J. Högel

发表

Relative risks of age, gender, nationality, smoking, and Helicobacter-pylori-infection in duodenal and gastric ulcer and interactions.

J. Högel, E. Schmid, G. Allmendinger, 1995, Zeitschrift für Gastroenterologie - German Journal of Gastroenterology.

Accelerated aging phenotype in mice with conditional deficiency for mitochondrial superoxide dismutase in the connective tissue

J. Chung, P. Maity, L. Claes, 2011, Aging cell.

Characterization of the genotoxic potential of formaldehyde in V79 cells.

J. Högel, G. Speit, P. Schütz, 2007, Mutagenesis.

The effect of smoking on DNA effects in the comet assay: a meta-analysis.

J. Högel, G. Speit, H. Hoffmann, 2005, Mutagenesis.

Clinicopathologic correlations of genomic gains and losses in follicular lymphoma.

R. Siebert, G. Ott, H. Döhner, 2002, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

Glimepiride treatment and IGF-I in adolescents with type 1 diabetes: a prospective, randomized, double-blind, placebo-controlled study.

J. Högel, P. Mullis, S. Wudy, 2003, Diabetes care.

Cardiac changes in fetuses secondary to immune hemolytic anemia and their relation to hemoglobin and catecholamine concentrations in fetal blood

J. Högel, R. Oberhoffer, D. Grab, 1999, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Hydrolysed protein accelerates the gastrointestinal transport of formula in preterm infants

F. Pohlandt, W. Mihatsch, J. Högel, 2001, Acta paediatrica.

Frequency of congenital dyserythropoietic anemias in Europe

K. Schwarz, H. Heimpel, S. Perrotta, 2010, European journal of haematology.

Evaluation of three risk scores to predict postoperative nausea and vomiting

A. Staack, M. Georgieff, J. Högel, 2000, Acta anaesthesiologica Scandinavica.

Immunohistochemical analysis of sex hormone receptors in squamous changes of the urothelium.

B. Wullich, M. Eckstein, R. Rieker, 2022, International journal of clinical and experimental pathology.

Reproducibility of measurements with a new slit lamp-mounted ocular blood flow tonograph

G. Lang, J. Högel, G. Lang, 1998, Graefe's Archive for Clinical and Experimental Ophthalmology.

Consumption of Imipenem Correlates with β-Lactam Resistance in Pseudomonas aeruginosa

J. Högel, P. Lepper, M. Trautmann, 2002, Antimicrobial Agents and Chemotherapy.

Influence of age, comorbidity, type of operation and other variables on lethality and duration of post-operative hospital stay in patients with peptic ulcer

J. Högel, R. Rieker, R. Eiselé, 2004, Langenbecks Archiv für Chirurgie.

High-dose cytosine arabinoside and daunorubicin postremission therapy in adults with de novo acute myeloid leukemia

H. Heimpel, J. Högel, W. Gaus, 1995, Annals of Hematology.

Cardiac and extracardiac complications in infants of diabetic mothers and their relation to parameters of carbohydrate metabolism

J. Högel, R. Oberhoffer, E. Kohne, 1997, European Journal of Pediatrics.

De novo FUS mutations are the most frequent genetic cause in early-onset German ALS patients

A. Ludolph, J. Högel, P. Nürnberg, 2015, Neurobiology of Aging.

Do Orofacial Clefts Represent Different Genetic Entities?

C. Maier, W. Vogel, S. Brosch, 2015, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

Comparison of conditional power criteria for early termination of clinical trials

Josef Högel, Martina Kron, M. Kron, 2004, Comput. Stat. Data Anal..

A Shift Algorithm for Exact Computation in Sequential Tests with Binary Outcome

J. Högel, J. Högel, 2000 .

Mutations in SPRTN cause early onset hepatocellular carcinoma, genomic instability and progeroid features

Peter Nürnberg, Ivan Dikic, Melanie Bahlo, 2014, Nature Genetics.

Extended runs of homozygosity at 17q11.2: an association with type‐2 NF1 deletions?

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2010, Human mutation.

Bioavailability of β-cryptoxanthin is greater from pasteurized orange juice than from fresh oranges - a randomized cross-over study.

R. Carle, J. Högel, N. Breusing, 2015, Molecular nutrition & food research.

Effect of aggregation form on bioavailability of zeaxanthin in humans: a randomised cross-over study

R. Carle, A. Bosy-Westphal, J. Hempel, 2017, British Journal of Nutrition.

Urinary excretion of Citrus flavanones and their major catabolites after consumption of fresh oranges and pasteurized orange juice: A randomized cross-over study.

R. Carle, J. Högel, A. Bosy-Westphal, 2016, Molecular nutrition & food research.

Carotenoids are more bioavailable from papaya than from tomato and carrot in humans: a randomised cross-over study

R. Carle, J. Högel, Patricia Esquivel, 2013, British Journal of Nutrition.

Lymphocytes of Type 2 Diabetic Women Carry a High Load of Stable Chromosomal Aberrations

W. März, B. Boehm, W. Renner, 2008, Diabetes.

Quantifying telomere lengths of human individual chromosome arms by centromere-calibrated fluorescence in situ hybridization and digital imaging.

