Phenome-wide and genome-wide analyses of quality of life in schizophrenia

por Pazoki, Raha, Lin, Bochao Danae, van Eijk, Kristel R., Schijven, Dick, de Zwarte, Sonja, Guloksuz, Sinan, Luykx, Jurjen J.
Publicado 2020

Phenome-wide and genome-wide analyses of quality of life in schizophrenia – ERRATUM

por Pazoki, Raha, Lin, Bochao Danae, van Eijk, Kristel R., Schijven, Dick, de Zwarte, Sonja, Guloksuz, Sinan, Luykx, Jurjen J.
Publicado 2021

Polygenic risk, familial liability and stress reactivity in psychosis: an experience sampling study

por Schick, Anita, van Winkel, Ruud, Lin, Bochao D., Luykx, Jurjen J., de Zwarte, Sonja M.C., van Eijk, Kristel R., Myin-Germeys, Inez, Reininghaus, Ulrich
Publicado 2023

Characterization of Genome-Methylome Interactions in 22 Nuclear Pedigrees

por Plongthongkum, Nongluk, van Eijk, Kristel R., de Jong, Simone, Wang, Tina, Sul, Jae Hoon, Boks, Marco P. M., Kahn, René S., Fung, Ho-Lim, Ophoff, Roel A., Zhang, Kun
Publicado 2014

Childhood maltreatment mediates the effect of the genetic background on psychosis risk in young adults

por Marchi, Mattia, Elkrief, Laurent, Alkema, Anne, van Gastel, Willemijn, Schubart, Chris D., van Eijk, Kristel R., Luykx, Jurjen J., Branje, Susan, Mastrotheodoros, Stefanos, Galeazzi, Gian M., van Os, Jim, Cecil, Charlotte A., Conrod, Patricia J., Boks, Marco P.
Publicado 2022

Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects

por van Eijk, Kristel R, de Jong, Simone, Boks, Marco PM, Langeveld, Terry, Colas, Fabrice, Veldink, Jan H, de Kovel, Carolien GF, Janson, Esther, Strengman, Eric, Langfelder, Peter, Kahn, René S, van den Berg, Leonard H, Horvath, Steve, Ophoff, Roel A
Publicado 2012

The Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis

por Tan, Harold H. G., Westeneng, Henk‐Jan, van der Burgh, Hannelore K., van Es, Michael A., Bakker, Leonhard A., van Veenhuijzen, Kevin, van Eijk, Kristel R., van Eijk, Ruben P. A., Veldink, Jan H., van den Berg, Leonard H.
Publicado 2020

Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

por McLaughlin, Russell L., Schijven, Dick, van Rheenen, Wouter, van Eijk, Kristel R., O'Brien, Margaret, Kahn, René S., Ophoff, Roel A., Goris, An, Bradley, Daniel G., Al-Chalabi, Ammar, van den Berg, Leonard H., Luykx, Jurjen J., Hardiman, Orla, Veldink, Jan H.
Publicado 2017

Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study

por van Rheenen, Wouter, Diekstra, Frank P., Harschnitz, Oliver, Westeneng, Henk-Jan, van Eijk, Kristel R., Saris, Christiaan G. J., Groen, Ewout J. N., van Es, Michael A., Blauw, Hylke M., van Vught, Paul W. J., Veldink, Jan H., van den Berg, Leonard H.
Publicado 2018

Age- and sex-specific associations between risk scores for schizophrenia and self-reported health in the general population

por Paquin, Vincent, Pries, Lotta-Katrin, ten Have, Margreet, Bak, Maarten, Gunther, Nicole, de Graaf, Ron, van Dorsselaer, Saskia, Lin, Bochao D., van Eijk, Kristel R., Kenis, Gunter, Richards, Alexander, O’Donovan, Michael C., Luykx, Jurjen J., Rutten, Bart P. F., van Os, Jim, Shah, Jai L., Guloksuz, Sinan
Publicado 2022

Analysis of FUS, PFN2, TDP-43, and PLS3 as potential disease severity modifiers in spinal muscular atrophy

por Wadman, Renske I., Jansen, Marc D., Curial, Chantall A.D., Groen, Ewout J.N., Stam, Marloes, Wijngaarde, Camiel A., Medic, Jelena, Sodaar, Peter, van Eijk, Kristel R., Huibers, Manon M.H., van Kuik, Joyce, Lemmink, Henny H., van Rheenen, Wouter, Veldink, Jan Herman, van den Berg, Leonard H., van der Pol, W. Ludo
Publicado 2019

The role of rare compound heterozygous events in autism spectrum disorder

por Lin, Bochao Danae, Colas, Fabrice, Nijman, Isaac J., Medic, Jelena, Brands, William, Parr, Jeremy R., van Eijk, Kristel R., Klauck, Sabine M., Chiocchetti, Andreas G., Freitag, Christine M., Maestrini, Elena, Bacchelli, Elena, Coon, Hilary, Vicente, Astrid, Oliveira, Guiomar, Pagnamenta, Alistair T., Gallagher, Louise, Ennis, Sean, Anney, Richard, Bourgeron, Thomas, Luykx, Jurjen J., Vorstman, Jacob
Publicado 2020

Enrichment of SARM1 alleles encoding variants with constitutively hyperactive NADase in patients with ALS and other motor nerve disorders

por Gilley, Jonathan, Jackson, Oscar, Pipis, Menelaos, Estiar, Mehrdad A, Al-Chalabi, Ammar, Danzi, Matt C, van Eijk, Kristel R, Goutman, Stephen A, Harms, Matthew B, Houlden, Henry, Iacoangeli, Alfredo, Kaye, Julia, Lima, Leandro, Ravits, John, Rouleau, Guy A, Schüle, Rebecca, Xu, Jishu, Züchner, Stephan, Cooper-Knock, Johnathan, Gan-Or, Ziv, Reilly, Mary M, Coleman, Michael P
Publicado 2021

Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis

por Dekker, Annelot M., Diekstra, Frank P., Pulit, Sara L., Tazelaar, Gijs H. P., van der Spek, Rick A., van Rheenen, Wouter, van Eijk, Kristel R., Calvo, Andrea, Brunetti, Maura, Damme, Philip Van, Robberecht, Wim, Hardiman, Orla, McLaughlin, Russell, Chiò, Adriano, Sendtner, Michael, Ludolph, Albert C., Weishaupt, Jochen H., Pardina, Jesus S. Mora, van den Berg, Leonard H., Veldink, Jan H.
Publicado 2019

Cross-reactive probes on Illumina DNA methylation arrays: a large study on ALS shows that a cautionary approach is warranted in interpreting epigenome-wide association studies

por Hop, Paul J, Zwamborn, Ramona A J, Hannon, Eilis J, Dekker, Annelot M, van Eijk, Kristel R, Walker, Emma M, Iacoangeli, Alfredo, Jones, Ashley R, Shatunov, Aleksey, Khleifat, Ahmad Al, Opie-Martin, Sarah, Shaw, Christopher E, Morrison, Karen E, Shaw, Pamela J, McLaughlin, Russell L, Hardiman, Orla, Al-Chalabi, Ammar, Van Den Berg, Leonard H, Mill, Jonathan, Veldink, Jan H
Publicado 2020

Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis

por de Groot, Evianne L., Ossewaarde–van Norel, Jeannette, de Boer, Joke H., Hiddingh, Sanne, Bakker, Bjorn, van Huet, Ramon A. C., ten Dam–van Loon, Ninette H., Thiadens, Alberta A. H. J., Meester-Smoor, Magda A., de Jong–Hesse, Yvonne, Los, Leonoor I., den Hollander, Anneke I., Boon, Camiel J. F., Kiemeney, Lambertus A., van Eijk, Kristel R., Bakker, Mark K., Hoyng, Carel B., Kuiper, Jonas J. W.
Publicado 2023

Author Correction: Integrative genetic analysis illuminates ALS heritability and identifies risk genes

por Megat, Salim, Mora, Natalia, Sanogo, Jason, Roman, Olga, Catanese, Alberto, Alami, Najwa Ouali, Freischmidt, Axel, Mingaj, Xhuljana, De Calbiac, Hortense, Muratet, François, Dirrig-Grosch, Sylvie, Dieterle, Stéphane, Van Bakel, Nick, Müller, Kathrin, Sieverding, Kirsten, Weishaupt, Jochen, Andersen, Peter Munch, Weber, Markus, Neuwirth, Christoph, Margelisch, Markus, Sommacal, Andreas, Van Eijk, Kristel R., Veldink, Jan H., Lautrette, Géraldine, Couratier, Philippe, Camuzat, Agnès, Le Ber, Isabelle, Grassano, Maurizio, Chio, Adriano, Boeckers, Tobias, Ludolph, Albert C., Roselli, Francesco, Yilmazer-Hanke, Deniz, Millecamps, Stéphanie, Kabashi, Edor, Storkebaum, Erik, Sellier, Chantal, Dupuis, Luc
Publicado 2023

