Inventor · disambiguated record
Corey D. Braastad
Also filed as: BRAASTAD COREY · BRAASTAD COREY D
10 granted patents·4 pending applications·12 citations·filing 2007–2025
84Inventor score
Top patents by PatentIndex Score
14 records- 0188US7704691B2Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)ATHENA DIAGNOSTICS INC·Filed 2007·Granted Apr 27, 2010·6 cites·19 claims
- 0284US8785122B2Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)BRAASTAD COREY D·Filed 2012·Granted Jul 22, 2014·3 cites·17 claims
- 0383US12497658B2Methods to detect a silent carrier genotypeATHENA DIAGNOSTICS INC·Filed 2023·Granted Dec 16, 2025·0 cites·11 claims
- 0483US8192933B2Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)BRAASTAD COREY D·Filed 2010·Granted Jun 5, 2012·3 cites·17 claims
- 0575US11512352B2Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)ATHENA DIAGNOSTICS INC·Filed 2019·Granted Nov 29, 2022·0 cites·8 claims
- 0672US10697016B2Methods to detect a silent carrier genotypeATHENA DIAGNOSTICS INC·Filed 2019·Granted Jun 30, 2020·0 cites·10 claims
- 0772US9611512B2Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)ATHENA DIAGNOSTICS INC·Filed 2014·Granted Apr 4, 2017·0 cites·7 claims
- 0867US2020385807A1Methods to detect a silent carrier genotypeATHENA DIAGNOSTICS INC·Filed 2020·Application pending·0 cites
- 0966US2017166970A1Methods of detecting mutations associated with ataxia-ocular apraxia 2 (aoa2)ATHENA DIAGNOSTICS INC·Filed 2017·Application pending·0 cites
- 1064US10762981B2Pathogenicity scoring system for human clinical geneticsATHENA DIAGNOSTICS INC·Filed 2014·Granted Sep 1, 2020·0 cites·13 claims
- 1162US10227650B2Methods to detect a silent carrier of a null allele genotypeATHENA DIAGNOSTICS INC·Filed 2015·Granted Mar 12, 2019·0 cites·32 claims
- 1261US2025232835A1Pathogenicity scoring system for human clinical geneticsATHENA DIAGNOSTICS INC·Filed 2025·Application pending·0 cites
- 1360US2020411134A1Pathogenicity scoring system for human clinical geneticsATHENA DIAGNOSTICS INC·Filed 2020·Application pending·0 cites
- 1459US7811762B2Identification of a novel gene underlying familial spastic paraplegiaUNIV DUKE·Filed 2007·Granted Oct 12, 2010·0 cites·20 claims
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →