Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorder

Elia, Josephine, Glessner, Joseph T, Wang, Kai, Takahashi, Nagahide, Shtir, Corina J, Hadley, Dexter, Sleiman, Patrick M A, Zhang, Haitao +56 more·2012·Nature Genetics
DOI 10.1038/ng.1013

Cited by (409)

Items 101–200 of 409

  1. Next-generation sequencing in drug development: target identification and genetically stratified clinical trials
    Abolfazl Doostparast Torshizi, Kai Wang · 2018 · Drug Discovery Today
  2. Association of AADAC Deletion and Gilles de la Tourette Syndrome in a Large European Cohort
    Birgitte Bertelsen, Hreinn Stefánsson, Lars R. Jensen, Linea Melchior, Nanette Mol Debes, Camilla Groth, Liselotte Skov, Thomas Mears Werge, Iordanis Karagiannidis, Zsanett Tárnok et al. · 2015 · Biological Psychiatry
  3. Neural stem cells in neuropsychiatric disorders
    Roberto Sacco, Emanuele Cacci, Gaia Novarino · 2017 · Current Opinion in Neurobiology
  4. Glutamatergic copy number variants and their role in attention‐deficit/hyperactivity disorder
    Glaucia Chiyoko Akutagava‐Martins, Angélica Salatino‐Oliveira, Júlia Pasqualini Genro, Verônica Contini, Guilherme V. Polanczyk, Cristian Zeni, Rodrigo Chazan, Christian Kieling, Luciana Anselmi, Ana Maria Baptista Menezes et al. · 2014 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  5. An epigenetic, transgenerational model of increased mental health disorders in children, adolescents and young adults
    Anthony P. Monaco · 2020 · European Journal of Human Genetics
  6. The electroretinogram b-wave amplitude: a differential physiological measure for Attention Deficit Hyperactivity Disorder and Autism Spectrum Disorder
    Irene Lee, David Skuse, Paul A. Constable, Fernando Marmolejo‐Ramos, Ludvig Renbo Olsen, Dorothy Thompson · 2022 · Journal of Neurodevelopmental Disorders
  7. Novel pharmacological targets for GABAergic dysfunction in ADHD
    Anthony S. Ferranti, Deborah Joyce Luessen, Colleen Marie Niswender · 2024 · Neuropharmacology
  8. From Rare Copy Number Variants to Biological Processes in ADHD
    Benjamin Harich, Monique van der Voet, Marieke Klein, Pavel Čížek, Michaela Fencková, Annette Schenck, Barbara Franke · 2020 · American Journal of Psychiatry
  9. Confluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world
    Scott I. Vrieze, William G. Iacono, Matt K. McGue · 2012 · Development and Psychopathology
  10. Genomic Disorders in Psychiatry-What Does the Clinician Need to Know?
    Lowther, Chelsea, Costain, Gregory, Baribeau, Danielle A., Bassett, Anne S. · 2017 · Current Psychiatry Reports
  11. Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity
    Robin G. Walters, Lachlan Coin, Aimo Ruokonen, Adam J. de Smith, Julia S. El-Sayed Moustafa, Sébastien Jacquemont, Paul Elliott, Tõnu Esko, Anna‐Liisa Hartikainen, Jaana H. Laitinen et al. · 2013 · PLoS ONE
  12. Allelic association, DNA resequencing and copy number variation at the metabotropic glutamate receptor GRM7 gene locus in bipolar disorder
    Radhika Kandaswamy, Andrew McQuillin, David Curtis, Hugh Gurling · 2014 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  13. Predicting attention deficit hyperactivity disorder using pregnancy and birth characteristics
    Schwenke, Eva, Fasching, Peter A., Faschingbauer, Florian, Pretscher, Jutta, Kehl, Sven, Peretz, Roberta, Keller, Andrea, Häberle, Lothar, Eichler, Anna, Irlbauer-Müller, Viktoria et al. · 2018 · Archives of Gynecology and Obstetrics
  14. Elevated endogenous GDNF induces altered dopamine signalling in mice and correlates with clinical severity in schizophrenia
