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.
98
days
Exome analysis of 22,319 individuals links extremely rare copy-number variants and 22q11.21 dosage to Alzheimer risk
Authors
Olivier Quenez; Catherine Schramm; Kévin Cassinari; Aude Nicolas; Joan Groeneveld; Guillaume Huguet; Benjamin Grenier-Boley; Marc Hulsman; G. Bragi Walters; Itziar de Rojas; Anne Rovelet-Lecrux; Sébastien Feuillette; Laetitia Miguel; Anne-Claire Richard; Stéphane Rousseau; Shahzad Ahmad; Najaf Amin; Philippe Amouyel; Olivia Belbin; Céline Bellenguez; Claudine Berr; Paola Bossù; Femke Bouwman; Jose Bras; Jordi Clarimon; Antonio Daniele; Jean-François Dartigues; Stéphanie Debette; Jean-François Deleuze; Nicola Denning; Oriol Dols-Icardo; Cornelia M. van Duijn; Juan Fortea; Nick C. Fox; Ruth Frikke-Schmidt; Daniela Galimberti; Roberta Ghidoni; Vilmantas Giedraitis; Johan J.P. Gille; Detelina Grozeva; Rita Guerreiro; Edna Grünblatt; John Hardy; Steffi G. Riedel-Heller; Mikko Hiltunen; Clive Holmes; Jakub Hort; Holger Hummerich; M. Arfan Ikram; M. Kamran Ikram; Martin Ingelsson; Iris E. Jansen; Amit Kawalia; Robert Kraaij; Patrick G. Kehoe; Marc Lathrop; Morgane Lacour; Afina W. Lemstra; Alberto Lleó; Lauren Luckcuck; Marcel M.A.M. Mannens; Rachel Marshall; Carlo Masullo; Simon Mead; Patrizia Mecocci; Alexandre de Mendonça; Alun Meggy; Shima Mehrabian; Merel O. Mol; Kevin Morgan; Alexandre Morin; Benedetta Nacmias; Penny J. Norsworthy; Robert Olaso; Florence Pasquier; Pau Pastor; Fabrizio Piras; Julius Popp; Alfredo Ramirez; Rachel Raybould; Richard Redon; Marcel J.T. Reinders; Fernando Rivadeneira; Jeroen G.J. van Rooij; Natalie S. Ryan; Salha Saad; Pascual Sanchez-Juan; Nikolaos Scarmeas; Philip Scheltens; Jonathan M. Schott; Davide Seripa; Daoud Sie; Rebecca Sims; Erik A. Sistermans; Sandro Sorbi; Kristel Sleegers; Resie van Spaendonk; John C. van Swieten; Niccolo’ Tesi; Betty M. Tijms; Magda Tsolaki; André G. Uitterlinden; Jort Vijverberg; Pieter Jelle Visser; Michael Wagner; Julie Williams; Aline Zarea; Emmanuelle Génin; Henne Holstege; Daniel F. Gudbjartsson; David Wallon; Magalie Lecourtois; Maria Victoria Fernandez; Hreinn Stefansson; Sébastien Jacquemont; Jean-Charles Lambert; Sven J. van der Lee; Camille Charbonnier; Gaël NicolasShow moreShow less
Affiliations
Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Genetics and CNRMAJ, 76000 Rouen, France; Univ Rouen Normandie, Normandie Univ, Inserm U1245, 76000 Rouen, France; Univ. Lille, Inserm, CHU Lille, Institut Pasteur de Lille, U1167-RID-AGE Facteurs de risque et déterminants moléculaires des maladies liées au vieillissement, Lille, France; Genomics of Neurodegenerative Diseases and Aging, Human Genetics, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, Amsterdam, the Netherlands; Alzheimer Center Amsterdam, Neurology, Vrije Universiteit Amsterdam, Amsterdam UMC location VUmc, Amsterdam, the Netherlands; Amsterdam Neuroscience, Neurodegeneration, Amsterdam, the Netherlands; Centre Hospitalier Universitaire Sainte-Justine Research Center, Montreal, QC, Canada; Delft Bioinformatics Lab, Delft University of Technology, Delft, the Netherlands; Amgen-deCODE Genetics, Sturlugata 8, 102, Reykjavik, Iceland; Ace Alzheimer Center Barcelona, Universitat Internacional de Catalunya, Barcelona, Spain; CIBERNED, Network Center for Biomedical Research in Neurodegenerative Diseases, National Institute of Health Carlos III, Madrid, Spain; Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, Esch-sur-Alzette, Luxembourg; Department of Epidemiology, Erasmus Medical Centre, Rotterdam, the Netherlands; Leiden Academic Centre for Drug Research, Leiden, the Netherlands; Nuffield Department of Population