Defining the genetic, genomic, cellular, and diagnostic architectures of psychiatric disorders

Sullivan, Patrick F., Geschwind, Daniel H.·2019·Cell

Cited by (476)

Items 201–300 of 476

  1. Functional Neurogenomics to Dissect Disease Mechanisms Across Models
    Xinhe Zheng, Jiwen Li, Xin Jin · 2025 · Annual Review of Genomics and Human Genetics
  2. Connecting genomic results for psychiatric disorders to human brain cell types and regions reveals convergence with functional connectivity
    Shuyang Yao, Arvid Harder, Fahimeh Darki, Yu-Wei Chang, Ang Li, Kasra Nikouei, Giovanni Volpe, Johan N. Lundström, Jian Zeng, Naomi R. Wray et al. · 2024 · medRxiv
  3. Understanding anhedonia from a genomic perspective
    E. Bondy, R. Bogdan · 2022 · Current topics in behavioral neurosciences
  4. Identifying age-specific gene signatures of the human cerebral cortex with joint analysis of transcriptomes and functional connectomes
    Xingzhong Zhao, Jingqi Chen, Peipei Xiao, Jianfeng Feng, Qing Hua Nie, Xing‐Ming Zhao · 2020 · Briefings in Bioinformatics
  5. Disrupted Timing of MET Signaling Derails the Developmental Maturation of Cortical Circuits and Leads to Altered Behavior in Mice
    Xiaokuang Ma, Jing Wei, Yuehua Cui, Baomei Xia, Le Zhang, Antoine Nehme, Yi Zuo, Deveroux Ferguson, Pat R. Levitt, Shenfeng Qiu · 2021 · Cerebral Cortex
  6. Transcriptome-wide gene-gene interaction associations elucidate pathways and functional enrichment of complex traits
    Luke M. Evans, Christopher H. Arehart, Andrew David Grotzinger, Travis J. Mize, Maizy S. Brasher, Jerry A. Stitzel, Marissa A. Ehringer, Charles A. Hoeffer · 2023 · PLoS Genetics
  7. Retrotransposon insertions associated with risk of neurologic and psychiatric diseases
    Hyo Won Ahn, Zelia Worman, Arianna Lechsinska, Lindsay M. Payer, Tongguang Wang, Nasir Malik, Wenxue Li, Kathleen H. Burns, Avindra Nath, Henry L. Levin · 2022 · EMBO Reports
  8. Intron retention as an excellent marker for diagnosing depression and for discovering new potential pathways for drug intervention
    Norihiro Okada, Kenshiro Oshima, Akiko Maruko, Mariko Sekine, Naoki Ito, Akino Wakasugi, Eiko Mori, Hiroshi Odaguchi, Yoshinori Kobayashi · 2024 · Frontiers in Psychiatry
  9. Transcriptional dysregulation in developing trigeminal sensory neurons in the LgDel mouse model of DiGeorge 22q11.2 deletion syndrome
    Thomas Michael Maynard, Anélia Horvath, James P. Bernot, Beverly A. Karpinski, André L. P. Tavares, Ankita Shah, Qianqian Zheng, Liam Flinn Spurr, Jacqueline Olender, Sally A. Moody et al. · 2020 · Human Molecular Genetics
