Identification of DLEC1 D215N Somatic Mutation in Formalin Fixed Paraffin Embedded Melanoma and Melanocytic Nevi Specimens

od Vieira, Ricardo, Simões, Maria José, Carmona, Susana, Egas, Conceição, Faro, Carlos, Figueiredo, Américo
Wydane 2013

AP4S1 splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyria

od Carmona, Susana, Marecos, Clara, Amorim, Marta, Ferreira, Ana C., Conceição, Carla, Brás, José, Duarte, Sofia T., Guerreiro, Rita
Wydane w Neurol Genet (2018)

Whole-exome sequencing of Finnish patients with vascular cognitive impairment

od Mönkäre, Saana, Kuuluvainen, Liina, Kun-Rodrigues, Celia, Carmona, Susana, Schleutker, Johanna, Bras, Jose, Pöyhönen, Minna, Guerreiro, Rita, Myllykangas, Liisa
Wydane w Eur J Hum Genet (2020)

MicroRNA-21 in lung cancer: overexpression in metastasis of pulmonary adenocarcinomas and squamous cell carcinomas

od Silva, Maria R, Santos, Paulo, Velada, Isabel, Gomes, Catarina, d’Aguiar, M João, Teixeira, Lia, Dinis, João, Carmona, Susana, Cortes, Luisa, Carvalho, Lina
Wydane 2010

Cortical morphometry in frontoparietal and default mode networks in math‐gifted adolescents

od Navas‐Sánchez, Francisco J., Carmona, Susana, Alemán‐Gómez, Yasser, Sánchez‐González, Javier, Guzmán‐de‐Villoria, Juan, Franco, Carolina, Robles, Olalla, Arango, Celso, Desco, Manuel
Wydane w Hum Brain Mapp (2016)

An AARS variant as the likely cause of Swedish type hereditary diffuse leukoencephalopathy with spheroids

od Sundal, Christina, Carmona, Susana, Yhr, Maria, Almström, Odd, Ljungberg, Maria, Hardy, John, Hedberg-Oldfors, Carola, Fred, Åsa, Brás, José, Oldfors, Anders, Andersen, Oluf, Guerreiro, Rita
Wydane w Acta Neuropathol Commun (2019)

An independent components and functional connectivity analysis of resting state fMRI data points to neural network dysregulation in adult ADHD

od Hoekzema, Elseline, Carmona, Susana, Ramos‐Quiroga, J. Antoni, Richarte Fernández, Vanesa, Bosch, Rosa, Soliva, Juan Carlos, Rovira, Mariana, Bulbena, Antonio, Tobeña, Adolf, Casas, Miguel, Vilarroya, Oscar
Wydane w Hum Brain Mapp (2013)

Response inhibition and reward anticipation in medication‐naïve adults with attention‐deficit/hyperactivity disorder: A within‐subject case‐control neuroimaging study

od Carmona, Susana, Hoekzema, Elseline, Ramos‐Quiroga, J. Antoni, Richarte, Vanesa, Canals, Clara, Bosch, Rosa, Rovira, Mariana, Carlos Soliva, Juan, Bulbena, Antonio, Tobeña, Adolf, Casas, Miguel, Vilarroya, Oscar
Wydane w Hum Brain Mapp (2011)

Sensation‐to‐cognition cortical streams in attention‐deficit/hyperactivity disorder

od Carmona, Susana, Hoekzema, Elseline, Castellanos, Francisco X., García‐García, David, Lage‐Castellanos, Agustín, Van Dijk, Koene R.A., Navas‐Sánchez, Francisco J., Martínez, Kenia, Desco, Manuel, Sepulcre, Jorge
Wydane w Hum Brain Mapp (2015)

Laminar Thickness Alterations in the Fronto-Parietal Cortical Mantle of Patients with Attention-Deficit/Hyperactivity Disorder

od Hoekzema, Elseline, Carmona, Susana, Ramos-Quiroga, J. Antoni, Fernández, Vanesa Richarte, Picado, Marisol, Bosch, Rosa, Soliva, Juan Carlos, Rovira, Mariana, Vives, Yolanda, Bulbena, Antonio, Tobeña, Adolf, Casas, Miguel, Vilarroya, Oscar
Wydane 2012

Correction: Laminar Thickness Alterations in the Fronto-Parietal Cortical Mantle of Patients with Attention-Deficit/Hyperactivity Disorder

od Hoekzema, Elseline, Carmona, Susana, Ramos-Quiroga, J. Antoni, Fernández, Vanesa Richarte, Picado, Marisol, Bosch, Rosa, Soliva, Juan Carlos, Rovira, Mariana, Vives, Yolanda, Bulbena, Antonio, Tobeña, Adolf, Casas, Miguel, Vilarroya, Oscar
Wydane 2013

