Catherine A Brownstein

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2018-2024
Publications (10 Years): 20

Top Venues

Advanced genetics (Hoboken, N.J.)

Genes

bioRxiv : the preprint server for biology

European journal of human genetics : EJHG

Boston Children's Hospital

Yale University Graduate School of Arts and Sciences (PHD)

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

Affiliation History

Boston Children's Hospital Nov 30 2011

United States

Assistant Professor :: Division of Genetics and Genomics

Education History

Yale University Graduate School of Arts and Sciences

United States

PHD :: Genetics

Publications

Caroline Dias, Alisa Mo, Chunhui Cai, Liang Sun, Kristen Cabral, Catherine A Brownstein, Shira Rockowitz, Christopher A Walsh
Cell-type-specific effects of autism-associated chromosome 15q11.2-13.1 duplications in human brain. bioRxiv : the preprint server for biology (2024)
Caroline Dias, Alisa Mo, Chunhui Cai, Liang Sun, Kristen Cabral, Catherine A Brownstein, Shira Rockowitz, Christopher A Walsh
Cell-type-specific effects of autism-associated chromosome 15q11.2-13.1 duplications in human brain. bioRxiv : the preprint server for biology (2024)
Caroline Dias, Alisa Mo, Chunhui Cai, Liang Sun, Kristen Cabral, Catherine A Brownstein, Shira Rockowitz, Christopher A Walsh
Cell-type-specific effects of autism-associated chromosome 15q11.2-13.1 duplications in human brain. bioRxiv : the preprint server for biology (2024)
Qifei Li, Rohan Agrawal, Klaus Schmitz-Abe, Casie A Genetti, Melissa A Fernandes, Noah L Fryou, Jill A Madden, Catherine A Brownstein, Edward C Smith, Farrah Rajabi, Alan H Beggs, Pankaj B Agrawal
Reanalysis of clinical exome identifies the second variant in two individuals with recessive disorders. European journal of human genetics : EJHG (2023)
Jenny Sun, Don Daniel Ocay, Meghan Halpin, Kimberly Lobo, Dafni F T Frohman, Carolina Donado, Catherine A Brownstein, Casie A Genetti, Anna Madden, Charles B Berde
Clinical Characterization of Pediatric Erythromelalgia: A Single-Center Case Series. Children (Basel, Switzerland) 10 (8) (2023)
Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Francis X Shen, Matthew L Baum, Nicole Martinez-Martin, Adam S Miner, Melissa Abraham, Catherine A Brownstein, Nathan Cortez, Barbara J Evans, Laura T Germine, David C Glahn, Christine Grady, Ingrid A Holm, Elisa A Hurley, Sara Kimble, Gabriel Lázaro-Muñoz, Kimberlyn Leary, Mason Marks, Patrick James Monette, Jukka-Pekka Onnela, P Pearl O'Rourke, Scott L Rauch, Carmel Shachar, Srijan Sen, Ipsit Vihang Vahia, Jason L Vassy, Justin T Baker, Barbara E Bierer, Benjamin C Silverman
Returning Individual Research Results from Digital Phenotyping in Psychiatry. The American journal of bioethics : AJOB (2023)
Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Margaret A Hojlo, Merhawi Ghebrelul, Casie A Genetti, Richard Scott Smith, Shira Rockowitz, Emma Deaso, Alan H Beggs, Pankaj B Agrawal, David C Glahn, Joseph Gonzalez-Heydrich, Catherine A Brownstein
Children with Early-Onset Psychosis Have Increased Burden of Rare GRIN2A Variants. Genes 14 (4) (2023)
Elicia Estrella, Shira Rockowitz, Marielle Thorne, Pressley Smith, Jeanette Petit, Veronica Zehnder, Richard N Yu, Stuart Bauer, Charles Berde, Pankaj B Agrawal, Alan H Beggs, Ali G Gharavi, Louis Kunkel, Catherine A Brownstein
