Works by Ozelius, Laurie

Results: 109

Olfactory identification in LRRK2 G2019S mutation carriers: a relevant marker?

Published in:

Annals of Clinical & Translational Neurology, 2014, v. 1, n. 9, p. 670, doi. 10.1002/acn3.95

By:

Saunders‐Pullman, Rachel;
Mirelman, Anat;
Wang, Cuiling;
Alcalay, Roy N.;
San Luciano, Marta;
Ortega, Robert;
Raymond, Deborah;
Mejia‐Santana, Helen;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Utreger, Avi;
Marder, Karen;
Giladi, Nir;
Bressman, Susan B.

Publication type:

Article

Progression in the LRRK2-Asssociated Parkinson Disease Population.

Published in:

JAMA Neurology, 2018, v. 75, n. 3, p. 312, doi. 10.1001/jamaneurol.2017.4019

By:

Saunders-Pullman, Rachel;
Mirelman, Anat;
Alcalay, Roy N.;
Wang, Cuiling;
Ortega, Roberto A.;
Raymond, Deborah;
Mejia-Santana, Helen;
Orbe-Reilly, Martha;
Johannes, Brooke A.;
Thaler, Avner;
Ozelius, Laurie;
Orr-Urtreger, Avi;
Marder, Karen S.;
Giladi, Nir;
Bressman, Susan B.

Publication type:

Article

Complex and Dynamic Chromosomal Rearrangements in a Family With Seemingly Non-Mendelian Inheritance of Dopa-Responsive Dystonia.

Published in:

JAMA Neurology, 2017, v. 74, n. 7, p. 806, doi. 10.1001/jamaneurol.2017.0666

By:

Lohmann, Katja;
Redin, Claire;
Tönnies, Holger;
Bressman, Susan B.;
Subero, Jose Ignacio Martin;
Wiegers, Karin;
Hinrichs, Frauke;
Hellenbroich, Yorck;
Rakovic, Aleksandar;
Raymond, Deborah;
Ozelius, Laurie J.;
Schwinger, Eberhard;
Siebert, Reiner;
Talkowski, Michael E.;
Saunders-Pullman, Rachel;
Klein, Christine

Publication type:

Article

Rapid-onset dystonia-parkinsonism is associated with reduced cerebral blood flow without gray matter changes.

Published in:

Frontiers in Neurology, 2023, v. 14, p. 1, doi. 10.3389/fneur.2023.1116723

By:

Whitlow, Christopher T.;
Atcheson, Kyle M.;
Snively, Beverly M.;
Cook, Jared F.;
Jeongchul Kim;
Haq, Ihtsham U.;
Sweadner, Kathleen J.;
Ozelius, Laurie J.;
Brashear, Allison

Publication type:

Article

Promise and challenges of dystonia brain banking: establishing a human tissue repository for studies of X-Linked Dystonia-Parkinsonism.

Published in:

Journal of Neural Transmission, 2021, v. 128, n. 4, p. 575, doi. 10.1007/s00702-020-02286-9

By:

Fernandez-Cerado, Cara;
Legarda, G. Paul;
Velasco-Andrada, M. Salvie;
Aguil, Abegail;
Ganza-Bautista, Niecy G.;
Lagarde, J. Benedict B.;
Soria, Jasmin;
Jamora, Roland Dominic G.;
Acuña, Patrick J.;
Vanderburg, Charles;
Sapp, Ellen;
DiFiglia, Marian;
Murcar, Micaela G.;
Campion, Lindsey;
Ozelius, Laurie J.;
Alessi, Amy K.;
Singh-Bains, Malvindar K.;
Waldvogel, Henry J.;
Faull, Richard L. M.;
Macalintal-Canlas, Regina

Publication type:

Article

Isolated dystonia: clinical and genetic updates.

Published in:

2021

By:

Domingo, Aloysius;
Yadav, Rachita;
Ozelius, Laurie J.

Publication type:

Literature Review

Mutations in GNAL cause primary torsion dystonia.

Published in:

Nature Genetics, 2013, v. 45, n. 1, p. 88, doi. 10.1038/ng.2496

By:

Fuchs, Tania;
Saunders-Pullman, Rachel;
Masuho, Ikuo;
Luciano, Marta San;
Raymond, Deborah;
Factor, Stewart;
Lang, Anthony E;
Liang, Tsao-Wei;
Trosch, Richard M;
White, Sierra;
Ainehsazan, Edmond;
Hervé, Denis;
Sharma, Nutan;
Ehrlich, Michelle E;
Martemyanov, Kirill A;
Bressman, Susan B;
Ozelius, Laurie J

Publication type:

Article

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia.

Published in:

Nature Genetics, 2009, v. 41, n. 3, p. 286, doi. 10.1038/ng.304

By:

Fuchs, Tania;
Gavarini, Sophie;
Saunders-Pullman, Rachel;
Raymond, Deborah;
Ehrlich, Michelle E.;
Bressman, Susan B.;
Ozelius, Laurie J.

Publication type:

Article

Phenotype- and genotype-specific structural alterations in spasmodic dysphonia.

Published in:

2017

By:

Bianchi, Serena;
Battistella, Giovanni;
Huddleston, Hailey;
Scharf, Rebecca;
Fleysher, Lazar;
Rumbach, Anna F.;
Frucht, Steven J.;
Blitzer, Andrew;
Ozelius, Laurie J.;
Simonyan, Kristina

Publication type:

journal article

GNAL mutation in isolated laryngeal dystonia.

Published in:

2016

By:

Putzel, Gregory G.;
Fuchs, Tania;
Battistella, Giovanni;
Rubien‐Thomas, Estee;
Frucht, Steven J.;
Blitzer, Andrew;
Ozelius, Laurie J.;
Simonyan, Kristina

Publication type:

journal article

REM sleep behavior disorder, as assessed by questionnaire, in G2019S LRRK2 mutation PD and carriers.

Published in:

2015

By:

Saunders‐Pullman, Rachel;
Alcalay, Roy N.;
Mirelman, Anat;
Wang, Cuiling;
Luciano, Marta San;
Ortega, Roberto A.;
Glickman, Amanda;
Raymond, Deborah;
Mejia‐Santana, Helen;
Doan, Nancy;
Johannes, Brooke;
Yasinovsky, Kira;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Utreger, Avi;
Marder, Karen;
Giladi, Nir;
Bressman, Susan B.

Publication type:

journal article

Nonmotor symptoms in healthy Ashkenazi Jewish carriers of the G2019S mutation in the LRRK2 gene.

Published in:

Movement Disorders, 2015, v. 30, n. 7, p. 981, doi. 10.1002/mds.26213

By:

Mirelman, Anat;
Alcalay, Roy N.;
Saunders‐Pullman, Rachel;
Yasinovsky, Kira;
Thaler, Avner;
Gurevich, Tanya;
Mejia‐Santana, Helen;
Raymond, Deborah;
Gana‐Weisz, Mali;
Bar‐Shira, Anat;
Ozelius, Laurie;
Clark, Lorraine;
Orr‐Urtreger, Avi;
Bressman, Susan;
Marder, Karen;
Giladi, Nir

Publication type:

Article

Novel compound heterozygous mutations in PRKRA cause pure dystonia.

Published in:

Movement Disorders, 2015, v. 30, n. 6, p. 877, doi. 10.1002/mds.26175

By:

de Carvalho Aguiar, Patricia;
Borges, Vanderci;
Ferraz, Henrique Ballalai;
Ozelius, Laurie Jean

Publication type:

Article

Heterogeneity in primary dystonia: Lessons from THAP1, GNAL, and TOR1A in Amish-Mennonites.

Published in:

Movement Disorders, 2014, v. 29, n. 6, p. 812, doi. 10.1002/mds.25818

By:

Saunders‐Pullman, Rachel;
Fuchs, Tania;
San Luciano, Marta;
Raymond, Deborah;
Brashear, Alison;
Ortega, Robert;
Deik, Andres;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Cognitive impairment in rapid-onset dystonia-parkinsonism.

Published in:

2014

By:

Cook, Jared F;
Hill, Deborah F;
Snively, Beverly M;
Boggs, Niki;
Suerken, Cynthia K;
Haq, Ihtsham;
Stacy, Mark;
McCall, W Vaughn;
Ozelius, Laurie J;
Sweadner, Kathleen J;
Brashear, Allison

Publication type:

journal article

Cognitive impairment in rapid-onset dystonia-parkinsonism.

Published in:

Movement Disorders, 2014, v. 29, n. 3, p. 344, doi. 10.1002/mds.25790

By:

Cook, Jared F.;
Hill, Deborah F.;
Snively, Beverly M.;
Boggs, Niki;
Suerken, Cynthia K.;
Haq, Ihtsham;
Stacy, Mark;
McCall, W. Vaughn;
Ozelius, Laurie J.;
Sweadner, Kathleen J.;
Brashear, Allison

Publication type:

Article

The endophenotype and the phenotype: Temporal discrimination and adult-onset dystonia.

