HuGE Literature Finder
Records 1-30
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Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease.
Neurobiology of aging 2019 Nov . Rosas Irene, Martínez Carmen, Clarimón Jordi, Lleó Alberto, Illán-Gala Ignacio, Dols-Icardo Oriol, Borroni Barbara, Almeida Maria Rosário, van der Zee Julie, Van Broeckhoven Christine, Bruni Amalia C, Anfossi Maria, Bernardi Livia, Maletta Raffaele, Serpente María, Galimberti Daniela, Scarpini Elio, Rossi Giacomina, Caroppo Paola, Benussi Luisa, Ghidoni Roberta, Binetti Giuliano, Nacmias Benedetta, Sorbi Sandro, Piaceri Irene, Bagnoli Silvia, Antonell Anna, Sánchez-Valle Raquel, De la Casa-Fages Beatriz, Grandas Francisco, Diez-Fairen Mónica, Pastor Pau, Ferrari Raffaele, Álvarez Victoria, Menéndez-González Manu |
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Rare homozygosity in amyotrophic lateral sclerosis suggests the contribution of recessive variants to disease genetics.
Journal of the neurological sciences 2019 May 402 62-68. Goldstein Orly, Kedmi Merav, Gana-Weisz Mali, Twito Shir, Nefussy Beatrice, Vainer Batel, Fainmesser Yaara, Abraham Alon, Nayshool Omri, Orr-Urtreger Avi, Drory Vivian |
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Prevalence of Carriers of Intermediate and Pathological Polyglutamine Disease-Associated Alleles Among Large Population-Based Cohorts.
JAMA neurology 2019 Apr . Gardiner Sarah L, Boogaard Merel W, Trompet Stella, de Mutsert Renée, Rosendaal Frits R, Gussekloo Jacobijn, Jukema J Wouter, Roos Raymund A C, Aziz N Ahm |
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DNA damage signatures in peripheral blood cells as biomarkers in prodromal huntington disease.
Annals of neurology 2019 Feb 85 (2): 296-301. Castaldo Imma, De Rosa Mariarosaria, Romano Antonella, Zuchegna Candida, Squitieri Ferdinando, Mechelli Rosella, Peluso Silvio, Borrelli Cristiana, Del Mondo Angelo, Salvatore Elena, Vescovi Luigi Angelo, Migliore Simone, De Michele Giuseppe, Ristori Giovanni, Romano Silvia, Avvedimento Enrico Vittorio, Porcellini Anton |
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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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Repeat length variations in ATXN1 and AR modify disease expression in Alzheimer's disease.
Neurobiology of aging 2018 Sep . Gardiner Sarah L, Harder Aster V E, Campman Yvonne J M, Trompet Stella, Gussekloo Jacobijn, van Belzen Martine J, Boogaard Merel W, Roos Raymund A C, Jansen Iris E, Pijnenburg Yolande A L, Scheltens Philip, van der Flier Wiesje M, Aziz N Ahm |
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A study of Huntington disease-like syndromes in black South African patients reveals a single SCA2 mutation and a unique distribution of normal alleles across five repeat loci.
Journal of the neurological sciences 2018 Jul 390 200-204. Baine Fiona K, Peerbhai Nabeelah, Krause Aman |
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Interactions Among Polymorphisms of Susceptibility Loci for Alzheimer's Disease or Depressive Disorder.
Medical science monitor : international medical journal of experimental and clinical research 2018 Apr 24 2599-2619. Kitzlerová Eva, Fišar Zdenek, Lelková Petra, Jirák Roman, Zverová Martina, Hroudová Jana, Manukyan Ada, Martásek Pavel, Raboch Ji |
Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.
The Lancet. Neurology 2017 Jun . Moss Davina J Hensman, Pardiñas Antonio F, Langbehn Douglas, Lo Kitty, Leavitt Blair R, Roos Raymund, Durr Alexandra, Mead Simon, , , Holmans Peter, Jones Lesley, Tabrizi Sarah |
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Study of the Huntington's disease IT-15 gene in different ethnic groups in Ecuador.
Clinical genetics 2017 Apr . Paz-Y-Miño César, Salazar Carolina, García-Cárdenas Jennyfer M, Cabrera-Andrade Alejandro, López-Cortés Andrés, Pavón-Realpe Víctor H, Eras Estefanía, Rodriguez P Carla, Domínguez Enríquez Juan P, Cusco Cuzco Cristian D, Navarrete Socasi Diana C, Leone Paola |
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Association Study and Meta-Analysis of Polymorphisms, Methylation Profiles, and Peripheral mRNA Expression of the Serotonin Transporter Gene in Patients with Alzheimer's Disease.
Dementia and geriatric cognitive disorders 2016 Jul 41 (5-6): 334-347. Yamazaki Kiyohiro, Yoshino Yuta, Mori Takaaki, Okita Mitsuo, Yoshida Taku, Mori Yoko, Ozaki Yuki, Sao Tomoko, Iga Jun-Ichi, Ueno Shu-Ic |
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Clinical manifestations of intermediate allele carriers in Huntington disease.
Neurology 2016 Jul . Cubo Esther, Ramos-Arroyo María A, Martinez-Horta Saul, Martínez-Descalls Asunción, Calvo Sara, Gil-Polo Cecilia, |
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Clinical-genetic model predicts incident impulse control disorders in Parkinson's disease.
Journal of neurology, neurosurgery, and psychiatry 2016 Apr . Kraemmer Julia, Smith Kara, Weintraub Daniel, Guillemot Vincent, Nalls Mike A, Cormier-Dequaire Florence, Moszer Ivan, Brice Alexis, Singleton Andrew B, Corvol Jean-Christop |
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Allele-specific reduction of the mutant huntingtin allele using transcription activator-like effectors in human Huntington's disease fibroblasts.
Cell transplantation 2016 Feb . Fink Kyle D, Deng Peter, Gutierrez Josh, Anderson Joseph S, Torrest Audrey, Komarla Anvita, Kalomoiris Stefanos, Cary Whitney, Anderson Johnathon D, Gruenloh William, Duffy Alexandra, Tempkin Teresa, Wheelock Vicki, Segal David J, Nolta Jan |
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The global prevalence of Huntington's disease: a systematic review and discussion.
Neurodegenerative disease management 2016 08 6 (4): 331-43. Baig Sheharyar Sajjad, Strong Mark, Quarrell Oliver |
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Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2015 Oct 168 (7): 573-85. Krause Amanda, Mitchell Claire, Essop Fahmida, Tager Susan, Temlett James, Stevanin Giovanni, Ross Christopher, Rudnicki Dobrila, Margolis Russe |
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Citalopram for the Treatment of Agitation in Alzheimer Dementia: Genetic Influences.
Journal of geriatric psychiatry and neurology 2015 Aug . Peters Matthew E, Vaidya Vijay, Drye Lea T, Devanand Davangere P, Mintzer Jacobo E, Pollock Bruce G, Porsteinsson Anton P, Rosenberg Paul B, Schneider Lon S, Shade David M, Weintraub Daniel, Yesavage Jerome, Lyketsos Constantine G, Avramopoulos Dimitri, |
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The role of tau in the pathological process and clinical expression of Huntington's disease.
Brain : a journal of neurology 2015 Jul 138 (Pt 7): 1907-18. Vuono Romina, Winder-Rhodes Sophie, de Silva Rohan, Cisbani Giulia, Drouin-Ouellet Janelle, , Spillantini Maria G, Cicchetti Francesca, Barker Roger |
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Prevalence of Huntington's disease gene CAG trinucleotide repeat alleles in patients with bipolar disorder.
Bipolar disorders 2015 Jun 17 (4): 403-8. Ramos Eliana Marisa, Gillis Tammy, Mysore Jayalakshmi S, Lee Jong-Min, Alonso Isabel, Gusella James F, Smoller Jordan W, Sklar Pamela, MacDonald Marcy E, Perlis Roy |
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Psychiatric and cognitive symptoms in Huntington's disease are modified by polymorphisms in catecholamine regulating enzyme genes.
Clinical genetics 2015 Jun . Vinther-Jensen T, Nielsen T T, Budtz-Jørgensen E, Larsen I U, Hansen M M, Hasholt L, Hjermind L E, Nielsen J E, Nørremølle |
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Defining neurodegeneration on Guam by targeted genomic sequencing.
Annals of neurology 2015 Mar 77 (3): 458-68. Steele John C, Guella Ilaria, Szu-Tu Chelsea, Lin Michelle K, Thompson Christina, Evans Daniel M, Sherman Holly E, Vilariño-Güell Carles, Gwinn Katrina, Morris Huw, Dickson Dennis W, Farrer Matthew |
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Functional genetic variation in the serotonin 5-HTTLPR modulates brain damage in frontotemporal dementia.
Neurobiology of aging 2015 Jan 36 (1): 446-51. Premi Enrico, Archetti Silvana, Pilotto Andrea, Seripa Davide, Paghera Barbara, Padovani Alessandro, Borroni Barba |
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A Study of a Geographical Cluster of Huntington's Disease in a Brazilian Town of Zona da Mata, Minas Gerais State.
European neurology 2015 74 (1-2): 62-8. Agostinho Luciana de Andrade, da Silva Iane Dos Santos, Maia Lorena Agostini, Azevedo Mariana de Almeida, Faria Távia Muniz Ribeiro de Oliveira, Apolinario Thays Andrade, Pereira Simão Pedro, Reis Rafael de Lima, Dos Santos Suely Rodrigues, Paiva Carmen Lúcia Ant |
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[Association of serotonin transporter linked polymorphic region 44 bp variable number of tandem repeat polymorphism with Tourette syndrome].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2014 Oct 31 (5): 646-9. Zhang Ying, Su Nailun, Wang Guiju, Cui Jiajia, Yi Mingji, Liu Shig |
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Alpha-theta border EEG abnormalities in preclinical Huntington's disease.
Journal of the neurological sciences 2014 Sep 344 (1-2): 114-20. Ponomareva Natalya, Klyushnikov Sergey, Abramycheva Natalya, Malina Daria, Scheglova Nadejda, Fokin Vitaly, Ivanova-Smolenskaia Irina, Illarioshkin Serg |
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Association between 5-HTTLPR polymorphism and Parkinson's disease: a meta analysis.
Molecular biology reports 2014 Sep 41 (9): 6071-82. Gao Lianbo, Gao Hongh |
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Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes.
Brain : a journal of neurology 2014 Sep 137 (Pt 9): 2444-55. Tezenas du Montcel Sophie, Durr Alexandra, Bauer Peter, Figueroa Karla P, Ichikawa Yaeko, Brussino Alessandro, Forlani Sylvie, Rakowicz Maria, Schöls Ludger, Mariotti Caterina, van de Warrenburg Bart P C, Orsi Laura, Giunti Paola, Filla Alessandro, Szymanski Sandra, Klockgether Thomas, Berciano José, Pandolfo Massimo, Boesch Sylvia, Melegh Bela, Timmann Dagmar, Mandich Paola, Camuzat Agnès, , , Goto Jun, Ashizawa Tetsuo, Cazeneuve Cécile, Tsuji Shoji, Pulst Stefan-M, Brusco Alfredo, Riess Olaf, Brice Alexis, Stevanin Giovan |
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Acute-phase proteins in relation to neuropsychiatric symptoms and use of psychotropic medication in Huntington's disease.
European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology 2014 Aug 24 (8): 1248-56. Bouwens J A, Hubers A A M, van Duijn E, Cobbaert C M, Roos R A C, van der Mast R C, Giltay E |
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Serotonin transporter polymorphic region 5-HTTLPR modulates risk for Parkinson's disease.
Neurobiology of aging 2014 Aug 35 (8): 1957.e9-1957.e14. Zhang Xiong, Cheng Xing, Hu Yan-Bing, Lai Jun-Mei, You Hui, Hu Pei-Long, Zou Ming, Zhu Jian-Ho |
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Evaluation of polyglutamine repeats in autosomal dominant Parkinson's disease.
Neurobiology of aging 2014 Jul 35 (7): 1779.e17-21. Yamashita Chikara, Tomiyama Hiroyuki, Funayama Manabu, Inamizu Saeko, Ando Maya, Li Yuanzhe, Yoshino Hiroyo, Araki Takehisa, Ichikawa Tadashi, Ehara Yoshiro, Ishikawa Kinya, Mizusawa Hidehiro, Hattori Nobuta |
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Determining the association of the 5HTTLPR polymorphism with delusions and hallucinations in Lewy body dementias.
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry 2014 Jun 22 (6): 580-6. Creese Byron, Ballard Clive, Aarsland Dag, Londos Elisabet, Sharp Sally, Jones Em |
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Huntingtin gene CAG repeat numbers in Chinese patients with Huntington's disease and controls.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2014 Apr 21 (4): 637-42. Jiang H, Sun Y M, Hao Y, Yan Y P, Chen K, Xin S H, Tang Y P, Li X H, Jun T, Chen Y Y, Liu Z J, Wang C R, Li H, Pei Z, Shang H F, Zhang B R, Gu W H, Wu Z Y, Tang B S, Burgunder J-M, |
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Investigation of association of serotonin transporter and monoamine oxidase-A genes with Alzheimer's disease and depression in the VITA study cohort: a 90-month longitudinal study.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2014 Mar 165B (2): 184-91. Scholz Claus-Jürgen, Jungwirth Susanne, Danielczyk Walter, Weber Heike, Wichart Ildiko, Tragl Karl Heinz, Fischer Peter, Riederer Peter, Deckert Jürgen, Grünblatt Ed |
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Clinical and genetic features of Huntington disease in Sri Lanka.
BMC neurology 2013 Dec 13 (1): 1. Sumathipala DS, Jayasekara RW, Dissanayake VH |
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High frequency of intermediate alleles on Huntington disease-associated haplotypes in British Columbia's general population.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Dec 162B (8): 864-71. Semaka Alicia, Kay Chris, Doty Crystal N, Collins Jennifer A, Tam Natalie, Hayden Michael |
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Modelling and inference reveal nonlinear length-dependent suppression of somatic instability for small disease associated alleles in myotonic dystrophy type 1 and Huntington disease.
Journal of the Royal Society, Interface / the Royal Society 2013 Nov 10 (88): 20130605. Higham Catherine F, Monckton Darren |
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CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease.
Journal of medical genetics 2013 Oct 50 (10): 696-703. Semaka Alicia, Kay Chris, Doty Crystal, Collins Jennifer A, Bijlsma Emilia K, Richards Fiona, Goldberg Y Paul, Hayden Michael |
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Huntington disease in the South African population occurs on diverse and ethnically distinct genetic haplotypes.
European journal of human genetics : EJHG 2013 Oct 21 (10): 1120-7. Baine Fiona K, Kay Chris, Ketelaar Maria E, Collins Jennifer A, Semaka Alicia, Doty Crystal N, Krause Amanda, Greenberg L Jacquie, Hayden Michael |
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Common and rare alleles of the serotonin transporter gene, SLC6A4, associated with Tourette's disorder.
Movement disorders : official journal of the Movement Disorder Society 2013 Aug 28 (9): 1263-70. Moya Pablo R, Wendland Jens R, Rubenstein Liza M, Timpano Kiara R, Heiman Gary A, Tischfield Jay A, King Robert A, Andrews Anne M, Ramamoorthy Samanda, McMahon Francis J, Murphy Dennis |
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Sociodemographic characteristics, clinical factors, and genetic polymorphisms associated with Alzheimer's disease.
International journal of geriatric psychiatry 2013 Jun 28 (6): 640-6. Bicalho Maria Aparecida Camargos, Pimenta Fausto Aloísio, Bastos-Rodrigues Luciana, de Oliveira Hansen Érika, Neves Samara Canguçu, Melo Marina, Rosa Daniela Valadão, Pedra de Souza Renan, Marques de Miranda Débora, Nunes de Moraes Edgar, Romano-Silva Marco Aurélio, De Marco Lu |
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Characterization of the Huntington intermediate CAG repeat expansion phenotype in PHAROS.
Neurology 2013 May 80 (22): 2022-7. Killoran Annie, Biglan Kevin M, Jankovic Joseph, Eberly Shirley, Kayson Elise, Oakes David, Young Anne B, Shoulson I |
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Serotonin transporter and serotonin receptor 2A gene polymorphisms in Alzheimer's disease.
Neuroscience letters 2013 Feb 534 233-6. Fehér Agnes, Juhász Anna, László Anna, Pákáski Magdolna, Kálmán János, Janka Zolt |
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The serotonin transporter gene locus in late-life major depressive disorder.
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry 2013 Jan 21 (1): 1. Seripa D, Panza F, D'Onofrio G, Paroni G, Bizzarro A, Fontana A, Paris F, Cascavilla L, Copetti M, Masullo C, Pilotto A |
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Brain-specific tryptophan hydroxylase, TPH2, and 5-HTTLPR are associated with frontal lobe symptoms in Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2013 35 (1): 67-73. Engelborghs Sebastiaan, Sleegers Kristel, Van der Mussele Stefan, Le Bastard Nathalie, Brouwers Nathalie, Van Broeckhoven Christine, De Deyn Peter Pa |
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Insulin sensitivity and early-phase insulin secretion in normoglycemic Huntington's disease patients.
Journal of Huntington's disease 2013 2 (4): 501-7. Russo Cinzia V, Salvatore Elena, Saccà Francesco, Tucci Tecla, Rinaldi Carlo, Sorrentino Pierpaolo, Massarelli Marco, Rossi Fabiana, Savastano Silvia, Di Maio Luigi, Filla Alessandro, Colao Annamaria, De Michele Giusep |
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Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease.
Journal of human genetics 2012 Dec 57 (12): 796-803. Agostinho Luciana de A, Rocha Catielly F, Medina-Acosta Enrique, Barboza Hazel N, da Silva Antônio F Alves, Pereira Simão P F, da Silva Iane Dos Santos, Paradela Eduardo R, Figueiredo André L dos S, Nogueira Eduardo de M, Alvarenga Regina M P, Hernan Cabello Pedro, dos Santos Suely R, Paiva Carmen L |
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Genetic Risk Factors for Depression in Alzheimer´s Disease Patients.
Current Alzheimer research 2012 Nov . Arlt S, Demiralay C, Tharun B, Geisel O, Storm N, Eichenlaub M, Lehmbeck JT, Wiedemann K, Leuenberger B, Jahn H |
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TAA repeat variation in the GRIK2 gene does not influence age at onset in Huntington's disease.
Biochemical and biophysical research communications 2012 Aug 424 (3): 404-8. Lee Ji-Hyun, Lee Jong-Min, Ramos Eliana Marisa, Gillis Tammy, Mysore Jayalakshmi S, Kishikawa Shotaro, Hadzi Tiffany, Hendricks Audrey E, Hayden Michael R, Morrison Patrick J, Nance Martha, Ross Christopher A, Margolis Russell L, Squitieri Ferdinando, Gellera Cinzia, Gomez-Tortosa Estrella, Ayuso Carmen, Suchowersky Oksana, Trent Ronald J, McCusker Elizabeth, Novelletto Andrea, Frontali Marina, Jones Randi, Ashizawa Tetsuo, Frank Samuel, Saint-Hilaire Marie-Helene, Hersch Steven M, Rosas Herminia D, Lucente Diane, Harrison Madaline B, Zanko Andrea, Abramson Ruth K, Marder Karen, Sequeiros Jorge, Landwehrmeyer G Bernhard, , Shoulson Ira, , Myers Richard H, MacDonald Marcy E, Gusella James |
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Chinese patients with Huntington's disease initially presenting with spinocerebellar ataxia.
Clinical genetics 2012 Jul 9999 (999A): 999A. Dong Y, Sun YM, Liu ZJ, Ni W, Shi SS, Wu ZY |
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Prevalence of Huntington's disease gene CAG repeat alleles in sporadic amyotrophic lateral sclerosis patients.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases 2012 May 13 (3): 265-9. Ramos Eliana Marisa, Keagle Pamela, Gillis Tammy, Lowe Patrick, Mysore Jayalakshmi S, Leclerc Ashley Lyn, Ratti Antonia, Ticozzi Nicola, Gellera Cinzia, Gusella James F, Silani Vincenzo, Alonso Isabel, Brown Robert H, MacDonald Marcy E, Landers John |
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Common SNP-based haplotype analysis of the 4p16.3 Huntington disease gene region.
American journal of human genetics 2012 Mar 90 (3): 434-44. Lee Jong-Min, Gillis Tammy, Mysore Jayalakshmi Srinidhi, Ramos Eliana Marisa, Myers Richard H, Hayden Michael R, Morrison Patrick J, Nance Martha, Ross Christopher A, Margolis Russell L, Squitieri Ferdinando, Griguoli Annamaria, Di Donato Stefano, Gomez-Tortosa Estrella, Ayuso Carmen, Suchowersky Oksana, Trent Ronald J, McCusker Elizabeth, Novelletto Andrea, Frontali Marina, Jones Randi, Ashizawa Tetsuo, Frank Samuel, Saint-Hilaire Marie-Helene, Hersch Steven M, Rosas Herminia D, Lucente Diane, Harrison Madaline B, Zanko Andrea, Abramson Ruth K, Marder Karen, Sequeiros Jorge, MacDonald Marcy E, Gusella James |
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Radioligand binding to brain dopamine and serotonin receptors and transporters in Parkinson's disease: relation to gene polymorphisms.
The International journal of neuroscience 2012 Mar 122 (3): 124-32. Güzey Cüneyt, Allard Per, Brännström Thomas, Spigset Ol |
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Clinical and genetic characteristics in patients with Huntington's Disease from Argentina.
Parkinsonism & related disorders 2012 Feb 18 (2): 166-9. Gatto Emilia, Parisi Virginia, Persi Gabriel, Converso Daniela Paola, Etcheverry José Luis, Varela Viviana, Lopez Ariel, Alba Liliana, Fretchel Gusta |
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Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data.
The Lancet. Neurology 2012 Jan 11 (1): 42-53. Tabrizi Sarah J, Reilmann Ralf, Roos Raymund A C, Durr Alexandra, Leavitt Blair, Owen Gail, Jones Rebecca, Johnson Hans, Craufurd David, Hicks Stephen L, Kennard Christopher, Landwehrmeyer Bernhard, Stout Julie C, Borowsky Beth, Scahill Rachael I, Frost Chris, Langbehn Douglas R, |
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The Serotonin Transporter Gene Locus in Late-Life Major Depressive Disorder.
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry 2012 Jan . Seripa D, Panza F, D?onofrio G, Paroni G, Bizzarro A, Fontana A, Paris F, Cascavilla L, Copetti M, Masullo C, Pilotto A |
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Sertraline for the treatment of depression in Alzheimer disease: genetic influences.
Journal of geriatric psychiatry and neurology 2011 Dec 24 (4): 222-8. Peters Matthew E, Vaidya Vijay, Drye Lea T, Rosenberg Paul B, Martin Barbara K, Porsteinsson Anton P, Frangakis Constantine E, Mintzer Jacobo, Weintraub Daniel, Schneider Lon S, Rabins Peter V, Munro Cynthia A, Meinert Curtis L, Lyketsos Constantine G, Avramopoulos Dimitri, Dimitri Avramopoulos, |
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HTT haplotypes contribute to differences in Huntington disease prevalence between Europe and East Asia.
European journal of human genetics : EJHG 2011 May 19 (5): 561-6. Warby Simon C, Visscher Henk, Collins Jennifer A, Doty Crystal N, Carter Catherine, Butland Stefanie L, Hayden Anna R, Kanazawa Ichiro, Ross Colin J, Hayden Michael |
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Differential genetic susceptibility in diphasic and peak-dose dyskinesias in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2011 Jan 26 (1): 73-9. Lee Jee-Young, Cho Jinwhan, Lee Eun-Kyung, Park Sung-Sup, Jeon Beom |
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Serotonin transporter and saitohin genes in risk of Alzheimer's disease and frontotemporal lobar dementia: preliminary findings.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2010 Dec 31 (6): 741-9. Lorenzi Cristina, Marcone Alessandra, Pirovano Adele, Marino Elena, Cordici Francesco, Cerami Chiara, Delmonte Dario, Cappa Stefano F, Bramanti Placido, Smeraldi Enri |
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Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.
Journal of the neurological sciences 2010 Nov 298 (1-2): 57-60. Ma Mingyi, Yang Yuan, Shang Huifang, Su Dan, Zhang Hao, Ma Yongxin, Liu Yunqiang, Tao Dachang, Zhang Sizho |
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Systemic energy homeostasis in Huntington's disease patients.
Journal of neurology, neurosurgery, and psychiatry 2010 Nov 81 (11): 1233-7. Aziz N Ahmad, Pijl Hanno, Frölich Marijke, Snel Marieke, Streefland Trea C M, Roelfsema Ferdinand, Roos Raymund A |
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A double blind evaluation of cognitive decline in a Norwegian cohort of asymptomatic carriers of Huntington's disease.
Journal of clinical and experimental neuropsychology 2010 Jul 32 (6): 590-8. van Walsem Marleen R, Sundet Kjetil, Retterstøl Lars, Sundseth Øyvi |
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Prevalence of incompletely penetrant Huntington's disease alleles among individuals with major depressive disorder.
The American journal of psychiatry 2010 May 167 (5): 574-9. Perlis Roy H, Smoller Jordan W, Mysore Jayalakshmi, Sun Mei, Gillis Tammy, Purcell Shaun, Rietschel Marcella, Nöthen Markus M, Witt Stephanie, Maier Wolfgang, Iosifescu Dan V, Sullivan Patrick, Rush A John, Fava Maurizio, Breiter Hans, Macdonald Marcy, Gusella Jam |
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A genetic variant of HTR2C may play a role in the manifestation of Tourette syndrome.
Psychiatric genetics 2010 Feb 20 (1): 35-8. Dehning Sandra, Müller Norbert, Matz Judith, Bender Andreas, Kerle Irina, Benninghoff Jens, Musil Richard, Spellmann Ilja, Bondy Brigitta, Möller Hans-Juergen, Riedel Michael, Zill Pet |
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Evaluation of IP-RP-HPLC for length determination of the trinucleotide repeat fragments in Huntington's disease.
Journal of chromatographic science 2010 Jan 48 (1): 55-8. Skrzypczak Marzena, Heinritz Wolfram, Schulz Anna M, Mierzejewski Marek, Froster Ursula |
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Normal and mutant HTT interact to affect clinical severity and progression in Huntington disease.
Neurology 2009 Oct 73 (16): 1280-5. Aziz N A, Jurgens C K, Landwehrmeyer G B, , van Roon-Mom W M C, van Ommen G J B, Stijnen T, Roos R A |
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Serotonergic system genes in psychosis of Alzheimer dementia: meta-analysis.
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry 2009 Oct 17 (10): 839-46. Ramanathan Seethalakshmi, Glatt Stephen |
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Somatic expansion of the Huntington's disease CAG repeat in the brain is associated with an earlier age of disease onset.
Human molecular genetics 2009 Aug 18 (16): 3039-47. Swami Meera, Hendricks Audrey E, Gillis Tammy, Massood Tiffany, Mysore Jayalakshmi, Myers Richard H, Wheeler Vanessa |
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A majority of Huntington's disease patients may be treatable by individualized allele-specific RNA interference.
Experimental neurology 2009 Jun 217 (2): 312-9. Lombardi Maria Stella, Jaspers Leonie, Spronkmans Christine, Gellera Cinzia, Taroni Franco, Di Maria Emilio, Donato Stefano Di, Kaemmerer William |
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Association of DRD3 and GRIN2B with impulse control and related behaviors in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009 Jun . Lee JY, Lee EK, Park SS, Lim JY, Kim HJ, Kim JS, Jeon BS |
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No association between polymorphism of serotonin transporter gene and depression in Parkinson's disease in Chinese.
Neuroscience letters 2009 May 455 (3): 155-8. Zhang Jing-Lin, Yang Jing-Fang, Chan P |
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4p16.3 haplotype modifying age at onset of Huntington disease.
Clinical genetics 2009 Mar 75 (3): 244-50. Nørremølle A, Budtz-Jørgensen E, Fenger K, Nielsen J E, Sørensen S A, Hasholt |
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CAG expansion in the Huntington disease gene is associated with a specific and targetable predisposing haplogroup.
American journal of human genetics 2009 Mar 84 (3): 351-66. Warby Simon C, Montpetit Alexandre, Hayden Anna R, Carroll Jeffrey B, Butland Stefanie L, Visscher Henk, Collins Jennifer A, Semaka Alicia, Hudson Thomas J, Hayden Michael |
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Relationship between CAG repeat length and brain volume in premanifest and early Huntington's disease.
Journal of neurology 2009 Feb 256 (2): 203-12. Henley Susie M D, Wild Edward J, Hobbs Nicola Z, Scahill Rachael I, Ridgway Gerard R, Macmanus David G, Barker Roger A, Fox Nick C, Tabrizi Sarah |
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Genetic risk factors and markers for Alzheimer's disease and/or depression in the VITA study.
Journal of psychiatric research 2009 Jan 43 (3): 298-308. Grünblatt Edna, Zehetmayer Sonja, Bartl Jasmin, Löffler Christiane, Wichart Ildiko, Rainer Michael K, Jungwirth Susanne, Bauer Peter, Danielczyk Walter, Tragl Karl-Heinz, Riederer Peter, Fischer Pet |
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Serotonin and dopamine transporter genes do not influence depression in Parkinson's disease.
