Výsledky vyhledávání - Reid Robison
- Zobrazuji výsledky 1 - 11 z 11
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Case report: Intramuscular ketamine or intranasal esketamine as a treatment in four patients with major depressive disorder and comorbid anorexia nervosa Autor Johanna Louise Keeler, Janet Treasure, Hubertus Himmerich, Madeline Brendle, Claire E. Moore, Reid Robison
Vydáno 2023Artigo -
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Ketamine as a Novel Psychopharmacotherapy for Eating Disorders: Evidence and Future Directions Autor Anya Ragnhildstveit, Matthew Slayton, Laura Jackson, Madeline Brendle, Sachin Ahuja, Willis Holle, Claire E. Moore, Kellie Sollars, Paul Seli, Reid Robison
Vydáno 2022Revisão -
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A case series of group-based ketamine-assisted psychotherapy for patients in residential treatment for eating disorders with comorbid depression and anxiety disorders Autor Reid Robison, Adèle Lafrance, Madeline Brendle, Michelle Smith, Claire E. Moore, Sachin Ahuja, Scott Richards, Nicole A. Hawkins, Erin J. Strahan
Vydáno 2022Artigo -
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Using VAAST to Identify an X-Linked Disorder Resulting in Lethality in Male Infants Due to N-Terminal Acetyltransferase Deficiency Autor Alan F. Rope, Kai Wang, Rune Evjenth, Jinchuan Xing, Jennifer J. Johnston, Jeffrey Swensen, W. Evan Johnson, Barry Moore, Chad D. Huff, Lynne M. Bird, John C. Carey, John M. Opitz, Cathy A. Stevens, Tao Jiang, Christa Schank, Heidi D. Fain, Reid Robison, Brian K. Dalley, Steven S. Chin, Sarah T. South, Theodore J. Pysher, Lynn B. Jorde, Hákon Hákonarson, Johan R. Lillehaug, Leslie G. Biesecker, Mark Yandell, Thomas Arnesen, Gholson J. Lyon
Vydáno 2011Artigo -
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Single-Dose Psilocybin Treatment for Major Depressive Disorder Autor Charles L. Raison, Gerard Sanacora, Joshua D. Woolley, Keith G. Heinzerling, Boadie W. Dunlop, Randall Brown, Rishi Kakar, Michael Hassman, Rupal Trivedi, Reid Robison, Natalie Gukasyan, Sandeep M. Nayak, Xiaojue Hu, Kelley C. O’Donnell, Benjamin Kelmendi, Jordan Sloshower, Andrew Penn, Ellen Bradley, Daniel F. Kelly, Tanja Mletzko, Christopher R. Nicholas, Paul R. Hutson, Gary Tarpley, Malynn Utzinger, Kelsey Lenoch, Kasia Warchol, Theraysa Gapasin, M. Davis, Courtney Nelson-Douthit, Steffanie H Wilson, Carrie Brown, William Linton, Matthew W. Johnson, Stephen Ross, Roland R. Griffiths
Vydáno 2023Artigo -
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TAF1 Variants Are Associated with Dysmorphic Features, Intellectual Disability, and Neurological Manifestations Autor Jason O'Rawe, Yiyang Wu, Max J. Dörfel, Alan F. Rope, Ping Yee Billie Au, Jillian S. Parboosingh, Sungjin Moon, Maria Kousi, Konstantina Kosma, Christopher Smith, Maria Tzetis, Jane L. Schuette, Robert B. Hufnagel, Carlos E. Prada, Francisco Martı́nez, Carmen Orellana, Jonathan Crain, Alfonso Caro‐Llopis, Silvestre Oltra, Sandra Monfort, Laura T. Jiménez-Barrón, Jeffrey Swensen, Sara Ellingwood, Rosemarie Smith, Han Fang, Sandra Ospina, Alexander P.A. Stegmann, Nicolette S. den Hollander, David Mittelman, Gareth Highnam, Reid Robison, Edward Yang, Laurence Faivre, Agathe Roubertie, Jean‐Baptiste Rivière, Kristin G. Monaghan, Kai Wang, Erica E. Davis, Nicholas Katsanis, Vera M. Kalscheuer, Edith H. Wang, Kay Metcalfe, Tjitske Kleefstra, A. Micheil Innes, Sophia Kitsiou‐Tzeli, Mónica Roselló, Catherine E. Keegan, Gholson J. Lyon
Vydáno 2015Artigo -
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Paralog Studies Augment Gene Discovery: DDX and DHX Genes Autor Ingrid S. Paine, Jennifer E. Posey, Christopher M. Grochowski, Shalini N. Jhangiani, Sarah Rosenheck, Robert Kleyner, Taylor Marmorale, Margaret S. Yoon, Kai Wang, Reid Robison, Gerarda Cappuccio, Michele Pinelli, Adriano Magli, Zeynep Coban‐Akdemir, Joannie Hui, Wai Lan Yeung, Bibiana K. Y. Wong, Lucia Ortega, Mir Reza Bekheirnia, Tatjana Bierhals, Maja Hempel, Jessika Johannsen, René Santer, Dilek Aktaş, Mehmet Alikaşifoĝlu, Sevcan Tuğ Bozdoğan, Hatip Aydın, Ender Karaca, Yavuz Bayram, Hadas Ityel, Michael O. Dorschner, Janson J. White, Ekkehard Wilichowski, Saskia B. Wortmann, Erasmo Barbante Casella, João Paulo Kitajima, Fernando Kok, Fabíola Paoli Monteiro, Donna M. Muzny, Michael J. Bamshad, Richard A. Gibbs, V. Reid Sutton, Hilde Van Esch, Nicola Brunetti‐Pierri, Friedhelm Hildebrandt, Ariel Brautbar, Ignatia B. Van den Veyver, Ian Glass, Davor Lessel, Gholson J. Lyon, James R. Lupski
Vydáno 2019Artigo -
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Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder Autor Josephine Elia, Joseph Glessner, Kai Wang, Nagahide Takahashi, Corina Shtir, Dexter Hadley, Patrick Sleiman, Haitao Zhang, Chong Ae Kim, Reid Robison, Gholson J. Lyon, James H. Flory, Jonathan P. Bradfield, Marcin Imieliński, Cuiping Hou, Edward C. Frackelton, Rosetta Chiavacci, Takeshi Sakurai, Cara Rabin, Frank A. Middleton, Kelly Thomas, Maria Garris, Frank Mentch, Christine M. Freitag, Hans‐Christoph Steinhausen, Alexandre A. Todorov, Andreas Reif, Aribert Rothenberger, Barbara Franke, Eric Mick, Herbert Roeyers, Jan K. Buitelaar, Klaus‐Peter Lesch, Tobias Banaschewski, Richard P. Ebstein, Fernando Mulas, Robert D. Oades, Joseph A. Sergeant, Edmund Sonuga‐Barke, Tobias Renner, Marcel Romanos, Jasmin Romanos, Andreas Warnke, Susanne Walitza, Jobst Meyer, Haukur Pálmason, Christiane Seitz, Sandra K. Loo, Susan L. Smalley, Joseph Biederman, Lindsey Kent, Philip Asherson, Richard Anney, J. William Gaynor, Philip Shaw, Marcella Devoto, Peter S. White, Struan F.A. Grant, Joseph D. Buxbaum, Judith L. Rapoport, Nigel Williams, Stanley F. Nelson, Stephen V. Faraone, Hákon Hákonarson
Vydáno 2011Artigo
Vyhledávací nástroje:
Související témata
Medicine
Psychiatry
Biology
Gene
Genetics
Dosing
Environmental health
Internal medicine
Psychology
Adverse effect
Anxiety
Clinical psychology
Depression (economics)
Economics
Genotype
Ketamine
Macroeconomics
Mood
Phenotype
Population
Single-nucleotide polymorphism
Developmental psychology
Eating disorders
Genome-wide association study
Hypotonia
Major depressive disorder
Tolerability
Acetylation
Acetyltransferase
Acrylate