83 research outputs found
Genetics and molecular mechanisms of resistance to powdery mildews in tomato (Solanum lycopersicum) and its wild relatives
- Author
- Publication venue
- Publication date
- 01/01/2013
- Field of study
Powdery mildews (PMs) cause disease in a wide range of plant species including important crops. Taking tomato as an example, here we review findings on the genetic basis and mechanisms of plant resistance to PMs. First, we present a summary of our research on tomato resistance to two PM species, with the focus on Oidium neolycopersici. We discuss the genetics of resistance to this pathogen in tomato. Then, we compare different forms of resistance mediated by different resistance genes based on molecular and cytological data. Also, we provide a comparison between these resistance genes in tomato with those in barley, Arabidopsis and wheat, in order to present a model for the genetic basis of resistance to PMs in plants. We try to accommodate these resistance mechanisms in the current model of plant innate immunity. At the end we discuss possibilities to translate these findings to practical approaches in breeding for resistance to PMs in crops
ZED1-related kinase 13 is required for resistance against Pseudoidium neolycopersici in Arabidopsis accession Bla-6
- Author
- Publication venue
- 'Frontiers Media SA'
- Publication date
- 01/03/2023
- Field of study
To explore specific components of resistance against the tomato-adapted powdery mildew pathogen Pseudoidium neolycopersici (On) in the model plant Arabidopsis, we performed a disease assay in 123 accessions. When testing the resistance in the F1 from crossings between resistant accessions with susceptible Col-0 or Sha, only the progeny of the cross between accession Bla-6 and Col-0 displayed a completely resistant phenotype. The resistance in Bla-6 is known to be specific for Pseudoidium neolycopersici. QTL analysis and fine-mapping through several rounds of recombinant screenings allowed us to locate a major resistance QTL in an interval on chromosome 1, containing two candidate genes and an intergenic insertion. Via CRISPR/Cas9 targeted mutagenesis, we could show that knocking out the ZED-1 RELATED KINASE 13 (ZRK13) gene compromised the On resistance in Bla-6. Several polymorphisms are observed in the ZRK13 allelic variant of Bla-6 when compared to the Col-0 protein
Identification of alleles of carotenoid pathway genes important for zeaxanthin accumulation in potato tubers
- Author
- A Kobayashi
- AB Lopez
- AM Anithakumari
- Anne-Marie A. Wolters
- B Kloosterman
- B Kloosterman
- BA Uijtewaal
- BA Uijtewaal
- BB D’hoop
- Bjorn A. Kloosterman
- C Fruwirth
- CM Andre
- CR Brown
- CR Brown
- CR Brown
- CR Brown
- CWB Bachem
- DE Breithaupt
- DM Snodderly
- E Jacobsen
- E Jacobsen
- E Marin
- E Ritter
- E Vries-Uijtewaal De
- G Burgos
- G Diretto
- GCL Johnson
- GJ Handelman
- GJ Lightbourn
- H Binding
- Herman J. van Eck
- J Kort
- Jan G. A. M. L. Uitdewilligen
- JE Bradshaw
- JG Beek Van der
- JHM Hovenkamp-Hermelink
- JM Seddon
- JME Jacobs
- JW Ooijen Van
- JW Ooijen Van
- MR Hanson
- MW Bonierbale
- N Galpaz
- N Nicot
- NI Krinsky
- O Sommerburg
- PC Ng
- RE Hanneman Jr
- Richard G. F. Visser
- RJ Bino
- Ronald C. B. Hutten
- S Gazzani
- S Nesterenko
- S Römer
- SC Duckham
- SD Michaels
- SE Vries De
- SM Moeller
- T Obukhanych
- TA Thorup
- TH Park
- TJH Hoogkamp
- VV Kapitonov
- W Iwanzik
- WL Morris
- Y Ohmori
- Y Tanaka
- YM Goo
- Publication venue
- Springer Netherlands
- Publication date
- 01/01/2010
- Field of study
We have investigated the genetics and molecular biology of orange flesh colour in potato (Solanum tuberosum L.). To this end the natural diversity in three genes of the carotenoid pathway was assessed by SNP analyses. Association analysis was performed between SNP haplotypes and flesh colour phenotypes in diploid and tetraploid potato genotypes. We observed that among eleven beta-carotene hydroxylase 2 (Chy2) alleles only one dominant allele has a major effect, changing white into yellow flesh colour. In contrast, none of the lycopene epsilon cyclase (Lcye) alleles seemed to have a large effect on flesh colour. Analysis of zeaxanthin epoxidase (Zep) alleles showed that all (diploid) genotypes with orange tuber flesh were homozygous for one specific Zep allele. This Zep allele showed a reduced level of expression. The complete genomic sequence of the recessive Zep allele, including the promoter, was determined, and compared with the sequence of other Zep alleles. The most striking difference was the presence of a non-LTR retrotransposon sequence in intron 1 of the recessive Zep allele, which was absent in all other Zep alleles investigated. We hypothesise that the presence of this large sequence in intron 1 caused the lower expression level, resulting in reduced Zep activity and accumulation of zeaxanthin. Only genotypes combining presence of the dominant Chy2 allele with homozygosity for the recessive Zep allele produced orange-fleshed tubers that accumulated large amounts of zeaxanthin
Assessing the genetic variation of Ty-1 and Ty-3 alleles conferring resistance to Tomato Yellow Leaf Curl Virus in a broad tomato germplasm
- Author
- A Pérez de Castro
- A Pérez de Castro
- Ana Pérez-de-Castro
- Anne-Marie A. Wolters
- B Pico
- CM Fauquet
- D Zamir
- F Vidavski
- H Agrama
- H Li
- H Li
- I Anbinder
- John W. Scott
- JT Robinson
- JW Scott
- K Tamura
- M Friedmann
- Maarten G. Verlaan
- Maria J. Díez
- MG Verlaan
- MG Verlaan
- Myluska Caro
- N Menda
- Olga Julián
- P Butterbach
- P Danecek
- PM Hanson
- PP Sahu
- R Vanitharani
- Richard Finkers
- Richard G. F. Visser
- Richard Kormelink
- S Cohen
- Samuel F. Hutton
- SF Hutton
- The 100 Tomato Genome Sequencing Consortium
- The Tomato Genome Consortium
- X Yang
- Y Bai
- Y Ji
- Y Ji
- Yuling Bai
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 01/01/2015
- Field of study
The online version of
this article (doi:10.1007/s11032-015-0329-y) contains supplementary
material, which is available to authorized users.[EN] Tomato yellow leaf curl virus (TYLCV) hampers tomato production worldwide. Our previous studies have focussed on mapping and ultimately cloning of the TYLCV resistance genes Ty-1 and Ty-3. Both genes are derived from Solanum chilense and were shown to be allelic. They code for an RNA-dependent RNA polymerase (RDR) belonging to the RDR gamma type defined by a DFDGD catalytic domain. In this study, we first fine-mapped the TYLCV resistance in S. chilense LA1932, LA1960 and LA1971. Results showed that chromosomal intervals of the causal genes in these TYLCV-resistant accessions overlap and cover the region where Ty-1/Ty-3 is located. Further, virus-induced gene silencing was used to silence Ty-1/Ty-3 in tomato lines carrying TYLCV resistance introgressed from S. chilense LA1932, LA1938 and LA1971. Results showed that silencing Ty-1/Ty-3 compromised the resistance in lines derived from S. chilense LA1932 and LA1938. The LA1971-derived material remained resistant upon silencing Ty-1/Ty-3. Further, we studied the allelic variation of the Ty-1/Ty-3 gene by examining cDNA sequences from nine S. chilense-derived lines/accessions and more than 80 tomato cultivars, landraces and accessions of related wild species. The DFDGD catalytic domain of the Ty-1/Ty-3 gene is conserved among all tomato lines and species analysed. In addition, the 12 base pair insertion at the 5-prime part of the Ty-1/Ty-3 gene was found not to be specific for the TYLCV resistance allele. However, compared with the susceptible ty-1 allele, the Ty-1/Ty-3 allele is characterized by three specific amino acids shared by seven TYLCV-resistant S. chilense accessions or derived lines. Thus, Ty-1/Ty-3-specific markers can be developed based on these polymorphisms. Elevated transcript levels were observed for all tested S. chilense RDR alleles (both Ty-1 and ty-1 alleles), demonstrating that elevated expression level is not a good selection criterion for a functional Ty-1/Ty-3 allele.The infectious TYLCV clone was kindly provided by Professor Eduardo Rodriguez Bejarano (Universidad de Malaga). We thank Dick Lohuis for his help with agro-infiltrations, Marc Hendriks and Marjon Arens for RNA isolation and sequencing. This project was financed by the Centre for BioSystems Genomics (CBSG), which is part of the Netherlands Genomics Initiative/Netherlands Organization for Scientific Research (http://www.cbsg.nl). Olga Julian was granted a scholarship by Generalitat Valenciana. Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.Caro, M.; Verlaan, MG.; Julián Rodríguez, O.; Finkers, R.; Wolters, AA.; Hutton, S.; Scott, JW.... (2015). Assessing the genetic variation of Ty-1 and Ty-3 alleles conferring resistance to Tomato Yellow Leaf Curl Virus in a broad tomato germplasm. Molecular Breeding. 35. doi:10.1007/s11032-015-0329-yS13235Agrama H, Scott J (2006) Quantitative trait loci for tomato yellow leaf curl virus and tomato mottle virus resistance in tomato. J Am Soc Hortic Sci 131:267–272Anbinder I, Reuveni M, Azari R, Paran I, Nahon S, Shlomo H, Chen L, Lapidot M, Levin I (2009) Molecular dissection of tomato leaf curl virus resistance in tomato line TY172 derived from Solanum peruvianum. Theor Appl Genet 119:519–530Bai Y, Van der Hulst R, Huang C, Wei L, Stam P, Lindhout P (2004) Mapping Ol-4, a gene conferring resistance to Oidium neolycopersici and originating from Lycopersicon peruvianum LA2172, requires multi-allelic, single-locus markers. Theor Appl Genet 109:1215–1223Butterbach P, Verlaan MG, Dullemans A, Lohuis D, Visser RGF, Bai Y, Kormelink R (2014) The TYLCV Resistance Gene Ty-1 confers resistance in tomato through enhanced transcriptional gene silencing. PNAS 111:12942–12947Cohen S, Lapidot M (2007) Appearance and expansion of TYLCV: a historical point of view. In: Czosnek H (ed) Tomato yellow leaf curl virus disease. Springer, The Netherlands, pp 3–12Danecek P, Auton A, Abecasis G, Albers CA, Banks E, DePristo MA, Handsaker RE, Lunter G, Marth GT, Sherry ST, McVean G, Durbin R, Group GPA (2011) The variant call format and VCFtools. Bioinformatics 27:2156–2158Fauquet CM, Briddon RW, Brown JK, Moriones E, Stanley J, Zerbini M, Zhou X (2008) Geminivirus strain demarcation and nomenclature. Arch Virol 153:783–821Friedmann M, Lapidot M, Cohen S, Pilowsky M (1998) A novel source of resistance to Tomato yellow leaf curl virus exhibiting a symptomless reaction to viral infection. J Am Soc Hortic Sci 123:1004–1007Hanson PM, Green SK, Kuo G (2006) Ty-2, a gene on chromosome 11 conditioning geminivirus resistance in tomato. Tomato Genet Coop Rep 56:17–18Hutton SF, Scott JW (2013) Fine-mapping and cloning of Ty-1 and Ty-3; and mapping of a new TYLCV resistance locus, “Ty-6”. In: Tomato breeders round table proceedings 2013, Chiang Mai, ThailandHutton SF, Scott JW, Schuster DJ (2012) Recessive resistance to tomato yellow leaf curl virus from the tomato cultivar tyking is located in the same region as Ty-5 on chromosome 4. HortScience 47:324–327Ji Y, Schuster DJ, Scott JW (2007) Ty-3, a begomovirus resistance locus near the Tomato yellow leaf curl virus resistance locus Ty-1 on chromosome 6 of tomato. Mol Breeding 20:271–284Ji Y, Scott JW, Schuster DJ, Maxwell DP (2009) Molecular mapping of Ty-4, a new tomato yellow leaf curl virus resistance locus on chromosome 3 of tomato. J Am Soc Hortic Sci 134:281–288Levin I, Karniel U, Fogel D, Reuveni M, Gelbart D, Evenor D, Chen L, Nahon S, Shlomo H, Machbosh Z, Lapidot M (2013) Cloning and analysis of the tomato yellow leaf curl virus resistance gene Ty-5. In: Tomato breeders round table proceedings 2013, Chiang Mai, ThailandLi H, Durbin R (2009) Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics 25:1754–1760Li H, Handsaker B, Wysoker A, Fennell T, Ruan J, Homer N, Marth G, Abecasis G, Durbin R (2009) The sequence alignment/map format and SAMtools. The sequence alignment/map format and SAMtools. Bioinformatics 25:2078–2079Mejía L, Teni RE, Vidavski F, Czosnek H, Lapidot M, Nakhla MK, Maxwell DP (2005) Evaluation of tomato germplasm and selection of breeding lines for resistance to begomoviruses in Guatemala. In: Momol MT, Ji P, Jones JB (eds) Proceedings 1st international symposium on tomato diseases. Acta Horticult 695:251–256Menda N, Strickler SR, Edwards JD, Bombarely A, Dunham DM, Martin GB, Mejia L, Hutton SF, Havey MJ, Maxwell DP, Mueller LA (2014) Analysis of wild-species introgressions in tomato inbreds uncovers ancestral origins. BMC Plant Biol 14(1):287Pérez de Castro A, Díez MJ, Nuez F (2007) Inheritance of Tomato yellow leaf curl virus resistance derived from Solanum pimpinellifolium UPV16991. Plant Dis 91:879–885Pérez de Castro A, Julián O, Díez M (2013) Genetic control and mapping of Solanum chilense LA1932, LA1960 and LA1971-derived resistance to tomato yellow leaf curl disease. Euphytica 190:203–214Pico B, Ferriol M, Diez MJ, Nuez F (1999) Developing tomato breeding lines resistant to tomato yellow leaf curl virus. Plant Breeding 118:537–542Robinson JT, Thorvaldsdottir H, Winckler W, Guttman M, Lander ES, Getz G, Mesirov JP (2011) Integrative genomics viewer. Nature. Biotech 29:24–26Sahu PP, Puranik S, Khan M, Prasad M (2012) Recent advances in tomato functional genomics: utilization of VIGS. Protoplasma 249(4):1017–1027Scott JW, Stevens MR, Barten JHM, Thome CR, Polston JE, Schuster DJ, Serra CA (1996) Introgression of resistance to whitefly-transmitted geminiviruses from Lycopersicon chilense to tomato. In: Gerling D, Mayer RT (eds) Bemisia 1995; taxonomy, biology, damage control, and management. Intercept Press, Andover, pp 357–367Tamura K, Peterson D, Peterson N, Stecher G, Nei M, Kumar S (2011) MEGA5: molecular evolutionary genetics analysis using maximum likelihood, evolutionary distance, and maximum parsimony methods. Mol Biol Evol 28:2731–2739The 100 Tomato Genome Sequencing Consortium (2014) Exploring genetic variation in the tomato (Solanum section Lycopersicon) clade by whole-genome sequencing. Plant J 80:136–148The Tomato Genome Consortium (2012) The tomato genome sequence provides insights into fleshy fruit evolution. Nature 485:635–641Vanitharani R, Chellappan P, Pita JS, Fauquet CM (2004) Differential roles of AC2 and AC4 of cassava geminiviruses in mediating synergism and suppression of posttranscriptional gene silencing. J Virol 78:9487–9498Verlaan MG, Szinay D, Hutton SF, de Jong H, Kormelink R, Visser RGF, Scott JW, Bai Y (2011) Chromosomal rearrangements between tomato and Solanum chilense hamper mapping and breeding of the TYLCV resistance gene Ty-1. Plant J 68:1093–1103Verlaan MG, Hutton SF, Ibrahem RM, Kormelink R, Visser RGF, Scott JW, Edwards JD, Bai Y (2013) The tomato yellow leaf curl virus resistance genes Ty-1 and Ty-3 are allelic and code for DFDGD-class RNA-dependent RNA polymerases. PLoS Genet 9(3):e1003399. doi: 10.1371/journal.pgen.1003399Vidavski F (2007) Exploitation of resistance genes found in wild tomato species to produce resistant cultivars; Pile up of Resistant Genes. In: Czosnek H (ed) Tomato yellow leaf curl virus disease. Springer, Netherlands, pp 363–372Willmann MR, Endres MW, Cook RT, Gregory BD (2011) The functions of RNA-dependent RNA polymerases in arabidopsis. In: The Arabidopsis Book, e0146Yang X, Caro M, Hutton SF, Scott JW, Guo Y, Wang X, Rashid MH, Szinay D, de Jong H, Visser RGF, Bai Y, Du Y (2014) Fine mapping of the tomato yellow leaf curl virus resistance gene Ty-2 on chromosome 11 of tomato. Mol Breeding 34:749–760Zamir D, Ekstein Michelson I, Zakay Y, Navot N, Zeidan M, Sarfatti M, Eshed Y, Harel E, Pleban T, van Oss H (1994) Mapping and introgression of a tomato yellow leaf curl virus tolerance gene, Ty-1. Theor Appl Genet 88:141–14
Global data on earthworm abundance, biomass, diversity and corresponding environmental properties
- Author
- Ammer Christian
- Ammer Sabine
- Arai Miwa
- Ayuke Fredrick O.
- Bach Elizabeth M.
- Baker Geoff H.
