Medical College of Wisconsin
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Jessica Scott Schwoerer MD

Jessica Scott Schwoerer MD profile photo picture

Associate Professor

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

image of /images/ORCIDiD_icon16x16.png   https://orcid.org/0000-0001-6106-8242


I am willing to collaborate on research projects.
I am willing to mentor a junior faculty member.

Publications (20)

  • Screening for Methylmalonic and Propionic Acidemia: Clinical Outcomes and Follow-Up Recommendations. (Held PK, Singh E, Scott Schwoerer J) Int J Neonatal Screen 2022 Feb 07;8(1) PMID: 35225935 PMCID: PMC8883915 SCOPUS ID: 2-s2.0-85124528103 03/01/2022       12 Citations
  • Rapid Transition to Telemedicine During the COVID-19 Pandemic: Medical Genetics Experience. (Zoran S, Turcott C, Whitehead A, Hrabik L, Harris A, Scott Schwoerer J) WMJ 2021 Oct;120(3):218-221 PMID: 34710304 10/29/2021    
  • No association between SCN9A and monogenic human epilepsy disorders. (Fasham J, Leslie JS, Harrison JW, Deline J, Williams KB, Kuhl A, Scott Schwoerer J, Cross HE, Crosby AH, Baple EL) PLoS Genet 2020 Nov;16(11):e1009161 PMID: 33216760 PMCID: PMC7717534 SCOPUS ID: 2-s2.0-85097156765 11/21/2020       9 Citations
  • A Survey of Eating Attitudes and Behaviors in Adolescents and Adults With Phenylalanine Hydroxylase Deficiency. (Luu S, Breunig T, Drilias N, Kuhl A, Scott Schwoerer J, Cody P) WMJ 2020 Mar;119(1):37-43 PMID: 32348070 SCOPUS ID: 2-s2.0-85084169892 04/30/2020       9 Citations
  • Neonatal Metabolic Crises: A Practical Approach. (Williams KB, Held PK, Scott Schwoerer J) Clin Perinatol 2020 Mar;47(1):155-170 PMID: 32000923 SCOPUS ID: 2-s2.0-85075899118 02/01/2020       2 Citations
  • Newborn Screening for Inherited Metabolic Disorders: Early Identification and Long-Term Care for Patients in the Plain Community, Wisconsin, 2011-2017. (Held PK, Rice GM, Kuhl A, Drilias N, Baker M, Deline J, Spicer G, Sandrock C, Seroogy CM, Schwoerer JS. ) Public Health Rep Public Health Rep. 2019 Nov/Dec;134(2_suppl):58S-63S. doi: 10.1177/0033354919878425. PubMed PMID: 31682555; PubMed Central PMCID: PMC6832032. 12/02/2019    
  • Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy. (18. Tam A, AlDhaheri NS, Mysore K, Tessier ME, Goss J, Fernandez LA, D'Alessandro AM, Schwoerer JS, Rice GM, Elsea SH, Scaglia F) Am J Med Genet A. 18. Tam A, AlDhaheri NS, Mysore K, Tessier ME, Goss J, Fernandez LA, D'Alessandro AM, Schwoerer JS, Rice GM, Elsea SH, Scaglia F. Improved clinical outcome following liver transplant in patients with ethylmalonic encephalopathy. Am J Med Genet A. 2019 Mar 12. doi: 10.1002/ajmg.a.61104. [Epub ahead of print] PMID: 30864297. 03/02/2019    
  • De Novo Mutations Affecting the Catalytic Cα Subunit of PP2A, PPP2CA, Cause Syndromic Intellectual Disability Resembling Other PP2A-Related Neurodevelopmental Disorders. (Reynhout S, Jansen S, Haesen D, van Belle S, de Munnik SA, Bongers EMHF, Schieving JH, Marcelis C, Amiel J, Rio M, Mclaughlin H, Ladda R, Sell S, Kriek M, Peeters-Scholte CMPCD, Terhal PA, van Gassen KL, Verbeek N, Henry S, Scott Schwoerer J, Malik S, Revencu N, Ferreira CR, Macnamara E, Braakman HMH, Brimble E, Ruzhnikov MRZ, Wagner M, Harrer P, Wieczorek D, Kuechler A, Tziperman B, Barel O, de Vries BBA, Gordon CT, Janssens V, Vissers LELM) Am J Hum Genet 2019 Jan 03;104(1):139-156 PMID: 30595372 PMCID: PMC6323609 SCOPUS ID: 2-s2.0-85059497872 01/01/2019       33 Citations
  • Long-term outcomes in Amish patients diagnosed with propionic acidemia. (Scott Schwoerer J, Clowes Candadai S, Held PK) Mol Genet Metab Rep 2018 Sep;16:36-38 PMID: 30013935 PMCID: PMC6019757 SCOPUS ID: 2-s2.0-85048739281 07/18/2018       16 Citations
  • Pegylated asparaginase as cause of fatal hyperammonemia in patient with latent urea cycle disorder. (15. Peters M, Zee-Cheng J, Kuhl A, Orozco J, Lally E, Scott Schwoerer J. ) Pediatr Blood Cancer 15. Peters M, Zee-Cheng J, Kuhl A, Orozco J, Lally E, Scott Schwoerer J. Pegylated asparaginase as cause of fatal hyperammonemia in patient with latent urea cycle disorder. Pediatr Blood Cancer. 2018 Sep;65(9):e27239. doi: 10.1002/pbc.27239. Epub 2018 May 18. PMID: 29775236. 05/02/2018    
