Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 53 Records) |
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Association between the valine/leucine247 polymorphism of ß2-glycoprotein I and susceptibility to anti-phospholipid syndrome: a meta-analysis. Lupus 2012 Jul 21 (8): 865-71. Lee Y H, Choi S J, Ji J D, Song G |
Functional properties of rare missense variants of human CDH13 found in adult attention deficit/hyperactivity disorder (ADHD) patients. PloS one 2013 8 (8): e71445. Mavroconstanti Thegna, Johansson Stefan, Winge Ingeborg, Knappskog Per M, Haavik J |
The haplotype M2 of the ANXA5 gene is not associated with antitrophoblast antibodies. Journal of assisted reproduction and genetics 2013 Jun 30 (5): 711-6. Rogenhofer Nina, Engels Laura, Bogdanova Nadja, Tüttelmann Frank, Markoff Arseni, Thaler Christian |
Anti-citrullinated glucose-6-phosphate isomerase peptide antibodies in patients with rheumatoid arthritis are associated with HLA-DRB1 shared epitope alleles and disease activity. Clinical and experimental immunology 2013 Apr 172 (1): 1. Umeda N, Matsumoto I, Ito I, Kawasaki A, Tanaka Y, Inoue A, Tsuboi H, Suzuki T, Hayashi T, Ito S, Tsuchiya N, Sumida T |
Recurrent pregnancy loss, plasminogen activator inhibitor-1 (-675) 4G/5G polymorphism and antiphospholipid antibodies in Czech women. American journal of reproductive immunology (New York, N.Y. : 1989) 2013 Jul 70 (1): 54-8. Subrt Ivan, Ulcova-Gallova Zdenka, Cerna Monika, Hejnalova Marketa, Slovanova Jitka, Bibkova Katarina, Micanova Zden |
Genetic determinants of plasma ß2-glycoprotein I levels: a genome-wide association study in extended pedigrees from Spain.
Journal of thrombosis and haemostasis : JTH 2013 Jan . Athanasiadis G, Sabater-Lleal M, Buil A, Souto JC, Borrell M, Lathrop M, Watkins H, Almasy L, Hamsten A, Soria JM |
Polymorphisms in the TNF-a, TNFR1 gene and risk of rheumatoid arthritis in Chinese Han population. International journal of immunogenetics 2014 Dec 41 (6): 499-502. Li F, Gao J, Sokolove J, Xu J, Zheng J, Zhu K, Pan |
The association of the vanin-1 N131S variant with blood pressure is mediated by endoplasmic reticulum-associated degradation and loss of function. PLoS genetics 2014 Sep 10 (9): e1004641. Wang Ya-Juan, Tayo Bamidele O, Bandyopadhyay Anupam, Wang Heming, Feng Tao, Franceschini Nora, Tang Hua, Gao Jianmin, Sung Yun Ju, , Elston Robert C, Williams Scott M, Cooper Richard S, Mu Ting-Wei, Zhu Xiaofe |
PIGA mutations cause early-onset epileptic encephalopathies and distinctive features. Neurology 2014 May 82 (18): 1587-96. Kato Mitsuhiro, Saitsu Hirotomo, Murakami Yoshiko, Kikuchi Kenjiro, Watanabe Shuei, Iai Mizue, Miya Kazushi, Matsuura Ryuki, Takayama Rumiko, Ohba Chihiro, Nakashima Mitsuko, Tsurusaki Yoshinori, Miyake Noriko, Hamano Shin-Ichiro, Osaka Hitoshi, Hayasaka Kiyoshi, Kinoshita Taroh, Matsumoto Naomic |
[Systemic lupus erythematous and CD24v]. Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993) 0 62 (4): 265-70. Jiménez-Uscanga Rubén Darío, Carsolio-Trujano Margarita, Herrera-Sánchez Diana Andrea, Castrejón-Vázquez María Isabel, Irazoque-Palacios Fedra, Vargas-Camaño María Eugenia, Martínez-Aguilar Nora, Chima-Galán María Carm |
[Mutation analysis of the pathogenic gene in a Chinese family with hereditary hemochromatosis]. Yi chuan = Hereditas 2015 1 36 (11): 1152-8. Yuanfeng Li, Hongxing Zhang, Haitao Zhang, Xiaobo Peng, Lili Bai, Fuchu He, Zewu Qiu, Gangqiao Zh |
Detection of new pathogenic mutations in patients with congenital haemolytic anaemia using next-generation sequencing. International journal of laboratory hematology 2016 Jul . Del Orbe Barreto R, Arrizabalaga B, De la Hoz A B, García-Orad Á, Tejada M I, Garcia-Ruiz J C, Fidalgo T, Bento C, Manco L, Ribeiro M |
Globus pallidus degeneration and clinicopathological features of Huntington disease. Annals of neurology 2016 Jun . Singh-Bains Malvindar K, Tippett Lynette J, Hogg Virginia M, Synek Beth J, Roxburgh Richard H, Waldvogel Henry J, Faull Richard L |
Genetic variants in glucose-6-phosphate isomerase gene as prognosis predictors in hepatocellular carcinoma. Clinics and research in hepatology and gastroenterology 2016 Jun . Lyu Zhuomin, Chen Yibing, Guo Xu, Zhou Feng, Yan Zhaoyong, Xing Jinliang, An Jiaze, Zhang Hongx |
Heterozygous mutants of TIRAP (S180L) polymorphism protect adult patients with Plasmodium falciparum infection against severe disease and mortality. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2016 May . Panda Aditya K, Das Bidyut K, Panda Abhinash, Tripathy Rina, Pattnaik Sarit S, Mahto Harishankar, Pied Sylviane, Pathak Sulabha, Sharma Shobhona, Ravindran Balachandr |
Correlation of EGFR or KRAS mutation status with 18F-FDG uptake on PET-CT scan in lung adenocarcinoma. PloS one 2017 12 (4): e0175622. Takamochi Kazuya, Mogushi Kaoru, Kawaji Hideya, Imashimizu Kota, Fukui Mariko, Oh Shiaki, Itoh Masayoshi, Hayashizaki Yoshihide, Ko Weijey, Akeboshi Masao, Suzuki Ken |
Evaluation of role of FV, FVIII and APLAs in the pathogenesis of APCR in FV Leiden negative DVT patients: a study in India. Journal of thrombosis and thrombolysis 2017 1 43 (2): 217-223. Sharma Amit, Singh Kanwaljeet, Biswas Arijit, Ranjan Ravi, Kishor Kamal, Kumar Ravi, Pandey Hareram, Kamal Vineet Kumar, Saxena Re |
A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle. The Journal of allergy and clinical immunology 2018 Jan . Stein Michelle M, Thompson Emma E, Schoettler Nathan, Helling Britney A, Magnaye Kevin M, Stanhope Catherine, Igartua Catherine, Morin Andréanne, Washington Charles, Nicolae Dan, Bønnelykke Klaus, Ober Caro |
Clonal Cell Proliferation in Paroxysmal Nocturnal Hemoglobinuria: Evaluation of PIGA Mutations and T-cell Receptor Clonality. Annals of laboratory medicine 2019 5 39 (5): 438-446. Park Joonhong, Kim Myungshin, Kim Yonggoo, Han Kyungja, Chung Nack Gyun, Cho Bin, Lee Sung Eun, Lee Jong Wo |
Genetic analyses identify GSDMB associated with asthma severity, exacerbations, and antiviral pathways. The Journal of allergy and clinical immunology 2020 8 147 (3): 894-909. Li Xingnan, Christenson Stephanie A, Modena Brian, Li Huashi, Busse William W, Castro Mario, Denlinger Loren C, Erzurum Serpil C, Fahy John V, Gaston Benjamin, Hastie Annette T, Israel Elliot, Jarjour Nizar N, Levy Bruce D, Moore Wendy C, Woodruff Prescott G, Kaminski Naftali, Wenzel Sally E, Bleecker Eugene R, Meyers Deborah A, |
Expression quantitative trait locus fine mapping of the 17q12-21 asthma locus in African American children: a genetic association and gene expression study. The Lancet. Respiratory medicine 2020 May 8 (5): 482-492. Ober Carole, McKennan Chris G, Magnaye Kevin M, Altman Matthew C, Washington Charles, Stanhope Catherine, Naughton Katherine A, Rosasco Mario G, Bacharier Leonard B, Billheimer Dean, Gold Diane R, Gress Lisa, Hartert Tina, Havstad Suzanne, Khurana Hershey Gurjit K, Hallmark Brian, Hogarth D Kyle, Jackson Daniel J, Johnson Christine C, Kattan Meyer, Lemanske Robert F, Lynch Susan V, Mendonca Eneida A, Miller Rachel L, Naureckas Edward T, O'Connor George T, Seroogy Christine M, Wegienka Ganesa, White Steven R, Wood Robert A, Wright Anne L, Zoratti Edward M, Martinez Fernando D, Ownby Dennis, Nicolae Dan L, Levin Albert M, Gern James E, |
