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Lista de obras de Per Hoffmann

16p11.2 600 kb Duplications confer risk for typical and atypical Rolandic epilepsy

artículo científico publicado en 2014

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

A common microdeletion affecting a hippocampus- and amygdala-specific isoform of tryptophan hydroxylase 2 is not associated with affective disorders

artículo científico publicado en 2014

A common variant in myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.

artículo científico publicado en 2013

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia

artículo científico publicado en 2007

Activation of invariant NK T cells in periodontitis lesions

artículo científico publicado en 2013

Altered expression of TGF-beta receptors in hepatocellular carcinoma--effects of a constitutively active TGF-beta type I receptor mutant

artículo científico publicado en 2005

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

artículo científico publicado en 2008

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of the Influence of microRNAs in Lithium Response in Bipolar Disorder.

artículo científico publicado en 2018

Analysis of the joint effect of SNPs to identify independent loci and allelic heterogeneity in schizophrenia GWAS data

artículo científico publicado en 2017

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

artículo científico publicado en 2019

Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample

artículo científico publicado en 2012

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

artículo científico publicado en 2011

Association between neuropeptide Y receptor Y2 promoter variant rs6857715 and major depressive disorder

artículo científico publicado en 2016

Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder

artículo científico publicado en 2012

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

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.

artículo científico publicado en 2017

Association of Whole-Genome and NETRIN1 Signaling Pathway–Derived Polygenic Risk Scores for Major Depressive Disorder and White Matter Microstructure in the UK Biobank

scholarly article by Miruna C. Barbu et al published July 2018 in Biological Psychiatry: Cognitive Neuroscience and Neuroimaging

Association of a Rare Variant with Mismatch Negativity in a Region Between KIAA0319 and DCDC2 in Dyslexia

scientific article published on 21 November 2010

Association of polygenic score for major depression with response to lithium in patients with bipolar disorder

artículo científico publicado en 2020

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

artículo científico publicado en 2015

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

scientific article published in Nature Communications

Autosomal-dominant non-syndromic anal atresia: sequencing of candidate genes, array-based molecular karyotyping, and review of the literature

artículo científico publicado en 2010

Bipolar multiplex families have an increased burden of common risk variants for psychiatric disorders

Brief report: no association between premorbid adjustment in adult-onset schizophrenia and genetic variation in Dysbindin

artículo científico publicado en 2008

Characterization of a family with rare deletions in CNTNAP5 and DOCK4 suggests novel risk loci for autism and dyslexia

artículo científico publicado en 2010

Common obesity risk alleles in childhood attention-deficit/hyperactivity disorder.

artículo científico publicado en 2013

Common variants in Alzheimer's disease and risk stratification by polygenic risk scores

artículo científico publicado en 2021

Common variants in the HLA-DQ region confer susceptibility to idiopathic achalasia.

artículo científico publicado en 2014

Common variation at 10p12.31 near MLLT10 influences meningioma risk

artículo científico publicado en 2011

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

scientific journal article

Complete homozygous deletion of CTSC in an Iranian family with Papillon-Lefèvre syndrome

artículo científico publicado en 2013

Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly

artículo científico publicado en 2018

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Copy number variants in German patients with schizophrenia

artículo científico publicado en 2013

Copy number variations in 375 patients with oesophageal atresia and/or tracheoesophageal fistula

artículo científico publicado en 2016

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

De novo duplication of 18p11.21-18q12.1 in a female with anorectal malformation

article published in 2011

Deep intronic APC mutations explain a substantial proportion of patients with familial or early-onset adenomatous polyposis.

artículo científico publicado en 2012

Defining the role of common variation in the genomic and biological architecture of adult human height

artículo científico publicado en 2014

Desaturase Activity and the Risk of Type 2 Diabetes and Coronary Artery Disease: A Mendelian Randomization Study

artículo científico publicado en 2020

Dihydroceramide- and ceramide-profiling provides insights into human cardiometabolic disease etiology

artículo científico publicado en 2022

Direct conversion of fibroblasts into stably expandable neural stem cells

artículo científico publicado en 2012

Disruption of the neurexin 1 gene is associated with schizophrenia

artículo científico publicado en 2009

Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance

artículo científico publicado en 2019

Evidence for linkage of the bladder exstrophy-epispadias complex on chromosome 4q31.21-22 and 19q13.31-41 from a consanguineous Iranian family

artículo científico publicado en 2010

Evidence for the involvement of ZNF804A in cognitive processes of relevance to reading and spelling

artículo científico publicado en 2012

Excitation-induced ataxin-3 aggregation in neurons from patients with Machado-Joseph disease

artículo científico publicado en 2011

Familial occurrence of the VATER/VACTERL association

artículo científico

First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children.

