Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: HOXA[original query] |
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High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009 Dec 24 (12): 2039-49. Yerges Laura M, Klei Lambertus, Cauley Jane A, Roeder Kathryn, Kammerer Candace M, Moffett Susan P, Ensrud Kristine E, Nestlerode Cara S, Marshall Lynn M, Hoffman Andrew R, Lewis Cora, Lang Thomas F, Barrett-Connor Elizabeth, Ferrell Robert E, Orwoll Eric S, Zmuda Joseph M, |
Altered transmission of HOX and apoptotic SNPs identify a potential common pathway for clubfoot. American journal of medical genetics. Part A 2009 Dec 149A (12): 2745-52. Ester Audrey R, Weymouth Katelyn S, Burt Amber, Wise Carol A, Scott Allison, Gurnett Christina A, Dobbs Matthew B, Blanton Susan H, Hecht Jacqueline |
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations.
American journal of human genetics 2013 Sep 93 (3): 545-54. Franceschini Nora, Fox Ervin, Zhang Zhaogong, Edwards Todd L, Nalls Michael A, Sung Yun Ju, Tayo Bamidele O, Sun Yan V, Gottesman Omri, Adeyemo Adebawole, Johnson Andrew D, Young J Hunter, Rice Ken, Duan Qing, Chen Fang, Li Yun, Tang Hua, Fornage Myriam, Keene Keith L, Andrews Jeanette S, Smith Jennifer A, Faul Jessica D, Guangfa Zhang, Guo Wei, Liu Yu, Murray Sarah S, Musani Solomon K, Srinivasan Sathanur, Velez Edwards Digna R, Wang Heming, Becker Lewis C, Bovet Pascal, Bochud Murielle, Broeckel Ulrich, Burnier Michel, Carty Cara, Chasman Daniel I, Ehret Georg, Chen Wei-Min, Chen Guanjie, Chen Wei, Ding Jingzhong, Dreisbach Albert W, Evans Michele K, Guo Xiuqing, Garcia Melissa E, Jensen Rich, Keller Margaux F, Lettre Guillaume, Lotay Vaneet, Martin Lisa W, Moore Jason H, Morrison Alanna C, Mosley Thomas H, Ogunniyi Adesola, Palmas Walter, Papanicolaou George, Penman Alan, Polak Joseph F, Ridker Paul M, Salako Babatunde, Singleton Andrew B, Shriner Daniel, Taylor Kent D, Vasan Ramachandran, Wiggins Kerri, Williams Scott M, Yanek Lisa R, Zhao Wei, Zonderman Alan B, Becker Diane M, Berenson Gerald, Boerwinkle Eric, Bottinger Erwin, Cushman Mary, Eaton Charles, Nyberg Fredrik, Heiss Gerardo, Hirschhron Joel N, Howard Virginia J, Karczewsk Konrad J, Lanktree Matthew B, Liu Kiang, Liu Yongmei, Loos Ruth, Margolis Karen, Snyder Michael, , Psaty Bruce M, Schork Nicholas J, Weir David R, Rotimi Charles N, Sale Michele M, Harris Tamara, Kardia Sharon L R, Hunt Steven C, Arnett Donna, Redline Susan, Cooper Richard S, Risch Neil J, Rao D C, Rotter Jerome I, Chakravarti Aravinda, Reiner Alex P, Levy Daniel, Keating Brendan J, Zhu Xiaofe |
Genome-wide copy number variation analysis of a Branchio-oto-renal syndrome cohort identifies a recombination hotspot and implicates new candidate genes. Human genetics 2013 Dec 132 (12): 1339-50. Brophy Patrick D, Alasti Fatemeh, Darbro Benjamin W, Clarke Jason, Nishimura Carla, Cobb Bryan, Smith Richard J, Manak J Robe |
Linking genomic lesions with minimal residual disease improves prognostic stratification in children with T-cell acute lymphoblastic leukaemia. Leukemia research 2013 Aug 37 (8): 928-35. La Starza Roberta, Lettieri Antonella, Pierini Valentina, Nofrini Valeria, Gorello Paolo, Songia Simona, Crescenzi Barbara, Te Kronnie Geertruy, Giordan Marco, Leszl Anna, Valsecchi Maria Grazia, Aversa Franco, Basso Giuseppe, Biondi Andrea, Conter Valentino, Cazzaniga Giovanni, Mecucci Cristi |
Mutation screening of HOXA7 and HOXA9 genes in Chinese women with Müllerian duct abnormalities. Reproductive biomedicine online 2014 Nov 29 (5): 595-9. Chen Xinxia, Mu Yulan, Li Chunyan, Li Guangyu, Zhao Hui, Qin Yingying, Chen Zi-Jia |
