METHOD FOR PREDICTION OF FETAL MONOGENIC GENETIC VARIATIONS USING MATERNAL SERUM DNA

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United States of America Patent

SERIAL NO

15313713

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Abstract

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The present invention provides a method for non-invasively detecting, expecting, or diagnosing fetal single nucleotide polymorphisms and the resultant monogenic disorders, through maternal cell-free DNA sequencing. The diagnosis method according to the present invention does not harm mothers or fetuses and is convenient, in that analysis is possible using maternal blood samples; and can be favorably used for a prenatal diagnosis method capable of determining at an early stage whether single nucleotide polymorphisms causing monogenic disorders occur or not

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Patent Owner(s)

Patent OwnerAddress
SK TELECOM CO LTDSK T-TOWER 65 EULJI-RO JUNG-GU SEOUL 04539

International Classification(s)

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  • 2015 Application Filing Year
  • C12Q Class
  • 3483 Applications Filed
  • 2244 Patents Issued To-Date
  • 64.43 % Issued To-Date
Click to zoom InYear of Issuance% of Matters IssuedCumulative IssuancesYearly Issuances201520162017201820192020202120222023202420250255075100

Inventor(s)

Inventor Name Address # of filed Patents Total Citations
NAMKUNG, Junghyun Seoul, KR 4 6

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  • 3 Citation Count
  • C12Q Class
  • 52.11 % this patent is cited more than
  • 8 Age
Citation count rangeNumber of patents cited in rangeNumber of patents cited in various citation count ranges2682212021779161049531101 - 1011 - 2021 - 3031 - 4041 - 5051 - 6061 - 7071 - 8081 - 9091 - 100100 +020040060080010001200140016001800200022002400260028003000

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