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Dennis Dooijes

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Judith A Groeneweg; Moniek G P J Cox; Rudolf A de Boer; Dennis Dooijes; Jan D H Jongbloed; William J McKenna; Jeroen F van der Heijden; Paul A van der Zwaag; J Peter van Tintelen; Toon A B van Veen; Arnold Vreeker; Richard N W Hauer
Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?
Maartje Noorman; Jeffrey E Saffitz; Michiel van der Heyden; Jasper J van der Smagt; Harold V M van Rijen; Leonie van Stuijvenberg; Andras Varro; Aryan Vink; Marc A Vos; Angeliki Asimaki; Halina Chkourko; Moniek G P J Cox; Jacques M T de Bakker; Nicolaas de Jonge; Roel A de Weger; Mario Delmar; Dennis Dooijes; Judith A Groeneweg; Sara Hakim; Richard N W Hauer; Thomas J Hund; Elise Kessler; Peter J Mohler; Toon A B van Veen
Remodeling of the cardiac sodium channel, connexin43, and plakoglobin at the intercalated disk in patients with arrhythmogenic cardiomyopathy.
Yvonne M Hoedemaekers; Titia E Cohen-Overbeek; Dennis Dooijes; Ingrid M E Frohn-Mulder; Danielle Majoor-Krakauer
Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy.

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2013: Judith A Groeneweg; Moniek G P J Cox; Rudolf A de Boer; Dennis Dooijes; Jan D H Jongbloed; William J McKenna; Jeroen F van der Heijden; Paul A van der Zwaag; J Peter van Tintelen; Toon A B van Veen; Arnold Vreeker; Richard N W Hauer
Left-dominant arrhythmogenic cardiomyopathy in a large family: associated desmosomal or nondesmosomal genotype?
Heart rhythm : the official journal of the Heart Rhythm Society 2013;10(4):548-59.
2013: Maartje Noorman; Jeffrey E Saffitz; Michiel van der Heyden; Jasper J van der Smagt; Harold V M van Rijen; Leonie van Stuijvenberg; Andras Varro; Aryan Vink; Marc A Vos; Angeliki Asimaki; Halina Chkourko; Moniek G P J Cox; Jacques M T de Bakker; Nicolaas de Jonge; Roel A de Weger; Mario Delmar; Dennis Dooijes; Judith A Groeneweg; Sara Hakim; Richard N W Hauer; Thomas J Hund; Elise Kessler; Peter J Mohler; Toon A B van Veen
Remodeling of the cardiac sodium channel, connexin43, and plakoglobin at the intercalated disk in patients with arrhythmogenic cardiomyopathy.
Heart rhythm : the official journal of the Heart Rhythm Society 2013;10(3):412-9.
2013: Yvonne M Hoedemaekers; Titia E Cohen-Overbeek; Dennis Dooijes; Ingrid M E Frohn-Mulder; Danielle Majoor-Krakauer
Prenatal ultrasound diagnosis of MYH7 non-compaction cardiomyopathy.
Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology 2013;41(3):336-9.
2013: Maartje Noorman; Maartje Papegaaij; Stefania Rizzo; Jeffrey E Saffitz; Leonie van Stuijvenberg; Toon A B van Veen; Aryan Vink; Angeliki Asimaki; Cristina Basso; Nicolaas de Jonge; Dennis Dooijes; Judith A Groeneweg; Richard N W Hauer
End stage of arrhythmogenic cardiomyopathy with severe involvement of the interventricular septum.
Heart rhythm : the official journal of the Heart Rhythm Society 2013;10(2):283-9.
2012: Iris C R M Kolder; Ronald H Lekanne Deprez; Danielle Majoor-Krakauer; Michelle Michels; Folkert J Ten Cate; Arthur A M Wilde; Michael W T Tanck; Connie R Bezzina; Imke Christiaans; Alexander Hessel Jan Danser; Dennis Dooijes
The role of renin-angiotensin-aldosterone system polymorphisms in phenotypic expression of MYBPC3-related hypertrophic cardiomyopathy.
European journal of human genetics : EJHG 2012;20(10):1071-7.