S. Perner, K. Nielsen, J. Högel, 2003, The American journal of pathology.

Randomized comparison of high-frequency ventilation with high-rate intermittent positive pressure ventilation in preterm infants with respiratory failure.

G. Lipowsky, J. Högel, O. Genzel‐Boroviczény, 1999, The Journal of pediatrics.

Sustained pressure—controlled inflation or intermittent mandatory ventilation in preterm infants in the delivery room? A randomized, controlled trial on initial respiratory support via nasopharyngeal tube

J. Högel, W. Lindner, F. Pohlandt, 2005, Acta paediatrica.

Polymerase chain reaction and Southern blot-based analysis of the C9orf72 hexanucleotide repeat in different motor neuron diseases

A. Ludolph, J. Högel, J. Dorst, 2014, Neurobiology of Aging.

Guidelines for the intramuscular positioning of EMG electrodes in the semispinalis capitis and cervicis muscles.

L Kinzl, L. Kinzl, M. Kramer, 2003, Journal of electromyography and kinesiology : official journal of the International Society of Electrophysiological Kinesiology.

T‐cell prolymphocytic leukemia is associated with deregulation of oncogenic microRNAs on transcriptional and epigenetic level

S. Bens, R. Siebert, E. Campo, 2022, Genes, chromosomes & cancer.

Long-term Follow Up of a Prospective Multicenter Trial with a High-Dose Cytosine Arabinoside and Daunorubicin Postremission Therapy in Adults with De Novo Acute Myeloid Leukemia

H. Heimpel, J. Högel, W. Gaus, 1997 .

The (−765 G→C) promoter variant of the COX-2/PTGS2 gene is associated with a lower risk for end-stage hip and knee osteoarthritis

H. Brenner, R. Brenner, E. Schneider, 2010, Annals of the rheumatic diseases.

Balanced designs for multiple crossover studies.

W. Gaus, J. Högel, 1992, Arzneimittel-Forschung.

SVA retrotransposon insertion-associated deletion represents a novel mutational mechanism underlying large genomic copy number changes with non-recurrent breakpoints

D. Cooper, C. Lázaro, J. Högel, 2014, Genome Biology.

Immune phenotypes predict survival in patients with glioblastoma multiforme

C. Wirtz, M. Georgieff, J. Högel, 2016, Journal of Hematology & Oncology.

Population-specific differences in gene conversion patterns between human SUZ12 and SUZ12P are indicative of the dynamic nature of interparalog gene conversion

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2014, Human Genetics.

Dysfunction of the MDM2/p53 axis is linked to premature aging.

C. Prives, J. Högel, David R. Tong, 2017, The Journal of clinical investigation.

Genetic and environmental risk factors for submucous cleft palate.

C. Maier, W. Vogel, G. Assum, 2012, European journal of oral sciences.

Right ventricle dimensions and function in response to acute hypoxia in healthy human subjects

K. Strohl, J. Högel, R. Schilz, 2017, Acta physiologica.

Gene synteny comparisons between different vertebrates provide new insights into breakage and fusion events during mammalian karyotype evolution

D. Cooper, C. Kemkemer, M. Kohn, 2009, BMC Evolutionary Biology.

Identification of recurrent type‐2 NF1 microdeletions reveals a mitotic nonallelic homologous recombination hotspot underlying a human genomic disorder

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2012, Human mutation.

Characterization of the nonallelic homologous recombination hotspot PRS3 associated with type‐3 NF1 deletions

Antje M Zickler, H. Kestler, D. Cooper, 2012, Human mutation.

Intrachromosomal mitotic nonallelic homologous recombination is the major molecular mechanism underlying type‐2 NF1 deletions

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2010, Human mutation.

Investigations of potential susceptibility toward formaldehyde-induced genotoxicity

G. Speit, J. Zeller, Regina Linsenmeyer, 2012, Archives of Toxicology.

Genetic polymorphisms and the effect of cigarette smoking in the comet assay.

J. Högel, G. Speit, H. Hoffmann, 2005, Mutagenesis.

Further investigations on the modified comet assay for measuring aphidicolin-block nucleotide excision repair.

J. Högel, G. Speit, Christine Leibiger, 2013, Mutagenesis.

Genotypes of amyotrophic lateral sclerosis in Mongolia

P. Andersen, A. Ludolph, A. Rosenbohm, 2019, Journal of Neurology, Neurosurgery, and Psychiatry.

C-reactive protein is a useful marker for guiding duration of antibiotic therapy in suspected neonatal bacterial infection.

S. Ehl, J. Högel, P. Bartmann, 1997, Pediatrics.

Analysis of a cohort of 101 CDAII patients: description of 24 new molecular variants and genotype‐phenotype correlations

K. Schwarz, H. Heimpel, A. Zanella, 2016, British journal of haematology.

The morphological diagnosis of congenital dyserythropoietic anemia: results of a quantitative analysis of peripheral blood and bone marrow cells

K. Schwarz, H. Heimpel, J. Högel, 2010, Haematologica.

Reconstruction of a 450-My-old ancestral vertebrate protokaryotype.

