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Human Molecular Genetics, Vol. 10, Iss. 16, 2001-08 ,pp. : 1619-1626

Oxford University Press

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Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration

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Oxford University Press

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The 2014 International Workshop on Statistical Genetic Methods for Human Complex Traits (Formerly the ‘Methodology of Twin and Family Studies Introductory Workshop’): March 3rd–March 7th, 2014

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Behavior Genetics, Vol. 43, Iss. 6, 2013-11 ,pp. : 559-560

Springer Publishing Company

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In vivo function of the orphan nuclear receptor NR2E3 in establishing photoreceptor identity during mammalian retinal development

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Human Molecular Genetics, Vol. 15, Iss. 17, 2006-09 ,pp. : 2588-2602

Oxford University Press

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The photoreceptor-specific nuclear receptor Nr2e3 interacts with Crx and exerts opposing effects on the transcription of rod versus cone genes

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Human Molecular Genetics, Vol. 14, Iss. 6, 2005-03 ,pp. : 747-764

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