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Change in Epigenome-Wide DNA Methylation Over 9 Years and Subsequent Mortality: Results From the InCHIANTI Study.
Published in:
2016
By:
- Zenobia Moore, Ann;
- Hernandez, Dena G.;
- Toshiko Tanaka;
- Pilling, Luke C.;
- Nalls, Mike A.;
- Bandinelli, Stefania;
- Singleton, Andrew B.;
- Ferrucci, Luigi;
- Moore, Ann Zenobia;
- Tanaka, Toshiko
Publication type:
journal article
Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction.
Published in:
Clinical Epigenetics, 2018, v. 10, n. 1, p. N.PAG, doi. 10.1186/s13148-018-0588-7
By:
- Ward-Caviness, Cavin K.;
- Agha, Golareh;
- Chen, Brian H.;
- Pfeiffer, Liliane;
- Wilson, Rory;
- Wolf, Petra;
- Gieger, Christian;
- Schwartz, Joel;
- Vokonas, Pantel S.;
- Hou, Lifang;
- Just, Allan C.;
- Bandinelli, Stefania;
- Hernandez, Dena G.;
- Singleton, Andrew B.;
- Prokisch, Holger;
- Meitinger, Thomas;
- Kastenmüller, Gabi;
- Ferrucci, Luigi;
- Baccarelli, Andrea A.;
- Waldenberger, Melanie
Publication type:
Article
Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic risk.
Published in:
2023
By:
- Bustos, Bernabe I;
- Billingsley, Kimberley;
- Blauwendraat, Cornelis;
- Gibbs, J Raphael;
- Gan-Or, Ziv;
- Krainc, Dimitri;
- Singleton, Andrew B;
- Lubbe, Steven J;
- (IPDGC), International Parkinson's Disease Genomics Consortium;
- International Parkinson’s Disease Genomics Consortium (IPDGC)
Publication type:
journal article
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
Published in:
2022
By:
- Zhu, William;
- Huang, Xiaoping;
- Yoon, Esther;
- Bandres-Ciga, Sara;
- Blauwendraat, Cornelis;
- Billingsley, Kimberly J;
- Cade, Joshua H;
- Wu, Beverly P;
- Williams, Victoria H;
- Schindler, Alice B;
- Brooks, Janet;
- Gibbs, J Raphael;
- Hernandez, Dena G;
- Ehrlich, Debra;
- Singleton, Andrew B;
- Narendra, Derek P
Publication type:
journal article
Clinical, pathological and functional characterization of riboflavin-responsive neuropathy.
Published in:
2017
By:
- Manole, Andreea;
- Jaunmuktane, Zane;
- Hargreaves, Iain;
- Ludtmann, Marthe H. R.;
- Salpietro, Vincenzo;
- Bello, Oscar D.;
- Pope, Simon;
- Pandraud, Amelie;
- Horga, Alejandro;
- Scalco, Renata S.;
- Abi Li;
- Ashokkumar, Balasubramaniem;
- Lourenc, Charles M.;
- Heales, Simon;
- Horvath, Rita;
- Chinnery, Patrick F.;
- Toro, Camilo;
- Singleton, Andrew B.;
- Jacques, Thomas S.;
- Abramov, Andrey Y.
Publication type:
journal article
Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literature.
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5740, doi. 10.1002/alz.13873
By:
- Jonson, Caroline;
- Levine, Kristin S.;
- Lake, Julie;
- Hertslet, Linnea;
- Jones, Lietsel;
- Patel, Dhairya;
- Kim, Jeff;
- Bandres‐Ciga, Sara;
- Terry, Nancy;
- Mata, Ignacio F.;
- Blauwendraat, Cornelis;
- Singleton, Andrew B.;
- Nalls, Mike A.;
- Yokoyama, Jennifer S.;
- Leonard, Hampton L.
Publication type:
Article
A cross‐sectional study of α‐synuclein seed amplification assay in Alzheimer's disease neuroimaging initiative: Prevalence and associations with Alzheimer's disease biomarkers and cognitive function.
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2024, v. 20, n. 8, p. 5114, doi. 10.1002/alz.13858
By:
- Tosun, Duygu;
- Hausle, Zachary;
- Iwaki, Hirotaka;
- Thropp, Pamela;
- Lamoureux, Jennifer;
- Lee, Edward B.;
- MacLeod, Karen;
- McEvoy, Sean;
- Nalls, Michael;
- Perrin, Richard J.;
- Saykin, Andrew J.;
- Shaw, Leslie M.;
- Singleton, Andrew B.;
- Lebovitz, Russ;
- Weiner, Michael W.;
- Blauwendraat, Cornelis
Publication type:
Article
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies.
Published in:
Nucleic Acids Research, 2013, v. 41, n. 7, p. e88, doi. 10.1093/nar/gkt069
By:
- Ramasamy, Adaikalavan;
- Trabzuni, Daniah;
- Gibbs, J. Raphael;
- Dillman, Allissa;
- Hernandez, Dena G.;
- Arepalli, Sampath;
- Walker, Robert;
- Smith, Colin;
- Ilori, Gigaloluwa Peter;
- Shabalin, Andrey A.;
- Li, Yun;
- Singleton, Andrew B.;
- Cookson, Mark R.;
- Hardy, John;
- Ryten, Mina;
- Weale, Michael E.
Publication type:
Article
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy.
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2017, v. 13, n. 8, p. 858, doi. 10.1016/j.jalz.2017.01.011
By:
- Capozzo, Rosa;
- Sassi, Celeste;
- Hammer, Monia B.;
- Arcuti, Simona;
- Zecca, Chiara;
- Barulli, Maria R.;
- Tortelli, Rosanna;
- Gibbs, J. Raphael;
- Crews, Cynthia;
- Seripa, Davide;
- Carnicella, Francesco;
- Dell'Aquila, Claudia;
- Rossi, Marco;
- Tamma, Filippo;
- Valluzzi, Francesco;
- Brancasi, Bruno;
- Panza, Francesco;
- Singleton, Andrew B.;
- Logroscino, Giancarlo
Publication type:
Article
A candidate gene study of genetic risk for dementia and mild cognitive impairment (MCI) in women aged >65 years: Results from the women's health initiative memory study (WHIMS).
Published in:
Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2014, v. 10, p. P787, doi. 10.1016/j.jalz.2014.05.1525
By:
- Driscoll, Ira;
- Snively, Beverly M.;
- Espeland, Mark A.;
- Shumaker, Sally A.;
- Rapp, Stephen R.;
- Goveas, Joseph S.;
- Casanova, Ramon;
- Wactawski-Wende, Jean;
- Manson, JoAnn E.;
- Rossom, Rebecca C.;
- Brooks, Janet;
- Hernandez, Dena G.;
- Singleton, Andrew B.;
- Resnick, Susan M.
Publication type:
Article
Erratum: Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
Published in:
2008
By:
- Houlden, Henry;
- Johnson, Janel;
- Gardner-Thorpe, Christopher;
- Lashley, Tammaryn;
- Hernandez, Dena;
- Worth, Paul;
- Singleton, Andrew B.;
- Hilton, David A.;
- Holton, Janice;
- Revesz, Tamas;
- Davis, Mary B.;
- Giunti, Paolo;
- Wood, Nicholas W.
Publication type:
Correction Notice
Mutations in TTBK2, encoding a kinase implicated in tau phosphorylation, segregate with spinocerebellar ataxia type 11.
Published in:
Nature Genetics, 2007, v. 39, n. 12, p. 1434, doi. 10.1038/ng.2007.43
By:
- Houlden, Henry;
- Johnson, Janel;
- Gardner-Thorpe, Christopher;
- Lashley, Tammaryn;
- Hernandez, Dena;
- Worth, Paul;
- Singleton, Andrew B.;
- Hilton, David A.;
- Holton, Janice;
- Revesz, Tamas;
- Davis, Mary B.;
- Giunti, Paolo;
- Wood, Nicholas W.
