Ivo Glynne Gut

Q: What Schools Are Affiliated With Ivo Glynne Gut

Ivo Glynne Gut is affiliated with the following schools: Stony Brook University, ETH Zurich, University of Basel, University of Geneva, Pompeu Fabra University, University of Zurich

Ivo Glynne Gut's AcademicInfluence.com Rankings

Ivo Glynne Gut

Chemistry

#3949

World Rank

#5000

Historical Rank

Organic Chemistry

#631

World Rank

#723

Historical Rank

chemistry Degrees

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Chemistry

Ivo Glynne Gut's Degrees

PhD Chemistry ETH Zurich
Masters Chemistry ETH Zurich
Bachelors Chemistry ETH Zurich

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Ivo Glynne Gut's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease (2008) (2621)
International network of cancer genome projects (2010) (1839)
SLCO1B1 variants and statin-induced myopathy--a genomewide study. (2008) (1819)
A large-scale, consortium-based genomewide association study of asthma. (2010) (1779)
Transcriptome and genome sequencing uncovers functional variation in humans (2013) (1758)
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma (2007) (1493)
Whole-genome sequencing identifies recurrent mutations in chronic lymphocytic leukaemia (2011) (1488)
Genome-wide association study identifies variants at CLU and CR1 associated with Alzheimer's disease (2009) (1476)
A susceptibility locus for lung cancer maps to nicotinic acetylcholine receptor subunit genes on 15q25 (2008) (1264)
Genome-wide association study identifies eight loci associated with blood pressure (2009) (1225)
A genome-wide association study of global gene expression (2007) (1021)
Exome sequencing identifies recurrent mutations of the splicing factor SF3B1 gene in chronic lymphocytic leukemia (2011) (993)
Great ape genetic diversity and population history (2013) (747)
Distinct DNA methylomes of newborns and centenarians (2012) (707)
Non-coding recurrent mutations in chronic lymphocytic leukaemia (2015) (654)
DNA methylation analysis by pyrosequencing (2007) (652)
Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4 (2007) (589)
Lung cancer susceptibility locus at 5p15.33 (2008) (562)
Towards complete and error-free genome assemblies of all vertebrate species (2020) (557)
Epigenomic analysis detects widespread gene-body DNA hypomethylation in chronic lymphocytic leukemia (2012) (534)
A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 (2007) (498)
Genome-wide association study identifies three loci associated with melanoma risk (2009) (444)
Whole-genome bisulfite sequencing of two distinct interconvertible DNA methylomes of mouse embryonic stem cells. (2013) (404)
Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations. (2014) (377)
Patterns of somatic structural variation in human cancer genomes (2020) (377)
β-Glucan Reverses the Epigenetic State of LPS-Induced Immunological Tolerance (2016) (368)
DNA Methylation Profiling of the Human Major Histocompatibility Complex: A Pilot Study for the Human Epigenome Project (2004) (364)
The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery (2016) (360)
Recommendations for the design and analysis of epigenome-wide association studies (2013) (336)
BLUEPRINT to decode the epigenetic signature written in blood (2012) (320)
Gibbon genome and the fast karyotype evolution of small apes (2014) (303)
Transcription initiation platforms and GTF recruitment at tissue-specific enhancers and promoters (2011) (288)
A high-density SNP-based linkage map of the chicken genome reveals sequence features correlated with recombination rate. (2009) (285)
A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium (2011) (278)
International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases (2017) (275)
De novo quantitative bisulfite sequencing using the pyrosequencing technology. (2004) (273)
Whole-genome fingerprint of the DNA methylome during human B cell differentiation (2015) (265)
Novel breast cancer susceptibility locus at 9q31.2: results of a genome-wide association study. (2011) (263)
Analysis and quantification of multiple methylation variable positions in CpG islands by Pyrosequencing. (2003) (261)
Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02). (2009) (255)
Reproducibility of high-throughput mRNA and small RNA sequencing across laboratories (2013) (254)
A comprehensive assessment of somatic mutation detection in cancer using whole-genome sequencing (2015) (250)
Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3 (2011) (246)
Morphometric, Behavioral, and Genomic Evidence for a New Orangutan Species (2017) (236)
Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy (2013) (235)
Automation in genotyping of single nucleotide polymorphisms (2001) (231)
Large-Scale Gene-Centric Analysis Identifies Novel Variants for Coronary Artery Disease (2011) (228)
Specific epigenetic alterations of IGF2-H19 locus in spermatozoa from infertile men (2010) (227)
Splicing enhances recruitment of methyltransferase HYPB/Setd2 and methylation of histone H3 Lys36 (2011) (225)
Analyses of non-coding somatic drivers in 2,658 cancer whole genomes (2020) (220)
HLA has strongest association with IgA nephropathy in genome-wide analysis. (2010) (216)
Making sense of big data in health research: Towards an EU action plan (2016) (205)
SPOTlight: seeded NMF regression to deconvolute spatial transcriptomics spots with single-cell transcriptomes (2020) (202)
Tuning of Natural Killer Cell Reactivity by NKp46 and Helios Calibrates T Cell Responses (2012) (201)
SNP and haplotype mapping for genetic analysis in the rat (2008) (200)
The Genome Response to Artificial Selection: A Case Study in Dairy Cattle (2009) (200)
CpG islands and GC content dictate nucleosome depletion in a transcription-independent manner at mammalian promoters (2012) (198)
Comprehensive molecular characterization of mitochondrial genomes in human cancers (2017) (197)
Chimpanzee genomic diversity reveals ancient admixture with bonobos (2016) (193)
Nested core collections maximizing genetic diversity in Arabidopsis thaliana. (2004) (186)
Transcriptome characterization by RNA sequencing identifies a major molecular and clinical subdivision in chronic lymphocytic leukemia (2014) (185)
Genome-wide nucleosome specificity and function of chromatin remodellers in ES cells (2015) (180)
Investigation of the fine structure of European populations with applications to disease association studies (2008) (178)
Epigenomic analysis detects aberrant super-enhancer DNA methylation in human cancer (2016) (177)
Development and Validation of a 20K Single Nucleotide Polymorphism (SNP) Whole Genome Genotyping Array for Apple (Malus × domestica Borkh) (2014) (177)
A whole genome Bayesian scan for adaptive genetic divergence in West African cattle (2009) (168)
RD-Connect: An Integrated Platform Connecting Databases, Registries, Biobanks and Clinical Bioinformatics for Rare Disease Research (2014) (164)
Genome sequence of the olive tree, Olea europaea (2016) (163)
Chromosome 7p11.2 (EGFR) variation influences glioma risk. (2011) (161)
Identification of regions correlating MGMT promoter methylation and gene expression in glioblastomas. (2009) (153)
Genotyping single nucleotide polymorphisms by MALDI mass spectrometry in clinical applications. (2005) (152)
Integrative epigenome-wide analysis demonstrates that DNA methylation may mediate genetic risk in inflammatory bowel disease (2016) (152)
Gene-environment interaction for childhood asthma and exposure to farming in Central Europe. (2011) (148)
Benchmarking single-cell RNA-sequencing protocols for cell atlas projects (2020) (147)
A novel procedure for efficient genotyping of single nucleotide polymorphisms. (2000) (145)
Threonine‐4 of mammalian RNA polymerase II CTD is targeted by Polo‐like kinase 3 and required for transcriptional elongation (2012) (144)
Variation in genomic landscape of clear cell renal cell carcinoma across Europe (2014) (142)
Genetic and Haplotypic Structure in 14 European and African Cattle Breeds (2007) (142)
Transcription Factors Drive Tet2-Mediated Enhancer Demethylation to Reprogram Cell Fate. (2018) (136)
Expressional and Epigenetic Alterations of Placental Serine Protease Inhibitors: SERPINA3 Is a Potential Marker of Preeclampsia (2007) (133)
DNA methylation profiling in doxorubicin treated primary locally advanced breast tumours identifies novel genes associated with survival and treatment response (2010) (132)
Mex3a Marks a Slowly Dividing Subpopulation of Lgr5+ Intestinal Stem Cells. (2017) (131)
The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia (2018) (131)
Epigenetic prediction of response to anti-PD-1 treatment in non-small-cell lung cancer: a multicentre, retrospective analysis. (2018) (130)
Whole genome sequencing of turbot (Scophthalmus maximus; Pleuronectiformes): a fish adapted to demersal life (2016) (129)
Spinal muscular atrophy associated with progressive myoclonic epilepsy is caused by mutations in ASAH1. (2012) (123)
Analysis and accurate quantification of CpG methylation by MALDI mass spectrometry. (2003) (122)
Genotyping single nucleotide polymorphisms by mass spectrometry. (2002) (121)
Benchmarking single-cell RNA-sequencing protocols for cell atlas projects (2019) (120)
Methylation profiling with a panel of cancer related genes: Association with estrogen receptor, TP53 mutation status and expression subtypes in sporadic breast cancer (2011) (120)
Increased DNA methylation variability in type 1 diabetes across three immune effector cell types (2016) (118)
Extreme genomic erosion after recurrent demographic bottlenecks in the highly endangered Iberian lynx (2016) (116)
Single-cell transcriptome conservation in cryopreserved cells and tissues (2017) (115)
Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03). (2009) (113)
DNA analysis by MALDI‐TOF mass spectrometry (2004) (111)
A whole-genome sequence and transcriptome perspective on HER2-positive breast cancers (2016) (110)
Whole-epigenome analysis in multiple myeloma reveals DNA hypermethylation of B cell-specific enhancers (2015) (109)
Mutation discovery in mice by whole exome sequencing (2011) (109)
Whole-exome sequencing in splenic marginal zone lymphoma reveals mutations in genes involved in marginal zone differentiation (2014) (105)
Unifying Candidate Gene and GWAS Approaches in Asthma (2010) (104)
Analysis of gene-specific DNA methylation patterns by pyrosequencing technology. (2007) (102)
Divergent transcription is associated with promoters of transcriptional regulators (2013) (101)
Runs of homozygosity reveal signatures of positive selection for reproduction traits in breed and non-breed horses (2015) (98)
Integrative pathway enrichment analysis of multivariate omics data (2018) (96)
Mutations in CNTNAP1 and ADCY6 are responsible for severe arthrogryposis multiplex congenita with axoglial defects. (2014) (96)
Interaction of Triplet Photosensitizers with Nucleotides and DNA in Aqueous Solution at Room Temperature (1996) (95)
Transient receptor potential genes, smoking, occupational exposures and cough in adults (2012) (95)
Transcriptome Analysis Describing New Immunity and Defense Genes in Peripheral Blood Mononuclear Cells of Rheumatoid Arthritis Patients (2009) (91)
Multiple-cohort genetic association study reveals CXCR6 as a new chemokine receptor involved in long-term nonprogression to AIDS. (2010) (91)
Decoding the DNA Methylome of Mantle Cell Lymphoma in the Light of the Entire B Cell Lineage. (2016) (91)
ProteinSeq: High-Performance Proteomic Analyses by Proximity Ligation and Next Generation Sequencing (2011) (89)
Eight blood pressure loci identified by genome-wide association study of 34,433 people of European ancestry (2009) (88)
Analysis of 14 Candidate Genes for Diabetic Nephropathy on Chromosome 3q in European Populations (2006) (88)
Reversion of a fungal genetic code alteration links proteome instability with genomic and phenotypic diversification (2013) (86)
Comprehensive characterization of complex structural variations in cancer by directly comparing genome sequence reads (2014) (82)
Modulation of imprinted gene network in placenta results in normal development of in vitro manipulated mouse embryos. (2010) (82)
Tyrosine phosphorylation of RNA polymerase II CTD is associated with antisense promoter transcription and active enhancers in mammalian cells (2014) (82)
Cancer LncRNA Census reveals evidence for deep functional conservation of long noncoding RNAs in tumorigenesis (2020) (80)
