• Samuel Huang

  • Physician - Genetics


    • MAR MC_Marshfield-Genetics
    • 1000 North Oak Ave. Marsh Main > (30292) Mfd Main Gr Genetics Marshfield, WI 54449

Education

2011:
BS, Molecular Biology, University of Wisconsin , Madison, WI
2016:
MD, University of Wisconsin School of Medicine and Public Health, Madison, WI
2019:
Residency, Pediatrics, Marshfiedl Clinic, Marshfield, WI
2022:
Residency and Fellowship, Medical Genetics, University of Washington and Seattle Children's Hospital, Seattle, WA

Work Experience

2022 to Present:
Physician - Genetics, Marshfield Clinic, Inc., Marshfield, WI
2023 to Present:
Department of Pediatrics - Adjunct Clinical Professor, University of Wisconsin School of Medicine and Public Health, Madison, WI

Board Certifications

2019 to Present:
American Board of Pediatrics
2021 to Present:
American Board of Medical Genetics

Select Publications

  • Huang SJ, Salsbery KT, Steiner RD. Porencephaly and Intracranial Calcifications in a Neonate. Pediatr Rev. 2020 October;41(10):543-545. doi: 10.1542/pir.2018-0309.
    PubMed ID: 33004666
  • Li Y, Huang SJ, McManus MJ. An 18-month-old Girl with a Fleshy Mass in the Ear Canal. Pediatr Rev. 2021 January;42(Suppl 1):S1-S3. doi: 10.1542/pir.2018-0325.
    PubMed ID: 33386348
  • Tayeh MK, Chen M, Fullerton SM, Gonzales PR, Huang SJ, Massingham LJ,...Evans BJ. The designated record set for clinical genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2023 March;25(3):100342. doi: 10.1016/j.gim.2022.11.010.
    PubMed ID: 36547466
  • Seaver LH, Chan P, Fleisher LD, Huang SJ, Klugman SD, Matalon DR. Points to consider for providing expert witness testimony for the specialty of medical genetics: A statement of the American College of Medical Genetics and Genomics (ACMG). Genet Med. 2024 October;26(10):101229. doi: 10.1016/j.gim.2024.101229.
    PubMed ID: 39240268
  • Blue EE, Huang SJ, Khan A, Golden-Grant K, Boyd B, Rosenthal EA,...Glass IA. Dual diagnosis of UQCRFS1-related mitochondrial complex III deficiency and recessive GJA8-related cataracts. Rare. 2024 August 14;2. doi: 10.1016/j.rare.2024.100040. PMCID: PMC11484756.
    PubMed ID: 39421685
  • Ryan CW, Regan SL, Sheingold JB, Goswami A, Mulhern M, Ploeger J,...Bielas SL [including Huang S.] RNF2 Missense Variants Disrupt Polycomb Repression and Enable Ectopic Mesenchymal Lineage Conversion During Human Neural Differentiation. Res Sq. 2025 August 11. doi: 10.21203/rs.3.rs-7143352/v1. PMCID: PMC12363927.
    PubMed ID: 40831499