Published in:

Movement Disorders, 2013, v. 28, n. 13, p. 1766, doi. 10.1002/mds.25676

By:

Hutchinson, Michael;
Kimmich, Okka;
Molloy, Anna;
Whelan, Robert;
Molloy, Fiona;
Lynch, Tim;
Healy, Daniel G.;
Walsh, Cathal;
Edwards, Mark J.;
Ozelius, Laurie;
Reilly, Richard B.;
O'Riordan, Seán

Publication type:

Article

Mutation in 5′ upstream region of GCHI gene causes familial dopa-responsive dystonia.

Published in:

Movement Disorders, 2011, v. 26, n. 11, p. 2140, doi. 10.1002/mds.23786

By:

Sharma, Nutan;
Armata, Ioanna A.;
Multhaupt-Buell, Trisha J.;
Ozelius, Laurie J.;
Xin, Winnie;
Sims, Katherine B.

Publication type:

Article

Mutation in 5' upstream region of GCHI gene causes familial dopa-responsive dystonia.

Published in:

2011

By:

Sharma N;
Armata IA;
Multhaupt-Buell TJ;
Ozelius LJ;
Xin W;
Sims KB;
Sharma, Nutan;
Armata, Ioanna A;
Multhaupt-Buell, Trisha J;
Ozelius, Laurie J;
Xin, Winnie;
Sims, Katherine B

Publication type:

Letter

Mood and cognition in leucine-rich repeat kinase 2 G2019S Parkinson's disease.

Published in:

Movement Disorders, 2011, v. 26, n. 10, p. 1875, doi. 10.1002/mds.23746

By:

Shanker, Vicki;
Groves, Mark;
Heiman, Gary;
Palmese, Christina;
Saunders-Pullman, Rachel;
Ozelius, Laurie;
Raymond, Deborah;
Bressman, Susan

Publication type:

Article

LRRK2 G2019S mutations may be increased in Puerto Ricans.

Published in:

Movement Disorders, 2011, v. 26, n. 9, p. 1771, doi. 10.1002/mds.23632

By:

Saunders-Pullman, Rachel;
Cabassa, Jose;
San Luciano, Marta;
Stanley, Kaili;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Milestones in dystonia.

Published in:

Movement Disorders, 2011, v. 26, n. 6, p. 1106, doi. 10.1002/mds.23775

By:

Ozelius, Laurie J.;
Lubarr, Naomi;
Bressman, Susan B.

Publication type:

Article

Substantia nigra hyperechogenicity with LRRK2 G2019S mutations.

Published in:

Movement Disorders, 2011, v. 26, n. 5, p. 885, doi. 10.1002/mds.23644

By:

Brüggemann, Norbert;
Hagenah, Johann;
Stanley, Kaili;
Klein, Christine;
Wang, Cuiling;
Raymond, Deborah;
Ozelius, Laurie;
Bressman, Susan;
Saunders-Pullman, Rachel

Publication type:

Article

Screening of Brazilian families with primary dystonia reveals a novel THAP1 mutation and a de novo TOR1A GAG deletion.

Published in:

Movement Disorders, 2010, v. 25, n. 16, p. 2854, doi. 10.1002/mds.23133

By:

De Carvalho Aguiar, Patricia;
Fuchs, Tania;
Borges, Vanderci;
Lamar, Kay-Marie;
Silva, Sonia Maria Azevedo;
Ferraz, Henrique Ballalai;
Ozelius, Laurie

Publication type:

Article

LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson disease.

Published in:

Movement Disorders, 2010, v. 25, n. 15, p. 2536, doi. 10.1002/mds.23314

By:

Saunders-Pullman, Rachel;
Barrett, Matthew J.;
Stanley, Kaili M.;
Luciano, Marta San;
Shanker, Vicki;
Severt, Lawrence;
Hunt, Ann;
Raymond, Deborah;
Ozelius, Laurie J.;
Bressman, Susan B.

Publication type:

Article

Clinical expression of LRRK2 G2019S mutations in the elderly.

Published in:

Movement Disorders, 2010, v. 25, n. 15, p. 2571, doi. 10.1002/mds.23330

By:

Luciano, Marta San;
Lipton, Richard B.;
Wang, Cuiling;
Katz, Mindy;
Zimmerman, Molly E.;
Sanders, Amy E.;
Ozelius, Laurie J.;
Bressman, Susan B.;
Saunders-Pullman, Rachel

Publication type:

Article

Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.

