Autosomal recessive inheritance of ADCY5-related generalized dystonia and myoclonus

by Barrett, Matthew J., Williams, Eli S., Chambers, Chelsea, Dhamija, Radhika
Published in Neurol Genet (2017)

Handedness and motor symptom asymmetry in Parkinson’s disease

by Barrett, Matthew J, Wylie, Scott A, Harrison, Madaline B, Wooten, G Frederick
Published 2010

Red blood cells stabilize flow in brain microvascular networks

by Schmid, Franca, Barrett, Matthew J. P., Obrist, Dominik, Weber, Bruno, Jenny, Patrick
Published in PLoS Comput Biol (2019)

The Relation Between Capillary Transit Times and Hemoglobin Saturation Heterogeneity. Part 2: Capillary Networks

by Lücker, Adrien, Secomb, Timothy W., Barrett, Matthew J. P., Weber, Bruno, Jenny, Patrick
Published in Front Physiol (2018)

Intravitreal AAV-Delivery of Genetically Encoded Sensors Enabling Simultaneous Two-Photon Imaging and Electrophysiology of Optic Nerve Axons

by Looser, Zoe J., Barrett, Matthew J. P., Hirrlinger, Johannes, Weber, Bruno, Saab, Aiman S.
Published in Front Cell Neurosci (2018)

Cytoarchitectonic Mapping of MRI Detects Rapid Changes in Alzheimer's Disease

by Blair, Jamie C., Lasiecka, Zofia M., Patrie, James, Barrett, Matthew J., Druzgal, T. Jason
Published in Front Neurol (2020)

Functional electrical stimulation for the treatment of lower extremity dystonia

by Barrett, Matthew J., Levy, Oren A., Fahn, Stanley, O'Dell, Michael, Bressman, Susan B.
Published 2011

Phase determination using chromosomal microarray and fluorescence in situ hybridization in a patient with early onset Parkinson disease and two deletions in PRKN

by Williams, Eli S., Barrett, Matthew J., Dhamija, Radhika, Toran, Lisa, Chambers, Chelsea, Mahadevan, Mani S., Golden, Wendy L.
Published in Mol Genet Genomic Med (2018)

Oxyphor 2P: A High-Performance Probe for Deep-Tissue Longitudinal Oxygen Imaging

by Esipova, Tatiana V., Barrett, Matthew J. P., Erlebach, Eva, Masunov, Artëm E., Weber, Bruno, Vinogradov, Sergei A.
Published in Cell Metab (2019)

The Effect of Education on Symptom Onset and Severity of Huntington's Disease

by Cain, Kristina K., Flanigan, Joseph L., Dalrymple, William Alex, Patrie, James, Harrison, Madaline B., Barrett, Matthew J.
Published in Mov Disord Clin Pract (2021)

Brain MRI Reveals Ascending Atrophy in Parkinson's Disease Across Severity

by Blair, Jamie C., Barrett, Matthew J., Patrie, James, Flanigan, Joseph L., Sperling, Scott A., Elias, W. Jeffrey, Druzgal, T. Jason
Published in Front Neurol (2019)

Selection of normative group affects rates of mild cognitive impairment in Parkinson disease

by Wyman-Chick, Kathryn A., Martin, Phillip K., Sperling, Scott A, Weintraub, Daniel, Erickson, Lauren O., Manning, Carol A, Barrett, Matthew J.
Published in Mov Disord (2018)

Comparison of Parkinson’s Disease Patients’ Characteristics by Indication for Deep Brain Stimulation: Men Are More Likely to Have DBS for Tremor

by Dalrymple, W. Alex, Pusso, Antonia, Sperling, Scott A., Flanigan, Joseph L., Huss, Diane S., Harrison, Madaline B., Elias, W. Jeffrey, Shah, Binit B., Barrett, Matthew J.
Published in Tremor Other Hyperkinet Mov (N Y) (2019)

Accelerated, First-Pass Cardiac Perfusion Pulse Sequence with Radial k-space Sampling, Compressed Sensing, and KWIC Reconstruction Tailored for Visual Analysis and Quantification o...

by Naresh, Nivedita K., Haji-Valizadeh, Hassan, Aouad, Pascale J., Barrett, Matthew J., Chow, Kelvin, Ragin, Ann B., Collins, Jeremy D., Carr, James C., Lee, Daniel C., Kim, Daniel
Published in Magn Reson Med (2018)

