HuGE Literature Finder
Records 1-13
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Demographic and genetic associations with markers of small and large fibre sensory neuropathy in HIV patients treated without stavudine.
Journal of acquired immune deficiency syndromes (1999) 2020 Sep . Yanuar Safri Ahmad, Gaff Jessica, Octaviana Fitri, Dewanto Setiawan Denise, Imran Darma, Cherry Catherine L, Laws Simon M, Price Patric |
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Polymorphisms in CAMKK2 associate with susceptibility to sensory neuropathy in HIV patients treated without stavudine.
Journal of neurovirology 2019 Jul . Gaff Jessica, Octaviana Fitri, Ariyanto Ibnu, Cherry Catherine, Laws Simon M, Price Patric |
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Polymorphisms in P2X4R and CAMKK2 may affect TNF? production: implications for a role in HIV-associated sensory neuropathy.
Human immunology 2018 Feb . Gaff Jessica, Halstrom Samuel, El Temple Suzanna, Baltic Svetlana, Kamerman Peter, Price Patric |
Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.
Nature communications 2018 01 9 (1): 321. Bonàs-Guarch Sílvia, Guindo-Martínez Marta, Miguel-Escalada Irene, Grarup Niels, Sebastian David, Rodriguez-Fos Elias, Sánchez Friman, Planas-Fèlix Mercè, Cortes-Sánchez Paula, González Santi, Timshel Pascal, Pers Tune H, Morgan Claire C, Moran Ignasi, Atla Goutham, González Juan R, Puiggros Montserrat, Martí Jonathan, Andersson Ehm A, Díaz Carlos, Badia Rosa M, Udler Miriam, Leong Aaron, Kaur Varindepal, Flannick Jason, Jørgensen Torben, Linneberg Allan, Jørgensen Marit E, Witte Daniel R, Christensen Cramer, Brandslund Ivan, Appel Emil V, Scott Robert A, Luan Jian'an, Langenberg Claudia, Wareham Nicholas J, Pedersen Oluf, Zorzano Antonio, Florez Jose C, Hansen Torben, Ferrer Jorge, Mercader Josep Maria, Torrents Dav |
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A haplotype spanning P2X7R, P2X4R and CAMKK2 may mark susceptibility to pulmonary non-tuberculous mycobacterial disease.
Immunogenetics 2017 Feb . Halstrom Samuel, Cherry Catherine L, Black Michael, Thomson Rachel, Goullee Hayley, Baltic Svetlana, Allcock Richard, Temple Suzanna E L, Price Patric |
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Genetic variants of increased waist circumference in psychosis.
Psychiatric genetics 2017 12 27 (6): 210-218. Hukic Dzana S, Ösby Urban, Olsson Eric, Hilding Agneta, Östenson Claes-Göran, Gu Harvest F, Ehrenborg Ewa, Edman Gunnar, Schalling Martin, Lavebratt Catharina, Frisén Loui |
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Utilizing the Dog Genome in the Search for Novel Candidate Genes Involved in Glioma Development-Genome Wide Association Mapping followed by Targeted Massive Parallel Sequencing Identifies a Strongly Associated Locus.
PLoS genetics 2016 May 12 (5): e1006000. Truvé Katarina, Dickinson Peter, Xiong Anqi, York Daniel, Jayashankar Kartika, Pielberg Gerli, Koltookian Michele, Murén Eva, Fuxelius Hans-Henrik, Weishaupt Holger, Swartling Fredrik J, Andersson Göran, Hedhammar Åke, Bongcam-Rudloff Erik, Forsberg-Nilsson Karin, Bannasch Danika, Lindblad-Toh Kerst |
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Effect of rs1063843 in the CAMKK2 gene on the dorsolateral prefrontal cortex.
Human brain mapping 2016 Mar . Yu Ping, Chen Xiongying, Zhao Wan, Zhang Zhifang, Zhang Qiumei, Han Bingqian, Zhai Jinguo, Chen Min, Du Boqi, Deng Xiaoxiang, Ji Feng, Wang Chuanyue, Xiang Yu-Tao, Li Dawei, Wu Hongjie, Li Jun, Dong Qi, Chen Chuanshe |
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Polymorphisms in CAMKK2 may predict sensory neuropathy in African HIV patients.
Journal of neurovirology 2016 Jan . Goullee Hayley, Wadley Antonia L, Cherry Catherine L, Allcock Richard J N, Black Michael, Kamerman Peter R, Price Patric |
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A genetic variant in CAMKK2 gene is possibly associated with increased risk of bipolar disorder.
Journal of neural transmission (Vienna, Austria : 1996) 2015 Sep . Atakhorrami Minoo, Rahimi-Aliabadi Simin, Jamshidi Javad, Moslemi Elham, Movafagh Abolfazl, Ohadi Mina, Mirabzadeh Arash, Emamalizadeh Babak, Ghaedi Hamid, Gholipour Fatemeh, Fazeli Atena, Motallebi Marzieh, Taghavi Shaghayegh, Ahmadifard Azadeh, Mohammadihosseinabad Saeed, Shafiei Zarneh Amir Ehtesham, Shahmohammadibeni Neda, Madadi Faranak, Andarva Monavvar, Darvish Hosse |
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Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene.
Molecular psychiatry 2014 Jul 19 (7): 774-83. Luo X-J, Li M, Huang L, Steinberg S, Mattheisen M, Liang G, Donohoe G, Shi Y, Chen C, Yue W, Alkelai A, Lerer B, Li Z, Yi Q, Rietschel M, Cichon S, Collier D A, Tosato S, Suvisaari J, Rujescu Dan, Golimbet V, Silagadze T, Durmishi N, Milovancevic M P, Stefansson H, Schulze T G, Nöthen M M, Chen C, Lyne R, Morris D W, Gill M, Corvin A, Zhang D, Dong Q, Moyzis R K, Stefansson K, Sigurdsson E, Hu F, , Su B, Gan |
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A common missense variant in the ATP receptor P2X7 is associated with reduced risk of cardiovascular events.
PloS one 2012 7 (5): e37491. Gidlöf Olof, Smith J Gustav, Melander Olle, Lövkvist Håkan, Hedblad Bo, Engström Gunnar, Nilsson Peter, Carlson Joyce, Berglund Göran, Olsson Sandra, Jood Katarina, Jern Christina, Norrving Bo, Lindgren Arne, Erlinge Dav |
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Analysis of single nucleotide polymorphisms in genes in the chromosome 12Q24.31 region points to P2RX7 as a susceptibility gene to bipolar affective disorder.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2006 Jun 141B (4): 374-82. Barden Nicholas, Harvey Mario, Gagné Bernard, Shink Eric, Tremblay Monique, Raymond Catherine, Labbé Michel, Villeneuve André, Rochette Denis, Bordeleau Lise, Stadler Herbert, Holsboer Florian, Müller-Myhsok Bertr |
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- Page last updated:Apr 15, 2021
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