Monocyte gene expression signature of patients with early onset coronary artery disease
Sivapalaratnam, Suthesh, Basart, Hanneke, Watkins, Nicholas A, Maiwald, Stepanie, Rendon, Augusto, Krishnan, Unni, Sondermeijer, Brigitte M, Creemers, Esther E, Pinto-Sietsma, Sara J, Hovingh, Kees, Ouwehand, Willem H, Kastelein, John J P, Goodall, Alison H, Trip, Mieke D
Published in PloS one (21.02.2012)
Published in PloS one (21.02.2012)
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Maps of open chromatin guide the functional follow-up of genome-wide association signals: application to hematological traits
Paul, Dirk S, Nisbet, James P, Yang, Tsun-Po, Meacham, Stuart, Rendon, Augusto, Hautaviita, Katta, Tallila, Jonna, White, Jacqui, Tijssen, Marloes R, Sivapalaratnam, Suthesh, Basart, Hanneke, Trip, Mieke D, Göttgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H, Deloukas, Panos
Published in PLoS genetics (01.06.2011)
Published in PLoS genetics (01.06.2011)
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Best Practices for the Diagnosis and Evaluation of Infants With Robin Sequence: A Clinical Consensus Report
Breugem, Corstiaan C, Evans, Kelly N, Poets, Christian F, Suri, Sunjay, Picard, Arnaud, Filip, Charles, Paes, Emma C, Mehendale, Felicity V, Saal, Howard M, Basart, Hanneke, Murthy, Jyotsna, Joosten, Koen F M, Speleman, Lucienne, Collares, Marcus V M, van den Boogaard, Marie-José H, Muradin, Marvick, Andersson, Maud Els-Marie, Kogo, Mikihiko, Farlie, Peter G, Don Griot, Peter, Mossey, Peter A, Slator, Rona, Abadie, Veronique, Hong, Paul
Published in JAMA pediatrics (01.09.2016)
Published in JAMA pediatrics (01.09.2016)
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Large-scale gene-centric analysis identifies novel variants for coronary artery disease
Butterworth, AS, Farrall, M, Hardwick, RJ, Saleheen, D, Peden, JF, Soranzo, N, Chambers, JC, Sivapalaratnam, S, Kleber, ME, Klopp, N, Erdmann, J, Assimes, TL, Ball, SG, Balmforth, AJ, Barnes, TA, Basart, H, Baumert, J, Bezzina, CR, Boerwinkle, E, Boehm, BO, Brocheton, J, Bugert, P, Cambien, F, Clarke, R, Codd, V, Collins, R, Couper, D, Cupples, LA, de Jong, JS, Diemert, P, Ejebe, K, Elbers, CC, Elliott, P, Fornage, M, Franzosi, MG, Frossard, P, Garner, S, Goel, A, Goodall, AH, Hengstenberg, C, Hunt, SE, Kastelein, JJP, Klungel, OH, Kluter, H, Koch, K, Konig, IR, Kooner, AS, Laaksonen, R, Lathrop, M, Li, MY, Liu, K, McPherson, R, Musameh, MD, Musani, S, Nelson, CP, O'Donnell, CJ, Ongen, H, Papanicolaou, G, Peters, A, Peters, BJM, Potter, S, Psaty, BM, Qu, LM, Rader, DJ, Rasheed, A, Rice, C, Scott, J, Seedorf, U, Sehmi, JS, Sotoodehnia, N, Stark, K, Stephens, J, van der Schoot, CE, van der Schouw, YT, Tomaszewski, M, van der Harst, P, Vasan, RS, Wilde, AAM, Willenborg, C, Winkelmann, BR, Zaidi, M, Zhang, WH, Ziegler, A, de Bakker, PIW, Koenig, W, Marz, W, Trip, MD, Reilly, MP, Kathiresan, S, Schunkert, H, Hamsten, A, Hall, AS, Kooner, JS, Thompson, SG, Thompson, JR, Deloukas, P, Ouwehand, WH, Watkins, H, Danesh, J, Samani, NJ
Published in PLoS genetics (01.09.2011)
Published in PLoS genetics (01.09.2011)