2012: Marka van Blitterswijk; Pierre R Bourque; Paul I W de Bakker; Marianne de Visser; Dennis Dooijes; Eric A M Hennekam; Jelena Medic; Helenius J Schelhaas; Anneke J van der Kooi; Michael A van Es; Wouter van Rheenen; Jan Veldink; Leonard H van den Berg
Evidence for an oligogenic basis of amyotrophic lateral sclerosis.
Human molecular genetics 2012;21(17):3776-84.
2012: Wouter van Rheenen; Jan Veldink; Lotte Vlam; Anneke J van der Kooi; W-Ludo van der Pol; Perry T C van Doormaal; Marianne de Visser; Dennis Dooijes; Mark H B Huisman; Jelena Medic; Joost Raaphorst; Helenius J Schelhaas; Meinie Seelen; Marka van Blitterswijk; Leonard H van den Berg
Hexanucleotide repeat expansions in C9ORF72 in the spectrum of motor neuron diseases.
Neurology 2012;79(9):878-82.
2012: Ewout J N Groen; Max Koppers; R Jeroen Pasterkamp; Leonard H Van den Berg; Perry T C van Doormaal; Wouter van Rheenen; Frank P Diekstra; Dennis Dooijes; Lotte Vlam; Jan Veldink
CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis.
Neurobiology of aging 2012;33(8):1852.e1-3.
2012: Marka van Blitterswijk; Marianne De Visser; Dennis Dooijes; Eric A M Hennekam; Helenius J Schelhaas; Anneke J van der Kooi; W-Ludo van der Pol; Michael A van Es; Jan Veldink; Lotte Vlam; Leonard H Van den Berg
Genetic overlap between apparently sporadic motor neuron diseases.
PloS one 2012;7(11):e48983.
2012: Jasper J van der Smagt; Paul A van der Zwaag; Irene van Langen; J Peter van Tintelen; Arthur A M Wilde; Dennis Dooijes; Frans Gerbens; Richard N W Hauer; F A M Hennekam; Amber Ummels; Hennie Bikker; Moniek G P J Cox; Pieter A Doevendans
Clinical and genetic characterization of patients with arrhythmogenic right ventricular dysplasia/cardiomyopathy caused by a plakophilin-2 splice mutation.
Cardiology 2012;123(3):181-9.
2012: Sabine J van Dijk; Marjon van Slegtenhorst; Nicky M Boontje; Lucie Carrier; Dennis Dooijes; Cris dos Remedios; Diederik W D Kuster; Michelle Michels; Aref Najafi; E Rosalie Paalberends; Sakthivel Sadayappan; Ger J M Stienen; Folkert J Ten Cate; Jolanda van der Velden
Contractile dysfunction irrespective of the mutant protein in human hypertrophic cardiomyopathy with normal systolic function.
Circulation. Heart failure 2012;5(1):36-46.
2011: Peter Elfferich; Sylvia A Eshuis; Ad Hovestadt; Klaus L Leenders; Saskia A J Lesnik-Oberstein; Leonardo Lopiano; JA Maat-Kievit; Jan-Pieter M Stroy; Cristina Tassorelli; Bart P C van de Warrenburg; Klaartje van Engelen; Wilson F Abdo; Vincenzo Bonifati; Agnita J W Boon; Dennis Dooijes; John C van Swieten; Marja C Verleun-Mooijman; Corien C Verschuuren-Bemelmans; Jan C M Zijlmans; Rick van Minkelen
Breakpoint mapping of 13 large parkin deletions/duplications reveals an exon 4 deletion and an exon 7 duplication as founder mutations.
Neurogenetics 2011;12(4):263-71.
2011: A van den Wijngaard; J Peter van Tintelen; Paul G A Volders; Maarten P van den Berg; Y H J M Arens; Dennis Dooijes; N Hofmann; Jan D H Jongbloed; Roselie J Jongbloed; R H Lekanne Deprez; M M A M Mannens; M Michels; M Slegtenhorst; B J M Smeets
Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy.
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2011;19(7-8):344-51.
2011: Moniek G P J Cox; Maarten J Cramer; Jacques M T de Bakker; Pieter A Doevendans; Dennis Dooijes; Douwe E Atsma; Zahurul A Bhuiyan; Arjan C Houweling; Jan D H Jongbloed; Luc Jordaens; Maartje Noorman; Arthur van den Wijngaard; Jasper J van der Smagt; Christian van der Werf; Paul A van der Zwaag; Irene van Langen; J Peter van Tintelen; Paul G A Volders; Ans C P Wiesfeld; Arthur A M Wilde; Richard N W Hauer
Arrhythmogenic right ventricular dysplasia/cardiomyopathy: pathogenic desmosome mutations in index-patients predict outcome of family screening: Dutch arrhythmogenic right ventricular dysplasia/cardiomyopathy genotype-phenotype follow-up study.
