Human Genome Epidemiology Literature Finder
Records 1 - 20 (of 20 Records) |
Query Trace: PLEKHA1[original query] |
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Hypothetical LOC387715 is a second major susceptibility gene for age-related macular degeneration, contributing independently of complement factor H to disease risk. Human molecular genetics 2005 Nov 14 (21): 3227-36. Rivera Andrea, Fisher Sheila A, Fritsche Lars G, Keilhauer Claudia N, Lichtner Peter, Meitinger Thomas, Weber Bernhard H |
CFH, ELOVL4, PLEKHA1 and LOC387715 genes and susceptibility to age-related maculopathy: AREDS and CHS cohorts and meta-analyses. Human molecular genetics 2006 Nov 15 (21): 3206-18. Conley Yvette P, Jakobsdottir Johanna, Mah Tammy, Weeks Daniel E, Klein Ronald, Kuller Lewis, Ferrell Robert E, Gorin Michael |
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration. Proceedings of the National Academy of Sciences of the United States of America 2007 Oct 104 (41): 16227-32. Kanda Atsuhiro, Chen Wei, Othman Mohammad, Branham Kari E H, Brooks Matthew, Khanna Ritu, He Shirley, Lyons Robert, Abecasis Gonçalo R, Swaroop Ana |
PLEKHA1-LOC387715-HTRA1 polymorphisms and exudative age-related macular degeneration in the French population. Molecular vision 2007 13 2153-9. Leveziel Nicolas, Souied Eric H, Richard Florence, Barbu Véronique, Zourdani Alain, Morineau Gilles, Zerbib Jennyfer, Coscas Gabriel, Soubrane Gisèle, Benlian Pasca |
The NEI/NCBI dbGAP database: genotypes and haplotypes that may specifically predispose to risk of neovascular age-related macular degeneration. BMC medical genetics 2008 9 (1): 51. Zhang Hong, Morrison Margaux A, Dewan Andy, Adams Scott, Andreoli Michael, Huynh Nancy, Regan Maureen, Brown Alison, Miller Joan W, Kim Ivana K, Hoh Josephine, Deangelis Margaret |
Alleles in the HtrA serine peptidase 1 gene alter the risk of neovascular age-related macular degeneration. Ophthalmology 2008 Jul 115 (7): 1209-1215.e7. Deangelis Margaret M, Ji Fei, Adams Scott, Morrison Margaux A, Harring Amanda J, Sweeney Meredith O, Capone Antonio, Miller Joan W, Dryja Thaddeus P, Ott Jurg, Kim Ivana |
Genome-wide association analyses of genetic, phenotypic, and environmental risks in the age-related eye disease study. Molecular vision 2010 16 2811-21. Ryu Euijung, Fridley Brooke L, Tosakulwong Nirubol, Bailey Kent R, Edwards Albert |
Integration of genome-wide association studies with biological knowledge identifies six novel genes related to kidney function. Human molecular genetics 2012 Dec 21 (24): 5329-43. Chasman Daniel I, Fuchsberger Christian, Pattaro Cristian, Teumer Alexander, Böger Carsten A, Endlich Karlhans, Olden Matthias, Chen Ming-Huei, Tin Adrienne, Taliun Daniel, Li Man, Gao Xiaoyi, Gorski Mathias, Yang Qiong, Hundertmark Claudia, Foster Meredith C, O'Seaghdha Conall M, Glazer Nicole, Isaacs Aaron, Liu Ching-Ti, Smith Albert V, O'Connell Jeffrey R, Struchalin Maksim, Tanaka Toshiko, Li Guo, Johnson Andrew D, Gierman Hinco J, Feitosa Mary F, Hwang Shih-Jen, Atkinson Elizabeth J, Lohman Kurt, Cornelis Marilyn C, Johansson Asa, Tönjes Anke, Dehghan Abbas, Lambert Jean-Charles, Holliday Elizabeth G, Sorice Rossella, Kutalik Zoltan, Lehtimäki Terho, Esko Tõnu, Deshmukh Harshal, Ulivi Sheila, Chu Audrey Y, Murgia Federico, Trompet Stella, Imboden Medea, Coassin Stefan, Pistis Giorgio, , , , , Harris Tamara B, Launer Lenore J, Aspelund Thor, Eiriksdottir Gudny, Mitchell Braxton D, Boerwinkle Eric, Schmidt Helena, Cavalieri Margherita, Rao Madhumathi, Hu Frank, Demirkan Ayse, Oostra Ben A, de Andrade Mariza, Turner Stephen T, Ding Jingzhong, Andrews Jeanette S, Freedman Barry I, Giulianini Franco, Koenig Wolfgang, Illig Thomas, Meisinger Christa, Gieger Christian, 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, Ketkar Shamika, 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, Kim Stuart K, 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, Siscovick David S, van Duijn Cornelia M, Borecki Ingrid B, 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, Parsa Afshin, Bochud Murielle, Heid Iris M, Kao W H Linda, Fox Caroline S, Köttgen An |
