Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans von Nadkarni, Girish N., MD, MPH, CPH, Galarneau, Geneviève, PhD, Ellis, Stephen B., MS, Nadukuru, Rajiv, MS, Zhang, Jinglan, PhD, Scott, Stuart A., PhD, Schurmann, Claudia, PhD, Li, Rongling, MD, PhD, MPH, Rasmussen-Torvik, Laura J., PhD, Kho, Abel N., MD, Hayes, M. Geoffrey, PhD, Pacheco, Jennifer A., MS, Manolio, Teri A., MD, PhD, Chisholm, Rex L., PhD, Roden, Dan M., MD, Denny, Joshua C., MD, MS, Kenny, Eimear E., PhD, Bottinger, Erwin P., MD

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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation von Galarneau, Geneviève, Palmer, Cameron D, Sankaran, Vijay G, Orkin, Stuart H, Hirschhorn, Joel N, Lettre, Guillaume

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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions von Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Møller, Peter L., Stefansdottir, Lilja, Galarneau, Geneviève, Turman, Constance, Danning, Rebecca, Law, Matthew H., Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Sobalska-Kwapis, Marta, Topbas-Selcuki, Nura F., Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S., Campbell, Archie, Cheuk, Cecilia S. K., DiVasta, Amy, Dorien, O., Donoghue, Jacqueline F., Fontanillas, Pierre, Geirsson, Reynir T., Girling, Jane E., Harkki, Paivi, Harris, Holly R., Heikinheimo, Oskari, Hostettler, Isabel C., Houlden, Henry, Houshdaran, Sahar, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H., Kettunen, Johannes, Kubo, Michiaki, Kulig, Bartosz, Laivuori, Hannele, Laufer, Marc R., Lindgren, Cecilia M., MacGregor, Stuart, Mangino, Massimo, Martin, Nicholas G., Matalliotakis, Michail, Murray, Alison D., Ndungu, Anne, Nezhat, Camran, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Peters, Maire, Polak, Grzegorz, Porteous, David J., Rexrode, Kathyrn M., Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J., Sen, Sushmita, Shafrir, Amy L., Siewierska-Górska, Anna, Smith, Blair H., Szaflik, Tomasz, Takahashi, Atsushi, Terry, Kathryn L., Tomassetti, Carla, Vanhie, Arne, Vincent, Katy, Vo, Kim C., Werring, David J., Zervou, Maria I., Adachi, Sosuke, Buring, Julie E., Ridker, Paul M., D’Hooghe, Thomas, Hapangama, Dharani K., Hayward, Caroline, Low, Siew-Kee, Martikainen, Hannu, Chasman, Daniel I., Saunders, Philippa T., Sirota, Marina, Spector, Tim, Strapagiel, Dominik, Tung, Joyce Y., Whiteman, David C., Velez-Edwards, Digna R., Uimari, Outi, Kraft, Peter, Salumets, Andres, Nyholt, Dale R., Stefansson, Kari, Becker, Christian M., Nyegaard, Mette, Missmer, Stacey A., Montgomery, Grant W., Morris, Andrew P.

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Gene-centric association study of acute chest syndrome and painful crisis in sickle cell disease patients von Galarneau, Geneviève, Coady, Sean, Garrett, Melanie E., Jeffries, Neal, Puggal, Mona, Paltoo, Dina, Soldano, Karen, Guasch, Antonio, Ashley-Koch, Allison E., Telen, Marilyn J., Kutlar, Abdullah, Lettre, Guillaume, Papanicolaou, George J.

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Genetic association analysis highlights new loci that modulate hematological trait variation in Caucasians and African Americans von Lo, Ken Sin, Wilson, James G, Lange, Leslie A, Folsom, Aaron R, Galarneau, Geneviève, Ganesh, Santhi K, Grant, Struan F. A, Keating, Brendan J, McCarroll, Steven A, Mohler III, Emile R, O'Donnell, Christopher J, Palmas, Walter, Tang, Weihong, Tracy, Russell P, Reiner, Alexander P, Lettre, Guillaume

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APOL1 renal risk variants are associated with obesity and body composition in African ancestry adults: An observational genotype–phenotype association study von Nadkarni, Girish N., Fei, Kezhen, Galarneau, Genevieve, Gao, Yan, Wilson, James G., Cooper, Richard, Madden, Ebony B., Denny, Joshua C., Richardson, Lynne D., Pollak, Martin, Loos, Ruth J. F., Horowitz, Carol R.

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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions von Rahmioglu, Nilufer, Mortlock, Sally, Ghiasi, Marzieh, Moller, Peter L, Stefansdottir, Lilja, Galarneau, Genevieve, Turman, Constance, Danning, Rebecca, Law, Matthew H, Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Blazej, Noukas, Margit, Perro, Danielle, Sliz, Eeva, Sobalska-Kwapis, Marta, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F, Vitonis, Allison, Westergaard, David, Arnadottir, Ragnheidur, Burgdorf, Kristoffer S, Campbell, Archie, Cheuk, Cecilia S.K, Clementi, Caterina, Cook, James, De Vivo, Immaculata, DiVasta, Amy, Dorien, O, Donoghue, Jacqueline F, Edwards, Todd, Fontanillas, Pierre, Fung, Jenny N, Geirsson, Reynir T, Girling, Jane E, Harkki, Paivi, Harris, Holly R, Healey, Martin, Heikinheimo, Oskari, Holdsworth-Carson, Sarah, Hostettler, Isabel C, Houlden, Henry, Houshdaran, Sahar, Irwin, Juan C, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H, Kepka, Ewa, Kettunen, Johannes, Kubo, Michiaki, Kulig, Bartosz, Kurra, Venla, Laivuori, Hannele, Laufer, Marc R, Lindgren, Cecilia M, MacGregor, Stuart, Mangino, Massimo, Martin, Nicholas G, Matalliotaki, Charoula, Matalliotakis, Michail, Murray, Alison D, Ndungu, Anne, Nezhat, Camran, Olsen, Catherine M, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Paranjpe, Manish, Peters, Maire, Polak, Grzegorz, Porteous, David J, Rabban, Joseph, Rexrode, Kathyrn M, Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J, Sen, Sushmita, Shafrir, Amy L, Siewierska-Gorska, Anna, Slomka, Marcin, Smith, Blair H, Smolarz, Beata, Szaflik, Tomasz, Szyllo, Krzysztof, Takahashi, Atsushi, Terry, Kathryn L, Tomassetti, Carla, Treloar, Susan A, Vanhie, Arne, Vincent, Katy, Vo, Kim C, Werring, David J, Zeggini, Eleftheria, Zervou, Maria, Stefansson, Kari

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The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions von Mortlock, Sally, Møller, Peter L, Law, Matthew H, Sapkota, Yadav, Christofidou, Paraskevi, Skarp, Sini, Giri, Ayush, Banasik, Karina, Krassowski, Michal, Lepamets, Maarja, Marciniak, Błażej, Nõukas, Margit, Thorleifsson, Gudmar, Topbas-Selcuki, Nura F, Westergaard, David, Cheuk, Cecilia SK, Clementi, Caterina, Cook, James, De Vivo, Immaculata, Dorien, O, Donoghue, Jacqueline F, Edwards, Todd, Fontanillas, Pierre, Harkki, Paivi, Harris, Holly R, Healey, Martin, Heikinheimo, Oskari, Holdsworth-Carson, Sarah, Houlden, Henry, Irwin, Juan C, Jarvelin, Marjo-Riitta, Kamatani, Yoichiro, Kennedy, Stephen H, Kepka, Ewa, Kettunen, Johannes, Kubo, Michiaki, Kurra, Venla, Laufer, Marc R, MacGregor, Stuart, Mangino, Massimo, Matalliotaki, Charoula, Matalliotakis, Michail, Murray, Alison D, Ndungu, Anne, Nezhat, Camran, Opoku-Anane, Jessica, Padmanabhan, Sandosh, Paranjpe, Manish, Peters, Maire, Polak, Grzegorz, Porteous, David J, Rabban, Joseph, Romanowicz, Hanna, Saare, Merli, Saavalainen, Liisu, Schork, Andrew J, Sen, Sushmita, Shafrir, Amy L, Siewierska-Górska, Anna, Słomka, Marcin, Smith, Blair H, Szaflik, Tomasz, Szyłło, Krzysztof, Takahashi, Atsushi, Terry, Kathryn L, Tomassetti, Carla, Treloar, Susan A, Vincent, Katy, Vo, Kim C, Werring, David J, Zeggini, Eleftheria, Zervou, Maria I, DBDS Genomic Consortium, FinnGen Study, FinnGen Endometriosis Taskforce, Celmatix Research Team, 23andMe Research Team, Adachi, Sosuke, Ridker, Paul M, D'Hooghe, Thomas, Goulielmos, George N, Hapangama, Dharani K, Hayward, Caroline, Horne, Andrew W, Low, Siew-Kee, Martikainen, Hannu, Chasman, Daniel I, Rogers, Peter AW, Saunders, Philippa T, Velez-Edwards, Digna R, Kraft, Peter, Salumets, Andres, Nyholt, Dale R, Mägi, Reedik, Stefansson, Kari, Becker, Christian M, Nyegaard, Mette, Montgomery, Grant W, Morris, Andrew P, Zondervan, Krina T

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METHODS FOR ASSESSING RISK OF INCREASED TIME-TO-FIRST-CONCEPTION von GALARNEAU, Genevieve, BEIM, Piraye

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METHODS FOR ASSESSING RISK OF INCREASED TIME-TO-FIRST-CONCEPTION von Beim, Piraye Yurttas, Galarneau, Genevieve

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Fine-mapping at three loci known to affect fetal hemoglobin levels explains additional genetic variation von Galarneau, Genevieve, Palmer, Cameron D, Sankaran, Vijay G, Orkin, Stuart H, Hirschhorn, Joel N, Lettre, Guillaume

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Examining the sensitivity of 18F-NaF PET for the imaging of cardiac amyloidosis von Martineau, Patrick, Finnerty, Vincent, Giraldeau, Geneviève, Authier, Sébastien, Harel, Francois, Pelletier-Galarneau, Matthieu

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Foreseeing the worst: Forecasting electricity DART spikes von Galarneau-Vincent, Rémi, Gauthier, Geneviève, Godin, Frédéric

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Comparison of 18F-sodium fluoride positron emission tomography imaging and 99mTc-pyrophosphate in cardiac amyloidosis von Zhang, Li Xin, Martineau, Patrick, Finnerty, Vincent, Giraldeau, Geneviève, Parent, Marie-Claude, Harel, François, Pelletier-Galarneau, Matthieu

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Venturing into uncharted territory: An extensible implied volatility surface model von François, Pascal, Galarneau‐Vincent, Rémi, Gauthier, Geneviève, Godin, Frédéric

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Increased glioma growth in mice depleted of macrophages von GALARNEAU, Hugo, VILLENEUVE, Jérome, GOWING, Geneviève, JULIEN, Jean-Pierre, VALLIERES, Luc

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Le nouveau programme formel de mentorat du Collège québécois des médecins de famille von Côté, Luc, Deschênes, Dominique, Hudon, Éveline, Galarneau, Sophie, Bolduc, Geneviève

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Quebec College of Family Physicians' new formal mentorship program von Côté, Luc, Deschênes, Dominique, Hudon, Éveline, Galarneau, Sophie, Bolduc, Geneviève

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Evaluation of the sensitivity of 18F-NaF PET for the imaging of cardiac amyloidosis von Martineau, Patrick, Finnerty, Vincent, Giraldeau, Genevieve, Authier, Sebastien, Harel, Francois, Pelletier-Galarneau, Matthieu

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Molecular Imaging of Cardiac Amyloidosis von Pelletier-Galarneau, Matthieu, Abikhzer, Gad, Giraldeau, Genevieve, Harel, Francois

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