Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: CDKN1C[original query] |
---|
An association between variants in the IGF2 gene and Beckwith-Wiedemann syndrome: interaction between genotype and epigenotype. Human molecular genetics 2004 Jan 13 (2): 247-55. Murrell Adele, Heeson Sarah, Cooper Wendy N, Douglas Eleanor, Apostolidou Sophia, Moore Gudrun E, Maher Eamonn R, Reik Wo |
Studies of variations of the cyclin-dependent kinase inhibitor 1C and the cyclin-dependent kinase 4 genes in relation to type 2 diabetes mellitus and related quantitative traits. Journal of molecular medicine (Berlin, Germany) 2005 May 83 (5): 353-61. Nielsen Eva-Maria D, Hansen Lars, Stissing Trine, Yanagisawa Keiko, Borch-Johnsen Knut, Poulsen Pernille, Vaag Allan, Hansen Torben, Pedersen Ol |
Role of the CDKN1A/p21, CDKN1C/p57, and CDKN2A/p16 genes in the risk of atherosclerosis and myocardial infarction. Cell cycle (Georgetown, Tex.) 2007 Mar 6 (5): 620-5. Rodríguez Isabel, Coto Eliecer, Reguero Julián R, González Pelayo, Andrés Vicente, Lozano Iñigo, Martín María, Alvarez Victoria, Morís Cés |
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 |
Germline and somatic mutations in cyclin-dependent kinase inhibitor genes CDKN1A, CDKN2B, and CDKN2C in sporadic parathyroid adenomas. Hormones & cancer 2013 Oct 4 (5): 301-7. Costa-Guda Jessica, Soong Chen-Pang, Parekh Vaishali I, Agarwal Sunita K, Arnold Andr |
Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance. Hormone research in pædiatrics 2013 80 (6): 457-65. Brioude F, Lacoste A, Netchine I, Vazquez M-P, Auber F, Audry G, Gauthier-Villars M, Brugieres L, Gicquel C, Le Bouc Y, Rossignol |
Genetic association of gastric cancer with miRNA clusters including the cancer-related genes MIR29, MIR25, MIR93 and MIR106: results from the EPIC-EURGAST study. International journal of cancer. Journal international du cancer 2014 Nov 135 (9): 2065-76. Espinosa-Parrilla Yolanda, Muñoz Xavier, Bonet Catalina, Garcia Nadia, Venceslá Adoración, Yiannakouris Nikos, Naccarati Alessio, Sieri Sabina, Panico Salvatore, Huerta José M, Barricarte Aurelio, Menéndez Virginia, Sánchez-Cantalejo Emilio, Dorronsoro Miren, Brennan Paul, Duarte-Salles Talita, B As Bueno-de-Mesquita H, Weiderpass Elisabete, Lund Eiliv, Clavel-Chapelon Françoise, Boutron-Ruault Marie-Christine, Racine Antoine, Numans Mattijs E, Tumino Rosario, Canzian Federico, Campa Daniele, Sund Malin, Johansson Mattias, Ohlsson Bodil, Lindkvist Björn, Overvad Kim, Tjønneland Anne, Palli Domenico, Travis Ruth C, Khaw Kay-Tee, Wareham Nick, Boeing Heiner, Nesi Gabriella, Riboli Elio, Gonzalez Carlos A, Sala Núr |
Association of breast cancer risk loci with breast cancer survival. International journal of cancer 2015 Jan . Barrdahl Myrto, Canzian Federico, Lindström Sara, Shui Irene, Black Amanda, Hoover Robert N, Ziegler Regina G, Buring Julie E, Chanock Stephen J, Diver W Ryan, Gapstur Susan M, Gaudet Mia M, Giles Graham G, Haiman Christopher, Henderson Brian E, Hankinson Susan, Hunter David J, Joshi Amit D, Kraft Peter, Lee I-Min, Le Marchand Loic, Milne Roger L, Southey Melissa C, Willett Walter, Gunter Marc, Panico Salvatore, Sund Malin, Weiderpass Elisabete, Sánchez María-José, Overvad Kim, Dossus Laure, Peeters Petra H, Khaw Kay-Tee, Trichopoulos Dimitrios, Kaaks Rudolf, Campa Danie |
