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1. Advances in intelligent signal processing and data mining
: theory and applications
by Georgieva, Petya and Mihaylova, Lyudmila and Jain, L. C
2013, Studies in computational intelligence, ISBN 9783642286957, Volume 410
Digital techniques | Signal processing | Data processing | Data mining
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2. Full Text De novo mutations in schizophrenia implicate synaptic networks
by Fromer, Menachem and Pocklington, Andrew J and Kavanagh, David H and Williams, Hywel J and Dwyer, Sarah and Gormley, Padhraig and Georgieva, Lyudmila and Rees, Elliott and Palta, Priit and Ruderfer, Douglas M and Carrera, Noa and Humphreys, Isla and Johnson, Jessica S and Roussos, Panos and Barker, Douglas D and Banks, Eric and Milanova, Vihra and Grant, Seth G and Hannon, Eilis and Rose, Samuel A and Chambert, Kimberly and Mahajan, Milind and Scolnick, Edward M and Moran, Jennifer L and Kirov, George and Palotie, Aarno and McCarroll, Steven A and Holmans, Peter and Sklar, Pamela and Owen, Michael J and Purcell, Shaun M and O'Donovan, Michael C
Nature, ISSN 0028-0836, 2014, Volume 506, Issue 7487, pp. 179 - 184
Inherited alleles account for most of the genetic risk for schizophrenia. However, new (de novo) mutations, in the form of large chromosomal copy number... 
INTELLECTUAL DISABILITY | RATES | COPY-NUMBER VARIANTS | GENE | MULTIDISCIPLINARY SCIENCES | DISEASE | COMPLEXITY | PATTERNS | MECHANISMS | AUTISM SPECTRUM DISORDERS | PLASTICITY | Schizophrenia - metabolism | Humans | RNA, Messenger - genetics | Receptors, N-Methyl-D-Aspartate - metabolism | Substrate Specificity | Mutation Rate | Fragile X Mental Retardation Protein - metabolism | Mutation - genetics | RNA, Messenger - metabolism | Intellectual Disability - genetics | Nerve Tissue Proteins - metabolism | Exome - genetics | Phenotype | Schizophrenia - genetics | Synapses - metabolism | Child Development Disorders, Pervasive - genetics | Schizophrenia - physiopathology | Nerve Net - metabolism | Neural Pathways - metabolism | Cytoskeletal Proteins - metabolism | Models, Neurological | Neural Pathways - physiopathology | Nerve Net - physiopathology | Psychological aspects | Neural circuitry | Gene mutations | Schizophrenia | Genetic aspects | Health aspects | Synapses | Studies | Autism | Mutation | Genes | Index Medicus
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3. Full Text Biological insights from 108 schizophrenia-associated genetic loci
by Ripke, Stephan and Neale, Benjamin M and Corvin, Aiden and Walters, James T. R and Farh, Kai-How and Holmans, Peter A and Lee, Phil and Bulik-Sullivan, Brendan and Collier, David A and Huang, Hailiang and Pers, Tune H and Agartz, Ingrid and Agerbo, Esben and Albus, Margot and Alexander, Madeline and Amin, Farooq and Bacanu, Silviu A and Begemann, Martin and Belliveau, Richard A and Bene, Judit and Bergen, Sarah E and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberly D and Chan, Raymond C. K and Chen, Ronald Y. L and Chen, Eric Y. H and Cheng, Wei and Cheung, Eric F. C and Chong, Siow Ann and Cloninger, C. Robert and Cohen, David and Cohen, Nadine and Cormican, Paul and Craddock, Nick and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and del Favero, Jurgen and Demontis, Ditte and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Durmishi, Naser and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedl, Marion and Friedman, Joseph I and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Golimbet, Vera and Gopal, Srihari and Gratten, Jacob and de Haan, Lieuwe and Hammer, Christian and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Hollegaard, Mads V and Hougaard, David M and Ikeda, Masashi and Joa, Inge and ... and Psychiat Genomics Consortium and Wellcome Trust Case-Control Consor and Psychosis Endophenotypes Int Conso and Schizophrenia Working Group of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature, ISSN 0028-0836, 2014, Volume 511, Issue 7510, pp. 421 - 427
Schizophrenia is a highly heritable disorder. Genetic risk is conferred by a large number of alleles, including common alleles of small effect that might be... 