Circulation 2011;123(23):2690-700.
2011: Imke Christiaans; Erwin Birnie; Gouke J Bonsel; marcel mannens; Michelle Michels; Daniëlle Majoor-Krakauer; Dennis Dooijes; J Peter van Tintelen; Maarten P van den Berg; Paul G A Volders; Yvonne H Arens; Arthur van den Wijngaard; Douwe E Atsma; Apollonia T J M Helderman-van den Enden; Arjan C Houweling; Karin de Boer; Jasper J van der Smagt; Richard N W Hauer; Carlo L M Marcelis; Janneke Timmermans; Irene M van Langen; Arthur A M Wilde
Manifest disease, risk factors for sudden cardiac death, and cardiac events in a large nationwide cohort of predictively tested hypertrophic cardiomyopathy mutation carriers: determining the best cardiological screening strategy.
European heart journal 2011;32(9):1161-70.
2010: P A van der Zwaag; M G P J Cox; C van der Werf; Ans C P Wiesfeld; Jan D H Jongbloed; Dennis Dooijes; H Bikker; R Jongbloed; A J H Suurmeijer; Maarten P van den Berg; R M W Hofstra; R N W Hauer; A A M Wilde; J Peter van Tintelen
Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2010;18(12):583-91.
2010: Georgy Bakalkin; Hiroyuki Watanabe; Justyna Jezierska; Cloë Depoorter; Corien Verschuuren-Bemelmans; Igor Bazov; Konstantin A Artemenko; Tatjana Yakovleva; Dennis Dooijes; Bart P C van de Warrenburg; Roman A Zubarev; Berry Kremer; Pamela E Knapp; Kurt F Hauser; Cisca Wijmenga; Fred Nyberg; Richard J Sinke; Dineke S Verbeek
Prodynorphin mutations cause the neurodegenerative disorder spinocerebellar ataxia type 23.
American journal of human genetics 2010;87(5):593-603.
2010: P A van der Zwaag; M G P J Cox; C van der Werf; Ans C P Wiesfeld; Jan D H Jongbloed; Dennis Dooijes; H Bikker; R Jongbloed; A J H Suurmeijer; Maarten P van den Berg; R M W Hofstra; R N W Hauer; A A M Wilde; J Peter van Tintelen
Recurrent and founder mutations in the Netherlands : Plakophilin-2 p.Arg79X mutation causing arrhythmogenic right ventricular cardiomyopathy/dysplasia.
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2010;18(12):583-91.
2010: Cornelis J J Boogerd; Dennis Dooijes; Aho Ilgun; Inge B Mathijssen; Roel Hordijk; Ingrid M B H van de Laar; Patrick Rump; Hermine E Veenstra-Knol; Antoon F M Moorman; Phil Barnett; Alex V Postma
Functional analysis of novel TBX5 T-box mutations associated with Holt-Oram syndrome.
Cardiovascular research 2010;88(1):130-9.
2010: Marijke Wasielewski; Muhammad Riaz; Joyce Vermeulen; Ans M W van den Ouweland; Ineke Labrijn-Marks; Renske Olmer; Linda van der Spaa; Jan G M Klijn; Hanne Meijers-Heijboer; Dennis Dooijes; Mieke Schutte
Association of rare MSH6 variants with familial breast cancer.
Breast cancer research and treatment 2010;123(2):315-20.
2010: Yvonne M Hoedemaekers; Kadir Caliskan; Michelle Michels; Ingrid Frohn-Mulder; Jasper J van der Smagt; Judith E Phefferkorn; Marja W Wessels; Folkert J Ten Cate; Eric J G Sijbrands; Dennis Dooijes; Danielle F Majoor-Krakauer
The importance of genetic counseling, DNA diagnostics, and cardiologic family screening in left ventricular noncompaction cardiomyopathy.
Circulation. Cardiovascular genetics 2010;3(3):232-9.
