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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, 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 |
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2023 Journal Article Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participantsGarcia-Marin, Luis M., Mulcahy, Aoibhe, Byrne, Enda M., Medland, Sarah E., Wray, Naomi R., Chafota, Freddy, Lind, Penelope A., Martin, Nicholas G., Hickie, Ian B., Rentería, Miguel E. and Campos, Adrian I. (2023). Discontinuation of antidepressant treatment: a retrospective cohort study on more than 20,000 participants. Annals of General Psychiatry, 22 (1) 49, 1-8. doi: 10.1186/s12991-023-00480-z |
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2023 Journal Article Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association studyRizig, Mie, Bandres-Ciga, Sara, Makarious, Mary B, Ojo, Oluwadamilola Omolara, Crea, Peter Wild, Abiodun, Oladunni Victoria, Levine, Kristin S, Abubakar, Sani Atta, Achoru, Charles Obiora, Vitale, Dan, Adeniji, Olaleye Akinmola, Agabi, Osigwe Paul, Koretsky, Mathew J, Agulanna, Uchechi, Hall, Deborah A, Akinyemi, Rufus Olusola, Xie, Tao, Ali, Mohammed Wulgo, Shamim, Ejaz A, Ani-Osheku, Ifeyinwa, Padmanaban, Mahesh, Arigbodi, Ohwotemu Michael, Standaert, David G, Bello, Abiodun Hamzat, Dean, Marissa N, Erameh, Cyril Oshomah, Elsayed, Inas, Farombi, Temitope Hannah, Okunoye, Olaitan ... Tavadyan, Zaruhi (2023). Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study. The Lancet Neurology, 22 (11), 1015-1025. doi: 10.1016/S1474-4422(23)00283-1 |
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2023 Journal Article Estimating the genetic contribution to astigmatism and myopia in the Mexican populationRomán-López, Talía V., García-Vilchis, Brisa, Murillo-Lechuga, Vanessa, Chiu-Han, Enrique, López-Camaño, Xanat, Aldana-Assad, Oscar, Diaz-Torres, Santiago, Caballero-Sánchez, Ulises, Ortega-Mora, Ivett, Ramírez-González, Diego, Zenteno, Diego, Espinosa-Valdés, Zaida, Tapia-Atilano, Andrea, Pradel-Jiménez, Sofía, Rentería, Miguel E., Medina-Rivera, Alejandra, Ruiz-Contreras, Alejandra E. and Alcauter, Sarael (2023). Estimating the genetic contribution to astigmatism and myopia in the Mexican population. Twin Research and Human Genetics, 26 (4-5), 1-9. doi: 10.1017/thg.2023.41 |
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2023 Journal Article Associations of comorbid substance use disorders with clinical outcomes in schizophrenia using electronic health record dataPatel, Rashmi, Chan, Kelly M.Y., Palmer, Emily O.C., Valko, Matthew, Guruswamy, Guruprabha, Ker, Sheryl, Batra, Gunjan, Rentería, Miguel E. and Kollins, Scott H. (2023). Associations of comorbid substance use disorders with clinical outcomes in schizophrenia using electronic health record data. Schizophrenia Research, 260, 191-197. doi: 10.1016/j.schres.2023.08.023 |
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2023 Journal Article GWAS meta-analysis of suicide attempt: identification of 12 genome-wide significant loci and implication of genetic risks for specific health factorsDocherty, Anna R., Mullins, Niamh, Ashley-Koch, Allison E., Qin, Xuejun, Coleman, Jonathan R.I., Shabalin, Andrey, Kang, JooEun, Murnyak, Balasz, Wendt, Frank, Adams, Mark, Campos, Adrian I., DiBlasi, Emily, Fullerton, Janice M., Kranzler, Henry R., Bakian, Amanda V., Monson, Eric T., Rentería, Miguel E., Walss-Bass, Consuelo, Andreassen, Ole A., Behera, Chittaranjan, Bulik, Cynthia M., Edenberg, Howard J., Kessler, Ronald C., Mann, J. John, Nurnberger, John I., Pistis, Giorgio, Streit, Fabian, Ursano, Robert J., Polimanti, Renato ... German Borderline Genomics Consortium (2023). GWAS meta-analysis of suicide attempt: identification of 12 genome-wide significant loci and implication of genetic risks for specific health factors. American Journal of Psychiatry, 180 (10), 723-738. doi: 10.1176/appi.ajp.21121266 |
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2023 Journal Article Associations of polygenic risk scores for smoking heaviness and lifetime cannabis use with tobacco and cannabis co-use trajectories among African AmericansRabinowitz, Jill A., Reboussin, Beth A., Sosnowski, David W., Kuo, Sally I-Chun, Strickland, Justin C., García-Marín, Luis M., Rentería, Miguel E., Gillespie, Nathan, Maher, Brion, Ialongo, Nicholas S., Thorpe, Roland J. and Uhl, George (2023). Associations of polygenic risk scores for smoking heaviness and lifetime cannabis use with tobacco and cannabis co-use trajectories among African Americans. Drug and Alcohol Dependence, 250 110895, 1-8. doi: 10.1016/j.drugalcdep.2023.110895 |
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2023 Journal Article Editorial: data mining and statistical methods for knowledge discovery in diseases based on multimodal omics, volume IIWang, Tao, Rentería, Miguel E., Tian, Zhen and Peng, Jiajie (2023). Editorial: data mining and statistical methods for knowledge discovery in diseases based on multimodal omics, volume II. Frontiers in Genetics, 14 1270862, 1-3. doi: 10.3389/fgene.2023.1270862 |
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2023 Journal Article Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk lociHan, Xikun, Gharahkhani, Puya, Hamel, Andrew R., Ong, Jue Sheng, Rentería, Miguel E., Mehta, Puja, Dong, Xianjun, Pasutto, Francesca, Hammond, Christopher, Young, Terri L., Hysi, Pirro, Lotery, Andrew J., Jorgenson, Eric, Choquet, Hélène, Hauser, Michael, Cooke Bailey, Jessica N., Nakazawa, Toru, Akiyama, Masato, Shiga, Yukihiro, Fuller, Zachary L., Wang, Xin, Hewitt, Alex W., Craig, Jamie E., Pasquale, Louis R., Mackey, David A., Wiggs, Janey L., Khawaja, Anthony P., Segrè, Ayellet V., MacGregor, Stuart ... International Glaucoma Genetics Consortium (2023). Large-scale multitrait genome-wide association analyses identify hundreds of glaucoma risk loci. Nature Genetics, 55 (7), 1116-1125. doi: 10.1038/s41588-023-01428-5 |
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2023 Journal Article Genetic overlap between cortical brain morphometry and frontotemporal dementia riskDiaz-Torres, Santiago, Ogonowski, Natalia, García-Marín, Luis M., Bonham, Luke W., Duran-Aniotz, Claudia, Yokoyama, Jennifer S. and Rentería, Miguel E. (2023). Genetic overlap between cortical brain morphometry and frontotemporal dementia risk. Cerebral Cortex, 33 (12), 7428-7435. doi: 10.1093/cercor/bhad049 |
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2023 Journal Article Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease riskGarcía-Marín, Luis M., Reyes-Pérez, Paula, Diaz-Torres, Santiago, Medina-Rivera, Alejandra, Martin, Nicholas G., Mitchell, Brittany L. and Rentería, Miguel E. (2023). Shared molecular genetic factors influence subcortical brain morphometry and Parkinson’s disease risk. npj Parkinson's Disease, 9 (1) 73, 73. doi: 10.1038/s41531-023-00515-y |
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2023 Journal Article Causal associations of sleep apnea, snoring with cardiovascular diseases, and the role of body mass index: a two-sample Mendelian randomization studyWang, Jiao, Campos, Adrian I., Rentería, Miguel E. and Xu, Lin (2023). Causal associations of sleep apnea, snoring with cardiovascular diseases, and the role of body mass index: a two-sample Mendelian randomization study. European Journal of Preventive Cardiology, 30 (7), 552-560. doi: 10.1093/eurjpc/zwad005 |
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2023 Journal Article Genetic impact of blood C-reactive protein levels on chronic spinal and widespread painFarrell, Scott F., Sterling, Michele, Klyne, David M., Mustafa, Sanam, Campos, Adrián I., Kho, Pik-Fang, Lundberg, Mischa, Rentería, Miguel E., Ngo, Trung Thanh and Cuéllar-Partida, Gabriel (2023). Genetic impact of blood C-reactive protein levels on chronic spinal and widespread pain. European Spine Journal, 32 (6), 2078-2085. doi: 10.1007/s00586-023-07711-7 |
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2023 Journal Article Life engagement improvement following initiation of brexpiprazole treatment in patients with mdd: a naturalistic, retrospective real-world studyWee, Soon Nan, Liman, Christian, Waters, Heidi C., Houle, Christy R., Renteria, Miguel, Mukherjee, Sankha S, Surendran, Subina, Marcovici, Joshua, Brubaker, Malaak, Rasmussen Meehan, Stine, de Jong-Laird, Anne, Rush, A John and Sarkar, Joydeep (2023). Life engagement improvement following initiation of brexpiprazole treatment in patients with mdd: a naturalistic, retrospective real-world study. ClinicoEconomics and Outcomes Research, 15, 195-208. doi: 10.2147/ceor.s395255 |
