Arvid Suls

Arvid Suls

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Arvid Suls

Arvid Suls

Publications by authors named "Arvid Suls"

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Large-scale analysis of methylation reveals its potential as biomarker for breast cancer.

Clin Epigenetics 2018 11;10:51. Epub 2018 Apr 11.

Center of Medical Genetics, University of Antwerp and Antwerp University Hospital, Prins Boudewijnlaan 43/6, BE-2650 Edegem, Antwerp Belgium.

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http://dx.doi.org/10.1186/s13148-018-0479-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896072PMC
May 2019

Methylation analysis of Gasdermin E shows great promise as a biomarker for colorectal cancer.

Cancer Med 2019 May 16;8(5):2133-2145. Epub 2019 Apr 16.

Centre of Medical Genetics, University of Antwerp and Antwerp University Hospital, Edegem, Belgium.

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https://onlinelibrary.wiley.com/doi/abs/10.1002/cam4.2103
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http://dx.doi.org/10.1002/cam4.2103DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6536921PMC
May 2019

Memory CD4 T cell receptor repertoire data mining as a tool for identifying cytomegalovirus serostatus.

Genes Immun 2019 03 15;20(3):255-260. Epub 2018 Jun 15.

AUDACIS, Antwerp Unit for Data Analysis and Computation in Immunology and Sequencing, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1038/s41435-018-0035-yDOI Listing
March 2019

Transcriptome profiling in blood before and after hepatitis B vaccination shows significant differences in gene expression between responders and non-responders.

Vaccine 2018 10 8;36(42):6282-6289. Epub 2018 Sep 8.

Department of Medical Genetics, University of Antwerp/Antwerp University Hospital, Edegem, Belgium; AUDACIS, Antwerp Unit for Data Analysis and Computation in Immunology and Sequencing, University of Antwerp, Antwerp, Belgium. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S0264410X183123
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http://dx.doi.org/10.1016/j.vaccine.2018.09.001DOI Listing
October 2018

On the feasibility of mining CD8+ T cell receptor patterns underlying immunogenic peptide recognition.

Immunogenetics 2018 03 4;70(3):159-168. Epub 2017 Aug 4.

Advanced Database Research and Modelling (ADReM), Department of Mathematics and Computer Science, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1007/s00251-017-1023-5DOI Listing
March 2018

Lessons learned from gene identification studies in Mendelian epilepsy disorders.

Eur J Hum Genet 2016 07 25;24(7):961-7. Epub 2015 Nov 25.

VIB-Department of Molecular Genetics, Neurogenetics Group, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1038/ejhg.2015.251DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070902PMC
July 2016

Simultaneous impairment of neuronal and metabolic function of mutated gephyrin in a patient with epileptic encephalopathy.

EMBO Mol Med 2015 Dec;7(12):1580-94

Department of Chemistry, Institute of Biochemistry University of Cologne, Cologne, Germany Center for Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany Cologne Excellence Cluster on Cellular Stress Responses in Aging-Associated Diseases (CECAD) University of Cologne, Cologne, Germany

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http://dx.doi.org/10.15252/emmm.201505323DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4693503PMC
December 2015

Do Glut1 (glucose transporter type 1) defects exist in epilepsy patients responding to a ketogenic diet?

Epilepsy Res 2015 Aug 1;114:47-51. Epub 2015 May 1.

Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany. Electronic address:

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http://dx.doi.org/10.1016/j.eplepsyres.2015.04.012DOI Listing
August 2015

Early and effective treatment of KCNQ2 encephalopathy.

Epilepsia 2015 May 16;56(5):685-91. Epub 2015 Apr 16.

Department of Neurology, University of California, San Francisco, San Francisco, California, U.S.A.

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http://dx.doi.org/10.1111/epi.12984DOI Listing
May 2015

DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsy.

Neurology 2014 Jun 9;82(23):2101-6. Epub 2014 May 9.

