MIRECC / CoE

2022 VISN 20 MIRECC Staff Research Articles and Presentations

VISN 20 MIRECC Staff Research Articles and Presentations

The findings of NW MIRECC research are disseminated through MIRECC Presents, lectures and presentations, and publications. Below is a list of publications and presentations by VISN 20 NW MIRECC researchers and fellowship program faculty that were published in 2022.

Adeniyi, P., Fopiano, K., Banine, F., Garcia, M., Gong, X., Keene, C., Sherman, L., Bagi, Z., & Back, S. (2022). Multispectral LEDs Eliminate Lipofuscin-Associated Autofluorescence for Immunohistochemistry and CD44 Variant Detection by in Situ Hybridization in Aging Human, non-Human Primate, and Murine Brain. ASN Neuro, 14, 175909142211231. doi:10.1177/17590914221123138

Alosco, M., Mariani, M., Adler, C., Balcer, L., Bernick, C., Au, R., Banks, S., Barr, W., Bouix, S., Cantu, R., Coleman, M., Dodick, D., Farrer, L., Geda, Y., Katz, D., Koerte, I., Kowall, N., Lin, A., Marcus, D., Marek, K., McClean, M., McKee, A., Mez, J., Palmisano, J., Peskind, E. R., Tripodis, Y., Turner, R., Wethe, J., Cummings, J., Reiman, E., Shenton, M., Stern, R., Adler, C., Alosco, M., Au, R., Balcer, L., Banks, S., Barr, W., Bernick, C., Bouix, S., Cantu, R., Chen, K., Coleman, M., Cummings, J., Dodick, D., Farrer, L., Fitzsimmons, J., Geda, Y., Goldberg, J., Helm, R., Johnson, K., Katz, D., Kirov, I., Koerte, I., Kowall, N., Lin, A., Lui, Y., Marcus, D., Marek, K., Mariani, M., Marmar, C., McClean, M., McKee, A., Mez, J., Miller, J., Palmisano, J., Pasternak, O., Peskind, E. R., Protas, H., Reiman, E., Ritter, A., Shenton, M., Stern, R., Su, Y., Tripodis, Y., Turner, R., Weller, J., & Wethe, J. (2021). Developing methods to detect and diagnose chronic traumatic encephalopathy during life: rationale, design, and methodology for the DIAGNOSE CTE Research Project. Alzheimer's Research and Therapy, 13 (1), 136. doi:10.1186/s13195-021-00872-x

Alosco, M., Su, Y., Stein, T., Protas, H., Cherry, J., Adler, C., Balcer, L., Bernick, C., Pulukuri, S., Abdolmohammadi, B., Coleman, M., Palmisano, J., Tripodis, Y., Mez, J., Rabinovici, G., Marek, K., Beach, T., Johnson, K., Huber, B., Koerte, I., Lin, A., Bouix, S., Cummings, J., Shenton, M., Reiman, E., McKee, A., Stern, R., Reiman, E., Su, Y., Chen, K., Protas, H., Boker, C., Alosco, M., Au, R., Cantu, R., Farrer, L., Helm, R., Katz, D., Kowall, N., Mez, J., Mercier, G., Otis, J., Stern, R., Weller, J., Simkin, I., Andino, A., Conneely, S., Diamond, C., Fagle, T., Haller, O., Hunt, T., Gullotti, N., Mariani, M., Mayville, B., McLaughlin, K., Nanna, M., Platt, T., Pulukuri, S., Rice, F., Sestak, M., McClean, M., Tripodis, Y., Annis, D., Chaisson, C., Dixon, D., Finney, C., Gallagher, K., Hartlage, K., Lu, J., Martin, B., Ojo, E., Palmisano, J., Pine, B., Ramachandran, J., Bouix, S., Fitzsimmons, J., Lin, A., Koerte, I., Pasternak, O., Shenton, M., Arcinieago, H., Billah, T., Bonke, E., Breedlove, K., Coello, E., Coleman, M., Jung, L., Liao, H., Loy, M., Rizzoni, E., Schultz, V., Silva, A., Vessey, B., Wiegand, T., Banks, S., Bernick, C., Miller, J., Ritter, A., Sabbagh, M., de la Cruz, R., Durant, J., Golceker, M., Harmon, N., Kaylegian, K., Long, R., Nance, C., Sandoval, P., Turner, R., Marek, K., Serrano, A., Adler, C., Dodick, D., Geda, Y., Wethe, J., Falk, B., Duffy, A., Howard, M., Montague, M., Osgood, T., Babcock, D., Bellgowan, P., Balcer, L., Barr, W., Goldberg, J., Wisniewski, T., Kirov, I., Lui, Y., Marmar, C., Hasanaj, L., Serrano, L., Al-Kharafi, A., George, A., Martin, S., Riley, E., Runge, W., Cummings, J., Peskind, E. R., Colasurdo, E., Marcus, D., Gurney, J., Greenwald, R., & Johnson, K. (2022). Associations between near end-of-life flortaucipir PET and postmortem CTE-related tau neuropathology in six former American football players. European Journal of Nuclear Medicine and Molecular Imaging. Advance online publication. doi:10.1007/s00259-022-05963-x

Ameen-Ali, K., Bretzin, A., Lee, E., Folkerth, R., Hazrati, L., Iacono, D., Keene, C., Kofler, J., Kovacs, G., Nolan, A., Perl, D., Priemer, D., Smith, D., Wiebe, D., Stewart, W., Al-Sarraj, S., Cortes, E., Crary, J., Dams-O’Connor, K., Diaz-Arrastia, R., Dollé, J., Edlow, B., Fischl, B., Hinds, C., Johnson, V., Manley, G., Meaney, D., Okonkwo, D., Schneider, A., Schneider, J., Troakes, C., Trojanowski, J., van der Kouwe, A., & Yaffe, K. (2022). Detection of astrocytic tau pathology facilitates recognition of chronic traumatic encephalopathy neuropathologic change. Acta Neuropathologica Communications, 10 (1), 1-50. doi:10.1186/s40478-022-01353-4

Bagi, Z., Kroenke, C., Fopiano, K., Tian, Y., Filosa, J., Sherman, L., Larson, E., Keene, C., Degener O’Brien, K., Adeniyi, P., & Back, S. (2022). Association of cerebral microvascular dysfunction and white matter injury in Alzheimer’s disease. GeroScience. Advance online publication. doi:10.1007/s11357-022-00585-5

Bakken, T., Jorstad, N., Hu, Q., Lake, B., Tian, W., Kalmbach, B., Crow, M., Hodge, R., Krienen, F., Sorensen, S., Eggermont, J., Yao, Z., Aevermann, B., Aldridge, A., Bartlett, A., Bertagnolli, D., Casper, T., Castanon, R., Crichton, K., Daigle, T., Dalley, R., Dee, N., Dembrow, N., Diep, D., Ding, S., Dong, W., Fang, R., Fischer, S., Goldman, M., Goldy, J., Graybuck, L., Herb, B., Hou, X., Kancherla, J., Kroll, M., Lathia, K., van Lew, B., Li, Y., Liu, C., Liu, H., Lucero, J., Mahurkar, A., McMillen, D., Miller, J., Moussa, M., Nery, J., Nicovich, P., Niu, S., Orvis, J., Osteen, J., Owen, S., Palmer, C., Pham, T., Plongthongkum, N., Poirion, O., Reed, N., Rimorin, C., Rivkin, A., Romanow, W., Sedeño-Cortés, A., Siletti, K., Somasundaram, S., Sulc, J., Tieu, M., Torkelson, A., Tung, H., Wang, X., Xie, F., Yanny, A., Zhang, R., Ament, S., Behrens, M., Bravo, H., Chun, J., Dobin, A., Gillis, J., Hertzano, R., Hof, P., Höllt, T., Horwitz, G., Keene, C., Kharchenko, P., Ko, A., Lelieveldt, B., Luo, C., Mukamel, E., Pinto-Duarte, A., Preissl, S., Regev, A., Ren, B., Scheuermann, R., Smith, K., Spain, W., White, O., Koch, C., Hawrylycz, M., Tasic, B., Macosko, E., McCarroll, S., Ting, J., Zeng, H., Zhang, K., Feng, G., Ecker, J., Linnarsson, S., & Lein, E. (2021). Comparative cellular analysis of motor cortex in human, marmoset and mouse. Nature, 598 (7879), 111-119. doi:10.1038/s41586-021-03465-8

Balba, N., McBride, A., Callahan, M., Mist, S., Jones, K., Butler, M., Lim, M., & Heinricher, M. (2022). Photosensitivity Is Associated with Chronic Pain following Traumatic Brain Injury. Journal of Neurotrauma, 39 (17-18), 1183-1194. doi:10.1089/neu.2022.0019

Baskin, B., Lee, S., Skillen, E., Wong, K., Rau, H., Hendrickson, R. C., Pagulayan, K. F., Raskind, M. A., Peskind, E. R., Phillips, P., Cook, D. G., & Schindler, A. (2021). Repetitive Blast Exposure Increases Appetitive Motivation and Behavioral Inflexibility in Male Mice. Frontiers in Behavioral Neuroscience, 15, 792648. doi:10.3389/fnbeh.2021.792648

Berg, J., Sorensen, S., Ting, J., Miller, J., Chartrand, T., Buchin, A., Bakken, T., Budzillo, A., Dee, N., Ding, S., Gouwens, N., Hodge, R., Kalmbach, B., Lee, C., Lee, B., Alfiler, L., Baker, K., Barkan, E., Beller, A., Berry, K., Bertagnolli, D., Bickley, K., Bomben, J., Braun, T., Brouner, K., Casper, T., Chong, P., Crichton, K., Dalley, R., de Frates, R., Desta, T., Lee, S., D’Orazi, F., Dotson, N., Egdorf, T., Enstrom, R., Farrell, C., Feng, D., Fong, O., Furdan, S., Galakhova, A., Gamlin, C., Gary, A., Glandon, A., Goldy, J., Gorham, M., Goriounova, N., Gratiy, S., Graybuck, L., Gu, H., Hadley, K., Hansen, N., Heistek, T., Henry, A., Heyer, D., Hill, D., Hill, C., Hupp, M., Jarsky, T., Kebede, S., Keene, L., Kim, L., Kim, M., Kroll, M., Latimer, C., Levi, B., Link, K., Mallory, M., Mann, R., Marshall, D., Maxwell, M., McGraw, M., McMillen, D., Melief, E., Mertens, E., Mezei, L., Mihut, N., Mok, S., Molnar, G., Mukora, A., Ng, L., Ngo, K., Nicovich, P., Nyhus, J., Olah, G., Oldre, A., Omstead, V., Ozsvar, A., Park, D., Peng, H., Pham, T., Pom, C., Potekhina, L., Rajanbabu, R., Ransford, S., Reid, D., Rimorin, C., Ruiz, A., Sandman, D., Sulc, J., Sunkin, S., Szafer, A., Szemenyei, V., Thomsen, E., Tieu, M., Torkelson, A., Trinh, J., Tung, H., Wakeman, W., Waleboer, F., Ward, K., Wilbers, R., Williams, G., Yao, Z., Yoon, J., Anastassiou, C., Arkhipov, A., Barzo, P., Bernard, A., Cobbs, C., de Witt Hamer, P., Ellenbogen, R., Esposito, L., Ferreira, M., Gwinn, R., Hawrylycz, M., Hof, P., Idema, S., Jones, A., Keene, C., Ko, A., Murphy, G., Ng, L., Ojemann, J., Patel, A., Phillips, J., Silbergeld, D., Smith, K., Tasic, B., Yuste, R., Segev, I., de Kock, C., Mansvelder, H., Tamas, G., Zeng, H., Koch, C., & Lein, E. (2021). Human neocortical expansion involves glutamatergic neuron diversification. Nature, 598 (7879), 151-158. doi:10.1038/s41586-021-03813-8

Boase, K., Machamer, J., Temkin, N., Dikmen, S., Wilson, L., Nelson, L., Barber, J., Bodien, Y., Giacino, J., Markowitz, A., McCrea, M., Satris, G., Stein, M., Taylor, S., Manley, G., Adeoye, O., Bullock, M., Corrigan, J., Diaz-Arrastia, R., Ellenbogen, R., Feeser, V., Ferguson, A., Gardner, R., Goldman, D., Gopinath, S., Hemphill, J., Keene, C., Korley, F., Kramer, J., Kreitzer, N., Levin, H., Lindsell, C., Madden, C., Martin, A., McAllister, T., Merchant, R., Mukherjee, P., Ngwenya, L., Noel, F., Nolan, A., Okonkwo, D., Palacios, E., Perl, D., Puccio, A., Rabinowitz, M., Robertson, C., Rosand, J., Sander, A., Schnyer, D., Seabury, S., Sherer, M., Toga, A., Valadka, A., Vassar, M., MS, R., Vespa, P., Wang, K., Yue, J., Yuh, E., & Zafonte, R. (2021). Central Curation of Glasgow Outcome Scale-Extended Data: Lessons Learned from TRACK-TBI. Journal of Neurotrauma, 38 (17), 2419-2434. doi:10.1089/neu.2020.7528

Boehnlein, J., & Kinzie, J. (2021). Experiencing Mental Illness: Suffering, Hope, and Healing. Narrative Inquiry in Bioethics, 11 (2), 189-194. doi:10.1353/nib.2021.0070

Bohr, T., Hjorth, P., Holst, S., Hrabetová, S., Kiviniemi, V., Lilius, T., Lundgaard, I., Mardal, K., Martens, E., Mori, Y., Nägerl, U., Nicholson, C., Tannenbaum, A., Thomas, J., Tithof, J., Benveniste, H., Iliff, J. J., Kelley, D., & Nedergaard, M. (2022). The glymphatic system: Current understanding and modeling. iScience, 25 (9), 104987. doi:10.1016/j.isci.2022.104987

Brett, B., Gardner, R., Godbout, J., Dams-O’Connor, K., & Keene, C. (2022). Traumatic Brain Injury and Risk of Neurodegenerative Disorder. Biological Psychiatry, 91(5), 498-507. doi:10.1016/j.biopsych.2021.05.025

Burke, B., Latimer, C., Keene, C., Sonnen, J., McCormick, W., Bowen, J., McCurry, S., Larson, E., & Crane, P. (2021). Theoretical impact of the AT(N) framework on dementia using a community autopsy sample. Alzheimer's & Dementia, 17(12), 1879-1891. doi:10.1002/alz.12348

Burke, J., Gugger, J., Ding, K., Kim, J., Foreman, B., Yue, J., Puccio, A., Yuh, E., Sun, X., Rabinowitz, M., Vassar, M., Taylor, S., Winkler, E., Deng, H., McCrea, M., Stein, M., Robertson, C., Levin, H., Dikmen, S., Temkin, N., Barber, J., Giacino, J., Mukherjee, P., Wang, K., Okonkwo, D., Markowitz, A., Jain, S., Lowenstein, D., Manley, G., Diaz-Arrastia, R., Badjatia, N., Duhaime, A., Feeser, V., Gaudette, E., Gopinath, S., Keene, C., Korley, F., Madden, C., Merchant, R., Schnyer, D., & Zafonte, R. (2021). Association of Posttraumatic Epilepsy With 1-Year Outcomes After Traumatic Brain Injury. JAMA Network Open, 4 (12), e2140191. doi:10.1001/jamanetworkopen.2021.40191

Callaway, E., Dong, H., Ecker, J., Hawrylycz, M., Huang, Z., Lein, E., Ngai, J., Osten, P., Ren, B., Tolias, A., White, O., Zeng, H., Zhuang, X., Ascoli, G., Behrens, M., Chun, J., Feng, G., Gee, J., Ghosh, S., Halchenko, Y., Hertzano, R., Lim, B., Martone, M., Ng, L., Pachter, L., Ropelewski, A., Tickle, T., Yang, X., Zhang, K., Bakken, T., Berens, P., Daigle, T., Harris, J., Jorstad, N., Kalmbach, B., Kobak, D., Li, Y., Liu, H., Matho, K., Mukamel, E., Naeemi, M., Scala, F., Tan, P., Ting, J., Xie, F., Zhang, M., Zhang, Z., Zhou, J., Zingg, B., Armand, E., Yao, Z., Bertagnolli, D., Casper, T., Crichton, K., Dee, N., Diep, D., Ding, S., Dong, W., Dougherty, E., Fong, O., Goldman, M., Goldy, J., Hodge, R., Hu, L., Keene, C., Krienen, F., Kroll, M., Lake, B., Lathia, K., Linnarsson, S., Liu, C., Macosko, E., McCarroll, S., McMillen, D., Nadaf, N., Nguyen, T., Palmer, C., Pham, T., Plongthongkum, N., Reed, N., Regev, A., Rimorin, C., Romanow, W., Savoia, S., Siletti, K., Smith, K., Sulc, J., Tasic, B., Tieu, M., Torkelson, A., Tung, H., van Velthoven, C., Vanderburg, C., Yanny, A., Fang, R., Hou, X., Lucero, J., Osteen, J., Pinto-Duarte, A., Poirion, O., Preissl, S., Wang, X., Aldridge, A., Bartlett, A., Boggeman, L., O’Connor, C., Castanon, R., Chen, H., Fitzpatrick, C., Luo, C., Nery, J., Nunn, M., Rivkin, A., Tian, W., Dominguez, B., Ito-Cole, T., Jacobs, M., Jin, X., Lee, C., Lee, K., Miyazaki, P., Pang, Y., Rashid, M., Smith, J., Vu, M., Williams, E., Biancalani, T., Booeshaghi, A., Crow, M., Dudoit, S., Fischer, S., Gillis, J., Hu, Q., Kharchenko, P., Niu, S., Ntranos, V., Purdom, E., Risso, D., de Bézieux, H., Somasundaram, S., Street, K., Svensson, V., Vaishnav, E., Van den Berge, K., Welch, J., An, X., Bateup, H., Bowman, I., Chance, R., Foster, N., Galbavy, W., Gong, H., Gou, L., Hatfield, J., Hintiryan, H., Hirokawa, K., Kim, G., Kramer, D., Li, A., Li, X., Luo, Q., Muñoz-Castañeda, R., Stafford, D., Feng, Z., Jia, X., Jiang, S., Jiang, T., Kuang, X., Larsen, R., Lesnar, P., Li, Y., Li, Y., Liu, L., Peng, H., Qu, L., Ren, M., Ruan, Z., Shen, E., Song, Y., Wakeman, W., Wang, P., Wang, Y., Wang, Y., Yin, L., Yuan, J., Zhao, S., Zhao, X., Narasimhan, A., Palaniswamy, R., Banerjee, S., Ding, L., Huilgol, D., Huo, B., Kuo, H., Laturnus, S., Li, X., Mitra, P., Mizrachi, J., Wang, Q., Xie, P., Xiong, F., Yu, Y., Eichhorn, S., Berg, J., Bernabucci, M., Bernaerts, Y., Cadwell, C., Castro, J., Dalley, R., Hartmanis, L., Horwitz, G., Jiang, X., Ko, A., Miranda, E., Mulherkar, S., Nicovich, P., Owen, S., Sandberg, R., Sorensen, S., Tan, Z., Allen, S., Hockemeyer, D., Lee, A., Veldman, M., Adkins, R., Ament, S., Bravo, H., Carter, R., Chatterjee, A., Colantuoni, C., Crabtree, J., Creasy, H., Felix, V., Giglio, M., Herb, B., Kancherla, J., Mahurkar, A., McCracken, C., Nickel, L., Olley, D., Orvis, J., Schor, M., Hood, G., Dichter, B., Grauer, M., Helba, B., Bandrowski, A., Barkas, N., Carlin, B., D’Orazi, F., Degatano, K., Gillespie, T., Khajouei, F., Konwar, K., Thompson, C., Kelly, K., Mok, S., & Sunkin, S. (2021). A multimodal cell census and atlas of the mammalian primary motor cortex. Nature, 598 (7879), 86-102. doi:10.1038/s41586-021-03950-0

Campagnola, L., Seeman, S., Chartrand, T., Kim, L., Hoggarth, A., Gamlin, C., Ito, S., Trinh, J., Davoudian, P., Radaelli, C., Kim, M., Hage, T., Braun, T., Alfiler, L., Andrade, J., Bohn, P., Dalley, R., Henry, A., Kebede, S., Alice, M., Sandman, D., Williams, G., Larsen, R., Teeter, C., Daigle, T., Berry, K., Dotson, N., Enstrom, R., Gorham, M., Hupp, M., Dingman Lee, S., Ngo, K., Nicovich, P., Potekhina, L., Ransford, S., Gary, A., Goldy, J., McMillen, D., Pham, T., Tieu, M., Siverts, L., Walker, M., Farrell, C., Schroedter, M., Slaughterbeck, C., Cobb, C., Ellenbogen, R., Gwinn, R., Keene, C., Ko, A., Ojemann, J., Silbergeld, D., Carey, D., Casper, T., Crichton, K., Clark, M., Dee, N., Ellingwood, L., Gloe, J., Kroll, M., Sulc, J., Tung, H., Wadhwani, K., Brouner, K., Egdorf, T., Maxwell, M., McGraw, M., Pom, C., Ruiz, A., Bomben, J., Feng, D., Hejazinia, N., Shi, S., Szafer, A., Wakeman, W., Phillips, J., Bernard, A., Esposito, L., D’Orazi, F., Sunkin, S., Smith, K., Tasic, B., Arkhipov, A., Sorensen, S., Lein, E., Koch, C., Murphy, G., Zeng, H., & Jarsky, T. (2022). Local connectivity and synaptic dynamics in mouse and human neocortex. Science, 375, 6585. doi:10.1126/science.abj5861

Cheng, Z., Lozier, C. C., Lewis, M., O’Neil, M., Luoma, J. B., & Morasco, B. (2021). Investigating the role of psychological inflexibility, mindfulness, and self -compassion in PTSD. Journal of Contextual Behavioral Science, 22, 102-107.

Clouston, S., Hall, C., Kritikos, M., Bennett, D., DeKosky, S., Edwards, J., Finch, C., Kreisl, W., Mielke, M., Peskind, E. R., Raskind, M. A., Richards, M., Sloan, R., Spiro, A., Vasdev, N., Brackbill, R., Farfel, M., Horton, M., Lowe, S., Lucchini, R., Prezant, D., Reibman, J., Rosen, R., Seil, K., Zeig-Owens, R., Deri, Y., Diminich, E., Fausto, B., Gandy, S., Sano, M., Bromet, E., & Luft, B. (2022). Cognitive impairment and World Trade Centre-related exposures. Nature Reviews Neurology, 18 (2), 103-116. doi:10.1038/s41582-021-00576-8

Coffey, K. R., Lesiak, A., Marx, R., Vo, E., Garden, G., & Neumaier, J. F. (2022). A cAMP-Related Gene Network in Microglia Is Inversely Regulated by Morphine Tolerance and Withdrawal. Biological Psychiatry Global Open Science, 2(2), 180-189. doi:10.1016/j.bpsgos.2021.07.011

Coffey, K. R., Venkat, V., West, M. O., & Barker, D. J. (2021). Lateral preoptic area neurons signal cocaine self-administration behaviors. European Journal of Neuroscience, 54(7), 6397-6405.

Course, M., Gudsnuk, K., Keene, C., Bird, T., Jayadev, S., & Valdmanis, P. (2022). Aberrant splicing of PSEN2, but not PSEN1, in individuals with sporadic Alzheimer's disease. Brain. Advance online publication. doi:10.1093/brain/awac294

Damodarasamy, M., Khaing, Z., Hyde, J., Keene, C., Bentov, I., Banks, W., & Reed, M. (2022). Viable human brain microvessels for the study of aging and neurodegenerative diseases. Microvascular Research, 140, 104282. doi:10.1016/j.mvr.2021.104282

Dickstein, D., De Gasperi, R., Gama Sosa, M., Perez-Garcia, G., Short, J., Sosa, H., Perez, G., Tschiffely, A., Dams-O’Connor, K., Pullman, M., Knesaurek, K., Knutsen, A., Pham, D., Soleimani, L., Jordan, B., Gordon, W., Delman, B., Shumyatsky, G., Shahim, P., DeKosky, S., Stone, J., Peskind, E. R., Blennow, K., Zetterberg, H., Chance, S., Torso, M., Kostakoglu, L., Sano, M., Hof, P., Ahlers, S., Gandy, S., & Elder, G. (2021). Brain and blood biomarkers of tauopathy and neuronal injury in humans and rats with neurobehavioral syndromes following blast exposure. Molecular Psychiatry, 26 (10), 5940-5954. doi:10.1038/s41380-020-0674-z

Djerdjaj, A., Ng, A. J., Rieger, N. S., & Christianson, J. P. (2022). The basolateral amygdala to posterior insular cortex tract is necessary for social interaction with stressed juvenile rats. Behavioural brain research, 435, 114050. doi:10.1016/j.bbr.2022

Edelman, W., Kiianitsa, K., Virmani, T., Martinez, R., Young, J., Keene, C., Bird, T., Raskind, W., & Korvatska, O. (2022). Reduced gene dosage is a common mechanism of neuropathologies caused by ATP6AP2 splicing mutations. Parkinsonism & Related Disorders, 101, 31-38. doi:10.1016/j.parkreldis.2022.06.015

Eissman, J., Dumitrescu, L., Mahoney, E., Smith, A., Mukherjee, S., Lee, M., Scollard, P., Choi, S., Bush, W., Engelman, C., Lu, Q., Fardo, D., Trittschuh, E., Mez, J., Kaczorowski, C., Hernandez Saucedo, H., Widaman, K., Buckley, R., Properzi, M., Mormino, E., Yang, H., Harrison, T., Hedden, T., Nho, K., Andrews, S., Tommet, D., Hadad, N., Sanders, R., Ruderfer, D., Gifford, K., Zhong, X., Raghavan, N., Vardarajan, B., Pericak-Vance, M., Farrer, L., Wang, L., Cruchaga, C., Schellenberg, G., Cox, N., Haines, J., Keene, C., Saykin, A., Larson, E., Sperling, R., Mayeux, R., Cuccaro, M., Bennett, D., Schneider, J., Crane, P., Jefferson, A., & Hohman, T. (2022). Sex differences in the genetic architecture of cognitive resilience to Alzheimer’s disease. Brain, 145 (7), 2541-2554. doi:10.1093/brain/awac177

Elliott, J., McBride, A., Balba, N., Thomas, S., Pattinson, C., Morasco, B., Wilkerson, A., Gill, J., & Lim, M. (2022). Feasibility and preliminary efficacy for morning bright light therapy to improve sleep and plasma biomarkers in US Veterans with TBI. A prospective, open-label, single-arm trial. PLOS ONE, 17 (4), e0262955. doi:10.1371/journal.pone.0262955

Evans, K., Barton, R., Hendrickson, R. C., & LaPlante, L. (2022). Creating Safe Spaces for Those Who Have Lived through Intimate Partner Violence. Journal of Aggression, Maltreatment & Trauma, NA, 1-16. doi:10.1080/10926771.2022.2099774

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Piantino, J., Iliff, J. J., & Lim, M. (2022). The Bidirectional Link Between Sleep Disturbances and Traumatic Brain Injury Symptoms: A Role for Glymphatic Dysfunction?. Biological Psychiatry, 91(5), 478-487. doi:10.1016/j.biopsych.2021.06.025

Prater, K., Green, K., Chiou, K., Smith, C., Sun, W., Shojaie, A., Heath, L., Rose, S., Keene, C., Logsdon, B., Snyder-Mackler, N., Blue, E., Young, J., Garden, G., & Jayadev, S. (2021). Microglia subtype transcriptomes differ between Alzheimer Disease and control human postmortem brain samples. Alzheimer's and Dementia, 17 (S2), e058474. doi:10.1002/alz.058474

