Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: CNP[original query] |
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Systematic screening of type B human natriuretic peptide receptor gene polymorphisms and association with essential hypertension. Journal of human hypertension 2001 Jul 15 (7): 471-4. Rahmutula D, Nakayama T, Soma M, Sato M, Izumi Y, Kanmatsuse K, Ozawa Y |
A single-nucleotide polymorphism in C-type natriuretic peptide gene may be associated with hypertension. Hypertension research : official journal of the Japanese Society of Hypertension 2002 Sep 25 (5): 727-30. Ono Koh, Mannami Toshifumi, Baba Shunroku, Tomoike Hitonobu, Suga Sin-ichi, Iwai Naoha |
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 2006 Aug 103 (33): 12469-74. Georgieva Lyudmila, Moskvina Valentina, Peirce Tim, Norton Nadine, Bray Nicholas J, Jones Lesley, Holmans Peter, Macgregor Stuart, Zammit Stanley, Wilkinson Jennifer, Williams Hywel, Nikolov Ivan, Williams Nigel, Ivanov Dobril, Davis Kenneth L, Haroutunian Vahram, Buxbaum Joseph D, Craddock Nick, Kirov George, Owen Michael J, O'Donovan Michael |
The 2',3'-cyclic nucleotide 3'-phosphodiesterase and oligodendrocyte lineage transcription factor 2 genes do not appear to be associated with schizophrenia in the Japanese population. Schizophrenia research 2006 Dec 88 (1-3): 245-50. Usui Hinako, Takahashi Nagahide, Saito Shinichi, Ishihara Ryoko, Aoyama Nagisa, Ikeda Masashi, Suzuki Tatsuyo, Kitajima Tsuyoshi, Yamanouchi Yoshio, Kinoshita Yoko, Yoshida Keizo, Iwata Nakao, Inada Toshiya, Ozaki Nor |
Convergent evidence for 2',3'-cyclic nucleotide 3'-phosphodiesterase as a possible susceptibility gene for schizophrenia. Archives of general psychiatry 2006 Jan 63 (1): 18-24. Peirce Timothy R, Bray Nicholas J, Williams Nigel M, Norton Nadine, Moskvina Valentina, Preece Anna, Haroutunian Vahram, Buxbaum Joseph D, Owen Michael J, O'Donovan Michael |
Case-control association study of the 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNP) gene and schizophrenia in the Han Chinese population. Neuroscience letters 2007 Apr 416 (2): 113-6. Tang Fulei, Qu Mei, Wang Lifang, Ruan Yan, Lu Tianlan, Zhang Handi, Liu Zhonghua, Yue Weihua, Zhang D |
A family-based association study of the myelin-associated glycoprotein and 2',3'-cyclic nucleotide 3'-phosphodiesterase genes with schizophrenia. Psychiatric genetics 2008 Jun 18 (3): 143-6. Voineskos Aristotle N, de Luca Vincenzo, Bulgin Natalie L, van Adrichem Quinton, Shaikh Sajid, Lang Donna J, Honer William G, Kennedy James |
Effect of a functional single nucleotide polymorphism in the 2',3'-cyclic nucleotide 3'-phosphodiesterase gene on the expression of oligodendrocyte-related genes in schizophrenia. Psychiatry and clinical neurosciences 2008 Feb 62 (1): 103-8. Iwamoto Kazuya, Ueda Junko, Bundo Miki, Nakano Yoko, Kato Tadafu |
No relationship between 2',3'-cyclic nucleotide 3'-phosphodiesterase and schizophrenia in the Chinese Han population: an expression study and meta-analysis. BMC medical genetics 2009 10 31. Che Ronglin, Tang Wei, Zhang Jing, Wei Zhiyun, Zhang Zhao, Huang Ke, Zhao Xinzhi, Gao Jianjun, Zhou Guoquan, Huang Peirong, He Lin, Shi Yongyo |
Association of genetic variation in the natriuretic peptide system with cardiovascular outcomes. Journal of molecular and cellular cardiology 2011 Apr 50 (4): 695-701. Ellis Katrina L, Newton-Cheh Christopher, Wang Thomas J, Frampton Chris M, Doughty Rob N, Whalley Gillian A, Ellis Chris J, Skelton Lorraine, Davis Nick, Yandle Tim G, Troughton Richard W, Richards A Mark, Cameron Vicky |
PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data. Genetic epidemiology 2011 Dec 35 (8): 831-44. Kumasaka Natsuhiko, Fujisawa Hironori, Hosono Naoya, Okada Yukinori, Takahashi Atsushi, Nakamura Yusuke, Kubo Michiaki, Kamatani Naoyu |
A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration. PloS one 2011 6 (10): e25598. Sivakumaran Theru A, Igo Robert P, Kidd Jeffrey M, Itsara Andy, Kopplin Laura J, Chen Wei, Hagstrom Stephanie A, Peachey Neal S, Francis Peter J, Klein Michael L, Chew Emily Y, Ramprasad Vedam L, Tay Wan-Ting, Mitchell Paul, Seielstad Mark, Stambolian Dwight E, Edwards Albert O, Lee Kristine E, Leontiev Dmitry V, Jun Gyungah, Wang Yang, Tian Liping, Qiu Feiyou, Henning Alice K, LaFramboise Thomas, Sen Parveen, Aarthi Manoharan, George Ronnie, Raman Rajiv, Das Manmath Kumar, Vijaya Lingam, Kumaramanickavel Govindasamy, Wong Tien Y, Swaroop Anand, Abecasis Goncalo R, Klein Ronald, Klein Barbara E K, Nickerson Deborah A, Eichler Evan E, Iyengar Sudha |
Genome-wide association study identified CNP12587 region underlying height variation in Chinese females. PloS one 2012 7 (9): e44292. Zhang Yin-Ping, Deng Fei-Yan, Yang Tie-Lin, Zhang Feng, Chen Xiang-Ding, Shen Hui, Zhu Xue-Zheng, Tian Qing, Deng Hong-W |
The association of white matter volume in psychotic disorders with genotypic variation in NRG1, MOG and CNP: a voxel-based analysis in affected individuals and their unaffected relatives. Translational psychiatry 2012 2 . Cannon DM, Walshe M, Dempster E, Collier DA, Marshall N, Bramon E, Murray RM, McDonald C |
Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population.
