Human Genome Epidemiology Literature Finder
Records 1 - 29 (of 29 Records) |
Query Trace: MECOM[original query] |
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Multiancestry Genome-Wide Association Study of Aortic Stenosis Identifies Multiple Novel Loci in the Million Veteran Program.
Circulation 2023 2 147 (12): 942-955. Small Aeron M, Peloso Gina M, Linefsky Jason, Aragam Jayashri, Galloway Ashley, Tanukonda Vidisha, Wang Lu-Chen, Yu Zhi, Sunitha Selvaraj Margaret, Farber-Eger Eric H, Baker Michael T, Setia-Verma Shefali, Lee Simon S K, Preuss Michael, Ritchie Marylyn D, Damrauer Scott M, Rader Daniel J, Wells Quinn S, Loos Ruth, Lubitz Steven A, Thanassoulis George, Cho Kelly, Wilson Peter W F, , Natarajan Pradeep, O'Donnell Christopher |
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Nature genetics 2011 Sep 43 (11): 1082-90. Soler Artigas María, Loth Daan W, Wain Louise V, Gharib Sina A, Obeidat Ma'en, Tang Wenbo, Zhai Guangju, Zhao Jing Hua, Smith Albert Vernon, Huffman Jennifer E, Albrecht Eva, Jackson Catherine M, Evans David M, Cadby Gemma, Fornage Myriam, Manichaikul Ani, Lopez Lorna M, Johnson Toby, Aldrich Melinda C, Aspelund Thor, Barroso Inês, Campbell Harry, Cassano Patricia A, Couper David J, Eiriksdottir Gudny, Franceschini Nora, Garcia Melissa, Gieger Christian, Gislason Gauti Kjartan, Grkovic Ivica, Hammond Christopher J, Hancock Dana B, Harris Tamara B, Ramasamy Adaikalavan, Heckbert Susan R, Heliövaara Markku, Homuth Georg, Hysi Pirro G, James Alan L, Jankovic Stipan, Joubert Bonnie R, Karrasch Stefan, Klopp Norman, Koch Beate, Kritchevsky Stephen B, Launer Lenore J, Liu Yongmei, Loehr Laura R, Lohman Kurt, Loos Ruth J F, Lumley Thomas, Al Balushi Khalid A, Ang Wei Q, Barr R Graham, Beilby John, Blakey John D, Boban Mladen, Boraska Vesna, Brisman Jonas, Britton John R, Brusselle Guy G, Cooper Cyrus, Curjuric Ivan, Dahgam Santosh, Deary Ian J, Ebrahim Shah, Eijgelsheim Mark, Francks Clyde, Gaysina Darya, Granell Raquel, Gu Xiangjun, Hankinson John L, Hardy Rebecca, Harris Sarah E, Henderson John, Henry Amanda, Hingorani Aroon D, Hofman Albert, Holt Patrick G, Hui Jennie, Hunter Michael L, Imboden Medea, Jameson Karen A, Kerr Shona M, Kolcic Ivana, Kronenberg Florian, Liu Jason Z, Marchini Jonathan, McKeever Tricia, Morris Andrew D, Olin Anna-Carin, Porteous David J, Postma Dirkje S, Rich Stephen S, Ring Susan M, Rivadeneira Fernando, Rochat Thierry, Sayer Avan Aihie, Sayers Ian, Sly Peter D, Smith George Davey, Sood Akshay, Starr John M, Uitterlinden André G, Vonk Judith M, Wannamethee S Goya, Whincup Peter H, Wijmenga Cisca, Williams O Dale, Wong Andrew, Mangino Massimo, Marciante Kristin D, McArdle Wendy L, Meibohm Bernd, Morrison Alanna C, North Kari E, Omenaas Ernst, Palmer Lyle J, Pietiläinen Kirsi H, Pin Isabelle, Pola Sbreve Ek Ozren, Pouta Anneli, Psaty Bruce M, Hartikainen Anna-Liisa, Rantanen Taina, Ripatti Samuli, Rotter Jerome I, Rudan Igor, Rudnicka Alicja R, Schulz Holger, Shin So-Youn, Spector Tim D, Surakka Ida, Vitart Veronique, Völzke Henry, Wareham Nicholas J, Warrington Nicole M, Wichmann H-Erich, Wild Sarah H, Wilk Jemma B, Wjst Matthias, Wright Alan F, Zgaga Lina, Zemunik Tatijana, Pennell Craig E, Nyberg Fredrik, Kuh Diana, Holloway John W, Boezen H Marike, Lawlor Debbie A, Morris Richard W, Probst-Hensch Nicole, , , Kaprio Jaakko, Wilson James F, Hayward Caroline, Kähönen Mika, Heinrich Joachim, Musk Arthur W, Jarvis Deborah L, Gläser Sven, Järvelin Marjo-Riitta, Ch Stricker Bruno H, Elliott Paul, O'Connor George T, Strachan David P, London Stephanie J, Hall Ian P, Gudnason Vilmundur, Tobin Martin |
Meta-analysis identifies a MECOM gene as a novel predisposing factor of osteoporotic fracture.
Journal of medical genetics 2013 Jan . Hwang JY, Lee SH, Go MJ, Kim BJ, Kou I, Ikegawa S, Guo Y, Deng HW, Raychaudhuri S, Kim YJ, Oh JH, Kim Y, Moon S, Kim DJ, Koo H, Cha MJ, Lee MH, Yun JY, Yoo HS, Kang YA, Cho EH, Kim SW, Oh KW, Kang MI, Son HY, Kim SY, Kim GS, Han BG, Cho YS, Cho MC, Lee JY, Koh JM |
Gene-smoking interactions identify several novel blood pressure loci in the Framingham Heart Study.
American journal of hypertension 2015 Mar 28 (3): 343-54. Sung Yun J, de Las Fuentes Lisa, Schwander Karen L, Simino Jeannette, Rao Dabeeru |
Genetic variation at MECOM, TERT, JAK2 and HBS1L-MYB predisposes to myeloproliferative neoplasms.
Nature communications 2015 6 6691. Tapper William, Jones Amy V, Kralovics Robert, Harutyunyan Ashot S, Zoi Katerina, Leung William, Godfrey Anna L, Guglielmelli Paola, Callaway Alison, Ward Daniel, Aranaz Paula, White Helen E, Waghorn Katherine, Lin Feng, Chase Andrew, Baxter E Joanna, Maclean Cathy, Nangalia Jyoti, Chen Edwin, Evans Paul, Short Michael, Jack Andrew, Wallis Louise, Oscier David, Duncombe Andrew S, Schuh Anna, Mead Adam J, Griffiths Michael, Ewing Joanne, Gale Rosemary E, Schnittger Susanne, Haferlach Torsten, Stegelmann Frank, Döhner Konstanze, Grallert Harald, Strauch Konstantin, Tanaka Toshiko, Bandinelli Stefania, Giannopoulos Andreas, Pieri Lisa, Mannarelli Carmela, Gisslinger Heinz, Barosi Giovanni, Cazzola Mario, Reiter Andreas, Harrison Claire, Campbell Peter, Green Anthony R, Vannucchi Alessandro, Cross Nicholas C |
A GWAS Meta-analysis and Replication Study Identifies a Novel Locus within CLPTM1L/TERT Associated with Nasopharyngeal Carcinoma in Individuals of Chinese Ancestry.
Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2015 Nov . Bei Jin-Xin, Su Wen-Hui, Ng Ching-Ching, Yu Kai, Chin Yoon-Ming, Lou Pei-Jen, Hsu Wan-Lun, McKay James D, Chen Chien-Jen, Chang Yu-Sun, Chen Li-Zhen, Chen Ming-Yuan, Cui Qian, Feng Fu-Tuo, Feng Qi-Shen, Guo Yun-Miao, Jia Wei-Hua, Khoo Alan Soo-Beng, Liu Wen-Sheng, Mo Hao-Yuan, Pua Kin-Choo, Teo Soo Hwang, Tse Ka-Po, Xia Yun-Fei, Zhang Hongxin, Zhou Gang-Qiao, Liu Jian-Jun, Zeng Yi-Xin, Hildesheim All |
Intratumoral Heterogeneity of Frameshift Mutations in MECOM Gene is Frequent in Colorectal Cancers with High Microsatellite Instability. Pathology oncology research : POR 2017 Jan 23 (1): 145-149. Choi Eun Ji, Kim Min Sung, Song Sang Yong, Yoo Nam Jin, Lee Sug Hyu |
Germline variations at JAK2, TERT, HBS1L-MYB and MECOM and the risk of myeloproliferative neoplasms in Taiwanese population. Oncotarget 2017 Sep 8 (44): 76204-76213. Chiang Yi-Hao, Chang Yu-Cheng, Lin Huan-Chau, Huang Ling, Cheng Chun-Chia, Wang Wei-Ting, Cheng Hung-I, Su Nai-Wen, Chen Caleb Gon-Shen, Lin Johnson, Chang Yi-Fang, Chang Ming-Chih, Hsieh Ruey-Kuen, Chou Wen-Chien, Lim Ken-Hong, Kuo Yuan-Y |
MECOM, HBS1L-MYB, THRB-RARB, JAK2, and TERT polymorphisms defining the genetic predisposition to myeloproliferative neoplasms: A study on 939 patients. American journal of hematology 2017 Oct . Trifa Adrian P, B?nescu Claudia, Bojan Anca S, Voina Cristian M, Popa ?tefana, Vi?an Simona, Ciubean Alina D, Tripon Florin, Dima Delia, Popov Viola M, Vesa ?tefan C, Andreescu Mihaela, Török-Vistai Tünde, Mih?il? Romeo G, Berbec Nicoleta, Macarie Ioan, Coli?? Andrei, Iordache Maria, C?tan? Alina C, Farca? Marius F, Tomuleasa Ciprian, Vasile Kinga, Truic? Cristina, Todinc? Adriana, Pop-Muntean Lavinia, Manolache Raluca, Bumbea Horia, Vl?d?reanu Ana-Maria, Gaman Mihaela, Ciufu Cristina M, Popp Radu |
Targeted Sequencing of Lung Function Loci in Chronic Obstructive Pulmonary Disease Cases and Controls. PloS one 2017 1 12 (1): e0170222. Artigas María Soler, Wain Louise V, Shrine Nick, McKeever Tricia M, , Sayers Ian, Hall Ian P, Tobin Martin |
Targeted next generation sequencing of well-differentiated/dedifferentiated liposarcoma reveals novel gene amplifications and mutations. Oncotarget 2018 Apr 9 (28): 19891-19899. Somaiah Neeta, Beird Hannah C, Barbo Andrea, Song Juhee, Mills Shaw Kenna R, Wang Wei-Lien, Eterovic Karina, Chen Ken, Lazar Alexander, Conley Anthony P, Ravi Vinod, Hwu Patrick, Futreal Andrew, Simon George, Meric-Bernstam Funda, Hong Dav |
Genetic alterations and PIK3CA gene mutations and amplifications analysis in cervical cancer by racial groups in the United States. International journal of health sciences 0 12 (1): 28-32. Femi Odekunle Floren |
Clinical and genetic risk factors for decreased bone mineral density in Japanese patients with inflammatory bowel disease.
Journal of gastroenterology and hepatology 2018 Mar . Naito Takeo, Yokoyama Naonobu, Kakuta Yoichi, Ueno Kazuko, Kawai Yosuke, Onodera Motoyuki, Moroi Rintaro, Kuroha Masatake, Kanazawa Yoshitake, Kimura Tomoya, Shiga Hisashi, Endo Katsuya, Nagasaki Masao, Masamune Atsushi, Kinouchi Yoshitaka, Shimosegawa Too |
High IL2RA mRNA expression is an independent adverse prognostic biomarker in core binding factor and intermediate-risk acute myeloid leukemia. Journal of translational medicine 2019 6 17 (1): 191. Du Wen, He Jing, Zhou Wei, Shu Simin, Li Juan, Liu Wei, Deng Yun, Lu Cong, Lin Shengyan, Ma Yaokun, He Yanli, Zheng Jine, Zhu Jiang, Bai Lijuan, Li Xiaoqing, Yao Junxia, Hu Dan, Gu Shengqing, Li Huiyu, Guo Anyuan, Huang Shiang, Feng Xiaolan, Hu Do |
Analytical and Potential Clinical Performance of Oncomine Myeloid Research Assay for Myeloid Neoplasms. Molecular diagnosis & therapy 2020 7 24 (5): 579-592. Park Joonhong, Kim Hoon Seok, Lee Jong-Mi, Jung Jin, Kang Dain, Choi Hayoung, Lee Gun Dong, Son Jungok, Park Silvia, Cho Byung-Sik, Kim Hee-Je, Kim Seongkoo, Lee Jae Wook, Chung Nack-Gyun, Cho Bin, Zhang Hua, Khazanov Nickolay A, Choi Jongpill, Jung Jae-Won, Kim Yonggoo, Kim Myungsh |
Prognosis of MECOM (EVI1)-rearranged MDS and AML patients rather depends on accompanying molecular mutations than on blast count. Leukemia & lymphoma 2020 3 61 (7): 1756-1759. Summerer Isolde, Haferlach Claudia, Meggendorfer Manja, Kern Wolfgang, Haferlach Torsten, Stengel An |
Integrated genomic profiling and modelling for risk stratification in patients with advanced oesophagogastric adenocarcinoma. Gut 2020 12 70 (11): 2055-2065. Hao Dapeng, He Siyuan, Harada Kazuto, Pizzi Melissa Pool, Lu Yang, Guan Pujun, Chen Lu, Wang Ruiping, Zhang Shaojun, Sewastjanow-Silva Matheus, Abdelhakeem Ahmed, Shanbhag Namita, Bhutani Manoop, Han Guangchun, Lee Jeffrey H, Zhao Shuangtao, Weston Brian, Blum Murphy Mariela, Waters Rebecca, Estrella Jeannelyn Santiano, Roy-Chowdhuri Sinchita, Gan Qiong, Lee Ju-Seog, Peng Guang, Hanash Samir M, Calin George Adrian, Song Xingzhi, Zhang Jianhua, Song Shumei, Wang Linghua, Ajani Jaffer |
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women.
Nature communications 2020 11 11 (1): 5976. Steinthorsdottir Valgerdur, McGinnis Ralph, Williams Nicholas O, Stefansdottir Lilja, Thorleifsson Gudmar, Shooter Scott, Fadista João, Sigurdsson Jon K, Auro Kirsi M, Berezina Galina, Borges Maria-Carolina, Bumpstead Suzannah, Bybjerg-Grauholm Jonas, Colgiu Irina, Dolby Vivien A, Dudbridge Frank, Engel Stephanie M, Franklin Christopher S, Frigge Michael L, Frisbaek Yr, Geirsson Reynir T, Geller Frank, Gretarsdottir Solveig, Gudbjartsson Daniel F, Harmon Quaker, Hougaard David Michael, Hegay Tatyana, Helgadottir Anna, Hjartardottir Sigrun, Jääskeläinen Tiina, Johannsdottir Hrefna, Jonsdottir Ingileif, Juliusdottir Thorhildur, Kalsheker Noor, Kasimov Abdumadjit, Kemp John P, Kivinen Katja, Klungsøyr Kari, Lee Wai K, Melbye Mads, Miedzybrodska Zosia, Moffett Ashley, Najmutdinova Dilbar, Nishanova Firuza, Olafsdottir Thorunn, Perola Markus, Pipkin Fiona Broughton, Poston Lucilla, Prescott Gordon, Saevarsdottir Saedis, Salimbayeva Damilya, Scaife Paula Juliet, Skotte Line, Staines-Urias Eleonora, Stefansson Olafur A, Sørensen Karina Meden, Thomsen Liv Cecilie Vestrheim, Tragante Vinicius, Trogstad Lill, Simpson Nigel A B, , , Aripova Tamara, Casas Juan P, Dominiczak Anna F, Walker James J, Thorsteinsdottir Unnur, Iversen Ann-Charlotte, Feenstra Bjarke, Lawlor Deborah A, Boyd Heather Allison, Magnus Per, Laivuori Hannele, Zakhidova Nodira, Svyatova Gulnara, Stefansson Kari, Morgan Lin |
Genome-Wide Gene-by-Smoking Interaction Study of Chronic Obstructive Pulmonary Disease.
American journal of epidemiology 2020 Oct . Kim Woori, Prokopenko Dmitry, Sakornsakolpat Phuwanat, Hobbs Brian D, Lutz Sharon M, Hokanson John E, Wain Louise V, Melbourne Carl A, Shrine Nick, Tobin Martin D, Silverman Edwin K, Cho Michael H, Beaty Terri |
Genome-wide association studies of antidepressant class response and treatment-resistant depression.
