Human Genome Epidemiology Literature Finder
Records 1 - 24 (of 24 Records) |
Query Trace: LAMC1[original query] |
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Evaluation of the ARMD1 locus on 1q25-31 in patients with age-related maculopathy: genetic variation in laminin genes and in exon 104 of HEMICENTIN-1. Ophthalmic genetics 2004 Jun 25 (2): 111-9. Hayashi M, Merriam J E, Klaver C C W, Zernant J, Bergen A A, Smith R T, Chang S, Merriam J C, Allikmets |
Is laminin gamma-1 a candidate gene for advanced pelvic organ prolapse? American journal of obstetrics and gynecology 2010 May 202 (5): 505.e1-5. Chen Chen, Hill Lori D, Schubert Christine M, Strauss Jerome F, Matthews Catherine |
Comprehensive analysis of LAMC1 genetic variants in advanced pelvic organ prolapse. American journal of obstetrics and gynecology 2012 May 206 (5): 447.e1-6. Wu Jennifer M, Visco Anthony G, Grass Elizabeth A, Craig Damian M, Fulton Rebekah G, Haynes Carol, Amundsen Cindy L, Shah Svati |
LAMC1 gene is associated with premature ovarian failure. Maturitas 2012 Feb . Pyun JA, Cha DH, Kwack K |
Laminin-1 (LM-111) in preeclampsia and systemic lupus erythematosus. Autoimmunity 2012 Oct . Páez MC, Matsuura E, Díaz LA, Shoenfeld Y, Serrano NC, Anaya JM |
Systematic review and metaanalysis of genetic association studies of urinary symptoms and prolapse in women. American journal of obstetrics and gynecology 2015 Feb 212 (2): 199.e1-24. Cartwright Rufus, Kirby Anna C, Tikkinen Kari A O, Mangera Altaf, Thiagamoorthy Gans, Rajan Prabhakar, Pesonen Jori, Ambrose Chris, Gonzalez-Maffe Juan, Bennett Phillip, Palmer Tom, Walley Andrew, Järvelin Marjo-Riitta, Chapple Chris, Khullar V |
Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
Human molecular genetics 2014 Sep 23 (17): 4729-37. Whiffin Nicola, Hosking Fay J, Farrington Susan M, Palles Claire, Dobbins Sara E, Zgaga Lina, Lloyd Amy, Kinnersley Ben, Gorman Maggie, Tenesa Albert, Broderick Peter, Wang Yufei, Barclay Ella, Hayward Caroline, Martin Lynn, Buchanan Daniel D, Win Aung Ko, Hopper John, Jenkins Mark, Lindor Noralane M, Newcomb Polly A, Gallinger Steve, Conti David, Schumacher Fred, Casey Graham, Liu Tao, , Campbell Harry, Lindblom Annika, Houlston Richard S, Tomlinson Ian P, Dunlop Malcolm |
A common variant association study in ethnic Saudi Arabs reveals novel susceptibility loci for hypertriglyceridemia.
Clinical genetics 2016 Sep . Ram Ramesh, Wakil Salma M, Muiya Nzioka P, Andres Editha, Mazhar Nejat, Hagos Samya, Alshahid Maie, Meyer Brian F, Morahan Grant, Dzimiri Ndu |
Genome-wide association study identifies three novel loci in Fuchs endothelial corneal dystrophy.
