UCONN

HEALTH

Photo of Robin C. Schwartz, M.S., C.G.C., L.G.C.

Robin C. Schwartz, M.S., C.G.C., L.G.C.

Assistant Professor, Genetics and Genome Sciences
Academic Office Location:
Genetics and Genome Sciences
UConn Health
263 Farmington Avenue
Farmington, CT 06030-7120
Phone: 860-679-6068
Fax: 860-679-0143
Email: rschwartz@uchc.edu

Ms. Schwartz received her bachelor’s degree in biology from Herbert H. Lehman College in 1973, and her master’s degree in genetic counseling from Rutgers University in 1976. A member of the National Society of Genetic Counseling since 1979, she was a coordinator in Clinical Genetics at Columbia University, a research associate at Rutgers University, and has been at UConn Health Center since 1987.

Education
DegreeInstitutionMajor
B.A.Herbert H. Lehman CollegeBiology
M.S.Rutgers UniversityGenetics and Genetic Counseling
Name & DescriptionCategoryRoleTypeScopeStart YearEnd Year
University of Connecticut, Professional Science Masters Program in Health Care GeneticsAdvisory CommitteeKey Faculty MemberUConn HealthUniversity2012
Education and Workforce Development, Genetic Advisory Committee, Connecticut Department of Public Health Advisory CommitteeCo-ChairUConn HealthUniversity2010
Expert Genomics Advisory Committee, CT Department of Public Health Advisory CommitteeMemberUConn HealthUniversity2008
Human Genetics Residency Program Research CommitteeAssociate DirectorUConn HealthUniversity2008
Education and Workforce Development, Connecticut Department of Public HealthAdvisory CommitteeMemberUConn HealthUniversity2007
National Society of Genetic Counselors Professional/Scientific OrganizationMemberExternalNational1980
American Society of Human GeneticsProfessional/Scientific OrganizationMemberExternalNational
American Board of Medical GeneticsProfessional/Scientific OrganizationDiplomateExternalNational
American Board of Genetic CounselingAdvisory CommitteeCharter MemberExternalNational
Commission on CancerOtherMember, Genetic Counselor RepresentativeUConn HealthNational
Ms. Schwartz strives to provide information to individuals with an increased risk to develop cancer, so that they, along with their health care providers, can activate personalized cancer prevention strategies. Genetic risk assessment can play a role in the early identification of families with a higher risk to develop cancer. Individuals in families with concerns about their cancer risk often seek guidance and information. Ms. Schwartz's goal is to answer their questions and support their decisions regarding the management of, and coping with, their familial cancer risk.

Journal Articles

Abstracts

  • Mild osteogenesis imperfecta is not always inherited as a dominant trait
    Tsipouras P,Flodman P, Schwartz RC, Quarrell O, Harper PS, Weksberg R Am J Hum Genet 1988 Jan;4397A
  • The evolving genetic heterogeneity in autosomal dominant osteogenesis imperfecta
    Tsipouras P, Schwartz RC Ped. Research 1988 Jan;23334A
  • First trimester prenatal diagnosis of autosomal dominant osteogenesis imperfecta type IV using restriction fragment length polymorphisms (RFLPs) in the COLIA2 gene
    Schwartz RC, Goldberg JD, Berkowitz RL, Tsipouras P Am J Hum Genet 1986 Jan;39265A
  • DNA Markers associated with the human procollagen genes
    Tsipouras P, Sangiorgi FO, Chu M-L, Weil D, Schwartz RC, Ramirez F Cytogenet and Cell Genetics 1985 Jan;40762-763
  • Genetic linkage to the Pro-al(III) collagen gene
    Schwartz RC, Byers PH, Chu M-L, Weil, Ramirez F, Tsipouras P Am J Hum Genet 1985 Jan;37173A
  • Linkage of mild Osteogenesis imperfecta OI type IV, to COLIA2
    Tsipouras P, Schwartz RC, Ramirez F, Falk CT Cytogenet and Cell Genetics 1985 Jan;40763
  • Familial distal trisomy 14q
    Sklower S, Jenkins E, Nolin S, Warburton D, Anyane-Yeboa K, Merkrebs A, Schwartz R, Wisnieski K, Stimson C, Brown T Am J Hum Genet 1982 Jan;34145A
  • Five Siblings with partial distal 13 Trisomy: delineation of a syndrome and implications for recurrence risks in translocation families
    Schwartz R, Johnson W, Warburton D, Fellman D Am. J. Hum. Genet 1982 Jan;34109A
  • Congenital sialidosis: biochemical studies, clinical spectrum in four sibs; two successful prenatal diagnoses
    Johnson WG, Thomas GH, Miranda AF, Driscoll JM, Wigger JJ, Yeh MN, Schwartz RC, Cohen CS, Berdon WE, Koenigsberb MR Am. J. Hum. Genet 1980 Jan;3243A
  • Donor Insemination: who should be screened for what? Tay-Sachs disease resulting from donor insemination
    Chutorian AM, Johnson WG, Schwartz RC Am. J. Hum. Genet 1980 Jan;32102A

Conference Papers

  • Direct-to-Consumer Marketing Of BRCA Testing: Assessing the Short Term impact on individuals at risk and the practice of cancer genetic counseling
    Schwartz R 2008 Jan;
  • Diagnosis of variant PKU in a child with the initial diagnosis of mild persisten hyperphenylalaninemia (MPH).
    Schwartz R 1994 Jan;
  • Genetic linkage study of Marfan syndrome with collagen genes and 41 other markers.
    Schwartz R 1990 Jan;
  • Linkage analysis of Marfan syndrome with 47 other markers.
    Schwartz R 1990 Jan;
  • An exclusion map for the Marfan syndrome (MS) locus.
    Schwartz R 1989 Jan;
  • Discordant segregation of the Type II collagen gene (COL2A1) in a family with Stickler syndrome using simple patterns of polymorphic restriction sites.
    Schwartz R 1989 Jan;
  • Genetic linkage studies in Marfan syndrome.
    Schwartz R 1989 Jan;
  • Non-allelic genetic heterogeneity in the vitreoretinal degenerations of the Stickler and Wagner types and evidence for intragenic recombination at the COL2A1 locus.
    Schwartz R 1989 Jan;
  • The use of linkage analysis using RFLP's in the heritable disorders of connective tissue.
    Schwartz R 1986 Jan;

Letters

Reviews

Title or AbstractTypeSponsor/EventDate/YearLocation
Genetic Counseling as a CareerLectureSimsbury High School 2013Simsbury CT
Carreers in Genetics TalkAvon High School SPARK2011
Hereditary and Familial Cancers Affecting WomenTalkUnicorn Perinatal Network Montlhy Series2010Charlotte Hugerford Hospital
Hereditary and Familial Cancers Affecting WomenTalkUCHC Unicorn Perinatal Network2010Windham Hospital
Hereditary and Familial Cancers Affecting WomenTalkUnicorn Perinatal Network Monthly Series2010Middlesex Hospital
Hereditary and Familial Cancers Affecting WomenTalkUCHC Unicorn Perinatal Network2010Midstate Medical Center
For Your Life For Your Health- Hereditary Breast Cancer Afffecting the Ashkenazi Jewish PopulationTalkTemple - Middletown CT2010Middletown Community
Ethical Considerations in Genetic Counseling and TestingTalkGPAH 5095, Dr. Judy Brown2010
Now We’re Cookin’: Quick and Easy Recipes for PKU Cooking. OtherUniversity of Connecticut Health Center1999UCHC