IDH1 p.R132 mutations may not be actively involved in the carcinogenesis of hepatocellular carcinoma. Medical science monitor : international medical journal of experimental and clinical research 2014 20 247-54. Lu Jun, Xu Ling, Zou Yang, Yang Run-Xiang, Fan Yu, Zhang Wen, Yu Dandan, Yao Yong-Ga |
Meta-analysis of correlated traits via summary statistics from GWASs with an application in hypertension. American journal of human genetics 2015 Jan 96 (1): 21-36. Zhu Xiaofeng, Feng Tao, Tayo Bamidele O, Liang Jingjing, Young J Hunter, Franceschini Nora, Smith Jennifer A, Yanek Lisa R, Sun Yan V, Edwards Todd L, Chen Wei, Nalls Mike, Fox Ervin, Sale Michele, Bottinger Erwin, Rotimi Charles, , Liu Yongmei, McKnight Barbara, Liu Kiang, Arnett Donna K, Chakravati Aravinda, Cooper Richard S, Redline Sus |
A functional variant in HOXA11-AS, a novel long non-coding RNA, inhibits the oncogenic phenotype of epithelial ovarian cancer. Oncotarget 2015 Sep . Richards Edward J, Permuth-Wey Jennifer, Li Yajuan, Chen Y Ann, Coppola Domenico, Reid Brett M, Lin Hui-Yi, Teer Jamie K, Berchuck Andrew, Birrer Michael J, Lawrenson Kate, Monteiro Alvaro N A, Schildkraut Joellen M, Goode Ellen L, Gayther Simon A, Sellers Thomas A, Cheng Jin |
DNA methylation analysis of Homeobox genes implicates HOXB7 hypomethylation as risk factor for neural tube defects. Epigenetics 2015 10 (1): 92-101. Rochtus Anne, Izzi Benedetta, Vangeel Elise, Louwette Sophie, Wittevrongel Christine, Lambrechts Diether, Moreau Yves, Winand Raf, Verpoorten Carla, Jansen Katrien, Van Geet Chris, Freson Kathle |
Deletions of the long arm of chromosome 5 define subgroups of T-cell acute lymphoblastic leukemia. Haematologica 2016 May . La Starza Roberta, Barba Gianluca, Demeyer Sofie, Pierini Valentina, Di Giacomo Danika, Gianfelici Valentina, Schwab Claire, Matteucci Caterina, Vicente Carmen, Cools Jan, Messina Monica, Crescenzi Barbara, Chiaretti Sabina, Foa' Robin, Basso Giuseppe, Harrison Christine J, Mecucci Cristi |
Variant Discovery and Fine Mapping of Genetic Loci Associated with Blood Pressure Traits in Hispanics and African Americans.
PloS one 2016 11 (10): e0164132. Franceschini Nora, Carty Cara L, Lu Yingchang, Tao Ran, Sung Yun Ju, Manichaikul Ani, Haessler Jeff, Fornage Myriam, Schwander Karen, Zubair Niha, Bien Stephanie, Hindorff Lucia A, Guo Xiuqing, Bielinski Suzette J, Ehret Georg, Kaufman Joel D, Rich Stephen S, Carlson Christopher S, Bottinger Erwin P, North Kari E, Rao D C, Chakravarti Aravinda, Barrett Paula Q, Loos Ruth J F, Buyske Steven, Kooperberg Charl |
Association of well-characterized lung cancer lncRNA polymorphisms with lung cancer susceptibility and platinum-based chemotherapy response. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2016 Jun 37 (6): 8349-58. Gong Wei-Jing, Yin Ji-Ye, Li Xiang-Ping, Fang Chao, Xiao Di, Zhang Wei, Zhou Hong-Hao, Li Xi, Liu Zhao-Qi |
Molecular synergy underlies the co-occurrence patterns and phenotype of NPM1-mutant acute myeloid leukemia. Blood 2017 8 130 (17): 1911-1922. Dovey Oliver M, Cooper Jonathan L, Mupo Annalisa, Grove Carolyn S, Lynn Claire, Conte Nathalie, Andrews Robert M, Pacharne Suruchi, Tzelepis Konstantinos, Vijayabaskar M S, Green Paul, Rad Roland, Arends Mark, Wright Penny, Yusa Kosuke, Bradley Allan, Varela Ignacio, Vassiliou George |
Association between long non-coding RNA polymorphisms and cancer risk: a meta-analysis. Bioscience reports 2018 May . Huang Xin, Zhang Weiyue, Shao Zeng |
Four novel polymorphisms in long non-coding RNA HOTTIP are associated with the risk and prognosis of colorectal cancer. Bioscience reports 2019 Apr . Lv Zhi, Xu Qian, Sun Liping, Wen Jing, Fang Xinxin, Xing Chengzhong, Yuan Yu |
Genome-wide association study of germline variants and breast cancer-specific mortality.
