Patents Assigned to deCODE genetics ehf.
  • Publication number: 20050196784
    Abstract: Association of Type II diabetes and a locus on chromosome 5 is disclosed. In particular, the gene KChIP1 within this locus is shown by linkage analysis to be a susceptibility gene for Type II diabetes. Pathway targeting for drug delivery and diagnosis applications in identifying those who have Type II diabetes or are at risk of developing Type II diabetes, in particular those that are non-obese are described.
    Type: Application
    Filed: January 5, 2005
    Publication date: September 8, 2005
    Applicant: deCODE genetics ehf.
    Inventors: Inga Reynisdottir, Jeffrey Gulcher, Struan Grant, Gudmar Thorleifsson
  • Publication number: 20050191272
    Abstract: The invention relates to methods for inducing a pro-asthma/pro-inflammatory like state in a resident tissue cell, comprising contacting the cell with one or more cytokines, e.g., IL-1?, TNF? or both. Methods are also disclosed for identifying genes that regulate responses to anti-inflammatory drugs, to methods for drug screening, and to methods for identifying genes that correlate with various pro-asthma/pro-inflammatory disease phenotypes.
    Type: Application
    Filed: December 22, 2004
    Publication date: September 1, 2005
    Applicants: deCODE genetics ehf., The Children's Hospital of Philadelphia
    Inventors: Hakon Hakonarson, Michael Grunstein
  • Publication number: 20050164220
    Abstract: A role of the human PDE4D gene in stroke is disclosed. Methods for diagnosis, prediction of clinical course and treatment for stroke using polymorphisms in the PDE4D gene are also disclosed.
    Type: Application
    Filed: June 14, 2004
    Publication date: July 28, 2005
    Applicant: deCODE genetics ehf.
    Inventors: Solveig Gretarsdottir, Gudmar Thorleifsson, Jeffrey Gulcher
  • Publication number: 20050113408
    Abstract: Linkage of myocardial infarction (MI) and a locus on chromosome 13q12 is disclosed. In particular, the FLAP gene within this locus is shown by genetic association analysis to be a susceptibility gene for MI and ACS, as well as stroke and PAOD. Pathway targeting for treatment and diagnostic applications in identifying those who are at risk of developing MI, ACS, stroke or PAOD, in particular are described.
    Type: Application
    Filed: April 22, 2004
    Publication date: May 26, 2005
    Applicant: deCODE genetics ehf.
    Inventors: Anna Helgadottir, Mark Gurney, Jeffrey Gulcher, Hakon Hakonarson
  • Publication number: 20050112611
    Abstract: Linkage of Myocardial Infarction (MI) to a locus on chromosome 13q12-13 is disclosed. In particular, the FLAP gene within this locus is shown by association analysis to be a susceptibility gene for MI and stroke. Pathway targeting for drug delivery and diagnosis applications in identifying those at risk of developing MI or stroke, in particular are described.
    Type: Application
    Filed: April 22, 2004
    Publication date: May 26, 2005
    Applicant: deCODE genetics ehf.
    Inventor: Anna Helgadottir
  • Patent number: 6897027
    Abstract: The present invention relates to a method for desalting nucleic acid samples. The method involves contacting a liquid sample comprising a nucleic acid and an ionic salt with an ion exchanger comprising an insoluble phosphate salt, removing said liquid, and eluting said nucleic acid from the ion exchanger. The desalted nucleic acids provided by the methods of the invention are suitable for a wide variety of analytic and diagnostic applications, including high-throughput assays.
    Type: Grant
    Filed: March 27, 2002
    Date of Patent: May 24, 2005
    Assignee: deCODE genetics ehf.
    Inventors: Sigurdur V. Smárason, Albert V. Smith
  • Patent number: 6893828
    Abstract: The present invention relates to methods for inducing a pro-asthma/pro-inflammatory like state in a resident tissue cell, comprising contacting the cell with IL-1?, TNF? or both. Methods are also disclosed for identifying genes that regulate responses to anti-inflammatory drugs, to methods for drug screening, and to methods for identifying genes that correlate with various pro-asthma/pro-inflammatory disease phenotypes.
