Selection and mutation in the “new” genetics: an emerging hypothesis Bruce GottliebLenore K. BeitelMark A. Trifiro Review Article 23 January 2010 Pages: 491 - 501
Significant association of glutamate receptor, ionotropic N-methyl-d-aspartate 3A (GRIN3A), with nicotine dependence in European- and African-American smokers Jennie Z. MaThomas J. PayneMing D. Li Original Investigation 19 January 2010 Pages: 503 - 512
Kalirin: a novel genetic risk factor for ischemic stroke Tiago KrugHelena MansoSofia A. Oliveira Original Investigation 28 January 2010 Pages: 513 - 523
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility Rebecca L. ZuvichJacob L. McCauleyJonathan L. Haines Original Investigation 30 January 2010 Pages: 525 - 535
Distinct breakpoints in two cases with deletion in the Yp11.2 region in Japanese population Reiko KumagaiYoshitoshi SasakiKoji Dewa Original Investigation 03 February 2010 Pages: 537 - 543
Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss Hui-Mei HongJiann-Jou YangShuan-Yow Li Original Investigation 04 February 2010 Pages: 545 - 551
Erratum to: Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss Hui-Mei HongJiann-Jou YangShuan-Yow Li Erratum 21 February 2010 Pages: 553 - 553
Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly Ute HehrDaniel E. Pineda-AlvarezMaximilian Muenke Original Investigation 16 February 2010 Pages: 555 - 561
Population description and its role in the interpretation of genetic association Stephanie M. FullertonJoon-Ho YuWylie Burke Original Investigation 16 February 2010 Pages: 563 - 572
Ultra deep sequencing detects a low rate of mosaic mutations in tuberous sclerosis complex Wei QinPiotr KozlowskiDavid J. Kwiatkowski Original Investigation 18 February 2010 Pages: 573 - 582
Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease Jean MullerC. StoetzelH. Dollfus Original Investigation 23 February 2010 Pages: 583 - 593
Analysis of the indel at the ARMS2 3′UTR in age-related macular degeneration Gaofeng WangKylee L. SpencerMargaret A. Pericak-Vance Original Investigation 25 February 2010 Pages: 595 - 602
Digging deeper into East African human Y chromosome lineages Verónica GomesPaula Sánchez-DizLeonor Gusmão Original Investigation 06 March 2010 Pages: 603 - 613
Keith DiPetrillo (ed): “Cardiovascular Genomics: Methods and Protocols”. Springer Protocols—Methods in Molecular Biology Dhavendra Kumar Book Review 03 March 2010 Pages: 617 - 617