Works matching AU van Duijn, Cornelia

Results: 346

Strengthening the Reporting of Genetic Risk Prediction Studies: The GRIPS Statement.

Published in:

PLoS Medicine, 2011, v. 8, n. 3, p. 1, doi. 10.1371/journal.pmed.1000420

By:

Janssens, A. Cecile J. W.;
Ioannidis, John P. A.;
van Duijn, Cornelia M.;
Little, Julian;
Khoury, Muin J.

Publication type:

Article

STrengthening the REporting of Genetic Association Studies (STREGA) An Extension of the STROBE Statement.

Published in:

PLoS Medicine, 2009, v. 6, n. 2, p. e1000022, doi. 10.1371/journal.pmed.1000022

By:

Little, Julian;
Higgins, Julian P.T;
Ioannidis, John P.A;
Moher, David;
Gagnon, France;
von Elm, Erik;
Khoury, Muin J;
Cohen, Barbara;
Davey-Smith, George;
Grimshaw, Jeremy;
Scheet, Paul;
Gwinn, Marta;
Williamson, Robin E;
Zou, Guang Yong;
Hutchings, Kim;
Johnson, Candice Y;
Tait, Valerie;
Wiens, Miriam;
Golding, Jean;
van Duijn, Cornelia

Publication type:

Article

STrengthening the REporting of Genetic Association Studies (STREGA)-an extension of the STROBE statement.

Published in:

Genetic Epidemiology, 2009, v. 33, n. 7, p. 581, doi. 10.1002/gepi.20410

By:

Little, Julian;
Higgins, Julian P. T.;
Ioannidis, John P. A.;
Moher, David;
Gagnon, France;
von Elm, Erik;
Khoury, Muin J.;
Cohen, Barbara;
Davey-Smith, George;
Grimshaw, Jeremy;
Scheet, Paul;
Gwinn, Marta;
Williamson, Robin E.;
Zou, Guang Yong;
Hutchings, Kim;
Johnson, Candice Y.;
Tait, Valerie;
Wiens, Miriam;
Golding, Jean;
van Duijn, Cornelia

Publication type:

Article

GenABEL: an R library for genome-wide association analysis.

Published in:

Bioinformatics, 2007, v. 23, n. 10, p. 1294, doi. 10.1093/bioinformatics/btm108

By:

Yurii S. Aulchenko;
Stephan Ripke;
Aaron Isaacs;
Cornelia M. van Duijn

Publication type:

Article

Genetic Complexities of Cerebral Small Vessel Disease, Blood Pressure, and Dementia.

Published in:

JAMA Network Open, 2024, v. 7, n. 5, p. e2412824, doi. 10.1001/jamanetworkopen.2024.12824

By:

Sargurupremraj, Muralidharan;
Soumaré, Aicha;
Bis, Joshua C.;
Surakka, Ida;
Jürgenson, Tuuli;
Joly, Pierre;
Knol, Maria J.;
Wang, Ruiqi;
Yang, Qiong;
Satizabal, Claudia L.;
Gudjonsson, Alexander;
Mishra, Aniket;
Bouteloup, Vincent;
Phuah, Chia-Ling;
van Duijn, Cornelia M.;
Cruchaga, Carlos;
Dufouil, Carole;
Chêne, Geneviève;
Lopez, Oscar L.;
Psaty, Bruce M.

Publication type:

Article

A Type 1 Diabetes Polygenic Score Is Not Associated With Prevalent Type 2 Diabetes in Large Population Studies.

Published in:

Journal of the Endocrine Society, 2023, v. 7, n. 11, p. 1, doi. 10.1210/jendso/bvad123

By:

Srinivasan, Shylaja;
Wu, Peitao;
Mercader, Josep M;
Udler, Miriam S;
Porneala, Bianca C;
Bartz, Traci M;
Floyd, James S;
Sitlani, Colleen;
Guo, Xiquing;
Haessler, Jeffrey;
Kooperberg, Charles;
Liu, Jun;
Ahmad, Shahzad;
Duijn, Cornelia van;
Liu, Ching-Ti;
Goodarzi, Mark O;
Florez, Jose C;
Meigs, James B;
Rotter, Jerome I;
Rich, Stephen S

Publication type:

Article

Whole genome sequencing of Caribbean Hispanic families with late‐onset Alzheimer's disease.

