S. Kerber

928 total citations
10 papers, 728 citations indexed

About

S. Kerber is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Physiology. According to data from OpenAlex, S. Kerber has authored 10 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pediatrics, Perinatology and Child Health, 4 papers in Genetics and 3 papers in Physiology. Recurrent topics in S. Kerber's work include Prenatal Screening and Diagnostics (4 papers), Nitric Oxide and Endothelin Effects (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). S. Kerber is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Nitric Oxide and Endothelin Effects (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). S. Kerber collaborates with scholars based in Germany, Croatia and Czechia. S. Kerber's co-authors include Malte Kelm, Katharina Schulz, André Dejam, Petra Kleinbongard, K. R. Held, Reinhart Willers, Rainer B. Zotz, Putrika Prastuti Ratna Gharini, Jan C. Balzer and Martin Feelisch and has published in prestigious journals such as Free Radical Biology and Medicine, Methods in enzymology on CD-ROM/Methods in enzymology and Human Genetics.

In The Last Decade

S. Kerber

10 papers receiving 710 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
S. Kerber Germany	8	262	179	162	106	89	10	728
Petr Mlejnek Czechia	18	336 1.3×	111 0.6×	489 3.0×	117 1.1×	52 0.6×	66	1.1k
Nelson N. Orie United Kingdom	14	227 0.9×	68 0.4×	272 1.7×	114 1.1×	91 1.0×	42	977
Anjana Sinha United States	18	187 0.7×	68 0.4×	250 1.5×	250 2.4×	51 0.6×	68	937
Nancy A. Sherman United States	12	180 0.7×	53 0.3×	232 1.4×	72 0.7×	37 0.4×	21	727
F. H. Schmidt United States	16	248 0.9×	122 0.7×	427 2.6×	63 0.6×	67 0.8×	45	1.3k
Yuko Yamazaki Japan	21	137 0.5×	112 0.6×	246 1.5×	192 1.8×	27 0.3×	59	1.0k
L. Thibault Canada	19	186 0.7×	84 0.5×	176 1.1×	45 0.4×	23 0.3×	45	844
Maria José de Carvalho Costa Brazil	18	352 1.3×	76 0.4×	312 1.9×	40 0.4×	20 0.2×	57	1.0k
Chun Yang United States	19	216 0.8×	97 0.5×	352 2.2×	183 1.7×	55 0.6×	47	917
Claudia Rodríguez Spain	16	117 0.4×	276 1.5×	561 3.5×	81 0.8×	47 0.5×	34	1.1k

Countries citing papers authored by S. Kerber

Since Specialization

Citations

This map shows the geographic impact of S. Kerber'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 S. Kerber with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S. Kerber more than expected).

Fields of papers citing papers by S. Kerber

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S. Kerber. 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 S. Kerber. The network helps show where S. Kerber may publish in the future.

Co-authorship network of co-authors of S. Kerber

This figure shows the co-authorship network connecting the top 25 collaborators of S. Kerber. A scholar is included among the top collaborators of S. Kerber 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 S. Kerber. S. Kerber is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

1.

Held, K. R., et al.. (2012). Der Stellenwert der „array comparative genomic hybridization“ in der Pränataldiagnostik. Medizinische Genetik. 24(2). 108–113. 2 indexed citations

2.

Köller, M., et al.. (2011). Hypoxämie 4 Monate nach rechtsseitiger Pneumektomie. Der Internist. 52(8). 1002–1005. 1 indexed citations

3.

Kleinbongard, Petra, André Dejam, Thomas E. Lauer, et al.. (2005). Plasma nitrite concentrations reflect the degree of endothelial dysfunction in humans. Free Radical Biology and Medicine. 40(2). 295–302. 303 indexed citations

4.

Kleinbongard, Petra, Tienush Rassaf, André Dejam, S. Kerber, & Malte Kelm. (2002). Griess method for nitrite measurement of aqueous and protein-containing samples. Methods in enzymology on CD-ROM/Methods in enzymology. 359. 158–168. 94 indexed citations

5.

Jenderny, J., et al.. (2001). Increased Nuchal Translucency, Hydrops fetalis or Hygroma colli. Fetal Diagnosis and Therapy. 16(4). 211–214. 8 indexed citations

6.

Schulz, Katharina, S. Kerber, & Malte Kelm. (1999). Reevaluation of the Griess Method for Determining NO/NO−2 in Aqueous and Protein-Containing Samples. Nitric Oxide. 3(3). 225–234. 144 indexed citations

7.

Meinecke, Peter, Dieter Meschede, Eberhard Nieschlag, et al.. (1996). Isochromosome Xq in Klinefelter syndrome: Report of 7 new cases. American Journal of Medical Genetics. 64(4). 580–582. 18 indexed citations

8.

Kerber, S. & K. R. Held. (1993). Early genetic amniocentesis—4 years' experience. Prenatal Diagnosis. 13(1). 21–27. 18 indexed citations

9.

Held, K. R., S. Kerber, Erin B. Kaminsky, et al.. (1992). Mosaicism in 45,X Turner syndrome: does survival in early pregnancy depend on the presence of two sex chromosomes?. Human Genetics. 88(3). 288–94. 133 indexed citations

10.

Hüneke, B., et al.. (1990). Frühzeitige Amniozentese zur zytogenetischen Diagnostik. Geburtshilfe und Frauenheilkunde. 50(12). 954–958. 7 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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