Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 63 Records) |
Query Trace: HMGA2[original query] |
---|
Single nucleotide polymorphisms in microRNA genes are associated with cervical cancer susceptibility in a population from Xinjiang Uygur. Oncotarget 2016 Sep . Yang Jie, Zhang Zegao, Guo Wen, Ma Yuhua, Muhammed Emin Raila, Abudubari Karima, Hayrat Glmira, Wali Hasiyet, Qi Xiaoli, Liu Chunhua, Ma Miaomiao, Nurbek Pul |
Epithelial-Myoepithelial Carcinoma: Frequent Morphologic and Molecular Evidence of Preexisting Pleomorphic Adenoma, Common HRAS Mutations in PLAG1-intact and HMGA2-intact Cases, and Occasional TP53, FBXW7, and SMARCB1 Alterations in High-grade Cases. The American journal of surgical pathology 2017 Nov . El Hallani Soufiane, Udager Aaron M, Bell Diana, Fonseca Isabel, Thompson Lester D R, Assaad Adel, Agaimy Abbas, Luvison Alyssa M, Miller Caitlyn, Seethala Raja R, Chiosea Simi |
Variant Alleles of the ESR1, PPARG, HMGA2, and MTHFR Genes Are Associated With Polycystic Ovary Syndrome Risk in a Chinese Population: A Case-Control Study. Frontiers in endocrinology 2018 9 504. Jiao Xianting, Chen Weiwei, Zhang Jun, Wang Weiye, Song Junjiao, Chen Dan, Zhu Wenting, Shi Yuhua, Yu Xiaod |
Admixture mapping and fine-mapping of birth weight loci in the Black Women's Health Study. Human genetics 2018 Jul . Ochs-Balcom Heather M, Shaw Holly, Preus Leah, Palmer Julie R, Haddad Stephen A, Rosenberg Lynn, Ruiz-Narváez Edward |
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 |
Genome-wide association study of offspring birth weight in 86?577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics.
Human molecular genetics 2018 Feb 27 (4): 742-756. Beaumont Robin N, Warrington Nicole M, Cavadino Alana, Tyrrell Jessica, Nodzenski Michael, Horikoshi Momoko, Geller Frank, Myhre Ronny, Richmond Rebecca C, Paternoster Lavinia, Bradfield Jonathan P, Kreiner-Møller Eskil, Huikari Ville, Metrustry Sarah, Lunetta Kathryn L, Painter Jodie N, Hottenga Jouke-Jan, Allard Catherine, Barton Sheila J, Espinosa Ana, Marsh Julie A, Potter Catherine, Zhang Ge, Ang Wei, Berry Diane J, Bouchard Luigi, Das Shikta, , Hakonarson Hakon, Heikkinen Jani, Helgeland Øyvind, Hocher Berthold, Hofman Albert, Inskip Hazel M, Jones Samuel E, Kogevinas Manolis, Lind Penelope A, Marullo Letizia, Medland Sarah E, Murray Anna, Murray Jeffrey C, Njølstad Pål R, Nohr Ellen A, Reichetzeder Christoph, Ring Susan M, Ruth Katherine S, Santa-Marina Loreto, Scholtens Denise M, Sebert Sylvain, Sengpiel Verena, Tuke Marcus A, Vaudel Marc, Weedon Michael N, Willemsen Gonneke, Wood Andrew R, Yaghootkar Hanieh, Muglia Louis J, Bartels Meike, Relton Caroline L, Pennell Craig E, Chatzi Leda, Estivill Xavier, Holloway John W, Boomsma Dorret I, Montgomery Grant W, Murabito Joanne M, Spector Tim D, Power Christine, Järvelin Marjo-Ritta, Bisgaard Hans, Grant Struan F A, Sørensen Thorkild I A, Jaddoe Vincent W, Jacobsson Bo, Melbye Mads, McCarthy Mark I, Hattersley Andrew T, Hayes M Geoffrey, Frayling Timothy M, Hivert Marie-France, Felix Janine F, Hyppönen Elina, Lowe William L, Evans David M, Lawlor Debbie A, Feenstra Bjarke, Freathy Rachel |
MED12 mutations and fumarate hydratase inactivation in uterine adenomyomas. Human reproduction open 2018 2018 (4): hoy020. Heikkinen Tuomas, Äyräväinen Anna, Hänninen Janne, Ahvenainen Terhi, Bützow Ralf, Pasanen Annukka, Vahteristo P |