Glucocerebrosidase Enzyme Activity in GBA Mutation Parkinson Disease

by Ortega, Roberto A., Torres, Paola A., Swan, Matthew, Nichols, William, Boschung, Sarah, Raymond, Deborah, Barrett, Matthew J., Johannes, Brooke A., Severt, Lawrence, Shanker, Vicki, Hunt, Ann L., Bressman, Susan, Pastores, Gregory M., Saunders-Pullman, Rachel
Published in J Clin Neurosci (2016)

Neuropsychiatric symptoms and cognitive abilities over the initial quinquennium of Parkinson disease

by Weintraub, Daniel, Caspell‐Garcia, Chelsea, Simuni, Tanya, Cho, Hyunkeun R., Coffey, Christopher S., Aarsland, Dag, Alcalay, Roy N., Barrett, Matthew J., Chahine, Lana M., Eberling, Jamie, Espay, Alberto J., Hamilton, Jamie, Hawkins, Keith A., Leverenz, James, Litvan, Irene, Richard, Irene, Rosenthal, Liana S., Siderowf, Andrew, York, Michele
Published in Ann Clin Transl Neurol (2020)

Design and performance of an ultra-flexible two-photon microscope for in vivo research

by Mayrhofer, Johannes M., Haiss, Florent, Haenni, Dominik, Weber, Stefan, Zuend, Marc, Barrett, Matthew J. P., Ferrari, Kim David, Maechler, Philipp, Saab, Aiman S., Stobart, Jillian L., Wyss, Matthias T., Johannssen, Helge, Osswald, Harald, Palmer, Lucy M., Revol, Vincent, Schuh, Claus-Dieter, Urban, Claus, Hall, Andrew, Larkum, Matthew E., Rutz-Innerhofer, Edith, Zeilhofer, Hanns Ulrich, Ziegler, Urs, Weber, Bruno
Published in Biomed Opt Express (2015)

Typical features of Parkinson disease and diagnostic challenges with microdeletion 22q11.2

by Boot, Erik, Butcher, Nancy J., Udow, Sean, Marras, Connie, Mok, Kin Y., Kaneko, Satoshi, Barrett, Matthew J., Prontera, Paolo, Berman, Brian D., Masellis, Mario, Dufournet, Boris, Nguyen, Karine, Charles, Perrine, Mutez, Eugénie, Danaila, Teodor, Jacquette, Aurélia, Colin, Olivier, Drapier, Sophie, Borg, Michel, Fiksinski, Ania M., Vergaelen, Elfi, Swillen, Ann, Vogels, Annick, Plate, Annika, Perandones, Claudia, Gasser, Thomas, Clerinx, Kristien, Bourdain, Frédéric, Mills, Kelly, Williams, Nigel M., Wood, Nicholas W., Booij, Jan, Lang, Anthony E., Bassett, Anne S.
Published in Neurology (2018)

Safety and Tolerability of SRX246, a Vasopressin 1a Antagonist, in Irritable Huntington’s Disease Patients—A Randomized Phase 2 Clinical Trial

by Brownstein, Michael J., Simon, Neal G., Long, Jeffrey D., Yankey, Jon, Maibach, Hilda T., Cudkowicz, Merit, Coffey, Christopher, Conwit, Robin A., Lungu, Codrin, Anderson, Karen E., Hersch, Steven M., Ecklund, Dixie J., Damiano, Eve M., Itzkowitz, Debra E., Lu, Shifang, Chase, Marianne K., Shefner, Jeremy M., McGarry, Andrew, Thornell, Brenda, Gladden, Catherine, Costigan, Michele, O’Suilleabhain, Padraig, Marshall, Frederick J., Chesire, Amy M., Deritis, Paul, Adams, Jamie L., Hedera, Peter, Lowen, Kelly, Rosas, H. Diana, Hiller, Amie L., Quinn, Joseph, Keith, Kellie, Duker, Andrew P., Gruenwald, Christina, Molloy, Angela, Jacob, Cara, Factor, Stewart, Sperin, Elaine, Bega, Danny, Brown, Zsazsa R., Seeberger, Lauren C., Sung, Victor W., Benge, Melanie, Kostyk, Sandra K., Daley, Allison M., Perlman, Susan, Suski, Valerie, Conlon, Patricia, Barrett, Matthew J., Lowenhaupt, Stephanie, Quigg, Mark, Perlmutter, Joel S., Wright, Brenton A., Most, Elaine, Schwartz, Guy J., Lamb, Jessica, Chuang, Rosalind S., Singer, Carlos, Marder, Karen, Moran, Joyce A., Singleton, John R., Zorn, Meghan, Wall, Paola V., Dubinsky, Richard M., Gray, Carolyn, Drazinic, Carolyn
Published in J Clin Med (2020)

