Camilynn I. Brannan

Biochemistry, Genetics and Molecular Biology · Life Sciences

36h-index12.7kcitations51works0.02yr avg
OpenAlex↗Google Scholar↗

Accepting Students?

No reports yet. Know if this professor is taking students?

Research Topics

Genetic Syndromes and Imprinting(12), Epigenetics and DNA Methylation(11), Neurofibromatosis and Schwannoma Cases(11), T-cell and B-cell Immunology(6), Prenatal Screening and Diagnostics(5)

Publications51 total

Pillars article: lymphoproliferation disorder in mice explained by defects in Fas antigen that mediates apoptosis. 1992.
PubMed·2012· 2 cited
Pillars Article: Lymphoproliferation Disorder in Mice Explained by Defects in Fas Antigen that MediatesApoptosis. <i>Nature</i>. 1992. 356: 314–317
The Journal of Immunology·2012
A targeted deletion upstream of Snrpn does not result in an imprinting defect
Mammalian Genome·2007· 13 cited
A human imprinting centre demonstrates conserved acquisition but diverged maintenance of imprinting in a mouse model for Angelman syndrome imprinting defects
Human Molecular Genetics·2005· 90 citedOpen Access
Evidence for genetic modifiers of postnatal lethality in PWS-IC deletion mice
Human Molecular Genetics·2004· 55 citedOpen Access
The Murine α1-Proteinase Inhibitor Gene Family: Polymorphism, Chromosomal Location, and Structure
Genomics·2002· 25 cited
The Murine α-Proteinase Inhibitor Gene Family: Polymorphism, Chromosomal Location, and Structure
Genomics·2002· 6 cited
Autosomal telomere exchange results in the rapid amplification and dispersion of Csf2ra genes in wild-derived mice
Mammalian Genome·2001· 7 cited
Retroviral Integration at the <i>Epi1</i> Locus Cooperates with <i>Nf1</i> Gene Loss in the Progression to Acute Myeloid Leukemia
Journal of Virology·2001· 22 citedOpen Access
The Prader–Willi Syndrome Imprinting Center Activates the Paternally Expressed Murine Ube3a Antisense Transcript but Represses Paternal Ube3a
Genomics·2001· 205 cited
Learning deficits, but normal development and tumor predisposition, in mice lacking exon 23a of Nf1
Nature Genetics·2001· 197 cited
Maternal methylation imprints on human chromosome 15 are established during or after fertilization
Nature Genetics·2001· 200 cited
Identification of brain-specific and imprinted small nucleolar RNA genes exhibiting an unusual genomic organization
Proceedings of the National Academy of Sciences·2000· 576 citedOpen Access
Dissection of the Pathogenesis of Neurofibromatosis Type 1-Associated Myeloid Leukemia
2000
De novo deletions of SNRPN exon 1 in early human and mouse embryos result in a paternal to maternal imprint switch
Nature Genetics·2000· 146 cited
Dissection of the Pathogenesis of Neurofibromatosis Type 1-Associated Myeloid Leukemia
1999
Analysis of murine Snrpn and human SNRPN gene imprinting in transgenic mice
Mammalian Genome·1999· 29 cited
Mechanisms of genomic imprinting
Current Opinion in Genetics & Development·1999· 200 citedOpen Access
A mouse model for Prader-Willi syndrome imprinting-centre mutations
Nature Genetics·1998· 301 cited
Nf1 deficiency causes Ras-Dediated granulocyte/macrophage colony stimulating factor hypersensitivity and chronic myeloid leukaemia
Nature Genetics·1996· 299 cited
page 1 of 3Next →

Frequent Co-authors

Neal G. Copeland(21), Nancy A. Jenkins(13), Nancy A. Jenkins(6), N.A. Jenkins(6), James L. Resnick(6), Shigekazu Nagata(5), Dirk Anderson(5), Rie Watanabe‐Fukunaga(4), N G Copeland(4), Nancy Ratner(4), N A Jenkins(4), Craig A. Smith(4), Tao Yang(4), Kristine S. Vogel(3), Michael L. Nordlund(3), Luis F. Parada(3), Karin Buiting(3), Terri Davis(3), Raymond G. Goodwin(3), Douglas E. Williams(3)