Efficient Computation of Significance Levels for Multiple Associations in Large Studies of Correlated Data, Including Genomewide Association Studies

gan Dudbridge, Frank, Koeleman, Bobby P. C.
Cyhoeddwyd 2004

Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy

gan Schijven, Dick, Stevelink, Remi, McCormack, Mark, van Rheenen, Wouter, Luykx, Jurjen J., Koeleman, Bobby P.C., Veldink, Jan H.
Cyhoeddwyd yn Neurobiol Aging (2020)

Assessing the genetic association between vitamin B6 metabolism and genetic generalized epilepsy

gan Stevelink, Remi, Pangilinan, Faith, Jansen, Floor E., Braun, Kees P.J., Molloy, Anne M., Brody, Lawrence C., Koeleman, Bobby P.C.
Cyhoeddwyd yn Mol Genet Metab Rep (2019)

Symptomatology of carbamazepine‐ and oxcarbazepine‐induced hyponatremia in people with epilepsy

gan Berghuis, Bianca, Hulst, Janic, Sonsma, Anja, McCormack, Mark, de Haan, Gerrit‐Jan, Sander, Josemir W., Lindhout, Dick, Koeleman, Bobby P. C.
Cyhoeddwyd yn Epilepsia (2021)

Febrile temperatures unmask biophysical defects in Na(v)1.1 epilepsy mutations supportive of seizure initiation

gan Volkers, Linda, Kahlig, Kristopher M., Das, Joost H.G., van Kempen, Marjan J.A., Lindhout, Dick, Koeleman, Bobby P.C., Rook, Martin B.
Cyhoeddwyd 2013

Implications of genetic diagnostics in epilepsy surgery candidates: A single‐center cohort study

gan Sanders, Maurits W. C. B., Lemmens, Cynthia M. C., Jansen, Floor E., Brilstra, Eva H., Koeleman, Bobby P. C., Braun, Kees P. J.
Cyhoeddwyd yn Epilepsia Open (2019)

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

gan van Eerde, Albertien M., Koeleman, Bobby P. C., van de Kamp, Jiddeke M., de Jong, Tom P. V. M., Wijmenga, Cisca, Giltay, Jacques C.
Cyhoeddwyd 2007

Clinical and genetic correlates of islet-autoimmune signatures in juvenile-onset type 1 diabetes

gan Claessens, Laura A., Wesselius, Joris, van Lummel, Menno, Laban, Sandra, Mulder, Flip, Mul, Dick, Nikolic, Tanja, Aanstoot, Henk-Jan, Koeleman, Bobby P. C., Roep, Bart O.
Cyhoeddwyd yn Diabetologia (2019)

Association study of genetic variants of pro-inflammatory chemokine and cytokine genes in systemic lupus erythematosus

gan Sánchez, Elena, Sabio, José M, Callejas, José L, de Ramón, Enrique, Garcia-Portales, Rosa, García-Hernández, Francisco J, Jiménez-Alonso, Juan, González-Escribano, Ma Francisca, Martín, Javier, Koeleman, Bobby P
Cyhoeddwyd 2006

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

gan Boshuisen, Kim, Brundel, Manon, de Kovel, Carolien G.F., Letteboer, Tom G., Rinkel, Gabriel J.E., Westermann, Cornelis J.J., Kim, Helen, Pawlikowska, Ludmila, Koeleman, Bobby P.C., Klijn, Catharina J.M.
Cyhoeddwyd 2012

Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease

gan Stevens, Kristen N., Hakonarson, Hakon, Kim, Cecilia E., Doevendans, Pieter A., Koeleman, Bobby P. C., Mital, Seema, Raue, Jennifer, Glessner, Joseph T., Coles, John G., Moreno, Victor, Granger, Anne, Gruber, Stephen B., Gruber, Peter J.
Cyhoeddwyd 2010

NaV1.1 and NaV1.6 selective compounds reduce the behavior phenotype and epileptiform activity in a novel zebrafish model for Dravet Syndrome

gan Weuring, Wout J., Singh, Sakshi, Volkers, Linda, Rook, Martin B., van ‘t Slot, Ruben H., Bosma, Marjolein, Inserra, Marco, Vetter, Irina, Verhoeven-Duif, Nanda M., Braun, Kees P. J., Rivara, Mirko, Koeleman, Bobby P. C.
Cyhoeddwyd yn PLoS One (2020)

Na(v)1.1 Dysfunction in Genetic Epilepsy with Febrile Seizures Plus or Dravet Syndrome

gan Volkers, Linda, Kahlig, Kristopher M., Verbeek, Nienke E., Das, Joost H.G., van Kempen, Marjan J.A., Stroink, Hans, Augustijn, Paul, van Nieuwenhuizen, Onno, Lindhout, Dick, George, Alfred L., Koeleman, Bobby P.C., Rook, Martin B.
Cyhoeddwyd 2011

A Genome-Wide Investigation of Copy Number Variation in Patients with Sporadic Brain Arteriovenous Malformation

gan Bendjilali, Nasrine, Kim, Helen, Weinsheimer, Shantel, Guo, Diana E., Kwok, Pui-Yan, Zaroff, Jonathan G., Sidney, Stephen, Lawton, Michael T., McCulloch, Charles E., Koeleman, Bobby P. C., Klijn, Catharina J. M., Young, William L., Pawlikowska, Ludmila
Cyhoeddwyd 2013

Modifier genes in SCN1A‐related epilepsy syndromes

gan de Lange, Iris M., Mulder, Flip, van 't Slot, Ruben, Sonsma, Anja C. M., van Kempen, Marjan J. A., Nijman, Isaac J., Ernst, Robert F., Knoers, Nine V. A. M., Brilstra, Eva H., Koeleman, Bobby P. C.
Cyhoeddwyd yn Mol Genet Genomic Med (2020)

Erratum to: Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

gan Boerma, Ragna S., Braun, Kees P., van den Broek, Marcel P. H., van Berkestijn, Frederique M. C., Swinkels, Marielle E., Hagebeuk, Eveline O., Lindhout, Dick, van Kempen, Marjan, Boon, Maartje, Nicolai, Joost, de Kovel, Carolien G., Brilstra, Eva H., Koeleman, Bobby P. C.
Cyhoeddwyd yn Neurotherapeutics (2015)

Remarkable Phenytoin Sensitivity in 4 Children with SCN8A-related Epilepsy: A Molecular Neuropharmacological Approach

gan Boerma, Ragna S., Braun, Kees P., van de Broek, Maarten P. H., van Berkestijn, Frederique M. C., Swinkels, Marielle E., Hagebeuk, Eveline O., Lindhout, Dick, van Kempen, Marjan, Boon, Maartje, Nicolai, Joost, de Kovel, Carolien G., Brilstra, Eva H., Koeleman, Bobby P. C.
Cyhoeddwyd yn Neurotherapeutics (2015)

Abnormal islet sphingolipid metabolism in type 1 diabetes

gan Holm, Laurits J., Krogvold, Lars, Hasselby, Jane P., Kaur, Simranjeet, Claessens, Laura A., Russell, Mark A., Mathews, Clayton E., Hanssen, Kristian F., Morgan, Noel G., Koeleman, Bobby P. C., Roep, Bart O., Gerling, Ivan C., Pociot, Flemming, Dahl-Jørgensen, Knut, Buschard, Karsten
Cyhoeddwyd yn Diabetologia (2018)

Evaluation of genetic risk loci for intracranial aneurysms in sporadic arteriovenous malformations of the brain

gan Kremer, Philip H. C., Koeleman, Bobby P. C., Pawlikowska, Ludmila, Weinsheimer, Shantel, Bendjilali, Nasrine, Sidney, Stephen, Zaroff, Jonathan G., Rinkel, Gabriel J. E., van den Berg, Leonard H., Ruigrok, Ynte M., de Kort, Gerard A. P., Veldink, Jan H., Kim, Helen, Klijn, Catharina J. M.
Cyhoeddwyd yn J Neurol Neurosurg Psychiatry (2014)

Characterization of a de novo SCN8A mutation in a patient with epileptic encephalopathy

gan de Kovel, Carolien G.F., Meisler, Miriam H., Brilstra, Eva H., van Berkestijn, Frederique M.C., van ‘t Slot, Ruben, van Lieshout, Stef, Nijman, Isaac J, O'Brien, Janelle E., Hammer, Michael F., Estacion, Mark, Waxman, Stephen G., Dib-Hajj, Sulayman D., Koeleman, Bobby P.C.
Cyhoeddwyd yn Epilepsy Res (2014)