Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 31 Records) |
| Query Trace: Disease and STAR[original query] |
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| Detection of His1069Gln mutation in Wilson disease by bidirectional PCR amplification of specific alleles (BI-PASA) test. General physiology and biophysics 2007 Jun 26 (2): 91-6. Poláková H, Katrincsáková B, Minárik G, Feráková E, Ficek A, Baldovic M, Kádasi |
| The FKBP5-gene in depression and treatment response--an association study in the Sequenced Treatment Alternatives to Relieve Depression (STAR*D) Cohort. Biological psychiatry 2008 Jun 63 (12): 1103-10. Lekman Magnus, Laje Gonzalo, Charney Dennis, Rush A John, Wilson Alexander F, Sorant Alexa J M, Lipsky Robert, Wisniewski Stephen R, Manji Husseini, McMahon Francis J, Paddock Silv |
| Extended tracts of homozygosity identify novel candidate genes associated with late-onset Alzheimer's disease. Neurogenetics 2009 Jul 10 (3): 183-90. Nalls M A, Guerreiro R J, Simon-Sanchez J, Bras J T, Traynor B J, Gibbs J R, Launer L, Hardy J, Singleton A |
| Isolated Addison's disease is unlikely to be caused by mutations in MC2R, MRAP or STAR, three genes responsible for familial glucocorticoid deficiency. European journal of endocrinology / European Federation of Endocrine Societies 2010 Feb 162 (2): 357-9. Dias R P, Chan L F, Metherell L A, Pearce S H S, Clark A J |
| Glycine and a glycine dehydrogenase (GLDC) SNP as citalopram/escitalopram response biomarkers in depression: pharmacometabolomics-informed pharmacogenomics. Clinical pharmacology and therapeutics 2011 Jan 89 (1): 97-104. Ji Y, Hebbring S, Zhu H, Jenkins G D, Biernacka J, Snyder K, Drews M, Fiehn O, Zeng Z, Schaid D, Mrazek D A, Kaddurah-Daouk R, Weinshilboum R |
Genome-wide pharmacogenomic study of citalopram-induced side effects in STAR*D.
Translational psychiatry 2012 2 e129. Adkins D E, Clark S L, Åberg K, Hettema J M, Bukszár J, McClay J L, Souza R P, van den Oord E J C |
| Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy. Neurology 2012 Jul 79 (2): 159-62. Bello Luca, Piva Luisa, Barp Andrea, Taglia Antonella, Picillo Esther, Vasco Gessica, Pane Marika, Previtali Stefano C, Torrente Yvan, Gazzerro Elisabetta, Motta Maria Chiara, Grieco Gaetano S, Napolitano Sara, Magri Francesca, D'Amico Adele, Astrea Guja, Messina Sonia, Sframeli Maria, Vita Gian Luca, Boffi Patrizia, Mongini Tiziana, Ferlini Alessandra, Gualandi Francesca, Soraru' Gianni, Ermani Mario, Vita Giuseppe, Battini Roberta, Bertini Enrico, Comi Giacomo P, Berardinelli Angela, Minetti Carlo, Bruno Claudio, Mercuri Eugenio, Politano Luisa, Angelini Corrado, Hoffman Eric P, Pegoraro Ele |
| Multiple regulatory variants modulate expression of 5-hydroxytryptamine 2A receptors in human cortex. Biological psychiatry 2012 Nov . Smith RM, Papp AC, Webb A, Ruble CL, Munsie LM, Nisenbaum LK, Kleinman JE, Lipska BK, Sadee W |
| Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study. European journal of human genetics : EJHG 2012 Oct . Tiziano FD, Lomastro R, Di Pietro L, Barbara Pasanisi M, Fiori S, Angelozzi C, Abiusi E, Angelini C, Sorarù G, Gaiani A, Mongini T, Vercelli L, Vasco G, Vita G, Luca Vita G, Messina S, Politano L, Passamano L, Di Gregorio G, Montomoli C, Orsi C, Campanella A, Mantegazza R, Morandi L |
| Origin and differential selection of allelic variation at TAS2R16 associated with salicin bitter taste sensitivity in Africa. Molecular biology and evolution 2014 Feb 31 (2): 288-302. Campbell Michael C, Ranciaro Alessia, Zinshteyn Daniel, Rawlings-Goss Renata, Hirbo Jibril, Thompson Simon, Woldemeskel Dawit, Froment Alain, Rucker Joseph B, Omar Sabah A, Bodo Jean-Marie, Nyambo Thomas, Belay Gurja, Drayna Dennis, Breslin Paul A S, Tishkoff Sarah |
