Human Genome Epidemiology Literature Finder
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Records 1 - 26 (of 26 Records) |
| Query Trace: Abnormalities and TAG[original query] |
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| Variation at the DAOA/G30 locus influences susceptibility to major mood episodes but not psychosis in schizophrenia and bipolar disorder. Archives of general psychiatry 2006 Apr 63 (4): 366-73. Williams Nigel M, Green Elaine K, Macgregor Stuart, Dwyer Sarah, Norton Nadine, Williams Hywel, Raybould Rachel, Grozeva Detelina, Hamshere Marian, Zammit Stanley, Jones Lisa, Cardno Alastair, Kirov George, Jones Ian, O'Donovan Michael C, Owen Michael J, Craddock Ni |
| LIPC variants in the promoter and intron 1 modify HDL-C levels in a sex-specific fashion. Atherosclerosis 2009 May 204 (1): 171-7. Feitosa Mary F, Myers Richard H, Pankow James S, Province Michael A, Borecki Ingrid |
| Angiogenesis in systemic sclerosis: impaired expression of vascular endothelial growth factor receptor 1 in endothelial progenitor-derived cells under hypoxic conditions. Arthritis and rheumatism 2008 Nov 58 (11): 3550-61. Avouac J, Wipff J, Goldman O, Ruiz B, Couraud P O, Chiocchia G, Kahan A, Boileau C, Uzan G, Allanore |
| High-frequency haplotypes in the X chromosome locus TLR8 are associated with both CD and UC in females. Inflammatory bowel diseases 2009 Mar 15 (3): 321-7. Saruta Masayuki, Targan Stephan R, Mei Ling, Ippoliti Andrew F, Taylor Kent D, Rotter Jerome |
| Association study of tardive dyskinesia and five DRD4 polymorphisms in schizophrenia patients. The pharmacogenomics journal 2009 Jun 9 (3): 168-74. Zai C C, Tiwari A K, Basile V, De Luca V, Müller D J, King N, Voineskos A N, Remington G, Meltzer H Y, Lieberman J A, Potkin S G, Kennedy J |
| Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia. Bipolar disorders 2009 Nov 11 (7): 701-10. Mansour Hader A, Talkowski Michael E, Wood Joel, Chowdari Kodavali V, McClain Lora, Prasad Konasale, Montrose Debra, Fagiolini Andrea, Friedman Edward S, Allen Michael H, Bowden Charles L, Calabrese Joseph, El-Mallakh Rif S, Escamilla Michael, Faraone Stephen V, Fossey Mark D, Gyulai Laszlo, Loftis Jennifer M, Hauser Peter, Ketter Terence A, Marangell Lauren B, Miklowitz David J, Nierenberg Andrew A, Patel Jayendra, Sachs Gary S, Sklar Pamela, Smoller Jordan W, Laird Nan, Keshavan Matcheri, Thase Michael E, Axelson David, Birmaher Boris, Lewis David, Monk Tim, Frank Ellen, Kupfer David J, Devlin Bernie, Nimgaonkar Vishwajit |
| Family-based association of YWHAH in psychotic bipolar disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Oct 150B (7): 977-83. Grover Deepak, Verma Ranjana, Goes Fernando S, Mahon Pamela L Belmonte, Gershon Elliot S, McMahon Francis J, Potash James B, , Gershon Elliot S, McMahon Francis J, Potash James |
| Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genetic epidemiology 2010 Sep 34 (6): 613-23. Locke Adam E, Dooley Kenneth J, Tinker Stuart W, Cheong Soo Yeon, Feingold Eleanor, Allen Emily G, Freeman Sallie B, Torfs Claudine P, Cua Clifford L, Epstein Michael P, Wu Michael C, Lin Xihong, Capone George, Sherman Stephanie L, Bean Lora J |
