Author

Felix W.M. de Rooij

Observed names: F W De Rooij, F W M D E Rooij, F W M de Rooij, F. W. M. DE ROOIJ, F. W. M. De Rooij, F. W. M. de Rooij, F. W.M. de Rooij, F.W.M. DE ROOIJ, F.W.M. De Rooij, F.W.M. de Rooij, FELIX W.M. DE ROOIJ, FWM de Rooij, Felix W M De Rooij, Felix W M de Rooij, Felix W. M. De Rooij, Felix W. M. de Rooij, Felix W.M de Rooij, Felix W.M. Rooij, Felix WM de Rooij

Institution: Erasmus MC

Observed institutions: Leiden University, Johns Hopkins University, Maastricht University Medical Centre, Erasmus MC, Amsterdam UMC Location University of Amsterdam, Maastricht University, Deventer Ziekenhuis, Academisch Ziekenhuis Rotterdam, University of Amsterdam, Erasmus University Rotterdam, Icahn School of Medicine at Mount Sinai

OpenAlex ID: A5111483086

Frequency and Spectrum of Cancers in the Peutz-Jeghers Syndrome

2006 · Nicholas Hearle, Valérie Schumacher, et al. · Clinical Cancer Research · 855

Afamelanotide for Erythropoietic Protoporphyria

2015 · Janneke G. Langendonk, Manisha Balwani, et al. · New England Journal of Medicine · 283

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High cancer risk and increased mortality in patients with Peutz–Jeghers syndrome

2011 · Margot G F van Lier, Anne Marie Westerman, et al. · Gut · 214

Peutz-Jeghers syndrome: 78-year follow-up of the original family

1999 · Anne Marie Westerman, Mark M Entius, et al. · The Lancet · 148

Long-Term Efficacy and Safety of Pegvisomant in Combination With Long-Acting Somatostatin Analogs in Acromegaly

2014 · S. J. C. M. M. Neggers, S. E. Franck, et al. · The Journal of Clinical Endocrinology & Metabolism · 125

5-Aminolaevulinic acid-induced protoporphyrin IX accumulation in tissues: pharmacokinetics after oral or intravenous administration

1998 · Jolanda van den Boogert, Richard van Hillegersberg, et al. · Journal of Photochemistry and Photobiology B Biology · 105

Novel mutations in theLKB1/STK11 gene in Dutch Peutz-Jeghers families

1999 · Anne Marie Westerman, Mark M. Entius, et al. · Human Mutation · 90

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Genetic defects underlying Peutz–Jeghers syndrome (PJS) and exclusion of the polarity‐associated MARK/Par1 gene family as potential PJS candidates

2007 · WWJ de Leng, M Jansen, et al. · Clinical Genetics · 58

Cyclooxygenase 2 expression and molecular alterations in Peutz-Jeghers hamartomas and carcinomas.

2003 · Wendy W J De Leng, Anne Marie Westerman, et al. · PubMed · 54

Bacterial infections in cirrhosis: role of proton pump inhibitors and intestinal permeability

2011 · Lotte G. van Vlerken, Ellen J. Huisman, et al. · European Journal of Clinical Investigation · 53

STK11 status and intussusception risk in Peutz-Jeghers syndrome

2006 · N Hearle, V Schumacher, et al. · Journal of Medical Genetics · 48

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Porphyrin biosynthesis in human Barrett's oesophagus and adenocarcinoma after ingestion of 5-aminolaevulinic acid

2000 · P Hinnen, F W M de Rooij, et al. · British Journal of Cancer · 45

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Card15 and Crohn's Disease: Healthy Homozygous Carriers of the 3020insC Frameshift Mutation

2003 · Klaas Linde, Patrick P.C. Boor, et al. · The American Journal of Gastroenterology · 44

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Systematic analysis of coproporphyrinogen oxidase gene defects in hereditary coproporphyria and mutation update

1999 · R. Rosipal, J. Lamoril, et al. · Human Mutation · 35

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Vitamin D deficiency in patients with erythropoietic protoporphyria

2009 · J. M. C. Spelt, F. W. M. de Rooij, et al. · Journal of Inherited Metabolic Disease · 34

Primary Bile Acid Malabsorption: A Pathophysiologic and Clinical Entity?

1992 · A. J. P. Van Tilburg, F. W. M. De Rooij, et al. · Scandinavian Journal of Gastroenterology · 34

Na+-dependent bile acid transport in the ileum: The balance between diarrhea and constipation

1990 · A.J.P. Van Tilburg, F.W.M. De Rooij, et al. · Gastroenterology · 33

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Kinetics, localization, and mechanism of 5-aminolevulinic acid-induced porphyrin accumulation in normal and Barrett's-like rat esophagus

1999 · Jolanda van den Boogert, Adriaan B. Houtsmuller, et al. · Lasers in Surgery and Medicine · 32

CARD15 mutations in Dutch familial and sporadic inflammatory bowel disease and an overview of European studies

2007 · Klaas van der Linde, Patrick P.C. Boor, et al. · European Journal of Gastroenterology & Hepatology · 31

Mutation analysis of three genes encoding novel LKB1-interacting proteins, BRG1, STRADα, and MO25α, in Peutz–Jeghers syndrome

2005 · P Alhopuro, P Katajisto, et al. · British Journal of Cancer · 30

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Failing beta-cell adaptation in South Asian families with a high risk of type 2 diabetes

2014 · Sjaam Jainandunsing, Behiye Özcan, et al. · Acta Diabetologica · 28

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Bile acids and Barrett's oesophagus: A sine qua non or coincidence?

2006 · Rudy R. Sital, Johannes G. Kusters, et al. · Scandinavian Journal of Gastroenterology · 26

Nasal polyposis in Peutz–Jeghers syndrome: a distinct histopathological and molecular genetic entity

2006 · Wendy W J de Leng, Anne Marie Westerman, et al. · Journal of Clinical Pathology · 24

Porphyria: A Diagnostic Approach

2003 · FELIX W.M. DE ROOIJ, ANNIE EDIXHOVEN, et al. · Elsevier eBooks · 24

STRAD in Peutz-Jeghers syndrome and sporadic cancers

2005 · W W J de Leng, J J Keller, et al. · Journal of Clinical Pathology · 23

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Works count: 62

Citation count: 2,718

H-index: 24

I10-index: 37