P

Inventor

EHRICH MATHIAS

US38 patents
⚠️ This page may combine multiple inventors who share the name “EHRICH MATHIAS”. Patents are grouped by organization below to help distinguish them — per-person disambiguation is on the roadmap.

SEQUENOM INC

25 patents
US9367663B2Jun 14, 2016

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC45 citations97
US9984198B2May 29, 2018

Reducing sequence read count error in assessment of complex genetic variations

SEQUENOM INC26 citations93
US9605313B2Mar 28, 2017

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC6 citations84
US10699800B2Jun 30, 2020

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC8 citations82
US10323268B2Jun 18, 2019

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC5 citations82
US11312997B2Apr 26, 2022

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC2 citations73
US10738359B2Aug 11, 2020

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC4 citations73
US11437121B2Sep 6, 2022

Methods and processes for non-invasive detection of a microduplication or a microdeletion with reduced sequence read count error

SEQUENOM INC2 citations72
US10738358B2Aug 11, 2020

Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses

SEQUENOM INC3 citations72
US10438691B2Oct 8, 2019

Non-invasive assessment of chromosome alterations using change in subsequence mappability

SEQUENOM INC3 citations72
US11560586B2Jan 24, 2023

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC3 citations71
US11462298B2Oct 4, 2022

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC2 citations71
US11365447B2Jun 21, 2022

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC2 citations71
US11060145B2Jul 13, 2021

Methods and compositions for identifying presence or absence of hypermethylation or hypomethylation locus

SEQUENOM INC2 citations71
US10612086B2Apr 7, 2020

Processes and compositions for methylation-based enrichment of fetal nucleic acid from a maternal sample useful for non-invasive prenatal diagnoses

SEQUENOM INC5 citations67
US11929146B2Mar 12, 2024

Systems for non-invasive assessment of chromosome alterations using changes in subsequence mappability

SEQUENOM INC0 citations62
US7608394B2Oct 27, 2009

Methods and compositions for phenotype identification based on nucleic acid methylation

SEQUENOM INC5 citations62
US12410475B2Sep 9, 2025

Methods and processes for non-invasive assessment of genetic variations

SEQUENOM INC0 citations60
US11697849B2Jul 11, 2023

Methods for non-invasive assessment of fetal genetic variations that factor experimental conditions

SEQUENOM INC1 citations58
US11180799B2Nov 23, 2021

Processes and kits for identifying aneuploidy

SEQUENOM INC0 citations55
US11694768B2Jul 4, 2023

Methods and processes for assessment of genetic variations

SEQUENOM INC1 citations53
US7867714B2Jan 11, 2011

Target-specific compomers and methods of use

SEQUENOM INC1 citations52
US7785843B2Aug 31, 2010

Target-specific compomers and methods of use

SEQUENOM INC0 citations52
US11515003B2Nov 29, 2022

Copy number alteration and reference genome mapping

SEQUENOM INC0 citations47
US11929145B2Mar 12, 2024

Methods for non-invasive assessment of genetic alterations

SEQUENOM INC0 citations45

EHRICH MATHIAS

9 patents

OETH PAUL A

1 patent

OETH PAUL ANDREW

1 patent

JUNO DIAGNOSTICS INC

1 patent

NUCLEIX LTD

1 patent