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The Distinct Traits of the UNC13A Polymorphism in Amyotrophic Lateral Sclerosis.
Published in:
2020
By:
- Tan, Harold H. G.;
- Westeneng, Henk‐Jan;
- Burgh, Hannelore K.;
- Es, Michael A.;
- Bakker, Leonhard A.;
- Veenhuijzen, Kevin;
- Eijk, Kristel R.;
- Eijk, Ruben P. A.;
- Veldink, Jan H.;
- Berg, Leonard H.;
- Westeneng, Henk-Jan;
- van der Burgh, Hannelore K;
- van Es, Michael A;
- van Veenhuijzen, Kevin;
- van Eijk, Kristel R;
- van Eijk, Ruben P A;
- van den Berg, Leonard H
Publication type:
journal article
DRD2 Schizophrenia-Risk Allele Is Associated With Impaired Striatal Functioning in Unaffected Siblings of Schizophrenia Patients.
Published in:
Schizophrenia Bulletin, 2016, v. 42, n. 3, p. 843, doi. 10.1093/schbul/sbv166
By:
- Vink, Matthijs;
- de Leeuw, Max;
- Luykx, Jurjen J.;
- van Eijk, Kristel R.;
- van den Munkhof, Hanna E.;
- van Buuren, Mariët;
- Kahn, René S.
Publication type:
Article
Associations Between Polygenic Risk Score Loading, Psychosis Liability, and Clozapine Use Among Individuals With Schizophrenia.
Published in:
JAMA Psychiatry, 2023, v. 80, n. 2, p. 181, doi. 10.1001/jamapsychiatry.2022.4234
By:
- Lin, Bochao D.;
- Pinzón-Espinosa, Justo;
- Blouzard, Elodie;
- van der Horst, Marte Z.;
- Okhuijsen-Pfeifer, Cynthia;
- van Eijk, Kristel R.;
- Guloksuz, Sinan;
- Peyrot, Wouter J.;
- Luykx, Jurjen J.
Publication type:
Article
Association of Recent Stressful Life Events With Mental and Physical Health in the Context of Genomic and Exposomic Liability for Schizophrenia.
Published in:
2020
By:
- Pries, Lotta-Katrin;
- van Os, Jim;
- ten Have, Margreet;
- de Graaf, Ron;
- van Dorsselaer, Saskia;
- Bak, Maarten;
- Lin, Bochao D.;
- van Eijk, Kristel R.;
- Kenis, Gunter;
- Richards, Alexander;
- O'Donovan, Michael C.;
- Luykx, Jurjen J.;
- Rutten, Bart P. F.;
- Guloksuz, Sinan
Publication type:
journal article
The role of rare compound heterozygous events in autism spectrum disorder.
Published in:
Translational Psychiatry, 2020, v. 10, n. 1, p. 1, doi. 10.1038/s41398-020-00866-7
By:
- 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
Publication type:
Article
Age- and sex-specific associations between risk scores for schizophrenia and self-reported health in the general population.
Published in:
Social Psychiatry & Psychiatric Epidemiology, 2023, v. 58, n. 1, p. 43, doi. 10.1007/s00127-022-02346-3
By:
- 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
Publication type:
Article
Characterization of Genome-Methylome Interactions in 22 Nuclear Pedigrees.
Published in:
PLoS ONE, 2014, v. 9, n. 7, p. 1, doi. 10.1371/journal.pone.0099313
By:
- 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
Publication type:
Article
Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.
Published in:
NPJ Genomic Medicine, 2022, v. 7, n. 1, p. 1, doi. 10.1038/s41525-021-00267-9
By:
- Al Khleifat, Ahmad;
- Iacoangeli, Alfredo;
- van Vugt, Joke J. F. A.;
- Bowles, Harry;
- Moisse, Matthieu;
- Zwamborn, Ramona A. J.;
- van der Spek, Rick A. A.;
- Shatunov, Aleksey;
- Cooper-Knock, Johnathan;
- Topp, Simon;
- Byrne, Ross;
- Gellera, Cinzia;
- López, Victoria;
- Jones, Ashley R.;
- Opie-Martin, Sarah;
- Vural, Atay;
- Campos, Yolanda;
- van Rheenen, Wouter;
- Kenna, Brendan;
- Van Eijk, Kristel R.
Publication type:
Article
Childhood maltreatment mediates the effect of the genetic background on psychosis risk in young adults.
Published in:
Translational Psychiatry, 2022, v. 12, n. 1, p. 1, doi. 10.1038/s41398-022-01975-1
By:
- 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.
Publication type:
Article
Identification of schizophrenia-associated loci by combining DNA methylation and gene expression data from whole blood.
Published in:
European Journal of Human Genetics, 2015, v. 23, n. 8, p. 1106, doi. 10.1038/ejhg.2014.245
By:
- van Eijk, Kristel R;
- de Jong, Simone;
- Strengman, Eric;
- Buizer-Voskamp, Jacobine E;
- Kahn, René S;
- Boks, Marco P;
- Horvath, Steve;
- Ophoff, Roel A
Publication type:
Article
Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes.
Published in:
European Journal of Human Genetics, 2012, v. 20, n. 9, p. 1004, doi. 10.1038/ejhg.2012.38
By:
- de Jong, Simone;
- van Eijk, Kristel R;
- Zeegers, Dave W L H;
- Strengman, Eric;
- Janson, Esther;
- Veldink, Jan H;
- van den Berg, Leonard H;
- Cahn, Wiepke;
- Kahn, René S;
- Boks, Marco P M;
- Ophoff, Roel A
Publication type:
Article
A Common Variant in ERBB4 Regulates GABA Concentrations in Human Cerebrospinal Fluid.
Published in:
Neuropsychopharmacology, 2012, v. 37, n. 9, p. 2088, doi. 10.1038/npp.2012.57
By:
- Luykx, Jurjen J;
- Vinkers, Christiaan H;
- Bakker, Steven C;
- Visser, Wouter F;
- van Boxmeer, Loes;
- Strengman, Eric;
- van Eijk, Kristel R;
- Lens, Judith A;
- Borgdorff, Paul;
- Keijzers, Peter;
- Kappen, Teus H;
- van Dongen, Eric P A;
- Bruins, Peter;
- Verhoeven, Nanda M;
- de Koning, Tom J;
- Kahn, René S;
- Ophoff, Roel A
Publication type:
Article
Association of Risk Variants in the CFH Gene With Elevated Levels of Coagulation and Complement Factors in Idiopathic Multifocal Choroiditis.
Published in:
JAMA Ophthalmology, 2023, v. 141, n. 8, p. 737, doi. 10.1001/jamaophthalmol.2023.2557
By:
- 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.
Publication type:
Article
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia.
Published in:
Nature Communications, 2017, v. 8, n. 3, p. 14774, doi. 10.1038/ncomms14774
By:
- 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.
Publication type:
Article
Genome‐wide association meta‐analysis of age at first cannabis use.
Published in:
Addiction, 2018, v. 113, n. 11, p. 2073, doi. 10.1111/add.14368
By:
- Minică, Camelia C.;
- Verweij, Karin J. H.;
- Most, Peter J.;
- Mbarek, Hamdi;
- Bernard, Manon;
- Eijk, Kristel R.;
- Lind, Penelope A.;
- Liu, Meng Zhen;
- Maciejewski, Dominique F.;
- Palviainen, Teemu;
- Sánchez‐Mora, Cristina;
- Sherva, Richard;
- Taylor, Michelle;
- Walters, Raymond K.;
- Abdellaoui, Abdel;
- Bigdeli, Timothy B.;
- Branje, Susan J. T.;
- Brown, Sandra A.;
- Casas, Miguel;
- Corley, Robin P.
Publication type:
Article
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Published in:
2020
By:
- van der Lee, Sven J.;
- Conway, Olivia J.;
- Jansen, Iris;
- Carrasquillo, Minerva M.;
- Kleineidam, Luca;
- van den Akker, Erik;
- Hernández, Isabel;
- van Eijk, Kristel R.;
- Stringa, Najada;
- Chen, Jason A.;
- Zettergren, Anna;
- Andlauer, Till F. M.;
- Diez-Fairen, Monica;
- Simon-Sanchez, Javier;
- Lleó, Alberto;
- Zetterberg, Henrik;
- Nygaard, Marianne;
- Blauwendraat, Cornelis;
- Savage, Jeanne E.;
- Mengel-From, Jonas
Publication type:
Correction Notice
A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
Published in:
Acta Neuropathologica, 2019, v. 138, n. 2, p. 237, doi. 10.1007/s00401-019-02026-8
By:
- van der Lee, Sven J.;
- Conway, Olivia J.;
- Jansen, Iris;
- Carrasquillo, Minerva M.;
- Kleineidam, Luca;
- van den Akker, Erik;
- Hernández, Isabel;
- van Eijk, Kristel R.;
- Stringa, Najada;
- Chen, Jason A.;
- Zettergren, Anna;
- Andlauer, Till F. M.;
- Diez-Fairen, Monica;
- Simon-Sanchez, Javier;
- Lleó, Alberto;
- Zetterberg, Henrik;
- Nygaard, Marianne;
- Blauwendraat, Cornelis;
- Savage, Jeanne E.;
- Mengel-From, Jonas
Publication type:
Article
Exome array analysis of rare and low frequency variants in amyotrophic lateral sclerosis.
Published in:
Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-42091-3
By:
- 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.
Publication type:
Article
Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS.
Published in:
Science Translational Medicine, 2022, v. 14, n. 633, p. 1, doi. 10.1126/scitranslmed.abj0264
By:
- Hop, Paul J.;
- Zwamborn, Ramona A.J.;
- Hannon, Eilis;
- Shireby, Gemma L.;
- Nabais, Marta F.;
- Walker, Emma M.;
- van Rheenen, Wouter;
- van Vugt, Joke J.F.A.;
- Dekker, Annelot M.;
- Westeneng, Henk-Jan;
- Tazelaar, Gijs H.P.;
- van Eijk, Kristel R.;
- Moisse, Matthieu;
- Baird, Denis;
- Al Khleifat, Ahmad;
- Iacoangeli, Alfredo;
- Ticozzi, Nicola;
- Ratti, Antonia;
- Cooper-Knock, Jonathan;
- Morrison, Karen E.
Publication type:
Article
Whole blood transcriptome analysis in amyotrophic lateral sclerosis: A biomarker study.
Published in:
PLoS ONE, 2018, v. 13, n. 6, p. 1, doi. 10.1371/journal.pone.0198874
By:
- 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.
Publication type:
Article
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects.
Published in:
BMC Genomics, 2012, v. 13, n. 1, p. 636, doi. 10.1186/1471-2164-13-636
By:
- van Eijk, Kristel R.;
- de Jong, Simone;
- Boks, Marco P. M.;
- Langeveld, Terry;
- Colas, Fabrice;
- Veldink, Jan H.;
- de Kovel, Carolien G. F.;
- Janson, Esther;
- Strengman, Eric;
- Langfelder, Peter;
- Kahn, Ren� S.;
- van den Berg, Leonard H.;
- Horvath, Steve;
- Ophoff, Roel A.
Publication type:
Article
Using genome-wide pathway analysis to unravel the etiology of complex diseases.
Published in:
Genetic Epidemiology, 2009, v. 33, n. 5, p. 419, doi. 10.1002/gepi.20395
By:
- Elbers, Clara C.;
- van Eijk, Kristel R.;
- Franke, Lude;
- Mulder, Flip;
- van der Schouw, Yvonne T.;
- Wijmenga, Cisca;
- Onland-Moret, N. Charlotte
Publication type:
Article

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