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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Merico, Daniele, Antaki, Danny, Shetty, Aniket, Gujral, Madhusudan, Brandler, William M, Malhotra, Dheeraj, Alexander, Madeline, Belliveau, Richard A, Bergen, Sarah E, Bertalan, Marcelo, Bevilacqua, Elizabeth, Cantor, Rita M, Carrera, Noa, Cormican, Paul, Crespo-Facorro, Benedicto, Curtis, David, Davidson, Michael, Degenhardt, Franziska, Del Favero, Jurgen, DeLisi, Lynn E, Dudbridge, Frank, Eichhammer, Peter, Eriksson, Johan, Essioux, Laurent, Farrell, Martilias S, Freedman, Robert, Freimer, Nelson B, Georgieva, Lyudmila, Gershon, Elliot S, Giegling, Ina, Godard, Stephanie, Goldstein, Jacqueline I, Hamshere, Marian L, Hartmann, Annette M, Hofman, Andrea, Kähler, Anna K, Kalaydjieva, Luba, Kelly, Brian J, Lee, S Hong, Legge, Sophie E, Lerer, Bernard, Levy, Deborah L, Maher, Brion S, Mattingsdal, Morten, McDonald, Colm, Metspalu, Andres, Milanova, Vihra, Morris, Derek W, Murray, Robin M, Nestadt, Gerald, Nicodemus, Kristin K, Nordin, Annelie, Oh, Sang-Yun, Olsen, Line, Van Os, Jim, Pantelis, Christos, Pers, Tune H, Powell, John, Price, Alkes, Pulver, Ann E, Purcell, Shaun M, Rasmussen, Henrik B, Richards, Alexander L, Roussos, Panos, Schall, Ulrich, Schwab, Sibylle G, Smoller, Jordan W, Spencer, Chris C A, Stahl, Eli A, Stroup, T Scott, Suvisaari, Jaana, Svrakic, Dragan M, Szatkiewicz, Jin P, Veijola, Juha, Waddington, John, Webb, Bradley T, Williams, Nigel M, Williams, Stephanie, Wolen, Aaron R, Adolfsson, Rolf, Blackwood, Douglas H R, Bramon, Elvira, Buxbaum, Joseph D, Collier, David A, Daly, Mark J, Darvasi, Ariel, Domenici, Enrico, Gill, Michael, Iwata, Nakao, Jablensky, Assen V, Jönsson, Erik G, Kirov, George, Knight, Jo, Levinson, Douglas F, Ophoff, Roel A, Owen, Michael J, Rietschel, Marcella, Rujescu, Dan, O'Donovan, Michael C, Neale, Benjamin M
Published in Nature genetics (01.01.2017)
Published in Nature genetics (01.01.2017)
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Epilepsy subtype-specific copy number burden observed in a genome-wide study of 17 458 subjects
Niestroj, Lisa-Marie, Perez-Palma, Eduardo, Howrigan, Daniel P, Zhou, Yadi, Cheng, Feixiong, Saarentaus, Elmo, Nürnberg, Peter, Stevelink, Remi, Daly, Mark J, Palotie, Aarno, Lal, Dennis, Feng, Yen-Chen Anne, Howrigan, Daniel P, Abbott, Liam E, Tashman, Katherine, Cerrato, Felecia, Lal, Dennis, Churchhouse, Claire, Gupta, Namrata, Neale, Benjamin M, Berkovic, Samuel F, Lerche, Holger, Goldstein, David B, Lowenstein, Daniel H, Cavalleri, Gianpiero L, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Dixon-Salazar, Tracy, Guerrini, Renzo, Hakonarson, Hakon, Heinzen, Erin L, Helbig, Ingo, Kwan, Patrick, Marson, Anthony G, Petrovski, Slavé, Kamalakaran, Sitharthan, Sisodiya, Sanjay M, Stewart, Randy, Weckhuysen, Sarah, Depondt, Chantal, Dlugos, Dennis J, Scheffer, Ingrid E, Striano, Pasquale, Freyer, Catharine, Krause, Roland, May, Patrick, McKenna, Kevin, Regan, Brigid M, Bellows, Susannah T, Leu, Costin, Bennett, Caitlin A, Johns, Esther C, Macdonald, Alexandra, Shilling, Hannah, Burgess, Rosemary, Weckhuysen, Dorien, Bahlo, Melanie, O’Brien, Terence J, Todaro, Marian, Stamberger, Hannah, Andrade, Danielle M, Sadoway, Tara R, Mo, Kelly, Krestel, Heinz, Gallati, Sabina, Papacostas, Savvas S, Kousiappa, Ioanna, Tanteles, George A, Šterbová, Katalin, Vlcková, Markéta, Sedlácková, Lucie, Laššuthová, Petra, Klein, Karl Martin, Rosenow, Felix, Reif, Philipp S, Knake, Susanne, Kunz, Wolfram S, Zsurka, Gábor, Elger, Christian E, Bauer, Jürgen, Rademacher, Michael, Pendziwiat, Manuela, Muhle, Hiltrud, Rademacher, Annika, van Baalen, Andreas, von Spiczak, Sarah, Stephani, Ulrich, Afawi, Zaid, Korczyn, Amos D, Kanaan, Moien, Canavati, Christina, Kurlemann, Gerhard, Müller-Schlüter, Karen, Kluger, Gerhard, Häusler, Martin, Blatt, Ilan, Lemke, Johannes R, Krey, Ilona, Weber, Yvonne G
