Human Genome Epidemiology Literature Finder
Records 1 - 19 (of 19 Records) |
Query Trace: Copy number variants[original query] |
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A genome-wide study of common SNPs and CNVs in cognitive performance in the CANTAB.
Human molecular genetics 2009 Dec 18 (23): 4650-61. Need Anna C, Attix Deborah K, McEvoy Jill M, Cirulli Elizabeth T, Linney Kristen L, Hunt Priscilla, Ge Dongliang, Heinzen Erin L, Maia Jessica M, Shianna Kevin V, Weale Michael E, Cherkas Lynn F, Clement Gail, Spector Tim D, Gibson Greg, Goldstein David |
Common variants on chromosome 6p22.1 are associated with schizophrenia.
Nature 2009 Aug 460 (7256): 753-7. Shi Jianxin, Levinson Douglas F, Duan Jubao, Sanders Alan R, Zheng Yonglan, Pe'er Itsik, Dudbridge Frank, Holmans Peter A, Whittemore Alice S, Mowry Bryan J, Olincy Ann, Amin Farooq, Cloninger C Robert, Silverman Jeremy M, Buccola Nancy G, Byerley William F, Black Donald W, Crowe Raymond R, Oksenberg Jorge R, Mirel Daniel B, Kendler Kenneth S, Freedman Robert, Gejman Pablo |
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Nature genetics 2009 Mar 41 (3): 334-41. , Kathiresan Sekar, Voight Benjamin F, Purcell Shaun, Musunuru Kiran, Ardissino Diego, Mannucci Pier M, Anand Sonia, Engert James C, Samani Nilesh J, Schunkert Heribert, Erdmann Jeanette, Reilly Muredach P, Rader Daniel J, Morgan Thomas, Spertus John A, Stoll Monika, Girelli Domenico, McKeown Pascal P, Patterson Chris C, Siscovick David S, O'Donnell Christopher J, Elosua Roberto, Peltonen Leena, Salomaa Veikko, Schwartz Stephen M, Melander Olle, Altshuler David, Ardissino Diego, Merlini Pier Angelica, Berzuini Carlo, Bernardinelli Luisa, Peyvandi Flora, Tubaro Marco, Celli Patrizia, Ferrario Maurizio, Fetiveau Raffaela, Marziliano Nicola, Casari Giorgio, Galli Michele, Ribichini Flavio, Rossi Marco, Bernardi Francesco, Zonzin Pietro, Piazza Alberto, Mannucci Pier M, Schwartz Stephen M, Siscovick David S, Yee Jean, Friedlander Yechiel, Elosua Roberto, Marrugat Jaume, Lucas Gavin, Subirana Isaac, Sala Joan, Ramos Rafael, Kathiresan Sekar, Meigs James B, Williams Gordon, Nathan David M, MacRae Calum A, O'Donnell Christopher J, Salomaa Veikko, Havulinna Aki S, Peltonen Leena, Melander Olle, Berglund Goran, Voight Benjamin F, Kathiresan Sekar, Hirschhorn Joel N, Asselta Rosanna, Duga Stefano, Spreafico Marta, Musunuru Kiran, Daly Mark J, Purcell Shaun, Voight Benjamin F, Purcell Shaun, Nemesh James, Korn Joshua M, McCarroll Steven A, Schwartz Stephen M, Yee Jean, Kathiresan Sekar, Lucas Gavin, Subirana Isaac, Elosua Roberto, Surti Aarti, Guiducci Candace, Gianniny Lauren, Mirel Daniel, Parkin Melissa, Burtt Noel, Gabriel Stacey B, Samani Nilesh J, Thompson John R, Braund Peter S, Wright Benjamin J, Balmforth Anthony J, Ball Stephen G, Hall Alistair S, , Schunkert Heribert, Erdmann Jeanette, Linsel-Nitschke Patrick, Lieb Wolfgang, Ziegler Andreas, König Inke, Hengstenberg Christian, Fischer Marcus, Stark Klaus, Grosshennig Anika, Preuss Michael, Wichmann H-Erich, Schreiber Stefan, Schunkert Heribert, Samani Nilesh J, Erdmann Jeanette, Ouwehand Willem, Hengstenberg Christian, Deloukas Panos, Scholz Michael, Cambien Francois, Reilly Muredach P, Li Mingyao, Chen Zhen, Wilensky Robert, Matthai William, Qasim Atif, Hakonarson Hakon H, Devaney Joe, Burnett Mary-Susan, Pichard Augusto D, Kent Kenneth M, Satler Lowell, Lindsay Joseph M, Waksman Ron, Knouff Christopher W, Waterworth Dawn M, Walker Max C, Mooser Vincent, Epstein Stephen E, Rader Daniel J, Scheffold Thomas, Berger Klaus, Stoll Monika, Huge Andreas, Girelli Domenico, Martinelli Nicola, Olivieri Oliviero, Corrocher Roberto, Morgan Thomas, Spertus John A, McKeown Pascal, Patterson Chris C, Schunkert Heribert, Erdmann Erdmann, Linsel-Nitschke Patrick, Lieb Wolfgang, Ziegler Andreas, König Inke R, Hengstenberg Christian, Fischer Marcus, Stark Klaus, Grosshennig Anika, Preuss Michael, Wichmann H-Erich, Schreiber Stefan, Hólm Hilma, Thorleifsson Gudmar, Thorsteinsdottir Unnur, Stefansson Kari, Engert James C, Do Ron, Xie Changchun, Anand Sonia, Kathiresan Sekar, Ardissino Diego, Mannucci Pier M, Siscovick David, O'Donnell Christopher J, Samani Nilesh J, Melander Olle, Elosua Roberto, Peltonen Leena, Salomaa Veikko, Schwartz Stephen M, Altshuler Dav |
A genome-wide association study of carotid atherosclerosis in HIV-infected men.
AIDS (London, England) 2010 Feb 24 (4): 583-92. Shrestha Sadeep, Irvin Marguerite R, Taylor Kent D, Wiener Howard W, Pajewski Nicholas M, Haritunians Talin, Delaney Joseph A C, Schambelan Morris, Polak Joseph F, Arnett Donna K, Chen Yii-Der Ida, Grunfeld Ca |
A genome-wide scan for common alleles affecting risk for autism.
Human molecular genetics 2010 Oct 19 (20): 4072-82. Anney Richard, Klei Lambertus, Pinto Dalila, Regan Regina, Conroy Judith, Magalhaes Tiago R, Correia Catarina, Abrahams Brett S, Sykes Nuala, Pagnamenta Alistair T, Almeida Joana, Bacchelli Elena, Bailey Anthony J, Baird Gillian, Battaglia Agatino, Berney Tom, Bolshakova Nadia, Bölte Sven, Bolton Patrick F, Bourgeron Thomas, Brennan Sean, Brian Jessica, Carson Andrew R, Casallo Guillermo, Casey Jillian, Chu Su H, Cochrane Lynne, Corsello Christina, Crawford Emily L, Crossett Andrew, Dawson Geraldine, de Jonge Maretha, Delorme Richard, Drmic Irene, Duketis Eftichia, Duque Frederico, Estes Annette, Farrar Penny, Fernandez Bridget A, Folstein Susan E, Fombonne Eric, Freitag Christine M, Gilbert John, Gillberg Christopher, Glessner Joseph T, Goldberg Jeremy, Green Jonathan, Guter Stephen J, Hakonarson Hakon, Heron Elizabeth A, Hill Matthew, Holt Richard, Howe Jennifer L, Hughes Gillian, Hus Vanessa, Igliozzi Roberta, Kim Cecilia, Klauck Sabine M, Kolevzon Alexander, Korvatska Olena, Kustanovich Vlad, Lajonchere Clara M, Lamb Janine A, Laskawiec Magdalena, Leboyer Marion, Le Couteur Ann, Leventhal Bennett L, Lionel Anath C, Liu Xiao-Qing, Lord Catherine, Lotspeich Linda, Lund Sabata C, Maestrini Elena, Mahoney William, Mantoulan Carine, Marshall Christian R, McConachie Helen, McDougle Christopher J, McGrath Jane, McMahon William M, Melhem Nadine M, Merikangas Alison, Migita Ohsuke, Minshew Nancy J, Mirza Ghazala K, Munson Jeff, Nelson Stanley F, Noakes Carolyn, Noor Abdul, Nygren Gudrun, Oliveira Guiomar, Papanikolaou Katerina, Parr Jeremy R, Parrini Barbara, Paton Tara, Pickles Andrew, Piven Joseph, Posey David J, Poustka Annemarie, Poustka Fritz, Prasad Aparna, Ragoussis Jiannis, Renshaw Katy, Rickaby Jessica, Roberts Wendy, Roeder Kathryn, Roge Bernadette, Rutter Michael L, Bierut Laura J, Rice John P, Salt Jeff, Sansom Katherine, Sato Daisuke, Segurado Ricardo, Senman Lili, Shah Naisha, Sheffield Val C, Soorya Latha, Sousa Inês, Stoppioni Vera, Strawbridge Christina, Tancredi Raffaella, Tansey Katherine, Thiruvahindrapduram Bhooma, Thompson Ann P, Thomson Susanne, Tryfon Ana, Tsiantis John, Van Engeland Herman, Vincent John B, Volkmar Fred, Wallace Simon, Wang Kai, Wang Zhouzhi, Wassink Thomas H, Wing Kirsty, Wittemeyer Kerstin, Wood Shawn, Yaspan Brian L, Zurawiecki Danielle, Zwaigenbaum Lonnie, Betancur Catalina, Buxbaum Joseph D, Cantor Rita M, Cook Edwin H, Coon Hilary, Cuccaro Michael L, Gallagher Louise, Geschwind Daniel H, Gill Michael, Haines Jonathan L, Miller Judith, Monaco Anthony P, Nurnberger John I, Paterson Andrew D, Pericak-Vance Margaret A, Schellenberg Gerard D, Scherer Stephen W, Sutcliffe James S, Szatmari Peter, Vicente Astrid M, Vieland Veronica J, Wijsman Ellen M, Devlin Bernie, Ennis Sean, Hallmayer Joach |
Genome-wide pharmacogenetics of antidepressant response in the GENDEP project.
The American journal of psychiatry 2010 May 167 (5): 555-64. Uher Rudolf, Perroud Nader, Ng Mandy Y M, Hauser Joanna, Henigsberg Neven, Maier Wolfgang, Mors Ole, Placentino Anna, Rietschel Marcella, Souery Daniel, Zagar Tina, Czerski Piotr M, Jerman Borut, Larsen Erik Roj, Schulze Thomas G, Zobel Astrid, Cohen-Woods Sarah, Pirlo Katrina, Butler Amy W, Muglia Pierandrea, Barnes Michael R, Lathrop Mark, Farmer Anne, Breen Gerome, Aitchison Katherine J, Craig Ian, Lewis Cathryn M, McGuffin Pet |
A pilot genome-wide association study shows genomic variants enriched in the non-tumor cells of patients with well-differentiated neuroendocrine tumors of the ileum.
Endocrine-related cancer 2011 Feb 18 (1): 171-80. Walsh Kyle M, Choi Murim, Oberg Kjell, Kulke Matthew H, Yao James C, Wu Chengqing, Jurkiewicz Magdalena, Hsu Ling-I, Hooshmand Susanne M, Hassan Manal, Janson Eva T, Cunningham Janet L, Vosburgh Evan, Sackler Richard S, Lifton Richard P, Dewan Andrew T, Hoh Josephi |
Association between ORMDL3, IL1RL1 and a deletion on chromosome 17q21 with asthma risk in Australia.
European journal of human genetics : EJHG 2011 Apr 19 (4): 458-64. Ferreira Manuel A R, McRae Allan F, Medland Sarah E, Nyholt Dale R, Gordon Scott D, Wright Margaret J, Henders Anjali K, Madden Pamela A, Visscher Peter M, Wray Naomi R, Heath Andrew C, Montgomery Grant W, Duffy David L, Martin Nicholas |
Genome-wide detection of allele specific copy number variation associated with insulin resistance in African Americans from the HyperGEN study.