J. Graves, W. Vogel, M. Kohn, 2006, Trends in genetics : TIG.

The impact of comorbidity on the overall survival and the cause of death in patients after colorectal cancer resection

J. Högel, E. Hammer, R. Rieker, 2002, Langenbeck’s Archives of Surgery.

Normobaric Intermittent Hypoxia over 8 Months Does Not Reduce Body Weight and Metabolic Risk Factors – a Randomized, Single Blind, Placebo-Controlled Study in Normobaric Hypoxia and Normobaric Sham Hypoxia

K. Strohl, M. Burtscher, M. Faulhaber, 2015, Obesity Facts.

Genetic variants in PSEN2 and correlation to CSF β-amyloid42 levels in AD

L. Bertram, J. Stingl, A. Ludolph, 2012, Neurobiology of Aging.

Insulin Resistance (HOMA) in Relation to Plasma Cortisol, IGF-I and IGFBP-3

M. Wabitsch, J. Högel, S. Wudy, 2002, Hormone Research in Paediatrics.

Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequences

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2018, Human Genetics.

Clinical characterisation of 29 neurofibromatosis type-1 patients with molecularly ascertained 1.4 Mb type-1 NF1 deletions

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2010, Journal of Medical Genetics.

Hydrolyzed protein accelerates feeding advancement in very low birth weight infants.

J. Högel, W. Mihatsch, F. Pohlandt, 2002, Pediatrics.

POLD1 Germline Mutations in Patients Initially Diagnosed with Werner Syndrome

J. Baldwin, W. Brown, J. Högel, 2015, Human mutation.

Accuracy Evaluation of Four Blood Glucose Monitoring Systems in Unaltered Blood Samples in the Low Glycemic Range and Blood Samples in the Concentration Range Defined by ISO 15197.

G. Freckmann, A. Baumstark, Manuela Link, 2015, Diabetes technology & therapeutics.

Reconstruction of the ancestral ferungulate karyotype by electronic chromosome painting (E-painting)

Horst Hameister, Josef Högel, Hildegard Kehrer-Sawatzki, 2006, Chromosome Research.

Different rates of telomere attrition in peripheral lymphocytes in a pair of dizygotic twins with hematopoietic chimerism

P. Möller, J. Högel, P. Wiegand, 2008, Aging cell.

Correlation of positive RT-PCR for tyrosinase in peripheral blood of malignant melanoma patients with clinical stage, survival and other risk factors

J. Högel, U. Keilholz, C. Voit, 1999, British Journal of Cancer.

A post GWAS association study of SNPs associated with cleft lip with or without cleft palate in submucous cleft palate

J. Högel, S. Brosch, C. Kubisch, 2015, American journal of medical genetics. Part A.

Tissue‐specific differences in the proportion of mosaic large NF1 deletions are suggestive of a selective growth advantage of hematopoietic del(+/−) stem cells

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2012, Human mutation.

Decreased accuracy of pulse oximetry measurements during low perfusion caused by sepsis: is the perfusion index of any value?

Josef Högel, H. Hummler, J. Högel, 2006, Intensive Care Medicine.

Consideration of the haplotype diversity at nonallelic homologous recombination hotspots improves the precision of rearrangement breakpoint identification

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2017, Human mutation.

The procedure of new drug application and the philosophy of critical rationalism or the limits of quality assurance with good clinical practice.

W. Gaus, J. Högel, 1999, Controlled clinical trials.

Evaluation of Meal Carbohydrate Counting Errors in Patients with Type 1 Diabetes.

G. Freckmann, Sina Buck, D. Waldenmaier, 2021, Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association.

Re-evaluation of a reported increased micronucleus frequency in lymphocytes of workers occupationally exposed to formaldehyde.

G. Speit, C. Ladeira, Regina Linsenmeyer, 2012, Mutation research.

Aberrant Single Exon Skipping is not Altered by Age in Exons of NF1, RABAC1, AATF or PCGF2 in Human Blood Cells and Fibroblasts

J. Högel, K. Mellert, Michael Uhl, 2011, Genes.

Lipids and amyotrophic lateral sclerosis: A two‐sample Mendelian randomization study

J. Dorst, Linjing Zhang, Kailin Xia, 2023, European journal of neurology.

Hemoglobin A1c and body mass index in children and adolescents with IDDM. An observational study from 1976-1995.

W. Gaus, S. Wudy, M. Grabert, 2000, Experimental and clinical endocrinology & diabetes.

Non-coding RNA ANRIL and the number of plexiform neurofibromas in patients with NF1 microdeletions

D. Cooper, J. Högel, H. Kehrer-Sawatzki, 2012, BMC Medical Genetics.

Population-specific differences in gene conversion patterns between human SUZ12 and SUZ12P are indicative of the dynamic nature of interparalog gene conversion

D. Cooper, H. Kehrer-Sawatzki, K. Bengesser, 2014, Human Genetics.