Dahal, P., Rauhala, O. J., Khodagholy, D., & Gelinas, J. N. (2023). Hippocampal–cortical coupling differentiates long-term memory processes. Proceedings of the National Academy of Sciences, 120(7). https://doi.org/10.1073/pnas.2207909120

Palmer, E. E., Pusch, M., Picollo, A., Forwood, C., Nguyen, M. H., Suckow, V., Gibbons, J., Hoff, A., Sigfrid, L., Megarbane, A., Nizon, M., Cogné, B., Beneteau, C., Alkuraya, F. S., Chedrawi, A., Hashem, M. O., Stamberger, H., Weckhuysen, S., Vanlander, A., … Kalscheuer, V. M. (2022). Functional and clinical studies reveal pathophysiological complexity of CLCN4-related neurodevelopmental condition. Molecular Psychiatry, 28(2), 668–697. https://doi.org/10.1038/s41380-022-01852-9

McGee, S. R., Rajamanickam, S., Adhikari, S., Falayi, O. C., Wilson, T. A., Shayota, B. J., Cooley Coleman, J. A., Skinner, C., Caylor, R. C., Stevenson, R. E., Quaio, C. R. D. A. C., Wilke, B. C., Bain, J. M., Anyane-Yeboa, K., Brown, K., Greally, J. M., Bijlsma, E. K., Ruivenkamp, C. A. L., Politi, K., … Jensik, P. J. (2022). Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders. Human Molecular Genetics, 32(3), 386–401. https://doi.org/10.1093/hmg/ddac200

Bianco, C., Sania, A., Kyle, M. H., Beebe, B., Barbosa, J., Bence, M., Coskun, L., Fields, A., Firestein, M. R., Goldman, S., Hane, A., Hott, V., Hussain, M., Hyman, S., Lucchini, M., Marsh, R., Mollicone, I., Myers, M., Ofray, D., … Amso, D. (2022). Pandemic beyond the virus: maternal COVID-related postnatal stress is associated with infant temperament. Pediatric Research, 93(1), 253–259. https://doi.org/10.1038/s41390-022-02071-2

Shen, M. Y., & Heshmati, A. (2023). Capsular Warning Syndrome Leading to Acute Ischemic Stroke in a Pediatric Patient Secondary to Varicella Zoster Virus. Child Neurology Open, 10, 2329048X2211499. https://doi.org/10.1177/2329048x221149961

Khodagholy, D., Ferrero, J. J., Park, J., Zhao, Z., & Gelinas, J. N. (2022). Large-scale, closed-loop interrogation of neural circuits underlying cognition. Trends in Neurosciences, 45(12), 968–983. https://doi.org/10.1016/j.tins.2022.10.003

Bain, J. M., Snyder, L. G., Helbig, K. L., Cooper, D. D., Chung, W. K., & Goodspeed, K. (2022). Consistency of parent-report SLC6A1 data in Simons Searchlight with Provider-Based Publications. Journal of Neurodevelopmental Disorders, 14(1). https://doi.org/10.1186/s11689-022-09449-7

Vitale, F., Gelinas, J. N., & Cabrera, L. Y. (2022). Neurotechnology: Bridging the dialogue between engineers, material scientists, clinicians, and ethicists. IScience, 25(11), 105432. https://doi.org/10.1016/j.isci.2022.105432

Chiriboga, C. A. (2022). Pharmacotherapy for Spinal Muscular Atrophy in Babies and Children: A Review of Approved and Experimental Therapies. Pediatric Drugs, 24(6), 585–602. https://doi.org/10.1007/s40272-022-00529-8

Tobochnik, S., Bateman, L. M., Akman, C. I., Anbarasan, D., Bazil, C. W., Bell, M., Choi, H., Feldstein, N. A., Kent, P. F., McBrian, D., McKhann, G. M., Mendiratta, A., Pack, A. M., Sands, T. T., Sheth, S. A., Srinivasan, S., & Schevon, C. A. (2021). Tracking Multisite Seizure Propagation Using Ictal High-Gamma Activity. Journal of Clinical Neurophysiology, 39(7), 592–601. https://doi.org/10.1097/wnp.0000000000000833

Lee, B. H., Deng, S., Chiriboga, C. A., Kay, D. M., Irumudomon, O., Laureta, E., Delfiner, L., Treidler, S. O., Anziska, Y., Sakonju, A., Kois, C., Farooq, O., Engelstad, K., Laurenzano, A., Hogan, K., Caggana, M., Saavedra-Matiz, C. A., Stevens, C. F., & Ciafaloni, E. (2022). Newborn Screening for Spinal Muscular Atrophy in New York State. Neurology, 99(14). https://doi.org/10.1212/wnl.0000000000200986

Hassan, A. R., Zhao, Z., Ferrero, J. J., Cea, C., Jastrzebska‐Perfect, P., Myers, J., Asman, P., Ince, N. F., McKhann, G., Viswanathan, A., Sheth, S. A., Khodagholy, D., & Gelinas, J. N. (2022). Translational Organic Neural Interface Devices at Single Neuron Resolution. Advanced Science, 9(27). Portico. https://doi.org/10.1002/advs.202202306

Lai, D., Gade, M., Yang, E., Koh, H. Y., Lu, J., Walley, N. M., Buckley, A. F., Sands, T. T., Akman, C. I., Mikati, M. A., McKhann, G. M., Goldman, J. E., Canoll, P., Alexander, A. L., Park, K. L., Von Allmen, G. K., Rodziyevska, O., Bhattacharjee, M. B., Lidov, H. G. W., … Heinzen, E. L. (2022). Somatic variants in diverse genes leads to a spectrum of focal cortical malformations. Brain, 145(8), 2704–2720. https://doi.org/10.1093/brain/awac117

Thakur, K. T., Chu, V. T., Hughes, C., Kim, C. Y., Fleck-Derderian, S., Barrett, C. E., Matthews, E., Balbi, A., Bilski, A., Chomba, M., Lieberman, O., Jacobson, S. D., Agarwal, S., Roh, D., Park, S., Ssonko, V., Silver, W. G., Vargas, W. D., Geneslaw, A., … Sejvar, J. (2022). Risk Factors for New Neurologic Diagnoses in Hospitalized Patients With COVID-19. Neurology Clinical Practice, 12(4). https://doi.org/10.1212/cpj.0000000000200006

Strauss, K. A., Farrar, M. A., Muntoni, F., Saito, K., Mendell, J. R., Servais, L., McMillan, H. J., Finkel, R. S., Swoboda, K. J., Kwon, J. M., Zaidman, C. M., Chiriboga, C. A., Iannaccone, S. T., Krueger, J. M., Parsons, J. A., Shieh, P. B., Kavanagh, S., Tauscher-Wisniewski, S., McGill, B. E., & Macek, T. A. (2022). Onasemnogene abeparvovec for presymptomatic infants with two copies of SMN2 at risk for spinal muscular atrophy type 1: the Phase III SPR1NT trial. Nature Medicine, 28(7), 1381–1389. https://doi.org/10.1038/s41591-022-01866-4

Strauss, K. A., Farrar, M. A., Muntoni, F., Saito, K., Mendell, J. R., Servais, L., McMillan, H. J., Finkel, R. S., Swoboda, K. J., Kwon, J. M., Zaidman, C. M., Chiriboga, C. A., Iannaccone, S. T., Krueger, J. M., Parsons, J. A., Shieh, P. B., Kavanagh, S., Wigderson, M., Tauscher-Wisniewski, S., … Macek, T. A. (2022). Onasemnogene abeparvovec for presymptomatic infants with three copies of SMN2 at risk for spinal muscular atrophy: the Phase III SPR1NT trial. Nature Medicine, 28(7), 1390–1397. https://doi.org/10.1038/s41591-022-01867-3

Pouliopoulos, A. N., Murillo, M. F., Noel, R. L., Batts, A. J., Ji, R., Kwon, N., Yu, H., Tong, C.-K., Gelinas, J. N., Araghy, D. K., Hussaini, S. A., & Konofagou, E. E. (2022). Non-invasive optogenetics with ultrasound-mediated gene delivery and red-light excitation. Brain Stimulation, 15(4), 927–941. https://doi.org/10.1016/j.brs.2022.06.007

Park, D. K., Kim, W., Thornburg, O. S., McBrian, D. K., McKhann, G. M., Feldstein, N. A., Maddocks, A. B., Gonzalez, E., Shen, M. Y., Akman, C., & Provenzano, F. A. (2022). Convolutional neural network‐aided tuber segmentation in tuberous sclerosis complex patients correlates with electroencephalogram. Epilepsia, 63(6), 1530–1541. Portico. https://doi.org/10.1111/epi.17227

Emmanuele, V., Ganesh, J., Vladutiu, G., Haas, R., Kerr, D., Saneto, R. P., Cohen, B. H., Van Hove, J. L. K., Scaglia, F., Hoppel, C., Rosales, X. Q., Barca, E., Buchsbaum, R., Thompson, J. L., DiMauro, S., & Hirano, M. (2022). Time to harmonize mitochondrial syndrome nomenclature and classification: A consensus from the North American Mitochondrial Disease Consortium (NAMDC). Molecular Genetics and Metabolism, 136(2), 125–131. https://doi.org/10.1016/j.ymgme.2022.05.001

Shuffrey, L. C., Firestein, M. R., Kyle, M. H., Fields, A., Alcántara, C., Amso, D., Austin, J., Bain, J. M., Barbosa, J., Bence, M., Bianco, C., Fernández, C. R., Goldman, S., Gyamfi-Bannerman, C., Hott, V., Hu, Y., Hussain, M., Factor-Litvak, P., Lucchini, M., … Dumitriu, D. (2022). Association of Birth During the COVID-19 Pandemic With Neurodevelopmental Status at 6 Months in Infants With and Without In Utero Exposure to Maternal SARS-CoV-2 Infection. JAMA Pediatrics, 176(6), e215563. https://doi.org/10.1001/jamapediatrics.2021.5563

Lines, M. A., Goldenberg, P., Wong, A., Srivastava, S., Bayat, A., Hove, H., Karstensen, H. G., Anyane‐Yeboa, K., Liao, J., Jiang, N., May, A., Guzman, E., Morleo, M., D’Arrigo, S., Ciaccio, C., Pantaleoni, C., Castello, R., McKee, S., … Dyment, D. A. (2022). Phenotypic spectrum of the recurrent TRPM3 p.(Val837Met) substitution in seven individuals with global developmental delay and hypotonia. American Journal of Medical Genetics Part A, 188(6), 1667–1675. Portico. https://doi.org/10.1002/ajmg.a.62673

Yamane, N., Snow, A. D., Fein, D., Naigles, L., & Goldman, S. (2022). Brief report: Parent-guided movements during play with children with autism spectrum disorder. Research in Autism Spectrum Disorders, 94, 101968. https://doi.org/10.1016/j.rasd.2022.101968

Aravamuthan, B. R., Shusterman, M., Green Snyder, L., Lemmon, M. E., Bain, J. M., & Gross, P. (2022). Diagnostic preferences include discussion of etiology for adults with cerebral palsy and their caregivers. Developmental Medicine & Child Neurology, 64(6), 723–733. Portico. https://doi.org/10.1111/dmcn.15164

Lippa, N., Bier, L., Revah-Politi, A., May, H., Kushary, S., Vena, N., Giordano, J. L., Rasouly, H. M., Cocchi, E., Sands, T. T., Wapner, R. J., Anyane-Yeboa, K., Gharavi, A. G., & Goldstein, D. B. (2022). Diagnostic sequencing to support genetically stratified medicine in a tertiary care setting. Genetics in Medicine, 24(4), 862–869. https://doi.org/10.1016/j.gim.2021.12.010

Wilson, J. L., Kim, Y.-M., O’Malley, J. A., Gelineau-Morel, R., Gilbert, L., Bain, J. M., & Aravamuthan, B. R. (2022). Cerebral Palsy in Child Neurology and Neurodevelopmental Disabilities Training: An Unmet Need. Journal of Child Neurology, 37(3), 194–201. https://doi.org/10.1177/08830738211072711

Fink, E. L., Robertson, C. L., Wainwright, M. S., Roa, J. D., Lovett, M. E., Stulce, C., Yacoub, M., Potera, R. M., Zivick, E., Holloway, A., Nagpal, A., Wellnitz, K., Czech, T., Even, K. M., Brunow de Carvalho, W., Rodriguez, I. S., Schwartz, S. P., Walker, T. C., Campos-Miño, S., … Schober, M. E. (2022). Prevalence and Risk Factors of Neurologic Manifestations in Hospitalized Children Diagnosed with Acute SARS-CoV-2 or MIS-C. Pediatric Neurology, 128, 33–44. https://doi.org/10.1016/j.pediatrneurol.2021.12.010

Knupp, K. G., Coryell, J., Singh, R. K., Gaillard, W. D., Shellhaas, R. A., Koh, S., Mitchell, W. G., Harini, C., Millichap, J. J., May, A., Dlugos, D., Nickels, K., Mytinger, J. R., Keator, C., Yozawitz, E., Singhal, N., Lockrow, J., Thomas, J. F., & Juarez-Colunga, E. (2022). Comparison of Cosyntropin, Vigabatrin, and Combination Therapy in New-Onset Infantile Spasms in a Prospective Randomized Trial. Journal of Child Neurology, 37(3), 186–193. https://doi.org/10.1177/08830738211073400

Kreienkamp, H.-J., Wagner, M., Weigand, H., McConkie-Rossell, A., McDonald, M., Keren, B., Mignot, C., Gauthier, J., Soucy, J.-F., Michaud, J. L., Dumas, M., Smith, R., Löbel, U., Hempel, M., Kubisch, C., Denecke, J., Campeau, P. M., Bain, J. M., & Lessel, D. (2021). Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males. Human Genetics, 141(2), 257–272. https://doi.org/10.1007/s00439-021-02412-x

