Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and HMGA2[original query] |
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Identification of common variants associated with human hippocampal and intracranial volumes.
Nature genetics 2012 May 44 (5): 552-61. Stein Jason L, Medland Sarah E, Vasquez Alejandro Arias, Hibar Derrek P, Senstad Rudy E, Winkler Anderson M, Toro Roberto, Appel Katja, Bartecek Richard, Bergmann Ørjan, Bernard Manon, Brown Andrew A, Cannon Dara M, Chakravarty M Mallar, Christoforou Andrea, Domin Martin, Grimm Oliver, Hollinshead Marisa, Holmes Avram J, Homuth Georg, Hottenga Jouke-Jan, Langan Camilla, Lopez Lorna M, Hansell Narelle K, Hwang Kristy S, Kim Sungeun, Laje Gonzalo, Lee Phil H, Liu Xinmin, Loth Eva, Lourdusamy Anbarasu, Mattingsdal Morten, Mohnke Sebastian, Maniega Susana Muñoz, Nho Kwangsik, Nugent Allison C, O'Brien Carol, Papmeyer Martina, Pütz Benno, Ramasamy Adaikalavan, Rasmussen Jerod, Rijpkema Mark, Risacher Shannon L, Roddey J Cooper, Rose Emma J, Ryten Mina, Shen Li, Sprooten Emma, Strengman Eric, Teumer Alexander, Trabzuni Daniah, Turner Jessica, van Eijk Kristel, van Erp Theo G M, van Tol Marie-Jose, Wittfeld Katharina, Wolf Christiane, Woudstra Saskia, Aleman Andre, Alhusaini Saud, Almasy Laura, Binder Elisabeth B, Brohawn David G, Cantor Rita M, Carless Melanie A, Corvin Aiden, Czisch Michael, Curran Joanne E, Davies Gail, de Almeida Marcio A A, Delanty Norman, Depondt Chantal, Duggirala Ravi, Dyer Thomas D, Erk Susanne, Fagerness Jesen, Fox Peter T, Freimer Nelson B, Gill Michael, Göring Harald H H, Hagler Donald J, Hoehn David, Holsboer Florian, Hoogman Martine, Hosten Norbert, Jahanshad Neda, Johnson Matthew P, Kasperaviciute Dalia, Kent Jack W, Kochunov Peter, Lancaster Jack L, Lawrie Stephen M, Liewald David C, Mandl René, Matarin Mar, Mattheisen Manuel, Meisenzahl Eva, Melle Ingrid, Moses Eric K, Mühleisen Thomas W, Nauck Matthias, Nöthen Markus M, Olvera Rene L, Pandolfo Massimo, Pike G Bruce, Puls Ralf, Reinvang Ivar, Rentería Miguel E, Rietschel Marcella, Roffman Joshua L, Royle Natalie A, Rujescu Dan, Savitz Jonathan, Schnack Hugo G, Schnell Knut, Seiferth Nina, Smith Colin, Steen Vidar M, Valdés Hernández Maria C, Van den Heuvel Martijn, van der Wee Nic J, Van Haren Neeltje E M, Veltman Joris A, Völzke Henry, Walker Robert, Westlye Lars T, Whelan Christopher D, Agartz Ingrid, Boomsma Dorret I, Cavalleri Gianpiero L, Dale Anders M, Djurovic Srdjan, Drevets Wayne C, Hagoort Peter, Hall Jeremy, Heinz Andreas, Jack Clifford R, Foroud Tatiana M, Le Hellard Stephanie, Macciardi Fabio, Montgomery Grant W, Poline Jean Baptiste, Porteous David J, Sisodiya Sanjay M, Starr John M, Sussmann Jessika, Toga Arthur W, Veltman Dick J, Walter Henrik, Weiner Michael W, , , , , Bis Joshua C, Ikram M Arfan, Smith Albert V, Gudnason Vilmundur, Tzourio Christophe, Vernooij Meike W, Launer Lenore J, DeCarli Charles, Seshadri Sudha, , Andreassen Ole A, Apostolova Liana G, Bastin Mark E, Blangero John, Brunner Han G, Buckner Randy L, Cichon Sven, Coppola Giovanni, de Zubicaray Greig I, Deary Ian J, Donohoe Gary, de Geus Eco J C, Espeseth Thomas, Fernández Guillén, Glahn David C, Grabe Hans J, Hardy John, Hulshoff Pol Hilleke E, Jenkinson Mark, Kahn René S, McDonald Colm, McIntosh Andrew M, McMahon Francis J, McMahon Katie L, Meyer-Lindenberg Andreas, Morris Derek W, Müller-Myhsok Bertram, Nichols Thomas E, Ophoff Roel A, Paus Tomas, Pausova Zdenka, Penninx Brenda W, Potkin Steven G, Sämann Philipp G, Saykin Andrew J, Schumann Gunter, Smoller Jordan W, Wardlaw Joanna M, Weale Michael E, Martin Nicholas G, Franke Barbara, Wright Margaret J, Thompson Paul M, |
| Transferability and fine mapping of type 2 diabetes loci in African Americans: the Candidate Gene Association Resource Plus Study. Diabetes 2013 Mar 62 (3): 965-76. Ng Maggie C Y, Saxena Richa, Li Jiang, Palmer Nicholette D, Dimitrov Latchezar, Xu Jianzhao, Rasmussen-Torvik Laura J, Zmuda Joseph M, Siscovick David S, Patel Sanjay R, Crook Errol D, Sims Mario, Chen Yii-Der I, Bertoni Alain G, Li Mingyao, Grant Struan F A, Dupuis Josée, Meigs James B, Psaty Bruce M, Pankow James S, Langefeld Carl D, Freedman Barry I, Rotter Jerome I, Wilson James G, Bowden Donald |
| Common variant in the HMGA2 gene increases susceptibility to nephropathy in patients with type 2 diabetes. Diabetologia 2012 Oct . Alkayyali S, Lajer M, Deshmukh H, Ahlqvist E, Colhoun H, Isomaa B, Rossing P, Groop L, Lyssenko V |
| Subsets of salivary duct carcinoma defined by morphologic evidence of pleomorphic adenoma, PLAG1 or HMGA2 rearrangements, and common genetic alterations. Cancer 2016 Jul . Chiosea Simion I, Thompson Lester D R, Weinreb Ilan, Bauman Julie E, Mahaffey Alyssa M, Miller Caitlyn, Ferris Robert L, Gooding William |
| A study of common Mendelian disease carriers across ageing British cohorts: meta-analyses reveal heterozygosity for alpha 1-antitrypsin deficiency increases respiratory capacity and height. Journal of medical genetics 2016 Feb . North Teri-Louise, Ben-Shlomo Yoav, Cooper Cyrus, Deary Ian J, Gallacher John, Kivimaki Mika, Kumari Meena, Martin Richard M, Pattie Alison, Sayer Avan Aihie, Starr John M, Wong Andrew, Kuh Diana, Rodriguez Santiago, Day Ian N |
| 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 |
| 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 |
| 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 |
| 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 |
| Genotype based Risk Predictors for Polycystic Ovary Syndrome in Western Saudi Arabia. Bioinformation 2019 15 (11): 812-819. Bakhashab Sherin, Ahmed Na |
| 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 |
| 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 |
| 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 |
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