Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: HOXB[original query] |
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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 |
Increased copy number of the DLX4 homeobox gene in breast axillary lymph node metastasis. Cancer genetics 2014 May 207 (5): 177-87. Torresan Clarissa, Oliveira Márcia M C, Pereira Silma R F, Ribeiro Enilze M S F, Marian Catalin, Gusev Yuriy, Lima Rubens S, Urban Cicero A, Berg Patricia E, Haddad Bassem R, Cavalli Iglenir J, Cavalli Luciane |
The role of polymorphisms associated with early tooth eruption in dental and occlusal traits in East Asian populations. Korean journal of orthodontics 2014 Mar 44 (2): 96-102. Yamaguchi Tetsutaro, Kawaguchi Akira, Kim Yong-Il, Haga Shugo, Katayama Koshu, Ishida Hajime, Park Soo-Byung, Maki Koutaro, Kimura Ryosu |
Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer. PLoS genetics 2014 Feb 10 (2): e1004129. Saunders Edward J, Dadaev Tokhir, Leongamornlert Daniel A, Jugurnauth-Little Sarah, Tymrakiewicz Malgorzata, Wiklund Fredrik, Al Olama Ali Amin, Benlloch Sara, Neal David E, Hamdy Freddie C, Donovan Jenny L, Giles Graham G, Severi Gianluca, Gronberg Henrik, Aly Markus, Haiman Christopher A, Schumacher Fredrick, Henderson Brian E, Lindstrom Sara, Kraft Peter, Hunter David J, Gapstur Susan, Chanock Stephen, Berndt Sonja I, Albanes Demetrius, Andriole Gerald, Schleutker Johanna, Weischer Maren, Nordestgaard Børge G, Canzian Federico, Campa Daniele, Riboli Elio, Key Tim J, Travis Ruth C, Ingles Sue A, John Esther M, Hayes Richard B, Pharoah Paul, Khaw Kay-Tee, Stanford Janet L, Ostrander Elaine A, Signorello Lisa B, Thibodeau Stephen N, Schaid Daniel, Maier Christiane, Kibel Adam S, Cybulski Cezary, Cannon-Albright Lisa, Brenner Hermann, Park Jong Y, Kaneva Radka, Batra Jyotsna, Clements Judith A, Teixeira Manuel R, Xu Jianfeng, Mikropoulos Christos, Goh Chee, Govindasami Koveela, Guy Michelle, Wilkinson Rosemary A, Sawyer Emma J, Morgan Angela, , , , , Easton Douglas F, Muir Ken, Eeles Rosalind A, Kote-Jarai Zsof |
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 |
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis.
The Lancet. Neurology 2017 Nov 16 (11): 898-907. Schormair Barbara, Zhao Chen, Bell Steven, Tilch Erik, Salminen Aaro V, Pütz Benno, Dauvilliers Yves, Stefani Ambra, Högl Birgit, Poewe Werner, Kemlink David, Sonka Karel, Bachmann Cornelius G, Paulus Walter, Trenkwalder Claudia, Oertel Wolfgang H, Hornyak Magdolna, Teder-Laving Maris, Metspalu Andres, Hadjigeorgiou Georgios M, Polo Olli, Fietze Ingo, Ross Owen A, Wszolek Zbigniew, Butterworth Adam S, Soranzo Nicole, Ouwehand Willem H, Roberts David J, Danesh John, Allen Richard P, Earley Christopher J, Ondo William G, Xiong Lan, Montplaisir Jacques, Gan-Or Ziv, Perola Markus, Vodicka Pavel, Dina Christian, Franke Andre, Tittmann Lukas, Stewart Alexandre F R, Shah Svati H, Gieger Christian, Peters Annette, Rouleau Guy A, Berger Klaus, Oexle Konrad, Di Angelantonio Emanuele, Hinds David A, Müller-Myhsok Bertram, Winkelmann Juliane, , |
Lung cancer susceptibility genetic variants modulate HOXB2 expression in the lung. The International journal of developmental biology 2019 1 62 (11-12): 857-864. Clemenceau Alisson, Boucherat Olivier, Landry-Truchon Kim, Lamontagne Maxime, Biardel Sabrina, Joubert Philippe, Gobeil Stéphane, Secco Blandine, Laplante Mathieu, Morissette Mathieu, Obeidat Ma'en, Timens Wim, Jeannotte Lucie, Bossé Yoh |
Prostate cancer risk variants of the HOXB genetic locus. Scientific reports 2021 May 11 (1): 11385. Dupont William D, Breyer Joan P, Johnson Spenser H, Plummer W Dale, Smith Jeffrey |
Determinants of Lung Fissure Completeness. American journal of respiratory and critical care medicine 2021 6 204 (7): 807-816. van der Molen Marieke C, Hartman Jorine E, Vermeulen Cornelis J, van den Berge Maarten, Faiz Alen, Kerstjens Huib A M, Charbonnier Jean-Paul, Vanfleteren Lowie E G W, Slebos Dirk-J |
Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases. Frontiers in genetics 2023 4 14 1164274. Zhu Xiaobo, Zou Yixin, Jia Linna, Ye Xiangyu, Zou Yanzheng, Tu Junlan, Li Juntong, Yu Rongbin, Yang Sheng, Huang Pe |
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- Page last updated:Mar 25, 2024
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