Mark Keating
30Patents
7h-index
33Co-inventors
69Inventor score
Filing activity: Mar 9, 1995 → Mar 4, 2024
Most-cited inventions
| Patent | Title | Area | Cited by | Status |
|---|---|---|---|---|
| US5599673A | Long QT syndrome genes | Emerging Cross-Sectional Technologies | 13 | Expired |
| US6274332A | Mutations in the KCNE1 gene encoding human minK which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene | Emerging Cross-Sectional Technologies | 11 | Expired |
| US6277978A | KVLQT1--a long QT syndrome gene | Chemistry; Metallurgy | 9 | Expired |
| US6207383A | Mutations in and genomic structure of HERG--a long QT syndrome gene | Chemistry; Metallurgy | 9 | Expired |
| US6787309B2 | Alterations in the long QT syndrome genes KVLQT1 and SCN5A and methods for detecting same | Chemistry; Metallurgy | 8 | Expired |
| US7125837B1 | Elastin-based compositions | Human Necessities | 7 | Expired |
| US6432644B1 | Mutations in the KCNE1 gene encoding human mink which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene | Emerging Cross-Sectional Technologies | 7 | Expired |
| US6323026A | Mutations in the KCNE1 gene encoding human mink which cause arrhythmia susceptibility thereby establishing KCNE1 as an LQT gene | Emerging Cross-Sectional Technologies | 6 | Expired |
| US5858662A | Diagnosis of Williams syndrome and Williams syndrome cognitive profile by analysis of the presence or absence of a LIM-kinase gene | Chemistry; Metallurgy | 5 | Expired |
| US6582913B1 | Diagnostic method for KVLQT1—a long QT syndrome gene | Chemistry; Metallurgy | 4 | Expired |
| US7208273B2 | Common polymorphism in scn5a implicated in drug-induced cardiac arrhythmia | Chemistry; Metallurgy | 4 | Expired |
| US6150104A | Homozygous mutation in KVLQT1 which causes Jervell and Lange Nielsen syndrome | Chemistry; Metallurgy | 4 | Expired |
| US5650282A | Diagnosis of Williams syndrome | Emerging Cross-Sectional Technologies | 3 | Expired |
| US6372958B1 | Transgenic mouse with endogenous endoglin gene disruption | Human Necessities | 3 | Expired |
| US6420124B1 | KVLQT1—a long qt syndrome gene | Chemistry; Metallurgy | 3 | Expired |
| US6451534B1 | KVLQT1—a long QT syndrome gene | Chemistry; Metallurgy | 3 | Expired |
| US6063576A | Actin mutations in dilated cardiomyopathy, a heritable form of heart failure | Chemistry; Metallurgy | 2 | Expired |
| US5840489A | Diagnosis and treatment of supravalvular aortic stenosis and Williams syndrome | Emerging Cross-Sectional Technologies | 2 | Expired |
| US6342357B1 | Alterations in the long QT syndrome genes KVLQT1 and SCN5A and methods for detecting same | Chemistry; Metallurgy | 2 | Expired |
| US6903244B1 | Mice which are +/− or −/− for the elastin gene as models for vascular disease | Human Necessities | 1 | Expired |
| US6864364B1 | MinK-related genes, formation of potassium channels and association with cardiac arrhythmia | Human Necessities | 1 | Expired |
| US6972176B2 | KVLQT1—a long QT syndrome gene | Chemistry; Metallurgy | 0 | Expired |
| US7297489B2 | Mutations in and genomic structure of HERG—a long QT syndrome gene | Chemistry; Metallurgy | 0 | Expired |
| US12331297B2 | Coagulation factor V (F5) iRNA compositions and methods of use thereof | Chemistry; Metallurgy | 0 | Active |
| US12365896B2 | Complement component C3 iRNA compositions and methods of use thereof | Chemistry; Metallurgy | 0 | Active |
Source: USPTO / EPO open patent data. Inventor disambiguation is heuristic; counts are objective bibliographic measures.