Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 205 Records) |
Query Trace: LRP5[original query] |
---|
Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR). Ophthalmic genetics 2020 12 42 (2): 200-203. Carrera William, Ng Caleb, Desler Caroline, Jumper J Michael, Agarwal Ani |
A Meta-Analysis of the Transferability of Bone Mineral Density Genetic Loci Associations From European to African Ancestry Populations. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2020 Nov . Yau Michelle S, Kuipers Allison L, Price Ryan, Nicolas Aude, Tajuddin Salman M, Handelman Samuel K, Arbeeva Liubov, Chesi Alessandra, Hsu Yi-Hsiang, Liu Ching-Ti, Karasik David, Zemel Babette S, Grant Struan Fa, Jordan Joanne M, Jackson Rebecca D, Evans Michele K, Harris Tamara B, Zmuda Joseph M, Kiel Douglas |
Associations of LRP5 Gene With Bone Mineral Density, Bone Turnover Markers, and Fractures in the Elderly With Osteoporosis. Frontiers in endocrinology 2020 10 11 571549. Wang Qi-Fei, Bi Hong-Sen, Qin Ze-Lian, Wang Pu, Nie Fang-Fei, Zhang Guang- |
The genetic polymorphisms of key genes in WNT pathway (LRP5 and AXIN1) was associated with osteoporosis susceptibility in Chinese Han population. Endocrine 2021 Sep . Cui Yongsheng, Hu Xinglv, Zhang Chen, Wang Kunzhe |
WNT3A rs752107(C > T) Polymorphism Is Associated With an Increased Risk of Essential Hypertension and Related Cardiovascular Diseases. Frontiers in cardiovascular medicine 2021 7 8 675222. Ren Huan, Luo Jian-Quan, Ouyang Fan, Cheng Li, Chen Xiao-Ping, Zhou Hong-Hao, Huang Wei-Hua, Zhang W |
Diagnostic utility of next-generation sequence genetic panel testing in children presenting with a clinically significant fracture history. Archives of osteoporosis 2021 6 16 (1): 88. Harrington Jennifer, AlSubaihin Abdulmajeed, Dupuis Lucie, Kannu Peter, Mendoza-Londono Roberto, Howard Andr |
More severe phenotype of early-onset osteoporosis associated with recessive form of LRP5 and combination with DKK1 or WNT3A. Molecular genetics & genomic medicine 2021 5 9 (6): e1681. Caetano da Silva Caroline, Ricquebourg Manon, Orcel Philippe, Fabre Stéphanie, Funck-Brentano Thomas, Cohen-Solal Martine, Collet Corin |
Integrative analysis of genetic and clinical risk factors for bone loss in a Korean population. Bone 2021 Mar 147 115910. Lee Ji Hyun, Park JooYong, Kim Jung Hee, Choi Ji-Yeob, Choi Hyung Jin, Ku Eu Jeong, Hong A Ram, Shin Chan Soo, Cho Nam |
Ocular Features and Mutation Spectrum of Patients With Familial Exudative Vitreoretinopathy. Investigative ophthalmology & visual science 2021 12 62 (15): 4. Tao Tianchang, Xu Ningda, Li Jiarui, Li Hongyan, Qu Jinfeng, Yin Hong, Liang Jianhong, Zhao Mingwei, Li Xiaoxin, Huang Lvzh |
Whole exome sequencing reveals potentially pathogenic variants in a small subset of premenopausal women with idiopathic osteoporosis. Bone 2021 11 154 116253. Cohen Adi, Hostyk Joseph, Baugh Evan H, Buchovecky Christie M, Aggarwal Vimla S, Recker Robert R, Lappe Joan M, Dempster David W, Zhou Hua, Kamanda-Kosseh Mafo, Bucovsky Mariana, Stubby Julie, Goldstein David B, Shane Elizabe |
Associations of LRP5 and MTHFR Gene Variants with Osteoarthritis Prevalence in Elderly Women: A Japanese Cohort Survey Randomly Sampled from a Basic Resident Registry. Therapeutics and clinical risk management 2021 17 1065-1073. Nakano Masaki, Yui Haruka, Kikugawa Shingo, Tokida Ryosuke, Sakai Noriko, Kondo Naoki, Endo Naoto, Haro Hirotaka, Shimodaira Hiroki, Suzuki Takako, Kato Hiroyuki, Takahashi Jun, Nakamura Yuk |
The Wnt/?-catenin signaling pathway has a healing ability for periapical periodontitis. Scientific reports 2021 10 11 (1): 19673. Naruse Haruna, Itoh Shousaku, Itoh Yuki, Kagioka Takumi, Abe Makoto, Hayashi Mika |
Identification of Rare LRP5 Variants in a Cohort of Males with Impaired Bone Mass. International journal of molecular sciences 2021 10 22 (19): . Rocca Maria Santa, Minervini Giovanni, Di Nisio Andrea, Merico Maurizio, Bueno Marinas Maria, De Toni Luca, Pilichou Kalliopi, Garolla Andrea, Foresta Carlo, Ferlin Alber |
Myelomeningocele genotype-phenotype correlation findings in cilia, HH, PCP, and WNT signaling pathways. Birth defects research 2021 Jan . Ortiz-Cruz Gabriela, Aguayo-Gómez Adolfo, Luna-Muñoz Leonora, Muñoz-Téllez Luis A, Mutchinick Osvaldo |
