Melissa A. Parisi

PTEN Mutation Spectrum and Genotype-Phenotype Correlations in Bannayan-Riley-Ruvalcaba Syndrome Suggest a Single Entity With Cowden Syndrome

Deborah J. Marsh, Jennifer B. Kum, Kathryn L. Lunetta et al. · Human Molecular Genetics · 1999 · 605 citations

Genotype-phenotype Correlations, Mendelian Disorder, Malignant Disease +15

The centrosomal protein nephrocystin-6 is mutated in Joubert syndrome and activates transcription factor ATF4

John A. Sayer, Edgar A. Otto, John F. O’Toole et al. · Nature Genetics · 2006 · 572 citations

Transcription Factor Atf4, Transcriptional Regulation, Developmental Biology +10

Similarity of Human Mitochondrial Transcription Factor 1 to High Mobility Group Proteins

Melissa A. Parisi, David A. Clayton · Science · 1991 · 540 citations

Transcriptional Regulation, Systems Biology, Mitochondrial Biogenesis +13

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Heleen H. Arts, Dan Doherty, Sylvia E. C. van Beersum et al. · Nature Genetics · 2007 · 321 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

DNA wrapping and bending by a mitochondrial high mobility group-like transcriptional activator protein.

Robert P. Fisher, Thomas Lisowsky, Melissa A. Parisi et al. · Journal of Biological Chemistry · 1992 · 318 citations · Full text

Chromatin, Mitophagy, Dna +14