Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: KCNQ1OT1[original query] |
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A novel tetranucleotide repeat polymorphism within KCNQ1OT1 confers risk for hepatocellular carcinoma. DNA and cell biology 2013 Nov 32 (11): 628-34. Wan Jiao, Huang Moli, Zhao Hua, Wang Chaoqun, Zhao Xiankun, Jiang Xinghong, Bian Shizhong, He Yan, Gao Yuzh |
Determinants of maternal pregnancy one-carbon metabolism and newborn human DNA methylation profiles. Reproduction (Cambridge, England) 2014 Dec 148 (6): 581-92. van Mil Nina H, Bouwland-Both Marieke I, Stolk Lisette, Verbiest Michael M P J, Hofman Albert, Jaddoe Vincent W V, Verhulst Frank C, Eilers Paul H C, Uitterlinden Andre G, Steegers Eric A P, Tiemeier Henning, Steegers-Theunissen Régine P |
High-dose folic acid supplementation alters the human sperm methylome and is influenced by the MTHFR C677T polymorphism. Human molecular genetics 2015 Aug . Aarabi Mahmoud, San Gabriel Maria C, Chan Donovan, Behan Nathalie A, Caron Maxime, Pastinen Tomi, Bourque Guillaume, MacFarlane Amanda J, Zini Armand, Trasler Jacquet |
Phenotype, cancer risk, and surveillance in Beckwith-Wiedemann syndrome depending on molecular genetic subgroups. American journal of medical genetics. Part A 2016 Jul . Maas Saskia M, Vansenne Fleur, Kadouch Daniel J M, Ibrahim Abdulla, Bliek Jet, Hopman Saskia, Mannens Marcel M, Merks Johannes H M, Maher Eamonn R, Hennekam Raoul |
Genome-wide DNA methylation analysis of transient neonatal diabetes type 1 patients with mutations in ZFP57. BMC medical genetics 2016 17 (1): 29. Bak Mads, Boonen Susanne E, Dahl Christina, Hahnemann Johanne M D, Mackay Deborah J D G, Tümer Zeynep, Grønskov Karen, Temple I Karen, Guldberg Per, Tommerup Nie |
Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT. Epigenomics 2017 Jul . Coto Eliecer, Calvo David, Reguero Julián R, Morís César, Rubín Jose M, Díaz-Corte Carmen, Gil-Peña Helena, Alosno Belén, Iglesias Sara, Gómez Ju |
Endurance Exercise Ability in the Horse: A Trait with Complex Polygenic Determinism. Frontiers in genetics 2017 8 89. Ricard Anne, Robert Céline, Blouin Christine, Baste Fanny, Torquet Gwendoline, Morgenthaler Caroline, Rivière Julie, Mach Nuria, Mata Xavier, Schibler Laurent, Barrey Er |
Sequence variants identification at the KCNQ1OT1:TSS differentially Methylated region in isolated omphalocele cases. BMC medical genetics 2017 10 18 (1): 115. Bedeschi Maria Francesca, Calvello Mariarosaria, Paganini Leda, Pezzani Lidia, Baccarin Marco, Fontana Laura, Sirchia Silvia M, Guerneri Silvana, Canazza Lorena, Leva Ernesto, Colombo Lorenzo, Lalatta Faustina, Mosca Fabio, Tabano Silvia, Miozzo Moni |
Genetic variation affecting DNA methylation and the human imprinting disorder, Beckwith-Wiedemann syndrome. Clinical epigenetics 2018 Aug 10 (1): 114. Dagar Vinod, Hutchison Wendy, Muscat Andrea, Krishnan Anita, Hoke David, Buckle Ashley, Siswara Priscillia, Amor David J, Mann Jeffrey, Pinner Jason, Colley Alison, Wilson Meredith, Sachdev Rani, McGillivray George, Edwards Matthew, Kirk Edwin, Collins Felicity, Jones Kristi, Taylor Juliet, Hayes Ian, Thompson Elizabeth, Barnett Christopher, Haan Eric, Freckmann Mary-Louise, Turner Anne, White Susan, Kamien Ben, Ma Alan, Mackenzie Fiona, Baynam Gareth, Kiraly-Borri Cathy, Field Michael, Dudding-Byth Tracey, Algar Elizabeth |
