Bobby P C Koeleman

Bobby P C Koeleman

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Bobby P C Koeleman

Publications by authors named "Bobby P C Koeleman"

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Liprin alfa 2 gene expression is increased by cannabis use and associated with neuropsychological function.

Eur Neuropsychopharmacol 2019 May 15;29(5):643-652. Epub 2019 Mar 15.

Department of Psychiatry, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.euroneuro.2019.03.004DOI Listing
May 2019

Outcomes and comorbidities of SCN1A-related seizure disorders.

Epilepsy Behav 2019 01 5;90:252-259. Epub 2018 Dec 5.

Department of Genetics, University Medical Center Utrecht, Utrecht University, the Netherlands.

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http://dx.doi.org/10.1016/j.yebeh.2018.09.041DOI Listing
January 2019

Rare coding variants in genes encoding GABA receptors in genetic generalised epilepsies: an exome-based case-control study.

Authors:
Patrick May Simon Girard Merle Harrer Dheeraj R Bobbili Julian Schubert Stefan Wolking Felicitas Becker Pamela Lachance-Touchette Caroline Meloche Micheline Gravel Cristina E Niturad Julia Knaus Carolien De Kovel Mohamad Toliat Anne Polvi Michele Iacomino Rosa Guerrero-López Stéphanie Baulac Carla Marini Holger Thiele Janine Altmüller Kamel Jabbari Ann-Kathrin Ruppert Wiktor Jurkowski Dennis Lal Raffaella Rusconi Sandrine Cestèle Benedetta Terragni Ian D Coombs Christopher A Reid Pasquale Striano Hande Caglayan Auli Siren Kate Everett Rikke S Møller Helle Hjalgrim Hiltrud Muhle Ingo Helbig Wolfram S Kunz Yvonne G Weber Sarah Weckhuysen Peter De Jonghe Sanjay M Sisodiya Rima Nabbout Silvana Franceschetti Antonietta Coppola Maria S Vari Dorothée Kasteleijn-Nolst Trenité Betul Baykan Ugur Ozbek Nerses Bebek Karl M Klein Felix Rosenow Dang K Nguyen François Dubeau Lionel Carmant Anne Lortie Richard Desbiens Jean-François Clément Cécile Cieuta-Walti Graeme J Sills Pauls Auce Ben Francis Michael R Johnson Anthony G Marson Bianca Berghuis Josemir W Sander Andreja Avbersek Mark McCormack Gianpiero L Cavalleri Norman Delanty Chantal Depondt Martin Krenn Fritz Zimprich Sarah Peter Marina Nikanorova Robert Kraaij Jeroen van Rooij Rudi Balling M Arfan Ikram André G Uitterlinden Giuliano Avanzini Stephanie Schorge Steven Petrou Massimo Mantegazza Thomas Sander Eric LeGuern Jose M Serratosa Bobby P C Koeleman Aarno Palotie Anna-Elina Lehesjoki Michael Nothnagel Peter Nürnberg Snezana Maljevic Federico Zara Patrick Cossette Roland Krause Holger Lerche

Lancet Neurol 2018 08 17;17(8):699-708. Epub 2018 Jul 17.

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http://dx.doi.org/10.1016/S1474-4422(18)30215-1DOI Listing
August 2018

Abnormal islet sphingolipid metabolism in type 1 diabetes.

Diabetologia 2018 07 18;61(7):1650-1661. Epub 2018 Apr 18.

The Bartholin Institute, Department of Pathology, Rigshospitalet, Copenhagen Biocenter, Ole Maaløes Vej 5, 2200, Copenhagen N, Denmark.

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http://dx.doi.org/10.1007/s00125-018-4614-2DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6445476PMC
July 2018

What do genetic studies tell us about the heritable basis of common epilepsy? Polygenic or complex epilepsy?

Neurosci Lett 2018 02 25;667:10-16. Epub 2017 Mar 25.

