Articles Accessed Most Frequently

These are the Top 20 Papers (by download) for the 30 days preceding May 17, 2008.

Article Information Date
1. The Dawn of Human Matrilineal Diversity
 Doron M. Behar, Richard Villems, Himla Soodyall, Jason Blue-Smith, Luisa Pereira, Ene Metspalu, Rosaria Scozzari, Heeran Makkan, Shay Tzur, David Comas et al.
Abstract | | | Supplemental Data
 9 May 2008
82(5)
2. Two Sources of the Russian Patrilineal Heritage in Their Eurasian Context
 Oleg Balanovsky, Siiri Rootsi, Andrey Pshenichnov, Toomas Kivisild, Michail Churnosov, Irina Evseeva, Elvira Pocheshkhova, Margarita Boldyreva, Nikolay Yankovsky, Elena Balanovska et al.
Abstract | |
10 January 2008
82(1)
3. On the Replication of Genetic Associations: Timing Can Be Everything!
 Jessica Lasky-Su, Helen N. Lyon, Valur Emilsson, Iris M. Heid, Cliona Molony, Benjamin A. Raby, Ross Lazarus, Barbara Klanderman, Manuel E. Soto-Quiros, Lydiana Avila et al.
Abstract | |
11 April 2008
82(4)
4. Bayesian Meta-Analysis of Genetic Association Studies with Different Sets of Markers
 Claudio Verzilli, Tina Shah, Juan P. Casas, Juliet Chapman, Manjinder Sandhu, Sally L. Debenham, Matthijs S. Boekholdt, Kay Tee Khaw, Nicholas J. Wareham, Richard Judson et al.
Abstract | | | Supplemental Data
 11 April 2008
82(4)
5. Y-Chromosomal Diversity in Lebanon Is Structured by Recent Historical Events
 Pierre A. Zalloua, Yali Xue, Jade Khalife, Nadine Makhoul, Labib Debiane, Daniel E. Platt, Ajay K. Royyuru, Rene J. Herrera, David F. Soria Hernanz, Jason Blue-Smith et al.
Abstract | | | Supplemental Data
 11 April 2008
82(4)
6. A Bayesian Evaluation of Human Mitochondrial Substitution Rates
 Phillip Endicott, Simon Y.W. Ho
Abstract | | | Supplemental Data
 11 April 2008
82(4)
7. Phenotypically Concordant and Discordant Monozygotic Twins Display Different DNA Copy-Number-Variation Profiles
 Carl E.G. Bruder, Arkadiusz Piotrowski, Antoinet A.C.J. Gijsbers, Robin Andersson, Stephen Erickson, Teresita Diaz de Ståhl, Uwe Menzel, Johanna Sandgren, Desiree von Tell, Andrzej Poplawski et al.
Abstract | | | Supplemental Data
 3 March 2008
82(3)
8. Mitochondrial Population Genomics Supports a Single Pre-Clovis Origin with a Coastal Route for the Peopling of the Americas
 Nelson J.R. Fagundes, Ricardo Kanitz, Roberta Eckert, Ana C.S. Valls, Mauricio R. Bogo, Francisco M. Salzano, David Glenn Smith, Wilson A. Silva, Marco A. Zago, Andrea K. Ribeiro-dos-Santos et al.
Abstract | |
3 March 2008
82(3)
9. Mapping of Small RNAs in the Human ENCODE Regions
 Christelle Borel, Maryline Gagnebin, Corinne Gehrig, Evgenia V. Kriventseva, Evgeny M. Zdobnov, Stylianos E. Antonarakis
Abstract | | | Supplemental Data
 11 April 2008
82(4)
10. Common Breast Cancer-Predisposition Alleles Are Associated with Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
 Antonis C. Antoniou, Amanda B. Spurdle, Olga M. Sinilnikova, Sue Healey, Karen A. Pooley, Rita K. Schmutzler, Beatrix Versmold, Christoph Engel, Alfons Meindl, Norbert Arnold et al.
