Patents by Inventor Jeffrey R. Gruen

Jeffrey R. Gruen 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: 20220243271
    Abstract: Described herein are the association BV677278 (READ1) with reading disability and language impairment, as well as the synergistic interaction of DCDC2 risk haplotypes or alleles with KIAA0319 risk allele.
    Type: Application
    Filed: September 8, 2021
    Publication date: August 4, 2022
    Applicant: Yale University
    Inventors: Jeffrey R. Gruen, Natalie Renee Powers
  • Patent number: 11155871
    Abstract: Described herein are the association BV677278 (READ1) with reading disability and language impairment, as well as the synergistic interaction of DCDC2 risk haplotypes or alleles with KIAA0319 risk allele.
    Type: Grant
    Filed: November 7, 2013
    Date of Patent: October 26, 2021
    Assignee: Yale University
    Inventors: Jeffrey R. Gruen, Natalie R. Powers
  • Publication number: 20180119224
    Abstract: The present invention relates to identification of a human gene, DCDC2 (MIM: 605755), associated with susceptibility for developing reading disability (RD), which is useful in identifying or aiding in identifying individuals at risk for developing RD, as well as for diagnosing or aiding in the diagnosis of RD.
    Type: Application
    Filed: November 6, 2017
    Publication date: May 3, 2018
    Applicant: Yale University
    Inventors: Jeffrey R. Gruen, Haiying Meng
  • Patent number: 9828639
    Abstract: The present invention relates to identification of a human gene, DCDC2 (MIM: 605755), associated with susceptibility for developing reading disability (RD), which is useful in identifying or aiding in identifying individuals at risk for developing RD, as well as for diagnosing or aiding in the diagnosis of RD.
    Type: Grant
    Filed: August 14, 2013
    Date of Patent: November 28, 2017
    Assignee: Yale University
    Inventors: Jeffrey R. Gruen, Haiying Meng
  • Publication number: 20170152558
    Abstract: Described herein are the association BV677278 (READ1) with reading disability and language impairment, as well as the synergistic interaction of DCDC2 risk haplotypes or alleles with KIAA0319 risk allele.
    Type: Application
    Filed: November 7, 2013
    Publication date: June 1, 2017
    Inventor: Jeffrey R. Gruen
  • Publication number: 20150299792
    Abstract: Described herein are the association BV677278 (READ1) with reading disability and language impairment, as well as the synergistic interaction of DCDC2 risk haplotypes or alleles with KIAA0319 risk allele.
    Type: Application
    Filed: November 7, 2013
    Publication date: October 22, 2015
    Inventor: Jeffrey R. Gruen
  • Publication number: 20140051076
    Abstract: The present invention relates to identification of a human gene, DCDC2 (MIM: 605755), associated with susceptibility for developing reading disability (RD), which is useful in identifying or aiding in identifying individuals at risk for developing RD, as well as for diagnosing or aiding in the diagnosis of RD.
    Type: Application
    Filed: August 14, 2013
    Publication date: February 20, 2014
    Applicant: Yale University
    Inventors: Jeffrey R. Gruen, Haiying Meng
  • Publication number: 20120115140
    Abstract: The present invention includes a rapid, selective, and accurate method of diagnosing a human subject with a triplet repeat genetic disorder of the FMR1 gene that leads to fragile X syndrome. The present invention also includes a rapid, selective, and accurate method of diagnosing a human subject at risk for developing a triplet repeat genetic disorder of the FMR1 gene that leads to fragile X syndrome, or at risk of passing such a disorder on to their progeny.
    Type: Application
    Filed: April 28, 2010
    Publication date: May 10, 2012
    Inventors: Scott A. Rivkees, Jeffrey R. Gruen, Seiyu Hosono, Karl Hager
  • Publication number: 20120100537
    Abstract: The present invention encompasses a method of diagnosing chromosomal trisomy in a human subject. In one embodiment, the method comprises pyrosequencing at least one single nucleotide polymorphism on a chromosome being assessed for trisomy, where the SNP comprises two alleles.
    Type: Application
    Filed: April 26, 2010
    Publication date: April 26, 2012
    Inventors: Scott A. Rivkees, Jeffrey R. Gruen, Seiyu Hosono, Karl Hager
  • Publication number: 20080318217
    Abstract: The present invention relates to identification of a human gene, DCDC2 (MIM: 605755), associated with susceptibility for developing reading disability (RD), which is useful in identifying or aiding in identifying individuals at risk for developing RD, as well as for diagnosing or aiding in the diagnosis of RD.
    Type: Application
    Filed: September 14, 2005
    Publication date: December 25, 2008
    Applicant: Yale University
    Inventors: Jeffrey R. Gruen, Haiying Meng