SFARI Gene: an evolving database for the autism research community

AutDB: a gene reference resource for autism research

Basu, S. N., Kollu, R., & Banerjee-Basu, S. (2009) · Nucleic Acids Research · doi:10.1093/nar/gkn835 · Cited by 394

Prenatal delta-9-tetrahydrocannabinol exposure is associated with changes in rhesus macaque DNA methylation enriched for autism genes

Shorey‐Kendrick, L. E., Roberts, V. H. J., D'Mello, R. J., Sullivan, E. L., Murphy, S. K., McCarty, O. J. T., Schust, D. J., Hedges, J. C., Mitchell, A. J., Terrobias, J. J. D., et al. (2023) · Clinical Epigenetics · doi:10.1186/s13148-023-01519-4 · Cited by 25

Preventable Forms of Autism?

Beaudet, A. L. (2012) · Science · doi:10.1126/science.1229178 · Cited by 24

A Consensus Network of Gene Regulatory Factors in the Human Frontal Lobe

Berto, S., Perdomo-Sabogal, Á., Wiegreffe, D., Qin, J., & Nowick, K. (2016) · Frontiers in Genetics · doi:10.3389/fgene.2016.00031 · Cited by 23

Integrated analysis of robust sex-biased gene signatures in human brain

Wapeesittipan, P., & Joshi, A. (2023) · Biology of Sex Differences · doi:10.1186/s13293-023-00515-w · Cited by 24

A comprehensive analysis towards exploring the promises of AI-related approaches in autism research

Pandya, S., Jain, S., & Verma, J. P. V. (2023) · Computers in Biology and Medicine · doi:10.1016/j.compbiomed.2023.107801 · Cited by 33

Neurocarta: aggregating and sharing disease-gene relations for the neurosciences

Portales-Casamar, É., Ch’ng, C., Lui, F., St-Georges, N., Zoubarev, A., Lai, A., Lee, M., Kwok, C., Kwok, W., Tseng, L., et al. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-129 · Cited by 26

A Foundational Atlas of Autism Protein Interactions Reveals Molecular ConvergencePreprint

Wang, B., Vartak, R. S., Zaltsman, Y., Naing, Z. Z. C., Hennick, K. M., Polacco, B. J., Bashir, A., Eckhardt, M., Bouhaddou, M., Xu, J., et al. (2023) · SSRN Electronic Journal · doi:10.1101/2023.12.03.569805 · Cited by 26

Compensation between FOXP transcription factors maintains proper striatal function

Ahmed, N. I., Khandelwal, N., Anderson, A. G., Oh, E., Vollmer, R. M., Kulkarni, A., Gibson, J. R., & Konopka, G. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114257 · Cited by 23

Ciliary biology intersects autism and congenital heart disease

Teerikorpi, N., McCluskey, K. E., Bader, E., Lasser, M. C., Wang, S., Nguyen, C. H., Schmidt, J. D., Kostyanovskaya, E., Sun, N., Dea, J., et al. (2025) · Development · doi:10.1242/dev.204295 · Cited by 22

Protein signatures of oxidative stress response in a patient specific cell line model for autism

Chiocchetti, A. G., Haslinger, D., Boesch, M., Karl, T., Wiemann, S., Freitag, C. M., Poustka, F., Scheibe, B., Bauer, J. W., Hintner, H., et al. (2014) · Molecular Autism · doi:10.1186/2040-2392-5-10 · Cited by 24

Gene-expression correlates of the oscillatory signatures supporting human episodic memory encoding

Berto, S., Fontenot, M. R., Seger, S. E., Ayhan, F., Caglayan, E., Kulkarni, A., Douglas, C., Tamminga, C. A., Lega, B. C., & Konopka, G. (2021) · Nature Neuroscience · doi:10.1038/s41593-021-00803-x · Cited by 24

Rare X-linked variants carry predominantly male risk in autism, Tourette syndrome, and ADHD

Wang, S., Wang, B., Drury, V., Drake, S., Sun, N., Alkhairo, H., Arbelaez, J., Duhn, C., Genetics), T. I. C. G. (., Bromberg, Y., et al. (2023) · Nature Communications · doi:10.1038/s41467-023-43776-0 · Cited by 26

A direct regulatory link between microRNA-137 and SHANK2: implications for neuropsychiatric disorders

Cortabitarte, A. D. S., Berkel, S., Cristian, F.-B., Fischer, C., & Rappold, G. (2018) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-018-9233-1 · Cited by 23

Using extended pedigrees to identify novel autism spectrum disorder (ASD) candidate genes

Woodbury‐Smith, M., Paterson, A. D., Thiruvahindrapduram, B., Lionel, A. C., Marshall, C. R., Merico, D., Fernandez, B. A., Duku, E., Sutcliffe, J. S., O’Conner, I., et al. (2014) · Human Genetics · doi:10.1007/s00439-014-1513-6 · Cited by 22

Autworks: a cross-disease network biology application for Autism and related disorders

Nelson, T. H., Jung, J.-Y., DeLuca, T. F., Hinebaugh, B. K., Gabriel, K. C. S., & Wall, D. P. (2012) · BMC Medical Genomics · doi:10.1186/1755-8794-5-56 · Cited by 22

brain-coX: investigating and visualising gene co-expression in seven human brain transcriptomic datasets

Freytag, S., Burgess, R., Oliver, K. L., & Bahlo, M. (2017) · Genome Medicine · doi:10.1186/s13073-017-0444-y · Cited by 20

Single-Cell RNA Sequencing Characterizes the Molecular Heterogeneity of the Larval Zebrafish Optic Tectum

Martin, A., Babbitt, A., Pickens, A. G., Pickett, B. E., Hill, J. T., & Suli, A. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.818007 · Cited by 22

Multi-View Design Patterns and Responsive Visualization for Genomics Data

L’Yi, S., & Gehlenborg, N. (2022) · IEEE Transactions on Visualization and Computer Graphics · doi:10.1109/tvcg.2022.3209398 · Cited by 24

A Brain Region-Specific Predictive Gene Map for Autism Derived by Profiling a Reference Gene Set

Kumar, A., Swanwick, C. C., Johnson, N., Menashe, I., Basu, S. N., Bales, M. E., & Banerjee‐Basu, S. (2011) · PLoS ONE · doi:10.1371/journal.pone.0028431 · Cited by 23

Curation of causal interactions mediated by genes associated with autism accelerates the understanding of gene-phenotype relationships underlying neurodevelopmental disorders

Iannuccelli, M., Vitriolo, A., Licata, L., Surdo, P. L., Contino, S., Cheroni, C., Capocefalo, D., Castagnoli, L., Testa, G., Cesareni, G., et al. (2023) · Molecular Psychiatry · doi:10.1038/s41380-023-02317-3 · Cited by 15

Synaptopathology in autism spectrum disorders: Complex effects of synaptic genes on neural circuits

Wang, X., Kéry, R., & Xiong, Q. (2017) · Progress in Neuro-Psychopharmacology and Biological Psychiatry · doi:10.1016/j.pnpbp.2017.09.026 · Cited by 24

mTOR-Dependent Spine Dynamics in Autism

Chaudry, S., & Vasudevan, N. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.877609 · Cited by 23

Convergent and distributed effects of the 3q29 deletion on the human neural transcriptome

Sefik, E., Purcell, R. H., The Emory 3q29 Project, Aberizk, K., Averbach, H., Black, E., Burrell, T. L., Cambala, S., Carlock, G., Caspary, T., et al. (2021) · Translational Psychiatry · doi:10.1038/s41398-021-01435-2 · Cited by 18

Characterization of cell-cell communication in autistic brains with single-cell transcriptomes

Astorkia, M., Lachman, H. M., & Zheng, D. (2022) · Journal of Neurodevelopmental Disorders · doi:10.1186/s11689-022-09441-1 · Cited by 19

Genetic mouse models of autism spectrum disorder present subtle heterogenous cardiac abnormalities

Assimopoulos, S., Hammill, C. F., Fernandes, D., Noakes, T. L. S., Zhou, Y., Nutter, L. M. J., Ellegood, J., Anagnostou, E. A., Sled, J. G., & Lerch, J. P. (2022) · Autism Research · doi:10.1002/aur.2728 · Cited by 19

Prenatal Sex Hormone Exposure Is Associated with the Development of Autism Spectrum Disorder

Li, M., Usui, N., & Shimada, S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24032203 · Cited by 24

The genetics of autism and steroid-related traits in prenatal and postnatal life

Tsompanidis, A., Warrier, V., & Baron‐Cohen, S. (2023) · Frontiers in Endocrinology · doi:10.3389/fendo.2023.1126036 · Cited by 21

KMT2C knockout generates ASD-like behaviors in mice

Brauer, B., Merino-Véliz, N., Ahumada-Marchant, C., Arriagada, G., & Bustos, F. J. (2023) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2023.1227723 · Cited by 18

Transcriptomic architecture of nuclei in the marmoset CNS

Lin, J., Kelly, H. M., Song, Y., Kawaguchi, R., Geschwind, D. H., Jacobson, S., & Reich, D. S. (2022) · Nature Communications · doi:10.1038/s41467-022-33140-z · Cited by 16

PhenoSV: interpretable phenotype-aware model for the prioritization of genes affected by structural variants

Xu, Z., Li, Q., Marchionni, L., & Wang, K. (2023) · Nature Communications · doi:10.1038/s41467-023-43651-y · Cited by 22

Cell-type-specific roles of FOXP1 in the excitatory neuronal lineage during early neocortical murine development

Ortiz, A., Ayhan, F., Khandelwal, N., Outland, E. H., Jankovic, M. J., Harper, M. J., & Konopka, G. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.115384 · Cited by 17

The cell-surface shared proteome of astrocytes and neurons and the molecular foundations of their multicellular interactions

Wu, L., Pandey, V., Hull, V. L., Qu, Z., Jami‐Alahmadi, Y., Gradinaru, V., Wohlschlegel, J. A., & Khakh, B. S. (2025) · Neuron · doi:10.1016/j.neuron.2025.05.019 · Cited by 19

Exome sequencing analysis of Japanese autism spectrum disorder case-control sample supports an increased burden of synaptic function-related genes

Kimura, H., Nakatochi, M., Aleksić, B., Guevara, J., Toyama, M., Hayashi, Y., Kato, H., Kushima, I., Morikawa, M., Ishizuka, K., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-02033-6 · Cited by 17

Interactive network visualization in Jupyter notebooks: visJS2jupyter

Rosenthal, S. B., Len, J., Webster, M., Gary, A., Birmingham, A., & Fisch, K. M. (2017) · Bioinformatics · doi:10.1093/bioinformatics/btx581 · Cited by 17

Analysis of neuroanatomical differences in mice with genetically modified serotonin transporters assessed by structural magnetic resonance imaging

Ellegood, J., Yee, Y., Kerr, T. M., Muller, C. L., Blakely, R., Henkelman, R. M., Veenstra-VanderWeele, J. M., & Lerch, J. P. (2018) · Molecular Autism · doi:10.1186/s13229-018-0210-z · Cited by 18

Convergent synaptic and circuit substrates underlying autism genetic risks

McGee, A. W., Li, G., Lu, Z., & Qiu, S. (2014) · Frontiers in Biology · doi:10.1007/s11515-014-1298-y · Cited by 17

Leveraging epigenetics to examine differences in developmental trajectories of social attention: A proof-of-principle study of DNA methylation in infants with older siblings with autism

Gui, A., Jones, E. J. H., Wong, C. C. Y., Meaburn, E. L., Xia, B., Pasco, G., Lloyd‐Fox, S., Charman, T., Bolton, P., & Johnson, M. H. (2020) · Infant Behavior and Development · doi:10.1016/j.infbeh.2019.101409 · Cited by 17

Genome-wide association meta-analysis of age at onset of walking in over 70,000 infants of European ancestry

Gui, A., Hollowell, A., Wigdor, E. M., MORGAN, M., Hannigan, L. J., Corfield, E. C., Odintsova, V. V., Hottenga, J., Wong, A., Pool, R., et al. (2025) · Nature Human Behaviour · doi:10.1038/s41562-025-02145-1 · Cited by 20

Autism Spectrum Disorder as a Multifactorial Disorder: The Interplay of Genetic Factors and Inflammation

Ayoub, G. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26136483 · Cited by 21

Resveratrol Prevents Cytoarchitectural and Interneuronal Alterations in the Valproic Acid Rat Model of Autism

Santos‐Terra, J., Deckmann, I., Carello‐Collar, G., Nunes, G. D., Bauer‐Negrini, G., Schwingel, G. B., Fontes‐Dutra, M., Riesgo, R. D. S., & Gottfried, C. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23084075 · Cited by 15

Coronally advanced flap associated with a connective tissue graft for the treatment of multiple recession defects in mandibular posterior teeth.

Sanctis, M. D., Baldini, N., Goracci, C., & Zucchelli, G. (2011) · PubMed · Cited by 14

Does Prenatal Valproate Interact with a Genetic Reduction in the Serotonin Transporter? A Rat Study on Anxiety and Cognition

Ellenbroek, B. A., August, C. L., & Youn, J. (2016) · Frontiers in Neuroscience · doi:10.3389/fnins.2016.00424 · Cited by 12

Gene network analysis reveals a role for striatal glutamatergic receptors in dysregulated risk-assessment behavior of autism mouse models

Oron, O., Getselter, D., Shohat, S., Reuveni, E., Lukić, I., Shifman, S., & Elliott, E. (2019) · Translational Psychiatry · doi:10.1038/s41398-019-0584-5 · Cited by 15

TrkB Signaling Influences Gene Expression in Cortistatin-Expressing Interneurons

Maynard, K. R., Kardian, A., Hill, J. L., Mai, Y., Barry, B. K., Hallock, H. L., Jaffe, A. E., & Martinowich, K. (2020) · eNeuro · doi:10.1523/eneuro.0310-19.2019 · Cited by 15

Krüppel-like Transcription Factor 7 Is a Causal Gene in Autism Development

Tian, H., Qiao, S., Zhao, Y., Jin, X., Cao, W. F., Wang, R. L., Wang, Y., Jiao, Y., Liu, Y., Zhang, B., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23063376 · Cited by 15

Genetic variants in DDX53 contribute to autism spectrum disorder associated with the Xp22.11 locus

Scala, M., Bradley, C. A., Howe, J., Trost, B., Salazar, N. B., Shum, C., de Aquino, M. M., Reuter, M. S., Anagnostou, E. A., MacDonald, J. R., et al. (2024) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2024.11.003 · Cited by 14

Dynamic subtype- and context-specific subcellular RNA regulation in growth cones of developing neurons of the cerebral cortex

Veeraraghavan, P., Engmann, A. K., Hatch, J. J., Itoh, Y., Nguyen, D., Addison, T. A., & Macklis, J. D. (2025) · Nature Neuroscience · doi:10.1038/s41593-025-02173-0 · Cited by 14

Using Machine Learning to Explore Shared Genetic Pathways and Possible Endophenotypes in Autism Spectrum Disorder

Giovanni, D. D., Enea, R., Micco, V. D., Benvenuto, A., Curatolo, P., & Gialloreti, L. E. (2023) · Genes · doi:10.3390/genes14020313 · Cited by 14

Rodent genetic models of neurodevelopmental disorders and epilepsy

Gonzalez‐Sulser, A. (2019) · European Journal of Paediatric Neurology · doi:10.1016/j.ejpn.2019.12.012 · Cited by 16