| UGT1A1 genetic analysis as a diagnostic aid for individuals with unconjugated hyperbilirubinemia. The Journal of pediatrics 2013 Jan . Skierka JM, Kotzer KE, Lagerstedt SA, O'Kane DJ, Baudhuin LM |
| DISC1-TSNAX and DAOA genes in major depression and citalopram efficacy. Journal of affective disorders 2014 Oct 168 91-7. Arias Bárbara, Fabbri Chiara, Serretti Alessandro, Drago Antonio, Mitjans Marina, Gastó Cristóbal, Catalán Rosa, Fañanás Lourd |
| The role of the potassium channel gene KCNK2 in major depressive disorder. Psychiatry research 2015 Feb 225 (3): 489-92. Congiu Chiara, Minelli Alessandra, Bonvicini Cristian, Bortolomasi Marco, Sartori Riccardo, Maj Carlo, Scassellati Catia, Maina Giuseppe, Trabucchi Luigi, Segala Matilde, Gennarelli Massi |
| What doesn't kill them makes them stronger: an association between elongation factor 1-a overdominance in the sea star Pisaster ochraceus and "sea star wasting disease". PeerJ 2016 4 e1876. Wares John P, Schiebelhut Lauren |
| Population genetic evidence for positive and purifying selection acting at the human IFN-? locus in Africa. Genes and immunity 2018 3 20 (2): 143-157. Campbell Michael C, Smith Lunden T, Harvey Jay |
| Longitudinal natural history in young boys with Duchenne muscular dystrophy. Neuromuscular disorders : NMD 2019 10 29 (11): 857-862. Coratti Giorgia, Brogna Claudia, Norcia Giulia, Ricotti Valeria, Abbott Lianne, D'Amico Adele, Berardinelli Angela, Vita Gian Luca, Lucibello Simona, Messina Sonia, Sansone Valeria, Albamonte Emilio, Colia Giulia, Salmin Francesca, Gardani Alice, Manzur Adnan, Main Marion, Baranello Giovanni, Arnoldi Maria Teresa, Parsons Julie, Carry Terri, Connolly Anne M, Bertini Enrico, Muntoni Francesco, Pane Marika, Mercuri Eugen |
| Association analysis of polymorphisms in STARD6 and near ECHDC3 in Alzheimer's disease patients carrying the APOE ?4 Allele. Neuropsychiatric disease and treatment 2019 15 213-218. Yin Jiajun, Feng Wei, Yuan Hongwei, Yuan Jianmin, Wu Yue, Liu Xiaowei, Jin Chunhui, Cheng Zaoh |
| Clinical Implication and the Hereditary Factors of NM23 in Hepatocellular Carcinoma Based on Bioinformatics Analysis and Genome-Wide Association Study. Journal of oncology 2019 1 2018 6594169. Yang Chengkun, Han Chuangye, Wang Xiangkun, Liao Xiwen, Liu Xiaoguang, Qin Wei, Yu Long, Zhu Guangzhi, Su Hao, Lu Sicong, Chen Zhiwei, Yu Tingdong, Liu Zhen, Huang Ketuan, Liu Zhengtao, Liang Yu, Huang Jianlu, Peng T |
| A novel prognostic two-gene signature for triple negative breast cancer. Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc 2020 5 33 (11): 2208-2220. Alsaleem Mansour A, Ball Graham, Toss Michael S, Raafat Sara, Aleskandarany Mohammed, Joseph Chitra, Ogden Angela, Bhattarai Shristi, Rida Padmashree C G, Khani Francesca, Davis Melissa, Elemento Olivier, Aneja Ritu, Ellis Ian O, Green Andrew, Mongan Nigel P, Rakha Em |
| Variable expression quantitative trait loci analysis of breast cancer risk variants. Scientific reports 2021 3 11 (1): 7192. Wiggins George A R, Black Michael A, Dunbier Anita, Merriman Tony R, Pearson John F, Walker Logan |
| Human APOE ?3 and APOE ?4 Alleles Have Differential Effects on Mouse Olfactory Epithelium. Journal of Alzheimer's disease : JAD 2021 12 85 (4): 1481-1494. Khan Naazneen, Alimova Yelena, Clark Sophie J, Vekaria Hemendra J, Walsh Adeline E, Williams Holden C, Hawk Gregory S, Sullivan Patrick G, Johnson Lance A, McClintock Timothy |
| An expanded set of genome-wide association studies of brain imaging phenotypes in UK Biobank.