HMGA2 gene polymorphisms and Wilms tumor susceptibility in Chinese children: a four-center case-control study. Biotechnology and applied biochemistry 2019 Nov . Cheng Jiwen, Zhuo Zhenjian, Yang Liu, Zhao Pu, Zhang Jiao, Zhou Haixia, He Jing, Li Pe |
SNPs of miR-23b, miR-107 and HMGA2 and their Relations with the Response to Medical Treatment in Acromegaly Patients. Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association 2020 Aug . Armagan Derya Metin, Akdemir Ayse Seda, Ozkaya Hande Mefkure, Korkmaz Ozge Polat, Gazioglu Nurperi, Kadioglu Pinar, Tanriover Necmettin, Dagistanli Kaya-Fatma, Dirican Ahmet, Ozturk Mel |
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 |
HMGA2 Gene rs8756 A>C Polymorphism Reduces Neuroblastoma Risk in Chinese Children: A Four-Center Case-Control Study. OncoTargets and therapy 2020 13 465-472. Liu Jiabin, Hua Rui-Xi, Cheng Yun, Zhu Jinhong, Zhang Jiao, Cheng Jiwen, Zhou Haixia, Xia Huimin, Bian Jun, He Ji |
Identification of potential genomic regions for egg weight by a haplotype-based genome-wide association study using Bayesian methods. British poultry science 2020 Feb . Khaltabadi Farahani A H, Mohammadi H, Moradi M H, Ghasemi H |
HMGA2 Polymorphisms and Hepatoblastoma Susceptibility: A Five-Center Case-Control Study. Pharmacogenomics and personalized medicine 2020 13 51-57. Li Li, Zhuo Zhenjian, Yang Zhen, Zhu Jinhong, He Xiaoli, Yang Zhonghua, Zhang Jiao, Xin Yijuan, He Jing, Zhang Tieso |
A Comprehensive Overview of Common Polymorphic Variants in Genes Related to Polycystic Ovary Syndrome. Reproductive sciences (Thousand Oaks, Calif.) 2020 Nov . Castillo-Higuera Tatiana, Alarcón-Granados María Camila, Marin-Suarez Johana, Moreno-Ortiz Harold, Esteban-Pérez Clara Inés, Ferrebuz-Cardozo Atilio Junior, Forero-Castro Maribel, Camargo-Vill Alba Glor |
The genetic map of diabetic nephropathy: evidence from a systematic review and meta-analysis of genetic association studies. Clinical kidney journal 2020 10 13 (5): 768-781. Tziastoudi Maria, Stefanidis Ioannis, Zintzaras Eli |
Genotype based Risk Predictors for Polycystic Ovary Syndrome in Western Saudi Arabia. Bioinformation 2019 15 (11): 812-819. Bakhashab Sherin, Ahmed Na |
Intravenous leiomyomatosis: molecular analysis of 17 cases. Pathology 2019 Dec . Lu Bingjian, Liu Qin, Tang Lanlan, Ma Yu, Shi Haiy |
HMGA2-WIF1 Rearrangements Characterize a Distinctive Subset of Salivary Pleomorphic Adenomas With Prominent Trabecular (Canalicular Adenoma-like) Morphology. The American journal of surgical pathology 2021 7 46 (2): 190-199. Agaimy Abbas, Ihrler Stephan, Ban??ková Martina, Costés Martineau Valérie, Mantsopoulos Konstantinos, Hartmann Arndt, Iro Heinrich, Stoehr Robert, Skálová Ale |
HMGA2 rs968697 T?>?C polymorphism is associated with the risk of colorectal cancer. Nucleosides, nucleotides & nucleic acids 2021 7 40 (8): 821-828. Gao Xueren, Wang Xiaoti |
Comprehensive Identification of Pathogenic Gene Variants in Patients With Neuroendocrine Disorders. The Journal of clinical endocrinology and metabolism 2021 Mar . Vishnopolska Sebastian Alexis, Mercogliano Maria Florencia, Camilletti Maria Andrea, Mortensen Amanda Helen, Braslavsky Debora, Keselman Ana, Bergadá Ignacio, Olivieri Federico, Miranda Lucas, Marino Roxana, Ramírez Pablo, Pérez Garrido Natalia, Patiño Mejia Helen, Ciaccio Marta, Di Palma Maria Isabel, Belgorosky Alicia, Martí Marcelo Adrian, Kitzman Jacob Otto, Camper Sally Ann, Pérez-Millán Maria In |
