The quest for genetic risk factors for Crohn's disease in the post-GWAS era

por Fransen, Karin, Mitrovic, Mitja, van Diemen, Cleo C, Weersma, Rinse K
Publicado 2011

ADAM33 Gene Polymorphisms and Mortality. A Prospective Cohort Study

por Figarska, Sylwia M., Vonk, Judith M., van Diemen, Cleo C., Postma, Dirkje S., Boezen, H. Marike
Publicado 2013

Decorin and TGF-β(1 )polymorphisms and development of COPD in a general population

por van Diemen, Cleo C, Postma, Dirkje S, Vonk, Judith M, Bruinenberg, Marcel, Nolte, Ilja M, Boezen, H Marike
Publicado 2006

A next-generation sequencing method for gene doping detection that distinguishes low levels of plasmid DNA against a background of genomic DNA

por de Boer, Eddy N., van der Wouden, Petra E., Johansson, Lennart F., van Diemen, Cleo C., Haisma, Hidde J.
Publicado 2019

Genetic Susceptibility and Predictors of Paradoxical Reactions in Buruli Ulcer

por Barogui, Yves Thierry, Klis, Sandor-Adrian, Johnson, Roch Christian, Phillips, Richard O., van der Veer, Eveline, van Diemen, Cleo, van der Werf, Tjip S., Stienstra, Ymkje
Publicado 2016

Limited Evidence for Parent-of-Origin Effects in Inflammatory Bowel Disease Associated Loci

por Fransen, Karin, Mitrovic, Mitja, van Diemen, Cleo C., B.K., Thelma, Sood, Ajit, Franke, Andre, Schreiber, Stefan, Midha, Vandana, Juyal, Garima, Potocnik, Uros, Fu, Jingyuan, Nolte, Ilja, Weersma, Rinse K.
Publicado 2012

PB1701: REPLACING THE CURRENT METHODS IN LEUKEMIA DIAGNOSTICS WITH OPTICAL GENOME MAPPING AND CAS9-DIRECTED NANOPORE SEQUENCING.

por Commandeur-Jan, Sabrina, van den Berg- de Ruiter, Eva, Vroom, Vincent, Scheper, Arjen, Johansson, Lennart, Bosscher, Laura, Rietema, Nettie, Drok, Gineke, Sikkema-Raddatz, Birgit, Knoers, Nine, van Diemen, Cleo, de Boer, Eddy
Publicado 2023

A pipeline‐friendly software tool for genome diagnostics to prioritize genes by matching patient symptoms to literature

por van der Velde, K. Joeri, van den Hoek, Sander, van Dijk, Freerk, Hendriksen, Dennis, van Diemen, Cleo C., Johansson, Lennart F., Abbott, Kristin M., Deelen, Patrick, Sikkema‐Raddatz, Birgit, Swertz, Morris A.
Publicado 2020

Copy Number Variant Analysis of Spinocerebellar Ataxia Genes in a Cohort of Dutch Patients With Cerebellar Ataxia

por Ghorbani, Fatemeh, de Boer, Eddy N., Benjamins-Stok, Marloes, Verschuuren-Bemelmans, Corien C., Knapper, Jurjen, de Boer-Bergsma, Jelkje, de Vries, Jeroen J., Sikkema-Raddatz, Birgit, Verbeek, Dineke S., Westers, Helga, van Diemen, Cleo C.
Publicado 2023

Occupational exposure to pesticides is associated with differential DNA methylation

por van der Plaat, Diana A, de Jong, Kim, de Vries, Maaike, van Diemen, Cleo C, Nedeljković, Ivana, Amin, Najaf, Kromhout, Hans, Vermeulen, Roel, Postma, Dirkje S, van Duijn, Cornelia M, Boezen, H Marike, Vonk, Judith M
Publicado 2018

From blood to lung tissue: effect of cigarette smoke on DNA methylation and lung function

por de Vries, Maaike, van der Plaat, Diana A, Nedeljkovic, Ivana, Verkaik-Schakel, Rikst Nynke, Kooistra, Wierd, Amin, Najaf, van Duijn, Cornelia M, Brandsma, Corry-Anke, van Diemen, Cleo C, Vonk, Judith M, Marike Boezen, H
Publicado 2018

Strategies in Rapid Genetic Diagnostics of Critically Ill Children: Experiences From a Dutch University Hospital

por Imafidon, Miriam E., Sikkema-Raddatz, Birgit, Abbott, Kristin M., Meems-Veldhuis, Martine T., Swertz, Morris A., van der Velde, K. Joeri, Beunders, Gea, Bos, Dennis K., Knoers, Nine V. A. M., Kerstjens-Frederikse, Wilhelmina S., van Diemen, Cleo C.
Publicado 2021

