Human Genome Epidemiology Literature Finder
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Records 1 - 12 (of 12 Records) |
| Query Trace: Disease and LMX1B[original query] |
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| The transcription factor PITX3 is associated with sporadic Parkinson's disease. Neurobiology of aging 2009 May 30 (5): 731-8. Fuchs Julia, Mueller Jakob C, Lichtner Peter, Schulte Claudia, Munz Marita, Berg Daniela, Wüllner Ullrich, Illig Thomas, Sharma Manu, Gasser Thom |
| Genetic risk for primary open-angle glaucoma determined by LMX1B haplotypes. Investigative ophthalmology & visual science 2009 Apr 50 (4): 1522-30. Park Soo, Jamshidi Yalda, Vaideanu Daniela, Bitner-Glindzicz Maria, Fraser Scott, Sowden Jane |
| Do polymorphisms in transcription factors LMX1A and LMX1B influence the risk for Parkinson's disease? Journal of neural transmission (Vienna, Austria : 1996) 2009 Mar 116 (3): 333-8. Bergman Olle, Håkansson Anna, Westberg Lars, Belin Andrea Carmine, Sydow Olof, Olson Lars, Holmberg Björn, Fratiglioni Laura, Bäckman Lars, Eriksson Elias, Nissbrandt Ha |
| Preliminary evidence that polymorphisms in dopamine-related transcription factors LMX1A, LMX1B and PITX3 are associated with schizophrenia. Progress in neuro-psychopharmacology & biological psychiatry 2010 Aug 34 (6): 1094-7. Bergman Olle, Westberg Lars, Nilsson Lars-Göran, Adolfsson Rolf, Eriksson Eli |
| SNP rs1533428 at 2p16.3 as a marker for late-onset primary open-angle glaucoma. Molecular vision 2012 18 1629-39. Chen Li Jia, Tam Pancy O S, Leung Dexter Y L, Fan Alex H, Zhang Mingzhi, Tham Clement C Y, Chiang Sylvia W Y, Fan Bao Jian, Wang Ningli, Pang Chi P |
Genome-wide association study identifies seven novel susceptibility loci for primary open-angle glaucoma.
Human molecular genetics 2018 Feb . Shiga Yukihiro, Akiyama Masato, Nishiguchi Koji M, Sato Kota, Shimozawa Nobuhiro, Takahashi Atsushi, Momozawa Yukihide, Hirata Makoto, Matsuda Koichi, Yamaji Taiki, Iwasaki Motoki, Tsugane Shoichiro, Oze Isao, Mikami Haruo, Naito Mariko, Wakai Kenji, Yoshikawa Munemitsu, Miyake Masahiro, Yamashiro Kenji, , Kashiwagi Kenji, Iwata Takeshi, Mabuchi Fumihiko, Takamoto Mitsuko, Ozaki Mineo, Kawase Kazuhide, Aihara Makoto, Araie Makoto, Yamamoto Tetsuya, Kiuchi Yoshiaki, Nakamura Makoto, Ikeda Yasuhiro, Sonoda Koh-Hei, Ishibashi Tatsuro, Nitta Koji, Iwase Aiko, Shirato Shiroaki, Oka Yoshitaka, Satoh Mamoru, Sasaki Makoto, Fuse Nobuo, Suzuki Yoichi, Cheng Ching-Yu, Khor Chiea Chuen, Baskaran Mani, Perera Shamira, Aung Tin, Vithana Eranga N, Cooke Bailey Jessica N, Kang Jae H, Pasquale Louis R, Haines Jonathan L, , Wiggs Janey L, Burdon Kathryn P, Gharahkhani Puya, Hewitt Alex W, Mackey David A, MacGregor Stuart, Craig Jamie E, Allingham R Rand, Hauser Micheal, Ashaye Adeyinka, Budenz Donald L, Akafo Stephan, Williams Susan E I, Kamatani Yoichiro, Nakazawa Toru, Kubo Michia |
| A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome. Annals of clinical and laboratory science 2019 7 49 (3): 330-337. Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw |
| An Exome Sequencing Study of 10 Families with IgA Nephropathy. Nephron 2019 Dec 1-12. Stapleton Caragh P, Kennedy Claire, Fennelly Neil K, Murray Susan L, Connaughton Dervla M, Dorman Anthony M, Doyle Brendan, Cavalleri Gianpiero L, Conlon Peter |
| Mutational landscape of TRPC6, WT1, LMX1B, APOL1, PTPRO, PMM2, LAMB2 and WT1 genes associated with Steroid resistant nephrotic syndrome. Molecular biology reports 2021 Sep . Thakor Jinal M, Parmar Glory, Mistry Kinnari N, Gang Sishir, Rank Dharamshibhai N, Joshi Chaitanya |
| Association analysis of variants rs35934224 in TXNRD2 and rs6478746 in LMX1B in primary angle-closure and pseudoexfoliation glaucoma. European journal of ophthalmology 2021 8 32 (4): 2249-2258. Kondkar Altaf A, Sultan Tahira, Alobaidan Abdullah S, Azad Taif A, Osman Essam A, Almobarak Faisal A, Lobo Glenn P, Al-Obeidan Saleh |
| Genetic Variations and Health-Related Quality of Life (HRQOL): A Genome-Wide Study Approach.
Cancers 2021 Feb 13 (4): . Adjei Araba A, Lopez Camden L, Schaid Daniel J, Sloan Jeff A, Le-Rademacher Jennifer G, Loprinzi Charles L, Norman Aaron D, Olson Janet E, Couch Fergus J, Beutler Andreas S, Vachon Celine M, Ruddy Kathryn |
| Exome sequencing of 1190 non-syndromic clubfoot cases reveals HOXD12 as a novel disease gene. Journal of medical genetics 2024 4 . Wu-Lin Charng, Momchil Nikolov, Isabel Shrestha, Mark A Seeley, Navya Shilpa Josyula, Anne E Justice, Matthew B Dobbs, Christina A Gurne |
- Page last reviewed:Feb 1, 2024
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