HuGE Literature Finder
Records 1-30
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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 |
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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 |
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Intravenous leiomyomatosis: molecular analysis of 17 cases.
Pathology 2019 Dec . Lu Bingjian, Liu Qin, Tang Lanlan, Ma Yu, Shi Haiy |
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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 |
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Genotype based Risk Predictors for Polycystic Ovary Syndrome in Western Saudi Arabia.
Bioinformation 2019 15 (11): 812-819. Bakhashab Sherin, Ahmed Na |
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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, Koichi Matsuda, 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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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Variations in the High Mobility Group-A2 Gene (HMGA2) Are Associated With Idiopathic Short Stature (ISS).
Pediatric research 2015 Nov . Fusco Ileana, Babu Deepak, Mellone Simona, Barizzone Nadia, Prodam Flavia, Fanelli Antonella, Muniswamy Ranjit, Petri Antonella, Bellone Simonetta, Bona Gianni, Giordano Ma |
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A splicing mutation of the HMGA2 gene is associated with Silver-Russell syndrome phenotype.
Journal of human genetics 2015 Jun 60 (6): 287-93. De Crescenzo Agostina, Citro Valentina, Freschi Andrea, Sparago Angela, Palumbo Orazio, Cubellis Maria Vittoria, Carella Massimo, Castelluccio Pia, Cavaliere Maria Luigia, Cerrato Flavia, Riccio Andr |
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HMGA2 expression pattern and TERT mutations in tumors of the vulva.
Oncology reports 2015 Jun 33 (6): 2675-80. Agostini Antonio, Panagopoulos Ioannis, Andersen Hege Kilen, Johannesen Lene Elisabeth, Davidson Ben, Tropé Claes Göran, Heim Sverre, Micci Frances |
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A novel common variant in DCST2 is associated with length in early life and height in adulthood.
Human molecular genetics 2015 Feb 24 (4): 1155-68. van der Valk Ralf J P, Kreiner-Møller Eskil, Kooijman Marjolein N, Guxens Mònica, Stergiakouli Evangelia, Sääf Annika, Bradfield Jonathan P, Geller Frank, Hayes M Geoffrey, Cousminer Diana L, Körner Antje, Thiering Elisabeth, Curtin John A, Myhre Ronny, Huikari Ville, Joro Raimo, Kerkhof Marjan, Warrington Nicole M, Pitkänen Niina, Ntalla Ioanna, Horikoshi Momoko, Veijola Riitta, Freathy Rachel M, Teo Yik-Ying, Barton Sheila J, Evans David M, Kemp John P, St Pourcain Beate, Ring Susan M, Davey Smith George, Bergström Anna, Kull Inger, Hakonarson Hakon, Mentch Frank D, Bisgaard Hans, Chawes Bo, Stokholm Jakob, Waage Johannes, Eriksen Patrick, Sevelsted Astrid, Melbye Mads, , van Duijn Cornelia M, Medina-Gomez Carolina, Hofman Albert, de Jongste Johan C, Taal H Rob, Uitterlinden André G, , Armstrong Loren L, Eriksson Johan, Palotie Aarno, Bustamante Mariona, Estivill Xavier, Gonzalez Juan R, Llop Sabrina, Kiess Wieland, Mahajan Anubha, Flexeder Claudia, Tiesler Carla M T, Murray Clare S, Simpson Angela, Magnus Per, Sengpiel Verena, Hartikainen Anna-Liisa, Keinanen-Kiukaanniemi Sirkka, Lewin Alexandra, Da Silva Couto Alves Alexessander, Blakemore Alexandra I, Buxton Jessica L, Kaakinen Marika, Rodriguez Alina, Sebert Sylvain, Vaarasmaki Marja, Lakka Timo, Lindi Virpi, Gehring Ulrike, Postma Dirkje S, Ang Wei, Newnham John P, Lyytikäinen Leo-Pekka, Pahkala Katja, Raitakari Olli T, Panoutsopoulou Kalliope, Zeggini Eleftheria, Boomsma Dorret I, Groen-Blokhuis Maria, Ilonen Jorma, Franke Lude, Hirschhorn Joel N, Pers Tune H, Liang Liming, Huang Jinyan, Hocher Berthold, Knip Mikael, Saw Seang-Mei, Holloway John W, Melén Erik, Grant Struan F A, Feenstra Bjarke, Lowe William L, Widén Elisabeth, Sergeyev Elena, Grallert Harald, Custovic Adnan, Jacobsson Bo, Jarvelin Marjo-Riitta, Atalay Mustafa, Koppelman Gerard H, Pennell Craig E, Niinikoski Harri, Dedoussis George V, Mccarthy Mark I, Frayling Timothy M, Sunyer Jordi, Timpson Nicholas J, Rivadeneira Fernando, Bønnelykke Klaus, Jaddoe Vincent W V, |
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Association Analysis of Genetic Variants with Type 2 Diabetes in a Mongolian Population in China.
Journal of diabetes research 2015 2015 613236. Bai Haihua, Liu Haiping, Suyalatu Suyalatu, Guo Xiaosen, Chu Shandan, Chen Ying, Lan Tianming, Borjigin Burenbatu, Orlov Yuriy L, Posukh Olga L, Yang Xiuqin, Guilan Guilan, Osipova Ludmila P, Wu Qizhu, Narisu Nari |
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Uterine fibroids: do we deal with more than one disease?
International journal of gynecological pathology : official journal of the International Society of Gynecological Pathologists 2014 Nov 33 (6): 568-72. Markowski Dominique N, Helmke Burkhard M, Bartnitzke Sabine, Löning Thomas, Bullerdiek Jö |
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Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.
PLoS genetics 2014 Aug 10 (8): e1004517. Ng Maggie C Y, Shriner Daniel, Chen Brian H, Li Jiang, Chen Wei-Min, Guo Xiuqing, Liu Jiankang, Bielinski Suzette J, Yanek Lisa R, Nalls Michael A, Comeau Mary E, Rasmussen-Torvik Laura J, Jensen Richard A, Evans Daniel S, Sun Yan V, An Ping, Patel Sanjay R, Lu Yingchang, Long Jirong, Armstrong Loren L, Wagenknecht Lynne, Yang Lingyao, Snively Beverly M, Palmer Nicholette D, Mudgal Poorva, Langefeld Carl D, Keene Keith L, Freedman Barry I, Mychaleckyj Josyf C, Nayak Uma, Raffel Leslie J, Goodarzi Mark O, Chen Y-D Ida, Taylor Herman A, Correa Adolfo, Sims Mario, Couper David, Pankow James S, Boerwinkle Eric, Adeyemo Adebowale, Doumatey Ayo, Chen Guanjie, Mathias Rasika A, Vaidya Dhananjay, Singleton Andrew B, Zonderman Alan B, Igo Robert P, Sedor John R, , Kabagambe Edmond K, Siscovick David S, McKnight Barbara, Rice Kenneth, Liu Yongmei, Hsueh Wen-Chi, Zhao Wei, Bielak Lawrence F, Kraja Aldi, Province Michael A, Bottinger Erwin P, Gottesman Omri, Cai Qiuyin, Zheng Wei, Blot William J, Lowe William L, Pacheco Jennifer A, Crawford Dana C, , , Grundberg Elin, , Rich Stephen S, Hayes M Geoffrey, Shu Xiao-Ou, Loos Ruth J F, Borecki Ingrid B, Peyser Patricia A, Cummings Steven R, Psaty Bruce M, Fornage Myriam, Iyengar Sudha K, Evans Michele K, Becker Diane M, Kao W H Linda, Wilson James G, Rotter Jerome I, Sale Michèle M, Liu Simin, Rotimi Charles N, Bowden Donald W, |
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Cross-ethnic meta-analysis of genetic variants for polycystic ovary syndrome.
The Journal of clinical endocrinology and metabolism 2013 Dec 98 (12): E2006-12. Louwers Yvonne V, Stolk Lisette, Uitterlinden André G, Laven Joop S |
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Genome-wide association study of primary tooth eruption identifies pleiotropic loci associated with height and craniofacial distances.
Human molecular genetics 2013 Sep 22 (18): 3807-17. Fatemifar Ghazaleh, Hoggart Clive J, Paternoster Lavinia, Kemp John P, Prokopenko Inga, Horikoshi Momoko, Wright Victoria J, Tobias Jon H, Richmond Stephen, Zhurov Alexei I, Toma Arshed M, Pouta Anneli, Taanila Anja, Sipila Kirsi, Lähdesmäki Raija, Pillas Demetris, Geller Frank, Feenstra Bjarke, Melbye Mads, Nohr Ellen A, Ring Susan M, St Pourcain Beate, Timpson Nicholas J, Davey Smith George, Jarvelin Marjo-Riitta, Evans David |
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Characterization of uterine leiomyomas by whole-genome sequencing.
The New England journal of medicine 2013 Jul 369 (1): 43-53. Mehine Miika, Kaasinen Eevi, Mäkinen Netta, Katainen Riku, Kämpjärvi Kati, Pitkänen Esa, Heinonen Hanna-Riikka, Bützow Ralf, Kilpivaara Outi, Kuosmanen Anna, Ristolainen Heikki, Gentile Massimiliano, Sjöberg Jari, Vahteristo Pia, Aaltonen Lauri |
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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 |
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New loci associated with birth weight identify genetic links between intrauterine growth and adult height and metabolism.
Nature genetics 2012 Dec . Horikoshi M, Yaghootkar H, Mook-Kanamori DO, Sovio U, Taal HR, Hennig BJ, Bradfield JP, St Pourcain B, Evans DM, Charoen P, Kaakinen M, Cousminer DL, Lehtimäki T, Kreiner-Møller E, Warrington NM, Bustamante M, Feenstra B, Berry DJ, Thiering E, Pfab T, Barton SJ, Shields BM, Kerkhof M, van Leeuwen EM, Fulford AJ, Kutalik Z, Zhao JH, den Hoed M, Mahajan A, Lindi V, Goh LK, Hottenga JJ, Wu Y, Raitakari OT, Harder MN, Meirhaeghe A, Ntalla I, Salem RM, Jameson KA, Zhou K, Monies DM, Lagou V, Kirin M, Heikkinen J, Adair LS, Alkuraya FS, Al-Odaib A, Amouyel P, Andersson EA, Bennett AJ, Blakemore AI, Buxton JL, Dallongeville J, Das S, de Geus EJ, Estivill X, Flexeder C, Froguel P, Geller F, Godfrey KM, Gottrand F, Groves CJ, Hansen T, Hirschhorn JN, Hofman A, Hollegaard MV, Hougaard DM, Hyppönen E, Inskip HM, Isaacs A, Jørgensen T, Kanaka-Gantenbein C, Kemp JP, Kiess W, Kilpeläinen TO, Klopp N, Knight BA, Kuzawa CW, McMahon G, Newnham JP, Niinikoski H, Oostra BA, Pedersen L, Postma DS, Ring SM, Rivadeneira F, Robertson NR, Sebert S, Simell O, Slowinski T, Tiesler CM, Tönjes A, Vaag A, Viikari JS, Vink JM, Vissing NH, Wareham NJ, Willemsen G, Witte DR, Zhang H, Zhao J, Wilson JF, Stumvoll M, Prentice AM, Meyer BF, Pearson ER, Boreham CA, Cooper C, Gillman MW, Dedoussis GV, Moreno LA, Pedersen O, Saarinen M, Mohlke KL, Boomsma DI, Saw SM, Lakka TA, Körner A, Loos RJ, Ong KK, Vollenweider P, van Duijn CM, Koppelman GH, Hattersley AT, Holloway JW, Hocher B, Heinrich J, Power C, Melbye M, Guxens M, Pennell CE, Bønnelykke K, Bisgaard H, Eriksson JG, Widén E, Hakonarson H, Uitterlinden AG, Pouta A, Lawlor DA, Smith GD, Frayling TM, McCarthy MI, Grant SF, Jaddoe VW, Jarvelin MR, Timpson NJ, Prokopenko I, Freathy RM |
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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 |
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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, |
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Genome-wide association study of body height in African Americans: the Women's Health Initiative SNP Health Association Resource (SHARe).
