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Author Details

Jochen Hecht
The Barcelona Institute of Science and Technology
2003
88
37
PMIDPaper TitleJournal TitlePublished Year
36221914Genomic Adaptations to an Endoparasitic Lifestyle in the Morphologically Atypical Crustacean Sacculina carcini (Cirripedia: Rhizocephala).Genome Biol Evol2022
35585074Citizen-science reveals changes in the oral microbiome in Spain through age and lifestyle factors.NPJ Biofilms Microbiomes2022
35670808Alternative splicing of BUD13 determines the severity of a developmental disorder with lipodystrophy and progeroid features.Genet Med2022
35711737Population dynamics and genetic connectivity in recent chimpanzee history.Cell Genom2022
36103953In vitro and in vivo evidence that the switch from calcineurin to mTOR inhibitors may be a strategy for immunosuppression in Epstein-Barr virus-associated post-transplant lymphoproliferative disorder.Kidney Int2022
33175145SARS-CoV-2 Seroprevalence and Antibody Kinetics Among Health Care Workers in a Spanish Hospital After 3 Months of Follow-up.J Infect Dis2021
34452462The Positive Rhinovirus/Enterovirus Detection and SARS-CoV-2 Persistence beyond the Acute Infection Phase: An Intra-Household Surveillance Study.Viruses2021
34104346Citizen-science based study of the oral microbiome in Cystic fibrosis and matched controls reveals major differences in diversity and abundance of bacterial and fungal species.J Oral Microbiol2021
34117224E2F6 initiates stable epigenetic silencing of germline genes during embryonic development.Nat Commun2021
33441425The intratumoral CXCR3 chemokine system is predictive of chemotherapy response in human bladder cancer.Sci Transl Med2021
32641730Seroprevalence of antibodies against SARS-CoV-2 among health care workers in a large Spanish reference hospital.Nat Commun2020
31832701Increased presence and differential molecular imprinting of transit amplifying cells in psoriasis.J Mol Med (Berl)2020
33456723Oral microbiome in down syndrome and its implications on oral health.J Oral Microbiol2020
30642251GOPHER: Generator Of Probes for capture Hi-C Experiments at high Resolution.BMC Genomics2019
31323892Computational Processing and Quality Control of Hi-C, Capture Hi-C and Capture-C Data.Genes (Basel)2019
30842609PAX5 biallelic genomic alterations define a novel subgroup of B-cell precursor acute lymphoblastic leukemia.Leukemia2019
31019503The Role of Pre-existing Cross-Reactive Central Memory CD4 T-Cells in Vaccination With Previously Unseen Influenza Strains.Front Immunol2019
29335546Transcription factors orchestrate dynamic interplay between genome topology and gene regulation during cell reprogramming.Nat Genet2018
30522523Citizen science charts two major "stomatotypes" in the oral microbiome of adolescents and reveals links with habits and drinking water composition.Microbiome2018
29499418Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta.Bone2018
29511024Genome-wide strategies identify downstream target genes of chick connective tissue-associated transcription factors.Development2018
29100093De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.Am J Hum Genet2017
28281571A De Novo Nonsense Mutation in MAGEL2 in a Patient Initially Diagnosed as Opitz-C: Similarities Between Schaaf-Yang and Opitz-C Syndromes.Sci Rep2017
28103242Genome-Wide Binding of Posterior HOXA/D Transcription Factors Reveals Subgrouping and Association with CTCF.PLoS Genet2017
28376765The germline variants in DNA repair genes in pediatric medulloblastoma: a challenge for current therapeutic strategies.BMC Cancer2017
28366934Acute myeloid leukemia in the elderly is characterized by a distinct genetic and epigenetic landscape.Leukemia2017
26799614An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing.Am J Med Genet A2016
26581570A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation.Am J Med Genet A2016
27814676Q-nexus: a comprehensive and efficient analysis pipeline designed for ChIP-nexus.BMC Genomics2016
27689917Generating Aptamers Interacting with Polymeric Surfaces for Biofunctionalization.Macromol Biosci2016
24916641Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome.Eur J Hum Genet2015
26249812Strategies to improve the performance of rare variant association studies by optimizing the selection of controls.Bioinformatics2015
26260076Key features and clinical variability of COG6-CDG.Mol Genet Metab2015
26163319Saturation analysis of ChIP-seq data for reproducible identification of binding peaks.Genome Res2015
26109426Selective cell targeting and lineage tracing of human induced pluripotent stem cells using recombinant avian retroviruses.Cell Mol Life Sci2015