Health, Oxford University, Oxford, UK; Department of Neurology, II B Sant Pau, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain; Biomedical Research Networking Center on Neurodegenerative Diseases, National Institute of Health Carlos III, Madrid, Spain; Université Montpellier, INSERM, Institute for Neurosciences of Montpellier, Montpellier, France; Experimental Neuro-psychobiology Laboratory, Department of Clinical and Behavioral Neurology, Istituto di Ricovero e Cura a Carattere Scientifico Santa Lucia Foundation, Rome, Italy; Department of Neurodegenerative Science, Van Andel Institute, Grand Rapids, MI, USA; Division of Psychiatry and Behavioral Medicine, Michigan State University College of Human Medicine, Grand Rapids, MI, USA; Department of Neuroscience, Catholic University of Sacred Heart, Fondazione Policlinico Universitario A. Gemelli Istituto di Ricovero e Cura a Carattere Scientifico, Rome, Italy; Université Bordeaux, INSERM, Bordeaux Population Health Research Center, Bordeaux, France; Department of Neurology, Bordeaux University Hospital, Bordeaux, France; Université Paris-Saclay, CEA, Centre National de Recherche en Génomique Humaine (CNRGH), 91057 Evry, France; UKDRI Cardiff, School of Medicine, Cardiff University, Cardiff, UK; Dementia Research Centre, University College London Queen Square Institute of Neurology, London, UK; Department of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark; Department of Clinical Biochemistry, Rigshospitalet, Copenhagen, Denmark; Fondazione Istituto di Ricovero e Cura a Carattere Scientifico C' Granda, Ospedale Policlinico, Milan, Italy; University of Milan, Milan, Italy; Molecular Markers Laboratory, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Brescia, Italy; Department of Public Health and Carins Sciences/Geriatrics, Uppsala University, Uppsala, Sweden; Genome Diagnostics, Department of Human Genetics, VU University, AmsterdamUMC (locationVUmc), Amsterdam, the Netherlands; Medical Research Council Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neuroscience, School of Medicine, Cardiff University, Cardiff, UK; Department of Child and Adolescent Psychiatry and Psychotherapy, Psychiatric University Hospital Zurich, University of Zurich, Zurich, Switzerland; Neuroscience Center Zurich, University of Zurich and ETH Zurich, Zurich, Switzerland; Zurich Center for Integrative Human Physiology, University of Zurich, Zurich, Switzerland; Reta Lila Weston Research Laboratories, Department of Molecular Neuroscience, University College London Institute of Neurology, London, UK; Institute of Social Medicine, Occupational Health and Public Health, University of Leipzig, Leipzig, Germany; Institute of Biomedicine, University of Eastern Finland, Kuopio, Finland; Clinical and Experimental Science, Faculty of Medicine, University of Southampton, Southampton, UK; Memory Clinic, Department of Neurology, Second Faculty of Medicine, Charles University, Motol University Hospital, Prague, Czech Republic; Medical Research Council Prion Unit at University College London, University College London Institute of Prion Diseases, London, UK; Department of Complex Trait Genetics, Center for Neurogenomics and Cognitive Research, Amsterdam Neuroscience, Vrije University, Amsterdam, the Netherlands; Division of Neurogenetics and Molecular Psychiatry, Department of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany; Department of Internal Medicine, Erasmus Medical Centre, Rotterdam, the Netherlands; Translational Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK; McGill University and Genome Quebec Innovation Centre, Montreal, QC, Canada; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Neurology