Human molecular genetics 2012 Feb 21 (3): 711-20. Carty Cara L, Johnson Nicholas A, Hutter Carolyn M, Reiner Alexander P, Peters Ulrike, Tang Hua, Kooperberg Charl |
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Large-Scale Gene-Centric Meta-Analysis across 39 studies Identifies Type 2 Diabetes Loci.
American journal of human genetics 2012 Feb . Saxena R, Elbers CC, Guo Y, Peter I, Gaunt TR, Mega JL, Lanktree MB, Tare A, Castillo BA, Li YR, Johnson T, Bruinenberg M, Gilbert-Diamond D, Rajagopalan R, Voight BF, Balasubramanyam A, Barnard J, Bauer F, Baumert J, Bhangale T, Böhm BO, Braund PS, Burton PR, Chandrupatla HR, Clarke R, Cooper-Dehoff RM, Crook ED, Davey-Smith G, Day IN, de Boer A, de Groot MC, Drenos F, Ferguson J, Fox CS, Furlong CE, Gibson Q, Gieger C, Gilhuijs-Pederson LA, Glessner JT, Goel A, Gong Y, Grant SF, Grobbee DE, Hastie C, Humphries SE, Kim CE, Kivimaki M, Kleber M, Meisinger C, Kumari M, Langaee TY, Lawlor DA, Li M, Lobmeyer MT, Maitland-van der Zee AH, Meijs MF, Molony CM, Morrow DA, Murugesan G, Musani SK, Nelson CP, Newhouse SJ, O'Connell JR, Padmanabhan S, Palmen J, Patel SR, Pepine CJ, Pettinger M, Price TS, Rafelt S, Ranchalis J, Rasheed A, Rosenthal E, Ruczinski I, Shah S, Shen H, Silbernagel G, Smith EN, Spijkerman AW, Stanton A, Steffes MW, Thorand B, Trip M, van der Harst P, van der A DL, van Iperen EP, van Setten J, van Vliet-Ostaptchouk JV, Verweij N, Wolffenbuttel BH, Young T, Zafarmand MH, Zmuda JM, Boehnke M, Altshuler D, McCarthy M, Kao WH, Pankow JS, Cappola TP, Caulfield M, Dominiczak A, Shields DC, Bhatt D, Zhang L, Curtis SP, Danesh J, Casas JP, van der Schouw YT, Onland-Moret NC, Doevendans PA, Dorn GW, Farrall M, Fitzgerald GA, Hamsten A, Hegele R, Hingorani AD, Hofker MH, Huggins GS, Illig T, Jarvik GP, Johnson JA, Klungel OH, Knowler WC, Koenig W, März W, Meigs JB, Melander O, Munroe PB, Mitchell BD, Bielinski SJ, Rader DJ, Reilly MP, Rich SS, Rotter JI, Saleheen D, Samani NJ, Schadt EE, Shuldiner AR, Silverstein R, Kottke-Marchant K, Talmud PJ, Watkins H, Asselbergs F, de Bakker PI, McCaffery J, Wijmenga C, Sabatine MS, Wilson JG, Reiner A, Bowden DW, Hakonarson H, Siscovick DS, Keating BJ |
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Lack of association of type 2 diabetes susceptibility genotypes and body weight on the development of islet autoimmunity and type 1 diabetes.
PloS one 2012 7 (4): e35410. Winkler Christiane, Raab Jennifer, Grallert Harald, Ziegler Anette-Gabrie |
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Confirmation that SNPs in the high mobility group-A2 gene (HMGA2) are associated with adult height in the Japanese population; wide-ranging population survey of height-related SNPs in HMGA2.
