Combining TerraSAR-X and time-lapse photography for seasonal sea ice monitoring: the case of Deception Bay, Nunavik von Dufour-Beausejour, Sophie, Wendleder, Anna, Gauthier, Yves, Bernier, Monique, Poulin, Jimmy, Gilbert, Veronique, Tuniq, Juupi, Rouleau, Amelie, Roth, Achim

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(Tables S4-S6) Break-up sequence observations in Nunavik's Deception Bay from TerraSAR-X and time-lapse photography (2016-2018) von Dufour-Beauséjour, Sophie, Wendleder, Anna, Gauthier, Yves, Bernier, Monique, Poulin, Jimmy, Gilbert, Véronique, Tuniq, Juupi, Rouleau, Amélie

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WHIM Syndrome-linked CXCR4 mutations drive osteoporosis von Anginot, Adrienne, Nguyen, Julie, Abou Nader, Zeina, Rondeau, Vincent, Bonaud, Amélie, Kalogeraki, Maria, Boutin, Antoine, Lemos, Julia P., Bisio, Valeria, Koenen, Joyce, Hanna Doumit Sakr, Lea, Picart, Amandine, Coudert, Amélie, Provot, Sylvain, Dulphy, Nicolas, Aurrand-Lions, Michel, Mancini, Stéphane J. C., Lazennec, Gwendal, McDermott, David H., Guidez, Fabien, Blin-Wakkach, Claudine, Murphy, Philip M., Cohen-Solal, Martine, Espéli, Marion, Rouleau, Matthieu, Balabanian, Karl

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Genome-wide meta-analyses of restless legs syndrome yield insights into genetic architecture, disease biology and risk prediction von Schormair, Barbara, Zhao, Chen, Bell, Steven, Didriksen, Maria, Nawaz, Muhammad S., Schandra, Nathalie, Stefani, Ambra, Högl, Birgit, Dauvilliers, Yves, Bachmann, Cornelius G., Kemlink, David, Sonka, Karel, Paulus, Walter, Trenkwalder, Claudia, Oertel, Wolfgang H., Hornyak, Magdolna, Teder-Laving, Maris, Metspalu, Andres, Hadjigeorgiou, Georgios M., Polo, Olli, Fietze, Ingo, Ross, Owen A., Wszolek, Zbigniew K., Ibrahim, Abubaker, Bergmann, Melanie, Kittke, Volker, Harrer, Philip, Dowsett, Joseph, Chenini, Sofiene, Ostrowski, Sisse Rye, Sørensen, Erik, Erikstrup, Christian, Pedersen, Ole B., Topholm Bruun, Mie, Nielsen, Kaspar R., Butterworth, Adam S., Soranzo, Nicole, Ouwehand, Willem H., Roberts, David J., Danesh, John, Burchell, Brendan, Furlotte, Nicholas A., Nandakumar, Priyanka, Earley, Christopher J., Ondo, William G., Xiong, Lan, Desautels, Alex, Perola, Markus, Vodicka, Pavel, Dina, Christian, Stoll, Monika, Franke, Andre, Lieb, Wolfgang, Stewart, Alexandre F. R., Shah, Svati H., Gieger, Christian, Peters, Annette, Rye, David B., Rouleau, Guy A., Berger, Klaus, Stefansson, Hreinn, Ullum, Henrik, Stefansson, Kari, Hinds, David A., Di Angelantonio, Emanuele, Oexle, Konrad, Winkelmann, Juliane

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Direct Measure of the De Novo Mutation Rate in Autism and Schizophrenia Cohorts von Awadalla, Philip, Gauthier, Julie, Myers, Rachel A., Casals, Ferran, Hamdan, Fadi F., Griffing, Alexander R., Côté, Mélanie, Henrion, Edouard, Spiegelman, Dan, Tarabeux, Julien, Piton, Amélie, Yang, Yan, Boyko, Adam, Bustamante, Carlos, Xiong, Lan, Rapoport, Judith L., Addington, Anjené M., DeLisi, J. Lynn E., Krebs, Marie-Odile, Joober, Ridha, Millet, Bruno, Fombonne, Éric, Mottron, Laurent, Zilversmit, Martine, Keebler, Jon, Daoud, Hussein, Marineau, Claude, Roy-Gagnon, Marie-Hélène, Dubé, Marie-Pierre, Eyre-Walker, Adam, Drapeau, Pierre, Stone, Eric A., Lafrenière, Ronald G., Rouleau, Guy A.