2010: Karin Y van Spaendonck-Zwarts; J Peter van Tintelen; Dirk J van Veldhuisen; Rik van der Werf; Jan D H Jongbloed; Walter J Paulus; Dennis Dooijes; Maarten P van den Berg
Peripartum cardiomyopathy as a part of familial dilated cardiomyopathy.
Circulation 2010;121(20):2169-75.
2010: I Christiaans; E A Nannenberg; Dennis Dooijes; R J E Jongbloed; M Michels; P G Postema; D Majoor-Krakauer; A van den Wijngaard; M M A M Mannens; J Peter van Tintelen; Irene M van Langen; A A M Wilde
Founder mutations in hypertrophic cardiomyopathy patients in the Netherlands.
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2010;18(5):248-54.
2010: Marja W Wessels; Brian Kuchinka; Rogier Heydanus; Bert J Smit; Dennis Dooijes; Ronald R de Krijger; Maarten H Lequin; Elisabeth M de Jong; Margreet Husen; Patrick J Willems; Brett Casey
Polyalanine expansion in the ZIC3 gene leading to X-linked heterotaxy with VACTERL association: a new polyalanine disorder?
Journal of medical genetics 2010;47(5):351-5.
2010: Ewout J N Groen; Michael A van Es; Paul van Vught; Wim G M Spliet; Jooyeon van Engelen-Lee; Marianne De Visser; J H J Wokke; H Jurgen Schelhaas; Roel A Ophoff; Katsumi Fumoto; R Jeroen Pasterkamp; Dennis Dooijes; Edwin Cuppen; Jan Veldink; Leonard H Van den Berg
FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.
Archives of neurology 2010;67(2):224-30.
2009: Yolande van Bever; Saskia J Gischler; Hans L J Hoeve; Liesbeth S Smit; Jeroen Nauta; Dennis Dooijes
Obstructive apneas and severe dysphagia in a girl with Townes-Brocks syndrome and atypical feet involvement.
European journal of medical genetics 2009;52(6):426-9.
2009: Michelle Michels; Osama Soliman; Judith Phefferkorn; Yvonne M Hoedemaekers; Marcel J M Kofflard; Dennis Dooijes; Danielle Majoor-Krakauer; Folkert J Ten Cate
Disease penetrance and risk stratification for sudden cardiac death in asymptomatic hypertrophic cardiomyopathy mutation carriers.
European heart journal 2009;30(21):2593-8.
2009: Ingrid Van de Laar; Marja Wessels; Ingrid Frohn-Mulder; Michiel Dalinghaus; Bianca de Graaf; Marianne van Tienhoven; Paul van der Moer; Margreet Husen-Ebbinge; Maarten H Lequin; Dennis Dooijes; Ronald R de Krijger; Ben A Oostra; Aida M Bertoli Avella
First locus for primary pulmonary vein stenosis maps to chromosome 2q.
European heart journal 2009;30(20):2485-92.
2009: Samantha R Riedijk; M F N Niermeijer; Dennis Dooijes; Aad Tibben
A decade of genetic counseling in frontotemporal dementia affected families: few counseling requests and much familial opposition to testing.
Journal of genetic counseling 2009;18(4):350-6.
2009: Irene C Joziasse; Jasper J van der Smagt; Martin Poot; Ron Hochstenbach; Marcel R Nelen; Marielle van Gijn; Dennis Dooijes; Barbara J M Mulder; Pieter A Doevendans
A duplication including GATA4 does not co-segregate with congenital heart defects.
American journal of medical genetics. Part A 2009;149A(5):1062-6.
2009: Sabine J van Dijk; Dennis Dooijes; Cris dos Remedios; Michelle Michels; Jos M J Lamers; Saul Winegrad; Saskia Schlossarek; Lucie Carrier; Folkert J Ten Cate; Ger J M Stienen; Jolanda van der Velden
Cardiac myosin-binding protein C mutations and hypertrophic cardiomyopathy: haploinsufficiency, deranged phosphorylation, and cardiomyocyte dysfunction.
Circulation 2009;119(11):1473-83.
2009: Peter C van den Akker; Raoul van de Graaf; Dennis Dooijes; Anthonie J van Essen
Somatic mosaicism for the SALL1 mutation p.Ser371X in full-blown Townes-Brocks syndrome with Duane anomaly.
American journal of medical genetics. Part A 2009;149A(4):812-5.
2009: Dewkoemar Ramsoekh; Anja Wagner; Monique E van Leerdam; Dennis Dooijes; Carli Tops; Ewout W Steyerberg; Ernst J Kuipers
Cancer risk in MLH1, MSH2 and MSH6 mutation carriers; different risk profiles may influence clinical management.
Hereditary cancer in clinical practice 2009;7(1):17.
2009: Susanne T de Bot; H P H Kremer; Dennis Dooijes; Marcel M Verbeek
CSF studies facilitate DNA diagnosis in familial Alzheimer's disease due to a presenilin-1 mutation.
Journal of Alzheimer's disease : JAD 2009;17(1):53-7.
2009: Michelle Michels; Osama Soliman; Marcel J Kofflard; Yvonne M Hoedemaekers; Dennis Dooijes; Danielle Majoor-Krakauer; Folkert J Ten Cate
Diastolic abnormalities as the first feature of hypertrophic cardiomyopathy in Dutch myosin-binding protein C founder mutations.
JACC. Cardiovascular imaging 2009;2(1):58-64.
2008: Dewkoemar Ramsoekh; Anja Wagner; Monique E van Leerdam; Winand N M Dinjens; Ewout W Steyerberg; D J J Halley; Ernst J Kuipers; Dennis Dooijes
A high incidence of MSH6 mutations in Amsterdam criteria II-negative families tested in a diagnostic setting.
Gut 2008;57(11):1539-44.
2008: H Seelaar; Wouter Kamphorst; Sonia M Rosso; Asma Azmani; R Masdjedi; Inge de Koning; JA Maat-Kievit; B Anar; L Donker Kaat; Guido J Breedveld; Dennis Dooijes; J M Rozemuller; Iraad F Bronner; Patrizia Rizzu; John C van Swieten
Distinct genetic forms of frontotemporal dementia.
Neurology 2008;71(16):1220-6.
2008: Hao Yun Wong; Jos W Hoogerbrugge; Kar Lok Pang; Marije van Leeuwen; Martin E van Royen; Michel Molier; Cor A Berrevoets; Dennis Dooijes; Hendrikus J Dubbink; Dennis J van de Wijngaart; Katja P Wolffenbuttel; Jan Trapman; Wim J Kleijer; Stenvert L S Drop; J Anton Grootegoed; Albert O Brinkmann
A novel mutation F826L in the human androgen receptor in partial androgen insensitivity syndrome; increased NH2-/COOH-terminal domain interaction and TIF2 co-activation.
Molecular and cellular endocrinology 2008;292(1-2):69-78.
2008: Marijke Wasielewski; H F A Vasen; Juul Wijnen; Maartje Hooning; Dennis Dooijes; Carli Tops; Jan G M Klijn; Hanne Meijers-Heijboer; Mieke Schutte
CHEK2 1100delC is a susceptibility allele for HNPCC-related colorectal cancer.
Clinical cancer research : an official journal of the American Association for Cancer Research 2008;14(15):4989-94.
2008: Marja W Wessels; Bianca de Graaf; Titia E Cohen-Overbeek; Silja E Spitaels; Lotte E de Groot-de Laat; Folkert J Ten Cate; Ingrid F M Frohn-Mulder; Ronald R de Krijger; Margot M Bartelings; Nienke Essed; Jury W Wladimiroff; Martinus F Niermeijer; Peter Heutink; Ben A Oostra; Dennis Dooijes; Aida M Bertoli Avella; Patrick J Willems
A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.
Human genetics 2008;122(6):595-603.
2007: Dewkoemar Ramsoekh; Monique E van Leerdam; Carli Tops; Dennis Dooijes; E W Steyerberg; Ernst J Kuipers; A Wagner
The use of genetic testing in hereditary colorectal cancer syndromes: genetic testing in HNPCC, (A)FAP and MAP.
Clinical genetics 2007;72(6):562-7.
2007: Ingrid Van de Laar; Dennis Dooijes; Lies Hoefsloot; Marleen Simon; Jeannette Hoogeboom; koenraad devriendt
Limb anomalies in patients with CHARGE syndrome: an expansion of the phenotype.
American journal of medical genetics. Part A 2007;143A(22):2712-5.
