Inventor · disambiguated record
John B. Vincent
Also filed as: VINCENT JOHN · VINCENT JOHN B · VINCENT JOHN BRYAN · VINCENT JOHN S
34 granted patents·15 pending applications·308 citations·filing 1993–2022
97Inventor score
Top patents by PatentIndex Score
49 records- 0194US6879424B2Electrochromic display device and compositions useful in making such devicesAVESO INC·Filed 2002·Granted Apr 12, 2005·71 cites·44 claims
- 0291US6639709B2Matrix addressable electrochromic display deviceDOW GLOBAL TECHNOLOGIES INC·Filed 2002·Granted Oct 28, 2003·47 cites·20 claims
- 0389US7670773B2MECP2E1 geneCAMH·Filed 2006·Granted Mar 2, 2010·10 cites·12 claims
- 0488US7354953B2Time-release compositions for delivery of [Cr3O(carboxylate)6(H2O)3]+UNIV ALABAMA·Filed 2006·Granted Apr 8, 2008·11 cites·7 claims
- 0588US6444231B2USE OF TRIAQUA-μ3-OXOHEXAKIS-μ-PROPIONATOTRICHROMIUM(1+), [CR3O(O2CCH2CH3)6(H2O)3]+, AS A NUTRITIONAL SUPPLEMENT OR IN TREATMENT OF MEDICAL CONDITIONSUNIV ALABAMA·Filed 2001·Granted Sep 3, 2002·20 cites·10 claims
- 0685US9851054B2Universal lamp supportVINCENT JOHN BRYAN·Filed 2014·Granted Dec 26, 2017·11 cites·15 claims
- 0785US7054050B2Electrochromic display deviceAVESO INC·Filed 2004·Granted May 30, 2006·27 cites·9 claims
- 0882US6744549B2Electrochromic display deviceDOW GLOBAL TECHNOLOGIES INC·Filed 2002·Granted Jun 1, 2004·22 cites·22 claims
- 0981US6881752B2USE OF TRIAQUA-μ3-OXOHEXAKIS-μ-PROPIONATOTRICHROMIUM(1+), [CR3O(O2CCH2CH3)6(H2O)3]+, AS A NUTRITIONAL SUPPLEMENT OR IN TREATMENT OF MEDICAL CONDITIONSUNIV ALABAMA·Filed 2002·Granted Apr 19, 2005·10 cites·15 claims
- 1079US12467093B2Biomarkers for autism spectrum disordersHOSPITAL FOR SICK CHILDREN·Filed 2022·Granted Nov 11, 2025·0 cites·6 claims
- 1179US8598330B2CC2D2A gene mutations associated with joubert syndrome and diagnostic methods for identifying the sameVINCENT JOHN B·Filed 2012·Granted Dec 3, 2013·2 cites·7 claims
- 1278US11254984B2Biomarkers for autism spectrum disordersHOSPITAL FOR SICK CHILDREN·Filed 2019·Granted Feb 22, 2022·0 cites·8 claims
- 1378US8119351B2CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the sameVINCENT JOHN B·Filed 2008·Granted Feb 21, 2012·4 cites·21 claims
- 1472US2020270695A1Mecp2e1 geneHOSPITAL FOR SICK CHILDREN·Filed 2020·Application pending·0 cites
- 1571US10577657B2MECP2E1 geneHOSPITAL FOR SICK CHILDREN·Filed 2018·Granted Mar 3, 2020·0 cites·6 claims
- 1671US9605314B2MECP2E1 geneHOSPITAL FOR SICK CHILDREN·Filed 2013·Granted Mar 28, 2017·0 cites·7 claims
- 1771US9096903B2CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the sameCAMH·Filed 2013·Granted Aug 4, 2015·0 cites·12 claims
- 1869US2010248235A1Biomarkers for autism spectrum disordersSCHERER STEPHEN W·Filed 2008·Application pending·0 cites
- 1969US2020270693A1Mecp2e1 geneHOSPITAL FOR SICK CHILDREN·Filed 2020·Application pending·0 cites
- 2068US2014227696A1Method and apparatus for predicting susceptibility to a developmental disorderCAMH·Filed 2014·Application pending·0 cites
- 2167US2017152564A1Mecp2e1 geneHOSPITAL FOR SICK CHILDREN·Filed 2017·Application pending·0 cites
- 2266US10024501B1Universal lamp supportPRINCIPAL LED LLC·Filed 2017·Granted Jul 17, 2018·1 cites·20 claims
- 2365US10577658B2MECP2E1 geneHOSPITAL FOR SICK CHILDREN·Filed 2018·Granted Mar 3, 2020·0 cites·6 claims
- 2465US10400960B1LED retrofit assembly with electrically biased support structurePRINCIPAL LIGHTING GROUP LLC·Filed 2018·Granted Sep 3, 2019·2 cites·20 claims
- 2564US9670544B2CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the sameCAMH·Filed 2015·Granted Jun 6, 2017·0 cites·11 claims
- 2664US9568484B2MECP2E1 geneMINASSIAN BERGE A·Filed 2008·Granted Feb 14, 2017·0 cites·9 claims
- 2763US10526653B2Biomarkers for autism spectrum disordersHOSPITAL FOR SICK CHILDREN·Filed 2015·Granted Jan 7, 2020·0 cites·3 claims
- 2863US6197816B1Use of triaqua-mu3-oxohexakis-mu-propionatotrichromium (1+), [CR3O(O2CCH2CH3)6(H2O) 3]+, as a nutritional supplement or in treatment of medical conditionsUNIV ALABAMA·Filed 1998·Granted Mar 6, 2001·19 cites·6 claims
- 2959US8716444B2Method and apparatus for predicting susceptibility to a developmental disorderVINCENT JOHN B·Filed 2010·Granted May 6, 2014·0 cites·4 claims
- 3059US2017137887A1Mecp2e1 geneHOSPITAL FOR SICK CHILDREN·Filed 2017·Application pending·0 cites
- 3157US9150923B2Methods of identifying FHL1 mutations associated with novel X-linked muscular myopathiesCAMH·Filed 2013·Granted Oct 6, 2015·0 cites·20 claims
- 3256US2015118687A1Method and apparatus for predicting susceptibility to a developmental disorderCAMH·Filed 2015·Application pending·0 cites
- 3355US5441643AProcess for recovering metals from solution utilizing metalloprotein affinity chromatographyUS ARMY·Filed 1993·Granted Aug 15, 1995·16 cites·3 claims
- 3455US2013116149A1Genetic Markers Associated with Intellectual DisabilityVINCENT JOHN B·Filed 2011·Application pending·0 cites
- 3554US2025044299A1Protein stability assayMEDICINES DISCOVERY CATAPULT LTD·Filed 2022·Application pending·0 cites
- 3653US7405313B2Method for the synthesis of basic chromium carboxylatesUNIV ALABAMA·Filed 2006·Granted Jul 29, 2008·0 cites·20 claims
- 3753US5872102AMethod for isolation of bovine low-molecular weight CR-binding substance and method of use of the sameUNIV ALABAMA·Filed 1996·Granted Feb 16, 1999·10 cites·7 claims
- 3853US2015315640A1Identification of the dcps gene on 11q24.2, which encodes the human decapping enzyme scavenger, in non-syndromic autosomal recessive mental retardation, diagnostic probes thereof and methods of identifying subjects with sameCAMH·Filed 2013·Application pending·0 cites
- 3952US9617320B2Nucleic acids encoding FHL1 mutations associated with novel X-linked muscular myopathies and methods of screening a subjectCAMH·Filed 2015·Granted Apr 11, 2017·0 cites·16 claims
- 4052US8637236B2MECP2E1 geneMINASSIAN BERGE A·Filed 2010·Granted Jan 28, 2014·0 cites·12 claims
- 4152US8580502B2Methods of screening a subject for FHL1 mutations associated with novel X-linked muscular myopathiesVINCENT JOHN B·Filed 2008·Granted Nov 12, 2013·0 cites·15 claims
- 4251US2015141287A1Genetic markers associated with intellectual disabilityCAMH·Filed 2015·Application pending·0 cites
- 4349US5567316AProcess for recovering metals from solution utilizing metalloprotein affinity chromatographyUS ARMY·Filed 1995·Granted Oct 22, 1996·13 cites·3 claims
- 4445US6149948AMethod of decreasing plasma cholesterol and triglycerides with a chromium-containing complexUNIV ALABAMA·Filed 1999·Granted Nov 21, 2000·7 cites·17 claims
- 4544US2012100995A1Biomarkers for Autism Spectrum DisordersSCHERER STEPHEN W·Filed 2011·Application pending·0 cites
- 4644US2013330422A1Methods for increasing insulin sensitivity and treating diabetes with a bioactive chromium binding peptideUNIV ALABAMA·Filed 2013·Application pending·0 cites
- 4739US2019186725A1Universal Light Emitting DeviceVINCENT JOHN BRYAN·Filed 2017·Application pending·0 cites
- 4830US2005118098A1Radioactive ionFiled 2002·Application pending·0 cites
- 4923US5875220AProcess for production of radiostrontiumINST YADERNYKH I ROSSIISKOI AK·Filed 1997·Granted Feb 23, 1999·5 cites·2 claims
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Identity basis: PatentsView inventor disambiguation (2025Q4-odp release). How scoring works →