Astrocyte regional heterogeneity revealed through machine learning‐based glial neuroanatomical assays
Blackburn, Jessica, Alves, Michele Joana, Aslan, Mehmet Tahir, Cevik, Lokman, Zhao, Jing, Czeisler, Catherine M., Otero, José Javier
Published in Journal of comparative neurology (1911) (01.07.2021)
Published in Journal of comparative neurology (1911) (01.07.2021)
Get full text
Journal Article
Information theory approaches to improve glioma diagnostic workflows in surgical neuropathology
Cevik, Lokman, Landrove, Marilyn Vazquez, Aslan, Mehmet Tahir, Khammad, Vasilii, Garagorry Guerra, Francisco Jose, Cabello‐Izquierdo, Yolanda, Wang, Wesley, Zhao, Jing, Becker, Aline Paixao, Czeisler, Catherine, Rendeiro, Anne Costa, Véras, Lucas Luis Sousa, Zanon, Maicon Fernando, Reis, Rui Manuel, Matsushita, Marcus de Medeiros, Ozduman, Koray, Pamir, M. Necmettin, Ersen Danyeli, Ayca, Pearce, Thomas, Felicella, Michelle, Eschbacher, Jennifer, Arakaki, Naomi, Martinetto, Horacio, Parwani, Anil, Thomas, Diana L., Otero, José Javier
Published in Brain pathology (Zurich, Switzerland) (01.09.2022)
Published in Brain pathology (Zurich, Switzerland) (01.09.2022)
Get full text
Journal Article
Neonatal apneic phenotype in a murine congenital central hypoventilation syndrome model is induced through non‐cell autonomous developmental mechanisms
Alzate‐Correa, Diego, Mei‐ling Liu, Jillian, Jones, Mikayla, Silva, Talita M., Alves, Michele Joana, Burke, Elizabeth, Zuñiga, Jessica, Kaya, Behiye, Zaza, Giuliana, Aslan, Mehmet Tahir, Blackburn, Jessica, Shimada, Marina Y., Fernandes‐Junior, Silvio A., Baer, Lisa A., Stanford, Kristin I., Kempton, Amber, Smith, Sakima, Szujewski, Caroline C., Silbaugh, Abby, Viemari, Jean‐Charles, Takakura, Ana C., Garcia, Alfredo J., Moreira, Thiago S., Czeisler, Catherine M., Otero, José J.
Published in Brain pathology (Zurich, Switzerland) (01.01.2021)
Published in Brain pathology (Zurich, Switzerland) (01.01.2021)
Get full text
Journal Article
Abstract 5222: Decoding >30 thousand individuals to analyze the most common genetic disorder: Hereditary hemochromatosis (HH)
Aslan, Mehmet Tahir, Mathew, Anita, Akova, Ferit, Metpally, Raghu, Carey, David J., Williams, Heinric, Williams, Marc S., Overton, John, Baras, Aris, Cook, Adam M., Colonie, Ryan D., Kip, Nefize Sertac
Published in Cancer research (Chicago, Ill.) (15.07.2016)
Published in Cancer research (Chicago, Ill.) (15.07.2016)
Get full text
Journal Article