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32199 publications found in the database

*2012 (1980)

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

2012 Publications

Transcription factors ETS2 and MESP1 transdifferentiate human dermal fibroblasts into cardiac progenitors
Islas, J. F. et al. Proceedings of the National Academy of Sciences of the United States of America 109(32), 13016-21, 2012, Mouse Genome 430A 2.0 Array  PubMed

No Association of a Set of Candidate Genes on Haloperidol Side Effects
Drago, A. et al. Plos One 7(10), NPG, 2012, Human Mapping 500K Array SetMapping 500K  PubMed

Two novel CCDC88C mutations confirm the role of DAPLE in autosomal recessive congenital hydrocephalus
Drielsma, A. et al. Journal of Medical Genetics 49(11), 708-12, 2012, Human Mapping 500K Array SetMapping 500K  PubMed

TCTN3 Mutations Cause Mohr-Majewski Syndrome
Thomas, S. et al. American Journal of Human Genetics 91(2), 372-8, 2012, Human Mapping 500K Array SetMapping 500K  PubMed

A Functional Copy-Number Variation in MAPKAPK2 Predicts Risk and Prognosis of Lung Cancer
Liu, B. et al. American Journal of Human Genetics 91(2), 384-90, 2012, Genome-Wide Human SNP Array 6.0  PubMed

Aberrant activation of ALK kinase by a novel truncated form ALK protein in neuroblastoma
Okubo, J. et al. Oncogene 31(44), 4667-76, 2012, Human Mapping 500K Array SetMapping 500K  PubMed

Genome-wide analysis of EGR2/SOX10 binding in myelinating peripheral nerve
Srinivasan, R. et al. Nucleic Acids Research 40(14), 6449-60, 2012, Rat Gene 1.0 ST Array  PubMed

Van Maldergem syndrome: further characterisation and evidence for neuronal migration abnormalities and autosomal recessive inheritance
Mansour, S. et al. European Journal of Human Genetics 20(10), 1024-31, 2012, Human Mapping 500K Array SetMapping 500K  PubMed

Copy-Number Gains of HUWE1 Due to Replication- and Recombination-Based Rearrangements
Froyen, G. et al. American Journal of Human Genetics 91(2), 252-64, 2012, Genome-Wide Human SNP Array 6.0  PubMed

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