Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 35 Records) |
| Query Trace: Disease and RELN[original query] |
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| Genetic variants in the RELN gene are associated with otosclerosis in multiple European populations. Human genetics 2010 Feb 127 (2): 155-62. Schrauwen Isabelle, Ealy Megan, Fransen Erik, Vanderstraeten Kathleen, Thys Melissa, Meyer Nicole C, Cosgarea Marcel, Huber Alex, Mazzoli Manuela, Pfister Markus, Smith Richard J H, Van Camp G |
| Genetic variants in RELN are associated with otosclerosis in a non-European population from Tunisia. Annals of human genetics 2010 Sep 74 (5): 399-405. Khalfallah Ayda, Schrauwen Isabelle, Mnaja Malek, Fransen Erik, Lahmar Imed, Ealy Megan, Dhouib Leila, Ayadi Hammadi, Charfedine Ilhem, Driss Nabil, Ghorbel Abdelmonem, Smith Richard J H, Masmoudi Saber, Van Camp G |
Alzheimer disease pathology in cognitively healthy elderly: a genome-wide study.
Neurobiology of aging 2011 Dec 32 (12): 2113-22. Kramer Patricia L, Xu Haiyan, Woltjer Randall L, Westaway Shawn K, Clark David, Erten-Lyons Deniz, Kaye Jeffrey A, Welsh-Bohmer Kathleen A, Troncoso Juan C, Markesbery William R, Petersen Ronald C, Turner R Scott, Kukull Walter A, Bennett David A, Galasko Douglas, Morris John C, Ott Ju |
| Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study. Current Alzheimer research 2012 Sep 9 (7): 801-14. Swaminathan Shanker, Shen Li, Kim Sungeun, Inlow Mark, West John D, Faber Kelley M, Foroud Tatiana, Mayeux Richard, Saykin Andrew J, , |
| Impact of the Reelin signaling cascade (ligands-receptors-adaptor complex) on cognition in schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2012 Jun 159B (4): 392-404. Verbrugghe Phebe, Bouwer Sonja, Wiltshire Steven, Carter Kim, Chandler David, Cooper Matthew, Morar Bharti, Razif Muhammad F M, Henders Anjali, Badcock Johanna C, Dragovic Milan, Carr Vaughan, Almeida Osvaldo P, Flicker Leon, Montgomery Grant, Jablensky Assen, Kalaydjieva Lu |
| Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals. PloS one 2012 7 (12): e50640. Swaminathan Shanker, Huentelman Matthew J, Corneveaux Jason J, Myers Amanda J, Faber Kelley M, Foroud Tatiana, Mayeux Richard, Shen Li, Kim Sungeun, Turk Mari, Hardy John, Reiman Eric M, Saykin Andrew J, |
| Genetic association analysis in a clinically and histologically confirmed otosclerosis population confirms association with the TGFB1 gene but suggests an association of the RELN gene with a clinically indistinguishable otosclerosis-like phenotype. Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2014 Jul 35 (6): 1058-64. Sommen Manou, Van Camp Guy, Liktor Balázs, Csomor Péter, Fransen Erik, Sziklai István, Schrauwen Isabelle, Karosi Tam |
| Genetic analysis of the RELN gene: Gender specific association with Alzheimer's disease. Psychiatry research 2015 Sep . Fehér Ágnes, Juhász Anna, Pákáski Magdolna, Kálmán János, Janka Zolt |
| Association studies of genomic variants with treatment response to risperidone, clozapine, quetiapine and chlorpromazine in the Chinese Han population. The pharmacogenomics journal 2015 Aug . Xu Q, Wu X, Li M, Huang H, Minica C, Yi Z, Wang G, Shen L, Xing Q, Shi Y, He L, Qin |
| Identification of RELN variation p.Thr3192Ser in a Chinese family with schizophrenia. Scientific reports 2016 6 24327. Zhou Zhifan, Hu Zhengmao, Zhang Lu, Hu Zhaoting, Liu Haihong, Liu Zhening, Du Juan, Zhao Jingping, Zhou Lin, Xia Kun, Tang Bengsha, Shen |