- Baretta Dilmar
- Barkusky Dietmar
- Bartz Marie L.C.
- Beauséjour Robin
- Bedano Jose C.
- Bennett Joanne M.
- Beugnon Rémy
- Birkhofer Klaus
- Blanchart Eric
- Blossey Bernd
- Bolger Thomas
- Bradley Robert L.
- Briones Maria J.I.
- Brose Ulrich
- Brossard Michel
- Brown George G.
- Burtis James C.
- Cameron Erin K.
- Capowiez Yvan
- Cavagnaro Timothy R.
- Choi Amy
- Clause Julia
- Cluzeau Daniel
- Coors Anja
- Cosín Darío J.Díaz
- Crotty Felicity V.
- Crumsey Jasmine M.
- de Valença Anne W.
- de Vries Franciska T.
- Decaëns Thibaud
- Dobson Annise M.
- Domínguez Anahí
- Duhour Andrés Esteban
- Dávalos Andrea
- Eisenhauer Nico
- Emmerling Christoph
- Falco Liliana B.
- Ferlian Olga
- Fernández Rosa
- Fonte Steven J.
- Fragoso Carlos
- Franco André L.C.
- Fusilero Abegail
- Geraskina Anna P.
- Gholami Shaieste
- Gongalsky Konstantin B.
- González Grizelle
- Guerra Carlos A.
- Gundale Michael J.
- Hackenberger Branimir K.
- Hackenberger Davorka K.
- Hernández Luis M.
- Hirth Jeff R.
- Hishi Takuo
- Holdsworth Andrew R.
- Holmstrup Martin
- Hopfensperger Kristine N.
- Huhta Veikko
- Hurisso Tunsisa T.
- Iannone Basil V.
- Iordache Madalina
- Irmler Ulrich
- Ivask Mari
- Jesús Juan B.
- Johnson-Maynard Jodi L.
- Joschko Monika
- Kaneko Nobuhiro
- Kanianska Radoslava
- Keith Aidan M.
- Kernecker Maria L.
- Koné Armand W.
- Kooch Yahya
- Krebs Julia J.
- Kukkonen Sanna T.
- König-Ries Birgitta
- Lalthanzara H.
- Lammel Daniel R.
- Lavelle Patrick
- Le Cadre Edith
- Lebedev Iurii M.
- Lincoln Noa K.
- Loreau Michel
- Loss Scott R.
- Lwanga Esperanza Huerta
- López Mónica Gutiérrez
- López-Hernández Danilo
- Marichal Raphael
- Mathieu Jérôme
- Matula Radim
- Minamiya Yukio
- Moos Jan Hendrik
- Moreno Gerardo
- Morón-Ríos Alejandro
- Motohiro Hasegawa
- Mujeeb Rahman P.
- Mulder Christian
- Muys Bart
- Neirynck Johan
- Norgrove Lindsey
- Novo Marta
- Nuutinen Visa
- Nuzzo Victoria
- Orgiazzi Alberto
- Pansu Johan
- Paudel Shishir
- Phillips Helen R.P.
- Ponge Jean François
- Prietzel Jörg
- Pérez-Camacho Lorenzo
- Pérès Guénola
- Ramirez Kelly S.
- Rapoport Irina B.
- Rashid Muhammad Imtiaz
- Rebollo Salvador
- Rillig Matthias C.
- Rodríguez Miguel
- Roth Alexander M.
- Rousseau Guillaume X.
- Rozen Anna
- Russell David J.
- Sayad Ehsan
- Scharenbroch Bryant
- Schirrmann Michael
- Schmidt Olaf
- Schröder Boris
- Schwarz Benjamin
- Seeber Julia
- Shashkov Maxim P.
- Singh Jaswinder
- Smith Sandy M.
- Steinwandter Michael
- Szlavecz Katalin
- Talavera José Antonio
- Thakur Madhav P.
- Trigo Dolores
- Tsukamoto Jiro
- Uribe-López Sheila
- van der Putten Wim H.
- van Eekeren Nick
- van Schaik Loes
- Virto Iñigo
- Wackett Adrian A.
- Wall Diana H.
- Wardle David A.
- Warren Matthew W.
- Webster Emily R.
- Wehr Nathaniel H.
- Whalen Joann K.
- Wironen Michael B.
- Wolters Volkmar
- Wu Pengfei
- Zenkova Irina V.
- Zhang Weixin
- Publication venue
- Publication date
- 01/01/2021
- Field of study
Publisher Copyright: © 2021, The Author(s).Earthworms are an important soil taxon as ecosystem engineers, providing a variety of crucial ecosystem functions and services. Little is known about their diversity and distribution at large spatial scales, despite the availability of considerable amounts of local-scale data. Earthworm diversity data, obtained from the primary literature or provided directly by authors, were collated with information on site locations, including coordinates, habitat cover, and soil properties. Datasets were required, at a minimum, to include abundance or biomass of earthworms at a site. Where possible, site-level species lists were included, as well as the abundance and biomass of individual species and ecological groups. This global dataset contains 10,840 sites, with 184 species, from 60 countries and all continents except Antarctica. The data were obtained from 182 published articles, published between 1973 and 2017, and 17 unpublished datasets. Amalgamating data into a single global database will assist researchers in investigating and answering a wide variety of pressing questions, for example, jointly assessing aboveground and belowground biodiversity distributions and drivers of biodiversity change.Peer reviewe
Recommended from our members
Global data on earthworm abundance, biomass, diversity and corresponding environmental properties
- Author
- Ammer Christian
- Ammer Sabine
- Arai Miwa
- Ayuke Fredrick O.
- Bach Elizabeth M.
- Baker Geoff H.
- Baretta Dilmar
- Barkusky Dietmar
- Bartz Marie L. C.
- Beauséjour Robin
- Bedano Jose C.
- Bennett Joanne M.
- Beugnon Rémy
- Birkhofer Klaus
- Blanchart Eric
- Blossey Bernd
- Bolger Thomas
- Bradley Robert L.
- Briones Maria J. I.
- Brose Ulrich
- Brossard Michel
- Brown George G.
- Burtis James C.
- Cameron Erin K.
- Capowiez Yvan
- Cavagnaro Timothy R.
- Choi Amy
- Clause Julia
- Cluzeau Daniel
- Coors Anja
- Cosín Darío J. Díaz
- Crotty Felicity V.
- Crumsey Jasmine M.
- de Valença Anne W.
- de Vries Franciska T.
- Decaëns Thibaud
- Dobson Annise M.
- Domínguez Anahí
- Duhour Andrés Esteban
- Dávalos Andrea
- Eisenhauer Nico
- Emmerling Christoph
- Falco Liliana B.
- Ferlian Olga
- Fernández Rosa
- Fonte Steven J.
- Fragoso Carlos
- Franco André L. C.
- Fusilero Abegail
- Geraskina Anna P.
- Gholami Shaieste
- Gongalsky Konstantin B.
- González Grizelle
- Guerra Carlos A.
- Gundale Michael J.
- Hackenberger Branimir K.
- Hackenberger Davorka K.
- Hernández Luis M.
- Hirth Jeff R.
- Hishi Takuo
- Holdsworth Andrew R.
- Holmstrup Martin
- Hopfensperger Kristine N.
- Huhta Veikko
- Hurisso Tunsisa T.
- Iannone Basil V.
- Iordache Madalina
- Irmler Ulrich
- Ivask Mari
- Jesús Juan B.
- Johnson-Maynard Jodi L.
- Joschko Monika
- Kaneko Nobuhiro
- Kanianska Radoslava
- Keith Aidan M.
- Kernecker Maria L.
- Koné Armand W.
- Kooch Yahya
- Krebs Julia J.
- Kukkonen Sanna T.
- König-Ries Birgitta
- Lalthanzara H.
- Lammel Daniel R.
- Lavelle Patrick
- Le Cadre Edith
- Lebedev Iurii M.
- Lincoln Noa K.
- Loreau Michel
- Loss Scott R.
- Lwanga Esperanza Huerta
- López Mónica Gutiérrez
- López-Hernández Danilo
- Marichal Raphael
- Mathieu Jérôme
- Matula Radim
- Minamiya Yukio
- Moos Jan Hendrik
- Moreno Gerardo
- Morón-Ríos Alejandro
- Motohiro Hasegawa
- Mujeeb Rahman P.
- Mulder Christian
- Muys Bart
- Neirynck Johan
- Norgrove Lindsey
- Novo Marta
- Nuutinen Visa
- Nuzzo Victoria
- Orgiazzi Alberto
- Pansu Johan
- Paudel Shishir
- Phillips Helen R. P.
- Ponge Jean-François
- Prietzel Jörg
- Pérez-Camacho Lorenzo
- Pérès Guénola
- Ramirez Kelly S.
- Rapoport Irina B.
- Rashid Muhammad Imtiaz
- Rebollo Salvador
- Rillig Matthias C.
- Rodríguez Miguel Á.
- Roth Alexander M.
- Rousseau Guillaume X.
- Rozen Anna
- Russell David J.
- Sayad Ehsan
- Scharenbroch Bryant
- Schirrmann Michael
- Schmidt Olaf
- Schröder Boris
- Schwarz Benjamin
- Seeber Julia
- Shashkov Maxim P.
- Singh Jaswinder
- Smith Sandy M.
- Steinwandter Michael
- Szlavecz Katalin
- Talavera José Antonio
- Thakur Madhav P.
- Trigo Dolores
- Tsukamoto Jiro
- Uribe-López Sheila
- van der Putten Wim H.
- van Eekeren Nick
- van Schaik Loes
- Virto Iñigo
- Wackett Adrian A.
- Wall Diana H.
- Wardle David A.
- Warren Matthew W.
- Webster Emily R.
- Wehr Nathaniel H.
- Whalen Joann K.
- Wironen Michael B.
- Wolters Volkmar
- Wu Pengfei
- Zenkova Irina V.
- Zhang Weixin
- Publication venue
- London : Nature Publ. Group
- Publication date
- 01/01/2021
- Field of study
Earthworms are an important soil taxon as ecosystem engineers, providing a variety of crucial ecosystem functions and services. Little is known about their diversity and distribution at large spatial scales, despite the availability of considerable amounts of local-scale data. Earthworm diversity data, obtained from the primary literature or provided directly by authors, were collated with information on site locations, including coordinates, habitat cover, and soil properties. Datasets were required, at a minimum, to include abundance or biomass of earthworms at a site. Where possible, site-level species lists were included, as well as the abundance and biomass of individual species and ecological groups. This global dataset contains 10,840 sites, with 184 species, from 60 countries and all continents except Antarctica. The data were obtained from 182 published articles, published between 1973 and 2017, and 17 unpublished datasets. Amalgamating data into a single global database will assist researchers in investigating and answering a wide variety of pressing questions, for example, jointly assessing aboveground and belowground biodiversity distributions and drivers of biodiversity change
The Youth Anxiety Measure for DSM-5 (YAM-5):Development and First Psychometric Evidence of a New Scale for Assessing Anxiety Disorders Symptoms of Children and Adolescents
- Author
- Albano Anne Marie
- Bar-Haim Yair
- Beesdo-Baum Katja
- Beidel Deborah
- Bender Patrick
- Borelli Jessica
- Bos Arjan
- Broeren Suzanne
- Cartwright-Hatton Sam
- Craske Michelle
- Crawford Erika
- Creswell Cathy
- DeSousa Diogo
- de Hullu Eva
- Dodd Helen
- Eley Thalia
- Farrell Lara
- Field Andy
- Fliek Lorraine
- Garcia-Lopez Luis Joaquin
- Grills Amie
- Hadwin Julie
- Hale William
- Hoff Esbjørn Barbara
- Hogendoorn Sanne
- Holly Lindsay
- Hudson Jennifer
- Huijding Jorg
- Ishikawa Shin ichi
- Kendall Philip
- Knappe Susanne
- LeBeau Richard
- Leikanger Einar
- Lester Kathryn
- Lijphart Hester
- Loxton Helene
- McLellan Lauren
- Meesters Cor
- Muris Peter
- Nauta Maaike
- Ollendick Thomas
- Pereira Ana
- Pina Armando
- Rapee Ron
- Sadeh Avi
- Schmeitz Kelly
- Simon Ellin
- Spence Susan
- Storch Eric A.
- Vreeke Leonie
- Waite Polly
- Wolters Lidewij
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 14/05/2016
- Field of study
The Youth Anxiety Measure for DSM-5 (YAM-5) is a new self- and parent-report questionnaire to assess anxiety disorder symptoms in children and adolescents in terms of the contemporary classification system. International panels of childhood anxiety researchers and clinicians were used to construct a scale consisting of two parts: part one consists of 28 items and measures the major anxiety disorders including separation anxiety disorder, selective mutism, social anxiety disorder, panic disorder, and generalized anxiety disorder, whereas part two contains 22 items that focus on specific phobias and (given its overlap with situational phobias) agoraphobia. In general, the face validity of the new scale was good; most of its items were successfully linked to the intended anxiety disorders. Notable exceptions were the selective mutism items, which were frequently considered as symptoms of social anxiety disorder, and some specific phobia items especially of the natural environment, situational and other type, that were regularly assigned to an incorrect category. A preliminary investigation of the YAM-5 in non-clinical (N = 132) and clinically referred (N = 64) children and adolescents indicated that the measure was easy to complete by youngsters. In addition, support was found for the psychometric qualities of the measure: that is, the internal consistency was good for both parts, as well as for most of the subscales, the parent-child agreement appeared satisfactory, and there was also evidence for the validity of the scale. The YAM-5 holds promise as a tool for assessing anxiety disorder symptoms in children and adolescents
Charged-particle distributions at low transverse momentum in s=13 TeV pp interactions measured with the ATLAS detector at the LHC
- Author
- Aad Georges
- Abbott Brad
- Abdallah Jalal
- Abdinov Ovsat
- Abeloos Baptiste
- Aben Rosemarie
- AbouZeid Ossama
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- Abramowicz Halina
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- Alexa Calin
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- Ali Babar
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- Allbrooke Benedict
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- Wang Wenxiao
- Wang Xiaoxiao
- Wanotayaroj Chaowaroj
- Warburton Andreas
- Ward Patricia
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- Washbrook Andrew
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- Watson Miriam
- Watts Gordon
- Watts Stephen
- Waugh Ben
- Webb Samuel
- Weber Michele
- Weber Stefan Wol
- Webster Jordan S
- Weidberg Anthony
- Weinert Benjamin
- Weingarten Jens
- Weiser Christian
- Weits Hartger
- Wells Phillippa
- Wenaus Torre
- Wengler Thorsten
- Wenig Siegfried
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- Whalen Kathleen
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- Wielers Monika
- Wienemann Peter
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- Wiik-Fuchs Liv Antje
- Wildauer Andreas
- Wilk Fabian
- Wilkens Henric Geo
- Williams Hugh
- Williams Sarah
- Willis Christophe
- Willocq Stephane
- Wilson John
- Wingerter-Seez Isabelle
- Winklmeier Frank
- Winston Oliver Jam
- Winter Benedict T
- Wittgen Matthias
- Wittkowski Josephine
- Wolter Marcin Wla
- Wolters Helmut
- Worm Steven D
- Wosiek Barbara
- Wotschack Jorg
- Woudstra Martin
- Wozniak Krzysztof
- Wu Mengqing
- Wu Miles
- Wu Sau Lan
- Wu Xin
- Wu Yusheng
- Wyatt Terry Rich
- Wynne Benjamin
- Xella Stefania
- Xu Da
- Xu Lailin
- Yabsley Bruce
- Yacoob Sahal
- Yakabe Ryota
- Yamaguchi Daiki
- Yamaguchi Yohei
- Yamamoto Akira
- Yamamoto Shimpei
- Yamanaka Takashi
- Yamauchi Katsuya
- Yamazaki Yuji
- Yan Zhen
- Yang Haijun
- Yang Hongtao
- Yang Yi
- Yang Zongchang
- Yao Weiming
- Yap Yee Chinn
- Yasu Yoshiji
- Yatsenko Elena
- Yau Wong Kaven Henr
- Ye Jingbo
- Ye Shuwei
- Yeletskikh Ivan
- Yen Andy L
- Yildirim Eda
- Yorita Kohei
- Yoshida Rikutaro
- Yoshihara Keisuke
- Young Charles
- Young Christophe
- Youssef Saul
- Yu David Ren-
- Yu Jaehoon
- Yu Jiaming
- Yu Jie
