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Refinado por: assunto: Genetic Variation remover Base de dados/Biblioteca: Springer Nature - Complete Springer Journals remover
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The ethics of characterizing difference: guiding principles on using racial categories in human genetics
The ethics of characterizing difference: guiding principles on using racial categories in human genetics
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The ethics of characterizing difference: guiding principles on using racial categories in human genetics

Lee, Sandra Soo-Jin ; Mountain, Joanna ; Koenig, Barbara ; Altman, Russ ; Brown, Melissa ; Camarillo, Albert ; Cavalli-Sforza, Luca ; Cho, Mildred ; Eberhardt, Jennifer ; Feldman, Marcus ; Ford, Richard ; Greely, Henry ; King, Roy ; Markus, Hazel ; Satz, Debra ; Snipp, Matthew ; Steele, Claude ; Underhill, Peter

Genome Biology (Online Edition), 2008-01, Vol.9 (7), p.404-404 [Periódico revisado por pares]

England: BioMed Central Ltd

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2
Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations
Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations
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Analysis of hereditary cancer syndromes by using a panel of genes: novel and multiple pathogenic mutations

Tsaousis, Georgios N ; Papadopoulou, Eirini ; Apessos, Angela ; Agiannitopoulos, Konstantinos ; Pepe, Georgia ; Kampouri, Stavroula ; Diamantopoulos, Nikolaos ; Floros, Theofanis ; Iosifidou, Rodoniki ; Katopodi, Ourania ; Koumarianou, Anna ; Markopoulos, Christos ; Papazisis, Konstantinos ; Venizelos, Vasileios ; Xanthakis, Ioannis ; Xepapadakis, Grigorios ; Banu, Eugeniu ; Eniu, Dan Tudor ; Negru, Serban ; Stanculeanu, Dana Lucia ; Ungureanu, Andrei ; Ozmen, Vahit ; Tansan, Sualp ; Tekinel, Mehmet ; Yalcin, Suayib ; Nasioulas, George

BMC cancer, 2019-06, Vol.19 (1), p.535-535, Article 535 [Periódico revisado por pares]

England: BioMed Central Ltd

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3
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects
Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects
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Genetic analysis of DNA methylation and gene expression levels in whole blood of healthy human subjects

van Eijk, Kristel R ; de Jong, Simone ; Boks, Marco P M ; Langeveld, Terry ; Colas, Fabrice ; Veldink, Jan H ; de Kovel, Carolien G F ; Janson, Esther ; Strengman, Eric ; Langfelder, Peter ; Kahn, René S ; van den Berg, Leonard H ; Horvath, Steve ; Ophoff, Roel A

BMC genomics, 2012-11, Vol.13 (1), p.636-636, Article 636 [Periódico revisado por pares]

England: BioMed Central Ltd

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4
Genetic architecture of fruit size and shape variation in cucurbits: a comparative perspective
Genetic architecture of fruit size and shape variation in cucurbits: a comparative perspective
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Genetic architecture of fruit size and shape variation in cucurbits: a comparative perspective

Pan, Yupeng ; Wang, Yuhui ; McGregor, Cecilia ; Liu, Shi ; Luan, Feishi ; Gao, Meiling ; Weng, Yiqun

Theoretical and applied genetics, 2020, Vol.133 (1), p.1-21 [Periódico revisado por pares]

Berlin/Heidelberg: Springer Berlin Heidelberg

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5
MAST: a flexible statistical framework for assessing transcriptional changes and characterizing heterogeneity in single-cell RNA sequencing data
MAST: a flexible statistical framework for assessing transcriptional changes and characterizing heterogeneity in single-cell RNA sequencing data
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MAST: a flexible statistical framework for assessing transcriptional changes and characterizing heterogeneity in single-cell RNA sequencing data

Finak, Greg ; McDavid, Andrew ; Yajima, Masanao ; Deng, Jingyuan ; Gersuk, Vivian ; Shalek, Alex K ; Slichter, Chloe K ; Miller, Hannah W ; McElrath, M Juliana ; Prlic, Martin ; Linsley, Peter S ; Gottardo, Raphael

Genome Biology, 2015-12, Vol.16 (1), p.278-278, Article 278 [Periódico revisado por pares]

England: BioMed Central Ltd

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6
Genome-based prediction of testcross values in maize
Genome-based prediction of testcross values in maize
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Genome-based prediction of testcross values in maize

Albrecht, Theresa ; Wimmer, Valentin ; Auinger, Hans-Jürgen ; Erbe, Malena ; Knaak, Carsten ; Ouzunova, Milena ; Simianer, Henner ; Schön, Chris-Carolin

Theoretical and applied genetics, 2011-07, Vol.123 (2), p.339-350 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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7
Patterns of molecular variation in a species-wide germplasm set of Brassica napus
Patterns of molecular variation in a species-wide germplasm set of Brassica napus
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Patterns of molecular variation in a species-wide germplasm set of Brassica napus

Bus, Anja ; Körber, Niklas ; Snowdon, Rod J. ; Stich, Benjamin

Theoretical and applied genetics, 2011-12, Vol.123 (8), p.1413-1423 [Periódico revisado por pares]

Berlin/Heidelberg: Springer-Verlag

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8
High throughput analysis of grape genetic diversity as a tool for germplasm collection management
High throughput analysis of grape genetic diversity as a tool for germplasm collection management
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High throughput analysis of grape genetic diversity as a tool for germplasm collection management

Laucou, V ; Lacombe, T ; Dechesne, F ; Siret, R ; Bruno, J.-P ; Dessup, M ; Dessup, T ; Ortigosa, P ; Parra, P ; Roux, C ; Santoni, S ; Varès, D ; Péros, J.-P ; Boursiquot, J.-M ; This, P

Theoretical and applied genetics, 2011-04, Vol.122 (6), p.1233-1245 [Periódico revisado por pares]

Berlin/Heidelberg: Berlin/Heidelberg : Springer-Verlag

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9
Host genetic variation impacts microbiome composition across human body sites
Host genetic variation impacts microbiome composition across human body sites
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Host genetic variation impacts microbiome composition across human body sites

Blekhman, Ran ; Goodrich, Julia K ; Huang, Katherine ; Sun, Qi ; Bukowski, Robert ; Bell, Jordana T ; Spector, Timothy D ; Keinan, Alon ; Ley, Ruth E ; Gevers, Dirk ; Clark, Andrew G

Genome Biology, 2015-09, Vol.16 (1), p.191, Article 191 [Periódico revisado por pares]

England: BioMed Central Ltd

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10
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders
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Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders

Gillentine, Madelyn A ; Wang, Tianyun ; Hoekzema, Kendra ; Rosenfeld, Jill ; Liu, Pengfei ; Guo, Hui ; Kim, Chang N ; De Vries, Bert B A ; Vissers, Lisenka E L M ; Nordenskjold, Magnus ; Kvarnung, Malin ; Lindstrand, Anna ; Nordgren, Ann ; Gecz, Jozef ; Iascone, Maria ; Cereda, Anna ; Scatigno, Agnese ; Maitz, Silvia ; Zanni, Ginevra ; Bertini, Enrico ; Zweier, Christiane ; Schuhmann, Sarah ; Wiesener, Antje ; Pepper, Micah ; Panjwani, Heena ; Torti, Erin ; Abid, Farida ; Anselm, Irina ; Srivastava, Siddharth ; Atwal, Paldeep ; Bacino, Carlos A ; Bhat, Gifty ; Cobian, Katherine ; Bird, Lynne M ; Friedman, Jennifer ; Wright, Meredith S ; Callewaert, Bert ; Petit, Florence ; Mathieu, Sophie ; Afenjar, Alexandra ; Christensen, Celenie K ; White, Kerry M ; Elpeleg, Orly ; Berger, Itai ; Espineli, Edward J ; Fagerberg, Christina ; Brasch-Andersen, Charlotte ; Hansen, Lars Kjærsgaard ; Feyma, Timothy ; Hughes, Susan ; Thiffault, Isabelle ; Sullivan, Bonnie ; Yan, Shuang ; Keller, Kory ; Keren, Boris ; Mignot, Cyril ; Kooy, Frank ; Meuwissen, Marije ; Basinger, Alice ; Kukolich, Mary ; Philips, Meredith ; Ortega, Lucia ; Drummond-Borg, Margaret ; Lauridsen, Mathilde ; Sorensen, Kristina ; Lehman, Anna ; Lopez-Rangel, Elena ; Levy, Paul ; Lessel, Davor ; Lotze, Timothy ; Madan-Khetarpal, Suneeta ; Sebastian, Jessica ; Vento, Jodie ; Vats, Divya ; Benman, L Manace ; Mckee, Shane ; Mirzaa, Ghayda M ; Muss, Candace ; Pappas, John ; Peeters, Hilde ; Romano, Corrado ; Elia, Maurizio ; Galesi, Ornella ; Simon, Marleen E H ; van Gassen, Koen L I ; Simpson, Kara ; Stratton, Robert ; Syed, Sabeen ; Thevenon, Julien ; Palafoll, Irene Valenzuela ; Vitobello, Antonio ; Bournez, Marie ; Faivre, Laurence ; Xia, Kun ; Earl, Rachel K ; Nowakowski, Tomasz ; Bernier, Raphael A ; Eichler, Evan E

Genome medicine, 2021-04, Vol.13 (1), p.63-63, Article 63 [Periódico revisado por pares]

England: BioMed Central Ltd

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