A mini-review: Bridging the gap between autism spectrum disorder and pain comorbidities

Brown, C. O., Uy, J. A., & Singh, K. K. (2020) · Canadian Journal of Pain · doi:10.1080/24740527.2020.1775486 · Cited by 12

Gene Module Analysis Reveals Cell-Type Specificity and Potential Target Genes in Autism’s Pathogenesis

Ji, G., Li, S., Ye, L., & Guan, J. (2021) · Biomedicines · doi:10.3390/biomedicines9040410 · Cited by 13

Investigating the impact of paternal aging on murine sperm miRNA profiles and their potential link to autism spectrum disorder

Miyahara, K., Tatehana, M., Kikkawa, T., & Osumi, N. (2023) · Scientific Reports · doi:10.1038/s41598-023-47878-z · Cited by 13

The spectrum of pre‐mRNA splicing in autism

Engal, E., Zhang, Z., Geminder, O., Jaffe‐Herman, S., Kay, G., Ben‐Hur, A., & Salton, M. (2024) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1838 · Cited by 14

Multi-omics study reveals differential expression and phosphorylation of autophagy-related proteins in autism spectrum disorder

Deri, E., Ojha, S. K., Kartawy, M., Khaliulin, I., & Amal, H. (2025) · Scientific Reports · doi:10.1038/s41598-025-95860-8 · Cited by 15

Genomic Strategies for Understanding the Pathophysiology of Autism Spectrum Disorder

Doi, M., Li, M., Usui, N., & Shimada, S. (2022) · Frontiers in Molecular Neuroscience · doi:10.3389/fnmol.2022.930941 · Cited by 13

A multi‐omic approach identifies an autism spectrum disorder ( ASD ) regulatory complex of functional epimutations in placentas from children born preterm

Freedman, A. N., Clark, J., Eaves, L. A., Roell, K. R., Oran, A., Koval, L. E., Rager, J. E., Junior, H. P. D. O. S., Kuban, K., Joseph, R. M., et al. (2023) · Autism Research · doi:10.1002/aur.2915 · Cited by 12

Cessation of chronic delta-9-tetrahydrocannabinol use partially reverses impacts on male fertility and the sperm epigenome in rhesus macaques

Hedges, J. C., Hanna, C. B., Shorey‐Kendrick, L. E., Boniface, E. R., Bash, J. C., Rice-Stitt, T. L., Burch, F. C., D'Mello, R. J., Morgan, T. K., Lima, A. C., et al. (2023) · Fertility and Sterility · doi:10.1016/j.fertnstert.2023.02.034 · Cited by 12

Maternal high-fat or low-protein diets promote autism-related behavior and altered social behavior within groups in offspring male mice

Zilkha, N., Chuartzman, S. G., Fishman, R., Ben‐Dor, S., & Kimchi, T. (2024) · Scientific Reports · doi:10.1038/s41598-024-70062-w · Cited by 14

Predicting causal genes from psychiatric genome-wide association studies using high-level etiological knowledge

Wainberg, M., Merico, D., Keller, M. C., Fauman, E. B., & Tripathy, S. J. (2022) · Molecular Psychiatry · doi:10.1038/s41380-022-01542-6 · Cited by 12

Somatic point mutations are enriched in non-coding RNAs with possible regulatory function in breast cancer

Rezaie, N., Bayati, M., Hamidi, M., Tahaei, M. S., Khorasani, S., Lovell, N. H., Breen, J., Rabiee, H. R., & Alinejad-Rokny, H. (2022) · Communications Biology · doi:10.1038/s42003-022-03528-0 · Cited by 12

RGS14 expression in CA2 hippocampus, amygdala, and basal ganglia: Implications for human brain physiology and disease

Montañez‐Miranda, C., Bramlett, S. N., & Hepler, J. R. (2022) · Hippocampus · doi:10.1002/hipo.23492 · Cited by 12

Systematic analysis of YFP traps reveals common mRNA/protein discordance in neural tissues

