المؤلفون: Victor Girard, Florence Jollivet, Oskar Knittelfelder, Marion Celle, Jean-Noel Arsac, Gilles Chatelain, Daan M Van den Brink, Thierry Baron, Andrej Shevchenko, Ronald P Kühnlein, Nathalie Davoust, Bertrand Mollereau

المصدر: PLoS Genetics, Vol 17, Iss 11, p e1009921 (2021)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

الوصول الحر: https://doaj.org/article/703475648ac1456b96f0b77a62b8af93Test

المؤلفون: Lesseur, Corina, Ferreiro-Iglesias, Aida, McKay, James D., Bossé, Yohan, Johansson, Mattias, Gaborieau, Valerie, Landi, Maria Teresa, Christiani, David C., Caporaso, Neil C., Bojesen, Stig E., Amos, Christopher I., Shete, Sanjay, Liu, Geoffrey, Rennert, Gadi, Albanes, Demetrios, Aldrich, Melinda C., Tardon, Adonina, Chen, Chu, Triantafillos, Liloglou, Field, John K., Teare, Marion Dawn, Kiemeney, Lambertus A., Diergaarde, Brenda, Ferris, Robert L., Zienolddiny, Shanbeh, Lam, Stephen, Olshan, Andrew F., Weissler, Mark C., Lacko, Martin, Risch, Angela, Bickeböller, Heike, Ness, Andy R., Thomas, Steve, Le Marchand, Loic, Schabath, Matthew B., Wünsch-Filho, Victor, Tajara, Eloiza H., Andrew, Angeline S., Clifford, Gary M., Lazarus, Philip, Grankvist, Kjell, Johansson, Mikael, Arnold, Susanne, Melander, Olle, Brunnström, Hans, Boccia, Stefania, Cadoni, Gabriella, Timens, Wim, Obeidat, Ma'en, Xiao, Xiangjun, Houlston, Richard S., Hung, Rayjean J., Brennan, Paul

المصدر: PLOS Genetics. 17(3)

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-181786Test
https://doi.org/10.1371/journal.pgen.1009254Test
https://umu.diva-portal.org/smash/get/diva2:1541557/FULLTEXT01.pdfTest

المؤلفون: Marion Herbette, Xiaolu Wei, Ching-Ho Chang, Amanda M Larracuente, Benjamin Loppin, Raphaëlle Dubruille

المصدر: PLoS Genetics, Vol 17, Iss 7, p e1009662 (2021)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

الوصول الحر: https://doaj.org/article/34761be6f8de43f3864747c2085ed363Test

المؤلفون: Corina Lesseur, Aida Ferreiro-Iglesias, James D McKay, Yohan Bossé, Mattias Johansson, Valerie Gaborieau, Maria Teresa Landi, David C Christiani, Neil C Caporaso, Stig E Bojesen, Christopher I Amos, Sanjay Shete, Geoffrey Liu, Gadi Rennert, Demetrius Albanes, Melinda C Aldrich, Adonina Tardon, Chu Chen, Liloglou Triantafillos, John K Field, Marion Dawn Teare, Lambertus A Kiemeney, Brenda Diergaarde, Robert L Ferris, Shanbeh Zienolddiny, Stephen Lam, Andrew F Olshan, Mark C Weissler, Martin Lacko, Angela Risch, Heike Bickeböller, Andy R Ness, Steve Thomas, Loic Le Marchand, Matthew B Schabath, Victor Wünsch-Filho, Eloiza H Tajara, Angeline S Andrew, Gary M Clifford, Philip Lazarus, Kjell Grankvist, Mikael Johansson, Susanne Arnold, Olle Melander, Hans Brunnström, Stefania Boccia, Gabriella Cadoni, Wim Timens, Ma'en Obeidat, Xiangjun Xiao, Richard S Houlston, Rayjean J Hung, Paul Brennan

المصدر: PLoS Genetics, Vol 17, Iss 3, p e1009254 (2021)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