British journal of cancer 2019 Mar 120 (6): 647-657. Escala-Garcia Maria, Guo Qi, Dörk Thilo, Canisius Sander, Keeman Renske, Dennis Joe, Beesley Jonathan, Lecarpentier Julie, Bolla Manjeet K, Wang Qin, Abraham Jean, Andrulis Irene L, Anton-Culver Hoda, Arndt Volker, Auer Paul L, Beckmann Matthias W, Behrens Sabine, Benitez Javier, Bermisheva Marina, Bernstein Leslie, Blomqvist Carl, Boeckx Bram, Bojesen Stig E, Bonanni Bernardo, Børresen-Dale Anne-Lise, Brauch Hiltrud, Brenner Hermann, Brentnall Adam, Brinton Louise, Broberg Per, Brock Ian W, Brucker Sara Y, Burwinkel Barbara, Caldas Carlos, Caldés Trinidad, Campa Daniele, Canzian Federico, Carracedo Angel, Carter Brian D, Castelao Jose E, Chang-Claude Jenny, Chanock Stephen J, Chenevix-Trench Georgia, Cheng Ting-Yuan David, Chin Suet-Feung, Clarke Christine L, , Cordina-Duverger Emilie, Couch Fergus J, Cox David G, Cox Angela, Cross Simon S, Czene Kamila, Daly Mary B, Devilee Peter, Dunn Janet A, Dunning Alison M, Durcan Lorraine, Dwek Miriam, Earl Helena M, Ekici Arif B, Eliassen A Heather, Ellberg Carolina, Engel Christoph, Eriksson Mikael, Evans D Gareth, Figueroa Jonine, Flesch-Janys Dieter, Flyger Henrik, Gabrielson Marike, Gago-Dominguez Manuela, Galle Eva, Gapstur Susan M, García-Closas Montserrat, García-Sáenz José A, Gaudet Mia M, George Angela, Georgoulias Vassilios, Giles Graham G, Glendon Gord, Goldgar David E, González-Neira Anna, Alnæs Grethe I Grenaker, Grip Mervi, Guénel Pascal, Haeberle Lothar, Hahnen Eric, Haiman Christopher A, Håkansson Niclas, Hall Per, Hamann Ute, Hankinson Susan, Harkness Elaine F, Harrington Patricia A, Hart Steven N, Hartikainen Jaana M, Hein Alexander, Hillemanns Peter, Hiller Louise, Holleczek Bernd, Hollestelle Antoinette, Hooning Maartje J, Hoover Robert N, Hopper John L, Howell Anthony, Huang Guanmengqian, Humphreys Keith, Hunter David J, Janni Wolfgang, John Esther M, Jones Michael E, Jukkola-Vuorinen Arja, Jung Audrey, Kaaks Rudolf, Kabisch Maria, Kaczmarek Katarzyna, Kerin Michael J, Khan Sofia, Khusnutdinova Elza, Kiiski Johanna I, Kitahara Cari M, Knight Julia A, Ko Yon-Dschun, Koppert Linetta B, Kosma Veli-Matti, Kraft Peter, Kristensen Vessela N, Krüger Ute, Kühl Tabea, Lambrechts Diether, Le Marchand Loic, Lee Eunjung, Lejbkowicz Flavio, Li Lian, Lindblom Annika, Lindström Sara, Linet Martha, Lissowska Jolanta, Lo Wing-Yee, Loibl Sibylle, Lubinski Jan, Lux Michael P, MacInnis Robert J, Maierthaler Melanie, Maishman Tom, Makalic Enes, Mannermaa Arto, Manoochehri Mehdi, Manoukian Siranoush, Margolin Sara, Martinez Maria Elena, Mavroudis Dimitrios, McLean Catriona, Meindl Alfons, Middha Pooja, Miller Nicola, Milne Roger L, Moreno Fernando, Mulligan