Human Genome Epidemiology Literature Finder
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Records 1 - 19 (of 19 Records) |
| Query Trace: Disease and LRP2[original query] |
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| A single nucleotide polymorphism in LRP2 is associated with susceptibility to Alzheimer's disease in the Chinese population. Clinica chimica acta; international journal of clinical chemistry 2011 Jan 412 (3-4): 268-70. Wang Li-Ling, Pan Xiao-Ling, Wang Ying, Tang Hui-Dong, Deng Yu-Lei, Ren Ru-Jing, Xu Wei, Ma Jian-Fang, Wang Gang, Chen Sheng- |
| Association between low density lipoprotein receptor-related protein 2 gene polymorphisms and bone mineral density variation in Chinese population. PloS one 2011 6 (12): e28874. Wang Chun, Hu Yi-Ming, He Jin-Wei, Gu Jie-Mei, Zhang Hao, Hu Wei-Wei, Yue Hua, Gao Gao, Xiao Wen-Jin, Yu Jin-Bo, Ke Yao-Hua, Hu Yun-Qiu, Li Miao, Liu Yu-Juan, Fu Wen-Zhen, Ren Ying, Zhang Zhen-L |
| Common variants in Mendelian kidney disease genes and their association with renal function. Journal of the American Society of Nephrology : JASN 2013 Dec 24 (12): 2105-17. Parsa Afshin, Fuchsberger Christian, Köttgen Anna, O'Seaghdha Conall M, Pattaro Cristian, de Andrade Mariza, Chasman Daniel I, Teumer Alexander, Endlich Karlhans, Olden Matthias, Chen Ming-Huei, Tin Adrienne, Kim Young J, Taliun Daniel, Li Man, Feitosa Mary, Gorski Mathias, Yang Qiong, Hundertmark Claudia, Foster Meredith C, Glazer Nicole, Isaacs Aaron, Rao Madhumathi, Smith Albert V, O'Connell Jeffrey R, Struchalin Maksim, Tanaka Toshiko, Li Guo, Hwang Shih-Jen, Atkinson Elizabeth J, Lohman Kurt, Cornelis Marilyn C, Johansson Asa, Tönjes Anke, Dehghan Abbas, Couraki Vincent, Holliday Elizabeth G, Sorice Rossella, Kutalik Zoltan, Lehtimäki Terho, Esko Tõnu, Deshmukh Harshal, Ulivi Sheila, Chu Audrey Y, Murgia Federico, Trompet Stella, Imboden Medea, Kollerits Barbara, Pistis Giorgio, Harris Tamara B, Launer Lenore J, Aspelund Thor, Eiriksdottir Gudny, Mitchell Braxton D, Boerwinkle Eric, Schmidt Helena, Hofer Edith, Hu Frank, Demirkan Ayse, Oostra Ben A, Turner Stephen T, Ding Jingzhong, Andrews Jeanette S, Freedman Barry I, Giulianini Franco, Koenig Wolfgang, Illig Thomas, Döring Angela, Wichmann H-Erich, Zgaga Lina, Zemunik Tatijana, Boban Mladen, Minelli Cosetta, Wheeler Heather E, Igl Wilmar, Zaboli Ghazal, Wild Sarah H, Wright Alan F, Campbell Harry, Ellinghaus David, Nöthlings Ute, Jacobs Gunnar, Biffar Reiner, Ernst Florian, Homuth Georg, Kroemer Heyo K, Nauck Matthias, Stracke Sylvia, Völker Uwe, Völzke Henry, Kovacs Peter, Stumvoll Michael, Mägi Reedik, Hofman Albert, Uitterlinden Andre G, Rivadeneira Fernando, Aulchenko Yurii S, Polasek Ozren, Hastie Nick, Vitart Veronique, Helmer Catherine, Wang Jie Jin, Stengel Bénédicte, Ruggiero Daniela, Bergmann Sven, Kähönen Mika, Viikari Jorma, Nikopensius Tiit, Province Michael, Colhoun Helen, Doney Alex, Robino Antonietta, Krämer Bernhard K, Portas Laura, Ford Ian, Buckley Brendan M, Adam Martin, Thun Gian-Andri, Paulweber Bernhard, Haun Margot, Sala Cinzia, Mitchell Paul, Ciullo Marina, Vollenweider Peter, Raitakari Olli, Metspalu Andres, Palmer Colin, Gasparini Paolo, Pirastu Mario, Jukema J Wouter, Probst-Hensch Nicole M, Kronenberg Florian, Toniolo Daniela, Gudnason Vilmundur, Shuldiner Alan R, Coresh Josef, Schmidt Reinhold, Ferrucci Luigi, van Duijn Cornelia M, Borecki Ingrid, Kardia Sharon L R, Liu Yongmei, Curhan Gary C, Rudan Igor, Gyllensten Ulf, Wilson James F, Franke Andre, Pramstaller Peter P, Rettig Rainer, Prokopenko Inga, Witteman Jacqueline, Hayward Caroline, Ridker Paul M, Bochud Murielle, Heid Iris M, Siscovick David S, Fox Caroline S, Kao W Linda, Böger Carsten |