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De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment von Hamdan, Fadi F., Daoud, Hussein, Rochefort, Daniel, Piton, Amélie, Gauthier, Julie, Langlois, Mathieu, Foomani, Gila, Dobrzeniecka, Sylvia, Krebs, Marie-Odile, Joober, Ridha, Lafrenière, Ronald G., Lacaille, Jean-Claude, Mottron, Laurent, Drapeau, Pierre, Beauchamp, Miriam H., Phillips, Michael S., Fombonne, Eric, Rouleau, Guy A., Michaud, Jacques L.

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Durvalumab compared to maintenance chemotherapy in metastatic breast cancer: the randomized phase II SAFIR02-BREAST IMMUNO trial von Bachelot, Thomas, Filleron, Thomas, Bieche, Ivan, Arnedos, Monica, Campone, Mario, Dalenc, Florence, Coussy, Florence, Sablin, Marie-Paule, Debled, Marc, Lefeuvre-Plesse, Claudia, Goncalves, Anthony, Reynier, Marie-Ange Mouret, Jacot, William, You, Benoit, Barthelemy, Philippe, Verret, Benjamin, Isambert, Nicolas, Tchiknavorian, Xavier, Levy, Christelle, Thery, Jean-Christophe, L’Haridon, Tifenn, Ferrero, Jean-Marc, Mege, Alice, Del Piano, Francesco, Rouleau, Etienne, Tran-Dien, Alicia, Adam, Julien, Lusque, Amelie, Jimenez, Marta, Jacquet, Alexandra, Garberis, Ingrid, Andre, Fabrice

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Montreal Cognitive Assessment and the Clock Drawing Test to Identify MCI and Predict Dementia in Isolated REM Sleep Behavior Disorder von Cogné, Émile, Postuma, Ronald B, Chasles, Marie-Joëlle, De Roy, Jessie, Montplaisir, Jacques, Pelletier, Amélie, Rouleau, Isabelle, Gagnon, Jean-François

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Mutations in the calcium-related gene IL1RAPL1 are associated with autism von Piton, Amélie, Michaud, Jacques L., Peng, Huashan, Aradhya, Swaroop, Gauthier, Julie, Mottron, Laurent, Champagne, Nathalie, Lafrenière, Ronald G., Hamdan, Fadi F., Joober, Ridha, Fombonne, Eric, Marineau, Claude, Cossette, Patrick, Dubé, Marie-Pierre, Haghighi, Pejmun, Drapeau, Pierre, Barker, Philip A., Carbonetto, Salvatore, Rouleau, Guy A.

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Does Hospitalization Influence Patients’ Medication Adherence and Community Pharmacists’ Interventions? von Beloin-Jubinville, Bianca, Joly-Mischlich, Thomas, Rouleau, Emilie Dufort, Noiseux, Pascale, Blais, Lucie, Forget, Amélie, Beauchesne, Marie-France

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Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia von Farazi Fard, Mohammad Ali, Rebelo, Adriana P., Buglo, Elena, Nemati, Hamid, Dastsooz, Hassan, Gehweiler, Ina, Reich, Selina, Reichbauer, Jennifer, Quintáns, Beatriz, Ordóñez-Ugalde, Andrés, Cortese, Andrea, Courel, Steve, Abreu, Lisa, Powell, Eric, Danzi, Matt C., Martuscelli, Nicole B., Bis-Brewer, Dana M., Tao, Feifei, Zarei, Fariba, Habibzadeh, Parham, Yavarian, Majid, Modarresi, Farzaneh, Silawi, Mohammad, Tabatabaei, Zahra, Yousefi, Masoume, Farpour, Hamid Reza, Kessler, Christoph, Mangold, Elisabeth, Kobeleva, Xenia, Tournev, Ivailo, Chamova, Teodora, Mueller, Amelie J., Haack, Tobias B., Tarnopolsky, Mark, Gan-Or, Ziv, Rouleau, Guy A., Synofzik, Matthis, Sobrido, María-Jesús, Jordanova, Albena, Schüle, Rebecca, Zuchner, Stephan, Faghihi, Mohammad Ali

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Genomics to select treatment for patients with metastatic breast cancer von Andre, Fabrice, Filleron, Thomas, Kamal, Maud, Mosele, Fernanda, Arnedos, Monica, Dalenc, Florence, Sablin, Marie-Paule, Campone, Mario, Bonnefoi, Hervé, Lefeuvre-Plesse, Claudia, Jacot, William, Coussy, Florence, Ferrero, Jean-Marc, Emile, George, Mouret-Reynier, Marie-Ange, Thery, Jean-Christophe, Isambert, Nicolas, Mege, Alice, Barthelemy, Philippe, You, Benoit, Hajjaji, Nawale, Lacroix, Ludovic, Rouleau, Etienne, Tran-Dien, Alicia, Boyault, Sandrine, Attignon, Valery, Gestraud, Pierre, Servant, Nicolas, Le Tourneau, Christophe, Cherif, Linda Larbi, Soubeyran, Isabelle, Montemurro, Filippo, Morel, Alain, Lusque, Amelie, Jimenez, Marta, Jacquet, Alexandra, Gonçalves, Anthony, Bachelot, Thomas, Bieche, Ivan