and CNRMAJ, 76000 Rouen, France; Department of Human Genetics, Amsterdam UMC, University of Amsterdam, Amsterdam Reproduction and Development Research Institute, Amsterdam, the Netherlands; Institute of Neurology, Catholic University of the Sacred Heart, Rome, Italy; Division of Gerontology and Geriatrics, Department of Medicine and Surgery, University of Perugia, Perugia, Italy; Division of Clinical Geriatrics, Department of Neurobiology, Care Sciences and Society, Karolinska Institutet, Stockholm, Sweden; Faculty of Medicine, University of Lisbon, Lisbon, Portugal; Department of Neurology, University Hospital “Alexandrovska,” 1431 Sofia, Bulgaria; Department of Clinical Genetics, Erasmus Medical Centre, Rotterdam, the Netherlands; Human Genetics, School of Life Sciences, University of Nottingham, Nottingham, UK; Department of Neuroscience, Psychology, Drug Research and Child Health, University of Florence, Florence, Italy; IRCCS Fondazione Don Carlo Gnocchi, Florence, Italy; Université Lille, INSERM, Centre Hospitalier Universitaire Lille, UMR1172, Resources and Research Memory Center (MRRC) of Distalz, Licend, Lille, France; Fundació Docència i Recerca MútuaTerrassa and Movement Disorders Unit, Department of Neurology, University Hospital MútuaTerrassa, Barcelona, Spain; Memory Disorders Unit, Department of Neurology, Hospital Universitari Mutua de Terrassa, Barcelona, Spain; Laboratory of Neuropsychiatry, Department of Clinical and Behavioral Neurology, Istituto di Ricovero e Cura a Carattere Scientifico, Santa Lucia Foundation, Rome, Italy; University Hospital of Psychiatry Zürich, University of Zürich, Zürich, Switzerland; Department of Psychiatry and Glenn Biggs Institute for Alzheimer’s and Neurodegenerative Diseases, San Antonio, TX, USA; Department of Neurodegenerative Diseases and Geriatric Psychiatry, University Hospital Bonn, Medical Faculty, Bonn, Germany; German Center for Neurodegenerative Diseases, Bonn, Germany; Cluster of Excellence Cellular Stress Responses in Aging-Associated Diseases, University of Cologne, Cologne, Germany; Université de Nantes, Centre Hospitalier Universitaire Nantes, Centre National de la Recherche Scientifique, INSERM, l’institut du Thorax, Nantes, France; Department of Neurology, Erasmus Medical Centre, Rotterdam, the Netherlands; Neurology Service, Marqués de Valdecilla University Hospital (University of Cantabria and IDIVAL), Santander, Spain; Department of Neurology, Aiginition Hospital, National and Kapodistrian University of Athens, 11528 Athens, Greece; Department of Neurology, Columbia University, New York, NY 10032, USA; Laboratory for Advanced Hematological Diagnostics, Department of Hematology and Stem Cell Transplant, Lecce, Italy; Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neuroscience, School of Medicine, Cardiff University, Cardiff, UK; Department of Human Genetics and Amsterdam Reproduction and Development Research Institute, Amsterdam UMC, location Vrije Universiteit Amsterdam, Amsterdam, the Netherlands; Complex Genetics of Alzheimer’s Disease Group, VIB Center for Molecular Neurology, VIB, Antwerp, Belgium; Laboratory of Neurogenetics, Institute Born-Bunge, Antwerp, Belgium; Department of Biomedical Sciences, University of Antwerp, Antwerp, Belgium; First Department of Neurology, Medical School, Aristotle University of Thessaloniki, Thessaloniki, Greece; Alzheimer Hellas, Thessaloniki, Greece; UK Dementia Research Institute, Cardiff University, Cardiff, UK; Université Brest, INSERM, Etablissement Français du Sang, Centre Hospitalier Universitaire Brest, Unité Mixte de Recherche 1078, GGB, Brest, France; School of Engineering and Natural Sciences, University of Iceland, Reykjavik, Iceland; Memory Clinic of Fundaciò ACE, Catalan Institute of Applied Neurosciences, 08028 Barcelona, Spain; Department of Pediatrics, Université de Montréal, Montreal, QC, Canada; Univ Rouen Normandie, Normandie Univ, Inserm U1245 and CHU Rouen, Department of Biostatistics and CNRMAJ, 76000 Rouen, FranceShow moreShow less