Evolutionary dynamics of non-coding sequences within the class II region of the human MHC. (1996) (78)
Genomic binding of Pol III transcription machinery and relationship with TFIIS transcription factor distribution in mouse embryonic stem cells (2011) (77)
Selective single molecule sequencing and assembly of a human Y chromosome of African origin (2018) (76)
Comparison of SNPs and microsatellites for assessing the genetic structure of chicken populations. (2012) (74)
Serial pyrosequencing for quantitative DNA methylation analysis. (2006) (74)
MetaTrans: an open-source pipeline for metatranscriptomics (2016) (74)
Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations. (2007) (74)
Fine Mapping of Quantitative Trait Loci Affecting Female Fertility in Dairy Cattle on BTA03 Using a Dense Single-Nucleotide Polymorphism Map (2008) (74)
Dynamics of Transcription Regulation in Human Bone Marrow Myeloid Differentiation to Mature Blood Neutrophils (2018) (71)
Full flexibility genotyping of single nucleotide polymorphisms by the GOOD assay. (2000) (71)
Shared Oncogenic Pathways Implicated in Both Virus-Positive and UV-Induced Merkel Cell Carcinomas. (2017) (71)
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity (2012) (70)
DNA sequencing - spanning the generations. (2012) (70)
Genetic analysis of an F2 intercross between two chicken lines divergently selected for body-weight (2009) (69)
Multiplex target protein imaging in tissue sections by mass spectrometry--TAMSIM. (2007) (68)
A DNA methylation map of human cancer at single base-pair resolution (2017) (68)
Influence of lung CT changes in chronic obstructive pulmonary disease (COPD) on the human lung microbiome (2017) (65)
Genetic heterogeneity of asthma phenotypes identified by a clustering approach (2013) (65)
Identification and quantification of differentially methylated loci by the pyrosequencing technology. (2009) (65)
RNA sequencing validation of the Complexity INdex in SARComas prognostic signature. (2016) (61)
Genotyping single-nucleotide polymorphisms by matrix-assisted laser-desorption/ionization time-of-flight mass spectrometry. (2002) (61)
A comprehensive DNA methylation profile of epithelial-to-mesenchymal transition. (2014) (61)
Hypermethylation of the IGF2 differentially methylated region 2 is a specific event in insulinomas leading to loss-of-imprinting and overexpression. (2009) (61)
Leveraging European infrastructures to access 1 million human genomes by 2022 (2019) (60)
In vivo binding of PRDM9 reveals interactions with noncanonical genomic sites. (2017) (56)
RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases (2018) (55)
Future potential of the Human Epigenome Project (2004) (55)
An efficient protocol for genomic DNA extraction from formalin-fixed paraffin-embedded tissues. (2009) (54)
GSTP1 promoter haplotypes affect DNA methylation levels and promoter activity in breast carcinomas. (2008) (53)
Molecular haplotyping at high throughput. (2002) (53)
G/T Substitution in Intron 1 of the UNC13B Gene Is Associated With Increased Risk of Nephropathy in Patients With Type 1 Diabetes (2008) (52)
Truncating Mutations of MAGEL2, a Gene within the Prader-Willi Locus, Are Responsible for Severe Arthrogryposis. (2015) (52)
bigSCale: an analytical framework for big-scale single-cell data (2017) (52)
Genomics of Ecological Adaptation in Cactophilic Drosophila (2014) (51)
Distinct Trends of DNA Methylation Patterning in the Innate and Adaptive Immune Systems (2016) (51)
Site- and allele-specific polycomb dysregulation in T-cell leukaemia (2015) (50)
Facile method for automated genotyping of single nucleotide polymorphisms by mass spectrometry. (2002) (49)
DNA analysis by mass spectrometry-past, present and future. (2006) (48)
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR1 as a Major Determinant of Coronary Artery Stenosis (2012) (48)
A single-cell tumor immune atlas for precision oncology (2020) (48)
Performance comparison of two microarray platforms to assess differential gene expression in human monocyte and macrophage cells (2008) (47)
Splenic diffuse red pulp small B-cell lymphoma displays increased expression of cyclin D3 and recurrent CCND3 mutations. (2017) (47)
Multi-scale computational models of the airways to unravel the pathophysiological mechanisms in asthma and chronic obstructive pulmonary disease (AirPROM) (2013) (46)
A mechanistic basis for amplification differences between samples and between genome regions (2012) (46)
The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild (2013) (46)
Gene expression profiling in insulinomas of Men1 β-cell mutant mice reveals early genetic and epigenetic events involved in pancreatic β-cell tumorigenesis (2006) (45)
From Wet‐Lab to Variations: Concordance and Speed of Bioinformatics Pipelines for Whole Genome and Whole Exome Sequencing (2016) (44)
Analysis of DNA by `Charge Tagging' and Matrix-assisted Laser Desorption/Ionization Mass Spectrometry (1997) (44)
A procedure for selective DNA alkylation and detection by mass spectrometry. (1995) (42)
Dynamics of genome architecture and chromatin function during human B cell differentiation and neoplastic transformation (2019) (42)
Sex differences in oncogenic mutational processes (2019) (41)
Emphysema- and airway-dominant COPD phenotypes defined by standardised quantitative computed tomography (2016) (41)
Loss of function mutations in EPHB4 are responsible for vein of Galen aneurysmal malformation (2018) (40)
Mutations in GLDN, Encoding Gliomedin, a Critical Component of the Nodes of Ranvier, Are Responsible for Lethal Arthrogryposis. (2016) (40)
Transcription Factors Drive Tet2-Mediated Enhancer Demethylation to Reprogram Cell Fate (2018) (39)
Benchmarking of Whole Exome Sequencing and Ad Hoc Designed Panels for Genetic Testing of Hereditary Cancer (2017) (39)
Examining Phylogenetic Relationships Among Gibbon Genera Using Whole Genome Sequence Data Using an Approximate Bayesian Computation Approach (2015) (39)
European rational approach for the genetics of diabetic complications--EURAGEDIC: patient populations and strategy. (2007) (38)
Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation (2018) (37)
Large-scale genotyping by mass spectrometry: experience, advances and obstacles. (2002) (36)
