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Author Details
Full Name
Andrea Hofmann
Affiliation
Institute of Human Genetics, University of Bonn and Department of Genomics
ORCID
Career Start Year
1991
Papers
61
H Index
27
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35225756
Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach.
Br J Psychiatry
2022
35505515
Using polygenic scores and clinical data for bipolar disorder patient stratification and lithium response prediction: machine learning approach - CORRIGENDUM.
Br J Psychiatry
2022
34803816
Children's Learning of Non-adjacent Dependencies Using a Web-Based Computer Game Setting.
Front Psychol
2021
32620862
Publisher Correction: Tumor-necrosis factor impairs CD4<sup>+</sup> T cell-mediated immunological control in chronic viral infection.
Nat Immunol
2020
30796272
Transcriptome-wide analysis of filarial extract-primed human monocytes reveal changes in LPS-induced PTX3 expression levels.
Sci Rep
2019
29121268
Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder: A Genome-Wide Association Study.
JAMA Psychiatry
2018
29438386
Doxycycline inhibits experimental cerebral malaria by reducing inflammatory immune reactions and tissue-degrading mediators.
PLoS One
2018
29080678
Genome-Wide MicroRNA Analysis Implicates miR-30b/d in the Etiology of Alopecia Areata.
J Invest Dermatol
2018
27306922
Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with MCHR2.
Exp Dermatol
2017
28166306
Identification of shared risk loci and pathways for bipolar disorder and schizophrenia.
PLoS One
2017
28371232
Investigation of SHANK3 in schizophrenia.
Am J Med Genet B Neuropsychiatr Genet
2017
29122006
Single nucleotide polymorphisms in the angiogenic and lymphangiogenic pathways are associated with lymphedema caused by Wuchereria bancrofti.
Hum Genomics
2017
26968009
Meta-analysis Reveals Genome-Wide Significance at 15q13 for Nonsyndromic Clefting of Both the Lip and the Palate, and Functional Analyses Implicate GREM1 As a Plausible Causative Gene.
PLoS Genet
2016
26631617
Gene expression variance in hippocampal tissue of temporal lobe epilepsy patients corresponds to differential memory performance.
Neurobiol Dis
2016
26608307
Genome-wide transcriptome induced by Porphyromonas gingivalis LPS supports the notion of host-derived periodontal destruction and its association with systemic diseases.
Innate Immun
2016
27668412
Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.
Psychiatr Genet
2016
27634931
The lncRNA HOTAIR impacts on mesenchymal stem cells via triple helix formation.
Nucleic Acids Res
2016
27477848
Genome-wide transcriptome induced by nickel in human monocytes.
Acta Biomater
2016
27329760
Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder.
Hum Mol Genet
2016
27384521
Further evidence for deletions in 7p14.1 contributing to nonsyndromic cleft lip with or without cleft palate.
Birth Defects Res A Clin Mol Teratol
2016
27138190
CNV analysis in 169 patients with bladder exstrophy-epispadias complex.
BMC Med Genet
2016
27315593
Genome-wide association study of pathological gambling.
Eur Psychiatry
2016
27283990
SOX2 is essential for in vivo reprogramming of seminoma-like TCam-2 cells to an embryonal carcinoma-like fate.
Oncotarget
2016
27281327
Targeted and Untargeted Approaches Unravel Novel Candidate Genes and Diagnostic SNPs for Quantitative Resistance of the Potato (Solanum tuberosum L.) to Phytophthora infestans Causing the Late Blight Disease.
PLoS One
2016
27018475
Sequencing the GRHL3 Coding Region Reveals Rare Truncating Mutations and a Common Susceptibility Variant for Nonsyndromic Cleft Palate.
Am J Hum Genet
2016
26806518
Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study.
Lancet
2016
26801514
Somatostatin treatment can induce extensive fibrosis in growth hormone-producing adenoma.
Acta Neurochir (Wien)
2016
27087860
Array-based molecular karyotyping in fetuses with isolated brain malformations identifies disease-causing CNVs.
J Neurodev Disord
2016
26680650
Array-based molecular karyotyping in fetal brain malformations: Identification of novel candidate genes and chromosomal regions.
Birth Defects Res A Clin Mol Teratol
2016
26926055
Resective surgery for medically refractory epilepsy using intraoperative MRI and functional neuronavigation: the Erlangen experience of 415 patients.
Neurosurg Focus
2016
26950238
Tumor-necrosis factor impairs CD4(+) T cell-mediated immunological control in chronic viral infection.
