Sally A Camper
Margery Shaw Distinguished University Professor of Human Genetics and Internal Medicine
Professor of Human Genetics
Professor of Internal Medicine
Human Genetics
1241 Catherine St.
Ann Arbor, MI 48109-5618
[email protected]

Available to mentor

Sally A Camper
Professor
  • About
  • Links
  • Qualifications
  • Center Memberships
  • Research Overview
  • Recent Publications
  • About

    Dr. Camper received her BA in Chemistry from U. Delaware, her PhD in Biochemistry from Michigan State University, and conducted postdoctoral work at Case Western Reserve University in Cleveland, OH, the Fox Chase Cancer Center in Philadelphia, PA, and at Princeton University in Princeton, NJ. She joined the faculty at University of Michigan in 1988 as an Assistant Professor, established the Transgenic Animal Model Core facility, and rose through the ranks to become the Margery W. Shaw Distinguished University Professor of Human Genetics, and she served as Department Chair for 11 years (2005-2015).

    Links
    • Human Genetics
    Qualifications
    • Postdoctoral fellow
      Princeton University, Princeton, 1998
    • Postdoctoral fellow
      Fox Chase Cancer Center, Philadelphia, 1996
    • PhD
      Michigan State University, East Lansing, 1983
    • BS
      University of Delaware, Newark, 1977
    Center Memberships
    • Center Member
      Center for Computational Medicine and Bioinformatics
    • Center Member
      Rogel Cancer Center
    • Center Member
      Center for Cell Plasticity and Organ Design
    • Center Member
      Biosciences Initiative
    Research Overview

    Dr. Camper studies the genetics of inherited birth defects, particularly those that affect neuroendocrine system development. She was among the pioneers in the use of transgenic mouse models to study developmentally regulated gene-expression that result in human genetic disorders. She studies human patients and genetically modified mice in collaboration with an international group of investigators. Her research seeks to identify genetic causes of hypopituitarism and understand pathophysiological mechanisms. She has contributed to understanding how transcription factors and signaling pathways regulate hypothalamic and pituitary gland development. She received the Roy O. Greep award for outstanding research from the Endocrine Society, a Merit award from the National Institutes of Health, and, from University of Michigan, the Faculty Recognition Award and the Distinguished Faculty Lectureship Award in Biomedical Research. She was elected as a Fellow for the American Academy for the Advancement of Science.

    Recent Publications See All Publications
    • Journal Article
      Pituitary stem cells: past, present and future perspectives.
      Pérez Millán MI, Cheung LYM, Mercogliano F, Camilletti MA, Chirino Felker GT, Moro LN, Miriuka S, Brinkmeier ML, Camper SA. Nat Rev Endocrinol, 2024 Feb; 20 (2): 77 - 92. DOI:10.1038/s41574-023-00922-4
      PMID: 38102391
    • Journal Article
      OR17-02 Combining Transcriptomics And Proteomics To Unveil Possible PROP1 Interactors During Embryonic Pituitary Development
      Garcia LI, Mercogliano MF, Schuster C, Cheung L, Camper SA, Marti M, Perez-Millan MI. Journal of the Endocrine Society, 2023 Oct 5; 7 (Supplement_1): bvad114.1308 DOI:10.1210/jendso/bvad114.1308
    • Journal Article
      THU119 Screening Publicly Available Data To Identify Candidate Genes For Congenital Hypopituitarism
      Brinkmeier ML, Mayer JJM, Ellsworth BS, Raetzman LT, Cheung L, Perez-Millan MI, Camper SA, Davis SW. Journal of the Endocrine Society, 2023 Oct 5; 7 (Supplement_1): bvad114.1197 DOI:10.1210/jendso/bvad114.1197
    • Journal Article
      Homozygous CDH2 variant may be associated with hypopituitarism without neurological disorders.
      Ferreira NGBP, Madeira JLO, Gergics P, Kertsz R, Marques JM, Trigueiro NSS, Benedetti AFF, Azevedo BV, Fernandes BHV, Bissegatto DD, Biscotto IP, Fang Q, Ma Q, Ozel AB, Li J, Camper SA, Jorge AAL, Mendonça BB, Arnhold IJP, Carvalho LR. Endocr Connect, 2023 Jul 5; 12 (8): DOI:10.1530/EC-22-0473
      PMID: 37166408
    • Journal Article
      Novel Candidate Regulators and Developmental Trajectory of Pituitary Thyrotropes.
      Cheung LYM, Menage L, Rizzoti K, Hamilton G, Dumontet T, Basham K, Daly AZ, Brinkmeier ML, Masser BE, Treier M, Cobb J, Delogu A, Lovell-Badge R, Hammer GD, Camper SA. Endocrinology, 2023 Apr 17; 164 (6): DOI:10.1210/endocr/bqad076
      PMID: 37183548
    • Journal Article
      Disruption of RNA Splicing Is an Important Contributor to Congenital Hypopituitarism and Other Human Genetic Diseases.
      Camper SA, Smith C, Kitzman JO. Endocrinology, 2023 Mar 13; 164 (5): DOI:10.1210/endocr/bqad039
      PMID: 36857601
    • Journal Article
      Pituitary Stem Cell Regulation by Zeb2 and BMP Signaling.
      Winningham AH, Camper SA. Endocrinology, 2023 Jan 9; 164 (3): DOI:10.1210/endocr/bqad016
      PMID: 36683433
    • Journal Article
      Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man.
      Bando H, Brinkmeier ML, Castinetti F, Fang Q, Lee M-S, Saveanu A, Albarel F, Dupuis C, Brue T, Camper SA. Hum Mol Genet, 2023 Jan 13; 32 (3): 367 - 385. DOI:10.1093/hmg/ddac192
      PMID: 35951005
    Featured News & Stories Panel presentation from 2024 Celebration of Women in Academic Medicine
    Medical School News
    Michigan Medicine celebrating, advancing women in medicine by doing more than “checking boxes”
    On Feb. 28, the Medical School hosted the second annual Celebration of Women in Academic Medicine.