Inventor · disambiguated record
Guy A. Rouleau
Also filed as: ROULEAU GUY · ROULEAU GUY A
12 granted patents·3 pending applications·50 citations·filing 2000–2017
89Inventor score
Files withUNIV MCGILL6HOSPITAL FOR SICK CHILDREN2ROULEAU GUY A2CT HOSPITALIER UNIVERSITAIRE SAINT JUSTINE1CT HOSPITALIER UNIVERSITAIRE SAINTE JUSTINE1
Top patents by PatentIndex Score
15 records- 0184US8143005B2Nucleic acids encoding sodium channel SCN1A alpha subunit proteins and mutations associated with epilepsyROULEAU GUY A·Filed 2009·Granted Mar 27, 2012·8 cites·19 claims
- 0279US7655460B2Nucleic acids encoding sodium channel SCN1A alpha subunit proteins with mutations associated with epilepsyUNIV MCGILL·Filed 2003·Granted Feb 2, 2010·12 cites·23 claims
- 0376US7485449B2Nucleic acids encoding sodium channel scn3a alpha subunitsUNIV MCGILL·Filed 2003·Granted Feb 3, 2009·7 cites·6 claims
- 0476US6828430B1Short GCG expansions in the PAB II gene for oculopharyngeal muscular dystrophy and diagnostic thereofUNIV MCGILL·Filed 2000·Granted Dec 7, 2004·6 cites·17 claims
- 0573US7364852B2Short GCG expansions in the PAB II gene for oculopharyngeal muscular dystrophy and diagnostic thereofUNIV MCGILL·Filed 2004·Granted Apr 29, 2008·4 cites·11 claims
- 0672US7528093B2SCN3A locus for idiopathic generalized epilepsy, mutations thereof and method using sameUNIV MCGILL·Filed 2003·Granted May 5, 2009·8 cites·10 claims
- 0771US9334539B2Lafora's disease geneHOSPITAL FOR SICK CHILDREN·Filed 2013·Granted May 10, 2016·0 cites·5 claims
- 0868US10969933B1Graphical representation of ordered model items based on solver informationMATHWORKS INC·Filed 2017·Granted Apr 6, 2021·2 cites·35 claims
- 0965US7951931B2Nucleic acid encoding sodium channel SCN3A alpha subunitsUNIV MCGILL·Filed 2009·Granted May 31, 2011·0 cites·14 claims
- 1064US2016215347A1LaFORA'S DISEASE GENEHOSPITAL FOR SICK CHILDREN·Filed 2016·Application pending·0 cites
- 1162US7989167B2Method of prognosing and diagnosing hereditary spastic paraplegia, mutant nucleic acid molecules and polypeptidesVAL CHUM L P·Filed 2007·Granted Aug 2, 2011·3 cites·58 claims
- 1257US9523698B2Method of prognosing and diagnosing hereditary spastic paraplegia, mutant nucleic acid molecules and polypeptidesUNIV MONTREAL·Filed 2013·Granted Dec 20, 2016·0 cites·14 claims
- 1354US2011229891A1Syngap1 dysfunctions and uses thereof in diagnostic and therapeutic applications for mental retardationCT HOSPITALIER UNIVERSITAIRE SAINT JUSTINE·Filed 2009·Application pending·0 cites
- 1452US2013065238A1Syngap1 dysfunctions and uses thereof in diagnostic and therapeutic applications for mental retardationCT HOSPITALIER UNIVERSITAIRE SAINTE JUSTINE·Filed 2012·Application pending·0 cites
- 1550US8518657B2Method of prognosing and diagnosing hereditary spastic paraplegia, mutant nucleic acid molecules and polypeptidesROULEAU GUY A·Filed 2011·Granted Aug 27, 2013·0 cites·24 claims
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →