Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: PURA[original query] |
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Lack of association between interleukin-6 promoter polymorphism at position -174 and Henoch-Schönlein pur pura. Clinical and experimental rheumatology 0 25 (1 Suppl 44): S6-9. Amoli M M, Martin J, Miranda-Filloy J A, Garcia-Porrua C, Ollier W E R, Gonzalez-Gay M |
Host genetic factors and vaccine-induced immunity to hepatitis B virus infection. PloS one 2008 3 (3): e1898. Hennig Branwen J, Fielding Katherine, Broxholme John, Diatta Mathurin, Mendy Maimuna, Moore Catrin, Pollard Andrew J, Rayco-Solon Pura, Sirugo Giorgio, van der Sande Marianne A, Waight Pauline, Whittle Hilton C, Zaman Syed M, Hill Adrian V, Hall Andrew |
Common polymorphic variation in the genetically diverse African insulin gene and its association with size at birth. Human genetics 2009 Sep 126 (3): 375-84. Petry Clive J, Rayco-Solon Pura, Fulford Anthony J C, Stead John D H, Wingate Dianne L, Ong Ken K, Sirugo Giorgio, Prentice Andrew M, Dunger David |
FTO gene variation and measures of body mass in an African population. BMC medical genetics 2009 10 (1): 21. Hennig Branwen J, Fulford Anthony J, Sirugo Giorgio, Rayco-Solon Pura, Hattersley Andrew T, Frayling Timothy M, Prentice Andrew |
Host genetic factors and vaccine-induced immunity to HBV infection: haplotype analysis. PloS one 2010 5 (8): e12273. Ryckman Kelli K, Fielding Katherine, Hill Adrian V, Mendy Maimuna, Rayco-Solon Pura, Sirugo Giorgio, van der Sande Marianne A, Waight Pauline, Whittle Hilton C, Hall Andrew J, Williams Scott M, Hennig Branwen |
[Autoimmune polyendocrine syndrome type 2 associated with autoimmune hypophysitis and coeliac disease]. Vnitrni lekarstvi 2011 1 56 (11): 1169-76. Hrubisková K, Jackuliak P, Vanuga P, Pura M, Payer |
PURA syndrome: clinical delineation and genotype-phenotype study in 32 individuals with review of published literature. Journal of medical genetics 2017 11 55 (2): 104-113. Reijnders Margot R F, Janowski Robert, Alvi Mohsan, Self Jay E, van Essen Ton J, Vreeburg Maaike, Rouhl Rob P W, Stevens Servi J C, Stegmann Alexander P A, Schieving Jolanda, Pfundt Rolph, van Dijk Katinke, Smeets Eric, Stumpel Connie T R M, Bok Levinus A, Cobben Jan Maarten, Engelen Marc, Mansour Sahar, Whiteford Margo, Chandler Kate E, Douzgou Sofia, Cooper Nicola S, Tan Ene-Choo, Foo Roger, Lai Angeline H M, Rankin Julia, Green Andrew, Lönnqvist Tuula, Isohanni Pirjo, Williams Shelley, Ruhoy Ilene, Carvalho Karen S, Dowling James J, Lev Dorit L, Sterbova Katalin, Lassuthova Petra, Neupauerová Jana, Waugh Jeff L, Keros Sotirios, Clayton-Smith Jill, Smithson Sarah F, Brunner Han G, van Hoeckel Ceciel, Anderson Mel, Clowes Virginia E, Siu Victoria Mok, Ddd Study The, Selber Paulo, Leventer Richard J, Nellaker Christoffer, Niessing Dierk, Hunt David, Baralle Dia |
Expanding the neurodevelopmental phenotype of PURA syndrome. American journal of medical genetics. Part A 2017 11 176 (1): 56-67. Lee Bo Hoon, Reijnders Margot R F, Abubakare Oluwatobi, Tuttle Emily, Lape Brynn, Minks Kelly Q, Stodgell Christopher, Bennetto Loisa, Kwon Jennifer, Fong Chin-To, Gripp Karen W, Marsh Eric D, Smith Wendy E, Huq Ahm M, Coury Stephanie A, Tan Wen-Hann, Solis Orestes, Mehta Rupal I, Leventer Richard J, Baralle Diana, Hunt David, Paciorkowski Alex |
Exome sequencing identified a de novo mutation of PURA gene in a patient with familial Xp22.31 microduplication. European journal of medical genetics 2018 6 62 (2): 103-108. Qiao Ying, Bagheri Hani, Tang Flamingo, Badduke Chansonette, Martell Sally, Lewis Suzanne M E, Robinson Wendy, Connolly Mary B, Arbour Laura, Rajcan-Separovic Evi |
