Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: NDE1[original query] |
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Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1. Human molecular genetics 2007 Mar 16 (5): 453-62. Hennah W, Tomppo L, Hiekkalinna T, Palo OM, Kilpinen H, Ekelund J, Tuulio-Henriksson A, Silander K, Partonen T, Paunio T, Terwilliger JD, Lönnqvist J, Peltonen L |
Elucidating the relationship between DISC1, NDEL1 and NDE1 and the risk for schizophrenia: evidence of epistasis and competitive binding. Human molecular genetics 2008 Aug 17 (16): 2462-73. Burdick Katherine E, Kamiya Atsushi, Hodgkinson Colin A, Lencz Todd, DeRosse Pamela, Ishizuka Koko, Elashvili Sarah, Arai Hiroyuki, Goldman David, Sawa Akira, Malhotra Anil |
No association between the NDE1 gene and schizophrenia in the Japanese population. Schizophrenia research 2008 Feb 99 (1-3): 367-9. Numata Shusuke, Ueno Shu-Ichi, Iga Jun-Ichi, Nakataki Masahito, Ohmori Tetsuro, Tanahashi Toshihito, Itakura Mitsuo, Sano Akira, Ohi Kazutaka, Hashimoto Ryota, Takeda Masatos |
Copy number variations of chromosome 16p13.1 region associated with schizophrenia. Molecular psychiatry 2011 Jan 16 (1): 17-25. Ingason A, Rujescu D, Cichon S, Sigurdsson E, Sigmundsson T, Pietiläinen O P H, Buizer-Voskamp J E, Strengman E, Francks C, Muglia P, Gylfason A, Gustafsson O, Olason P I, Steinberg S, Hansen T, Jakobsen K D, Rasmussen H B, Giegling I, Möller H-J, Hartmann A, Crombie C, Fraser G, Walker N, Lonnqvist J, Suvisaari J, Tuulio-Henriksson A, Bramon E, Kiemeney L A, Franke B, Murray R, Vassos E, Toulopoulou T, Mühleisen T W, Tosato S, Ruggeri M, Djurovic S, Andreassen O A, Zhang Z, Werge T, Ophoff R A, , Rietschel M, Nöthen M M, Petursson H, Stefansson H, Peltonen L, Collier D, Stefansson K, St Clair D |
Association between genes of Disrupted in schizophrenia 1 (DISC1) interactors and schizophrenia supports the role of the DISC1 pathway in the etiology of major mental illnesses. Biological psychiatry 2009 Jun 65 (12): 1055-62. Tomppo Liisa, Hennah William, Lahermo Päivi, Loukola Anu, Tuulio-Henriksson Annamari, Suvisaari Jaana, Partonen Timo, Ekelund Jesper, Lönnqvist Jouko, Peltonen Lee |
Evidence of statistical epistasis between DISC1, CIT and NDEL1 impacting risk for schizophrenia: biological validation with functional neuroimaging. Human genetics 2010 Apr 127 (4): 441-52. Nicodemus Kristin K, Callicott Joseph H, Higier Rachel G, Luna Augustin, Nixon Devon C, Lipska Barbara K, Vakkalanka Radhakrishna, Giegling Ina, Rujescu Dan, St Clair David, Muglia Pierandrea, Shugart Yin Yao, Weinberger Daniel |
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population. PloS one 2011 6 (8): e23450. Moens Lotte N, De Rijk Peter, Reumers Joke, Van den Bossche Maarten J A, Glassee Wim, De Zutter Sonia, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, Medina Castello Ignacio, Norrback Karl-Fredrik, Goossens Dirk, Van Steen Kristel, Adolfsson Rolf, Del-Favero Jurg |
Male-biased autosomal effect of 16p13.11 copy number variation in neurodevelopmental disorders. PloS one 2013 8 (4): e61365. Tropeano Maria, Ahn Joo Wook, Dobson Richard J B, Breen Gerome, Rucker James, Dixit Abhishek, Pal Deb K, McGuffin Peter, Farmer Anne, White Peter S, Andrieux Joris, Vassos Evangelos, Ogilvie Caroline Mackie, Curran Sarah, Collier David |