Mutations in TYROBP are not a common cause of dementia in a Turkish cohort

od Darwent, Lee, Carmona, Susana, Lohmann, Ebba, Guven, Gamze, Kun-Rodrigues, Celia, Bilgic, Basar, Hanagasi, Hasmet, Gurvit, Hakan, Erginel-Unaltuna, Nihan, Pak, Meltem, Hardy, John, Singleton, Andrew, Brás, Jose, Guerreiro, Rita
Wydane w Neurobiol Aging (2017)

Study Protocol—Coping With the Pandemics: What Works Best to Reduce Anxiety and Depressive Symptoms

od Fortea, Lydia, Solanes, Aleix, Pomarol-Clotet, Edith, Garcia-Leon, Maria Angeles, Fortea, Adriana, Torrent, Carla, Varo, Cristina, Bonnin, C. Mar, Montejo, Laura, Alonso, Jordi, Carmona, Susana, Soldevila-Matías, Pau, Alustiza, Irene, Arbós, Daniel, Hidalgo-Mazzei, Diego, Grande, Iria, Vieta, Eduard, Fullana, Miquel Àngel, Radua, Joaquim
Wydane w Front Psychiatry (2021)

SVEP1 as a Genetic Modifier of TEK-Related Primary Congenital Glaucoma

od Young, Terri L., Whisenhunt, Kristina N., Jin, Jing, LaMartina, Sarah M., Martin, Sean M., Souma, Tomokazu, Limviphuvadh, Vachiranee, Suri, Fatemeh, Souzeau, Emmanuelle, Zhang, Xue, Dan, Yongwook, Anagnos, Evie, Carmona, Susana, Jody, Nicole M., Stangel, Nickie, Higuchi, Emily C., Huang, Samuel J., Siggs, Owen M., Simões, Maria José, Lawson, Brendan M., Martin, Jacob S., Elahi, Elahe, Narooie-Nejad, Mehrnaz, Motlagh, Behzad Fallahi, Quaggin, Susan E., Potter, Heather D., Silva, Eduardo D., Craig, Jamie E., Egas, Conceição, Maroofian, Reza, Maurer-Stroh, Sebastian, Bradfield, Yasmin S., Tompson, Stuart W.
Wydane w Invest Ophthalmol Vis Sci (2020)

A comprehensive screening of copy number variability in dementia with Lewy bodies

od Kun-Rodrigues, Celia, Orme, Tatiana, Carmona, Susana, Hernandez, Dena G., Ross, Owen A., Eicher, John D., Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G., Scholz, Sonja W., Troncoso, Juan C., Pletnikova, Olga, Dawson, Ted, Rosenthal, Liana, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S., Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, George-Hyslop, Peter St., Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E., Beach, Thomas G., Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F., Petersen, Ronald C., Ferman, Tanis J., Escott-Price, Valentina, Graff-Radford, Neill, Cairns, Nigel J., Morris, John C., Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M., Hardy, John, Trojanowski, John Q., Dickson, Dennis W., Singleton, Andrew, Stone, David J., Guerreiro, Rita, Bras, Jose
Wydane w Neurobiol Aging (2018)

Heritability and genetic variance of dementia with Lewy bodies

od Guerreiro, Rita, Escott-Price, Valentina, Hernandez, Dena G., Kun-Rodrigues, Celia, Ross, Owen A., Orme, Tatiana, Neto, Joao Luis, Carmona, Susana, Dehghani, Nadia, Eicher, John D., Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G., Scholz, Sonja W., Troncoso, Juan C., Pletnikova, Olga, Dawson, Ted, Rosenthal, Liana, Ansorge, Olaf, Clarimon, Jordi, Lleo, Alberto, Morenas-Rodriguez, Estrella, Clark, Lorraine, Honig, Lawrence S, Marder, Karen, Lemstra, Afina, Rogaeva, Ekaterina, George-Hyslop, Peter St., Londos, Elisabet, Zetterberg, Henrik, Barber, Imelda, Braae, Anne, Brown, Kristelle, Morgan, Kevin, Troakes, Claire, Al-Sarraj, Safa, Lashley, Tammaryn, Holton, Janice, Compta, Yaroslau, Van Deerlin, Vivianna, Serrano, Geidy E, Beach, Thomas G, Lesage, Suzanne, Galasko, Douglas, Masliah, Eliezer, Santana, Isabel, Pastor, Pau, Diez-Fairen, Monica, Aguilar, Miquel, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Revesz, Tamas, Lees, Andrew, Boeve, Brad F, Petersen, Ronald C., Ferman, Tanis J, Graff-Radford, Neill, Cairns, Nigel J., Morris, John C., Pickering-Brown, Stuart, Mann, David, Halliday, Glenda M., Hardy, John, Trojanowski, John Q., Dickson, Dennis W., Singleton, Andrew, Stone, David J., Bras, Jose
Wydane w Neurobiol Dis (2019)