Publication type:
Article
Comparing Spatial Maps of Human Population-Genetic Variation Using Procrustes Analysis.
Published in:
Statistical Applications in Genetics & Molecular Biology, 2010, v. 9, n. 1, p. 1, doi. 10.2202/1544-6115.1493
By:
- Chaolong Wang;
- Szpiech, Zachary A.;
- Degnan, James H.;
- Jakobsson, Mattias;
- Pemberton, Trevor J.;
- Hardy, John A.;
- Singleton, Andrew B.;
- Rosenberg, Noah A.
Publication type:
Article
Imputation of Variants from the 1000 Genomes Project Modestly Improves Known Associations and Can Identify Low-frequency Variant - Phenotype Associations Undetected by HapMap Based Imputation
Published in:
PLoS ONE, 2013, v. 8, n. 5, p. 1, doi. 10.1371/journal.pone.0064343
By:
- Wood, Andrew R.;
- Perry, John R. B.;
- Tanaka, Toshiko;
- Hernandez, Dena G.;
- Zheng, Hou-Feng;
- Melzer, David;
- Gibbs, J. Raphael;
- Nalls, Michael A.;
- Weedon, Michael N.;
- Spector, Tim D.;
- Richards, J. Brent;
- Bandinelli, Stefania;
- Ferrucci, Luigi;
- Singleton, Andrew B.;
- Frayling, Timothy M.
Publication type:
Article
Genome Wide Assessment of Young Onset Parkinson's Disease from Finland.
Published in:
2012
By:
- Hernandez, Dena G.;
- Nalls, Michael A.;
- Ylikotila, Pauli;
- Keller, Margaux;
- Hardy, John A.;
- Majamaa, Kari;
- Singleton, Andrew B.
Publication type:
Case Study
Cooperative Genome-Wide Analysis Shows Increased Homozygosity in Early Onset Parkinson's Disease.
Published in:
PLoS ONE, 2012, v. 7, n. 3, p. 1, doi. 10.1371/journal.pone.0028787
By:
- Simón-Sánchez, Javier;
- Kilarski, Laura L.;
- Nalls, Michael A.;
- Martinez, Maria;
- Schulte, Claudia;
- Holmans, Peter;
- Gasser, Thomas;
- Hardy, John;
- Singleton, Andrew B.;
- Wood, Nicholas W.;
- Brice, Alexis;
- Heutink, Peter;
- Williams, Nigel;
- Morris, Huw R.
Publication type:
Article
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia.
Published in:
2017
By:
- Bettencourt, Conceição;
- Salpietro, Vincenzo;
- Efthymiou, Stephanie;
- Chelban, Viorica;
- Hughes, Deborah;
- Pittman, Alan M.;
- Federoff, Monica;
- Bourinaris, Thomas;
- Spilioti, Martha;
- Deretzi, Georgia;
- Kalantzakou, Triantafyllia;
- Houlden, Henry;
- Singleton, Andrew B.;
- Xiromerisiou, Georgia
Publication type:
journal article
SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families.
Published in:
Neurodegenerative Diseases, 2017, v. 17, n. 4/5, p. 208, doi. 10.1159/000464445
By:
- Hammer, Monia B.;
- Ding, Jinhui;
- Mochel, Fanny;
- Eleuch-Fayache, Ghada;
- Charles, Perrine;
- Coutelier, Marie;
- Gibbs, J. Raphael;
- arepalli, Sampath K.;
- Chong, Sean B.;
- Hernandez, Dena G.;
- Majounie, Elisa;
- Clipman, Steven;
- Bouhlal, Yosr;
- Nehdi, Houda;
- Brice, alexis;
- Hentati, Faycal;
- Stevanin, Giovanni;
- amouri, Rim;
- Durr, alexandra;
- Singleton, andrew B.
Publication type:
Article
Using DNA Methylation to Understand Biological Consequences of Genetic Variability.
Published in:
Neurodegenerative Diseases, 2012, v. 9, n. 2, p. 53, doi. 10.1159/000333097
By:
- Hernandez, Dena G.;
- Singleton, Andrew B.
Publication type:
Article
Comprehensive Screening of a North American Parkinson’s Disease Cohort for LRRK2 Mutation.
Published in:
Neurodegenerative Diseases, 2007, v. 4, n. 5, p. 386, doi. 10.1159/000105160
By:
- Johnson, Janel;
- Paisán-Ruíz, Coro;
- Lopez, Grisel;
- Crews, Cynthia;
- Britton, Angela;
- Malkani, Roniel;
- Evans, E.Whitney;
- McInerney-Leo, Aideen;
- Jain, Shushant;
- Nussbaum, Robert L.;
- Foote, Kelly D.;
- Mandel, Ronald J.;
- Crawley, Anthony;
- Reimsnider, Sharon;
- Fernandez, Hubert H.;
- Okun, Michael S.;
- Gwinn-Hardy, Katrina;
- Singleton, Andrew B.
Publication type:
Article
A common genetic factor for Parkinson disease in ethnic Chinese population in Taiwan.
Published in:
BMC Neurology, 2006, v. 6, p. 47, doi. 10.1186/1471-2377-6-47
By:
- Hon-Chung Fung;
- Chiung-Mei Chen;
- Hardy, John;
- Singleton, Andrew B.;
- Yih-Ru Wu
Publication type:
Article
Lack of evidence for a genetic association between FGF20 and Parkinson's disease in Finnish and Greek patients.
Published in:
BMC Neurology, 2005, v. 5, p. 1, doi. 10.1186/1471-2377-5-11
By:
- Clarimon, Jordi;
- Xiromerisiou, Georgia;
- Eerola, Johanna;
- Gourbali, Vanesa;
- Hellström, Olli;
- Dardiotis, Euthimios;
- Peuralinna, Terhi;
- Papadimitriou, Alexandros;
- Hadjigeorgiou, George M.;
- Tienari, Pentti J.;
- Singleton, Andrew B.
Publication type:
Article
Clinical and Neuropathological Correlates of Apolipoprotein E Genotype in Dementia with Lewy Bodies.
Published in:
Dementia & Geriatric Cognitive Disorders, 2002, v. 14, n. 4, p. 167, doi. 10.1159/000066022
By:
- Singleton, Andrew B.;
- Wharton, Anna;
- O'Brien, Kirsty K.;
- Walker, Matthew P.;
- McKeith, Ian G.;
- Ballard, Clive G.;
- O'Brien, John;
- Perry, Robert H.;
- Ince, Paul G.;
- Edwardson, James A.;
- Morris, Christopher M.
Publication type:
Article
Genome-wide association study confirms extant PD risk loci among the Dutch.
Published in:
European Journal of Human Genetics, 2011, v. 19, n. 6, p. 655, doi. 10.1038/ejhg.2010.254
By:
- Simón-Sánchez, Javier;
- van Hilten, Jacobus J.;
- van de Warrenburg, Bart;
- Post, Bart;
- Berendse, Henk W.;
- Arepalli, Sampath;
- Hernandez, Dena G.;
- de Bie, Rob M. A.;
- Velseboer, Daan;
- Scheffer, Hans;
- Bloem, Bas;
- van Dijk, Karin D.;
- Rivadeneira, Fernando;
- Hofman, Albert;
- Uitterlinden, André G.;
- Rizzu, Patrizia;
- Bochdanovits, Zoltan;
- Singleton, Andrew B.;
- Heutink, Peter
Publication type:
Article
Genetic variability at the PARK16 locus.
Published in:
European Journal of Human Genetics, 2010, v. 18, n. 12, p. 1356, doi. 10.1038/ejhg.2010.125
By:
- Tucci, Arianna;
- Nalls, Mike A.;
- Houlden, Henry;
- Revesz, Tamas;
- Singleton, Andrew B.;
- Wood, Nicholas W.;
- Hardy, John;
- Paisán-Ruiz, Coro
Publication type:
Article
Association of integrin α2 gene variants with ischemic stroke.
Published in:
Journal of Cerebral Blood Flow & Metabolism, 2008, v. 28, n. 1, p. 81, doi. 10.1038/sj.jcbfm.9600508
By:
- Matarin, Mar;
- Brown, W. Mark;
- Hardy, John A.;
- Rich, Stephen S.;
- Singleton, Andrew B.;
- Brown Jr., Robert D.;
- Brott, Thomas G.;
- Worrall, Bradford B.;
- Meschia, James F.
Publication type:
Article
Assessment of Genetic Association Between Parkinson Disease and Bipolar Disorder.
Published in:
JAMA Neurology, 2020, v. 77, n. 8, p. 1034, doi. 10.1001/jamaneurol.2020.0248
By:
- Bandres-Ciga, Sara;
- Blauwendraat, Cornelis;
- Singleton, Andrew B.
Publication type:
Article
Common Premutations in the General Population.
Published in:
2019
By:
- Hammer, Monia B.;
- Singleton, Andrew B.
Publication type:
Opinion
Genome-Wide Analysis of the Heritability of Amyotrophic Lateral Sclerosis.
Published in:
JAMA Neurology, 2014, v. 71, n. 9, p. 1123, doi. 10.1001/jamaneurol.2014.1184
By:
- Keller, Margaux F.;
- Ferrucci, Luigi;
- Singleton, Andrew B.;
- Tienari, Pentti J.;
- Laaksovirta, Hannu;
- Restagno, Gabriella;
- Chiò, Adriano;
- Traynor, Bryan J.;
- Nalls, Michael A.
Publication type:
Article
A 6.4 Mb Duplication of the a-Synuclein Locus Causing Frontotemporal Dementia and Parkinsonism Phenotype-Genotype Correlations.
Published in:
JAMA Neurology, 2014, v. 71, n. 9, p. 1162, doi. 10.1001/jamaneurol.2014.994
By:
- Kara, Eleanna;
- Kiely, Aoife P.;
- Proukakis, Christos;
- Giffin, Nicola;
- Love, Seth;
- Hehir, Jason;
- Rantell, Khadija;
- Pandraud, Amelie;
- Hernandez, Dena G.;
- Nacheva, Elizabeth;
- Pittman, Alan M.;
- Nalls, Mike A.;
- Singleton, Andrew B.;
- Revesz, Tamas;
- Bhatia, Kailash P.;
- Quinn, Niall;
- Hardy, John;
- Holton, Janice L.;
- Houlden, Henry
Publication type:
Article
Finnish Parkinson's disease study integrating protein-protein interaction network data with exome sequencing analysis.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. 1, doi. 10.1038/s41598-019-55479-y
By:
- Siitonen, Ari;
- Kytövuori, Laura;
- Nalls, Mike A.;
- Gibbs, Raphael;
- Hernandez, Dena G.;
- Ylikotila, Pauli;
- Peltonen, Markku;
- Singleton, Andrew B.;
- Majamaa, Kari
Publication type:
Article
Parkinson's Disease and Low Frequency Alleles Found Together Throughout LRRK2.
Published in:
Annals of Human Genetics, 2009, v. 73, n. 4, p. 391, doi. 10.1111/j.1469-1809.2009.00524.x
By:
- Paisán-Ruiz, Coro;
- Washecka, Nicole;
- Nath, Priti;
- Singleton, Andrew B.;
- Corder, Elizabeth H.
Publication type:
Article
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease.