Titlow, J., Kiourlappou, M., Palanca, A., Lee, Y. S., Gala, D., Ennis, D., Yu, J. J. S., Young, F. L., Pinto, D. M. S., Garforth, S., et al. (2022) · The Journal of Cell Biology · doi:10.1083/jcb.202205129 · Cited by 15

Cord blood DNA methylome in newborns later diagnosed with autism spectrum disorder reflects early dysregulation of neurodevelopmental and X-linked genesPreprint

Mordaunt, C. E., Jianu, J. M., Laufer, B. I., Zhu, Y., Dunaway, K. W., Bakulski, K. M., Feinberg, J. I., Volk, H. E., Lyall, K., Croen, L., et al. (2019) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/850529 · Cited by 12

Cullin-RING Ubiquitin Ligases in Neurodevelopment and Neurodevelopmental Disorders

Ashitomi, H., Nakagawa, T., Nakagawa, M., & Hosoi, T. (2025) · Biomedicines · doi:10.3390/biomedicines13040810 · Cited by 10

Hippocampal and peripheral blood DNA methylation signatures correlate at the gene and pathway level in a mouse model of autism

Alberca, C. D., Papale, L. A., Madrid, A., & Alisch, R. S. (2023) · Human Molecular Genetics · doi:10.1093/hmg/ddad137 · Cited by 12

Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variants

Einson, J. E., Glinos, D. A., Boerwinkle, E., Castaldi, P. J., Darbar, D., de Andrade, M., Ellinor, P. T., Fornage, M., Gabriel, S., Germer, S., et al. (2023) · Genetics · doi:10.1093/genetics/iyad115 · Cited by 10

microRNA as a Maternal Marker for Prenatal Stress-Associated ASD, Evidence from a Murine Model

Woo, T., King, C., Ahmed, N. I., Cordes, M., Nistala, S., Will, M. J., Bloomer, C., Kibiryeva, N., Rivera, R. M., Talebizadeh, Z., et al. (2023) · Journal of Personalized Medicine · doi:10.3390/jpm13091412 · Cited by 12

Role of FPR2 antagonism in alleviating social isolation-induced depression and protecting blood-brain barrier integrity

Zheng, J., Wang, H., Wu, W., Wang, L., Qin, M., Zhu, L., Liu, Z., Chen, Y., & Yu, Y. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03408-4 · Cited by 12

A Study of the Genomic Variations Associated with Autistic Spectrum Disorders in a Russian Cohort of Patients Using Whole-Exome Sequencing

Gibitova, E. A., Dobrynin, P. V., Pomerantseva, E. A., Musatova, E. V., Kostareva, A. A., Evsyukov, I., Rychkov, S. Y., Zhukova, O. V., Naumova, O. Y., & Grigorenko, E. L. (2022) · Genes · doi:10.3390/genes13050920 · Cited by 9

A synaptic molecular dependency network in knockdown of autism- and schizophrenia-associated genes revealed by multiplexed imaging

Falkovich, R., Danielson, E., de Arce, K. P., Wamhoff, E., Strother, J., Lapteva, A. P., Sheng, M., Cottrell, J. R., & Bathe, M. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112430 · Cited by 10

dbMDEGA: a database for meta-analysis of differentially expressed genes in autism spectrum disorder

Zhang, S., Deng, L., Jia, Q., Huang, S., Gu, J., Zhou, F., Gao, M., Sun, X., Feng, C., & Fan, G. (2017) · BMC Bioinformatics · doi:10.1186/s12859-017-1915-2 · Cited by 10

Heterozygous Nexmif female mice demonstrate mosaic NEXMIF expression, autism-like behaviors, and abnormalities in dendritic arborization and synaptogenesis

O’Connor, M. G., Qiao, H., Odamah, K., Cerdeira, P. C., & Man, H. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e24703 · Cited by 9

Loss of NSD2 causes dysregulation of synaptic genes and altered H3K36 dimethylation in mice