- Yuan Li
- Yuen Stephanie
- Yusuff Imran
- Zabinski Bartlomiej
- Zaidan Remi
- Zaitsev Alexander
- Zakharchuk Nataliia
- Zalieckas Justas
- Zaman Aungshuman
- Zambito Stefano
- Zanello Lucia
- Zanzi Daniele
- Zeitnitz Christian
- Zeman Martin
- Zemla Andrzej
- Zeng Jian Cong
- Zeng Qi
- Zengel Keith
- Zenin Oleg
- Zerwas Dirk
- Zhang Dongliang
- Zhang Fangzhou
- Zhang Guangyi
- Zhang Huijun
- Zhang Jinlong
- Zhang Lei
- Zhang Rui
- Zhang Ruiqi
- Zhang Xueyao
- Zhang Zhiqing
- Zhao Xiandong
- Zhao Yongke
- Zhao Zhengguo
- Zhemchugov Alexey
- Zhong Jiahang
- Zhou Bing
- Zhou Chen
- Zhou Lei
- Zhou Li
- Zhou Mingliang
- Zhou Ning
- Zhu Cheng Guan
- Zhu Hongbo
- Zhu Junjie
- Zhu Yingchun
- Zhuang Xuai
- Zhukov Konstantin
- Zibell Andre
- Zieminska Daria
- Zimine Nikolai
- Zimmermann Christoph
- Zimmermann Stephanie
- Zinonos Zinonas
- Zinser Markus
- Ziolkowski Michael
- Zobernig Georg
- Zoccoli Antonio
- zur Nedden Martin
- Zwalinski Lukasz
- Åkesson Torsten Pa
- Åsman Barbro
- Ženiš Tibor
- Živković Lidija
- Άlvarez Piqueras Damián
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 15/09/2016
- Field of study
Measurements of top-quark pair differential cross-sections in the eμ channel in pp collisions at s=13 TeV using the ATLAS detector
- Author
- Aad Georges
- Abbott Brad
- Abdallah Jalal
- Abdinov Ovsat
- Abeloos Baptiste
- Aben Rosemarie
- AbouZeid Ossama
- Abraham Nicola
- Abramowicz Halina
- Abreu Henso
- Abreu Ricardo
- Abulaiti Yiming
- Acharya Bobby Sami
- Adachi Shunsuke
- Adamczyk Leszek
- Adams David
- Adelman Jahred
- Adomeit Stefanie
- Adye Tim
- Affolder Tony
- Agatonovic-Jovin Tatjana
- Aguilar-Saavedra Juan Anton
- Ahlen Steven
- Ahmadov Faig
- Aielli Giulio
- Akerstedt Henrik
- Akimov Andrei
- Alberghi Gian Luigi
- Albert Justin
- Albrand Solveig
- Alconada Verzini Maria Jose
- Aleksa Martin
- Aleksandrov Igor
- Alexa Calin
- Alexander Gideon
- Alexopoulos Theodoros
- Alhroob Muhammad
- Ali Babar
- Aliev Malik
- Alimonti Gianluca
- Alison John
- Alkire Steven Pat
- Allbrooke Benedict
- Allen Benjamin W
- Allport Phillip
- Aloisio Alberto
- Alonso Alejandro
- Alonso Francisco
- Alpigiani Cristiano
- Alshehri Azzah Aziz
- Alstaty Mahmoud
- Alvarez Gonzalez Barbara
- Alviggi Mariagrazi
- Amadio Brian Thom
- Amako Katsuya
- Amaral Coutinho Yara
- Amelung Christoph
- Amidei Dante
- Amor Dos Santos Susana Pat
- Amorim Antonio
- Amoroso Simone
- Amundsen Glenn
- Anastopoulos Christos
- Ancu Lucian Ste
- Andari Nansi
- Andeen Timothy
- Anders Christoph
- Anders Gabriel
- Anders John Kenne
- Anderson Kelby
- Andreazza Attilio
- Andrei George Vic
- Angelidakis Stylianos
- Angelozzi Ivan
- Angerami Aaron
- Anghinolfi Francis
- Anisenkov Alexey
- Anjos Nuno
- Annovi Alberto
- Antel Claire
- Antonelli Mario
- Antonov Alexey
- Anulli Fabio
- Aoki Masato
- Aperio Bella Ludovica
- Arabidze Giorgi
- Arai Yasuo
- Araque Juan Pedro
- Arce Ayana
- Arduh Francisco
- Arguin Jean-Franc
- Argyropoulos Spyridon
- Arik Metin
- Armbruster Aaron Jame
- Armitage Lewis Jame
- Arnaez Olivier
- Arnold Hannah
- Arratia Miguel
- Arslan Ozan
- Artamonov Andrei
- Artoni Giacomo
- Artz Sebastian
- Asai Shoji
- Asbah Nedaa
- Ashkenazi Adi
- Asquith Lily
- Assamagan Ketevi
- Astalos Robert
- Atkinson Markus
- Atlay Naim Bora
- Augsten Kamil
- Avolio Giuseppe
- Axen Bradley
- Ayoub Mohamad Ka
- Azuelos Georges
- Baak Max
- Baas Alessandra
- Baca Matthew Jo
- Bachacou Henri
- Bachas Konstantin
- Backes Moritz
- Backhaus Malte
- Bagiacchi Paolo
- Bagnaia Paolo
- Bai Yu
- Baines John
- Baker Oliver Kei
- Baldin Evgenii
- Balek Petr
- Balestri Thomas
- Balli Fabrice
- Balunas William Ke
- Banas Elzbieta
- Banerjee Swagato
- Bannoura Arwa A E
- Barak Liron
- Barberio Elisabetta
- Barberis Dario
- Barbero Marlon
- Barillari Teresa
- Barisits Martin-Ste
- Barklow Timothy
- Barlow Nick
- Barnes Sarah Loui
- Barnett Bruce
- Barnett Michael
- Barnovska-Blenessy Zuzana
- Baroncelli Antonio
- Barone Gaetano
- Barr Alan
- Barranco Navarro Laura
- Barreiro Guimarães da Costa João
- Barreiro Fernando
- Barros do Vale Maria Alin
- Bartoldus Rainer
- Barton Adam Edwar
- Bartos Pavol
- Basalaev Artem
- Bassalat Ahmed
- Bates Richard
- Batista Santiago J
- Batley Richard
- Battaglia Marco
- Bauce Matteo
- Bauer Florian
- Bawa Harinder S
- Beacham James
- Beattie Michael Da
- Beau Tristan
- Beauchemin Pierre-Hug
- Bechtle Philip
- Beck Hans~Peter
- Becker Kathrin
- Becker Maurice
- Beckingham Matthew
- Becot Cyril
- Beddall Andrew
- Beddall Ayda
- Bednyakov Vadim
- Bedognetti Matteo
- Bee Christophe
- Beemster Lars
- Beermann Thomas
- Begel Michael
- Behr Janna Kath
- Belanger-Champagne Camille
- Bell Andrew Stu
- Bella Gideon
- Bellagamba Lorenzo
- Bellerive Alain
- Bellomo Massimilia
- Belotskiy Konstantin
- Beltramello Olga
- Belyaev Nikita
- Benary Odette
- Benchekroun Driss
- Bender Michael
- Bendtz Katarina
- Benekos Nektarios
- Benhammou Yan
- Benhar Noccioli Eleonora
- Benitez Jose
- Benjamin Douglas
- Bensinger James
- Bentvelsen Stan
- Beresford Lydia
- Beretta Matteo
- Berge David
- Bergeaas Kuutmann Elin
- Berger Nicolas
- Beringer Jürg
- Berlendis Simon
- Bernard Nathan Rog
- Bernius Catrin
- Bernlochner Florian Ur
- Berry Tracey
- Berta Peter
- Bertella Claudia
- Bertoli Gabriele
- Bertolucci Federico
- Bertram Iain Alexa
- Bertsche Carolyn
- Bertsche David
- Besjes Geert-Jan
- Bessidskaia Bylund Olga
- Bessner Martin Flo
- Besson Nathalie
- Betancourt Christophe
- Bethani Agni
- Bethke Siegfried
- Bevan Adrian Joh
- Bianchi Riccardo-M
- Bianchini Louis
- Bianco Michele
- Biebel Otmar
- Biedermann Dustin
- Bielski Rafal
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- Biglietti Michela
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- Blazek Tomas
- Bloch Ingo
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- Bobbink Gerjan
- Bobrovnikov Victor
- Bocchetta Simona Ser
- Bocci Andrea
- Bock Christophe
- Boehler Michael
- Boerner Daniela
- Bogaerts Joannes An
- Bogavac Danijela
- Bogdanchikov Alexander
- Bohm Christian
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- Borissov Guennadi
- Bortfeldt Jonathan
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- Bortolotto Valerio
- Bos Kors
- Boscherini Davide
- Bosman Martine
- Bossio Sola Jonathan D
- Boudreau Joseph
- Bouffard Julian
- Bouhova-Thacker Evelina Va
- Boumediene Djamel Edd
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- Brandt Andrew
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- Bruncko Dusan
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- Burmeister Ingo
- Burr Jonathan T
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- Carminati Leonardo
- Carney Rebecca
- Caron Sascha
- Carquin Edson
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- Carter Janet
- Carvalho João
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- Chomont Arthur Ren
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- Chromek-Burckhart Doris
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- Ciubancan Mihai
- Clark Allan G
- Clark Brian Lee
- Clark Michael
- Clark Philip Jam
- Clarke Robert
- Clement Christophe
- Coadou Yann
