Empirical validity of Leonhard's psychoses: A long-term follow-up study of first-episode psychosis patients

Autor: Ballesteros, A., Hernández, R., Janda, L., Lorente, R., Peralta, D., Ribeiro, M., Rosero, A., Cuesta, M.J., Sánchez-Torres, A.M., García de Jalón, E., Moreno-Izco, L., Gil-Berrozpe, G.J., Zarzuela, A., Papiol, S., Fañanás, L., Peralta, V.

Publikováno v: In Schizophrenia Research January 2024 263:237-245

Neurocognitive correlates of the varied domains of outcomes at 20 year follow-up of first-episode psychosis

Autor: Ballesteros, A., Fañanás, L., Hernández, R., Janda, L., Lorente, R., Papiol, S., Peralta, D., Ribeiro, M., Rosero, A., Zandio, M., Cuesta, M.J., Sánchez-Torres, A.M., Moreno-Izco, L., García de Jalón, E., Gil-Berrozpe, G.J., Zarzuela, A., Peralta, V.

Publikováno v: In Psychiatry Research December 2022 318

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Genomic answers for children: Dynamic analyses of >1000 pediatric rare disease genomes

Autor: Ana S.A. Cohen, Emily G. Farrow, Ahmed T. Abdelmoity, Joseph T. Alaimo, Shivarajan M. Amudhavalli, John T. Anderson, Lalit Bansal, Lauren Bartik, Primo Baybayan, Bradley Belden, Courtney D. Berrios, Rebecca L. Biswell, Pawel Buczkowicz, Orion Buske, Shreyasee Chakraborty, Warren A. Cheung, Keith A. Coffman, Ashley M. Cooper, Laura A. Cross, Tom Curran, Thuy Tien T. Dang, Mary M. Elfrink, Kendra L. Engleman, Erin D. Fecske, Cynthia Fieser, Keely Fitzgerald, Emily A. Fleming, Randi N. Gadea, Jennifer L. Gannon, Rose N. Gelineau-Morel, Margaret Gibson, Jeffrey Goldstein, Elin Grundberg, Kelsee Halpin, Brian S. Harvey, Bryce A. Heese, Wendy Hein, Suzanne M. Herd, Susan S. Hughes, Mohammed Ilyas, Jill Jacobson, Janda L. Jenkins, Shao Jiang, Jeffrey J. Johnston, Kathryn Keeler, Jonas Korlach, Jennifer Kussmann, Christine Lambert, Caitlin Lawson, Jean-Baptiste Le Pichon, James Steven Leeder, Vicki C. Little, Daniel A. Louiselle, Michael Lypka, Brittany D. McDonald, Neil Miller, Ann Modrcin, Annapoorna Nair, Shelby H. Neal, Christopher M. Oermann, Donna M. Pacicca, Kailash Pawar, Nyshele L. Posey, Nigel Price, Laura M.B. Puckett, Julio F. Quezada, Nikita Raje, William J. Rowell, Eric T. Rush, Venkatesh Sampath, Carol J. Saunders, Caitlin Schwager, Richard M. Schwend, Elizabeth Shaffer, Craig Smail, Sarah Soden, Meghan E. Strenk, Bonnie R. Sullivan, Brooke R. Sweeney, Jade B. Tam-Williams, Adam M. Walter, Holly Welsh, Aaron M. Wenger, Laurel K. Willig, Yun Yan, Scott T. Younger, Dihong Zhou, Tricia N. Zion, Isabelle Thiffault, Tomi Pastinen

Publikováno v: Genetics in Medicine. 24:1336-1348

This study aimed to provide comprehensive diagnostic and candidate analyses in a pediatric rare disease cohort through the Genomic Answers for Kids program.Extensive analyses of 960 families with suspected genetic disorders included short-read exome

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0fae080f2e98a691a62cb07ca295bd7e
https://doi.org/10.1016/j.gim.2022.02.007

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