1. Selection and mutation in the “new” genetics: an emerging hypothesis

   • Bruce Gottlieb
   • Lenore K. Beitel
   • Mark A. Trifiro

   Review Article 23 January 2010 Pages: 491 - 501

   

2. Significant association of glutamate receptor, ionotropic N-methyl-d-aspartate 3A (GRIN3A), with nicotine dependence in European- and African-American smokers

   • Jennie Z. Ma
   • Thomas J. Payne
   • Ming D. Li

   Original Investigation 19 January 2010 Pages: 503 - 512

   

3. Kalirin: a novel genetic risk factor for ischemic stroke

   • Tiago Krug
   • Helena Manso
   • Sofia A. Oliveira

   Original Investigation 28 January 2010 Pages: 513 - 523

   

4. Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility

   • Rebecca L. Zuvich
   • Jacob L. McCauley
   • Jonathan L. Haines

   Original Investigation 30 January 2010 Pages: 525 - 535

5. Distinct breakpoints in two cases with deletion in the Yp11.2 region in Japanese population

   • Reiko Kumagai
   • Yoshitoshi Sasaki
   • Koji Dewa

   Original Investigation 03 February 2010 Pages: 537 - 543

   

6. Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss

   • Hui-Mei Hong
   • Jiann-Jou Yang
   • Shuan-Yow Li

   Original Investigation 04 February 2010 Pages: 545 - 551

   

7. Erratum to: Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss

   • Hui-Mei Hong
   • Jiann-Jou Yang
   • Shuan-Yow Li

   Erratum 21 February 2010 Pages: 553 - 553

8. Heterozygous mutations in SIX3 and SHH are associated with schizencephaly and further expand the clinical spectrum of holoprosencephaly

   • Ute Hehr
   • Daniel E. Pineda-Alvarez
   • Maximilian Muenke

   Original Investigation 16 February 2010 Pages: 555 - 561

   

9. Population description and its role in the interpretation of genetic association

   • Stephanie M. Fullerton
   • Joon-Ho Yu
   • Wylie Burke

   Original Investigation 16 February 2010 Pages: 563 - 572

10. Ultra deep sequencing detects a low rate of mosaic mutations in tuberous sclerosis complex

    • Wei Qin
    • Piotr Kozlowski
    • David J. Kwiatkowski

    Original Investigation 18 February 2010 Pages: 573 - 582

    

11. Identification of 28 novel mutations in the Bardet–Biedl syndrome genes: the burden of private mutations in an extensively heterogeneous disease

    • Jean Muller
    • C. Stoetzel
    • H. Dollfus

    Original Investigation 23 February 2010 Pages: 583 - 593

    

12. Analysis of the indel at the ARMS2 3′UTR in age-related macular degeneration

    • Gaofeng Wang
    • Kylee L. Spencer
    • Margaret A. Pericak-Vance

    Original Investigation 25 February 2010 Pages: 595 - 602

    

13. Digging deeper into East African human Y chromosome lineages

    • Verónica Gomes
    • Paula Sánchez-Diz
    • Leonor Gusmão

    Original Investigation 06 March 2010 Pages: 603 - 613

    

14. Peter Harper: Myotonic dystrophy

    • Sandeep Jayawant

    Book Review 16 February 2010 Pages: 615 - 615

15. Keith DiPetrillo (ed): “Cardiovascular Genomics: Methods and Protocols”. Springer Protocols—Methods in Molecular Biology

    • Dhavendra Kumar

    Book Review 03 March 2010 Pages: 617 - 617