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D. Grozeva · SciRah

Researcher profile · Semantic Scholar

D. Grozeva

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D. Grozeva — researcher profile on SciRah

h-index: 50
Works: 119
Citations: 27K

Most-cited papers

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Brian W. Kunkle, B. Grenier-Boley, R. Sims, J. Bis +464 more
2019Nature Genetics2,491 citations Open access
Semantic Scholar
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
S. H. S. B. M. S. V. S. M. R. H. B. Lee Ripke Neale Faraone Purcell Perlis Mowry Thapa, Hong S. Lee, S. Ripke, B. Neale +367 more
2013Nature Genetics2,210 citations Open access
Semantic Scholar
The UK10K project identifies rare variants in health and disease
Klaudia Walter, Josine L. Min, Jie Huang, L. Crooks +238 more
2015Nature1,070 citations Open access
Semantic Scholar
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
G. Kirov, AJ Pocklington, P. Holmans, D. Ivanov +26 more
2011Molecular Psychiatry880 citations Open access
Semantic Scholar
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
Colm Lizzy Phil H Laramie Neelroop N Stephen Stephan Be O'Dushlaine Rossin Lee Duncan Parikshak Newhouse R, C. O'Dushlaine, L. Rossin, P. Lee +372 more
2015Nature Neuroscience765 citations Open access
Semantic Scholar
Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls
Nick Craddock, M. Hurles, Niall J. Cardin, R. Pearson +213 more
2010Nature706 citations Open access
Semantic Scholar
Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease.
K. Carss, G. Arno, M. Erwood, Jonathan Stephens +33 more
2017American Journal of Human Genetics478 citations Open access
Semantic Scholar
Common variants in Alzheimer’s disease and risk stratification by polygenic risk scores
I. de Rojas, S. Moreno-Grau, N. Tesi, B. Grenier-Boley +496 more
2021Nature Communications295 citations Open access
Semantic Scholar
Genome wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC
M. Hamshere, J. Walters, R. Smith, A. Richards +19 more
2012Molecular Psychiatry233 citations Open access
Semantic Scholar
Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder
R. Maier, G. Moser, Guo-Bo Chen, S. Ripke +373 more
2015American Journal of Human Genetics226 citations Open access
Semantic Scholar
Mutations in the histone methyltransferase gene KMT2B cause complex early-onset dystonia
E. Meyer, K. Carss, J. Rankin, John M. E. Nichols +66 more
2016Nature Genetics219 citations Open access
Semantic Scholar
Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder
You-Fang Liu, D. Blackwood, S. Caesar, E. de Geus +40 more
2011Molecular Psychiatry198 citations Open access
Semantic Scholar
Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries.
H. Williams, N. Craddock, G. Russo, M. Hamshere +8 more
2011Human Molecular Genetics196 citations Open access
Semantic Scholar
Rare Copy Number Variants
D. Grozeva, G. Kirov, D. Ivanov, I. Jones +11 more
2010Archives of General Psychiatry194 citations Open access
Semantic Scholar
Targeted Next‐Generation Sequencing Analysis of 1,000 Individuals with Intellectual Disability
D. Grozeva, K. Carss, O. Spasic-Boskovic, M. Tejada +19 more
2015Human Mutation189 citations Open access
Semantic Scholar
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer’s disease
H. Holstege, M. Hulsman, C. Charbonnier, B. Grenier-Boley +103 more
2022Nature Genetics181 citations Open access
Semantic Scholar
Copy number variation in bipolar disorder
E. Green, E. Rees, J. Walters, Kgc Smith +14 more
2015Molecular Psychiatry180 citations Open access
Semantic Scholar
Complex structural variants in Mendelian disorders: identification and breakpoint resolution using short- and long-read genome sequencing
