| | Human Genome Variation is an online, open access journal with accompanying database publishing articles and reports about variation and variability in the human genome. The journal was born from a demand by the community for a place to publish important discoveries, observations and analysis about research on the human genome. We are delighted that Human Genome Variation is now covered by PubMed Central (PMC) allowing all published articles data to be made available for search and across on the journals' page on PMC. Its inclusion confirms the potential and importance of high quality content, and it will provide increased international visibility and recognition for our journal contributors. Check out some of the top-accessed articles from the last 12 months: | | | | Novel rare variations of the oxytocin receptor (OXTR) gene in autism spectrum disorder individuals | Xiaoxi Liu, Minae Kawashima, Taku Miyagawa, Takeshi Otowa, Khun Zaw Latt, Myo Thiri, Hisami Nishida, Toshiro Sugiyama, Yoshinori Tsurusaki, Naomichi Matsumoto, Akihiko Mabuchi, Katsushi Tokunaga & Tsukasa Sasaki | | | | | Genomic architecture of inflammatory bowel disease in five families with multiple affected individuals | Anna B Stittrich, Justin Ashworth, Mude Shi, Max Robinson, Denise Mauldin, Mary E Brunkow, Shameek Biswas, Jin-Man Kim, Ki-Sun Kwon, Jae U Jung, David Galas, Kyle Serikawa, Richard H Duerr, Stephen L Guthery, Jacques Peschon, Leroy Hood, Jared C Roach & Gustavo Glusman | | | | | | | | Publish in Human Genome Variation - a quality, peer-reviewed journal with further discoverability. It is a home for your work and a resource for the community. Learn more about author benefit | | | | | |
No comments:
Post a Comment
Keep a civil tongue.