Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 40 Records) |
| Query Trace: PRDM16[original query] |
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Identification of three novel genetic variations associated with electrocardiographic traits (QRS duration and PR interval) in East Asians.
Human molecular genetics 2014 Dec 23 (24): 6659-67. Hong Kyung-Won, Lim Ji Eun, Kim Jong Wook, Tabara Yasuharu, Ueshima Hirotsugu, Miki Tetsuro, Matsuda Fumihiko, Cho Yoon Shin, Kim Yeonjung, Oh Bermse |
| Large-scale analysis reveals a functional single-nucleotide polymorphism in the 5'-flanking region of PRDM16 gene associated with lean body mass. Aging cell 2014 Aug 13 (4): 739-43. Urano Tomohiko, Shiraki Masataka, Sasaki Noriko, Ouchi Yasuyoshi, Inoue Satos |
| Replication study of previous migraine genome-wide association study findings in a Spanish sample of migraine with aura. Cephalalgia : an international journal of headache 2015 Aug 35 (9): 776-82. Sintas Cèlia, Fernández-Morales Jèssica, Vila-Pueyo Marta, Narberhaus Bernat, Arenas Concepció, Pozo-Rosich Patricia, Macaya Alfons, Cormand B |
| Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology.
PLoS genetics 2016 Aug 12 (8): e1006149. Shaffer John R, Orlova Ekaterina, Lee Myoung Keun, Leslie Elizabeth J, Raffensperger Zachary D, Heike Carrie L, Cunningham Michael L, Hecht Jacqueline T, Kau Chung How, Nidey Nichole L, Moreno Lina M, Wehby George L, Murray Jeffrey C, Laurie Cecelia A, Laurie Cathy C, Cole Joanne, Ferrara Tracey, Santorico Stephanie, Klein Ophir, Mio Washington, Feingold Eleanor, Hallgrimsson Benedikt, Spritz Richard A, Marazita Mary L, Weinberg Seth |
| PPARGC1? gene DNA methylation variations in human placenta mediate the link between maternal hyperglycemia and leptin levels in newborns. Clinical epigenetics 2016 8 72. Côté Sandra, Gagné-Ouellet Valérie, Guay Simon-Pierre, Allard Catherine, Houde Andrée-Anne, Perron Patrice, Baillargeon Jean-Patrice, Gaudet Daniel, Guérin Renée, Brisson Diane, Hivert Marie-France, Bouchard Lui |
| An adaptive variant of TRIB2, rs1057001, is associated with higher expression levels of thermogenic genes in human subcutaneous and visceral adipose tissues. Journal of physiological anthropology 2017 Feb 36 (1): 16. Nakayama Kazuhiro, Iwamoto Sadahi |
| Multilocus analysis reveals three candidate genes for Chinese migraine susceptibility. Clinical genetics 2017 Jan . An X-K, Fang J, Yu Z-Z, Lin Q, Lu C-X, Qu H-L, Ma Q |
| Detection of genetic alterations in gastric cancer patients from Saudi Arabia using comparative genomic hybridization (CGH). PloS one 2018 9 13 (9): e0202576. Bibi Fehmida, Ali Isse, Naseer Muhammad Imran, Ali Mohamoud Hussein Sheikh, Yasir Muhammad, Alvi Sana Akhtar, Jiman-Fatani Asif Ahmed, Sawan Ali, Azhar Esam Ibrahe |
| PRDM16 Gene Polymorphism Is Associated with Obesity and Blood Lipids Profiles in Saudi Population. Journal of clinical medicine 2018 Jun 7 (6): . AlAmrani Aishah, AbdelKarim Mouaadh, AlZoghaibi Mohamm |
| [Associations among PRDM16 polymorphisms, environmental exposure factors during mother's pregnancy, and nonsyndromic cleft lip with or without cleft palate]. Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology 2018 Oct 36 (5): 503-507. Yin Bin, Shi Bing, Jia Zhong-L |
| Implications for the migraine SNP rs1835740 in a Swedish cluster headache population. The journal of headache and pain 2018 Nov 19 (1): 100. Ran Caroline, Fourier Carmen, Zinnegger Margret, Steinberg Anna, Sjöstrand Christina, Waldenlind Elisabet, Belin Andrea Carmi |
| Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort.
