Human Genome Epidemiology Literature Finder
Records 1 - 9 (of 9 Records) |
Query Trace: MAP1B[original query] |
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Identification of candidate oncogenes in human colorectal cancers with microsatellite instability. Gastroenterology 2013 Sep 145 (3): 540-3.e22. Gylfe Alexandra E, Kondelin Johanna, Turunen Mikko, Ristolainen Heikki, Katainen Riku, Pitkänen Esa, Kaasinen Eevi, Rantanen Ville, Tanskanen Tomas, Varjosalo Markku, Lehtonen Heli, Palin Kimmo, Taipale Minna, Taipale Jussi, Renkonen-Sinisalo Laura, Järvinen Heikki, Böhm Jan, Mecklin Jukka-Pekka, Ristimäki Ari, Kilpivaara Outi, Tuupanen Sari, Karhu Auli, Vahteristo Pia, Aaltonen Lauri |
MAP1B and NOS1 genes are associated with working memory in youths with attention-deficit/hyperactivity disorder. European archives of psychiatry and clinical neuroscience 2015 Aug . Salatino-Oliveira Angélica, Wagner Flávia, Akutagava-Martins Glaucia C, Bruxel Estela M, Genro Júlia P, Zeni Cristian, Kieling Christian, Polanczyk Guilherme V, Rohde Luis A, Hutz Mara |
NOS1 and SNAP25 polymorphisms are associated with Attention-Deficit/Hyperactivity Disorder symptoms in adults but not in children. Journal of psychiatric research 2016 Jan 75 75-81. Salatino-Oliveira Angélica, Akutagava-Martins Glaucia C, Bruxel Estela M, Genro Julia P, Polanczyk Guilherme V, Zeni Cristian, Kieling Christian, Karam Rafael G, Rovaris Diego L, Contini Verônica, Cupertino Renata B, Mota Nina R, Grevet Eugenio H, Bau Claiton H, Rohde Luis A, Hutz Mara |
MAP1B mutations cause intellectual disability and extensive white matter deficit. Nature communications 2018 8 9 (1): 3456. Walters G Bragi, Gustafsson Omar, Sveinbjornsson Gardar, Eiriksdottir Valgerdur K, Agustsdottir Arna B, Jonsdottir Gudrun A, Steinberg Stacy, Gunnarsson Arni F, Magnusson Magnus I, Unnsteinsdottir Unnur, Lee Amy L, Jonasdottir Adalbjorg, Sigurdsson Asgeir, Jonasdottir Aslaug, Skuladottir Astros, Jonsson Lina, Nawaz Muhammad S, Sulem Patrick, Frigge Mike, Ingason Andres, Love Askell, Norddhal Gudmundur L, Zervas Mark, Gudbjartsson Daniel F, Ulfarsson Magnus O, Saemundsen Evald, Stefansson Hreinn, Stefansson Ka |
De novo and inherited private variants in MAP1B in periventricular nodular heterotopia. PLoS genetics 2018 5 14 (5): e1007281. Heinzen Erin L, O'Neill Adam C, Zhu Xiaolin, Allen Andrew S, Bahlo Melanie, Chelly Jamel, Chen Ming Hui, Dobyns William B, Freytag Saskia, Guerrini Renzo, Leventer Richard J, Poduri Annapurna, Robertson Stephen P, Walsh Christopher A, Zhang Mengqi, , |
Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetes.
Cardiovascular diabetology 2018 Apr 17 (1): 61. Charmet Romain, Duffy Seamus, Keshavarzi Sareh, Gyorgy Beata, Marre Michel, Rossing Peter, McKnight Amy Jayne, Maxwell Alexander P, Ahluwalia Tarun Veer Singh, Paterson Andrew D, Trégouët David-Alexandre, Hadjadj Sa |
The genomic profile of parathyroid carcinoma based on whole-genome sequencing. International journal of cancer 2020 6 147 (9): 2446-2457. Hu Ya, Zhang Xiang, Wang Ou, Bi Yalan, Xing Xiaoping, Cui Ming, Wang Mengyi, Tao Wei, Liao Quan, Zhao Yup |
Epilepsy phenotypes associated with MAP1B-related brain malformations. Epileptic disorders : international epilepsy journal with videotape 2021 3 23 (2): 392-396. Arya Ravindra, Spaeth Christine, Zhang Wenyi |
Meta-analysis of genome-wide association studies identifies ancestry-specific associations underlying circulating total tau levels.
Communications biology 2022 4 5 (1): 336. Sarnowski Chloé, Ghanbari Mohsen, Bis Joshua C, Logue Mark, Fornage Myriam, Mishra Aniket, Ahmad Shahzad, Beiser Alexa S, Boerwinkle Eric, Bouteloup Vincent, Chouraki Vincent, Cupples L Adrienne, Damotte Vincent, DeCarli Charles S, DeStefano Anita L, Djoussé Luc, Fohner Alison E, Franz Carol E, Kautz Tiffany F, Lambert Jean-Charles, Lyons Michael J, Mosley Thomas H, Mukamal Kenneth J, Pase Matthew P, Portilla Fernandez Eliana C, Rissman Robert A, Satizabal Claudia L, Vasan Ramachandran S, Yaqub Amber, Debette Stephanie, Dufouil Carole, Launer Lenore J, Kremen William S, Longstreth William T, Ikram M Arfan, Seshadri Sud |
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- Page last updated:Apr 22, 2024
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