L. Georgieva

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Aliases
L. Georgieva, Lyudmila B Georgieva, Lyudmila Georgieva
Publication record
69 papers · 21,645 citations · H-index 38

PAPERS

Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions
202328 citationsauthor #58
in a large
20230 citationsauthor #19
in a large
20230 citationsauthor #19
Distinct genetic liability profiles define clinically relevant patient strata across common diseases
20236 citationsauthor #88
A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts.
2021155 citationsauthor #90
Population-based identity-by-descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia
20201 citationsauthor #145
Complement genes contribute sex-biased vulnerability in diverse illnesses
2020163 citationsauthor #91
Complement genes contribute sex-biased vulnerability in diverse disorders
202062 citationsauthor #91
CORRIGENDUM
20190 citationsauthor #7
Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
2019174 citationsauthor #115
First Report of DHA-1 Producing Enterobacter cloacae Complex Isolate in Bulgaria.
20193 citationsauthor #5
A polygenic resilience score moderates the genetic risk for schizophrenia
201955 citationsauthor #103
Publisher Correction: Gene expression imputation across multiple brain regions provides insights into schizophrenia risk
20190 citationsauthor #115
The Analysis of FFPE Samples by Next-Generation Sequencing (NGS) of Key Genes for Research into Breast and Ovarian Cancer
20180 citationsauthor #3
Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes.
2018659 citationsauthor #162
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
20173 citationsauthor #2
Age at first birth in women is genetically associated with increased risk of schizophrenia
201723 citationsauthor #82
The Analysis of Myeloproliferative Neoplasm (MPN) Samples Using a Rapid Hybridisation-Based (30 Minute Hybridisation) Enrichment Protocol for Next-Generation Sequencing (NGS)
20170 citationsauthor #2
Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes
20170 citationsauthor #178
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
2017134 citationsauthor #221
VKučinskas-2001-2016
20160 citationsauthor #109
Parental Origin of Interstitial Duplications at 15q11.2-q13.3 in Schizophrenia and Neurodevelopmental Disorders
201661 citationsauthor #11
A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects: CNV Analysis Group and the Schizophrenia Working Group of the Psychiatric Genomics Consortium
20161,257 citationsauthor #80
Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
2016961 citationsauthor #93
Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women.
201655 citationsauthor #38
New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis.
201561 citationsauthor #34
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
2015225 citationsauthor #105
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
2015747 citationsauthor #116
Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia
201535 citationsauthor #11
Analysis of copy number variations at 15 schizophrenia-associated loci
2014194 citationsauthor #3
De novo CNVs in bipolar affective disorder and schizophrenia
201485 citationsauthor #1
De novo mutations in schizophrenia implicate synaptic networks
20141,604 citationsauthor #7
Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.
2014584 citationsauthor #98
schizophrenia-associated loci Analysis of copy number variations at 15
2014255 citationsauthor #8
The penetrance of copy number variations for schizophrenia and developmental delay.
2014368 citationsauthor #5
Biological Insights From 108 Schizophrenia-Associated Genetic Loci
20147,324 citationsauthor #77
CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1
201391 citationsauthor #7
Risk variant of oligodendrocyte lineage transcription factor 2 is associated with reduced white matter integrity
201318 citationsauthor #6
Rare exonic deletions implicate the synaptic organizer Gephyrin (GPHN) in risk for autism, schizophrenia and seizures.
2013147 citationsauthor #19
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
20132,194 citationsauthor #108
Schizophrenia genetic variants are not associated with intelligence | NOVA. The University of Newcastle's Digital Repository
20130 citationsauthor #179
Schizophrenia genetic variants are not associated with intelligence
201352 citationsauthor #81
Absence of de novo point mutations in exons of GRIN2B in a large schizophrenia trio sample.
20125 citationsauthor #2
Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder
2011283 citationsauthor #7
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
2011865 citationsauthor #11
Fine mapping of ZNF 804 A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder
201149 citationsauthor #7
Effect of olig2 in white matter integrity in healthy subjects and patients with schizophrenia
20100 citationsauthor #6
Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha
201036 citationsauthor #8
Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples
200915 citationsauthor #7
A genome-wide association study in 574 schizophrenia trios using DNA pooling
2009180 citationsauthor #3
Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2
200977 citationsauthor #9
A network of dopaminergic gene variations implicated as risk factors for schizophrenia.
2008155 citationsauthor #4
A genome-wide association study for late-onset Alzheimer's disease using DNA pooling
2008194 citationsauthor #6
Support for neuregulin 1 as a susceptibility gene for bipolar disorder and schizophrenia.
2008112 citationsauthor #1
Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping
200831 citationsauthor #2
P3‐265: Testing for association between Alzheimer's disease with psychosis and variants identified as influencing risk of schizophrenia
20080 citationsauthor #9
P3‐196: A genome‐wide association study for late‐onset Alzheimer's disease using DNA pooling
20087 citationsauthor #2
Identification of loci associated with schizophrenia by genome-wide association and follow-up
20081,100 citationsauthor #10
Comparative genome hybridization suggests a role for NRXN1 and APBA2 in schizophrenia.
2007397 citationsauthor #5
Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia
2006133 citationsauthor #1
Genetic variation in the seven‐pass transmembrane cadherin CELSR1: lack of association with schizophrenia
20038 citationsauthor #1
Variation in the protocadherin γ A gene cluster
200312 citationsauthor #2
Variation in the protocadherin gamma A gene cluster.
200312 citationsauthor #2
Major psychiatric disorders and the serotonin transporter gene (SLC6A4): family-based association studies
200212 citationsauthor #2
Screening the human protocadherin 8 (PCDH8) gene in schizophrenia
200234 citationsauthor #5
Screening the protocadherin 8 (PCDH8) gene in schizophrenia [Conference Abstract]
20020 citationsauthor #5
Dopamine transporter gene (DAT1) VNTR polymorphism in major psychiatric disorders: family‐based association study in the Bulgarian population
200242 citationsauthor #1
Prevalence of enzootic bovine leukosis in South-eastern Bulgaria during the period 1998-2000
20013 citationsauthor #7

TIMELINE

2001 3 citations

2002 88 citations

2003 32 citations

2006 133 citations

2007 397 citations

2008 1,599 citations

2009 272 citations

2010 36 citations

2011 1,197 citations

2012 5 citations

2013 2,502 citations

2014 10,414 citations

2015 1,068 citations

2016 2,334 citations

2017 160 citations

2018 659 citations

2019 232 citations

2020 226 citations

2021 155 citations

2023 34 citations

L. Georgieva

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