Heredity - Table of Contents alert Volume 120 Issue 1

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TABLE OF CONTENTS Volume 120, Issue 1 (January 2018) In this issue Articles Also new AOP   Sign up for e-alerts Recommend to your library Web feed Subscribe Articles The mutational decay of male-male and hermaphrodite-hermaphrodite competitive fitness in the androdioecious nematode C. elegans Shu-Dan Yeh, Ayush Shekhar Saxena, Timothy A. Crombie, Dorian Feistel, Lindsay M. Johnson et al. Heredity 2017 120: 1 - 12; November 14, 2017; 10.1038/s41437-017-0003-8   Abstract | Full Text The IICR (inverse instantaneous coalescence rate) as a summary of genomic diversity: insights into demographic inference and model choice Lounès Chikhi, Willy Rodríguez, Simona Grusea, Patrícia Santos, Simon Boitard et al. Heredity 2017 120: 13 - 24; November 08, 2017; 10.1038/s41437-017-0005-6   Abstract | Full Text Influence of historical land use and modern agricultural expansion on the spatial and ecological divergence of sugarcane borer, Diatraea saccharalis (Lepidoptera: Crambidae) in Brazil   Heredity 2017 120: 25 - 37; November 20, 2017; 10.1038/s41437-017-0018-1   Abstract | Full Text Environmental and genetic determinants of transcriptional plasticity in Chinook salmon Kyle W. Wellband, John W. Heath& Daniel D. Heath Heredity 2017 120: 38 - 50; November 10, 2017; 10.1038/s41437-017-0009-2   Abstract | Full Text Characterization of hybridization within a secondary contact region of the inshore fish, Bostrychus sinensis, in the East China Sea   Heredity 2017 120: 51 - 62; November 10, 2017; 10.1038/s41437-017-0011-8   Abstract | Full Text Porcine Y-chromosome variation is consistent with the occurrence of paternal gene flow from non-Asian to Asian populations   Heredity 2017 120: 63 - 76; November 20, 2017; 10.1038/s41437-017-0002-9   Abstract | Full Text The SETDB2 locus: evidence for a genetic link between handedness and atopic disease Bernard Crespi, Silven Read& Peter Hurd Heredity 2017 120: 77 - 82; November 10, 2017; 10.1038/s41437-017-0004-7   Abstract | Full Text A missense point mutation in COL10A1 identified with whole-genome deep sequencing in a 7-generation Pakistan dwarf family Chao Zhang, Jiaojiao Liu, Furhan Iqbal, Yan Lu, Saima Mustafa et al. Heredity 2017 120: 83 - 89; November 10, 2017; 10.1038/s41437-017-0021-6   Abstract | Full Text Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. The contents of the Natureevents Directory are now live. The digital version is available here. Find the latest scientific conferences, courses, meetings and symposia on natureevents.com. For event advertising opportunities across the Nature Publishing Group portfolio please contact natureevents@nature.com More Nature Events Please note that you need to be a subscriber or site-licence holder to enjoy full-text access to Heredity. In order to do so, please purchase a subscription. You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/nams/svc/myaccount (You will need to log in to be recognised as a nature.com registrant). For further technical assistance, please contact our registration department. For print subscription enquiries, please contact our subscription department. For other enquiries, please contact our customer feedback department. Springer Nature |One New York Plaza, Suite 4500 | New York | NY 10004-1562 | USA Springer Nature's worldwide offices: London - Paris - Munich - New Delhi - Tokyo - Melbourne San Diego - San Francisco - Washington - New York - Boston Macmillan Publishers Limited is a company incorporated in England and Wales under company number 785998 and whose registered office is located at The Campus, 4 Crinan Street, London, N1 9XW. © 2017 Macmillan Publishers Limited, part of Springer Nature. All Rights Reserved.