One test for all: whole exome sequencing significantly improves the diagnostic yield in growth retarded patients referred for molecular testing for Silver-Russell syndrome. Orphanet journal of rare diseases 2021 1 16 (1): 42. Meyer Robert, Begemann Matthias, Hübner Christian Thomas, Dey Daniela, Kuechler Alma, Elgizouli Magdeldin, Schara Ulrike, Ambrozaityte Laima, Burnyte Birute, Schröder Carmen, Kenawy Asmaa, Kroisel Peter, Demuth Stephanie, Fekete Gyorgy, Opladen Thomas, Elbracht Miriam, Eggermann Thom |
Population history and genome wide association studies of birth weight in a native high altitude Ladakhi population. PloS one 2022 9 17 (9): e0269671. Bhandari Sushil, Dolma Padma, Mukerji Mitali, Prasher Bhavana, Montgomery Hugh, Kular Dalvir, Jain Vandana, Dadhwal Vatsla, Williams David J, Bhattacharyaa Aniket, Gilbert Edmund, Cavalleri Gianpiero L, Hillman Sara |
Molecular Landscape and Prognostic Biomarker Analysis of Advanced Pancreatic Cancer and Predictors of Treatment Efficacy of AG Chemotherapy. Frontiers in oncology 2022 12 844527. Du Juan, Qiu Xin, Lu Changchang, Zhu Yahui, Kong Weiwei, Xu Mian, Zhang Xin, Tang Min, Chen Jun, Li Qi, Li Aimei, He Jian, Gu Qing, Wang Lei, Qiu Yudong, Liu Baor |
Large scale across-breed genome-wide association study reveals a variant in HMGA2 associated with inguinal cryptorchidism risk in dogs. PloS one 2022 5 17 (5): e0267604. Blades Matthew, Freyer Jamie, Donner Jonas, Chodroff Foran Rebecca, Forman Oliver |
Shared genetic architectures of subjective well-being in East Asian and European ancestry populations.
Nature human behaviour 2022 May . Kim Soyeon, Kim Kiwon, Hwang Mi Yeong, Ko Hyunwoong, Jung Sang-Hyuk, Shim Injeong, Cha Soojin, Lee Hyewon, Kim Beomsu, Yoon Joohyun, Ha Tae Hyon, Kim Doh Kwan, Kim Jinho, Park Woong-Yang, Okbay Aysu, Kim Bong-Jo, Kim Young Jin, Myung Woojae, Won Hong-H |
Evaluation of an HMGA2 variant contribution to height and basal insulin concentrations in ponies. Journal of veterinary internal medicine 2023 5 . Brianna L Clark, Nicholas J Bamford, Allison J Stewart, Molly E McCue, Aaron Rendahl, Simon R Bailey, François-René Bertin, Elaine M Nort |
Prevalence and clinical significance of co-existing mutations in MED12 and FH in uterine fibroids of Australian women. Frontiers in reproductive health 2023 4 5 1081092. M Fairuz B Jamaluddin, Prathima B Nagendra, Yi-An Ko, Preety Bajwa, Rodney J Scott, Pravin Nahar, Pradeep S Tanw |
Inherited mutations affecting the SRCAP complex are central in moderate-penetrance predisposition to uterine leiomyomas. American journal of human genetics 2023 2 110 (3): 460-474. Välimäki Niko, Jokinen Vilja, Cajuso Tatiana, Kuisma Heli, Taira Aurora, Dagnaud Olivia, Ilves Sini, Kaukomaa Jaana, Pasanen Annukka, Palin Kimmo, Heikinheimo Oskari, Bützow Ralf, Aaltonen Lauri A, Karhu Au |
Genetic Variants of Steroidogenesis and Gonadotropin Pathways and Polycystic Ovary Syndrome Susceptibility: A Systematic Review and Meta-analysis. Metabolic syndrome and related disorders 2023 10 . Priya Sharma, Abhilash Kumar Singh, Sabyasachi Senapati, Harmanpreet Singh Kapoor, Lajya Devi Goyal, Balpreet Kaur, Pooja Kamra, Preeti Khetarp |
Bioinformatics analysis and experimental validation identified HMGA2/microRNA-200c-3p/LSAMP/Wnt axis as an immunological factor of patients with colorectal cancer. American journal of cancer research 2023 10 13 (9): 3898-3920. Xi Xu, Chaoju Gong, Yunfeng Wang, Zhidong Yin, Xiaogang Wang, Yanyan Hu, Zejun Fa |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: