Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 99 Records) |
Query Trace: NOS1AP[original query] |
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The genetic variation rs12143842 in NOS1AP increases idiopathic ventricular tachycardia risk in Chinese Han populations. Scientific reports 2017 Aug 7 (1): 8356. Zhang Ronfeng, Chen Feifei, Yu Honjiu, Gao Lianjun, Yin Xiaomeng, Dong Yingxue, Yang Yanzong, Xia Yunlo |
Ethnic Differences in Genetic Ion Channelopathies Associated with Sudden Cardiac Death: A Systematic Review and Meta-Analysis. Annals of clinical and laboratory science 2017 Aug 47 (4): 481-490. Kong Tim, Feulefack Joseph, Ruether Kim, Shen Fan, Zheng Wang, Chen Xing-Zhen, Sergi Consola |
NOS1AP genetic variation is associated with impaired healing of diabetic foot ulcers and diminished response to healing of circulating stem/progenitor cells. Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society 2017 08 25 (4): 733-736. Margolis David J, Hampton Michelle, Hoffstad Ole, Mala D Scot, Mirza Ziad, Woltereck Diana, Shannon Steven, Troiano Michael A, Mitra Nandita, Yang Ming, Bhopale Veena M, Thom Stephen |
Sex is a moderator of the association between NOS1AP sequence variants and QTc in two long QT syndrome founder populations: a pedigree-based measured genotype association analysis. BMC medical genetics 2017 07 18 (1): 74. Winbo Annika, Stattin Eva-Lena, Westin Ida Maria, Norberg Anna, Persson Johan, Jensen Steen M, Rydberg Anni |
GWAS of the electrocardiographic QT interval in Hispanics/Latinos generalizes previously identified loci and identifies population-specific signals.
Scientific reports 2017 Dec 7 (1): 17075. Méndez-Giráldez Raúl, Gogarten Stephanie M, Below Jennifer E, Yao Jie, Seyerle Amanda A, Highland Heather M, Kooperberg Charles, Soliman Elsayed Z, Rotter Jerome I, Kerr Kathleen F, Ryckman Kelli K, Taylor Kent D, Petty Lauren E, Shah Sanjiv J, Conomos Matthew P, Sotoodehnia Nona, Cheng Susan, Heckbert Susan R, Sofer Tamar, Guo Xiuqing, Whitsel Eric A, Lin Henry J, Hanis Craig L, Laurie Cathy C, Avery Christy |
The interaction of NOS1AP, DISC1, DAOA, and GSK3B confers susceptibility of early-onset schizophrenia in Chinese Han population. Progress in neuro-psychopharmacology & biological psychiatry 2017 Oct . Hu Guoqin, Yang Chengqing, Zhao Lei, Fan Yong, Lv Qinyu, Zhao Jing, Zhu Minghuan, Guo Xiangqing, Bao Chenxi, Xu Ahong, Jie Yong, Jiang Yaqing, Zhang Chen, Yu Shunying, Wang Zuowei, Li Zezhi, Yi Zhengh |
QT length during methadone maintenance treatment: gene × dose interaction. Fundamental & clinical pharmacology 2018 Aug . Zerdazi El-Hadi, Vorspan Florence, Marees Andries T, Naccache François, Lepine Jean-Pierre, Laplanche Jean-Louis, Prince Nathalie, Marie-Claire Cynthia, Bellivier Frank, Mouly Stéphane, Bloch Vanes |
QTc prolongation in short-term treatment of schizophrenia patients: effects of different antipsychotics and genetic factors. European archives of psychiatry and clinical neuroscience 2018 Feb . Spellmann Ilja, Reinhard Matthias A, Veverka Diana, Zill Peter, Obermeier Michael, Dehning Sandra, Schennach Rebecca, Müller Norbert, Möller Hans-Jürgen, Riedel Michael, Musil Richa |
Corrected QT Interval Prolongation in Psychopharmacological Treatment and Its Modulation by Genetic Variation. Neuropsychobiology 2019 77 (2): 67-72. Corponi Filippo, Fabbri Chiara, Boriani Giuseppe, Diemberger Igor, Albani Diego, Forloni Gianluigi, Serretti Alessand |
Insights into the genetics of blood pressure in black South African individuals: the Birth to Twenty cohort.
BMC medical genomics 2018 Jan 11 (1): 2. Hendry Liesl M, Sahibdeen Venesa, Choudhury Ananyo, Norris Shane A, Ramsay Michèle, Lombard Zané, |
Systematic Meta-Analysis of the Association Between a Common NOS1AP Genetic Polymorphism, the QTc Interval, and Sudden Death. International heart journal 2019 Aug . Zang Xiaobiao, Li Sisi, Zhao Yonghui, Chen Ke, Wang Xianqing, Song Weifeng, Ma Jifang, Tu Xin, Xia Yunlong, Zhang Shulong, Gao Chuan |
Generation of two human induced pluripotent stem cell (hiPSC) lines from a long QT syndrome South African founder population. Stem cell research 2019 8 39 101510. Mura Manuela, Pisano Federica, Stefanello Manuela, Ginevrino Monia, Boni Marina, Calabrò Federica, Crotti Lia, Valente Enza Maria, Schwartz Peter J, Brink Paul A, Gnecchi Massimilia |
Generation of the human induced pluripotent stem cell (hiPSC) line PSMi007-A from a Long QT Syndrome type 1 patient carrier of two common variants in the NOS1AP gene. Stem cell research 2019 3 36 101416. Mura Manuela, Pisano Federica, Stefanello Manuela, Ginevrino Monia, Boni Marina, Calabrò Federica, Crotti Lia, Valente Enza Maria, Schwartz Peter J, Brink Paul A, Gnecchi Massimilia |
Effect of Sex and Underlying Disease on the Genetic Association of QT Interval and Sudden Cardiac Death. Journal of the American Heart Association 2019 Dec 8 (23): e013751. Mitchell Rebecca N, Ashar Foram N, Jarvelin Marjo-Riitta, Froguel Philippe, Sotoodehnia Nona, Brody Jennifer A, Sebert Sylvain, Huikuri Heikki, Rioux John, Goyette Philippe, Newcomb Charles E, Junttila M Juhani, Arking Dan |
Effects of interaction of NOS1AP gene polymorphisms and childhood abuse on paranoid personality disorder features among male violent offenders in China. Journal of psychiatric research 2020 Aug 130 180-186. Wang Qiuyu, Liu Gang, Li Jinyang, Zhang Min, Chen Haocheng, Chen Chen, Wang Chun, Liu Na, Zhang Ni |
Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome.
Circulation 2020 Jul 142 (4): 324-338. Lahrouchi Najim, Tadros Rafik, Crotti Lia, Mizusawa Yuka, Postema Pieter G, Beekman Leander, Walsh Roddy, Hasegawa Kanae, Barc Julien, Ernsting Marko, Turkowski Kari L, Mazzanti Andrea, Beckmann Britt M, Shimamoto Keiko, Diamant Ulla-Britt, Wijeyeratne Yanushi D, Kucho Yu, Robyns Tomas, Ishikawa Taisuke, Arbelo Elena, Christiansen Michael, Winbo Annika, Jabbari Reza, Lubitz Steven A, Steinfurt Johannes, Rudic Boris, Loeys Bart, Shoemaker M Ben, Weeke Peter E, Pfeiffer Ryan, Davies Brianna, Andorin Antoine, Hofman Nynke, Dagradi Federica, Pedrazzini Matteo, Tester David J, Bos J Martijn, Sarquella-Brugada Georgia, Campuzano Óscar, Platonov Pyotr G, Stallmeyer Birgit, Zumhagen Sven, Nannenberg Eline A, Veldink Jan H, van den Berg Leonard H, Al-Chalabi Ammar, Shaw Christopher E, Shaw Pamela J, Morrison Karen E, Andersen Peter M, Müller-Nurasyid Martina, Cusi Daniele, Barlassina Cristina, Galan Pilar, Lathrop Mark, Munter Markus, Werge Thomas, Ribasés Marta, Aung Tin, Khor Chiea C, Ozaki Mineo, Lichtner Peter, Meitinger Thomas, van Tintelen J Peter, Hoedemaekers Yvonne, Denjoy Isabelle, Leenhardt Antoine, Napolitano Carlo, Shimizu Wataru, Schott Jean-Jacques, Gourraud Jean-Baptiste, Makiyama Takeru, Ohno Seiko, Itoh Hideki, Krahn Andrew D, Antzelevitch Charles, Roden Dan M, Saenen Johan, Borggrefe Martin, Odening Katja E, Ellinor Patrick T, Tfelt-Hansen Jacob, Skinner Jonathan R, van den Berg Maarten P, Olesen Morten Salling, Brugada Josep, Brugada Ramón, Makita Naomasa, Breckpot Jeroen, Yoshinaga Masao, Behr Elijah R, Rydberg Annika, Aiba Takeshi, Kääb Stefan, Priori Silvia G, Guicheney Pascale, Tan Hanno L, Newton-Cheh Christopher, Ackerman Michael J, Schwartz Peter J, Schulze-Bahr Eric, Probst Vincent, Horie Minoru, Wilde Arthur A, Tanck Michael W T, Bezzina Connie |
NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis. Cardiovascular research 2020 2 117 (2): 472-483. Ronchi Carlotta, Bernardi Joyce, Mura Manuela, Stefanello Manuela, Badone Beatrice, Rocchetti Marcella, Crotti Lia, Brink Paul, Schwartz Peter J, Gnecchi Massimiliano, Zaza Anton |