| Common variants in cardiac ion channel genes are associated with sudden cardiac death. Circulation. Arrhythmia and electrophysiology 2010 Jun 3 (3): 222-9. Albert Christine M, MacRae Calum A, Chasman Daniel I, VanDenburgh Martin, Buring Julie E, Manson JoAnn E, Cook Nancy R, Newton-Cheh Christoph |
| Cannabinoid receptor 1 gene polymorphisms and marijuana misuse interactions on white matter and cognitive deficits in schizophrenia. Schizophrenia research 2011 May 128 (1-3): 66-75. Ho Beng-Choon, Wassink Thomas H, Ziebell Steven, Andreasen Nancy |
| Genetic variation in GREM1 is a risk factor for fibrosis in pulmonary sarcoidosis. Tissue antigens 2011 Feb 77 (2): 112-7. Heron M, van Moorsel C H M, Grutters J C, Huizinga T W J, van der Helm-van Mil A H M, Nagtegaal M M, Ruven H J T, van den Bosch J M |
| MAPK14 and CNR1 gene variant interactions: effects on brain volume deficits in schizophrenia patients with marijuana misuse. Psychological medicine 2013 Mar 43 (3): 619-31. Onwuameze O E, Nam K W, Epping E A, Wassink T H, Ziebell S, Andreasen N C, Ho B |
| Gender, body mass index, and PPAR? polymorphism are good indicators in hyperuricemia prediction for Han Chinese. Genetic testing and molecular biomarkers 2013 Jan 17 (1): 1. Lee MF, Liou TH, Wang W, Pan WH, Lee WJ, Hsu CT, Wu SF, Chen HH |
| Association of the iPLA2ß gene with bipolar disorder and assessment of its interaction with TRPM2 gene polymorphisms. Psychiatric genetics 2012 Dec . Xu C, Warsh JJ, Wang KS, Mao CX, Kennedy JL |
| Common genetic variants and risk of brain injury after preterm birth. Pediatrics 2014 Jun 133 (6): e1655-63. Boardman James P, Walley Andrew, Ball Gareth, Takousis Petros, Krishnan Michelle L, Hughes-Carre Laurelle, Aljabar Paul, Serag Ahmed, King Caroline, Merchant Nazakat, Srinivasan Latha, Froguel Philippe, Hajnal Jo, Rueckert Daniel, Counsell Serena, Edwards A Dav |
| Association of a single nucleotide polymorphism in HOXB9 with developmental dysplasia of the hip: a case-control study. Journal of orthopaedic research : official publication of the Orthopaedic Research Society 2014 Feb 32 (2): 179-82. Hao Zheng, Dai Jin, Shi Dongquan, Xu Zhihong, Chen Dongyang, Zhao Baocheng, Teng Huajian, Jiang Qi |
| Family-based association study of common variants, rare mutation study and epistatic interaction detection in HDAC genes in schizophrenia. Schizophrenia research 2014 Dec 160 (1-3): 97-103. Kebir Oussama, Chaumette Boris, Fatjó-Vilas Mar, Ambalavanan Amirthagowri, Ramoz Nicolas, Xiong Lan, Mouaffak Fayçal, Millet Bruno, Jaafari Nematollah, DeLisi Lynn E, Levinson Douglas, Joober Ridha, Fañanás Lourdes, Rouleau Guy, Dubertret Caroline, Krebs Marie-Odi |
| An integrated genomic-transcriptomic approach supports a role for the proto-oncogene BCL3 in atherosclerosis. Thrombosis and haemostasis 2015 Mar 113 (3): 655-63. Marchetti Giovanna, Girelli Domenico, Zerbinati Carlotta, Lunghi Barbara, Friso Simonetta, Meneghetti Silvia, Coen Matteo, Gagliano Teresa, Guastella Giuseppe, Bochaton-Piallat Marie-Luce, Pizzolo Francesca, Mascoli Francesco, Malerba Giovanni, Bovolenta Matteo, Ferracin Manuela, Olivieri Oliviero, Bernardi Francesco, Martinelli Nico |