Department of Genetics, UMC Utrecht, Utrecht, The Netherlands. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S03043940173027
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http://dx.doi.org/10.1016/j.neulet.2017.03.042DOI Listing
February 2018

Carbamazepine- and oxcarbazepine-induced hyponatremia in people with epilepsy.

Epilepsia 2017 07 24;58(7):1227-1233. Epub 2017 May 24.

Stichting Epilepsie Instellingen Nederland (SEIN), Zwolle, The Netherlands.

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http://dx.doi.org/10.1111/epi.13777DOI Listing
July 2017

Identification of coagulation gene 3'UTR variants that are potentially regulated by microRNAs.

Br J Haematol 2017 06 26;177(5):782-790. Epub 2017 Apr 26.

Servicio de Hematología y Oncología Médica. Hospital Universitario Morales Meseguer y Centro Regional de Hemodonación, IMIB-Arrixaca, Universidad de Murcia, Murcia, Spain.

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http://dx.doi.org/10.1111/bjh.14629DOI Listing
June 2017

Genetics of common forms of epilepsy.

Lancet Neurol 2017 02;16(2):101-102

Department of Genetics, University Medical Centre Utrecht, Universiteitsweg 100, 3584CX, Netherland. Electronic address:

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http://dx.doi.org/10.1016/S1474-4422(16)30400-8DOI Listing
February 2017

Genome-wide association study of sporadic brain arteriovenous malformations.

J Neurol Neurosurg Psychiatry 2016 09 27;87(9):916-23. Epub 2016 Jan 27.

Department of Anesthesia and Perioperative Care, Center for Cerebrovascular Research, University of California, San Francisco, California, USA Department of Epidemiology and Biostatistics, University of California, San Francisco, California, USA Institute for Human Genetics, University of California, San Francisco, California, USA.

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http://dx.doi.org/10.1136/jnnp-2015-312272DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963303PMC
September 2016

Autosomal dominant epilepsy with auditory features: a new LGI1 family including a phenocopy with cortical dysplasia.

J Neurol 2016 Jan 12;263(1):11-6. Epub 2015 Oct 12.

Department of Neuropediatrics, Christian-Albrechts-University of Kiel and University Medical Center Schleswig-Holstein, Kiel, Germany.

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http://dx.doi.org/10.1007/s00415-015-7921-2DOI Listing
January 2016

Complex SCN8A DNA-abnormalities in an individual with therapy resistant absence epilepsy.

Epilepsy Res 2015 Sep 15;115:141-4. Epub 2015 Jun 15.

Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.eplepsyres.2015.06.007DOI Listing
September 2015

Genetic Factors for the Severity of ACPA-negative Rheumatoid Arthritis in 2 Cohorts of Early Disease: A Genome-wide Study.

J Rheumatol 2015 Aug 15;42(8):1383-91. Epub 2015 Jun 15.

From the Department of Rheumatology, and the Department of Medical Statistics, Leiden University Medical Center, Leiden, the Netherlands; the Section of Rheumatology at the Institution of Clinical Science, Lund University, Skåne University Hospital, Lund, Sweden, for the BARFOT study group; the Department of Genetics, University Medical Center Groningen and University of Groningen, Groningen, The Netherlands; Center of Experimental Rheumatology, University Hospital Zurich, Schlieren, Switzerland; the Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.D.P. de Rooy, LLM, MD, PhD, Department of Rheumatology, Leiden University Medical Center; R. Tsonaka, PhD, Department of Medical Statistics, Leiden University Medical Center; M.L. Andersson, BMS, PhD; K. Forslind, Associate Professor, Senior Consultant, Section of Rheumatology at the Institution of Clinical Science, Lund University, Skåne University Hospital, for the BARFOT study group; A. Zhernakova, MD, PhD, Department of Rheumatology, Leiden University Medical Center, and Department of Genetics, University Medical Center Groningen and University of Groningen; M. Frank-Bertoncelj, MD, PhD, Center of Experimental Rheumatology, University Hospital Zurich; C.G. de Kovel, PhD; B.P. Koeleman, PhD, Department of Medical Genetics, University Medical Center Utrecht; D.M. van der Heijde, MD, PhD; T.W. Huizinga, MD, PhD; R.E. Toes, PhD, Department of Rheumatology, Leiden University Medical Center; J.J. Houwing-Duistermaat, PhD, PD, Department of Medical Statistics, Leiden University Medical Center; C. Ospelt, MD, PhD, Center of Experimental Rheumatology, University Hospital Zurich; B. Svensson, MD, PhD, Section of Rheumatology at the Institution of Clinical Science, Lund University, Skåne University Hospital, for the BARFOT study group; A.H. van der Helm-van Mil, MD, PhD, Department of Rheumatology, Leiden University Medical Center.