COMMON VARIANTS | MUTATIONS | MULTIDISCIPLINARY SCIENCES | CONFERRING RISK | GENOME-WIDE ASSOCIATION | Schizophrenia | Genetic research | Research | Health aspects | Analysis | Studies | Confidence intervals | Hypotheses | Genealogy | Sample size | Genomics | Genetics | Trends | Index Medicus | Clinical Medicine | Psykiatri | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap | Psychiatry
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4. Full Text The Penetrance of Copy Number Variations for Schizophrenia and Developmental Delay
by Kirov, George|Rees, Elliott|Walters, James T.R.|Escott-Price, Valentina|Georgieva, Lyudmila|Richards, Alexander L.|Chambert, Kimberly D.|Davies, Gerwyn|Legge, Sophie E.|Moran, Jennifer L.|McCarroll, Steven A.|O’Donovan, Michael C.|Owen, Michael J
Biological Psychiatry, ISSN 0006-3223, 2014, Volume 75, Issue 5, pp. 378 - 385
Background Several recurrent copy number variants (CNVs) have been shown to increase the risk of developing schizophrenia (SCZ), developmental delay (DD),... 
Psychiatry | developmental delay | CNV | schizophrenia | selection | Autism spectrum disorder | penetrance | POPULATION | DUPLICATIONS | MENTAL-RETARDATION | INCREASE RISK | VARIANTS | PSYCHIATRY | RARE CHROMOSOMAL DELETIONS | DISORDERS | PREVALENCE | NEUROSCIENCES | CHILDREN | AUTISM-SPECTRUM | Genetic Predisposition to Disease | Schizophrenia - genetics | Humans | Chromosome Aberrations | Female | Male | Penetrance | DNA Copy Number Variations - genetics | Developmental Disabilities - genetics | Genetic research | Schizophrenia | Development and progression | Birth defects | Analysis | Index Medicus | autism spectrum disorder
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5. Full Text Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia
by Kirov, George and Gumus, Dilihan and Chen, Wei and Norton, Nadine and Georgieva, Lyudmila and Sari, Murat and O'Donovan, Michael C and Erdogan, Fikret and Owen, Michael J and Ropers, Hans-Hilger and Ullmann, Reinhard
Human Molecular Genetics, ISSN 0964-6906, 2/2008, Volume 17, Issue 3, pp. 458 - 465
Copy number variations (CNVs) account for a substantial proportion of human genomic variation, and have been shown to cause neurodevelopmental disorders. We... 
AUTISM | MENTAL-RETARDATION | GENE | BIOCHEMISTRY & MOLECULAR BIOLOGY | SYNAPTIC-TRANSMISSION | CA2+ CHANNELS | GENETICS & HEREDITY | NEUREXINS | COPY-NUMBER VARIATIONS | CHROMOSOMAL-ABNORMALITIES | ARRAY CGH | CARDIO-FACIAL SYNDROME | Autistic Disorder - genetics | Glycoproteins - genetics | Nucleic Acid Hybridization | Humans | Middle Aged | Male | Gene Dosage | Chromosomes, Human, Pair 15 - genetics | Nerve Tissue Proteins - genetics | Case-Control Studies | Intellectual Disability - genetics | Schizophrenia - etiology | Genetic Variation | Carrier Proteins - genetics | Schizophrenia - genetics | Adolescent | Adult | Female | Neuropeptides - genetics | Cadherins - genetics | Index Medicus
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6. Full Text Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
by Marshall, Christian R and Howrigan, Daniel P and Merico, Daniele and Thiruvahinapuram, Bhooma and Wu, Wenting and Greer, Douglas S and Antaki, Danny and Shetty, Aniket and Holmans, Peter A and Pinto, Dalila and Gujral, Madhusudan and Brandler, William M and Malhotra, Dheeraj and Wang, Zhouzhi and Fajarado, Karin V Fuentes and Maile, Michelle S and Ripke, Stephan and Agartz, Ingrid and Albus, Margot and Alexander, Madeline and Amin, Farooq and Atkins, Joshua and Bacanu, Silviu A and Belliveau, Richard A and Bergen, Sarah E and Bertalan, Marcelo and Bevilacqua, Elizabeth and Bigdeli, Tim B and Black, Donald W and Bruggeman, Richard and Buccola, Nancy G and Buckner, Randy L and Bulik-Sullivan, Brendan and Byerley, William and Cahn, Wiepke and Cai, Guiqing and Cairns, Murray J and Campion, Dominique and Cantor, Rita M and Carr, Vaughan J and Carrera, Noa and Catts, Stanley V and Chambert, Kimberley D