HuGE Literature Finder
Records 1-30
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HTT gene intermediate alleles in neurodegeneration: evidence for association with Alzheimer's disease.
Neurobiology of aging 2019 04 76 215.e9-215.e14. Menéndez-González Manuel, Clarimón Jordi, Rosas-Allende Irene, Blázquez Marta, San Martín Esther Suárez, García-Fernández Ciara, Lleó Alberto, Dols-Icardo Oriol, Illán-Gala Ignacio, Morís Germán, Ribacoba Renée, Álvarez Victoria, Martínez Carm |
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Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype.
Acta neuropathologica 2018 Jun . Koga Shunsuke, Kouri Naomi, Walton Ronald L, Ebbert Mark T W, Josephs Keith A, Litvan Irene, Graff-Radford Neill, Ahlskog J Eric, Uitti Ryan J, van Gerpen Jay A, Boeve Bradley F, Parks Adam, Ross Owen A, Dickson Dennis |
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ATXN1 intermediate-length polyglutamine expansions are associated with amyotrophic lateral sclerosis.
Neurobiology of aging 2018 04 64 157.e1-157.e5. Lattante Serena, Pomponi Maria Grazia, Conte Amelia, Marangi Giuseppe, Bisogni Giulia, Patanella Agata Katia, Meleo Emiliana, Lunetta Christian, Riva Nilo, Mosca Lorena, Carrera Paola, Bee Marco, Zollino Marcella, Sabatelli Mar |
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Case-control analysis of leucine-rich repeat kinase 2 protective variants in Alzheimer's disease.
Neurobiology of aging 2018 04 64 157.e7-157.e9. Ng Adeline S L, Ng Ebonne Y L, Tan Yi Jayne, Kandiah Nagaendran, Zhou Juan, Hameed Shahul, Ting Simon K S, Tan Eng-Ki |
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Dysregulation of C-X-C motif ligand 10 during aging and association with cognitive performance.
Neurobiology of aging 2018 03 63 54-64. Bradburn Steven, McPhee Jamie, Bagley Liam, Carroll Michael, Slevin Mark, Al-Shanti Nasser, Barnouin Yoann, Hogrel Jean-Yves, Pääsuke Mati, Gapeyeva Helena, Maier Andrea, Sipilä Sarianna, Narici Marco, Robinson Andrew, Mann David, Payton Antony, Pendleton Neil, Butler-Browne Gillian, Murgatroyd Chr |
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Epoxyeicosatrienoic Acids are Mediated by EPHX2 Variants and may be a Predictor of Early Neurological Deterioration in Acute Minor Ischemic Stroke.
Journal of atherosclerosis and thrombosis 2017 Aug . Yi Xingyang, Lin Jing, Li Jie, Zhou Qiang, Han Zh |
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Tumor necrosis factor alpha polymorphisms are associated with Parkinson's disease age at onset.
Neuroscience letters 2017 Aug 658 133-136. Lindenau Juliana D, Altmann Vivian, Schumacher-Schuh Artur F, Rieder Carlos R, Hutz Mara |
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A genome wide association study identifies a lncRna as risk factor for pathological inflammatory responses in leprosy.
PLoS genetics 2017 Feb 13 (2): e1006637. Fava Vinicius M, Manry Jeremy, Cobat Aurélie, Orlova Marianna, Van Thuc Nguyen, Moraes Milton O, Sales-Marques Carolinne, Stefani Mariane M A, Latini Ana Carla P, Belone Andrea F, Thai Vu Hong, Abel Laurent, Alcaïs Alexandre, Schurr Erw |
Differential Aging Analysis in Human Cerebral Cortex Identifies Variants in TMEM106B and GRN that Regulate Aging Phenotypes.
Cell systems 2017 04 4 (4): 404-415.e5. Rhinn Herve, Abeliovich A |
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CYP Genetic Variants, CYP Metabolite Levels, and Neurologic Deterioration in Acute Ischemic Stroke in Chinese Population.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2016 Dec . Yi Xingyang, Lin Jing, Wang Chun, Zhou Qia |
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Globus pallidus degeneration and clinico-pathological features of Huntington's disease.
Annals of neurology 2016 Jun . Singh-Bains Malvindar K, Tippett Lynette J, Hogg Virginia M, Synek Beth J, Roxburgh Richard H, Waldvogel Henry J, Faull Richard L |
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Genome-wide association study of serum coenzyme Q10 levels identifies susceptibility loci linked to neuronal diseases.
Human molecular genetics 2016 May . Degenhardt Frauke, Niklowitz Petra, Szymczak Silke, Jacobs Gunnar, Lieb Wolfgang, Menke Thomas, Laudes Matthias, Esko Tõnu, Weidinger Stephan, Franke Andre, Döring Frank, Onur Simo |
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Impact of SORL1 genetic variations on MRI markers in non-demented elders.
Oncotarget 2016 May . Yin Rui-Hua, Li Jun, Tan Lin, Wang Hui-Fu, Tan Meng-Shan, Yu Wan-Jiang, Tan Chen-Chen, Yu Jin-Tai, Tan Lan, |
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Bridging Integrator 1 (BIN1) Genotypes Mediate Alzheimer's Disease Risk by Altering Neuronal Degeneration.
Journal of Alzheimer's disease : JAD 2016 Mar . Wang Hui-Fu, Wan Yu, Hao Xiao-Ke, Cao Lei, Zhu Xi-Chen, Jiang Teng, Tan Meng-Shan, Tan Lin, Zhang Dao-Qiang, Tan Lan, Yu Jin-Tai, |
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White matter hyperintensities characterize monogenic frontotemporal dementia with granulin mutations.
Neurobiology of aging 2016 Feb 38 176-80. Paternicò Donata, Premi Enrico, Gazzina Stefano, Cosseddu Maura, Alberici Antonella, Archetti Silvana, Cotelli Maria S, Micheli Anna, Turla Marinella, Gasparotti Roberto, Padovani Alessandro, Borroni Barba |
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A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin.
Neurobiology of aging 2015 Sep . Deming Yuetiva, Xia Jian, Cai Yefei, Lord Jenny, Holmans Peter, Bertelsen Sarah, Holtzman David, Morris John C, Bales Kelly, Pickering Eve H, Kauwe John, Goate Alison, Cruchaga Carlos, |
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Genetic modification of the relationship between phosphorylated tau and neurodegeneration.
Alzheimer's & dementia : the journal of the Alzheimer's Association 2014 Nov 10 (6): 637-645.e1. Hohman Timothy J, Koran Mary Ellen I, Thornton-Wells Tricia A, |
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Extended phenotypic spectrum of KIF5A mutations: From spastic paraplegia to axonal neuropathy.
Neurology 2014 Aug 83 (7): 612-9. Liu Yo-Tsen, Laurá Matilde, Hersheson Joshua, Horga Alejandro, Jaunmuktane Zane, Brandner Sebastian, Pittman Alan, Hughes Deborah, Polke James M, Sweeney Mary G, Proukakis Christos, Janssen John C, Auer-Grumbach Michaela, Zuchner Stephan, Shields Kevin G, Reilly Mary M, Houlden Hen |
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CDKN2B-AS1 Genotype-Glaucoma Feature Correlations in Primary Open-Angle Glaucoma Patients From the United States.
American journal of ophthalmology 2012 Oct . Pasquale LR, Loomis SJ, Kang JH, Yaspan BL, Abdrabou W, Budenz DL, Chen TC, Delbono E, Friedman DS, Gaasterland D, Gaasterland T, Grosskreutz CL, Lee RK, Lichter PR, Liu Y, McCarty CA, Moroi SE, Olson LM, Realini T, Rhee DJ, Schuman JS, Singh K, Vollrath D, Wollstein G, Zack DJ, Allingham RR, Pericak-Vance MA, Weinreb RN, Zhang K, Hauser MA, Richards JE, Haines JL, Wiggs JL |
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Ninjurin1 single nucleotide polymorphism and nerve damage in leprosy.
Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases 2012 Feb . Graça CR, Paschoal VD, Cordeiro-Soubhia RM, Tonelli-Nardi SM, Machado RL, Kouyoumdjian JA, Baptista Rossit AR |
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Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS genetics 2012 8 (4): e1002654. Wiggs Janey L, Yaspan Brian L, Hauser Michael A, Kang Jae H, Allingham R Rand, Olson Lana M, Abdrabou Wael, Fan Bao J, Wang Dan Y, Brodeur Wendy, Budenz Donald L, Caprioli Joseph, Crenshaw Andrew, Crooks Kristy, Delbono Elizabeth, Doheny Kimberly F, Friedman David S, Gaasterland Douglas, Gaasterland Terry, Laurie Cathy, Lee Richard K, Lichter Paul R, Loomis Stephanie, Liu Yutao, Medeiros Felipe A, McCarty Cathy, Mirel Daniel, Moroi Sayoko E, Musch David C, Realini Anthony, Rozsa Frank W, Schuman Joel S, Scott Kathleen, Singh Kuldev, Stein Joshua D, Trager Edward H, Vanveldhuisen Paul, Vollrath Douglas, Wollstein Gadi, Yoneyama Sachiko, Zhang Kang, Weinreb Robert N, Ernst Jason, Kellis Manolis, Masuda Tomohiro, Zack Don, Richards Julia E, Pericak-Vance Margaret, Pasquale Louis R, Haines Jonathan |
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Ataxin-2 repeat-length variation and neurodegeneration.
Human molecular genetics 2011 Aug 20 (16): 3207-12. Ross Owen A, Rutherford Nicola J, Baker Matt, Soto-Ortolaza Alexandra I, Carrasquillo Minerva M, DeJesus-Hernandez Mariely, Adamson Jennifer, Li Ma, Volkening Kathryn, Finger Elizabeth, Seeley William W, Hatanpaa Kimmo J, Lomen-Hoerth Catherine, Kertesz Andrew, Bigio Eileen H, Lippa Carol, Woodruff Bryan K, Knopman David S, White Charles L, Van Gerpen Jay A, Meschia James F, Mackenzie Ian R, Boylan Kevin, Boeve Bradley F, Miller Bruce L, Strong Michael J, Uitti Ryan J, Younkin Steven G, Graff-Radford Neill R, Petersen Ronald C, Wszolek Zbigniew K, Dickson Dennis W, Rademakers Ro |
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Diabetes and neurodegeneration in Wolfram syndrome: a multicenter study of phenotype and genotype.
Diabetes care 2011 Jul 34 (7): 1503-10. Rohayem Julia, Ehlers Christian, Wiedemann Bärbel, Holl Reinhard, Oexle Konrad, Kordonouri Olga, Salzano Giuseppina, Meissner Thomas, Burger Walter, Schober Edith, Huebner Angela, Lee-Kirsch Min Ae, |
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No association of psychosis in Alzheimer disease with neurodegenerative pathway genes.
Neurobiology of aging 2011 Mar 32 (3): 555.e9-11. DeMichele-Sweet Mary Ann A, Klei Lambertus, Devlin Bernie, Ferrell Robert E, Weamer Elise A, Emanuel James E, Lopez Oscar L, Sweet Robert |
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The thermolabile variant of 5,10-methylenetetrahydrofolate reductase is a possible risk factor for amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2011 Mar 12 (2): 136-9. Kühnlein Peter, Jung Hans, Farkas Melinda, Keskitalo Salla, Ineichen Benjamin, Jelcic Ilijas, Petersen Jens, Semmler Alexander, Weller Michal, Ludolph Albert Christian, Linnebank Micha |
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Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease.