| Identification of two maternal transmission ratio distortion loci in pedigrees of the Framingham heart study. Scientific reports 2013 3 2147. Liu Yang, Zhang Liangliang, Xu Shuhua, Hu Landian, Hurst Laurence D, Kong Xiangy |
| Genetic variants in vitamin d pathway genes and risk of pancreas cancer; results from a population-based case-control study in ontario, Canada. PloS one 2013 8 (6): e66768. Anderson Laura N, Cotterchio Michelle, Knight Julia A, Borgida Ayelet, Gallinger Steven, Cleary Sean |
| Common variants of a urate-associated gene LRP2 are not associated with gout susceptibility. Rheumatology international 2014 Apr 34 (4): 473-6. Nakayama Akiyoshi, Matsuo Hirotaka, Shimizu Toru, Takada Yuzo, Nakamura Takahiro, Shimizu Seiko, Chiba Toshinori, Sakiyama Masayuki, Naito Mariko, Morita Emi, Ichida Kimiyoshi, Shinomiya Nariyos |
| Sequencing of LRP2 reveals multiple rare variants associated with urinary trefoil factor-3. Journal of the American Society of Nephrology : JASN 2014 Dec 25 (12): 2896-905. McMahon Gearoid M, Olden Matthias, Garnaas Maija, Yang Qiong, Liu Xuan, Hwang Shih-Jen, Larson Martin G, , Goessling Wolfram, Fox Caroline |
| Common Variants in LRP2 and COMT Genes Affect the Susceptibility of Gout in a Chinese Population. PloS one 2015 10 (7): e0131302. Dong Zheng, Zhao Dongbao, Yang Chengde, Zhou Jingru, Qian Qiaoxia, Ma Yanyun, He Hongjun, Ji Hengdong, Yang Yajun, Wang Xiaofeng, Xu Xia, Pang Yafei, Zou Hejian, Jin Li, Wang Jiuc |
| Identification of a homozygous missense mutation in LRP2 and a hemizygous missense mutation in TSPYL2 in a family with mild intellectual disability. Psychiatric genetics 2015 Nov . Vasli Nasim, Ahmed Iltaf, Mittal Kirti, Ohadi Mehrnaz, Mikhailov Anna, Rafiq Muhammad A, Bhatti Attya, Carter Melissa T, Andrade Danielle M, Ayub Muhammad, Vincent John B, John Pet |
Genetic variation in the gene LRP2 increases relapse risk in multiple sclerosis.
Journal of neurology, neurosurgery, and psychiatry 2017 Jul . Zhou Yuan, Graves Jennifer S, Simpson Steve, Charlesworth Jac C, Mei Ingrid van der, Waubant Emmanuelle, Barcellos Lisa F, Belman Anita, Krupp Lauren, Lucas Robyn, Ponsonby Anne-Louise, Taylor Bruce V, |
| Prevalence, determinants and clinical correlates of vitamin D deficiency in patients with Chronic Obstructive Pulmonary Disease in London, UK. The Journal of steroid biochemistry and molecular biology 2018 01 175 138-145. Jolliffe David A, James Wai Yee, Hooper Richard L, Barnes Neil C, Greiller Claire L, Islam Kamrul, Bhowmik Angshu, Timms Peter M, Rajakulasingam Raj K, Choudhury Aklak B, Simcock David E, Hyppönen Elina, Walton Robert T, Corrigan Christopher J, Griffiths Christopher J, Martineau Adrian |
| Genome-wide association analysis identifies multiple loci associated with kidney disease-related traits in Korean populations.
