Annals of Human Genetics

A Genome-wide Association Study of Autism Reveals a Common Novel Risk Locus at 5p14.1
pp. 263-273(11)
Authors: Ma, Deqiong; Salyakina, Daria; Jaworski, James M.; Konidari, Ioanna; Whitehead, Patrice L.; Andersen, Ashley N.; Hoffman, Joshua D.; Slifer, Susan H.; Hedges, Dale J.; Cukier, Holly N.; Griswold, Anthony J.; McCauley, Jacob L.; Beecham, Gary W.; Wright, Harry H.; Abramson, Ruth K.; Martin, Eden R.; Hussman, John P.; Gilbert, John R.; Cuccaro, Michael L.; Haines, Jonathan L.; Pericak-Vance, Margaret A.

SNP Discovery and Haplotype Analysis in the Segmentally Duplicated DRD5 Coding Region
pp. 274-282(9)
Authors: Housley, Donna J. E.; Nikolas, Molly; Venta, Patrick J.; Jernigan, Kathrine A.; Waldman, Irwin D.; Nigg, Joel T.; Friderici, Karen H.

New Mutations of EXT1 and EXT2 Genes in German Patients with Multiple Osteochondromas
pp. 283-291(9)
Authors: Heinritz, Wolfram; Hüffmeier, Ulrike; Strenge, Sibylle; Miterski, Bianca; Zweier, Christiane; Leinung, Steffen; Bohring, Axel; Mitulla, Beate; Peters, Usha; Froster, Ursula G.

High-resolution Melting Facilitates Mutation Screening of PYGM in Patients with McArdle Disease
pp. 292-297(6)
Authors: Duno, Morten; Quinlivan, Ros; Vissing, John; Schwartz, Marianne

Revisiting MSUD in Portuguese Gypsies: Evidence for a Founder Mutation and for a Mutational Hotspot within the BCKDHA Gene
pp. 298-303(6)
Authors: Quental, Sofia; Gusmão, Alfredo; Rodríguez-Pombo, Pilar; Ugarte, Magdalena; Vilarinho, Laura; Amorim, António; Prata, Maria J.

Genetic Admixture in Brazilians Exposed to Infection with Leishmania chagasi
pp. 304-313(10)
Authors: Ettinger, Nicholas A.; Duggal, Priya; Braz, Regina F. S.; Nascimento, Eliana T.; Beaty, Terri H.; Jeronimo, Selma M. B.; Pearson, Richard D.; Blackwell, Jenefer M.; Moreno, Lina; Wilson, Mary E.

Inter- and Extra-Indian Admixture and Genetic Diversity in Reunion Island Revealed by Analysis of Mitochondrial DNA
pp. 314-334(21)
Authors: Dubut, Vincent; Murail, Pascal; Pech, Nicolas; Thionville, Marie-Dominique; Cartault, François

Refined Geographic Distribution of the Oriental ALDH2*504Lys (nee 487Lys) Variant
pp. 335-345(11)
Authors: Li, Hui; Borinskaya, Svetlana; Yoshimura, Kimio; Kal'ina, Nina; Marusin, Andrey; Stepanov, Vadim A.; Qin, Zhendong; Khaliq, Shagufta; Lee, Mi-Young; Yang, Yajun; Mohyuddin, Aisha; Gurwitz, David; Mehdi, Syed Qasim; Rogaev, Evgeny; Jin, Li; Yankovsky, Nikolay K.; Kidd, Judith R.; Kidd, Kenneth K.

Using Case-parent Triads to Estimate Relative Risks Associated with a Candidate Haplotype
pp. 346-359(14)
Authors: Shi, Min; Umbach, David M.; Weinberg, Clarice R.

Evaluating the Ability of Tree-Based Methods and Logistic Regression for the Detection of SNP-SNP Interaction
pp. 360-369(10)
Authors: García-Magariños, M.; López-de-Ullibarri, I.; Cao, R.; Salas, A.

The Cost Effectiveness of Duplicate Genotyping for Testing Genetic Association
pp. 370-378(9)
Authors: Tintle, Nathan; Gordon, Derek; Van Bruggen, Dirk; Finch, Stephen

CALHM1 Polymorphism is not Associated with Late-onset Alzheimer Disease
pp. 379-381(3)
Authors: Beecham, Gary W.; Schnetz-Boutaud, Nathalie; Haines, Jonathan L.; Pericak-Vance, Margaret A.

Spastic Paraplegia, Optic Atrophy, and Neuropathy: New Observations, Locus Refinement, and Exclusion of Candidate Genes
pp. 382-387(6)
Authors: Macedo-Souza, Lúcia Inês; Kok, Fernando; Santos, Silvana; Licinio, Luciana; Lezirovitz, Karina; Cavaçana, Natale; Bueno, Clarissa; Amorim, Simone; Pessoa, André; Graciani, Zodja; Ferreira, Áurea; Prazeres, Abdísio; de Melo, Áurea Nogueira; Otto, Paulo Alberto; Zatz, Mayana