NeuroImage 2010 Jun 51 (2): 542-54. Stein Jason L, Hua Xue, Morra Jonathan H, Lee Suh, Hibar Derrek P, Ho April J, Leow Alex D, Toga Arthur W, Sul Jae Hoon, Kang Hyun Min, Eskin Eleazar, Saykin Andrew J, Shen Li, Foroud Tatiana, Pankratz Nathan, Huentelman Matthew J, Craig David W, Gerber Jill D, Allen April N, Corneveaux Jason J, Stephan Dietrich A, Webster Jennifer, DeChairo Bryan M, Potkin Steven G, Jack Clifford R, Weiner Michael W, Thompson Paul M, |
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Temporal lobe grey matter volume in schizophrenia is associated with a genetic polymorphism influencing glycogen synthase kinase 3-? activity.
Genes, brain, and behavior 2010 Jun 9 (4): 365-71. Benedetti F, Poletti S, Radaelli D, Bernasconi A, Cavallaro R, Falini A, Lorenzi C, Pirovano A, Dallaspezia S, Locatelli C, Scotti G, Smeraldi |
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Genetic screening reveals high frequency of PARK2 mutations and reduced Parkin expression conferring risk for Parkinsonism in North West India.
Journal of neurology, neurosurgery, and psychiatry 2010 Feb 81 (2): 166-70. Vinish Monika, Prabhakar Sudesh, Khullar Madhu, Verma Indu, Anand Aksh |
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Upregulation of persistent sodium conductances in familial ALS.
Journal of neurology, neurosurgery, and psychiatry 2010 Feb 81 (2): 222-7. Vucic Steve, Kiernan Matthew |
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Cancer linked to Alzheimer disease but not vascular dementia.
Neurology 2010 Jan 74 (2): 2. Roe CM, Fitzpatrick AL, Xiong C, Sieh W, Kuller L, Miller JP, Williams MM, Kopan R, Behrens MI, Morris JC |
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PITX3 polymorphism is associated with early onset Parkinson's disease.
Neurobiology of aging 2010 Jan 31 (1): 114-7. Bergman Olle, Håkansson Anna, Westberg Lars, Nordenström Kajsa, Carmine Belin Andrea, Sydow Olof, Olson Lars, Holmberg Björn, Eriksson Elias, Nissbrandt Ha |
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Association of MAPT haplotype-tagging SNPs with sporadic Parkinson's disease.
Neurobiology of aging 2009 Sep 30 (9): 1477-82. Vandrovcova Jana, Pittman Alan M, Malzer Elke, Abou-Sleiman Patrick M, Lees Andrew J, Wood Nicholas W, de Silva Roh |
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Tracking of the genetic deafness associated to the aging in Brazilian patients.
Neurobiology of aging 2009 Jul 30 (7): 1173-4. Piatto Vânia Belintani, Pereira Márcio Coimbra, da Silva Magali A O M, Maniglia José Vict |
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Association of distinct variants in SORL1 with cerebrovascular and neurodegenerative changes related to Alzheimer disease.
Archives of neurology 2008 Dec 65 (12): 1640-8. T Cuenco Karen, Lunetta Kathryn L, Baldwin Clinton T, McKee Ann C, Guo Jianping, Cupples L Adrienne, Green Robert C, St George-Hyslop Peter H, Chui Helena, DeCarli Charles, Farrer Lindsay A, |
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Apolipoprotein E highly correlates with AbetaPP- and tau-related markers in human cerebrospinal fluid.
Journal of Alzheimer's disease : JAD 2008 Nov 15 (3): 409-17. Vuletic Simona, Li Ge, Peskind Elaine R, Kennedy Hal, Marcovina Santica M, Leverenz James B, Petrie Eric C, Lee Virginia M-Y, Galasko Douglas, Schellenberg Gerard D, Albers John |
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Neurofibrillary tau pathology modulated by genetic variation of alpha-synuclein.
Annals of neurology 2008 Sep 64 (3): 348-52. Peuralinna Terhi, Oinas Minna, Polvikoski Tuomo, Paetau Anders, Sulkava Raimo, Niinistö Leena, Kalimo Hannu, Hernandez Dena, Hardy John, Singleton Andrew, Tienari Pentti J, Myllykangas Lii |
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CCL5 and CCR5 genotypes modify clinical, radiological and pathological features of multiple sclerosis.
