of Minnesota, Minneapolis, MN; Department of Clinical Genetics, Guy's Hospital London, London, United Kingdom; Department of Genetics and Genomics. Fundación Jiménez Díaz University Hospital & Health Research Institute-Fundación Jiménez Díaz University Hospital, Universidad Autónoma de Madrid (IIS-FJD, UAM), Madrid, Spain; CIBERER (Biomedical Research Network Center for Rare Diseases), Carlos III Health Institute (ISCIII), Madrid, Spain; North West Thames Regional Genetics Service, London North West Healthcare NHS Trust, London, United Kingdom; Section of Genetics and Genomics, Department of Metabolism Digestion and Reproduction, Faculty of Medicine, Imperial College, London, United Kingdom; Division of Clinical and Metabolic Genetics, Department of Pediatrics, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada; Division of Clinical Genetics, NYU Grossman Long Island School of Medicine, Garden City, New York, NY; Department of Genetics, 12 de Octubre University Hospital, Madrid, Spain; Group of Rare, Mitochondrial and Neuromuscular Diseases (RMND), 12 de Octubre University Hospital Research Institute (i+12), Madrid, Spain; UDISGEN (Dysmorphology and Genetics Unit), 12 de Octubre University Hospital, Madrid, Spain; Epilepsy-vEEG Unit, Neurology Department, 12 Octubre University Hospital, Madrid, Spain; Department of Pediatric Endocrinology, 12 Octubre University Hospital, Madrid, Spain; University of Zurich, Institute of Medical Genetics, Wagistrasse 12, Schlieren, Switzerland; University Children’s Hospital Zurich, Zurich, Switzerland; Medical Genetics Department, Timone Children’s Hospital, APHM, Marseille, France; Aix Marseille Univ, INSERM, Marseille Medical Genetics, U1251, Marseille, France; Center for Neurogenetics, Weill Cornell Medicine, New York, NY; Department of Pediatrics, Weill Cornell Medicine, New York, NY; Centre de Génétique, CRMRs "Anomalies du Développement et syndromes malformatifs" et "Déficiences Intellectuelles de causes rares", "GenoPsy" et "Neurogène", FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France; Université Bourgogne Europe, CHU Dijon Bourgogne, Laboratoire de Génomique Médicale, Centre Neomics, FHU-TRANSLAD, Centre de recherche Translationnelle en Médecine moléculaire – Inserm UMR1231 équipe GAD, Dijon, France; Center for Human Genetics, University Hospitals Cleveland Medical Center and Case Western Reserve University School of Medicine, Cleveland, OH; Department of Pediatrics, University of California San Francisco, San Francisco, CA; Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio; Clinical Genetics unit, National Center of Genetics, Laboratoire national de santé, Dudelange, Luxembourg; Foetopathologie, National Center of Pathologie, Laboratoire national de santé, Dudelange, Luxembourg; Division of Clinical Genetics, Department of Pediatrics, Columbia University Irving Medical Center, New York, NY; Department of Pathology, University of Missouri, Columbia, MO; Department of Clinical Genetics, Southern California Kaiser Permanente, Los Angeles, CA; Department of Pediatrics, University of California San Diego, San Diego, CA; Division of Genetics/Dysmorphology, Rady Children’s Hospital San Diego, San Diego, CA; GeneDx, LLC, Gaithersburg, MD; Bioscience Program, Biological and Environmental Science and Engineering Division, Computational Bioscience Research Center, King Abdullah University of Science and Technology (KAUST), Thuwal, Saudi Arabia; Centre de Biologie Structurale, CNRS, INSERM, Université de Montpellier, Montpellier, France; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, GermanyShow moreShow less
252
days
Decision-making criteria in polygenic embryo screening: A survey of reproductive medicine physicians
Authors
Rémy A. Furrer; Aayushi Gandhi; Dorit Barlevy; Shai Carmi; Todd Lencz; Stacey Pereira; Gabriel Lázaro-MuñozShow moreShow less
Affiliations
Department of Neurosurgery, Massachusetts General Hospital, Boston, MA; Harvard Medical School, Boston, MA; Stanford University, Stanford, CA; Center for Medical Ethics and Health Policy, Baylor College of Medicine, Houston, TX; Braun School of Public Health and Community Medicine, The Hebrew University of Jerusalem, Jerusalem, Israel; Institute of Behavioral Science, The Feinstein Institutes for Medical Research, Northwell Health, Manhasset, NY; Departments of Psychiatry and Molecular Medicine, Zucker School of Medicine at Hofstra/Northwell, Hempstead, NY; Division of Research, Department of Psychiatry, The Zucker Hillside Hospital Division of Northwell Health, Glen Oaks, NY; Department of Psychiatry, Massachusetts General Hospital, Boston, MAShow moreShow less
211
days
Clinical utility of exome sequencing: Post-exome testing decision changes in the management of children with suspected rare genetic disease
Authors
Toni Tagimacruz; Trevor Adam Seeger; Koen Degeling; Katharine Fooks; Viji Venkataramanan; Francois P. Bernier; Kym M. Boycott; Roberto Mendoza-Londono; Taila Hartley; Robin Z. Hayeems; Deborah A. MarshallShow moreShow less
Affiliations
Department of Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, AB, Canada; Cancer Health Services Research, Centre for Health Policy & Centre for Cancer Research, Faculty of Medicine, Dentistry and Health Sciences, The University of Melbourne, Melbourne, Australia; Child Health Evaluative Sciences, The Hospital for Sick Children, Toronto, ON, Canada; Department of Medical Genetics, University of Calgary, AB, Canada; One Child Every Child, University of Calgary, Calgary, AB, Canada; Alberta Children’s Hospital Research Institute, University of Calgary, Calgary, AB, Canada; Children’s Hospital of Eastern Ontario Research Institute, University of Ottawa Ottawa, ON, Canada; Department of Genetics, Children’s Hospital of Eastern Ontario, Ottawa, ON, Canada; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, ON, Canada; Institute of Health Policy, Management and Evaluation, The University of Toronto, Toronto, ON, CanadaShow moreShow less
Expert Matching · Case Demo
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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