JacobAndersonReissMD

PubMed

• 5 citations
  Implementation of a systematic tumor screening program for Lynch Syndrome in an integrated health care setting
  Elizabeth V. Clarke, Kristin R. Muessig, Jamilyn M. Zepp, Jessica Ezzell Hunter, Sapna Syngal, Louise S. Acheson, Georgia L. Wiesner, Susan K. Peterson, Kellene M. Ber...> ;Familial Cancer. 2019 Jul 1
• A case for expanding carrier testing to include actionable X-linked disorders.
  Alan F. Rope, Tia L. Kauffman, Pat Himes, Laura M. Amendola, Sumit Punj, Yassmine Akkari, Amiee Potter, James V. Davis, Jennifer L. Schneider, Jacob A. Reiss, Mari J. ...> ;Clinical Case Reports. 2018 Sep 19
• 23 citations
  Time Costs for Genetic Counseling in Preconception Carrier Screening with Genome Sequencing.
  Frances L. Lynch, Patricia Himes, Marian J. Gilmore, Elissa Morris, Jennifer L. Schneider, Tia L. Kauffman, Elizabeth Shuster, Jacob A. Reiss, John F. Dickerson, Micha...> ;Journal of Genetic Counseling. 2018 Feb 8
• 24 citations
  Genome sequencing and carrier testing: decisions on categorization and whether to disclose results of carrier testing
  Patricia Himes, Tia L. Kauffman, Kristin R. Muessig, Laura M. Amendola, Jonathan S. Berg, Michael O. Dorschner, Marian J. Gilmore, Deborah A. Nickerson, Jacob A. Reiss...> ;Genetics in Medicine. 2017 Jan 12
• 22 citations
  Generating a taxonomy for genetic conditions relevant to reproductive planning.
  Diane M. Korngiebel, Carmit K. McMullen, Laura M. Amendola, Jonathan S. Berg, James V. Davis, Marian J. Gilmore, Cary O. Harding, Patricia Himes, Gail P. Jarvik, Tia L...> ;American Journal of Medical Genetics. Part A. 2016 Mar 1
• 32 citations
  Stakeholder perspectives on implementing a universal Lynch syndrome screening program: a qualitative study of early barriers and facilitators
  Jennifer L. Schneider, James V. Davis, Tia L. Kauffman, Jacob A. Reiss, Cheryl Mcginley, Kathleen Arnold, Jamilyn M. Zepp, Marian J. Gilmore, Kristin R. Muessig, Sapna...> ;Genetics in Medicine. 2016 Feb 1
• 38 citations
  “Is It Worth Knowing?” Focus Group Participants’ Perceived Utility of Genomic Preconception Carrier Screening
  Jennifer L. Schneider, Katrina A.B. Goddard, James V. Davis, Benjamin S. Wilfond, Tia L. Kauffman, Jacob A. Reiss, Marian J. Gilmore, Patricia Himes, Frances L. Lynch,...> ;Journal of Genetic Counseling. 2016 Feb 1
• 17 citations
  Patients' ratings of genetic conditions validate a taxonomy to simplify decisions about preconception carrier screening via genome sequencing.
  Michael C. Leo, Carmit K. McMullen, Benjamin S. Wilfond, Frances L. Lynch, Jacob A. Reiss, Marian J. Gilmore, Patricia Himes, Tia L. Kauffman, James V. Davis, Gail P. ...> ;American Journal of Medical Genetics. Part A. 2016 Mar 1
• 14 citations
  Heritability of serum iron measures in the hemochromatosis and iron overload screening (HEIRS) family study.
  Christine E. McLaren, James C. Barton, John H. Eckfeldt, Gordon D. McLaren, Ronald T. Acton, Paul C. Adams, Leora Henkin, Victor R. Gordeuk, Chris D. Vulpe, Emily L. H...> ;American Journal of Hematology. 2010 Feb 1
• 33 citations
  Deletion of an enhancer near DLX5 and DLX6 in a family with hearing loss, craniofacial defects, and an inv(7)(q21.3q35)
  Kerry K. Brown, Jacob A. Reiss, Kate Crow, Heather L. Ferguson, Chantal Kelly, Bernd Fritzsch, Cynthia C. Morton> ;Human Genetics. 2010 Jan 1
• 10 citations
  Screening for hemochromatosis and iron overload: satisfaction with results notification and understanding of mailed results in unaffected participants of the HEIRS study.
  Helen Harrison, Barbara Harrison, Ann P. Walker, Kurt Lohman, Shellie D. Ellis, Mark A. Hall, Jacob A. Reiss, Paul C. Adams, Joan Holup, Ronald T. Acton, Thomas C. Ben...> ;Genetic Testing. 2008 Dec 15
• 15 citations
  Combined Retinal Hamartomas Leading to the Diagnosis of Neurofibromatosis Type 2
  Elizabeth A. Grant, Karmen M Trzupek, Jacob A. Reiss, Kate Crow, Ludwine Messiaen, Richard G. Weleber> ;Ophthalmic Genetics. 2008 Sep 1
• 37 citations
  Serum ferritin concentrations and body iron stores in a multicenter, multiethnic primary-care population.