Journal of neuroimmunology 2007 Oct 190 (1-2): 157-64. van Veen Tineke, Nielsen Jessica, Berkhof Johannes, Barkhof Frederik, Kamphorst Wouter, Bö Lars, Ravid Rivka, Verweij Cor L, Huitinga Inge, Polman Chris H, Uitdehaag Bernard M |
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Differential CSF butyrylcholinesterase levels in Alzheimer's disease patients with the ApoE epsilon4 allele, in relation to cognitive function and cerebral glucose metabolism.
Neurobiology of disease 2006 Nov 24 (2): 326-33. Darreh-Shori T, Brimijoin S, Kadir A, Almkvist O, Nordberg |
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Association study of the Ubiquilin gene with Alzheimer's disease.
Neurobiology of disease 2006 Jun 22 (3): 691-3. Bensemain Faiza, Chapuis Julien, Tian Jinzhou, Shi Jing, Thaker Uma, Lendon Corinne, Iwatsubo Takeshi, Amouyel Philippe, Mann David, Lambert Jean-Charl |
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Association of the H63D polymorphism in the hemochromatosis gene with sporadic ALS.
Neurology 2005 Sep 65 (6): 934-7. Goodall E F, Greenway M J, van Marion I, Carroll C B, Hardiman O, Morrison K |
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SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS.
Neurology 2005 Sep 65 (6): 820-5. Veldink J H, Kalmijn S, Van der Hout A H, Lemmink H H, Groeneveld G J, Lummen C, Scheffer H, Wokke J H J, Van den Berg L |
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Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family.
Proceedings of the National Academy of Sciences of the United States of America 2004 Nov 101 (44): 15688-93. Li Yonghong, Nowotny Petra, Holmans Peter, Smemo Scott, Kauwe John S K, Hinrichs Anthony L, Tacey Kristina, Doil Lisa, van Luchene Ryan, Garcia Veronica, Rowland Charles, Schrodi Steve, Leong Diane, Gogic Goran, Chan Joanne, Cravchik Anibal, Ross David, Lau Kit, Kwok Shirley, Chang Sheng-Yung, Catanese Joe, Sninsky John, White Thomas J, Hardy John, Powell John, Lovestone Simon, Morris John C, Thal Leon, Owen Michael, Williams Julie, Goate Alison, Grupe Andr |
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A polymorphism in the angiotensin 1-converting enzyme gene is associated with damage to cerebral cortical white matter in Alzheimer's disease.
Neuroscience letters 2004 Jan 354 (2): 103-6. Tian J, Shi J, Bailey K, Harris J M, Pritchard A, Lambert J-C, Chartier-Harlin M-C, Pickering-Brown S M, Lendon C L, Mann D M |
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Parkinson's disease, CYP2D6 polymorphism, and age.
Neurology 2001 May 56 (10): 1363-70. Payami H, Lee N, Zareparsi S, Gonzales McNeal M, Camicioli R, Bird T D, Sexton G, Gancher S, Kaye J, Calhoun D, Swanson P D, Nutt |
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The Apolipoprotein E genotype in patients affected by syndromes with focal cortical atrophy.
Neuroscience letters 2001 May 303 (2): 87-90. Masullo C, Daniele A, Fazio V M, Seripa D, Gravina C, Filippini V, Grossi D, Fragassi N, Nichelli P, Leone M, Gainotti |
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Correlation of the clinical severity of Alzheimer's disease with an aberration in mitochondrial DNA (mtDNA).
Journal of molecular neuroscience : MN 2001 Feb 16 (1): 41-8. Brown A M, Sheu R K, Mohs R, Haroutunian V, Blass J |
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No evidence for the presence of apolipoprotein epsilon4, interleukin-lalpha allele 2 and interleukin-1beta allele 2 cause an increase in programmed cell death following traumatic brain injury in humans.
Clinical neuropathology 0 25 (6): 255-64. Johnson V E, Murray L, Raghupathi R, Stewart J, Nicoll J A R, MacKinnon M A, McIntosh T K, Graham D |
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- Page last updated:Sep 18, 2020
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