    Kärt Mätlik, Daniel R. Garton, Ana Montaño-Rodriguez, Soophie Olfat, Feride Eren, Laoise Casserly, Anastasios E. Damdimopoulos, Anne E. Panhelainen, L. Lauriina Porokuokka, Jaakko J. Kopra et al. · 2022 · Molecular Psychiatry
  15. A selective review of glutamate pharmacological therapy in obsessive–compulsive and related disorders
    Marco A. Grados, Elizabeth Atkins, Kovacikova GI, Erin L. McVicar · 2015 · Psychology Research and Behavior Management
  16. Phenotypic profiling of mGlu7 knockout mice reveals new implications for neurodevelopmental disorders
    Nicole M. Fisher, Robert W. Gould, Rocco G. Gogliotti, Annalise J. McDonald, Hana Badivuku, Susmita Chennareddy, Aditi B. Buch, Annah M. Moore, Matthew T. Jenkins, W Hudson Robb et al. · 2020 · Genes Brain & Behavior
  17. Discovery of VU6005649, a CNS Penetrant mGlu7/8 Receptor PAM Derived from a Series of Pyrazolo[1,5-a]pyrimidines
    Masahito Abe, Mabel Seto, Rocco G. Gogliotti, Matthew T. Loch, Katrina A. Bollinger, Sichen Chang, Eileen M. Engelberg, Vincent B. Luscombe, Joel M. Harp, Michael Bubser et al. · 2017 · ACS Medicinal Chemistry Letters
  18. Attention and Impulsivity
    Joel T. Nigg · 2016 · Wiley eBooks
  19. Research models of neurodevelopmental disorders: The right model in the right place
    Eleni Damianidou, Lidia Mouratidou, Christina Kyrousi · 2022 · Frontiers in Neuroscience
  20. Protein interaction networks: centrality, modularity, dynamics, and applications
    Xiangmao Meng, Wen-Kai Li, Xiaoqing Peng, Yaohang Li, Min Li · 2021 · Frontiers of Computer Science
  21. Attention-Deficit Hyperactivity Disorder and Pharmacotherapy—Past, Present, and Future: A Review of the Changing Landscape of Drug Therapy
    John J. Connolly, Joseph Glessner, Charlly Kao, Josephine Elia, Hakon H. Hakonarson · 2015 · Therapeutic Innovation & Regulatory Science
  22. Is there a role for endogenous retroviruses to mediate long-term adaptive phenotypic response upon environmental inputs?
    Jafar Sharif, Yoichi Shinkai, Haruhiko Koseki · 2012 · Philosophical Transactions of the Royal Society B Biological Sciences
  23. High resolution chromosomal microarray analysis in paediatric obsessive-compulsive disorder
    Edna Grünblatt, Beatrice Oneda, Arif Bülent Ekici, Juliane Ball, Julia M. Geissler, Steffen Uebe, Marcel Romanos, Anita M. Rauch, Susanne Walitza · 2017 · BMC Medical Genomics
  24. Small rare recurrent deletions and reciprocal duplications in 2q21.1, including brain-specific ARHGEF4 and GPR148
    Avinash V. Dharmadhikari, S.-H. L. Kang, Przemysław Szafrański, Richard Person, S. Sampath, Siddharth K. Prakash, Patricia I. Bader, J. A. Phillips, Vickie Hannig, M. Williams et al. · 2012 · Human Molecular Genetics
  25. Rare DNA variants in the brain-derived neurotrophic factor gene increase risk for attention-deficit hyperactivity disorder: a next-generation sequencing study
    Z. Hawi, Tdr Cummins, J. Tong, M. Arcos-Burgos, Q. Zhao, N. Matthews, Daniel P. Newman, B. Johnson, A. Vance, H. Heussler et al. · 2017 · Molecular Psychiatry
  26. Pathogenic GRM7 Mutations Associated with Neurodevelopmental Disorders Impair Axon Outgrowth and Presynaptic Terminal Development
    Jae‐man Song, Minji Kang, Da-ha Park, Sun-Ha Park, Sanghyeon Lee, Young Ho Suh · 2021 · Journal of Neuroscience
  27. Anterior cingulate cortex glutamate and its association with striatal functioning during cognitive control
    Jilly Naaijen, David J. Lythgoe, Marcel P. Zwiers, Catharina Annette Hartman, Pieter J. Hoekstra, Jan K. Buitelaar, Esther Aarts · 2018 · European Neuropsychopharmacology
