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Clinical chemistry, ISSN 0009-9147, 01/2019, Volume 65, Issue 1, pp. 146 - 152
Journal Article
01/2014, ISBN 9781321225914
Schizophrenia is a severe psychiatric disorder that affects roughly 1% of the general population. It has been clearly demonstrated that the disease possesses a... 
Genetics
Dissertation
by Davis, Lea K and Yu, Dongmei and Keenan, Clare L and Gamazon, Eric R and Konkashbaev, Anuar I and Derks, Eske M and Neale, Benjamin M and Yang, Jian and Lee, S. Hong and Evans, Patrick and Barr, Cathy L and Bellodi, Laura and Benarroch, Fortu and Berrio, Gabriel Bedoya and Bienvenu, Oscar J and Bloch, Michael H and Blom, Rianne M and Bruun, Ruth D and Budman, Cathy L and Camarena, Beatriz and Campbell, Desmond and Cappi, Carolina and Cardona Silgado, Julio C and Cath, Danielle C and Cavallini, Maria C and Chavira, Denise A and Chouinard, Sylvain and Conti, David V and Cook, Edwin H and Coric, Vladimir and Cullen, Bernadette A and Deforce, Dieter and Delorme, Richard and Dion, Yves and Edlund, Christopher K and Egberts, Karin and Falkai, Peter and Fernandez, Thomas V and Gallagher, Patience J and Garrido, Helena and Geller, Daniel and Girard, Simon L and Grabe, Hans J and Grados, Marco A and Greenberg, Benjamin D and Gross-Tsur, Varda and Haddad, Stephen and Heiman, Gary A and Hemmings, Sian M. J and Hounie, Ana G and Illmann, Cornelia and Jankovic, Joseph and Jenike, Michael A and Kennedy, James L and King, Robert A and Kremeyer, Barbara and Kurlan, Roger and Lanzagorta, Nuria and Leboyer, Marion and Leckman, James F and Lennertz, Leonhard and Liu, Chunyu and Lochner, Christine and Lowe, Thomas L and Macciardi, Fabio and McCracken, James T and McGrath, Lauren M and Mesa Restrepo, Sana C and Moessner, Rainald and Morgan, Jubel and Muller, Heike and Murphy, Dennis L and Naarden, Allan L and Ochoa, William Cornejo and Ophoff, Roel A and Osiecki, Lisa and Pakstis, Anew J and Pato, Michele T and Pato, Carlos N and Piacentini, John and Pittenger, Christopher and Pollak, Yehuda and Rauch, Scott L and Renner, Tobias J and Reus, Victor I and Richter, Margaret A and Riddle, Mark A and Robertson, Mary M and Romero, Roxana and Rosàrio, Maria C and Rosenberg, David and Rouleau, Guy A and Ruhrmann, Stephan and Ruiz-Linares, Anes and Sampaio, Aline S and Samuels, Jack and Sandor, Paul and Sheppard, Brooke and Singer, Harvey S and Smit, Jan H and ...
PLoS genetics, ISSN 1553-7390, 2013, Volume 9, Issue 10, p. e1003864
Journal Article
Journal Article
by Hamdan, Fadi F and Myers, Candace T and Cossette, Patrick and Lemay, Philippe and Spiegelman, Dan and Laporte, Alexandre Dionne and Nassif, Christina and Diallo, Ousmane and Monlong, Jean and Cadieux-Dion, Maxime and Dobrzeniecka, Sylvia and Meloche, Caroline and Retterer, Kyle and Cho, Megan T and Rosenfeld, Jill A and Bi, Weimin and Massicotte, Christine and Miguet, Marguerite and Brunga, Ledia and Regan, Brigid M and Mo, Kelly and Tam, Cory and Schneider, Amy and Hollingsworth, Georgie and FitzPatrick, David R and Donaldson, Alan and Canham, Natalie and Blair, Edward and Kerr, Bronwyn and Fry, Andrew E and Thomas, Rhys H and Shelagh, Joss and Hurst, Jane A and Brittain, Helen and Blyth, Moira and Lebel, Robert Roger and Gerkes, Erica H and Davis-Keppen, Laura and Stein, Quinn and Chung, Wendy K and Dorison, Sara J and Benke, Paul J and Fassi, Emily and Corsten-Janssen, Nicole and Kamsteeg, Erik-Jan and Mau-Them, Frederic T and Bruel, Ange-Line and Verloes, Alain and Õunap, Katrin and Wojcik, Monica H and Albert, Dara V.F and Venkateswaran, Sunita and Ware, Tyson and Jones, Dean and Liu, Yu-Chi and Mohammad, Shekeeb S and Bizargity, Peyman and Bacino, Carlos A and Leuzzi, Vincenzo and Martinelli, Simone and Dallapiccola, Bruno and Tartaglia, Marco and Blumkin, Lubov and Wierenga, Klaas J and Purcarin, Gabriela and O’Byrne, James J and Stockler, Sylvia and Lehman, Anna and Keren, Boris and Nougues, Marie-Christine and Mignot, Cyril and Auvin, Stéphane and Nava, Caroline and Hiatt, Susan M and Bebin, Martina and Shao, Yunru and Scaglia, Fernando and Lalani, Seema R and Frye, Richard E and Jarjour, Imad T and Jacques, Stéphanie and Boucher, Renee-Myriam and Riou, Emilie and Srour, Myriam and Carmant, Lionel and Lortie, Anne and Major, Philippe and Diadori, Paola and Dubeau, François and D’Anjou, Guy and Bourque, Guillaume and Berkovic, Samuel F and Sadleir, Lynette G and Campeau, Philippe M and Kibar, Zoha and Lafrenière, Ronald G and Girard, Simon L and Mercimek-Mahmutoglu, Saadet and Boelman, Cyrus and Rouleau, Guy A and ... and Deciphering Dev Disorders Study and Deciphering Developmental Disorders Study
The American Journal of Human Genetics, ISSN 0002-9297, 11/2017, Volume 101, Issue 5, pp. 664 - 685
Journal Article
Nucleic Acids Research, ISSN 0305-1048, 08/2018, Volume 46, Issue 14, pp. 7236 - 7249
Abstract Copy number variants (CNVs) are known to affect a large portion of the human genome and have been implicated in many diseases. Although whole-genome... 