166
days
Distinct mutational landscapes for germline and somatic cancer variants in forty tumor suppressor genes
Authors
Suhasini D. Lulla; Deborah I. Ritter; Chimene Kesserwan; Sharon E. PlonShow moreShow less
Affiliations
Department of Pediatrics, Baylor College of Medicine, Houston, TX 77030, USA; Texas Children’s Cancer and Hematology Center, Houston, TX 77030, USA; Memorial Sloan Kettering Cancer Center, New York, NY 10065, USAShow moreShow less
166
days
RNA splicing evidence enables robust classification of BRCA1 exon 18 variants: Results from the ENIGMA consortium
Authors
Joanna Domènech-Vivó; Hélène Tubeuf; Romy L.S. Mesman; Aurelie Drouet; Mélanie Girardi; María Concepción Alonso-Cerezo; Diana Baralle; Nadia Boutry-Kryza; David J. Bunyan; Helen J. Byers; Sandrine M. Caputo; Kathleen B.M. Claes; Miguel De la Hoya; D. Gareth Evans; Laure Frésard; Sophie Krieger; Conxi Lázaro; Mélanie Leone; Eva Macháčková; Mireia Menéndez; Alejandro Moles-Fernández; Gemma Montalban; Erin Mundt; Marcy E. Richardson; Elke M. Van Veen; Jamie Weyandt; Judith Balmaña; Amanda B. Spurdle; Orland Diez; Maaike P.G. Vreeswijk; Alexandra Martins; Sara Gutiérrez-EnríquezShow moreShow less
Affiliations
Hereditary Cancer Genetics Group, Vall d’Hebron Institute of Oncology (VHIO), Vall d’Hebron Barcelona Hospital Campus, Barcelona, Spain; Programa de Doctorat en Biomedicina, Universitat de Barcelona (UB), Barcelona, Spain; Area of Clinical and Molecular Genetics, Vall d'Hebron Hospital Universitari, Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain; Medicine Genetics Group, Vall d'Hebron Institut de Recerca (VHIR), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain; University Rouen Normandie, Inserm U1245, 76000 Rouen, France; Interactive Biosoftware, Rouen, France; Department of Human Genetics, Leiden University Medical Center, Leiden, the Netherlands; Genética Clínica, Servicio de Oncología Médica, Hospital Universitario de la Princesa, Madrid, Spain; Faculty of Medicine, University of Southampton, Southampton, UK; University Hospital Southampton, Southampton, UK; Plateforme mixte de génétique moléculaire Hospices Civils de Lyon, Centre Léon Bérard, Lyon, France; Wessex Genomics Laboratory Service (Salisbury), Salisbury District Hospital, Salisbury, UK; Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Manchester, UK; Division of Evolution, Infection and Genomic Sciences, School of Biological Sciences, Faculty of Biology, Medicine and Health, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK; Service de Génétique, Institut Curie, 26 rue d'Ulm, Paris, France; Paris Sciences and Lettres (PSL) University, Paris, France; Center for Medical Genetics, Ghent University Hospital, Department of Biomolecular Medicine, Ghent University, CRIG (Cancer Research Institute Ghent), Ghent, Belgium; Molecular Oncology Laboratory, Hospital Clínico San Carlos, IdISSC, Madrid, Spain; Manchester Centre for Genomic Medicine, Manchester Academic Health Science Centre, Division of Evolution and Genomic Medicine, University of Manchester, St Mary’s Hospital, Manchester Universities NHS Foundation Trust, Manchester, UK; Labcorp Genetics Inc, 1400 16th Street, San Francisco, CA, USA; Laboratoire de Biologie et Génétique du Cancer, Centre François Baclesse, Caen, France; UNICAEN, Normandie Université, Caen, France; Hereditary