artículo científico publicado en 2009

GWAS of Suicide Attempt in Psychiatric Disorders and Association With Major Depression Polygenic Risk Scores.

artículo científico publicado en 2019

Gene expression is stable in a complete CIB1 knockout keratinocyte model

scientific article published on 11 September 2020

Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder

artículo científico publicado en 2017

Genetic Contribution to Alcohol Dependence: Investigation of a Heterogeneous German Sample of Individuals with Alcohol Dependence, Chronic Alcoholic Pancreatitis, and Alcohol-Related Cirrhosis

artículo científico

Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort

artículo científico publicado en 2013

Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization

artículo científico publicado en 2014

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic risk factors for nonsyndromic cleft lip with or without cleft palate in a Mesoamerican population: Evidence for IRF6 and variants at 8q24 and 10q25.

artículo científico publicado en 2010

Genetic variants associated with response to lithium treatment in bipolar disorder: a genome-wide association study

artículo científico publicado en 2016

Genetic variants including markers from the exome chip and metabolite traits of type 2 diabetes

artículo científico publicado en 2017

Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia

artículo científico publicado en 2012

Genetics of dyslexia: the evolving landscape

artículo científico publicado en 2007

Genome-wide Association Analysis of Psoriatic Arthritis and Cutaneous Psoriasis Reveals Differences in Their Genetic Architecture

artículo científico publicado en 2015

Genome-wide CNV analysis in 221 unrelated patients and targeted high-throughput sequencing reveal novel causative candidate genes for colorectal adenomatous polyposis

artículo científico publicado en 2014

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

artículo científico publicado en 2012

Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression.

artículo científico publicado en 2018

Genome-wide association analysis identifies a meningioma risk locus at 11p15.5

Genome-wide association meta-analysis of coronary artery disease and periodontitis reveals a novel shared risk locus

scientific article published in Scientific Reports

Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia

artículo científico publicado en 2019

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies multiple susceptibility loci for multiple myeloma ⬇️

artículo científico publicado en 2016

Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia. ⬇️

artículo científico publicado en 2018

Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2009

Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma

artículo científico publicado en 2018

Genome-wide association study in German patients with attention deficit/hyperactivity disorder

artículo científico publicado en 2011

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

artículo científico publicado en 2016

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

article

Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

artículo científico publicado en 2017

Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.

artículo científico publicado en 2017

Genome-wide association study of monoclonal gammopathy of unknown significance (MGUS): comparison with multiple myeloma

artículo científico publicado en 2019

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression

scientific article published on 11 November 2019

Genome-wide association study on differentiated thyroid cancer

scientific journal article

Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

artículo científico publicado en 2020

Genome-wide association study reveals two new risk loci for bipolar disorder

artículo científico publicado en 2014

Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci

scientific journal article

Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster

artículo científico publicado en 2011

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Hammerhead ribozymes with cleavage site specificity for NUH and NCH display significant anti-hepatitis C viral effect in vitro and in recombinant HepG2 and CCL13 cells

artículo científico publicado en 2005

Human Platelet Lysate versus Fetal Calf Serum: These Supplements Do Not Select for Different Mesenchymal Stromal Cells.

artículo científico publicado en 2017

IRF6 gene variants in Central European patients with non-syndromic cleft lip with or without cleft palate

artículo científico publicado en 2009

Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity.

artículo científico publicado en 2012

Identification of ADHD risk genes in extended pedigrees by combining linkage analysis and whole-exome sequencing

article

Identification of loci associated with schizophrenia by genome-wide association and follow-up

artículo científico publicado en 2008

Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

scientific article published in Nature Communications

Identification of pleiotropy at the gene level between psychiatric disorders and related traits

artículo científico publicado en 2021

Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2.

scientific article published on 23 September 2016

Identification of shared risk loci and pathways for bipolar disorder and schizophrenia

artículo científico publicado en 2017

Imaging genetics of FOXP2 in dyslexia

artículo científico publicado en 2011

Imaging genetics of FOXP2 in dyslexia

artículo científico publicado en 2012

Impact of atopy on risk of glioma: a Mendelian randomisation study.

artículo científico publicado en 2018

Infection fatality rate of SARS-CoV2 in a super-spreading event in Germany

artículo científico publicado en 2020

Influence of obesity-related risk factors in the aetiology of glioma.

artículo científico publicado en 2018

Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

artículo científico publicado en 2014

Inhibition of hepatitis C virus RNA translation by antisense bile acid conjugated phosphorothioate modified oligodeoxynucleotides (ODN).

artículo científico publicado en 2012

Inhibition of hepatitis C virus gene expression by adenoviral vectors encoding antisense RNA in vitro and in vivo

artículo científico publicado en 2010

Investigating polygenic burden in age at disease onset in bipolar disorder: Findings from an international multicentric study

