Tsapanou, A., Lee, S., Chapman, S., Mourtzi, N., Habeck, C., & Stern, Y. (2024). Sleep Genetics and Cognitive Changes over Time: The Moderating Effect of Age and the Role of Brain. Genes, 16(1), 21. https://doi.org/10.3390/genes16010021

Vanderscheldon, R. K., Sukov, W. R., Gardner, J.-A., Rehder, C. W., Levy, B., Velagaleti, G. V., Toydemir, R. M., Tang, G., Boles, B., Cao, Y., Mixon, C., Zou, Y. S., Astbury, C., Tsuchiya, K. D., & Peterson, J. F. (2024). Conventional Cytogenetic Analysis of Solid Tumor Abnormalities: A 25-Year Review of Proficiency Test Results from the College of American Pathologists/American College of Medical Genetics and Genomics Cytogenetics Committee. Genes, 15(12), 1612. https://doi.org/10.3390/genes15121612

Beckers, L., Rashid, M., Lee, A. J., Chatila, Z. K., Tamucci, K. A., Talcoff, R. C., Hall, J. L., Bennett, D. A., Vardarajan, B. N., & Bradshaw, E. M. (2024). CD33 and SHP-1/PTPN6 Interaction in Alzheimer’s Disease. Genes, 15(9), 1204. https://doi.org/10.3390/genes15091204

Shani, S., Gana-Weisz, M., Bar-Shira, A., Thaler, A., Gurevich, T., Mirelman, A., Giladi, N., Alcalay, R. N., Goldstein, O., & Orr-Urtreger, A. (2023). MAPT Locus in Parkinson’s Disease Patients of Ashkenazi Origin: A Stratified Analysis. Genes, 15(1), 46. https://doi.org/10.3390/genes15010046

Tsapanou, A., Gacheru, M., Lee, S., Mourtzi, N., Gazes, Y., Habeck, C., Belsky, D. W., & Stern, Y. (2023). Association of Cognitive Polygenic Index and Cognitive Performance with Age in Cognitively Healthy Adults. Genes, 14(9), 1814. https://doi.org/10.3390/genes14091814

Bi, X., Mulhern, M. S., Spiegel, E., Wapner, R. J., Levy, B., Bain, J. M., & Liao, J. (2023). 3′ UTR Deletion of FBXO28 in a Patient with Brain Abnormalities and Developmental Delay. Genes, 14(9), 1687. https://doi.org/10.3390/genes14091687

Gonzalez, J. N., Goldman, S., Carter, M. T., & Bain, J. M. (2023). Rett-like Phenotypes in HNRNPH2-Related Neurodevelopmental Disorder. Genes, 14(6), 1154. https://doi.org/10.3390/genes14061154

Juárez-Rendón, K. J., Castro-García, M. A., Prada-Ortega, D. G., Rivera, G., Ruíz-Godoy, L. M., Enríquez-Cárcamo, V. I., & Reyes-Lopez, M. A. (2023). Variants Identified in the HOXC13 and HOXD13 Genes Suggest Association with Cervical Cancer in a Cohort of Mexican Women. Genes, 14(2), 358. https://doi.org/10.3390/genes14020358

Esposito, F., Osiceanu, A. M., Sorosina, M., Ottoboni, L., Bollman, B., Santoro, S., Bettegazzi, B., Zauli, A., Clarelli, F., Mascia, E., Calabria, A., Zacchetti, D., Capra, R., Ferrari, M., Provero, P., Lazarevic, D., Cittaro, D., Carrera, P., Patsopoulos, N., … Martinelli Boneschi, F. (2022). A Whole-Genome Sequencing Study Implicates GRAMD1B in Multiple Sclerosis Susceptibility. Genes, 13(12), 2392. https://doi.org/10.3390/genes13122392

Zada, A., Ali, A., Binjawhar, D., Abdel-Hameed, U., Shah, A., Gill, S., Hussain, I., Abbas, Z., Ullah, Z., Sher, H., & Ali, I. (2022). Molecular and Physiological Evaluation of Bread Wheat (Triticum aestivum L.) Genotypes for Stay Green under Drought Stress. Genes, 13(12), 2261. https://doi.org/10.3390/genes13122261

Tawalbeh, M., Aburizeg, D., Abu Alragheb, B. O., Alaqrabawi, W. S., Dardas, Z., Srour, L., Altarayra, B. H., Zayed, A. A., El Omari, Z., & Azab, B. (2022). SLC26A4 Phenotypic Variability Influences Intra- and Inter-Familial Diagnosis and Management. Genes, 13(12), 2192. https://doi.org/10.3390/genes13122192

Azab, B., Rabab’h, O., Aburizeg, D., Mohammad, H., Dardas, Z., Mustafa, L., Khasawneh, R. A., Awad, H., Hatmal, M. M., & Altamimi, E. (2022). Potential Composite Digenic Contribution of NPC1 and NOD2 Leading to Atypical Lethal Niemann-Pick Type C with Initial Crohn’s Disease-like Presentation: Genotype-Phenotype Correlation Study. Genes, 13(6), 973. https://doi.org/10.3390/genes13060973

Cornejo-Sanchez, D. M., Acharya, A., Bharadwaj, T., Marin-Gomez, L., Pereira-Gomez, P., Nouel-Saied, L. M., Nickerson, D. A., Bamshad, M. J., Mefford, H. C., Schrauwen, I., Carrizosa-Moog, J., Cornejo-Ochoa, W., Pineda-Trujillo, N., & Leal, S. M. (2022). SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families. Genes, 13(5), 754. https://doi.org/10.3390/genes13050754

Liaqat, K., Hussain, S., Acharya, A., Nasir, A., Bharadwaj, T., Ansar, M., Basit, S., Schrauwen, I., Ahmad, W., & Leal, S. M. (2022). Phenotype Expansion for Atypical Gaucher Disease Due to Homozygous Missense PSAP Variant in a Large Consanguineous Pakistani Family. Genes, 13(4), 662. https://doi.org/10.3390/genes13040662

Kadlubowska, M. K., & Schrauwen, I. (2022). Methods to Improve Molecular Diagnosis in Genomic Cold Cases in Pediatric Neurology. Genes, 13(2), 333. https://doi.org/10.3390/genes13020333

Nagy, D., Verheyen, S., Wigby, K. M., Borovikov, A., Sharkov, A., Slegesky, V., Larson, A., Fagerberg, C., Brasch-Andersen, C., Kibæk, M., Bader, I., Hernan, R., High, F. A., Chung, W. K., Schieving, J. H., Behunova, J., Smogavec, M., Laccone, F., Witsch-Baumgartner, M., … Weis, D. (2022). Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring. Genes, 13(1), 154. https://doi.org/10.3390/genes13010154

Tsapanou, A., Mourtzi, N., Charisis, S., Hatzimanolis, A., Ntanasi, E., Kosmidis, M. H., Yannakoulia, M., Hadjigeorgiou, G., Dardiotis, E., Sakka, P., Stern, Y., & Scarmeas, N. (2021). Sleep Polygenic Risk Score Is Associated with Cognitive Changes over Time. Genes, 13(1), 63. https://doi.org/10.3390/genes13010063

Ye, Z., Mo, C., Ke, H., Yan, Q., Chen, C., Kochunov, P., Hong, L. E., Mitchell, B. D., Chen, S., & Ma, T. (2021). Meta-Analysis of Transcriptome-Wide Association Studies across 13 Brain Tissues Identified Novel Clusters of Genes Associated with Nicotine Addiction. Genes, 13(1), 37. https://doi.org/10.3390/genes13010037

Farooqi, N., Metherell, L. A., Schrauwen, I., Acharya, A., Khan, Q., Nouel Saied, L. M., Ali, Y., El-Serehy, H. A., Jalil, F., & Leal, S. M. (2021). Exome Sequencing Identifies a Novel FBN1 Variant in a Pakistani Family with Marfan Syndrome That Includes Left Ventricle Diastolic Dysfunction. Genes, 12(12), 1915. https://doi.org/10.3390/genes12121915