From the Department of Neurology (F.P.), and Service of Genetic Medicine (S.E.A.), University Hospitals of Geneva; Department of Genetic Medicine and Development (P.M.), and iGE3, Institute of Genetics and Genomics of Geneva (S.E.A.), University of Geneva, Switzerland; Institut national de la santé et de la recherche médicale (INSERM) (V.N., S.I., C.D., I.A.-G., M.V., M.B., E.L., S.B.), U1127, ICM, Paris, F-75013 Paris; Sorbonne Universités, UPMC Univ Paris 06, UMR S 1127, F-75013 Paris (V.N., S.I., C.D., I.A.-G., M.V., M.B., E.L., S.B.), Paris; CNRS (V.N., S.I., C.D., I.A.-G., M.V., M.B., E.L., S.B.), UMR7225, Hôpital de la Pitié-Salpêtrière, Paris; Epilepsy Unit (V.N., I.A.-G., M.V., M.B.), ICM, Paris, F-75013 Paris, France (V.N., S.I., C.D., I.A.-G., M.V., M.B., E.L., S.B.), and Département de Génétique et de Cytogénétique (C.D., E.L.), AP-HP Groupe hospitalier Pitié-Salpêtrière, Paris; Epilepsy, Sleep and Pediatric Neurophysiology (J.d.B.), University Hospitals of Lyon; Hospices Civils de Lyon (D.V.), HFME, centre de référence déficiences intellectuelles de causes rares et sclérose tubéreuse de Bourneville, Bron, France; Neurogenetics Group (S.W., A.S., P.D.J.), Department of Molecular Genetics, VIB, Antwerp; Laboratory of Neurogenetics (S.W., A.S., P.D.J.), Institute Born-Bunge, University of Antwerp, Belgium; Epilepsy Centre Kempenhaeghe (S.W.), Oosterhout, the Netherlands; Algemeen Stedelijk Ziekenhuis (E.F.), Aalst; Division of Neurology (P.D.J.), Antwerp University Hospital, Antwerp University, Belgium; Centre hospitalier général de Valence (M.V.R.); Department of Medical Genetics (G.L.), Hospices Civils de Lyon; Claude Bernard Lyon I University (G.L.); CRNL (G.L.), CNRS UMR 5292, INSERM U1028, Lyon; Centre de référence épilepsies rares et Sclérose tubéreuse de Bourneville (I.A.-G., M.B.); Genotyping and Sequencing Platform, ICM (E.M.), and DNA and Cell Bank (P.C.), Hôpital Pitié-Salpêtrière, Paris, France; Department of Surge

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http://dx.doi.org/10.1212/WNL.0000000000000488DOI Listing
June 2014

GABRA1 and STXBP1: novel genetic causes of Dravet syndrome.

Neurology 2014 Apr 12;82(14):1245-53. Epub 2014 Mar 12.

From the Division of Genetic Medicine, Department of Pediatrics (G.L.C., C.H., J.C., E.G., H.C.M.), and the Department of Genome Sciences (J.S.), University of Washington, Seattle; Neurogenetics Group (S.W.), Department of Molecular Genetics, VIB, Antwerp; Laboratory of Neurogenetics (S.W., A.S., P.D.J.), Institute Born-Bunge, University of Antwerp, Belgium; Epilepsy Centre Kempenhaeghe (S.W.), Oosterhout, the Netherlands; Epilepsy Research Centre (J.M.M., S.F.B., I.E.S.), Department of Medicine, University of Melbourne, Austin Health, Australia; Department of Neuropediatrics (C.H., H.M., S.v.S., I.H.), University Medical Center, Schleswig-Holstein, Christian-Albrechts University, Kiel, Germany; Danish Epilepsy Centre (R.S.M., H.H., M.N.), Dianalund; Institute for Regional Health Services (H.H., M.N.), University of Southern Denmark, Odense, Denmark; Department of Molecular and Medical Genetics (B.J.O.), Oregon Health and Science University, Portland; Florey Institute (S.P., A.C., E.V.G., I.E.S.), Victoria; TY Nelson Department of Neurology (D.G.), The Children's Hospital at Westmead, Sydney, NSW, Australia; Department of Paediatrics (L.G.S.), School of Medicine and Health Sciences, University of Otago, Wellington, New Zealand; Epilepsy Research Program (B.L.H., L.M.D.), School of Pharmacy and Medical Sciences, University of South Australia, Adelaide; Division of Neurology (P.D.J.), Antwerp University Hospital, Belgium; and the Department of Paediatrics (I.E.S.), University of Melbourne, Royal Children's Hospital, Australia.

