Increased exonic de novo mutation rate in individuals with schizophrenia
Girard, Simon L, Gauthier, Julie, Noreau, Anne, Xiong, Lan, Zhou, Sirui, Jouan, Loubna, Dionne-Laporte, Alexandre, Spiegelman, Dan +14 more·2011·Nature Genetics
DOI 10.1038/ng.886
Cited by (435)
Items 201–300 of 435
- RNA-Seq methods for imperfect samples: development, evaluation and applicationsXian Adiconis, Lin Fan, David S. DeLuca, Andrey Sivachenko, Nathalie L.M.M. Pochet, Aaron M. Berlin, Sarah Young, Gad A. Getz, Aviv Regev, Chad Nusbaum et al. · 2011 · Genome biology
- The genetic basis of onset age in schizophrenia: evidence and modelsNa Zhan, Pak Chung Sham, Hon‐Cheong So, Simon S. Y. Lui · 2023 · Frontiers in Genetics
- De novo non-synonymous TBL1XR1 mutation alters Wnt signaling activityAkira Nishi, Shusuke Numata, Atsushi Tajima, Xiaolei Zhu, Koki Ito, Atsushi Saito, Yusuke Kato, Makoto Kinoshita, Shinji Shimodera, Shinji Ono et al. · 2017 · Scientific Reports
- Integrating Clinical Data and Imputed Transcriptome from GWAS to Uncover Complex Disease Subtypes: Applications in Psychiatry and CardiologyLiangying Yin, Carlos Kwan‐Long Chau, Pak Chung Sham, Hon‐Cheong So · 2019 · The American Journal of Human Genetics
- Deep resequencing of 17 glutamate system genes identifies rare variants in DISC1 and GRIN2B affecting risk of opioid dependencePingxing Xie, Henry R. Kranzler, John Harrison Krystal, Lindsay A. Farrer, Hongyu Zhao, Joel E. Gelernter · 2013 · Addiction Biology
- The Impact of Improved Microarray Coverage and Larger Sample Sizes on Future Genome‐Wide Association StudiesKarla J. Lindquist, Eric Jorgenson, Thomas J. Hoffmann, John S. Witte · 2013 · Genetic Epidemiology
- A new era in the discovery of de novomutations underlying human genetic diseaseChee‐Seng Ku, Vasilis Vasiliou, D.N. Cooper · 2012 · Human Genomics
- Next-generation sequencing approaches for genetic mapping of complex diseasesFerrán Casals, Youssef Idaghdour, Julie Hussin, Philip Awadalla · 2012 · Journal of Neuroimmunology
- Rare Risk Variants Identification by Identity-by-Descent Mapping and Whole-Exome Sequencing Implicates Neuronal Development Pathways in Schizophrenia and Bipolar DisorderCecilia Salvoro, Stefania Bortoluzzi, Alessandro Coppe, Giorgio Valle, Erika Feltrin, Maria Luisa Mostacciuolo, Giovanni Vazza · 2018 · Molecular Neurobiology
- Prioritization of Variants Detected by Next Generation Sequencing According to the Mutation Tolerance and Mutational Architecture of the Corresponding GenesIria Roca, Ana Fernández Marmiesse, Sofía Gouveia, Marta Segovia, María Luz Couce · 2018 · International Journal of Molecular Sciences
- Exome array analysis suggests an increased variant burden in families with schizophreniaNina S. McCarthy, Phillip E. Melton, Sarah V. Ward, Spencer M. Allan, Milan Dragović, Melanie L. Clark, Bharti Morar, Justin P. Rubio, John Blangero, Johanna Claire Badcock et al. · 2016 · Schizophrenia Research
- CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmiaXiao‐Rong Liu, Ting‐Ting Ye, Wen‐Jun Zhang, Xuan Guo, Jie Wang, Shaoping Huang, Longshan Xie, Xing‐Wang Song, Wei‐Wen Deng, Bing-Mei Li et al. · 2021 · CNS Neuroscience & Therapeutics
- Mutation Burden of Rare Variants in Schizophrenia Candidate GenesSimon Girard, Patrick A. Dion, Cynthia V. Bourassa, Steve Geoffroy, Pamela Lachance‐Touchette, Amina Barhdadi, Mathieu Langlois, Ridha Joober, Marie‐Odile Krebs, Marie‐Pierre Dubé et al. · 2015 · PLoS ONE
- No evidence that runs of homozygosity are associated with schizophrenia in an Irish genome-wide association datasetElizabeth A. Heron, Paul Cormican, Gary J Donohoe, F. Anthony O’Neill, Kenneth S. Kendler, Brien P. Riley, Michael Gill, Aiden Peter Corvin, Derek W. Morris · 2014 · Schizophrenia Research
- Convergent roles of de novo mutations and common variants in schizophrenia in tissue-specific and spatiotemporal co-expression networkPeilin Jia, Xiangning Chen, Ayman H. Fanous, Zhongming Zhao · 2018 · Translational Psychiatry
- Effects of Importin α1/KPNA1 deletion and adolescent social isolation stress on psychiatric disorder-associated behaviors in miceKoki Sakurai, Taichi Itou, Makiko Morita, Emiko Kasahara, Tetsuji Moriyama, Tom Macpherson, Takaaki Ozawa, Yoichi Miyamoto, Yoshihiro Yoneda, Atsuo Sekiyama et al. · 2021 · PLoS ONE
- In vitro fluorescence assay to measure GDP/GTP exchange of guanine nucleotide exchange factors of Rho family GTPasesAlyssa M. Blaise, Ellen E Corcoran, Eve S. Wattenberg, Yan-Ling Zhang, Jeffrey R. Cottrell, Anthony J. Koleske · 2021 · Biology Methods and Protocols
- Patterns of Variation Influencing Antipsychotic Treatment Outcomes in South African First-Episode Schizophrenia PatientsBritt I. Drögemöller, Dana J.H. Niehaus, Bonginkosi Chiliza, Lize van der Merwe, Laila Asmal, Anil K. Malhotra, Galen E.B. Wright, Robin Alexander Emsley, Louise Warnich · 2014 · Pharmacogenomics
- Investigation of the role of TCF4 rare sequence variants in schizophreniaFitnat Buket Basmanav, Andreas J. Forstner, Heide Loehlein Fier, Stefan Herms, Sandra Meier, Franziska Degenhardt, Per Hoffmann, Sandra Barth, Nadine Fricker, Jana Strohmaier et al. · 2015 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Sequencing-based high throughput mutation detection in bread wheatGaganjot Sidhu, Amita Mohan, Ping Zheng, Amandeep Kaur Dhaliwal, Dorrie Main, Kulvinder Singh Gill · 2015 · BMC Genomics
- Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic CasesLinlin Wang, Aiguo Ren, Tian Tian, Nan Li, Xuanye Cao, Peng Zhang, Lei Jin, Zhiwen Li, Yan Shen, Bo Zhang et al. · 2019 · Frontiers in Neuroscience
- Jumping on the Train of Personalized Medicine: A Primer for Non-Geneticist Clinicians: Part 2. Fundamental Concepts in Genetic EpidemiologyAihua Li, David Meyre · 2014 · Current Psychiatry Reviews
- Evolution and dysfunction of human cognitive and social traits: A transcriptional regulation perspectiveRoman Zug, Tobias Uller · 2022 · Evolutionary Human Sciences
- Future possibilities in migraine geneticsLaura Aviaja Rudkjøbing, Ann-Louise Esserlind, J. Olesen · 2012 · The Journal of Headache and Pain
- Precise detection of de novo single nucleotide variants in human genomesLaura Gómez-Romero, Kim Palacios-Flores, José Luis Reyes, Delfino García, Margareta Boege, Guillermo Dávila, Margarita Flores, Michael C. Schatz, Rafael Palacios · 2018 · Proceedings of the National Academy of Sciences
- Developmental disruption to the cortical transcriptome and synaptosome in a model of SETD1A loss-of-functionNicholas E. Clifton, Matthew L. Bosworth, Niels Haan, Elliott Rees, Peter Holmans, Lawrence S. Wilkinson, Anthony R Isles, Mark O. Collins, Jérémy Hall · 2022 · Human Molecular Genetics
- De novo mutations in neurological and psychiatric disorders: effects, diagnosis and preventionJulie Gauthier, Guy Armand Rouleau · 2012 · Genome Medicine
- Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample setsFranziska Degenhardt, Lutz Priebe, S Meier, Leonhard Lennertz, Fabian Streit, Stephanie H. Witt, A Hofmann, Tim Becker, Rainald Mößner, Wolfgang Maier et al. · 2013 · Translational Psychiatry
- Whole exome sequencing identifies hemizygous deletions in the UGT2B28 and USP17L2 genes in a three‑generation family with endometriosisHans Albertsen, Charoula Matalliotaki, Michail Matalliotakis, Maria I. Zervou, Ioannis Matalliotakis, Demetrios A. Spandidos, Rakesh Chettier, Kenneth J. Ward, George N. Goulielmos · 2019 · Molecular Medicine Reports
- Antipsychotics and the Dopamine–Serotonin ConnectionB. Ellenbroek, A. Cesura · 2014 · Topics in medicinal chemistry
- Rare Variants in Tissue Inhibitor of Metalloproteinase 2 as a Risk Factor for Schizophrenia: Evidence From Familial and Cohort AnalysisJibin John, Aditya Kumar Sharma, Prachi Kukshal, Triptish Bhatia A, Vishwajit Laxmikant Nimgaonkar, Smita Neelkanth Deshpande, Bittianda Kuttapa Thelma · 2017 · Schizophrenia Bulletin
- Relationship between polymorphisms in the proline dehydrogenase gene and schizophrenia riskFariba Ghasemvand, Eskandar Omidinia, Zivar Salehi, Saeid Rahmanzadeh · 2015 · Genetics and Molecular Research
- Assessment of de novo copy-number variations in Italian patients with schizophrenia: Detection of putative mutations involving regulatory enhancer elementsG. Piluso, P. Monteleone, S. Galderisi, Teresa Giugliano, A. Bertolino, P. Rocca, A. Rossi, A. Mucci, E. Aguglia, I. Andriola et al. · 2019 · World Journal of Biological Psychiatry
- Investigation of Schizophrenia with Human Induced Pluripotent Stem CellsSamuel K. Powell, Callan P. O’Shea, Sara Rose Shannon, Schahram Akbarian, Kristen Brennand · 2020 · Advances in neurobiology
- Novel rare variants in F-box protein 45 (FBXO45) in schizophreniaChenyao Wang, Takayoshi Koide, Hiroki Kimura, Shohko Kunimoto, Akira Yoshimi, Yukako Nakamura, Itaru Kushima, Masahiro Banno, Naoko Kawano, Yuto Takasaki et al. · 2014 · Schizophrenia Research
- Next-generation sequencing diagnostics for neurological diseases/disorders: from a clinical perspectiveJia Nee Foo, Jianjun Liu, Eng‐King Tan · 2013 · Human Genetics
- Genetic Evaluation of Schizophrenia Using the Illumina HumanExome ChipTim Moons, Marc D. Binder, Gellens Edith, Gielen Leen, Kim Sweers, Jacqmaert Sigrun, Ruud van Winkel, Philippe G. Vandekerckhove, Stephan J. Claes · 2016 · PLoS ONE
- A pipeline combining multiple strategies for prioritizing heterozygous variants for the identification of candidate genes in exome datasetsTeresa Requena, Alvaro Gallego‐Martinez, Jose Antonio Lopez-Escamez · 2017 · Human Genomics
- Phelan‐McDermid syndrome data network: Integrating patient reported outcomes with clinical notes and curated genetic reportsCartik R. Kothari, Maxime Wack, Claire Hassen‐Khodja, Sean Finan, Guergana Savova, Megan O'Boyle, Geraldine Bliss, Andria Cornell, Elizabeth J. Horn, Rebecca Davis et al. · 2017 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Evaluating Rare Variants in Complex Disorders Using Next-Generation SequencingMatthew N. Ezewudo, Michael E. Zwick · 2013 · Current Psychiatry Reports
- Post‐zygotic genomic changes in glutamate and dopamine pathway genes may explain discordance of monozygotic twins for schizophreniaChristina A. Castellani, Melkaye G. Melka, J. L. Gui, Anthony J. Gallo, R.L. O’Reilly, Shiva M. Singh · 2017 · Clinical and Translational Medicine
- Genetics of schizophrenia from a clinicial perspectivePrachi Kukshal, Bittianda Kuttapa Thelma, Vishwajit Laxmikant Nimgaonkar, Smita Neelkanth Deshpande · 2012 · International Review of Psychiatry
- Plastome sequencing of Myripnois dioica and comparison within AsteraceaeNan Lin, Xu Zhang, Tao Deng, Jianwen Zhang, Aiping Meng, Hengchang Wang, Hang Sun, Yanxia Sun · 2019 · Acta Botanica Yunnanica
- False Negatives Are a Significant Feature of Next Generation Sequencing CallsetsDean Bobo, Mikhail Lipatov, Juan L. Rodríguez-Flores, Adam Auton, Brenna M. Henn · 2016 · bioRxiv (Cold Spring Harbor Laboratory)
- Challenges for Implementing Next-Generation Sequencing-Based Genome Diagnostics: It‘s Also the People, Not Just the MachinesJoris A. Veltman, Edwin P. J. G. Cuppen, Terry Vrijenhoek · 2013 · Personalized Medicine
- Schizophrenia and Bipolar DisorderAlastair G. Cardno, Edward J. Pepper · 2014 · Springer eBooks
- Common variants of IRF3 conferring risk of schizophreniaXiao Li, Wen Zhang, Todd Lencz, Ariel Darvasi, Anna Alkelai, Bernard Lerer, Hongyan Jiang, Dengfeng Zhang, Li Yu, Xiufeng Xu et al. · 2015 · Journal of Psychiatric Research
- Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approachElena Michaelovsky, Miri Carmel, Amos Frisch, Mali Salmon‐Divon, Metsada Pasmanik, Abraham Weizman, Doron Gothelf · 2019 · Translational Psychiatry
- Introduction to Epigenetics in PsychiatryRichard S. Lee, Dimitrios Avramopoulos · 2014 · Elsevier eBooks
- Rare variants in Protein tyrosine phosphatase, receptor type A (PTPRA) in schizophrenia: Evidence from a family based studyJibin John, Prachi Kukshal, Aditya Kumar Sharma, Triptish Bhatia A, Vishwajit Laxmikant Nimgaonkar, S.N. Deshpande, Bittianda Kuttapa Thelma · 2018 · Schizophrenia Research
- Rare germline variants in individuals diagnosed with schizophrenia within multiplex familiesShangzhong Li, Lynn E. DeLisi, Stefan I. McDonough · 2021 · Psychiatry Research
- Translating exome sequencing from research to clinical diagnosticsEmily M. Coonrod, Rebecca L. Margraf, Karl V. Voelkerding · 2011 · Clinical Chemistry and Laboratory Medicine (CCLM)
- Genetics of Schizophrenia and other Psychotic DisordersEdward J. Pepper, Alastair G. Cardno · 2014 · Current Psychiatry Reviews
- Double hits in schizophreniaJacob A. S. Vorstman, Loes M. Olde Loohuis, GROUP Investigators, René S. Kahn, Roel A. Ophoff, GROUP investigators, Behrooz Z. Alizadeh, Agna A. Bartels‐Velthuis, Nico J.M. van Beveren, Richard Bruggeman et al. · 2018 · Human Molecular Genetics
- Derivation, Expansion, Cryopreservation and Characterization of Brain Microvascular Endothelial Cells from Human Induced Pluripotent Stem CellsSovannarath Pong, Paulo L. Lizano, Rakesh Karmacharya · 2020 · Journal of Visualized Experiments
- Paternal-age-related de novo mutations and risk for five disordersJacob L. Taylor, Jean-Christophe Debost, Sarah U. Morton, Emilie M. Wigdor, Henrike Heyne, Dennis Lal, Daniel P. Howrigan, Alex Bloemendal, Janne Tidselbak Larsen, Jack A. Kosmicki et al. · 2017 · bioRxiv (Cold Spring Harbor Laboratory)
- Identification of genetic variants of LGI 1 and RTN 4R (NgR1) linked to schizophrenia that are defective in NgR1– LGI 1 signalingRhalena A. Thomas, Amirthagowri Ambalavanan, Guy Armand Rouleau, Philip A. Barker · 2016 · Molecular Genetics & Genomic Medicine
- Biomarker Identification Through Integrating fMRI and EpigeneticsYuntong Bai, Pascal Zillé, Wenxing Hu, Vince D. Calhoun, Yu‐Ping Wang · 2019 · IEEE Transactions on Biomedical Engineering
- Génétique et épigénétique de la schizophrénie et des psychosesBoris Chaumette, Oussama Kébir, Marie‐Odile Krebs · 2017 · Biologie Aujourd hui
- Genes positively regulated by Mef2c in cortical neurons are enriched for common genetic variation associated with IQ and educational attainmentLaura Fahey, Deema Ali, Gary J Donohoe, Pilib Ó Broin, Derek W. Morris · 2023 · Human Molecular Genetics
- Using whole-exome sequencing to identify variants inherited from mosaic parentsJonathan J. Rios, Mauricio R. Delgado · 2014 · European Journal of Human Genetics
- GWAS, Cytomegalovirus Infection, and SchizophreniaJakob Grove, Anders Dupont Børglum, Brad D. Pearce · 2014 · Current Behavioral Neuroscience Reports
- Paradoxical Improvement of Schizophrenic Symptoms by a Dopaminergic Agonist: An Example of Personalized Psychiatry in a Copy Number Variation–Carrying PatientCharlotte Danset-Alexandre, Boris Chaumette, Gilles Martínez, Laurence Christa, Jean‐Michel Dupont, Oussama Kébir, Raphaël Gaillard B, Isabelle Amado, Marie‐Odile Krebs · 2015 · Biological Psychiatry
- Exome sequences of multiplex, multigenerational families reveal schizophrenia risk loci with potential implications for neurocognitive performanceMark Z. Kos, Melanie A. Carless, Juan M. Peralta, Joanne E. Curran, Ellen E. Quillen, Marcio Almeida, August N. Blackburn, Lucy Blondell, David R. Roalf, Michael F. Pogue‐Geile et al. · 2017 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Selected rapporteur summaries from the XX world congress of psychiatric genetics, Hamburg, Germany, october 14–18, 2012Heike Anderson‐Schmidt, Olga Beltcheva, Mariko D. Brandon, Enda M. Byrne, Eric Chater‐Diehl, Laramie E. Duncan, Suzanne Gonzalez, Eilis J. Hannon, Katri Kantojärvi, Iordanis Karagiannidis et al. · 2013 · American Journal of Medical Genetics Part B Neuropsychiatric Genetics
- Rare truncating variations and risk of schizophrenia: Whole-exome sequencing in three families with affected siblings and a three-stage follow-up study in a Japanese populationYuichiro Watanabe, Ayako Nunokawa, Masako Shibuya, Masashi Ikeda, Akitoyo Hishimoto, Kenji Kondo, Jun Egawa, Naoshi Kaneko, Tatsuyuki Muratake, Takeo Saito et al. · 2015 · Psychiatry Research
- The search for susceptibility genes in lumbar disc degeneration : focus on young individualsPasi J Eskola · 2012
- Genetics: Finding Genes for SchizophreniaJonathan Flint C, Marcus Robert Munafo · 2014 · Current Biology
- Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophreniaSaeko Yokotsuka, Masayuki Nakamura, Yoko Tomiyasu, Mio Nagai, Yuko Kato, Akiyuki Tomiyasu, Hiromi Umehara, Takehiro Hayashi, Natsuki Sasaki, Shuichi Ueno et al. · 2021 · Journal of Human Genetics
- The complete chloroplast genome of Ulmus mianzhuensis with insights into structural variations, adaptive evolution, and phylogenetic relationships of Ulmus (Ulmaceae)Nan Lin, Rui Liu, Yakun Wang, Peng Guo, Yihan Wang, Yanpei Liu, Fude Shang · 2023 · BMC Genomics
- Effect of illness expression and liability on familial associations of clinical and subclinical psychosis phenotypesTineke Lataster, Kim H. W. Verweij, Wolfgang Viechtbauer, GROUP · 2013 · Acta Psychiatrica Scandinavica
- DNA Methylation Differences in Cortical Grey and White Matter in SchizophreniaAmber Berdenis van Berlekom, Nina Notman, Marjolein A. M. Sneeboer, Gijsje J. L. Snijders, Lotte C. Houtepen, Danny M. Nispeling, Yujie He, Stella M. Dracheva, Elly M. Hol, René S. Kahn et al. · 2021 · Epigenomics
- Personalized Medicine in the Genomics Era: Highlights From an International Symposium On Childhood Heart DiseaseNatalie Farra, Ashok Kumar Manickaraj, James Ellis, Seema R. Mital · 2012 · Future Cardiology
- Analysis of 2,440 human exomes highlights the evolution and functional impact of rare coding variationJoshua M. Akey · 2011 · Genome biology
- Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2Franziska Degenhardt, Barbara Heinemann, Jana Strohmaier, Marvin A. Pfohl, Ina Giegling, Andrea Hofmann, Kerstin U. Ludwig, Stephanie H. Witt, Michael Ludwig, Andreas J. Forstner et al. · 2016 · Psychiatric Genetics
- Determination of candidate genes involved in schizophrenia using the whole-exome sequencingO. Senormanci, S. Karatas Celik, E. Valipour, V Dogan, G. Senormanci · 2018 · Bratislavské lekárske listy/Bratislava medical journal
- Massively parallel sequencing identifies a previously unrecognized X-linked disorder resulting in lethality in male infants owing to amino-terminal acetyltransferase deficiencyAlan F. Rope, Kai Wang, Rune Evjenth, Jinchuan Xing, Jennifer J. Johnston, Jeffrey J. Swensen, William Evan Johnson, Barry Moore, Chad Daniel Huff, Lynne M. Bird et al. · 2011 · Genome biology
- A new conceptual framework for investigating complex genetic diseaseShobbir Hussain · 2015 · Frontiers in Genetics
- Rare genetic variants and schizophreniaJonathan Flint C · 2016 · Nature Neuroscience
- VARPRISM: incorporating variant prioritization in tests of de novo mutation associationHao Hu, Hilary H Coon, Man Li, Mark D. Yandell, Chad Daniel Huff · 2016 · Genome Medicine
- Down Regulation of MIR-320 Gene Family Members in the Peripheral Blood of Schizophrenia PatientsTihomir Iliev Vachev, Nikolay Todorov Popov, Vili Krasteva Stoyanova, Hristo Yordanov Ivanov, Danail Savov Minchev · 2016 · International Journal of Current Microbiology and Applied Sciences
- COSMIC: the catalogue of somatic mutations in cancerNidhi Bindal, Simon Andrew Forbes, David M. Beare, Prasad Gunasekaran, Kenric Leung, Chai Yin Kok, Mingming Jia, Sally Bamford, Charlotte G. Cole, Sari A. Ward et al. · 2011 · Genome biology
- Neurodevelopmental predictors of treatment response in schizophrenia and bipolar disorderAnton Iftimovici, Emma Krebs, William Dalfin, Adrien Legrand, Linda Scoriels, Gilles Martínez, Narjès Bendjemaa, Édouard Duchesnay, Boris Chaumette, Marie‐Odile Krebs · 2024 · Psychological Medicine
- Genomics of Behavioral DiseasesEvgeny Ivanovich Rogaev · 2012 · Frontiers in Genetics
- Targeted resequencing of regulatory regions at schizophrenia risk loci: Role of rare functional variants at chromatin repressive statesJavier González‐Peñas, Jorge Amigo, Luis Santomé, Beatriz Sobrino, Julio Brenlla, Santiago Agra, Eduardo Paz, Mario Páramo, Ángel Carracedo, Manuel Arrojo et al. · 2016 · Schizophrenia Research
- Rare Variants in Complex Traits: Novel Identification Strategies and the Role of de novo MutationsLoubna Jouan, Julie Gauthier, Patrick A. Dion, Guy Armand Rouleau · 2012 · Human Heredity
