JEFFREY R GRUEN, MD
Medical Practice in New Haven, CT
License number
Connecticut 025237
Category
Medical Practice
Type
Neonatal-Perinatal Medicine
Address
Address
20 WEST Pavilion - FLOOR 2ND, New Haven, CT 06504
Phone
(203) 688-2320
(203) 688-5426 (Fax)
(203) 688-5426 (Fax)
Personal information
See more information about JEFFREY R GRUEN at radaris.comName
Address
Phone
151 Harmon St, Hamden, CT 06517
151 Harmon St, Hamden, CT 06517
Organization information
See more information about JEFFREY R GRUEN at bizstanding.comYale Neonatalogy - Jeffrey R Gruen MD
20 York St #4, New Haven, CT 06510
Categories:
Physicians & Surgeons
Phone:
(203) 688-2320 (Phone)
Professional information
See more information about JEFFREY R GRUEN at trustoria.com
Professor At Yale Medical School
Professor At Yale Medical School
Position:
Professor at Yale Medical School
Location:
New Haven, Connecticut
Industry:
Research
Work:
Yale Medical School
- New Haven, CT since Jun 1988
-
Professor
Education:
Tulane University School of Medicine 1977 - 1981
Dr. Jeffrey R Gruen, New Haven CT - MD (Doctor of Medicine)
Dr. Jeffrey R Gruen, New Haven CT - MD (Doctor of Medicine)
Specialties:
Neonatal Medicine
Address:
Yale Neonatologist Group
20 York St SUITE 493, New Haven 06510
(203) 688-2320 (Phone)
20 York St SUITE 493, New Haven 06510
(203) 688-2320 (Phone)
Certifications:
Pediatrics, 1986, Perinatal Medicine & Neonatal Medicine, 1997
Awards:
Healthgrades Honor Roll
Languages:
English
Hospitals:
Yale Neonatologist Group
20 York St SUITE 493, New Haven 06510
Yale - New Haven Hospital
20 York St, New Haven 06510
20 York St SUITE 493, New Haven 06510
Yale - New Haven Hospital
20 York St, New Haven 06510
Education:
Medical School
Northwestern Center Feinberg School of Medicine
Graduated: 1980
Tulane University of Louisiana
Graduated: 1981
Yale New Haven Hospital
Northwestern Center Feinberg School of Medicine
Graduated: 1980
Tulane University of Louisiana
Graduated: 1981
Yale New Haven Hospital
Identification Of Gene Associated With Reading Disability And Uses Therefor
Identification Of Gene Associated With Reading Disability And Uses Therefor
US Patent:
2008031, Dec 25, 2008
Filed:
Sep 14, 2005
Appl. No.:
11/662325
Inventors:
Jeffrey R. Gruen - Hamden CT, US
Haiying Meng - New Haven CT, US
Haiying Meng - New Haven CT, US
Assignee:
Yale University - New Haven CT
International Classification:
C12Q 1/68, C07H 21/04
US Classification:
435 6, 536 2431, 536 2433
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.
Dna Diagnostic Screening For Turner Syndrome And Sex Chromosome Disorders
Dna Diagnostic Screening For Turner Syndrome And Sex Chromosome Disorders
US Patent:
2006029, Dec 28, 2006
Filed:
Apr 12, 2006
Appl. No.:
11/402775
Inventors:
Scott Rivkees - Orange CT, US
Jeffrey Gruen - Hamden CT, US
Jeffrey Gruen - Hamden CT, US
International Classification:
C12Q 1/68, C07H 21/04
US Classification:
435006000, 536024300
Abstract:
The present invention encompasses methods, assays and kits for the diagnosis, screening and identification of Turner syndrome and other disorders of sexual differentiation in a human using single nucleotide polymorphisms present on the X and Y chromosomes.
Molecular Diagnosis Of Fragile X Syndrome Associated With Fmr1 Gene
Molecular Diagnosis Of Fragile X Syndrome Associated With Fmr1 Gene
US Patent:
2012011, May 10, 2012
Filed:
Apr 28, 2010
Appl. No.:
13/266434
Inventors:
Scott A. Rivkees - Orange CT, US
Jeffrey R. Gruen - Hamden CT, US
Seiyu Hosono - Rye NY, US
Karl Hager - Branford CT, US
Jeffrey R. Gruen - Hamden CT, US
Seiyu Hosono - Rye NY, US
Karl Hager - Branford CT, US
International Classification:
C12Q 1/68
US Classification:
435 611, 435 612
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.
Dna Diagnostic Screening For Turner Syndrome And Sex Chromosome Disorders
Dna Diagnostic Screening For Turner Syndrome And Sex Chromosome Disorders
US Patent:
2011022, Sep 22, 2011
Filed:
Feb 17, 2011
Appl. No.:
13/029963
Inventors:
Scott Rivkees - Orange CT, US
Jeffrey Gruen - Hamden CT, US
Jeffrey Gruen - Hamden CT, US
International Classification:
C12Q 1/68
US Classification:
435 612
Abstract:
The present invention encompasses methods, assays and kits for the diagnosis, screening and identification of Turner syndrome and other disorders of sexual differentiation in a human using single nucleotide polymorphisms present on the X and Y chromosomes.
Dna Diagnostic Screening For Turner Syndrome And Sex Chromosome Disorders
Dna Diagnostic Screening For Turner Syndrome And Sex Chromosome Disorders
US Patent:
2010019, Aug 5, 2010
Filed:
Nov 20, 2007
Appl. No.:
11/986165
Inventors:
Scott Rivkees - Orange CT, US
Jeffrey Gruen - Hamden CT, US
Jeffrey Gruen - Hamden CT, US
Assignee:
Yale University - New Haven CT
International Classification:
C12Q 1/68, C07H 21/04
US Classification:
435 6, 536 2433
Abstract:
The present invention encompasses methods, assays and kits for the diagnosis, screening and identification of Turner syndrome and other disorders of sexual differentiation in a human using single nucleotide polymorphisms present on the X and Y chromosomes.