Published in Brain (London, England : 1878) (01.07.2020)
Published in Brain (London, England : 1878) (01.07.2020)
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Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects
Kendall, Kimberley M., Rees, Elliott, Escott-Price, Valentina, Einon, Mark, Thomas, Rhys, Hewitt, Jonathan, O’Donovan, Michael C., Owen, Michael J., Walters, James T.R., Kirov, George
Published in Biological psychiatry (1969) (15.07.2017)
Published in Biological psychiatry (1969) (15.07.2017)
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Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associations
Li, Yun Rose, Glessner, Joseph T., Coe, Bradley P., Li, Jin, Mohebnasab, Maede, Chang, Xiao, Connolly, John, Kao, Charlly, Wei, Zhi, Bradfield, Jonathan, Kim, Cecilia, Hou, Cuiping, Khan, Munir, Mentch, Frank, Qiu, Haijun, Bakay, Marina, Cardinale, Christopher, Lemma, Maria, Abrams, Debra, Bridglall-Jhingoor, Andrew, Behr, Meckenzie, Harrison, Shanell, Otieno, George, Thomas, Alexandria, Wang, Fengxiang, Chiavacci, Rosetta, Wu, Lawrence, Hadley, Dexter, Goldmuntz, Elizabeth, Elia, Josephine, Maris, John, Grundmeier, Robert, Devoto, Marcella, Keating, Brendan, March, Michael, Pellagrino, Renata, Grant, Struan F. A., Sleiman, Patrick M. A., Li, Mingyao, Eichler, Evan E., Hakonarson, Hakon
Published in Nature communications (14.01.2020)
Published in Nature communications (14.01.2020)
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Contribution of copy number variations to education, socioeconomic status and cognition from a genome-wide study of 305,401 subjects
Wu, Xin-Rui, Wu, Bang-Sheng, Kang, Ju-Jiao, Chen, Li-Min, Deng, Yue-Ting, Chen, Shi-Dong, Dong, Qiang, Feng, Jian-Feng, Cheng, Wei, Yu, Jin-Tai
Published in Molecular psychiatry (01.03.2025)
Published in Molecular psychiatry (01.03.2025)
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Frequency of sex chromosome involvement in a large cohort of subjects with two copy number variants (CNVs)
Vara, Autumn, Smith, Janice L, Hashmi, S Shahrukh, Wagner, Victoria F, Gunther, Kathryn, Rodriguez-Buritica, David F
Published in Cytogenetic and genome research (18.05.2023)
Published in Cytogenetic and genome research (18.05.2023)
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Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia
Bergen, Sarah E, Ploner, Alexander, Howrigan, Daniel, O’Donovan, Michael C, Smoller, Jordan W, Sullivan, Patrick F, Sebat, Jonathan, Neale, Benjamin, Kendler, Kenneth S
Published in The American journal of psychiatry (01.01.2019)
Published in The American journal of psychiatry (01.01.2019)
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Copy number variation in bipolar disorder
Green, E K, Rees, E, Walters, J T R, Smith, K-G, Forty, L, Grozeva, D, Moran, J L, Sklar, P, Ripke, S, Chambert, K D, Genovese, G, McCarroll, S A, Jones, I, Jones, L, Owen, M J, O'Donovan, M C, Craddock, N, Kirov, G
Published in Molecular psychiatry (01.01.2016)
Published in Molecular psychiatry (01.01.2016)
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Leukocyte telomere length, mitochondrial DNA copy number, and coronary artery disease risk and severity: A two-stage case-control study of 3064 Chinese subjects
Wang, Xue-bin, Cui, Ning-hua, Zhang, Shuai, Liu, Ze-jin, Ma, Jun-fen, Ming, Liang
Published in Atherosclerosis (01.05.2019)
Published in Atherosclerosis (01.05.2019)
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Copy Number Variations and Schizophrenia
Szecówka, Kamila, Misiak, Błażej, Łaczmańska, Izabela, Frydecka, Dorota, Moustafa, Ahmed A.
Published in Molecular neurobiology (01.04.2023)
Published in Molecular neurobiology (01.04.2023)
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Gene Copy-Number Variation and Associated Polymorphisms of Complement Component C4 in Human Systemic Lupus Erythematosus (SLE): Low Copy Number Is a Risk Factor for and High Copy Number Is a Protective Factor against SLE Susceptibility in European Americans
Yang, Yan, Chung, Erwin K., Wu, Yee Ling, Savelli, Stephanie L., Nagaraja, Haikady N., Zhou, Bi, Hebert, Maddie, Jones, Karla N., Shu, Yaoling, Kitzmiller, Kathryn, Blanchong, Carol A., McBride, Kim L., Higgins, Gloria C., Rennebohm, Robert M., Rice, Robert R., Hackshaw, Kevin V., Roubey, Robert A.S., Grossman, Jennifer M., Tsao, Betty P., Birmingham, Daniel J., Rovin, Brad H., Hebert, Lee A., Yung Yu, C.
Published in American journal of human genetics (01.06.2007)
Published in American journal of human genetics (01.06.2007)
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Classification of cancers based on copy number variation landscapes
Zhang, Ning, Wang, Meng, Zhang, Peiwei, Huang, Tao
Published in Biochimica et biophysica acta (01.11.2016)
Published in Biochimica et biophysica acta (01.11.2016)
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Elevated basal serum tryptase identifies a multisystem disorder associated with increased TPSAB1 copy number
Lyons, Jonathan J, Yu, Xiaomin, Hughes, Jason D, Le, Quang T, Jamil, Ali, Bai, Yun, Ho, Nancy, Zhao, Ming, Liu, Yihui, O'Connell, Michael P, Trivedi, Neil N, Nelson, Celeste, DiMaggio, Thomas, Jones, Nina, Matthews, Helen, Lewis, Katie L, Oler, Andrew J, Carlson, Ryan J, Arkwright, Peter D, Hong, Celine, Agama, Sherene, Wilson, Todd M, Tucker, Sofie, Zhang, Yu, McElwee, Joshua J, Pao, Maryland, Glover, Sarah C, Rothenberg, Marc E, Hohman, Robert J, Stone, Kelly D, Caughey, George H, Heller, Theo, Metcalfe, Dean D, Biesecker, Leslie G, Schwartz, Lawrence B, Milner, Joshua D
Published in Nature genetics (01.12.2016)
Published in Nature genetics (01.12.2016)
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Human Salivary Amylase Gene Copy Number Impacts Oral and Gut Microbiomes
Poole, Angela C., Goodrich, Julia K., Youngblut, Nicholas D., Luque, Guillermo G., Ruaud, Albane, Sutter, Jessica L., Waters, Jillian L., Shi, Qiaojuan, El-Hadidi, Mohamed, Johnson, Lynn M., Bar, Haim Y., Huson, Daniel H., Booth, James G., Ley, Ruth E.
Published in Cell host & microbe (10.04.2019)
Published in Cell host & microbe (10.04.2019)
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Minimal, encapsulated proteomic-sample processing applied to copy-number estimation in eukaryotic cells
Kulak, Nils A, Pichler, Garwin, Paron, Igor, Nagaraj, Nagarjuna, Mann, Matthias
Published in Nature methods (01.03.2014)
Published in Nature methods (01.03.2014)
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Exploring mitochondrial DNA copy number in circulating cell‐free DNA and extracellular vesicles across cardiovascular health status: A prospective case–control pilot study
Rucci, Chiara, Simone, Gaia, Salathia, Saniya, Casadidio, Cristina, Censi, Roberta, Bordoni, Laura
Published in The FASEB journal (31.05.2024)
Published in The FASEB journal (31.05.2024)
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Alterations in mitochondrial DNA copy number and the activities of electron transport chain complexes and pyruvate dehydrogenase in the frontal cortex from subjects with autism
Gu, F, Chauhan, V, Kaur, K, Brown, W T, LaFauci, G, Wegiel, J, Chauhan, A
Published in Translational psychiatry (01.09.2013)
Published in Translational psychiatry (01.09.2013)
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Alpha globin gene copy number and hypertension risk among Black Americans
Ruhl, A. Parker, Jeffries, Neal, Yang, Yu, Gutierrez, Orlando M., Muntner, Paul, Naik, Rakhi P., Pecker, Lydia H., Mott, Bryan T., Zakai, Neil A., Safford, Monika M., Lange, Leslie A., Winkler, Cheryl A., Irvin, Marguerite R., Cushman, Mary, Ackerman, Hans C.
Published in PloS one (14.07.2022)
Published in PloS one (14.07.2022)
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Circulating cell-free mitochondrial DNA, but not leukocyte mitochondrial DNA copy number, is elevated in major depressive disorder
Lindqvist, Daniel, Wolkowitz, Owen M., Picard, Martin, Ohlsson, Lars, Bersani, Francesco S., Fernström, Johan, Westrin, Åsa, Hough, Christina M., Lin, Jue, Reus, Victor I., Epel, Elissa S., Mellon, Synthia H.
Published in Neuropsychopharmacology (New York, N.Y.) (01.06.2018)
Published in Neuropsychopharmacology (New York, N.Y.) (01.06.2018)
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