High‐Density SNP genotyping defines 17 distinct haplotypes of the TNF block in the Caucasian population: Implications for haplotype tagging (2004) (36)
Common and Rare Variant Analysis in Early-Onset Bipolar Disorder Vulnerability (2014) (36)
Information recovery from low coverage whole-genome bisulfite sequencing (2016) (36)
Ketonization equilibria of phenol in aqueous solution (1999) (36)
Tracking of Antibiotic Resistance Transfer and Rapid Plasmid Evolution in a Hospital Setting by Nanopore Sequencing (2019) (35)
Replication of the tumor necrosis factor receptor-associated factor 1/complement component 5 region as a susceptibility locus for rheumatoid arthritis in a European family-based study. (2008) (35)
New sequencing technologies (2013) (34)
Dynamic recruitment of Ets1 to both nucleosome-occupied and -depleted enhancer regions mediates a transcriptional program switch during early T-cell differentiation (2015) (34)
Single cell RNA-seq identifies the origins of heterogeneity in efficient cell transdifferentiation and reprogramming (2019) (34)
Systems biology of infectious diseases: a focus on fungal infections. (2011) (34)
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases (2021) (33)
A high-resolution linkage map for the Z chromosome in chicken reveals hot spots for recombination (2007) (33)
Early-onset chronic axonal neuropathy, strokes, and hemolysis (2015) (32)
Combined burden and functional impact tests for cancer driver discovery using DriverPower (2020) (31)
gemBS: high throughput processing for DNA methylation data from bisulfite sequencing (2018) (31)
Mitochondrial Complex I Is a Global Regulator of Secondary Metabolism, Virulence and Azole Sensitivity in Fungi (2016) (30)
The EvA study: aims and strategy (2012) (30)
Chromatin-Based Classification of Genetically Heterogeneous AMLs into Two Distinct Subtypes with Diverse Stemness Phenotypes (2019) (30)
Towards a European health research and innovation cloud (HRIC) (2020) (29)
Evolution of Robustness to Protein Mistranslation by Accelerated Protein Turnover (2015) (29)
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (29)
Seventh international meeting on single nucleotide polymorphism and complex genome analysis: ‘ever bigger scans and an increasingly variable genome’ (2006) (29)
Rapid identification of promoter hypermethylation in hepatocellular carcinoma by pyrosequencing of etiologically homogeneous sample pools. (2007) (29)
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (2021) (28)
Myelin Basic Protein as a Novel Genetic Risk Factor in Rheumatoid Arthritis—A Genome-Wide Study Combined with Immunological Analyses (2011) (28)
Impact of DNA methylation on 3D genome structure (2020) (28)
Morphometric, Behavioral, and Genomic Evidence for a New Orangutan Species (2017) (28)
Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (2021) (28)
Relationship between genome and epigenome - challenges and requirements for future research (2014) (28)
The evolution and diversity of TNF block haplotypes in European, Asian and Australian Aboriginal populations (2009) (27)
Tumour necrosis factor haplotypes associated with sensory neuropathy in Asian and Caucasian human immunodeficiency virus patients. (2011) (26)
Gene expression profiling in insulinomas of Men1 beta-cell mutant mice reveals early genetic and epigenetic events involved in pancreatic beta-cell tumorigenesis. (2006) (26)
The Phenol ⇌ 2,4‐Cyclohexadienone Equilibrium in Aqueous Solution (1986) (26)
Saturation analysis for whole-genome bisulfite sequencing data (2016) (26)
Mutational Profile of Aggressive, Localised Prostate Cancer from African Caribbean Men Versus European Ancestry Men. (2019) (25)
Genomic evidence for recurrent genetic admixture during the domestication of Mediterranean olive trees (Olea europaea L.) (2020) (25)
Analysis of negatively 'charge tagged' DNA by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry. (1999) (25)
Single-nucleotide polymorphisms: analysis by mass spectrometry (2006) (25)
10th Anniversary of the European Association for Predictive, Preventive and Personalised (3P) Medicine - EPMA World Congress Supplement 2020 (2020) (24)
Site-specific methylation and acetylation of lysine residues in the C-terminal domain (CTD) of RNA polymerase II (2015) (24)
Blood eosinophil count and airway epithelial transcriptome relationships in COPD versus asthma (2019) (24)
ERBB2 in Cat Mammary Neoplasias Disclosed a Positive Correlation between RNA and Protein Low Expression Levels: A Model for erbB-2 Negative Human Breast Cancer (2013) (23)
Recessive variants of MuSK are associated with late onset CMS and predominant limb girdle weakness (2018) (23)
Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (22)
Systemic inflammation in pre-clinical ulcerative colitis. (2021) (22)
Extension of the GOOD assay for genotyping single nucleotide polymorphisms by matrix-assisted laser desorption/ionization mass spectrometry. (2003) (22)
Sequence variation between 462 human individuals fine-tunes functional sites of RNA processing (2016) (22)
Chromatin activation as a unifying principle underlying pathogenic mechanisms in multiple myeloma (2019) (22)
Adaptive Mistranslation Accelerates the Evolution of Fluconazole Resistance and Induces Major Genomic and Gene Expression Alterations in Candida albicans (2017) (21)
Duplicating SNPs (2004) (20)
Detection of early seeding of Richter transformation in chronic lymphocytic leukemia (2022) (20)
Identification of IL7RA risk alleles for rapid progression during HIV-1 infection: a comprehensive study in the GRIV cohort. (2012) (20)
SNP genotyping using alkali cleavage of RNA/DNA chimeras and MALDI time-of-flight mass spectrometry (2006) (20)
Lung microbiome composition and bronchial epithelial gene expression in patients with COPD versus healthy individuals: a bacterial 16S rRNA gene sequencing and host transcriptomic analysis. (2021) (20)
Genomic and Phenotypic Variation in Morphogenetic Networks of Two Candida albicans Isolates Subtends Their Different Pathogenic Potential (2018) (19)
TNF block haplotypes associated with conserved MHC haplotypes in European, Asian and Australian Aboriginal donors. (2009) (19)
Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region (2006) (19)
Blueprint of human thymopoiesis reveals molecular mechanisms of stage-specific TCR enhancer activation (2020) (19)
Somatic Embryonic FGFR2 Mutations in Keratinocytic Epidermal Nevi. (2016) (18)
Quantitative DNA Methylation Analysis at Single-Nucleotide Resolution by Pyrosequencing®. (2018) (18)
Mex 3 a Marks a Slowly Dividing Subpopulation of Lgr 5 + Intestinal Stem Cells (2018) (17)
PRKG1 and genetic diagnosis of early‐onset thoracic aortic disease (2016) (17)
DNA sequencing by MALDI-TOF MS using alkali cleavage of RNA/DNA chimeras (2007) (17)
Involvement of a citrus meiotic recombination TTC-repeat motif in the formation of gross deletions generated by ionizing radiation and MULE activation (2015) (16)
Similarity in recombination rate and linkage disequilibrium at CYP2C and CYP2D cytochrome P450 gene regions among Europeans indicates signs of selection and no advantage of using tagSNPs in population isolates (2012) (16)
Pheno-seq – linking visual features and gene expression in 3D cell culture systems (2019) (16)
Activity of imipenem/relebactam against a Spanish nationwide collection of carbapenemase-producing Enterobacterales. (2021) (16)
Sequence Variants and Haplotype Analysis of Cat ERBB2 Gene: A Survey on Spontaneous Cat Mammary Neoplastic and Non-Neoplastic Lesions (2012) (16)
Loss-of-Function Mutations in LGI4, a Secreted Ligand Involved in Schwann Cell Myelination, Are Responsible for Arthrogryposis Multiplex Congenita. (2017) (16)
Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita (2021) (16)
Does a central MHC gene in linkage disequilibrium with HLA-DRB1*0401 affect susceptibility to type 1 diabetes? (2005) (15)
Common colorectal cancer risk alleles contribute to the multiple colorectal adenoma phenotype, but do not influence colonic polyposis in FAP (2014) (15)
Characterisation of TNF block haplotypes affecting the production of TNF and LTA. (2011) (15)
Depurination of DNA and matrix-assisted laser desorption/ionization mass spectrometry (1997) (15)
Genome-wide linkage disequilibrium in the Blonde d'Aquitaine cattle breed. (2013) (15)
Exploration of associations between phospholipase A2 gene family polymorphisms and AIDS progression using the SNPlex method. (2008) (15)
Recurrent somatic mutations reveal new insights into consequences of mutagenic processes in cancer (2019) (14)
Two-photon absorption cross sections of guanosine 5'-monophosphate and uridine 5'-monophosphate at 532 nm (1993) (14)
Improved Diagnosis of Rare Disease Patients through Systematic Detection of Runs of Homozygosity (2020) (13)
The Fungus Candida albicans Tolerates Ambiguity at Multiple Codons (2016) (13)
Alternative Enhancer Usage and Targeted Polycomb Marking Hallmark Promoter Choice during T Cell Differentiation. (2020) (13)
Multi-omics profiling reveals a distinctive epigenome signature for high-risk acute promyelocytic leukemia (2018) (13)
The Genome Sequence of the Eastern Woodchuck (Marmota monax) – A Preclinical Animal Model for Chronic Hepatitis B (2019) (13)
matchSCore: Matching Single-Cell Phenotypes Across Tools and Experiments (2018) (12)
Erratum to: Making sense of big data in health research: towards an EU action plan (2016) (12)
New technologies for DNA analysis--a review of the READNA Project. (2016) (12)
Characterization of tumor necrosis factor-α block haplotypes associated with susceptibility to chronic venous leg ulcers in Caucasian patients. (2010) (12)
Transcription-Dependent Generation of a Specialized Chromatin Structure at the TCRβ Locus (2015) (12)
Resistome analyses of sputum from COPD and healthy subjects reveals bacterial load-related prevalence of target genes (2019) (11)
Colorectal Adenomas Contain Multiple Somatic Mutations That Do Not Coincide with Synchronous Adenocarcinoma Specimens (2015) (11)
Detection and characterization of interleukin-6 gene variants in Canis familiaris: association studies with periodontal disease. (2011) (10)
A family-based genome-wide association study reveals an association of spondyloarthritis with MAPK14 (2015) (10)
A comprehensive multicenter comparison of whole genome sequencing pipelines using a uniform tumor-normal sample pair (2014) (10)
A roadmap for the generation of benchmarking resources for antimicrobial resistance detection using next generation sequencing (2021) (9)
Quantification of target proteins using hydrogel antibody arrays and MALDI time-of-flight mass spectrometry (A2M2S). (2009) (9)
Systems Genetics of Hepatic Metabolome Reveals Octopamine as a Target for Non-Alcoholic Fatty Liver Disease Treatment (2019) (9)
Whole-genome single nucleotide polymorphism-based linkage analysis in spondyloarthritis multiplex families reveals a new susceptibility locus in 13q13 (2015) (9)
Applications of second generation sequencing technologies in complex disorders. (2012) (9)
Labelled regulatory elements are pervasive features of the macrophage genome and are dynamically utilized by classical and alternative polarization signals (2019) (8)
Emergence of 16S rRNA methyltransferases among carbapenemase-producing Enterobacterales in Spain studied by WGS. (2021) (8)
Sequence variation and mRNA expression of the TWIST1 gene in cats with mammary hyperplasia and neoplasia. (2012) (8)
DNA Methylation Analysis by MALDI Mass Spectrometry (2012) (8)
Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis (2017) (8)
A Comprehensive Assessment of Somatic Mutation Calling in Cancer Genomes (2014) (7)
Specific hypomethylated CpGs at the IGF2 locus act as an epigenetic biomarker for familial adenomatous polyposis colorectal cancer. (2010) (7)
Correction: A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium (2011) (7)
Clonal dynamics monitoring during clinical evolution in chronic lymphocytic leukaemia (2019) (7)
, SERPINA 3 Is a Potential Marker of Preeclampsia Expressional and Epigenetic Alterations of Placental Serine Protease Inhibitors (2006) (7)
Combined HAT/EZH2 modulation leads to cancer-selective cell death (2018) (7)
Deciphering the mechanism of action of 089, a compound impairing the fungal cell cycle (2018) (7)
Framework for quality assessment of whole genome cancer sequences (2017) (7)
Overview of Genotyping (2011) (7)
Molecular Techniques for DNA Methylation Studies (2017) (6)