A. Sanchis-Juan, J. Stephens, Courtney E. French, Nicholas S. Gleadall +18 more
2018Genome Medicine158 citations Open access
Semantic Scholar
Exome sequencing of Pakistani consanguineous families identifies 30 novel candidate genes for recessive intellectual disability
S. Riazuddin, Mureed Hussain, Attia Razzaq, Zafar Iqbal +29 more
2016Molecular Psychiatry150 citations Open access
Semantic Scholar
Replication of bipolar disorder susceptibility alleles and identification of 2 novel genome-wide significant associations in a new bipolar disorder case-control sample
E. Green, M. Hamshere, L. Forty, K. Gordon-Smith +13 more
2012Molecular Psychiatry150 citations Open access
Semantic Scholar
Phenotypic insights into ADCY5‐associated disease
F. Chang, A. Westenberger, R. Dale, Martin Smith +21 more
2016Movement Disorders121 citations Open access
Semantic Scholar
De novo loss-of-function mutations in SETD5, encoding a methyltransferase in a 3p25 microdeletion syndrome critical region, cause intellectual disability.
D. Grozeva, K. Carss, O. Spasic-Boskovic, M. Parker +11 more
2014American Journal of Human Genetics117 citations Open access
Semantic Scholar
Association at SYNE1 in both bipolar disorder and recurrent major depression
E. Green, D. Grozeva, L. Forty, K. Gordon-Smith +12 more
2013Molecular Psychiatry95 citations Open access
Semantic Scholar
Identification of a human synaptotagmin-1 mutation that perturbs synaptic vesicle cycling.
K. Baker, Sarah L. Gordon, D. Grozeva, M. van Kogelenberg +10 more
2015Journal of Clinical Investigation94 citations Open access
Semantic Scholar
Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia
D. Grozeva, D. Conrad, Chris P. Barnes, M. Hurles +4 more
2012Schizophrenia Research91 citations Open access
Semantic Scholar
Comparative performances of machine learning methods for classifying Crohn Disease patients using genome-wide genotyping data
A. Romagnoni, S. Jégou, K. van Steen, G. Wainrib +341 more
2019Scientific Reports88 citations Open access
Semantic Scholar
Author Correction: Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing
Brian W. Kunkle, B. Grenier-Boley, R. Sims, J. Bis +464 more
2019Nature Genetics85 citations Open access
Semantic Scholar
Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC
M. Hamshere, J. Walters, R. Smith, A. Richards +19 more
2013Molecular Psychiatry85 citations Open access
Semantic Scholar
Reciprocal duplication of the Williams-Beuren syndrome deletion on chromosome 7q11.23 is associated with schizophrenia
J. Mulle, A. Pulver, J. McGrath, P. Wolyniec +26 more
2013Biological Psychiatry76 citations Open access
Semantic Scholar
Polygenic dissection of the bipolar phenotype
M. Hamshere, M. O'Donovan, I. Jones, L. Jones +17 more
2011British Journal of Psychiatry70 citations Open access
Semantic Scholar
Polymorphism of the 5-HT transporter and response to antidepressants: randomised controlled trial
G. Lewis, J. Mulligan, N. Wiles, P. Cowen +10 more
2011British Journal of Psychiatry65 citations Open access
Semantic Scholar
Cancer symptom experience and help-seeking behaviour during the COVID-19 pandemic in the UK: a cross-sectional population survey
H. Quinn-Scoggins, R. Cannings-John, Yvonne Moriarty, V. Whitelock +13 more
2021BMJ Open64 citations Open access
Semantic Scholar
Rare Variant Analysis of Human and Rodent Obesity Genes in Individuals with Severe Childhood Obesity
A. Hendricks, E. Bochukova, G. Marenne, J. Keogh +266 more
2017Scientific Reports61 citations Open access
Semantic Scholar
Clinical and molecular consequences of disease-associated de novo mutations in SATB2
Hemant Bengani, Mark T. Handley, M. Alvi, R. Ibitoye +29 more