Published in:

Annals of Clinical & Translational Neurology, 2018, v. 5, n. 4, p. 406, doi. 10.1002/acn3.537

By:

Vardarajan, Badri N.;
Barral, Sandra;
Jaworski, James;
Beecham, Gary W.;
Blue, Elizabeth;
Tosto, Giuseppe;
Reyes‐Dumeyer, Dolly;
Medrano, Martin;
Lantigua, Rafael;
Naj, Adam;
Thornton, Timothy;
DeStefano, Anita;
Martin, Eden;
Wang, Li‐San;
Brown, Lisa;
Bush, William;
van Duijn, Cornelia;
Goate, Allison;
Farrer, Lindsay;
Haines, Jonathan L.

Publication type:

Article

Association of Rare APOE Missense Variants V236E and R251G With Risk of Alzheimer Disease.

Published in:

JAMA Neurology, 2022, v. 79, n. 7, p. 652, doi. 10.1001/jamaneurol.2022.1166

By:

Le Guen, Yann;
Belloy, Michael E.;
Grenier-Boley, Benjamin;
de Rojas, Itziar;
Castillo-Morales, Atahualpa;
Jansen, Iris;
Nicolas, Aude;
Bellenguez, Céline;
Dalmasso, Carolina;
Küçükali, Fahri;
Eger, Sarah J.;
Rasmussen, Katrine Laura;
Thomassen, Jesper Qvist;
Deleuze, Jean-François;
He, Zihuai;
Napolioni, Valerio;
Amouyel, Philippe;
Jessen, Frank;
Kehoe, Patrick G.;
van Duijn, Cornelia

Publication type:

Article

Analysis of Whole-Exome Sequencing Data for Alzheimer Disease Stratified by APOE Genotype.

Published in:

JAMA Neurology, 2019, v. 76, n. 9, p. 1099, doi. 10.1001/jamaneurol.2019.1456

By:

Ma, Yiyi;
Jun, Gyungah R.;
Zhang, Xiaoling;
Chung, Jaeyoon;
Naj, Adam C.;
Chen, Yuning;
Bellenguez, Celine;
Hamilton-Nelson, Kara;
Martin, Eden R.;
Kunkle, Brian W.;
Bis, Joshua C.;
Debette, Stéphanie;
DeStefano, Anita L.;
Fornage, Myriam;
Nicolas, Gaël;
van Duijn, Cornelia;
Bennett, David A.;
De Jager, Philip L.;
Mayeux, Richard;
Haines, Jonathan L

Publication type:

Article

Genes predict village of origin in rural Europe.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 11, p. 1269, doi. 10.1038/ejhg.2010.92

By:

O'Dushlaine, Colm;
McQuillan, Ruth;
Weale, Michael E.;
Crouch, Daniel J. M.;
Johansson, Åsa;
Aulchenko, Yurii;
Franklin, Christopher S.;
Pola&;#x0161;ek, Ozren;
Fuchsberger, Christian;
Corvin, Aiden;
Hicks, Andrew A.;
Vitart, Veronique;
Hayward, Caroline;
Wild, Sarah H.;
Meitinger, Thomas;
van Duijn, Cornelia M.;
Gyllensten, Ulf;
Wright, Alan F.;
Campbell, Harry;
Pramstaller, Peter P.

Publication type:

Article

Comparison of participant information and informed consent forms of five European studies in genetic isolated populations.

Published in:

European Journal of Human Genetics, 2010, v. 18, n. 3, p. 296, doi. 10.1038/ejhg.2009.155

By:

Mascalzoni, Deborah;
Janssens, A. Cecile J. W.;
Stewart, Alison;
Pramstaller, Peter;
Gyllensten, Ulf;
Rudan, Igor;
van Duijn, Cornelia M.;
Wilson, James F.;
Campbell, Harry;
Quillan, Ruth Mc

Publication type:

Article

Predicting human height by Victorian and genomic methods.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 8, p. 1070, doi. 10.1038/ejhg.2009.5

By:

Aulchenko, Yurii S.;
Struchalin, Maksim V.;
Belonogova, Nadezhda M.;
Axenovich, Tatiana I.;
Weedon, Michael N.;
Hofman, Albert;
Uitterlinden, Andre G.;
Kayser, Manfred;
Oostra, Ben A.;
van Duijn, Cornelia M.;
Janssens, A. Cecile J. W.;
Borodin, Pavel M.

Publication type:

Article

Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 7, p. 958, doi. 10.1038/ejhg.2008.260

By:

Amin, Najaf;
Aulchenko, Yuri S.;
Dekker, Marieke C.;
Ferdinand, Robert F.;
van Spreeken, Alwin;
Temmink, Alfons H.;
Verhulst, Frank C.;
Oostra, Ben A.;
van Duijn, Cornelia M.

Publication type:

Article

The expression of type III hyperlipoproteinemia: involvement of lipolysis genes.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 5, p. 620, doi. 10.1038/ejhg.2008.202

By:

Henneman, Peter;
van der Sman-de Beer, Femke;
Moghaddam, Payman Hanifi;
Huijts, Petra;
Stalenhoef, Anton F. H.;
Kastelein, John J. P.;
van Duijn, Cornelia M.;
Havekes, Louis M.;
Frants, Rune R.;
van Dijk, Ko Willems;
Smelt, Augustinus H. M.

Publication type:

Article

GENESTAT: an information portal for design and analysis of genetic association studies.

Published in:

European Journal of Human Genetics, 2009, v. 17, n. 4, p. 533, doi. 10.1038/ejhg.2008.216

By:

Ripatti, Samuli;
Becker, Tim;
Bickeböller, Heike;
Dominicus, Annica;
Fischer, Christine;
Humphreys, Keith;
Jonasdottir, Gudrun;
Moreau, Yves;
Olsson, Marita;
Ploner, Alexander;
Sheehan, Nuala;
Van Steen, Kristel;
Baur, Max;
van Duijn, Cornelia;
Palmgren, Juni

Publication type:

Article

Familial aggregation of preeclampsia and intrauterine growth restriction in a genetically isolated population in The Netherlands.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 12, p. 1437, doi. 10.1038/ejhg.2008.118

By:

Berends, Anne L.;
Steegers, Eric A.;
Isaacs, Aaron;
Aulchenko, Y. S.;
Fan Liu;
de Groot, Christianne J.;
Oostra, Ben A.;
van Duijn, Cornelia M.

Publication type:

Article

An approach for cutting large and complex pedigrees for linkage analysis.

Published in:

European Journal of Human Genetics, 2008, v. 16, n. 7, p. 854, doi. 10.1038/ejhg.2008.24

By:

Liu, Fan;
Kirichenko, Anatoliy;
Axenovich, Tatiana I.;
van Duijn, Cornelia M.;
Aulchenko, Yurii S.

Publication type:

Article

Mutation analysis of candidate genes within the 2q33.3 linkage area for familial early-onset generalised osteoarthritis.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 7, p. 791, doi. 10.1038/sj.ejhg.5201829

By:

Min, Josine L;
Meulenbelt, Ingrid;
Kloppenburg, Margreet;
van Duijn, Cornelia M;
Slagboom, P Eline

Publication type:

Article

Angiotensinogen M235T polymorphism and the risk of myocardial infarction and stroke among hypertensive patients on ACE-inhibitors or β-blockers.

Published in:

European Journal of Human Genetics, 2007, v. 15, n. 4, p. 478, doi. 10.1038/sj.ejhg.5201789

By:

Schelleman, Hedi;
Klungel, Olaf H.;
Witteman, Jacqueline C. M.;
Breteler, Monique M. B.;
Yazdanpanah, Moygan;
Danser, A. H. Jan;
Hofman, Albert;
van Duijn, Cornelia M.;
de Boer, Anthonius;
Stricker, Bruno H. Ch

Publication type:

Article

Strong linkage on 2q33.3 to familial early-onset generalized osteoarthritis and a consideration of two positional candidate genes.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 12, p. 1280, doi. 10.1038/sj.ejhg.5201704

By:

Meulenbelt, Ingrid;
Min, Josine L.;
van Duijn, Cornelia M.;
Kloppenburg, Margreet;
Breedveld, Ferdinand C.;
Slagboom, P. Eline

Publication type:

Article

The influence of the alpha-adducin G460W polymorphism and angiotensinogen M235T polymorphism on antihypertensive medication and blood pressure.

Published in:

European Journal of Human Genetics, 2006, v. 14, n. 7, p. 860, doi. 10.1038/sj.ejhg.5201632

By:

Schelleman, Hedi;
Klungel, Olaf H.;
Witteman, Jacqueline C. M.;
Hofman, Albert;
van Duijn, Cornelia M.;
de Boer, Anthonius;
Stricker, Bruno H. C. H.

Publication type:

Article

Linkage disequilibrium in young genetically isolated Dutch population.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 7, p. 527, doi. 10.1038/sj.ejhg.5201188

By:

Aulchenko, Yurii S.;
Heutink, Peter;
Mackay, Ian;
Bertoli-Avella, Aida M.;
Pullen, Jan;
Vaessen, Norbert;
Rademaker, Tessa AM;
Sandkuijl, Lodewijk A.;
Cardon, Lon;
Oostra, Ben;
van Duijn, Cornelia M.

Publication type:

Article

Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease.

Published in:

European Journal of Human Genetics, 2004, v. 12, n. 5, p. 389, doi. 10.1038/sj.ejhg.5201161

By:

Croes, Esther A.;
Alizadeh, Behrooz Z.;
Bertoli-Avella, Aida M.;
Rademaker, Tessa;
Vergeer-Drop, Jeannette;
Dermaut, Bart;
Houwing-Duistermaat, Jeanine J.;
Wientjens, Dorothee P. W. M.;
Hofman, Albert;
Van Broeckhoven, Christine;
van Duijn, Cornelia M.

Publication type:

Article

A population-based study of the effect of the HFE C282Y and H63D mutations on iron metabolism.

Published in:

European Journal of Human Genetics, 2003, v. 11, n. 3, p. 225, doi. 10.1038/sj.ejhg.5200955

By:

Njajou, Omer T;
Houwing-Duistermaat, Jeanine J;
Osborne, Richard H;
Vaessen, Norbert;
Vergeer, Jeanette;
Heeringa, Jan;
Pols, Huibert AP;
Hofman, Albert;
van Duijn, Cornelia M

Publication type:

Article

Genetic association of the presenilin-1 regulatory region with early-onset Alzheimer's disease in a population-based sample.

Published in:

European Journal of Human Genetics, 1999, v. 7, n. 7, p. 801, doi. 10.1038/sj.ejhg.5200373

By:

Duijn, Cornelia M van;
Cruts, Marc;
Theuns, Jessie;
Van Gassen, Geert;
Backhovens, Hubert;
van den Broeck, Marleen;
Wehnert, Anita;
Serneels, Sally;
Hofman, Albert;
Van Broeckhoven, Christine

Publication type:

Article

Association of metformin, sulfonylurea and insulin use with brain structure and function and risk of dementia and Alzheimer’s disease: Pooled analysis from 5 cohorts.

Published in:

PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0212293

By:

Weinstein, Galit;
Davis-Plourde, Kendra L.;
Conner, Sarah;
Himali, Jayandra J.;
Beiser, Alexa S.;
Lee, Anne;
Rawlings, Andreea M.;
Sedaghat, Sanaz;
Ding, Jie;
Moshier, Erin;
van Duijn, Cornelia M.;
Beeri, Michal S.;
Selvin, Elizabeth;
Ikram, M. Arfan;
Launer, Lenore J.;
Haan, Mary N.;
Seshadri, Sudha

Publication type:

Article

A combined linkage, microarray and exome analysis suggests <italic>MAP3K11</italic> as a candidate gene for left ventricular hypertrophy.

