Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
   dataset        GWAS Only
Filtered By:

Previous    

Records 1 - 13 (of 13 Records)

Query Trace: Disease and ACTN4[original query]
Genome-wide Association Studies of Retinal Vessel Tortuosity Identify Numerous Novel Loci Revealing Genes and Pathways Associated With Ocular and Cardiometabolic Diseases. GWAS Catalog
Ophthalmology science 2023 5 3 (3): 100288.
Tomasoni Mattia, Beyeler Michael Johannes, Vela Sofia Ortin, Mounier Ninon, Porcu Eleonora, Corre Tanguy, Krefl Daniel, Button Alexander Luke, Abouzeid Hana, Lazaros Konstantinidis, Bochud Murielle, Schlingemann Reinier, Bergin Ciara, Bergmann Sv
Molecular analysis of NPHS2 and ACTN4 genes in a series of 33 Italian patients affected by adult-onset nonfamilial focal segmental glomerulosclerosis.
Nephron. Clinical practice 2005 1 99 (2): c31-6.
Aucella Filippo, De Bonis Patrizia, Gatta Giuseppe, Muscarella Lucia Anna, Vigilante Mimmo, di Giorgio Giuseppe, D'Errico Michele, Zelante Leopoldo, Stallone Carmine, Bisceglia Lui
Mutations in the INF2 gene account for a significant proportion of familial but not sporadic focal and segmental glomerulosclerosis.
Kidney international 2013 Feb 83 (2): 316-22.
Barua Moumita, Brown Elizabeth J, Charoonratana Victoria T, Genovese Giulio, Sun Hua, Pollak Martin
Relevance of the ACTN4 gene in African-Americans with non-diabetic end-stage renal disease.
American journal of nephrology 2012 36 (3): 252-60.
Bostrom Meredith A, Perlegas Peter, Lu Lingyi, Hicks Pamela J, Hawkins Greg, Ng Maggie C Y, Langefeld Carl D, Freedman Barry I, Bowden Donald
Mutations in podocyte genes are a rare cause of primary FSGS associated with ESRD in adult patients.
Clinical nephrology 2012 Jul 78 (1): 47-53.
Büscher Anja K, Konrad Martin, Nagel Mato, Witzke Oliver, Kribben Andreas, Hoyer Peter F, Weber Stefan
Mutational analysis of ACTN4, encoding a-actinin 4, in patients with focal segmental glomerulosclerosis using HRM method.
Folia biologica 2013 59 (3): 110-5.
Safa?íková M, Reiterová J, Safránková H, Stekrová J, Zidková A, Obeidová L, Kohoutová M, Tesa?
Screening of ACTN4 and TRPC6 mutations in a Chinese cohort of patients with adult-onset familial focal segmental glomerulosclerosis.
Contributions to nephrology 2013 181 91-100.
Zhang Qianying, Ma Jun, Xie Jingyuan, Wang Zhaohui, Zhu Bin, Hao Xu, Yang Li, Ren Hong, Chen N
Genetic screening in adolescents with steroid-resistant nephrotic syndrome.
Kidney international 2013 Jul 84 (1): 206-13.
Lipska Beata S, Iatropoulos Paraskevas, Maranta Ramona, Caridi Gianluca, Ozaltin Fatih, Anarat Ali, Balat Ayse, Gellermann Jutta, Trautmann Agnes, Erdogan Ozlem, Saeed Bassam, Emre Sevinc, Bogdanovic Radovan, Azocar Marta, Balasz-Chmielewska Irena, Benetti Elisa, Caliskan Salim, Mir Sevgi, Melk Anette, Ertan Pelin, Baskin Esra, Jardim Helena, Davitaia Tinatin, Wasilewska Anna, Drozdz Dorota, Szczepanska Maria, Jankauskiene Augustina, Higuita Lina Maria Serna, Ardissino Gianluigi, Ozkaya Ozan, Kuzma-Mroczkowska Elzbieta, Soylemezoglu Oguz, Ranchin Bruno, Medynska Anna, Tkaczyk Marcin, Peco-Antic Amira, Akil Ipek, Jarmolinski Tomasz, Firszt-Adamczyk Agnieszka, Dusek Jiri, Simonetti Giacomo D, Gok Faysal, Gheissari Alaleh, Emma Francesco, Krmar Rafael T, Fischbach Michel, Printza Nikoleta, Simkova Eva, Mele Caterina, Ghiggeri Gian Marco, Schaefer Franz,
A Systematic Analysis of Major Susceptible Genes in Childhood-onset Steroid-resistant Nephrotic Syndrome.
Annals of clinical and laboratory science 2019 7 49 (3): 330-337.
Li Yongzhen, He Qingnan, Wang Ying, Dang Xiqiang, Wu Xiaochuan, Li Xiaoyan, Shuai Lanjun, Yi Zhuw
Novel Genetic Locus Influencing Retinal Venular Tortuosity Is Also Associated With Risk of Coronary Artery Disease. GWAS Catalog
Arteriosclerosis, thrombosis, and vascular biology 2019 Dec 39 (12): 2542-2552.
Veluchamy Abirami, Ballerini Lucia, Vitart Veronique, Schraut Katharina E, Kirin Mirna, Campbell Harry, Joshi Peter K, Relan Devanjali, Harris Sarah, Brown Ellie, Vaidya Suraj S, Dhillon Baljean, Zhou Kaixin, Pearson Ewan R, Hayward Caroline, Polasek Ozren, Deary Ian J, MacGillivray Thomas, Wilson James F, Trucco Emanuele, Palmer Colin N A, Doney Alexander S
Auxiliary genetic analysis in a Chinese adolescent NPH family by single nucleotide polymorphism screening.
Molecular medicine reports 2020 1 21 (3): 1115-1124.
Tang Chunrong, Zhou Daoyuan, Tan Rongshao, Zhong Xiaoshi, Xiao Xiao, Qin Danping, Liu Yun, Hu Jianguang, Liu Y
Genetic Risk Factors Associated With Preeclampsia and Hypertensive Disorders of Pregnancy. GWAS Catalog
JAMA cardiology 2023 6 .
Jaakko S Tyrmi, Tea Kaartokallio, A Inkeri Lokki, Tiina Jääskeläinen, Eija Kortelainen, Sanni Ruotsalainen, Juha Karjalainen, Samuli Ripatti, Anna Kivioja, Triin Laisk, Johannes Kettunen, Anneli Pouta, Katja Kivinen, Eero Kajantie, Seppo Heinonen, Juha Kere, Hannele Laivuori,
Differential Expression of Peripheral Circulating MicroRNA-146a Between Patients with Atherosclerotic Vulnerable Plaque and Stable Plaque.
International heart journal 2023 10 64 (5): 847-855.
Yenwen Song, Lei Zhang, Ye Hua
TOP