Electrophoresis 2011 Jul 32 (14): 1844-51. Takeshita Haruo, Fujihara Junko, Soejima Mikiko, Koda Yoshiro, Kimura-Kataoka Kaori, Ono Rei-Ichiro, Yuasa Isao, Iida Reiko, Ueki Misuzu, Nagao Masataka, Yasuda Toshihi |
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Type 2 diabetes risk allele near CENTD2 is associated with decreased glucose-stimulated insulin release.
Diabetologia 2011 May 54 (5): 1052-6. Nielsen T, Sparsø T, Grarup N, Jørgensen T, Pisinger C, Witte D R, , Hansen T, Pedersen |
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Association of new loci identified in European genome-wide association studies with susceptibility to type 2 diabetes in the Japanese.
PloS one 2011 6 (10): e26911. Ohshige Toshihiko, Iwata Minoru, Omori Shintaro, Tanaka Yasushi, Hirose Hiroshi, Kaku Kohei, Maegawa Hiroshi, Watada Hirotaka, Kashiwagi Atsunori, Kawamori Ryuzo, Tobe Kazuyuki, Kadowaki Takashi, Nakamura Yusuke, Maeda Shi |
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Genetic variation in candidate genes like the HMGA2 gene in the extremely tall.
Hormone research in pædiatrics 2011 76 (5): 307-13. Hendriks A E J, Brown M R, Boot A M, Oostra B A, Drop S L S, Parks J |
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Genome-wide association study of height and body mass index in Australian twin families.
Twin research and human genetics : the official journal of the International Society for Twin Studies 2010 Apr 13 (2): 179-93. Liu Jimmy Z, Medland Sarah E, Wright Margaret J, Henders Anjali K, Heath Andrew C, Madden Pamela A F, Duncan Alexis, Montgomery Grant W, Martin Nicholas G, McRae Allan |
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Genome-wide association study reveals multiple loci associated with primary tooth development during infancy.
PLoS genetics 2010 Feb 6 (2): e1000856. Pillas Demetris, Hoggart Clive J, Evans David M, O'Reilly Paul F, Sipilä Kirsi, Lähdesmäki Raija, Millwood Iona Y, Kaakinen Marika, Netuveli Gopalakrishnan, Blane David, Charoen Pimphen, Sovio Ulla, Pouta Anneli, Freimer Nelson, Hartikainen Anna-Liisa, Laitinen Jaana, Vaara Sarianna, Glaser Beate, Crawford Peter, Timpson Nicholas J, Ring Susan M, Deng Guohong, Zhang Weihua, McCarthy Mark I, Deloukas Panos, Peltonen Leena, Elliott Paul, Coin Lachlan J M, Smith George Davey, Jarvelin Marjo-Riit |
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HMGA2 is confirmed to be associated with human adult height.
Annals of human genetics 2010 Jan 74 (1): 11-6. Yang Tie-Lin, Guo Yan, Zhang Li-Shu, Tian Qing, Yan Han, Guo Yan-Fang, Deng Hong-W |
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The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
BMC medical genetics 2010 11 (1): 96. Zhao Jianhua, Li Mingyao, Bradfield Jonathan P, Zhang Haitao, Mentch Frank D, Wang Kai, Sleiman Patrick M, Kim Cecilia E, Glessner Joseph T, Hou Cuiping, Keating Brendan J, Thomas Kelly A, Garris Maria L, Deliard Sandra, Frackelton Edward C, Otieno F George, Chiavacci Rosetta M, Berkowitz Robert I, Hakonarson Hakon, Grant Struan F |
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Association of a high mobility group gene (HMGA2) variant with bone mineral density.