PloS one 2011 6 (8): e24052. Irvin Marguerite R, Wineinger Nathan E, Rice Treva K, Pajewski Nicholas M, Kabagambe Edmond K, Gu Charles C, Pankow Jim, North Kari E, Wilk Jemma B, Freedman Barry I, Franceschini Nora, Broeckel Uli, Tiwari Hemant K, Arnett Donna |
Genome-wide association study of serious blistering skin rash caused by drugs.
The pharmacogenomics journal 2012 Apr 12 (2): 96-104. Shen Y, Nicoletti P, Floratos A, Pirmohamed M, Molokhia M, Geppetti P, Benemei S, Giomi B, Schena D, Vultaggio A, Stern R, Daly M J, John S, Nelson M R, Pe'er I, |
Genome-wide association study of multiplex schizophrenia pedigrees.
The American journal of psychiatry 2012 Sep 169 (9): 963-73. Levinson Douglas F, Shi Jianxin, Wang Kai, Oh Sang, Riley Brien, Pulver Ann E, Wildenauer Dieter B, Laurent Claudine, Mowry Bryan J, Gejman Pablo V, Owen Michael J, Kendler Kenneth S, Nestadt Gerald, Schwab Sibylle G, Mallet Jacques, Nertney Deborah, Sanders Alan R, Williams Nigel M, Wormley Brandon, Lasseter Virginia K, Albus Margot, Godard-Bauché Stephanie, Alexander Madeline, Duan Jubao, O'Donovan Michael C, Walsh Dermot, O'Neill Anthony, Papadimitriou George N, Dikeos Dimitris, Maier Wolfgang, Lerer Bernard, Campion Dominique, Cohen David, Jay Maurice, Fanous Ayman, Eichhammer Peter, Silverman Jeremy M, Norton Nadine, Zhang Nancy, Hakonarson Hakon, Gao Cynthia, Citri Ami, Hansen Mark, Ripke Stephan, , Dudbridge Frank, Holmans Peter |
Genome-wide association study in a Swedish population yields support for greater CNV and MHC involvement in schizophrenia compared with bipolar disorder.
Molecular psychiatry 2012 Sep 17 (9): 880-6. Bergen S E, O'Dushlaine C T, Ripke S, Lee P H, Ruderfer D M, Akterin S, Moran J L, Chambert K D, Handsaker R E, Backlund L, Ösby U, McCarroll S, Landen M, Scolnick E M, Magnusson P K E, Lichtenstein P, Hultman C M, Purcell S M, Sklar P, Sullivan P |
Polygenic transmission and complex neuro developmental network for attention deficit hyperactivity disorder: genome-wide association study of both common and rare variants.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2013 Jul 162B (5): 419-30. Yang Li, Neale Benjamin M, Liu Lu, Lee S Hong, Wray Naomi R, Ji Ning, Li Haimei, Qian Qiujin, Wang Dongliang, Li Jun, Faraone Stephen V, Wang Yufeng, , Doyle Alysa E, Reif Andreas, Rothenberger Aribert, Franke Barbara, Sonuga-Barke Edmund J S, Steinhausen Hans-Christoph, Buitelaar Jan K, Kuntsi Jonna, Biederman Joseph, Lesch Klaus-Peter, Kent Lindsey, Asherson Philip, Oades Robert D, Loo Sandra K, Nelson Stan F, Faraone Stephen V, Smalley Susan L, Banaschewski Tobias, Arias Vasquez Alejandro, Todorov Alexandre, Charach Alice, Miranda Ana, Warnke Andreas, Thapar Anita, Neale Benjamin M, Cormand Bru, Freitag Christine, Mick Eric, Mulas Fernando, Middleton Frank, HakonarsonHakonarson Hakon, Palmason Haukur, Schäfer Helmut, Roeyers Herbert, McGough James J, Romanos Jasmin, Crosbie Jennifer, Meyer Jobst, Ramos-Quiroga Josep Antoni, Sergeant Joseph, Elia Josephine, Langely Kate, Nisenbaum Laura, Romanos Marcel, Daly Mark J, Ribasés Marta, Gill Michael, O'Donovan Michael, Owen Michael, Casas Miguel, Bayés Mònica, Lambregts-Rommelse Nanda, Williams Nigel, Holmans Peter, Anney Richard J L, Ebstein Richard P, Schachar Russell, Medland Sarah E, Ripke Stephan, Walitza Susanne, Nguyen Thuy Trang, Renner Tobias J, Hu Xiaol |
Genome-wide association study of pre-eclampsia detects novel maternal single nucleotide polymorphisms and copy-number variants in subsets of the Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study cohort.
Annals of human genetics 2013 Jul 77 (4): 277-87. Zhao Linlu, Bracken Michael B, DeWan Andrew |
Genome-wide association analysis identifies common variants influencing infant brain volumes.
Translational psychiatry 2017 Aug 7 (8): e1188. Xia K, Zhang J, Ahn M, Jha S, Crowley J J, Szatkiewicz J, Li T, Zou F, Zhu H, Hibar D, Thompson P, , Sullivan P F, Styner M, Gilmore J H, Knickmeyer R |
The coexistence of copy number variations (CNVs) and single nucleotide polymorphisms (SNPs) at a locus can result in distorted calculations of the significance in associating SNPs to disease.
Human genetics 2018 Jul 137 (6-7): 553-567. Liu Jiaqi, Zhou Yangzhong, Liu Sen, Song Xiaofei, Yang Xin-Zhuang, Fan Yanhui, Chen Weisheng, Akdemir Zeynep Coban, Yan Zihui, Zuo Yuzhi, Du Renqian, Liu Zhenlei, Yuan Bo, Zhao Sen, Liu Gang, Chen Yixin, Zhao Yanxue, Lin Mao, Zhu Qiankun, Niu Yuchen, Liu Pengfei, Ikegawa Shiro, Song You-Qiang, Posey Jennifer E, Qiu Guixing, , Zhang Feng, Wu Zhihong, Lupski James R, Wu N |
17p12 Influences Hematoma Volume and Outcome in Spontaneous Intracerebral Hemorrhage.
Stroke 2018 Jun . Marini Sandro, Devan William J, Radmanesh Farid, Miyares Laura, Poterba Timothy, Hansen Björn M, Norrving Bo, Jimenez-Conde Jordi, Giralt-Steinhauer Eva, Elosua Roberto, Cuadrado-Godia Elisa, Soriano Carolina, Roquer Jaume, Kourkoulis Christina E, Ayres Alison M, Schwab Kristin, Tirschwell David L, Selim Magdy, Brown Devin L, Silliman Scott L, Worrall Bradford B, Meschia James F, Kidwell Chelsea S, Montaner Joan, Fernandez-Cadenas Israel, Delgado Pilar, Greenberg Steven M, Lindgren Arne, Matouk Charles, Sheth Kevin N, Woo Daniel, Anderson Christopher D, Rosand Jonathan, Falcone Guido J, |
Genome-wide survey of copy number variants finds MAPT duplications in progressive supranuclear palsy.
Movement disorders : official journal of the Movement Disorder Society 2019 May . Chen Zhongbo, Chen Jason A, Shatunov Aleksey, Jones Ashley R, Kravitz Stephanie N, Huang Alden Y, Lawrence Lauren, Lowe Jennifer K, Lewis Cathryn M, Payan Christine A M, Lieb Wolfgang, Franke Andre, Deloukas Panagiotis, Amouyel Philippe, Tzourio Christophe, Dartigues Jean-François, , Ludolph Albert, Bensimon Gilbert, Leigh P Nigel, Bronstein Jeff M, Coppola Giovanni, Geschwind Daniel H, Al-Chalabi Amm |
Both rare and common genetic variants contribute to autism in the Faroe Islands.
NPJ genomic medicine 2019 4 1. Leblond Claire S, Cliquet Freddy, Carton Coralie, Huguet Guillaume, Mathieu Alexandre, Kergrohen Thomas, Buratti Julien, Lemière Nathalie, Cuisset Laurence, Bienvenu Thierry, Boland Anne, Deleuze Jean-François, Stora Tormodur, Biskupstoe Rannva, Halling Jónrit, Andorsdóttir Guðrið, Billstedt Eva, Gillberg Christopher, Bourgeron Thom |
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