| Variants in MTHFR gene and neural tube defects susceptibility in China. Metabolic brain disease 2015 Aug 30 (4): 1017-26. Wang Yongxin, Liu Yuan, Ji Wenyu, Qin Hu, Wu Hao, Xu Danshu, Turtuohut Tukebai, Wang Zenglia |
| The Nsun7 (A11337)-deletion mutation, causes reduction of its protein rate and associated with sperm motility defect in infertile men. Journal of assisted reproduction and genetics 2015 May 32 (5): 807-15. Khosronezhad Nahid, Hosseinzadeh Colagar Abasalt, Mortazavi Seyed Mohs |
| Association study between Van der Woude Syndrome causative gene GRHL3 and nonsyndromic cleft lip with or without cleft palate in a Chinese cohort. Gene 2016 Apr . Wang Yirui, Sun Yimin, Huang Yongqing, Pan Yongchu, Jia Zhonglin, Ma Lijuan, Ma Lan, Lan Feifei, Zhou Yuxi, Shi Jiayu, Yang Xiong, Zhang Lei, Jiang Hongbing, Jiang Min, Yin Aihua, Cheng Jing, Wang Lin, Yang Yinxue, Shi Bi |
| Polymorphisms and haplotypes of the CYP2B6 detoxification gene in the predisposition of Acute Myeloid Leukemia (AML) and induction of its cytogenetic abnormalities. Cancer genetics 2016 Nov 209 (11): 525-533. Daraki Aggeliki, Kakosaiou Katerina, Zachaki Sophia, Sambani Constantina, Aleporou-Marinou Vassiliki, Kollia Panagoula, Manola Kalliopi |
| Voltage-gated calcium channel activity and complex related genes and schizophrenia: A systematic investigation based on Han Chinese population. Journal of psychiatric research 2018 10 106 99-105. Zhang Tianxiao, Zhu Li, Ni Tong, Liu Dan, Chen Gang, Yan Zhilan, Lin Huali, Guan Fanglin, Rice John |
| ALDH1A1 Genetic Variations May Modulate Risk of Parkinson's Disease in Han Chinese Population. Frontiers in neuroscience 2021 4 15 620929. Fan Hui-Hui, Guo Qing, Zheng Jing, Lian Yi-Zhi, Huang Shi-Shi, Sun Yue, Zou Ming, Zhu Jian-Hong, Zhang Xio |
| The HIF1? polymorphism rs2301104 is associated with obesity and obesity-related cytokines in Han Chinese population. Acta diabetologica 2022 11 60 (2): 285-292. Zheng Xiaoya, Ma Jiani, Long Jian, Wei Qiang, Ren W |
| Contribution of TEX15 genetic variants to the risk of developing severe non-obstructive oligozoospermia. Frontiers in cell and developmental biology 2023 1 10 1089782. Guzmán-Jiménez Andrea, González-Muñoz Sara, Cerván-Martín Miriam, Rivera-Egea Rocío, Garrido Nicolás, Luján Saturnino, Santos-Ribeiro Samuel, Castilla José A, Gonzalvo M Carmen, Clavero Ana, Vicente F Javier, Maldonado Vicente, Villegas-Salmerón Javier, Burgos Miguel, Jiménez Rafael, Pinto Maria Graça, Pereira Isabel, Nunes Joaquim, Sánchez-Curbelo Josvany, López-Rodrigo Olga, Pereira-Caetano Iris, Marques Patricia Isabel, Carvalho Filipa, Barros Alberto, Bassas Lluís, Seixas Susana, Gonçalves João, Lopes Alexandra M, Larriba Sara, Palomino-Morales Rogelio J, Carmona F David, Bossini-Castillo Lara, , |
- Page last reviewed:Feb 1, 2023
- Page last updated:May 22, 2023
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