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32199 publications found in the database

*2011 (1784)

*Starting in 2010, coverage has been refocused on core journals.

2011 Publications

A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases
Ostergaard, E. et al. Molecular Vision 17(167), 1485-92, 2011, Mapping 100K Set  PubMed

Genome-Wide Association Study of Schizophrenia in Japanese Population
Yamada, K. et al. Plos One 6(6), NPG, 2011, Mapping 100K Set  PubMed

RDH12 retinopathy: novel mutations and phenotypic description
Mackay, D. S. et al. Molecular Vision 17(293-95), 2706-16, 2011, Mapping 100K Set  PubMed

Population Genetic Structure of Peninsular Malaysia Malay Sub-Ethnic Groups
Hatin, W. I. et al. Plos One 6(4), NPG, 2011, Mapping 100K Set  PubMed

A novel 1-bp deletion in PITX3 causing congenital posterior polar cataract
Berry, V. et al. Molecular Vision 17(140), 1249-53, 2011, Mapping 100K Set  PubMed

Identification of Close Relatives in the HUGO Pan-Asian SNP Database
Yang, X. et al. Plos One 6(12), NPG, 2011, Mapping 100K Set  PubMed

Ancestry of the Iban Is Predominantly Southeast Asian: Genetic Evidence from Autosomal, Mitochondrial, and Y Chromosomes
Simonson, T. S. et al. Plos One 6(1), NPG, 2011, Mapping 100K Set  PubMed

A genome-wide analysis of population structure in the Finnish Saami with implications for genetic association studies
Huyghe, J. R. et al. European Journal of Human Genetics 19(3), 347-52, 2011, Mapping 100K Set  PubMed

FAF1, a Gene that Is Disrupted in Cleft Palate and Has Conserved Function in Zebrafish
Ghassibe-Sabbagh, M. et al. American Journal of Human Genetics 88(2), 150-61, 2011, Mapping 100K Set  PubMed

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