Published in:

BMC Medical Genomics, 2018, v. 11, p. 1, doi. 10.1186/s12920-018-0339-9

By:

Silva, Claudia Tamar;
Zorkoltseva, Irina V.;
Niemeijer, Maartje N.;
van den Berg, Marten E.;
Amin, Najaf;
Demirkan, Ayşe;
van Leeuwen, Elisa;
Iglesias, Adriana I.;
Piñeros-Hernández, Laura B.;
Restrepo, Carlos M.;
Kors, Jan A.;
Kirichenko, Anatoly V.;
Willemsen, Rob;
Oostra, Ben A.;
Stricker, Bruno H.;
Uitterlinden, André G.;
Axenovich, Tatiana I.;
van Duijn, Cornelia M.;
Isaacs, Aaron

Publication type:

Article

Genome-wide patterns and properties of de novo mutations in humans.

Published in:

Nature Genetics, 2015, v. 47, n. 7, p. 822, doi. 10.1038/ng.3292

By:

Francioli, Laurent C;
Menelaou, Androniki;
Renkens, Ivo;
Kloosterman, Wigard P;
Guryev, Victor;
Arndt, Peter F;
de Bakker, Paul I W;
Polak, Paz P;
Chun, Sung;
Sunyaev, Shamil R;
Koren, Amnon;
van Duijn, Cornelia M;
Swertz, Morris;
Wijmenga, Cisca;
van Ommen, Gertjan;
Slagboom, P Eline;
Boomsma, Dorret I;
Ye, Kai

Publication type:

Article

The impact of low-frequency and rare variants on lipid levels.

Published in:

Nature Genetics, 2015, v. 47, n. 6, p. 589, doi. 10.1038/ng.3300

By:

Surakka, Ida;
Sarin, Antti-Pekka;
Kettunen, Johannes;
Hottenga, Jouke-Jan;
de Geus, Eco J;
Willemsen, Gonneke;
Boomsma, Dorret I;
Isaacs, Aaron;
van Duijn, Cornelia M;
Ladenvall, Claes;
Beekman, Marian;
Deelen, Joris;
Slagboom, P Eline;
Esko, Tõnu;
Ried, Janina S;
Nelson, Christopher P;
Samani, Nilesh J;
Willenborg, Christina;
Erdmann, Jeanette;
Blades, Matthew

Publication type:

Article

Rapid variance components-based method for whole-genome association analysis.

Published in:

Nature Genetics, 2012, v. 44, n. 10, p. 1166, doi. 10.1038/ng.2410

By:

Svishcheva, Gulnara R;
Axenovich, Tatiana I;
Belonogova, Nadezhda M;
van Duijn, Cornelia M;
Aulchenko, Yurii S

Publication type:

Article

A genome-wide association study identifies a susceptibility locus for refractive errors and myopia at 15q14.

Published in:

Nature Genetics, 2010, v. 42, n. 10, p. 897, doi. 10.1038/ng.663

By:

Solouki, Abbas M.;
Verhoeven, Virginie J. M.;
van Duijn, Cornelia M.;
Verkerk, Annemieke J. M. H.;
Ikram, M. Kamran;
Hysi, Pirro G.;
Despriet, Dominiek D. G.;
van Koolwijk, Leonieke M.;
Lintje Ho;
Ramdas, Wishal D.;
Czudowska, Monika;
Kuijpers, Robert W. A. M.;
Amin, Najaf;
Struchalin, Maksim;
Aulchenko, Yurii S.;
van Rij, Gabriel;
Riemslag, Frans C. C.;
Young, Terri L.;
Mackey, David A.;
Spector, Timothy D.

Publication type:

Article

A genome-wide association study for myopia and refractive error identifies a susceptibility locus at 15q25.

Published in:

Nature Genetics, 2010, v. 42, n. 10, p. 902, doi. 10.1038/ng.664

By:

Hysi, Pirro G.;
Young, Terri L.;
Mackey, David A.;
Andrew, Toby;
Fernández-Medarde, Alberto;
Solouki, Abbas M.;
Hewitt, Alex W.;
Macgregor, Stuart;
Vingerling, Johannes R.;
Yi-Ju Li;
Ikram, M. Kamran;
Lee Yiu Fai;
Sham, Pak C.;
Manyes, Lara;
Porteros, Angel;
Lopes, Margarida C.;
Carbonaro, Francis;
Fahy, Samantha J.;
Martin, Nicholas G.;
van Duijn, Cornelia M.

Publication type:

Article

Reply to “Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis”.

Published in:

2010

By:

Hintzen, Rogier Q.;
Aulchenko, Yurii S.;
Ramagopalan, Sriram;
Ebers, George;
van Duijn, Cornelia M.

Publication type:

Letter

Meta-analyses of genome-wide association studies identify multiple loci associated with pulmonary function.

Published in:

Nature Genetics, 2010, v. 42, n. 1, p. 45, doi. 10.1038/ng.500

By:

Hancock, Dana B.;
Eijgelsheim, Mark;
Wilk, Jemma B.;
Gharib, Sina A.;
Loehr, Laura R.;
Marciante, Kristin D.;
Franceschini, Nora;
van Durme, Yannick M. T. A.;
Ting-hsu Chen;
Barr, R. Graham;
Schabath, Matthew B.;
Couper, David J.;
Brusselle, Guy G.;
Psaty, Bruce M.;
van Duijn, Cornelia M.;
Rotter, Jerome I.;
Uitterlinden, André G.;
Hofman, Albert;
Punjabi, Naresh M.;
Rivadeneira, Fernando

Publication type:

Article

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.

Published in:

Nature Genetics, 2008, v. 40, n. 12, p. 1402, doi. 10.1038/ng.251

By:

Aulchenko, Yurii S.;
Hoppenbrouwers, Ilse A.;
Ramagopalan, Sreeram V.;
Broer, Linda;
Jafari, Naghmeh;
Hillert, Jan;
Link, Jenny;
Lundström, Wangko;
Greiner, Eva;
Dessa Sadovnick, A;
Goossens, Dirk;
Van Broeckhoven, Christine;
Del-Favero, Jurgen;
Ebers, George C.;
Oostra, Ben A.;
van Duijn, Cornelia M.;
Hintzen, Rogier Q.

Publication type:

Article

Susceptibility loci for intracranial aneurysm in European and Japanese populations.

Published in:

Nature Genetics, 2008, v. 40, n. 12, p. 1472, doi. 10.1038/ng.240

By:

Bilguvar, Kaya;
Yasuno, Katsuhito;
Niemelä, Mika;
Ruigrok, Ynte M.;
von und zu Fraunberg, Mikael;
van Duijn, Cornelia M.;
van den Berg, Leonard H.;
Mane, Shrikant;
Mason, Christopher E.;
Choi, Murim;
Gaál, Emília;
Bayri, Yasar;
Kolb, Luis;
Arlier, Zulfikar;
Ravuri, Sudhakar;
Ronkainen, Antti;
Tajima, Atsushi;
Laakso, Aki;
Hata, Akira;
Kasuya, Hidetoshi

Publication type:

Article

Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies.

Published in:

Nature Genetics, 2006, v. 38, n. 5, p. 556, doi. 10.1038/ng1770

By:

Service, Susan;
DeYoung, Joseph;
Karayiorgou, Maria;
Roos, J. Louw;
Pretorious, Herman;
Bedoya, Gabriel;
Ospina, Jorge;
Ruiz-Linares, Andres;
Macedo, António;
Palha, Joana Almeida;
Heutink, Peter;
Aulchenko, Yurii;
Oostra, Ben;
van Duijn, Cornelia;
Jarvelin, Marjo-Riitta;
Varilo, Teppo;
Peddle, Lynette;
Rahman, Proton;
Piras, Giovanna;
Monne, Maria

Publication type:

Article

Low-penetrance susceptibility to breast cancer due to CHEK2<sup>*</sup>1100delC in noncarriers of BRCA1 or BRCA2 mutations.

Published in:

Nature Genetics, 2002, v. 31, n. 1, p. 55

By:

Meijers-Heijboer, Hanne;
van den Ouweland, Ans;
Klijn, Jan;
Wasielewski, Marijke;
de Snoo, Anja;
Oldenburg, Rogier;
Hollestelle, Antoinette;
Houben, Mark;
Crepin, Ellen;
van Veghel-Plandsoen, Monique;
Elstrodt, Fons;
van Duijn, Cornelia;
Bartels, Carina;
Meijers, Carel;
Schutte, Mieke;
McGuffog, Lesley;
Thompson, Deborah;
Easton, Douglas F.;
Sodha, Nayanta

Publication type:

Article

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis.

Published in:

Nature Genetics, 2001, v. 28, n. 3, p. 213, doi. 10.1038/90038

By:

Njajou, Omer T.;
Vaessen, Norbert;
Joosse, Marijke;
Berghuis, Bianca;
van Dongen, Jeroen W.F.;
Breuning, Martijn H.;
Snijders, Pieter J.L.M.;
Rutten, Wim P.F.;
Sandkuijl, Lodewijk A.;
Oostra, Ben A.;
van Duijn, Cornelia M.;
Heutink, Peter

Publication type:

Article

Epistatic Effect of Cholesteryl Ester Transfer Protein and Hepatic Lipase on Serum High-Density Lipoprotein Cholesterol Levels.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2007, v. 92, n. 7, p. 2680, doi. 10.1210/jc.2007-0269

By:

Isaacs, Aaron;
Aulchenko, Yurii S.;
Hofman, Albert;
Sijbrands, Eric J. G.;
Sayed-Tabatabaei, Fakhredin A.;
Klungel, Olaf H.;
Maitland-van der Zee, Anke-Hilse;
Stricker, Bruno H. Ch.;
Oostra, Ben A.;
Witteman, Jacqueline C. M.;
van Duijn, Cornelia M.

Publication type:

Article

The –514 C→T Hepatic Lipase Promoter Region Polymorphism and Plasma Lipids: A Meta-Analysis.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2004, v. 89, n. 8, p. 3858, doi. 10.1210/jc.2004-0188

By:

ISAACS, AARON;
SAYED-TABATABAEI, FAKHREDIN A.;
NJAJOU, OMER T.;
WITTEMAN, JACQUELINE C. M.;
VAN DUIJN, CORNELIA M.

Publication type:

Article

Association between an Insulin-Like Growth Factor I Gene Promoter Polymorphism and Bone Mineral Density in the Elderly: The Rotterdam Study.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2003, v. 88, n. 8, p. 3878, doi. 10.1210/jc.2002-021813

By:

RIVADENEIRA, FERNANDO;
HOUWING-DUISTERMAAT, JEANINE J.;
VAESSEN, NORBERT;
VERGEER-DROP, JEANNETTE M.;
HOFMAN, ALBERT;
POLS, HUIBERT A. P.;
VAN DUIJN, CORNELIA M.;
UITTERLINDEN, ANDRÉ G.

Publication type:

Article

Polymorphism in the IGF-I Gene: Clinical Relevance for Short Children Born Small for Gestational Age (SGA).

Published in:

Journal of Clinical Endocrinology & Metabolism, 2002, v. 87, n. 6, p. 2720, doi. 10.1210/jcem.87.6.8673

By:

ARENDS, NICOLETTE;
JOHNSTON, LINDA;
HOKKEN-KOELEGA, ANITA;
VAN DUIJN, CORNELIA;
DE RIDDER, MARIA;
SAVAGE, MARTIN;
CLARK, ADRIAN

Publication type:

Article

Automated workflow-based exploitation of pathway databases provides new insights into genetic associations of metabolite profiles.

Published in:

BMC Genomics, 2013, v. 14, n. 1, p. 1, doi. 10.1186/1471-2164-14-865

By:

Dharuri, Harish;
Henneman, Peter;
Demirkan, Ayse;
van Klinken, Jan Bert;
Mook-Kanamori, Dennis Owen;
Wang-Sattler, Rui;
Gieger, Christian;
Adamski, Jerzy;
Hettne, Kristina;
Roos, Marco;
Suhre, Karsten;
Van Duijn, Cornelia M.;
van Dijk, Ko Willems;
't Hoen, Peter A. C.

Publication type:

Article

Polymorphisms in metabolic genes, their combination andinteraction with tobacco smoke and alcohol consumption and riskof gastric cancer: a case-control study in an Italian population.

Published in:

BMC Cancer, 2007, v. 7, p. 206, doi. 10.1186/1471-2407-7-206

By:

Boccia, Stefania;
Sayed-Tabatabaei, Fakhredin A.;
Persiani, Roberto;
Gianfagna, Francesco;
Rausei, Stefano;
Arzani, Dario;
La Greca, Antonio;
D'Ugo, Domenico;
La Torre, Giuseppe;
van Duijn, Cornelia M.;
Ricciardi, Gualtiero

Publication type:

Article

The first two patients with dura mater associated Creutzfeldt-Jakob disease in the Netherlands.

Published in:

Journal of Neurology, 2001, v. 248, n. 10, p. 877, doi. 10.1007/s004150170073

By:

Croes, Esther A.;
Jansen, Gerard H.;
Lemstra, Afina W.;
Frijns, Catharina J.M.;
van Gool, Willem A.;
van Duijn, Cornelia M.

Publication type:

Article

Suggestive linkage to chromosome 19 in a large Cuban family with late-onset Parkinson's disease.

Published in:

Movement Disorders, 2003, v. 18, n. 11, p. 1240, doi. 10.1002/mds.10534

By:

Aida M. Bertoli-Avella;
Jose L. Giroud-Benitez;
Vincenzo Bonifati;
Eduardo Alvarez-Gonzalez;
Luis Heredero-Baute;
Cornelia M. Van Duijn;
Peter Heutink

Publication type:

Article

Clinical features and neuroimaging of PARK7-linked parkinsonism.

Published in:

2003

By:

Dekker, Marieke;
Bonifati, Vincenzo;
van Swieten, John;
Leenders, Nico;
Galjaard, Robert-Jan;
Snijders, Pieter;
Horstink, Marten;
Heutink, Peter;
Oostra, Ben;
van Duijn, Cornelia

Publication type:

journal article

CYP2D6 polymorphism in Parkinson's disease: The Rotterdam study.

Published in:

Movement Disorders, 2001, v. 16, n. 2, p. 290, doi. 10.1002/mds.1041

By:

Harhangi, B. Sanjay;
Oostra, Ben A.;
Heutink, Peter;
van Duijn, Cornelia M.;
Hofman, Albert;
Breteler, Monique M.B.

Publication type:

Article

CYP1A1, CYP2E1, GSTM1, GSTT1, EPHX1 exons 3 and 4, and NAT2 polymorphisms, smoking, consumption of alcohol and fruit and vegetables and risk of head and neck cancer.

Published in:

Journal of Cancer Research & Clinical Oncology, 2008, v. 134, n. 1, p. 93, doi. 10.1007/s00432-007-0254-5

By:

Boccia, Stefania;
Cadoni, Gabriella;
Sayed-Tabatabaei, Fakhredin A.;
Volante, Mariangela;
Arzani, Dario;
De Lauretis, Angelo;
Cattel, Caterina;
Almadori, Giovanni;
van Duijn, Cornelia M.;
Paludetti, Gaetano;
Ricciardi, Gualtiero

Publication type:

Article