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Neuronal Nitric Oxide Synthase (nNOS, NOS1) rs693534 and rs7977109 Variants and Risk for Migraine

Headache, 2015-10, Vol.55 (9), p.1209-1217

2015

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Variability in histamine receptor genes HRH1, HRH2 and HRH4 in patients with hypersensitivity to NSAIDs

Pharmacogenomics, 2013-11, Vol.14 (15), p.1871-1878

2013

Volltextzugriff (PDF)

Mitochondrial superoxide dismutase and glutathione peroxidase in idiosyncratic drug‐induced liver injury

Hepatology (Baltimore, Md.), 2010-07, Vol.52 (1), p.303-312

2010

Volltextzugriff (PDF)

High frequency of mutations related to impaired CYP2C9 metabolism in a Caucasian population

European journal of clinical pharmacology, 2001-04, Vol.57 (1), p.47-49

2001

Volltextzugriff (PDF)

Loss-of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome

American journal of human genetics, 2010-06, Vol.86 (6), p.957-962

2010

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The differential effect of NAT2 variant alleles permits refinement in phenotype inference and identifies a very slow acetylation genotype

PloS one, 2012-09, Vol.7 (9), p.e44629-e44629

2012

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Gender and functional CYP2C and NAT2 polymorphisms determine the metabolic profile of metamizole

Biochemical pharmacology, 2014-12, Vol.92 (3), p.457-466

2014

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Drug metabolism and hypersensitivity reactions to drugs

Current opinion in allergy and clinical immunology, 2015-08, Vol.15 (4), p.277-284

2015

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LINGO1 and risk for essential tremor: Results of a meta-analysis of rs9652490 and rs11856808

Journal of the neurological sciences, 2012-06, Vol.317 (1), p.52-57

2012

Volltextzugriff (PDF)

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

Journal of Neural Transmission, 2017-03, Vol.124 (3), p.285-291

2017

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Influence of age and gender in motor performance in healthy subjects

Journal of the neurological sciences, 2011-03, Vol.302 (1), p.72-80

2011

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CYP2W1 variant alleles in Caucasians and association of the CYP2W1 G541A (Ala181Thr) polymorphism with increased colorectal cancer risk

Pharmacogenomics, 2010-07, Vol.11 (7), p.919-925

2010

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Delta‐amino‐levulinic acid dehydratase gene and essential tremor

European journal of clinical investigation, 2017-05, Vol.47 (5), p.348-356

2017

Volltextzugriff (PDF)

Pharmacogenomics of cyclooxygenases

Pharmacogenomics, 2015-04, Vol.16 (5), p.501-522

2015

Volltextzugriff (PDF)

NAT2 polymorphisms and risk for Parkinson's disease: a systematic review and meta-analysis

Expert opinion on drug metabolism & toxicology, 2016-08, Vol.12 (8), p.937-946

2016

Volltextzugriff (PDF)

Clinical pharmacogenomic testing of KRAS, BRAF and EGFR mutations by high resolution melting analysis and ultra-deep pyrosequencing

BMC cancer, 2011-09, Vol.11 (1), p.406-406

2011

Volltextzugriff (PDF)

The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

Cellular & molecular immunology, 2015-11, Vol.12 (6), p.777-779

2015

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Interethnic and intraethnic variability of CYP2C8 and CYP2C9 polymorphisms in healthy individuals

Molecular diagnosis & therapy, 2006, Vol.10 (1), p.29-40

2006

Volltextzugriff (PDF)

SLC1A2 rs3794087 variant and risk for migraine

Journal of the neurological sciences, 2014-03, Vol.338 (1), p.92-95

2014

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Genetic variability of histamine receptors in patients with Parkinson's disease

BMC medical genetics, 2008-03, Vol.9 (1), p.15-15, Article 15

2008

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Diamine Oxidasers10156191 and rs2052129 Variants Are Associated With the Risk for Migraine

Headache, 2015-02, Vol.55 (2), p.276-286

2015

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Alcohol Dehydrogenase 2 Genotype and Risk for Migraine

Headache, 2010-01, Vol.50 (1), p.85-91

2010

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MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome

Journal of Neural Transmission, 2013-03, Vol.120 (3), p.463-467

2013

Volltextzugriff (PDF)

Genetic variability in CYP3A4 and CYP3A5 in primary liver, gastric and colorectal cancer patients

BMC cancer, 2007-07, Vol.7 (1), p.118-118

2007

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Neuronal Nitric Oxide Synthase (nNOS, NOS1) rs693534 and rs7977109 Variants and Risk for Migraine

Variability in histamine receptor genes HRH1, HRH2 and HRH4 in patients with hypersensitivity to NSAIDs

Mitochondrial superoxide dismutase and glutathione peroxidase in idiosyncratic drug‐induced liver injury

High frequency of mutations related to impaired CYP2C9 metabolism in a Caucasian population

Loss-of-Function Mutations in HPSE2 Cause the Autosomal Recessive Urofacial Syndrome

The differential effect of NAT2 variant alleles permits refinement in phenotype inference and identifies a very slow acetylation genotype

Exome-wide rare variant analysis in familial essential tremor

Gender and functional CYP2C and NAT2 polymorphisms determine the metabolic profile of metamizole

Drug metabolism and hypersensitivity reactions to drugs

LINGO1 and risk for essential tremor: Results of a meta-analysis of rs9652490 and rs11856808

Thr105Ile (rs11558538) polymorphism in the histamine-1-methyl-transferase (HNMT) gene and risk for restless legs syndrome

Influence of age and gender in motor performance in healthy subjects

CYP2W1 variant alleles in Caucasians and association of the CYP2W1 G541A (Ala181Thr) polymorphism with increased colorectal cancer risk

Delta‐amino‐levulinic acid dehydratase gene and essential tremor

Pharmacogenomics of cyclooxygenases

NAT2 polymorphisms and risk for Parkinson's disease: a systematic review and meta-analysis

Clinical pharmacogenomic testing of KRAS, BRAF and EGFR mutations by high resolution melting analysis and ultra-deep pyrosequencing

The GSTP1 gene variant rs1695 is not associated with an increased risk of multiple sclerosis

Interethnic and intraethnic variability of CYP2C8 and CYP2C9 polymorphisms in healthy individuals

SLC1A2 rs3794087 variant and risk for migraine

Genetic variability of histamine receptors in patients with Parkinson's disease

Diamine Oxidasers10156191 and rs2052129 Variants Are Associated With the Risk for Migraine

Alcohol Dehydrogenase 2 Genotype and Risk for Migraine

MAPT1 gene rs1052553 variant is unrelated with the risk for restless legs syndrome

Genetic variability in CYP3A4 and CYP3A5 in primary liver, gastric and colorectal cancer patients

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