Academic Journal
Q2Genetics in Medicine Open
About Genetics in Medicine Open
Genetics in Medicine Open is a scholarly journal published by Elsevier B.V.. SCImago 2025 lists it in Q2, with an SJR of 0.823 and H-index of 10.
Coverage: 2023-2026. Research categories: Biochemistry, Genetics and Molecular Biology (miscellaneous) (Q2); Genetics (Q2); Cell Biology (Q3); Molecular Biology (Q3).
Open-access policies and author information
Reported in the official DOAJ public CSV snapshot (2026-09-01), downloaded 2026-10-03. Record updated 2026-04-27. This snapshot does not establish today’s listing status or fee quotation.
Publisher policy links recorded by DOAJ
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Source: DOAJ journal record. Journal metadata is distributed by DOAJ under CC0. Confirm current fees, tax, eligibility and waiver terms with the publisher.
Source-backed journal facts
Topics in published research
Genomics and Rare Diseases; BRCA gene mutations in cancer; Genomic variations and chromosomal abnormalities; Metabolism and Genetic Disorders; Prenatal Screening and Diagnostics; Cancer Genomics and Diagnostics.
OpenAlex classifies topics from published works. These topics are not the publisher’s official aims and scope.
Source: OpenAlex source record. Retrieved 2026-10-03. Source record updated 2026-10-02. OpenAlex metrics are different from SCImago metrics and the Clarivate Journal Impact Factor.
Journal Metrics
Quartile, SJR and the listed SCImago H-index use the 2025 imported SCImago dataset. A quartile may vary by subject category. Values without a source or reporting year are unverified historical entries. Verify the current Journal Impact Factor with Clarivate or the publisher before using it.
Aims & Scope
The publisher’s official aims and scope have not yet been verified for this profile. Use the journal website to check subject fit and accepted article types before submitting.
Recent Research Articles
Latest publications matched automatically by ISSN.
Classical Homocystinuria Unmasked by Segmental Uniparental Isodisomy in a Child with Ectopia Lentis and Autism Spectrum Disorder
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2026-10 · DOI: 10.1016/j.gimo.2026.104497Retrospective Application of Genome-Based Newborn Screening Platforms Identifies Diagnoses in Critically Ill Children
Erica Sanford Kobayashi, Edwin F. Juarez Rosales, Laura E. Tobin, Ofelia Vargas Shiraishi et al.
2026-10 · DOI: 10.1016/j.gimo.2026.104500Promoting diversity in the genomics workforce: A funded collaborative summer internship model supports genetic counseling graduate admission
Rebecca Mueller, Lisa Kessler, Isaac Elysee, Meron Azage et al.
2026-10 · DOI: 10.1016/j.gimo.2026.104502Publisher's Correction
2026-09 · DOI: 10.1016/j.gimo.2026.104492New Developments in Fragile X Premutation-Associated Conditions: Consensus Perspectives from the 6th International Conference on FMR1 Premutation
Federica Alice Maria Montanaro, Paolo Alfieri, Emily Graves Allen, Holley Arnold et al.
2026-09 · DOI: 10.1016/j.gimo.2026.104496Comparing patients’ perceptions and cognitive and emotional responses to pre-test cancer genetic services delivered via chatbot versus standard of care: findings from the BRIDGE trial
Yang Yi, Jemar R. Bather, Melody S. Goodman, Rachelle Lorenz Chambers et al.
2026-09 · DOI: 10.1016/j.gimo.2026.104498Recommendations for the re-analysis of existing genomic data from epilepsy patients
Alan J. Robertson, Natalie B. Tan, Pei Dai, Carmen Bennett et al.
2026-09 · DOI: 10.1016/j.gimo.2026.104494The Case for Long Read Sequencing for the Future of Genomic Newborn Screening
Seth I. Berger, Laura M. Amendola, Susan Toomey, Changrui Xiao et al.
2026-09 · DOI: 10.1016/j.gimo.2026.104495Public Preferences for Investigative Genetic Genealogy (IGG) Programs: A Discrete Choice Experiment
Nijole P. Tjader, Natalie Riva Smith, Nicola B. Campoamor, Amy L. McGuire et al.
2026-09 · DOI: 10.1016/j.gimo.2026.104499Zevaskyn (prademagene zamikeracel) for wound treatment in individuals with recessive dystrophic epidermolysis bullosa: A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG)
Amanda Thomas-Wilson, Marek Svoboda, Vanina Taliercio, Noura S. Abul-Husn et al.
2026-08 · DOI: 10.1016/j.gimo.2026.104408DNA methylation episignature for White-Sutton syndrome due to POGZ variants
Sadegheh Haghshenas, Brittany N. Simpson, Amelle Shillington, Aurore Garde et al.
2026-08 · DOI: 10.1016/j.gimo.2026.104489Diazoxide choline (Vykat XR) for treatment of hyperphagia and obesity in Prader-Willi syndrome: A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG)
Nadia Merchant, Juanita Neira, Allyson Derry, Andrea L. Gropman et al.
2026-08 · DOI: 10.1016/j.gimo.2026.104412Newborn screening: past, present, and future
Cynthia M. Powell
2026-07 · DOI: 10.1016/j.gimo.2026.104482When the newborn screening works: And why the system around families must still evolve
Yojana Rodriguez-Humbert
2026-06 · DOI: 10.1016/j.gimo.2026.104414Kebilidi (eladocagene exuparvovec-tneq) for adults and children with aromatic L-amino acid decarboxylase (AADC) deficiency: A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG)
Julie M. Porter, Andrés Morales Corado, Kuntal Sen, Sarah H. Elsea et al.
2026-06 · DOI: 10.1016/j.gimo.2025.103471Sepiapterin approved for children and adults with phenylketonuria (PKU): A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG)
Irene J. Chang, Danny E. Miller, Andres Morales Corado, Juanita Neira et al.
2026-06 · DOI: 10.1016/j.gimo.2026.104399Mavorixafor (Xolremdi) for individuals with warts, hypogammaglobulinemia, infections, and myelokathexis (WHIM) syndrome: A therapeutics bulletin of the American College of Medical Genetics and Genomics (ACMG)
Mark Dulchavsky, Xiao Peng, Mark Hannibal, Harry Lesmana et al.
2026-06 · DOI: 10.1016/j.gimo.2026.104398CLN2 Batten disease diagnosed via newborn genome screening
Patrick O’Connell, Luca Fierro, Rachel Kaplan, Lilian Liou Cohen et al.
2026-06 · DOI: 10.1016/j.gimo.2026.104415P043: RNA sequencing aids in the molecular diagnosis of mucopolysaccharidosis IVA: A case report
Jay Shaw, Shoji Yano, James Zdrodowski, Mitchell Dillon et al.
2026 · DOI: 10.1016/j.gimo.2026.103534P166: Characterization of phenotype and effect on diagnostic yield in a patient population undergoing clinical genome wide sequencing
Anna Szuto, Caitlin Chisholm, Meredith Gillespie, Lynette Lau et al.
2026 · DOI: 10.1016/j.gimo.2026.103660Reviews
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October 4, 2026 at 9:04 pm
October 2, 2026