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2015/02/03

Human Genome Variation: Open for submissions


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Human Genome Variation (HGV) is an online, open access journal that contains articles and reports about variation and variability in human genomes.

As a key part of the journal, HGV publishes Data Reports, or short reports which describe disease-causing variation and/ or their frequencies. Data Reports are fully peer reviewed, and follow a rapid publication pathway.

Read some of the Data Reports recently published in the journal:

Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer’s disease
E C Schulte, A Kurz, P Alexopoulos, H Hampel, A Peters, C Gieger, D Rujescu, J Diehl-Schmid and J Winkelmann

A novel KCNT1 mutation in a Japanese patient with epilepsy of infancy with migrating focal seizures
S Shimada, Y Hirano, S Ito, H Oguni, S Nagata, K Shimojima and T Yamamoto

Osteogenesis imperfecta IIC caused by a novel heterozygous mutation in the C-propeptide region of COL1A1
M Takagi, M Matsushita, G Nishimura and T Hasegawa

A novel PTCH1 mutation in a patient with Gorlin syndrome
N Okamoto, T Naruto, T Kohmoto, T Komori and I Imoto

Additionally, the journal hosts a fully searchable database of genomic variation which contains relevant data from the published Data Reports. Try it now!
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Submit your next manuscript to Human Genome Variation and benefit from:

  • Human Genome Variation is an official journal of the Japanese Society of Human Genetics, and builds upon the success of its sister journal: Journal of Human Genetics, the leading genetics journal based in the Asia-Pacific region.
  • An online submission system, developed to speed up the submission process.
  • Assurance of the highest possible publishing, editorial and production standards.
  • High visibility for your research: a recent study indicates that open access articles are viewed three times more often than articles only available to subscribers.*
  • Wide dissemination: articles are published under a Creative Commons License, permanently and freely available for all to read, use and cite without restriction.
  • Compliance with many open access funder mandates.
  • Article Processing Charge for Data Reports waived in the initial development phase.

View our Submission Guide.


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*Research Information Network (RIN), 2014

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