  10. Relationship Between Problematic Alcohol Use and Various Psychiatric Disorders: A Genetically Informed Study.
    Yeeun Ahn, Jaehyun Kim, Kyeongmin Jung, Dong June Lee, Jin-Young Jung, Yewon Eom, Sanghyeon Park, Jaeyoung Kim, Hyejin Kim, Hyeonbin Jo et al. · 2025 · American Journal of Psychiatry
  11. Pediatric Tuina in children with autism spectrum disorder: a study protocol for a randomized controlled trial
    Xiang Feng, Quanrui Jiang, Yuxing Zhang, Tao Li, Wei Wei, Jun Yu, Wu Li, Jiangshan Li · 2022 · Trials
  12. Association of polygenic scores for depression and neuroticism with perceived stress in daily life during a long‐lasting stress period
    Hannah L. Peter, Marina Giglberger, Fabian Streit, Josef Frank, Ludwig Kreuzpointner, Marcella Rietschel, Brigitte M. Kudielka, Stefan Wüst · 2023 · Genes Brain & Behavior
  13. Human Brain Organoids: Development and Applications
    Wu Hongxi, Wang Ruting, Liu Yiyang, Huang Qinglian, Chen Jibing, Jiang Feng · 2025 · Journal of Microbiology and Biotechnology
  14. Using genetic designs to identify likely causal environmental contributions to psychopathology
    Ruth Sellers, Lucy Riglin, Gordon T. Harold, Anita Thapar · 2022 · Development and Psychopathology
  15. Leveraging interindividual variability of regulatory activity for refining genetic regulation of gene expression in schizophrenia
    Maris Alver, Nikolaos M. R. Lykoskoufis, Anna Ramisch, Emmanouil T. Dermitzakis, Halit Ongen · 2022 · Molecular Psychiatry
  16. Transcriptional enhancers in human neuronal differentiation provide clues to neuronal disorders
    Masahito Yoshihara, Andrea Coschiera, Jörg A. Bachmann et al. · 2025 · EMBO Reports
  17. One Single Nucleotide Polymorphism of the TRPM2 Channel Gene Identified as a Risk Factor in Bipolar Disorder Associates With Autism Spectrum Disorder in a Japanese Population
    Naila Al Mahmuda, Shigeru Yokoyama, Toshio Munesue, Kenshi Hayashi, Kunimasa Yagi, Chiharu Tsuji, Haruhiro Higashida · 2020 · Diseases
  18. A multi-regional human brain atlas of chromatin accessibility and gene expression facilitates promoter-isoform resolution genetic fine-mapping
    Pengfei Dong, Liting Song, Jaroslav M. Bendl, Ruth Misir, Zhiping Shao, Jonathan Edelstien, David A. Davis, Vahram H. Haroutunian, William K. Scott, Susanne Acker et al. · 2024 · Nature Communications
  19. Non-additive effects of schizophrenia risk genes reflect convergent downstream function
    PJ Michael Deans, Carina Seah, Jessica Johnson, Judit García‐González, Kayla G. Townsley, Evan Cao, Nadine Schrode, Eli A. Stahl, Paul F. O’Reilly, Laura M. Huckins et al. · 2023 · medRxiv
  20. Human brain prefrontal cortex proteomics identifies compromised energy metabolism and neuronal function in Schizophrenia
    Frank Koopmans, Anke A. Dijkstra, Wei-Ping Li, Remco V. Klaassen, Yvonne Gouwenberg, Shuyang Yao, Lisa Bast, Matthijs Verhage, Robert Karlsson, Andrew J. Dwork et al. · 2026 · Nature Communications
  21. Multivariate genome-wide association study identifies 780 unique genetic loci associated with cortical morphology
    2020
  22. A resource of induced pluripotent stem cell (iPSC) lines including clinical, genomic, and cellular data from genetically isolated families with mood and psychotic disorders
    Sevilla D. Detera‐Wadleigh, Layla Kassem, Emily Besancon, Fabiana L. Lopes, Nirmala Akula, Heejong Sung, Meghan Blattner, Laura Sheridan, Ley Nadine Lacbawan, Joshua Garcia et al. · 2023 · Translational Psychiatry
  23. Testing single/combined clinical categories on 5110 Italian patients with developmental phenotypes to improve array‐based detection rate