PPARD rs2016520 (T/C) and NOS1AP rs12742393 (A/C) polymorphisms affect therapeutic efficacy of nateglinide in Chinese patients with type 2 diabetes mellitus. BMC medical genomics 2021 Nov 14 (1): 267. Wang Tao, Song Jin-Fang, Zhou Xue-Yan, Li Cheng-Lin, Yin Xiao-Xing, Lu Qi |
A NOS1AP gene variant is associated with a paradoxical increase of the QT-interval shortening effect of digoxin. The pharmacogenomics journal 2021 Oct . Soroush Negin, Aarnoudse Albert-Jan, Kavousi Maryam, Kors Jan A, Ikram M Arfan, Newton-Cheh Christopher, Ahmadizar Fariba, Stricker Bruno |
Genome-Wide Association Study for Idiopathic Ventricular Tachyarrhythmias Identifies Key Role of CCR7 and PKN2 in Calcium Homeostasis and Cardiac Rhythm Maintenance. Circulation. Genomic and precision medicine 2022 Jul 101161CIRCGEN121003603. Fang Chen, Wang Pengxia, Yu Dong, Zhang Xiaoyu, Gou Dongzhi, Liang Lina, Bai Xuemei, Xie Wen, Li Hui, Pu Jielin, Yao Yufeng, Wang Binbin, Ren Xiang, Ke Tie, Tu Xin, Xu Chengqi, Wang Qing |
Influence of NOS1AP Risk Variants on the Corrected QT (QTc) Interval in the Pharmacotherapy of Schizophrenia. Pharmacopsychiatry 2022 Jun . Esen-Sehir Dilhan, Kopf Juliane, Hägele Sandra, Plichta Michael M, Reif Andreas, Freudenberg Flori |
Association of a Common NOS1AP Variant with Attenuation of QTc Prolongation in Men with Heroin Dependence Undergoing Methadone Treatment. Journal of personalized medicine 2022 5 12 (5): . Chang Kuan-Cheng, Chen Ke-Wei, Huang Chieh-Liang, Liao Wen-Ling, Wu Mei-Yao, Lin Yu-Kai, Shiao Yi-Tzone, Chung Wei-Hsin, Lin Yen-Nien, Lane Hsien-Yu |
Association of nitric oxide synthase 1 adaptor protein gene polymorphisms with schizophrenia in a Chinese Han population. Indian journal of psychiatry 0 64 (2): 130-137. Yang Xueping, Zhou Jing, Yuan Zhen, Lin Ailu, Li Xin, Cong Zhengtu, He Ru, Zhu Ga |
Evaluating Common NOS1AP Variants in Patients with Implantable Cardioverter Defibrillators for Secondary Prevention : Evaluating SNPs in NOS1AP. Journal of interventional cardiac electrophysiology : an international journal of arrhythmias and pacing 2022 3 64 (3): 793-800. Zang Xiaobiao, Zhang Shulong, Li Sisi, Wang Xianqing, Song Weifeng, Chen Ke, Ma Jifang, Tu Xin, Xia Yunlong, Zhao Yonghui, Gao Chuan |
The influence of NOS1AP gene polymorphisms and childhood abuse on antisocial personality disorder in Chinese male violent inmates. Personality and mental health 2022 12 . Li Jinyang, Ouyang Lichen, Liu Xinyao, Wang Qiuyu, Min Zhang, Liu Gang, Zhong Yuan, Zhang Ning, Wang Chun, Liu |
Genetic Analysis of RASD1 as a Candidate Gene for Schizophrenia. Balkan medical journal 2022 10 39 (6): 422-428. Durmaz Ceren Damla, Karabulut Halil Gürhan, Saka Meram Can, Sucularl? Ceren, Gümü? Akay Güvem, Atba?o?lu Cem, Ilg?n Ruhi Hati |
Uncovering associations between mental illness diagnosis, nitric oxide synthase gene variation, and peripheral nitric oxide concentration. Brain, behavior, and immunity 2022 1 101 275-283. McNeill Rhiannon V, Kehrwald Christopher, Brum Murielle, Knopf Katrin, Brunkhorst-Kanaan Nathalie, Etyemez Semra, Koreny Carolin, Bittner Robert A, Freudenberg Florian, Herterich Sabine, Reif Andreas, Kittel-Schneider Sar |
Genetic variants and effect modifiers of QT interval prolongation in patients with sickle cell disease. Gene 2023 9 890 147824. Mengna Zhang, William B Hillegass, Xue Yu, Suvankar Majumdar, J Daryl Pollard, Erin Jackson, Jarrod Knudson, Douglas Wolfe, Gregory J Kato, Joseph F Maher, Hao M |
Molecular and in silico analyses of SYN III gene variants in autism spectrum disorder. Irish journal of medical science 2023 5 . Remzi Oguz Baris, Nilfer Sahin, Ay?egül Demirtas Bilgic, Cilem Ozdemir, Tuba Gokdogan Edgun |
An improved clinical and genetics-based prediction model for diabetic foot ulcer healing. Advances in wound care 2024 1 . Gary Hettinger, Nandita Mitra, Stephen R Thom, David Margol |
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- Page last updated:Mar 25, 2024
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