Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
de Kovel, C. G. F., Trucks, H., Helbig, I., Mefford, H. C., Baker, C., Leu, C., Kluck, C., Muhle, H., von Spiczak, S., Ostertag, P., Obermeier, T., Kleefuss-Lie, A. A., Hallmann, K., Steffens, M., Gaus, V., Klein, K. M., Hamer, H. M., Rosenow, F., Brilstra, E. H., Kasteleijn-Nolst Trenite, D., Swinkels, M. E. M., Weber, Y. G., Unterberger, I., Zimprich, F., Urak, L., Feucht, M., Fuchs, K., Moller, R. S., Hjalgrim, H., De Jonghe, P., Suls, A., Ruckert, I.-M., Wichmann, H.-E., Franke, A., Schreiber, S., Nurnberg, P., Elger, C. E., Lerche, H., Stephani, U., Koeleman, B. P. C., Lindhout, D., Eichler, E. E., Sander, T.·2010·Brain
Cited by (446)
Items 301–400 of 446
- Nomo1 deficiency causes autism-like behavior in zebrafishQi Zhang, Fei Li, Tingting Li, Jia Lin, Jing Jian, Yinglan Zhang, Xudong Chen, Ting Liu, Shenglan Gou, Yawen Zhang et al. · 2024 · EMBO Reports
- Evidence for the multiple hits genetic theory for inherited language impairment: a case studyTracy Michelle Centanni, Jordan R. Green, Jenya Iuzzini-Seigel, Christopher W. Bartlett, Tiffany P. Hogan · 2015 · Frontiers in Genetics
- Copy number variation analysis in 83 children with early-onset developmental and epileptic encephalopathy after targeted resequencing of a 109-epilepsy gene panelKyoko Hirabayashi, Daniela Tiaki Uehara, Hidetoshi Abe, Atsushi Ishii, Keiji Moriyama, Shinichi Hirose, Johji Inazawa · 2019 · Journal of Human Genetics
- SNP array and phenotype correlation shows that FLI1 deletion per se is not responsible for thrombocytopenia development in Jacobsen syndromeMarie Trková, Vera Becvarova, Martin Hynek, Lenka Hnykova, Eva Hlavova, Gabriela Křečková, E Kulovaný, David Čutka, Jitka Zatloukalova, Kristyna Markova et al. · 2012 · American Journal of Medical Genetics Part A
- Deletions and Other Structural Abnormalities of the AutosomesNancy Bettina Spinner, Laura Kathleen Conlin, Surabhi Mulchandani, Beverly S. Emanuel · 2013 · Elsevier eBooks
- Prenatal diagnosis of 15q11.2 microdeletion fetuses in Eastern China: 21 case series and literature reviewXia-Li Jiang, Bin Liang, Wantong Zhao, Na Lin, Hailong Huang, Meiying Cai, Liangpu Xu · 2023 · The Journal of Maternal-Fetal & Neonatal Medicine
- Analysis of a Protein Network Related to Copy Number Variations in Autism Spectrum DisorderJaqueline Bohrer Schuch, Vanessa Rodrigues Paixão‐Côrtes, Dânae Longo, Tatiana Roman, Rudimar dos Santos Riesgo, Josiane Ranzan, Michele Michelin Becker, Mariluce Riegel, Lavínia Schüler‐Faccini · 2019 · Journal of Molecular Neuroscience
- Genetics of epilepsy: successes, problems and development prospectsRimma Gamirova, R. R. Gamirova, Radiy Germanovich Esin · 2020 · S S Korsakov Journal of Neurology and Psychiatry
- 15q13.3 microdeletions in a prospectively recruited cohort of patients with idiopathic generalized epilepsy in BulgariaAndrey Kirov, Petia S Dimova, Албена Тодорова, Heather C. Mefford, Tihomir Todorov, Gergana Saraylieva, Veneta Bojinova, Vanio Mitev, Ingo Helbig · 2013 · Epilepsy Research
- Expression Analysis of CYFIP1 and CAMKK2 Genes in the Blood of Epileptic and Schizophrenic PatientsArezou Sayad, Fatemeh Ranjbaran, Soudeh Ghafouri‐Fard, Shahram Arsang‐Jang, Mohammad Naser Taheri · 2018 · Journal of Molecular Neuroscience
- Chromosome 16p13.11 Microdeletion Syndrome in a Newborn: A Case StudyAmanda Elizabeth Smith, Amy J. Jnah, Desi Newberry · 2018 · Neonatal Network The Journal of Neonatal Nursing
- Pathophysiology of EpilepsyKenneth A. Jenrow, Kost V. Elisevich · 2019 · Cambridge University Press eBooks
- Global characterization of copy number variants in epilepsy patients from whole genome sequencingJean Monlong, Simon Girard, Caroline Meloche, Maxime Cadieux‐Dion, Danielle Molinari Andrade, Ron G. Lafrenière, Micheline Gravel, Dan Spiegelman, Alexandre Dionne‐Laporte, Cyrus G. Boelman et al. · 2017 · bioRxiv (Cold Spring Harbor Laboratory)
- The newly identified migration inhibitory protein regulates the radial migration in the developing neocortexSuxiang Zhang, Yoshitaka Kanemitsu, Masashi Fujitani, Toshihide Yamashita · 2014 · Scientific Reports
- Genetic mechanisms in generalized epilepsiesXiaoqian Wang, Xueyi Rao, Jia Zhang, Jing Gan · 2023 · Acta Epileptologica
- Structural Variation Evolution at the 15q11-q13 Disease-Associated LocusAnnalisa Paparella, Alberto L’Abbate, Donato Palmisano, Gerardina Chirico, David Porubskỳ, Claudia Rita Catacchio, Mario Ventura, Evan E. Eichler, Flavia Angela Maria Maggiolini, Francesca Antonacci · 2023 · International Journal of Molecular Sciences
- 16p13.11 Microdeletion in a Patient With Hemiconvulsion-Hemiplegia-Epilepsy SyndromeChristina Miteff, Robert L. Smith, Nicole L. Bain, Gopinath Musuwadi Subramanian, Janis E. Brown, Ben Kamien · 2014 · Journal of Child Neurology
- Clinical and molecular delineation of a 16p13.2p13.13 microduplicationElisa Tassano, Maria Giannina Alpigiani, Andrea Calcagno, Pietro Salvati, L. De Miglio, Patrizia Fiorio, Cristina Cuoco, Giorgio Gimelli · 2015 · European Journal of Medical Genetics
- Epilepsy Genetics: Advancements in the Field and Impact on Clinical PracticeSenyene Eyo Hunter, Elizabeth Jalazo, Thomas Felton, Erin L. Heinzen, Yael Shiloh‐Malawsky · 2022 · Epilepsy
- Neuropsychiatric connections of ADHD genesJ. Peter H. Burbach · 2010 · The Lancet
- Copy number variation in genetic epilepsy with febrile seizures plusOlivier Fortin, Christian Vincelette, Sébastien Chénier, Ahmad Ghais, Michael Israel Shevell, Elisabeth Simard‐Tremblay, Kenneth Alexis Myers · 2020 · European Journal of Paediatric Neurology
- Clinical phenotype of the 16p.13.11 microdeletion: a case report with a mini review of the literatureRoberto Palumbi, Emanuela Ponzi, Stefania Micella, Mara Pascali, Roberta Bucci, Mattia Gentile, Lucia Margari, Marta Simone · 2024 · Frontiers in Genetics
- Application of Array-Based Comparative Genomic Hybridization to Pediatric Neurologic DiseasesJung Hye Byeon, Eunsim Shin, Gun-Ha Kim, Kyungok Lee, Young Sook Hong, Joo Won Lee, Baik‐Lin Eun · 2013 · Yonsei Medical Journal
- Genome-Wide Association Analysis of Neonatal White Matter MicrostructureJ Zhang, Kai Xia, Mihye Ahn, Shaili C. Jha, Reid Blanchett, James J. Crowley, Jin Szatkiewicz, Fei Zou, Hongtu Zhu B, Martin Andreas Styner et al. · 2020 · Cerebral Cortex
