Pharmacotherapy for mental health problems in people with intellectual disability

Autor: Robert L. Findling, Na Young Ji

Publikováno v: Current Opinion in Psychiatry. 29:103-125

Psychotropic medications are commonly prescribed to people with intellectual disability. We reviewed current evidence-based pharmacotherapy options and recent updates to guide clinicians in their medication management plans.Antipsychotics, particular

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c134cc312f3377158a4f288fe43b8520
https://doi.org/10.1097/yco.0000000000000233

Pervasive within-Mitochondrion Single-Nucleotide Variant Heteroplasmy as Revealed by Single-Mitochondrion Sequencing

Autor: Morris, Jacqueline, Na, Young-Ji, Zhu, Hua, Lee, Jae-Hee, Giang, Hoa, Ulyanova, Alexandra V., Baltuch, Gordon H., Brem, Steven, Chen, H. Isaac, Kung, David K., Lucas, Timothy H., O’Rourke, Donald M., Wolf, John A., Grady, M. Sean, Sul, Jai-Yoon, Kim, Junhyong, Eberwine, James

Publikováno v: In Cell Reports 5 December 2017 21(10):2706-2713

Erratum: Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018))

Autor: Sanna-Cherchi, Simone, Khan, Kamal, Westland, Rik, Krithivasan, Priya, Fievet, Lorraine, Rasouly, Hila Milo, Ionita-Laza, Iuliana, Capone, Valentina P., Fasel, David A., Kiryluk, Krzysztof, Kamalakaran, Sitharthan, Bodria, Monica, Otto, Edgar A., Sampson, Matthew G., Gillies, Christopher E., Vega-Warner, Virginia, Vukojevic, Katarina, Pediaditakis, Igor, Makar, Gabriel S., Mitrotti, Adele, Verbitsky, Miguel, Martino, Jeremiah, Liu, Qingxue, Na, Young Ji, Goj, Vinicio, Ardissino, Gianluigi, Gigante, Maddalena, Gesualdo, Loreto, Janezcko, Magdalena, Zaniew, Marcin, Mendelsohn, Cathy Lee, Shril, Shirlee, Hildebrandt, Friedhelm, van Wijk, Joanna A.E., Arapovic, Adela, Saraga, Marijan, Allegri, Landino, Izzi, Claudia, Scolari, Francesco, Tasic, Velibor, Ghiggeri, Gian Marco, Latos-Bielenska, Anna, Materna-Kiryluk, Anna, Mane, Shrikant, Goldstein, David B., Lifton, Richard P., Katsanis, Nicholas, Davis, Erica E., Gharavi, Ali G.

Publikováno v: American journal of human genetics, 101(6). Cell Press
Sanna-Cherchi, S, Khan, K, Westland, R, Krithivasan, P, Fievet, L, Rasouly, H M, Ionita-Laza, I, Capone, V P, Fasel, D A, Kiryluk, K, Kamalakaran, S, Bodria, M, Otto, E A, Sampson, M G, Gillies, C E, Vega-Warner, V, Vukojevic, K, Pediaditakis, I, Makar, G S, Mitrotti, A, Verbitsky, M, Martino, J, Liu, Q, Na, Y J, Goj, V, Ardissino, G, Gigante, M, Gesualdo, L, Janezcko, M, Zaniew, M, Mendelsohn, C L, Shril, S, Hildebrandt, F, van Wijk, J A E, Arapovic, A, Saraga, M, Allegri, L, Izzi, C, Scolari, F, Tasic, V, Ghiggeri, G M, Latos-Bielenska, A, Materna-Kiryluk, A, Mane, S, Goldstein, D B, Lifton, R P, Katsanis, N, Davis, E E & Gharavi, A G 2017, ' Erratum : Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations (The American Journal of Human Genetics (2017) 101(5) (789–802) (S0002929717303877) (10.1016/j.ajhg.2017.09.018)) ', American journal of human genetics, vol. 101, no. 6, pp. 1034 . https://doi.org/10.1016/j.ajhg.2017.11.003

(The American Journal of Human Genetics 101, 789–802; November 2, 2017) In the version of this paper originally published, the author's name Anna Materna-Kiryluk was incorrectly hyphenated. It appears correctly here and online. The authors apologiz

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::f0cb8c904b03a947091fe2a0fbb8cca2
https://research.vumc.nl/en/publications/ee38b299-0eb4-471c-a6c7-642a353b2475

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Autism spectrum disorder in Down syndrome: cluster analysis of Aberrant Behaviour Checklist data supports diagnosis

Autor: G. T. Capone, Na Young Ji, W. E. Kaufmann

Publikováno v: Journal of Intellectual Disability Research. 55:1064-1077

Background The diagnostic validity of autism spectrum disorder (ASD) based on Diagnostic and Statistical Manual of Mental Disorders (DSM) has been challenged in Down syndrome (DS), because of the high prevalence of cognitive impairments in this popul

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::1932be06338416b2e6ebffa9b03948c0
https://doi.org/10.1111/j.1365-2788.2011.01465.x