  28. Peripheral biomarkers of attention-deficit hyperactivity disorder: Current status and future perspective
    Nagahide Takahashi, Kanako Ishizuka, Toshiya Inada · 2021 · Journal of Psychiatric Research
  29. Rare de novo deletion of metabotropic glutamate receptor 7 (GRM7) gene in a patient with autism spectrum disorder
    Yi Liu, Yanqing Zhang, Dongmei Zhao, Rui Dong, Xiaomeng Yang, Kristiina Tammimies, Mohammed J. Uddin, Stephen W. Scherer, Zhongtao Gai · 2015 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
  30. Cross-species models of attention-deficit/hyperactivity disorder and autism spectrum disorder
    Elisa Dalla Vecchia, Niall Mortimer, Viola Stella Palladino, Sarah Kittel‐Schneider, Klaus‐Peter Lesch, Andreas Reif, Annette Schenck, William Norton · 2018 · Psychiatric Genetics
  31. A GRM7 mutation associated with developmental delay reduces mGlu7 expression and produces neurological phenotypes
    Nicole M. Fisher, Aqeela H. Alhashim, Aditi B. Buch, Hana Badivuku, Manar M. Samman, Kelly Weiss, Gabriela I. Cestero, Mark D. Does, Jerri M. Rook, Craig W. Lindsley et al. · 2021 · JCI Insight
  32. Mapping the cortico-striatal transcriptome in attention deficit hyperactivity disorder
    Gustavo P. Sudre, Derek E. Gildea, Gauri G. Shastri, Wendy S. Sharp, Benjamin Jung, Qing Xu, Pavan Kumar Auluck, Laura L. Elnitski, Andreas D. Baxevanis, Stefano Marenco et al. · 2022 · Molecular Psychiatry
  33. Educational Psychology
    Adar Ben‐Eliyahu, Moshe Zeidner · 2020 · Cambridge University Press eBooks
  34. Mental health dished up—the use of iPSC models in neuropsychiatric research
    Rhiannon Victoria McNeill, Georg Christoph Ziegler, Franziska Radtke, Matthias Nieberler, Klaus‐Peter Lesch, Sarah Kittel‐Schneider · 2020 · Journal of Neural Transmission
  35. Functional Properties of Rare Missense Variants of Human CDH13 Found in Adult Attention Deficit/Hyperactivity Disorder (ADHD) Patients
    Thegna Mavroconstanti, Stefan Johansson, Ingeborg Winge, Per Morten Knappskog, Jan Haavik · 2013 · PLoS ONE
  36. Background, clinical features and treatment of attention deficit hyperactivity disorder in children
    N. Warikoo, S. Faraone · 2013 · Expert Opinion on Pharmacotherapy
  37. SLC 2A3 single‐nucleotide polymorphism and duplication influence cognitive processing and population‐specific risk for attention‐deficit/hyperactivity disorder
    Sören Merker, Andreas Reif, Georg Christoph Ziegler, Heike Weber, Ute Mayer, Ann‐Christine Ehlis, Annette Conzelmann, Stefan Johansson, C. Müller‐Reible, Indrajit Nanda et al. · 2017 · Journal of Child Psychology and Psychiatry
  38. Modeling and Predicting Developmental Trajectories of Neuropsychiatric Dimensions Associated With Copy Number Variations
    Noboru Hiroi, Takahira Yamauchi · 2019 · The International Journal of Neuropsychopharmacology
  39. Biallelic GRM7 variants cause epilepsy, microcephaly, and cerebral atrophy
    Dana Marafi, Tadahiro Mitani, Sedat Işıkay, Jozef Hertecant, Mohammed Almannai, Kandamurugu Manickam, Rami Abou Jamra, Ayman W. El‐Hattab, Jaishen Rajah, Jawid M. Fatih et al. · 2020 · Annals of Clinical and Translational Neurology
  40. Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay
    Yi Liu, Yuqiang Lv, Mehdi Zarrei, Rui Dong, Xiaomeng Yang, Edward J. Higginbotham, Yue Li, Dongmei Zhao, Fengling Song, Yali Yang et al. · 2022 · npj Genomic Medicine
  41. Recent developments in the genetics of attention‐deficit hyperactivity disorder