Movement disorders : official journal of the Movement Disorder Society 2009 Jan 24 (1): 111-5. Dissanayaka Nadeeka N W, Silburn Peter A, O'Sullivan John D, Mellick George |
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The genetics of Alzheimer's disease in Brazil: 10 years of analysis in a unique population.
Journal of molecular neuroscience : MN 2009 Jan 37 (1): 74-9. Oliveira J R M, Nishimura A L, Lemos R R, Zatz |
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Genetic analysis of Alzheimer's disease in the Uppsala Longitudinal Study of Adult Men.
Dementia and geriatric cognitive disorders 2009 27 (1): 59-68. Giedraitis Vilmantas, Kilander Lena, Degerman-Gunnarsson Malin, Sundelöf Johan, Axelsson Tomas, Syvänen Ann-Christine, Lannfelt Lars, Glaser An |
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Psychotic symptoms in Alzheimer's disease and 5-HTTLPR polymorphism of the serotonin transporter gene: evidence for an association.
Journal of Alzheimer's disease : JAD 2009 16 (1): 173-80. Quaranta Davide, Bizzarro Alessandra, Marra Camillo, Vita Maria Gabriella, Seripa Davide, Pilotto Alberto, Sebastiani Valeria, Mecocci Patrizia, Masullo Car |
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Serotonin transporter gene polymorphic element 5-HTTLPR increases the risk of sporadic Parkinson's disease in Italy.
European neurology 2009 62 (2): 120-3. Albani Diego, Vittori Angelica, Batelli Sara, Polito Letizia, De Mauro Stefania, Galimberti Daniela, Scarpini Elio, Lovati Carlo, Mariani Claudio, Forloni Gianlui |
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The serotonin transporter promoter polymorphic region is not a risk factor for Alzheimer's disease related behavioral disturbances.
Journal of Alzheimer's disease : JAD 2009 18 (1): 125-30. Albani Diego, Prato Francesca, Tettamanti Mauro, Lovati Carlo, Galimberti Daniela, Restelli Ilaria, Mariani Claudio, Quadri Pier Luigi, Scarpini Elio, Lucca Ugo, Forloni Gianlui |
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Impact of serotonin transporter and catechol-O-methyl transferase genes polymorphism on gastrointestinal dysfunction in Swedish and Japanese familial amyloidotic polyneuropathy patients.
Clinica chimica acta; international journal of clinical chemistry 2008 Dec 398 (1-2): 10-4. Obayashi Konen, Olsson Malin, Anan Intissar, Ueda Mitsuharu, Nakamura Masaaki, Okamoto Sadahisa, Yamashita Taro, Miida Takashi, Ando Yukio, Suhr Ole |
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Cross-sectional study on prevalences of psychiatric disorders in mutation carriers of Huntington's disease compared with mutation-negative first-degree relatives.
The Journal of clinical psychiatry 2008 Nov 69 (11): 1804-10. van Duijn Erik, Kingma Elisabeth M, Timman Reinier, Zitman Frans G, Tibben Aad, Roos Raymund A C, van der Mast Rose |
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Huntington CAG repeat size does not modify onset age in familial Parkinson's disease: the GenePD study.
Movement disorders : official journal of the Movement Disorder Society 2008 Aug 23 (11): 1596-601. McNicoll Christopher F, Latourelle Jeanne C, MacDonald Marcy E, Lew Mark F, Suchowersky Oksana, Klein Christine, Golbe Lawrence I, Mark Margery H, Growdon John H, Wooten G Frederick, Watts Ray L, Guttman Mark, Racette Brad A, Perlmutter Joel S, Ahmed Anwar, Shill Holly A, Singer Carlos, Saint-Hilaire Marie H, Massood Tiffany, Huskey Karen W, DeStefano Anita L, Gillis Tammy, Mysore Jayalakshmi, Goldwurm Stefano, Pezzoli Gianni, Baker Kenneth B, Itin Ilia, Litvan Irene, Nicholson Garth, Corbett Alastair, Nance Martha, Drasby Edward, Isaacson Stuart, Burn David J, Chinnery Patrick F, Pramstaller Peter P, Al-Hinti Jomana, Moller Anette T, Ostergaard Karen, Sherman Scott J, Roxburgh Richard, Snow Barry, Slevin John T, Cambi Franca, Gusella James F, Myers Richard |
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Effect of CAG repeat length on psychiatric disorders in Huntington's disease.
Journal of psychiatric research 2008 Jun 42 (7): 544-9. Vassos Evangelos, Panas Marios, Kladi Athina, Vassilopoulos Dimitri |
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Polymorphism C in the serotonin transporter gene (SLC6A4) in questionable dementia and Alzheimer's disease.
