Mallhi, A. K., Kiely, K., Roy, V., Ovchinsky, N., Woo Baidal, J. A., Rochani, H., & Zhang, J. (2025). The change of alanine aminotransferase distributions among US youths, NHANES 1988–2020. Journal of Pediatric Gastroenterology and Nutrition. Portico. https://doi.org/10.1002/jpn3.12460

Kraal, A. Z., McFarlane, H. V., Pyne, J. D., Turney, I. C., Lao, P. J., Mazen, J., Brickman, A. M., & Manly, J. J. (2024). Does socioeconomic status modify the association between glycemic level and MRI markers of ADRD risk in middle‐aged adults? Alzheimer’s & Dementia, 20(S9). Portico. https://doi.org/10.1002/alz.094021

Sourander, A., Silwal, S., Surcel, H.-M., Hinkka-Yli-Salomäki, S., Cheslack-Postava, K., Upadhyaya, S., McKeague, I. W., & Brown, A. S. (2025). Maternal vitamin B12 during pregnancy and schizophrenia in offspring. Psychiatry Research, 344, 116284. https://doi.org/10.1016/j.psychres.2024.116284

VandeBunte, A. M., Lee, H., Paolillo, E. W., Hsiung, G. R., Staffaroni, A. M., Saloner, R., Tartaglia, C., Yaffe, K., Knopman, D. S., Ramos, E. M., Rascovsky, K., Bozoki, A. C., Wong, B., Domoto‐Reilly, K., Snyder, A., Pressman, P., Mendez, M. F., Litvan, I., … Fields, J. A. (2024). Better cardiovascular health is associated with slowed clinical progression in autosomal dominant frontotemporal lobar degeneration variant carriers. Alzheimer’s & Dementia. Portico. https://doi.org/10.1002/alz.14172

Chen, Q., Aguirre, L., Liang, G., Zhao, H., Dong, T., Borrego, F., de Rojas, I., Hu, Q., Reyes, C., Su, L.-Y., Zhang, B., Lechleiter, J. D., Göring, H. H. H., De Jager, P. L., Kleinman, J. E., Hyde, T. M., Li, P. P., Ruiz, A., Weinberger, D. R., … Ma, L. (2024). Identification of a specific APOE transcript and functional elements associated with Alzheimer’s disease. Molecular Neurodegeneration, 19(1). https://doi.org/10.1186/s13024-024-00751-7

Carter, R. C. (2024). The critical need for novel precision medicine methodologies in fetal alcohol spectrum disorders. The American Journal of Clinical Nutrition, 119(1), 5–6. https://doi.org/10.1016/j.ajcnut.2023.10.027

Yang, H., Mukherjee, S., Latimer, C. S., Teng, L., White, C. C., Yu, L., Sperling, R. A., Larson, E. B., Crane, P. K., Keene, C. D., Bennett, D. A. A., Schneider, J. A., & De Jager, P. L. (2023). A genome‐wide association study of LATE‐NC (limbic‐predominant age‐related TDP‐43 encephalopathy neuropathologic change) reveals a distinct genetic architecture. Alzheimer’s & Dementia, 19(S12). Portico. https://doi.org/10.1002/alz.079393

Mann, J. J., Hur, K., Lavigne, J. E., & Gibbons, R. D. (2023). Folic acid prescription and suicide attempt prevention: effect of past suicidal behaviour, psychiatric diagnosis and psychotropic medication. BJPsych Open, 9(5). https://doi.org/10.1192/bjo.2023.549

Martinez-Calle, M., Courbon, G., Hunt-Tobey, B., Francis, C., Spindler, J., Wang, X., dos Reis, L. M., Martins, C. S. W., Salusky, I. B., Malluche, H., Nickolas, T. L., Moyses, R. M. A., Martin, A., & David, V. (2023). Transcription factor HNF4α2 promotes osteogenesis and prevents bone abnormalities in mice with renal osteodystrophy. Journal of Clinical Investigation, 133(11). https://doi.org/10.1172/jci159928

Monfrini, E., Pesini, A., Biella, F., Sobreira, C. F. R., Emmanuele, V., Brescia, G., Lopez, L. C., Tadesse, S., Hirano, M., Comi, G. P., Quinzii, C. M., & Di Fonzo, A. (2023). Whole-Exome Sequencing Study of Fibroblasts Derived From Patients With Cerebellar Ataxia Referred to Investigate CoQ10 Deficiency. Neurology Genetics, 9(2). https://doi.org/10.1212/nxg.0000000000200058

Zhu, J., Chen, C., Lu, L., Shikany, J. M., D’Alton, M. E., & Kahe, K. (2023). Folate, Vitamin B6, and Vitamin B12Status in Association With Metabolic Syndrome Incidence. JAMA Network Open, 6(1), e2250621. https://doi.org/10.1001/jamanetworkopen.2022.50621

Caspa Gokulan, R., Paulrasu, K., Azfar, J., El-Rifai, W., Que, J., Boutaud, O. G., Ban, Y., Gao, Z., Buitrago, M. G., Dikalov, S. I., & Zaika, A. I. (2023). Protein adduction causes non-mutational inhibition of p53 tumor suppressor. Cell Reports, 42(1), 112024. https://doi.org/10.1016/j.celrep.2023.112024

Moore, A., Busch, M. P., Dziewulska, K., Francis, R. O., Hod, E. A., Zimring, J. C., D’Alessandro, A., & Page, G. P. (2022). Genome-wide metabolite quantitative trait loci analysis (mQTL) in red blood cells from volunteer blood donors. Journal of Biological Chemistry, 298(12), 102706. https://doi.org/10.1016/j.jbc.2022.102706

Oussalah, A., Siblini, Y., Hergalant, S., Chéry, C., Rouyer, P., Cavicchi, C., Guerrini, R., Morange, P.-E., Trégouët, D., Pupavac, M., Watkins, D., Pastinen, T., Chung, W. K., Ficicioglu, C., Feillet, F., Froese, D. S., Baumgartner, M. R., Benoist, J.-F., Majewski, J., … Guéant, J.-L. (2022). Epimutations in both the TESK2 and MMACHC promoters in the Epi-cblC inherited disorder of intracellular metabolism of vitamin B12. Clinical Epigenetics, 14(1). https://doi.org/10.1186/s13148-022-01271-1

Tahir, U. A., Katz, D. H., Avila-Pachecho, J., Bick, A. G., Pampana, A., Robbins, J. M., Yu, Z., Chen, Z.-Z., Benson, M. D., Cruz, D. E., Ngo, D., Deng, S., Shi, X., Zheng, S., Eisman, A. S., Farrell, L., Hall, M. E., Correa, A., Tracy, R. P., … Gerszten, R. E. (2022). Whole Genome Association Study of the Plasma Metabolome Identifies Metabolites Linked to Cardiometabolic Disease in Black Individuals. Nature Communications, 13(1). https://doi.org/10.1038/s41467-022-32275-3

Subbanna, S., & Basavarajappa, B. S. (2022). Binge-like Prenatal Ethanol Exposure Causes Impaired Cellular Differentiation in the Embryonic Forebrain and Synaptic and Behavioral Defects in Adult Mice. Brain Sciences, 12(6), 793. https://doi.org/10.3390/brainsci12060793

Ullal, J., Kutney, K., Williams, K. M., & Weber, D. R. (2022). Treatment of cystic fibrosis related bone disease. Journal of Clinical & Translational Endocrinology, 27, 100291. https://doi.org/10.1016/j.jcte.2021.100291

Paolino, J. D., Flamand, Y., Stevenson, K. E., Koch, V., Athale, U. H., Cole, P. D., Gennarini, L. M., Kahn, J. M., Kelly, K. M., Laverdiere, C., Leclerc, J.-M., Michon, B., Place, A. E., Supko, J. G., Tran, T. H., Welch, J. J. G., Neuberg, D. S., Sallan, S. E., Silverman, L. B., & Vrooman, L. M. (2021). Impact of Age, Body Surface Area, and Body Mass Index on Pegaspargase Toxicity and Pharmacokinetics: A Report from the DFCI ALL Consortium. Blood, 138(Supplement 1), 3396–3396. https://doi.org/10.1182/blood-2021-151313

Walters, M. C., Tisdale, J. F., Mapara, M. Y., Krishnamurti, L., Kwiatkowski, J. L., Aygun, B., Kasow, K. A., Rifkin-Zenenberg, S., Jaroscak, J., Garbinsky, D., Chirila, C., Gallagher, M. E., Zhang, X., Ho, P.-R., Thompson, A. A., & Kanter, J. (2021). Sustained Improvements in Patient-Reported Quality of Life up to 24 Months Post-Treatment with LentiGlobin for Sickle Cell Disease (bb1111) Gene Therapy. Blood, 138(Supplement 1), 7–7. https://doi.org/10.1182/blood-2021-146905

Towheed, A., Hietanen, C. L., Kamath, V. G., Singh, L. N., Ho, A., Engelstad, K., Cornett, K., Montes, J., & De Vivo, D. (2021). Hypotonia–cystinuria 2p21 deletion syndrome: Intrafamilial variability of clinical expression. Annals of Clinical and Translational Neurology, 8(11), 2199–2204. Portico. https://doi.org/10.1002/acn3.51464