    Ilaria Catusi, Maria Paola Recalcati, Ilaria Bestetti et al. · 2019 · Molecular Genetics & Genomic Medicine
  24. Inferring cell-type-specific causal gene regulatory networks during human neurogenesis
    Nil Aygün, Dan Liang, Wesley L. Crouse, Gregory R. Keele, Michael I. Love, Jason L. Stein · 2022 · bioRxiv (Cold Spring Harbor Laboratory)
  25. The conserved ASTN2/BRINP1 locus at 9q33.1–33.2 is associated with major psychiatric disorders in a large pedigree from Southern Spain
    Josep Pol-Fuster, Francesca Cañellas, Laura Ruiz-Guerra, Aina Medina-Dols, Bàrbara Bisbal-Carrió, Bernat Ortega-Vila, Jaume Llinàs, Jessica Hernández-Rodríguez, Jerònia Lladó, Gabriel Olmos et al. · 2021 · Scientific Reports
  26. Leveraging iPSC technology to assess neuro-immune interactions in neurological and psychiatric disorders
    Christina Michalski, Zhexing Wen · 2023 · Frontiers in Psychiatry
  27. Genomic Chaos Begets Psychiatric Disorder
    Donard S. Dwyer · 2020 · Complex Psychiatry
  28. ADHD: Progressing From Genetic Discoveries to Biological Insights
    Anita Thapar · 2020 · American Journal of Psychiatry
  29. The Promise and Peril of Genetics
    Danielle M. Dick · 2022 · Current Directions in Psychological Science
  30. Biomarkers in psychiatric disorders
    Jemmyson Romário de Jesus, Tatianny de Araújo Andrade, Eduardo Costa Figueiredo · 2023 · Advances in clinical chemistry
  31. Is Depression Nature or Nurture? Yes
    Myrna M. Weissman · 2020 · American Journal of Psychiatry
  32. Elucidation of molecular pathogenesis and drug development for psychiatric disorders from rare disease-susceptibility variants
    Hiroki Kimura, Daisuke Mori, Branko Aleksić, Norio Ozaki · 2020 · Neuroscience Research
  33. The architecture of brain co-expression reveals the brain-wide basis of disease susceptibility
    Christopher Hartl, Gokul Ramaswami, William G. Pembroke, Sandrine Muller, Greta Pintacuda, Ashis Saha, Princy Parsana, Alexis J. Battle, Kasper Lage, Daniel H. Geschwind · 2020 · bioRxiv (Cold Spring Harbor Laboratory)
  34. Underlying causes for prevalent false positives and false negatives in STARR-seq data
    Pengyu Ni, Siwen Wu, Zhengchang Su · 2023 · NAR Genomics and Bioinformatics
  35. Cheminformatics and Bioinformatics at the Interface with Systems Biology
    Aman Chandra Kaushik, Aamir Mehmood, Dong‐Qing Wei, Sadia Nawab, Shakti Sahi, Ajay Kumar · 2023 · Royal Society of Chemistry eBooks
  36. Dynamic convergence of neurodevelopmental disorder risk genes across neurodevelopment
    Meilín Fernández García, Kayla G. Townsley, April Pruitt, Elizabeth Davidson, Novin Balafkan, Jonathan Warrell, Tzu-Chieh Huang, Alfred Kibowen, Zhiyuan Chu, Yi Dai et al. · 2024 · bioRxiv (Cold Spring Harbor Laboratory)
  37. Wnt activity reveals context-specific genetic effects on gene regulation in neural progenitors
    Nana Matoba, Brandon D. Le, Jordan M. Valone, Justin M. Wolter, Jessica T. Mory, Dan Liang, Nil Aygün, K. Alaine Broadaway, Marielle L. Bond, Karen L. Mohlke et al. · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
  38. The First Large GWAS Meta-Analysis for Postpartum Depression
    Jessica Ann May Adams, Prabha S. Chandra, Divya Mehta · 2023 · American Journal of Psychiatry
  39. Large-scale whole-exome sequencing of neuropsychiatric diseases and traits in 350,770 adults
    Yue‐Ting Deng, Bang‐Sheng Wu, Liu Yang, Xiao‐Yu He, Jujiao Kang, Weishi Liu, Ze-Yu Li, Xinrui Wu, Ya-Ru Zhang, Shi-Dong Chen et al. · 2024 · Nature Human Behaviour
  40. Playing the genome card
    A. Berkowitz · 2019 · Journal of neurogenetics