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An international randomised placebo-controlled trial of a four-component combination pill ("polypill") in people with raised cardiovascular risk
Rodgers, Anthony, Patel, Anushka, Berwanger, Otavio, Bots, Michiel, Grimm, Richard, Grobbee, Diederick E, Jackson, Rod, Neal, Bruce, Neaton, Jim, Poulter, Neil, Rafter, Natasha, Raju, P Krishnam, Reddy, Srinath, Thom, Simon, Vander Hoorn, Stephen, Webster, Ruth
Published in PloS one (25.05.2011)
Published in PloS one (25.05.2011)
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Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals
Guo, Yiran, Lanktree, Matthew B, Taylor, Kira C, Hakonarson, Hakon, Lange, Leslie A, Keating, Brendan J
Published in Human molecular genetics (01.01.2013)
Published in Human molecular genetics (01.01.2013)
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Optimised treatment of patients with enlarged lateral lymph nodes in rectal cancer: protocol of an international, multicentre, prospective registration study after extensive multidisciplinary training (LaNoReC)
Sluckin, Tania C, Intven, Martijn, Lange, Marilyne M, Taggart, Melissa W, Beets-Tan, Regina G H, Konishi, Tsuyoshi, Tanis, Pieter J, Kusters, Miranda, Geijsen, Elisabeth D., Hompes, Roel, Meijnen, Philip, Stoker, Jaap, Bruijnzeel, Ingrid M., Lamme, Bas, Alberts, Femke M., Crolla, Rogier M. P. H., Verdult, Joanne, van Kessel, Charlotte S., Mulder, Erik Jan, Hulshoff, Jan Binne, Cherepanin, Ivan M., Fabry, Hans F. J., Kemper, Frank J. M., Cnossen, Jeltsje S., Nederend, Joost, de Bie, Shira H., Bosker, Robbert J. I., Boogerd, Leonora S. F., Govaert, Marc J. P. M., Antonisse, Imogeen E., Rothbarth, Joost, Vries, Marianne de, Ribbert, Marcel A. H., Borg, Susan ter, Verseveld, Maria, de Korte, Fleur I., Marinelli, Andreas W. K. S., Westerterp, Marinke, Aukema, Tjeerd S., van Bockel, Liselotte W., van Tilborg, Aukje A. J. M., Rozema, Tom, Hoogendoorn, Stefan, Offerman, Saskia R., Vos, Hanneke, van Westreenen, Henderik L., Leijtens, Jeroen W. A., Peeters, Koen C.M.J., Velema, Laura A., Els, L, Meerten, van Persijn van, Bakers, Frans C. H., Šefčovičová, Nina, Berbée, Maaike, Rouw, Dennis B., René Arensman, L., Basart, Hanneke, Consten, Esther C. J., Verheijen, Paul M., Fassaert, Thomas A., Hoff, Christiaan, van Duyn, Eino B., Hendriksen, Ellen M., Grotenhuis, Brechtje A., van Geel, Anne M., Meischl, Christof, Hermien Schreurs, W., Spruit, Patty H., Gerhards, Michael F., Karsten, Thomas M., Peringa, Jan, Koeverden, Sebastiaan van, Bremers, Andre J. A., Rütten, Heidi, de Wilt, Johannes H. W., Hartogh, Mariska den, Muller, Karin, Oppedijk, Vera, Dekker, Jan Willem T., Eschbach-Zandbergen, Debora, Gerbrands, Krista, Roos, Daphne, Jan, Ernst, Knijn, Nikki, de Roos, Marnix A. J., Dop, Ilse van, Croft, Michael, Ruszkiewicz, Andrew, Wilks, Michael, Oosterling, Steven J., Tielbeek, Jeroen A. W., Vuylsteke, Ronald J. C. L. M., van der Hoeven, Erik J. R. J., Braat, Manon N. G. J. A., van Grevenstein, Wilhelmina M. U., Richir, Milan C., Leseman, Tilly, Belgers, Eric H. J., Krdzalic, Jasenko, Vliegen, Roy F. A.
Published in BMJ open (16.10.2024)
Published in BMJ open (16.10.2024)
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Meta-analysis of Gene-Level Associations for Rare Variants Based on Single-Variant Statistics
Berndt, Sonja I., Wheeler, Eleanor, Croteau-Chonka, Damien C., Day, Felix R., Esko, Tõnu, Jackson, Anne U., Vedantam, Sailaja, Wood, Andrew R., Workalemahu, Tsegaselassie, Hu, Yi-Juan, Thorleifsson, Gudmar, den Heijer, Martin, Kanoni, Stavroula, Lecoeur, Cecile, Li, Guo, Paternoster, Lavinia, Rose, Lynda M., Strawbridge, Rona J., Teumer, Alexander, Van Vliet-Ostaptchouk, Jana V., Waite, Lindsay L., Absher, Devin, Attwood, Antony P., Campbell, Harry, Connell, John M., de Vegt, Femmie, Edkins, Sarah, Evans, David M., Farrall, Martin, Grallert, Harald, Grönberg, Henrik, Gudnason, Vilmundur, Hall, Per, Hayward, Caroline, Heath, Andrew C., Hebebrand, Johannes, Homuth, Georg, Hu, Frank B., Jansson, John-Olov, Jula, Antti, Kathiresan, Sekar, Kuulasmaa, Kari, Kuusisto, Johanna, Launer, Lenore J., Lorentzon, Mattias, Madden, Pamela A., Magnusson, Patrik K., März, Winfried, Montgomery, Grant W., Mühleisen, Thomas W., Munroe, Patricia B., Narisu, Narisu, Peden, John F., Pedersen, Nancy, Pramstaller, Peter P., Pütter, Carolin, Raitakari, Olli, Sambrook, Jennifer G., Sanna, Serena, Stančáková, Alena, Stark, Klaus, Stephens, Jonathan C., Swift, Amy J., Theodoraki, Eirini V., Thorand, Barbara, van Meurs, Joyce B.J., Viikari, Jorma, Virtamo, Jarmo, Waeber, Gérard, Wolffenbuttel, Bruce H.R., Boerwinkle, Eric, Cupples, L. Adrienne, Eriksson, Johan G., Gieger, Christian, Hengstenberg, Christian, Hinney, Anke, Jöckel, Karl-Heinz, Kiemeney, Lambertus A., Martin, Nicholas G., Nieminen, Markku S., Njølstad, Inger, Penninx, Brenda, Power, Chris, Province, Michael A., Qi, Lu, Samani, Nilesh J., Sørensen, Thorkild I.A., Vollenweider, Peter, Borecki, Ingrid B., Deloukas, Panos, Groop, Leif C., Karpe, Fredrik, Moffatt, Miriam, O’Connell, Jeffrey R., Pawitan, Yudi, Schlessinger, David, Di Blasio, Anna Maria, Scherag, André, Ingelsson, Erik, Lin, Dan-Yu
Published in American journal of human genetics (08.08.2013)
Published in American journal of human genetics (08.08.2013)
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Objectifying Micrognathia Using Three-Dimensional Photogrammetric Analysis
Basart, Hanneke, Suttie, Michael, Ibrahim, Amel, Ferretti, Patrizia, van der Horst, Chantal M A M, Hennekam, Raoul C, Hammond, Peter
Published in The Journal of craniofacial surgery (01.11.2018)
Published in The Journal of craniofacial surgery (01.11.2018)
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Etiology and pathogenesis of robin sequence in a large Dutch cohort
Basart, Hanneke, Paes, Emma C., Maas, Saskia M., van den Boogaard, Marie-Jose H., van Hagen, Johanna M., Breugem, Corstiaan C., Cobben, Jan Maarten, Don Griot, J. Peter W., Lachmeijer, Augusta M. A., Lichtenbelt, Klaske D., van Nunen, Daan P. F., van der Horst, Chantal M., Hennekam, Raoul C.
Published in American journal of medical genetics. Part A (01.09.2015)
Published in American journal of medical genetics. Part A (01.09.2015)
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Birth prevalence of Robin sequence in the Netherlands from 2000-2010: a retrospective population-based study in a large Dutch cohort and review of the literature
Paes, Emma C., van Nunen, Daan P. F., Basart, Hanneke, Don Griot, J. Peter W., van Hagen, Johanna M., van der Horst, Chantal M. A. M., van den Boogaard, Marie-José H., Breugem, Corstiaan C.
Published in American journal of medical genetics. Part A (01.09.2015)
Published in American journal of medical genetics. Part A (01.09.2015)
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Health‐related quality of life in children with Robin sequence
Basart, Hanneke, van Oers, Hedy A., Paes, Emma C., Breugem, Corstiaan C., Don Griot, J. Peter W., van der Horst, Chantal M. A. M., Haverman, Lotte, Hennekam, Raoul C.
Published in American journal of medical genetics. Part A (01.01.2017)
Published in American journal of medical genetics. Part A (01.01.2017)
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Will the right Robin patient rise, please? Definitions and criteria during management of Robin sequence patients in the Netherlands and Belgium
Basart, Hanneke, Kruisinga, Frea H, Breugem, Corstiaan C, Don Griot, J. Peter W, Hennekam, Raoul C, Van der Horst, Chantal M.A.M
Published in Journal of cranio-maxillo-facial surgery (01.01.2015)
Published in Journal of cranio-maxillo-facial surgery (01.01.2015)
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Frontometaphyseal dysplasia and keloid formation without FLNA mutations
Basart, Hanneke, van de Kar, Annekatrien, Adès, Lesley, Cho, Tae-Joon, Carter, Erin, Maas, Saskia M., Wilson, Louise C., van der Horst, Chantal M. A. M., Wade, Emma M., Robertson, Stephen P., Hennekam, Raoul C.
Published in American journal of medical genetics. Part A (01.06.2015)
Published in American journal of medical genetics. Part A (01.06.2015)
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Correction: Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits
Dirk S. Paul, James P. Nisbet, Tsun-Po Yang, Stuart Meacham, Augusto Rendon, Katta Hautaviita, Jonna Tallila, Jacqui White, Marloes R. Tijssen, Suthesh Sivapalaratnam, Hanneke Basart, Mieke D. Trip, Berthold Göttgens, Nicole Soranzo, Willem H. Ouwehand, Panos Deloukas
Published in PLoS genetics (01.07.2011)
Published in PLoS genetics (01.07.2011)
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Sex-stratified Genome-wide Association Studies Including 270,000 Individuals Show Sexual Dimorphism in Genetic Loci for Anthropometric Traits: e1003500
Winkler, Thomas W, Monda, Keri L, Mägi, Reedik, Workalemahu, Tsegaselassie, Croteau-Chonka, Damien C, Steinthorsdottir, Valgerdur, Dimas, Antigone S, Clegg, Deborah J, Person, Thomas, Krohn, Jon P, Buechler, Christa, Eisinger, Kristina, Froguel, Philippe, Hottenga, Jouke-Jan, Harris, Tamara B, Chen, Yii-Der Ida, Johnson, Toby, Thorsteinsdottir, Unnur, Teder-Laving, Maris, Amin, Najaf, Oostra, Ben A, Province, Michael A, Kaprio, Jaakko, Saramies, Jouko, Jula, Antti, Loley, Christina, Schunkert, Heribert, Wichmann, H Erich, Albrecht, Eva, Gieger, Christian, Hicks, Andrew A, Speliotes, Elizabeth K, Hartikainen, Anna-Liisa, Jarvelin, Marjo-Riitta, Gyllensten, Ulf, Campbell, Harry, Farrall, Martin, Rivadeneira, Fernando, Hofman, Albert, Zillikens, M Carola, Heijer, Martin den, Kiemeney, Lambertus A, Maschio, Andrea, Tyrer, Jonathan, Kovacs, Peter, Attwood, Antony Paul, Lokki, Marja-Liisa, Sinisalo, Juha, Ohlsson, Claes, Snieder, Harold, Gejman, Pablo V, Shi, Jianxin, Navis, Gerjan, Medland, Sarah E, Montgomery, Grant W, Yang, Jian, Chasman, Daniel I, Ridker, Paul M, Rose, Lynda M, Lehtimäki, Terho, Iribarren, Carlos, Hovingh, Kees G, Anderson, Denise, Sager, Hendrik, Lindström, Jaana, Uusitupa, Matti, Rauramaa, Rainer, Fowkes, Gerry, Fischer, Krista, Luan, an, Keinanen-Kiukaanniemi, Sirkka M, Morris, Andrew David, Palmer, Colin NA, Hveem, Kristian, Narisu, Narisu, Humphries, Steve E, Grallert, Harald, Illig, Thomas, Müller-Nurasyid, Martina, Peters, Annette, Kleber, Marcus E, März, Winfried, Winkelmann, Bernhard R, Laakso, Markku, Kuulasmaa, Kari, Virtamo, Jarmo, Yarnell, John WG, Faire, Ulf de, Magnusson, Patrik KE, Dimitriou, Maria, Stirrups, Kathleen, Ganna, Andrea, Rehnberg, Emil, Assimes, Themistocles L, Fox, Caroline S, Groop, Leif C, Duijn, Cornelia Mvan, Qi, Lu, North, Kari E, Heid, Iris M
Published in PLoS genetics (01.06.2013)
Published in PLoS genetics (01.06.2013)
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Correction: Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits
Paul, Dirk S., Nisbet, James P., Yang, Tsun-Po, Meacham, Stuart, Rendon, Augusto, Hautaviita, Katta, Tallila, Jonna, White, Jacqui, Tijssen, Marloes R., Sivapalaratnam, Suthesh, Basart, Hanneke, Trip, Mieke D., Göttgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H., Deloukas, Panos
Published in PLoS genetics (21.07.2011)
Published in PLoS genetics (21.07.2011)
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Maps of Open Chromatin Guide the Functional Follow-Up of Genome-Wide Association Signals: Application to Hematological Traits: e1002139
Paul, Dirk S, Nisbet, James P, Yang, Tsun-Po, Meacham, Stuart, Rendon, Augusto, Hautaviita, Katta, Tallila, Jonna, White, Jacqui, Tijssen, Marloes R, Sivapalaratnam, Suthesh, Basart, Hanneke, Trip, Mieke D, Göttgens, Berthold, Soranzo, Nicole, Ouwehand, Willem H, Deloukas, Panos, Cardiogenics, Consortium, MuTHER, Consortium
Published in PLoS genetics (01.06.2011)
Published in PLoS genetics (01.06.2011)
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