Journal of autoimmunity 2018 Jan . Sharma Ashok, Liu Xiang, Hadley David, Hagopian William, Chen Wei-Min, Onengut-Gumuscu Suna, Törn Carina, Steck Andrea K, Frohnert Brigitte I, Rewers Marian, Ziegler Anette-G, Lernmark Åke, Toppari Jorma, Krischer Jeffrey P, Akolkar Beena, Rich Stephen S, She Jin-Xiong, |
| Association of rs2651899 Polymorphism in the Positive Regulatory Domain 16 and Common Migraine Subtypes: A Meta-Analysis. Headache 2019 Sep . Lee Hsun-Hua, Chen Chih-Chung, Ong Jiann-Ruey, Lin Yuan-Feng, Lee Fei-Peng, Hu Chaur-Jong, Wang Yuan-Hu |
| Association between PRDM16, MEF2D, TRPM8, LRP1 gene polymorphisms and migraine susceptibility in the She ethnic population in China. Clinical and investigative medicine. Medecine clinique et experimentale 2019 Mar 42 (1): E21-E30. Fu Xianguo, Yang Jing, Wu Xiaoyang, Lin Qifang, Zeng Yuli, Xia Qiaoqing, Cao Luoyuan, Huang Baoying, Huang Genb |
| Editors' Note to: EDAR, LYPLAL1, PRDM16, PAX3, DKK1, TNFSF12, CACNA2D3, and SUPT3H gene variants influence facial morphology in a Eurasian population. Human genetics 2019 Dec . Authors are not available |
| rs2651899 variant is associated with risk for migraine without aura from North Indian population. Molecular biology reports 2019 Jan . Kaur Sukhvinder, Ali Arif, Ahmad Uzair, Pandey A K, Singh Balkir |
| High PRDM16 expression predicts poor outcomes in adult acute myeloid leukemia patients with intermediate cytogenetic risk: a comprehensive cohort study from a single Chinese center. Leukemia & lymphoma 2020 9 62 (1): 185-193. Dao Feng-Ting, Chen Wen-Min, Long Ling-Yu, Li Ling-Di, Yang Lu, Wang Jun, Liu Yan-Rong, Jiang Hao, Zhang Xiao-Hui, Jiang Qian, Qin Ya-Zh |
| Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation. American journal of medical genetics. Part A 2020 4 182 (6): 1387-1399. Coban-Akdemir Zeynep H, Charng Wu-Lin, Azamian Mahshid, Paine Ingrid S, Punetha Jaya, Grochowski Christopher M, Gambin Tomasz, Valdes Santiago O, Cannon Bryan, Zapata Gladys, Hernandez Patricia P, Jhangiani Shalini, Doddapaneni Harsha, Hu Jianhong, Boricha Fatima, Muzny Donna M, Boerwinkle Eric, Yang Yaping, Gibbs Richard A, Posey Jennifer E, Wehrens Xander H T, Belmont John W, Kim Jeffrey J, Miyake Christina Y, Lupski James R, Lalani Seema |
| PRDM16, LRP1 and TRPM8 genetic polymorphisms are risk factor for Pakistani migraine patients. Saudi journal of biological sciences 2021 Oct 28 (10): 5793-5799. Zafar R, Saleem T, Sheikh N, Maqbool H, Mukhtar M, Abbasi M |
| Retraction Note: EDAR, LYPLAL1, PRDM16, PAX3, DKK1, TNFSF12, CACNA2D3, and SUPT3H gene variants influence facial morphology in a Eurasian population. Human genetics 2021 8 140 (10): 1499. Li Yi, Zhao Wenting, Li Dan, Tao Xianming, Xiong Ziyi, Liu Jing, Zhang Wei, Ji Anquan, Tang Kun, Liu Fan, Li Caix |
| Profiling of somatic mutations and fusion genes in acute myeloid leukemia patients with FLT3-ITD or FLT3-TKD mutation at diagnosis reveals distinct evolutionary patterns. Experimental hematology & oncology 2021 4 10 (1): 27. Guan Wei, Zhou Lei, Li Yan, Yang Erna, Liu Yangyang, Lv Na, Fu Lin, Ding Yi, Wang Nan, Fang Nan, Liu Qian, Wang Binan, Li Fuwei, Zhang Juan, Wang Maoquan, Wang Lili, Jing Yu, Li Yonghui, Yu |
