Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 138 Records) |
| Query Trace: ENPP1[original query] |
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| Gender differences in the association of ENPP1 polymorphisms with type 2 diabetes in a Chinese population. Gene 2017 Sep . Chen Lulin, Qin Yingfen, Liang Danyan, Liang Xinghuan, Liang Yaojie, Li Li, Xian Jing, Zhang Lulu, Tong Lei, Li Hong, Zhang Haiyi |
| The ENPP1 K121Q polymorphism modulates developing of bone disorders in type 2 diabetes: A cross sectional study. Gene 2017 Sep . Neamati Nahid, Hosseini Seyed Reza, Hajiahmadi Mahmood, Halalkhor Sohrab, Nooreddini Hajighorban, Niaki Haleh Akhavan, Korani Bahare, Parsian Ha |
| ENPP1 121Q functional variant enhances susceptibility to coronary artery disease in South Indian patients with type 2 diabetes mellitus. Molecular and cellular biochemistry 2017 May . Sumi S, Ramachandran Surya, RamanKutty V, Patel Maulin M, Anand T N, Mullasari Ajit S, Kartha C |
| Condylar geometry variation is associated with ENPP1 variant in a population of patients with dento-facial deformities. Journal of cranio-maxillo-facial surgery : official publication of the European Association for Cranio-Maxillo-Facial Surgery 2017 Mar . Constant Marion, Nicot Romain, Vieira Alexandre R, Raoul Gwenael, Sciote James J, Ferri Jo |
| ENPP1 and ESR1 genotypes associated with subclassifications of craniofacial asymmetry and severity of temporomandibular disorders. American journal of orthodontics and dentofacial orthopedics : official publication of the American Association of Orthodontists, its constituent societies, and the American Board of Orthodontics 2017 11 152 (5): 631-645. Chung Kay, Richards Tabitha, Nicot Romain, Vieira Alexandre R, Cruz Christiane V, Raoul Gwénaël, Ferri Joel, Sciote James |
| [The analysis of association between ENPP1 K121Q polymorphism and risk factors of type 2 diabetes mellitus in ukrainian population]. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2018 71 (4): 815-820. Marchenko Irina V, Dubovyk Yevhen I, Matlai Olha I, Biesiedina Antonina A, Kniazkova Polina V, Harbuzova Yelizaveta |
| ENPP1 K121Q (rs1044498?C?>?A) genetic polymorphism confers a high risk of susceptibility to coronary heart disease: A PRISMA-compliant article. Medicine 2018 Jul 97 (27): e11236. Di Jia-Yin, Dai Meng-Lu, Zhang Zong-X |
| Association and in silico studies of ENPP1 gene variants with type 2 diabetes mellitus in a Northern Iranian population. Gene 2018 Jun . Sharafshah Alireza, Keshavarz Parvaneh, Rezaei Sajjad, Farhadian Nastar |
| [The association between enpp1 rs997509 polymorphism and type 2 diabetes mellitus development in ukrainian population]. Wiadomosci lekarskie (Warsaw, Poland : 1960) 2018 71 (3 pt 1): 490-495. Marchenko Irina V, Dubovyk Yevhen I, Tkach Gennadii F, Maksymova Olena S, Matlai Olha I, Ataman Alexander V, Harbuzova Viktoriia |
| Genetic determinants of steatosis and fibrosis progression in paediatric non-alcoholic fatty liver disease. Liver international : official journal of the International Association for the Study of the Liver 2019 Mar 39 (3): 540-556. Hudert Christian A, Selinski Silvia, Rudolph Birgit, Bläker Hendrik, Loddenkemper Christoph, Thielhorn Ria, Berndt Nikolaus, Golka Klaus, Cadenas Cristina, Reinders Jörg, Henning Stephan, Bufler Philip, Jansen Peter L M, Holzhütter Hermann-Georg, Meierhofer David, Hengstler Jan G, Wiegand Susan |
| [Mutation analysis of four pedigrees affected with hypophosphatemic rickets through targeted next-generation sequencing]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2018 10 35 (5): 638-643. Bai Ying, Liu Ning, Shao Mingwei, Qin Guijun, Gao Xu, Kong Xiangdo |
| MC4R and ENPP1 gene polymorphisms and their implication in maternal and neonatal risk for obesity. Scientific reports 2019 Jul 9 (1): 10858. M?rginean Claudiu, M?rginean Cristina Oana, Iancu Mihaela, Meli? Lorena Elena, Tripon Florin, B?nescu Claud |
| K121Q polymorphism in the Ectonucleotide Pyrophosphatase/Phosphodiesterase 1 gene is associated with acute kidney rejection. PloS one 2019 14 (7): e0219062. Sortica Denise A, Crispim Daisy, Bauer Andrea C, Nique Pamela S, Nicoletto Bruna B, Crestani Ricieli P, Staehler Jennifer T, Manfro Roberto C, Canani Luis |
| Genetic variants in cardiac calcification in Northern Sweden. Medicine 2019 4 98 (15): e15065. Hellman Urban, Mörner Stellan, Henein Micha |
| An observational study of the risk of neonatal macrosomia, and early gestational diabetes associated with selected candidate genes for type 2 diabetes mellitus polymorphisms in women with gestational diabetes mellitus. Ginekologia polska 2019 1 89 (12): 705-710. Zawiejska Agnieszka, Wender-Ozegowska Ewa, Bogacz Anna, Iciek Rafal, Mikolajczak Przemyslaw, Brazert Jac |
| Condyle modeling stability, craniofacial asymmetry and ACTN3 genotypes: Contribution to TMD prevalence in a cohort of dentofacial deformities. PloS one 2020 7 15 (7): e0236425. Nicot Romain, Chung Kay, Vieira Alexandre R, Raoul Gwénaël, Ferri Joël, Sciote James |
| Heritability and Genetics of Type 2 Diabetes Mellitus in Sub-Saharan Africa: A Systematic Review and Meta-Analysis. Journal of diabetes research 2020 7 2020 3198671. Asamoah Evans Adu, Obirikorang Christian, Acheampong Emmanuel, Annani-Akollor Max Efui, Laing Edwin Ferguson, Owiredu Eddie-Williams, Anto Enoch Oda |
| Biomarkers and genetic modulators of cerebral vasculopathy in sub-Saharan ancestry children with sickle cell anemia. Blood cells, molecules & diseases 2020 Jul 83 102436. Silva Marisa, Vargas Sofia, Coelho Andreia, Ferreira Emanuel, Mendonça Joana, Vieira Luís, Maia Raquel, Dias Alexandra, Ferreira Teresa, Morais Anabela, Soares Isabel Mota, Lavinha João, Silva Rita, Kjöllerström Paula, Faustino Pau |
| Genetic landscape of autism spectrum disorder in Vietnamese children. Scientific reports 2020 3 10 (1): 5034. Tran Kien Trung, Le Vinh Sy, Bui Hoa Thi Phuong, Do Duong Huy, Ly Ha Thi Thanh, Nguyen Hieu Thi, Dao Lan Thi Mai, Nguyen Thanh Hong, Vu Duc Minh, Ha Lien Thi, Le Huong Thi Thanh, Mukhopadhyay Arijit, Nguyen Liem Tha |
| The genetic map of diabetic nephropathy: evidence from a systematic review and meta-analysis of genetic association studies. Clinical kidney journal 2020 10 13 (5): 768-781. Tziastoudi Maria, Stefanidis Ioannis, Zintzaras Eli |
| Single locus and haplotype association of ENPP1 gene variants with the development of retinopathy among type 2 diabetic patients. International ophthalmology 2020 Jan . Gohari-Lasaki Sahar, Sharafshah Alireza, Abbaspour Saima, Keshavarz Parvan |
| Influence of Single Nucleotide Polymorphism of ENPP1 and ADIPOQ on Insulin Resistance and Obesity: A Case-Control Study in a Javanese Population. Life (Basel, Switzerland) 2021 Jun 11 (6): . Arianti Rini, Ariani Nia Lukita, Muhammad Al Azhar, Sadewa Ahmad Hamim, Farmawati Arta, Sunarti , Hastuti Pramudji, Kristóf End |
| Type 2 diabetes is associated with the MTNR1B gene, a genetic bridge between circadian rhythm and glucose metabolism, in a Turkish population. Molecular biology reports 2021 Jun . Arikoglu Hilal, Erkoc-Kaya Dudu, Ipekci Suleyman Hilmi, Gokturk Fatma, Iscioglu Funda, Korez Muslu Kazim, Baldane Suleyman, Gonen Mustafa Sa |
| Genetic associated complications of type 2 diabetes mellitus. Panminerva medica 2021 10 64 (2): 274-288. Wong Yee H, Wong Shen H, Wong Xiao T, Yap Qiao Y, Yip Khar Y, Wong Liang Z, Chellappan Dinesh K, Bhattamisra Subrat K, Candasamy Mayur |
| Association of the ENPP1/ENTPD1 Polymorphisms in Hemodialysis Patients. International journal of general medicine 2021 14 6401-6408. Zhang Xi, Wan Ziming, Cheng Si, Gan H |
| Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders. The Journal of clinical endocrinology and metabolism 2022 3 107 (7): e3048-e3057. Oheim Ralf, Tsourdi Elena, Seefried Lothar, Beller Gisela, Schubach Max, Vettorazzi Eik, Stürznickel Julian, Rolvien Tim, Ehmke Nadja, Delsmann Alena, Genest Franca, Krüger Ulrike, Zemojtel Tomasz, Barvencik Florian, Schinke Thorsten, Jakob Franz, Hofbauer Lorenz C, Mundlos Stefan, Kornak U |
| The Contribution of Deleterious Rare Alleles in ENPP1 and Osteomalacia Causative Genes to Atypical Femoral Fracture. The Journal of clinical endocrinology and metabolism 2022 1 107 (5): e1890-e1898. Furukawa Hiroshi, Oka Shomi, Kondo Naoki, Nakagawa Yasuaki, Shiota Naofumi, Kumagai Kenji, Ando Keiji, Takeshita Tsutao, Oda Takenori, Takahashi Yoshinori, Izawa Kazutaka, Iwasaki Yoichi, Hasegawa Kazuhiro, Arino Hiroshi, Minamizaki Takeshi, Yoshikawa Norie, Takata Shinjiro, Yoshihara Yasuo, Tohma Shige |
| Role of ENPP1 Gene Variants in the Susceptibility to Diabetic Nephropathy in Patients with type 2 Diabetes Mellitus. Biochemical genetics 2023 5 . Niloofar Faraji, Saima Abbaspour, Farzam Ajamian, Parvaneh Keshava |
| Correlation between ENPP1 Gene rs1044498 Polymorphism with the Risk of Type 2 Diabetes Mellitus: A Meta-Analysis. The Tohoku journal of experimental medicine 2024 7 . Chunlin Li, Li L |
| Vascular calcification in chronic kidney disease associated with pathogenic variants in ABCC6. Gene 2024 6 927 148731. Clara Schott, Allison A Dilliott, Jian Wang, Adam D McIntyre, Surim Son, Samantha Colaiacovo, Cadence Baker, Lakshman Gunaratnam, Andrew A House, Shih-Han Susan Huang, Hariharan Iyer, John Johnson, Khaled Lotfy, Mario Masellis, Douglas P Munoz, Faisal Rehman, Pavel S Roshanov, Richard H Swartz, Matthew A Weir, Robert A Hegele, Dervla M Connaught |
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