  41. Schizophrenia: Developmental Variability Interacts with Risk Factors to Cause the Disorder
    Andreı̈ Szöke, Baptiste Pignon, Sarah Boster, Stéphane Jamain, Franck Schürhoff · 2020 · BioEssays
  42. Cross-trait prediction accuracy of high-dimensional ridge-type estimators in genome-wide association studies
    Bingxin Zhao, Hongtu Zhu B · 2019 · arXiv (Cornell University)
  43. Disentangling chromatin architecture to gain insights into the etiology of brain disorders
    Janine M. Lamonica, Zhaolan Zhou · 2019 · Current Opinion in Genetics & Development
  44. Integration with systems biology approaches and -omics data to characterize risk variation
    Hannah E. Young, Alanna C. Cote, Laura M. Huckins · 2022 · Elsevier eBooks
  45. Formulating treatment of major psychiatric disorders: algorithm targets the dominantly affected brain cell-types
    Jeffrey Fessel · 2023 · Discover Mental Health
  46. Replicating extensive brain structural heterogeneity in individuals with schizophrenia and bipolar disorder
    Thomas Wolfers, Jaroslav Rokicki, Dag Alnæs et al. · 2020 · medRxiv
  47. Feasibility and application of polygenic score analysis to the morphology of human-induced pluripotent stem cells
    J. Coleman · 2020 · Zeitschrift für Induktive Abstammungs- und Vererbungslehre
  48. Psychiatric Genetics in Clinical Practice: Essential Knowledge for Mental Health Professionals
    Aaron D. Besterman, Mohamed Abdalhameed Alnor, Mauricio Castaño, Lynn E. DeLisi, Dorothy E. Grice, Falk W. Lohoff, Christel Maria Middeldorp, Daniel J. Müller, Diego Quattrone, John I. Nürnberger et al. · 2025 · American Journal of Psychiatry
  49. Refining patterns of MEF2C effects in white matter microstructure and psychiatric features
    Maria Eduarda Tavares, Renata Basso Cupertino, Cibele Edom Bandeira, Bruna Santos da Silva, Eduardo Schneider Vitola, Carlos Alberto Iglesias Salgado, Robson dos Santos Soares, Felipe Almeida Picon, Luís Augusto Rohde, Diego Luiz Rovaris et al. · 2023 · Journal of Neural Transmission
  50. CellGO: a novel deep learning-based framework and webserver for cell-type-specific gene function interpretation
    Peilong Li, Junfeng Wei, Ying Zhu · 2023 · Briefings in Bioinformatics
  51. Neuron-Specific Deletion of Scrib in Mice Leads to Neuroanatomical and Locomotor Deficits
    Jérôme Ezan, Maïté Marie Moreau, Tamrat M. Mamo, Miki Shimbo, Maureen Decroo, Nathalie Sans, Mireille Montcouquiol · 2022 · Frontiers in Genetics
  52. Gene co-expression architecture in peripheral blood in a cohort of remitted first-episode schizophrenia patients
    Natàlia Rodríguez, Patricia Gassó, Albert Martínez-Pinteño, Àlex G. Segura, Gisela Mezquida, Lucía Moreno-Izco, Javier González‐Peñas, Eric P. Zorrilla, Marta Martín-Subero, Natàlia Rodríguez et al. · 2022 · Schizophrenia
  53. Resequencing and association analysis of GAP43 with autism spectrum disorder and schizophrenia in a Japanese population
    Reza K. Arta, Yuichiro Watanabe, Emiko Inoue, Yoshihiro Nawa, Ryo Morikawa, Jun Egawa, Itaru Kushima, Hirofumi Igeta, Satoshi Hoya, Atsunori Sugimoto et al. · 2021 · Research in Autism
  54. Perspective on Beyond Statistical Significance: Finding Meaningful Effects
    Howard J. Edenberg · 2021 · Complex Psychiatry
  55. Polygenic profiles define aspects of clinical heterogeneity in ADHD
    A. Schork, S. LaBianca, Isabell Brickell, D. Helenius, R. Loughnan, J. Mefford, C. Palmer, Rebecca L. Walker, J. Gådin, M. Krebs et al. · 2021 · medRxiv
  56. Phenotypic complexities of rare heterozygous neurexin-1 deletions