GENOMIC STRUCTURAL VARIATION | DUPLICATIONS | REPEAT | RARE CHROMOSOMAL DELETIONS | DNA | BIOCHEMISTRY & MOLECULAR BIOLOGY | LONG-READ ALIGNMENT | DISEASE | MECHANISMS | ALGORITHMS | SEQUENCING DATA | Genomics
Journal Article
by Yu, Dongmei and Mathews, Carol A and Scharf, Jeremiah M and Neale, Benjamin M and Davis, Lea K and Gamazon, Eric R and Derks, Eske M and Evans, Patrick and Edlund, Christopher K and Crane, Jacquelyn and Fagerness, Jesen A and Osiecki, Lisa and Gallagher, Patience and Gerber, Gloria and Haddad, Stephen and Illmann, Cornelia and McGrath, Lauren M and Mayerfeld, Catherine and Arepalli, Sampath and Barlassina, Cristina and Barr, Cathy L and Bellodi, Laura and Benarroch, Fortu and Berrió, Gabriel Bedoya and Bienvenu, O. Joseph and Black, Donald W and Bloch, Michael H and Brentani, Helena and Bruun, Ruth D and Budman, Cathy L and Camarena, Beatriz and Campbell, Desmond D and Cappi, Carolina and Silgado, Julio C. Cardona and Cavallini, Maria C and Chavira, Denise A and Chouinard, Sylvain and Cook, Edwin H and Cookson, M. R and Coric, Vladimir and Cullen, Bernadette and Cusi, Daniele and Delorme, Richard and Denys, Damiaan and Dion, Yves and Eapen, Valsama and Egberts, Karin and Falkai, Peter and Fernandez, Thomas and Fournier, Eduardo and Garrido, Helena and Geller, Daniel and Gilbert, Donald L and Girard, Simon L and Grabe, Hans J and Grados, Marco A and Greenberg, Benjamin D and Gross-Tsur, Varda and Grünblatt, Edna and Hardy, John and Heiman, Gary A and Hemmings, Sian M. J and Herrera, Luis D and Hezel, Dianne M and Hoekstra, Pieter J and Jankovic, Joseph and Kennedy, James L and King, Robert A and Konkashbaev, Anuar I and Kremeyer, Barbara and Kurlan, Roger and Lanzagorta, Nuria and Leboyer, Marion and Leckman, James F and Lennertz, Leonhard and Liu, Chunyu and Lochner, Christine and Lowe, Thomas L and Lupoli, Sara and Macciardi, Fabio and Maier, Wolfgang and Manunta, Paolo and Marconi, Maurizio and McCracken, James T and Mesa Restrepo, Sana C and Moessner, Rainald and Moorjani, Priya and Morgan, Jubel and Muller, Heike and Murphy, Dennis L and Naarden, Allan L and Nurmi, Erika and Ochoa, William Cornejo and Ophoff, Roel A and Pakstis, Anew J and Pato, Michele T and Pato, Carlos N and Piacentini, John and Pittenger, Christopher and Pollak, Yehuda and ...
American journal of psychiatry, ISSN 0002-953X, 2015, Volume 172, Issue 1, pp. 82 - 93
Journal Article
Lancet Neurology, The, ISSN 1474-4422, 2014, Volume 13, Issue 7, pp. 643 - 644
  To better understand the complex genetic architecture of FTD, Raffaele Ferrari and colleagues completed the largest genome-wide association study (GWAS) of... 
Neurology | TAU | MUTATIONS | CLINICAL NEUROLOGY | FRONTOTEMPORAL DEMENTIA | Frontotemporal Dementia - genetics | Humans | Female | Genotype | Male | Frontotemporal Dementia - diagnosis | Genome-Wide Association Study - methods | Genetic research | Genomics | Florists | Studies | Gene loci | Genomes | Dementia
Journal Article