Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 106 Records) |
Query Trace: PLCE1[original query] |
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Migraine, Stroke, and Cervical Arterial Dissection: Shared Genetics for a Triad of Brain Disorders With Vascular Involvement.
Neurology. Genetics 2022 2 8 (1): e653. Daghals Iyas, Sargurupremraj Muralidharan, Danning Rebecca, Gormley Padhraig, Malik Rainer, Amouyel Philippe, Metso Tiina, Pezzini Alessandro, Kurth Tobias, Debette Stéphanie, Chasman Dani |
Polygenic prediction of preeclampsia and gestational hypertension.
Nature medicine 2023 5 29 (6): 1540-1549. Honigberg Michael C, Truong Buu, Khan Raiyan R, Xiao Brenda, Bhatta Laxmi, Vy Ha My T, Guerrero Rafael F, Schuermans Art, Selvaraj Margaret Sunitha, Patel Aniruddh P, Koyama Satoshi, Cho So Mi Jemma, Vellarikkal Shamsudheen Karuthedath, Trinder Mark, Urbut Sarah M, Gray Kathryn J, Brumpton Ben M, Patil Snehal, Zöllner Sebastian, Antopia Mariah C, Saxena Richa, Nadkarni Girish N, Do Ron, Yan Qi, Pe'er Itsik, Verma Shefali Setia, Gupta Rajat M, Haas David M, Martin Hilary C, van Heel David A, Laisk Triin, Natarajan Prade |
Insights into the genetic basis of retinal detachment.
Human molecular genetics 2020 Mar 29 (4): 689-702. Boutin Thibaud S, Charteris David G, Chandra Aman, Campbell Susan, Hayward Caroline, Campbell Archie, , Nandakumar Priyanka, Hinds David, , Mitry Danny, Vitart Veroniq |
Estimation of associations between 10 common gene polymorphisms and gastric cancer: evidence from a meta-analysis. Journal of clinical pathology 2019 11 73 (6): 318-321. Xie Zongjing, Wang Bingmei, Chai Yongjie, Chen Juny |
The Correlation between Phospholipase C Epsilon (PLCE1) Gene Polymorphisms and Risk of Gastric Adenocarcinoma in Iranian Population. International journal of hematology-oncology and stem cell research 2019 10 13 (3): 108-115. Shekarriz Ramin, Faghani Sahar, Tafazoli Alireza, Hashemi-Soteh Mohammad Bagh |
Genetic variants in GHR and PLCE1 genes are associated with susceptibility to esophageal cancer. Molecular genetics & genomic medicine 2020 Aug e1474. Wang Rong, Si Lining, Zhu Derui, Shen Guoping, Long Qifu, Zhao Yan |
Predictive model for risk of gastric cancer using genetic variants from genome-wide association studies and high-evidence meta-analysis. Cancer medicine 2020 Aug . Qiu Lixin, Qu Xiaofei, He Jing, Cheng Lei, Zhang Ruoxin, Sun Menghong, Yang Yajun, Wang Jiucun, Wang Mengyun, Zhu Xiaodong, Guo Weiji |
The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population. PloS one 2020 6 15 (6): e0234547. Soltész Beáta, Pikó Péter, Sándor János, Kósa Zsigmond, Ádány Róza, Fiatal Szilv |
The PLCE1 rs2274223 variant is associated with the risk of laryngeal squamous cell carcinoma. International journal of medical sciences 2020 11 17 (17): 2826-2830. Zhang Yi, Li Wei, Wang Ying, Wang Ning |
Cumulative Evidence for Associations between Genetic Variants and Risk of Esophageal Cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2020 Jan . Li Gaoming, Song Qiuyue, Jiang Yuxing, Cai Angsong, Tang Yong, Tang Ning, Yi Dali, Zhang Rui, Wei Zeliang, Liu Dingxin, Chen Jia, Zhang Yanqi, Liu Ling, Wu Yazhou, Zhang Ben, Yi Do |
Auxiliary genetic analysis in a Chinese adolescent NPH family by single nucleotide polymorphism screening. Molecular medicine reports 2020 1 21 (3): 1115-1124. Tang Chunrong, Zhou Daoyuan, Tan Rongshao, Zhong Xiaoshi, Xiao Xiao, Qin Danping, Liu Yun, Hu Jianguang, Liu Y |
Identification and epidemiological evaluation of gastric cancer risk factors: based on a field synopsis and meta-analysis in Chinese population. Aging 2021 Sep 13 (undefined): . Duan Fujiao, Song Chunhua, Shi Jiachen, Wang Peng, Ye Hua, Dai Liping, Zhang Jianying, Wang Kaiju |