    Michael B. Fernando, Yu Fan, Yanchun Zhang et al. · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
  57. Distal‐to‐proximal etiologically relevant variables associated with the general ( p ) and specific factors of psychopathology
    Jonah Ormel, Melissa Vos, Odilia M. Laceulle, Charlotte Vrijen, Camiel M. van der Laan, Ilja Maria Nolte, Catharina Annette Hartman · 2024 · Journal of Child Psychology and Psychiatry
  58. Transcriptomic networks implicate neuronal energetic abnormalities in three mouse models harboring autism and schizophrenia-associated mutations
    Aaron Gordon, Annika Grønborg-Forsingdal, Ib Vestergaard Klewe · 2019 · bioRxiv (Cold Spring Harbor Laboratory)
  59. Transcriptomic and phenotypic convergence of neurodevelopmental disorder risk genes in vitro and in vivo
    Meilín Fernández García, Kayla G. Townsley, April Pruitt, Elizabeth Davidson, Novin Balafkan, Jonathan Warrell, Tzu-Chieh Huang, Alfred Kibowen, Zhiyuan Chu, Yi Dai et al. · 2026 · Nature Neuroscience
  60. Transcriptome and chromatin accessibility landscapes across 25 distinct human brain regions expand the susceptibility gene set for neuropsychiatric disorders
    P. Dong, J. Bendl, Ruth Misir et al. · 2022 · bioRxiv
  61. Use of the epigenetic toolbox to contextualize common variants associated with schizophrenia risk
    Prashanth Rajarajan, Schahram Akbarian · 2019 · Dialogues in Clinical Neuroscience
  62. Population-level variation of enhancer expression identifies novel disease mechanisms in the human brain
    Pengfei Dong, Gabriel E. Hoffman, Pasha Apontes et al. · 2021 · bioRxiv (Cold Spring Harbor Laboratory)
  63. Selective vulnerability of the ventral hippocampus-prelimbic cortex axis parvalbumin interneuron network underlies learning deficits of fragile X mice
    Komal Bhandari, Harsh Kanodia, Flavio Donato, Pico Caroni · 2024 · Cell Reports
  64. Obsessive-Compulsive Symptoms, Polygenic Risk Score, and Thalamic Development in Children From the Brazilian High-Risk Cohort for Mental Conditions (BHRCS)
    Ana Beatriz Ravagnani Salto, Marcos Leite Santoro, Marcelo Q. Hoexter, Andrea Parolin Jackowski, Pedro Mário Pan, Maria Conceição do Rosário, Sintia Iole Belangero, Pedro Gomes de Alvarenga, Victoria Fogaça Doretto, A Fumo et al. · 2021 · Frontiers in Psychiatry
  65. Executive dysfunction as a transdiagnostic mechanism of psychopathology: a neurocognitive framework for diagnosis and intervention
    Sandra Carvalho · 2026 · Frontiers in Human Neuroscience
  66. Whole genome sequencing study of identical twins discordant for psychosis
    Cathal Ormond, Niamh Ryan, Anna M. Hedman, Tyrone D. Cannon, Patrick F. Sullivan, Michael Gill, Christina M. Hultman, Elizabeth A. Heron, Viktoria Johansson, Aiden Peter Corvin · 2024 · Translational Psychiatry
  67. Joint-Tissue Integrative Analysis Identified Hundreds of Schizophrenia Risk Genes
    Yong Wu, Xiaolin Yu, Xiao Xiao, Ming Li, Yi Li · 2021 · Molecular Neurobiology
  68. Social work, psychiatry the biopsychosocial model and mental health reform
    John Pullman, Luke Molloy, Paul Beckett, Steven J. Campbell · 2024 · Social Work in Mental Health
  69. Molecular genetics of human developmental neurocranial anomalies: towards “precision surgery”
    Phan Q. Duy, Andrew T. Timberlake, Richard P. Lifton, Kristopher Thomas Kahle · 2022 · Cerebral Cortex
  70. Intron retention: a novel method for evaluating the response to ketamine in patients with treatment-resistant depression
    Norihiro Okada, Kenshiro Oshima, Akiko Maruko, Yoshinori Kobayashi · 2025 · npj Mental Health Research
