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Sally Camper, Ph. D.

Affiliations: 
Human Genetics University of Michigan, Ann Arbor, Ann Arbor, MI 
Area:
Pituitary developement
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"Sally Camper"
Mean distance: 16.06 (cluster 32)
 
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Parents

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Fritz Rottman grad student 1983 Michigan State
Shirley Tilghman post-doc Princeton

Children

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Amy Cristine Lossie research assistant 1991-1994 University of Michigan Medical School Ann Arbor (DevTree)
Marion S. Buckwalter grad student 1990-1996 University of Michigan Medical School
Heather L. Burrows grad student 2000 University of Michigan
Kristin R. Douglas grad student 2000 University of Michigan
Lisa J. Cushman grad student 2001 University of Michigan
Frank J. Probst grad student 2001 University of Michigan
Igor O. Nasonkin grad student 2002 University of Michigan
Hoonkyo Suh grad student 1996-2002 University of Michigan
Michael A. Charles grad student 2005 University of Michigan
Kelly B. Cha grad student 2006 University of Michigan

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Publications

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Cheung LYM, Menage L, Rizzoti K, et al. (2023) Novel candidate regulators and developmental trajectory of pituitary thyrotropes. Endocrinology
Winningham AH, Camper SA. (2023) Pituitary Stem Cell Regulation by Zeb2 and BMP Signaling. Endocrinology. 164
Bando H, Brinkmeier ML, Castinetti F, et al. (2022) Heterozygous variants in SIX3 and POU1F1 cause pituitary hormone deficiency in mouse and man. Human Molecular Genetics
Brinkmeier ML, Bando H, Camarano AC, et al. (2020) Rathke's cleft-like cysts arise from Isl1 deletion in murine pituitary progenitors. The Journal of Clinical Investigation
Bando H, Gergics P, Bohnsack BL, et al. (2020) otx2b mutant zebrafish have pituitary, eye and mandible defects that model mammalian disease. Human Molecular Genetics
Cheung L, Daly A, Brinkmeier M, et al. (2020) OR16-05 Single-Cell Sequencing Identifies Novel Regulators of Thyrotrope Populations and POU1F1-Independent Thyroid-Stimulating Hormone Expression Journal of the Endocrine Society. 4
Brinkmeier M, Camper SA. (2020) SAT-288 Pituitary Developmental Defects Caused by Haploinsufficiency for the Transcription Factor SIX3 Are Worsened by POU1F1 Deficiency Journal of the Endocrine Society. 4
Dudley LA, Daley AZ, Mortensen AH, et al. (2020) MON-715 How Heterogeneous Are Pituitary Thyrotropes? Journal of the Endocrine Society. 4
Pereira Ferreira NGB, Madeira JLdO, Kertsz R, et al. (2020) SAT-LB58 Molecular Investigation of Recessive Inheritance by Exome Sequencing of Patients With Congenital Hypopituitarism Journal of the Endocrine Society. 4
Vishnopolska SA, Braslavsky D, Keselman AC, et al. (2020) MON-717 Novel GLI2 Mutations Identified in Pediatric Patients with Combined Pituitary Hormone Deficiency: One Gene, Various Genotypes Journal of the Endocrine Society. 4
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