Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
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High resolution linkage and linkage disequilibrium analyses of chromosome 1p36 SNPs identify new positional candidate genes for low bone mineral density. Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2009 Feb 20 (2): 341-6. Zhang H, Sol-Church K, Rydbeck H, Stabley D, Spotila L D, Devoto |
Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.
The New England journal of medicine 2010 May 362 (18): 1686-97. Jin Ying, Birlea Stanca A, Fain Pamela R, Gowan Katherine, Riccardi Sheri L, Holland Paulene J, Mailloux Christina M, Sufit Alexandra J D, Hutton Saunie M, Amadi-Myers Anita, Bennett Dorothy C, Wallace Margaret R, McCormack Wayne T, Kemp E Helen, Gawkrodger David J, Weetman Anthony P, Picardo Mauro, Leone Giovanni, Taïeb Alain, Jouary Thomas, Ezzedine Khaled, van Geel Nanny, Lambert Jo, Overbeck Andreas, Spritz Richard |
Association between genetic variants associated with vertical cup-to-disc ratio and phenotypic features of primary open-angle glaucoma. Ophthalmology 2012 Sep 119 (9): 1819-25. Mabuchi Fumihiko, Sakurada Yoichi, Kashiwagi Kenji, Yamagata Zentaro, Iijima Hiroyuki, Tsukahara Shig |
A genetic risk score for thyroid peroxidase antibodies associates with clinical thyroid disease in community-based populations. The Journal of clinical endocrinology and metabolism 2015 May 100 (5): E799-807. Schultheiss Ulla T, Teumer Alexander, Medici Marco, Li Yong, Daya Natalie, Chaker Layal, Homuth Georg, Uitterlinden Andre G, Nauck Matthias, Hofman Albert, Selvin Elizabeth, Völzke Henry, Peeters Robin P, Köttgen An |
Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. International journal of cardiology 2015 Nov 204 115-121. Costain Gregory, Lionel Anath C, Ogura Lucas, Marshall Christian R, Scherer Stephen W, Silversides Candice K, Bassett Anne |
Copy number analysis of whole-genome data using BIC-seq2 and its application to detection of cancer susceptibility variants. Nucleic acids research 2016 Jun . Xi Ruibin, Lee Semin, Xia Yuchao, Kim Tae-Min, Park Peter |
Single nucleotide polymorphisms of the DGKB and VCAM1 genes are associated with granulocyte colony stimulating factor-mediated peripheral blood stem cell mobilization. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2016 Oct . Mishima Seiji, Matsuda Chikashi, Ishihara Tomoko, Nagase Mayumi, Taketani Takeshi, Nagai Atsus |
Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2016 Oct . Whitton Laura, Cosgrove Donna, Clarkson Christopher, Harold Denise, Kendall Kimberley, Richards Alex, Mantripragada Kiran, Owen Michael J, O'Donovan Michael C, Walters James, Hartmann Annette, Konte Betina, Rujescu Dan, , Gill Michael, Corvin Aiden, Rea Stephen, Donohoe Gary, Morris Derek |
Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study. International journal of cancer 2017 Nov . Brandt Jasmine, Borgquist Signe, Almgren Peter, Försti Asta, Huss Linnea, Melander Olle, Manjer Jon |
Genetic effects on white matter integrity in drug-naive patients with major depressive disorder: a diffusion tensor imaging study of 17 genetic loci associated with depressive symptoms. Neuropsychiatric disease and treatment 2019 15 375-383. Kakeda Shingo, Watanabe Keita, Katsuki Asuka, Sugimoto Koichiro, Ueda Issei, Igata Natsuki, Kishi Taro, Iwata Nakao, Abe Osamu, Yoshimura Reiji, Korogi Yukuno |
A single-nucleotide polymorphism influences brain morphology in drug-naïve patients with major depressive disorder. Neuropsychiatric disease and treatment 2019 15 2425-2432. Katsuki Asuka, Kakeda Shingo, Watanabe Keita, Igata Ryohei, Otsuka Yuka, Kishi Taro, Nguyen LeHoa, Ueda Issei, Iwata Nakao, Korogi Yukunori, Yoshimura Rei |
Exon Coverage Variations Between Cancer Tissues and Adjacent Non-Cancerous Tissues are Prognostic Factors in Gastric Cancer. OncoTargets and therapy 2020 13 61-70. Pan Xuan, Wang Yajing, Li Chenchen, Zhou Zhaofei, Zhong Yuejiao, Feng Jifeng, Lu Jianw |
Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank.