Published in:

Movement Disorders, 2010, v. 25, n. 13, p. 2183, doi. 10.1002/mds.23225

By:

Sharma, Nutan;
Franco, Ramon A.;
Kuster, John K.;
Mitchell, Adele A.;
Fuchs, Tania;
Saunders-Pullman, Rachel;
Raymond, Deborah;
Brin, Mitchell F.;
Blitzer, Andrew;
Bressman, Susan B.;
Ozelius, Laurie J.

Publication type:

Article

Gaucher disease ascertained through a Parkinson's center: Imaging and clinical characterization.

Published in:

Movement Disorders, 2010, v. 25, n. 10, p. 1364, doi. 10.1002/mds.23046

By:

Saunders-Pullman, Rachel;
Hagenah, Johann;
Dhawan, Vijay;
Stanley, Kaili;
Pastores, Gregory;
Sathe, Swati;
Tagliati, Michele;
Condefer, Kelly;
Palmese, Christina;
Brüggemann, Norbert;
Klein, Christine;
Roe, AM;
Kornreich, Ruth;
Ozelius, Laurie;
Bressman, Susan

Publication type:

Article

Responsiveness to levodopa in epsilon-sarcoglycan deletions.

Published in:

Movement Disorders, 2009, v. 24, n. 3, p. 425, doi. 10.1002/mds.22375

By:

Luciano, Marta San;
Ozelius, Laurie;
Sims, Katherine;
Raymond, Deborah;
Liu, Liu;
Saunders-Pullman, Rachel

Publication type:

Article

Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with ε-sarcoglycan mutations.

Published in:

Movement Disorders, 2008, v. 23, n. 4, p. 588, doi. 10.1002/mds.21785

By:

Raymond, Deborah;
Saunders-Pullman, Rachel;
de Carvalho Aguiar, Patricia;
Schule, Birgitt;
Kock, Norman;
Friedman, Jennifer;
Harris, Juliette;
Ford, Blair;
Frucht, Steven;
Heiman, Gary A.;
Jennings, Danna;
Doheny, Dana;
Brin, Mitchell F.;
de Leon Brin, Deborah;
Multhaupt-Buell, Trisha;
Lang, Anthony E.;
Kurlan, Roger;
Klein, Christine;
Ozelius, Laurie;
Bressman, Susan

Publication type:

Article

ATP1A3 mutation in the first asian case of rapid-onset dystonia-parkinsonism.

Published in:

Movement Disorders, 2007, v. 22, n. 12, p. 1808, doi. 10.1002/mds.21638

By:

Lee, Jee-Young;
Gollamudi, Seema;
Ozelius, Laurie J.;
Kim, Ji-Young;
Jeon, Beom S.

Publication type:

Article

Heterogeneity of presentation and outcome in the Irish rapid-onset dystonia-parkinsonism kindred.

Published in:

2007

By:

McKeon, Andrew;
Ozelius, Laurie J.;
Hardiman, Oria;
Greenway, Matthew J.;
Pittock, Sean J.

Publication type:

journal article

Novel and de novo mutations of the SGCE gene in Brazilian patients with myoclonus-dystonia.

Published in:

Movement Disorders, 2007, v. 22, n. 8, p. 1208, doi. 10.1002/mds.21380

By:

Borges, Vanderci;
Aguiar, Patricia de Carvalho;
Ferraz, Henrique Ballalai;
Ozelius, Laurie J.

Publication type:

Article

G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy.

Published in:

2007

By:

Ozelius, Laurie J.;
Foroud, Tatiana;
May, Susanne;
Senthil, Geetha;
Sandroni, Paola;
Low, Phillip A.;
Reich, Stephen;
Colcher, Amy;
Stern, Matthew B.;
Ondo, William G.;
Jankovic, Joseph;
Huang, Neng;
Tanner, Caroline M.;
Novak, Peter;
Gilman, Sid;
Marshall, Frederick J.;
Wooten, G. Frederick;
Chelimsky, Thomas C.;
Shults, Clifford W.;
North American Multiple System Atrophy Study Group

Publication type:

journal article

Inherited myoclonus-dystonia and epilepsy: Further evidence of an association?

Published in:

Movement Disorders, 2004, v. 19, n. 12, p. 1456, doi. 10.1002/mds.20224

By:

O'Riordan, Sean;
Ozelius, Laurie J.;
De Carvalho Aguiar, Patricia;
Hutchinson, Michael;
King, Mary;
Lynch, Tim

Publication type:

Article

Rapid-onset dystonia-parkinsonism: A fourth family consistent with linkage to chromosome 19q13.

