Attachment styles in college students and depression: The mediating role of self differentiation von Simon, Heather L. Monaghan, DiPlacido, Joanne, Conway, James M.

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Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot von Page, Donna J, Miossec, Matthieu J, Williams, Simon G, Monaghan, Richard M, Fotiou, Elisavet, Cordell, Heather J, Sutcliffe, Louise, Topf, Ana, Bourgey, Mathieu, Bourque, Guillaume, Eveleigh, Robert, Dunwoodie, Sally L, Winlaw, David S, Bhattacharya, Shoumo, Breckpot, Jeroen, Devriendt, Koenraad, Gewillig, Marc, Brook, J David, Setchfield, Kerry J, Bu’Lock, Frances A, O’Sullivan, John, Stuart, Graham, Bezzina, Connie R, Mulder, Barbara J.M, Postma, Alex V, Bentham, James R, Baron, Martin, Bhaskar, Sanjeev S, Black, Graeme C, Newman, William G, Hentges, Kathryn E, Lathrop, G Mark, Santibanez-Koref, Mauro, Keavney, Bernard D

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Triple Therapy for Cystic Fibrosis Phe508del–Gating and –Residual Function Genotypes von Barry, Peter J, Mall, Marcus A, Álvarez, Antonio, Colombo, Carla, de Winter-de Groot, Karin M, Fajac, Isabelle, McBennett, Kimberly A, McKone, Edward F, Ramsey, Bonnie W, Sutharsan, Sivagurunathan, Taylor-Cousar, Jennifer L, Tullis, Elizabeth, Ahluwalia, Neil, Jun, Lucy S, Moskowitz, Samuel M, Prieto-Centurion, Valentin, Tian, Simon, Waltz, David, Xuan, Fengjuan, Zhang, Yaohua, Rowe, Steven M, Polineni, Deepika

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Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot von Page, Donna J, Miossec, Matthieu J, Williams, Simon G, Monaghan, Richard M, Fotiou, Elisavet, Cordell, Heather J, Sutcliffe, Louise, Topf, Ana, Bourgey, Mathieu, Bourque, Guillaume, Eveleigh, Robert, Dunwoodie, Sally L, Winlaw, David S, Bhattacharya, Shoumo, Breckpot, Jeroen, Devriendt, Koenraad, Gewillig, Marc, Brook, J David, Setchfield, Kerry J, Bu'Lock, Frances A, O'Sullivan, John, Stuart, Graham, Bezzina, Connie R, Mulder, Barbara J M, Postma, Alex V, Bentham, James R, Baron, Martin, Bhaskar, Sanjeev S, Black, Graeme C, Newman, William G, Hentges, Kathryn E, Lathrop, G Mark, Santibanez-Koref, Mauro, Keavney, Bernard D

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Whole Exome Sequencing Reveals the Major Genetic Contributors to Non-Syndromic Tetralogy of Fallot von Page, Donna J., Miossec, Matthieu J., Williams, Simon G., Monaghan, Richard M., Fotiou, Elisavet, Cordell, Heather J., Sutcliffe, Louise, Topf, Ana, Bourgey, Mathieu, Bourque, Guillaume, Eveleigh, Robert, Dunwoodie, Sally L., Winlaw, David S., Bhattacharya, Shoumo, Breckpot, Jeroen, Devriendt, Koenraad, Gewillig, Marc, Brook, J. David, Setchfield, Kerry J., Bu'Lock, Frances A., O’Sullivan, John, Stuart, Graham, Bezzina, Connie R., Mulder, Barbara J.M., Postma, Alex V., Bentham, James R., Baron, Martin, Bhaskar, Sanjeev S., Black, Graeme C., Newman, William G., Hentges, Kathryn E., Lathrop, G. Mark, Santibanez-Koref, Mauro, Keavney, Bernard D.

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Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot von Page, Donna J, Miossec, Matthieu J, Williams, Simon G, Monaghan, Richard M, Fotiou, Elisavet, Cordell, Heather J, Sutcliffe, Louise, Topf, Ana, Bourgey, Mathieu, Bourque, Guillaume, Eveleigh, Robert, Dunwoodie, Sally L, Winlaw, David S, Bhattacharya, Shoumo, Breckpot, Jeroen, Devriendt, Koenraad, Gewillig, Marc, Brook, J. David, Setchfield, Kerry J, Bu'Lock, Frances A, O'Sullivan, John, Stuart, Graham, Bezzina, Connie R, Mulder, Barbara J.M, Postma, Alex V, Bentham, James R, Baron, Martin, Bhaskar, Sanjeev S, Black, Graeme C, Newman, William G, Hentges, Kathryn E, Lathrop, G. Mark, Santibanez-Koref, Mauro, Keavney, Bernard D