- Cannabis and Psychosis: A Systematic Review of Genetic StudiesVera Uliana, Annarita Tomassini, R. Pollice, Massimo Gennarelli, Francesca Faravelli, MASSIMO CASACCHIA, Emilio Di Maria · 2013 · Current Psychiatry Reviews
- A rigorous in silico genomic interrogation at 1p13.3 reveals 16 autosomal dominant candidate genes in syndromic neurodevelopmental disordersAfif Ben‐Mahmoud, Kyung Ran Jun, Vijay R. Gupta, Pinang Shastri, Alberto de la Fuente, Yongsoo Park, Kyung Chul Shin, Chong Ae Kim, Aparecido Divino da Cruz, Irene Plaza Pinto et al. · 2022 · Frontiers in Molecular Neuroscience
- Discovery of rare variants implicated in schizophrenia using next-generation sequencingRaina E. Rhoades, Fatimah L. C. Jackson, Shaolei Teng · 2019 · Journal of Translational Genetics and Genomics
- De novo damaging coding mutations are strongly associated with obsessive-compulsive disorder and overlap with autismCarolina Cappi, Melody E. Oliphant, Zsanett Péter, Gwyneth C. Zai, Catherine A.W. Sullivan, Abha R. Gupta, Ellen J. Hoffman, Manmeet Virdee, Arthur Jeremy Willsey, Roseli Gedanke Shavitt et al. · 2017 · bioRxiv (Cold Spring Harbor Laboratory)
- Importin α4 deficiency induces psychiatric disorder-related behavioral deficits and neuroinflammation in miceKoki Sakurai, Makiko Morita, Yoshiatsu Aomine, Mitsunobu Matsumoto, Tetsuji Moriyama, Emiko Kasahara, Atsuo Sekiyama, Mayumi Otani, Rieko Oshima, Kate L. Loveland et al. · 2024 · Translational Psychiatry
- Whole-exome sequencing: discovering genetic causes of orthopaedic disorders.N. Paria, L. Copley, J. Herring, Harry K. W. Kim, B. Richards, D. Sucato, C. Wise, J. Rios · 2013 · Journal of Bone and Joint Surgery. American volume
- ‘Sifting the significance from the data’ - the impact of high-throughput genomic technologies on human genetics and health careAngus John Clarke, D.N. Cooper, Michael Krawczak, Chris Tyler‐Smith, Helen M Wallace, Andrew O.M. Wilkie, Frances Lucy Raymond, RUTH F. CHADWICK, Nick J. Craddock, Rosalind M. John et al. · 2012 · Human Genomics
- Involvement of strawberry notch homologue 1 in neurite outgrowth of cortical neuronsMunkhsoyol Erkhembaatar, Iroha Yamamoto, Fuduki Inoguchi, Kosuke Taki, Satoru Yamagishi, Leanne M. Delaney, Mariko Nishibe, Takaya Abe, Hiroshi Kiyonari, Carina Hanashima et al. · 2022 · Development Growth & Differentiation
- The Genetics of SchizophreniaJames N. Samson, Albert H.C. Wong · 2015 · Royal Society of Chemistry eBooks
- The Analysis of Ethnic MixturesXiaofeng Zhu · 2011 · Methods in molecular biology
- Failure to Identify Somatic Mutations in Monozygotic Twins Discordant for Schizophrenia by Whole Exome SequencingNan Lyu, Li-Li Guan, Hong Ma, Xijin Wang, Baoming Wu, Fan-Hong Shang, Dan Wang, Hong Wen, Xin Yu · 2016 · Chinese Medical Journal
- Genetics of SchizophreniaDavid Roofeh, Divya Tumuluru, Sona Shilpakar, Vishwajit Laxmikant Nimgaonkar · 2013 · International Journal of Mental Health
- Exom-Sequenzierung zur Identifizierung von KrankheitsgenenKornelia Neveling, Alexander Hoischen · 2012 · Medizinische Genetik
- Schizophrenia risk conferred by protein-coding de novo mutationsDaniel P. Howrigan, Samuel A. Rose, Kaitlin E. Samocha, Menachem Fromer, Felecia E. Cerrato, Wei J. Chen, Claire L. Churchhouse, Kimberly Chambert, Sharon D. Chandler, Mark J. Daly et al. · 2018 · bioRxiv (Cold Spring Harbor Laboratory)