Homozygosity Mapping Reveals Null Mutations in FAM161A as a Cause of Autosomal-Recessive Retinitis Pigmentosa

Primer3 on the WWW for General Users and for Biologist Programmers

Steve Rozen, Helen Skaletsky · Humana Press eBooks · 2003 · 15K citations

Engineering, Genetics, Molecular Biology +24

A Human Protein-Protein Interaction Network: A Resource for Annotating the Proteome

Ulrich Stelzl, Uwe Worm, Christian Haenig et al. · Cell · 2005 · 2.4K citations · Full text

Proteomic Technology, Functional Genomics, Interactomics +13

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

Thaddeus P. Dryja, Terri L. McGee, Elias Reichel et al. · Nature · 1990 · 1.1K citations

Retinitis Pigmentosa, Genetics, Pathogenesis +5

Crx, a Novel otx-like Homeobox Gene, Shows Photoreceptor-Specific Expression and Regulates Photoreceptor Differentiation

Takahisa Furukawa, Eric M. Morrow, Constance L. Cepko · Cell · 1997 · 904 citations · Full text

Photoreceptor Cell, Developmental Biology, Molecular Physiology +10

Mutations in the CEP290 (NPHP6) Gene Are a Frequent Cause of Leber Congenital Amaurosis

Anneke I. den Hollander, Robert K. Koenekoop, Suzanne Yzer et al. · The American Journal of Human Genetics · 2006 · 670 citations · Full text

Developmental Biology, Genetic Disorder, Genetics +7