- Concomitant deletion of chromosome 16p13.11 and triplication of chromosome 19p13.3 in a child with developmental disorders, intellectual disability, and epilepsyElisa Tassano, Lucia De Santis, Maria Corona, Stefano Parmigiani, Dalila Zanetti, Simona Porta, Giorgio Gimelli, Cristina Cuoco · 2015 · Molecular Cytogenetics
- Cloning of the promoter of NDE1, a gene implicated in psychiatric and neurodevelopmental disorders through copy number variationNicholas J. Bradshaw · 2016 · Neuroscience
- Neuropsychiatric genomics in precision medicine: diagnostics, gene discovery, and translationAnna C. Need, David B. Goldstein · 2016 · Dialogues in Clinical Neuroscience
- Monogenic Epilepsies in Adult Epilepsy Clinics and Gene-Driven Approaches to TreatmentLisa M. S. Clayton, Angeliki Vakrinou, Simona Balestrini, Sanjay M. Sisodiya · 2025 · Current Neurology and Neuroscience Reports
- Translation of genetic findings to clinical practice in juvenile myoclonic epilepsyRhys Huw Thomas, Seo‐Kyung Chung, Khalid Hamandi, Mark I. Rees, Michael Kerr · 2012 · Epilepsy & Behavior
- Chromosomal microarray and exome sequencing in unexplained early infantile epileptic encephalopathies in a highly consanguineous populationDilşad Türkdoğan, Ayberk Türkyılmaz, Güneş Sağer, Gülten Öztürk, Olcay I. Unver, Merve Say · 2021 · International Journal of Neuroscience
- Assessment of burden and segregation profiles of CNVs in patients with epilepsyClaudia Moreau, Frédérique Tremblay, Stefan Wolking, Alexandre Girard, Catherine Laprise, Fadi F. Hamdan, Jacques L. Michaud, Berge Arakel Minassian, Patrick Cossette, Simon Girard · 2022 · Annals of Clinical and Translational Neurology
- The role of copy number variants in the genetic architecture of common familial epilepsiesEpi4K Consortium · 2023 · Epilepsia
- New technologies in molecular geneticsIngo Helbig · 2014 · Progress in brain research
- Mode of transmission of schizophreniaRex N. Ponnudurai, J Jayakar · 2010 · Asian Journal of Psychiatry
- Infantile spasms and 15q11.2q13.1 chromosome duplication in two successive generationsRaili Riikonen, Tiina Wallden, Hannaleena Kokkonen · 2015 · European Journal of Paediatric Neurology
- Expanding role of GABAA receptors in generalised epilepsiesHeather C. Mefford · 2018 · The Lancet Neurology
- Performance of Chromosomal Microarray Analysis for Detection of Copy Number Variations in Fetal Echogenic BowelXiangqun Fan, Hailong Huang, Xiyao Lin, Huili Xue, Meiying Cai, Na Lin, Liangpu Xu · 2021 · Risk Management and Healthcare Policy
- Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetusChih‐Ping Chen, Tsang‐Ming Ko, Schu‐Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun‐Yi Chen, Dai‐Dyi Town, Lifeng Chen, Wayseen Wang · 2021 · Taiwanese Journal of Obstetrics and Gynecology
- Idiopathische generalisierte EpilepsienYG Weber, T. Sander, Holger Lerche · 2011 · Clinical Epileptology