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http://www.washington.edu/medicine/pediatrics/meflab/doc/201
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http://www.neurology.org/cgi/doi/10.1212/WNL.000000000000029
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http://dx.doi.org/10.1212/WNL.0000000000000291DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4001207PMC
April 2014

Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.

Ann Neurol 2014 Mar 18;75(3):382-94. Epub 2014 Mar 18.

Department of Neurology and Epileptology, Hertie Institute for Clinical Brain Research, University of Tübingen, Tübingen, Germany.

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http://dx.doi.org/10.1002/ana.24080DOI Listing
March 2014

Extending the KCNQ2 encephalopathy spectrum: clinical and neuroimaging findings in 17 patients.

Neurology 2013 Nov 9;81(19):1697-703. Epub 2013 Oct 9.

From the Neurogenetics Group (S.W., R.H., A.S., P.D.J.), Department of Molecular Genetics, VIB, Antwerp; Laboratory of Neurogenetics (S.W., R.H., A.S., P.D.J.), Institute Born-Bunge, University of Antwerp, Belgium; Epilepsy Centre Kempenhaeghe (S.W.), Oosterhout, the Netherlands; Department of Paediatrics (V.I.), University Hospital Centre Zagreb, Croatia; Division of Pediatric Neurology and Metabolism (R.V.C.), Department of Pediatrics, University Hospital Ghent, Belgium; Danish Epilepsy Centre (H.H., R.S.M.), Dianalund; Institute for Regional Health Research (H.H.), University of Southern Denmark, Odense; Department of Child Neurology (S.G.), Juliane Marie Center, Rigshospital, Copenhagen, Denmark; Pediatric Neurology (A.-S.S., B.C.), Department of Neurology (A.-S.S., B.C., P.D.J.), Antwerp University Hospital, Antwerp University, Antwerp, Belgium; Epilepsy Research Centre (S.B.H., S.M., I.S.), Department of Medicine, University of Melbourne, Austin Health, Australia; Great Ormond Street Hospital (C.E.), London; Institute of Genetic Medicine (R.H.), Newcastle University, UK; Child Neurology and Neurorehabilitation Unit (G.C., M.A.), Department of Pediatrics, Central Hospital of Bolzano; Neurology Unit and laboratories (T.P., R.G., C.M.), A. Meyer Children's Hospital, Florence; Child Neuropsychiatry Unit (L.G.), Spedali Civili, Brescia, Italy; Pädiatrie I (K.R., E.H.), Division of Pediatric Neurology, University Hospital Innsbruck, Austria; University Hospital Essen (B.A.), University Duisburg-Essen; Department of Paediatric Neurology and Developmental Medicine (A.B.), University Children's Hospital Tübingen, Eberhard Karls University of Tübingen; Center for Child Neurology (I.B.), Sana Krankenhaus Gerresheim, Düsseldorf; Department of Neuropediatrics (S.S.), Hospital for Children and Adolescents, University of Leipzig, Germany; Department of Neurology (B.S., A.P.), Boston Children's Hospital, Harvard School of Medicine; Department of Biology (B.S.), Brandeis U

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http://dx.doi.org/10.1212/01.wnl.0000435296.72400.a1DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3812107PMC
November 2013

Duplications of 17q12 can cause familial fever-related epilepsy syndromes.

Neurology 2013 Oct 18;81(16):1434-40. Epub 2013 Sep 18.

From the Neurogenetics Group (K.H., S.W., P.H., P.D.J., A.S.), Department of Molecular Genetics, VIB, Antwerp; Laboratory of Neurogenetics (K.H., S.W., P.H., P.D.J., A.S.), Institute Born-Bunge, University of Antwerp; Department of Neurology (E.P., W.V.P.), University Hospital Gasthuisberg, Leuven; Center for Human Genetics (H.V.E.), University Hospitals Leuven, KU Leuven; and Division of Neurology (P.D.J.), Antwerp University Hospital, Antwerp, Belgium.