Ray, L., Pike, M., Simon, M., Iliff, J. J., & Heys, J. (2021). Quantitative analysis of macroscopic solute transport in the murine brain. Fluids and Barriers of the CNS, 18 (1), 55. doi:10.1186/s12987-021-00290-z

Rieger, N. S., Guoynes, C. D., Monari, P. K., Hammond, E. R., Malone, C. L., & Marler, C. A. (2022). Neuroendocrine mechanisms of aggression in rodents. Motivation Science, 8(2), 81-105. Retrieved from https://doi.org/10.1037/mot0000260

Rieger, N. S., Varela, J. A., Ng, A. J., Granata, L., Djerdjaj, A., Brenhouse, H. C., & Christianson, J. P. (2022). Insular cortex corticotropin-releasing factor integrates stress signaling with social affective behavior. Neuropsychopharmacology, 47(6), 1156-1168. doi:10.1038/s41386-022-01292-7

Rieger, N. S., Worley, N., Ng, A., & Christianson, J. (2022). Insular cortex modulates social avoidance of sick rats. Behavioural Brain Research, 416, 113541. doi:10.1016/j.bbr.2021.113541

Salman, M., Kitchen, P., Halsey, A., Wang, M., Törnroth-Horsefield, S., Conner, A., Badaut, J., Iliff, J. J., & Bill, R. (2022). Emerging roles for dynamic aquaporin-4 subcellular relocalization in CNS water homeostasis. Brain, 145 (1), 64-75. doi:10.1093/brain/awab311

Schindler, A. G., Baskin, B., Juarez, B., Janet Lee, S., Hendrickson, R., Pagulayan, K., Zweifel, L. S., Raskind, M. A., Phillips, P. E. M., Peskind, E. R., & Cook, D. G. (2021). Repetitive blast mild traumatic brain injury increases ethanol sensitivity in male mice and risky drinking behavior in male combat veterans. Alcoholism, clinical and experimental research, 45(5), 1051–1064. doi:10.1111/acer.14605

Schneider, L., Bennett, D., Farlow, M., Peskind, E. R., Raskind, M. A., Sano, M., Stern, Y., Haneline, S., Welsh-Bohmer, K., O’Neil, J., Walter, R., Maresca, S., Culp, M., Alexander, R., Saunders, A., Burns, D., & Chiang, C. (2022). Adjudicating Mild Cognitive Impairment Due to Alzheimer’s Disease as a Novel Endpoint Event in the TOMMORROW Prevention Clinical Trial. The Journal of Prevention of Alzheimer's Disease, 9(4), 625-634. doi:10.14283/jpad.2022.72

Sheppard, D., Rau, H., Trittschuh, E., Werhane, M., Schindler, A., Hendrickson, R. C., Peskind, E. R., & Pagulayan, K. F. (2022). Poorer prospective memory performance is associated with reduced time monitoring among OEF/OIF/OND Veterans with a history of blast-related mild traumatic brain injury. The Clinical Neuropsychologist. doi:10.1080/13854046.2022.2068455

Sheppard, D., Rau, H., Werhane, M., Fonseca, L., Chaytor, N., Peskind, E. R., & Pagulayan, K. F. (2022). Associations between Intra-Individual Neurocognitive Variability and Prospective Memory in Veterans with Mild Traumatic Brain Injury History and Posttraumatic Stress Disorder. Archives of Clinical Neuropsychology, 37(6), 1221-1227. doi:10.1093/arclin/acac014

Simon, M., Wang, M., Ismail, O., Braun, M., Schindler, A., Reemmer, J., Wang, Z., Haveliwala, M., O’Boyle, R., Han, W., Roese, N., Grafe, M., Woltjer, R., Boison, D., & Iliff, J. J. (2022). Loss of perivascular aquaporin-4 localization impairs glymphatic exchange and promotes amyloid ß plaque formation in mice. Alzheimer's Research and Therapy, 14 (1), 59. doi:10.1186/s13195-022-00999-5

Somohano, V., Kaplan, J., Newman, A., O’Neil, M., & Lovejoy, T. (2022). Formal mindfulness practice predicts reductions in PTSD symptom severity following a mindfulness-based intervention for women with co-occurring PTSD and substance use disorder. Addiction Science & Clinical Practice, 17 (1), 51. doi:10.1186/s13722-022-00333-2

Somohano, V., Shank, T., Manuel, J., Mallik, D., Rehder, K., & Bowen, S. (2021). The Role of Pretreatment Expectancy on Substance Use Outcomes in Women Mandated to Mindfulness-Based Relapse Prevention. The Journal of Alternative and Complementary Medicine. doi:10.1089/acm.2021.0123

Sorg, S., Werhane, M., Merritt, V., Clark, A., Holiday, K., Hanson, K., Jak, A. J., Schiehser, D. M., & Delano-Wood, L. (2021). Research letter: PTSD symptom severity and multiple traumatic brain injuries are associated with elevated memory complaints in veterans with histories of mild TBI. Journal of Head Trauma Rehabilitation, 36 (6), 418-423. doi:10.1097/HTR.0000000000000659

Sun, D., Rakesh, G., Clarke-Rubright, E., Haswell, C., Logue, M. W., O’Leary, E., Cotton, A., Xie, H., Dennis, E., Jahanshad, N., Salminen, L., Thomopoulos, S., Rashid, F., Ching, C., Koch, S., Frijling, J., Nawijn, L., van Zuiden, M., Zhu, X., Suarez-Jimenez, B., Sierk, A., Walter, H., Manthey, A., Stevens, J., Fani, N., van Rooij, S., Stein, M., Bomyea, J., Koerte, I., Choi, K., van de Werff, S., Vermeiren, R., Herzog, J., Lebois, L., Baker, J., Ressler, K., Olson, E., Straube, T., Korgaonkar, M., Andrew, E., Zhu, Y., Li, G., Ipser, J., Hudson, A., Peverill, M., Sambrook, K., Gordon, E., Baugh, L., Forster, G., Simons, R., Simons, J., Magnotta, V., Maron-Katz, A., du Plessis, S., Disner, S., Davenport, N., Grupe, D., Nitschke, J., deRoon-Cassini, T., Fitzgerald, J., Krystal, J. H., Levy, I., Olff, M., Veltman, D., Wang, L., Neria, Y., De Bellis, M., Jovanovic, T., Daniels, J., Shenton, M., van de Wee, N., Schmahl, C., Kaufman, M., Rosso, I., Sponheim, S., Hofmann, D., Bryant, R., Fercho, K., Stein, D., Mueller, S., Phan, L., McLaughlin, K., Davidson, R., Larson, C., May, G., Nelson, S., Abdallah, C., Gomaa, H., Etkin, A., Seedat, S., Harpaz-Rotem, I., Liberzon, I., Wang, X., Thompson, P., & Morey, R. (2022). Remodeling of the cortical structural connectome in posttraumatic stress disorder: Results from the ENIGMA-PGC PTSD consortium. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. Advance online publication. doi:10.1016/j.bpsc.2022.02.008

Sytsma, T., Chen, D., Rolf, B., Dorschner, M., Jayadev, S., Keene, C., Zhang, J., Bird, T., & Latimer, C. (2022). Spinal cord-predominant neuropathology in an adult-onset case of POLR3A-related spastic ataxia. Neuropathology, 42 (1), 58-65. doi:10.1111/neup.12775

Tian, C., Stewart, T., Hong, Z., Guo, Z., Aro, P., Soltys, D., Pan, C., Peskind, E. R., Zabetian, C., Shaw, L., Galasko, D., Quinn, J., Shi, M., & Zhang, J. (2022). Blood extracellular vesicles carrying synaptic function- and brain-related proteins as potential biomarkers for Alzheimer's disease. Alzheimer's & Dementia. doi:10.1002/alz.12723

Torres, E., Luo, J., Boehnlein, J., Towns, D., Kinzie, J., DeBarber, A., & Raber, J. (2022). Apolipoprotein E Isoform-specific changes related to stress and trauma exposure. Translational Psychiatry, 12 (1), 125-135. doi:10.1038/s41398-022-01848-7

Uneri, A., Niere, F., Macauley, S., Ma, T., Keene, C., Craft, S., & Raab-Graham, K. (2021). mRNA-Binding Protein DJ-1 as a pivotal protein in AD pathology. Alzheimer's and Dementia, 17 (S2), e058602. doi:10.1002/alz.058602

Williams, R. G., Li, K., & Phillips, P. (2022). The Influence of Stress on Decision-Making: Effects of CRF and Dopamine Antagonism in the Nucleus Accumbens. Frontiers in Psychiatry, 12, 113541. doi:10.3389/fpsyt.2021.814218

Wyse, J., Mackey, K., Lovejoy, T., Kansagara, D., Tuepker, A., Gordon, A., Todd Korthuis, P., Herreid-O’Neill, A., Williams, B., & Morasco, B. (2022). Expanding access to medications for opioid use disorder through locally-initiated implementation. Addiction Science & Clinical Practice, 17 (1), 32. doi:10.1186/s13722-022-00312-7

Wyse, J., Morasco, B., Dougherty, J., Edwards, B., Kansagara, D., Gordon, A., Korthuis, P., Tuepker, A., Lindner, S., Mackey, K., Williams, B., Herreid-O’Neill, A., Paynter, R., & Lovejoy, T. (2021). Adjunct interventions to standard medical management of buprenorphine in outpatient settings: A systematic review of the evidence. Drug and Alcohol Dependence, 228, 108923. doi:10.1016/j.drugalcdep.2021.108923

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Use of these Materials and Finding VA Health Care

Please note that the health care information provided in these materials is for educational purposes only. It does not replace the role of a medical practitioner for advice on care and treatment. If you are looking for professional medical care, find your local VA healthcare center by using the VA Facilities Locator & Directory. This page may contain links that will take you outside of the Department of Veterans Affairs website. VA does not endorse and is not responsible for the content of the linked websites.

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VA Regional Offices

The Veterans Benefits Administration (VBA) helps service members transition out of military service, and assists with Veterans with education, home loans, life insurance and much more. Service members, Veterans, their families, and Survivors are invited to request information on VA Benefits including disability compensation, pension, fiduciary, education, Veteran Readiness and Employment (VR&E), Home Loans, and Insurance. In addition to information on VA Benefits Veterans may initiate an intent to file and request assistance with filing compensation and pension claims. Visit regional office websites to learn about the services the regional office provides, directions to the facility, hours of operation, and the leadership team that serves the regional office.

Find out if you can get VA health care as a Veteran

The following four categories of Veterans are not required to enroll but are urged to do so to permit better planning of health resources:

1. Veterans with a service-connected (SC) disability rated at 50% or more.
2. Veterans seeking care for a disability the military determined was incurred or aggravated in the line of duty, but which VA has not yet rated, within 12 months of discharge.
3. Veterans seeking care for a SC disability only or under a special treatment authority.
4. Veterans seeking health registry examinations. VA’s health registry evaluation is a free, voluntary medical assessment for Veterans who may have been exposed to certain environmental hazards during military service. The evaluations alert Veterans to possible long-term health problems that may be related to exposure to specific environmental hazards during their military service. VA has established several health registries to track and monitor the health of specific groups of Veterans. You may be eligible to participate in one or more of these health registries: Agent Orange Registry, Airborne Hazards and Open Burn Pit Registry, Gulf War Registry (includes Operations Iraqi Freedom and New Dawn), Ionizing Radiation Registry, Depleted Uranium Follow-Up Program, and Toxic Embedded Fragment Surveillance Center. Use the chart below to help determine your eligibility.