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort. Advanced genetics (Hoboken, N.J.) 4 (1) (2022)
Elicia Estrella, Shira Rockowitz, Marielle Thorne, Pressley Smith, Jeanette Petit, Veronica Zehnder, Richard N Yu, Stuart Bauer, Charles Berde, Pankaj B Agrawal, Alan H Beggs, Ali G Gharavi, Louis Kunkel, Catherine A Brownstein
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort. Advanced genetics (Hoboken, N.J.) 4 (1) (2022)
Catherine A Brownstein, Elise Douard, Robin L Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan, Bree Martin, Sanda Alexandrescu, Elisabeth A Haas, Sara O Vargas, Monica H Wojcik, Sébastien Jacquemont, Annapurna H Poduri, Richard D Goldstein, Ingrid A Holm
Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age. Advanced genetics (Hoboken, N.J.) 4 (1) (2022)
Elicia Estrella, Shira Rockowitz, Marielle Thorne, Pressley Smith, Jeanette Petit, Veronica Zehnder, Richard N Yu, Stuart Bauer, Charles Berde, Pankaj B Agrawal, Alan H Beggs, Ali G Gharavi, Louis Kunkel, Catherine A Brownstein
Mendelian Disorders in an Interstitial Cystitis/Bladder Pain Syndrome Cohort. Advanced genetics (Hoboken, N.J.) 4 (1) (2022)
Catherine A Brownstein, Elise Douard, Robin L Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan, Bree Martin, Sanda Alexandrescu, Elisabeth A Haas, Sara O Vargas, Monica H Wojcik, Sébastien Jacquemont, Annapurna H Poduri, Richard D Goldstein, Ingrid A Holm
Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of Age. Advanced genetics (Hoboken, N.J.) 4 (1) (2022)
Ange-Line Bruel, Antonio Vitobello, Isabelle Thiffault, Linda Manwaring, Marcia Willing, Pankaj B Agrawal, Carolina Alvarez, Thomas M Kitzler, Catherine A Brownstein, Casie A Genetti, Joseph Gonzalez-Heydrich, Parul Jayakar, Jacob W Zyskind, Zehua Zhu, Clemence Vachet, Gena R Wilson, Brianna Pruniski, Anne-Marie Goyette, Yannis Duffourd, Christel Thauvin-Robinet, Christophe Philippe, Laurence Faivre
ITSN1: a novel candidate gene involved in autosomal dominant neurodevelopmental disorder spectrum. European journal of human genetics : EJHG (2021)
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)
Catherine A Brownstein, Richard S Smith, Lance H Rodan, Mark P Gorman, Margaret A Hojlo, Emily A Garvey, Jianqiao Li, Kristin Cabral, Joshua J Bowen, Abhijit S Rao, Casie A Genetti, Devon Carroll, Emma A Deaso, Pankaj B Agrawal, Jill Anne Rosenfeld, Weimin Bi, Jennifer Howe, Dimitri J Stavropoulos, Adam W Hansen, Hesham M Hamoda, Ferne Pinard, Annmarie Caracansi, Christopher A Walsh, Eugene J D'Angelo, Alan H Beggs, Mehdi Zarrei, Richard A Gibbs, Stephen W Scherer, David C Glahn, Joseph Gonzalez-Heydrich
RCL1 copy number variants are associated with a range of neuropsychiatric phenotypes. Molecular psychiatry 26 (5) (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)
Chrystal F Mavros, Catherine A Brownstein, Roshni Thyagrajan, Casie A Genetti, Sahil Tembulkar, Kelsey Graber, Quinn Murphy, Kristin Cabral, Grace E VanNoy, Matthew Bainbridge, Jiahai Shi, Pankaj B Agrawal, Alan H Beggs, Eugene D'Angelo, Joseph Gonzalez-Heydrich
De novo variant of TRRAP in a patient with very early onset psychosis in the context of non-verbal learning disability and obsessive-compulsive disorder: a case report. BMC medical genetics 19 (1) (2018)

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Publication Activity (10 Years)

Top Topics

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Catherine A Brownstein