Published in:
Brain: A Journal of Neurology, 2012, v. 135, n. 9, p. 2875, doi. 10.1093/brain/aws161
By:
- Johnson, Janel O.;
- Gibbs, J. Raphael;
- Megarbane, Andre;
- Urtizberea, J. Andoni;
- Hernandez, Dena G.;
- Foley, A. Reghan;
- Arepalli, Sampath;
- Pandraud, Amelie;
- Simón-Sánchez, Javier;
- Clayton, Peter;
- Reilly, Mary M.;
- Muntoni, Francesco;
- Abramzon, Yevgeniya;
- Houlden, Henry;
- Singleton, Andrew B.
Publication type:
Article
Another locus, a new method.
Published in:
Brain: A Journal of Neurology, 2010, v. 133, n. 12, p. 3492, doi. 10.1093/brain/awq331
By:
- Singleton, Andrew B.;
- Gibbs, J. Raphael
Publication type:
Article
Genomewide scans in North American families reveal genetic linkage of essential tremor to a region on chromosome 6p23.
Published in:
Brain: A Journal of Neurology, 2006, v. 129, n. 9, p. 2318, doi. 10.1093/brain/awl120
By:
- Alexey Shatunov;
- Nyamkhishig Sambuughin;
- Joseph Jankovic;
- Rodger Elble;
- Hee Suk Lee;
- Andrew B. Singleton;
- Ayush Dagvadorj;
- Jay Ji;
- Yiping Zhang;
- Virginia E. Kimonis;
- John Hardy;
- Mark Hallett;
- Lev G. Goldfarb
Publication type:
Article
Profiling complex repeat expansions in RFC1 in Parkinson's disease.
Published in:
NPJ Parkinson's Disease, 2024, v. 10, n. 1, p. 1, doi. 10.1038/s41531-024-00723-0
By:
- Alvarez Jerez, Pilar;
- Daida, Kensuke;
- Miano-Burkhardt, Abigail;
- Iwaki, Hirotaka;
- Malik, Laksh;
- Cogan, Guillaume;
- Makarious, Mary B.;
- Sullivan, Roisin;
- Vandrovcova, Jana;
- Ding, Jinhui;
- Gibbs, J. Raphael;
- Markham, Androo;
- Nalls, Mike A.;
- Kesharwani, Rupesh K.;
- Sedlazeck, Fritz J.;
- Casey, Bradford;
- Hardy, John;
- Houlden, Henry;
- Blauwendraat, Cornelis;
- Singleton, Andrew B.
Publication type:
Article
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2).
Published in:
NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00533-w
By:
- Towns, Clodagh;
- Richer, Madeleine;
- Jasaityte, Simona;
- Stafford, Eleanor J.;
- Joubert, Julie;
- Antar, Tarek;
- Martinez-Carrasco, Alejandro;
- Makarious, Mary B.;
- Casey, Bradford;
- Vitale, Dan;
- Levine, Kristin;
- Leonard, Hampton;
- Pantazis, Caroline B.;
- Screven, Laurel A.;
- Hernandez, Dena G.;
- Wegel, Claire E.;
- Solle, Justin;
- Nalls, Mike A.;
- Blauwendraat, Cornelis;
- Singleton, Andrew B.
Publication type:
Article
Genome-wide case-only analysis of gene-gene interactions with known Parkinson's disease risk variants reveals link between LRRK2 and SYT10.
Published in:
NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00550-9
By:
- Aleknonytė-Resch, Milda;
- Trinh, Joanne;
- Leonard, Hampton;
- Delcambre, Sylvie;
- Leitão, Elsa;
- Lai, Dongbing;
- Smajić, Semra;
- Orr-Urtreger, Avi;
- Thaler, Avner;
- Blauwendraat, Cornelis;
- Sharma, Arunabh;
- Makarious, Mary B.;
- Kim, Jonggeol Jeff;
- Lake, Julie;
- Rahmati, Pegah;
- Freitag-Wolf, Sandra;
- Seibler, Philip;
- Foroud, Tatiana;
- Singleton, Andrew B.;
- Grünewald, Anne
Publication type:
Article
Exploring the genetic and genomic connection underlying neurodegeneration with brain iron accumulation and the risk for Parkinson's disease.
