|
2026 Journal Article Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations (npj Parkinson's Disease, (2025), 11, 1, (348), 10.1038/s41531-025-01180-z)Sun, Wenhua, Schulte, Claudia, Gasser, Thomas, Tan, Manuela, Atadzhanov, Masharip, Nguyen, Toan, Nguyen, Duan, Foroud, Tatiana, Xie, Tao, Walker, Ruth, Alcalay, Roy, Albin, Roger, Shulman, Lisa, Dean, Marissa, Ruffrage, Lauren, Chahine, Lana M., Marek, Kenneth, Markopoulou, Katerina, Kieburtz, Karl, Nuytemans, Karen, Shulman, Joshua, Inca-Martinez, Miguel, Jankovic, Joseph, Lubbe, Steven, Mencacci, Niccolò E., Sarmiento, Ignacio Juan Keller, Chen, Honglei, Beach, Thomas, Serrano, Geidy E. ... Pihlstrøm, Lasse (2026). Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations (npj Parkinson's Disease, (2025), 11, 1, (348), 10.1038/s41531-025-01180-z). npj Parkinson's Disease, 12 (1) 93. doi: 10.1038/s41531-026-01351-6 |
|
2026 Journal Article Cumulative traumatic brain injury as a predictor of Parkinson's disease with sex-related differencesLázaro-Figueroa, Alejandra, Garza-Flores, Stephanie, Reyes-Pérez, Paula, Morales De Arcia, Andrés, Esquivias, Juan, Caballero-Sánchez, Ulises, Guerra-Galicia, Carlos M., Estrada-Bellmann, Ingrid, Oropeza, Dante, Matuk-Pérez, Yamil, Morelos-Figaredo, Eugenia, Gandarilla-Martínez, Nadia A., Portillo-Sánchez, Antinea, Salinas-Barboza, Karla, López-Pintor, Araliz, Angulo-Arrieta, Ana, Nolasco-López, Miriam, Zayas-Del Moral, Alejandra, Rentería, Miguel E., Alcauter, Sarael, Hernandez-Ponce, Fatima, González-González, Mirna, Luna-Rangel, Francisco A., Medina-Rivera, Alejandra, Martinez-Ramirez, Daniel and Ruiz-Contreras, Alejandra E. (2026). Cumulative traumatic brain injury as a predictor of Parkinson's disease with sex-related differences. Parkinsonism and Related Disorders, 148 108334, 1-6. doi: 10.1016/j.parkreldis.2026.108334 |
|
2026 Journal Article Proteomic and genetic insights into ancestry‐specific associations in Parkinson's diseaseLim, Amanda Wei‐Yin, Foo, Jia‐Nee, Chew, Elaine Guo‐Yan, Lim, Shen‐Yang, Tan, Ai Huey, Hwang, Liang‐Dar, MacGregor, Stuart, Rentería, Miguel E. and Ong, Jue‐Sheng (2026). Proteomic and genetic insights into ancestry‐specific associations in Parkinson's disease. Movement Disorders, 41 (4) mds.70169, 981-991. doi: 10.1002/mds.70169 |
|
2026 Journal Article Relationship between neurologic symptoms and signs and FMR1 genotype in premutation carriersTassone, Flora, Chafota, Freddy, Renteria, Miguel E., Hagerman, Randi J., Santos, Ellery, Atkinson, Anna, Martin, Nicholas G., Storey, Elsdon and Loesch, Danuta Z. (2026). Relationship between neurologic symptoms and signs and FMR1 genotype in premutation carriers. Annals of Clinical and Translational Neurology acn3.70375. doi: 10.1002/acn3.70375 |
|
2026 Journal Article CD8+ T cells sustain vaccination-induced immunity against dissemination of contained tuberculosis in immunosuppressed hostsMiranda-Hernandez, Socorro, Kumar, Manoharan, Henderson, Alec, Graham, Erin, Tan, Xiao, Taylor, Jim, Meehan, Michael T., Ceja, Zuriel, del Pozo-Ramos, Lidia, Pan, Yi, Tsui, Ellen, Donovan, Meg L., Rentería, Miguel E., Flores-Valdez, Mario Alberto, Blumenthal, Antje, Nguyen, Quan, Subbian, Selvakumar, Field, Matt A. and Kupz, Andreas (2026). CD8+ T cells sustain vaccination-induced immunity against dissemination of contained tuberculosis in immunosuppressed hosts. Nature Communications, 17 (1) 4476, 1-17. doi: 10.1038/s41467-026-70911-4 |
|
2026 Journal Article Unique and shared internalizing and externalizing genetic factors associated with suicidal thoughts and behaviors: Findings from the adolescent brain cognitive development studyThomas, Nathaniel S., Hung, I-Tzu, Ceja, Zuriel, García-Marín, Luis M., Stephenson, Mallory, Castro-de-Araujo, Luis Silva, Lannoy, Séverine, Thorp, Jackson, Rentería, Miguel E., Edwards, Alexis C. and Rabinowitz, Jill A. (2026). Unique and shared internalizing and externalizing genetic factors associated with suicidal thoughts and behaviors: Findings from the adolescent brain cognitive development study. Journal of Affective Disorders, 397 120931, 1-11. doi: 10.1016/j.jad.2025.120931 |
|
2026 Journal Article Genome-wide assessment reveals ancestral differences in homozygosity patterns potentially linked to Parkinson's Disease etiologyStep, Kathryn, Hernández, Carlos F., Khani, Marzieh, Eltaraifee, Esraa, Hernández-Medrano, Ana Jimena, Kung, Pin-Jui, Ostrožovičová, Miriam, Zirra, Alexandra, Pérez-Palma, Eduardo, Mencacci, Niccolò E., Keller Sarmiento, Ignacio J., Morris, Huw R., Mata, Ignacio F., Acosta-Uribe, Juliana, Fang, Zih-Hua, Bandres-Ciga, Sara, Mecheri, Yasser, Sofiane, Bouchetara Mohamed, Traki, Benhassine, Gatto, Emilia Mabel, Kauffman, Marcelo, Capparelli, Federico, Muller, Maria Valentina, Tela, Marcela Susana, Adamec, Dario Sergio, Avila, Cesar, Khachatryan, Samson, Tavadyan, Zaruhi, Isayan, Mariam ... Atadzhanov, Masharip (2026). Genome-wide assessment reveals ancestral differences in homozygosity patterns potentially linked to Parkinson's Disease etiology. Movement Disorders, 41 (5), 1128-1140. doi: 10.1002/mds.70182 |
|
2026 Journal Article Insights from a cross-sectional population-based study of 10,929 Australians living with Parkinson's disease: risk factors, comorbidities, and sex differencesCao, Fangyuan, McAloney, Kerrie, Ogonowski, Natalia S., García-Marín, Luis M., Díaz-Torres, Santiago, Flores-Ocampo, Victor, Ceja, Zuriel, Chafota, Freddy, Parker, Richard, Ferguson, Mary, Cicero, Rebekah A., List-Armitage, Susan E., Miller, Vicki, Campbell, Clyde, Sue, Carolyn M., Kumar, Kishore R., Mellick, George D., Martin, Nicholas G. and Rentería, Miguel E. (2026). Insights from a cross-sectional population-based study of 10,929 Australians living with Parkinson's disease: risk factors, comorbidities, and sex differences. The Lancet Regional Health - Western Pacific, 68 101816, 1-14. doi: 10.1016/j.lanwpc.2026.101816 |
|
2026 Journal Article CRISPR screens identify PRMT7 as a therapeutic target to enhance T cell-mediated killing in breast cancerShi, Wei, Luo, Yi, Wang, Yizhuo, Burrows, Jacqueline M., Black, Debra, Civitarese, Andrew, Perlaza-Jimenez, Laura, Zhang, Ping, Manning, Murray, Tuano, Natasha, Rentería, Miguel E., Xiao, Christos, Tey, Siok-Keen, Rosenbluh, Joseph, Smith, Corey, Chenevix-Trench, Georgia and Beesley, Jonathan (2026). CRISPR screens identify PRMT7 as a therapeutic target to enhance T cell-mediated killing in breast cancer. npj Breast Cancer, 12 (1) 24. doi: 10.1038/s41523-025-00888-8 |
|
2026 Journal Article Genetic exploration of the relationship between liability to psychiatric disorders and acne vulgarisMitchell, Brittany L., Lupton, Michelle K., Rentería, Miguel E., Simpson, Michael A. and Reay, William R. (2026). Genetic exploration of the relationship between liability to psychiatric disorders and acne vulgaris. European Journal of Human Genetics, 34 (4) PMID 9302235, 565-573. doi: 10.1038/s41431-026-02028-7 |
|