  71. Mutational landscape of risk variants in comorbid depression and obesity: a next-generation sequencing approach
    Ana María Pérez-Gutiérrez, Rosario Carmona, Carlos Loucera, Jorge Antonio Cervilla, Blanca Gutiérrez, Esther Molina, Daniel López-López, Javier Pérez-Florido, Juan Antonio Zarza-Rebollo, Elena López‐Isac et al. · 2024 · Molecular Psychiatry
  72. Subtyping Schizophrenia Using Psychiatric Polygenic Scores
    Yi Lu, K. Kowalec, Jie Song, Robert Karlsson, A. Harder, P. Giusti-Rodríguez, Patrick F. Sullivan, Shu-Yang Yao · 2023 · medRxiv
  73. Mapping, clustering, and analysis of research in psychiatric genomics
    Sabita Yadav, Ayushi Chhabra, G. Mahesh · 2022 · Psychiatric Genetics
  74. Beyond out-of-sample: robust and generalizable multivariate neuroanatomical patterns of psychiatric problems in youth
    Bing Xu, Hao Wang, Lorenza Dall’Aglio, Mannan Luo, Yingzhe Zhang, Ryan L. Muetzel, Henning W. Tiemeier · 2024 · Molecular Psychiatry
  75. Disrupted long-range gene regulations elucidate shared tissue-specific mechanisms of neuropsychiatric disorders
    Jingqi Chen, Liting Song, Anyi Yang, Guiying Dong, Xing‐Ming Zhao · 2022 · Molecular Psychiatry
  76. Novel missense SETD1A variants in Japanese patients with schizophrenia: Resequencing and association analysis
    Ryo Morikawa, Yuichiro Watanabe, Hirofumi Igeta, Reza K. Arta, Masashi Ikeda, Satoshi Okazaki, Satoshi Hoya, Takeo Saito, Ikuo Otsuka, Jun Egawa et al. · 2022 · Psychiatry Research
  77. Toward a Pathway-Driven Clinical-Molecular Framework for Classifying Autism Spectrum Disorders
    Catherine A. Ziats, Owen M. Rennert, Mark N. Ziats · 2019 · Pediatric Neurology
  78. The predicament of heritable confounders
    Na Cai, Andy W. Dahl, Richard Border, Aditya Gorla, Jolien Rietkerk, Joel Mefford, Noah Zaitlen, Morten Dybdahl Krebs, Andrew Joseph Schork, Kenneth S. Kendler et al. · 2026 · Nature Genetics
  79. Genetic testing in psychiatry, the perceptions of healthcare workers and patients: a mini review
    Kyriakos I. Ioannou, Anastasia Constantinidou, Andreas Chatzittofis · 2024 · Frontiers in Public Health
  80. Modern Psychiatry: from Theory to Practice
    Н. Н. Петрова · 2024 · Personalized Psychiatry and Neurology
  81. Neurite outgrowth deficits caused by rare PLXNB1 mutation in pediatric bipolar disorder
    Guang Yang, Ethan Parker, Bushra Gorsi, M. Libowitz, Colin T. Maguire, J. King, H. Coon, M. Lopez-Larson, Jeffrey S. Anderson, M. Yandell et al. · 2022 · medRxiv
  82. Gene and schizophrenia in the pregenome and postgenome-wide association studies era: a bibliometric analysis and network visualization
    Wan Nur Amalina Zakaria, Teguh Haryo Sasongko, Badryia Al-Rahbi, Noorah Saleh Al‐Sowayan, Asma Hayati Ahmad, Rahimah Zakaria, Aidi Ahmi, Zahiruddin Othman · 2023 · Psychiatric Genetics
  83. Role of Immature Choroid Plexus in the Pathology of Autism Spectrum Disorder
    Motoi Tanabe, Yuga Saito, Ayaka Takasaki et al. · 2023 · bioRxiv (Cold Spring Harbor Laboratory)
  84. Improved functional mapping with GSA-MiXeR implicates biologically specific gene-sets and estimates enrichment magnitude
    Oleksandr Frei, Guy Hindley, Alexey A. Shadrin, Dennis van der Meer, Bayram Cevdet Akdeniz, Weiqiu Cheng, Kevin Sean O’Connell, Shahram Bahrami, Nadine Parker, Olav Bjerkehagen Smeland et al. · 2022 · medRxiv
  85. Naturalistic follow-up study of rehospitalization rates and assigned disability status of patients with first-episode schizophrenia spectrum psychosis in South East Latvia: preliminary results
    Liene Sīle, Karīna Bezina, Dmitrijs Kvartalovs, Renārs Erts, S. Kikuste, Inna Šapele, Elmārs Rancāns · 2020 · Nordic Journal of Psychiatry