Find out how to apply for VA health care benefits as a Veteran or service member. For other mental health services, contact a VA medical center for information on eligibility and treatment options.

Vet Centers in VISN 20

Vet Centers in VISN 20 are community-based counseling centers that provide a wide range of social and psychological services, including professional readjustment counseling to eligible Veterans, active-duty Army, Navy, Marine Corp, Air Force, Space Force, and Coast Guard service members, including National Guard and Reserve components, and their families. 1-877-927-8387 is an around the clock confidential call center where combat Veterans and their families can call to talk about their military experience or any other issue they are facing in their readjustment to civilian life. The staff is comprised of combat Veterans from several eras as well as families members of combat Veterans. This benefit is prepaid through the Veteran’s military service.

Alaska

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Washington

Plan your trip to VA

In 1946, Veterans Canteen Service (VCS) was established by law to provide comfort and well-being to America’s Veterans. With our many retail stores, cafés and coffee shops across the country, we serve those who have served our country. We are a self-sustaining entity providing merchandise and services to Veterans enrolled in VA’s healthcare system, their families, caregivers, VA employees, volunteers and visitors. We are honored to give back to the VA community through many programs established for the health and well-being of our nation’s heroes. Revenues generated from VCS are used to support a variety of programs, such as VA’s Rehabilitation Games, Fisher Houses, Poly-Trauma Centers for OIF/OEF/OND Veterans, disaster relief efforts, Substance Abuse Cessation, VA’s Homelessness initiatives, Women Veterans, Veteran Suicide Prevention and other activities.

Hospital Service Directory

To find out whether there is a van near you use the Disabled American Veterans (DAV) Hospital Service Coordinator Directory to contact your nearest HSC for information or assistance. Please remember that the DAV Transportation Network is staffed by volunteers; therefore, it is unable to cover every community. The vans are driven by volunteers, and the rides coordinated by more than 133 Hospital Service Coordinators around the country. Our nation’s heroes travel around the globe to protect our freedoms—it’s only right that we return their dedication. Volunteering to drive a Vet ensures that even those living remotely from VA hospitals can make their appointments and never go without the treatment they need. Learn more about the DAV transportation network through the VISN 20 NewsFlash Resources section.

Today's VHA - the largest of the three administrations that comprise the VA - continues to meet Veterans' changing medical, surgical, and quality-of-life needs. VHA is the largest integrated health care system in the United States, providing care at 1,321 health care facilities, including 172 VA Medical Centers and 1,138 outpatient sites of care of varying complexity (VHA outpatient clinics) to over 9 million Veterans enrolled in the VA health care program. There are 18 Veterans Integrated Service Networks (VISNs) in VHA operating as regional systems of care to better meet local health care needs and provides greater access to care. In the Pacific Northwest, VISN 20 serves Veterans in Alaska, Oregon, Washington, most of Idaho, and one county each in California and Montana. Spanning 23% of the US land mass, VISN 20 is the largest geographic region of VA. Operating across three time zones over 817,417 square miles, VISN 20 is home to 273 federally recognized American Indian and Alaskan Native tribes. According to DoD, American Indians and Alaska Natives have one of the highest representations in the United States Armed Forces. VA consults with American Indian and Alaska Native tribal governments to develop partnerships that enhance access to services and benefits by Veterans and their families. VA is committed to ensuring that Native American Veterans and their families are able to utilize all benefits and services they are entitled to receive. As of the end of FY2024, 39% of VISN 20 enrollees resided in rural or highly rural areas.

Community Care (Mission Act)

The MISSION Act became law in 2018, bringing the VA’s previous Veterans Choice Program to an end and establishing the Community Care Program. VA provides health care for Veterans from providers in your local community outside of VA. Veterans may be eligible to receive care from a community provider when VA cannot provide the care needed. This care is provided on behalf of and paid for by VA. Community care is also available to Veterans based on certain conditions and eligibility requirements, and in consideration of a Veteran’s specific needs and circumstances. VA offers urgent care services to eligible Veterans at in-network urgent care clinics to treat minor injuries and illnesses that are not life-threatening, such as colds, strep throat, sprained muscles, and skin and ear infections. Community care must be first authorized by VA before a Veteran can receive care from a community provider.

Browse facilities by state

VA Puget Sound Health Care System (VAPSHCS) serves Veterans from a five-state area in the Pacific Northwest with two main divisions: American Lake VA Medical Center and Seattle VA Medical Center. Veterans Medical Centers are also located in Spokane, Vancouver, and Walla Walla. VA Outpatient Clinics and Vet Centers are located in Bellingham, Bellevue, Bremerton, Edmunds, Everett, Federal Way, Lacey, Mount Vernon, Olympia, Port Angeles, Puyallup, Richland, Renton, Silverdale, Seattle, Spokane, Union Gap, Vancouver, Walla Walla, Wenatchee, and Yakima.

VA Portland Health Care System (VAPORHCS) serves Veterans in Oregon and Southwest Washington with two main divisions: Portland VA Medical Center and Vancouver VA Medical Center. Veterans Medical Centers are also located in Roseburg, White City, and Vancouver, Washington. VA Outpatient Clinics and Vet Centers are located in Astoria, Bend, Boardman, Brookings, Eugene, Fairview, Grants Pass, Hines, Hillsboro, Klamath Falls, LaGrande, Lincoln City, Newport, Portland, Salem, The Dalles, and West Linn.