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Author Details

Ulrike Kr??ger
Berlin Institute of Health (BIH)
2007
25
20
PMIDPaper TitleJournal TitlePublished Year
35276006Genetic Diagnostics in Routine Osteological Assessment of Adult Low Bone Mass Disorders.J Clin Endocrinol Metab2022
35418979The Host Peritoneal Cavity Harbors Prominent Memory Th2 and Early Recall Responses to an Intestinal Nematode.Front Immunol2022
34490415Increased risk of severe clinical course of COVID-19 in carriers of HLA-C*04:01.EClinicalMedicine2021
32482712Association between Subcutaneous Adipose Tissue Inflammation, Insulin Resistance, and Calorie Restriction in Obese Females.J Immunol2020
31832701Increased presence and differential molecular imprinting of transit amplifying cells in psoriasis.J Mol Med (Berl)2020
31781089Multi-Parameter Analysis of Biobanked Human Bone Marrow Stromal Cells Shows Little Influence for Donor Age and Mild Comorbidities on Phenotypic and Functional Properties.Front Immunol2019
29491455Hematopoietic lineage distribution and evolutionary dynamics of clonal hematopoiesis.Leukemia2018
29499418Diagnostic strategies and genotype-phenotype correlation in a large Indian cohort of osteogenesis imperfecta.Bone2018
29100093De Novo Mutations in SLC25A24 Cause a Craniosynostosis Syndrome with Hypertrichosis, Progeroid Appearance, and Mitochondrial Dysfunction.Am J Hum Genet2017
26320891Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa.Am J Hum Genet2015
24129430Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome.Eur J Hum Genet2014
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
23561847PGAP2 mutations, affecting the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation syndrome.Am J Hum Genet2013
23733340A case of paroxysmal nocturnal hemoglobinuria caused by a germline mutation and a somatic mutation in PIGT.Blood2013
22127862The allele distribution in next-generation sequencing data sets is accurately described as the result of a stochastic branching process.Nucleic Acids Res2012
22683086Mutations in PIGO, a member of the GPI-anchor-synthesis pathway, cause hyperphosphatasia with mental retardation.Am J Hum Genet2012
22169203Autophagic degradation of tau in primary neurons and its enhancement by trehalose.Neurobiol Aging2012
20023429Synergy and antagonism of macroautophagy and chaperone-mediated autophagy in a cell model of pathological tau aggregation.Autophagy2010
20173337Generation of tau aggregates and clearance by autophagy in an inducible cell model of tauopathy.Neurodegener Dis2010
19654187Tau fragmentation, aggregation and clearance: the dual role of lysosomal processing.Hum Mol Genet2009
18515483Evaluation of major types of Shiga toxin 2E-producing Escherichia coli bacteria present in food, pigs, and the environment as potential pathogens for humans.Appl Environ Microbiol2008
17449692DNA microarray-based identification of serogroups and virulence gene patterns of Escherichia coli isolates associated with porcine postweaning diarrhea and edema disease.Appl Environ Microbiol2007
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Collaborators

The Barcelona Institute of Science and Technology
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Max Planck Institute for Molecular Genetics
Co-authored papers 11
Institute for Genomic Statistics and Bioinformatics, University of Bonn
Co-authored papers 10
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 10
Institute of Medical and Human Genetics, Charite - Universitatsmedizin Berlin
Co-authored papers 6
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Co-authored papers 6
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Co-authored papers 5
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Co-authored papers 4
Berlin Institute of Health at Charite - Universitatsmedizin Berlin
Co-authored papers 4
Charite Universitatsmedizin Berlin
Co-authored papers 3
Charite Universitaetsmedizin Berlin
Co-authored papers 2
Albert Einstein College of Medicine
Co-authored papers 2
Albert Einstein College of Medicine
Co-authored papers 2
American Medical Informatics Association, Oregon Health and Science University, Oregon State University, University of Colorado Anschutz Medical Campus, University of North Carolina at Chapel Hill, University of Wisconsin-Madison
Co-authored papers 1
MassGeneral Hospital for Children
Co-authored papers 1
Berlin Institute of Health of Health at Charite - Universitatsmedizin Berlin
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Vanderbilt University Medical Center
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Institut fur Klinische Genetik, Technische Universitat Dresden
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Division of Emergency Medicine University of Calgary Calgary Alberta Canada.
Co-authored papers 1
NIHR Biomedical Research Centre, University of Oxford
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Lawrence Berkeley National Laboratory
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University of California San Francisco
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Cell Therapy Institute, Paracelsus Medical University (PMU)
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Max Planck Institute for Molecular Genetics
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College of Medicine and Health Sciences, United Arab Emirates University
Co-authored papers 1
Kyoto University
Co-authored papers 1