Identification of acquired PIGA mutations and additional variants by next-generation sequencing in paroxysmal nocturnal hemoglobinuria. International journal of laboratory hematology 2020 5 42 (4): 473-481. Li Jing, Lin Yani, Chen Long, Qin Li, Tan Hao, Zou Junyan, Zhang Donglei, Nie Yanbo, Wang Guangjuan, Zhang Hong, Liu Enbin, Chen Xuejing, Ru K |
Polymorphisms in Glycolysis-Related Genes Are Associated with Clinical Outcomes of Paclitaxel-Cisplatin Chemotherapy in Non-Small Cell Lung Cancer. Oncology 2020 4 98 (7): 468-477. Choi Sun Ha, Jin Cheng Cheng, Do Sook Kyung, Lee Shin Yup, Choi Jin Eun, Kang Hyo-Gyoung, Kim Ji Hyun, Lee Jang Hyuck, Hong Mi Jeong, Lee Won Kee, Jeong Ji Yun, Shin Kyung Min, Lee Yong Hoon, Seo Hyewon, Yoo Seung Soo, Lee Jaehee, Cha Seung Ick, Kim Chang Ho, Park Jae Yo |
Significantly different clinical phenotypes associated with mutations in synthesis and transamidase+remodeling glycosylphosphatidylinositol (GPI)-anchor biosynthesis genes. Orphanet journal of rare diseases 2020 2 15 (1): 40. Carmody Leigh C, Blau Hannah, Danis Daniel, Zhang Xingman A, Gourdine Jean-Philippe, Vasilevsky Nicole, Krawitz Peter, Thompson Miles D, Robinson Peter |
The Asthma-associated PER1-like domain-containing protein 1 (PERLD1) Haplotype Influences Soluble Glycosylphosphatidylinositol Anchor Protein (sGPI-AP) Levels in Serum and Immune Cell Proliferation. Scientific reports 2020 Jan 10 (1): 715. Sio Yang Yie, Anantharaman Ramani, Lee Sean Qiu En, Matta Sri Anusha, Ng Yu Ting, Chew Fook T |
Clinical Relevance of Gastroesophageal Cancer Associated SNPs for Oncologic Outcome After Curative Surgery. Annals of surgical oncology 2021 Sep . Jung Jin-On, Wirsik Naita Maren, Nienhüser Henrik, Peters Leila, Müller-Stich Beat Peter, Hess Timo, Schüller Vitalia, Schumacher Johannes, Schmidt Thom |
The Efficacy and Predictors of Using GPi-DBS to Treat Early-Onset Dystonia: An Individual Patient Analysis. Neural plasticity 2021 5 2021 9924639. Chen Wenxiu, Fan Houyou, Lu Guoh |
YTGT: A new high-prevalence antigen in the Yt blood group system in two unrelated Native Americans and transfusion management. Transfusion 2022 Sep 62 (9): 1917-1922. Van Buren Nancy L, Gillen Barbara, Lomas-Francis Christine, Burgos Anna, Pease Daniel, Beaver Maria, Imbryk Adam, Dugger Julia, Fugate Alexandra, Hebel Eric, Lodermeier Michelle, Vege Sunitha, Westhoff Connie |
Functional Annotation and Gene Set Analysis of Gastric Cancer Risk Loci in a Korean Population. Cancer research and treatment 2023 6 . Hyojin Pyun, Madhawa Gunathilake, Jeonghee Lee, Il Ju Choi, Young-Il Kim, Joohon Sung, Jeongseon K |
Post-viral idiopathic purpura fulminans is associated with inherited thrombophilia and anti-cardiolipin antibodies. Frontiers in pediatrics 2023 6 11 1197795. A Theron, S Ayadi, E Boissier, O Dautremay, J-F Schved, N Sirvent, I Diaz, G Captier, C Biron-Andreani, E Jeziors |
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- Page last updated:Apr 16, 2024
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