- Intrauterine ultrasound phenotyping, molecular characteristics, and postnatal follow-up of fetuses with the 15q11.2 BP1-BP2 microdeletion syndrome: a single-center, retrospective clinical studyMeiying Cai, Aixiang Lv, Wantong Zhao, Liangpu Xu, Na Lin, Hailong Huang · 2024 · BMC Pregnancy and Childbirth
- Altered development and network connectivity in a human neuronal model of 15q11.2 deletion-related neurodevelopmental disordersChrista Whelan Habela, Shiyu Liu, Arens Taga, Sean Oddoye, Raha Maryam Dastgheyb, Norman J. Haughey, Dwight E. Bergles, Hongjun Song, Guo‐li Ming, Nicholas John Maragakis · 2025 · Translational Psychiatry
- 15q13.3 MicrodeletionBregje W.M. van Bon, Heather C. Mefford, Bert B A De Vries · 2015 · Europe PMC (PubMed Central)
- Exome sequencing and arrayCGH detection of gene sequence and copy number variation between ILS and ISS mouse strainsLaura Dumas, Charles Michael Dickens, Nathan Anderson, Jonathan M. Davis, Beth Bennett, Richard A. Radcliffe, James M. Sikela · 2014 · Mammalian Genome
- Submicroscopic aberrations of chromosome 16 in prenatal diagnosisXiaoqing Wu, Liangpu Xu, Ying Li, Na Lin, Linjuan Su, Meiying Cai, Xiaorui Xie, Lin Zheng, Hailong Huang, Yuan Lin · 2019 · Molecular Cytogenetics
- Genetics and Epigenetics of Autism Spectrum DisordersThomas Bourgeron · 2012 · Research and perspectives in neurosciences
- Genetics of Psychiatric Disorders: Advances in Genetic Epidemiology and Molecular GeneticsKathleen Ries Merikangas, Maria Karayiorgou · 2015 · Wiley eBooks
- Faculty Opinions recommendation of Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies.Michael Johnston · 2011 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Impact of copy number variants in epilepsy plus neurodevelopment disordersS João, Rita Quental, Joel Pinto, Carolina Almeida, Helena Santos, Sofia Dória · 2024 · Seizure
- A channel for precision diagnosis and treatment in genetic epilepsyAnnapurna Poduri · 2014 · Annals of Neurology
- Clarifying the role of the 22q11.2 microdeletion in juvenile myoclonic epilepsyIngo Helbig, Corinna Hartmann, Heather C. Mefford · 2013 · Epilepsy & Behavior
- What Epilepsy Comorbidities Are Important to Model in the Laboratory? Clinical PerspectivesSimon D. Shorvon · 2014 · Advances in experimental medicine and biology
- Genetic variations and associated pathophysiology in the management of epilepsyLeanne M. Dibbens, Mulley · 2011 · The Application of Clinical Genetics
- Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5–6.0 Hz polyspike wavesJenny E. Wight, Viet-Huong V. Nguyen, Marco Tulio Medina, Christopher Patterson, Reyna M. Durón, Yolly Molina, Yuchen Lin, Iris Enriqueta Martínez-Juárez, Adriana Ochoa, Aurelio Jara‐Prado et al. · 2016 · Molecular Genetics & Genomic Medicine
- Genetik der idiopathischen EpilepsienYG Weber, Holger Lerche · 2013 · Der Nervenarzt
- Genetic generalized epilepsy in three siblings with 8q21.13-q22.2 duplicationArezoo Rezazadeh, Felippe Borlot, Hanna Faghfoury, Danielle Molinari Andrade · 2017 · Seizure
- Genetic mechanisms of neurodevelopmental disordersPing Yee Billie Au, Alison J. Eaton, David Alexandre Dyment · 2020 · Handbook of clinical neurology
- Copy Number Variation and Structural Genomic Findings in 116 Cases of Sudden Unexplained Death between 1 and 28 Months of AgeCatherine A. Brownstein, Elise A. Douard, Robin Lynn Haynes, Hyun Yong Koh, Alireza Haghighi, Christine Keywan, Bree E. Martin, Sanda Alexandrescu, Elisabeth A. Haas, Sara O. Vargas et al. · 2022 · Advanced Genetics
- Evaluation of copy number burden in specific epilepsy types from a genome-wide study of 18,564 subjectsLisa‐Marie Niestroj, Daniel P. Howrigan, Eduardo Pérez‐Palma, Elmo Saarentaus, Peter Nürnberg, Remi Stevelink, Mark J. Daly, Aarno V. Palotie, Dennis Lal, Epi25 Collaborative · 2019 · bioRxiv (Cold Spring Harbor Laboratory)
- Congenital Arthrogryposis: An Extension of the 15q11.2 BP1-BP2 Microdeletion Syndrome?Usrey, K. M., Williams, C. A., Dasouki, M., Fairbrother, L. C., Butler, M. G. · 2014 · Case Reports in Genetics
- Copy Number Variation and Epilepsy: State of the Art in the Era of High-Throughput Sequencing—A Multicenter Cohort StudySarah Baer, Audrey Schalk, Marguerite Miguet, Élise Schaefer, Salima El Chehadeh, Emmanuelle Ginglinger, Anne de Saint Martin, Marie‐Thérèse Abi‐Warde, Vincent Laugel, Yvan de Féraudy et al. · 2024 · Pediatric Neurology
- Psychoses of Epilepsy: Unravelling the Phenotypic and Genotypic FeaturesGenevieve Rayner, Eliza Honybun, Melanie Bahlo, Karen L. Oliver, Ingrid Eileen Scheffer · 2025 · Annals of Neurology
- Beyond the Copy Number Differences: The Phenotypic Diversity of Children With 15q11.2 Microdeletions and MicroduplicationsGünce Başarır, Irmak Erdoğan, Berk Özyılmaz, Pınar Gençpınar, Nihal Olgaç Dündar · 2025 · Journal of Child Neurology
- Microdeletion/microduplication of proximal 15q11.2 between BP1 and BP2: a susceptibility region for neurological dysfunction including developmental and language delay Rachel D. BurnsideRomela PasionFady M. MikhailAndrew J. CarrollNathaniel H. Robin • Erin L. YoungsInder K. GadiElizabeth KeitgesVikram L. JaswaneyPeter R. Papenhausen • Venkateswara R. PotluriHiba RishegBrooke RushJanice L. SmithStuart Schwartz •Rachel D. Burnside, Romela M. Pasion, Inder K. Gadi, Vikram L. Jaswaney, Papenhausen B. Rush, Stuart Schwartz, James H. Tepperberg, Fady M. Mikhail, Andrew J. Carroll, Nathaniel H. Robin et al. · 2011
- Integrative Multi-Omics Research in Cerebral Palsy: Current Progress and Future ProspectsChengqi Xin, Xin Guan, Liang Wang, Jing Liu · 2022 · Neurochemical Research
- Midbrain structure volume, estimated myelin and functional connectivity in idiopathic generalised epilepsyAndrea McKavanagh, Adam Ridzuan-Allen, Barbara A. K. Kreilkamp, Yachin Chen, José V. Manjón, Pierrick Coupé A, Robert Martyn Bracewell, Kumar Das, Peter N. Taylor, Anthony Guy Marson et al. · 2023 · Epilepsy & Behavior
- Examining neurodevelopmental problems in 15q11.2 ( BP1‐BP2 ) copy number variation carriers at ages 9/12 and 18 in a Swedish twin sampleLina Jönsson, Joanna Martin, Paul Lichtenstein, Patrik K. E. Magnusson, Sebastian Lundström, Lars Westberg, Kristiina Tammimies · 2023 · Molecular Genetics & Genomic Medicine
- Copy number variants associated with epilepsy from gene expression microarraysDong Wang, Xia Li, Shanshan Jia, Yan Wang, Zhijing Wang, Xixiao Song, Liang Liu · 2015 · Journal of Clinical Neuroscience
- Copy-number variants as modulators of common disease susceptibilityChiara Auwerx, Maarja Jõeloo, Marie C. Sadler, Nicolò Tesio, Sven E. Ojavee, Charlie J. Clark, Reedik Mägi, Alexandre Reymond, Zoltán Kutalik · 2023 · medRxiv
- Molecular Architecture and Neurobiology of the EpilepsiesRyan S. Dhindsa, Daniel H. Lowenstein, David B. Goldstein · 2016 · Elsevier eBooks
- Gene–gene interaction network analysis indicates CNTN2 is a candidate gene for idiopathic generalized epilepsyZhi-Jian Lin, Junwei He, Sheng-Yin Zhu, Li-Hong Xue, Jianfeng Zheng, Li-Qin Zheng, Bixia Huang, Guozhang Chen, Peng-Xing Lin · 2024 · Neurogenetics
- Idiopathic epilepsySimon D. Shorvon, Frédérick Andermann, Renzo Guerrini · 2011 · Cambridge University Press eBooks
- Familial 15q11.2 Micro deletions are not Fully Penetrant in Two Cases with Hereditary Spastic Paraplegia and Dysmorphic FeaturesEwelina Elert‐Dobkowska · 2014 · Journal of Genetic Syndromes & Gene Therapy
- Whole-exome sequencing of patients with juvenile myoclonic epilepsyТимечко Елена Евгеньевна, Шилкина Ольга Сергеевна, Natalya V. Oreshkova, V. O. Kobanenko, E. A. Osipova, Natalia Alekseevna Shnayder, Д. В. Дмитренко · 2022 · Epilepsy and Paroxysmal Conditions
- Systematic Review and Meta-Analyses of Aminopeptidases as Prognostic Biomarkers in Amyotrophic Lateral SclerosisBárbara Teruel-Peña, José Luis Gómez‐Urquiza, Nora Suleiman‐Martos, Isabel Prieto, Francisco Jose Garcia-Cozar, Manuel Ramírez‐Sánchez, Carmen María Fernández-Martos, Germán Domínguez-Vías · 2023 · International Journal of Molecular Sciences
- The NDE1 genomic locus can affect treatment of psychiatric illness through gene expression changes related to MicroRNA-484Nicholas J. Bradshaw, Liisa Ukkola-Vuoti, Maiju Pankakoski, Amanda B. Zheutlin, Alfredo Ortega-Alonso, Minna Torniainen‐Holm, Vishal Sinha, Sebastian Therman, Tiina Paunio, Jaana Suvisaari et al. · 2016 · bioRxiv (Cold Spring Harbor Laboratory)
- Haploinsufficiency of the psychiatric risk gene Cyfip1 causes abnormal postnatal hippocampal neurogenesis through microglial and Arp2/3 mediated actin dependent mechanismsNiels Haan, Laura J Westacott, Jenny Carter, Michael John Owen, William P Gray, Jérémy Hall, Lawrence S Wilkinson · 2018 · bioRxiv (Cold Spring Harbor Laboratory)
- Childhood Absence EpilepsyLuigi Vetri, Carola Costanza, Margherita Siciliano, Francesco Precenzano, Beatrice Gallai, Marco Carotenuto · 2024 · IntechOpen eBooks
- Epilepsy: Epidemiology, Molecular Pathogenesis, and Clinical ManagementJian Liu, Xinyan Wu, Ting Yin, Feining Huang, Manqi Kong, Yi Yang, Z.H. Liu, Jiabin Yu, Tianpeng Zhang · 2026 · MedComm
- Strategies for studying the epilepsy genomeThomas N. Ferraro, José María Serratosa, Deb K. Pal, Guy Armand Rouleau, Russell J. Buono · 2010 · Epilepsia
- Die historische Entwicklung genetischer EpilepsiediagnostikHenrike Heyne, Johannes R. Lemke · 2015 · Clinical Epileptology
