JV

John B. Vincent

CH Centre For Addiction And Mental Health: 15 patents #1 of 49Top 3%
HC Hospital For Sick Children: 8 patents #13 of 239Top 6%
UA University Of Alabama: 7 patents #7 of 324Top 3%
Dow Global Technologies: 2 patents #1,896 of 4,534Top 45%
UI US Dept of the Interior: 2 patents #49 of 508Top 10%
📍 Toronto, CA: #126 of 9,482 inventorsTop 2%
Overall (All Time): #107,314 of 4,157,543Top 3%
33
Patents All Time

Issued Patents All Time

Showing 1–25 of 33 patents

Patent #TitleCo-InventorsDate
11254984 Biomarkers for autism spectrum disorders Stephen Scherer 2022-02-22
10577657 MECP2E1 gene Berge A. Minassian 2020-03-03
10577658 MECP2E1 gene Berge A. Minassian 2020-03-03
10526653 Biomarkers for autism spectrum disorders Stephen Scherer 2020-01-07
10400960 LED retrofit assembly with electrically biased support structure Nicholas Keith Kadlacek 2019-09-03
10024501 Universal lamp support 2018-07-17
9851054 Universal lamp support 2017-12-26
9670544 CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the same Muhammad Ayub 2017-06-06
9617320 Nucleic acids encoding FHL1 mutations associated with novel X-linked muscular myopathies and methods of screening a subject Christian Windpassinger, Stefan Quasthoff 2017-04-11
9605314 MECP2E1 gene Berge A. Minassian 2017-03-28
9568484 MECP2E1 gene Berge A. Minassian 2017-02-14
9150923 Methods of identifying FHL1 mutations associated with novel X-linked muscular myopathies Christian Windpassinger, Stefan Quasthoff 2015-10-06
9096903 CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the same Muhammad Ayub 2015-08-04
8716444 Method and apparatus for predicting susceptibility to a developmental disorder 2014-05-06
8637236 MECP2E1 gene Berge A. Minassian 2014-01-28
8598330 CC2D2A gene mutations associated with joubert syndrome and diagnostic methods for identifying the same Muhammad Ayub 2013-12-03
8580502 Methods of screening a subject for FHL1 mutations associated with novel X-linked muscular myopathies Christian Windpassinger, Stefan Quasthoff 2013-11-12
8119351 CC2D2A gene mutations associated with Joubert syndrome and diagnostic methods for identifying the same Muhammad Ayub 2012-02-21
7670773 MECP2E1 gene Berge A. Minassian 2010-03-02
7405313 Method for the synthesis of basic chromium carboxylates 2008-07-29
7354953 Time-release compositions for delivery of [Cr3O(carboxylate)6(H2O)3]+ 2008-04-08
7054050 Electrochromic display device Derrick W. Flick 2006-05-30
6881752 USE OF TRIAQUA-μ3-OXOHEXAKIS-μ-PROPIONATOTRICHROMIUM(1+), [CR3O(O2CCH2CH3)6(H2O)3]+, AS A NUTRITIONAL SUPPLEMENT OR IN TREATMENT OF MEDICAL CONDITIONS Catherine Davis 2005-04-19
6879424 Electrochromic display device and compositions useful in making such devices Susan J. Babinec, Daniel L. Dermody, Yu-Fan Chen 2005-04-12
6744549 Electrochromic display device Derrick W. Flick 2004-06-01