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C Identification of the major genetic contributors to tetralogy of fallot von Page, Donna J, Miossec, Matthieu J, Williams, Simon G, Monaghan, Richard M, Fotiou, Elisavet, Cordell, Heather J, Sutcliffe, Louise, Topf, Ana, Bourgey, Mathieu, Bourque, Guillaume, Eveleigh, Robert, Dunwoodie, Sally L, Winlaw, David S, Bhattacharya, Shoumo, Breckpot, Jeroen, Devriendt, Koenraad, Gewillig, Marc, Brook, David, Setchfield, Kerry, Bu’Lock, Frances A, O’Sullivan, John, Stuart, Graham, Bezzina, Connie, Mulder, Barbara JM, Postma, Alex V, Bentham, James R, Baron, Martin, Bhaskar, Sanjeev S, Black, Graeme C, Newman, William G, Hentges, Kathryn E, Lathrop, Mark, Santibanez-Koref, Mauro, Keavney, Bernard D

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Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, van de Kamp, Jiddeke, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Lüttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Küry, Sébastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Õunap, Katrin, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vøllo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Schrier Vergano, Samantha A, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla Sirera, Natàlia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon, Bhoj, Elizabeth J, Universitat Autònoma de Barcelona

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Histone H3.3 beyond cancer : Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, van de Kamp, Jiddeke, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Lüttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Õunap, Katrin, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vøllo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Schrier Vergano, Samantha A, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla Sirera, Natàlia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon, Bhoj, Elizabeth J, Universitat Autònoma de Barcelona

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Histone H3.3 beyond cancer: Germline mutations in Histone 3 Family 3A and 3B cause a previously unidentified neurodegenerative disorder in 46 patients von Bryant, Laura, Li, Dong, Marchione, Dylan, Joiner, Evan F, Wilson, Khadija, Lee, Pearl, March, Michael E, Nair, Divya, Sherr, Elliott, Fregeau, Brieana, Wadley, Alexandrea, Mancini, Grazia M. S, Powell-Hamilton, Nina, Kamp, Jiddeke van de, Dean, John, Ross, Alison, Crawford, Heather P, Powis, Zoe, Cho, Megan T, Willing, Marcia C, Manwaring, Linda, Schot, Rachel, Nava, Caroline, Lessel, Davor, Wagner, Matias, Winkelmann, Juliane, Schuette, Jane L, Innis, Jeffrey W, Pizzino, Amy, Luttgen, Sabine, Strom, Tim M, Monaghan, Kristin G, Dubbs, Holly, Bend, Renee, Lee, Jennifer A, Lyons, Michael J, Hoefele, Julia, Reutter, Heiko, Radtke, Kelly, Sherbini, Omar, Mrokse, Cameron, Helbig, Katherine L, Odent, Sylvie, Cogne, Benjamin, Mercier, Sandra, Besnard, Thomas, Kury, Sebastien, Redon, Richard, Reinson, Karit, Wojcik, Monica H, Ilves, Pilvi, Innes, A. Micheil, Kernohan, Kristin D, Meyn, M. Stephen, Lehman, Anna, Kitson, Hilary, Martin, Martin G, Martinez-Agosto, Julian A, Palmer, Christina G. S, Papp, Jeanette C, Parker, Neil H, Vilain, Eric, Wan, Jijun, Yoon, Amanda J, Ferrero, Giovanni Battista, Radio, Francesca Clementina, Carli, Diana, Barresi, Sabina, Brusco, Alfredo, Thomas, Jennifer Muncy, Stuurman, K. E, Thompson, Michelle L, McWalter, Kirsty, Stegmann, Alexander P. A, Tveten, Kristian, Vollo, Arve, Prescott, Trine, Fagerberg, Christina, Laulund, Lone Walentin, Larsen, Martin J, Byler, Melissa, Lebel, Robert Roger, Dean, Joy, Vergano, Samantha A. Schrier, Norman, Jennifer, Mercimek-Andrews, Saadet, Neira, Juanita, Allen, Margot van, Longo, Nicola, Sellars, Elizabeth, Louie, Raymond J, Cathey, Sara S, Heron, Delphine, Vanderver, Adeline, Simon, Celeste, Padilla, Natalia, Chung, Wendy, Garcia, Benjamin, Hakonarson, Hakon H, Bhoj, Elizabeth J

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