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Verbal and Visual Memory Impairments Among Young Offspring and Healthy Adult Relatives of Patients With Schizophrenia and Bipolar Disorder: Selective Generational Patterns Indicate... von Maziade, Michel, Rouleau, Nancie, Mérette, Chantal, Cellard, Caroline, Battaglia, Marco, Marino, Cecilia, Jomphe, Valérie, Gilbert, Elsa, Achim, Amélie, Bouchard, Roch-Hugo, Paccalet, Thomas, Paradis, Marie-Eve, Roy, Marc-André

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De Novo Truncating Mutation in Kinesin 17 Associated with Schizophrenia von Tarabeux, Julien, Champagne, Nathalie, Brustein, Edna, Hamdan, Fadi F, Gauthier, Julie, Lapointe, Mathieu, Maios, Claudia, Piton, Amélie, Spiegelman, Dan, Henrion, Édouard, Millet, Bruno, Rapoport, Judith L, DeLisi, Lynn E, Joober, Ridha, Fathalli, Ferid, Fombonne, Éric, Mottron, Laurent, Forget-Dubois, Nadine, Boivin, Michel, Michaud, Jacques L, Lafrenière, Ronald G, Drapeau, Pierre, Krebs, Marie-Odile, Rouleau, Guy A

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SCARB2 variants and glucocerebrosidase activity in Parkinson’s disease von Alcalay, Roy N, Levy, Oren A, Wolf, Pavlina, Oliva, Petra, Zhang, Xiaokui Kate, Waters, Cheryl H, Fahn, Stanley, Kang, Un Jung, Liong, Christopher, Ford, Blair, Mazzoni, Pietro, Kuo, Sheng, Johnson, Amelie, Xiong, Lan, Rouleau, Guy A, Chung, Wendy K, Marder, Karen S, Gan-Or, Ziv

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Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability von Hamdan, Fadi F., Gauthier, Julie, Araki, Yoichi, Lin, Da-Ting, Yoshizawa, Yuhki, Higashi, Kyohei, Park, A-reum, Spiegelman, Dan, Dobrzeniecka, Sylvia, Piton, Amélie, Tomitori, Hideyuki, Daoud, Hussein, Massicotte, Christine, Henrion, Edouard, Diallo, Ousmane, Shekarabi, Masoud, Marineau, Claude, Shevell, Michael, Maranda, Bruno, Mitchell, Grant, Nadeau, Amélie, D'Anjou, Guy, Vanasse, Michel, Srour, Myriam, Lafrenière, Ronald G., Drapeau, Pierre, Lacaille, Jean Claude, Kim, Eunjoon, Lee, Jae-Ran, Igarashi, Kazuei, Huganir, Richard L., Rouleau, Guy A., Michaud, Jacques L.

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Genetic markers of Restless Legs Syndrome in Parkinson disease von Gan-Or, Ziv, Alcalay, Roy N, Bar-Shira, Anat, Leblond, Claire S, Postuma, Ronald B, Ben-Shachar, Shay, Waters, Cheryl, Johnson, Amelie, Levy, Oren, Mirelman, Anat, Gana-Weisz, Mali, Dupré, Nicolas, Montplaisir, Jacques, Giladi, Nir, Fahn, Stanley, Xiong, Lan, Dion, Patrick A, Orr-Urtreger, Avi, Rouleau, Guy A

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Analysis of CAG repeat expansions in restless legs syndrome von DESAUTELS, Alex, TURECKI, Gustavo, MONTPLAISIR, Jacques, BRISEBOIS, Katéri, DESAUTELS, Amelie K, ADAM, Benoit, ROULEAU, Guy A

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Whole Exome Sequencing of Affected Individuals From Large Consanguineous Pedigrees With Psychotic/Affective Disorders From Pakistan von He, Qin, Hajji, Ilyass, Jimenez, Daniel, Benbetka, Souhila, Johnson, Amelie, Dionne-Laporte, Alexandre, Spiegelman, Dan, Joober, Ridha, Dubé, Marie-Pierre, DeLisi, Lynn, Rouleau, Guy A., Xiong, Lan

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Analysis of the effects of rare variants on splicing identifies alterations in GABA sub(A) receptor genes in autism spectrum disorder individuals von Piton, Amelie, Jouan, Loubna, Rochefort, Daniel, Dobrzeniecka, Sylvia, Lachapelle, Karine, Dion, Patrick A, Gauthier, Julie, Rouleau, Guy A

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