Flash photolytic generation of two keto tautomers of 1-naphthol in aqueous solution: kinetics and equilibria of enolization. (2010) (6)
Analysis of new lactotransferrin gene variants in a case–control study related to periodontal disease in dog (2012) (6)
The RD‐Connect Genome‐Phenome Analysis Platform: Accelerating diagnosis, research, and gene discovery for rare diseases (2022) (6)
Gene expression proﬁling in insulinomas of Men1 b -cell mutant mice reveals early genetic and epigenetic events involved in pancreatic b -cell tumorigenesis (2006) (6)
THE GOOD ASSAY (2001) (5)
Population genomics of Saccharomyces cerevisiae human isolates: passengers, colonizers, invaders (2014) (5)
Gender specific airway gene expression in COPD sub-phenotypes supports a role of mitochondria and of different types of leukocytes (2021) (5)
Non-random, individual-specific methylation profiles are present at the sixth CTCF binding site in the human H19/IGF2 imprinting control region. (2006) (5)
DNA sequencing of the MHC class II region and the chromosome 6 sequencing effort at the Sanger Centre. (1996) (5)
Epigenetic Alterations at Diagnosis Predict Susceptibility, Prognosis and Treatment Escalation in Inflammatory Bowel Disease and IBD Character (2017) (4)
An Overview of Genotyping and Single Nucleotide Polymorphisms (SNP) (2005) (4)
Variation in predicted COVID-19 risk among lemurs and lorises (2021) (4)
A method for multiplexed full-length single-molecule sequencing of the human mitochondrial genome (2022) (4)
GEMBS – high through-put processing for DNA methylation data from Whole Genome Bisulfite Sequencing (WGBS) (2017) (4)
Author Correction: Leveraging European infrastructures to access 1 million human genomes by 2022 (2019) (4)
Epigenetic alterations in inflammatory bowel disease: the complex interplay between genome-wide methylation alterations, germline variation, and gene expression (2017) (4)
Occurrence of the p019 Gene in the blaKPC-Harboring Plasmids: Adverse Clinical Impact for Direct Tracking of KPC-Producing Klebsiella pneumoniae by Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry (2021) (4)
The ELIXIR Human Copy Number Variations Community: building bioinformatics infrastructure for research (2020) (4)
Solving unsolved rare neurological diseases—a Solve-RD viewpoint (2021) (4)
TWIST1 Gene: First Insights in Felis catus (2010) (3)
Genome-Wide Association Study in a Lebanese Cohort Confirms PHACTR 1 as a Major Determinant of Coronary Artery Stenosis (2012) (3)
Comparative analysis of neutrophil and monocyte epigenomes (2017) (3)
A revisit of high collision energy effects on collision-induced dissociation spectra using matrix-assisted laser desorption/ionization tandem time-of-flight mass spectrometry (MALDI-LIFT-TOF/TOF): application to the sequencing of RNA/DNA chimeras. (2014) (3)
Upper excited-state photochemistry of DNA and nucleotides (1992) (3)
An Improved Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry Data Analysis Pipeline for the Identification of Carbapenemase-Producing Klebsiella pneumoniae (2021) (3)
Variation in predicted COVID‐19 risk among lemurs and lorises (2021) (3)
DNA methylation oscillation defines classes of enhancers (2018) (3)
Inference of genomic spatial organization from a whole genome bisulfite sequencing sample (2018) (3)
Structural studies of the sBBI/trypsin non-covalent complex using covalent modification and mass spectrometry. (2014) (2)
PLCγ1/PKCθ Downstream Signaling Controls Cutaneous T-Cell Lymphoma Development And Progression. (2021) (2)
Differentiation power of SNPs for assessing the phylogenetic structure of populations (2014) (2)
2nd generation DNA sequencing meets functional genomics (2010) (2)
Bronchial epithelial gene expression of NOX isoforms are related to important clinical characteristics in COPD (2016) (2)
Extreme genomic erosion after recurrent demographic bottlenecks in the highly endangered Iberian lynx (2016) (2)
Possible conformational change within the desolvated and cationized sBBI/trypsin non-covalent complex during the collision-induced dissociation process. (2011) (2)
An Atlas of Cells in the Human Tonsil (2022) (2)
Systematic Collaborative Reanalysis of Genomic Data Improves Diagnostic Yield in Neurologic Rare Diseases. (2022) (2)
A global catalog of whole-genome diversity from 233 primate species (2023) (2)
Genomic evidence for recurrent genetic admixture during domestication mediterranean olive trees (Olea europaea) (2020) (2)
Genome-Wide Analysis Identifies Strong Association Between HLA and IgA Nephropathy (2010) (2)
Resolution-dependent methylome feature analysis of whole-genome bisulfite sequencing data (2016) (1)
Author Correction: Pan-cancer analysis of whole genomes (2023) (1)
Author Correction: Pathway and network analysis of more than 2500 whole cancer genomes (2020) (1)
Correction: Colorectal Adenomas Contain Multiple Somatic Mutations That Do Not Coincide with Synchronous Adenocarcinoma Specimens (2015) (1)
Mitogenomic analysis of extant condor species provides insight into the molecular evolution of vultures (2021) (1)
Divergent transcription is associated with promoters of transcriptional regulators (2013) (1)
Whole-genome sequencing identifies recurrent mutations in chronic lymphocyticleukaemia (2011) (1)
Relationship between genome and epigenome - challenges and requirements for future research (2014) (1)
mulTI-cohorT GeneTIc assocIaTIon sTudy reVeals cXcr 6 as a new chemokIne recePTor InVolVed In aIds lonG-Term non-ProGressIon (2011) (1)
An improved MALDI-TOF MS data analysis pipeline for the identification of carbapenemase-producing Klebsiella pneumoniae. (2021) (1)
Author Correction: Integrative pathway enrichment analysis of multivariate omics data (2020) (1)
A mechanistic basis for amplification differences between samples and between genome regions (2012) (1)
Author Correction: Combined burden and functional impact tests for cancer driver discovery using DriverPower (2020) (1)
Optical properties of Er-doped As-S-Ge chalcogenide glasses (2009) (1)
Keeping up with Genome Sequence and Expression (2014) (1)
The ulcerative colitis-associated gene FUT8 regulates the quantity and quality of secreted mucins (2021) (1)
