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Modifier genes in SCN1A‐related epilepsy syndromes.
Published in:
Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 4, p. 1, doi. 10.1002/mgg3.1103
By:
- de Lange, Iris M.;
- Mulder, Flip;
- Slot, Ruben;
- Sonsma, Anja C. M.;
- Kempen, Marjan J. A.;
- Nijman, Isaac J.;
- Ernst, Robert F.;
- Knoers, Nine V. A. M.;
- Brilstra, Eva H.;
- Koeleman, Bobby P. C.
Publication type:
Article
Clinical and genetic correlates of islet-autoimmune signatures in juvenile-onset type 1 diabetes.
Published in:
Diabetologia, 2020, v. 63, n. 2, p. 351, doi. 10.1007/s00125-019-05032-3
By:
- 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.
Publication type:
Article
A Gene Co-Expression Network in Whole Blood of Schizophrenia Patients Is Independent of Antipsychotic- Use and Enriched for Brain-Expressed Genes.
Published in:
PLoS ONE, 2012, v. 7, n. 6, p. 1, doi. 10.1371/journal.pone.0039498
By:
- de Jong, Simone;
- Boks, Marco P. M.;
- Fuller, Tova F.;
- Strengman, Eric;
- Janson, Esther;
- de Kovel, Carolien G. F.;
- Ori, Anil P. S.;
- Vi, Nancy;
- Mulder, Flip;
- Blom, Jan Dirk;
- Glenthøj, Birte;
- Schubart, Chris D.;
- Cahn, Wiepke;
- Kahn, René S.;
- Horvath, Steve;
- Ophoff, Roel A.
Publication type:
Article
Increased paternal age and the influence on burden of genomic copy number variation in the general population.
Published in:
Human Genetics, 2013, v. 132, n. 4, p. 443, doi. 10.1007/s00439-012-1261-4
By:
- Buizer-Voskamp, Jacobine;
- Blauw, Hylke;
- Boks, Marco;
- Eijk, Kristel;
- Veldink, Jan;
- Hennekam, Eric;
- Vorstman, Jacob;
- Mulder, Flip;
- Tiemeier, Henning;
- Uitterlinden, André;
- Kiemeney, Lambertus;
- den Berg, Leonard;
- Kahn, René;
- Sabatti, Chiara;
- Ophoff, Roel
Publication type:
Article
Mosaicism of de novo pathogenic SCN1A variants in epilepsy is a frequent phenomenon that correlates with variable phenotypes.
Published in:
Epilepsia (Series 4), 2018, v. 59, n. 3, p. 690, doi. 10.1111/epi.14021
By:
- de Lange, Iris M.;
- Koudijs, Marco J.;
- van ’t Slot, Ruben;
- Gunning, Boudewijn;
- Sonsma, Anja C. M.;
- van Gemert, Lisette J. J. M.;
- Mulder, Flip;
- Carbo, Ellen C.;
- van Kempen, Marjan J. A.;
- Verbeek, Nienke E.;
- Nijman, Isaac J.;
- Ernst, Robert F.;
- Savelberg, Sanne M. C.;
- Knoers, Nine V. A. M.;
- Brilstra, Eva H.;
- Koeleman, Bobby P. C.
Publication type:
Article
Influence of common SCN1A promoter variants on the severity of SCN1A‐related phenotypes.
Published in:
Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 7, p. N.PAG, doi. 10.1002/mgg3.727
By:
- Lange, Iris M.;
- Weuring, Wout;
- 't Slot, Ruben;
- Gunning, Boudewijn;
- Sonsma, Anja C. M.;
- McCormack, Mark;
- Kovel, Carolien;
- Gemert, Lisette J. J. M.;
- Mulder, Flip;
- Kempen, Marjan J. A.;
- Knoers, Nine V. A. M.;
- Brilstra, Eva H.;
- Koeleman, Bobby P. C.
Publication type:
Article
A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 22, p. 6081, doi. 10.1093/hmg/ddu307
By:
- Kuiper, Jonas J.W.;
- Van Setten, Jessica;
- Ripke, Stephan;
- Van ‘T Slot, Ruben;
- Mulder, Flip;
- Missotten, Tom;
- Baarsma, G. Seerp;
- Francioli, Laurent C.;
- Pulit, Sara L.;
- De Kovel, Carolien G.F.;
- Ten Dam-Van Loon, Ninette;
- Den Hollander, Anneke I.;
- Huis in het Veld, Paulien;
- Hoyng, Carel B.;
- Cordero-Coma, Miguel;
- Martín, Javier;
- Llorenç, Victor;
- Arya, Bharti;
- Thomas, Dhanes;
- Bakker, Steven C.
Publication type:
Article
Exome-Wide Association Analysis of Coronary Artery Disease in the Kingdom of Saudi Arabia Population.
Published in:
PLoS ONE, 2016, v. 11, n. 2, p. 1, doi. 10.1371/journal.pone.0146502
By:
- de Kovel, Carolien G.;
- Mulder, Flip;
- van Setten, Jessica;
- van ‘t Slot, Ruben;
- Al-Rubaish, Abdullah;
- Alshehri, Abdullah M.;
- Al Faraidy, Khalid;
- Al-Ali, Abdullah;
- Al-Madan, Mohammed;
- Al Aqaili, Issa;
- Larbi, Emmanuel;
- Al-Ali, Rudaynah;
- Alzahrani, Alhusain;
- Asselbergs, Folkert W.;
- Koeleman, Bobby P. C.;
- Al-Ali, Amein
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
ATG16L1 and IL23R Are Associated With Inflammatory Bowel Diseases but Not With Celiac Disease in The Netherlands.
Published in:
American Journal of Gastroenterology (Springer Nature), 2008, v. 103, n. 3, p. 621, doi. 10.1111/j.1572-0241.2007.01660.x
By:
- Weersma, Rinse K.;
- Zhernakova, Alexandra;
- Nolte, Ilja M.;
- Lefebvre, Céline;
- Rioux, John D.;
- Mulder, Flip;
- van Dullemen, Hendrik M.;
- Kleibeuker, Jan H.;
- Wijmenga, Cisca;
- Dijkstra, Gerard
Publication type:
Article
Long RNA Sequencing and Ribosome Profiling of Inflamed β-Cells Reveal an Extensive Translatome Landscape.
Published in:
2021
By:
- Thomaidou, Sofia;
- Slieker, Roderick C.;
- van der Slik, Arno R.;
- Boom, Jasper;
- Mulder, Flip;
- Munoz-Garcia, Amadeo;
- 't Hart, Leen M.;
- Koeleman, Bobby;
- Carlotti, Françoise;
- Hoeben, Rob C.;
- Roep, Bart O.;
- Mei, Hailiang;
- Zaldumbide, Arnaud
Publication type:
journal article

Found: 11