    Oliver Grimm, Sarah Kittel‐Schneider, Andreas Reif · 2018 · Psychiatry and Clinical Neurosciences
  42. An electronic health record (EHR) phenotype algorithm to identify patients with attention deficit hyperactivity disorders (ADHD) and psychiatric comorbidities
    Isabella Slaby, Heather S. Hain, Debra J. Abrams, Frank D. Mentch, Joseph Glessner, Patrick M. Abou‐Sleiman, Hakon H. Hakonarson · 2022 · Journal of Neurodevelopmental Disorders
  43. Neurobiology of Attention Deficit Hyperactivity Disorder
    Stephen V. Faraone, Nevena V. Radonjić · 2023 · Springer eBooks
  44. Machine learning derived risk prediction of anorexia nervosa
    Yiran Guo, Zhi Wei, Brendan J. Keating, Hakon H. Hakonarson · 2015 · BMC Medical Genomics
  45. A null mutation in TNIK defines a novel locus for intellectual disability
    Shams Anazi, Hanan E. Shamseldin, Dhekra Alnaqeb, Mohamed Ibrahim Abouelhoda, Dorota Monies, Mustafa Abdalla M Salih, Khalid A Al-Rubeaan, Fowzan Sami Alkuraya · 2016 · Human Genetics
  46. Decoding the non‐coding genome: elucidating genetic risk outside the coding genome
    Cathy L. Barr, Virginia L. Misener · 2015 · Genes Brain & Behavior
  47. ADGRL3 rs6551665 as a Common Vulnerability Factor Underlying Attention-Deficit/Hyperactivity Disorder and Autism Spectrum Disorder
    Djenifer B. Kappel, Jaqueline Bohrer Schuch, Diego Luiz Rovaris, Bruna Santos da Silva, Diana Müller, Vitor Breda, Stefania Pigatto Teche, Rudimar dos Santos Riesgo, Lavínia Schüler‐Faccini, Luís Augusto Rohde et al. · 2019 · NeuroMolecular Medicine
  48. Genetic characterization of HIV-1 epidemic in Anhui Province, China
    Dong Zhang, Jianjun Wu, Yu Zhang, Yuelan Shen, Sheying Dai, Xiaolin Wang, Hui Qin Xing, Jin Lin, Jingwan Han, Jingyun Li et al. · 2020 · Virology Journal
  49. Personality Neuroscience
    Colin G. DeYoung, Scott D. Blain · 2020 · Cambridge University Press eBooks
  50. Genome-Wide Association Studies of Autism
    Joseph Glessner, John J. Connolly, Hakon H. Hakonarson · 2014 · Current Behavioral Neuroscience Reports
  51. Attention-Deficit/Hyperactivity Disorder Genomics: Update for Clinicians
    Josephine Elia, Jillan Cantor Sackett, Terri Turner, Martin Schardt, Shih-Ching Tang, Nicole Kurtz, Maura Dunfey, Nadia A. McFarlane, Aita Susi, David Danish et al. · 2012 · Current Psychiatry Reports
  52. Clinical relevance of small copy-number variants in chromosomal microarray clinical testing
    Dana Hollenbeck, Crescenda L. Williams, Kathryn T. Drazba, Maria D. Descartes, Bruce R. Korf, S. Lane Rutledge, Edward J. Lose, Nathaniel H. Robin, Andrew J. Carroll, Fady M. Mikhail · 2016 · Genetics in Medicine
  53. Genome-wide copy-number variation study of psychosis in Alzheimer’s disease
    Xiaojing Zheng, F. Yesim Demirci, M. Michael Barmada, Gale A. Richardson, Oscar L. López, Robert A. Sweet, M. Ilyas Kamboh, Eleanor Feingold · 2015 · Translational Psychiatry
  54. l -Carnosine as Adjunctive Therapy in Children and Adolescents with Attention-Deficit/Hyperactivity Disorder: A Randomized, Double-Blind, Placebo-Controlled Clinical Trial
    Alireza Ghajar, Farinaz Aghajan-Nashtaei, Mohsen Afarideh, Mohammad-Reza Mohammadi, Shahin Akhondzadeh · 2018 · Journal of Child and Adolescent Psychopharmacology
  55. Child Development and Structural Variation in the Human Genome
    Ying Zhang, Rajini Haraksingh, Fabian Grubert, Alexej S. Abyzov, Mark Gerstein, Sherman M. Weissman, Alexander Eckehart Urban · 2013 · Child Development
  56. An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity Disorder
    Leandro de Araújo Lima, Ana Cecília Feio dos Santos, Sintia Iole Belangero, Ary Gadelha, Rodrigo A. Bressan, Giovanni Abrahão Salum, Pedro Mário Pan, Tais Silveira Moriyama, Ana Soledade Graeff‐Martins, Ana Carina Tamanaha et al. · 2016 · Scientific Reports
  57. A 7q31.33q32.1 microdeletion including LRRC4 and GRM8 is associated with severe intellectual disability and characteristics of autism
    Noriko Sangu, Keiko Yamamoto Shimojima, Yuya Takahashi, Tsukasa Ohashi, Jun Tohyama, Toshiyuki Yamamoto · 2017 · Human Genome Variation
  58. Atomoxetine produces oxidative stress and alters mitochondrial function in human neuron-like cells
    Juan Carlos Corona, Sonia Carreón-Trujillo, Raquel González-Pérez, Denise Gómez-Bautista, Daniela Vázquez-González, Marcela Salazar–García · 2019 · Scientific Reports
  59. Copy Number Variants and Polygenic Risk Scores Predict Need of Care in Autism and/or ADHD Families
    Sonja LaBianca, Jette LaBianca, Anne Katrine Pagsberg, Klaus D. Jakobsen, Vivek Appadurai, Alfonso Buil, Thomas Mears Werge · 2020 · Journal of Autism and Developmental Disorders
  60. A comprehensive benchmarking of WGS-based deletion structural variant callers
    Varuni Sarwal, Sebastian Niehus, Ram Ayyala, Minyoung Kim, Aditya Prasad Sarkar, Sei Chang, Angela Lu, Neha Rajkumar, Nicholas Darci-Maher, Russell Littman et al. · 2022 · Briefings in Bioinformatics
  61. Molecular Mechanisms Underlying NMDARs Dysfunction and Their Role in ADHD Pathogenesis
    Justyna Kuś, Kamil Saramowicz, Maria Czerniawska, Wojciech Wiese, Natalia Siwecka, Wioletta Rozpędek‐Kamińska, Aleksandra Kucharska-Lusina, Dominik Strzelecki, Ireneusz Majsterek · 2023 · International Journal of Molecular Sciences
  62. Investigating the effects of copy number variants on reading and language performance
    Alessandro Gialluisi, Alessia Visconti, Erik G. Willcutt, Shelley D. Smith, Bruce F. Pennington, Mario Falchi, John C. DeFries, Richard K. Olson, Clyde Francks, Simon E. Fisher · 2016 · Journal of Neurodevelopmental Disorders
  63. Basolateral amygdala, nicotinic cholinergic receptors, and nicotine: Pharmacological effects and addiction in animal models and humans
    Burt M. Sharp · 2018 · European Journal of Neuroscience
  64. Lrrc7 mutant mice model developmental emotional dysregulation that can be alleviated by mGluR5 allosteric modulation
    Chi Ho Chong, Qi Li, Priscilla Hoi Shan Mak, Cypress Chun Pong Ng, Eva Hin Wa Leung, Vicky Huiqi Tan, Anthony Kin Wang Chan, Grainne Mary McAlonan, Siu Yuen Chan · 2019 · Translational Psychiatry
  65. Identification of structural variation in mouse genomes
    Thomas Keane, Kim Wong, David J. Adams, Jonathan Flint, Alexandre Reymond, Binnaz Yalcin · 2014 · Frontiers in Genetics
  66. Genome-wide association study identifies RBFOX1 locus influencing brain glucose metabolism
    Alzheimer’s Disease Neuroimaging Initiative, Lingli Kong, Dan Miao, Lin Tan, Shulei Liu, Jieqiong Li, Xi‐Peng Cao, Lan Tan · 2018 · Annals of Translational Medicine
  67. Personality and Emotion
    Rainer Reisenzein, Andrea Hildebrandt, Hannelore Weber · 2020 · Cambridge University Press eBooks
  68. Methylphenidate HCL for the treatment of ADHD in children and adolescents
    Ann Catherine Childress · 2016 · Expert Opinion on Pharmacotherapy
  69. Integrative genomic analysis of methylphenidate response in attention-deficit/hyperactivity disorder
    M. Pagerols, V. Richarte, C. Sánchez-Mora, P. Rovira, M. Soler Artigas, I. Garcia-Martínez, Eva Calvo-Sánchez, M. Corrales, B. D. da Silva, N. Mota et al. · 2018 · Scientific Reports