GAVIN: Gene-Aware Variant INterpretation for medical sequencing

por van der Velde, K. Joeri, de Boer, Eddy N., van Diemen, Cleo C., Sikkema-Raddatz, Birgit, Abbott, Kristin M., Knopperts, Alain, Franke, Lude, Sijmons, Rolf H., de Koning, Tom J., Wijmenga, Cisca, Sinke, Richard J., Swertz, Morris A.
Publicado 2017

A Genome-Wide Linkage Study for Chronic Obstructive Pulmonary Disease in a Dutch Genetic Isolate Identifies Novel Rare Candidate Variants

por Nedeljkovic, Ivana, Terzikhan, Natalie, Vonk, Judith M., van der Plaat, Diana A., Lahousse, Lies, van Diemen, Cleo C., Hobbs, Brian D., Qiao, Dandi, Cho, Michael H., Brusselle, Guy G., Postma, Dirkje S., Boezen, H. M., van Duijn, Cornelia M., Amin, Najaf
Publicado 2018

Feasibility of Follow-Up Studies and Reclassification in Spinocerebellar Ataxia Gene Variants of Unknown Significance

por Ghorbani, Fatemeh, Alimohamed, Mohamed Z., Vilacha, Juliana F., Van Dijk, Krista K., De Boer-Bergsma, Jelkje, Fokkens, Michiel R., Lemmink, Henny, Sijmons, Rolf H., Sikkema-Raddatz, Birgit, Groves, Matthew R., Verschuuren-Bemelmans, Corien C., Verbeek, Dineke S., Van Diemen, Cleo C., Westers, Helga
Publicado 2022

Limited overlap in significant hits between genome-wide association studies on two airflow obstruction definitions in the same population

por van der Plaat, Diana A., Vonk, Judith M., Lahousse, Lies, de Jong, Kim, Faiz, Alen, Nedeljkovic, Ivana, Amin, Najaf, van Diemen, Cleo C., Brusselle, Guy G., Bossé, Yohan, Brandsma, Corry-Anke, Hao, Ke, Paré, Peter D., van Duijn, Cornelia M., Postma, Dirkje S., Boezen, H. Marike
Publicado 2019

Prevalence of intronic repeat expansions in RFC1 in Dutch patients with CANVAS and adult-onset ataxia

por Ghorbani, Fatemeh, de Boer-Bergsma, Jelkje, Verschuuren-Bemelmans, Corien C., Pennings, Maartje, de Boer, Eddy N., Kremer, Berry, Vanhoutte, Els K., de Vries, Jeroen J., van de Berg, Raymond, Kamsteeg, Erik-Jan, van Diemen, Cleo C., Westers, Helga, van de Warrenburg, Bart P., Verbeek, Dineke S.
Publicado 2022

Occupational exposure to gases/fumes and mineral dust affect DNA methylation levels of genes regulating expression

por van der Plaat, Diana A, Vonk, Judith M, Terzikhan, Natalie, de Jong, Kim, de Vries, Maaike, La Bastide-van Gemert, Sacha, van Diemen, Cleo C, Lahousse, Lies, Brusselle, Guy G, Nedeljkovic, Ivana, Amin, Najaf, Kromhout, Hans, Vermeulen, Roel C H, Postma, Dirkje S, van Duijn, Cornelia M, Boezen, H Marike
Publicado 2019

CAPICE: a computational method for Consequence-Agnostic Pathogenicity Interpretation of Clinical Exome variations

por Li, Shuang, van der Velde, K. Joeri, de Ridder, Dick, van Dijk, Aalt D. J., Soudis, Dimitrios, Zwerwer, Leslie R., Deelen, Patrick, Hendriksen, Dennis, Charbon, Bart, van Gijn, Marielle E., Abbott, Kristin, Sikkema-Raddatz, Birgit, van Diemen, Cleo C., Kerstjens-Frederikse, Wilhelmina S., Sinke, Richard J., Swertz, Morris A.
Publicado 2020

A prospective study on rapid exome sequencing as a diagnostic test for multiple congenital anomalies on fetal ultrasound

por Corsten‐Janssen, Nicole, Bouman, Katelijne, Diphoorn, Janouk C. D., Scheper, Arjen J., Kinds, Rianne, el Mecky, Julia, Breet, Hanna, Verheij, Joke B. G. M., Suijkerbuijk, Ron, Duin, Leonie K., Manten, Gwendolyn T. R., van Langen, Irene M., Sijmons, Rolf H., Sikkema‐Raddatz, Birgit, Westers, Helga, van Diemen, Cleo C.
Publicado 2020