Prenatal sonographic features can accurately determine parental origin in triploid pregnancies

par Lugthart, Malou A., Horenblas, Judith, Kleinrouweler, Emily C., Engels, Melanie, Knegt, Alida C., Huijsdens, Karin, van Leeuwen, Elisabeth, Pajkrt, Eva
Publié dans Prenat Diagn (2020)

Oral‐facial‐digital syndrome type 1 in males: Congenital heart defects are included in its phenotypic spectrum

par Bouman, Arjan, Alders, Mariëlle, Oostra, Roelof Jan, van Leeuwen, Elisabeth, Thuijs, Nikki, van der Kevie‐Kersemaekers, Anne‐Marie, van Maarle, Merel
Publié dans Am J Med Genet A (2017)

Lack of Detection of XMRV in Seminal Plasma from HIV-1 Infected Men in The Netherlands

par Cornelissen, Marion, Zorgdrager, Fokla, Blom, Petra, Jurriaans, Suzanne, Repping, Sjoerd, van Leeuwen, Elisabeth, Bakker, Margreet, Berkhout, Ben, van der Kuyl, Antoinette C.
Publié 2010

Development of placental abnormalities in location and anatomy

par Jansen, Charlotte H. J. R., Kastelein, Arnoud W., Kleinrouweler, C. Emily, Van Leeuwen, Elisabeth, De Jong, Kees H., Pajkrt, Eva, Van Noorden, Cornelis J. F.
Publié dans Acta Obstet Gynecol Scand (2020)

Preconception use of cART by HIV-positive pregnant women increases the risk of infants being born small for gestational age

par Snijdewind, Ingrid J. M., Smit, Colette, Godfried, Mieke H., Bakker, Rachel, Nellen, Jeannine F. J. B., Jaddoe, Vincent W. V., van Leeuwen, Elisabeth, Reiss, Peter, Steegers, Eric A. P., van der Ende, Marchina E.
Publié dans PLoS One (2018)

A Combined Linkage and Exome Sequencing Analysis for Electrocardiogram Parameters in the Erasmus Rucphen Family Study

par Silva, Claudia T., Zorkoltseva, Irina V., Amin, Najaf, Demirkan, Ayşe, van Leeuwen, Elisabeth M., Kors, Jan A., van den Berg, Marten, Stricker, Bruno H., Uitterlinden, André G., Kirichenko, Anatoly V., Witteman, Jacqueline C. M., Willemsen, Rob, Oostra, Ben A., Axenovich, Tatiana I., van Duijn, Cornelia M., Isaacs, Aaron
Publié dans Front Genet (2016)

Improved imputation quality of low-frequency and rare variants in European samples using the ‘Genome of The Netherlands'

par Deelen, Patrick, Menelaou, Androniki, van Leeuwen, Elisabeth M, Kanterakis, Alexandros, van Dijk, Freerk, Medina-Gomez, Carolina, Francioli, Laurent C, Hottenga, Jouke Jan, Karssen, Lennart C, Estrada, Karol, Kreiner-Møller, Eskil, Rivadeneira, Fernando, van Setten, Jessica, Gutierrez-Achury, Javier, Westra, Harm-Jan, Franke, Lude, van Enckevort, David, Dijkstra, Martijn, Byelas, Heorhiy, van Duijn, Cornelia M, de Bakker, Paul I W, Wijmenga, Cisca, Swertz, Morris A
Publié 2014

Clinical manifestations, risk factors, and maternal and perinatal outcomes of coronavirus disease 2019 in pregnancy: living systematic review and meta-analysis

par Allotey, John, Fernandez, Silvia, Bonet, Mercedes, Stallings, Elena, Yap, Magnus, Kew, Tania, Zhou, Dengyi, Coomar, Dyuti, Sheikh, Jameela, Lawson, Heidi, Ansari, Kehkashan, Attarde, Shruti, Littmoden, Megan, Banjoko, Adeolu, Barry, Kathryn, Akande, Oluwadamilola, Sambamoorthi, Dharshini, van Wely, Madelon, van Leeuwen, Elisabeth, Kostova, Elena, Kunst, Heinke, Khalil, Asma, Tiberi, Simon, Brizuela, Vanessa, Broutet, Nathalie, Kara, Edna, Kim, Caron Rahn, Thorson, Anna, Escuriet, Ramón, Gottlieb, Sami, Tong, Van T, Ellington, Sascha, Oladapo, Olufemi T, Mofenson, Lynne, Zamora, Javier, Thangaratinam, Shakila
Publié dans BMJ (2020)

Clinical manifestations, prevalence, risk factors, outcomes, transmission, diagnosis and treatment of COVID-19 in pregnancy and postpartum: a living systematic review protocol

par Yap, Magnus, Debenham, Luke, Kew, Tania, Chatterjee, Shaunak Rhiju, Allotey, John, Stallings, Elena, Coomar, Dyuti, Lee, Siang Ing, Qiu, Xiu, Yuan, Mingyang, Clavé Llavall, Anna, Dixit, Anushka, Zhou, Dengyi, Balaji, Rishab, van Wely, Madelon, Kostova, Elena, van Leeuwen, Elisabeth, Mofenson, Lynne, Kunst, Heinke, Khalil, Asma, Tiberi, Simon, Thomas, James, Brizuela, Vanessa, Broutet, Nathalie, Kara, Edna, Kim, Caron, Thorson, Anna, Rayco-Solon, Pura, Pardo-Hernandez, Hector, Oladapo, Olufemi Taiwo, Zamora, Javier, Bonet, Mercedes, Thangaratinam, Shakila
Publié dans BMJ Open (2020)

The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels

par van Leeuwen, Elisabeth M., Smouter, Françoise A. S., Kam-Thong, Tony, Karbalai, Nazanin, Smith, Albert V., Harris, Tamara B., Launer, Lenore J., Sitlani, Colleen M., Li, Guo, Brody, Jennifer A., Bis, Joshua C., White, Charles C., Jaiswal, Alok, Oostra, Ben A., Hofman, Albert, Rivadeneira, Fernando, Uitterlinden, Andre G., Boerwinkle, Eric, Ballantyne, Christie M., Gudnason, Vilmundur, Psaty, Bruce M., Cupples, L. Adrienne, Järvelin, Marjo-Riitta, Ripatti, Samuli, Isaacs, Aaron, Müller-Myhsok, Bertram, Karssen, Lennart C., van Duijn, Cornelia M.
Publié 2014

Diagnostic Yield of Sequencing Familial Hypercholesterolemia Genes in Severe Hypercholesterolemia

par Khera, Amit V., Won, Hong-Hee, Peloso, Gina M., Lawson, Kim S., Bartz, Traci M., Deng, Xuan, van Leeuwen, Elisabeth M., Natarajan, Pradeep, Emdin, Connor A., Bick, Alexander G., Morrison, Alanna C., Brody, Jennifer A., Gupta, Namrata, Nomura, Akihiro, Kessler, Thorsten, Duga, Stefano, Bis, Joshua C., van Duijn, Cornelia M., Cupples, L. Adrienne, Psaty, Bruce, Rader, Daniel J., Danesh, John, Schunkert, Heribert, McPherson, Ruth, Farrall, Martin, Watkins, Hugh, Lander, Eric, Wilson, James G., Correa, Adolfo, Boerwinkle, Eric, Merlini, Piera Angelica, Ardissino, Diego, Saleheen, Danish, Gabriel, Stacey, Kathiresan, Sekar
Publié dans J Am Coll Cardiol (2016)

Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA

par Kettunen, Johannes, Demirkan, Ayşe, Würtz, Peter, Draisma, Harmen H.M., Haller, Toomas, Rawal, Rajesh, Vaarhorst, Anika, Kangas, Antti J., Lyytikäinen, Leo-Pekka, Pirinen, Matti, Pool, René, Sarin, Antti-Pekka, Soininen, Pasi, Tukiainen, Taru, Wang, Qin, Tiainen, Mika, Tynkkynen, Tuulia, Amin, Najaf, Zeller, Tanja, Beekman, Marian, Deelen, Joris, van Dijk, Ko Willems, Esko, Tõnu, Hottenga, Jouke-Jan, van Leeuwen, Elisabeth M, Lehtimäki, Terho, Mihailov, Evelin, Rose, Richard J., de Craen, Anton J.M., Gieger, Christian, Kähönen, Mika, Perola, Markus, Blankenberg, Stefan, Savolainen, Markku J., Verhoeven, Aswin, Viikari, Jorma, Willemsen, Gonneke, Boomsma, Dorret I., van Duijn, Cornelia M., Eriksson, Johan, Jula, Antti, Järvelin, Marjo-Riitta, Kaprio, Jaakko, Metspalu, Andres, Raitakari, Olli, Salomaa, Veikko, Slagboom, P. Eline, Waldenberger, Melanie, Ripatti, Samuli, Ala-Korpela, Mika
Publié dans Nat Commun (2016)

Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels

par Draisma, Harmen H.M., Pool, René, Kobl, Michael, Jansen, Rick, Petersen, Ann-Kristin, Vaarhorst, Anika A.M., Yet, Idil, Haller, Toomas, Demirkan, Ayşe, Esko, Tõnu, Zhu, Gu, Böhringer, Stefan, Beekman, Marian, van Klinken, Jan Bert, Römisch-Margl, Werner, Prehn, Cornelia, Adamski, Jerzy, de Craen, Anton J.M., van Leeuwen, Elisabeth M., Amin, Najaf, Dharuri, Harish, Westra, Harm-Jan, Franke, Lude, de Geus, Eco J.C., Hottenga, Jouke Jan, Willemsen, Gonneke, Henders, Anjali K., Montgomery, Grant W., Nyholt, Dale R., Whitfield, John B., Penninx, Brenda W., Spector, Tim D., Metspalu, Andres, Slagboom, P. Eline, van Dijk, Ko Willems, ‘t Hoen, Peter A.C., Strauch, Konstantin, Martin, Nicholas G., van Ommen, Gert-Jan B., Illig, Thomas, Bell, Jordana T., Mangino, Massimo, Suhre, Karsten, McCarthy, Mark I., Gieger, Christian, Isaacs, Aaron, van Duijn, Cornelia M., Boomsma, Dorret I.
Publié dans Nat Commun (2015)

The Genome of the Netherlands: design, and project goals

par Boomsma, Dorret I, Wijmenga, Cisca, Slagboom, Eline P, Swertz, Morris A, Karssen, Lennart C, Abdellaoui, Abdel, Ye, Kai, Guryev, Victor, Vermaat, Martijn, van Dijk, Freerk, Francioli, Laurent C, Hottenga, Jouke Jan, Laros, Jeroen F J, Li, Qibin, Li, Yingrui, Cao, Hongzhi, Chen, Ruoyan, Du, Yuanping, Li, Ning, Cao, Sujie, van Setten, Jessica, Menelaou, Androniki, Pulit, Sara L, Hehir-Kwa, Jayne Y, Beekman, Marian, Elbers, Clara C, Byelas, Heorhiy, de Craen, Anton J M, Deelen, Patrick, Dijkstra, Martijn, den Dunnen, Johan T, de Knijff, Peter, Houwing-Duistermaat, Jeanine, Koval, Vyacheslav, Estrada, Karol, Hofman, Albert, Kanterakis, Alexandros, Enckevort, David van, Mai, Hailiang, Kattenberg, Mathijs, van Leeuwen, Elisabeth M, Neerincx, Pieter B T, Oostra, Ben, Rivadeneira, Fernanodo, Suchiman, Eka H D, Uitterlinden, Andre G, Willemsen, Gonneke, Wolffenbuttel, Bruce H, Wang, Jun, de Bakker, Paul I W, van Ommen, Gert-Jan, van Duijn, Cornelia M
Publié 2014

Meta-analysis of Genome-Wide Association Studies Identifies Novel Loci Associated With Optic Disc Morphology

par Springelkamp, Henriët, Mishra, Aniket, Hysi, Pirro G., Gharahkhani, Puya, Höhn, René, Khor, Chiea-Chuen, Cooke Bailey, Jessica N., Luo, Xiaoyan, Ramdas, Wishal D., Vithana, Eranga, Koh, Victor, Yazar, Seyhan, Xu, Liang, Forward, Hannah, Kearns, Lisa S., Amin, Najaf, Iglesias, Adriana I., Sim, Kar-Seng, van Leeuwen, Elisabeth M., Demirkan, Ayse, van der Lee, Sven, Loon, Seng-Chee, Rivadeneira, Fernando, Nag, Abhishek, Sanfilippo, Paul G., Schillert, Arne, de Jong, Paulus T. V. M., Oostra, Ben A., Uitterlinden, André G., Hofman, Albert, Zhou, Tiger, Burdon, Kathryn P., Spector, Timothy D., Lackner, Karl J., Saw, Seang-Mei, Vingerling, Johannes R., Teo, Yik-Ying, Pasquale, Louis R., Wolfs, Roger C. W., Lemij, Hans G., Tai, E-Shyong, Jonas, Jost B., Cheng, Ching-Yu, Aung, Tin, Jansonius, Nomdo M., Klaver, Caroline C. W., Craig, Jamie E., Young, Terri L., Haines, Jonathan L., MacGregor, Stuart, Mackey, David A., Pfeiffer, Norbert, Wong, Tien-Yin, Wiggs, Janey L., Hewitt, Alex W., van Duijn, Cornelia M., Hammond, Christopher J.
Publié dans Genet Epidemiol (2015)