Cancer Risk in Beckwith-Wiedemann Syndrome: A Systematic Review and Meta-Analysis Outlining a Novel (Epi)Genotype Specific Histotype Targeted Screening Protocol. The Journal of pediatrics 2016 Jun . Mussa Alessandro, Molinatto Cristina, Baldassarre Giuseppina, Riberi Evelise, Russo Silvia, Larizza Lidia, Riccio Andrea, Ferrero Giovanni Battis |
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 |
Primary hyperparathyroidism in young patients in Russia: high frequency of hyperparathyroidism-jaw tumor syndrome. Endocrine connections 2017 9 6 (8): 557-565. Mamedova Elizaveta, Mokrysheva Natalya, Vasilyev Evgeny, Petrov Vasily, Pigarova Ekaterina, Kuznetsov Sergey, Kuznetsov Nikolay, Rozhinskaya Liudmila, Melnichenko Galina, Dedov Ivan, Tiulpakov Anato |
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 Disorders in Prenatal Onset Syndromic Short Stature Identified by Exome Sequencing. The Journal of pediatrics 2019 10 215 192-198. Homma Thais Kataoka, Freire Bruna Lucheze, Honjo Kawahira Rachel Sayuri, Dauber Andrew, Funari Mariana Ferreira de Assis, Lerario Antônio Marcondes, Nishi Mirian Yumie, Albuquerque Edoarda Vasco de, Vasques Gabriela de Andrade, Collett-Solberg Paulo Ferrez, Miura Sugayama Sofia Mizuho, Bertola Debora Romeo, Kim Chong Ae, Arnhold Ivo Jorge Prado, Malaquias Alexsandra Christianne, Jorge Alexander Augusto de Li |
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 |
Integrated analysis of cell cycle-related genes in HR+/HER2- breast cancer. Breast cancer (Tokyo, Japan) 2021 8 29 (1): 121-130. Lai Jianguo, Chen Bo, Li Yingzi, Lin Xiaoyi, Li Min, Liu Jing, Liao Ni |
Pathogenic Germline Variants in Cancer Susceptibility Genes in Children and Young Adults With Rhabdomyosarcoma. JCO precision oncology 2021 5 . Kim Jung, Light Nicholas, Subasri Vallijah, Young Erin L, Wegman-Ostrosky Talia, Barkauskas Donald A, Hall David, Lupo Philip J, Patidar Rajesh, Maese Luke D, Jones Kristine, Wang Mingyi, Tavtigian Sean V, Wu Dongjing, Shlien Adam, Telfer Frank, Goldenberg Anna, Skapek Stephen X, Wei Jun S, Wen Xinyu, Catchpoole Daniel, Hawkins Douglas S, Schiffman Joshua D, Khan Javed, Malkin David, Stewart Douglas |
Genetic variants of cell cycle pathway genes are associated with head and neck squamous cell carcinoma in the Chinese population. Carcinogenesis 2021 Oct . Chen Mo, Xu Wen-Mao, Wang Gui-Yang, Hou Ya-Xuan, Tian Ting-Ting, Li Yu-Qing, Qi Hong-Jiao, Zhou Meng, Kong Wei-Jia, Lu Mei-X |
Genomic Profiling Identified Prognostic Biomarkers of Definitive Chemo-Radiotherapy Response in Esophageal Carcinoma. International journal of radiation oncology, biology, physics 2021 Nov 111 (3S): S13. Li L, Yuan S, Sun J, Yin Y, Cui J, Zhang J, Chen Y, Pang J, Yin J, Shao Y, Yu |
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 |
Deciphering Epigenetic Backgrounds in a Korean Cohort with Beckwith-Wiedemann Syndrome. Annals of laboratory medicine 2022 Nov 42 (6): 668-677. Kim Hwa Young, Shin Choong Ho, Lee Young Ah, Shin Chang Ho, Kim Gu-Hwan, Ko Jung M |
Multigene testing panels reveal pathogenic variants in sporadic breast cancer patients in northern China. Frontiers in genetics 2023 11 14 1271710. Yinfeng Liu, Jie Zheng, Yue Xu, Ji Lv, Zizheng Wu, Kai Feng, Jiani Liu, Weitao Yan, Liguang Wei, Jiangman Zhao, Lisha Jiang, Meng H |
- Page last reviewed:Feb 1, 2024
- Page last updated:Jun 03, 2024
- Content source: