Human Genome Epidemiology Literature Finder
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Records 1 - 15 (of 15 Records) |
| Query Trace: Disease and PIK3CD[original query] |
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| Pooled analysis of phosphatidylinositol 3-kinase pathway variants and risk of prostate cancer. Cancer research 2010 Mar 70 (6): 2389-96. Koutros Stella, Schumacher Fredrick R, Hayes Richard B, Ma Jing, Huang Wen-Yi, Albanes Demetrius, Canzian Federico, Chanock Stephen J, Crawford E David, Diver W Ryan, Feigelson Heather Spencer, Giovanucci Edward, Haiman Christopher A, Henderson Brian E, Hunter David J, Kaaks Rudolf, Kolonel Laurence N, Kraft Peter, Le Marchand Loïc, Riboli Elio, Siddiq Afshan, Stampfer Mier J, Stram Daniel O, Thomas Gilles, Travis Ruth C, Thun Michael J, Yeager Meredith, Berndt Sonja |
| Genetic Diagnosis Using Whole Exome Sequencing in Common Variable Immunodeficiency. Frontiers in immunology 2016 7 220. Maffucci Patrick, Filion Charles A, Boisson Bertrand, Itan Yuval, Shang Lei, Casanova Jean-Laurent, Cunningham-Rundles Charlot |
| Integrative Analysis to Identify Common Genetic Markers of Metabolic Syndrome, Dementia, and Diabetes. Medical science monitor : international medical journal of experimental and clinical research 2017 12 23 5885-5891. Zhang Weihong, Xin Linlin, Lu Yi |
| Autoimmunity/inflammation in a monogenic primary immunodeficiency cohort. Clinical & translational immunology 2017 10 6 (9): e155. Rae William, Ward Daniel, Mattocks Christopher J, Gao Yifang, Pengelly Reuben J, Patel Sanjay V, Ennis Sarah, Faust Saul N, Williams Anthony |
| Associations of high-altitude polycythemia with polymorphisms in PIK3CD and COL4A3 in Tibetan populations. Human genomics 2018 Jul 12 (1): 37. Fan Xiaowei, Ma Lifeng, Zhang Zhiying, Li Yi, Hao Meng, Zhao Zhipeng, Zhao Yiduo, Liu Fang, Liu Lijun, Luo Xingguang, Cai Peng, Li Yansong, Kang Long |
| Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes. Blood 2019 Apr . Hadjadj Jérôme, Aladjidi Nathalie, Fernandes Helder, Leverger Guy, Magérus-Chatinet Aude, Mazerolles Fabienne, Stolzenberg Marie-Claude, Jacques Sidonie, Picard Capucine, Rosain Jérémie, Fourrage Cécile, Hanein Sylvain, Zarhrate Mohammed, Pasquet Marlène, Abou Chahla Wadih, Barlogis Vincent, Bertrand Yves, Pellier Isabelle, Colomb Bottollier Elodie, Fouyssac Fanny, Blouin Pascale, Thomas Caroline, Cheikh Nathalie, Dore Eric, Pondarre Corinne, Plantaz Dominique, Jeziorski Eric, Millot Frédéric, Garcelon Nicolas, Ducassou Stéphane, Perel Yves, Leblanc Thierry, Neven Bénédicte, Fischer Alain, Rieux-Laucat Frédéric, |
| Integrated characterisation of cancer genes identifies key molecular biomarkers in stomach adenocarcinoma. Journal of clinical pathology 2020 2 73 (9): 579-586. Wang Haifeng, Shen Liyijing, Li Yaoqing, Lv Jieqi |
| Clinical Manifestations and Outcomes of Activated Phosphoinositide 3-Kinase ? Syndrome from the USIDNET Cohort. The journal of allergy and clinical immunology. In practice 2021 8 9 (11): 4095-4102. Oh Jessica, Garabedian Elizabeth, Fuleihan Ramsay, Cunningham-Rundles Charlot |
| The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-? (PI3K?) Syndrome (APDS). Immunological investigations 2021 1 51 (3): 644-659. Fekrvand Saba, Delavari Samaneh, Chavoshzadeh Zahra, Sherkat Roya, Mahdaviani Seyed Alireza, Sadeghi Shabestari Mahnaz, Azizi Gholamreza, Arzanian Mohammad Taghi, Shahin Shamsian Bibi, Eskandarzadeh Shabnam, Eslami Narges, Rae William, Condino-Neto Antonio, Mohammadi Javad, Abolhassani Hassan, Yazdani Reza, Aghamohammadi Asgh |
| Establishing the Molecular Diagnoses in a Cohort of 291 Patients With Predominantly Antibody Deficiency by Targeted Next-Generation Sequencing: Experience From a Monocentric Study. Frontiers in immunology 2022 1 12 786516. Rojas-Restrepo Jessica, Caballero-Oteyza Andrés, Huebscher Katrin, Haberstroh Hanna, Fliegauf Manfred, Keller Baerbel, Kobbe Robin, Warnatz Klaus, Ehl Stephan, Proietti Michele, Grimbacher Bo |
| NTRK expression is common in xanthogranuloma and is associated with the solitary variant. Journal of cutaneous pathology 2023 8 . B Umphress, M Kuhar, R Kowal, A K Alomari, L A Baldridge, A J Ross, S J Warr |
| Clinical Features and Genetic Analysis of Taiwanese Primary Immunodeficiency Patients with Prolonged Diarrhea and Monogenetic Inflammatory Bowel Disease. Journal of clinical immunology 2023 5 . Wen-I Lee, Chien-Chang Chen, Shih-Hsiang Chen, Wan-Tz Lai, Tang-Her Jaing, Liang-Shiou Ou, Chi-Jou Liang, Chen-Chen Kang, Jing-Long Hua |
| Clinical characteristics of early-onset paediatric systemic lupus erythematosus in a single centre in China. Rheumatology (Oxford, England) 2023 2 . Hou Yipei, Wang Li, Luo Chong, Tang Wenjing, Dai Rongxin, An Yunfei, Tang Xuem |
| B-cells absence in patients diagnosed as inborn errors of immunity: a registry-based study. Immunogenetics 2024 4 . Razieh Khoshnevisan, Shakiba Hassanzadeh, Christoph Klein, Meino Rohlfs, Bodo Grimbacher, Newsha Molavi, Aryana Zamanifar, Ali Khoshnevisan, Mahbube Jafari, Bahram Bagherpour, Mahdiyeh Behnam, Somayeh Najafi, Roya Sherk |
| Bioinformatic analysis reveals the clinical value of SASH3 in survival prognosis and immune infiltration of acute myelocytic leukemia (AML). American journal of translational research 2024 1 15 (12): 6858-6866. Yufei Li, Lin Wang, Xueyuan Jia, Yanru Yang, Zhengqi Q |
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