LRP5 BIALLELIC MUTATIONS CAUSE A HIGHER INCIDENCE OF SEVERE PHENOTYPE COMPARED WITH LRP5 MONOALLELIC MUTATION. Retina (Philadelphia, Pa.) 2022 8 42 (10): 1958-1964. Chen Chunli, Zhang Xiang, Peng Xiaoyan, Hu Feng, Cheng Yizhe, Zhao Peiqu |
Genomic selection applications can improve the environmental performance of aquatics: A case study on the heat tolerance of abalone. Evolutionary applications 2022 7 15 (6): 992-1001. Liu Junyu, Peng Wenzhu, Yu Feng, Shen Yawei, Yu Wenchao, Lu Yisha, Lin Weihong, Zhou Muzhi, Huang Zekun, Luo Xuan, You Weiwei, Ke Caihu |
Mutation spectrum in a cohort with familial exudative vitreoretinopathy. Molecular genetics & genomic medicine 2022 Jul e2021. Qu Ning, Li Wei, Han Dong-Ming, Gao Jia-Yu, Yang Zheng-Tao, Jiang Li, Liu Tian-Bin, Chen Yan-Xian, Jiang Xiao-Sen, Zhou Liang, Wu Ji-Hong, Huang X |
Genotype-phenotype associations in familial exudative vitreoretinopathy: A systematic review and meta-analysis on more than 3200 individuals. PloS one 2022 7 17 (7): e0271326. Wang Xiaona, Chen Jun, Xiong Hui, Yu Xuh |
Association between the LRP5 rs556442 gene polymorphism and the risks of NAFLD and CHD in a Chinese Han population. BMC gastroenterology 2022 Jun 22 (1): 305. Han Dongli, Zhang Haiying, Liu Shousheng, Zhuang Likun, Zhao Zhenzhen, Ding Hongguang, Xin Yongni |
Germline Mutations Related to Primary Hyperparathyroidism Identified by Next-Generation Sequencing. Frontiers in endocrinology 2022 5 13 853171. Park Hye-Sun, Lee Yeon Hee, Hong Namki, Won Dongju, Rhee Yum |
Update on the Phenotypic and Genotypic Spectrum of KIF11-Related Retinopathy. Genes 2022 4 13 (4): . Wang You, Zhang Zhaotian, Huang Li, Sun Limei, Li Songshan, Zhang Ting, Ding Xiaoy |
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 |
Clinical relevance of genetic polymorphisms in WNT signaling pathway (SFRP1, WNT3A, CTNNB1, WIF-1, DKK-1, LRP5, LRP6) on pulmonary tuberculosis in a Chinese population. Frontiers in immunology 2022 12 13 1011700. Huang Qian, Wang Chao-Cai, Liu Yun-Guang, Zhao Chang-Ming, Zhang Tian-Ping, Liu Yan, Wang H |
Single nucleotide polymorphisms (rs3736228 and rs4988321) in low-density lipoprotein receptor-related protein-5 gene with predisposition to rheumatoid arthritis. Gene 2022 11 851 147025. Zehra Sitwat, Ghouri Maham, Jafari Halima, Saleem Saima, Fatima Sehrish, Azhar Ab |
The relationship between LRP5 rs556442 and rs638051 polymorphisms and mutations and their influence on bone metabolism in postmenopausal Xinjiang women with type 2 diabetes. Advances in clinical and experimental medicine : official organ Wroclaw Medical University 2022 11 . Li Jun, Song Minli, Li Siyuan, Wang Xiling, Zhao Huirong, Hou Zex |
Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy. Annals of medicine 2022 11 54 (1): 3286-3298. Mao Jianbo, Chen Yijing, Fang Yuyan, Shao Yirun, Xiang Ziyi, Li Hanxiao, Zhao Shixin, Chen Yiqi, Shen Lij |
Gene Network of Susceptibility to Atypical Femoral Fractures Related to Bisphosphonate Treatment. Genes 2022 01 13 (1): . Garcia-Giralt Natalia, Roca-Ayats Neus, Abril Josep F, Martinez-Gil Nuria, Ovejero Diana, Castañeda Santos, Nogues Xavier, Grinberg Daniel, Balcells Susanna, Rabionet Raqu |
LRP5-/6 gene polymorphisms and its association with risk of abnormal bone mass in postmenopausal women. Journal of orthopaedic surgery and research 2023 5 18 (1): 369. Jun Li, Zebing Liu, Yanxia Ren, Han Shao, Siyuan |
LDL receptor-related protein 5 rs648438 polymorphism is associated with the risk of skeletal fluorosis. International journal of environmental health research 2023 1 1-10. Zhang Meichen, Xu Haili, Lou Qun, Yin Fanshuo, Guo Ning, Wu Liaowei, Huang Wei, Ji Yi, Yang Liu, Li Qiao, Wang Sa, Guan Zhizhong, YanMei Yang, Yanhui G |
Clinical and genetic risk factors underlying severe consequence identified in 75 families with unilateral high myopia. Journal of translational medicine 2024 1 22 (1): 75. Yi Jiang, Xueshan Xiao, Wenmin Sun, Yingwei Wang, Shiqiang Li, Xiaoyun Jia, Panfeng Wang, J Fielding Hejtmancik, Qingjiong Zha |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 16, 2024
- Content source: