Maria H Chahrour (Maria Chahrour)

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 8

Top Venues

The Journal of neuroscience : the official journal of the Society for Neuroscience

American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics

Proceedings of the National Academy of Sciences of the United States of America

University of Texas Southwestern Medical Center

Baylor College of Medicine (PHD)

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

Affiliation History

University of Texas Southwestern Medical Center Jan 5o 2015

United States

Assistant professor :: McDermott Center for Human Growth and Development, Neuroscience, Psychiatry

Education History

Baylor College of Medicine

United States

PHD :: Molecular and Human Genetics

Publications

Lauretta El Hayek, Darlene DeVries, Ashlesha Gogate, Ariel Aiken, Kiran Kaur, Maria H Chahrour
Disruption of the autism gene and chromatin regulator KDM5A alters hippocampal cell identity. Science advances 9 (47) (2023)
Shayal Vashisth, Maria H Chahrour
Genomic strategies to untangle the etiology of autism: A primer. Autism research : official journal of the International Society for Autism Research (2022)
Islam Oguz Tuncay, Nancy L Parmalee, Raida Khalil, Kiran Kaur, Ashwani Kumar, Mohamed Jimale, Jennifer L Howe, Kimberly Goodspeed, Patricia Evans, Loai Alzghoul, Chao Xing, Stephen W Scherer, Maria H Chahrour
Analysis of recent shared ancestry in a familial cohort identifies coding and noncoding autism spectrum disorder variants. NPJ genomic medicine 7 (1) (2022)
Lauretta El Hayek, Islam Oguz Tuncay, Nadine Nijem, Jamie Russell, Sara Ludwig, Kiran Kaur, Xiaohong Li, Priscilla Anderton, Miao Tang, Amanda Gerard, Anja Heinze, Pia Zacher, Hessa S Alsaif, Aboulfazl Rad, Kazem Hassanpour, Mohammad Reza Abbaszadegan, Camerun Washington, Barbara R DuPont, Raymond J Louie, null null, Madeline Couse, Maha Faden, R Curtis Rogers, Rami Abou Jamra, Ellen R Elias, Reza Maroofian, Henry Houlden, Anna Lehman, Bruce Beutler, Maria H Chahrour
KDM5A mutations identified in autism spectrum disorder using forward genetics. eLife 9 (2020)
Solmi Cheon, Kiran Kaur, Nadine Nijem, Islam Oguz Tuncay, Pooja Kumar, Milan Dean, Jane Juusola, Maria J Guillen-Sacoto, Emma Bedoukian, Lynne Ierardi-Curto, Paige Kaplan, G Bradley Schaefer, Prashant Mishra, Maria H Chahrour
The ubiquitin ligase UBE3B, disrupted in intellectual disability and absent speech, regulates metabolic pathways by targeting BCKDK. Proceedings of the National Academy of Sciences of the United States of America 116 (9) (2019)
Raida Khalil, Connor Kenny, R Sean Hill, Ganeshwaran H Mochida, Ramzi Nasir, Jennifer N Partlow, Brenda J Barry, Muna Al-Saffar, Chloe Egan, Christine R Stevens, Stacey B Gabriel, A James Barkovich, Jay W Ellison, Lihadh Al-Gazali, Christopher A Walsh, Maria H Chahrour
PSMD12 haploinsufficiency in a neurodevelopmental disorder with autistic features. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 177 (8) (2018)
Hsiang-Chih Lu, Qiumin Tan, Maxime W C Rousseaux, Wei Wang, Ji-Yoen Kim, Ronald Richman, Ying-Wooi Wan, Szu-Ying Yeh, Jay M Patel, Xiuyun Liu, Tao Lin, Yoontae Lee, John D Fryer, Jing Han, Maria H Chahrour, Richard H Finnell, Yunping Lei, Maria E Zurita-Jimenez, Priyanka Ahimaz, Kwame Anyane-Yeboa, Lionel Van Maldergem, Daphne Lehalle, Nolwenn Jean-Marcais, Anne-Laure Mosca-Boidron, Julien Thevenon, Margot A Cousin, Della E Bro, Brendan C Lanpher, Eric W Klee, Nora Alexander, Matthew N Bainbridge, Harry T Orr, Roy V Sillitoe, M Cecilia Ljungberg, Zhandong Liu, Christian Patrick Schaaf, Huda Y Zoghbi
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. Nature genetics 49 (4) (2017)
Maria H Chahrour, Brian J O'Roak, Emanuela Santini, Rodney C Samaco, Robin J Kleiman, M Chiara Manzini
Current Perspectives in Autism Spectrum Disorder: From Genes to Therapy. The Journal of neuroscience : the official journal of the Society for Neuroscience 36 (45) (2017)

Maria H Chahrour.css-eqlu8i{font-size:small;padding-left:4px;} (Maria Chahrour)

Publication Activity (10 Years)

Top Topics

Top Venues

Maria H Chahrour (Maria Chahrour)