Annals of Human Genetics

mtDNA Lineages Reveal Coronary Artery Disease-Associated Structures in the Lebanese Population
pp. 1-8(8)
Authors: Haber, Marc; Youhanna, Sonia C.; Balanovsky, Oleg; Saade, Stephanie; Martínez-Cruz, Begoña; Ghassibe-Sabbagh, Michella; Shasha, Nabil; Osman, Raed; el Bayeh, Hamid; Koshel, Sergey; Zaporozhchenko, Valery; Balanovska, Elena; Soria-Hernanz, David F.; Platt, Daniel E.; Zalloua, Pierre A.

Meta Analysis of the Association between <i>MTHFR</i> C677T Polymorphism and the Risk of Congenital Heart Defects
pp. 9-16(8)
Authors: Yin, Meng; Dong, Lingyan; Zheng, Jinghao; Zhang, Haibo; Liu, Jinfen; Xu, Zhiwei

Common Variants in <i>FTO</i> Are Not Significantly Associated with Obesity-Related Phenotypes among Samoans of Polynesia
pp. 17-24(8)
Authors: Karns, Rebekah; Viali, Satupaitea; Tuitele, John; Sun, Guangyun; Cheng, Hong; Weeks, Daniel E.; McGarvey, Stephen T.; Deka, Ranjan

Association of the Methylenetetrahydrofolate Reductase Gene A1298C Polymorphism with Male Infertility: A Meta-Analysis
pp. 25-32(8)
Authors: Shen, Ouxi; Liu, Renping; Wu, Wei; Yu, Lugang; Wang, Xinru

A Genome-Wide Search for Non-<i>UGT1A1</i> Markers Associated with Unconjugated Bilirubin Level Reveals Significant Association with a Polymorphic Marker Near a Gene of the Nucleoporin Family
pp. 33-41(9)
Authors: Datta, Shalini; Chowdhury, Abhijit; Ghosh, Malay; Das, Kaushik; Jha, Pankaj; Colah, Roshan; Mukerji, Mitali; Majumder, Partha P.

Differentiating Population Stratification from Genotyping Error Using Family Data
pp. 42-52(11)
Authors: Sebro, Ronnie; Lange, Christoph; Laird, Nan M.; Rogus, John J.; Risch, Neil J.

TRM: A Powerful Two-Stage Machine Learning Approach for Identifying SNP-SNP Interactions
pp. 53-62(10)
Authors: Lin, Hui-Yi; Ann Chen, Y.; Tsai, Ya-Yu; Qu, Xiaotao; Tseng, Tung-Sung; Park, Jong Y.

On the Validity of the Likelihood Ratio Test and Consistency of Resulting Parameter Estimates in Joint Linkage and Linkage Disequilibrium Analysis under Improperly Specified Parametric Models
pp. 63-73(11)
Authors: Hiekkalinna, Tero; Göring, Harald H. H.; Terwilliger, Joseph D.

Testing Rare Variants for Association with Diseases: A Bayesian Marker Selection Approach
pp. 74-85(12)
Authors: Zhang, Lei; Pei, Yu-Fang; Hai, Rong; Lin, Yong; Deng, Hong-Wen

Necessary and Sufficient Conditions for Equality of Sibling and Parent-Offspring Risk of a Disease Endophenotype in Case Families
pp. 86-91(6)
Authors: Sung, Heejong; Mendell, Nancy R.

Y-chromosome O3 Haplogroup Diversity in Sino-Tibetan Populations Reveals Two Migration Routes into the Eastern Himalayas
pp. 92-99(8)
Authors: Kang, Longli; Lu, Yan; Wang, Chuanchao; Hu, Kang; Chen, Feng; Liu, Kai; Li, Shilin; Jin, Li; Li, Hui; The Genographic Consortiumcr10,