Assignee
ATHENA DIAGNOSTICS INC
US·20 granted patents·7 pending applications·39 citations·filing 1996–2025
Top patents by PatentIndex Score
27 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
- 0283US12497658B2Methods to detect a silent carrier genotypeATHENA DIAGNOSTICS INC·Filed 2023·Granted Dec 16, 2025·0 cites·11 claims
- 0379US7521190B2Compositions and methods for genetic analysis of polycystic kidney diseaseATHENA DIAGNOSTICS INC·Filed 2007·Granted Apr 21, 2009·2 cites·14 claims
- 0476US7273701B2Compositions and methods for genetic analysis of polycystic kidney diseaseATHENA DIAGNOSTICS INC·Filed 2003·Granted Sep 25, 2007·6 cites·18 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
- 0675US6916619B2Compositions and methods for genetic analysis of polycystic kidney diseaseATHENA DIAGNOSTICS INC·Filed 2002·Granted Jul 12, 2005·6 cites·23 claims
- 0773US7824860B2Application of aprataxin gene to diagnosis and treatment for early-onset spinocerebellar ataxia (EAOH)ATHENA DIAGNOSTICS INC·Filed 2006·Granted Nov 2, 2010·2 cites·13 claims
- 0873US2023374593A1Pkd mutations and evaluation of sameATHENA DIAGNOSTICS INC·Filed 2023·Application pending·0 cites
- 0972US10697016B2Methods to detect a silent carrier genotypeATHENA DIAGNOSTICS INC·Filed 2019·Granted Jun 30, 2020·0 cites·10 claims
- 1072US9611512B2Methods of detecting mutations associated with ataxia-ocular apraxia 2 (AOA2)ATHENA DIAGNOSTICS INC·Filed 2014·Granted Apr 4, 2017·0 cites·7 claims
- 1170US7119186B2Application of aprataxin gene to diagnosis and treatment for early-onset spinocerebellar ataxia (EAOH)ATHENA DIAGNOSTICS INC·Filed 2002·Granted Oct 10, 2006·5 cites·8 claims
- 1267US2020385807A1Methods to detect a silent carrier genotypeATHENA DIAGNOSTICS INC·Filed 2020·Application pending·0 cites
- 1366US11655508B2PKD mutations and evaluation of sameATHENA DIAGNOSTICS INC·Filed 2020·Granted May 23, 2023·0 cites·4 claims
- 1466US2017166970A1Methods of detecting mutations associated with ataxia-ocular apraxia 2 (aoa2)ATHENA DIAGNOSTICS INC·Filed 2017·Application pending·0 cites
- 1565US10760128B2PKD mutations and evaluation of sameATHENA DIAGNOSTICS INC·Filed 2014·Granted Sep 1, 2020·0 cites·6 claims
- 1664US10762981B2Pathogenicity scoring system for human clinical geneticsATHENA DIAGNOSTICS INC·Filed 2014·Granted Sep 1, 2020·0 cites·13 claims
- 1762US10227650B2Methods to detect a silent carrier of a null allele genotypeATHENA DIAGNOSTICS INC·Filed 2015·Granted Mar 12, 2019·0 cites·32 claims
- 1861US2025232835A1Pathogenicity scoring system for human clinical geneticsATHENA DIAGNOSTICS INC·Filed 2025·Application pending·0 cites
- 1960US2020411134A1Pathogenicity scoring system for human clinical geneticsATHENA DIAGNOSTICS INC·Filed 2020·Application pending·0 cites
- 2057US6824999B1Detection of antibodies to gangliosides using solid-phase reactants coated with carbonyl groupsATHENA DIAGNOSTICS INC·Filed 2000·Granted Nov 30, 2004·3 cites·19 claims
- 2153US7799529B2Nephrin gene and proteinATHENA DIAGNOSTICS INC·Filed 2006·Granted Sep 21, 2010·0 cites·13 claims
- 2252US6951763B2Detection of antibodies to glycosphingolipids using solid-phase reactants coated with carbonyl groupsATHENA DIAGNOSTICS INC·Filed 2003·Granted Oct 4, 2005·1 cites·8 claims
- 2347US2005233384A1Detection of antibodies to gangliosides using solid-phase reactants coated with carbonyl groupsATHENA DIAGNOSTICS INC·Filed 2004·Application pending·0 cites
- 2443US2016115544A1Molecular barcoding for multiplex sequencingATHENA DIAGNOSTICS INC·Filed 2014·Application pending·0 cites
- 2532US6001576AMutations relating to X-linked charcot-marie-tooth diseaseATHENA DIAGNOSTICS INC·Filed 1998·Granted Dec 14, 1999·2 cites·15 claims
- 2631US6599756B1Detection of antibodies to glycosphingolipids using solid-phase reactants coated with carbonyl groupsATHENA DIAGNOSTICS INC·Filed 2000·Granted Jul 29, 2003·2 cites·10 claims
- 2730US5691144AMethods of detecting novel mutations relating to X-linked Charcot-Marie-Tooth diseaseATHENA DIAGNOSTICS INC·Filed 1996·Granted Nov 25, 1997·4 cites·15 claims
Counts cover granted patents and pending applications in the PatentIndex corpus. How scoring works →