  • Genotypes of patients with phenylalanine hydroxylase deficiency in the Wisconsin Amish. (Scott Schwoerer J, Drilias N, Kuhl A, Mochal S, Baker M. ) Mol Genet Metab Rep. Scott Schwoerer J, Drilias N, Kuhl A, Mochal S, Baker M. Genotypes of patients with phenylalanine hydroxylase deficiency in the Wisconsin Amish. Mol Genet Metab Rep. 2018 Mar 8;15:75-77. doi: 10.1016/j.ymgmr.2018.02.005. eCollection 2018 Jun. PMID: 29560316. 03/02/2018    
  • Successful pregnancy and delivery in a woman with propionic acidemia from the Amish community. (Scott Schwoerer J, van Calcar S, Rice GM, Deline J) Mol Genet Metab Rep 2016 Sep;8:4-7 PMID: 28649556 PMCID: PMC5471548 SCOPUS ID: 2-s2.0-84971501135 06/27/2017       10 Citations
  • Biallelic Mutations in MITF Cause Coloboma, Osteopetrosis, Microphthalmia, Macrocephaly, Albinism, and Deafness. (George A, Zand DJ, Hufnagel RB, Sharma R, Sergeev YV, Legare JM, Rice GM, Scott Schwoerer JA, Rius M, Tetri L, Gamm DM, Bharti K, Brooks BP) Am J Hum Genet 2016 Dec 01;99(6):1388-1394 PMID: 27889061 PMCID: PMC5142105 SCOPUS ID: 2-s2.0-85003956518 11/28/2016       71 Citations
  • Comparison of Methods of Initial Ascertainment in 58 Cases of Propionic Acidemia Enrolled in the Inborn Errors of Metabolism Information System Reveals Significant Differences in Time to Evaluation and Symptoms at Presentation. (McCrory NM, Edick MJ, Ahmad A, Lipinski S, Scott Schwoerer JA, Zhai S, Justice K, Cameron CA, Berry SA, Pena LD, Inborn Errors of Metabolism Collaborative) J Pediatr 2017 Jan;180:200-205.e8 PMID: 27776753 PMCID: PMC5183466 SCOPUS ID: 2-s2.0-85006150266 10/26/2016       14 Citations
  • Development of carrier testing for common inborn errors of metabolism in the Wisconsin Plain population. (Kuhl A, van Calcar S, Baker M, Seroogy CM, Rice G, Scott Schwoerer J) Genet Med 2017 Mar;19(3):352-356 PMID: 27513192 SCOPUS ID: 2-s2.0-85014857899 08/12/2016       6 Citations
  • Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency. (Scott Schwoerer J, Cooper G, van Calcar S) Mol Genet Metab Rep 2015 Jun;3:39-41 PMID: 26937394 PMCID: PMC4750558 SCOPUS ID: 2-s2.0-84925711135 03/05/2016       6 Citations
  • MECP2 duplication: possible cause of severe phenotype in females. (Scott Schwoerer J, Laffin J, Haun J, Raca G, Friez MJ, Giampietro PF) Am J Med Genet A 2014 Apr;164A(4):1029-34 PMID: 24458799 SCOPUS ID: 2-s2.0-84896316139 01/25/2014       22 Citations
  • Thirteen new patients with guanidinoacetate methyltransferase deficiency and functional characterization of nineteen novel missense variants in the GAMT gene. (Mercimek-Mahmutoglu S, Ndika J, Kanhai W, de Villemeur TB, Cheillan D, Christensen E, Dorison N, Hannig V, Hendriks Y, Hofstede FC, Lion-Francois L, Lund AM, Mundy H, Pitelet G, Raspall-Chaure M, Scott-Schwoerer JA, Szakszon K, Valayannopoulos V, Williams M, Salomons GS) Hum Mutat 2014 Apr;35(4):462-9 PMID: 24415674 SCOPUS ID: 2-s2.0-84896114525 01/15/2014       38 Citations
  • Analysis of maternal risk factors associated with congenital vertebral malformations. (Hesemann J, Lauer E, Ziska S, Noonan K, Nemeth B, Scott-Schwoerer J, McCarty C, Rasmussen K, Goldberg JM, Sund S, Eickhoff J, Raggio CL, Giampietro PF) Spine (Phila Pa 1976) 2013 Mar 01;38(5):E293-8 PMID: 23446706 PMCID: PMC3959640 SCOPUS ID: 2-s2.0-84875025443 03/01/2013       5 Citations
  • 5. Scott Schwoerer JA, Obernolte L, Van Calcar S, Heighway S, Bankowski B, Williams P and Rice G (5. Scott Schwoerer JA, Obernolte L, Van Calcar S, Heighway S, Bankowski B, Williams P and Rice G. ) JIMD Reports. Scott Schwoerer JA, Obernolte L, Van Calcar S, Heighway S, Bankowski B, Williams P and Rice G. Use of a gastrostomy tube to prevent maternal PKU syndrome. JIMD Reports. 2012; 6:15-20. PMID: 23430933. doi: 10.1007/8904_2011_95. 11/02/2012    
    • Last update: 08/14/2023