PloS one 2018 13 (3): e0194044. Lee Jeonghwan, Lee Young, Park Boram, Won Sungho, Han Jin Suk, Heo Nam |
| Sequence variants associating with urinary biomarkers.
Human molecular genetics 2019 04 28 (7): 1199-1211. Benonisdottir Stefania, Kristjansson Ragnar P, Oddsson Asmundur, Steinthorsdottir Valgerdur, Mikaelsdottir Evgenia, Kehr Birte, Jensson Brynjar O, Arnadottir Gudny A, Sulem Gerald, Sveinbjornsson Gardar, Kristmundsdottir Snaedis, Ivarsdottir Erna V, Tragante Vinicius, Gunnarsson Bjarni, Runolfsdottir Hrafnhildur Linnet, Arthur Joseph G, Deaton Aimee M, Eyjolfsson Gudmundur I, Davidsson Olafur B, Asselbergs Folkert W, Hreidarsson Astradur B, Rafnar Thorunn, Thorleifsson Gudmar, Edvardsson Vidar, Sigurdsson Gunnar, Helgadottir Anna, Halldorsson Bjarni V, Masson Gisli, Holm Hilma, Onundarson Pall T, Indridason Olafur S, Benediktsson Rafn, Palsson Runolfur, Gudbjartsson Daniel F, Olafsson Isleifur, Thorsteinsdottir Unnur, Sulem Patrick, Stefansson Ka |
| Exonic variants of genes related to the vitamin D signaling pathway in the families of familial multiple sclerosis using whole-exome next generation sequencing. Brain and behavior 2019 3 9 (4): e01272. Pytel Vanesa, Matías-Guiu Jordi A, Torre-Fuentes Laura, Montero-Escribano Paloma, Maietta Paolo, Botet Javier, Álvarez Sara, Gómez-Pinedo Ulises, Matías-Guiu Jor |
| Cancer gene mutations in congenital pulmonary airway malformation patients. ERJ open research 2019 2 5 (1): . Hsu Jacob Shujui, Zhang Ruizhong, Yeung Fanny, Tang Clara S M, Wong John K L, So Man-Ting, Xia Huimin, Sham Pak, Tam Paul K, Li Miaoxin, Wong Kenneth K Y, Garcia-Barcelo Maria-Mer |
| Genetic Analyses in Dent Disease and Characterization of CLCN5 Mutations in Kidney Biopsies. International journal of molecular sciences 2020 1 21 (2): . Gianesello Lisa, Ceol Monica, Bertoldi Loris, Terrin Liliana, Priante Giovanna, Murer Luisa, Peruzzi Licia, Giordano Mario, Paglialonga Fabio, Cantaluppi Vincenzo, Musetti Claudio, Valle Giorgio, Del Prete Dorella, Anglani Franca, Network Dent Disease Itali |
| Smoking, cardiovascular risk factors and LRP2 gene variation: Associations with disease severity, cognitive function and brain structure in primary progressive multiple sclerosis. Multiple sclerosis and related disorders 2021 10 56 103296. Chow Helene Højsgaard, Talbot Jacob, Marstrand Lisbet, Lundell Henrik, Roman Siebner Hartwig, Bach Søndergaard Helle, Sellebjerg Fi |
| Identification of recurrent pathogenic alleles using exome sequencing data: Proof-of-concept study of Russian subjects. European journal of medical genetics 2022 1 65 (2): 104426. Orlov Igor E, Laidus Tatiana A, Tumakova Anastasia V, Yanus Grigoriy A, Iyevleva Aglaya G, Sokolenko Anna P, Bizin Ilya V, Imyanitov Evgeny N, Suspitsin Evgeny |
| Clinical Exome Gene Panel Analysis of a Cohort of Urothelial Bladder Cancer Patients from Sri Lanka. Asian Pacific journal of cancer prevention : APJCP 2023 5 24 (5): 1533-1542. Ajith Malalasekera, Nilaksha Neththikumara, Praveenan Somasundaram, Sajeewani Pathirana, Chathumadavi Ediriweera, Dileepa Ediriweera, Serozsha As Goonewardena, Neville D Perera, Anuruddha Abeygunasekara, Rohan W Jayasekara, Kalum Wettasinghe, M Dilani S Lokuhetty, Vajira H W Dissanaye |
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