Inventor · disambiguated record
Akiko Noma
Also filed as: NOMA AKIKO
7 granted patents·2 pending applications·11 citations·filing 2018–2024
78Inventor score
Files withCRISPR THERAPEUTICS AG9
Top patents by PatentIndex Score
9 records- 0191US12122998B2Materials and methods for treatment of usher syndrome type 2A and/or non-syndromic autosomal recessive retinitis pigmentosa (ARRP)CRISPR THERAPEUTICS AG·Filed 2021·Granted Oct 22, 2024·2 cites·22 claims
- 0289US11072792B2Materials and methods for treatment of usher syndrome type 2ACRISPR THERAPEUTICS AG·Filed 2020·Granted Jul 27, 2021·2 cites·16 claims
- 0388US11118177B2Materials and methods for treatment of Usher syndrome type 2A and/or non-syndromic autosomal recessive retinitis pigmentosa (ARRP)CRISPR THERAPEUTICS AG·Filed 2020·Granted Sep 14, 2021·3 cites·2 claims
- 0487US10662425B2Materials and methods for treatment of autosomal dominant retinitis pigmentosaCRISPR THERAPEUTICS AG·Filed 2018·Granted May 26, 2020·3 cites·30 claims
- 0586US12215316B2Materials and methods for treatment of usher syndrome type 2ACRISPR THERAPEUTICS AG·Filed 2021·Granted Feb 4, 2025·1 cites·7 claims
- 0679US2025122497A1Materials and methods for treatment of usher syndrome type 2a and/or non-syndromic autosomal recessive retinitis pigmentosa (arrp)CRISPR THERAPEUTICS AG·Filed 2024·Application pending·0 cites
- 0761US12247201B2Materials and methods for treatment of autosomal dominant retinitis pigmentosaCRISPR THERAPEUTICS AG·Filed 2020·Granted Mar 11, 2025·0 cites·30 claims
- 0860US10995328B2Materials and methods for treatment of autosomal dominant cone-rod dystrophyCRISPR THERAPEUTICS AG·Filed 2020·Granted May 4, 2021·0 cites·16 claims
- 0959US2022081680A1Materials and methods for treatment of autosomal dominant cone-rod dystrophyCRISPR THERAPEUTICS AG·Filed 2021·Application pending·0 cites
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →