MON-208 Association Study of AMH Promoter Polymorphisms and Serum AMH Levels in PCOS Patients

por Moolhuijsen, Loes, Meun, Cindy, Louwers, Yvonne, Broer, Linda, Uitterlinden, André, Laven, Joop, Visser, Jenny
Publicado 2019

Perspectives on the Use of Multiple Sclerosis Risk Genes for Prediction

por Jafari, Naghmeh, Broer, Linda, van Duijn, Cornelia M., Janssens, A. Cecile J. W., Hintzen, Rogier Q.
Publicado 2011

Burden of genetic risk variants in multiple sclerosis families in the Netherlands

por Mescheriakova, Julia Y, Broer, Linda, Wahedi, Simin, Uitterlinden, André G, van Duijn, Cornelia M, Hintzen, Rogier Q
Publicado 2016

Reduced penetrance of pathogenic ACMG variants in a deeply phenotyped cohort study and evaluation of ClinVar classification over time

por van Rooij, Jeroen, Arp, Pascal, Broer, Linda, Verlouw, Joost, van Rooij, Frank, Kraaij, Robert, Uitterlinden, André, Verkerk, Annemieke J. M. H.
Publicado 2020

Telomere Length and the Risk of Alzheimer’s Disease: The Rotterdam Study

por Fani, Lana, Hilal, Saima, Sedaghat, Sanaz, Broer, Linda, Licher, Silvan, Arp, Pascal P., van Meurs, Joyce B.J., Ikram, M. Kamran, Ikram, M. Arfan
Publicado 2020

Association of heat shock proteins with Parkinson’s disease

por Broer, Linda, Koudstaal, Peter J., Amin, Najaf, Rivadeneira, Fernando, Uitterlinden, Andre G., Hofman, Albert, Oostra, Ben A., Breteler, Monique M. B., Ikram, M. Arfan, van Duijn, Cornelia M.
Publicado 2011

Helicobacter pylori colonization and obesity – a Mendelian randomization study

por den Hollander, Wouter J., Broer, Linda, Schurmann, Claudia, Meyre, David, den Hoed, Caroline M., Mayerle, Julia, Hofman, Albert, Homuth, Georg, Uitterlinden, André G., Lerch, Markus M., Kuipers, Ernst J.
Publicado 2017

Association between an AMH promoter polymorphism and serum AMH levels in PCOS patients

por Moolhuijsen, Loes M E, Louwers, Yvonne V, McLuskey, Anke, Broer, Linda, Uitterlinden, Andre G, Verdiesen, Renée M G, Sisk, Ryan K, Dunaif, Andrea, Laven, Joop S E, Visser, Jenny A
Publicado 2022

A bioinformatics pipeline for estimating mitochondrial DNA copy number and heteroplasmy levels from whole genome sequencing data

por Battle, Stephanie L, Puiu, Daniela, Verlouw, Joost, Broer, Linda, Boerwinkle, Eric, Taylor, Kent D, Rotter, Jerome I, Rich, Stephan S, Grove, Megan L, Pankratz, Nathan, Fetterman, Jessica L, Liu, Chunyu, Arking, Dan E
Publicado 2022

Risk Assessment for Hip and Knee Osteoarthritis Using Polygenic Risk Scores

por Sedaghati‐Khayat, Bahar, Boer, Cindy G., Runhaar, Jos, Bierma‐Zeinstra, Sita M. A., Broer, Linda, Ikram, M. Arfan, Zeggini, Eleftheria, Uitterlinden, André G., van Rooij, Jeroen G. J., van Meurs, Joyce B. J.
Publicado 2022

Unraveling Dexamethasone-Induced Neurobehavioral and Sleep Problems in Children With ALL: Which Determinants Are Important?

por van Hulst, Annelienke M., Grootenhuis, Martha A., Verwaaijen, Emma J., van Litsenburg, Raphaële R.L., Li, Letao, van Zelst, Bertrand D., Broer, Linda, Pluijm, Saskia M.F., Pieters, Rob, Fiocco, Marta, van den Akker, Erica L.T., van den Heuvel-Eibrink, Marry M.
Publicado 2023

Genome-wide association of phenotypes based on clustering patterns of hand osteoarthritis identify WNT9A as novel osteoarthritis gene

por Boer, Cindy Germaine, Yau, Michelle S, Rice, Sarah J, Coutinho de Almeida, Rodrigo, Cheung, Kathleen, Styrkarsdottir, Unnur, Southam, Lorraine, Broer, Linda, Wilkinson, Jeremy Mark, Uitterlinden, André G, Zeggini, Eleftheria, Felson, David, Loughlin, John, Young, Mariel, Capellini, Terence Dante, Meulenbelt, Ingrid, van Meurs, Joyce BJ
Publicado 2021

A comparison of genotyping arrays

por Verlouw, Joost A. M., Clemens, Eva, de Vries, Jard H., Zolk, Oliver, Verkerk, Annemieke J. M. H., am Zehnhoff-Dinnesen, Antoinette, Medina-Gomez, Carolina, Lanvers-Kaminsky, Claudia, Rivadeneira, Fernando, Langer, Thorsten, van Meurs, Joyce B. J., van den Heuvel-Eibrink, Marry M., Uitterlinden, André G., Broer, Linda
Publicado 2021

Single nucleotide polymorphisms in CRTC1 and BARX1 are associated with esophageal adenocarcinoma

por van Nistelrooij, Anna M. J., van der Korput, Hetty A. G. M., Broer, Linda, van Marion, Ronald, van Berge Henegouwen, Mark I., van Noesel, Carel J., Biermann, Katharina, Spaander, Manon C. W., Tilanus, Hugo W., van Lanschot, J. Jan B., Hofman, Albert, Uitterlinden, André G., Wijnhoven, Bas P. L., Dinjens, Winand N. M.
Publicado 2015

Leukocyte telomere length associates with prospective mortality independent of immune-related parameters and known genetic markers

por Deelen, Joris, Beekman, Marian, Codd, Veryan, Trompet, Stella, Broer, Linda, Hägg, Sara, Fischer, Krista, Thijssen, Peter E, Suchiman, H Eka D, Postmus, Iris, Uitterlinden, André G, Hofman, Albert, de Craen, Anton J M, Metspalu, Andres, Pedersen, Nancy L, van Duijn, Cornelia M, Wouter Jukema, J, Houwing-Duistermaat, Jeanine J, Samani, Nilesh J, Eline Slagboom, P
Publicado 2014

Exome Sequencing Analysis Identifies Rare Variants in ATM and RPL8 That Are Associated With Shorter Telomere Length

por van der Spek, Ashley, Warner, Sophie C., Broer, Linda, Nelson, Christopher P., Vojinovic, Dina, Ahmad, Shahzad, Arp, Pascal P., Brouwer, Rutger W. W., Denniff, Matthew, van den Hout, Mirjam C. G. N., van Rooij, Jeroen G. J., Kraaij, Robert, van IJcken, Wilfred F. J., Samani, Nilesh J., Ikram, M. Arfan, Uitterlinden, André G., Codd, Veryan, Amin, Najaf, van Duijn, Cornelia M.
Publicado 2020

Rapid Low-Cost Microarray-Based Genotyping for Genetic Screening in Primary Immunodeficiency

por Suratannon, Narissara, van Wijck, Rogier T. A., Broer, Linda, Xue, Laixi, van Meurs, Joyce B. J., Barendregt, Barbara H., van der Burg, Mirjam, Dik, Willem A., Chatchatee, Pantipa, Langerak, Anton W., Swagemakers, Sigrid M. A., Goos, Jacqueline A. C., Mathijssen, Irene M. J., Dalm, Virgil A. S. H., Suphapeetiporn, Kanya, Heezen, Kim C., Drabwell, Jose, Uitterlinden, André G., van der Spek, Peter J., van Hagen, P. Martin
Publicado 2020

Causal mechanisms and balancing selection inferred from genetic associations with polycystic ovary syndrome

por Day, Felix R., Hinds, David A., Tung, Joyce Y., Stolk, Lisette, Styrkarsdottir, Unnur, Saxena, Richa, Bjonnes, Andrew, Broer, Linda, Dunger, David B., Halldorsson, Bjarni V., Lawlor, Debbie A., Laval, Guillaume, Mathieson, Iain, McCardle, Wendy L., Louwers, Yvonne, Meun, Cindy, Ring, Susan, Scott, Robert A., Sulem, Patrick, Uitterlinden, André G., Wareham, Nicholas J., Thorsteinsdottir, Unnur, Welt, Corrine, Stefansson, Kari, Laven, Joop S. E., Ong, Ken K., Perry, John R. B.
Publicado 2015

Genetic variation in gonadal impairment in female survivors of childhood cancer: a PanCareLIFE study protocol

por van der Kooi, Anne-Lotte L. F., Clemens, Eva, Broer, Linda, Zolk, Oliver, Byrne, Julianne, Campbell, Helen, van den Berg, Marleen, Berger, Claire, Calaminus, Gabriele, Dirksen, Uta, Winther, Jeanette Falck, Fosså, Sophie D, Grabow, Desiree, Haupt, Riccardo, Kaiser, Melanie, Kepak, Tomas, Kremer, Leontien, Kruseova, Jarmila, Modan-Moses, Dalit, Ranft, Andreas, Spix, Claudia, Kaatsch, Peter, Laven, Joop S. E., van Dulmen-den Broeder, Eline, Uitterlinden, André G., van den Heuvel-Eibrink, Marry M.
Publicado 2018

Genetic Determinants of Ototoxicity During and After Childhood Cancer Treatment: Protocol for the PanCareLIFE Study

por Clemens, Eva, Meijer, Annelot JM, Broer, Linda, Langer, Thorsten, van der Kooi, Anne-Lotte LF, Uitterlinden, André G, de Vries, Andrica, Kuehni, Claudia E, Garrè, Maria L, Kepak, Tomas, Kruseova, Jarmila, Winther, Jeanette F, Kremer, Leontien C, van Dulmen-den Broeder, Eline, Tissing, Wim JE, Rechnitzer, Catherine, Kenborg, Line, Hasle, Henrik, Grabow, Desiree, Parfitt, Ross, Binder, Harald, Carleton, Bruce C, Byrne, Julianne, Kaatsch, Peter, am Zehnhoff-Dinnesen, Antoinette, Zolk, Oliver, van den Heuvel-Eibrink, Marry M
Publicado 2019