Both rare and de novo copy number variants are prevalent in agenesis of the corpus callosum but not in cerebellar hypoplasia or polymicrogyria. PLoS genetics 2013 9 (10): e1003823. Sajan Samin A, Fernandez Liliana, Nieh Sahar Esmaeeli, Rider Eric, Bukshpun Polina, Wakahiro Mari, Christian Susan L, Rivière Jean-Baptiste, Sullivan Christopher T, Sudi Jyotsna, Herriges Michael J, Paciorkowski Alexander R, Barkovich A James, Glessner Joseph T, Millen Kathleen J, Hakonarson Hakon, Dobyns William B, Sherr Elliott |
Analysis of MTHFR and MTRR Gene Polymorphisms in Iranian Ventricular Septal Defect Subjects. International journal of molecular sciences 2013 14 (2): 2. Pishva SR, Vasudevan R, Etemad A, Heidari F, Komara M, Ismail P, Othman F, Karimi A, Sabri MR |
Identification of Rare, Single-Nucleotide Mutations in NDE1 and Their Contributions to Schizophrenia Susceptibility. Schizophrenia bulletin 2015 May 41 (3): 744-53. Kimura Hiroki, Tsuboi Daisuke, Wang Chenyao, Kushima Itaru, Koide Takayoshi, Ikeda Masashi, Iwayama Yoshimi, Toyota Tomoko, Yamamoto Noriko, Kunimoto Shohko, Nakamura Yukako, Yoshimi Akira, Banno Masahiro, Xing Jingrui, Takasaki Yuto, Yoshida Mami, Aleksic Branko, Uno Yota, Okada Takashi, Iidaka Tetsuya, Inada Toshiya, Suzuki Michio, Ujike Hiroshi, Kunugi Hiroshi, Kato Tadafumi, Yoshikawa Takeo, Iwata Nakao, Kaibuchi Kozo, Ozaki Nor |
An interaction between NDE1 and high birth weight increases schizophrenia susceptibility. Psychiatry research 2015 Sep . Wegelius Asko, Pankakoski Maiju, Tomppo Liisa, Lehto Ulriika, Lönnqvist Jouko, Suvisaari Jaana, Paunio Tiina, Hennah Willi |
Copy Number Variations in DISC1 and DISC1-Interacting Partners in Major Mental Illness. Molecular neuropsychiatry 2015 Oct 1 (3): 175-190. Johnstone Mandy, Maclean Alan, Heyrman Lien, Lenaerts An-Sofie, Nordin Annelie, Nilsson Lars-Göran, De Rijk Peter, Goossens Dirk, Adolfsson Rolf, St Clair David M, Hall Jeremy, Lawrie Stephen M, McIntosh Andrew M, Del-Favero Jurgen, Blackwood Douglas H R, Pickard Benjamin |
The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to microRNA-484. Open biology 2017 11 7 (11): . Bradshaw Nicholas J, Ukkola-Vuoti Liisa, Pankakoski Maiju, Zheutlin Amanda B, Ortega-Alonso Alfredo, Torniainen-Holm Minna, Sinha Vishal, Therman Sebastian, Paunio Tiina, Suvisaari Jaana, Lönnqvist Jouko, Cannon Tyrone D, Haukka Jari, Hennah Willi |
Rare germline alterations in cancer-related genes associated with the risk of multiple primary tumor development. Journal of molecular medicine (Berlin, Germany) 2017 Jan . Villacis Rolando A R, Basso Tatiane R, Canto Luisa M, Pinheiro Maísa, Santiago Karina M, Giacomazzi Juliana, de Paula Cláudia A A, Carraro Dirce M, Ashton-Prolla Patrícia, Achatz Maria I, Rogatto Silvia |
Whole Exome Sequencing in 16p13.11 Microdeletion Patients Reveals New Variants Through Deductive and Systems Medicine Approaches. Frontiers in genetics 2022 4 13 798607. Granata Paola, Cocciadiferro Dario, Zito Alessandra, Pessina Chiara, Bassani Alessandro, Zambonin Fabio, Novelli Antonio, Fasano Mauro, Casalone Rosar |
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