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

artículo científico publicado en 2008

Investigation of the DCDC2 intron 2 deletion/compound short tandem repeat polymorphism in a large German dyslexia sample

artículo científico publicado en 2008

Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia

artículo científico publicado en 2014

Investigation of the role of TCF4 rare sequence variants in schizophrenia

artículo científico publicado en 2015

Isolated bladder exstrophy associated with a de novo 0.9 Mb microduplication on chromosome 19p13.12.

artículo científico publicado en 2013

Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24.

artículo científico publicado en 2009

LAMP-Seq enables sensitive, multiplexed COVID-19 diagnostics using molecular barcoding

artículo científico publicado en 2021

Low-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibility

artículo científico publicado en 2015

Mapping for dyslexia and related cognitive trait loci provides strong evidence for further risk genes on chromosome 6p21

article

Mendelian randomisation study of the relationship between vitamin D and risk of glioma

artículo científico publicado en 2018

Microduplications at 22q11.21 are associated with non-syndromic classic bladder exstrophy

Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum

artículo científico publicado en 2022

Mutations in GRIN2A cause idiopathic focal epilepsy with rolandic spikes

artículo científico publicado en 2013

No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder

artículo científico publicado en 2013

Patient-derived dendritic cells transduced with an a-fetoprotein-encoding adenovirus and co-cultured with autologous cytokine-induced lymphocytes induce a specific and strong immune response against hepatocellular carcinoma cells

Promoter variants determine γ-aminobutyric acid homeostasis-related gene transcription in human epileptic hippocampi.

artículo científico publicado en 2011

Publisher Correction: Mendelian randomisation study of the relationship between vitamin D and risk of glioma

scientific article published on 23 May 2019

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Recent patents on experimental therapy for hepatitis C virus infection (1999 ? 2002)

Replication of novel susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 in Estonian and Lithuanian patients

article published in 2009

Resequencing of VAX1 in patients with nonsyndromic cleft lip with or without cleft palate

artículo científico publicado en 2012

Risk loci for coronary artery calcification replicated at 9p21 and 6q24 in the Heinz Nixdorf Recall Study

artículo científico publicado en 2013

Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue.

artículo científico publicado en 2013

SUCLG2 identified as both a determinator of CSF Aβ1-42 levels and an attenuator of cognitive decline in Alzheimer's disease

artículo científico publicado en 2014

SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients

article

Shared genetic etiology between alcohol dependence and major depressive disorder.

artículo científico publicado en 2018

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome

artículo científico publicado en 2011

Stimulation of MMP-1 and CCL2 by NAMPT in PDL cells.

artículo científico publicado en 2013

Supporting evidence for LRRTM1 imprinting effects in schizophrenia.

artículo científico publicado en 2009

Susceptibility locus for non-syndromic cleft lip with or without cleft palate on chromosome 10q25 confers risk in Estonian patients

artículo científico publicado en 2010

Systematic Evaluation of Pleiotropy Identifies 6 Further Loci Associated With Coronary Artery Disease ⬇️

artículo científico publicado en 2017

The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells

artículo científico publicado en 2014

The 9p21.3 risk of childhood acute lymphoblastic leukaemia is explained by a rare high-impact variant in CDKN2A ⬇️

artículo científico publicado en 2015

The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

artículo científico publicado en 2013

The DISC locus and schizophrenia: evidence from an association study in a central European sample and from a meta-analysis across different European populations

artículo científico publicado en 2009

The aromatase gene CYP19A1: several genetic and functional lines of evidence supporting a role in reading, speech and language

artículo científico publicado en 2012

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

artículo científico publicado en 2020

The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis

article published in 2018

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

artículo científico publicado en 2018

Transcriptome-Wide Association Study Identifies New Candidate Susceptibility Genes for Glioma

artículo científico publicado en 2019

Transethnic meta-analysis of rare coding variants in PLCG2, ABI3, and TREM2 supports their general contribution to Alzheimer's disease

artículo científico publicado en 2019

Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent

artículo científico publicado en 2009

Translation of mouse model to human gives insights into periodontitis etiology

artículo científico publicado en 2020

VATER/VACTERL association: identification of seven new twin pairs, a systematic review of the literature, and a classical twin analysis

artículo científico publicado en 2012

Variation in GRIN2B contributes to weak performance in verbal short-term memory in children with dyslexia.

artículo científico publicado en 2010

Whole-exome sequencing of 81 individuals from 27 multiply affected bipolar disorder families

scientific article published on 04 February 2020

XRCC5 as a risk gene for alcohol dependence: evidence from a genome-wide gene-set-based analysis and follow-up studies in Drosophila and humans

artículo científico publicado en 2014

αCaMKII autophosphorylation controls the establishment of alcohol drinking behavior

artículo científico publicado en 2013

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