Published in:

Movement Disorders, 2004, v. 19, n. 12, p. 1506, doi. 10.1002/mds.20258

By:

Zaremba, Jacek;
Mierzewska, Hanna;
Lysiak, Zofia;
Kramer, Patricia;
Ozelius, Laurie J.;
Brashear, Allison

Publication type:

Article

Distribution, type, and origin of Parkin mutations: Review and case studies.

Published in:

Movement Disorders, 2004, v. 19, n. 10, p. 1146, doi. 10.1002/mds.20234

By:

Hedrich, Katja;
Eskelson, Cordula;
Wilmot, Beth;
Marder, Karen;
Harris, Juliette;
Garrels, Jennifer;
Meija-Santana, Helen;
Vieregge, Peter;
Jacobs, Helfried;
Bressman, Susan B.;
Lang, Anthony E.;
Kann, Martin;
Abbruzzese, Giovanni;
Martinelli, Paolo;
Schwinger, Eberhard;
Ozelius, Laurie J.;
Pramstaller, Peter P.;
Klein, Christine;
Kramer, Patricia

Publication type:

Article

Examination of the SGCE gene in Tourette syndrome patients with obsessive-compulsive disorder.

Published in:

Movement Disorders, 2004, v. 19, n. 10, p. 1237, doi. 10.1002/mds.20156

By:

De Carvalho Aguiar, Patricia;
Fazzari, Melissa;
Jankovic, Joseph;
Ozelius, Laurie J.

Publication type:

Article

Intrafamilial phenotypic variability of the DYT1 dystonia: From asymptomatic TOR1A gene carrier status to dystonic storm.

Published in:

Movement Disorders, 2002, v. 17, n. 2, p. 339, doi. 10.1002/mds.10096

By:

Opal, Puneet;
Tintner, Ron;
Jankovic, Joseph;
Leung, Joanne;
Breakefield, Xandra O.;
Friedman, Jennifer;
Ozelius, Laurie

Publication type:

Article

Phenotypic variability in a large kindred (Family LA) with deletions in the parkin gene.

Published in:

Movement Disorders, 2002, v. 17, n. 2, p. 424, doi. 10.1002/mds.10071

By:

Pramstaller, Peter P.;
Kis, Bernhard;
Eskelson, Cordula;
Hedrich, Katja;
Scherer, Monika;
Schwinger, Eberhard;
Breakefield, Xandra O.;
Kramer, Patricia L.;
Ozelius, Laurie J.;
Klein, Christine

Publication type:

Article

Concordant late onset of craniocervical dystonia in a pair of monozygotic twins.

Published in:

Movement Disorders, 1999, v. 14, n. 6, p. 1040, doi. 10.1002/1531-8257(199911)14:6<1040::AID-MDS1025>3.0.CO;2-9

By:

Sieberer, Marcel G.;
Vieregge, Peter;
Klein, Christine;
Ozelius, Laurie J.;
Wandinger, Klaus-Peter

Publication type:

Article

Rapid-onset dystonia-parkinsonism associated with the I758S mutation of the ATP1A3 gene: a neuropathologic and neuroanatomical study of four siblings.

Published in:

Acta Neuropathologica, 2014, v. 128, n. 1, p. 81, doi. 10.1007/s00401-014-1279-x

By:

Oblak, Adrian;
Hagen, Matthew;
Sweadner, Kathleen;
Haq, Ihtsham;
Whitlow, Christopher;
Maldjian, Joseph;
Epperson, Francine;
Cook, Jared;
Stacy, Mark;
Murrell, Jill;
Ozelius, Laurie;
Brashear, Allison;
Ghetti, Bernardino

Publication type:

Article

Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression.

Published in:

JAMA Network Open, 2021, v. 4, n. 4, p. e215845, doi. 10.1001/jamanetworkopen.2021.5845

By:

Ortega, Roberto A.;
Wang, Cuiling;
Raymond, Deborah;
Bryant, Nicole;
Scherzer, Clemens R.;
Thaler, Avner;
Alcalay, Roy N.;
West, Andrew B.;
Mirelman, Anat;
Kuras, Yuliya;
Marder, Karen S.;
Giladi, Nir;
Ozelius, Laurie J.;
Bressman, Susan B.;
Saunders-Pullman, Rachel

Publication type:

Article

Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's disease.

