Casie A Genetti (Casie Genetti)

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 3

Top Topics

Attention Deficit Hyperactivity Disorder

Interstitial Lung Disease

Tyrosine Kinase

Gene Expression

Top Venues

Journal of medical Internet research

This page only lists publications with an associated author ORCID identifier.

Publications

Yoel Gofin, Tianyun Wang, Madelyn A Gillentine, Tiana M Scott, Aliska M Berry, Mahshid S Azamian, Casie A Genetti, Pankaj B Agrawal, Jonathan Picker, Monica Hsiung Wojcik, Mauricio R Delgado, Sally-Ann Lynch, Stephen W Scherer, Jennifer L Howe, Carlos A Bacino, Stephanie DiTroia, Grace E VanNoy, Anne H O'Donnell-Luria, Seema R Lalani, William D Graf, Jill Anne Rosenfeld, Evan E Eichler, Rachel K Earl, Daryl A Scott
Delineation of a novel neurodevelopmental syndrome associated with PAX5 haploinsufficiency. Human mutation 43 (4) (2022)
Qifei Li, Michal Dibus, Alicia M H Casey, Christina S K Yee, Sara O Vargas, Shiyu Luo, Samantha M Rosen, Jill A Madden, Casie A Genetti, Jan Brabek, Catherine A Brownstein, Shideh Kazerounian, Benjamin A Raby, Klaus Schmitz-Abe, John C Kennedy, Martha P Fishman, Mary P Mullen, Joan M Taylor, Daniel Rosel, Pankaj B Agrawal
A homozygous stop-gain variant in ARHGAP42 is associated with childhood interstitial lung disease, systemic hypertension, and immunological findings. PLoS genetics 17 (7) (2021)
Jianqiao Li, Margaret A Hojlo, Sampath Chennuri, Nitin Gujral, Heather L Paterson, Kent A Shefchek, Casie A Genetti, Emily L Cohn, Kara C Sewalk, Emily A Garvey, Elizabeth D Buttermore, Nickesha C Anderson, Alan H Beggs, Pankaj B Agrawal, John S Brownstein, Melissa A Haendel, Ingrid A Holm, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Underrepresentation of Phenotypic Variability of 16p13.11 Microduplication Syndrome Assessed With an Online Self-Phenotyping Tool (Phenotypr): Cohort Study. Journal of medical Internet research 23 (3) (2021)