Patents by Inventor Jonathan Segal

Jonathan Segal has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20100144538
    Abstract: The present invention relates to the selection of a set of polymorphism markers for use in genome wide association studies based on linkage disequilibrium mapping. In particular, the invention relates to the fields of pharmacogenomics, diagnostics, patient therapy and the use of genetic haplotype information to predict an individual's susceptibility to SCHIZOPHRENIA disease and/or their response to a particular drug or drugs.
    Type: Application
    Filed: March 10, 2008
    Publication date: June 10, 2010
    Inventors: Abdelmajid Belouchi, John Verner Raelson, Walter Edward Bradley, Bruno Paquin, Helene Fournier, Pascal Croteau, Nouzha Paquin, Daniel Dubois, Vanessa Bruat, Paul Van Eerdewegh, Jonathan Segal, Randall David Little, Tim Keith
  • Publication number: 20100120628
    Abstract: The present invention relates to the selection of a set of polymorphism markers for use in genome wide association studies based on linkage disequilibrium mapping. In particular, the invention relates to the fields of pharmacogenomics, diagnostics, patient therapy and the use of genetic haplotype information to predict an individual's susceptibility to ADHD disease and/or their response to a particular drug or drugs.
    Type: Application
    Filed: February 6, 2008
    Publication date: May 13, 2010
    Applicant: GENIZON BIOSCIENCES INC.
    Inventors: Abdelmajid Belouchi, Vanessa Bruat, Pascal Croteau, Daniel Dubois, Randall David Little, Bruno Paquin, John Verner Raelson, Jonathan Segal, Paul Van Eerdewegh, Sandie Briand, Sem Kebache, Tim Keith
  • Publication number: 20100120627
    Abstract: The present invention relates to the selection of a set of polymorphism markers for use in genome wide association studies based on linkage disequilibrium mapping. In particular, the invention relates to the fields of pharmacogenomics, diagnostics, patient therapy and the use of genetic haplotype information to predict an individual's susceptibility to psoriasis disease and/or their response to a particular drug or drugs.
    Type: Application
    Filed: August 2, 2006
    Publication date: May 13, 2010
    Inventors: Abdelmajid Belouchi, John Verner Raelson, Walter Edward Bradley, Bruno Paquian, Quynh Nguyen-Huu, Pascal Croteau, Rene Allard, Randall David Little, Johanne Cousineau, Sophie Debrus, Tim Keith, Natali Henderson, Daniel Dubois, Paul Van Eerdewegh, Jonathan Segal
  • Publication number: 20100081129
    Abstract: The present invention relates to the selection of a set of polymorphism markers for use in genome wide association studies based on linkage disequilibrium mapping. In particular, the invention relates to the fields of pharmacogenomics, diagnostics, patient therapy and the use of genetic haplotype information to predict an individual's susceptibility to Crohn's disease and/or their response to a particular drug or drugs.
    Type: Application
    Filed: May 1, 2006
    Publication date: April 1, 2010
    Inventors: Abdelmajid Belouchi, John Verner Raelson, Walter Edward Bradley, Bruno Paquin, Hélene Fournier, Quynh Nguyen-Huu, Pascal Croteau, Réne Allard, Sophie Debrus, Valerie Serre, Paul Van Eerdewegh, Randall David Little, Jonathan Segal, Tim Keith
  • Publication number: 20090305900
    Abstract: The present invention relates to the selection of a set of SNP markers for use in genome wide association studies based on linkage disequilibrium mapping. In particular, the invention relates to the fields of pharmacogenomics, diagnostics, patient therapy and the use of genetic haplotype information to predict an individual's longevity, their protection against age-related diseases and/or their response to a particular drug or drugs.
    Type: Application
    Filed: June 19, 2006
    Publication date: December 10, 2009
    Inventors: Abdelmajid Belouchi, John Verner Raelson, Walter Edward Bradley, Bruno Paquin, Quynh Nguyen-Huu, Pascal Croteau, Rene Allard, Johanne Cousineau, Nouzha Paquin, Paul Van Eerdewegh, Randall David Little, Tim Keith, Jonathan Segal
  • Publication number: 20090181380
    Abstract: The present invention relates to the selection of a set of polymorphism makers for use in genome wide association studies based on linkage disequilibrium mapping. In particular, the invention relates to the fields of pharmacogenomics, diagnostics, patient therapy and the use of genetic haplotype information to predict an individual's susceptibility to IBD (ex: Chrohn's disease) and/or their response to a particular drug or drugs.
    Type: Application
    Filed: December 19, 2006
    Publication date: July 16, 2009
    Inventors: Abdelmajid Belouchi, John Verner Raelson, Walter Edward Bradley, Bruno Paquin, Helene Fournier, Quynh Nguyen-Huu, Pascal Croteau, Rene Allard, Sandie Briand, Paul Van Eerdewegh, Randall David Little, Jonathan Segal, Tim Keith
  • Publication number: 20090081658
    Abstract: The present invention relates to the selection of a set of polymorphism markers for use in genome wide association studies based on linkage disequilibrium mapping. In particular, the invention relates to the fields of pharmacogenomics, diagnostics, patient therapy and the use of genetic haplotype information to predict an individual's susceptibility to Crohn's disease and/or their response to a particular drug or drugs.
    Type: Application
    Filed: August 24, 2006
    Publication date: March 26, 2009
    Inventors: Abdelmajid Belouchi, John Verner Raelson, Walter Edward Bradley, Bruno Paquin, Helene Fournier, Quynh Nguyen-Huu, Pascal Croteau, Rene Allard, Sophie Debrus, Valerie Serre, Paul Van Eerdewegh, Randall David Little, Tim Keith, Jonathan Segal, Tim Keith
  • Publication number: 20030200033
    Abstract: The invention provides an automated method of simultaneously identifying sequence information extending a plurality of seed sequences. The method consists of: (a) searching a plurality of target sequences with a multiplex query comprising a plurality of seed sequences; (b) identifying a plurality of target sequences substantially aligning with a plurality of seed sequences; (c) selecting a plurality of substantially aligned target sequences containing sequence extending information for a plurality of seed sequences, and (d) repeating steps (a) through (c) using the selected plurality of substantially aligned target sequences as a plurality of seed sequences. Also provided is an automated method of simultaneous identifying a plurality of gene sequences within a plurality of genomic region sequences.
    Type: Application
    Filed: April 12, 2002
    Publication date: October 23, 2003
    Inventors: Jonathan Segal, Hui Huang