Translational psychiatry 2020 10 10 (1): 360. Li Qingqin S, Tian Chao, Hinds David, |
Sex-specific genetic factors affect the risk of early-onset periodontitis in Europeans.
Journal of clinical periodontology 2021 Aug . Freitag-Wolf Sandra, Munz Matthias, Junge Olaf, Graetz Christian, Jockel-Schneider Yvonne, Staufenbiel Ingmar, Bruckmann Corinna, Lieb Wolfgang, Franke Andre, Loos Bruno G, Jepsen Søren, Dommisch Henrik, Schaefer Arne |
Comparison of myeloid neoplasms with nonclassic 3q26.2/MECOM versus classic inv(3)/t(3;3) rearrangements reveals diverse clinicopathologic features, genetic profiles, and molecular mechanisms of MECOM activation. Genes, chromosomes & cancer 2021 10 61 (2): 71-80. Gao Juehua, Gurbuxani Sandeep, Zak Taylor, Kocherginsky Masha, Ji Peng, Wehbe Firas, Chen Qing, Chen Yi-Hua, Lu Xinyan, Jennings Lawrence, Frankfurt Olga, Altman Jessica, Sukhanova Madi |
High-resolution structural variant profiling of myelodysplastic syndromes by optical genome mapping uncovers cryptic aberrations of prognostic and therapeutic significance. Leukemia 2022 8 36 (9): 2306-2316. Yang Hui, Garcia-Manero Guillermo, Sasaki Koji, Montalban-Bravo Guillermo, Tang Zhenya, Wei Yue, Kadia Tapan, Chien Kelly, Rush Diana, Nguyen Ha, Kalia Awdesh, Nimmakayalu Manjunath, Bueso-Ramos Carlos, Kantarjian Hagop, Medeiros L Jeffrey, Luthra Rajyalakshmi, Kanagal-Shamanna Rash |
Clinical and Genomic Profiles of Korean Patients with MECOM Rearrangement and the t(3;21)(q26.2;q22.1) Translocation. Annals of laboratory medicine 2022 4 42 (5): 590-596. Lee Jikyo, Kim Sung Min, Kim Soonok, Yun Jiwon, Jeong Dajeong, Lee Young Eun, Roh Eun-Youn, Lee Dong So |
MECOM-related disorder: Radioulnar synostosis without hematological aberration due to unique variants. Genetics in medicine : official journal of the American College of Medical Genetics 2022 2 24 (5): 1139-1147. Shen Fang, Yang Yongjia, Zheng Yu, Li Pengcheng, Luo Zhenqing, Fu Yuyan, Zhu Guanghui, Mei Haibo, Chen Shanlin, Zhu Yim |
COL4A1/COL4A2 and inherited platelet disorder gene variants in fetuses showing intracranial hemorrhage. Prenatal diagnosis 2022 2 42 (5): 601-610. Coste Thibault, Vincent-Delorme Catherine, Stichelbout Morgane, Devisme Louise, Gelot Antoinette, Deryabin Igor, Pelluard Fanny, Aloui Chaker, Leutenegger Anne-Louise, Jouannic Jean-Marie, Héron Delphine, Gould Douglas B, Tournier-Lasserve Elisabe |
A family case series of inherited thrombocytopenia. Proceedings (Baylor University. Medical Center) 2022 12 36 (1): 93-95. Borkowski Artur, Gawry? Jakub, Iwanek Gracjan, Dybko Jaros? |
A signature of cuproptosis-related lncRNAs predicts prognosis and provides basis for future anti-tumor drug development in breast cancer. Translational cancer research 2023 7 12 (6): 1392-1410. Hao Yu, Yanbiao Liu, Wenrong Zhang, Ziqi Peng, Xinmiao Yu, Feng J |
Copy number variants landscape of multiple cancers and clinical applications based on NGS gene panel. Annals of medicine 2023 11 55 (2): 2280708. Kangpeng Yan, Li Niu, Boyu Wu, Chongwu He, Lei Deng, Chuan Chen, Zhangzhang Lan, Chao Lin, Weihua Kuang, Huihong Lin, Jun Zou, Wenyong Zhang, Zhiqiang L |
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- Page last updated:Apr 22, 2024
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