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Jeroen van Dongen

Research Profile

Concepts & Ideas

Physiology

Genes & Molecular Sequences

Procedures

Physical Chromosome Mapping

Disorders

Chemicals & Drugs

Anatomy

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Publications

TOP 3
Vincenzo Bonifati; Patrizia Rizzu; Marijke J van Baren; Onno Schaap; Guido J Breedveld; Elmar Krieger; Marieke C J Dekker; Ferdinando Squitieri; Pablo Ibanez; Marijke Joosse; Jeroen W F van Dongen; Nicola Vanacore; John C van Swieten; Alexis Brice; Giuseppe Meco; C.M. Duijn; Ben A Oostra; Peter Heutink
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.
Guido J Breedveld; Jeroen W F van Dongen; Cesare Danesino; Andrea Guala; Alan K Percy; Leon S Dure; Peter Harper; Lazarus P Lazarou; Herma C van der Linde; Marijke Joosse; Annette Grüters; Marcy E MacDonald; Bert B A de Vries; W F M Arts; Ben A Oostra; Heiko Krude; Peter Heutink
Mutations in TITF-1 are associated with benign hereditary chorea.
Omer T Njajou; Norbert Vaessen; Marijke Joosse; B Berghuis; Jeroen W F van Dongen; Martijn H Breuning; Pieter J L M Snijders; W P Rutten; Lodewijk A Sandkuijl; Ben A Oostra; C.M. Duijn; Peter Heutink
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

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All Publications

2003: Vincenzo Bonifati; Patrizia Rizzu; Marijke J van Baren; Onno Schaap; Guido J Breedveld; Elmar Krieger; Marieke C J Dekker; Ferdinando Squitieri; Pablo Ibanez; Marijke Joosse; Jeroen W F van Dongen; Nicola Vanacore; John C van Swieten; Alexis Brice; Giuseppe Meco; C.M. Duijn; Ben A Oostra; Peter Heutink
Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism.
Science (New York, N.Y.) 2003;299(5604):256-9.
2002: Guido J Breedveld; Jeroen W F van Dongen; Cesare Danesino; Andrea Guala; Alan K Percy; Leon S Dure; Peter Harper; Lazarus P Lazarou; Herma C van der Linde; Marijke Joosse; Annette Grüters; Marcy E MacDonald; Bert B A de Vries; W F M Arts; Ben A Oostra; Heiko Krude; Peter Heutink
Mutations in TITF-1 are associated with benign hereditary chorea.
Human molecular genetics 2002;11(8):971-9.
2001: Omer T Njajou; Norbert Vaessen; Marijke Joosse; B Berghuis; Jeroen W F van Dongen; Martijn H Breuning; Pieter J L M Snijders; W P Rutten; Lodewijk A Sandkuijl; Ben A Oostra; C.M. Duijn; Peter Heutink
A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.
Nature genetics 2001;28(3):213-4.

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