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2024 Journal Article Parkinson's disease polygenic risk score and neurological involvement in carriers of the FMR1 premutation allele: a case for genetic modifierLoesch, Danuta Z., Chafota, Freddy, Bui, Minh Q., Storey, Elsdon, Atkinson, Anna, Martin, Nicholas G., Gordon, Scott D., Rentería, Miguel E., Hagerman, Randi J. and Tassone, Flora (2024). Parkinson's disease polygenic risk score and neurological involvement in carriers of the FMR1 premutation allele: a case for genetic modifier. Molecular Genetics and Genomic Medicine, 12 (11) e70043. doi: 10.1002/mgg3.70043 |
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2024 Journal Article Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysisDiaz-Torres, Santiago, Lee, Samantha Sze-Yee, García-Marín, Luis M., Campos, Adrian I., Lingham, Garreth, Ong, Jue-Sheng, Mackey, David A., Burdon, Kathryn P., Hunter, Michael, Dong, Xianjun, MacGregor, Stuart, Gharahkhani, Puya and Rentería, Miguel E. (2024). Uncovering genetic loci and biological pathways associated with age-related cataracts through GWAS meta-analysis. Nature Communications, 15 (1) 9116, 1-10. doi: 10.1038/s41467-024-53212-6 |
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2024 Journal Article Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestriesGarcía-Marín, Luis M., Campos, Adrian I., Diaz-Torres, Santiago, Rabinowitz, Jill A., Ceja, Zuriel, Mitchell, Brittany L., Grasby, Katrina L., Thorp, Jackson G., Agartz, Ingrid, Alhusaini, Saud, Ames, David, Amouyel, Philippe, Andreassen, Ole A., Arfanakis, Konstantinos, Arias-Vasquez, Alejandro, Armstrong, Nicola J., Athanasiu, Lavinia, Bastin, Mark E., Beiser, Alexa S., Bennett, David A., Bis, Joshua C., Boks, Marco P. M., Boomsma, Dorret I., Brodaty, Henry, Brouwer, Rachel M., Buitelaar, Jan K., Burkhardt, Ralph, Cahn, Wiepke, Calhoun, Vince D. ... Rentería, Miguel E. (2024). Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries. Nature Genetics, 56 (11), 2333-2344. doi: 10.1038/s41588-024-01951-z |
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2024 Journal Article Macular structural integrity estimates are associated with Parkinson’s disease genetic riskDiaz-Torres, Santiago, Lee, Samantha Sze-Yee, Ogonowski, Natalia S., Mackey, David A., MacGregor, Stuart, Gharahkhani, Puya and Renteria, Miguel E. (2024). Macular structural integrity estimates are associated with Parkinson’s disease genetic risk. Acta Neuropathologica Communications, 12 (1) 130, 130. doi: 10.1186/s40478-024-01841-9 |
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2024 Journal Article Building national patient registries in Mexico: insights from the MexOMICS ConsortiumReyes-Pérez, Paula, Hernández-Ledesma, Ana Laura, Román-López, Talía V., García-Vilchis, Brisa, Ramírez-González, Diego, Lázaro-Figueroa, Alejandra, Martinez, Domingo, Flores-Ocampo, Victor, Espinosa-Méndez, Ian M., Tinajero-Nieto, Lizbet, Peña-Ayala, Angélica, Morelos-Figaredo, Eugenia, Guerra-Galicia, Carlos M., Torres-Valdez, Estefania, Gordillo-Huerta, María Vanessa, Gandarilla-Martínez, Nadia A, Salinas-Barboza, Karla, Félix-Rodríguez, Guillermo, Frontana-Vázquez, Gabriel, Matuk-Pérez, Yamil, Estrada-Bellmann, Ingrid, Alpizar-Rodríguez, Deshiré, Rodríguez-Violante, Mayela, Rentería, Miguel E., Ruíz-Contreras, Alejandra E., Alcauter, Sarael and Medina-Rivera, Alejandra (2024). Building national patient registries in Mexico: insights from the MexOMICS Consortium. Frontiers in Digital Health, 6 1344103, 1-14. doi: 10.3389/fdgth.2024.1344103 |
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2024 Journal Article Genetic variants for head size share genes and pathways with cancerKnol, Maria J., Poot, Raymond A., Evans, Tavia E., Satizabal, Claudia L., Mishra, Aniket, Sargurupremraj, Muralidharan, van der Auwera, Sandra, Duperron, Marie-Gabrielle, Jian, Xueqiu, Hostettler, Isabel C., van Dam-Nolen, Dianne H.K., Lamballais, Sander, Pawlak, Mikolaj A., Lewis, Cora E., Carrion-Castillo, Amaia, van Erp, Theo G.M., Reinbold, Céline S., Shin, Jean, Scholz, Markus, Håberg, Asta K., Kämpe, Anders, Li, Gloria H.Y., Avinun, Reut, Atkins, Joshua R., Hsu, Fang-Chi, Amod, Alyssa R., Lam, Max, Tsuchida, Ami, Teunissen, Mariël W.A. ... The Enhancing NeuroImaging Genetics through Meta-Analysis (ENIGMA) Consortium (2024). Genetic variants for head size share genes and pathways with cancer. Cell Reports Medicine, 5 (5) 101529, 101529. doi: 10.1016/j.xcrm.2024.101529 |
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2024 Journal Article TwinsMX: exploring the genetic and environmental influences on health traits in the Mexican populationGarcía-Vilchis, Brisa, Román-López, Talia V., Ramírez-González, Diego, López-Camaño, Xanat J., Murillo-Lechuga, Vanessa, Díaz-Téllez, Xóchitl, Sánchez-Moncada, C. Itzamná, Espinosa-Méndez, Ian M., Zenteno-Morales, Diego, Espinosa-Valdes, Zaida X., Pradel-Jiménez, Sofia, Tapia-Atilano, Andrea, Zanabria-Pérez, Ana V., Livas-Gangas, Federica, Aldana-Assad, Oscar, Caballero-Sánchez, Ulises, Dominguez-Frausto, César A., Rentería, Miguel E., Medina-Rivera, Alejandra, Alcauter, Sarael and Ruiz-Contreras, Alejandra E. (2024). TwinsMX: exploring the genetic and environmental influences on health traits in the Mexican population. Twin Research and Human Genetics, 27 (2), 85-96. doi: 10.1017/thg.2024.18 |
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2024 Journal Article Fighting plastic pollution with a circular economy roadmap and strategy: Addressed to the United Nations Environment ProgrammeGarcía-Marín, Luis M. and Rentería, Miguel E. (2024). Fighting plastic pollution with a circular economy roadmap and strategy: Addressed to the United Nations Environment Programme. Journal of Science Policy & Governance, 24 (1), 1-11. doi: 10.38126/jspg240107 |
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2024 Journal Article Impact of genetic predisposition to late-onset neurodegenerative diseases on early life outcomes and brain structureOgonowski, Natalia S., García-Marín, Luis M., Fernando, Amali S., Flores-Ocampo, Victor and Rentería, Miguel E. (2024). Impact of genetic predisposition to late-onset neurodegenerative diseases on early life outcomes and brain structure. Translational Psychiatry, 14 (1) 185, 185. doi: 10.1038/s41398-024-02898-9 |
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2024 Journal Article Investigating the shared genetic etiology between Parkinson’s disease and depressionReyes-Pérez, Paula, García-Marín, Luis M., Aman, Asma M., Antar, Tarek, Flores-Ocampo, Victor, Mitchell, Brittany L., Medina-Rivera, Alejandra and Rentería, Miguel E. (2024). Investigating the shared genetic etiology between Parkinson’s disease and depression. Journal of Parkinson's Disease, 14 (3), 483-493. doi: 10.3233/jpd-230176 |