PLCE1 Polymorphisms Are Associated With Gastric Cancer Risk: The Changes in Protein Spatial Structure May Play a Potential Role. Frontiers in genetics 2021 9 12 714915. Hu Xi'e, Jia Jintong, Yang Zhenyu, Chen Songhao, Xue Jingyi, Duan Sensen, Yang Ping, Peng Shujia, Yang Lin, Yuan Lijuan, Bao Guoqia |
Independent and opposing associations of dietary phytosterols intake and PLCE1 rs2274223 polymorphisms on esophageal squamous cell carcinoma risk. European journal of nutrition 2021 May . Wang Shuyi, Zhao Wenjing, Sun Liping, Xiao Su-Mei, Lin Sihao, Zhao Jin, Xiao Hengyi, Xing Xiangbin, Lao Xiang Qian, Chen Yu-Ming, Liu Xudo |
Next-Generation Sequencing for Congenital Nephrotic Syndrome: A Multi-Center Cross-Sectional Study from India. Indian pediatrics 2021 5 58 (5): 445-451. Joshi Aditi, Sinha Aditi, Sharma Aakanksha, Shamim Uzma, Uppilli Bharathram, Sharma Pooja, Zahra Sana, Parveen Shaista, Mathur Aradhana, Chandan Monica, Tewari Prachi, Khandelwal Priyanka, Hari Pankaj, Mukerji Mitali, Faruq Mohammed, Bagga Arvind, |
Next-generation sequencing in patients with familial FSGS: first report of collagen gene mutations in Tunisian patients. Journal of human genetics 2021 3 66 (8): 795-803. Ammar Sawssan, Kanoun Houda, Kammoun Khawla, Domingo-Gallego Andrea, Ruiz Patricia, Lorente-Grandoso Laura, Pybus Marc, Maalej Bayen, Boudawara Tahya, Kamoun Hassen, Ben Hmida Mohamed, Ars Elisabet, Jarraya Faiç |
Causal and putative pathogenic mutations identified in 39% of children with primary steroid-resistant nephrotic syndrome in South Africa. European journal of pediatrics 2022 Oct 181 (10): 3595-3606. Nandlal Louansha, Winkler Cheryl A, Bhimma Rajendra, Cho Sungkweon, Nelson George W, Haripershad Sudesh, Naicker Thajasvar |
Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes. Frontiers in genetics 2022 8 13 886038. Alaamery Manal, Alghamdi Jahad, Massadeh Salam, Alsawaji Mona, Aljawini Nora, Albesher Nour, Alghamdi Bader, Almutairi Mansour, Hejaili Fayez, Alfadhel Majid, Baz Batoul, Almuzzaini Bader, Almutairi Adel F, Abdullah Mubarak, Quintana Francisco J, Sayyari Abdull |
Polymorphisms in immune-mediator genes and the risk of dengue virus infection: Lights from a systematic revaluation by Bayesian approaches. Cytokine 2022 Jul 157 155955. Leal Alessandro Luiz Araújo Bentes, da Silva Fyama Araújo, Shin Jae Il, Jeong Gwang Hun, Ferreira Gustavo Portela, Vasconcelos Daniel Fernando Pereira, Monteiro José Rogério Souza, de Sousa Aline Andrade, da Silva Felipe Rodolfo Pereira, da Cunha Pereira Anna Carolina Tole |
The Frequency of Genetic Mutations in Pediatric Patients Diagnosed with Nephrotic Syndrome: A Single-Center Retrospective Study in Saudi Arabia. Saudi journal of kidney diseases and transplantation : an official publication of the Saudi Center for Organ Transplantation, Saudi Arabia 2022 2 32 (3): 798-805. Almokali Khamisa, Alyami Ali, Ajeebi Abdulaziz, Almutairi Turki, Aldriwesh Mar |
[Association of GSTP1 and PLCE1 gene polymorphisms with primary esophageal cancer]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 11 39 (11): 1283-1289. Han Wenjie, Li Weiyan, He Zhangbi |
Polymorphisms of hypertension susceptibility genes as a risk factors of preeclampsia in the Caucasian population of central Russia. Placenta 2022 Sep 129 51-61. Churnosov Mikhail, Abramova Maria, Reshetnikov Evgeny, Lyashenko Igor V, Efremova Olesya, Churnosova Maria, Ponomarenko Iri |
Aggregation of Genome-Wide Association Data from FinnGen and UK Biobank Replicates Multiple Risk Loci for Pregnancy Complications.