  Victor R. Gordeuk, David M. Reboussin, Christine E. McLaren, James C. Barton, Ronald T. Acton, Gordon D. McLaren, Emily L. Harris, Jacob A. Reiss, Paul C. Adams, Mark ...> ;American Journal of Hematology. 2008 Aug 1
• 11 citations
  Accuracy of Family History of Hemochromatosis or Iron Overload: The Hemochromatosis and Iron Overload Screening Study
  Ronald T. Acton, James C. Barton, Leah Passmore, Paul C. Adams, Gordon D. McLaren, Catherine Leiendecker–Foster, Mark Speechley, Emily L. Harris, Oswaldo L. Castro, Ja...> ;Clinical Gastroenterology and Hepatology. 2008 Aug 1
• 6 citations
  Characteristics of participants with self‐reported hemochromatosis or iron overload at HEIRS study initial screening
  James C. Barton, Ronald T. Acton, Catherine Leiendecker-Foster, Laura C. Lovato, Paul C. Adams, John H. Eckfeldt, Christine E. McLaren, Jacob A. Reiss, Gordon D. McLar...> ;American Journal of Hematology. 2008 Feb 1
• 12 citations
  Results communication and patient education after screening for possible hemochromatosis and iron overload: experience from the HEIRS Study of a large ethnically and l...
  Ann P. Walker, Diane C. Tucker, Mark A. Hall, Kurt Lohman, Helen Harrison, Barbara Harrison, Jacob A. Reiss, Ronald T. Acton, Paul C. Adams, Sharmin Diaz, Joan Holup, ...> ;Genetics in Medicine. 2007 Nov 1
• 6 citations
  HFE C282Y homozygotes aged 25-29 years at HEIRS Study initial screening.
  James C. Barton, Ronald T. Acton, Catherine Leiendecker-Foster, Laura C. Lovato, Paul C. Adams, Gordon D. McLaren, John H. Eckfeldt, Christine E. McLaren, David M. Reb...> ;Genetic Testing. 2007 Oct 21
• 6 citations
  Health-related quality of life in a racially diverse population screened for hemochromatosis: results from the Hemochromatosis and Iron Overload Screening (HEIRS) study.
  Lari Wenzel, Roger T. Anderson, Diane C. Tucker, Shana L. Palla, Elizabeth J. Thomson, Mark Speechley, Helen Harrison, Ometha Lewis-Jack, Margaret Fadojutimi-Akinsiku,...> ;Genetics in Medicine. 2007 Oct 1
• 21 citations
  Genetic screening for iron overload: No evidence of discrimination at 1 year.
  Mark A. Hall, James C. Barton, Paul C. Adams, Christine E. McLaren, Jacob A. Reiss, Oswaldo Castro, Andrea Ruggiero, Ronald T. Acton, Tara E Power, Thomas C. Bent> ;The Journal of Family Practice. 2007 Oct 1
• 8 citations
  Predictors of belief that genetic test information about hemochromatosis should be shared with family members.
  Diane C. Tucker, Ronald T. Acton, Nancy Press, Andrea Ruggiero, Jacob A. Reiss, Ann P. Walker, Lari Wenzel, Barbara Harrison, Margaret Fadojutimi-Akinsiku, Helen Harri...> ;Genetic Testing. 2006 Mar 17
• 74 citations
  Concerns in a primary care population about genetic discrimination by insurers
  Mark A. Hall, Jean E. McEwen, James C. Barton, Ann P. Walker, Edmund G Howe, Jacob A. Reiss, Tara E Power, Shellie D. Ellis, Diane C. Tucker, Barbara Harrison, Gordon ...> ;Genetics in Medicine. 2005 May 1
• 272 citations
  Interstitial deletion of (17)(p11.2p11.2) in nine patients
  Ann C. M. Smith, Loris McGavran, Jeannie Robinson, Gail Waldstein, Jean Macfarlane, Jon Zonona, Jacob A. Reiss, Martin Lahr, L. Allen, Ellen Magenis, John M. Opitz, Ja...> ;American Journal of Medical Genetics. 1986 Jul 1
• 19 citations
  The 8p- syndrome.
  Jacob A. Reiss, J. Chamberlin, R E Magenis, Everett W. Lovrien> ;Human Genetics. 1979 Mar 12
• A mutation in the gene for the neurotransmitter receptor-clustering protein gephyrin causes a novel form of molybdenum cofactor deficiency.
  Reiss, J., Gross-Hardt, S., Christensen, E., Schmidt, P., Mendel, R. R., Schwarz, G.> ;Am J Hum Genet. 2001 Jan
• A cystic fibrosis patient homozygous for the nonsense mutation R553X.
  Bal, J., Stuhrmann, M., Schloesser, M., Schmidtke, J., Reiss, J.> ;J Med Genet. 1991 Oct
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