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2024 Journal Article Associations of externalizing polygenic scores with externalizing disorders among Mexican youthMartinez-Levy, Gabriela A., Maya-Martínez, Mateo, García-Marín, Luis M., Díaz-Torres, Santiago, Gómez, Lina M., Benjet, Corina, Rentería, Miguel E., Cruz-Fuentes, Carlos S. and Rabinowitz, Jill A. (2024). Associations of externalizing polygenic scores with externalizing disorders among Mexican youth. Journal of Psychiatric Research, 171, 346-353. doi: 10.1016/j.jpsychires.2024.01.030 |
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2024 Journal Article Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inferenceMeng, Xiangrui, Navoly, Georgina, Giannakopoulou, Olga, Levey, Daniel F., Koller, Dora, Pathak, Gita A., Koen, Nastassja, Lin, Kuang, Adams, Mark J., Rentería, Miguel E., Feng, Yanzhe, Gaziano, J. Michael, Stein, Dan J., Zar, Heather J., Campbell, Megan L., van Heel, David A., Trivedi, Bhavi, Finer, Sarah, McQuillin, Andrew, Bass, Nick, Chundru, V. Kartik, Martin, Hilary C., Huang, Qin Qin, Valkovskaya, Maria, Chu, Chia-Yi, Kanjira, Susan, Kuo, Po-Hsiu, Chen, Hsi-Chung, Tsai, Shih-Jen ... BioBank Japan Project (2024). Multi-ancestry genome-wide association study of major depression aids locus discovery, fine mapping, gene prioritization and causal inference. Nature Genetics, 56 (2), 222-233. doi: 10.1038/s41588-023-01596-4 |
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2024 Journal Article Psychometric evaluation and linking of the PHQ-9, QIDS-C, and VQIDS-C in a real-world population with major depressive disorderPalmer, Emily OC, Ker, Sheryl, Rentería, Miguel E., Carmody, Thomas and Rush, A. John (2024). Psychometric evaluation and linking of the PHQ-9, QIDS-C, and VQIDS-C in a real-world population with major depressive disorder. Neuropsychiatric Disease and Treatment, 20, 671-687. doi: 10.2147/NDT.S444223 |
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2024 Journal Article Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?Lázaro-Figueroa, Alejandra, Hernández-Medrano, Ana Jimena, Ramírez-Pineda, Diana Berenice, Navarro Cadavid, Andrés, Makarious, Mary, Foo, Jia Nee, Alvarado, Chelsea X., Bandres-Ciga, Sara, Periñan, Maria Teresa, Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie, Kumar, Kishore, Ellis, Melina, Rentería, Miguel E., Koks, Sulev, Zimprich, Alexander, Schumacher-Schuh, Artur F., Rieder, Carlos, Awad, Paula Saffie, Tumas, Vitor, Camargos, Sarah, Fon, Edward A., Monchi, Oury, Fon, Ted, Galleguillos, Benjamin Pizarro ... Atadzhanov, Masharip (2024). Is SH3GL2 p.G276V the Causal Functional Variant Underlying Parkinson's Disease Risk at this Locus?. Movement Disorders, 39 (11), 2117-2119. doi: 10.1002/mds.29719 |
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2024 Journal Article Fructose intake from sugar-sweetened beverages is associated with a greater risk of hyperandrogenism in women: UK Biobank cohort studyChen, Huadong, Buziau, Amée M., Rentería, Miguel E., Simons, Pomme I. H. G. and Brouwers, Martijn C. G. J. (2024). Fructose intake from sugar-sweetened beverages is associated with a greater risk of hyperandrogenism in women: UK Biobank cohort study. European Journal of Endocrinology, 190 (1), 104-112. doi: 10.1093/ejendo/lvae006 |