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- Cochran James H
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- Cole Brian
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- Collot Johann
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- Da Cunha Sargedas De Sousa Mario Jose
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- Dale Orjan
- Dallaire Frederick
- Dallapiccola Carlo
- Dam Mogens
- Dandoy Jeffrey
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- Daniells Andrew Chr
- Dann Nicholas S
- Danninger Matthias
- Dano Hoffmann Maria
- Dao Valerio
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- de Asmundis Riccardo
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- Duffield Emily Mari
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- Eckardt Christoph
- Ecker Katharina
- Edgar Ryan Chris
- Edwards Nicholas C
- Eifert Till
- Eigen Gerald
- Einsweiler Kevin
- Ekelof Tord
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- Ellajosyula Venugopal
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- Gauthier Lea
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- Gee Norman
- Geich-Gimbel Christoph
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- Gilles Geoffrey
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- Giorgi Filippo Ma
- Giorgi Francesco
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- Gkaitatzis Stamatios
- Gkialas Ioannis
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- Glaysher Paul
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- Godlewski Jan
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- Golling Tobias
- Golubkov Dmitry
- Gomes Agostinho
- Goncalves Pinto Firmino Da Costa Joao
- Gonella Giulia
- Gonella Laura
- Gongadze Alexi
- Gonzalez-Sevilla Sergio
- González de la Hoz Santiago
- Gonçalo Ricardo
- Goossens Luc
- Gorbounov Petr Andre
- Gordon Howard
- Gorelov Igor
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- Gorini Edoardo
- Gorišek Andrej
- Gornicki Edward
- Goshaw Alfred
- Gostkin Mikhail Iv
- Goudet Christophe
- Goujdami Driss
- Goussiou Anna
- Govender Nicolin
- Gozani Eitan
- Graber Lars
- Grabowska-Bold Iwona
- Gradin Per Olov J
- Grafström Per
- Gramling Johanna
- Gramstad Eirik
- Grancagnolo Sergio
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- Gravila Paul Mirce
- Gray Heather
- Graziani Enrico
- Greenwood Zeno Dixon
- Grefe Christian
- Gregersen Kristian
- Gregor Ingrid-Mar
- Grenier Philippe
- Grevtsov Kirill
- Griffiths Justin
- Grillo Alexander
- Grimm Kathryn
- Grinstein Sebastian
- Gris Philippe L
- Grivaz Jean-Franc
- Groh Sabrina
- Gross Eilam
- Grosse-Knetter Joern
- Grossi Giulio Cor
- Grout Zara Jane
- Guan Liang
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- Gul Umar
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- Gupta Shaun
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- Gutierrez Ortiz Nicolas Gi
- Gutierrez Phillip
- Gutschow Christian
- Guyot Claude
- Gwenlan Claire
- Gwilliam Carl
- Gössling Claus
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- Hadavand Haleh Khan
- Haddad Nacim
- Hadef Asma
- Hageböck Stephan
- Hagihara Mutsuto
- Hajduk Zbigniew
- Hakobyan Hrachya
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- Haley Joseph
- Halladjian Garabed
- Hallewell Gregory Da
- Hamacher Klaus
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- Hamity Guillermo
- Hamnett Phillip Ge
- Han Liang
- Hanagaki Kazunori
- Hanawa Keita
- Hance Michael
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- Hansen Jorn Dines
- Hansen Jørgen Be
- Hansen Maike Chri
- Hansen Peter Henr
- Hara Kazuhiko
- Hard Andrew
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- Harrison Paul Frase
- Hartjes Fred
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- Hasegawa Yoji
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- Hauser Reiner
- Hauswald Lorenz
- Havranek Miroslav
- Hawkes Christophe
- Hawkings Richard Jo
- Hayakawa Daiki
- Hayden Daniel
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- Hays Jonathan M
- Hayward Helen
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- Henderson Robert
- Heng Yang
- Henkelmann Steffen
- Henriques Correia Ana Maria
- Henrot-Versille Sophie
- Herbert Geoffrey H
- Herde Hannah
- Herget Verena
- Hernández Jiménez Yesenia
- Herten Gregor
- Hertenberger Ralf
- Hervas Luis
- Hesketh Gavin Gran
- Hessey Nigel
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- Hickling Robert
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- Hoecker Andreas
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- Hohn David
- Holmes Tova Ray
- Homann Michael
- Honda Takuya
- Hong Tae Min
- Hooberman Benjamin H
- Hopkins Walter
- Horii Yasuyuki
- Horton Arthur Jam
- Hostachy Jean-Yves
- Hou Suen
- Hoummada Abdeslam
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- Hrabovsky Miroslav
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- Jones Roger
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- Kaplan Benjamin
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- Kar Deepak
- Karakostas Konstantin
- Karamaoun Andrew
- Karastathis Nikolaos
- Kareem Mohammad J
- Karentzos Efstathios
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- Karpov Sergey
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- Kartvelishvili Vakhtang
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- Kasahara Kota
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- Willocq Stephane
- Wilson John
- Wingerter-Seez Isabelle
- Winklmeier Frank
- Winston Oliver Jam
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- Wittgen Matthias
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- Wolf Tim Michae
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- Yamanaka Takashi
- Yamauchi Katsuya
- Yamazaki Yuji
- Yan Zhen
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- Yang Zongchang
- Yao Weiming
- Yap Yee Chinn
- Yasu Yoshiji
- Yatsenko Elena
- Yau Wong Kaven Henr
- Ye Jingbo
- Ye Shuwei
- Yeletskikh Ivan
- Yildirim Eda
- Yorita Kohei
- Yoshida Rikutaro
- Yoshihara Keisuke
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- Yu Jaehoon
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- Yu Jie
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- Yuen Stephanie
- Yusuff Imran
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- Zaidan Remi
- Zaitsev Alexander
- Zakharchuk Nataliia
- Zalieckas Justas
- Zaman Aungshuman
- Zambito Stefano
- Zanello Lucia
- Zanzi Daniele
- Zeitnitz Christian
- Zeman Martin
- Zemla Andrzej
- Zeng Jian Cong
- Zeng Qi
- Zenin Oleg
- Zerwas Dirk
- Zhang Dongliang
- Zhang Fangzhou
- Zhang Guangyi
- Zhang Huijun
- Zhang Jinlong
- Zhang Lei
- Zhang Matt
- Zhang Rui
- Zhang Ruiqi
- Zhang Xueyao
- Zhang Zhiqing
- Zhao Xiandong
- Zhao Yongke
- Zhao Zhengguo
- Zhemchugov Alexey
- Zhong Jiahang
- Zhou Bing
- Zhou Chen
- Zhou Lei
- Zhou Li
- Zhou Mingliang
- Zhou Ning
- Zhu Cheng Guan
- Zhu Hongbo
- Zhu Junjie
- Zhu Yingchun
- Zhuang Xuai
- Zhukov Konstantin
- Zibell Andre
- Zieminska Daria
- Zimine Nikolai
- Zimmermann Christoph
- Zimmermann Stephanie
- Zinonos Zinonas
- Zinser Markus
- Ziolkowski Michael
- Zobernig Georg
- Zoccoli Antonio
- zur Nedden Martin
- Zwalinski Lukasz
- Åkesson Torsten Pa
- Åsman Barbro
- Ženiš Tibor
- Živković Lidija
- Άlvarez Piqueras Damián
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 08/05/2017
- Field of study
Measurement of the W boson polarisation in ttˉ events from pp collisions at s = 8 TeV in the lepton + jets channel with ATLAS
- Author
- Aad Georges
- Abbott Brad
- Abdallah Jalal
- Abdinov Ovsat
- Abeloos Baptiste
- AbouZeid Ossama
- Abraham Nicola
- Abramowicz Halina
- Abreu Henso
- Abreu Ricardo
- Abulaiti Yiming
- Acharya Bobby Sami
- Adachi Shunsuke
- Adamczyk Leszek
- Adams David
- Adelman Jahred
- Adomeit Stefanie
- Adye Tim
- Affolder Tony
- Agatonovic-Jovin Tatjana
- Aguilar-Saavedra Juan Anton
- Ahlen Steven
- Ahmadov Faig
- Aielli Giulio
- Akerstedt Henrik
- Akimov Andrei
- Alberghi Gian Luigi
- Albert Justin
- Albrand Solveig
- Alconada Verzini Maria Jose
- Aleksa Martin
- Aleksandrov Igor
- Alexa Calin
- Alexander Gideon
- Alexopoulos Theodoros
- Alhroob Muhammad
- Ali Babar
- Aliev Malik
- Alimonti Gianluca
- Alison John
- Alkire Steven Pat
- Allbrooke Benedict
- Allen Benjamin W
- Allport Phillip
- Aloisio Alberto
- Alonso Alejandro
- Alonso Francisco
- Alpigiani Cristiano
- Alshehri Azzah Aziz
- Alstaty Mahmoud
- Alvarez Gonzalez Barbara
- Alviggi Mariagrazi
- Amadio Brian Thom
- Amaral Coutinho Yara
- Amelung Christoph
- Amidei Dante
- Amor Dos Santos Susana Pat
- Amorim Antonio
- Amoroso Simone
- Amundsen Glenn
- Anastopoulos Christos
- Ancu Lucian Ste
- Andari Nansi
- Andeen Timothy
- Anders Christoph
- Anders John Kenne
- Anderson Kelby
- Andreazza Attilio
- Andrei George Vic
- Angelidakis Stylianos
- Angelozzi Ivan
- Angerami Aaron
- Anghinolfi Francis
- Anisenkov Alexey
- Anjos Nuno
- Annovi Alberto
- Antel Claire
- Antonelli Mario
- Antonov Alexey
- Antrim Daniel Jos
- Anulli Fabio
- Aoki Masato
- Aperio Bella Ludovica
- Arabidze Giorgi
- Arai Yasuo
- Araque Juan Pedro
- Araujo Ferraz Victor
- Arce Ayana
- Arduh Francisco
- Arguin Jean-Franc
- Argyropoulos Spyridon
- Arik Metin
- Armbruster Aaron Jame
- Armitage Lewis Jame
- Arnaez Olivier
- Arnold Hannah
- Arratia Miguel
- Arslan Ozan
- Artamonov Andrei
- Artoni Giacomo
- Artz Sebastian
- Asai Shoji
- Asbah Nedaa
- Ashkenazi Adi
- Asquith Lily
- Assamagan Ketevi
- Astalos Robert
- Atkinson Markus
- Atlay Naim Bora
- Augsten Kamil
- Avolio Giuseppe
- Axen Bradley
- Ayoub Mohamad Ka
- Azuelos Georges
- Baak Max
- Baas Alessandra
- Baca Matthew Jo
- Bachacou Henri
- Bachas Konstantin
- Backes Moritz
- Backhaus Malte
- Bagiacchi Paolo
- Bagnaia Paolo
- Bai Yu
- Baines John
- Bajic Milena
- Baker Oliver Kei
- Baldin Evgenii
- Balek Petr
- Balestri Thomas
- Balli Fabrice
- Balunas William Ke
- Banas Elzbieta
- Banerjee Swagato
- Bannoura Arwa A E
- Barak Liron
- Barberio Elisabetta
- Barberis Dario
- Barbero Marlon
- Barillari Teresa
- Barisits Martin-Ste
- Barklow Timothy
- Barlow Nick
- Barnes Sarah Loui
- Barnett Bruce
- Barnett Michael
- Barnovska-Blenessy Zuzana
- Baroncelli Antonio
- Barone Gaetano
- Barr Alan
- Barranco Navarro Laura
- Barreiro Guimarães da Costa João
- Barreiro Fernando
- Barros do Vale Maria Alin
- Bartoldus Rainer
- Barton Adam Edwar
- Bartos Pavol
- Basalaev Artem
- Bassalat Ahmed
- Bates Richard
- Batista Santiago J
- Batley Richard
- Battaglia Marco
- Bauce Matteo
- Bauer Florian
- Bawa Harinder S
- Beacham James
- Beattie Michael Da
- Beau Tristan
- Beauchemin Pierre-Hug
- Bechtle Philip
- Beck Hans~Peter
- Becker Kathrin
- Becker Maurice
- Beckingham Matthew
- Becot Cyril
- Beddall Andrew
- Beddall Ayda
- Bednyakov Vadim
- Bedognetti Matteo
- Bee Christophe
- Beemster Lars
- Beermann Thomas
- Begel Michael
- Behr Janna Kath
- Bell Andrew Stu
- Bella Gideon
- Bellagamba Lorenzo
- Bellerive Alain
- Bellomo Massimilia
- Belotskiy Konstantin
- Beltramello Olga
- Belyaev Nikita
- Benary Odette
- Benchekroun Driss
- Bender Michael
- Bendtz Katarina
- Benekos Nektarios
- Benhammou Yan
- Benhar Noccioli Eleonora
- Benitez Jose
- Benjamin Douglas
- Bensinger James
- Bentvelsen Stan
- Beresford Lydia
- Beretta Matteo
- Berge David
- Bergeaas Kuutmann Elin
- Berger Nicolas
- Beringer Jürg
- Berlendis Simon
- Bernard Nathan Rog
- Bernius Catrin
- Bernlochner Florian Ur
- Berry Tracey
- Berta Peter
- Bertella Claudia
- Bertoli Gabriele
- Bertolucci Federico
- Bertram Iain Alexa
- Bertsche Carolyn
- Bertsche David
- Besjes Geert-Jan
- Bessidskaia Bylund Olga
- Bessner Martin Flo
- Besson Nathalie
- Betancourt Christophe
- Bethani Agni
- Bethke Siegfried
- Bevan Adrian Joh
- Bianchi Riccardo-M
- Bianco Michele
- Biebel Otmar
- Biedermann Dustin
- Bielski Rafal
- Biesuz Nicolo Vla
- Biglietti Michela
- Bilbao De Mendizabal Javier
- Billoud Thomas Rem
- Bilokon Halina
- Bindi Marcello
- Bingul Ahmet
- Bini Cesare
- Biondi Silvia
- Bisanz Tobias
- Bjergaard David Mart
- Black Curtis
- Black James
- Black Kevin
- Blackburn Daniel
- Blair Robert
- Blazek Tomas
- Bloch Ingo
- Blocker Craig
- Blue Andrew
- Blum Walter
- Blumenschein Ulrike
- Blunier Sylvain
- Bobbink Gerjan
- Bobrovnikov Victor
- Bocchetta Simona Ser
- Bocci Andrea
- Bock Christophe
- Boehler Michael
- Boerner Daniela
- Bogaerts Joannes An
- Bogavac Danijela
- Bogdanchikov Alexander
- Bohm Christian
- Boisvert Veronique
- Bokan Petar
- Bold Tomasz
- Boldyrev Alexey
- Bomben Marco
- Bona Marcella
- Boonekamp Maarten
- Borisov Anatoly
- Borissov Guennadi
- Bortfeldt Jonathan
- Bortoletto Daniela
- Bortolotto Valerio
- Bos Kors
- Boscherini Davide
- Bosman Martine
- Bossio Sola Jonathan D
- Boudreau Joseph
- Bouffard Julian
- Bouhova-Thacker Evelina Va
- Boumediene Djamel Edd
- Bourdarios Claire
- Boutle Sarah Kate
- Boveia Antonio
- Boyd James
- Boyko Igor
- Bracinik Juraj
- Brandt Andrew
- Brandt Gerhard
- Brandt Oleg
- Bratzler Uwe
- Brau Benjamin
- Brau James
- Breaden Madden William Dm
- Brendlinger Kurt
- Brennan Amelia Jea
- Brenner Lydia
- Brenner Richard
- Bressler Shikma
- Bristow Timothy Mi
- Britton Dave
- Britzger Daniel
- Brochu Frederic
- Brock Ian
- Brock Raymond
- Brooijmans Gustaaf
- Brooks Timothy
- Brooks William
- Brosamer Jacquelyn
- Brost Elizabeth
- Broughton James
- Bruckman de Renstrom Pawel
- Bruncko Dusan
- Bruneliere Renaud
- Bruni Alessia
- Bruni Graziano
- Bruni Lucrezia S
- Brunt Benjamin
- Bruschi Marco
- Bruscino Nello
- Bryant Patrick
- Bryngemark Lene
- Buanes Trygve
- Buat Quentin
- Buchholz Peter
- Buckley Andrew
- Budagov Ioulian
- Buehrer Felix
- Bugge Magnar Kop
- Bulekov Oleg
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- Burghgrave Blake
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- Burmeister Ingo
- Burr Jonathan T
- Busato Emmanuel
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- Buttar Craig
- Butterworth Jonathan
- Butti Pierfrance
- Buttinger William
- Buzatu Adrian
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- Büscher Daniel
- Büscher Volker
- Cabrera Urbán Susana
- Caforio Davide
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- Calace Noemi
- Calafiura Paolo
- Calandri Alessandro
- Calderini Giovanni
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- Calvet David
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- Camarda Stefano
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- Cameron David
- Caminal Armadans Roger
- Camincher Clement
- Campana Simone
- Campanelli Mario
- Camplani Alessandra
- Campoverde Angel
- Canale Vincenzo
- Canepa Anadi
- Cano Bret Marc
- Cantero Josu
- Cao Tingting
- Capeans Garrido Maria Del
- Caprini Irinel
- Caprini Mihai
- Capua Marcella
- Carbone Ryne Micha
- Cardarelli Roberto
- Cardillo Fabio
- Carli Ina
- Carli Tancredi
- Carlino Gianpaolo
- Carlson Benjamin T
- Carminati Leonardo
- Carney Rebecca
- Caron Sascha
- Carquin Edson
- Carrillo-Montoya German D
- Carter Janet
- Carvalho João
- Casadei Diego
- Casado Maria Pila
- Casolino Mirkoanton
- Casper David Will
- Castaneda-Miranda Elizabeth
- Castelijn Remco
- Castelli Angelanton
- Castillo Gimenez Victoria
- Castro Nuno Filip
- Catinaccio Andrea
- Catmore James
- Cattai Ariella
- Caudron Julien
- Cavaliere Viviana
- Cavallaro Emanuele
- Cavalli Donatella
- Cavalli-Sforza Matteo
- Cavasinni Vincenzo
- Ceradini Filippo
- Cerda Alberich Leonor
- Cerri Alessandro
- Cerrito Lucio
- Cerutti Fabio
- Cervelli Alberto
- Cetin Serkant Al
- Chafaq Aziz
- Chakraborty Dhiman
- Chan Stephen Ka
- Chan Yat Long
- Chang Philip
- Chapman John Derek
- Charlton Dave
- Chatterjee Avishek
- Chau Chav Chhiv
- Chavez Barajas Carlos Alb
- Che Siinn
- Cheatham Susan
- Chegwidden Andrew
- Chekanov Sergei
- Chekulaev Sergey
- Chelkov Gueorgui
- Chelstowska Magda Anna
- Chen Chunhui
- Chen Hucheng
- Chen Shenjian
- Chen Shion
- Chen Xin
- Chen Ye
- Cheng Hok Chuen
- Cheng Huajie
- Cheng Yangyang
- Cheplakov Alexander
- Cheremushkina Evgenia
- Cherkaoui El Moursli Rajaa
- Chernyatin Valeriy
- Cheu Elliott
- Chevalier Laurent
- Chiarella Vitaliano
- Chiarelli Giorgio
- Chiodini Gabriele
- Chisholm Andrew
- Chitan Adrian
- Chizhov Mihail
- Choi Kyungeon
- Chomont Arthur Ren
- Chouridou Sofia
- Chow Bonnie Kar
- Christodoulou Valentinos
- Chromek-Burckhart Doris
- Chudoba Jiri
- Chuinard Annabelle
- Chwastowski Janusz
- Chytka Ladislav
- Ciftci Abbas Kena
- Cinca Diane
- Cindro Vladimir
- Cioara Irina Anto
- Ciocca Claudia
- Ciocio Alessandra
- Cirotto Francesco
- Citron Zvi Hirsh
- Citterio Mauro
- Ciubancan Mihai
- Clark Allan G
- Clark Brian Lee
- Clark Michael
- Clark Philip Jam
- Clarke Robert
- Clement Christophe
- Coadou Yann
- Cobal Marina
- Coccaro Andrea
- Cochran James H
- Colasurdo Luca
- Cole Brian
- Colijn Auke-Piete
- Collot Johann
- Colombo Tommaso
- Conde Muiño Patricia
- Coniavitis Elias
- Connell Simon Henr
- Connelly Ian
- Consorti Valerio
- Constantinescu Serban
- Conti Geraldine
- Conventi Francesco
- Cooke Mark
- Cooper Ben
- Cooper-Sarkar Amanda
- Cormier Felix
- Cormier Kyle James
- Cornelissen Thijs
- Corradi Massimo
- Corriveau Francois
- Cortes-Gonzalez Arely
- Cortiana Giorgio
- Costa Giuseppe
- Costa María Jos
- Costanzo Davide
- Cottin Giovanna
- Cowan Glen
- Cox Brian
- Cranmer Kyle
- Crawley Samuel Jos
- Cree Graham
- Crescioli Francesco
- Cribbs Wayne Alle
- Crispin Ortuzar Mireia
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- Daniells Andrew Chr
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- Grabowska-Bold Iwona
- Gradin Per Olov J
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- Kareem Mohammad J
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- LeBlanc Matthew Ed
- LeCompte Thomas
- Ledroit-Guillon Fabienne A
- Lee Claire Ale
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- Vlachos Sotirios
- Vlasak Michal
- Vogel Marcelo
- Vokac Petr
- Volpi Guido
- Volpi Matteo
- von der Schmitt Hans
- von Toerne Eckhard
- Vorobel Vit
- Vorobev Konstantin
- Vos Marcel
- Voss Rudiger
- Vossebeld Joost
- Vranjes Milosavljevic Marija
- Vranjes Nenad
- Vrba Vaclav
- Vreeswijk Marcel
- Vuillermet Raphael
- Vukotic Ilija
- Wagner Peter
- Wagner Wolfgang
- Wahlberg Hernan
- Wahrmund Sebastian
- Wakabayashi Jun
- Walder James
- Walker Rodney
- Walkowiak Wolfgang
- Wallangen Veronica
- Wang Chao
- Wang Fuquan
- Wang Haichen
- Wang Hulin
- Wang Jike
- Wang Jin
- Wang Kuhan
- Wang Qing
- Wang Rui
- Wang Song-Ming
- Wang Tingting
- Wang Wenxiao
- Wanotayaroj Chaowaroj
- Warburton Andreas
- Ward Patricia
- Wardrope David Robe
- Washbrook Andrew
- Watkins Peter
- Watson Alan
- Watson Miriam
- Watts Gordon
- Watts Stephen
- Waugh Ben
- Webb Samuel
- Weber Michele
- Weber Stefan Wol
- Weber Stephen
- Webster Jordan S
- Weidberg Anthony
- Weinert Benjamin
- Weingarten Jens
- Weiser Christian
- Weits Hartger
- Wells Phillippa
- Wenaus Torre
- Wengler Thorsten
- Wenig Siegfried
- Wermes Norbert
- Werner Michael Da
- Werner Per
- Wessels Martin
- Wetter Jeffrey
- Whalen Kathleen
- Whallon Nikola Laz
- Wharton Andrew Mar
- White Andrew
- White Martin
- White Ryan
- Whiteson Daniel
- Wickens Fred
- Wiedenmann Werner
- Wielers Monika
- Wiglesworth Craig
- Wiik-Fuchs Liv Antje
- Wildauer Andreas
- Wilk Fabian
- Wilkens Henric Geo
- Williams Hugh
- Williams Sarah
- Willis Christophe
- Willocq Stephane
- Wilson John
- Wingerter-Seez Isabelle
- Winklmeier Frank
- Winston Oliver Jam
- Winter Benedict T
- Wittgen Matthias
- Wobisch Markus
- Wolf Tim Michae
- Wolff Robert
- Wolter Marcin Wla
- Wolters Helmut
- Worm Steven D
- Wosiek Barbara
- Wotschack Jorg
- Woudstra Martin
- Wozniak Krzysztof
- Wu Mengqing
- Wu Miles
- Wu Sau Lan
- Wu Xin
- Wu Yusheng
- Wyatt Terry Rich
- Wynne Benjamin
- Xella Stefania
- Xi Zhaoxu
- Xu Da
- Xu Lailin
- Yabsley Bruce
- Yacoob Sahal
- Yamaguchi Daiki
- Yamaguchi Yohei
- Yamamoto Akira
- Yamamoto Shimpei
- Yamanaka Takashi
- Yamauchi Katsuya
- Yamazaki Yuji
- Yan Zhen
- Yang Haijun
- Yang Hongtao
- Yang Yi
- Yang Zongchang
- Yao Weiming
- Yap Yee Chinn
- Yasu Yoshiji
- Yatsenko Elena
- Yau Wong Kaven Henr
- Ye Jingbo
- Ye Shuwei
- Yeletskikh Ivan
- Yildirim Eda
- Yorita Kohei
- Yoshida Rikutaro
- Yoshihara Keisuke
- Young Charles
- Young Christophe
- Youssef Saul
- Yu David Ren-
- Yu Jaehoon
- Yu Jiaming
- Yu Jie
- Yuan Li
- Yuen Stephanie
- Yusuff Imran
- Zabinski Bartlomiej
- Zaidan Remi
- Zaitsev Alexander
- Zakharchuk Nataliia
- Zalieckas Justas
- Zaman Aungshuman
- Zambito Stefano
- Zanzi Daniele
- Zeitnitz Christian
- Zeman Martin
- Zemla Andrzej
- Zeng Jian Cong
- Zeng Qi
- Zenin Oleg
- Zerwas Dirk
- Zhang Dongliang
- Zhang Fangzhou
- Zhang Guangyi
- Zhang Huijun
- Zhang Jinlong
- Zhang Lei
- Zhang Liqing
- Zhang Matt
- Zhang Rui
- Zhang Ruiqi
- Zhang Xueyao
- Zhang Zhiqing
- Zhao Xiandong
- Zhao Yongke
- Zhao Zhengguo
- Zhemchugov Alexey
- Zhong Jiahang
- Zhou Bing
- Zhou Chen
- Zhou Lei
- Zhou Li
- Zhou Maosen
- Zhou Mingliang
- Zhou Ning
- Zhu Cheng Guan
- Zhu Hongbo
- Zhu Junjie
- Zhu Yingchun
- Zhuang Xuai
- Zhukov Konstantin
- Zibell Andre
- Zieminska Daria
- Zimine Nikolai
- Zimmermann Christoph
- Zimmermann Stephanie
- Zinonos Zinonas
- Zinser Markus
- Ziolkowski Michael
- Zobernig Georg
- Zoccoli Antonio
- zur Nedden Martin
- Zwalinski Lukasz
- Åkesson Torsten Pa
- Åsman Barbro
- Ženiš Tibor
- Živković Lidija
- Άlvarez Piqueras Damián
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- 26/04/2017
- Field of study
- …