Christopher C. Glenn

Allen Institute for Brain Science — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

12h-index1.7kcitations18works0.02yr avg
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Research Topics

Genetic Syndromes and Imprinting(15), Epigenetics and DNA Methylation(10), Prenatal Screening and Diagnostics(6), Genetics and Neurodevelopmental Disorders(2), Genetic diversity and population structure(1)

Publications18 total

Up‐regulation of tissue‐type transglutaminase after traumatic 
brain injury
Journal of Neurochemistry·2002· 35 cited
Stretch Injury Causes Calpain and Caspase-3 Activation and Necrotic and Apoptotic Cell Death in Septo-Hippocampal Cell Cultures
Journal of Neurotrauma·2000· 101 cited
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader-Willi syndromes and imprinting
Prenatal Diagnosis·2000· 70 cited
DNA methylation analysis with respect to prenatal diagnosis of the Angelman and Prader–Willi syndromes and imprinting
Prenatal Diagnosis·2000· 2 cited
A High-Density Integrated Genetic Linkage and Radiation Hybrid Map of the Laboratory Rat
Genome Research·1999· 203 citedOpen Access
A Novel Imprinted Gene, Encoding a RING Zinc-Finger Protein, and Overlapping Antisense Transcript in the Prader-Willi Syndrome Critical Region
Human Molecular Genetics·1999· 229 cited
Genomic imprinting: potential function and mechanisms revealed by the Prader-Willi and Angelman syndromes
Molecular Human Reproduction·1997· 148 citedOpen Access
Clinical spectrum and molecular diagnosis of Angelman and Prader‐Willi syndrome patients with an imprinting mutation
American Journal of Medical Genetics·1997· 3 cited
Clinical spectrum and molecular diagnosis of Angelman and Prader-Willi syndrome patients with an imprinting mutation
American Journal of Medical Genetics·1997· 141 cited
Familial cryptic translocation resulting in Angelman syndrome:implications for imprinting or location of the Angelman gene?
PubMed·1996· 26 cited
Multiple Imprinted Genes Associated with Prader-Willi Syndrome and Location of an Imprinting Control Element
Acta geneticae medicae et gemellologiae twin research·1996Open Access
Gene structure, DNA methylation, and imprinted expression of the human SNRPN gene.
PubMed·1996· 236 cited
Molecular pathogenesis of Prader-Willi syndrome
1996· 4 cited
The putative imprinted locus D15S9 within the common deletion region for the Prader-Willi and Angelman syndromes encodes two overlapping mRNAs transcribed from opposite strands
The American Journal of Human Genetics·1994
Expression and DNA methylation analysis of SNRPN in Prader-Willi patients
The American Journal of Human Genetics·1994
Functional imprinting and epigenetic modification of the human <i>SNRPN</i> gene
Human Molecular Genetics·1993· 156 cited
Modification of 15q11 — q13 DNA methylation imprints in unique Angelman and Prader — Willi patients
Human Molecular Genetics·1993· 140 citedOpen Access
A DNA methylation imprint, determined by the sex of the parent, distinguishes the angelman and Prader-Willi syndromes
Genomics·1992· 211 cited

Frequent Co-authors

Daniel J. Driscoll(14), Shinji Saitoh(8), Robert D. Nicholls(8), M T Jong(6), Charles A. Williams(3), James M. Gabriel(3), Peter K. Rogan(3), Karin Buiting(2), Suzanne B. Cassidy(2), Jeffrey M. Conroy(2), Gabriele Gillessen‐Kaesbach(2), Louise R. Greenswag(2), Bernhard Horsthemke(2), Ikuko Kondo(2), Katsuko Kuwajima(2), Norio Niikawa(2), Stuart Schwartz(2), James R. Seip(2), G. Bruce Pike(2), Ronald L. Hayes(2)