Medical College of Wisconsin
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Erin Syverson MGC

Director, Assistant Professor

Institution: Medical College of Wisconsin
Department: Institute for Health and Equity
Division: Genetics
Program: Genetic Counseling Education

Clinical Expertise

  • Genetic Counseling
  • Human Genetics

    • Publications (5)

  • TCEAL1 loss-of-function results in an X-linked dominant neurodevelopmental syndrome and drives the neurological disease trait in Xq22.2 deletions. (Hijazi H, Reis LM, Pehlivan D, Bernstein JA, Muriello M, Syverson E, Bonner D, Estiar MA, Gan-Or Z, Rouleau GA, Lyulcheva E, Greenhalgh L, Tessarech M, Colin E, Guichet A, Bonneau D, van Jaarsveld RH, Lachmeijer AMA, Ruaud L, Levy J, Tabet AC, Ploski R, Rydzanicz M, Kępczyński Ł, Połatyńska K, Li Y, Fatih JM, Marafi D, Rosenfeld JA, Coban-Akdemir Z, Bi W, Gibbs RA, Hobson GM, Hunter JV, Carvalho CMB, Posey JE, Semina EV, Lupski JR) Am J Hum Genet 2022 Nov 07 PMID: 36368327 11/12/2022    
  • Genetic counseling for congenital heart disease - Practice resource of the National Society of Genetic Counselors. (Ison HE, Griffin EL, Parrott A, Shikany AR, Meyers L, Thomas MJ, Syverson E, Demo EM, Fitzgerald KK, Fitzgerald-Butt S, Ziegler KL, Schartman AF, Stone KM, Helm BM) J Genet Couns 2022 Feb;31(1):9-33 PMID: 34510635 SCOPUS ID: 2-s2.0-85114855852 09/13/2021       5 Citations
  • Does Supply Equal Demand? The Workforce of Direct Patient Care Genetic Counselors in Wisconsin. (Dawson C, Syverson E, Chelius TH, Linn S, Reiser C, Stuewe K, Zoran S, Geurts JL) WMJ 2020 Sep;119(3):158-164 PMID: 33091282 SCOPUS ID: 2-s2.0-85094155867 10/23/2020       3 Citations
  • Three year experience of a clinical cardiovascular genetics program for infants with congenital heart disease. (Geddes GC, Syverson E, Earing MG) Congenit Heart Dis 2019 Sep;14(5):832-837 PMID: 31222963 PMCID: PMC6851694 SCOPUS ID: 2-s2.0-85067900893 06/22/2019       4 Citations
  • DNA Polymerase Epsilon Deficiency Causes IMAGe Syndrome with Variable Immunodeficiency. (Logan CV, Murray JE, Parry DA, Robertson A, Bellelli R, Tarnauskaitė Ž, Challis R, Cleal L, Borel V, Fluteau A, Santoyo-Lopez J, SGP Consortium, Aitman T, Barroso I, Basel D, Bicknell LS, Goel H, Hu H, Huff C, Hutchison M, Joyce C, Knox R, Lacroix AE, Langlois S, McCandless S, McCarrier J, Metcalfe KA, Morrissey R, Murphy N, Netchine I, O'Connell SM, Olney AH, Paria N, Rosenfeld JA, Sherlock M, Syverson E, White PC, Wise C, Yu Y, Zacharin M, Banerjee I, Reijns M, Bober MB, Semple RK, Boulton SJ, Rios JJ, Jackson AP) Am J Hum Genet 2018 Dec 06;103(6):1038-1044 PMID: 30503519 PMCID: PMC6288413 SCOPUS ID: 2-s2.0-85058605364 12/07/2018       39 Citations
    • Last update: 11/15/2022