Abstract | | | Supplemental Data
 11 April 2008
82(4)
11. Genetic Architecture of Transcript-Level Variation in Humans
 Shiwei Duan, R. Stephanie Huang, Wei Zhang, Wasim K. Bleibel, Cheryl A. Roe, Tyson A. Clark, Tina X. Chen, Anthony C. Schweitzer, John E. Blume, Nancy J. Cox et al.
Abstract | | | Supplemental Data
 9 May 2008
82(5)
12. A Critical Appraisal of the Scientific Basis of Commercial Genomic Profiles Used to Assess Health Risks and Personalize Health Interventions
 A. Cecile J.W. Janssens, Marta Gwinn, Linda A. Bradley, Ben A. Oostra, Cornelia M. van Duijn, Muin J. Khoury
Abstract | | | Supplemental Data
 3 March 2008
82(3)
13. SNP Arrays in Heterogeneous Tissue: Highly Accurate Collection of Both Germline and Somatic Genetic Information from Unpaired Single Tumor Samples
 Guillaume Assié, Thomas LaFramboise, Petra Platzer, Jérôme Bertherat, Constantine A. Stratakis, Charis Eng
Abstract | | | Supplemental Data
 11 April 2008
82(4)
14. SLC9A6 Mutations Cause X-Linked Mental Retardation, Microcephaly, Epilepsy, and Ataxia, a Phenotype Mimicking Angelman Syndrome
 Gregor D. Gilfillan, Kaja K. Selmer, Ingrid Roxrud, Raffaella Smith, Mårten Kyllerman, Kristin Eiklid, Mette Kroken, Morten Mattingsdal, Thore Egeland, Harald Stenmark et al.
Abstract | | | Supplemental Data
 11 April 2008
82(4)
15. Mutations in the GIGYF2 (TNRC15) Gene at the PARK11 Locus in Familial Parkinson Disease
 Corinne Lautier, Stefano Goldwurm, Alexandra Dürr, Barbara Giovannone, William G. Tsiaras, Gianni Pezzoli, Alexis Brice, Robert J. Smith
Abstract | |
11 April 2008
82(4)
16. Walking the Interactome for Prioritization of Candidate Disease Genes
 Sebastian Köhler, Sebastian Bauer, Denise Horn, Peter N. Robinson
Abstract | | | Supplemental Data
 11 April 2008
82(4)
17. Analysis of Genomic Admixture in Uyghur and Its Implication in Mapping Strategy
 Shuhua Xu, Wei Huang, Ji Qian, Li Jin
Abstract | | | Supplemental Data
 11 April 2008
82(4)
18. Identification of the SPG15 Gene, Encoding Spastizin, as a Frequent Cause of Complicated Autosomal-Recessive Spastic Paraplegia, Including Kjellin Syndrome
 Sylvain Hanein, Elodie Martin, Amir Boukhris, Paula Byrne, Cyril Goizet, Abdelmadjid Hamri, Ali Benomar, Alexander Lossos, Paola Denora, José Fernandez et al.
Abstract | | | Supplemental Data
 11 April 2008
82(4)
19. Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Is a Fully Penetrant, Lethal Arrhythmic Disorder Caused by a Missense Mutation in the TMEM43 Gene
 Nancy D. Merner, Kathy A. Hodgkinson, Annika F.M. Haywood, Sean Connors, Vanessa M. French, Jörg-Detlef Drenckhahn, Christine Kupprion, Kalina Ramadanova, Ludwig Thierfelder, William McKenna et al.
Abstract | | | Supplemental Data
 11 April 2008
82(4)
20. Estimating Odds Ratios in Genome Scans: An Approximate Conditional Likelihood Approach
 Arpita Ghosh, Fei Zou, Fred A. Wright
Abstract | | | Supplemental Data
 9 May 2008
82(5)