品尝你的人
发表于 2025-3-28 17:07:40
rceived by the citing author. The collective view of a large number of citing authors regarding the relationships between documents represented by citations, that is the ., can therefore be analyzed to study the intellectual structures of research fields, and to inform knowledge organization and inf
艰苦地移动
发表于 2025-3-28 20:23:33
Manorama Bhargava or research field during a certain time period. The first step in a citation network analysis study is therefore to collect a set of citing papers (along with their reference lists) to represent a defined scholarly community or research field within a specified time period (which is called a .). Th
形状
发表于 2025-3-29 01:54:58
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pessimism
发表于 2025-3-29 04:54:26
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预定
发表于 2025-3-29 08:45:51
Manorama Bhargavaale citation analysis, even without special access to special data collections. Exciting new developments are emerging this way in many aspects of citation analysis. This book critically examines both theory and practical techniques of citation network analysis and visualization, one of the two main
OVERT
发表于 2025-3-29 12:51:01
Manorama Bhargavaation that arises in any network utility maximization. .In the high power regime, a simple characterization of the obtained performance becomes possible due to the fact that the weighted sum rate utility conver978-3-642-43634-5978-3-642-31692-0Series ISSN 1863-8538 Series E-ISSN 1863-8546
Transfusion
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烦忧
发表于 2025-3-29 23:05:46
Acute Myeloid Leukemiaive AML: AML with mutated NPM1 and AML with biallelic CEBPA mutations. AML with RUNX1 mutation and AML with BCR-ABL1 fusion have been added as provisional entities in the WHO classification (2016)..The following 33 case studies include all categories seen in AML: Recurrent cytogenetic abnormalities,
懒惰民族
发表于 2025-3-30 00:49:47
Myelodysplastic Syndromeence of diagnostic morphologic features of MDS. del(5q) remains as the only cytogenetic abnormality that defines a specific MDS subtype..The following case studies on MDS describe the various permutations and combinations of genetic abnormalities conforming to the WHO classification for MDS (2016) (