Emotion processing in Alzheimer's disease von CADIEUX, NICOLE L., GREVE, KEVIN W.

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Hyperphagia and obesity in female rats with temporal lobe lesions von King, Bruce M., Kass, Jenny M., Cadieux, Nicole L., Sam, Hoan, Neville, Katherine L., Arceneaux, Elizabeth R.

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CLINICAL COMMENTS von Rife, John C., Smith, Charles E., Bissett, Bruce, Greve, Kevin W., Cadieux, Nicole, Hale, Mary Anne, Gafner, George, Coolidge, Frederick L., Janitell, Patricia M., Griego, Jacqueline A., McGreevey, John F., Miller, Barbara Kopp, McSweeney, A. John, Hicks, Barbara, Brink, T. L., Features Submission, Haworth Continuing

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IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans von Bakey, Zeineb, Cabrera, Oscar A, Hoefele, Julia, Antony, Dinu, Wu, Kaman, Stuck, Michael W, Micha, Dimitra, Eguether, Thibaut, Smith, Abigail O, van der Wel, Nicole N, Wagner, Matias, Strittmatter, Lara, Beales, Philip L, Jonassen, Julie A, Thiffault, Isabelle, Cadieux-Dion, Maxime, Boyes, Laura, Sharif, Saba, Tüysüz, Beyhan, Dunstheimer, Desiree, Niessen, Hans W M, Devine, William, Lo, Cecilia W, Mitchison, Hannah M, Schmidts, Miriam, Pazour, Gregory J

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Pharmacological Inhibition of Endogenous Hydrogen Sulfide Production Slows Bladder Cancer Progression in an Intravesical Murine Model von Relouw, Sydney, Dugbartey, George J, McLeod, Patrick, Knier, Natasha N, Santiesteban, Francisco Martinez, Foster, Paula J, Cadieux-Pitre, Heather-Anne, Hague, Nicole M, Caine, Jenna, Belletti, Kaitlin, Major, Sally, O'Neil, Caroline, Gabril, Manal Y, Moussa, Madeleine, Huynh, Melissa J, Haeryfar, S M Mansour, Sener, Alp

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Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report von Cadieux-Dion, Maxime, Safina, Nicole P, Engleman, Kendra, Saunders, Carol, Repnikova, Elena, Raje, Nikita, Canty, Kristi, Farrow, Emily, Miller, Neil, Zellmer, Lee, Thiffault, Isabelle

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TESS discovery of a sub-Neptune orbiting a mid-M dwarf TOI-2136 von Gan, Tianjun, Soubkiou, Abderahmane, Wang, Sharon X, Benkhaldoun, Zouhair, Mao, Shude, Artigau, Étienne, Fouqué, Pascal, Arnold, Luc, Giacalone, Steven, Theissen, Christopher A, Aganze, Christian, Burgasser, Adam, Collins, Karen A, Shporer, Avi, Barkaoui, Khalid, Ghachoui, Mourad, Howell, Steve B, Lamman, Claire, Demangeon, Olivier D S, Burdanov, Artem, Cadieux, Charles, Chouqar, Jamila, Collins, Kevin I, Cook, Neil J, Delrez, Laetitia, Demory, Brice-Olivier, Doyon, René, Dransfield, Georgina, Dressing, Courtney D, Ducrot, Elsa, Fan, Jiahao, Garcia, Lionel, Gill, Holden, Gillon, Michaël, Gnilka, Crystal L, Gómez Maqueo Chew, Yilen, Günther, Maximilian N, Henze, Christopher E, Huang, Chelsea X, Jehin, Emmanuel, Jensen, Eric L N, Lin, Zitao, Manset, Nadine, McCormac, James, Murray, Catriona A, Niraula, Prajwal, Pedersen, Peter P, Pozuelos, Francisco J, Queloz, Didier, Rackham, Benjamin V, Savel, Arjun B, Schanche, Nicole, Schwarz, Richard P, Sebastian, Daniel, Thompson, Samantha, Timmermans, Mathilde, Triaud, Amaury H M J, Vezie, Michael, Wells, Robert D, de Wit, Julien, Ricker, George R, Vanderspek, Roland, Latham, David W, Seager, Sara, Winn, Joshua N, Jenkins, Jon M