Kim, W., Shen, M. Y., Provenzano, F. A., Lowenstein, D. B., McBrian, D. K., Mandel, A. M., Sands, T. T., Riviello, J. J., McKhann, G. M., Feldstein, N. A., & Akman, C. I. (2022). The role of stereo-electroencephalography to localize the epileptogenic zone in children with nonlesional brain magnetic resonance imaging. Epilepsy Research, 179, 106828. https://doi.org/10.1016/j.eplepsyres.2021.106828

Schmaedick, M. J., Midura, D., Gerall, C. D., Garey, D., Middlesworth, W., & Bain, J. M. (2022). Neurologic Complications of Extracorporeal Cardiopulmonary Resuscitation in Neonates and Infants. Child Neurology Open, 9. https://doi.org/10.1177/2329048x221114970

Ardalan, A., Yamane, N., Rao, A. K., Montes, J., & Goldman, S. (2021). Analysis of gait synchrony and balance in neurodevelopmental disorders using computer vision techniques. Health Informatics Journal, 27(4). https://doi.org/10.1177/14604582211055650

Salazar, R., Beenders, S., LaMarca, N. M., Thornburg, O., Rubin-Thompson, L., Snow, A., Goldman, S., Chung, W. K., & Bain, J. M. (2021). Cross-sectional, quantitative analysis of motor function in females with HNRNPH2-related disorder. Research in Developmental Disabilities, 119, 104110. https://doi.org/10.1016/j.ridd.2021.104110

Vasquez, A., Farias-Moeller, R., Sánchez-Fernández, I., Abend, N. S., Amengual-Gual, M., Anderson, A., Arya, R., Brenton, J. N., Carpenter, J. L., Chapman, K., Clark, J., Gaillard, W. D., Glauser, T., Goldstein, J. L., Goodkin, H. P., Guerriero, R. M., Lai, Y.-C., McDonough, T. L., … Mikati, M. A. (2021). Super-Refractory Status Epilepticus in Children: A Retrospective Cohort Study. Pediatric Critical Care Medicine, 22(12), e613–e625. https://doi.org/10.1097/pcc.0000000000002786

Lippa, N. C., Barua, S., Aggarwal, V., Pereira, E., & Bain, J. M. (2021). A novel de novo KDM5C variant in a female with global developmental delay and ataxia: a case report. BMC Neurology, 21(1). https://doi.org/10.1186/s12883-021-02380-9

White‐Brown, A. M., Lemire, G., Ito, Y. A., Thornburg, O., Bain, J. M., & Dyment, D. A. (2021). A disease‐causing variant in HNRNPH2 inherited from an unaffected mother with skewed X‐inactivation. American Journal of Medical Genetics Part A, 188(2), 668–671. Portico. https://doi.org/10.1002/ajmg.a.62549

Sheehan, T., Amengual‐Gual, M., Vasquez, A., Abend, N. S., Anderson, A., Appavu, B., Arya, R., Barcia Aguilar, C., Brenton, J. N., Carpenter, J. L., Chapman, K. E., Clark, J., Farias‐Moeller, R., Gaillard, W. D., Gaínza‐Lein, M., Glauser, T. A., Goldstein, J. L., Goodkin, H. P., … Guerriero, R. M. (2021). Benzodiazepine administration patterns before escalation to second‐line medications in pediatric refractory convulsive status epilepticus. Epilepsia, 62(11), 2766–2777. Portico. https://doi.org/10.1111/epi.17043

Gaínza‐Lein, M., Barcia Aguilar, C., Piantino, J., Chapman, K. E., Sánchez Fernández, I., Amengual‐Gual, M., Anderson, A., Appavu, B., Arya, R., Brenton, J. N., Carpenter, J. L., Clark, J., Farias‐Moeller, R., Gaillard, W. D., Glauser, T. A., Goldstein, J. L., Goodkin, H. P., Huh, L., … Kahoud, R. (2021). Factors associated with long‐term outcomes in pediatric refractory status epilepticus. Epilepsia, 62(9), 2190–2204. Portico. https://doi.org/10.1111/epi.16984

Bain, J. M., Dyer, C.-A., Galvin, M., Goldman, S., Selman, J., Silver, W. G., & Tom, S. E. (2021). How Providers in Child Neurology Transitioned to Telehealth During COVID-19 Pandemic. Child Neurology Open, 8. https://doi.org/10.1177/2329048x211022976

Cornet, M., Morabito, V., Lederer, D., Glass, H. C., Ferrao Santos, S., Numis, A. L., Ferriero, D. M., Sands, T. T., & Cilio, M. R. (2021). Neonatal presentation of genetic epilepsies: Early differentiation from acute provoked seizures. Epilepsia, 62(8), 1907–1920. Portico. https://doi.org/10.1111/epi.16957