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http://dx.doi.org/10.1212/WNL.0b013e3182a84163DOI Listing
October 2013

Head stereotypies in STXBP1 encephalopathy.

Dev Med Child Neurol 2013 Aug 13;55(8):769-72. Epub 2013 Jun 13.

Department of Medicine, Epilepsy Research Centre, The University of Melbourne, Austin Health, Melbourne, Vic., Australia.

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http://dx.doi.org/10.1111/dmcn.12197DOI Listing
August 2013

The role of SLC2A1 in early onset and childhood absence epilepsies.

Epilepsy Res 2013 Jul 8;105(1-2):229-33. Epub 2013 Jan 8.

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

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http://dx.doi.org/10.1016/j.eplepsyres.2012.11.004DOI Listing
July 2013

Do mutations in SCN1B cause Dravet syndrome?

Epilepsy Res 2013 Jan 20;103(1):97-100. Epub 2012 Nov 20.

Epilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, Melbourne, Australia.

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http://dx.doi.org/10.1016/j.eplepsyres.2012.10.009DOI Listing
January 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
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http://dx.doi.org/10.1093/hmg/dds373DOI Listing
December 2012

A novel autosomal dominant GDAP1 mutation in an Italian CMT2 family.

J Peripher Nerv Syst 2012 Sep;17(3):351-5

Department of Neurological Sciences, University Federico II of Naples, Naples, Italy.

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http://doi.wiley.com/10.1111/j.1529-8027.2012.00414.x
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http://dx.doi.org/10.1111/j.1529-8027.2012.00414.xDOI Listing
September 2012

Neonatal seizures associated with a severe neonatal myoclonus like dyskinesia due to a familial KCNQ2 gene mutation.

Eur J Paediatr Neurol 2012 Jul 14;16(4):356-60. Epub 2011 Dec 14.

Pediatric Neurology Unit, Wolfson Medical Center, Holon, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel.

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http://dx.doi.org/10.1016/j.ejpn.2011.11.004DOI Listing
July 2012

Glucose transporter 1 deficiency as a treatable cause of myoclonic astatic epilepsy.

Arch Neurol 2011 Sep 9;68(9):1152-5. Epub 2011 May 9.

Epilepsy Research Centre, Department of Medicine, University of Melbourne, Melbourne, Australia.

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http://dx.doi.org/10.1001/archneurol.2011.102DOI Listing
September 2011

"Benign" myoclonic epilepsy of infancy as the initial presentation of glucose transporter-1 deficiency.

Epileptic Disord 2011 Sep;13(3):300-3

Department of Pediatric Neurology, ULB-Erasme Hospital, Brussels, Belgium.

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http://www.john-libbey-eurotext.fr/medline.md?doi=10.1684/ep
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http://dx.doi.org/10.1684/epd.2011.0452DOI Listing
September 2011

The genetics of Dravet syndrome.

Epilepsia 2011 Apr;52 Suppl 2:24-9

Pediatric Neurology Unit and Laboratories, Children's Hospital A Meyer - University of Florence, Florence, Italy.

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http://dx.doi.org/10.1111/j.1528-1167.2011.02997.xDOI Listing
April 2011

The SCN1A variant database: a novel research and diagnostic tool.

Hum Mutat 2009 Oct;30(10):E904-20

Neurogenetics Group, VIB Department of Molecular Genetics, University of Antwerp, Antwerp, Belgium.

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http://dx.doi.org/10.1002/humu.21083DOI Listing
October 2009

Epilepsy as part of the phenotype associated with ATP1A2 mutations.

Epilepsia 2008 Mar 19;49(3):500-8. Epub 2007 Nov 19.

Neurogenetics Group, Department of Molecular Genetics, VIB; Antwerpen, Belgium.

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http://dx.doi.org/10.1111/j.1528-1167.2007.01415.xDOI Listing
March 2008