Growing community of inventors

Alston, MA, United States of America

Igor Splawski

Average Co-Inventor Count = 3.06

ph-index = 6

The patent ph-index is calculated by counting the number of publications for which an author has been cited by other authors at least that same number of times.

Forward Citations = 70

Igor SplawskiMark T Keating (16 patents)Igor SplawskiMichael C Sanguinetti (9 patents)Igor SplawskiTimothy C Burn (5 patents)Igor SplawskiTimothy D Connors (5 patents)Igor SplawskiGregory M Landes (5 patents)Igor SplawskiMark E Curran (5 patents)Igor SplawskiQing K Wang (1 patent)Igor SplawskiGeoffrey W Abbott (1 patent)Igor SplawskiFederico Sesti (1 patent)Igor SplawskiSteve A N Goldstein (1 patent)Igor SplawskiIgor Splawski (16 patents)Mark T KeatingMark T Keating (25 patents)Michael C SanguinettiMichael C Sanguinetti (12 patents)Timothy C BurnTimothy C Burn (17 patents)Timothy D ConnorsTimothy D Connors (14 patents)Gregory M LandesGregory M Landes (10 patents)Mark E CurranMark E Curran (6 patents)Qing K WangQing K Wang (3 patents)Geoffrey W AbbottGeoffrey W Abbott (1 patent)Federico SestiFederico Sesti (1 patent)Steve A N GoldsteinSteve A N Goldstein (1 patent)
..
Inventor’s number of patents
..
Strength of working relationships

Company Filing History:

1. University of Utah Research Foundation (11 from 1,645 patents)

2. Other (4 from 832,843 patents)

3. Yale University (1 from 1,327 patents)

4. Genzyme Corporation (1 from 789 patents)

5. Univ. of Utah Research Foundation (1 from 3 patents)


16 patents:

1. 7297489 - [object Object]

2. 7247436 - Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene

3. 7208273 - Common polymorphism in scn5a implicated in drug-induced cardiac arrhythmia

4. 6972176 - KVLQT1—a long QT syndrome gene

5. 6864364 - MinK-related genes, formation of potassium channels and association with cardiac arrhythmia

6. 6787309 - Alterations in the long QT syndrome genes KVLQT1 and SCN5A and methods for detecting same

7. 6582913 - Diagnostic method for KVLQT1—a long QT syndrome gene

8. 6451534 - KVLQT1—a long QT syndrome gene

9. 6432644 - Mutations in the KCNE1 gene encoding human mink which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene

10. 6420124 - KVLQT1—a long qt syndrome gene

11. 6342357 - Alterations in the long QT syndrome genes KVLQT1 and SCN5A and methods for detecting same

12. 6323026 - Mutations in the KCNE1 gene encoding human mink which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene

13. 6277978 - KVLQT1—a long QT syndrome gene

14. 6274332 - Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene

15. 6207383 - Mutations in and genomic structure of HERG—a long QT syndrome gene

Please report any incorrect information to support@idiyas.com
idiyas.com
as of
12/26/2025
Loading…