  70. Glutamate receptor metabotropic 7 (GRM7) gene polymorphisms in mood disorders and attention deficit hyperactive disorder
    Rezvan Noroozi, Mohammad Naser Taheri, Mir Davood Omrani, Soudeh Ghafouri‐Fard · 2019 · Neurochemistry International
  71. Organization of TNIK in dendritic spines
    Alain C. Burette, Kristen D. Phend, Susan Burette, Qingcong Lin, Musen Liang, Gretchen M. Foltz, Noël Taylor, Qi Wang, Nicholas J. Brandon, Brian Bates et al. · 2015 · The Journal of Comparative Neurology
  72. Trans-Synaptic Regulation of Metabotropic Glutamate Receptors by Elfn Proteins in Health and Disease
    Hayato Matsunaga, Jun Aruga · 2021 · Frontiers in Neural Circuits
  73. CNV analysis in Chinese children of mental retardation highlights a sex differentiation in parental contribution to de novo and inherited mutational burdens
    Binbin Wang, Taoyun Ji, Xueya Zhou, Jing Wang, Xi Wang, Jingmin Wang, Dingliang Zhu, Xuejun Zhang, Pak Chung Sham, Xuegong Zhang et al. · 2016 · Scientific Reports
  74. Correction: RBFOX1 and RBFOX3 Mutations in Rolandic Epilepsy
    Dennis Lal, Eva Maria Reinthaler, Janine Altmüller, Mohammad Reza Toliat, Hölger Thiele, Peter NÃ ⁄ rnberg, Holger Lerche, Andreas Hahn, Rikke Steensbjerre Møller, Hiltrud Muhle et al. · 2013 · PLoS ONE
  75. GRM7 gene mutations and consequences for neurodevelopment
    Geanne A. Freitas, Colleen Marie Niswender · 2023 · Pharmacology Biochemistry and Behavior
  76. Detection and correction of artefacts in estimation of rare copy number variants and analysis of rare deletions in type 1 diabetes
    Nicholas J. Cooper, Corina J. Shtir, Deborah J. Smyth, Hui Guo, Austin D.-E. Swafford, Manuela Zanda, Matthew E. Hurles, Neil M Walker, Vincent Plagnol, Jason D. Cooper et al. · 2014 · Human Molecular Genetics
  77. Genome-wide CNV analysis revealed variants associated with growth traits in African indigenous goats
    Mei Liu, M. Jennifer Woodward-Greene, Xiaolong Kang, Michael G. Pan, Benjamin D. Rosen, Curtis P. Van Tassell, Hong Chen, George E. Liu · 2019 · Genomics
  78. Neuromorphological and Neurofunctional Correlates of ADHD and ADD in the Auditory Cortex of Adults
    Bettina Lara Serrallach, Christine Groß, Markus Christiner, Simon Wildermuth, Peter T. Schneider · 2022 · Frontiers in Neuroscience
  79. Potential Inflammatory Biomarker in Patients with Attention Deficit Hyperactivity Disorder
    Ji Hyun Park · 2022 · International Journal of Molecular Sciences
  80. No Association Between General Cognitive Ability and Rare Copy Number Variation
    Allan F. McRae, Margaret J. Wright, Narelle K. Hansell, Grant W. Montgomery, Nicholas G. Martin · 2013 · Behavior Genetics
  81. Mitochondrial DNA haplogroups and risk of attention deficit and hyperactivity disorder in European Americans
    Xiao Chang, Yichuan Liu, Frank D. Mentch, Joseph Glessner, Hui‐Qi Qu, Kenny Nguyen, Patrick M. Abou‐Sleiman, Hakon H. Hakonarson · 2020 · Translational Psychiatry
  82. Folate Metabolism Gene 5,10-Methylenetetrahydrofolate Reductase (MTHFR) Is Associated with ADHD in Myelomeningocele Patients
    Catherine J. Spellicy, Hope Northrup, Jack McKay Fletcher, Paul T. Cirino, Maureen Dennis, Alanna C. Morrison, Carla Ann Martinez, Kit Sing Au · 2012 · PLoS ONE
  83. The role of rs2237781 withinGRM8in eating behavior
    Marie‐Therese Gast, Anke Tönjes, Maria Keller, Annette Horstmann, Nanette Steinle, Markus R. Scholz, I. Müller, Arno Villringer, Michael Stümvoll, Peter Louis Kovacs et al. · 2013 · Brain and Behavior
