Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: TBX2[original query] |
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ERBB2, TBX2, RPS6KB1, and MYC alterations in breast tissues of BRCA1 and BRCA2 mutation carriers. Genes, chromosomes & cancer 2004 Sep 41 (1): 1-11. Adem Camilo, Soderberg Cheryl L, Hafner Kari, Reynolds Carol, Slezak Jeffrey M, Sinclair Colleen S, Sellers Thomas A, Schaid Daniel J, Couch Fergus, Hartmann Lynn C, Jenkins Robert |
Genetic variation in the chromosome 17q23 amplicon and breast cancer risk. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009 Jun 18 (6): 1864-8. Kelemen Linda E, Wang Xianshu, Fredericksen Zachary S, Pankratz V Shane, Pharoah Paul D P, Ahmed Shahana, Dunning Alison M, Easton Douglas F, Vierkant Robert A, Cerhan James R, Goode Ellen L, Olson Janet E, Couch Fergus |
Novel and functional sequence variants within the TBX2 gene promoter in ventricular septal defects. Biochimie 2013 Sep 95 (9): 1807-9. Pang Shuchao, Liu Yumei, Zhao Zhongqing, Huang Wenhui, Chen Dongfeng, Yan |
TBX4 mutations (small patella syndrome) are associated with childhood-onset pulmonary arterial hypertension. Journal of medical genetics 2013 Aug 50 (8): 500-6. Kerstjens-Frederikse Wilhelmina S, Bongers Ernie M H F, Roofthooft Marcus T R, Leter Edward M, Douwes J Menno, Van Dijk Arie, Vonk-Noordegraaf Anton, Dijk-Bos Krista K, Hoefsloot Lies H, Hoendermis Elke S, Gille Johan J P, Sikkema-Raddatz Birgit, Hofstra Robert M W, Berger Rolf M |
Associations between menarche-related genetic variants and pubertal growth in male and female adolescents. The Journal of adolescent health : official publication of the Society for Adolescent Medicine 2015 Jan 56 (1): 66-72. Tu Wanzhu, Wagner Erin K, Eckert George J, Yu Zhangsheng, Hannon Tamara, Pratt J Howard, He Chuny |
Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation.
Nature genetics 2015 Sep . Kato Norihiro, Loh Marie, Takeuchi Fumihiko, Verweij Niek, Wang Xu, Zhang Weihua, Kelly Tanika N, Saleheen Danish, Lehne Benjamin, Leach Irene Mateo, Drong Alexander W, Abbott James, Wahl Simone, Tan Sian-Tsung, Scott William R, Campanella Gianluca, Chadeau-Hyam Marc, Afzal Uzma, Ahluwalia Tarunveer S, Bonder Marc Jan, Chen Peng, Dehghan Abbas, Edwards Todd L, Esko Tõnu, Go Min Jin, Harris Sarah E, Hartiala Jaana, Kasela Silva, Kasturiratne Anuradhani, Khor Chiea-Chuen, Kleber Marcus E, Li Huaixing, Yu Mok Zuan, Nakatochi Masahiro, Sapari Nur Sabrina, Saxena Richa, Stewart Alexandre F R, Stolk Lisette, Tabara Yasuharu, Teh Ai Ling, Wu Ying, Wu Jer-Yuarn, Zhang Yi, Aits Imke, Da Silva Couto Alves Alexessander, Das Shikta, Dorajoo Rajkumar, Hopewell Jemma C, Kim Yun Kyoung, Koivula Robert W, Luan Jian'an, Lyytikäinen Leo-Pekka, Nguyen Quang N, Pereira Mark A, Postmus Iris, Raitakari Olli T, Scannell Bryan Molly, Scott Robert A, Sorice Rossella, Tragante Vinicius, Traglia Michela, White Jon, Yamamoto Ken, Zhang Yonghong, Adair Linda S, Ahmed Alauddin, Akiyama Koichi, Asif Rasheed, Aung Tin, Barroso Inês, Bjonnes Andrew, Braun Timothy R, Cai Hui, Chang Li-Ching, Chen Chien-Hsiun, Cheng Ching-Yu, Chong Yap-Seng, Collins Rory, Courtney Regina, Davies Gail, Delgado Graciela, Do Loi D, Doevendans Pieter A, Gansevoort Ron T, Gao Yu-Tang, Grammer Tanja B, Grarup Niels, Grewal Jagvir, Gu Dongfeng, Wander Gurpreet S, Hartikainen Anna-Liisa, Hazen Stanley L, He Jing, Heng Chew-Kiat, Hixson James E, Hofman Albert, Hsu Chris, Huang Wei, Husemoen Lise L N, Hwang Joo-Yeon, Ichihara Sahoko, Igase Michiya, Isono Masato, Justesen Johanne M, Katsuya Tomohiro, Kibriya Muhammad G, Kim Young Jin, Kishimoto Miyako, Koh Woon-Puay, Kohara Katsuhiko, Kumari Meena, Kwek Kenneth, Lee Nanette R, Lee Jeannette, Liao Jiemin, Lieb Wolfgang, Liewald David C M, Matsubara Tatsuaki, Matsushita Yumi, Meitinger Thomas, Mihailov Evelin, Milani Lili, Mills Rebecca, Mononen Nina, Müller-Nurasyid Martina, Nabika Toru, Nakashima Eitaro, Ng Hong Kiat, Nikus Kjell, Nutile Teresa, Ohkubo Takayoshi, Ohnaka Keizo, Parish Sarah, Paternoster Lavinia, Peng Hao, Peters Annette, Pham Son T, Pinidiyapathirage Mohitha J, Rahman Mahfuzar, Rakugi Hiromi, Rolandsson Olov, Ann Rozario Michelle, Ruggiero Daniela, Sala Cinzia F, Sarju Ralhan, Shimokawa Kazuro, Snieder Harold, Sparsø Thomas, Spiering Wilko, Starr John M, Stott David J, Stram Daniel O, Sugiyama Takao, Szymczak Silke, Tang W H Wilson, Tong Lin, Trompet Stella, Turjanmaa Väinö, Ueshima Hirotsugu, Uitterlinden André G, Umemura Satoshi, Vaarasmaki Marja, van Dam Rob M, van Gilst Wiek H, van Veldhuisen Dirk J, Viikari Jorma S, Waldenberger Melanie, Wang Yiqin, Wang Aili, Wilson Rory, Wong Tien-Yin, Xiang Yong-Bing, Yamaguchi Shuhei, Ye Xingwang, Young Robin D, Young Terri L, Yuan Jian-Min, Zhou Xueya, Asselbergs Folkert W, Ciullo Marina, Clarke Robert, Deloukas Panos, Franke Andre, Franks Paul W, Franks Steve, Friedlander Yechiel, Gross Myron D, Guo Zhirong, Hansen Torben, Jarvelin Marjo-Riitta, Jørgensen Torben, Jukema J Wouter, Kähönen Mika, Kajio Hiroshi, Kivimaki Mika, Lee Jong-Young, Lehtimäki Terho, Linneberg Allan, Miki Tetsuro, Pedersen Oluf, Samani Nilesh J, Sørensen Thorkild I A, Takayanagi Ryoichi, Toniolo Daniela, , , , , Ahsan Habibul, Allayee Hooman, Chen Yuan-Tsong, Danesh John, Deary Ian J, Franco Oscar H, Franke Lude, Heijman Bastiaan T, Holbrook Joanna D, Isaacs Aaron, Kim Bong-Jo, Lin Xu, Liu Jianjun, März Winfried, Metspalu Andres, Mohlke Karen L, Sanghera Dharambir K, Shu Xiao-Ou, van Meurs Joyce B J, Vithana Eranga, Wickremasinghe Ananda R, Wijmenga Cisca, Wolffenbuttel Bruce H W, Yokota Mitsuhiro, Zheng Wei, Zhu Dingliang, Vineis Paolo, Kyrtopoulos Soterios A, Kleinjans Jos C S, McCarthy Mark I, Soong Richie, Gieger Christian, Scott James, Teo Yik-Ying, He Jiang, Elliott Paul, Tai E Shyong, van der Harst Pim, Kooner Jaspal S, Chambers John |
Genome-wide Analysis of Body Proportion Classifies Height-Associated Variants by Mechanism of Action and Implicates Genes Important for Skeletal Development.
American journal of human genetics 2015 May 96 (5): 695-708. Chan Yingleong, Salem Rany M, Hsu Yu-Han H, McMahon George, Pers Tune H, Vedantam Sailaja, Esko Tonu, Guo Michael H, Lim Elaine T, , Franke Lude, Smith George Davey, Strachan David P, Hirschhorn Joel |
Rare copy number variants implicated in posterior urethral valves. American journal of medical genetics. Part A 2015 Dec . Boghossian Nansi S, Sicko Robert J, Kay Denise M, Rigler Shannon L, Caggana Michele, Tsai Michael Y, Yeung Edwina H, Pankratz Nathan, Cole Benjamin R, Druschel Charlotte M, Romitti Paul A, Browne Marilyn L, Fan Ruzong, Liu Aiyi, Brody Lawrence C, Mills James |
Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3' untranslated region in the Han Chinese population. Pediatric research 2018 Sep . Wang Jie, Zhang Ran-Ran, Cai Ke, Yang Qian, Duan Wen-Yuan, Zhao Jian-Yuan, Gui Yong-Hao, Wang Fe |
HIRA directly targets the enhancers of selected cardiac transcription factors during in vitro differentiation of mouse embryonic stem cells. Molecular biology reports 2018 7 45 (5): 1001-1011. Saleh Rasha Noureldin M, Dilg Daniel, Abou Zeid Abla A, Hashad Doaa I, Scambler Peter J, Chapgier Ariane L |
Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations.
PloS one 2018 13 (3): e0194044. Lee Jeonghwan, Lee Young, Park Boram, Won Sungho, Han Jin Suk, Heo Nam |
A regulatory variant in TBX2 promoter is related to the decreased susceptibility of congenital heart disease in the Han Chinese population. Molecular genetics & genomic medicine 2019 02 7 (2): e00530. Zhang Ran-Ran, Cai Ke, Liu Lian, Yang Qian, Zhang Ping, Gui Yong-Hao, Wang Fe |
Insights Figure for ''Susceptibility to congenital heart defects associated with a polymorphism in TBX2 3' untranslated region in the Han Chinese population''. Pediatric research 2019 Feb 85 (3): 255. Wang Fe |
ASCL1 is a MYCN- and LMO1-dependent member of the adrenergic neuroblastoma core regulatory circuitry. Nature communications 2019 12 10 (1): 5622. Wang Lu, Tan Tze King, Durbin Adam D, Zimmerman Mark W, Abraham Brian J, Tan Shi Hao, Ngoc Phuong Cao Thi, Weichert-Leahey Nina, Akahane Koshi, Lawton Lee N, Rokita Jo Lynne, Maris John M, Young Richard A, Look A Thomas, Sanda Takao |
Size matters: Large copy number losses in Hirschsprung disease patients reveal genes involved in enteric nervous system development. PLoS genetics 2021 8 17 (8): e1009698. Kuil Laura E, MacKenzie Katherine C, Tang Clara S, Windster Jonathan D, Le Thuy Linh, Karim Anwarul, de Graaf Bianca M, van der Helm Robert, van Bever Yolande, Sloots Cornelius E J, Meeussen Conny, Tibboel Dick, de Klein Annelies, Wijnen René M H, Amiel Jeanne, Lyonnet Stanislas, Garcia-Barcelo Maria-Mercè, Tam Paul K H, Alves Maria M, Brooks Alice S, Hofstra Robert M W, Brosens Erw |
Clinical and Genetic Characteristics of Preeclampsia. Archives of Razi Institute 2022 02 77 (1): 293-299. Golovchenko O V, Abramova M Y, Orlova V S, Batlutskaya I V, Sorokina I |
Polymorphisms of hypertension susceptibility genes as a risk factors of preeclampsia in the Caucasian population of central Russia. Placenta 2022 Sep 129 51-61. Churnosov Mikhail, Abramova Maria, Reshetnikov Evgeny, Lyashenko Igor V, Efremova Olesya, Churnosova Maria, Ponomarenko Iri |
Association of T-box gene polymorphisms with the risk of Wolff-Parkinson-White syndrome in a Han Chinese population. Medicine 2022 Aug 101 (32): e30046. Han Bing, Wang Yongxiang, Zhao Jing, Lan Qingsu, Zhang Jin, Meng Xiaoxue, Jin Jianjian, Bai Ming, Zhang Zhe |
Analysis of pathogenic variants in 605 Chinese children with non-syndromic cardiac conotruncal defects based on targeted sequencing. Genomics 2023 7 115 (5): 110676. JiaJun Ye, Yiwei Niu, Yongxuan Peng, Jihong Huang, Huiying Wang, Qihua Fu, Fen Li, Rang Xu, Sun Chen, Yuejuan Xu, Kun S |
Risk Effects of rs1799945 Polymorphism of the HFE Gene and Intergenic Interactions of GWAS-Significant Loci for Arterial Hypertension in the Caucasian Population of Central Russia. International journal of molecular sciences 2023 5 24 (9): . Tatiana Ivanova, Maria Churnosova, Maria Abramova, Irina Ponomarenko, Evgeny Reshetnikov, Inna Aristova, Inna Sorokina, Mikhail Churnos |
Sex-Specific Features of the Correlation between GWAS-Noticeable Polymorphisms and Hypertension in Europeans of Russia. International journal of molecular sciences 2023 5 24 (9): . Tatiana Ivanova, Maria Churnosova, Maria Abramova, Denis Plotnikov, Irina Ponomarenko, Evgeny Reshetnikov, Inna Aristova, Inna Sorokina, Mikhail Churnos |
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