Inke R König


Ontology type: schema:Person     


Person Info

NAME

Inke R

SURNAME

König

Publications in SciGraph latest 50 shown

  • 2019-02 Can we predict cognitive decline after initial diagnosis of multiple sclerosis? Results from the German National early MS cohort (KKNMS) in JOURNAL OF NEUROLOGY
  • 2018-12 Evaluating the current state of Mendelian randomization studies: a protocol for a systematic review on methodological and clinical aspects using neurodegenerative disorders as outcome in SYSTEMATIC REVIEWS
  • 2018-12 Evaluation of body position in upper airway stimulation for obstructive sleep apnea—is continuous voltage sufficient enough? in SLEEP AND BREATHING
  • 2018-12 The all age asthma cohort (ALLIANCE) - from early beginnings to chronic disease: a longitudinal cohort study in BMC PULMONARY MEDICINE
  • 2018-12 Correction to: The all age asthma cohort (ALLIANCE) - from early beginnings to chronic disease: a longitudinal cohort study in BMC PULMONARY MEDICINE
  • 2017-02 Rückenlage- und REM-Bezug bei obstruktiver Schlafapnoe. Kritische Modellbetrachtungen in HNO
  • 2017-01 Supine position and REM dependence in obstructive sleep apnea in HNO
  • 2016-12 Machine learning and data mining in complex genomic data—a review on the lessons learned in Genetic Analysis Workshop 19 in BMC GENETICS
  • 2016-12 No Association of Coronary Artery Disease with X-Chromosomal Variants in Comprehensive International Meta-Analysis in SCIENTIFIC REPORTS
  • 2016-12 Do little interactions get lost in dark random forests? in BMC BIOINFORMATICS
  • 2016-12 Male-specific association between MT-ND4 11719 A/G polymorphism and ulcerative colitis: a mitochondria-wide genetic association study in BMC GASTROENTEROLOGY
  • 2016-10 Identification of interactions using model-based multifactor dimensionality reduction in BMC PROCEEDINGS
  • 2016-10 Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals in BMC PROCEEDINGS
  • 2016-01-21 Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function in NATURE COMMUNICATIONS
  • 2015-12 Patient selection for upper airway stimulation: is concentric collapse in sleep endoscopy predictable? in SLEEP AND BREATHING
  • 2015-10 A comprehensive 1000 Genomes–based genome-wide association meta-analysis of coronary artery disease in NATURE GENETICS
  • 2015-10 Genetic variants associated with celiac disease and the risk for coronary artery disease in MOLECULAR GENETICS AND GENOMICS
  • 2015-03 Is there a male-specific effect on hypertension? in HUMAN GENETICS
  • 2014-06 Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees in BMC PROCEEDINGS
  • 2014-06 A comparison of two collapsing methods in different approaches in BMC PROCEEDINGS
  • 2013-12 A unifying framework for robust association testing, estimation, and genetic model selection using the generalized linear model in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2013-07 Pregnancy risk factors for very premature delivery: what role do hypertension, obesity and diabetes play? in ARCHIVES OF GYNECOLOGY AND OBSTETRICS
  • 2013-06 Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis in NATURE GENETICS
  • 2013-05 Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture in NATURE GENETICS
  • 2013-01 Large-scale association analysis identifies new risk loci for coronary artery disease in NATURE GENETICS
  • 2012-10 Risk estimation and risk prediction using machine-learning methods in HUMAN GENETICS
  • 2012-07 No association of vitamin D metabolism-related polymorphisms and melanoma risk as well as melanoma prognosis: a case–control study in ARCHIVES OF DERMATOLOGICAL RESEARCH
  • 2011-12 Identifying rare variants from exome scans: the GAW17 experience in BMC PROCEEDINGS
  • 2011-12 Comparison of collapsing methods for the statistical analysis of rare variants in BMC PROCEEDINGS
  • 2011-10 Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure in NATURE GENETICS
  • 2011-04 Risk for antipsychotic-induced extrapyramidal symptoms: influence of family history and genetic susceptibility in PSYCHOPHARMACOLOGY
  • 2011-04 Basal ganglia hyperechogenicity does not distinguish between patients with primary dystonia and healthy individuals in JOURNAL OF NEUROLOGY
  • 2011-03-06 Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease in NATURE GENETICS
  • 2010-11 Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index in NATURE GENETICS
  • 2010-10 Hundreds of variants clustered in genomic loci and biological pathways affect human height in NATURE
  • 2010-08 Biological, clinical and population relevance of 95 loci for blood lipids in NATURE
  • 2009-12 Evaluation of single-nucleotide polymorphism imputation using random forests in BMC PROCEEDINGS
  • 2009-12 ACPA: automated cluster plot analysis of genotype data in BMC PROCEEDINGS
  • 2009-12 Look who is calling: a comparison of genotype calling algorithms in BMC PROCEEDINGS
  • 2009-11 A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium in NATURE GENETICS
  • 2009-09 Distal and proximal interleukin (IL)-10 promoter polymorphisms associated with risk of cutaneous melanoma development: a case–control study in GENES & IMMUNITY
  • 2009-09 Assessment of transmission distortion on chromosome 6p in healthy individuals using tagSNPs in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-07 Analysis of a functional serotonin transporter promoter polymorphism in psoriasis vulgaris in ARCHIVES OF DERMATOLOGICAL RESEARCH
  • 2009-03 Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease in NATURE GENETICS
  • 2009-03 Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants in NATURE GENETICS
  • 2009-03 New susceptibility locus for coronary artery disease on chromosome 3q22.3 in NATURE GENETICS
  • 2009-03 Predicting recovery after intracerebral hemorrhage – An external validation in patients from controlled clinical trials in JOURNAL OF NEUROLOGY
  • 2009-01 MDR1 variants and risk of Parkinson disease in JOURNAL OF NEUROLOGY
  • 2008-11 Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample in JOURNAL OF NEURAL TRANSMISSION
  • 2008-10 Lack of association of genetic variants in the LRP8 gene with familial and sporadic myocardial infarction in JOURNAL OF MOLECULAR MEDICINE
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