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http://dx.doi.org/10.3899/jrheum.140741DOI Listing
August 2015

Effect of vaccinations on seizure risk and disease course in Dravet syndrome.

Neurology 2015 Aug 22;85(7):596-603. Epub 2015 Jul 22.

From the Department of Medical Genetics (N.E.V., A.C.M.S., E.I., M.v.K., C.G.F.d.K., B.P.C.K., N.V.K., D.L., E.H.B.) and Department of Child Neurology, Brain Center Rudolf Magnus (F.E.J., K.P.B.), University Medical Center Utrecht; Centre for Infectious Disease Control (N.A.T.v.d.M., P.E.V.-d.B., J.M.K.), National Institute for Public Health and Environment-RIVM, Bilthoven; Stichting Epilepsie Instellingen Nederland (E.H., W.B.G.), Zwolle; Stichting Epilepsie Instellingen Nederland (H.H.G., P.B.A.), Heemstede; Epilepsy Center Kempenhaeghe (A.d.L.), Heeze; Department of Child Neurology (R.F.N.), Erasmus Medical Centre, Rotterdam; Department of Child Neurology (J.H.S.), Radboud Medical Centre, Nijmegen; Department of Neurology (H.S.), Canisius-Wilhelmina Hospital, Nijmegen; Department of Child Neurology (R.J.V.), VU Medical Centre, Amsterdam; Department of Child Neurology (J.N.), Maastricht University Medical Centre; and Department of Neurology (O.F.B.), University of Groningen, University Medical Centre of Groningen, the Netherlands.

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http://dx.doi.org/10.1212/WNL.0000000000001855DOI Listing
August 2015

A large-scale genetic analysis reveals a strong contribution of the HLA class II region to giant cell arteritis susceptibility.

Am J Hum Genet 2015 Apr 26;96(4):565-80. Epub 2015 Mar 26.

Instituto de Parasitología y Biomedicina "López-Neyra," CSIC, PTS Granada, Granada 18016, Spain.

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http://dx.doi.org/10.1016/j.ajhg.2015.02.009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385191PMC
April 2015

Febrile temperatures unmask biophysical defects in Nav1.1 epilepsy mutations supportive of seizure initiation.

J Gen Physiol 2013 Dec;142(6):641-53

Department of Medical Genetics, Division of Biomedical Genetics, and 2 Department of Medical Physiology, Division of Heart and Lungs, University Medical Center Utrecht, 3508 AB Utrecht, Netherlands.

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http://dx.doi.org/10.1085/jgp.201311042DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840920PMC
December 2013

Epilepsy, hippocampal sclerosis and febrile seizures linked by common genetic variation around SCN1A.

Brain 2013 Oct 6;136(Pt 10):3140-50. Epub 2013 Sep 6.

1 NIHR University College London Hospitals Biomedical Research Centre, Department of Clinical and Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London, WC1N 3BG, UK.

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https://academic.oup.com/brain/article/136/10/3140/330027
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http://dx.doi.org/10.1093/brain/awt233DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3784283PMC
October 2013

The quest for juvenile myoclonic epilepsy genes.

Epilepsy Behav 2013 Jul;28 Suppl 1:S52-7

Epilepsy Genetics/Genomics Laboratories, Neurology and Research Services, VA GLAHS-West Los Angeles, CA, USA.

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http://dx.doi.org/10.1016/j.yebeh.2012.06.033DOI Listing
July 2013

Photoparoxysmal EEG response and genetic dissection of juvenile myoclonic epilepsy.