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Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia von Guissart, Claire, Latypova, Xenia, Rollier, Paul, Khan, Tahir N., Stamberger, Hannah, McWalter, Kirsty, Cho, Megan T., Kjaergaard, Susanne, Weckhuysen, Sarah, Lesca, Gaetan, Besnard, Thomas, Õunap, Katrin, Schema, Lynn, Chiocchetti, Andreas G., McDonald, Marie, de Bellescize, Julitta, Vincent, Marie, Van Esch, Hilde, Sattler, Shannon, Forghani, Irman, Thiffault, Isabelle, Freitag, Christine M., Barbouth, Deborah Sara, Cadieux-Dion, Maxime, Willaert, Rebecca, Guillen Sacoto, Maria J., Safina, Nicole P., Dubourg, Christèle, Grote, Lauren, Carré, Wilfrid, Saunders, Carol, Pajusalu, Sander, Farrow, Emily, Boland, Anne, Karlowicz, Danielle Hays, Deleuze, Jean-François, Wojcik, Monica H., Pressman, Rena, Isidor, Bertrand, Vogels, Annick, Van Paesschen, Wim, Al-Gazali, Lihadh, Al Shamsi, Aisha Mohamed, Claustres, Mireille, Pujol, Aurora, Sanders, Stephan J., Rivier, François, Leboucq, Nicolas, Cogné, Benjamin, Sasorith, Souphatta, Sanlaville, Damien, Retterer, Kyle, Odent, Sylvie, Katsanis, Nicholas, Bézieau, Stéphane, Koenig, Michel, Davis, Erica E., Pasquier, Laurent, Küry, Sébastien

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A Classification and Regression Tree for Predicting Recurrent Falling among Community-dwelling Seniors Using Home-care Services von Leclerc, Bernard S., Bégin, Claude, Cadieux, Élizabeth, Goulet, Lise, Allaire, Jean-François, Meloche, Julie, Leduc, Nicole, Kergoat, Marie-Jeanne

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Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia von Guissart, Claire, Latypova, Xenia, Rollier, Paul, Khan, Tahir N, Stamberger, Hannah, McWalter, Kirsty, Cho, Megan T, Kjaergaard, Susanne, Weckhuysen, Sarah, Lesca, Gaetan, Besnard, Thomas, Õunap, Katrin, Schema, Lynn, Chiocchetti, Andreas G, McDonald, Marie, de Bellescize, Julitta, Vincent, Marie, Van Esch, Hilde, Sattler, Shannon, Forghani, Irman, Thiffault, Isabelle, Freitag, Christine M, Barbouth, Deborah Sara, Cadieux-Dion, Maxime, Willaert, Rebecca, Guillen Sacoto, Maria J, Safina, Nicole P, Dubourg, Christèle, Grote, Lauren, Carré, Wilfrid, Saunders, Carol, Pajusalu, Sander, Farrow, Emily, Boland, Anne, Karlowicz, Danielle Hays, Deleuze, Jean-François, Wojcik, Monica H, Pressman, Rena, Isidor, Bertrand, Vogels, Annick, Van Paesschen, Wim, Al-Gazali, Lihadh, Al Shamsi, Aisha Mohamed, Claustres, Mireille, Pujol, Aurora, Sanders, Stephan J, Rivier, François, Leboucq, Nicolas, Cogné, Benjamin, Sasorith, Souphatta, Sanlaville, Damien, Retterer, Kyle, Odent, Sylvie, Katsanis, Nicholas, Bézieau, Stéphane, Koenig, Michel, Davis, Erica E, Pasquier, Laurent, Küry, Sébastien

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IFT74 variants cause skeletal ciliopathy and motile cilia defects in mice and humans von Bakey, Zeineb, Cabrera, Oscar A, Hoefele, Julia, Antony, Dinu, Wu, Kaman, Stuck, Michael W, Micha, Dimitra, Eguether, Thibaut, Smith, Abigail O, van der Wel, Nicole N, Wagner, Matias, Strittmatter, Lara, Beales, Philip L, Jonassen, Julie A, Thiffault, Isabelle, Cadieux-Dion, Maxime, Boyes, Laura, Sharif, Saba, Tüysüz, Beyhan, Dunstheimer, Desiree, Niessen, Hans WM, Devine, William, Lo, Cecilia W, Mitchison, Hannah M, Schmidts, Miriam, Pazour, Gregory J

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TESS discovery of a sub-Neptune orbiting a mid-M dwarf TOI-2136 von Gan, Tianjun, Soubkiou, Abderahmane, Wang, Sharon X, Benkhaldoun, Zouhair, Mao, Shude, Artigau, Étienne, Fouqué, Pascal, Giacalone, Steven, Theissen, Christopher A, Aganze, Christian, Collins, Karen A, Shporer, Avi, Barkaoui, Khalid, Ghachoui, Mourad, Howell, Steve B, Lamman, Claire, Demangeon, Olivier D S, Burdanov, Artem, Cadieux, Charles, Chouqar, Jamila, Collins, Kevin I, Cook, Neil J, Delrez, Laetitia, Brice-Olivier Demory, Doyon, René, Dransfield, Georgina, Dressing, Courtney D, Ducrot, Elsa, Fan, Jiahao, Garcia, Lionel, Holden, Gill, Gillon, Michaël, Gnilka, Crystal L, Yilen Gómez Maqueo Chew, Günther, Maximilian N, Henze, Christopher E, Huang, Chelsea X, Jehin, Emmanuel, Jensen, Eric L N, Lin, Zitao, McCormac, James, Murray, Catriona A, Niraula, Prajwal, Pedersen, Peter P, Pozuelos, Francisco J, Queloz, Didier, Rackham, Benjamin V, Savel, Arjun B, Schanche, Nicole, Schwarz, Richard P, Sebastian, Daniel, Thompson, Samantha, Timmermans, Mathilde, Amaury H M J Triaud, Vezie, Michael, Wells, Robert D, de Wit, Julien, Ricker, George R, Vanderspek, Roland, Latham, David W, Seager, Sara, Winn, Joshua N, Jenkins, Jon M

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Dual Molecular Effects of Dominant RORA Mutations Cause Two Variants of Syndromic Intellectual Disability with Either Autism or Cerebellar Ataxia von Guissart, Claire, Latypova, Xenia, Rollier, Paul, Khan, Tahir N, Stamberger, Hannah, McWalter, Kirsty, Cho, Megan T, Kjaergaard, Susanne, Weckhuysen, Sarah, Lesca, Gaetan, Besnard, Thomas, Õunap, Katrin, Schema, Lynn, Chiocchetti, Andreas G, Mcdonald, Marie, Bellescize, Julitta de, Vincent, Marie, Van Esch, Hilde, Sattler, Shannon, Forghani, Irman, Thiffault, Isabelle, Freitag, Christine M, Barbouth, Deborah Sara, Cadieux-Dion, Maxime, Willaert, Rebecca, Guillen Sacoto, Maria J, Safina, Nicole P, Dubourg, Christèle, Grote, Lauren, Carre, Wilfrid, Saunders, Carol, Pajusalu, Sander, Farrow, Emily, Boland, Anne, Karlowicz, Danielle Hays, Deleuze, Jean-François, Wojcik, Monica H, Pressman, Rena, Isidor, Bertrand, Vogels, Annick, Van Paesschen, Wim, Al-Gazali, Lihadh, Mohamed Al Shamsi, Aisha, Claustres, Mireille, Pujol Onofre, Aurora, Sanders, Stephan, Rivier, François, Leboucq, Nicolas, Cogne, Benjamin, Sasorith, Souphatta, Sanlaville, Damien, Retterer, Kyle, Odent, Sylvie, Katsanis, Nicholas, Bézieau, Stéphane, Koenig, Michel, Davis, Erica E, Pasquier, Laurent, Küry, Sébastien

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TESS discovery of a sub-Neptune orbiting a mid-M dwarf TOI-2136 von Gan, Tianjun, Soubkiou, Abderahmane, Wang, Sharon X., Benkhaldoun, Zouhair, Mao, Shude, Artigau, Étienne, Fouqué, Pascal, Giacalone, Steven, Theissen, Christopher A., Aganze, Christian, Collins, Karen A., Shporer, Avi, Barkaoui, Khalid, Ghachoui, Mourad, Howell, Steve B., Lamman, Claire, Olivier D. S. Demangeon, Burdanov, Artem, Cadieux, Charles, Chouqar, Jamila, Collins, Kevin I., Cook, Neil J., Delrez, Laetitia, Demory, Brice-Olivier, Doyon, René, Dransfield, Georgina, Dressing, Courtney D., Ducrot, Elsa, Fan, Jiahao, Garcia, Lionel, Gill, Holden, Gillon, Michaël, Gnilka, Crystal L., Gómez Maqueo Chew, Yilen, Günther, Maximilian N., Henze, Christopher E., Huang, Chelsea X., Jehin, Emmanuel, Eric L. N. Jensen, Lin, Zitao, McCormac, James, Murray, Catriona A., Niraula, Prajwal, Pedersen, Peter P., Pozuelos, Francisco J., Queloz, Didier, Rackham, Benjamin V., Savel, Arjun B., Schanche, Nicole, Schwarz, Richard P., Sebastian, Daniel, Thompson, Samantha, Timmermans, Mathilde, Amaury H. M. J. Triaud, Vezie, Michael, Wells, Robert D., de Wit, Julien, Ricker, George R., Vanderspek, Roland, Latham, David W., Seager, Sara, Winn, Joshua N., Jenkins, Jon M.

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Additional file 3: of Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report von Cadieux-Dion, Maxime, Safina, Nicole, Engleman, Kendra, Saunders, Carol, Repnikova, Elena, Raje, Nikita, Canty, Kristi, Farrow, Emily, Miller, Neil, Zellmer, Lee, Thiffault, Isabelle

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Additional file 2: of Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report von Cadieux-Dion, Maxime, Safina, Nicole, Engleman, Kendra, Saunders, Carol, Repnikova, Elena, Raje, Nikita, Canty, Kristi, Farrow, Emily, Miller, Neil, Zellmer, Lee, Thiffault, Isabelle

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Additional file 1: of Novel heterozygous pathogenic variants in CHUK in a patient with AEC-like phenotype, immune deficiencies and 1q21.1 microdeletion syndrome: a case report von Cadieux-Dion, Maxime, Safina, Nicole, Engleman, Kendra, Saunders, Carol, Repnikova, Elena, Raje, Nikita, Canty, Kristi, Farrow, Emily, Miller, Neil, Zellmer, Lee, Thiffault, Isabelle

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