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

by Chia, Ruth, Sabir, Marya S., Bandres-Ciga, Sara, Saez-Atienzar, Sara, Reynolds, Regina H., Gustavsson, Emil, Walton, Ronald L., Ahmed, Sarah, Viollet, Coralie, Ding, Jinhui, Makarious, Mary B., Diez-Fairen, Monica, Portley, Makayla K., Shah, Zalak, Abramzon, Yevgeniya, Hernandez, Dena G., Blauwendraat, Cornelis, Stone, David J., Eicher, John, Parkkinen, Laura, Ansorge, Olaf, Clark, Lorraine, Honig, Lawrence S., Marder, Karen, Lemstra, Afina, St George-Hyslop, Peter, Londos, Elisabet, Morgan, Kevin, Lashley, Tammaryn, Warner, Thomas T., Jaunmuktane, Zane, Galasko, Douglas, Santana, Isabel, Tienari, Pentti J., Myllykangas, Liisa, Oinas, Minna, Cairns, Nigel J., Morris, John C., Halliday, Glenda M., Van Deerlin, Vivianna M., Trojanowski, John Q., Grassano, Maurizio, Calvo, Andrea, Mora, Gabriele, Canosa, Antonio, Floris, Gianluca, Bohannan, Ryan C., Brett, Francesca, Gan-Or, Ziv, Geiger, Joshua T., Moore, Anni, May, Patrick, Krüger, Rejko, Goldstein, David S., Lopez, Grisel, Tayebi, Nahid, Sidransky, Ellen, Norcliffe-Kaufmann, Lucy, Palma, Jose-Alberto, Kaufmann, Horacio, Shakkottai, Vikram G., Perkins, Matthew, Newell, Kathy L., Gasser, Thomas, Schulte, Claudia, Landi, Francesco, Salvi, Erika, Cusi, Daniele, Masliah, Eliezer, Kim, Ronald C., Caraway, Chad A., Monuki, Edwin S., Brunetti, Maura, Dawson, Ted M., Rosenthal, Liana S., Albert, Marilyn S., Pletnikova, Olga, Troncoso, Juan C., Flanagan, Margaret E., Mao, Qinwen, Bigio, Eileen H., Rodríguez-Rodríguez, Eloy, Infante, Jon, Lage, Carmen, González-Aramburu, Isabel, Sanchez-Juan, Pascual, Ghetti, Bernardino, Keith, Julia, Black, Sandra E., Masellis, Mario, Rogaeva, Ekaterina, Duyckaerts, Charles, Brice, Alexis, Lesage, Suzanne, Xiromerisiou, Georgia, Barrett, Matthew J., Tilley, Bension S., Gentleman, Steve, Logroscino, Giancarlo, Serrano, Geidy E., Beach, Thomas G., McKeith, Ian G., Thomas, Alan J., Attems, Johannes, Morris, Christopher M., Palmer, Laura, Love, Seth, Troakes, Claire, Al-Sarraj, Safa, Hodges, Angela K., Aarsland, Dag, Klein, Gregory, Kaiser, Scott M., Woltjer, Randy, Pastor, Pau, Bekris, Lynn M., Leverenz, James B., Besser, Lilah M., Kuzma, Amanda, Renton, Alan E., Goate, Alison, Bennett, David A., Scherzer, Clemens R., Morris, Huw R., Ferrari, Raffaele, Albani, Diego, Pickering-Brown, Stuart, Faber, Kelley, Kukull, Walter A., Morenas-Rodriguez, Estrella, Lleó, Alberto, Fortea, Juan, Alcolea, Daniel, Clarimon, Jordi, Nalls, Mike A., Ferrucci, Luigi, Resnick, Susan M., Tanaka, Toshiko, Foroud, Tatiana M., Graff-Radford, Neill R., Wszolek, Zbigniew K., Ferman, Tanis, Boeve, Bradley F., Hardy, John A., Topol, Eric J., Torkamani, Ali, Singleton, Andrew B., Ryten, Mina, Dickson, Dennis W., Chiò, Adriano, Ross, Owen A., Gibbs, J. Raphael, Dalgard, Clifton L., Traynor, Bryan J., Scholz, Sonja W.
Published in Nat Genet (2021)