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

par Iotchkova, Valentina, Huang, Jie, Morris, John A., Jain, Deepti, Barbieri, Caterina, Walter, Klaudia, Min, Josine L., Chen, Lu, Astle, William, Cocca, Massimilian, Deelen, Patrick, Elding, Heather, Farmaki, Aliki-Eleni, Franklin, Christopher S., Franberg, Mattias, Gaunt, Tom R., Hofman, Albert, Jiang, Tao, Kleber, Marcus E., Lachance, Genevieve, Luan, Jian'an, Malerba, Giovanni, Matchan, Angela, Mead, Daniel, Memari, Yasin, Ntalla, Ioanna, Panoutsopoulou, Kalliope, Pazoki, Raha, Perry, John R.B., Rivadeneira, Fernando, Sabater-Lleal, Maria, Sennblad, Bengt, Shin, So-Youn, Southam, Lorraine, Traglia, Michela, van Dijk, Freerk, van Leeuwen, Elisabeth M., Zaza, Gianluigi, Zhang, Weihua, Amin, Najaf, Butterworth, Adam, Chambers, John C., Dedoussis, George, Dehghan, Abbas, Franco, Oscar H., Franke, Lude, Frontini, Mattia, Gambaro, Giovanni, Gasparini, Paolo, Hamsten, Anders, Issacs, Aaron, Kooner, Jaspal S., Kooperberg, Charles, Langenberg, Claudia, Marz, Winfried, Scott, Robert A., Swertz, Morris A., Toniolo, Daniela, Uitterlinden, Andre G., van Duijn, Cornelia M., Watkins, Hugh, Zeggini, Eleftheria, Maurano, Mathew T., Timpson, Nicholas J., Reiner, Alexander P., Auer, Paul L., Soranzo, Nicole
Publié dans Nat Genet (2016)

Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

par Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart
Publié dans Nat Commun (2018)

Author Correction: Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases

par Iglesias, Adriana I., Mishra, Aniket, Vitart, Veronique, Bykhovskaya, Yelena, Höhn, René, Springelkamp, Henriët, Cuellar-Partida, Gabriel, Gharahkhani, Puya, Bailey, Jessica N. Cooke, Willoughby, Colin E., Li, Xiaohui, Yazar, Seyhan, Nag, Abhishek, Khawaja, Anthony P., Polašek, Ozren, Siscovick, David, Mitchell, Paul, Tham, Yih Chung, Haines, Jonathan L., Kearns, Lisa S., Hayward, Caroline, Shi, Yuan, van Leeuwen, Elisabeth M., Taylor, Kent D., Bonnemaijer, Pieter, Rotter, Jerome I., Martin, Nicholas G., Zeller, Tanja, Mills, Richard A., Souzeau, Emmanuelle, Staffieri, Sandra E., Jonas, Jost B., Schmidtmann, Irene, Boutin, Thibaud, Kang, Jae H., Lucas, Sionne E. M., Wong, Tien Yin, Beutel, Manfred E., Wilson, James F., Uitterlinden, André G., Vithana, Eranga N., Foster, Paul J., Hysi, Pirro G., Hewitt, Alex W., Khor, Chiea Chuen, Pasquale, Louis R., Montgomery, Grant W., Klaver, Caroline C. W., Aung, Tin, Pfeiffer, Norbert, Mackey, David A., Hammond, Christopher J., Cheng, Ching-Yu, Craig, Jamie E., Rabinowitz, Yaron S., Wiggs, Janey L., Burdon, Kathryn P., van Duijn, Cornelia M., MacGregor, Stuart
Publié dans Nat Commun (2019)

Genome of the Netherlands population-specific imputations identify an ABCA6 variant associated with cholesterol levels

par van Leeuwen, Elisabeth M., Karssen, Lennart C., Deelen, Joris, Isaacs, Aaron, Medina-Gomez, Carolina, Mbarek, Hamdi, Kanterakis, Alexandros, Trompet, Stella, Postmus, Iris, Verweij, Niek, van Enckevort, David J., Huffman, Jennifer E., White, Charles C., Feitosa, Mary F., Bartz, Traci M., Manichaikul, Ani, Joshi, Peter K., Peloso, Gina M., Deelen, Patrick, van Dijk, Freerk, Willemsen, Gonneke, de Geus, Eco J., Milaneschi, Yuri, Penninx, Brenda W.J.H., Francioli, Laurent C., Menelaou, Androniki, Pulit, Sara L., Rivadeneira, Fernando, Hofman, Albert, Oostra, Ben A., Franco, Oscar H., Leach, Irene Mateo, Beekman, Marian, de Craen, Anton J.M., Uh, Hae-Won, Trochet, Holly, Hocking, Lynne J., Porteous, David J., Sattar, Naveed, Packard, Chris J., Buckley, Brendan M., Brody, Jennifer A., Bis, Joshua C., Rotter, Jerome I., Mychaleckyj, Josyf C., Campbell, Harry, Duan, Qing, Lange, Leslie A., Wilson, James F., Hayward, Caroline, Polasek, Ozren, Vitart, Veronique, Rudan, Igor, Wright, Alan F., Rich, Stephen S., Psaty, Bruce M., Borecki, Ingrid B., Kearney, Patricia M., Stott, David J., Adrienne Cupples, L., Jukema, J. Wouter, van der Harst, Pim, Sijbrands, Eric J., Hottenga, Jouke-Jan, Uitterlinden, Andre G., Swertz, Morris A., van Ommen, Gert-Jan B., de Bakker, Paul I.W., Eline Slagboom, P., Boomsma, Dorret I., Wijmenga, Cisca, van Duijn, Cornelia M.
Publié dans Nat Commun (2015)

Discovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density Imputation

par Horikoshi, Momoko, Mӓgi, Reedik, van de Bunt, Martijn, Surakka, Ida, Sarin, Antti-Pekka, Mahajan, Anubha, Marullo, Letizia, Thorleifsson, Gudmar, Hӓgg, Sara, Hottenga, Jouke-Jan, Ladenvall, Claes, Ried, Janina S., Winkler, Thomas W., Willems, Sara M., Pervjakova, Natalia, Esko, Tõnu, Beekman, Marian, Nelson, Christopher P., Willenborg, Christina, Wiltshire, Steven, Ferreira, Teresa, Fernandez, Juan, Gaulton, Kyle J., Steinthorsdottir, Valgerdur, Hamsten, Anders, Magnusson, Patrik K. E., Willemsen, Gonneke, Milaneschi, Yuri, Robertson, Neil R., Groves, Christopher J., Bennett, Amanda J., Lehtimӓki, Terho, Viikari, Jorma S., Rung, Johan, Lyssenko, Valeriya, Perola, Markus, Heid, Iris M., Herder, Christian, Grallert, Harald, Müller-Nurasyid, Martina, Roden, Michael, Hypponen, Elina, Isaacs, Aaron, van Leeuwen, Elisabeth M., Karssen, Lennart C., Mihailov, Evelin, Houwing-Duistermaat, Jeanine J., de Craen, Anton J. M., Deelen, Joris, Havulinna, Aki S., Blades, Matthew, Hengstenberg, Christian, Erdmann, Jeanette, Schunkert, Heribert, Kaprio, Jaakko, Tobin, Martin D., Samani, Nilesh J., Lind, Lars, Salomaa, Veikko, Lindgren, Cecilia M., Slagboom, P. Eline, Metspalu, Andres, van Duijn, Cornelia M., Eriksson, Johan G., Peters, Annette, Gieger, Christian, Jula, Antti, Groop, Leif, Raitakari, Olli T., Power, Chris, Penninx, Brenda W. J. H., de Geus, Eco, Smit, Johannes H., Boomsma, Dorret I., Pedersen, Nancy L., Ingelsson, Erik, Thorsteinsdottir, Unnur, Stefansson, Kari, Ripatti, Samuli, Prokopenko, Inga, McCarthy, Mark I., Morris, Andrew P.
Publié dans PLoS Genet (2015)