Nature communications 2017 Mar 8 14898. Afshari Natalie A, Igo Robert P, Morris Nathan J, Stambolian Dwight, Sharma Shiwani, Pulagam V Lakshmi, Dunn Steven, Stamler John F, Truitt Barbara J, Rimmler Jacqueline, Kuot Abraham, Croasdale Christopher R, Qin Xuejun, Burdon Kathryn P, Riazuddin S Amer, Mills Richard, Klebe Sonja, Minear Mollie A, Zhao Jiagang, Balajonda Elmer, Rosenwasser George O, Baratz Keith H, Mootha V Vinod, Patel Sanjay V, Gregory Simon G, Bailey-Wilson Joan E, Price Marianne O, Price Francis W, Craig Jamie E, Fingert John H, Gottsch John D, Aldave Anthony J, Klintworth Gordon K, Lass Jonathan H, Li Yi-Ju, Iyengar Sudha |
Identification of a functional polymorphism affecting microRNA binding in the susceptibility locus 1q25.3 for colorectal cancer. Molecular carcinogenesis 2017 Mar . Ke Juntao, Tian Jianbo, Li Jiaoyuan, Gong Yajie, Yang Yang, Zhu Ying, Zhang Yi, Zhong Rong, Chang Jiang, Gong Ji |
Estrogen receptor and laminin genetic polymorphism among women with pelvic organ prolapse. Taiwanese journal of obstetrics & gynecology 2017 Dec 56 (6): 750-754. Nakad Bothaina, Fares Fuad, Azzam Naiel, Feiner Benjamin, Zilberlicht Ariel, Abramov Yor |
A functional polymorphism located at transcription factor binding sites, rs6695837 near LAMC1 gene, confers risk of colorectal cancer in Chinese populations. Carcinogenesis 2016 Dec . Lou Jiao, Gong Jing, Ke Juntao, Tian Jianbo, Zhang Yi, Li Jiaoyuan, Yang Yang, Zhu Ying, Gong Yajie, Li Lu, Chang Jiang, Zhong Rong, Miao Xiaopi |
Gene expression in the corneal endothelium of Fuchs endothelial corneal dystrophy patients with and without expansion of a trinucleotide repeat in TCF4. PloS one 2018 13 (7): e0200005. Wieben Eric D, Aleff Ross A, Tang Xiaojia, Kalari Krishna R, Maguire Leo J, Patel Sanjay V, Baratz Keith H, Fautsch Michael |
Analysis of candidate genes ZEB1 and LOXHD1 in late-onset Fuchs' endothelial corneal dystrophy in an Indian cohort. Ophthalmic genetics 2018 May 1-7. Rao Bhavna S, Ansar Samdani, Arokiasamy Tharigopala, Sudhir Rachapalli R, Umashankar Vetrivel, Rajagopal Rama, Soumittra Nagasa |
Correlation of the predisposition of Chinese children to cerebral palsy with nucleotide variation in pri-miR-124 that alters the non-canonical apoptosis pathway. Acta pharmacologica Sinica 2018 May . Li Hui, Wang Xiu-Li, Wu Yan-Qiu, Liu Xiu-Mei, Li Ai-M |
Common variants in LAMC1 confer risk for pelvic organ prolapse in Chinese population. Hereditas 2020 Jul 157 (1): 26. Chen Juan, Li Lei, Lang Jinghe, Zhu L |
A novel regQTL-SNP and the risk of lung cancer: a multi-dimensional study. Archives of toxicology 2021 Oct . Yu Yuhui, Mao Liping, Cheng Zhounan, Zhu Xiaoqi, Cui Jiahua, Fu Xiaoyu, Cheng Jingwen, Zhou Yan, Qiu Anni, Dong Yang, Zhuang Xun, Lu Yihua, Lian Yulong, Tian Tian, Wu Shuangshuang, Chu Minj |
Genetics of agenesis/hypoplasia of the uterus and vagina: narrowing down the number of candidate genes for Mayer-Rokitansky-Küster-Hauser Syndrome. Human genetics 2021 1 140 (4): 667-680. Mikhael Sasha, Dugar Sonal, Morton Madison, Chorich Lynn P, Tam Kerlene Berwick, Lossie Amy C, Kim Hyung-Goo, Knight James, Taylor Hugh S, Mukherjee Souhrid, Capra John A, Phillips John A, Friez Michael, Layman Lawrence |
Association of miRNA targetome variants in LAMC1 and GNB3 genes with colorectal cancer and obesity. Cancer medicine 2022 4 11 (21): 3923-3938. Gholami Morteza, Zoughi Marziyeh, Behboo Roobic, Taslimi Reza, Kazemeini Alireza, Bastami Milad, Hasani-Ranjbar Shirin, Larijani Bagher, Amoli Mahsa |
Fuchs Endothelial Corneal Dystrophy associated risk variant, rs3768617 in LAMC1 shows allele specific binding of GFI1B. Gene 2022 1 817 146179. Chakraborty Maynak, Das Rajesh Kumar, Samal Sujata, Das Sujata, Alone Debasmita Pank |
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 |
Using multi-tissue transcriptome-wide association study to identify candidate susceptibility genes for respiratory infectious diseases. Frontiers in genetics 2023 4 14 1164274. Zhu Xiaobo, Zou Yixin, Jia Linna, Ye Xiangyu, Zou Yanzheng, Tu Junlan, Li Juntong, Yu Rongbin, Yang Sheng, Huang Pe |
LAMC1, LAMA2 and LAMA3 gene polymorphisms and the risk for severe pelvic organ prolapse. Science bulletin 2023 1 64 (7): 466-468. Li Lei, Kang Jia, Zhang Ye, Mao Meng, Yang Yuxiang, Lang Jinghe, Sun Zhijing, Chen Juan, Zhu L |
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 |
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- Page last updated:Apr 22, 2024
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