Human Genome Epidemiology Literature Finder
Records 1 - 18 (of 18 Records) |
Query Trace: LAMA5[original query] |
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Association of a common LAMA5 variant with anthropometric and metabolic traits in an Italian cohort of healthy elderly subjects. Experimental gerontology 2011 Jan 46 (1): 60-4. De Luca Maria, Crocco Paolina, Wiener Howard, Tiwari Hemant K, Passarino Giuseppe, Rose Giuseppi |
Common variants in the LAMA5 gene associate with fasting plasma glucose and serum triglyceride levels in a cohort of pre-and early pubertal children. Journal of pediatric genetics 2012 Oct 1 (4): 4. De Luca M, Chandler-Laney PC, Wiener H, Fernandez JR |
Association of the Laminin, Alpha 5 (LAMA5) rs4925386 with height and longevity in an elderly population from Southern Italy. Mechanisms of ageing and development 2016 Mar . De Luca Maria, Crocco Paolina, De Rango Francesco, Passarino Giuseppe, Rose Giuseppi |
Colorectal cancer susceptibility loci as predictive markers of rectal cancer prognosis after surgery. Genes, chromosomes & cancer 2017 11 57 (3): 140-149. Hu Yue, Gaedcke Jochen, Emons Georg, Beissbarth Tim, Grade Marian, Jo Peter, Yeager Meredith, Chanock Stephen J, Wolff Hendrik, Camps Jordi, Ghadimi B Michael, Ried Thom |
New candidate genes associated to endometriosis. Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2018 Jul 1-4. Christofolini Denise Maria, Mafra Fernanda Abani, Catto Michelle Cristina, Bianco Bianca, Barbosa Caio Paren |
Host Genetic and Gut Microbial Signatures in Familial Inflammatory Bowel Disease. Clinical and translational gastroenterology 2020 8 11 (7): e00213. Park Yoo Min, Ha Eunji, Gu Ki-Nam, Shin Ga Young, Lee Chang Kyun, Kim Kwangwoo, Kim Hyo Jo |
Genome-Wide Association Study for the Identification of Novel Genetic Variants Associated with the Risk of Neuroblastoma in Korean Children.
Cancer research and treatment 2020 Oct 52 (4): 1251-1261. Bae Joon Seol, Lee Ji Won, Yoo Jung Eun, Joung Je-Gun, Yoo Keon Hee, Koo Hong Hoe, Song Yun-Mi, Sung Ki Woo |
Gene-based association analysis reveals involvement of LAMA5 and cell adhesion pathways in nicotine dependence in African- and European-American samples.
Addiction biology 2020 Apr e12898. Fan Rongli, Cui Wenyan, Chen Jiali, Ma Yunlong, Yang Zhongli, Payne Thomas J, Ma Jennie Z, Li Ming |
Colorectal cancer genetic variants are also associated with serrated polyposis syndrome susceptibility. Journal of medical genetics 2020 3 57 (10): 677-682. Arnau-Collell Coral, Soares de Lima Yasmin, Díaz-Gay Marcos, Muñoz Jenifer, Carballal Sabela, Bonjoch Laia, Moreira Leticia, Lozano Juan José, Ocaña Teresa, Cuatrecasas Miriam, Díaz de Bustamante Aranzazu, Castells Antoni, Capellà Gabriel, Bujanda Luis, Cubiella Joaquin, Rodríguez-Alcalde Daniel, Balaguer Francesc, Ruiz-Ponte Clara, Valle Laura, Moreno Victor, Castellvi-Bel Ser |
Whole-Exome Sequencing Reveals Rare Germline Mutations in Patients With Hemifacial Microsomia. Frontiers in genetics 2021 6 12 580761. Chen Xiaojun, Liu Fatao, Mar Aung Zin, Zhang Yan, Chai Ga |
Recessive LAMA5 Variants Associated With Partial Epilepsy and Spasms in Infancy. Frontiers in molecular neuroscience 2022 6 15 825390. Luo Sheng, Liu Zhi-Gang, Wang Juan, Luo Jun-Xia, Ye Xing-Guang, Li Xin, Zhai Qiong-Xiang, Liu Xiao-Rong, Wang Jie, Gao Liang-Di, Liu Fu-Li, Ye Zi-Long, Li Huan, Gao Zai-Fen, Guo Qing-Hui, Li Bing-Mei, Yi Yong-Hong, Liao Wei-Pi |
Using whole exome sequencing to identify susceptibility genes associated with nonsyndromic cleft lip with or without cleft palate. Molecular genetics and genomics : MGG 2022 11 298 (1): 107-118. Fu Zhenzhen, Yue Jin, Xue Lingfa, Xu Yaoxiang, Ding Qian, Xiao Wenl |
Contribution of common and rare variants to Asian neovascular age-related macular degeneration subtypes. Nature communications 2023 9 14 (1): 5574. Qiao Fan, Hengtong Li, Xiaomeng Wang, Yih-Chung Tham, Kelvin Yi Chong Teo, Masayuki Yasuda, Weng Khong Lim, Yuet Ping Kwan, Jing Xian Teo, Ching-Jou Chen, Li Jia Chen, Jeeyun Ahn, Sonia Davila, Masahiro Miyake, Patrick Tan, Kyu Hyung Park, Chi Pui Pang, Chiea Chuan Khor, Tien Yin Wong, Yasuo Yanagi, Chui Ming Gemmy Cheung, Ching-Yu Che |
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort. Biomedicines 2023 8 11 (8): . Aurora Santin, Beatrice Spedicati, Anna Morgan, Stefania Lenarduzzi, Paola Tesolin, Giuseppe Giovanni Nardone, Daniela Mazzà, Giovanni Di Lorenzo, Federico Romano, Francesca Buonomo, Alessandro Mangogna, Maria Pina Concas, Gabriella Zito, Giuseppe Ricci, Giorgia Girot |
Multi-ancestry GWAS of Fuchs corneal dystrophy highlights roles of laminins, collagen, and endothelial cell regulation. Research square 2023 5 . Neal Peachey, Bryan Gorman, Michael Francis, Cari Nealon, Christopher Halladay, Nalvi Duro, Kyriacos Markianos, Giulio Genovese, Pirro Hysi, Hélène Choquet, Natalie Afshari, Yi-Ju Li, J Michael Gaziano, Adriana Hung, Wen-Chih Wu, Paul Greenberg, Saiju Pyarajan, Jonathan Lass, Sudha Iyeng |
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 |
A multi-ancestry GWAS of Fuchs corneal dystrophy highlights the contributions of laminins, collagen, and endothelial cell regulation. Communications biology 2024 4 7 (1): 418. Bryan R Gorman, Michael Francis, Cari L Nealon, Christopher W Halladay, Nalvi Duro, Kyriacos Markianos, Giulio Genovese, Pirro G Hysi, Hélène Choquet, Natalie A Afshari, Yi-Ju Li, , J Michael Gaziano, Adriana M Hung, Wen-Chih Wu, Paul B Greenberg, Saiju Pyarajan, Jonathan H Lass, Neal S Peachey, Sudha K Iyeng |
Characterization of cell cycle, inflammation, and oxidative stress signaling role in non-communicable diseases: Insights into genetic variants, microRNAs and pathways. Computers in biology and medicine 2024 4 174 108346. Salvatore D'Antona, Danilo Porro, Francesca Gallivanone, Gloria Berto |
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- Page last updated:Apr 16, 2024
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