Medical College of Wisconsin
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Gabrielle Christine Geddes MD

Assistant Professor

Institution: Medical College of Wisconsin
Department: Pediatrics
Division: Genetics

Member of the Genomic Sciences and Precision Medicine Center (GSPMC)


  • Inheritance of a Balanced t(12;20)(q24.33;p12.2) and Unbalanced der(13)t(7;13)(p21.3;q33.2) from a Maternally Derived Double Balanced Translocation Carrier. (Peterson JF, Geddes GC, Basel DG, Schippman D, Grignon JW Jr, vanTuinen P, Kappes UP) J Pediatr Genet 2018 Mar;7(1):35-39 PMID: 29441220 PMCID: PMC5809171 02/15/2018    
  • The spectrum of manifestations in desmoplakin gene (DSP) spectrin repeat 6 domain mutations: Immunophenotyping and response to ustekinumab. (Paller AS, Czarnowicki T, Renert-Yuval Y, Holland K, Huynh T, Sadlier M, McAleer MA, Tran G, Geddes GC, Irvine AD, Guttman-Yassky E) J Am Acad Dermatol 2018 03;78(3):498-505.e2 PMID: 29066275 10/27/2017       6 Citations
  • Genetic Testing Protocol Reduces Costs and Increases Rate of Genetic Diagnosis in Infants with Congenital Heart Disease. (Geddes GC, Basel D, Frommelt P, Kinney A, Earing M) Pediatr Cardiol 2017 Oct;38(7):1465-1470 PMID: 28725922 PMCID: PMC5628185 07/21/2017       1 Citations
  • Ciliopathy variant burden and developmental delay in children with hypoplastic left heart syndrome. (Geddes GC, Stamm K, Mitchell M, Mussatto KA, Tomita-Mitchell A) Genet Med 2016 Oct 27 PMID: 27787502 10/28/2016    
  • Concomitant 11p15.4-p15.5 duplication and terminal 22q13.33 deletion in a patient with features of Beckwith-Wiedemann syndrome. (Peterson JF, Bick DP, Geddes GC, McCarrier J, Grignon JW Jr, Chirempes B, Broeckel U, Abidi F, Rogers RC, Boccuto L, DuPont B, vanTuinen P) Am J Med Genet A 2016 Dec;170(12):3348-3351 PMID: 27549580 08/24/2016       2 Citations
  • Bacteremia in Patients with Heterotaxy: A Review and Implications for Management. (Loomba RS, Geddes GC, Basel D, Benson DW, Leuthner SR, Hehir DA, Ghanayem N, Shillingford AJ) Congenit Heart Dis 2016 Dec;11(6):537-547 PMID: 27425254 07/19/2016       4 Citations
  • BAG3 myofibrillar myopathy presenting with cardiomyopathy. (Konersman CG, Bordini BJ, Scharer G, Lawlor MW, Zangwill S, Southern JF, Amos L, Geddes GC, Kliegman R, Collins MP) Neuromuscul Disord 2015 May;25(5):418-22 PMID: 25728519 03/03/2015       34 Citations
  • A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia. (Geddes GC, Dimmock DP, Hehir DA, Helbling DC, Kirkpatrick E, Loomba R, Southern J, Waknitz M, Scharer G, Konduri GG) J Perinatol 2015 Feb;35(2):155-7 PMID: 25627281 01/30/2015       1 Citations
  • FISH for 22q11.2 deletion not cost-effective for infants with congenital heart disease with microarray. (Geddes GC, Butterly M, Sajan I) Pediatr Cardiol 2015 Mar;36(3):531-6 PMID: 25304247 10/12/2014       4 Citations
  • Multicellular redox regulation in an early-evolving animal treated with glutathione. (Doolen JF, Geddes GC, Blackstone NW) Physiol Biochem Zool 2007 May-Jun;80(3):317-25 PMID: 17390287 03/29/2007       7 Citations
  • Redox signaling in colonial hydroids: many pathways for peroxide. (Blackstone NW, Bivins MJ, Cherry KS, Fletcher RE, Geddes GC) J Exp Biol 2005 Jan;208(Pt 2):383-90 PMID: 15634856 01/07/2005       17 Citations
  • Last update: 01/18/2019
    jenkins-FCD Prod-300 626508253d14e4184314fb9f66322a03a5906796