الوصول الحر: https://doaj.org/article/1d4a61d6236e418ea99298d8bce6bf87Test

المؤلفون: Davis, Lea K, Yu, Dongmei, Keenan, Clare L, Gamazon, Eric R, Konkashbaev, Anuar I, Derks, Eske M, Neale, Benjamin M, Yang, Jian, Lee, S. Hong, Evans, Patrick, Barr, Cathy L, Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel Bedoya, Bienvenu, Oscar J, Bloch, Michael H, Blom, Rianne M, Bruun, Ruth D, Budman, Cathy L, Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio C, Cath, Danielle C, Cavallini, Maria C, Chavira, Denise A, Chouinard, Sylvain, Conti, David V, Cook, Edwin H, Coric, Vladimir, Cullen, Bernadette A, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher K, Egberts, Karin, Falkai, Peter, Fernandez, Thomas V, Gallagher, Patience J, Garrido, Helena, Geller, Daniel, Girard, Simon L, Grabe, Hans J, Grados, Marco A, Greenberg, Benjamin D, Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary A, Hemmings, Sian M. J, Hounie, Ana G, Illmann, Cornelia, Jankovic, Joseph, Jenike, Michael A, Kennedy, James L, King, Robert A, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James F, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Lowe, Thomas L, Macciardi, Fabio, McCracken, James T, McGrath, Lauren M, Mesa Restrepo, Sandra C, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis L, Naarden, Allan L, Ochoa, William Cornejo, Ophoff, Roel A, Osiecki, Lisa, Pakstis, Andrew J, Pato, Michele T, Pato, Carlos N, Piacentini, John, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott L, Renner, Tobias J, Reus, Victor I, Richter, Margaret A, Riddle, Mark A, Robertson, Mary M, Romero, Roxana, Rosàrio, Maria C, Rosenberg, David, Rouleau, Guy A, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline S, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey S, Smit, Jan H

المصدر: PLoS Genetics. 9(10)

مصطلحات موضوعية: Missing Heritability, Tic Disorders, Neuropsychiatric Disorders, Complex Diseases, Common Snps, Gilles, Family, Brain, Expression, Autism

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/21h67097Test

المؤلفون: Chouinard, Sylvain, Conti, David, Cook, Edwin, Coric, Vladimir, Cullen, Bernadette, Deforce, Dieter, Delorme, Richard, Dion, Yves, Edlund, Christopher, Egberts, Karin, Falkai, Peter, Fernandez, Thomas, Gallagher, Patience, Garrido, Helena, Geller, Daniel, Girard, Simon, Grabe, Hans, Grados, Marco, Greenberg, Benjamin, Gross-Tsur, Varda, Haddad, Stephen, Heiman, Gary, Hemmings, Sian, Hounie, Ana, Illmann, Cornelia, Jankovic, Joseph, Jenike, Michael, Kennedy, James, King, Robert, Kremeyer, Barbara, Kurlan, Roger, Lanzagorta, Nuria, Leboyer, Marion, Leckman, James, Lennertz, Leonhard, Liu, Chunyu, Lochner, Christine, Davis, Lea, Yu, Dongmei, Keenan, Clare, Gamazon, Eric, Konkashbaev, Anuar, Derks, Eske, Neale, Benjamin, Yang, Jian, Lee, S, Evans, Patrick, Barr, Cathy, Bellodi, Laura, Benarroch, Fortu, Berrio, Gabriel, Bienvenu, Oscar, Bloch, Michael, Blom, Rianne, Bruun, Ruth, Budman, Cathy, Camarena, Beatriz, Campbell, Desmond, Cappi, Carolina, Cardona Silgado, Julio, Cath, Danielle, Cavallini, Maria, McCracken, James, McGrath, Lauren, Mesa Restrepo, Sandra, Moessner, Rainald, Morgan, Jubel, Muller, Heike, Murphy, Dennis, Naarden, Allan, Ochoa, William, Osiecki, Lisa, Pakstis, Andrew, Pato, Michele, Pato, Carlos, Pittenger, Christopher, Pollak, Yehuda, Rauch, Scott, Renner, Tobias, Richter, Margaret, Riddle, Mark, Robertson, Mary, Romero, Roxana, Rosàrio, Maria, Rosenberg, David, Rouleau, Guy, Ruhrmann, Stephan, Ruiz-Linares, Andres, Sampaio, Aline, Samuels, Jack, Sandor, Paul, Sheppard, Brooke, Singer, Harvey, Smit, Jan, Stein, Dan, Strengman, E, Tischfield, Jay, Valencia Duarte, Ana, Vallada, Homero, Van Nieuwerburgh, Filip