| A replication study separates polymorphisms behind migraine with and without depression. PloS one 2021 12 16 (12): e0261477. Petschner Peter, Baksa Daniel, Hullam Gabor, Torok Dora, Millinghoffer Andras, Deakin J F William, Bagdy Gyorgy, Juhasz Gabriel |
| Adipose tissue expression of UCP1 and PRDM16 genes and their association with postprandial triglyceride metabolism and glucose intolerance. Diabetes research and clinical practice 2021 10 182 109115. Mishra B K, Madhu S V, Aslam M, Agarwal V, Banerjee B |
| Systematic large-scale assessment of the genetic architecture of left ventricular noncompaction reveals diverse etiologies. Genetics in medicine : official journal of the American College of Medical Genetics 2021 Jan . Mazzarotto Francesco, Hawley Megan H, Beltrami Matteo, Beekman Leander, de Marvao Antonio, McGurk Kathryn A, Statton Ben, Boschi Beatrice, Girolami Francesca, Roberts Angharad M, Lodder Elisabeth M, Allouba Mona, Romeih Soha, Aguib Yasmine, Baksi A John, Pantazis Antonis, Prasad Sanjay K, Cerbai Elisabetta, Yacoub Magdi H, O'Regan Declan P, Cook Stuart A, Ware James S, Funke Birgit, Olivotto Iacopo, Bezzina Connie R, Barton Paul J R, Walsh Rod |
| Novel association of SNP rs2297828 in PRDM16 gene with predisposition to type 2 diabetes. Gene 2022 Sep 849 146916. Zhang Hongmei, Guan Qiuyue, Wang Ruyi, Yang Shanshan, Yu Xiaoqian, Cui Daxin, Su Zhigua |
| Germline Variants Associated with Nasopharyngeal Carcinoma Predisposition Identified through Whole-Exome Sequencing. Cancers 2022 Jul 14 (15): . Lee Ning-Yuan, Hum Melissa, Ong Pei-Yi, Myint Matthew Khine, Ong Enya H W, Low Kar-Perng, Li Zheng, Goh Boon-Cher, Tay Joshua K, Loh Kwok-Seng, Chua Melvin L K, Lee Soo-Chin, Khor Chiea-Chuen, Lee Ann S |
| Impact of HOXB4 and PRDM16 Gene Expressions on Prognosis and Treatment Response in Acute Myeloid Leukemia Patients. Pharmacogenomics and personalized medicine 2022 7 15 663-674. El-Meligui Yomna M, Hassan Naglaa M, Kassem Amira B, Gouda Nora A, Mohanad Marwa, Hamouda Manal A, Salahuddin Ahm |
| Deciphering the Role of the rs2651899, rs10166942, and rs11172113 Polymorphisms in Migraine: A Meta-Analysis. Medicina (Kaunas, Lithuania) 2022 4 58 (4): . Siokas Vasileios, Liampas Ioannis, Aloizou Athina-Maria, Papasavva Maria, Bakirtzis Christos, Lavdas Eleftherios, Liakos Panagiotis, Drakoulis Nikolaos, Bogdanos Dimitrios P, Dardiotis Efthimi |
| UBTF-internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia. Genes, chromosomes & cancer 2022 11 62 (4): 202-209. Kaburagi Taeko, Shiba Norio, Yamato Genki, Yoshida Kenichi, Tabuchi Ken, Ohki Kentaro, Ishikita Etsuko, Hara Yusuke, Shiraishi Yuichi, Kawasaki Hirohide, Sotomatsu Manabu, Takizawa Takumi, Taki Tomohiko, Kiyokawa Nobutaka, Tomizawa Daisuke, Horibe Keizo, Miyano Satoru, Taga Takashi, Adachi Souichi, Ogawa Seishi, Hayashi Yasuhi |
| Improved polygenic risk prediction in migraine-first patients. The journal of headache and pain 2024 9 25 (1): 161. Dora Torok, Peter Petschner, Daniel Baksa, Gabriella Juha |
- Page last reviewed:Feb 1, 2024
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