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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 7 (of 7 Records)

Query Trace: Disease and SKIV2L[original query]
Role of RDBP and SKIV2L variants in the major histocompatibility complex class III region in polypoidal choroidal vasculopathy etiology.
Ophthalmology 2009 Aug 116 (8): 1502-9.
Kondo Naoshi, Honda Shigeru, Kuno Shin-ichi, Negi Aki
Pleiotropic genes for metabolic syndrome and inflammation.
Molecular genetics and metabolism 2014 Aug 112 (4): 317-38.
Kraja Aldi T, Chasman Daniel I, North Kari E, Reiner Alexander P, Yanek Lisa R, Kilpeläinen Tuomas O, Smith Jennifer A, Dehghan Abbas, Dupuis Josée, Johnson Andrew D, Feitosa Mary F, Tekola-Ayele Fasil, Chu Audrey Y, Nolte Ilja M, Dastani Zari, Morris Andrew, Pendergrass Sarah A, Sun Yan V, Ritchie Marylyn D, Vaez Ahmad, Lin Honghuang, Ligthart Symen, Marullo Letizia, Rohde Rebecca, Shao Yaming, Ziegler Mark A, Im Hae Kyung, , , , , , , , , , , , Schnabel Renate B, Jørgensen Torben, Jørgensen Marit E, Hansen Torben, Pedersen Oluf, Stolk Ronald P, Snieder Harold, Hofman Albert, Uitterlinden Andre G, Franco Oscar H, Ikram M Arfan, Richards J Brent, Rotimi Charles, Wilson James G, Lange Leslie, Ganesh Santhi K, Nalls Mike, Rasmussen-Torvik Laura J, Pankow James S, Coresh Josef, Tang Weihong, Linda Kao W H, Boerwinkle Eric, Morrison Alanna C, Ridker Paul M, Becker Diane M, Rotter Jerome I, Kardia Sharon L R, Loos Ruth J F, Larson Martin G, Hsu Yi-Hsiang, Province Michael A, Tracy Russell, Voight Benjamin F, Vaidya Dhananjay, O'Donnell Christopher J, Benjamin Emelia J, Alizadeh Behrooz Z, Prokopenko Inga, Meigs James B, Borecki Ingrid
Low-frequency coding variants in CETP and CFB are associated with susceptibility of exudative age-related macular degeneration in the Japanese population.
Human molecular genetics 2016 Nov 25 (22): 5027-5034.
Momozawa Yukihide, Akiyama Masato, Kamatani Yoichiro, Arakawa Satoshi, Yasuda Miho, Yoshida Shigeo, Oshima Yuji, Mori Ryusaburo, Tanaka Koji, Mori Keisuke, Inoue Satoshi, Terasaki Hiroko, Yasuma Tetsuhiro, Honda Shigeru, Miki Akiko, Inoue Maiko, Fujisawa Kimihiko, Takahashi Kanji, Yasukawa Tsutomu, Yanagi Yasuo, Kadonosono Kazuaki, Sonoda Koh-Hei, Ishibashi Tatsuro, Takahashi Atsushi, Kubo Michia
Prevalence of age-related macular degeneration associated genetic risk factors and 4-year progression data in the Irish population.
The British journal of ophthalmology 2018 2 102 (12): 1691-1695.
Connolly Emma, Rhatigan Maedbh, O'Halloran Aisling M, Muldrew Katherine Alyson, Chakravarthy Usha, Cahill Mark, Kenny Rose Anne, Doyle Sarah
Genome-wide analysis of disease progression in age-related macular degeneration. GWAS Catalog
Human molecular genetics 2018 Mar 27 (5): 929-940.
Yan Qi, Ding Ying, Liu Yi, Sun Tao, Fritsche Lars G, Clemons Traci, Ratnapriya Rinki, Klein Michael L, Cook Richard J, Liu Yu, Fan Ruzong, Wei Lai, Abecasis Gonçalo R, Swaroop Anand, Chew Emily Y, , Weeks Daniel E, Chen W
Genetic Association of Age-Related Macular Degeneration and Polypoidal Choroidal Vasculopathy.
Asia-Pacific journal of ophthalmology (Philadelphia, Pa.) 2020 3 9 (2): 104-109.
Chen Li J
Genetic diagnosis of fetal microcephaly at a single tertiary center in China.
Frontiers in genetics 2023 5 14 1112153.
You Wang, Fang Fu, Tingying Lei, Li Zhen, Qiong Deng, Hang Zhou, Chunling Ma, Ken Cheng, Ruibin Huang, Ru Li, Qiuxia Yu, Lushan Li, Jin Han, Xin Yang, Dongzhi Li, Can Li
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