Published in:
NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00496-y
By:
- Alvarez Jerez, Pilar;
- Alcantud, Jose Luis;
- de los Reyes-Ramírez, Lucia;
- Moore, Anni;
- Ruz, Clara;
- Vives Montero, Francisco;
- Rodriguez-Losada, Noela;
- Saini, Prabhjyot;
- Gan-Or, Ziv;
- Alvarado, Chelsea X.;
- Makarious, Mary B.;
- Billingsley, Kimberley J.;
- Blauwendraat, Cornelis;
- Noyce, Alastair J.;
- Singleton, Andrew B.;
- Duran, Raquel;
- Bandres-Ciga, Sara
Publication type:
Article
Identification and prediction of Parkinson's disease subtypes and progression using machine learning in two cohorts.
Published in:
NPJ Parkinson's Disease, 2022, v. 8, n. 1, p. 1, doi. 10.1038/s41531-022-00439-z
By:
- Dadu, Anant;
- Satone, Vipul;
- Kaur, Rachneet;
- Hashemi, Sayed Hadi;
- Leonard, Hampton;
- Iwaki, Hirotaka;
- Makarious, Mary B.;
- Billingsley, Kimberley J.;
- Bandres‐Ciga, Sara;
- Sargent, Lana J.;
- Noyce, Alastair J.;
- Daneshmand, Ali;
- Blauwendraat, Cornelis;
- Marek, Ken;
- Scholz, Sonja W.;
- Singleton, Andrew B.;
- Nalls, Mike A.;
- Campbell, Roy H.;
- Faghri, Faraz
Publication type:
Article
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
Published in:
2018
By:
- Pihlstrøm, Lasse;
- Blauwendraat, Cornelis;
- Cappelletti, Chiara;
- Berge‐seidl, Victoria;
- Langmyhr, Margrete;
- Henriksen, Sandra Pilar;
- Van De Berg, Wilma D. J.;
- Gibbs, J. Raphael;
- Cookson, Mark R.;
- The International Parkinson Disease Genomics Consortium;
- The North American Brain Expression Consortium;
- Singleton, Andrew B.;
- Nalls, Mike A.;
- Toft, Mathias;
- Berge-Seidl, Victoria;
- International Parkinson Disease Genomics Consortium;
- North American Brain Expression Consortium
Publication type:
journal article
Is the MC1R variant p.R160W associated with Parkinson's?
Published in:
2016
By:
- Lubbe, Steven J.;
- Escott‐Price, Valentina;
- Brice, Alexis;
- Gasser, Thomas;
- Hardy, John;
- Heutink, Peter;
- Sharma, Manu;
- Wood, Nicholas W.;
- Nalls, Mike;
- Singleton, Andrew B.;
- Williams, Nigel M.;
- Morris, Huw R.;
- Escott-Price, Valentina;
- International Parkinson's Disease Genomics Consortium
Publication type:
Letter
Polygenic risk of Parkinson disease is correlated with disease age at onset.
Published in:
Annals of Neurology, 2015, v. 77, n. 4, p. 582, doi. 10.1002/ana.24335
By:
- Escott‐Price, Valentina;
- Nalls, Mike A.;
- Morris, Huw R.;
- Lubbe, Steven;
- Brice, Alexis;
- Gasser, Thomas;
- Heutink, Peter;
- Wood, Nicholas W.;
- Hardy, John;
- Singleton, Andrew B.;
- Williams, Nigel M.
Publication type:
Article
Clinical heterogeneity of α‐synuclein gene duplication in Parkinson's disease.
