Alexandra K. Blomfield

Also affiliated with Upstate University Hospital

Biochemistry, Genetics and Molecular BiologyMedicineNeuroscience

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 6 papers. Top paper: “Ectopic Rod Photoreceptor Development in Mice with Genetic Deficiency of WNT2B”.

Ectopic Rod Photoreceptor Development in Mice with Genetic Deficiency of WNT2B

Cells(2023)10.3390/cells12071033

N/A

0.208DataRank · unranked

3 citations

Meenakshi Maurya, Kiran Bora, Madeline C. Pavlovich, Felix Yemanyi, Shuo Huang +4 more

Genetic deficiency of ribosomal rescue factor HBS1L causes retinal dystrophy associated with Pelota and EDF1 depletion

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.10.18.562924

N/A

0.104DataRank · unranked

1 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more

Wnt Signaling in Inner Blood–Retinal Barrier Maintenance

International Journal of Molecular Sciences(2021)10.3390/ijms222111877

N/A

0DataRank · unranked

45 citations

Kiran Bora, Alexandra K. Blomfield, Zhongxiao Wang, Jing Chen, Felix Yemanyi

Endothelial Cell Transcytosis Assay as an In Vitro Model to Evaluate Inner Blood-Retinal Barrier Permeability

Journal of Visualized Experiments(2022)10.3791/64076

N/A

0DataRank · unranked

6 citations

Zhongxiao Wang, Felix Yemanyi, Meenakshi Maurya, Alexandra K. Blomfield, Yohei Tomita +2 more

Genetic deficiency and pharmacological modulation of RORα regulate laser-induced choroidal neovascularization

Aging(2023)10.18632/aging.204480

N/A

0DataRank · unranked

5 citations

Felix Yemanyi, Kiran Bora, Neetu Kushwah, Alexandra K. Blomfield, Theodore M. Kamenecka +5 more

HBS1L deficiency causes retinal dystrophy in a child and in a mouse model associated with defective development of photoreceptor cells

Disease Models & Mechanisms(2024)10.1242/dmm.050557

N/A

0DataRank · unranked

3 citations

Bilal K. AlWattar, Qifei Li, Kiran Bora, Alexandra K. Blomfield, Jasmine Lin +4 more