Integrative genetic analysis illuminates ALS heritability and identifies risk genes

por Megat, Salim, Mora, Natalia, Sanogo, Jason, Roman, Olga, Catanese, Alberto, Alami, Najwa Ouali, Freischmidt, Axel, Mingaj, Xhuljana, De Calbiac, Hortense, Muratet, François, Dirrig-Grosch, Sylvie, Dieterle, Stéphane, Van Bakel, Nick, Müller, Kathrin, Sieverding, Kirsten, Weishaupt, Jochen, Andersen, Peter Munch, Weber, Markus, Neuwirth, Christoph, Margelisch, Markus, Sommacal, Andreas, Van Eijk, Kristel R., Veldink, Jan H., Lautrette, Géraldine, Couratier, Philippe, Camuzat, Agnès, Le Ber, Isabelle, Grassano, Maurizio, Chio, Adriano, Boeckers, Tobias, Ludolph, Albert C., Roselli, Francesco, Yilmazer-Hanke, Deniz, Millecamps, Stéphanie, Kabashi, Edor, Storkebaum, Erik, Sellier, Chantal, Dupuis, Luc
Publicado 2023

Whole-genome sequencing reveals that variants in the Interleukin 18 Receptor Accessory Protein 3′UTR protect against ALS

por Eitan, Chen, Siany, Aviad, Barkan, Elad, Olender, Tsviya, van Eijk, Kristel R., Moisse, Matthieu, Farhan, Sali M. K., Danino, Yehuda M., Yanowski, Eran, Marmor-Kollet, Hagai, Rivkin, Natalia, Yacovzada, Nancy Sarah, Hung, Shu-Ting, Cooper-Knock, Johnathan, Yu, Chien-Hsiung, Louis, Cynthia, Masters, Seth L., Kenna, Kevin P., van der Spek, Rick A. A., Sproviero, William, Al Khleifat, Ahmad, Iacoangeli, Alfredo, Shatunov, Aleksey, Jones, Ashley R., Elbaz-Alon, Yael, Cohen, Yahel, Chapnik, Elik, Rothschild, Daphna, Weissbrod, Omer, Beck, Gilad, Ainbinder, Elena, Ben-Dor, Shifra, Werneburg, Sebastian, Schafer, Dorothy P., Brown, Robert H., Shaw, Pamela J., Van Damme, Philip, van den Berg, Leonard H., Phatnani, Hemali, Segal, Eran, Ichida, Justin K., Al-Chalabi, Ammar, Veldink, Jan H., Hornstein, Eran
Publicado 2022

Telomere length analysis in amyotrophic lateral sclerosis using large-scale whole genome sequence data

por Al Khleifat, Ahmad, Iacoangeli, Alfredo, Jones, Ashley R., van Vugt, Joke J. F. A., Moisse, Matthieu, Shatunov, Aleksey, Zwamborn, Ramona A. J., van der Spek, Rick A. A., Cooper-Knock, Johnathan, Topp, Simon, van Rheenen, Wouter, Kenna, Brendan, Van Eijk, Kristel R., Kenna, Kevin, Byrne, Ross, López, Victoria, Opie-Martin, Sarah, Vural, Atay, Campos, Yolanda, Weber, Markus, Smith, Bradley, Fogh, Isabella, Silani, Vincenzo, Morrison, Karen E., Dobson, Richard, van Es, Michael A., McLaughlin, Russell L., Vourc’h, Patrick, Chio, Adriano, Corcia, Philippe, de Carvalho, Mamede, Gotkine, Marc, Panades, Monica Povedano, Mora, Jesus S., Shaw, Pamela J., Landers, John E., Glass, Jonathan D., Shaw, Christopher E., Basak, Nazli, Hardiman, Orla, Robberecht, Wim, Van Damme, Philip, van den Berg, Leonard H., Veldink, Jan H., Al-Chalabi, Ammar
Publicado 2022