2017Genetics in Medicine60 citations Open access
Semantic Scholar
TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport
M. Schmidts, Yu-Qing Hou, Claudio R. Cortés, D. A. Mans +183 more
2015Nature Communications55 citations Open access
Semantic Scholar
Bi-allelic Loss-of-Function CACNA1B Mutations in Progressive Epilepsy-Dyskinesia.
K. Gorman, E. Meyer, D. Grozeva, E. Spinelli +27 more
2019American Journal of Human Genetics54 citations Open access
Semantic Scholar
Bipolar Disorder is associated with the rs6971 polymorphism in the gene encoding 18 kDa Translocator Protein (TSPO)
A. Colasanti, David R. Owen, D. Grozeva, E. Rabiner +3 more
2013Psychoneuroendocrinology52 citations Open access
Semantic Scholar
Affective temperaments across the bipolar-unipolar spectrum: examination of the TEMPS-A in 927 patients and controls.
A. Di Florio, M. Hamshere, L. Forty, E. Green +8 more
2010Journal of Affective Disorders46 citations
Semantic Scholar
An inherited duplication at the gene p21 Protein-Activated Kinase 7 (PAK7) is a risk factor for psychosis
D. Morris, R. Pearson, P. Cormican, E. Kenny +52 more
2014Human Molecular Genetics44 citations Open access
Semantic Scholar
DNAJC6 Mutations Disrupt Dopamine Homeostasis in Juvenile Parkinsonism‐Dystonia
J. Ng, E. Cortés-Saladelafont, L. Abela, P. Termsarasab +21 more
2020Movement Disorders38 citations Open access
Semantic Scholar
Meta-analysis of genetic association with diagnosed Alzheimer’s disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing
R. Sims, M. Vronskaya, A. Frizatti, Nandini Badarinarayan +18 more
2018bioRxiv38 citations Open access
Semantic Scholar
Genome Wide Linkage Analysis of 972 Bipolar Pedigrees Using Single Nucleotide Polymorphisms
J. Badner, D. Koller, T. Foroud, H. Edenberg +29 more
2011Molecular Psychiatry37 citations Open access
Semantic Scholar
Identification of high risk DISC1 protein structural variants in patients with bipolar spectrum disorder.
Wen-Jia Song, Wen-Yan Li, Katie Noltner, Jin Yan +7 more
2010Neuroscience Letters36 citations
Semantic Scholar
Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha
L. Carroll, Nigel M. Williams, V. Moskvina, E. Russell +20 more
2010Molecular Psychiatry35 citations
Semantic Scholar
Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A
C. Steward, Jolien Roovers, M. Suner, J. Gonzalez +32 more
2019npj Genomic Medicine32 citations Open access
Semantic Scholar
Reduced burden of very large and rare CNVs in bipolar affective disorder.
D. Grozeva, G. Kirov, D. Conrad, Chris P. Barnes +4 more
2013Bipolar Disorders32 citations
Semantic Scholar
Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer’s disease
E. Baker, R. Sims, G. Leonenko, Aura Frizzati +32 more
2019PLoS ONE31 citations Open access
Semantic Scholar
Novel ATP2A2 mutations in a large sample of individuals with Darier disease
E. Green, K. Gordon-Smith, S. Burge, D. Grozeva +4 more
2013Journal of dermatology (Print)31 citations Open access
Semantic Scholar
Identification of a CACNA2D4 deletion in late onset bipolar disorder patients and implications for the involvement of voltage‐dependent calcium channels in psychiatric disorders
M. V. D. Van Den Bossche, Mojca Strazisar, S. De Bruyne, C. Bervoets +14 more
2012American Journal of Medical Genetics Part B: Neuropsychiatric Genetics31 citations
Semantic Scholar
Genotype–phenotype correlations in Darier disease: A focus on the neuropsychiatric phenotype
K. Gordon-Smith, E. Green, D. Grozeva, S. Tavadia +2 more
2018American Journal of Medical Genetics Part B: Neuropsychiatric Genetics29 citations Open access
Semantic Scholar

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