LifeTime and improving European healthcare through cell-based interceptive medicine (2020) (1)
Approaches to measuring linear and nonlinear acoustic properties of biological material (1994) (1)
High-throughput DNA analysis (2013) (1)
Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (1)
Correction: Mitochondrial Complex I Is a Global Regulator of Secondary Metabolism, Virulence and Azole Sensitivity in Fungi (2017) (1)
Chapter 14 – Molecular Techniques for DNA Methylation Studies (2010) (1)
Tackling the translational challenges of multi-omics research in the realm of European personalised medicine: A workshop report (2022) (1)
Whose genes are they and how can we identify them? (1996) (1)
The landscape of tolerated genetic variation in humans and primates (2023) (1)
OC-047 Epigenetic alterations at diagnosis predict susceptibility, prognosis and treatment escalation in inflammatory bowel disease – ibd character (2017) (1)
The Complete Mutatome and Clonal Architecture of Del(5q) (2015) (1)
The genome sequencing of an albino Western lowland gorilla reveals inbreeding in the wild (2013) (1)
Single-cell transcriptome conservation in cryopreserved cells and tissues (2016) (1)
Analysis of new lactotransferrin gene variants in a case–control study related to periodontal disease in dog (2011) (1)
A Genetic code alteration accelerates the acquisition of antifungal drug resistance in Candida albicans (2015) (0)
Making sense of big data in health research: Towards an EU action plan (2016) (0)
Genetic polymorphisms in the 5' flanking region of glutathione S-transferase P1 affect promoter methylation (2005) (0)
Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over (2015) (0)
Haplotyping method by mass spectrometry. (2001) (0)
An Approximate Bayesian Computation Approach to Examining the Phylogenetic Relationships among the Four Gibbon Genera using Whole Genome Sequence Data (2014) (0)
Partially methylated domains are hypervariable in breast cancer and fuel widespread CpG island hypermethylation (2019) (0)
Selective single molecule sequencing and assembly of a human Y chromosome of African origin (2019) (0)
samples and between genome regions. (2012) (0)
2174 / 138920210791110933 TWIST 1 Gene : First Insights in Felis catus (2012) (0)
pheno-seq – linking 3D phenotypes of clonal tumor spheroids to gene expression (2018) (0)
RD-Connect, NeurOmics and EURenOmics: collaborative European initiative for rare diseases (2018) (0)
Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (0)
Publisher Correction: Mutations in Vps15 perturb neuronal migration in mice and are associated with neurodevelopmental disease in humans (2018) (0)
Mo1115 WHOLE-BLOOD EXPRESSION PROFILES IN INFLAMMATORY BOWEL DISEASE REVEAL TRANSCRIPTION FACTOR INVOLVEMENT (2020) (0)
Scientific Business Abstracts of the 112th Annual Meeting of the Association of Physicians of Great Britain and Ireland. (2018) (0)
Systems Genetics of Hepatic Metabolome Reveals Octopamine as a Target for Non-Alcoholic Fatty Liver Disease Treatment (2019) (0)
PLCγ1/PKCθ and its downstream effectors in cutaneous T-cell lymphoma development and progression (2021) (0)
Scientific Business Abstracts of the 112th Annual Meeting of the Association of Physicians of Great Britain and Ireland. (2018) (0)
Ten simple rules for a successful international consortium in big data omics (2022) (0)
MITOCHONDRIAL DISEASES (Posters) P.193Unexpected genetic diagnosis of mitochondrial disease in three consanguineous Turkish families (2018) (0)
Deciphering the mechanism of action of 089, a compound impairing the fungal cell cycle (2018) (0)
Decreased Prevotella and Increased Moraxella Genera Abundance in Bronchial Epithelial Brushes Differentiates COPD from Health and Is Associated with Epithelial Host Defense and Pro-Inflammatory Gene Expression (2020) (0)
Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (2021) (0)
Association of COPD Bronchial Brush Microbiome Profile with Lung Function and Host Gene Expression (2020) (0)
A Multimodal Single Cell Atlas of Human Tonsils Reveals New Insights into T and B Cell Differentiation (2022) (0)
Association of Proteobacteria Phylum with Emphysema- and Airway-Dominant COPD Phenotypes Defined by Computed Tomography (2021) (0)
Remote visualization of large-scale genomic alignments for collaborative clinical research and diagnosis of rare diseases (2023) (0)
Author response: Single cell RNA-seq identifies the origins of heterogeneity in efficient cell transdifferentiation and reprogramming (2019) (0)
Author Correction: Patterns of somatic structural variation in human cancer genomes (2020) (0)
Abstract 3795: Early seeding of Richter transformation in chronic lymphocytic leukemia (2022) (0)
P061 Epigenetic alterations at diagnosis predict susceptibility, prognosis and treatment escalation in inflammatory bowel disease - IBD Character. (2017) (0)
EURAGEDIC; European consortium for the genetics of diabetic nephropathy: strategy and first results. (2003) (0)
Association of COPD Bronchial Brush Microbiome-Determined γProteobacteria:Firmicutes (γP:f) Ratio with Gold Grade, Symptoms, and Host Inflammatory Response (2020) (0)
Whole-Genome DNA Methylation Analysis of Mantle Cell Lymphoma: Biological and Clinical Implications (2014) (0)
Erratum to: Making sense of big data in health research: towards an EU action plan (2016) (0)
DNA methylation in human gastric epithelial cells defines regional identity without restricting lineage plasticity (2022) (0)
Dissecting the origin of heterogeneity in uterine and ovarian carcinosarcomas (2023) (0)
Author Correction: The evolutionary history of 2,658 cancers (2023) (0)
Proteobacteria phylum association with airway- and emphysema-dominant COPD phenotypes defined by computed tomography (2021) (0)
A process for the removal of biological samples (1997) (0)
Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (2021) (0)
G.O.21 Relapsing immune mediated polyneuropathy, strokes and chronic haemolysis due to inherited CD59 deficiency (2014) (0)
The prevalence and transcriptional activity of the mucosal microbiota of ulcerative colitis patients (2018) (0)
Clonal dynamics monitoring during clinical evolution in chronic lymphocytic leukaemia (2019) (0)
Differential bronchial epithelial gene expression in COPD versus controls (2016) (0)