    Type: Grant
    Filed: September 6, 2001
    Date of Patent: May 17, 2005
    Assignees: deCODE genetics ehf., The Children's Hospital of Philadelphia
    Inventors: Hakon Hakonarson, Michael M. Grunstein
  • Publication number: 20050050030
    Abstract: The present invention relates to the usage pattern, commonly found in many software applications, of defining sets of objects based on object attributes. A specifically designed set definition language for defining sets, called SDL, is described and a software system that implements this language efficiently on top of a standard relational database management system (RDBMS) is presented. The unique features of the SDL language are the implicit constraints that are enforced on the relational data that belong to the objects. Unique to the SDL system is also the logical metadata of dimensions that enables the SDL system to enforce these constraints across relations. The SDL system utilizes several optimization techniques to enable efficient implementation on top of RDBMS. It is also shown how the SDL language and the SQL language can be merged with bidirectional inlining using syntactic gates. Query composition tools are also described that facilitate the creation of SDL expressions.
    Type: Application
    Filed: July 20, 2004
    Publication date: March 3, 2005
    Applicant: deCODE genetics ehf.
    Inventors: Hakon Gudbjartsson, Thorvaldur Arnarson, Pavol Rovensky, Vilmundur Palmason
  • Publication number: 20040153435
    Abstract: The present invention relates to the usage pattern, commonly found in many software applications, of defining sets of objects based on object attributes. A specifically designed set definition language for defining sets, called SDL, is described and a software system that implements this language efficiently on top of a standard relational database management system (RDBMS) is presented. The unique features of the SDL language are the implicit constraints that are enforced on the relational data that belong to the objects. Unique to the SDL system is also the logical metadata of dimensions that enables the SDL system to enforce these constraints across relations. The SDL system utilizes several optimization techniques to enable efficient implementation on top of RDBMS. It is also shown how the SDL language and the SQL language can be merged with bidirectional inlining using syntactic gates. Query composition tools are also described that facilitate the creation of SDL expressions.
    Type: Application
    Filed: June 24, 2003
    Publication date: August 5, 2004
    Applicant: deCODE genetics ehf.
    Inventors: Hakon Gudbjartsson, Thorvaldur S. Arnarson, Pavol Rovensky, Vilmundur Palmason
  • Publication number: 20040091865
    Abstract: A role of the human PDE4D gene in stroke is disclosed. Methods for diagnosis, prediction of clinical course and treatment for stroke using polymorphisms in the PDE4D gene are also disclosed.
    Type: Application
    Filed: September 25, 2002
    Publication date: May 13, 2004
    Applicant: deCODE genetics ehf.
    Inventors: Solveig Gretarsdottir, Sif Jonsdottir, Sigridur Th. Reynisdottir, Gudmar Thorleifsson
  • Publication number: 20040014099
    Abstract: A role of the human PDE4D gene in stroke is disclosed. Methods for diagnosis, prediction of clinical course and treatment for stroke using polymorphisms in the PDE4D gene are also disclosed.
    Type: Application
    Filed: April 18, 2003
    Publication date: January 22, 2004
    Applicant: deCODE genetics ehf.
    Inventors: Solveig Gretarsdottir, Sif Jonsdottir, Sigridur Th. Reynisdottir, Gudmar Thorleifsson, Jeffrey R. Gulcher
  • Publication number: 20030224393
    Abstract: A role of the human PAOD1 gene in peripheral arterial occlusive disease is disclosed. Methods for diagnosis, prediction of clinical course and treatment for peripheral arterial occlusive disease using polymorphisms in the PAOD1 gene are also disclosed.
    Type: Application
    Filed: January 29, 2003
    Publication date: December 4, 2003
    Applicant: deCODE genetics ehf.
    Inventor: Gudmundur Gudmundsson
  • Publication number: 20030203380
    Abstract: A role of the human MATN3 gene in osteoarthritis is disclosed. Methods for diagnosis, prediction of clinical course and treatment for osteoarthritis using polymorphisms in the MATN3 gene are also disclosed.
    Type: Application
    Filed: January 24, 2003
    Publication date: October 30, 2003
    Applicant: deCODE genetics ehf.