| Contribution of Common Variants in GABRG2, RELN and NRG3 and Interaction Networks to the Risk of Hirschsprung Disease. Cellular physiology and biochemistry : international journal of experimental cellular physiology, biochemistry, and pharmacology 2016 40 (3-4): 509-526. Wang Yang, Wang Jun, Zhou Ying, Wei Zhiyun, Xiao Yongtao, Zhou Kejun, Wen Jie, Yan Junkai, Cai W |
| Meta-analyses of RELN variants in neuropsychiatric disorders. Behavioural brain research 2017 May . Chen Na, Bao Yanping, Xue Yanxue, Sun Yan, Hu Die, Meng Shiqiu, Lu Lin, Shi J |
| Evidence of distinct RELN and TGFB1 genetic associations in familial and non-familial otosclerosis in a British population. Human genetics 2018 May . Mowat Andrew J, Crompton Michael, Ziff Joanna L, Aldren Christopher P, Lavy Jeremy A, Saeed Shakeel R, Dawson Sally |
| Common genetic variants in GAL, GAP43 and NRSN1 and interaction networks confer susceptibility to Hirschsprung disease. Journal of cellular and molecular medicine 2018 Apr . Wang Yang, Yan Weihui, Wang Jun, Zhou Ying, Chen Jie, Gu Beilin, Cai W |
| A Genetic Study of Psychosis in Huntington's Disease: Evidence for the Involvement of Glutamate Signaling Pathways. Journal of Huntington's disease 2018 7 (1): 51-59. Tsuang Debby W, Greenwood Tiffany A, Jayadev Suman, Davis Marie, Shutes-David Andrew, Bird Thomas |
| Patterns of Mutation Enrichment in Metastatic Triple-Negative Breast Cancer. Clinical Medicine Insights. Oncology 2019 13 1179554919868482. Saravia César H, Flores Claudio, Schwarz Luis J, Bravo Leny, Zavaleta Jenny, Araujo Jhajaira, Neciosup Silvia, Pinto Joseph |
| Variants at potential loci associated with Sjogren's syndrome in Koreans: A genetic association study. Clinical immunology (Orlando, Fla.) 2019 7 207 79-86. Shen Qingxia, Lee Kwanghwan, Han Seong Kyu, Ahn Hyung-Joon, Kim Sanguk, Lee Jae Ho |
| Identification of exon skipping events associated with Alzheimer's disease in the human hippocampus. BMC medical genomics 2019 2 12 (Suppl 1): 13. Han Seonggyun, Miller Jason E, Byun Seyoun, Kim Dokyoon, Risacher Shannon L, Saykin Andrew J, Lee Younghee, Nho Kwangsik, |
| Reelin Signaling Controls the Preference for Social Novelty in Zebrafish. Frontiers in behavioral neuroscience 2019 13 214. Vecchia Elisa Dalla, Donato Vincenzo Di, Young Andrew M J, Bene Filippo Del, Norton William H |
| Genetic variants in RET, ARHGEF3 and CTNNAL1, and relevant interaction networks, contribute to the risk of Hirschsprung disease. Aging 2020 3 12 (5): 4379-4393. Wang Yang, Jiang Qian, Cai Hao, Xu Ze, Wu Wenjie, Gu Beilin, Li Long, Cai W |
| Acquired mutations and transcriptional remodeling in long-term estrogen-deprived locoregional breast cancer recurrences. Breast cancer research : BCR 2021 1 23 (1): 1. Priedigkeit Nolan, Ding Kai, Horne William, Kolls Jay K, Du Tian, Lucas Peter C, Blohmer Jens-Uwe, Denkert Carsten, Machleidt Anna, Ingold-Heppner Barbara, Oesterreich Steffi, Lee Adrian |
| Evaluation of candidate genes in a Chinese cohort of atypical Rolandic epilepsy. Epileptic disorders : international epilepsy journal with videotape 2021 Jul . Hu Xiaoyue, Tang Jihong, Hua Ying, Wang Yanping, Huang Ji |
| Whole genome analysis in APOE4 homozygotes identifies the DAB1-RELN pathway in Alzheimer's disease pathogenesis.