25880334Missense variant in CCDC22 causes X-linked recessive intellectual disability with features of Ritscher-Schinzel/3C syndrome.Eur J Hum Genet2015
25966950Inhibition of histone methyltransferases SUV39H1 and G9a leads to neuroprotection in an in vitro model of cerebral ischemia.J Cereb Blood Flow Metab2015
25987567IMSEQ--a fast and error aware approach to immunogenetic sequence analysis.Bioinformatics2015
25961942PDE3A mutations cause autosomal dominant hypertension with brachydactyly.Nat Genet2015
25959774Disruptions of topological chromatin domains cause pathogenic rewiring of gene-enhancer interactions.Cell2015
25712132Molecular mechanism of CHRDL1-mediated X-linked megalocornea in humans and in Xenopus model.Hum Mol Genet2015
25595890Mutational spectrum of adult T-ALL.Oncotarget2015
25293717Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient.Eur J Hum Genet2015
23842424PAX5 overexpression is not enough to reestablish the mature B-cell phenotype in classical Hodgkin lymphoma.Leukemia2014
25480037Homozygous and compound-heterozygous mutations in TGDS cause Catel-Manzke syndrome.Am J Hum Genet2014
25534655European sea bass genome and its variation provide insights into adaptation to euryhalinity and speciation.Nat Commun2014
25333064Screening for single nucleotide variants, small indels and exon deletions with a next-generation sequencing based gene panel approach for Usher syndrome.Mol Genet Genomic Med2014
25331754First description of a patient with Vici syndrome due to a mutation affecting the penultimate exon of EPG5 and review of the literature.Am J Med Genet A2014
25186178Effective diagnosis of genetic disease by computational phenotype analysis of the disease-associated genome.Sci Transl Med2014
24439110Mutations in PGAP3 impair GPI-anchor maturation, causing a subtype of hyperphosphatasia with mental retardation.Am J Hum Genet2014
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Collaborators

Stefan Mundlos
Max Planck Institute for Molecular Genetics
Co-authored papers 42
Peter N Robinson
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 32
Peter M Krawitz
Institute for Genomic Statistics and Bioinformatics, University of Bonn
Co-authored papers 31
Uwe Kornak
Institute of Human Genetics, University Medical Center Gottingen
Co-authored papers 13
Denise Horn
Institute of Medical and Human Genetics, Charite - Universitatsmedizin Berlin
Co-authored papers 12
Ulrike Kr??ger
Berlin Institute of Health (BIH)
Co-authored papers 11
Peter Hansen
Institute of Medical Genetics and Human Genetics, Charite-Universitatsmedizin Berlin
Co-authored papers 8
Bj??rn Fischer-Zirnsak
Max Planck Institute for Molecular Genetics FG Development and Disease
Co-authored papers 8
Malte Spielmann
Max Planck Institute for Molecular Genetics
Co-authored papers 7
Marten J??ger
Charite Universitatsmedizin Berlin
Co-authored papers 6
Eva Klopocki
Institute for Human Genetics, University of Wurzburg
Co-authored papers 6
Sebastian Bauer
Institute for Medical Genetics and Human Genetics, Charite-Universitatsmedizin Berlin
Co-authored papers 5
Nadja Ehmke
Berlin Institute of Health at Charite - Universitatsmedizin Berlin
Co-authored papers 5
Tomasz Zemojtel
Berlin Institute of Health (BIH)
Co-authored papers 5
Toni Gabald??n
Catalan Institution for Research and Advanced Studies
Co-authored papers 4
Sandra C Doelken
Institute for Medical Genetics and Human Genetics, Charite Universitatsmedizin Berlin
Co-authored papers 4
Albert J Poustka
Max-Planck-Institut fur Molekulare Genetik
Co-authored papers 3
Michal R Schweiger
Institute for Translational Epigenetics, University of Cologne
Co-authored papers 3
Luitgard Graul-Neumann
Charite Universitaetsmedizin Berlin
Co-authored papers 3
Luisa Mackenroth
Institut fur Klinische Genetik, Technische Universitat Dresden
Co-authored papers 2
Tony Roscioli
Prince of Wales Hospital
Co-authored papers 2
Jonas Ibn-Salem
Max-Planck Institute for Molecular Genetics, Johannes Gutenberg University of Mainz
Co-authored papers 2
Sebastian K??hler
Division of Emergency Medicine University of Calgary Calgary Alberta Canada.
Co-authored papers 2
Andreas Vilcinskas
Fraunhofer Institute for Molecular Biology and Applied Ecology
Co-authored papers 2
Georgia Panopoulou
Max-Planck Institut fur Molekulare Genetik
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H??lya Kayserili
Istanbul University
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Christoph R??llig
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Rainer Spang
University of Regensburg
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John A Phillips
Vanderbilt University Medical Center
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Release 1.2