Annals of Human Genetics

An Analysis Paradigm for Investigating Multi-locus Effects in Complex Disease: Examination of Three GABA_A Receptor Subunit Genes on 15q11-q13 as Risk Factors for Autistic Disorder.
pp. 281-292(12)
Authors: Ashley-Koch, A. E.; Mei, H.; Jaworski, J.; Ma, D. Q.; Ritchie, M. D.; Menold, M. M.; Delong, G. R.; Abramson, R. K.; Wright, H. H.; Hussman, J. P.; Cuccaro, M. L.; Gilbert, J. R.; Martin, E. R.; Pericak-Vance, M. A.

Obesity is Associated with Genetic Variants That Alter Dopamine Availability
pp. 293-303(11)
Authors: Need, A. C.; Ahmadi, K. R.; Spector, T. D.; Goldstein, D. B.

A Frequent Partial AZFc Deletion does not Render an Increased Risk of Spermatogenic Impairment in East Asians
pp. 304-313(10)
Authors: Zhang, F.; Li, Z.; Wen, B.; Jiang, J.; Shao, M.; Zhao, Y.; He, Y.; Song, X.; Qian, J.; Lu, D.; Jin, L.

Quality Assessment of DNA Sequence Data: Autopsy of A Mis-Sequenced mtDNA Population Sample
pp. 314-326(13)
Authors: Bandelt, H.-J.; Kivisild, T.

The Patient is Not Dead Yet: Premature Autopsy of a mtDNA Data Set
pp. 327-331(5)
Authors: Stoneking, M.; Nasidze, I.

Design and Analysis of Genetic Association Studies to Finely Map a Locus Identified by Linkage Analysis: Sample Size and Power Calculations
pp. 332-349(18)
Authors: Hanson, R. L.; Looker, H. C.; Ma, L.; Muller, Y. L.; Baier, L. J.; Knowler, W. C.

A Comparison of Individual Genotyping and Pooled DNA Analysis for Polymorphism Validation Prior to Large-Scale Genetic Studies
pp. 350-359(10)
Authors: Yang, H.-C.; Lin, C.-H.; Hung, S.-I.; Fann, C. S. J.

Appropriate Use of Information on Family History of Disease in Recruitment for Linkage Analysis Studies
pp. 360-371(12)
Authors: Wallace, C.; Clayton, D.G.

Multiple Imputation of Missing Genotype Data for Unrelated Individuals
pp. 372-381(10)
Authors: Souverein, O. W.; Zwinderman, A. H.; Tanck, M. W. T.

Case-parent Triads: Estimating Single- and Double-dose Effects of Fetal and Maternal Disease Gene Haplotypes
pp. 382-396(15)
Authors: GJESSING, H. K.; LIE, R. T.

Detecting linkage disequilibrium in the presence of locus heterogeneity
pp. 397-409(13)
Authors: Wang, D.; Huang, J.

Study of the PVRL1 Gene in Italian Nonsyndromic Cleft Lip Patients with or without Cleft Palate
pp. 410-413(4)
Authors: Scapoli, L.; Palmieri, A.; Martinelli, M.; Vaccari, C.; Marchesini, J.; Pezzetti, F.; Baciliero, U.; Padula, E.; Carinci, P.; Carinci, F.

Myotilin is not the Causative Gene for Vocal Cord and Pharyngeal Weakness with Distal Myopathy (VCPDM)
pp. 414-416(3)
Authors: Garvey, Sean M.; Senderek, Jan; Beckmann, Jacques S.; Seboun, Eric; Jackson, Charles E.; Hauser, Michael A.