PloS one 2012 7 (9): e44507. Kumasaka Natsuhiko, Aoki Masayuki, Okada Yukinori, Takahashi Atsushi, Ozaki Kouichi, Mushiroda Taisei, Hirota Tomomitsu, Tamari Mayumi, Tanaka Toshihiro, Nakamura Yusuke, Kamatani Naoyuki, Kubo Michia |
Copy number polymorphisms near SLC2A9 are associated with serum uric acid concentrations. BMC genetics 2014 15 81. Scharpf Robert B, Mireles Lynn, Yang Qiong, Köttgen Anna, Ruczinski Ingo, Susztak Katalin, Halper-Stromberg Eitan, Tin Adrienne, Cristiano Stephen, Chakravarti Aravinda, Boerwinkle Eric, Fox Caroline S, Coresh Josef, Linda Kao Wen Ho |
Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients. Journal of human genetics 2015 Aug . Brkušanin Miloš, Kosa? Ana, Jovanovi? Vladimir, Pešovi? Jovan, Brajuškovi? Goran, Dimitrijevi? Nikola, Todorovi? Slobodanka, Romac Stanka, Mili? Raši? Vedrana, Savi?-Pavi?evi? Dušan |
Are HLA-E*0103 alleles predictive markers for nasopharyngeal cancer risk? Pathology, research and practice 2016 Apr 212 (4): 345-9. Douik Hayet, Romdhane Neila Attia, Guemira Fet |
New Insights into Cardiac and Vascular Natriuretic Peptides: Findings from Young Adults Born with Very Low Birth Weight. Clinical chemistry 2017 11 64 (2): 363-373. Prickett Timothy C R, Darlow Brian A, Troughton Richard W, Cameron Vicky A, Elliott John M, Martin Julia, Horwood L John, Espiner Eric |
Genome-Wide Association of Copy Number Polymorphisms and Kidney Function. PloS one 2017 12 (1): e0170815. Li Man, Carey Jacob, Cristiano Stephen, Susztak Katalin, Coresh Josef, Boerwinkle Eric, Kao Wen Hong L, Beaty Terri H, Köttgen Anna, Scharpf Robert |
Human genotyping and an experimental model reveal NPR-C as a possible contributor to morbidity in coarctation of the aorta. Physiological genomics 2019 4 51 (6): 177-185. LaDisa John F, Tomita-Mitchell Aoy, Stamm Karl, Bazan Kathleen, Mahnke Donna K, Goetsch Mary A, Wegter Brandon J, Gerringer Jesse W, Repp Kathryn, Palygin Oleg, Zietara Adrian P, Krolikowski Mary M, Eddinger Thomas J, Alli Abdel A, Mitchell Michael |
Role of NPR2 mutation in idiopathic short stature: Identification of two novel mutations. Molecular genetics & genomic medicine 2020 1 8 (3): e1146. Hwang Il Tae, Mizuno Yusuke, Amano Naoko, Lee Hye Jin, Shim Young Suk, Nam Hyo-Kyoung, Rhie Young-Jun, Yang Seung, Lee Kee-Hyoung, Hasegawa Tomonobu, Kang Min J |
Morphometric and Nanomechanical Features of Platelets from Women with Early Pregnancy Loss Provide New Evidence of the Impact of Inherited Thrombophilia. International journal of molecular sciences 2021 8 22 (15): . Andreeva Tonya, Komsa-Penkova Regina, Langari Ariana, Krumova Sashka, Golemanov Georgi, Georgieva Galya B, Taneva Stefka G, Giosheva Ina, Mihaylova Nikolina, Tchorbanov Andrey, Todinova Svet |
Residential surrounding greenness and DNA methylation: An epigenome-wide association study. Environment international 2021 4 154 106556. Xu Rongbin, Li Shuai, Li Shanshan, Wong Ee Ming, Southey Melissa C, Hopper John L, Abramson Michael J, Guo Yumi |
A splice site and copy number variant responsible for TTC25-related primary ciliary dyskinesia. European journal of medical genetics 2021 3 64 (5): 104193. Backman K, Mears W E, Waheeb A, Beaulieu Bergeron M, McClintock J, de Nanassy J, Reisman J, Osmond M, Hartley T, Mears A J, Kernohan K D, |
Atezolizumab plus carboplatin and nab-paclitaxel versus carboplatin and nab-paclitaxel as treatments for Chinese, treatment-naïve, stage IV, non-squamous, non-small-cell lung cancer patients: A retrospective analysis. Pharmacology research & perspectives 2022 5 10 (3): e00941. Chen Yingkai, Kang Shizhou, Yan Mi |
Genetic evidence implicating natriuretic peptide receptor-3 in cardiovascular disease risk: a Mendelian randomization study. BMC medicine 2023 4 21 (1): 158. Héléne T Cronjé, Ville Karhunen, G Kees Hovingh, Ken Coppieters, Jens O Lagerstedt, Michael Nyberg, Dipender Gi |
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- Page last updated:Apr 22, 2024
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