Year |
Citation |
Score |
2022 |
Parra MM, Spoth E, Ronquillo CC, Henderson R, Hartnett ME. Multimodal Retinal Imaging Findings in Two Cousins With VCAN-Related Vitreoretinopathy or Wagner Disease. Ophthalmic Surgery, Lasers & Imaging Retina. 53: 639-643. PMID 36378611 DOI: 10.3928/23258160-20221026-01 |
0.333 |
|
2019 |
Ronquillo CC, Sauer L, Morgan D, Heckzo JB, Creel DJ, Mamalis N, DeAngelis MM, Hagemann GS, Bernstein PS. ABSENCE OF MACULAR DEGENERATION IN A PATIENT WITH ACERULOPLASMINEMIA. Retina (Philadelphia, Pa.). PMID 31356495 DOI: 10.1097/Iae.0000000000002628 |
0.319 |
|
2018 |
Ronquillo CC, Wegner K, Calvo CM, Bernstein PS. Genetic Penetrance of Macular Telangiectasia Type 2. Jama Ophthalmology. PMID 30098143 DOI: 10.1001/Jamaophthalmol.2018.3283 |
0.319 |
|
2016 |
Ronquillo CC, Hanke-Gogokhia C, Revelo MP, Frederick JM, Jiang L, Baehr W. Ciliopathy-associated IQCB1/NPHP5 protein is required for mouse photoreceptor outer segment formation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. PMID 27328943 DOI: 10.1096/Fj.201600511R |
0.543 |
|
2016 |
Rao KN, Zhang W, Li L, Ronquillo C, Baehr W, Khanna H. Ciliopathy-associated protein CEP290 modifies the severity of retinal degeneration due to loss of RPGR. Human Molecular Genetics. PMID 26936822 DOI: 10.1093/Hmg/Ddw075 |
0.637 |
|
2015 |
Jiang L, Wei Y, Ronquillo CC, Marc RE, Yoder BK, Frederick JM, Baehr W. Heterotrimeric kinesin-2 (KIF3) mediates transition zone and axoneme formation of mouse photoreceptors. The Journal of Biological Chemistry. 290: 12765-78. PMID 25825494 DOI: 10.1074/Jbc.M115.638437 |
0.623 |
|
2012 |
Ronquillo CC, Bernstein PS, Baehr W. Senior-Løken syndrome: a syndromic form of retinal dystrophy associated with nephronophthisis. Vision Research. 75: 88-97. PMID 22819833 DOI: 10.1016/J.Visres.2012.07.003 |
0.603 |
|
2008 |
Tong Z, Yang Z, Patel S, Chen H, Gibbs D, Yang X, Hau VS, Kaminoh Y, Harmon J, Pearson E, Buehler J, Chen Y, Yu B, Tinkham NH, Zabriskie NA, ... ... Ronquillo CC, et al. Promoter polymorphism of the erythropoietin gene in severe diabetic eye and kidney complications. Proceedings of the National Academy of Sciences of the United States of America. 105: 6998-7003. PMID 18458324 DOI: 10.1073/Pnas.0800454105 |
0.588 |
|
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