Kinoshita, S., Kojima, K., Ohnishi, E., Takayama, Y., Kikuchi, H., Takada, S., Nakabayashi, K., Kawai, T., & Hata, K. (2024) · Frontiers in Genetics · doi:10.3389/fgene.2024.1308234 · Cited by 9

Prenatal stress alters mouse offspring dorsal striatal development and placental function in sex-specific ways

Maurer, S. V., Hing, B. W. Q., Lussier, S. J., Radhakrishna, S., Davis, J. L.-B., Abbott, P. W., Michaelson, J. J., & Stevens, H. E. (2025) · Journal of Psychiatric Research · doi:10.1016/j.jpsychires.2024.12.048 · Cited by 9

Sex-specific DNA methylation signatures of autism spectrum disorder from whole genome bisulfite sequencing of newborn blood

Mouat, J. S., Krigbaum, N. Y., Hakam, S. M., Thrall, E., Kuodza, G. E., Mellis, J., Yasui, D. H., Cirillo, P. M., Ludeña, Y., Schmidt, R. J., et al. (2025) · Biology of Sex Differences · doi:10.1186/s13293-025-00712-9 · Cited by 9

Cell-type-specific DNA methylation dynamics in the prenatal and postnatal human cortex

Franklin, A., Davies, J. P., Clifton, N. E., Blake, G. E. T., Bamford, R. A., Walker, E., Chioza, B. A., Frith, M., Baron‐Cohen, S., Allison, C., et al. (2025) · Cell Genomics · doi:10.1016/j.xgen.2025.101010 · Cited by 13

A chromosomal microdeletion of 15q in a female patient with epilepsy, ID , and autism spectrum disorder: a case report

Ahram, D. F., Al-Sarraj, Y. A., Taha, R. Z., Elhag, S. F., Alshaban, F. A. W., El‐Shanti, H., & Kambouris, M. (2017) · Clinical Case Reports · doi:10.1002/ccr3.945 · Cited by 9

Targeted Tshz3 deletion in corticostriatal circuit components segregates core autistic behaviors

Caubit, X., Gubellini, P., Roubertoux, P. L., Carlier, M., Molitor, J., Chabbert, D., Metwaly, M., Salin, P., Fatmi, A., Belaïdouni, Y., et al. (2022) · Translational Psychiatry · doi:10.1038/s41398-022-01865-6 · Cited by 10

Analyzing aggregation propensities of clinically relevant PTEN mutants: a new culprit in pathogenesis of cancer and other PTENopathies

Palumbo, E., Zhao, B., Xue, B., Uversky, V. N., & Davé, V. (2019) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2019.1630005 · Cited by 9

Rare Pathogenic Variants Identified in Whole Exome Sequencing of Monozygotic Twins With Autism Spectrum Disorder

Anitha, A., Banerjee, M., Thanseem, I., Prakash, A., Melempatt, N., Sumitha, P. S., Iype, M., & Thomas, S. V. (2024) · Pediatric Neurology · doi:10.1016/j.pediatrneurol.2024.06.003 · Cited by 8

A quantitative description of the peptide sharing between poliovirus and Homo sapiens

Novello, G., Capone, G., Fasano, C., Bavaro, S. L., Polito, A. N., & Kanduc, D. (2011) · Immunopharmacology and Immunotoxicology · doi:10.3109/08923973.2011.608360 · Cited by 8

Evolution is in the details: Regulatory differences in modern human and Neanderthal

Barker, H. R., Parkkila, S., & Tolvanen, M. E. E. (2025) · Computational and Structural Biotechnology Journal · doi:10.1016/j.csbj.2025.05.052 · Cited by 10

PTEN controls alternative splicing of autism spectrum disorder-associated transcripts in primary neurons

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Age-related differences in axon pruning and myelination may alter neural signaling in autism spectrum disorder

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Simons Foundation

(2020) · Palgrave Macmillan UK eBooks · doi:10.1057/978-1-349-95988-4_100304