Epilepsy Behav 2013 Jul;28 Suppl 1:S69-71

Department of Medical Genetics, University Medical Center Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.yebeh.2012.07.016DOI Listing
July 2013

Polymorphisms in ACVRL1 and endoglin genes are not associated with sporadic and HHT-related brain AVMs in Dutch patients.

Transl Stroke Res 2013 Jun 29;4(3):375-378. Epub 2012 Nov 29.

Department of Neurology and Neurosurgery, Rudolf Magnus Institute of Neurosciences, University Medical Center Utrecht, Heidelberglaan 100, 3484CX, The Netherlands.

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http://dx.doi.org/10.1007/s12975-012-0231-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4038301PMC
June 2013

Genome-wide association analysis of genetic generalized epilepsies implicates susceptibility loci at 1q43, 2p16.1, 2q22.3 and 17q21.32.

Hum Mol Genet 2012 Dec 4;21(24):5359-72. Epub 2012 Sep 4.

Institute for Medical Biometry, Informatic and Epidemiology, University of Bonn, Bonn, Germany.

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http://hmg.oxfordjournals.org/content/21/24/5359.full.pdf
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http://www.hmg.oxfordjournals.org/cgi/doi/10.1093/hmg/dds373
Publisher Site
http://dx.doi.org/10.1093/hmg/dds373DOI Listing
December 2012

Transfer of regulatory properties from tolerogenic to proinflammatory dendritic cells via induced autoreactive regulatory T cells.

J Immunol 2011 Dec 14;187(12):6357-64. Epub 2011 Nov 14.

Department of Immunohematology and Blood Transfusion, Leiden University Medical Center, 2333 ZA Leiden, The Netherlands.

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http://dx.doi.org/10.4049/jimmunol.1101638DOI Listing
December 2011

Nav 1.1 dysfunction in genetic epilepsy with febrile seizures-plus or Dravet syndrome.

Eur J Neurosci 2011 Oct 22;34(8):1268-75. Epub 2011 Aug 22.

Division of Biomedical Genetics, Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1111/j.1460-9568.2011.07826.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3195841PMC
October 2011

Identification of novel genetic markers associated with clinical phenotypes of systemic sclerosis through a genome-wide association strategy.

PLoS Genet 2011 Jul 14;7(7):e1002178. Epub 2011 Jul 14.

Department of Epidemiology, M. D. Anderson Cancer Center, Houston, Texas, USA.

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http://dx.doi.org/10.1371/journal.pgen.1002178DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3136437PMC
July 2011

Endocrine autoimmune disease: genetics become complex.

Eur J Clin Invest 2010 Dec 16;40(12):1144-55. Epub 2010 Aug 16.

Department of Endocrinology, University Medical Centre Utrecht, Utrecht, the Netherlands.

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http://dx.doi.org/10.1111/j.1365-2362.2010.02366.xDOI Listing
December 2010

Association of IL-2RA/CD25 with type 1 diabetes in the Belgian population.

Hum Immunol 2010 Dec 16;71(12):1233-7. Epub 2010 Sep 16.

Diabetes Research Center, Faculty of Medicine and Pharmacy, Brussels Free University-Vrije Universiteit Brussel (VUB), Brussels, Belgium.

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http://dx.doi.org/10.1016/j.humimm.2010.09.006DOI Listing
December 2010

Association study of TRPC4 as a candidate gene for generalized epilepsy with photosensitivity.

Neuromolecular Med 2010 Sep 24;12(3):292-9. Epub 2010 Jun 24.

Department of Neuropediatrics, University Hospital Schleswig-Holstein, Campus Kiel, Arnold-Heller-Str.3, Building 9, Kiel, Germany.

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http://dx.doi.org/10.1007/s12017-010-8122-xDOI Listing
September 2010

Association analysis of myosin IXB and type 1 diabetes.

Hum Immunol 2010 Jun 1;71(6):598-601. Epub 2010 Apr 1.