  86. Drosophila functional screening of de novo variants in autism uncovers deleterious variants and facilitates discovery of rare neurodevelopmental diseases
    Paul C. Marcogliese, Samantha L. Deal, Jonathan C. Andrews et al. · 2021 · bioRxiv (Cold Spring Harbor Laboratory)
  87. Neuropeptidases in Psychiatric Disorders
    João Victor Silva Nani, Priscila G.C. Almeida, Mirian A.F. Hayashi · 2021 · Elsevier eBooks
  88. Association of CDH11 with ASD revealed by matched-gene co-expression analysis and mouse behavioral studies
    Nan Wu, Yue Wang, Jing-Yan Jia, Yi-Hsuan Pan, Xiao‐bing Yuan · 2020 · bioRxiv (Cold Spring Harbor Laboratory)
  89. Systematic exploration of a decade of publications on psychiatric genetics in Latin America
    Diana Garro-Núñez, María Jesús Picado-Martínez, Erika Espinoza-Campos, Daniela Ugalde-Araya, Gabriel Macaya, Henriette Raventós, Gabriela Chavarría-Soley · 2023 · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics
  90. Distinguishing different psychiatric disorders using DDx-PRS
    Wouter J. Peyrot, Georgia Panagiotaropoulou, Loes M. Olde Loohuis, Mark J. Adams, Swapnil Awasthi, Tian Ge, Andrew Mark McIntosh, Brittany L. Mitchell, Niamh Mullins, Kevin Sean O’Connell et al. · 2024 · medRxiv
  91. Transcriptomic Evidence Reveals the Dysfunctional Mechanism of Synaptic Plasticity Control in ASD
    Chao Kong, Zhitong Bing, Lei Yang, Zi‐Gang Huang, Wen-Xu Wang, Celso Grebogi · 2024 · Genes
  92. Genetics of cell-type-specific post-transcriptional gene regulation during human neurogenesis
    Nil Aygün, Celine K. Vuong, Oleh Krupa, Jessica T. Mory, Brandon D. Le, Jordan M. Valone, Dan Liang, Beck Shafie, Pan Zhang, Angelo Salinda et al. · 2024 · The American Journal of Human Genetics
  93. Motivating and Discouraging Factors for Bipolar Patient Participation in Genomic Research
    Eric J. Vallender, Mark E. Ladner, Margaret O. Akinhanmi, Felicia V. Caples, Mark A. Frye, Joyce E. Balls‐Berry · 2021 · Public Health Genomics
  94. Related Disorders (Intellectual, Attention, and Language Disorders) and ASD
    Mary F. S. Dieckhaus, Rebecca P. Thomas, MaryKate Frisch, Maria Paula Moreno, Joyce Suh, DEBORAH A. FEIN · 2024 · Autism and child psychopathology series
  95. Development of colorimetric recombinase polymerase amplification (RPA) assay for rapid detection of Tuta absoluta
    Arindam Kumar, Damini Diksha, Susheel Kumar Sharma · 2025 · Phytoparasitica
  96. Genomics-driven integrative analysis highlights immune-related plasma proteins for psychiatric disorders
    Weiming Gong, Ping Guo, Lu Liu, Ran Yan, Shuai Liu, Shukang Wang, Fuzhong Xue, Xiang Zhou, Xiubin Sun, Zhongshang Yuan · 2024 · Journal of Affective Disorders
  97. The association between family history and genomic burden with schizophrenia mortality: a Swedish population-based register and genetic sample study
    Kaarina Kowalec, Yi Lu, Jie Song, Christina Dalman, Christina M. Hultman, Henrik Larsson, Paul Lichtenstein, Patrick F. Sullivan · 2021 · Translational Psychiatry
  98. Insufficient Evidence for “Autism-Specific” Genes
    Scott M. Myers, Thomas D. Challman, Raphael Bernier et al. · 2020
  99. Estimating disorder probability based on polygenic prediction using the BPC approach
    Emil Uffelmann, Cathryn M. Lewis, Andrew Mark McIntosh, Micheal C. O’Donovan, James Walters, Alkes L. Price, Daniëlle Posthuma, Wouter J. Peyrot · 2025 · Nature Communications
  100. A Blueprint for Next Generation of Clinical Trials in Precision Psychiatry
    Kay T. Pham, Jony Sheynin, Israel Liberzon · 2023 · Elsevier eBooks