RNA sequencing reveals PNN and KCNQ1OT1 as predictive biomarkers of clinical outcome in stage III colorectal cancer patients treated with adjuvant chemotherapy. International journal of cancer 2019 Apr . Mini Enrico, Lapucci Andrea, Perrone Gabriele, D'Aurizio Romina, Napoli Cristina, Brugia Marco, Landini Ida, Tassi Renato, Picariello Lucia, Simi Lisa, Mancini Irene, Messerini Luca, Magi Alberto, Pinzani Pamela, Mazzei Teresita, Tonelli Francesco, Nobili Stefan |
The Somatic Mutation Landscape and RNA Prognostic Markers in Stomach Adenocarcinoma. OncoTargets and therapy 2020 8 13 7735-7746. Zhang Xiulei, Zheng Peiming, Li Zhen, Gao Shanjun, Liu Guangz |
Contribution of gene mutations to Silver-Russell syndrome phenotype: multigene sequencing analysis in 92 etiology-unknown patients. Clinical epigenetics 2020 6 12 (1): 86. Inoue Takanobu, Nakamura Akie, Iwahashi-Odano Megumi, Tanase-Nakao Kanako, Matsubara Keiko, Nishioka Junko, Maruo Yoshihiro, Hasegawa Yukihiro, Suzumura Hiroshi, Sato Seiji, Kobayashi Yoshiyuki, Murakami Nobuyuki, Nakabayashi Kazuhiko, Yamazawa Kazuki, Fuke Tomoko, Narumi Satoshi, Oka Akira, Ogata Tsutomu, Fukami Maki, Kagami Masa |
Association study between KCNQ1 and KCNQ1OT1 genetic polymorphisms and gastric cancer susceptibility and survival in a Chinese Han population: a case-control study. Annals of translational medicine 2021 Jan 9 (2): 156. Yang Zhenyu, Yuan Lijuan, Yang Lin, Peng Shujia, Yang Ping, He Xianli, Bao Guoqia |
Clinical Spectrum and Tumour Risk Analysis in Patients with Beckwith-Wiedemann Syndrome Due to CDKN1C Pathogenic Variants. Cancers 2022 8 14 (15): . Cardoso Leila Cabral de Almeida, Parra Alejandro, Gil Cristina Ríos, Arias Pedro, Gallego Natalia, Romanelli Valeria, Kantaputra Piranit Nik, Lima Leonardo, Llerena Júnior Juan Clinton, Arberas Claudia, Guillén-Navarro Encarna, Nevado Julián, Spanish OverGrowth Registry Initiative , Tenorio-Castano Jair, Lapunzina Pab |
Germline variants in genes of the subcortical maternal complex and Multilocus Imprinting Disturbance are associated with miscarriage/infertility or Beckwith-Wiedemann progeny. Clinical epigenetics 2022 3 14 (1): 43. Tannorella Pierpaola, Calzari Luciano, Daolio Cecilia, Mainini Ester, Vimercati Alessandro, Gentilini Davide, Soli Fiorenza, Pedrolli Annalisa, Bonati Maria Teresa, Larizza Lidia, Russo Silv |
KCNQ1OT1 polymorphism rs35622507 and methylation status of KCNQ1OT1 promoter influence the drug resistance to L-OHP. Aging 2022 2 14 (4): 1836-1847. Zhang Caihong, Wang Yongl |
SNPs in lncRNA KCNQ1OT1 Modulate Its Expression and Confer Susceptibility to Salt Sensitivity of Blood Pressure in a Chinese Han Population. Nutrients 2022 10 14 (19): . Xie Yunyi, Qi Han, Peng Wenjuan, Li Bingxiao, Wen Fuyuan, Zhang Fengxu, Zhang Li |
Discovery of genomic and transcriptomic pleiotropy between kidney function and soluble receptor for advanced glycation end-products using correlated meta-analyses: The Long Life Family Study (LLFS). medRxiv : the preprint server for health sciences 2024 1 . Mary F Feitosa, Shiow J Lin, Sandeep Acharya, Bharat Thyagarajan, Mary K Wojczynski, Allison L Kuipers, Alexander Kulminski, Kaare Christensen, Joseph M Zmuda, Michael R Brent, Michael A Provin |
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- Page last updated:Mar 25, 2024
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