2026 Journal Article Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onsetLim, Kai Shi, Periñan, Maria Teresa, Chew, Elaine Guo Yan, Lee, Paul Suhwan, Akçimen, Fulya, Lim, Jia Lun, Koretsky, Mathew J., Funayama, Manabu, Yoshino, Hiroyo, Hattori, Nobutaka, Kaiyrzhanov, Rauan, Houlden, Henry, Isayan, Mariam, Tay, Yi Wen, Toh, Tzi Shin, Lit, Lei-Cheng, Khairul Anuar, Anis Nadhirah, Ding, Hans Xing, Screven, Laurel, Ibrahim, Norlinah Mohamed, Lin, Chin-Hsien, Kim, Han-Joon, Lee, Jee-Young, Chung, Sun Ju, Foo, Jia Nee, Tan, Eng-King, Lim, Shen-Yang, Tan, Ai Huey, Bandres-Ciga, Sara ... Yan Chew, Elaine Guo (2026). Association of LRRK2 p.A419V with Parkinson’s Disease in East Asians and analysis of age at onset. npj Parkinson's Disease, 12 (1) 51. doi: 10.1038/s41531-026-01265-3 |
|
2026 Journal Article Transdiagnostic comparison of sleep measures across chronic physical and mental health disorders using FitBit data in the All of Us datasetHuang, X., Hsieh, C., Nguyen, Q., Rentería, M.E. and Gharahkhani, P. (2026). Transdiagnostic comparison of sleep measures across chronic physical and mental health disorders using FitBit data in the All of Us dataset. Sleep Medicine, 138 108633, 108633. doi: 10.1016/j.sleep.2025.108633 |
|
2026 Journal Article Genetic analysis of APOE reveals distinct origins and distribution of ancestry-enrichment haplotypes in the Mexican BiobankBarberena-Jonas, Carmina, Flores-Ocampo, Victor, Ogonowski, Natalia S., Piña-Escudero, Stefanie Danielle, Mata, Ignacio F., Yokoyama, Jennifer S., García-García, Lourdes, Aguilar Salinas, Carlos Alberto, Tusié-Luna, María Teresa, Moreno-Estrada, Andrés and Rentería, Miguel E. (2026). Genetic analysis of APOE reveals distinct origins and distribution of ancestry-enrichment haplotypes in the Mexican Biobank. Genes and Diseases, 13 (1) 101542, 1-4. doi: 10.1016/j.gendis.2025.101542 |
|
2026 Journal Article Genome-wide meta-analyses of non-response to antidepressants provide insights into underlying molecular genetics and suggest potential pharmacotherapiesKoch, Elise, Puusepp, Tuuli, Einarsson, Guðmundur, Mitchell, Brittany L., Harder, Arvid, Lin, Yuhao, García-Marín, Luis M., Krebs, Kristi, Shadrin, Alexey A., Xiong, Ying, Estonian Biobank Research Team, Metspalu, Andres, Esko, Tõnu, Mägi, Reedik, Nelis, Mari, Hudjashov, Georgi, Frei, Oleksandr, Lu, Yi, Hägg, Sara, Rentería, Miguel E., Medland, Sarah E., Wray, Naomi R., Martin, Nicholas G., Hübel, Christopher, Breen, Gerome, Thorgeirsson, Thorgeir, Stefánsson, Hreinn, Stefánsson, Kári, Lehto, Kelli ... O’Connell, Kevin S. (2026). Genome-wide meta-analyses of non-response to antidepressants provide insights into underlying molecular genetics and suggest potential pharmacotherapies. Molecular Psychiatry, 31 (4), 2005-2013. doi: 10.1038/s41380-025-03357-7 |
|
2026 Journal Article Decoding chronic pain: integrating genetics, neuroimaging, and AI for precision managementUckac, Bade, Ogonowski, Natalia S., García-Marín, Luis M., Diaz-Torres, Santiago, Farrell, Scott F., Nyholt, Dale R. and Rentería, Miguel E. (2026). Decoding chronic pain: integrating genetics, neuroimaging, and AI for precision management. Frontiers in Pain Research, 7 1747942, 7. doi: 10.3389/fpain.2026.1747942 |
|
2025 Journal Article TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populationsSun, Wenhua, Schulte, Claudia, Gasser, Thomas, Tan, Manuela, Atadzhanov, Masharip, Nguyen, Toan, Nguyen, Duan, Foroud, Tatiana, Xie, Tao, Walker, Ruth, Alcalay, Roy, Albin, Roger, Shulman, Lisa, Dean, Marissa, Ruffrage, Lauren, Chahine, Lana M., Marek, Kenneth, Markopoulou, Katerina, Kieburtz, Karl, Nuytemans, Karen, Shulman, Joshua, Inca-Martinez, Miguel, Jankovic, Joseph, Lubbe, Steven, Mencacci, Niccolò E., Sarmiento, Ignacio Juan Keller, Chen, Honglei, Beach, Thomas, Serrano, Geidy E. ... Pihlstrøm, Lasse (2025). TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations. npj Parkinson's Disease, 11 (1) 348. doi: 10.1038/s41531-025-01180-z |
|
2025 Journal Article The LRRK2 p.L1795F variant causes Parkinson’s disease in the European populationLange, Lara M., Levine, Kristin, Fox, Susan H., Marras, Connie, Ahmed, Nazish, Kuznetsov, Nicole, Vitale, Dan, Iwaki, Hirotaka, Lohmann, Katja, Marsili, Luca, Espay, Alberto J., Bauer, Peter, Beetz, Christian, Martin, Jessica, Factor, Stewart A., Higginbotham, Lenora A., Chen, Honglei, Leonard, Hampton, Nalls, Mike A., Mencacci, Niccolo E., Morris, Huw R., Singleton, Andrew B., Klein, Christine, Blauwendraat, Cornelis, Fang, Zih-Hua, Atadzhanov, Masharip, Nguyen, Toan, Nguyen, Duan, Koretsky, Mathew ... Gatto, Emilia M. (2025). The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population. npj Parkinson's Disease, 11 (1) 58. doi: 10.1038/s41531-025-00896-2 |
|
2025 Journal Article Unravelling the causal link between gut microbiota and acne risk using a genetic approachCao, Fangyuan, Ogonowski, Natalia S., Díaz-Torres, Santiago, Mitchell, Brittany L., Gharhakhani, Puya, Martin, Nicholas G., Simpson, Michael A., Ong, Jue-Sheng and Rentería, Miguel E. (2025). Unravelling the causal link between gut microbiota and acne risk using a genetic approach. Skin Health and Disease, 5 (6), 448-459. doi: 10.1093/skinhd/vzaf077 |
|
2025 Journal Article Transdiagnostic alterations in white matter microstructure associated with suicidal thoughts and behaviours in the ENIGMA Suicidal Thoughts and Behaviours consortiumvan Velzen, Laura S., Colic, Lejla, Ceja, Zuriel, Dauvermann, Maria R., Villa, Luca M., Savage, Hannah S., Toenders, Yara J., Dehestani, Niousha, Zhu, Alyssa H., Campos, Adrian I., Salminen, Lauren E., Alda, Martin, Agartz, Ingrid, Alexander, Nina, Ayesa-Arriola, Rosa, Ballard, Elizabeth D., Banaj, Nerisa, Barkhau, Carlotta, Başgöze, Zeynep, Bauer, Jochen, Benedetti, Francesco, Berger, Klaus, Besteher, Bianca, Brosch, Katharina, Canal-Rivero, Manuel, Cervenka, Simon, Colle, Romain, Connolly, Colm G., Corruble, Emmanuelle ... Schmaal, Lianne (2025). Transdiagnostic alterations in white matter microstructure associated with suicidal thoughts and behaviours in the ENIGMA Suicidal Thoughts and Behaviours consortium. Translational Psychiatry, 15 (1) 429, 1-11. doi: 10.1038/s41398-025-03602-1 |
|
2025 Journal Article Functional genomics studies of psychiatric disorders in individuals of Latin American populations: a scoping reviewPorras, Luz M., Rodríguez-Lausell, Isabelle, Iglesias-Maldonado, Gabriel, Tuliao, Emily Val F., Martínez, Gabriela, Leveque, Chelsey, Tobon, Julian, Eloy, Rachel, Belangero, Sintia, Bulik, Cynthia M., Loureiro, Camila M., Carvalho, Carolina Muniz, Ota, Vanessa, Rovaris, Diego Luiz, Storch, Eric A., Vacuan, Eva Maria Trujillo-Chi, Velasquez, Maria M., Acero González, Ángela R., Adams, Amy Maldonado, Albino, Elinette, Alliey-Rodríguez, Ney, Alvarado, Angel T., Amador, Francisco, Ambite, Jose-Luis, Andrade-Brito, Diego, Pascualli, Paola Arguello, Arnold, Paul, Atkinson, Elizabeth, Bhattacharyya, Upasana ... Giusti-Rodríguez, Paola (2025). Functional genomics studies of psychiatric disorders in individuals of Latin American populations: a scoping review. American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics, 201 (4), 227-245. doi: 10.1002/ajmg.b.33063 |