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2024 Journal Article Investigating the genetic relationship of intracranial and subcortical brain volumes with depression and other psychiatric disordersGarcía-Marín, Luis M., Ogonowski, Natalia S., Han, Laura K.M., Maya-Martínez, Mateo, Mitchell, Brittany L., Schmaal, Lianne, Martin, Nicholas G. and Rentería, Miguel E. (2024). Investigating the genetic relationship of intracranial and subcortical brain volumes with depression and other psychiatric disorders. Imaging Neuroscience, 2 imag-2-00291, 1-16. doi: 10.1162/imag_a_00291 |
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2024 Journal Article Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundityMbarek, Hamdi, Gordon, Scott D., Duffy, David L., Hubers, Nikki, Mortlock, Sally, Beck, Jeffrey J., Hottenga, Jouke-Jan, Pool, René, Dolan, Conor V., Actkins, Ky’Era V., Gerring, Zachary F., Van Dongen, Jenny, Ehli, Erik A., Iacono, William G., Mcgue, Matt, Chasman, Daniel I., Gallagher, C. Scott, Schilit, Samantha L. P., Morton, Cynthia C., Paré, Guillaume, Willemsen, Gonneke, Whiteman, David C., Olsen, Catherine M., Derom, Catherine, Vlietinck, Robert, Gudbjartsson, Daniel, Cannon-Albright, Lisa, Krapohl, Eva, Plomin, Robert ... Martin, Nicholas G. (2024). Genome-wide association study meta-analysis of dizygotic twinning illuminates genetic regulation of female fecundity. Human Reproduction, 39 (1), 240-257. doi: 10.1093/humrep/dead247 |
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2023 Journal Article Multi-ancestry genome-wide association meta-analysis of Parkinson’s diseaseKim, Jonggeol Jeffrey, Vitale, Dan, Otani, Diego Véliz, Lian, Michelle Mulan, Heilbron, Karl, Aslibekyan, Stella, Auton, Adam, Babalola, Elizabeth, Bell, Robert K., Bielenberg, Jessica, Bryc, Katarzyna, Bullis, Emily, Cannon, Paul, Coker, Daniella, Partida, Gabriel Cuellar, Dhamija, Devika, Das, Sayantan, Elson, Sarah L., Eriksson, Nicholas, Filshtein, Teresa, Fitch, Alison, Fletez-Brant, Kipper, Fontanillas, Pierre, Freyman, Will, Granka, Julie M., Hernandez, Alejandro, Hicks, Barry, Hinds, David A., Jewett, Ethan M. ... Mata, Ignacio (2023). Multi-ancestry genome-wide association meta-analysis of Parkinson’s disease. Nature Genetics, 56 (1), 27-36. doi: 10.1038/s41588-023-01584-8 |
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2023 Journal Article Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9)Lange, Lara M., Avenali, Micol, Ellis, Melina, Illarionova, Anastasia, Keller Sarmiento, Ignacio J., Tan, Ai-Huey, Madoev, Harutyun, Galandra, Caterina, Junker, Johanna, Roopnarain, Karisha, Solle, Justin, Wegel, Claire, Fang, Zih-Hua, Heutink, Peter, Kumar, Kishore R., Lim, Shen-Yang, Valente, Enza Maria, Nalls, Mike, Blauwendraat, Cornelis, Singleton, Andrew, Mencacci, Niccolo, Lohmann, Katja, Klein, Christine, Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie ... Atadzhanov, Masharip (2023). Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2) (npj Parkinson's Disease, (2023), 9, 1, (100), 10.1038/s41531-023-00526-9). npj Parkinson's Disease, 9 (1) 133. doi: 10.1038/s41531-023-00560-7 |
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2023 Journal Article Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)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., Tan, Manuela M. X., Iwaki, Hirotaka, Morris, Huw R., Gatto, Emilia M., Kauffman, Marcelo, Khachatryan, Samson, Tavadyan, Zaruhi, Shepherd, Claire E., Hunter, Julie ... Atadzhanov, Masharip (2023). Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2). npj Parkinson's Disease, 9 (1) 131. doi: 10.1038/s41531-023-00533-w |
