Exome sequencing findings in children with annular pancreas

por Pitsava, Georgia, Pankratz, Nathan, Lane, John, Yang, Wei, Rigler, Shannon, Shaw, Gary M., Mills, James L.
Publicado 2023

Requirement of FAT and DCHS protocadherins during hypothalamic-pituitary development

por Lodge, Emily J., Xekouki, Paraskevi, Silva, Tatiane S., Kochi, Cristiane, Longui, Carlos A., Faucz, Fabio R., Santambrogio, Alice, Mills, James L., Pankratz, Nathan, Lane, John, Sosnowska, Dominika, Hodgson, Tina, Patist, Amanda L., Francis-West, Philippa, Helmbacher, Françoise, Stratakis, Constantine A., Andoniadou, Cynthia L.
Publicado 2020

Somatic USP8 Gene Mutations Are a Common Cause of Pediatric Cushing Disease

por Faucz, Fabio R., Tirosh, Amit, Tatsi, Christina, Berthon, Annabel, Hernández-Ramírez, Laura C., Settas, Nikolaos, Angelousi, Anna, Correa, Ricardo, Papadakis, Georgios Z., Chittiboina, Prashant, Quezado, Martha, Pankratz, Nathan, Lane, John, Dimopoulos, Aggeliki, Mills, James L., Lodish, Maya, Stratakis, Constantine A.
Publicado 2017

Associations between teacher training and measures of physical literacy among Canadian 8- to 12-year-old students

por Law, Barbi, Bruner, Brenda, Scharoun Benson, Sara M., Anderson, Kristal, Gregg, Melanie, Hall, Nathan, Lane, Kirstin, MacDonald, Dany J., Saunders, Travis J., Sheehan, Dwayne, Stone, Michelle R., Woodruff, Sarah J., Belanger, Kevin, Barnes, Joel D., Longmuir, Patricia E., Tremblay, Mark S.
Publicado 2018

Mitochondrial DNA copy number and incident atrial fibrillation

por Zhao, Di, Bartz, Traci M., Sotoodehnia, Nona, Post, Wendy S., Heckbert, Susan R., Alonso, Alvaro, Longchamps, Ryan J., Castellani, Christina A., Hong, Yun Soo, Rotter, Jerome I., Lin, Henry J., O’Rourke, Brian, Pankratz, Nathan, Lane, John A., Yang, Stephanie Y., Guallar, Eliseo, Arking, Dan E.
Publicado 2020

THU214 Exploratory Study Of The Association Of Genetic Factors With Recovery Of Hypothalamic-Pituitary-Adrenal Axis In Cushing Disease

por Nguyen, Matthew H, Zhang, Wei, Pankratz, Nathan, Lane, John, Chittiboina, Prashant, Faucz, Fabio R, Liu, Aiyi, Mills, James L, Stratakis, Constantine A, Tatsi, Christina
Publicado 2023

OR06-01 The Role of Germline Defects in Cushing’s Disease

por Hernández-Ramírez, Laura C, Pankratz, Nathan, Lane, John, Faucz, Fabio R, Chittiboina, Prashant, Denise, Kay M, Mills, James L, Stratakis, Constantine A
Publicado 2020

Potential Role for the RASD1 Glucocorticoid-Responsive Gene in Corticotroph Tumorigenesis

por Hernández-Ramírez, Laura C, Pankratz, Nathan, Lane, John, Hu, Mingming, Faucz, Fabio R, Chittiboina, Prashant, Denise, Kay M, Mills, James L, Stratakis, Constantine A
Publicado 2021

OR2802 A Novel CABLES1 Missense Variant Associated With Cushing's Disease Disrupts Protein Structure And Stability

por Franco-Álvarez, Alexa L, Morán, Mariana Torres, Rebollar-Vega, Rosa G, Pankratz, Nathan, Lane, John, Faucz, Fabio R, Chittiboina, Prashant, Kay, Denise M, Mills, James L, Stratakis, Constantine A, Hernández-Ramírez, Laura C
Publicado 2023

RF01 | PMON167 Isolated Cushing's Disease Associated With Rare Germline SDHx Variants

por Chittiboina, Prashant, Kay, Denise M, Mills, James L, Stratakis, Constantine A, Hernãndez-Ramírez, Laura C, Pankratz, Nathan, Lane, John, Faucz, Fabio R
Publicado 2022