Published in:

NPJ Parkinson's Disease, 2023, v. 9, n. 1, p. 1, doi. 10.1038/s41531-023-00599-6

By:

Miltenberger-Miltenyi, Gabriel;
Ortega, Roberto A.;
Domingo, Aloysius;
Yadav, Rachita;
Nishiyama, Ayumi;
Raymond, Deborah;
Katsnelson, Viktoriya;
Urval, Nikita;
Swan, Matthew;
Shanker, Vicki;
Miravite, Joan;
Walker, Ruth H.;
Bressman, Susan B.;
Ozelius, Laurie J.;
Cabassa, José C.;
Saunders-Pullman, Rachel

Publication type:

Article

Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.

Published in:

Annals of Neurology, 1990, v. 27, n. 2, p. 114, doi. 10.1002/ana.410270203

By:

Kramer, Patricia L.;
De Leon, Deborah;
Ozelius, Laurie;
Risch, Neil;
Bressman, Susan B.;
Brin, Mitchell F.;
Schuback, Deborah E.;
Burke, Robert E.;
Kwiatkowski, David J.;
Shale, Heidi;
Gusella, James F.;
Breakefield, Xandra O.;
Fahn, Stanley

Publication type:

Article

ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia.

Published in:

Developmental Medicine & Child Neurology, 2012, v. 54, n. 11, p. 1065, doi. 10.1111/j.1469-8749.2012.04421.x

By:

BRASHEAR, ALLISON;
MINK, JONATHAN W;
HILL, DEBORAH F;
BOGGS, NIKI;
MCCALL, W VAUGHN;
STACY, MARK A;
SNIVELY, BEVERLY;
LIGHT, LANEY S;
SWEADNER, KATHLEEN J;
OZELIUS, LAURIE J;
MORRISON, LESLIE

Publication type:

Article

Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.

Published in:

Genetic Epidemiology, 1988, v. 5, n. 6, p. 375, doi. 10.1002/gepi.1370050602

By:

Haines, Jonathan L.;
Ozelius, Laurie;
George-Hyslop, Peter St;
Wexler, Nancy S.;
Gusella, James F.;
Conneally, P. Michael;
Vogler, G. P.

Publication type:

Article

Establishing a natural history of X-linked dystonia parkinsonism.

Published in:

Brain Communications, 2023, v. 5, n. 3, p. 1, doi. 10.1093/braincomms/fcad106

By:

Acuna, Patrick;
Supnet-Wells, Melanie Leigh;
Spencer, Neil A.;
de Guzman, Jan Kristoper;
Russo, Massimiliano;
Hunt, Ann;
Stephen, Christopher;
Go, Criscely;
Carr, Samuel;
Ganza, Niecy Grace;
Lagarde, John Benedict;
Begalan, Shin;
Multhaupt-Buell, Trisha;
Aldykiewicz, Gabrielle;
Paul, Lisa;
Ozelius, Laurie;
Bragg, D. Cristopher;
Perry, Bridget;
Green, Jordan R.;
Miller, Jeffrey W.

Publication type:

Article

Abnormalities of motor function, transcription and cerebellar structure in mouse models of THAP1 dystonia.

Published in:

Human Molecular Genetics, 2015, v. 24, n. 25, p. 7159, doi. 10.1093/hmg/ddv384

By:

Ruiz, Marta;
Garcia, Georgina Perez;
Virumbrales, Maitane Ortiz;
Méneret, Aurelie;
Morant, Andrika;
Kottwitz, Jessica;
Fuchs, Tania;
Bonet, Justine;
Alegre, Pedro Gonzalez;
Hof, Patrick R.;
Ozelius, Laurie J.;
Ehrlich, Michelle E.

Publication type:

Article

Genome-wide mapping of IBD segments in an Ashkenazi PD cohort identifies associated haplotypes.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 17, p. 4693, doi. 10.1093/hmg/ddu158

By:

Vacic, Vladimir;
Ozelius, Laurie J.;
Clark, Lorraine N.;
Bar-Shira, Anat;
Gana-Weisz, Mali;
Gurevich, Tanya;
Gusev, Alexander;
Kedmi, Merav;
Kenny, Eimear E.;
Liu, Xinmin;
Mejia-Santana, Helen;
Mirelman, Anat;
Raymond, Deborah;
Saunders-Pullman, Rachel;
Desnick, Robert J.;
Atzmon, Gil;
Burns, Edward R.;
Ostrer, Harry;
Hakonarson, Hakon;
Bergman, Aviv

Publication type:

Article