Neuroscience letters 2008 Jun 438 (3): 335-9. Seripa Davide, Franceschi Marilisa, D'Onofrio Grazia, Panza Francesco, Cascavilla Leandro, Paris Francesco, Placentino Giuliana, Matera Maria Giovanna, Solfrizzi Vincenzo, Pilotto Alber |
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Neuropsychological deficits in Huntington's disease gene carriers and correlates of early "conversion".
The Journal of neuropsychiatry and clinical neurosciences 2008 20 (4): 466-72. Brandt Jason, Inscore Anjeli B, Ward Julianna, Shpritz Barnett, Rosenblatt Adam, Margolis Russell L, Ross Christopher |
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Are cognitive changes progressive in prediagnostic HD?
Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology 2007 Dec 20 (4): 212-8. Stout Julie C, Weaver Marjorie, Solomon Andrea C, Queller Sarah, Hui Siu, Johnson Shannon A, Gray Jacqueline, Beristain Xabier, Wojcieszek Joanne, Foroud Tatia |
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Cognitive changes in asymptomatic carriers of the Huntington disease mutation gene.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2007 Dec 14 (12): 1344-50. Verny C, Allain P, Prudean A, Malinge M-C, Gohier B, Scherer C, Bonneau D, Dubas F, Le Gall |
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Serotonin transporter gene polymorphism and BPSD in mild Alzheimer's disease.
Journal of Alzheimer's disease : JAD 2007 Nov 12 (3): 245-53. Ueki Akinori, Ueno Hideo, Sato Noriko, Shinjo Hidetaka, Morita Yosh |
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Visual hallucinations in Parkinson's disease are not influenced by polymorphisms of serotonin 5-HT2A receptor and transporter genes.
Neuroscience letters 2007 Jul 422 (3): 228-31. Kiferle Lorenzo, Ceravolo Roberto, Petrozzi Lucia, Rossi Carlo, Frosini Daniela, Rocchi Anna, Siciliano Gabriele, Bonuccelli Ubaldo, Murri Lui |
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Reduced penetrance alleles for Huntington's disease: a multi-centre direct observational study.
Journal of medical genetics 2007 Mar 44 (3): e68. Quarrell Oliver W J, Rigby Alan S, Barron L, Crow Y, Dalton A, Dennis N, Fryer A E, Heydon F, Kinning E, Lashwood A, Losekoot M, Margerison L, McDonnell S, Morrison P J, Norman A, Peterson M, Raymond F L, Simpson S, Thompson E, Warner |
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Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder.
Biological psychiatry 2007 Feb 61 (3): 322-9. Dickel Diane E, Veenstra-VanderWeele Jeremy, Bivens Nancy Chiu, Wu Xiaolin, Fischer Daniel J, Van Etten-Lee Michelle, Himle Joseph A, Leventhal Bennett L, Cook Edwin H, Hanna Gregory |
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Early cognitive deficits in Swedish gene carriers of Huntington's disease.
Neuropsychology 2007 Jan 21 (1): 31-44. Robins Wahlin Tarja-Brita, Lundin Anders, Dear Kei |
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Role of serotonin transporter polymorphisms in the behavioural and psychological symptoms in probable Alzheimer disease patients.
Dementia and geriatric cognitive disorders 2007 24 (3): 201-6. Pritchard Antonia L, Pritchard Colin W, Bentham Peter, Lendon Corinne |
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No evidence for allelic association of serotonin 2A receptor and transporter gene polymorphisms with depression in Alzheimer disease.
Journal of Alzheimer's disease : JAD 2006 Dec 10 (4): 371-8. Micheli D, Bonvicini C, Rocchi A, Ceravolo R, Mancuso M, Tognoni G, Gennarelli M, Siciliano G, Murri |
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Genetic correlates of behavioral endophenotypes in Alzheimer disease: role of COMT, 5-HTTLPR and APOE polymorphisms.
Neurobiology of aging 2006 Nov 27 (11): 1595-603. Borroni B, Grassi M, Agosti C, Costanzi C, Archetti S, Franzoni S, Caltagirone C, Di Luca M, Caimi L, Padovani |
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Association study of polymorphisms in LRP1, tau and 5-HTT genes and Alzheimer's disease in a sample of Colombian patients.
Journal of neural transmission (Vienna, Austria : 1996) 2006 Sep 113 (9): 1253-62. Forero D A, Arboleda G, Yunis J J, Pardo R, Arboleda |
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Allelic variation of a functional polymorphism in the serotonin transporter gene and depression in Parkinson's disease.
Parkinsonism & related disorders 2006 Apr 12 (3): 139-41. Burn David J, Tiangyou Watcharee, Allcock Liesl M, Davison Jill, Chinnery Patrick |
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Cumulative effect of COMT and 5-HTTLPR polymorphisms and their interaction with disease severity and comorbidities on the risk of psychosis in Alzheimer disease.
The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry 2006 Apr 14 (4): 343-51. Borroni Barbara, Grassi Mario, Agosti Chiara, Archetti Silvana, Costanzi Chiara, Cornali Cristina, Caltagirone Carlo, Caimi Luigi, Di Luca Monica, Padovani Alessand |
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- Page last updated:Mar 30, 2020
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