  84. Genetics and hypertension: is it time to change my practice?
    Delles, Christian, Padmanabhan, Sandosh · 2012 · Canadian Journal of Cardiology
  85. Identification of Copy Number Variants from SNP Arrays Using PennCNV
    Fang Li, Kai Wang · 2018 · Methods in molecular biology
  86. A polymorphism in the glutamate metabotropic receptor 7 is associated with cognitive deficits in the early phases of psychosis
    Boris Chaumette, Sarojini M. Sengupta, Martín Lepage, ASHOK K. MALLA, Srividya N. Iyer, Oussama Kébir, Patrick A. Dion, Guy Armand Rouleau, Marie‐Odile Krebs, Jai L. Shah et al. · 2020 · Schizophrenia Research
  87. Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American Ancestry
    Yichuan Liu, Xiao Chang, Hui‐Qi Qu, Lifeng Tian, Joseph Glessner, Jingchun Qu, Dong Li, Haijun Qiu, Patrick M. Abou‐Sleiman, Hakon H. Hakonarson · 2021 · Genes
  88. Neurobiology of Attention Deficit Hyperactivity Disorder
    Stephen V. Faraone, Pradeep G. Bhide, Joseph Biederman · 2017 · Oxford University Press eBooks
  89. Review of the association between obesity and ADHD.
    R. Martínez de Velasco, Eduardo Barbudo, Josefa Pérez-Templado, Belén Silveira, Javier Quintero · 2015 · Actas Españolas de Psiquiatría
  90. Energy Metabolism Disturbances in Cell Models of PARK2 CNV Carriers with ADHD
    V. S. Palladino, A. Chiocchetti, Lukas Frank, Denise Haslinger, R. McNeill, F. Radtke, A. Till, S. Haupt, O. Brüstle, Katharina Günther et al. · 2020 · Journal of Clinical Medicine
  91. Intragenic CNTN4 copy number variants associated with a spectrum of neurobehavioral phenotypes
    Stephanie Q. Zhang, Julie A. Fleischer, Hussam Al‐Kateb, Yoshiko Mito, Ina E. Amarillo, Marwan S. Shinawi · 2019 · European Journal of Medical Genetics
  92. Early Developmental Cues for Diagnosis of Attention Deficit/Hyperactivity Disorder in Young Children
    Itai Berger, Yoram Nevo · 2011 · Developmental Disabilities Research Reviews
  93. Rare copy number variants in patients with congenital conotruncal heart defects
    Hongbo Michael Xie, Petra Werner, Dwight Stambolian, Joan Wilson, Hakon H. Hakonarson, Peter S. White, Deanne M. Taylor, Elizabeth Goldmuntz · 2017 · Birth Defects Research
  94. Copy number variation analysis in the context of electronic medical records and large-scale genomics consortium efforts
    John J. Connolly, Joseph Glessner, Berta Almoguera, David R. Crosslin, Gail Pairitz Jarvik, Patrick M. Abou‐Sleiman, Hakon H. Hakonarson · 2014 · Frontiers in Genetics
  95. Association between the group III metabotropic glutamate receptor gene polymorphisms and attention-deficit/hyperactivity disorder and functional exploration of risk loci
    Qi Zhang, Xinzhen Chen, Shanyawen Li, Ting Yao, Jing Wu · 2020 · Journal of Psychiatric Research
  96. Annual Research Review: Rare genotypes and childhood psychopathology – uncovering diverse developmental mechanisms of ADHD risk
    Gaia Scerif, Kate Baker · 2014 · Journal of Child Psychology and Psychiatry
  97. Genetic factors underlying attention and impulsivity: mouse models of attention-deficit/hyperactivity disorder
    Shigeyoshi Itohara, Yuki Kobayashi, Toshiaki Nakashiba · 2014 · Current Opinion in Behavioral Sciences
  98. De novo mutations in neurological and psychiatric disorders: effects, diagnosis and prevention
    Julie Gauthier, Guy Armand Rouleau · 2012 · Genome Medicine
  99. Discovery of VU6027459: A First-in-Class Selective and CNS Penetrant mGlu7 Positive Allosteric Modulator Tool Compound
    Carson W. Reed, Jacob J. Kalbfleisch, Madison J. Wong, Jordan P. Washecheck, Ashton Hunter, Alice L. Rodriguez, Anna Louise Blobaum, Peter Jeffrey Conn, Colleen Marie Niswender, Craig W. Lindsley · 2020 · ACS Medicinal Chemistry Letters
  100. Personality and the Self
    Michael D. Robinson, Constantine Sedikides · 2020 · Cambridge University Press eBooks