    Inventor: Stefan E. Stefansson
  • Patent number: 6630304
    Abstract: A role of the human BMP2 gene in osteoporosis is disclosed. Methods for diagnosis, prediction of clinical course and treatment for osteoporosis using polymorphisms in the BMP2 gene are also disclosed.
    Type: Grant
    Filed: September 14, 2000
    Date of Patent: October 7, 2003
    Assignee: deCODE genetics ehf.
    Inventors: Unnur Styrkarsdottir, Vala Drofn Johannsdottir
  • Publication number: 20030186247
    Abstract: The present invention relates to a method for desalting nucleic acid samples. The method involves contacting a liquid sample comprising a nucleic acid and an ionic salt with an ion exchanger comprising an insoluble phosphate salt, removing said liquid, and eluting said nucleic acid from the ion exchanger. The desalted nucleic acids provided by the methods of the invention are suitable for a wide variety of analytic and diagnostic applications, including high-throughput assays.
    Type: Application
    Filed: March 27, 2002
    Publication date: October 2, 2003
    Applicant: deCODE genetics ehf.
    Inventors: Sigurdur V. Smarason, Albert V. Smith
  • Publication number: 20030176344
    Abstract: A role of the human BMP2 nucleic acid in osteoporosis is disclosed. Methods for diagnosis, prediction of clinical course and treatment for osteoporosis or a susceptibility to osteoporosis using polymorphisms in the BMP2 nucleic acid, alone or in combination with other assays, are also disclosed.
    Type: Application
    Filed: January 16, 2003
    Publication date: September 18, 2003
    Applicant: deCODE genetics ehf.
    Inventors: Unnur Styrkarsdottir, Vala Drofn Johannsdottir
  • Publication number: 20030166904
    Abstract: The gene for hypocretin (orexin) receptor 2 (HCRTR2), which is associated with narcolepsy, is disclosed. Also described are methods of diagnosis of narcolepsy, pharmaceutical compositions comprising nucleic acids comprising the HCRTR2 gene, as well as methods of therapy of narcolepsy.
    Type: Application
    Filed: June 21, 2002
    Publication date: September 4, 2003
    Applicant: deCODE genetics ehf.
    Inventors: Berglind Ran Olafsdottir, Jeffrey Gulcher
  • Publication number: 20030163461
    Abstract: The present invention relates to the usage pattern, commonly found in many software applications, of defining sets of objects based on object attributes. A specifically designed set-definition language for defining sets, called SDL, is described and a software system that implements this language efficiently on top of a standard relational database management system (RDMS) is presented. The unique features of the SDL language are the implicit constraints that are enforced on the relational data that belong to the objects. Unique to the SDL system is also the logical metadata of dimensions that enables the SDL system to enforce these constraints across relations. The SDL system utilizes several optimization techniques to enable efficient implementation on top of RDMS. Query composition tools are also described and facilitate the creation of SDL expressions.
    Type: Application
    Filed: January 30, 2003
    Publication date: August 28, 2003
    Applicant: deCODE genetics, ehf.
    Inventors: Hakon Gudbjartsson, Thorvaldur S. Arnarson, Pavol Rovensky, Vilmundur Palmason
  • Publication number: 20030157599
    Abstract: A role of the human PAOD1 gene in peripheral arterial occlusive disease is disclosed. Methods for diagnosis, prediction of clinical course and treatment for peripheral arterial occlusive disease using polymorphisms in the PAOD1 gene are also disclosed.
    Type: Application
    Filed: January 30, 2002
    Publication date: August 21, 2003
    Applicant: deCODE genetics ehf
    Inventor: Gudmundur Gudmundsson
  • Publication number: 20030154189
    Abstract: The invention discloses a system and methods that facilitate efficient querying of tables referencing spatial object types. The methods enable meaningful indexing of the tables as well as rewriting of queries with respect to the spatial structures. Dynamic schema extraction using efficient proper coloring algorithms for large sets of spatial objects is disclosed that structures the data in such a way that complex spatial queries and grouping of objects is replaced with traditional relational joins. This enables a relational database system to harness its entire query optimizing capability when querying tables referencing spatial objects.
    Type: Application
    Filed: February 13, 2003
    Publication date: August 14, 2003
    Applicant: deCODE genetics, ehf.
    Inventors: Agust Sverrir Egilsson, Hakon Gudbjartsson