and Cheng, Wei and Cloninger, C Robert and Cohen, David and Cormican, Paul and Craddock, Nick and Crespo-Facorro, Benedicto and Crowley, James J and Curtis, David and Davidson, Michael and Davis, Kenneth L and Degenhardt, Franziska and Del Favero, Jurgen and DeLisi, Lynn E and Dikeos, Dimitris and Dinan, Timothy and Djurovic, Srdjan and Donohoe, Gary and peau, Elodie and Duan, Jubao and Dudbridge, Frank and Eichhammer, Peter and Eriksson, Johan and Escott-Price, Valentina and Essioux, Laurent and Fanous, Ayman H and Farh, Kai-How and Farrell, Martilias S and Frank, Josef and Franke, Lude and Freedman, Robert and Freimer, Nelson B and Friedman, Joseph I and Forstner, Aneas J and Fromer, Menachem and Genovese, Giulio and Georgieva, Lyudmila and Gershon, Elliot S and Giegling, Ina and Giusti-Roíguez, Paola and Godard, Stephanie and Goldstein, Jacqueline I and Gratten, Jacob and de Haan, Lieuwe and Hamshere, Marian L and Hansen, Mark and Hansen, Thomas and Haroutunian, Vahram and Hartmann, Annette M and Henskens, Frans A and Herms, Stefan and Hirschhorn, Joel N and Hoffmann, Per and Hofman, Anea and Huang, Hailiang and Ikeda, Masashi and Joa, Inge and Kähler, Anna K and ... and Schizophrenia Working Grp and Psychosis Endophenotypes and CNV and Psychosis Endophenotypes International Consortium and CNV and Schizophrenia Working Groups of the Psychiatric Genomics Consortium and Medicinska fakulteten and Institutionen för klinisk vetenskap and Psykiatri and Umeå universitet
Nature Genetics, ISSN 1061-4036, 01/2017, Volume 49, Issue 1, pp. 27 - 35
Copy number variants (CNVs) have been strongly implicated in the genetic etiology of schizophrenia (SCZ). However, genome-wide investigation of the... 
DUPLICATIONS | AUTISM | GENE | CNVS | GENETICS & HEREDITY | RISK | DISORDERS | 16P11.2 | PHENOTYPES | MUTATIONS | REARRANGEMENTS | Genetic Predisposition to Disease | Genome-Wide Association Study | Schizophrenia - genetics | Genetic Markers - genetics | Humans | Risk Factors | Genetic Loci - genetics | Female | Genotype | Male | DNA Copy Number Variations - genetics | Case-Control Studies | Schizophrenia | Genome-wide association studies | Genetic aspects | Copy number variations | Analysis | Studies | Consortia | Datasets | Working groups | Pipelines | Genomics | Quality control | Data processing | Genomes | Meta-analysis | Index Medicus | Clinical Medicine | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Cell and Molecular Biology | Psykiatri | Klinisk medicin | Psychiatry | Cell- och molekylärbiologi
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7. Full Text Identification of loci associated with schizophrenia by genome-wide association and follow-up
by Georgieva, Lyudmila and Shifman, Sagiv and Quinn, Emma M and Peirce, Timothy and Giegling, Ina and He, Lin and Duan, Jubao and Leung, Hin-Tak and Shi, YongYong and Schumacher, Johannes and Moskvina, Valentina and Schulze, Thomas G and Craddock, Nicholas and Kirov, George and Levinson, Douglas F and Gill, Michael and Rujescu, Dan and O'Donovan, Michael C and Corvin, Aiden and Marchini, Jonathan L and Zammit, Stanley and Owen, Michael J and Williams, Hywel and Möller, Hans-Jürgen and Vasilescu, Catalina and Spencer, Chris C A and Nöthen, Markus M and Howie, Bryan and Rietschel, Marcella and Norton, Nadine and Nikolov, Ivan and Williams, Nigel M and Gejman, Pablo V and Iwata, Nakao and Hartmann, Annette M and Carroll, Liam and Hoffmann, Per and Darvasi, Ariel and Cichon, Sven and Morris, Derek W and Sanders, Alan R and Feng, GuoYin and Ikeda, Masashi and Propping, Peter and Dwyer, Sarah and Holmans, Peter and Hamshere, Marian and Maier, Wolfgang and Mol Genetics Of Schizophrenia Coll and Molecular Genetics of Schizophrenia Collaboration
Nature Genetics, ISSN 1061-4036, 09/2008, Volume 40, Issue 9, pp. 1053 - 1055
We carried out a genome-wide association study of schizophrenia (479 cases, 2,937 controls) and tested loci with P < 10−5 in up to 16,726 additional subjects.... 
