Konstantin Miller

2.2k total citations
56 papers, 1.5k citations indexed

About

Konstantin Miller is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Konstantin Miller has authored 56 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 16 papers in Pediatrics, Perinatology and Child Health and 15 papers in Genetics. Recurrent topics in Konstantin Miller's work include Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (11 papers) and Image and Video Quality Assessment (8 papers). Konstantin Miller is often cited by papers focused on Prenatal Screening and Diagnostics (16 papers), Genomic variations and chromosomal abnormalities (11 papers) and Image and Video Quality Assessment (8 papers). Konstantin Miller collaborates with scholars based in Germany, Netherlands and Italy. Konstantin Miller's co-authors include Adam Wolisz, Emanuele Quacchio, Sylvia Merkert, Silke Glage, Alexandra Haase, Ulrich Martin, Ruth Olmer, Stefan Wagner, Hans R. Schöler and Johann Meyer and has published in prestigious journals such as Cell stem cell, Experimental Cell Research and Operations Research.

In The Last Decade

Konstantin Miller

55 papers receiving 1.4k citations

Peers

Konstantin Miller

CVPR

SURGE

GENET

CNC

Jing Ya China

Frédéric Sala United States

Xiaona Lin China

Chih‐Hung Lin Taiwan

Masanobu Abe Japan

Hiroyuki Yamaguchi Japan

Hironobu Yamashita Japan

Xiaohua Qian China

Yuqing Chen China

Darya Chudova United States

Jing Ya China

Konstantin Miller

704 ×1.0

112 ×0.4

CVPR

111 ×0.5

SURGE

198 ×0.8

GENET

109 ×0.5

CNC

Citations per year, relative to Konstantin Miller Konstantin Miller (= 1×) peers Jing Ya

Countries citing papers authored by Konstantin Miller

Since Specialization

Citations

This map shows the geographic impact of Konstantin Miller's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Konstantin Miller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Konstantin Miller more than expected).

Fields of papers citing papers by Konstantin Miller

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Konstantin Miller. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Konstantin Miller. The network helps show where Konstantin Miller may publish in the future.

Co-authorship network of co-authors of Konstantin Miller

This figure shows the co-authorship network connecting the top 25 collaborators of Konstantin Miller. A scholar is included among the top collaborators of Konstantin Miller based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Konstantin Miller. Konstantin Miller is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Miller, Konstantin, et al.. (2017). Adaptive low-delay video streaming in heterogeneous wireless networks using MPRTP. 14–19. 10 indexed citations

Claustres, Mireille, Viktor Kožich, Elisabeth Dequeker, et al.. (2013). Recommendations for reporting results of diagnostic genetic testing (biochemical, cytogenetic and molecular genetic). European Journal of Human Genetics. 22(2). 160–170. 70 indexed citations

Carapinha, Jorge, et al.. (2011). Quality of service in the Future Internet. 1–8. 2 indexed citations

Dittmar, Kurt E.J., Oliver Schön, Wilhelm G. Dirks, et al.. (2010). Quality of Cell Products: Authenticity, Identity, Genomic Stability and Status of Differentiation. Transfusion Medicine and Hemotherapy. 37(2). 2–2. 17 indexed citations

Olmer, Ruth, Alexandra Haase, Sylvia Merkert, et al.. (2010). Long term expansion of undifferentiated human iPS and ES cells in suspension culture using a defined medium. Stem Cell Research. 5(1). 51–64. 128 indexed citations

Haase, Alexandra, Ruth Olmer, Kristin Schwanke, et al.. (2009). Generation of Induced Pluripotent Stem Cells from Human Cord Blood. Cell stem cell. 5(4). 434–441. 359 indexed citations

Staboulidou, I., et al.. (2008). Prenatal Diagnosis of an Epignathus Associated with a 49,XXXXY Karyotype – A Case Report. Fetal Diagnosis and Therapy. 24(3). 313–317. 21 indexed citations

Sieberer, Marcel, et al.. (2005). Basal ganglia calcification and psychosis in 22q11.2 deletion syndrome. European Psychiatry. 20(8). 567–569. 13 indexed citations

Miller, Konstantin, Brigitte Pabst, Peter Nürnberg, et al.. (2003). Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin. Human Genetics. 112(4). 343–347. 12 indexed citations

10.

Pabst, Brigitte, et al.. (2002). Reciprocal translocation between Y chromosome long arm euchromatin and the short arm of chromosome 1. Annales de Génétique. 45(1). 5–8. 8 indexed citations

11.

Harms, Wolfgang, et al.. (2001). Characterization of Human Myocardial Fibroblasts Immortalized by HPV16 E6–E7 Genes. Experimental Cell Research. 268(2). 252–261. 16 indexed citations

12.

Coerdt, Wiltrud, Konstantin Miller, Wolfgang Holzgreve, et al.. (1997). Neural tube defects in chromosomally normal and abnormal human embryos. Ultrasound in Obstetrics and Gynecology. 10(6). 410–415. 29 indexed citations

13.

Fuchs, Jörg, Dagmar Schmidt, Torsten Pietsch, Konstantin Miller, & Dietrich von Schweinitz. (1996). Successful transplantation of human hepatoblastoma into immunodeficient mice. Journal of Pediatric Surgery. 31(9). 1241–1246. 24 indexed citations

14.

Miller, Konstantin. (1991). Clastogenic effects of bleomycin, cyclophosphamide, and ethyl methanesulfonate on resting and proliferating human B- and T-lymphocytes. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 251(2). 241–251. 12 indexed citations

15.

Miller, Konstantin. (1991). Sister-chromatid exchange in human B- and T-lymphocytes exposed to bleomycin, cyclophosphamide, and ethyl methanesulfonate. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 247(1). 175–182. 19 indexed citations

16.

Miller, Konstantin, et al.. (1990). Cell proliferation in chorionic villi at different gestational ages, as analyzed by premature chromosome condensation. Cytogenetic and Genome Research. 54(3-4). 127–131. 4 indexed citations

17.

Miller, Konstantin. (1988). Spontaneous sister-chromatid exchange frequencies in human B and T lymphocytes at BrdU borderline concentrations for sister-chromatid differentiation. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 202(1). 97–101. 9 indexed citations

18.

Peter, H. H., et al.. (1988). The DiGeorge syndrome. European Journal of Pediatrics. 147(5). 496–502. 79 indexed citations

19.

Schulze, Bernd, et al.. (1987). Chromosomal mosaicism confined to chorionic tissue. Prenatal Diagnosis. 7(6). 451–453. 11 indexed citations

20.

Miller, Konstantin. (1987). Proliferation kinetics of human B‐ and T‐lymphocytes. Cell Proliferation. 20(6). 611–615. 5 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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