pheno-seq – linking morphological features to gene expression in 3D cell culture systems (2018) (0)
Publisher Correction: LifeTime and improving European healthcare through cell-based interceptive medicine (2021) (0)
TWIST1 oncogene: Comparative Studies, Sequence Variations and mRNA expression in Cat Mammary Gland Carcinomas (2010) (0)
PLC g 1/PKC q Downstream Signaling Controls Cutaneous T-Cell Lymphoma Development and Progression (2022) (0)
High degree of polyclonality hinders somatic mutation calling in lung brush samples of COPD cases and controls (2019) (0)
Integrative and Computational Biology Joint symposium (2014) (0)
Device for preparing biological samples for DNA analysis (1999) (0)
Comparing The Full Genome Sequence Derived Of Blood And Bronchial Brush Cells From COPD Patients (2012) (0)
Whose genes are they and how can we identify them? (1996) (0)
Runs of homozygosity reveal signatures of positive selection for reproduction traits in breed and non-breed horses (2015) (0)
Towards a European health research and innovation cloud (HRIC) (2020) (0)
Epigenomic analysis detects aberrant super-enhancer DNA methylation in human cancer (2016) (0)
Reproducible mRNA and small RNA sequencing across different laboratories (2013) (0)
Phenol ‐ 2,4‐Cyclohexadienone Equilibrium in Aqueous Solution. (1986) (0)
Cancer-om-atics: Multilevel interpretation of cancer genome data (2011) (0)
OP0203 A Family-Based Genome-Wide Association Study Reveals an Association of Spondyloarthritis with MAPK14 (2015) (0)
leukemia major molecular and clinical subdivision in chronic lymphocytic Transcriptome characterization by RNA sequencing identifies a Material (2014) (0)
A novel quantitative trait locus controlling fetal haemoglobin on chromosome 2p15 (2008) (0)
COPD bronchial brush microbiome association with lung function and bronchial gene expression (2020) (0)
Association between COPD bronchial brush microbiome-determined ?Proteobacteria:Firmicutes (G:F) ratio and GOLD grade and symptoms (2019) (0)
Locus β Specialized Chromatin Structure at the TCR Transcription-Dependent Generation of a Andrau (2015) (0)
Genotyping Methods and Disease Gene Identification (2006) (0)
Device for sampling and identification of a living (1997) (0)
766 Comprehensive Epigenome-Wide DNA Methylation Profiling in Inflammatory Bowel Disease (2016) (0)
B1MG D3.1 - Quality metrics for sequencing (2021) (0)
Revolutionary Approaches and Devices for Nucleic Acid analysis (2010) (0)
Nucleic acid detection ribonucleotides labeled with labels (2009) (0)
Aberrant Expression of the SOX11 Oncogene in Mantle Cell Lymphoma Is Associated with Activation and De Novo 3D Looping of a Distant Enhancer Element (2016) (0)
Whole-Exome Sequencing in Myelodysplastic Syndromes with 5q Deletion (2014) (0)
The reference epigenome and regulatory chromatin landscape of chronic lymphocytic leukemia (2018) (0)
Chromosome 7p11.2(EGFR) and 7q36.1(XRCC2) variants influence glioma risk (2011) (0)
Copy number variation identified on chromosome 5p13. (2014) (0)
The Strepsirrhine and Tarsier genome sequencing initiative : conservation genomics of the non-anthropoid primate (2021) (0)
Correction to: Solving patients with rare diseases through programmatic reanalysis of genome-phenome data (2021) (0)
Genetic studies of diabetic nephropathy in three European populations (EURAGEDIC consortium): analyses of 14 candidate genes on chromosome 3q (2005) (0)
Whole-genome epigenomic analysis in multiple myeloma reveals DNA hypermethylation of b-cell specific enhancers (2014) (0)
DNA methylation in human gastric epithelial cells allows cell type-related plasticity and defines regional identity (2022) (0)
Author Correction: Inferring structural variant cancer cell fraction (2022) (0)
Characterization of Subclonal Changes Along Progression in Multiple Myeloma. (2012) (0)
EURAGEDIC study: analyses of 144 candidate genes for diabetic nephropathy (2006) (0)
Contents Vol. 117, 2007 (2007) (0)
704 IDENTIFICATION OF CANDIDATE GENES IN DIET INDUCED NON-ALCOHOLIC FATTY LIVER DISEASE IN INBRED MICE (2009) (0)
Mutation analysis by mass spectrometry (1998) (0)
ELIXIR Rare Disease Use Case: ELIXIR infrastructure for rare disease research (2017) (0)
A Draft Assembly of the Almond Genome: abstract (2016) (0)
Correction: Solving unsolved rare neurological diseases—a Solve-RD viewpoint (2021) (0)
Mutational Status of Splenic Marginal Zone Lymphoma Revealed by Whole Exome Sequencing. (2012) (0)
1 of Genotyping (2012) (0)
Characterization of the DNA Methylome during Human B-Cell Differentiation (2014) (0)
EURAGEDIC study: identification of new candidate genes for diabetic nephropathy (2007) (0)
Development and Validation of a 20K Single Nucleotide Polymorphism (SNP) Whole Genome Genotyping Array for Apple (Malus 6 domestica Borkh) (2014) (0)
Genomic characterization of mutant laboratory mouse strains by exome sequencing and annotation lift-over (2015) (0)
Mutational Status of Splenic Diffuse Red Pulp Small B-Cell Lymphoma Revealed By Whole Exome Sequencing (2015) (0)
Single cell expression analysis uncouples transdifferentiation and reprogramming (2018) (0)
Prevotella genera abundance in bronchial brush samples differentiates COPD from health and is associated with gene expression (2019) (0)
Author Correction: Retrospective evaluation of whole exome and genome mutation calls in 746 cancer samples (2020) (0)
Evaluation of a panel of SNP markers for the traceability of cattle (2004) (0)
A roadmap for the generation of benchmarking resources for antimicrobial resistance detection using next generation sequencing. (2021) (0)
Regions associated at P<5×10−5 with early-onset BD in meta-analysis. (2014) (0)
1 Overview of Genotyping (0)
Epigenomic and functional dynamics of human bone marrow myeloid differentiation to mature blood neutrophils (2018) (0)
Mex 3 a Marks a Slowly Div iding Subpopulation of Lgr 5 + Intestinal Stem Cells Graphical Abstract Highlights (2017) (0)

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What Schools Are Affiliated With Ivo Glynne Gut?

Ivo Glynne Gut is affiliated with the following schools:

Stony Brook University
ETH Zurich
University of Basel
University of Geneva
Pompeu Fabra University
University of Zurich