Cumulative association between age-related macular degeneration and less studied genetic variants in PLEKHA1/ARMS2/HTRA1: a meta and gene-cluster analysis. Molecular biology reports 2013 Oct 40 (10): 5551-61. Yu Weihong, Dong Shuqian, Zhao Chuntao, Wang Haina, Dai Fei, Yang Jingy |
Study of Polymorphisms in CX3CR1, PLEKHA1 and VEGF genes as risk factors for age-related macular degeneration in Indian patients. Archives of medical research 2014 Aug 45 (6): 489-94. Gupta Divya, Gupta Vani, Singh Vinita, Chawla Shobhit, Parveen Farah, Agrawal Suraksha, Phadke Shubha |
Specific correlation between the major chromosome 10q26 haplotype conferring risk for age-related macular degeneration and the expression of HTRA1. Molecular vision 2017 23 318-333. Liao Sha-Mei, Zheng Wei, Zhu Jiang, Lewis Casey A, Delgado Omar, Crowley Maura A, Buchanan Natasha M, Jaffee Bruce D, Dryja Thaddeus |
Bivariate Genome-Wide Association Study of Depressive Symptoms With Type 2 Diabetes and Quantitative Glycemic Traits. Psychosomatic medicine 2017 Dec . Haljas Kadri, Amare Azmeraw T, Alizadeh Behrooz Z, Hsu Yi-Hsiang, Mosley Thomas, Newman Anne, Murabito Joanne, Tiemeier Henning, Tanaka Toshiko, van Duijn Cornelia, Ding Jingzhong, Llewellyn David J, Bennett David A, Terracciano Antonio, Launer Lenore, Ladwig Karl-Heinz, Cornelis Marylin C, Teumer Alexander, Grabe Hans, Kardia Sharon L R, Ware Erin B, Smith Jennifer A, Snieder Harold, Eriksson Johan G, Groop Leif, Räikkönen Katri, Lahti Ja |
Polymorphisms in Selected Genes and Their Association with Age-Related Macular Degeneration in a Chinese Population. Medical science monitor : international medical journal of experimental and clinical research 2018 Mar 24 1693-1700. Huang Qing, Xiang |
Identification of non-HLA genes associated with development of islet autoimmunity and type 1 diabetes in the prospective TEDDY cohort.
Journal of autoimmunity 2018 Jan . Sharma Ashok, Liu Xiang, Hadley David, Hagopian William, Chen Wei-Min, Onengut-Gumuscu Suna, Törn Carina, Steck Andrea K, Frohnert Brigitte I, Rewers Marian, Ziegler Anette-G, Lernmark Åke, Toppari Jorma, Krischer Jeffrey P, Akolkar Beena, Rich Stephen S, She Jin-Xiong, |
Rare Genetic Variants in Jewish Patients Suffering from Age-Related Macular Degeneration. Genes 2019 10 10 (10): . Shoshany Nadav, Weiner Chen, Safir Margarita, Einan-Lifshitz Adi, Pokroy Russell, Kol Ayala, Modai Shira, Shomron Noam, Pras Er |
Assessment of genetic risk of type 2 diabetes among Pakistanis based on GWAS-implicated loci. Gene 2021 Mar 783 145563. Sabiha Bibi, Bhatti Attya, Fan Kang-Hsien, John Peter, Aslam Muhammad Muaaz, Ali Johar, Feingold Eleanor, Demirci F Yesim, Kamboh M Ily |
The genomic landscape of pediatric renal cell carcinomas. iScience 2022 4 25 (4): 104167. Beck Pengbo, Selle Barbara, Madenach Lukas, Jones David T W, Vokuhl Christian, Gopisetty Apurva, Nabbi Arash, Brecht Ines B, Ebinger Martin, Wegert Jenny, Graf Norbert, Gessler Manfred, Pfister Stefan M, Jäger Natal |
De novo mutations within metabolism networks of amino acid/protein/energy in Chinese autistic children with intellectual disability. Human genomics 2022 11 16 (1): 52. Chen Wen-Xiong, Liu Bin, Zhou Lijie, Xiong Xiaoli, Fu Jie, Huang Zhi-Fang, Tan Ting, Tang Mingxi, Wang Jun, Tang Ya-Pi |
Genetic Overlap Analysis Identifies a Shared Etiology between Migraine and Headache with Type 2 Diabetes.
Genes 2022 10 13 (10): . Islam Md Rafiqul, The International Headache Genetics Consortium Ihgc , Nyholt Dale |
Type 2 diabetes mellitus and the risk of male infertility: a Mendelian randomization study. Frontiers in endocrinology 2023 12 14 1279058. Xiao-Bin Zhu, Zhi-Hong Niu, Wei-Min Fan, Chang-Sheng Sheng, Qian Ch |
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- Page last updated:Apr 22, 2024
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