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GENETICS IN MEDICINE

Elsevier SCIE Non-OA
2026 Emerging Zone 12025 CAS Zone 1 TOP2025 JCR Q1
257.5Average days
224.5Median days
139Fastest days
543Longest days
2352025 publications

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.

139 days

“It didn’t feel like anything unusual because we had already been through so much”: Disability-related research experiences of families with children enrolled in the undiagnosed diseases network

AuthorsKevin T. Mintz; Elisa N. Altamirano; Meghan C. Halley; Krysta S. Barton; Mildred K. Cho; Jonathan A. Bernstein; Jennefer N. Carter; Holly K. Tabor

AffiliationsStanford Department of Pediatrics, Stanford School of Medicine, Stanford, CA; The Laurie J. Girand Center for Biomedical Ethics, Stanford School of Medicine, Stanford, CA; Department of Medicine, Stanford School of Medicine, Stanford, CA; Center for Undiagnosed Diseases, Stanford School of Medicine, Stanford, CA

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140 days

Genotype-phenotype relationships in phenylalanine hydroxylase deficiency: Functional annotation-enhanced analysis of 23,427 individuals

AuthorsNenad Blau; Nastassja Himmelreich

AffiliationsDivision 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, Germany

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336 days

Extended newborn screening using DNA methylation testing for fragile X syndrome in 17,107 infants

AuthorsDavid E. Godler; Ling Ling; Dinusha Gamage; Minh Bui; Michael J. Field; David J. Amor

AffiliationsDepartment 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, Australia

Source PDF DOI Publisher page
324 days

Evaluation of electrical impedance myography as a noninvasive musculoskeletal biomarker in infantile- and late-onset Pompe disease

AuthorsRaquel 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 Upadhyay

AffiliationsDepartment 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, CA

Source PDF DOI Publisher page
181 days

Delineating the clinical and molecular spectrum of the neurodevelopmental disorder associated with SET

AuthorsYuwei 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 Barakat

AffiliationsDepartment 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, Germany

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252 days

Decision-making criteria in polygenic embryo screening: A survey of reproductive medicine physicians

AuthorsRémy A. Furrer; Aayushi Gandhi; Dorit Barlevy; Shai Carmi; Todd Lencz; Stacey Pereira; Gabriel Lázaro-Muñoz

AffiliationsDepartment 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, MA

Source PDF DOI Publisher page
211 days

Clinical utility of exome sequencing: Post-exome testing decision changes in the management of children with suspected rare genetic disease

AuthorsToni 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. Marshall

AffiliationsDepartment 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, Canada

Source PDF DOI Publisher page
543 days

MAJIQ-CLIN: A novel tool to help identify Mendelian disease-causing variants from RNA-seq data

AuthorsJoseph K. Aicher; Dina Issakova; Barry Slaff; San Jewell; Nicholas F. Lahens; Gregory R. Grant; Diana Baralle; Jill A. Rosenfeld; Daryl A. Scott; Elizabeth J. Bhoj; Yoseph Barash

AffiliationsDepartment of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA; Department of Biology, School of Arts and Sciences, University of Pennsylvania, Philadelphia, PA; Department of Computer and Information Sciences, School of Engineering, University of Pennsylvania, Philadelphia, PA; Faculty of Medicine, University of Southampton, Southampton, United Kingdom; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX; Children’s Hospital of Philadelphia, Philadelphia, PA

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238 days

ACMG/AMP variant classification specifications from the ClinGen Epilepsy Sodium Channel Variant Curation Expert Panel

AuthorsLacey Smith; Emily Bonkowski; Anna Prentice; Stacey Cohen; Laina Lusk; Shridhar Parthasarathy; Brendan Burns; Elizabeth Butler; Yanmin Chen; Kathleen Dady; Sarah Dugger; Alexander Ing; Rhonda Lassiter; David Lewis-Smith; Maureen Mulhern; Jimmy N.H. Nguyen; Jonathan Olival; Samin A. Sajan; Christopher H. Thompson; Alfred L. George; Jacy Wagnon; Katie Yergert; Jan H. Magielski; Jillian L. McKee; Erin Riggs; Kimberly Wiltrout; Annapurna Poduri; Ingo Helbig; Heather C. Mefford

