Breast-Feeding Modifies the Association of PPARγ2 Polymorphism Pro12Ala With Growth in Early Life: The Generation R Study

Por Mook-Kanamori, Dennis O., Steegers, Eric A.P., Uitterlinden, Andre G., Moll, Henriëtte A., van Duijn, Cornelia M., Hofman, Albert, Jaddoe, Vincent W.V.
Publicado em 2009

Heritability Estimates of Body Size in Fetal Life and Early Childhood

Por Mook-Kanamori, Dennis O., van Beijsterveldt, Catharina E. M., Steegers, Eric A. P., Aulchenko, Yurii S., Raat, Hein, Hofman, Albert, Eilers, Paul H., Boomsma, Dorret I., Jaddoe, Vincent W. V.
Publicado em 2012

Type 2 diabetes gene TCF7L2 polymorphism is not associated with fetal and postnatal growth in two birth cohort studies

Por Mook-Kanamori, Dennis O, de Kort, Sandra WK, van Duijn, Cornelia M, Uitterlinden, Andre G, Hofman, Albert, Moll, Henriëtte A, Steegers, Eric AP, Hokken-Koelega, Anita CS, Jaddoe, Vincent WV
Publicado em 2009

Elevated HbA1c levels in individuals not diagnosed with type 2 diabetes in Qatar: a pilot study

Por Mook-Kanamori, Marjonneke J., El-Din Selim, Mohammed M., Takiddin, Ahmed H., Al-Mahmoud, Khoulood A.S., Al-Homsi, Hala, McKeon, Cindy, Al Muftah, Wadha A., Kader, Sara Abdul, Mook-Kanamori, Dennis O., Suhre, Karsten
Publicado no Qatar Med J (2014)

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

Por 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 AC
Publicado em 2013

LysoPC-acyl C16:0 is associated with brown adipose tissue activity in men

Por Boon, Mariëtte R., Bakker, Leontine E. H., Prehn, Cornelia, Adamski, Jerzy, Vosselman, Maarten J., Jazet, Ingrid M., Arias-Bouda, Lenka M. Pereira, van Lichtenbelt, Wouter D. Marken, van Dijk, Ko Willems, Rensen, Patrick C. N., Mook-Kanamori, Dennis O.
Publicado no Metabolomics (2017)

Gender-specific pathway differences in the human serum metabolome

Por Krumsiek, Jan, Mittelstrass, Kirstin, Do, Kieu Trinh, Stückler, Ferdinand, Ried, Janina, Adamski, Jerzy, Peters, Annette, Illig, Thomas, Kronenberg, Florian, Friedrich, Nele, Nauck, Matthias, Pietzner, Maik, Mook-Kanamori, Dennis O., Suhre, Karsten, Gieger, Christian, Grallert, Harald, Theis, Fabian J., Kastenmüller, Gabi
Publicado no Metabolomics (2015)

Ethnic and gender differences in advanced glycation end products measured by skin auto-fluorescence

Por Mook-Kanamori, Marjonneke J, Selim, Mohammed M El-Din, Takiddin, Ahmed H, Al-Homsi, Hala, Al-Mahmoud, Khoulood A S, Al-Obaidli, Amina, Zirie, Mahmoud A, Rowe, Jillian, Gherbi, Wafaa Sekkal, Chidiac, Omar M, Kader, Sara Abdul, Al Muftah, Wadha A, McKeon, Cindy, Suhre, Karsten, Mook-Kanamori, Dennis O
Publicado em 2013

A systems view of type 2 diabetes-associated metabolic perturbations in saliva, blood and urine at different timescales of glycaemic control

Por Yousri, Noha A., Mook-Kanamori, Dennis O., Selim, Mohammed M. El-Din, Takiddin, Ahmed H., Al-Homsi, Hala, Al-Mahmoud, Khoulood A. S., Karoly, Edward D., Krumsiek, Jan, Do, Kieu Thinh, Neumaier, Ulrich, Mook-Kanamori, Marjonneke J., Rowe, Jillian, Chidiac, Omar M., McKeon, Cindy, Al Muftah, Wadha A., Kader, Sara Abdul, Kastenmüller, Gabi, Suhre, Karsten
Publicado no Diabetologia (2015)

Erratum to: A systems view of type 2 diabetes-associated metabolic perturbations in saliva, blood and urine at different timescales of glycaemic control

Por Yousri, Noha A., Mook-Kanamori, Dennis O., El-Din Selim, Mohammed M., Takiddin, Ahmed H., Al-Homsi, Hala, Al-Mahmoud, Khoulood A. S., Karoly, Edward D., Krumsiek, Jan, Do, Kieu Trinh, Neumaier, Ulrich, Mook-Kanamori, Marjonneke J., Rowe, Jillian, Chidiac, Omar M., McKeon, Cindy, Al Muftah, Wadha A., Kader, Sara Abdul, Kastenmüller, Gabi, Suhre, Karsten
Publicado no Diabetologia (2015)

Connecting genetic risk to disease end points through the human blood plasma proteome

Por Suhre, Karsten, Arnold, Matthias, Bhagwat, Aditya Mukund, Cotton, Richard J., Engelke, Rudolf, Raffler, Johannes, Sarwath, Hina, Thareja, Gaurav, Wahl, Annika, DeLisle, Robert Kirk, Gold, Larry, Pezer, Marija, Lauc, Gordan, El-Din Selim, Mohammed A., Mook-Kanamori, Dennis O., Al-Dous, Eman K., Mohamoud, Yasmin A., Malek, Joel, Strauch, Konstantin, Grallert, Harald, Peters, Annette, Kastenmüller, Gabi, Gieger, Christian, Graumann, Johannes
Publicado no Nat Commun (2017)

Erratum: Connecting genetic risk to disease end points through the human blood plasma proteome

Por Suhre, Karsten, Arnold, Matthias, Bhagwat, Aditya Mukund, Cotton, Richard J., Engelke, Rudolf, Raffler, Johannes, Sarwath, Hina, Thareja, Gaurav, Wahl, Annika, DeLisle, Robert Kirk, Gold, Larry, Pezer, Marija, Lauc, Gordan, El-Din Selim, Mohammed A., Mook-Kanamori, Dennis O., Al-Dous, Eman K., Mohamoud, Yasmin A., Malek, Joel, Strauch, Konstantin, Grallert, Harald, Peters, Annette, Kastenmüller, Gabi, Gieger, Christian, Graumann, Johannes
Publicado no Nat Commun (2017)

Association between Common Variation at the FTO Locus and Changes in Body Mass Index from Infancy to Late Childhood: The Complex Nature of Genetic Association through Growth and De...

Por Sovio, Ulla, Mook-Kanamori, Dennis O., Warrington, Nicole M., Lawrence, Robert, Briollais, Laurent, Palmer, Colin N. A., Cecil, Joanne, Sandling, Johanna K., Syvänen, Ann-Christine, Kaakinen, Marika, Beilin, Lawrie J., Millwood, Iona Y., Bennett, Amanda J., Laitinen, Jaana, Pouta, Anneli, Molitor, John, Davey Smith, George, Ben-Shlomo, Yoav, Jaddoe, Vincent W. V., Palmer, Lyle J., Pennell, Craig E., Cole, Tim J., McCarthy, Mark I., Järvelin, Marjo-Riitta, Timpson, Nicholas J.
Publicado em 2011

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

Por Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceshini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.
Publicado no Am J Hum Genet (2016)

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

Por Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.
Publicado no Am J Hum Genet (2016)

Common variants at 6q22 and 17q21 are associated with intracranial volume

Por Ikram, M. Arfan, Fornage, Myriam, Smith, Albert V., Seshadri, Sudha, Schmidt, Reinhold, Debette, Stéphanie, Vrooman, Henri A., Sigurdsson, Sigurdur, Ropele, Stefan, Taal, H. Rob, Mook-Kanamori, Dennis O., Coker, Laura H., Longstreth, W.T., Niessen, Wiro J., DeStefano, Anita L., Beiser, Alexa, Zijdenbos, Alex P., Struchalin, Maksim, Jack, Clifford R., Rivadeneira, Fernando, Uitterlinden, Andre G., Knopman, David S., Hartikainen, Anna-Liisa, Pennell, Craig E., Thiering, Elisabeth, Steegers, Eric A.P., Hakonarson, Hakon, Heinrich, Joachim, Palmer, Lyle J, Jarvelin, Marjo-Riitta, McCarthy, Mark I., Grant, Struan F.A., St Pourcain, Beate, Timpson, Nicholas J, Smith, George Davey, Sovio, Ulla, Nalls, Mike A., Au, Rhoda, Hofman, Albert, Gudnason, Haukur, van der Lugt, Aad, Harris, Tamara B., Meeks, William M., Vernooij, Meike W., van Buchem, Mark A., Catellier, Diane, Jaddoe, Vincent W.V., Gudnason, Vilmundur, Windham, B. Gwen, Wolf, Philip A., van Duijn, Cornelia M., Mosley, Thomas H., Schmidt, Helena, Launer, Lenore J., Breteler, Monique M.B., DeCarli, Charles
Publicado em 2012

Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight

Por Freathy, Rachel M, Mook-Kanamori, Dennis O, Sovio, Ulla, Prokopenko, Inga, Timpson, Nicholas J, Berry, Diane J, Warrington, Nicole M, Widen, Elisabeth, Hottenga, Jouke Jan, Kaakinen, Marika, Lange, Leslie A, Bradfield, Jonathan P, Kerkhof, Marjan, Marsh, Julie A, Mägi, Reedik, Chen, Chih-Mei, Lyon, Helen N, Kirin, Mirna, Adair, Linda S, Aulchenko, Yurii S, Bennett, Amanda J, Borja, Judith B, Bouatia-Naji, Nabila, Charoen, Pimphen, Coin, Lachlan J M, Cousminer, Diana L, de Geus, Eco J. C., Deloukas, Panos, Elliott, Paul, Evans, David M, Froguel, Philippe, Glaser, Beate, Groves, Christopher J, Hartikainen, Anna-Liisa, Hassanali, Neelam, Hirschhorn, Joel N, Hofman, Albert, Holly, Jeff M P, Hyppönen, Elina, Kanoni, Stavroula, Knight, Bridget A, Laitinen, Jaana, Lindgren, Cecilia M, McArdle, Wendy L, O'Reilly, Paul F, Pennell, Craig E, Postma, Dirkje S, Pouta, Anneli, Ramasamy, Adaikalavan, Rayner, Nigel W, Ring, Susan M, Rivadeneira, Fernando, Shields, Beverley M, Strachan, David P, Surakka, Ida, Taanila, Anja, Tiesler, Carla, Uitterlinden, Andre G, van Duijn, Cornelia M, Wijga, Alet H, Willemsen, Gonneke, Zhang, Haitao, Zhao, Jianhua, Wilson, James F, Steegers, Eric A P, Hattersley, Andrew T, Eriksson, Johan G, Peltonen, Leena, Mohlke, Karen L, Grant, Struan F A, Hakonarson, Hakon, Koppelman, Gerard H, Dedoussis, George V, Heinrich, Joachim, Gillman, Matthew W, Palmer, Lyle J, Frayling, Timothy M, Boomsma, Dorret I, Smith, George Davey, Power, Chris, Jaddoe, Vincent W V, Jarvelin, Marjo-Riitta, McCarthy, Mark I
Publicado em 2010

A genome-wide association meta-analysis identifies new childhood obesity loci

Por Bradfield, Jonathan P., Taal, H. Rob, Timpson, Nicholas J., Scherag, André, Lecoeur, Cecile, Warrington, Nicole M., Hypponen, Elina, Holst, Claus, Valcarcel, Beatriz, Thiering, Elisabeth, Salem, Rany M., Schumacher, Fredrick R., Cousminer, Diana L., Sleiman, Patrick M.A., Zhao, Jianhua, Berkowitz, Robert I., Vimaleswaran, Karani S., Jarick, Ivonne, Pennell, Craig E., Evans, David M., St. Pourcain, Beate, Berry, Diane J., Mook-Kanamori, Dennis O, Hofman, Albert, Rivadeinera, Fernando, Uitterlinden, André G., van Duijn, Cornelia M., van der Valk, Ralf J.P., de Jongste, Johan C., Postma, Dirkje S., Boomsma, Dorret I., Gauderman, William J., Hassanein, Mohamed T., Lindgren, Cecilia M., Mägi, Reedik, Boreham, Colin A.G., Neville, Charlotte E., Moreno, Luis A., Elliott, Paul, Pouta, Anneli, Hartikainen, Anna-Liisa, Li, Mingyao, Raitakari, Olli, Lehtimäki, Terho, Eriksson, Johan G., Palotie, Aarno, Dallongeville, Jean, Das, Shikta, Deloukas, Panos, McMahon, George, Ring, Susan M., Kemp, John P., Buxton, Jessica L., Blakemore, Alexandra I.F., Bustamante, Mariona, Guxens, Mònica, Hirschhorn, Joel N., Gillman, Matthew W., Kreiner-Møller, Eskil, Bisgaard, Hans, Gilliland, Frank D., Heinrich, Joachim, Wheeler, Eleanor, Barroso, Inês, O'Rahilly, Stephen, Meirhaeghe, Aline, Sørensen, Thorkild I.A., Power, Chris, Palmer, Lyle J., Hinney, Anke, Widen, Elisabeth, Farooqi, I. Sadaf, McCarthy, Mark I., Froguel, Philippe, Meyre, David, Hebebrand, Johannes, Jarvelin, Marjo-Riitta, Jaddoe, Vincent W.V., Smith, George Davey, Hakonarson, Hakon, Grant, Struan F.A.
Publicado em 2012

Common variants at 12q15 and 12q24 are associated with infant head circumference

Por Taal, H Rob, Pourcain, Beate St, Thiering, Elisabeth, Das, Shikta, Mook-Kanamori, Dennis O, Warrington, Nicole M, Kaakinen, Marika, Kreiner-Møller, Eskil, Bradfield, Jonathan P, Freathy, Rachel M, Geller, Frank, Guxens, Mònica, Cousminer, Diana L, Kerkhof, Marjan, Timpson, Nicholas J, Ikram, M Arfan, Beilin, Lawrence J, Bønnelykke, Klaus, Buxton, Jessica L, Charoen, Pimphen, Chawes, Bo Lund Krogsgaard, Eriksson, Johan, Evans, David M, Hofman, Albert, Kemp, John P, Kim, Cecilia E, Klopp, Norman, Lahti, Jari, Lye, Stephen J, McMahon, George, Mentch, Frank D, Müller, Martina, O’Reilly, Paul F, Prokopenko, Inga, Rivadeneira, Fernando, Steegers, Eric A P, Sunyer, Jordi, Tiesler, Carla, Yaghootkar, Hanieh, Breteler, Monique M B, Debette, Stephanie, Fornage, Myriam, Gudnason, Vilmundur, Launer, Lenore J, van der Lugt, Aad, Mosley, Thomas H, Seshadri, Sudha, Smith, Albert V, Vernooij, Meike W, Blakemore, Alexandra IF, Chiavacci, Rosetta M, Feenstra, Bjarke, Fernandez-Benet, Julio, Grant, Struan F A, Hartikainen, Anna-Liisa, van der Heijden, Albert J, Iñiguez, Carmen, Lathrop, Mark, McArdle, Wendy L, Mølgaard, Anne, Newnham, John P, Palmer, Lyle J, Palotie, Aarno, Pouta, Annneli, Ring, Susan M, Sovio, Ulla, Standl, Marie, Uitterlinden, Andre G, Wichmann, H-Erich, Vissing, Nadja Hawwa, DeCarli, Charles, van Duijn, Cornelia M, McCarthy, Mark I, Koppelman, Gerard H., Estivill, Xavier, Hattersley, Andrew T, Melbye, Mads, Bisgaard, Hans, Pennell, Craig E, Widen, Elisabeth, Hakonarson, Hakon, Smith, George Davey, Heinrich, Joachim, Jarvelin, Marjo-Riitta, Jaddoe, Vincent W V
Publicado em 2012

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Por van Leeuwen, Elisabeth M, Sabo, Aniko, Bis, Joshua C, Huffman, Jennifer E, Manichaikul, Ani, Smith, Albert V, Feitosa, Mary F, Demissie, Serkalem, Joshi, Peter K, Duan, Qing, Marten, Jonathan, van Klinken, Jan B, Surakka, Ida, Nolte, Ilja M, Zhang, Weihua, Mbarek, Hamdi, Li-Gao, Ruifang, Trompet, Stella, Verweij, Niek, Evangelou, Evangelos, Lyytikäinen, Leo-Pekka, Tayo, Bamidele O, Deelen, Joris, van der Most, Peter J, van der Laan, Sander W, Arking, Dan E, Morrison, Alanna, Dehghan, Abbas, Franco, Oscar H, Hofman, Albert, Rivadeneira, Fernando, Sijbrands, Eric J, Uitterlinden, Andre G, Mychaleckyj, Josyf C, Campbell, Archie, Hocking, Lynne J, Padmanabhan, Sandosh, Brody, Jennifer A, Rice, Kenneth M, White, Charles C, Harris, Tamara, Isaacs, Aaron, Campbell, Harry, Lange, Leslie A, Rudan, Igor, Kolcic, Ivana, Navarro, Pau, Zemunik, Tatijana, Salomaa, Veikko, Kooner, Angad S, Kooner, Jaspal S, Lehne, Benjamin, Scott, William R, Tan, Sian-Tsung, de Geus, Eco J, Milaneschi, Yuri, Penninx, Brenda W J H, Willemsen, Gonneke, de Mutsert, Renée, Ford, Ian, Gansevoort, Ron T, Segura-Lepe, Marcelo P, Raitakari, Olli T, Viikari, Jorma S, Nikus, Kjell, Forrester, Terrence, McKenzie, Colin A, de Craen, Anton J M, de Ruijter, Hester M, Pasterkamp, Gerard, Snieder, Harold, Oldehinkel, Albertine J, Slagboom, P Eline, Cooper, Richard S, Kähönen, Mika, Lehtimäki, Terho, Elliott, Paul, van der Harst, Pim, Jukema, J Wouter, Mook-Kanamori, Dennis O, Boomsma, Dorret I, Chambers, John C, Swertz, Morris, Ripatti, Samuli, Willems van Dijk, Ko, Vitart, Veronique, Polasek, Ozren, Hayward, Caroline, Wilson, James G, Wilson, James F, Gudnason, Vilmundur, Rich, Stephen S, Psaty, Bruce M, Borecki, Ingrid B, Boerwinkle, Eric, Rotter, Jerome I, Cupples, L Adrienne, van Duijn, Cornelia M
Publicado no J Med Genet (2016)