Department Immunohematology and Blood Transfusion, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1016/j.humimm.2010.03.002DOI Listing
June 2010

Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.

Neurosci Lett 2009 Oct 25;462(1):24-9. Epub 2009 Jun 25.

Complex Genetics Section, DBG-Department of Medical Genetics, University Medical Center Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.neulet.2009.06.064DOI Listing
October 2009

Genetic polymorphisms in susceptibility to Type 1 Diabetes.

Clin Chim Acta 2008 Jan 2;387(1-2):9-17. Epub 2007 Oct 2.

Complex Genetics Section, Department of Medical Genetics, University Medical Center Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.cca.2007.09.021DOI Listing
January 2008

Linkage study of 14 candidate genes and loci in four large Dutch families with vesico-ureteral reflux.

Pediatr Nephrol 2007 Aug 12;22(8):1129-33. Epub 2007 May 12.

Department of Medical Genetics KC.04.084.2, University Medical Centre Utrecht, P.O. Box 85090, 3508 AB, Utrecht, The Netherlands.

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http://link.springer.com/10.1007/s00467-007-0492-4
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http://dx.doi.org/10.1007/s00467-007-0492-4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1915619PMC
August 2007

TNFa microsatellite polymorphism modulates the risk of type 1 diabetes in the Belgian population, independent of HLA-DQ.

Hum Immunol 2007 Aug 11;68(8):690-7. Epub 2007 Jun 11.

Diabetes Research Center, Molecular Diagnosis Unit, Vrije Universiteit Brussel, Brussels, Belgium.

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http://dx.doi.org/10.1016/j.humimm.2007.05.001DOI Listing
August 2007

MICA marks additional risk factors for Type 1 diabetes on extended HLA haplotypes: an association and meta-analysis.

Mol Immunol 2007 Apr 12;44(11):2806-12. Epub 2007 Mar 12.

Complex Genetic Section, Department of Medical Genetics, University Medical Center Utrecht, P.O. Box 85060, 3508 AB Utrecht, The Netherlands.

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http://dx.doi.org/10.1016/j.molimm.2007.01.032DOI Listing
April 2007

Explorative two-locus linkage analysis suggests a multiplicative interaction between the 7q32 and 16p13 myoclonic seizures-related photosensitivity loci.

Genet Epidemiol 2007 Jan;31(1):42-50

Complex Genetics Section, DBG-Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.

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http://dx.doi.org/10.1002/gepi.20190DOI Listing
January 2007

Heterogeneity at the JME 6p11-12 locus: absence of mutations in the EFHC1 gene in linked Dutch families.

Epilepsia 2006 Oct;47(10):1743-6

Complex Genetics Section, DBG-Department of Medical Genetics, University Medical Center Utrecht, Utrecht, the Netherlands.

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http://dx.doi.org/10.1111/j.1528-1167.2006.00676.xDOI Listing
October 2006

MICA is associated with type 1 diabetes in the Belgian population, independent of HLA-DQ.

Hum Immunol 2006 Jan-Feb;67(1-2):94-101. Epub 2006 Mar 31.

Diabetes Research Center, Molecular Diagnosis Unit, Vrije Universteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium.

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http://dx.doi.org/10.1016/j.humimm.2006.02.032DOI Listing
August 2006

CTLA4 is differently associated with autoimmune diseases in the Dutch population.

Hum Genet 2006 Mar;119(1-2):225

Department of Medical Genetics, University Medical Centre, Wilhelmina Children's Hospital, PO Box 85090, 3508 AB, Utrecht, The Netherlands.

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http://dx.doi.org/10.1007/s00439-005-0087-8DOI Listing
March 2006

Oligogenic inheritance in photosensitive juvenile myoclonic epilepsy?

Epileptic Disord 2006 Mar;8(1):32-6

Epilepsy Institute of the Netherlands SEIN, Heemstede, The Netherlands.

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March 2006

Detecting multiple associations in genome-wide studies.

Hum Genomics 2006 Mar;2(5):310-7

MRC Biostatistics Unit, Cambridge, UK.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3500180PMC
March 2006