GENETICS & HEREDITY | Genetic Predisposition to Disease | Genome-Wide Association Study | Schizophrenia - genetics | Follow-Up Studies | Humans | Chromosome Mapping | Polymorphism, Single Nucleotide | Bipolar Disorder - genetics | Kruppel-Like Transcription Factors - genetics | Case-Control Studies | Schizophrenia | Genetic aspects | Research | Genetic susceptibility | Genetic variation | Risk factors | Medical research | Genetics | Quality control | Meta-analysis | Index Medicus
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8. Full Text The Analysis of Myeloproliferative Neoplasm (MPN) Samples Using a Rapid Hybridisation-Based (30 Minute Hybridisation) Enrichment Protocol for Next-Generation Sequencing (NGS)
by Speight, Graham|Georgieva, Lyudmila|Uddin, Ezam|Cross, Nick
Cancer Genetics, ISSN 2210-7762, 2017, Volume 214, pp. 51 - 51
Hematology, Oncology and Palliative Medicine | Medical Education | Analysis | Tumors
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9. Full Text The Accurate Detection by Next-Generation Sequencing (NGS) of Difficult to Sequence Genes (CALR, CEBPA, FLT3) Associated With Myeloid Disorders Using a Hybridisation-Based Enrichment Approach
by Speight, Graham|Georgieva, Lyudmila|Uddin, Ezam|Cross, Nick
Cancer Genetics, ISSN 2210-7762, 2017, Volume 214, pp. 50 - 51
Hematology, Oncology and Palliative Medicine | Medical Education
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10. Full Text Phytochemical analysis of Vietnamese propolis produced by the stingless bee Lisotrigona cacciae
by Georgieva, K and Popova, M and Dimitrova, L and Trusheva, B and Phuong, DTL and Lien, NTP and Najdenski, H and Bankova, V and Thanh, LN
PLOS ONE, ISSN 1932-6203, 04/2019, Volume 14, Issue 4, pp. e0216074 - e0216074
Propolis produced by the stingless bee Lisotrigona cacciae was studied for the first time. Using different chromatographic procedures, a total of eighteen... 
THAILAND | RESIN | DRACAENA-COCHINCHINENSIS | PROFILES | ORIGIN | CHEMICAL-CONSTITUENTS | PHENOLIC-COMPOUNDS | MULTIDISCIPLINARY SCIENCES | HYMENOPTERA APIDAE MELIPONINI | XANTHONES | DRAGONS BLOOD | Saponins | Terpenes | Analysis | Chromatography | Gas chromatography | Usage | Phytochemicals | Research | Mass spectrometry | Bees | Triterpenes | Scavenging | Propolis | Cytotoxicity | Antimicrobial agents | Mass spectroscopy | Ecology | Antioxidants | Organic chemistry | Constituents | Minimum inhibitory concentration | Phenols | Hydroxyl groups
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11. Full Text A Beamformer-Particle Filter Framework for Localization of Correlated EEG Sources
by Georgieva, Petia and Bouaynaya, Nidhal and Silva, Filipe and Mihaylova, Lyudmila and Jain, Lakhmi C
IEEE Journal of Biomedical and Health Informatics, ISSN 2168-2194, 05/2016, Volume 20, Issue 3, pp. 880 - 892
Electroencephalography (EEG)-based brain computer interface (BCI) is the most studied noninvasive interface to build a direct communication pathway between the... 
EEG inverse problem | Bayesian estimation | Estimation | particle filtering | spatial-temporal brain source localization | multicore beamformer | Position measurement | Brain models | Electroencephalography | Noise measurement | Brain-Computer Interfaces | Young Adult | Algorithms | Evoked Potentials, Visual - physiology | Humans | Bayes Theorem | Signal Processing, Computer-Assisted | Adult | Female | Male | Electroencephalography - methods | Visual Cortex - physiology | Brain | Construction | Correlation | Beamforming | Human-computer interface | Waveforms | Position (location) | Index Medicus
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12. Full Text Support for Neuregulin 1 as a Susceptibility Gene for Bipolar Disorder and Schizophrenia
by Georgieva, Lyudmila|Dimitrova, Albena|Ivanov, Dobril|Nikolov, Ivan|Williams, Nigel M.|Grozeva, Detelina|Zaharieva, Irina|Toncheva, Draga|Owen, Michael J.|Kirov, George|O'Donovan, Michael C
Biological Psychiatry, ISSN 0006-3223, 2008, Volume 64, Issue 5, pp. 419 - 427
Background There is support that Neuregulin 1 ( NRG1 ) plays a role in susceptibility to schizophrenia but limited evidence for its involvement in bipolar... 
Psychiatry | Bipolar disorder | polymorphism | family based association | haplotype | schizophrenia | trios | METAANALYSIS | PSYCHIATRY | SCOTTISH POPULATION | FAMILY-BASED ASSOCIATION | NEUROSCIENCES | AT-RISK HAPLOTYPE | NO ASSOCIATION | NRG1 GENE | bipolar disorder | LINKAGE DISEQUILIBRIUM | POLYMORPHISMS | NEUROBIOLOGY | EXPRESSION | Genetic Predisposition to Disease | Gene Frequency | Humans | Family Health | Genotype | Male | Bipolar Disorder - genetics | Neuregulin-1 - genetics | Linkage Disequilibrium | Polymorphism, Genetic | Schizophrenia - genetics | DNA Mutational Analysis | Female | Schizophrenia | Disease susceptibility | Genetic aspects | Index Medicus
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