JS GENETICS, LLC

Basic Information

RICHARD CHAMPAGNE
397 POST ROAD, SUITE 203
DARIEN, CT, -

Company Profile

n/a

Additional Details

Field Value
DUNS: 149516101
Hubzone Owned: N
Socially and Economically Disadvantaged: N
Woman Owned: N
Number of Employees: n/a


  1. Identification of Oligodendrocyte Stimulators

    Amount: $708,235.00

    DESCRIPTION (provided by applicant): Oligodendrocytes (OLs) are the myelinating cells of the central nervous system and play a critical role in white matter formation. Serious clinical disorders affec ...

    SBIR Phase II 2010 Department of Health and Human Services
  2. Development of Novel Diagnostics for Fragile X Syndrome

    Amount: $1,069,800.00

    DESCRIPTION (provided by applicant): Fragile X Syndrome (FRAX) is the most common genetic cause of mental retardation in males. FRAX is caused by the expansion of a CGG trinucleotide repeat of the ...

    SBIR Phase II 2010 Department of Health and Human Services
  3. Development of Novel Diagnostics for Fragile X Syndrome

    Amount: $117,700.00

    DESCRIPTION (provided by applicant): Fragile X Syndrome (FRAX), is the most common cause of mental retardation in males. The incidence of FRAX is 1 per 4000 in males and 1 per 8000 in females. FRAX i ...

    SBIR Phase I 2008 Department of Health and Human Services
  4. Identification of Oligodendrocyte Stimulators

    Amount: $150,854.00

    DESCRIPTION (provided by applicant): Abstract Oligodendrocytes (OLs) are the myelinating cells of the central nervous system and play a critical role in white matter formation and white matter stabili ...

    SBIR Phase I 2008 Department of Health and Human Services
  5. Molecular Diagnosis of Dyslexia

    Amount: $122,164.00

    DESCRIPTION (provided by applicant): Reading disability (RD), also known as dyslexia, is the most common learning disability affecting school children. In the US, Canada, Europe and countries where it ...

    SBIR Phase I 2007 Department of Health and Human Services
  6. Newborn Screening for Sex Chromosome Disorders

    Amount: $464,396.00

    DESCRIPTION (provided by applicant): Turner syndrome (TS) is the most common genetic problem affecting women and occurs when an entire, or a portion of an X-chromosome is deleted. The incidence of TS ...

    STTR Phase II 2007 Department of Health and Human Services
  7. Newborn Screening for Sex Chromosome Disorders

    Amount: $129,953.00

    DESCRIPTION (provided by applicant): Turner syndrome (TS) is the most common genetic problem effecting women, with an incidence of 1 in 1,500 to 2,000 live female births and occurs when an entire, or ...

    STTR Phase I 2006 Department of Health and Human Services

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