Published in:
Annals of Neurology, 2006, v. 59, n. 2, p. 298
By:
- Kenya Nishioka;
- Shin Hayashi;
- Matthew J. Farrer;
- Andrew B. Singleton;
- Hiroyo Yoshino;
- Hisamasa Imai;
- Toshiaki Kitami;
- Kenichi Sato;
- Ryu Kuroda;
- Hiroyuki Tomiyama;
- Koichi Mizoguchi;
- Miho Murata;
- Tatsushi Toda;
- Issei Imoto;
- Johji Inazawa;
- Yoshikuni Mizuno;
- Nobutaka Hattori
Publication type:
Article
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2.
Published in:
Annals of Neurology, 2005, v. 57, n. 3, p. 453
By:
- Dena G. Hernandez;
- Coro Paisán‐Ruíz;
- Aideen McInerney‐Leo;
- Shushant Jain;
- Andreas Meyer‐Lindenberg;
- E. Whitney Evans;
- Karen F. Berman;
- Janel Johnson;
- Georg Auburger;
- Alejandro A. Schäffer;
- Grisel J. Lopez;
- Robert L. Nussbaum;
- Andrew B. Singleton
Publication type:
Article
Case-Control study of the extended tau gene haplotype in Parkinson's disease.
Published in:
2001
By:
- Maraganore, Demetrius M.;
- Hernandez, Dena G.;
- Singleton, Andrew B.;
- Farrer, Matthew J.;
- McDonnell, Shannon K.;
- Hutton, Michael L.;
- Hardy, John A.;
- Rocca, Walter A.;
- Maraganore, D M;
- Hernandez, D G;
- Singleton, A B;
- Farrer, M J;
- McDonnell, S K;
- Hutton, M L;
- Hardy, J A;
- Rocca, W A
Publication type:
journal article
Genetics in Parkinson disease: Mendelian versus non-Mendelian inheritance.
Published in:
Journal of Neurochemistry, 2016, v. 139, p. 59, doi. 10.1111/jnc.13593
By:
- Hernandez, Dena G.;
- Reed, Xylena;
- Singleton, Andrew B.
Publication type:
Article
Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p.
Published in:
Journal of Neurology, 2011, v. 258, n. 4, p. 647, doi. 10.1007/s00415-010-5815-x
By:
- Pearson, Justin P.;
- Williams, Nigel M.;
- Majounie, Elisa;
- Waite, Adrian;
- Stott, Jennifer;
- Newsway, Victoria;
- Murray, Alex;
- Hernandez, Dena;
- Guerreiro, Rita;
- Singleton, Andrew B.;
- Neal, James;
- Morris, Huw R.
Publication type:
Article
Investigation of the genetic aetiology of Lewy body diseases with and without dementia.
Published in:
Brain Communications, 2024, v. 6, n. 4, p. 1, doi. 10.1093/braincomms/fcae190
By:
- Wu, Lesley Yue;
- Real, Raquel;
- Martinez-Carrasco, Alejandro;
- Chia, Ruth;
- Lawton, Michael A;
- Shoai, Maryam;
- Bresner, Catherine;
- Blauwendraat, Cornelis;
- Singleton, Andrew B;
- Ryten, Mina;
- Consortium, International Lewy Body Dementia Genomics;
- Scholz, Sonja W;
- Traynor, Bryan J;
- Williams, Nigel M;
- Hu, Michele T M;
- Ben-Shlomo, Yoav;
- Grosset, Donald G;
- Hardy, John;
- Morris, Huw R
Publication type:
Article
Analysis of Y chromosome haplogroups in Parkinson's disease.
Published in:
Brain Communications, 2022, v. 4, n. 6, p. 1, doi. 10.1093/braincomms/fcac277
By:
- Grenn, Francis P.;
- Makarious, Mary B.;
- Bandres-Ciga, Sara;
- Hirotaka Iwaki;
- Singleton, Andrew B.;
- Nalls, Mike A.;
- Blauwendraat, Cornelis
Publication type:
Article

Found: 122