Bone 2009 Aug 45 (2): 295-300. Kuipers Allison, Zhang Yingze, Cauley Jane A, Nestlerode Cara S, Chu Yanxia, Bunker Clareann H, Patrick Alan L, Wheeler Victor W, Hoffman Andrew R, Orwoll Eric S, Zmuda Joseph |
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Smallness for gestational age interacts with high mobility group A2 gene genetic variation to modulate height.
European journal of endocrinology / European Federation of Endocrine Societies 2009 Apr 160 (4): 557-60. Bouatia-Naji Nabila, Marchand Marion, Cavalcanti-Proença Christine, Daghmoun Samia, Durand Emmanuelle, Tichet Jean, Marre Michel, Balkau Beverley, Froguel Philippe, Lévy-Marchal Clai |
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Uterine leiomyomata and decreased height: a common HMGA2 predisposition allele.
Human genetics 2009 Apr 125 (3): 257-63. Hodge Jennelle C, T Cuenco Karen, Huyck Karen L, Somasundaram Priya, Panhuysen Carolien I M, Stewart Elizabeth A, Morton Cynthia |
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Genome-wide association analysis identifies 20 loci that influence adult height.
Nature genetics 2008 May 40 (5): 575-83. Weedon Michael N, Lango Hana, Lindgren Cecilia M, Wallace Chris, Evans David M, Mangino Massimo, Freathy Rachel M, Perry John R B, Stevens Suzanne, Hall Alistair S, Samani Nilesh J, Shields Beverly, Prokopenko Inga, Farrall Martin, Dominiczak Anna, , , Johnson Toby, Bergmann Sven, Beckmann Jacques S, Vollenweider Peter, Waterworth Dawn M, Mooser Vincent, Palmer Colin N A, Morris Andrew D, Ouwehand Willem H, , Zhao Jing Hua, Li Shengxu, Loos Ruth J F, Barroso Inês, Deloukas Panagiotis, Sandhu Manjinder S, Wheeler Eleanor, Soranzo Nicole, Inouye Michael, Wareham Nicholas J, Caulfield Mark, Munroe Patricia B, Hattersley Andrew T, McCarthy Mark I, Frayling Timothy |
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Common variants in the GDF5-UQCC region are associated with variation in human height.
Nature genetics 2008 Feb 40 (2): 198-203. Sanna Serena, Jackson Anne U, Nagaraja Ramaiah, Willer Cristen J, Chen Wei-Min, Bonnycastle Lori L, Shen Haiqing, Timpson Nicholas, Lettre Guillaume, Usala Gianluca, Chines Peter S, Stringham Heather M, Scott Laura J, Dei Mariano, Lai Sandra, Albai Giuseppe, Crisponi Laura, Naitza Silvia, Doheny Kimberly F, Pugh Elizabeth W, Ben-Shlomo Yoav, Ebrahim Shah, Lawlor Debbie A, Bergman Richard N, Watanabe Richard M, Uda Manuela, Tuomilehto Jaakko, Coresh Josef, Hirschhorn Joel N, Shuldiner Alan R, Schlessinger David, Collins Francis S, Davey Smith George, Boerwinkle Eric, Cao Antonio, Boehnke Michael, Abecasis Gonçalo R, Mohlke Karen |
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A common variant of HMGA2 is associated with adult and childhood height in the general population.
Nature genetics 2007 Oct 39 (10): 1245-50. Weedon Michael N, Lettre Guillaume, Freathy Rachel M, Lindgren Cecilia M, Voight Benjamin F, Perry John R B, Elliott Katherine S, Hackett Rachel, Guiducci Candace, Shields Beverley, Zeggini Eleftheria, Lango Hana, Lyssenko Valeriya, Timpson Nicholas J, Burtt Noel P, Rayner Nigel W, Saxena Richa, Ardlie Kristin, Tobias Jonathan H, Ness Andrew R, Ring Susan M, Palmer Colin N A, Morris Andrew D, Peltonen Leena, Salomaa Veikko, , , Davey Smith George, Groop Leif C, Hattersley Andrew T, McCarthy Mark I, Hirschhorn Joel N, Frayling Timothy |
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