Nat Immunol
2016
26974007
Analysis of five chronic inflammatory diseases identifies 27 new associations and highlights disease-specific patterns at shared loci.
Nat Genet
2016
25219767
Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis.
Int J Cancer
2015
26556287
Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder.
Transl Psychiatry
2015
26226633
BMP Inhibition in Seminomas Initiates Acquisition of Pluripotency via NODAL Signaling Resulting in Reprogramming to an Embryonal Carcinoma.
PLoS Genet
2015
26088384
Destabilization of the human epigenome: consequences of foreign DNA insertions.
Epigenomics
2015
25887883
Genomic architecture of potato resistance to Synchytrium endobioticum disentangled using SSR markers and the 8.3k SolCAP SNP genotyping array.
BMC Genet
2015
25571874
Aberrant NMDA receptor DNA methylation detected by epigenome-wide analysis of hippocampus and prefrontal cortex in major depression.
Eur Arch Psychiatry Clin Neurosci
2015
24272960
Efficient strategy for detecting gene ÿ gene joint action and its application in schizophrenia.
Genet Epidemiol
2014
25327457
Characterizing the genetic basis of innate immune response in TLR4-activated human monocytes.
Nat Commun
2014
23184149
X-linked dystonia parkinsonism syndrome (XDP, lubag): disease-specific sequence change DSC3 in TAF1/DYT3 affects genes in vesicular transport and dopamine metabolism.
Hum Mol Genet
2013
26151896
Duplications in RB1CC1 are associated with schizophrenia; identification in large European sample sets.
Transl Psychiatry
2013
23132931
Keratin 1 maintains skin integrity and participates in an inflammatory network in skin through interleukin-18.
J Cell Sci
2012
21704280
RNA-stabilized whole blood samples but not peripheral blood mononuclear cells can be stored for prolonged time periods prior to transcriptome analysis.
J Mol Diagn
2011
21841785
Repression of the genome organizer SATB1 in regulatory T cells is required for suppressive function and inhibition of effector differentiation.
Nat Immunol
2011
21558400
Blood-based gene expression signatures in non-small cell lung cancer.
Clin Cancer Res
2011
20532675
Higher frequency of thyroid tumors in the right lobe.
Endocr Pathol
2010
18820854
Incidence and predictability of amiodarone-induced thyrotoxicosis and hypothyroidism.
Wien Klin Wochenschr
2008
17492353
Vascular endothelial growth factor in thyroid cyst fluids.
Wien Klin Wochenschr
2007
16952488
A positron emission tomography microdosing study with a potential antiamyloid drug in healthy volunteers and patients with Alzheimer's disease.
Clin Pharmacol Ther
2006
1 - 50 of 61
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row(s) 1 - 30 of 30
Collaborators
Markus M N??then
Institute of Human Genetics, University Hospital Bonn
Co-authored papers
21
Franziska Degenhardt
University of Duisburg-Essen
Co-authored papers
15
Marcella Rietschel
Central Institute of Mental Health, University of Mannheim
Co-authored papers
12
Per Hoffmann
Institute of Human Genetics, University of Bonn and University Hospital Bonn
Co-authored papers
12
Andreas J Forstner
University of Bonn, School of Medicine & University Hospital Bonn.
Co-authored papers
10
Stephanie H Witt
Central Institute of Mental Health, Heidelberg University
Co-authored papers
10
Stefan Herms
Institute of Human Genetics, University of Bonn
Co-authored papers
9
Sven Cichon
University Hospital Basel and University of Basel
Co-authored papers
9
Martin Alda
Dalhousie University
Co-authored papers
7
Andrea Pfennig
University Hospital, TUD Dresden University of Technology
Co-authored papers
7
Johannes Schumacher
Philipps University of Marburg
Co-authored papers
7
Maria Grigoroiu-Serbanescu
Alexandru Obregia Clinical Psychiatric Hospital.
Co-authored papers
7
Gustavo Turecki
Douglas Institute, McGill University
Co-authored papers
7
Thomas G Schulze
SUNY Upstate Medical University
Co-authored papers
7
Piotr M Czerski
Poznan University of Medical Sciences
Co-authored papers
7
Philip B Mitchell
University of New South Wales
Co-authored papers
7
Joanna Hauser
Poznan University of Medical Sciences
Co-authored papers
7
Janice M Fullerton
University of New South Wales
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7
Michael Bauer
Carl Gustav Carus University Hospital, Technische Universitat Dresden
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7
Cristiana Cruceanu
Max Plank Institute for Psychiatry.
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Peter R Schofield
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Guy A Rouleau
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