Genes 2022 12 13 (12): . Changalidis Anton I, Maksiutenko Evgeniia M, Barbitoff Yury A, Tkachenko Alexander A, Vashukova Elena S, Pachuliia Olga V, Nasykhova Yulia A, Glotov Andrey |
Genome-wide association study of esophageal squamous cell cancer identifies shared and distinct risk variants in African and Chinese populations. American journal of human genetics 2023 9 . Wenlong Carl Chen, Jean-Tristan Brandenburg, Ananyo Choudhury, Mahtaab Hayat, Dhriti Sengupta, Yaniv Swiel, Chantal Babb de Villiers, Lucien Ferndale, Colleen Aldous, Cassandra C Soo, Sang Lee, Charles Curtis, Rob Newton, Tim Waterboer, Freddy Sitas, Debbie Bradshaw, Christian C Abnet, Michele Ramsay, M Iqbal Parker, Elvira Singh, Cathryn M Lewis, Christopher G Math |
Copy number variation analysis in 138 families with steroid-resistant nephrotic syndrome identifies causal homozygous deletions in PLCE1 and NPHS2 in two families. Pediatric nephrology (Berlin, Germany) 2023 9 . Dalia Pantel, Nils D Mertens, Ronen Schneider, Selina Hölzel, Jameela A Kari, Sherif El Desoky, Mohamed A Shalaby, Tze Y Lim, Simone Sanna-Cherchi, Shirlee Shril, Friedhelm Hildebran |
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy.
JAMA cardiology 2023 6 . Jaakko S Tyrmi, Tea Kaartokallio, A Inkeri Lokki, Tiina Jääskeläinen, Eija Kortelainen, Sanni Ruotsalainen, Juha Karjalainen, Samuli Ripatti, Anna Kivioja, Triin Laisk, Johannes Kettunen, Anneli Pouta, Katja Kivinen, Eero Kajantie, Seppo Heinonen, Juha Kere, Hannele Laivuori, |
Risk Effects of rs1799945 Polymorphism of the HFE Gene and Intergenic Interactions of GWAS-Significant Loci for Arterial Hypertension in the Caucasian Population of Central Russia. International journal of molecular sciences 2023 5 24 (9): . Tatiana Ivanova, Maria Churnosova, Maria Abramova, Irina Ponomarenko, Evgeny Reshetnikov, Inna Aristova, Inna Sorokina, Mikhail Churnos |
Sex-Specific Features of the Correlation between GWAS-Noticeable Polymorphisms and Hypertension in Europeans of Russia. International journal of molecular sciences 2023 5 24 (9): . Tatiana Ivanova, Maria Churnosova, Maria Abramova, Denis Plotnikov, Irina Ponomarenko, Evgeny Reshetnikov, Inna Aristova, Inna Sorokina, Mikhail Churnos |
Idiopathic collapsing glomerulopathy is associated with APOL1 high-risk genotypes or Mendelian variants in most affected individuals in a highly admixed population. Kidney international 2023 12 . Precil D Neves, Andreia Watanabe, Elieser H Watanabe, Amanda M Narcizo, Kelly Nunes, Antonio M Lerario, Frederico Moraes Ferreira, Lívia B Cavalcante, Janewit Wongboonsin, Denise M Malheiros, Lectícia B Jorge, Matthew G Sampsom, Irene L Noronha, Luiz F Onuch |
Genetic Association Studies of MICB and PLCE1 with Severity of Dengue in Indonesian and Taiwanese Populations. Diagnostics (Basel, Switzerland) 2023 11 13 (21): . Imaniar Noor Faridah, Haafizah Dania, Rita Maliza, Wan-Hsuan Chou, Wen-Hung Wang, Yen-Hsu Chen, Dyah Aryani Perwitasari, Wei-Chiao Cha |
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- Page last updated:Apr 22, 2024
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