AffiliationsDepartment of Neurology, Boston Children’s Hospital, Boston, MA; Center for Pediatric Neurological Disease Research, Department of Cell & Molecular Biology, St Jude Children’s Research Hospital, Memphis, TN; Department of Neurology, Children’s Hospital of Philadelphia, Philadelphia, PA; Division of Translational Medicine and Human Genetics, Hospital of the University of Pennsylvania, Philadelphia, PA; QIAGEN, Germantown, MD; GeneDx, Gaithersburg, MD; Labcorp, San Francisco, CA; Ambry Genetics, 1 Enterprise Aliso Viejo, CA; Division of Genetics, Genomics, and Metabolism, Ann & Robert H. Lurie Children’s Hospital of Chicago, Chicago, IL; Neurology Department, North Bristol Trust, Southmead Hospital Bristol, Bristol, United Kingdom; Department of Neurology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY; Department of Pathology and Cell Biology, Vagelos College of Physicians and Surgeons, Columbia University, New York, NY; Program in Genetics and Genome Biology, The Hospital for Sick Children, Toronto, ON, Canada; Department of Molecular Genetics, University of Toronto, Toronto, ON, Canada; Laboratory of Neurogenetics and Molecular Medicine, Institut de Recerca Sant Joan de Déu, Barcelona, Spain; Department of Pharmacology, Feinberg School of Medicine, Northwestern University, Chicago, IL; Department of Neuroscience, Ohio State University Wexner Medical Center, Columbus, OH; Autism & Developmental Medicine Institute, Geisinger, Danville, PA

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211 days

Multimodal genotype-phenotype analysis in SMARCB1-associated developmental disorders

AuthorsRamy Saad; Clementina Cobolli Gigli; Pleuntje J. van der Sluijs; Jon R. Wilson; Tzung-Chien Hsieh; Vivienne P.M. McConnell; Carlos A. Bacino; Lynne M. Bird; Shelin Adam; Lorne Clarke; Jan M. Cobben; André M. Travessa; Laurence Faivre; Stense Farholt; Pernille A. Gregersen; Jos van Hasselt; Nayana Lahiri; Elizabeth E. Palmer; Ruth Sheffer; Jill Clayton-Smith; Yael Wilnai; Charu Deshpande; Jenny E.V. Morton; Emma Clement; Gijs W.E. Santen; Cristina Dias

AffiliationsDepartment of Twin Research & Genetic Epidemiology, King’s College London, London, United Kingdom; Clinical Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom; Neural Stem Cell Biology Lab, The Francis Crick Institute, London, United Kingdom; Department of Medical and Molecular Genetics, School of Basic & Medical Biosciences, King’s College London, London, United Kingdom; Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands; Structural Biology of Disease Processes Laboratory, The Francis Crick Institute, London, United Kingdom; Institute for Genomic Statistics and Bioinformatics, University Hospital Bonn, Rheinische Friedrich-Wilhelms-Universität Bonn, Bonn, Germany; Northern Ireland Regional Genetics Service, Belfast City Hospital, Belfast Health & Social Care Trust, Belfast, Northern Ireland, United Kingdom; Department of Molecular and Human Genetics, Baylor College of Medicine, Genetics Service, Texas Children’s Hospital, Houston, TX; Department of Pediatrics, University of California San Diego, Division of Dysmorphology and Genetics, Rady Children’s Hospital San Diego, San Diego, CA; Department of Medical Genetics and the British Columbia Children’s Hospital Research Institute, University of British Columbia, Vancouver, BC, Canada; North West Thames Regional Genetics Service, NHS, Northwick Park & St Mark’s Hospitals, London, Harrow, United Kingdom; Serviço de Genética Médica, Centro Hospitalar Universitário Lisboa Norte, Hospital de Santa Maria, Lisbon, Portugal; Inserm, UMR1231, Equipe GAD, Bâtiment B3, Université de Bourgogne Franche Comté, Dijon Cedex, France; Centre de Référence Maladies Rares "Anomalies du développement et syndromes malformatifs", Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU Dijon Bourgogne, Dijon, France; Department of Clinical Genetics, Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark; Pediatrics and Adolescent Medicine, Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark; ‘ s Heeren Loo Zorggroep, Advisium, Ermelo, The Netherlands; St George’s University Hospitals NHS Foundation Trust & St Georges, University of London, IMBE, London, United Kingdom; Department of Molecular and Biomedical Sciences, City St, University of London, London, United Kingdom; Discipline of Paediatrics and Child Health, School of Clinical Medicine, Faculty of Medicine and Health, University of New South Wales, Sydney, NSW, Australia; Centre for Clinical Genetics, Sydney Children’s Hospitals Network, Randwick, NSW, Australia; Department of Human Genetics, Hadassah University Hospital, Jerusalem, Israel; Manchester Centre for Genomic Medicine, Manchester University Hospitals NHS Foundation Trust, Saint Mary’s Hospital, Oxford Road, Manchester, United Kingdom; Genetic Institute, Tel Aviv Sourasky Medical Center, Tel Aviv, Israel; Department of Clinical Genetics, Guy’s & St Thomas NHS Foundation Trust, London, United Kingdom; West Midlands Regional Clinical Genetics Service and Birmingham Health Partners, Birmingham Women’s and Children’s Hospitals NHS Foundation Trust, Birmingham, United Kingdom

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Average review96.4 days

Median77 days

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