Immediate Impact

12 standout
Sub-graph 1 of 6

Citing Papers

Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes
2024 Standout
Engineered virus-like particles for transient delivery of prime editor ribonucleoprotein complexes in vivo
2024 Standout
4 intermediate papers

Works of Raúl Ayala-Ramírez being referenced

ABCA4 mutational spectrum in Mexican patients with Stargardt disease: Identification of 12 novel mutations and evidence of a founder effect for the common p.A1773V mutation
2013
A new autosomal recessive syndrome consisting of posterior microphthalmos, retinitis pigmentosa, foveoschisis, and optic disc drusen is caused by a MFRP gene mutation.
2006
and 3 more

Author Peers

Author Last Decade Papers Cites
Raúl Ayala-Ramírez 193 207 150 12 320
Ayse G. Koçak-Altintas 98 154 138 10 341
Jan-Willem R. Pott 172 284 70 8 327
Ilangovan Raju 49 181 42 12 324
Sanaa Muheisen 58 235 119 14 290
Jean-Louis Dufier 82 170 61 8 282
Sara Moore 99 92 117 10 330
Carla J. Ramos 137 183 56 12 368
Luísa Coutinho Santos 139 213 154 11 362
Kaoru Tsujikawa 134 149 29 15 346
David F. Gilmour 142 216 48 13 354

All Works

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Rankless by CCL
2026