2007: Yvonne M Hoedemaekers; Kadir Caliskan; Danielle Majoor-Krakauer; Ingrid Van de Laar; Michelle Michels; Maarten Witsenburg; Folkert J Ten Cate; Maarten L Simoons; Dennis Dooijes
Cardiac beta-myosin heavy chain defects in two families with non-compaction cardiomyopathy: linking non-compaction to hypertrophic, restrictive, and dilated cardiomyopathies.
European heart journal 2007;28(22):2732-7.
2007: Michelle Michels; Yvonne M Hoedemaekers; Marcel J M Kofflard; Ingrid M E Frohn-Mulder; Dennis Dooijes; Danielle Majoor-Krakauer; Folkert J Ten Cate
Familial screening and genetic counselling in hypertrophic cardiomyopathy: the Rotterdam experience.
Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation 2007;15(5):184-90.
2006: Wenxia Chai; Yvonne M Hoedemaekers; Ron van Schaik; Marianne van Fessem; Ingrid M Garrelds; Jasper J Saris; Dennis Dooijes; Folkert J Ten Cate; Marcel M J Kofflard; Alexander Hessel Jan Danser
Cardiac aldosterone in subjects with hypertrophic cardiomyopathy.
Journal of the renin-angiotensin-aldosterone system : JRAAS 2006;7(4):225-30.
2005: Dominique Marcus-Soekarman; Jos P M Offermans; Ans M W van den Ouweland; A L M Mulder; N Muntjewerff; M Vossen; W Kleijer; C T R M Schrander-Stumpel; Dennis Dooijes
Hyperechogenic fetal bowel: counseling difficulties.
European journal of medical genetics 2005;48(4):421-5.
2005: Dineke S Verbeek; Bart P C van de Warrenburg; F A M Hennekam; Dennis Dooijes; PF Ippel; Corien C Verschuuren-Bemelmans; H P H Kremer; Richard J Sinke
Gly118Asp is a SCA14 founder mutation in the Dutch ataxia population.
Human genetics 2005;117(1):88-91.
2005: Arzu Umar; Cor A Berrevoets; N Mai Van; Marije van Leeuwen; Michael Verbiest; Wim J Kleijer; Dennis Dooijes; J Anton Grootegoed; Stenvert L S Drop; Albert O Brinkmann
Functional analysis of a novel androgen receptor mutation, Q902K, in an individual with partial androgen insensitivity.
The Journal of clinical endocrinology and metabolism 2005;90(1):507-15.
2003: Esther van Herpen; Sonia M Rosso; Lies-Anne Serverijnen; Hirotaka Yoshida; Guido J Breedveld; Raoul van de Graaf; Wouter Kamphorst; Rivka Ravid; Rob Willemsen; Dennis Dooijes; Danielle Majoor-Krakauer; Johan M Kros; R Anthony Crowther; Michel Goedert; Peter Heutink; John C van Swieten
Variable phenotypic expression and extensive tau pathology in two families with the novel tau mutation L315R.
Annals of neurology 2003;54(5):573-81.
2003: Marielle Alders; Roselie J Jongbloed; Wout Deelen; Arthur van den Wijngaard; Pieter A Doevendans; Folkert J Ten Cate; Vera Regitz-Zagrosek; Hans-Peter Vosberg; Irene M van Langen; Arthur Wilde; Dennis Dooijes; marcel mannens
The 2373insG mutation in the MYBPC3 gene is a founder mutation, which accounts for nearly one-fourth of the HCM cases in the Netherlands.
European heart journal 2003;24(20):1848-53.
2003: Sonia M Rosso; Laura Donker Kaat; Timo Baks; Marijke Joosse; Inge de Koning; Y A L Pijnenburg; Danielle De Jong; Dennis Dooijes; Wouter Kamphorst; Rivka Ravid; Martinus F Niermeijer; Frans Verheij; H P H Kremer; Philip scheltens; C.M. Duijn; Peter Heutink; John C van Swieten
Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population-based study.
Brain : a journal of neurology 2003;126(Pt 9):2016-22.
2003: Alice S Brooks; Dennis Dooijes
[From gene to disease: arteriohepatic dysplasia or Alagille syndrome].
Nederlands tijdschrift voor geneeskunde 2003;147(25):1213-5.
2003: John C van Swieten; Esther Brusse; Bianca de Graaf; Elmar Krieger; Raoul van de Graaf; Inge de Koning; anneke maat-kievit; Peter Leegwater; Dennis Dooijes; Ben A Oostra; Peter Heutink
A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected].
American journal of human genetics 2003;72(1):191-9.
2002: Bart P C van de Warrenburg; Richard J Sinke; C C Verschuuren-Bemelmans; Hans Scheffer; Ewout R Brunt; PF Ippel; JA Maat-Kievit; Dennis Dooijes; Nicolette C Notermans; Dick Lindhout; Nine V A M Knoers; H P H Kremer
Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis.
Neurology 2002;58(5):702-8.
2002: Sonia M Rosso; Esther van Herpen; Wout Deelen; Wouter Kamphorst; Lies-Anne Severijnen; Rob Willemsen; Rivka Ravid; Martinus F Niermeijer; Dennis Dooijes; Michael J Smith; Michel Goedert; Peter Heutink; John C van Swieten
A novel tau mutation, S320F, causes a tauopathy with inclusions similar to those in Pick's disease.
Annals of neurology 2002;51(3):373-6.
2001: A de Goede-Bolder; MH Cnossen; Dennis Dooijes; Ans M W van den Ouweland; Martinus F Niermeijer
[From gene to disease; neurofibromatosis type 1].
Nederlands tijdschrift voor geneeskunde 2001;145(36):1736-8.
2000: Moniek van Beest; Dennis Dooijes; Marc van de Wetering; Søren Kjaerulff; Alexandre Bonvin; Olaf Nielsen; Hans Clevers
Sequence-specific high mobility group box factors recognize 10-12-base pair minor groove motifs.
The Journal of biological chemistry 2000;275(35):27266-73.
1998: Dennis Dooijes; Moniek van Beest; Marc van de Wetering; G Boulanger; Tamara Jones; Hans Clevers; Mark A Mortin
Genomic organization of the segment polarity gene pan in Drosophila melanogaster.
Molecular & general genetics : MGG 1998;258(1-2):45-52.
1997: Søren Kjaerulff; Dennis Dooijes; Hans Clevers; Olaf Nielsen
Cell differentiation by interaction of two HMG-box proteins: Mat1-Mc activates M cell-specific genes in S.pombe by recruiting the ubiquitous transcription factor Ste11 to weak binding sites.
The EMBO journal 1997;16(13):4021-33.
1997: Dennis Dooijes; Hans Clevers
Control of gene expression during lymphoid development: targeted gene disruption provides new clues.
APMIS : acta pathologica, microbiologica, et immunologica Scandinavica 1997;105(5):337-44.
1997: Marc van de Wetering; R Cavallo; Dennis Dooijes; Moniek van Beest; Johan H van Es; Joseph Loureiro; A Ypma; Deborah A Hursh; Tamara Jones; Amy Bejsovec; Mark Peifer; Mark A Mortin; Hans Clevers
Armadillo coactivates transcription driven by the product of the Drosophila segment polarity gene dTCF.
Cell 1997;88(6):789-99.
1993: Dennis Dooijes; Marc van de Wetering; L Knippels; Hans Clevers
The Schizosaccharomyces pombe mating-type gene mat-Mc encodes a sequence-specific DNA-binding high mobility group box protein.
The Journal of biological chemistry 1993;268(33):24813-7.
1993: L van Houte; A van Oers; Marc van de Wetering; Dennis Dooijes; R Kaptein; Hans Clevers
The sequence-specific high mobility group 1 box of TCF-1 adopts a predominantly alpha-helical conformation in solution.
The Journal of biological chemistry 1993;268(24):18083-7.
1991: M Oosterwegel; Marc van de Wetering; Dennis Dooijes; L Klomp; A Winoto; K Georgopoulos; F Meijlink; Hans Clevers
Cloning of murine TCF-1, a T cell-specific transcription factor interacting with functional motifs in the CD3-epsilon and T cell receptor alpha enhancers.
The Journal of experimental medicine 1991;173(5):1133-42.
1991: Marc van de Wetering; M Oosterwegel; Dennis Dooijes; Hans Clevers
Identification and cloning of TCF-1, a T lymphocyte-specific transcription factor containing a sequence-specific HMG box.
The EMBO journal 1991;10(1):123-32.