Human Genome Epidemiology Literature Finder
Records 1 - 15 (of 15 Records) |
Query Trace: NTNG1[original query] |
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Association of polymorphisms in the haplotype block spanning the alternatively spliced exons of the NTNG1 gene at 1p13.3 with schizophrenia in Japanese populations. Neuroscience letters 2008 Apr 435 (3): 194-7. Ohtsuki T, Horiuchi Y, Koga M, Ishiguro H, Inada T, Iwata N, Ozaki N, Ujike H, Watanabe Y, Someya T, Arinami |
Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3). Human genetics 2009 Jun 125 (5-6): 581-90. van Kuilenburg André B P, Meijer Judith, Mul Adri N P M, Hennekam Raoul C M, Hoovers Jan M N, de Die-Smulders Christine E M, Weber Peter, Mori Andrea Capone, Bierau Jörgen, Fowler Brian, Macke Klaus, Sass Jörn Oliver, Meinsma Rutger, Hennermann Julia B, Miny Peter, Zoetekouw Lida, Vijzelaar Raymon, Nicolai Joost, Ylstra Bauke, Rubio-Gozalbo M Este |
A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.
Molecular psychiatry 2011 Sep 16 (9): 949-59. Wang K, Zhang H, Bloss C S, Duvvuri V, Kaye W, Schork N J, Berrettini W, Hakonarson H, |
Functional variants of the genes involved in neurodevelopment and susceptibility to schizophrenia in an Armenian population. Human immunology 2011 Sep 72 (9): 746-8. Zakharyan Roksana, Boyajyan Anna, Arakelyan Arsen, Gevorgyan Anaida, Mrazek Frantisek, Petrek Mart |
The netrin G1 gene rs628117 polymorphism is associated with ischemic stroke. Neuroscience letters 2013 Aug 549 74-7. Stepanyan Ani, Zakharyan Roksana, Boyajyan An |
Replication of NTNG1 association in schizophrenia. Psychiatric genetics 2014 Dec 24 (6): 266-8. Wilcox James A, Quadri Sy |
A prognostic mutation panel for predicting cancer recurrence in stages II and III colorectal cancer. Journal of surgical oncology 2017 Aug . Sho Shonan, Court Colin M, Winograd Paul, Russell Marcia M, Tomlinson James |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
The Lancet. Neurology 2017 Nov 16 (11): 898-907. Schormair Barbara, Zhao Chen, Bell Steven, Tilch Erik, Salminen Aaro V, Pütz Benno, Dauvilliers Yves, Stefani Ambra, Högl Birgit, Poewe Werner, Kemlink David, Sonka Karel, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Teder-Laving Maris, Metspalu Andres, Hadjigeorgiou Georgios M, Polo Olli, Fietze Ingo, Ross Owen A, Wszolek Zbigniew, Butterworth Adam S, Soranzo Nicole, Ouwehand Willem H, Roberts David J, Danesh John, Allen Richard P, Earley Christopher J, Ondo William G, Xiong Lan, Montplaisir Jacques, Gan-Or Ziv, Perola Markus, Vodicka Pavel, Dina Christian, Franke Andre, Tittmann Lukas, Stewart Alexandre F R, Shah Svati H, Gieger Christian, Peters Annette, Rouleau Guy A, Berger Klaus, Oexle Konrad, Di Angelantonio Emanuele, Hinds David A, Müller-Myhsok Bertram, Winkelmann Juliane, , |
Netrin G1: its downregulation in the nucleus accumbens of cocaine-conditioned mice and genetic association in human cocaine dependence. Addiction biology 2017 Jan . Kelaï Sabah, Ramoz Nicolas, Moalic Jean-Marie, Noble Florence, Mechawar Naguib, Imbeaud Sandrine, Turecki Gustavo, Simonneau Michel, Gorwood Philip, Maussion Gill |
Identification of Restless Legs Syndrome Genes by Mutational Load Analysis. Annals of neurology 2019 Dec . Tilch Erik, Schormair Barbara, Zhao Chen, Salminen Aaro V, Antic Nikolic Ana, Holzknecht Evi, Högl Birgit, Poewe Werner, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Fietze Ingo, Berger Klaus, Lichtner Peter, Gieger Christian, Peters Annette, Müller-Myhsok Bertram, Hoischen Alexander, Winkelmann Juliane, Oexle Konr |
A logical relationship for schizophrenia, bipolar, and major depressive disorder. Part 1: Evidence from chromosome 1 high density association screen. The Journal of comparative neurology 2020 4 528 (15): 2620-2635. Zhang Zhihua, Chen Ga |
Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways. Omics : a journal of integrative biology 2020 2 24 (3): 160-171. Aldosary Mazhor, Al-Bakheet AlBandary, Al-Dhalaan Hesham, Almass Rawan, Alsagob Maysoon, Al-Younes Banan, AlQuait Laila, Mustafa Osama Mufid, Bulbul Mustafa, Rahbeeni Zuhair, Alfadhel Majid, Chedrawi Aziza, Al-Hassnan Zuhair, AlDosari Mohammed, Al-Zaidan Hamad, Al-Muhaizea Mohammad A, AlSayed Moeenaldeen D, Salih Mustafa A, AlShammari Mai, Faiyaz-Ul-Haque Muhammad, Chishti Mohammad Azhar, Al-Harazi Olfat, Al-Odaib Ali, Kaya Namik, Colak Dil |
Genetically predicted circulating protein biomarkers and ovarian cancer risk. Gynecologic oncology 2020 Nov . Considine Daniel P C, Jia Guochong, Shu Xiang, Schildkraut Joellen M, Pharoah Paul D P, Zheng Wei, Kar Siddhartha P, |
A Genetic Study of Cerebral Atherosclerosis Reveals Novel Associations with NTNG1 and CNOT3. Genes 2021 May 12 (6): . Vattathil Selina M, Liu Yue, Harerimana Nadia V, Lori Adriana, Gerasimov Ekaterina S, Beach Thomas G, Reiman Eric M, De Jager Philip L, Schneider Julie A, Bennett David A, Seyfried Nicholas T, Levey Allan I, Wingo Aliza P, Wingo Thomas |
Genome-wide interrogation of structural variation reveals novel African-specific prostate cancer oncogenic drivers. Genome medicine 2022 Aug 14 (1): 100. Gong Tingting, Jaratlerdsiri Weerachai, Jiang Jue, Willet Cali, Chew Tracy, Patrick Sean M, Lyons Ruth J, Haynes Anne-Maree, Pasqualim Gabriela, Brum Ilma Simoni, Stricker Phillip D, Mutambirwa Shingai B A, Sadsad Rosemarie, Papenfuss Anthony T, Bornman Riana M S, Chan Eva K F, Hayes Vanessa |
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- Page last updated:Apr 22, 2024
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