Neurobiology of aging 2022 8 119 67-76. Bracher-Smith Matthew, Leonenko Ganna, Baker Emily, Crawford Karen, Graham Andrew C, Salih Dervis A, Howell Brian W, Hardy John, Escott-Price Valenti |
| Targeted Resequencing of Otosclerosis Patients from Different Populations Replicates Results from a Previous Genome-Wide Association Study. Journal of clinical medicine 2022 12 11 (23): . Tavernier Lisse J M, Vanpoucke Thomas, Schrauwen Isabelle, Van Camp Guy, Fransen Er |
| Targeted Next-Generation Sequencing Identifies Additional Mutations Other than BCR?ABL in Chronic Myeloid Leukemia Patients: A Chinese Monocentric Retrospective Study. Cancers 2022 12 14 (23): . Hu Shiwei, Chen Dan, Xu Xiaofei, Zhang Lan, Wang Shengjie, Jin Keyi, Zheng Yan, Zhu Xiaoqiong, Jin Jie, Huang Ji |
| Reeling from news that reelin defends the brain against Alzheimer's. Cell reports. Medicine 2023 7 4 (7): 101111. Edmond N Mouofo, Tara L Spires-Jon |
| Characteristics of molecular genetic mutations and their correlation with prognosis in adolescent and adult patients with ALL. Oncology 2023 7 . Xue Sun, Xiaoqian Liu, Ying Li, Xue Shi, Yahan Li, Ran Tan, Yujie Jiang, Xiaohui Sui, Xueling Ge, Hongzhi Xu, Xin Wang, Xiaosheng Fa |
| Resilience to autosomal dominant Alzheimer's disease in a Reelin-COLBOS heterozygous man. Nature medicine 2023 5 29 (5): 1243-1252. Francisco Lopera, Claudia Marino, Anita S Chandrahas, Michael O'Hare, Nelson David Villalba-Moreno, David Aguillon, Ana Baena, Justin S Sanchez, Clara Vila-Castelar, Liliana Ramirez Gomez, Natalia Chmielewska, Gabriel M Oliveira, Jessica Lisa Littau, Kristin Hartmann, Kyungeun Park, Susanne Krasemann, Markus Glatzel, Dorothee Schoemaker, Lucia Gonzalez-Buendia, Santiago Delgado-Tirado, Said Arevalo-Alquichire, Kahira L Saez-Torres, Dhanesh Amarnani, Leo A Kim, Randall C Mazzarino, Harper Gordon, Yamile Bocanegra, Andres Villegas, Xiaowu Gai, Moiz Bootwalla, Jianling Ji, Lishuang Shen, Kenneth S Kosik, Yi Su, Yinghua Chen, Aaron Schultz, Reisa A Sperling, Keith Johnson, Eric M Reiman, Diego Sepulveda-Falla, Joseph F Arboleda-Velasquez, Yakeel T Quir |
| Bayesian mixed model analysis uncovered 21 risk loci for chronic kidney disease in boxer dogs. PLoS genetics 2023 1 19 (1): e1010599. Lingaas Frode, Tengvall Katarina, Jansen Johan Høgset, Pelander Lena, Hurst Maria H, Meuwissen Theo, Karlsson Åsa, Meadows Jennifer R S, Sundström Elisabeth, Thoresen Stein Istre, Arnet Ellen Frøysadal, Guttersrud Ole Albert, Kierczak Marcin, Hytönen Marjo K, Lohi Hannes, Hedhammar Åke, Lindblad-Toh Kerstin, Wang Ch |
| MYLK*FLNB and DOCK1*LAMA2 gene-gene interactions associated with rheumatoid arthritis in the focal adhesion pathway. Frontiers in genetics 2024 5 15 1375036. Maëva Veyssiere, Maria Del Pilar Rodriguez Ordonez, Smahane Chalabi, Laetitia Michou, François Cornelis, Anne Boland, Robert Olaso, Jean-François Deleuze, Elisabeth Petit-Teixeira, Valérie Chaud |
- Page last reviewed:Feb 1, 2024
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