Anna Marie, Mulot Claire, Nassir Rami, Neuhausen Susan L, Newman William T, Nielsen Sune F, Nordestgaard Børge G, Norman Aaron, Olsson Håkan, Orr Nick, Pankratz V Shane, Park-Simon Tjoung-Won, Perez Jose I A, Pérez-Barrios Clara, Peterlongo Paolo, Petridis Christos, Pinchev Mila, Prajzendanc Karoliona, Prentice Ross, Presneau Nadege, Prokofieva Darya, Pylkäs Katri, Rack Brigitte, Radice Paolo, Ramachandran Dhanya, Rennert Gadi, Rennert Hedy S, Rhenius Valerie, Romero Atocha, Roylance Rebecca, Saloustros Emmanouil, Sawyer Elinor J, Schmidt Daniel F, Schmutzler Rita K, Schneeweiss Andreas, Schoemaker Minouk J, Schumacher Fredrick, Schwentner Lukas, Scott Rodney J, Scott Christopher, Seynaeve Caroline, Shah Mitul, Simard Jacques, Smeets Ann, Sohn Christof, Southey Melissa C, Swerdlow Anthony J, Talhouk Aline, Tamimi Rulla M, Tapper William J, Teixeira Manuel R, Tengström Maria, Terry Mary Beth, Thöne Kathrin, Tollenaar Rob A E M, Tomlinson Ian, Torres Diana, Truong Thérèse, Turman Constance, Turnbull Clare, Ulmer Hans-Ulrich, Untch Michael, Vachon Celine, van Asperen Christi J, van den Ouweland Ans M W, van Veen Elke M, Wendt Camilla, Whittemore Alice S, Willett Walter, Winqvist Robert, Wolk Alicja, Yang Xiaohong R, Zhang Yan, Easton Douglas F, Fasching Peter A, Nevanlinna Heli, Eccles Diana M, Pharoah Paul D P, Schmidt Marjanka |
Unraveling the cellular origin and clinical prognostic markers of infant B-cell acute lymphoblastic leukemia using genome-wide analysis. Haematologica 2019 1 104 (6): 1176-1188. Agraz-Doblas Antonio, Bueno Clara, Bashford-Rogers Rachael, Roy Anindita, Schneider Pauline, Bardini Michela, Ballerini Paola, Cazzaniga Gianni, Moreno Thaidy, Revilla Carlos, Gut Marta, Valsecchi Maria G, Roberts Irene, Pieters Rob, De Lorenzo Paola, Varela Ignacio, Menendez Pablo, Stam Ronald |
The Influence of rs1859168 Polymorphism on Serum Expression of HOTTIP and Its Target miR-615-3p in Egyptian Patients with Breast Cancer. Biomolecules 2021 May 11 (5): . Abdelaleem Omayma O, Shaker Olfat G, AbdelHafez Marwa N, Abdelghaffar Noha K, Eid Hanaa M, Zaidan Mohamed, Khalefa Abeer A, Ahmed Naglaa A, Hemeda Nada F, Zaki Othman M, Awaji Aeshah Ali A, Mohammed Shereen |
Association of Genetic Polymorphisms in Long Noncoding RNA HOTTIP with Risk of Idiopathic Recurrent Spontaneous Abortion. Biochemical genetics 2023 12 . Shekoufeh Mirinejad, Saeedeh Salimi, Saman Sargazi, Milad Heidari Nia, Roghayeh Sheervalilou, Mahdi Majidpour, Mahdiyeh Harati-Sadegh, Mohammad Sarhadi, Sheida Shahraki, Marzieh Ghase |
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- Page last updated:Apr 22, 2024
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