Communications biology 2021 Jun 4 (1): 700. Valette Kim, Li Zhonglin, Bon-Baret Valentin, Chignon Arnaud, Bérubé Jean-Christophe, Eslami Aida, Lamothe Jennifer, Gaudreault Nathalie, Joubert Philippe, Obeidat Ma'en, van den Berge Maarten, Timens Wim, Sin Don D, Nickle David C, Hao Ke, Labbé Catherine, Godbout Krystelle, Côté Andréanne, Laviolette Michel, Boulet Louis-Philippe, Mathieu Patrick, Thériault Sébastien, Bossé Yoh |
Causal influences of neuroticism on mental health and cardiovascular disease. Human genetics 2021 May . Zhang Fuquan, Baranova Ancha, Zhou Chao, Cao Hongbao, Chen Jiu, Zhang Xiangrong, Xu Mingqi |
Relationship between Gene Polymorphisms and Urine Iodine Levels on Susceptibility to Thyroid Peroxidase Antibody Positivity in the Chinese Population. European thyroid journal 2021 Mar 10 (1): 79-85. Han Bing, Chen Chi, Chen Yi, Wang Ningjian, Yu Jie, Cheng Jing, Chen Yingchao, Zhu Chunfang, Lu Ying |
Genome-wide meta-analysis identifies 127 open-angle glaucoma loci with consistent effect across ancestries.
Nature communications 2021 (1): 1258. Gharahkhani Puya, Jorgenson Eric, Hysi Pirro, Khawaja Anthony P, Pendergrass Sarah, Han Xikun, Ong Jue Sheng, Hewitt Alex W, Segrè Ayellet V, Rouhana John M, Hamel Andrew R, Igo Robert P, Choquet Helene, Qassim Ayub, Josyula Navya S, Cooke Bailey Jessica N, Bonnemaijer Pieter W M, Iglesias Adriana, Siggs Owen M, Young Terri L, Vitart Veronique, Thiadens Alberta A H J, Karjalainen Juha, Uebe Steffen, Melles Ronald B, Nair K Saidas, Luben Robert, Simcoe Mark, Amersinghe Nishani, Cree Angela J, Hohn Rene, Poplawski Alicia, Chen Li Jia, Rong Shi-Song, Aung Tin, Vithana Eranga Nishanthie, , , , , , , , Tamiya Gen, Shiga Yukihiro, Yamamoto Masayuki, Nakazawa Toru, Currant Hannah, Birney Ewan, Wang Xin, Auton Adam, Lupton Michelle K, Martin Nicholas G, Ashaye Adeyinka, Olawoye Olusola, Williams Susan E, Akafo Stephen, Ramsay Michele, Hashimoto Kazuki, Kamatani Yoichiro, Akiyama Masato, Momozawa Yukihide, Foster Paul J, Khaw Peng T, Morgan James E, Strouthidis Nicholas G, Kraft Peter, Kang Jae H, Pang Chi Pui, Pasutto Francesca, Mitchell Paul, Lotery Andrew J, Palotie Aarno, van Duijn Cornelia, Haines Jonathan L, Hammond Chris, Pasquale Louis R, Klaver Caroline C W, Hauser Michael, Khor Chiea Chuen, Mackey David A, Kubo Michiaki, Cheng Ching-Yu, Craig Jamie E, MacGregor Stuart, Wiggs Janey |
A comprehensive meta-analysis and prioritization study to identify vitiligo associated coding and non-coding SNV candidates using web-based bioinformatics tools. Scientific reports 2022 8 12 (1): 14543. Dutta Tithi, Mitra Sayantan, Saha Arpan, Ganguly Kausik, Pyne Tushar, Sengupta Main |
A novel prognostic signature based on N7-methylguanosine-related long non-coding RNAs in breast cancer. Frontiers in genetics 2022 10 13 1030275. Huang Zhidong, Lou Kaixin, Liu Ho |
Genome-wide association study on 13?167 individuals identifies regulators of blood CD34+cell levels.
Blood 2022 1 139 (11): 1659-1669. Lopez de Lapuente Portilla Aitzkoa, Ekdahl Ludvig, Cafaro Caterina, Ali Zain, Miharada Natsumi, Thorleifsson Gudmar, Žemaitis Kristijonas, Lamarca Arrizabalaga Antton, Thodberg Malte, Pertesi Maroulio, Dhapola Parashar, Bao Erik, Niroula Abhishek, Bali Divya, Norddahl Gudmundur, Ugidos Damboriena Nerea, Sankaran Vijay G, Karlsson Göran, Thorsteinsdottir Unnur, Larsson Jonas, Stefansson Kari, Nilsson Bjö |
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