المصدر: PLoS Genetics. 9(10)

مصطلحات موضوعية: Gene Frequency, Genome-Wide Association Study, Humans, Obsessive-Compulsive Disorder, Phenotype, Polymorphism, Single Nucleotide, Quantitative Trait, Heritable, Tourette Syndrome

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/7qz8p8mfTest
https://escholarship.org/content/qt7qz8p8mf/qt7qz8p8mf.pdfTest

المؤلفون: Couch, Fergus J, Wang, Xianshu, McGuffog, Lesley, Lee, Andrew, Olswold, Curtis, Kuchenbaecker, Karoline B, Soucy, Penny, Fredericksen, Zachary, Barrowdale, Daniel, Dennis, Joe, Gaudet, Mia M, Dicks, Ed, Kosel, Matthew, Healey, Sue, Sinilnikova, Olga M, Lee, Adam, Bacot, François, Vincent, Daniel, Hogervorst, Frans BL, Peock, Susan, Stoppa-Lyonnet, Dominique, Jakubowska, Anna, kConFab Investigators, Radice, Paolo, Schmutzler, Rita Katharina, SWE-BRCA, Domchek, Susan M, Piedmonte, Marion, Singer, Christian F, Friedman, Eitan, Thomassen, Mads, Ontario Cancer Genetics Network, Hansen, Thomas VO, Neuhausen, Susan L, Szabo, Csilla I, Blanco, Ignacio, Greene, Mark H, Karlan, Beth Y, Garber, Judy, Phelan, Catherine M, Weitzel, Jeffrey N, Montagna, Marco, Olah, Edith, Andrulis, Irene L, Godwin, Andrew K, Yannoukakos, Drakoulis, Goldgar, David E, Caldes, Trinidad, Nevanlinna, Heli, Osorio, Ana, Terry, Mary Beth, Daly, Mary B, van Rensburg, Elizabeth J, Hamann, Ute, Ramus, Susan J, Toland, Amanda Ewart, Caligo, Maria A, Olopade, Olufunmilayo I, Tung, Nadine, Claes, Kathleen, Beattie, Mary S, Southey, Melissa C, Imyanitov, Evgeny N, Tischkowitz, Marc, Janavicius, Ramunas, John, Esther M, Kwong, Ava, Diez, Orland, Balmaña, Judith, Barkardottir, Rosa B, Arun, Banu K, Rennert, Gad, Teo, Soo-Hwang, Ganz, Patricia A, Campbell, Ian, van der Hout, Annemarie H, van Deurzen, Carolien HM, Seynaeve, Caroline, Gómez Garcia, Encarna B, van Leeuwen, Flora E, Meijers-Heijboer, Hanne EJ, Gille, Johannes JP, Ausems, Margreet GEM, Blok, Marinus J, Ligtenberg, Marjolijn JL, Rookus, Matti A, Devilee, Peter, Verhoef, Senno, van Os, Theo AM, Wijnen, Juul T, HEBON, EMBRACE, Frost, Debra, Ellis, Steve, Fineberg, Elena, Platte, Radka, Evans, D Gareth, Izatt, Louise, Eeles, Rosalind A, Adlard, Julian

المصدر: PLoS genetics. 9(3)

مصطلحات موضوعية: kConFab Investigators, SWE-BRCA, Ontario Cancer Genetics Network, HEBON, EMBRACE, GEMO Study Collaborators, BCFR, CIMBA, Humans, Breast Neoplasms, Ovarian Neoplasms, Genetic Predisposition to Disease, BRCA1 Protein, BRCA2 Protein, Prognosis, Risk Factors, Genotype, Heterozygote, Mutation, Polymorphism, Single Nucleotide, Middle Aged, Female, Genome-Wide Association Study, Polymorphism, Single Nucleotide, Developmental Biology, Genetics

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/3n33s4t6Test

المؤلفون: Kryvokhyzha, Dmytro, Milesi, Pascal, Duan, Tianlin, Orsucci, Marion, Wright, Stephen I., Glemin, Sylvain, Lascoux, Martin

المصدر: PLOS Genetics. 15(5)

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-387963Test
https://doi.org/10.1371/journal.pgen.1008131Test
https://uu.diva-portal.org/smash/get/diva2:1331994/FULLTEXT01.pdfTest

المؤلفون: Tomlinson, Ian PM, Carvajal-Carmona, Luis G, Dobbins, Sara E, Tenesa, Albert, Jones, Angela M, Howarth, Kimberley, Palles, Claire, Broderick, Peter, Jaeger, Emma EM, Farrington, Susan, Lewis, Annabelle, Prendergast, James GD, Pittman, Alan M, Theodoratou, Evropi, Olver, Bianca, Walker, Marion, Penegar, Steven, Barclay, Ella, Whiffin, Nicola, Martin, Lynn, Ballereau, Stephane, Lloyd, Amy, Gorman, Maggie, Lubbe, Steven, COGENT Consortium, CORGI Collaborators, EPICOLON Consortium, Howie, Bryan, Marchini, Jonathan, Ruiz-Ponte, Clara, Fernandez-Rozadilla, Ceres, Castells, Antoni, Carracedo, Angel, Castellvi-Bel, Sergi, Duggan, David, Conti, David, Cazier, Jean-Baptiste, Campbell, Harry, Sieber, Oliver, Lipton, Lara, Gibbs, Peter, Martin, Nicholas G, Montgomery, Grant W, Young, Joanne, Baird, Paul N, Gallinger, Steven, Newcomb, Polly, Hopper, John, Jenkins, Mark A, Aaltonen, Lauri A, Kerr, David J, Cheadle, Jeremy, Pharoah, Paul, Casey, Graham, Houlston, Richard S, Dunlop, Malcolm G

المصدر: PLoS genetics. 7(6)

مصطلحات موضوعية: COGENT Consortium, CORGI Collaborators, EPICOLON Consortium, Humans, Colorectal Neoplasms, Genetic Predisposition to Disease, Intercellular Signaling Peptides and Proteins, Case-Control Studies, Signal Transduction, Gene Frequency, Quantitative Trait, Heritable, Polymorphism, Single Nucleotide, Aged, Middle Aged, Male, Genetic Variation, Genome-Wide Association Study, Bone Morphogenetic Protein 2, Bone Morphogenetic Protein 4, Polymorphism, Single Nucleotide, Quantitative Trait, Heritable, Genetics, Developmental Biology

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/8hg5z5bpTest

المؤلفون: Fasil Tekola-Ayele, Cuilin Zhang, Jing Wu, Katherine L Grantz, Mohammad L Rahman, Deepika Shrestha, Marion Ouidir, Tsegaselassie Workalemahu, Michael Y Tsai

المصدر: PLoS Genetics, Vol 16, Iss 5, p e1008747 (2020)

مصطلحات موضوعية: Genetics, QH426-470

وصف الملف: electronic resource

العلاقة: https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test

الوصول الحر: https://doaj.org/article/0e162cb92f8447d2817ffe9e76969529Test