Human Genome Epidemiology Literature Finder
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Records 1 - 10 (of 10 Records) |
| Query Trace: Syndrome and ATXN2[original query] |
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| Screening for premutation in the FMR1 gene in male patients suspected of spinocerebellar ataxia. Neurologia i neurochirurgia polska 0 42 (6): 497-504. Rajkiewicz Marta, Su?ek-Piatkowska Anna, Krysa Wioletta, Zdzienicka Elzbieta, Szirkowiec Walentyna, Zaremba Jac |
| Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. Clinical genetics 2013 Mar 83 (3): 279-83. Lindquist S G, Duno M, Batbayli M, Puschmann A, Braendgaard H, Mardosiene S, Svenstrup K, Pinborg L H, Vestergaard K, Hjermind L E, Stokholm J, Andersen B B, Johannsen P, Nielsen J |
| CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis. Neurobiology of aging 2012 Aug 33 (8): 1852.e1-3. Groen Ewout J N, van Rheenen Wouter, Koppers Max, van Doormaal Perry T C, Vlam Lotte, Diekstra Frank P, Dooijes Dennis, Pasterkamp R Jeroen, van den Berg Leonard H, Veldink Jan |
| Thrombotic antiphospholipid syndrome shows strong haplotypic association with SH2B3-ATXN2 locus. PloS one 2013 8 (7): e67897. Ochoa Eguzkine, Iriondo Mikel, Bielsa Ana, Ruiz-Irastorza Guillermo, Estonba Andone, Zubiaga Ana |
| 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 |
| Ataxin-2 as potential disease modifier in C9ORF72 expansion carriers. Neurobiology of aging 2014 Oct 35 (10): 2421.e13-7. van Blitterswijk Marka, Mullen Bianca, Heckman Michael G, Baker Matthew C, DeJesus-Hernandez Mariely, Brown Patricia H, Murray Melissa E, Hsiung Ging-Yuek R, Stewart Heather, Karydas Anna M, Finger Elizabeth, Kertesz Andrew, Bigio Eileen H, Weintraub Sandra, Mesulam Marsel, Hatanpaa Kimmo J, White Charles L, Neumann Manuela, Strong Michael J, Beach Thomas G, Wszolek Zbigniew K, Lippa Carol, Caselli Richard, Petrucelli Leonard, Josephs Keith A, Parisi Joseph E, Knopman David S, Petersen Ronald C, Mackenzie Ian R, Seeley William W, Grinberg Lea T, Miller Bruce L, Boylan Kevin B, Graff-Radford Neill R, Boeve Bradley F, Dickson Dennis W, Rademakers Ro |
| Analysis of CACNA1A CAG repeat lengths in patients with familial ALS. Neurobiology of aging 2018 10 74 235.e5-235.e8. Brenner David, Müller Kathrin, Gastl Regina, Gorges Martin, Otto Markus, Pinkhardt Elmar H, Kassubek Jan, Weishaupt Jochen H, Ludolph Albert |
| Multiple Gene Polymorphisms Associated with Exfoliation Syndrome in the Uygur Population. Journal of ophthalmology 2019 2019 9687823. Ma Yi-Nu, Xie Ting-Yu, Chen Xue- |
| Effect of CAG repeats on the age at onset of patients with spinocerebellar ataxia type 2 in China. Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences 2021 9 46 (8): 793-799. Li Yu, Liu Zhen, Hou Xiaorong, Chen Zhao, Shen Lu, Xia Kun, Tang Beisha, Jiang Hong, Wang Junli |
| Pediatric Non-Alcoholic Fatty Liver Disease is Affected by Genetic Variants Involved in Lifespan/Healthspan. Journal of pediatric gastroenterology and nutrition 2021 Mar . Crudele Annalisa, Dato Serena, Re Oriana Lo, Maugeri Andrea, Sanna Paola, Giallongo Sebastiano, Oben Jude, Panera Nadia, De Rango Francesco, Mosca Antonella, Rose Giuseppina, Passarino Giuseppe, Alisi Anna, Vinciguerra Manl |
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
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