- Review article Epilepsy associated with autism and attention deficit hyperactivity disorder: Is there a genetic link?Adriana Lo‐Castro, Paolo Curatolo · 2014
- 16p13.11 deletion variants associated with neuropsychiatric disorders cause morphological and synaptic changes in induced pluripotent stem cell-derived neuronsElizabeth D. Buttermore, Nickesha Camille Anderson, Pin-Fang Chen, Nina R. Makhortova, Kristina H. Kim, Syed M.A. Wafa, Sean Dwyer, John M. Micozzi, Kellen Diamond Winden, Bo Zhang et al. · 2022 · Frontiers in Psychiatry
- Neue Entwicklungen der Epileptogenese und therapeutische PerspektivenHolger Lerche, Annamaria Vezzani, Heinz Beck, Ingmar Blümcke, Yvonne G. Weber, Christian Erich Elger · 2011 · Der Nervenarzt
- The genetics of schizophreniaHugh Gurling, Andrew McQuillin · 2012 · Cambridge University Press eBooks
- Idiopathische generalisierte Epilepsien und FotosensitivitätNatalie Winter, Hiltrud Muhle, Holger Lerche · 2015 · Clinical Epileptology
- Aspetti genetici delle epilessieGaëtan Lesca · 2018 · EMC - Neurologia
- Molecular genetic management of epilepsyDavid Lewis‐Smith, Donald P. Craig, Naomi Thomas, Khalid Hamandi, Rhys Huw Thomas · 2019 · Elsevier eBooks
- SNP Variants at 16p13.11 Clarify the Role of the NDE1/miR-484 Locus in Major Mental Illness in FinlandVishal Sinha, Alfredo Ortega‐Alonso, Liisa Ukkola‐Vuoti, Outi Mantere, Amanda B. Zheutlin, Minna Torniainen‐Holm, Sebastian Therman, Annamari Tuulio‐Henriksson, Pekka J. Jylhä, Jaakko A. Kaprio et al. · 2020 · Schizophrenia Bulletin Open
- Genetic Aspects of Human EpilepsyA.N. Prasad, Chitra Prasad · 2014 · Elsevier eBooks
- Genetic studies of the common epilepsies: genome-wide association studies in the partial epilepsiesClaudia B. Catarino · 2014 · UCL Discovery (University College London)
- Genetic Counselling in EpilepsyFederico Zara · 2009 · Wiley eBooks
- Magnetic Resonance Spectroscopy as applied to epilepsyRobert J. Simister · 2012 · UCL Discovery (University College London)
- The interictal state in epilepsy and behaviorDaniel T. Barkmeier · 2010 · Human Biology
- Large-scale examination of neuropsychiatric, cognitive and cardiovascular phenotypic associations with 15q11.2 BP1-BP2 deletion in ∼500,000 UK Biobank individualsSimon G. Williams, Apostol Nakev, Hui Guo, Simon Frain, Gennadiy Tenin, Anna Liakhovitskaia, Priyanka Saha, James Rush Priest, Kathryn E. Hentges, Bernard D. Keavney · 2019 · bioRxiv (Cold Spring Harbor Laboratory)
- Current World Literature2011 · Current Opinion in Neurology
- Faculty Opinions recommendation of Analysis of shared heritability in common disorders of the brain.Donna K. Slonim · 2018 · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature
- Recurrent CNVs in the Etiology of Epigenetic Neurodevelopmental DisordersJanine M. LaSalle, Mohammad Saharul Islam · 2013 · Springer eBooks
- Structural genomic variants in pediatric seizure disordersJohanna A. Jähn, Ingo Helbig · 2015 · Journal of Pediatric Epilepsy
- Genetische Untersuchungen bei EpilepsienHolger Lerche, Bernd Axel Neubauer · 2011 · Clinical Epileptology
- Genomic copy number variation in schizophreniaDanielle S. Rudd · 2014