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UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls

The pharmacogenomics journal, 2008-02, Vol.8 (1), p.34-41

2008

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Long-term olive oil-based parenteral nutrition sustains innate immune function in home patients without active underlying disease

Clinical nutrition (Edinburgh, Scotland), 2013-08, Vol.32 (4), p.643-649

2013

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Nav1.7-related small fiber neuropathy: impaired slow-inactivation and DRG neuron hyperexcitability

Neurology, 2012-05, Vol.78 (21), p.1635

2012

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Hepatic cyst penetration of cefazolin in patients receiving aspiration sclerotherapy

Journal of antimicrobial chemotherapy, 2016-09, Vol.71 (9), p.2547-2552

2016

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Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia

British journal of dermatology (1951), 2005-07, Vol.153 (1), p.174-177

2005

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Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis

Netherlands journal of medicine, 2011-07, Vol.69 (7-8), p.330-334

2011

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Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis

British journal of surgery, 2008-04, Vol.95 (4), p.499-505

2008

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Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63

Clinical genetics, 2010-07, Vol.78 (1), p.47-56

2010

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Prevalence of hepatitis C in the general population in the Netherlands

Netherlands journal of medicine, 2008, Vol.66 (1), p.13-17

2008

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Genetic polymorphisms in UDP-glucuronosyltransferases and glutathione S-transferases and colorectal cancer risk

Carcinogenesis (New York), 2004-12, Vol.25 (12), p.2407-2415

2004

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Genetic polymorphism in UDP-glucuronosyltransferase 2B7 and colorectal cancer risk

Oncology research, 2009, Vol.17 (7), p.323

2009

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Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases

Journal of medical genetics, 2005-10, Vol.42 (10), p.e62-e62

2005

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No genetic association between EPHX1 and Crohn’s disease

Gut, 2005-11, Vol.54 (11), p.1659-1660

2005

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Haptoglobin and its association with the HELLP syndrome

Journal of medical genetics, 2003-03, Vol.40 (3), p.214-216

2003

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Short mucin 6 alleles are associated with H pylori infection

World journal of gastroenterology : WJG, 2006-10, Vol.12 (37), p.6021

2006

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From gene to disease; primary erythermalgia--a neuropathic disease as a consequence of mutations in a sodium pump gene

Nederlands tijdschrift voor geneeskunde, 2006-01, Vol.150 (4), p.194

2006

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From gene to disease; hepatocystin and autosomal dominant polycystic liver disease

Nederlands tijdschrift voor geneeskunde, 2003-07, Vol.147 (29), p.1408

2003

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Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis

Proceedings of the National Academy of Sciences - PNAS, 2014-04, Vol.111 (14), p.5343-5348

2014

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Novel GANAB variants associated with polycystic liver disease

Orphanet journal of rare diseases, 2020-10, Vol.15 (1), p.302-302, Article 302

2020

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SCN9A Mutations Define Primary Erythermalgia as a Neuropathic Disorder of Voltage Gated Sodium Channels

Journal of investigative dermatology, 2005-06, Vol.124 (6), p.1333-1338

2005

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Paroxysmal extreme pain disorder: a molecular lesion of peripheral neurons

Nature reviews. Neurology, 2011-01, Vol.7 (1), p.51

2011

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LRP5 variants may contribute to ADPKD

European journal of human genetics : EJHG, 2016-02, Vol.24 (2), p.237-242

2016

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Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease

Nature genetics, 2003-03, Vol.33 (3), p.345-347

2003

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Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes

European journal of human genetics : EJHG, 2016-12, Vol.24 (12), p.1707-1714

2016

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UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls

Long-term olive oil-based parenteral nutrition sustains innate immune function in home patients without active underlying disease

Nav1.7-related small fiber neuropathy: impaired slow-inactivation and DRG neuron hyperexcitability

Hepatic cyst penetration of cefazolin in patients receiving aspiration sclerotherapy

Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia

Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis

Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis

Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63

Prevalence of hepatitis C in the general population in the Netherlands

Genetic polymorphisms in UDP-glucuronosyltransferases and glutathione S-transferases and colorectal cancer risk

Genetic polymorphism in UDP-glucuronosyltransferase 2B7 and colorectal cancer risk

Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases

No genetic association between EPHX1 and Crohn’s disease

Haptoglobin and its association with the HELLP syndrome

Short mucin 6 alleles are associated with H pylori infection

From gene to disease; primary erythermalgia--a neuropathic disease as a consequence of mutations in a sodium pump gene

From gene to disease; hepatocystin and autosomal dominant polycystic liver disease

Whole-exome sequencing reveals LRP5 mutations and canonical Wnt signaling associated with hepatic cystogenesis

Novel GANAB variants associated with polycystic liver disease

Chymotrypsin C (CTRC) variants that diminish activity or secretion are associated with chronic pancreatitis

SCN9A Mutations Define Primary Erythermalgia as a Neuropathic Disorder of Voltage Gated Sodium Channels

Paroxysmal extreme pain disorder: a molecular lesion of peripheral neurons

LRP5 variants may contribute to ADPKD

Germline mutations in PRKCSH are associated with autosomal dominant polycystic liver disease

Chromosomal abnormalities in hepatic cysts point to novel polycystic liver disease genes

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