Pharmacogenetics and prediction of adverse events in prescription opioid use disorder patients. Basic & clinical pharmacology & toxicology 2018 12 124 (4): 439-448. Muriel Javier, Margarit César, Barrachina Jordi, Ballester Pura, Flor Andrea, Morales Domingo, Horga José F, Fernández Eduardo, Peiró Ana |
Genetic Contribution in Low Back Pain: A Prospective Genetic Association Study. Pain practice : the official journal of World Institute of Pain 2019 7 19 (8): 836-847. Margarit César, Roca Reyes, Inda María-Del-Mar, Muriel Javier, Ballester Pura, Moreu Rocío, Conte Anna Lucia, Nuñez Angela, Morales Domingo, Peiró Ana |
Gender based differences, pharmacogenetics and adverse events in chronic pain management. The pharmacogenomics journal 2019 Nov . Planelles Beatriz, Margarit César, Inda María-Del-Mar, Ballester Pura, Muriel Javier, Barrachina Jordi, Ajo Raquel, Esteban María-Dolores, Peiró Ana |
[Erectile dysfunction in patients with cardiovascular disease and the potential influence of genetic markers]. Revista internacional de andrologia 2020 Aug . Ors Diego, Segura Ana, Arrarte Vicente, Ballester Pura, Muriel Javier, Fernández Guillermina, Soriano Josefa, Peiró Ana |
Endothelial nitric oxide synthase gene polymorphisms and erectile dysfunction in chronic pain. Gene: X 2020 6 1 100005. Segura Ana, Ballester Pura, Ajo Raquel, Inda María-Del-Mar, Urbano Antonio, Muriel Javier, Ochando Isabel, Margarit César, Martinez Emi, Peiró Ana |
Endothelial nitric oxide synthase gene polymorphisms and erectile dysfunction in chronic pain. Gene 2021 9 721S 100005. Segura Ana, Ballester Pura, Ajo Raquel, Inda María-Del-Mar, Urbano Antonio, Muriel Javier, Ochando Isabel, Margarit César, Martinez Emi, Peiró Ana |
Association between ethnicity and hypertension in Northern Colombia in 2015. Clinical hypertension 2022 6 28 (1): 18. Smith Drew H, Grewal Jaskaran, Mehboob Saba, Mohan Shiva, Pombo Luisa F, Rodriguez Pura, Gonzalez Juan Carlos, Zevallos Juan, Barengo Noël |
CYP2D6 phenotypes and opioid metabolism: the path to personalized analgesia. Expert opinion on drug metabolism & toxicology 2022 6 18 (4): 261-275. Ballester Pura, Muriel Javier, Peiró Ana |
A 25 Mainland Chinese cohort of patients with PURA-related neurodevelopmental disorders: clinical delineation and genotype-phenotype correlations. European journal of human genetics : EJHG 2022 11 31 (1): 112-121. Dai Weiqian, Sun Yu, Fan Yanjie, Gao Yan, Zhan Yongkun, Wang Lili, Xiao Bing, Qiu Wenjuan, Gu Xuefan, Sun Kun, Yu Yongguo, Xu |
CYP2D6 Genotype and Pharmacovigilance Impact on Autism Spectrum Disorder: A Naturalistic Study with Extreme Phenotype Analysis. Pharmaceuticals (Basel, Switzerland) 2023 7 16 (7): . Pura Ballester, Cristina Espadas, Susana Almenara, Jordi Barrachina, Javier Muriel, Enrique Ramos, Natalia Toral, César Belda, Ana M Pei |
Detecting Low-Variant Allele Frequency Mosaic Pathogenic Variants of NF1, TSC2, and AKT3 Genes from Blood in Patients with Neurodevelopmental Disorders. The Journal of molecular diagnostics : JMD 2023 4 . Se Hee Kim, Soon Sung Kwon, Mi Ri Park, Hyeon Ah Lee, Ji Hun Kim, JiHoon Cha, Sangwoo Kim, Seung Tae Baek, Se Hoon Kim, Joon Soo Lee, Heung Dong Kim, Jong Rak Choi, Seung-Tae Lee, Hoon-Chul Ka |
Pharmacogenetics May Prevent Psychotropic Adverse Events in Autism Spectrum Disorder: An Observational Pilot Study. Pharmaceuticals (Basel, Switzerland) 2023 10 16 (10): . Laura de Miguel, Pura Ballester, Cecilia Egoavil, María Luisa Sánchez-Ocaña, Ana María García-Muñoz, Begoña Cerdá, Pilar Zafrilla, Enrique Ramos, Ana M Pei |
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- Page last updated:Mar 25, 2024
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