Cancer Program, Oncobell, IDIBELL, Catalan Institute of Oncology, Hospitalet de Llobregat, Barcelona, Spain; Centro de Investigación Biomédica en Red de Cáncer (CIBERONC), Madrid, Spain; Department of Cancer Epidemiology and Genetics, Masaryk Memorial Cancer Institute, Brno, Czech Republic; Myriad Genetics, Inc., Salt Lake City, UT, USA; Ambry Genetics, Aliso Viejo, CA, USA; Medical Oncology Department, Vall d’Hebron Hospital Universitari, Vall d’Hebron Barcelona Hospital Campus, Barcelona, Spain; QIMR Berghofer, Brisbane, QLD, AustraliaShow moreShow less
270
days
Long-read transcriptome analysis using IsoRanker for identifying pathogenic variants in Mendelian conditions
Authors
Yong-Han Hank Cheng; Adriana E. Sedeño-Cortés; Jane E. Ranchalis; Katherine M. Munson; Mitchell R. Vollger; Elsa Balton; Casie A. Genetti; Jenny L. Wilson; Monica H. Wojcik; Alan H. Beggs; Michael J. Bamshad; Chia-Lin Wei; Katrina M. Dipple; Runjun D. Kumar; Mark D. Fleming; Ian A. Glass; Elizabeth E. Blue; Gail Jarvik; Jessica X. Chong; Daniela M. Witten; Anne O’Donnell-Luria; Andrew B. StergachisShow moreShow less
Affiliations
Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA; Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA, USA; The Manton Center for Orphan Disease Research, Division of Genetics and Genomics, Boston Children’s Hospital, Harvard Medical School, Boston, MA, USA; Division of Pediatric Neurology, Department of Pediatrics, Oregon Health & Science University, Portland, OR, USA; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA; Division of Genetic Medicine, Department of Pediatrics, University of Washington, Seattle, WA, USA; Brotman Baty Institute for Precision Medicine, Seattle, WA, USA; The Northwest Genomics Center, University of Washington, Seattle, WA, USA; Seattle Children’s Research Institute, Center for Clinical and Translational Research, Seattle, WA, USA; Department of Laboratory Medicine & Pathology, University of Washington, Seattle, WA, USA; Department of Pathology, Boston Children’s Hospital, Harvard Medical School, Boston, MA, USA; Department of Pediatrics, University of Washington, Seattle, WA, USA; Institute for Public Health Genetics, University of Washington, Seattle, WA, USA; Departments of Statistics & Biostatistics, University of Washington, Seattle, WA, USAShow moreShow less
107
days
Shared inheritance reveals landscape of somatic and germline cancer risk in TP53
Authors
Hamish A.J. MacGregor; Jamie R. Blundell; Douglas F. EastonShow moreShow less
Affiliations
Early Cancer Institute, University of Cambridge, Cambridge, UK; Centre for Cancer Genetic Epidemiology, Department of Public Health and Primary Care, University of Cambridge, Cambridge, UKShow moreShow less
140
days
Examining gaps in institutional policies for clinical genomic data sharing: A cross-jurisdictional study
Authors
Zhaoping Ju; Yunhe Xue; Abby Rud; Juliann M. Savatt; Jordan Lerner-Ellis; Heidi L. Rehm; Yann Joly; Diya UberoiShow moreShow less
Affiliations
Centre of Genomics and Policy, McGill University, Montreal, QC, Canada; Department of Pathology, McGill University, Montreal, QC, Canada; Department of Genomic Health, Geisinger, Danville, PA, USA; Pathology and Laboratory Medicine, Mount Sinai Hospital, Toronto, ON, Canada; Department of Laboratory Medicine and Pathobiology, Mount Sinai Hospital, Toronto, ON, Canada; Lunenfeld-Tanenbaum Research Institute, Toronto, ON, Canada; Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA; Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA; Independent Researcher, Montreal, QC, CanadaShow moreShow less
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 review62 days
Median65 days