Nature neuroscience 2021 4 24 (5): 737-745. Smith Stephen M, Douaud Gwenaëlle, Chen Winfield, Hanayik Taylor, Alfaro-Almagro Fidel, Sharp Kevin, Elliott Lloyd |
| Comprehensive Analysis of Congenital Adrenal Hyperplasia Using Long-Read Sequencing. Clinical chemistry 2022 6 68 (7): 927-939. Liu Yingdi, Chen Miaomiao, Liu Jing, Mao Aiping, Teng Yanling, Yan Huiming, Zhu Huimin, Li Zhuo, Liang Desheng, Wu Lingqi |
| Characteristics of disease progression and genetic correlation in ambulatory Iranian boys with Duchenne muscular dystrophy. BMC neurology 2022 5 22 (1): 162. Zamani Gholamreza, Hosseinpour Sareh, Ashrafi Mahmoud Reza, Mohammadi Mahmoud, Badv Reza Shervin, Tavasoli Ali Reza, Akbari Masood Ghahvechi, Bereshneh Ali Hosseini, Malamiri Reza Azizi, Heidari Morte |
| The frequencies of CYP2D6 alleles and their impact on clinical outcomes of adjuvant tamoxifen therapy in Syrian breast cancer patients. BMC cancer 2022 Oct 22 (1): 1067. Ismail Al-Khalil Wouroud, Al-Salhi Lana, Rijjal Sara, Aljamali Majd, Youssef Lama |
| Association between CYP2D6 phenotype and recurrence of Plasmodium vivax infection in south Korean patients. Malaria journal 2022 Oct 21 (1): 289. Choi Sungim, Choi Heun, Park Seong Yeon, Kwak Yee Gyung, Song Je Eun, Shin So Youn, Baek Ji Hyeon, Shin Hyun-Il, Cho Shin-Hyung, Lee Sang-Eun, Kwon Jeong-Ran, Park Sookkyung, Kim Miyoung, Oh Hong Sang, Kim Yong Chan, Kim Min Jae, Yeom Joon-S |
| Development of a novel dementia risk prediction model in the general population: A large, longitudinal, population-based machine-learning study. EClinicalMedicine 2022 Nov 53 101665. You Jia, Zhang Ya-Ru, Wang Hui-Fu, Yang Ming, Feng Jian-Feng, Yu Jin-Tai, Cheng W |
| Caffeine intake interacts with Asian gene variants in Parkinson's disease: a study in 4488 subjects. The Lancet regional health. Western Pacific 2023 9 40 100877. Yi-Lin Ong, Xiao Deng, Hui-Hua Li, K Narasimhalu, Ling-Ling Chan, Kumar M Prakash, Wing-Lok Au, Pavanni Ratnagopal, Louis C S Tan, Eng-King T |
| Longitudinal study of Alzheimer's disease biomarkers, allostatic load, and cognition among memory clinic patients. Brain, behavior, & immunity - health 2023 2 28 100592. Adedeji Dickson O, Holleman Jasper, Juster Robert-Paul, Udeh-Momoh Chinedu T, Kåreholt Ingemar, Hagman Göran, Aspö Malin, Adagunodo Sofia, Håkansson Krister, Kivipelto Miia, Solomon Alina, Sindi Shire |
| Association of rheumatoid factor, anti-citrullinated protein antibodies and shared epitope with clinical response to initial treatment in patients with early rheumatoid arthritis: data from a randomised controlled trial. Annals of the rheumatic diseases 2024 7 . Kristina Lend, Jon Lampa, Leonid Padyukov, Merete Lund Hetland, Marte Schrumpf Heiberg, Dan C Nordström, Michael T Nurmohamed, Anna Rudin, Mikkel Østergaard, Espen A Haavardsholm, Kim Hørslev-Petersen, Till Uhlig, Tuulikki Sokka-Isler, Bjorn Gudbjornsson, Gerdur Grondal, Giulia Frazzei, Jeroen Christiaans, Gertjan Wolbink, Theo Rispens, Jos W R Twisk, Ronald F van Vollenhov |
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