C. Ström

1.7k total citations
33 papers, 993 citations indexed

About

C. Ström is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, C. Ström has authored 33 papers receiving a total of 993 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Pediatrics, Perinatology and Child Health, 16 papers in Genetics and 8 papers in Molecular Biology. Recurrent topics in C. Ström's work include Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic Syndromes and Imprinting (6 papers). C. Ström is often cited by papers focused on Prenatal Screening and Diagnostics (19 papers), Genomic variations and chromosomal abnormalities (8 papers) and Genetic Syndromes and Imprinting (6 papers). C. Ström collaborates with scholars based in United States and Russia. C. Ström's co-authors include Yury Verlinsky, Anver Kuliev, V. Ivakhnenko, Svetlana Rechitsky, Oleg Verlinsky, Norman Ginsberg, George Wolf, J. Cieslak, Melody White and V. I. Kukharenko and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and Human Reproduction.

In The Last Decade

C. Ström

33 papers receiving 924 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
C. Ström United States	17	709	392	225	208	180	33	993
Aaron Lifchez United States	15	829 1.2×	393 1.0×	295 1.3×	185 0.9×	212 1.2×	24	1.0k
Barbara Pertl Austria	20	969 1.4×	497 1.3×	62 0.3×	241 1.2×	126 0.7×	51	1.2k
Anıl Biricik Italy	18	1.2k 1.7×	614 1.6×	468 2.1×	315 1.5×	146 0.8×	41	1.5k
B. Eiben Germany	18	753 1.1×	449 1.1×	175 0.8×	129 0.6×	168 0.9×	65	969
Andrea Nuccitelli Italy	10	446 0.6×	256 0.7×	104 0.5×	104 0.5×	75 0.4×	16	593
Vincenzo Cirigliano Spain	18	817 1.2×	550 1.4×	57 0.3×	210 1.0×	111 0.6×	46	1.0k
Muhterem Bahçe Türkiye	11	711 1.0×	423 1.1×	281 1.2×	171 0.8×	112 0.6×	34	898
Sara Bono Italy	12	1.1k 1.5×	554 1.4×	357 1.6×	229 1.1×	93 0.5×	17	1.2k
Andrew Dorfmann United States	14	677 1.0×	425 1.1×	387 1.7×	166 0.8×	99 0.6×	30	1.1k
Necati Fındıklı Türkiye	19	401 0.6×	153 0.4×	372 1.7×	198 1.0×	96 0.5×	60	855

Countries citing papers authored by C. Ström

Since Specialization

Citations

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

Fields of papers citing papers by C. Ström

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of C. Ström

This figure shows the co-authorship network connecting the top 25 collaborators of C. Ström. A scholar is included among the top collaborators of C. Ström 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 C. Ström. C. Ström 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

Mikula, Mario, et al.. (2011). The importance of β globin deletion analysis in the evaluation of patients with β thalassemia. International Journal of Laboratory Hematology. 33(3). 310–317. 1 indexed citations

Monaghan, Kristin G., W. Edward Highsmith, J. Amos, et al.. (2004). Genotype-phenotype correlation and frequency of the 3199del6 cystic fibrosis mutation among I148T carriers: Results from a collaborative study. Genetics in Medicine. 6(5). 421–425. 24 indexed citations

Verlinsky, Yury, Svetlana Rechitsky, Oleg Verlinsky, et al.. (2002). Polar body-based preimplantation diagnosis for X-linked disorders. Reproductive BioMedicine Online. 4(1). 38–42. 34 indexed citations

Ginsberg, Norman, C. Ström, & Yury Verlinsky. (2001). Crown–rump lengths in missed miscarriages and trisomy 21. Ultrasound in Obstetrics and Gynecology. 18(5). 488–490. 3 indexed citations

Verlinsky, Yury, Svetlana Rechitsky, Oleg Verlinsky, C. Ström, & Anver Kuliev. (2000). Preimplantation diagnosis for ornithine transcarbamylase deficiency. Reproductive BioMedicine Online. 1(2). 45–47. 8 indexed citations

Verlinsky, Yury, Svetlana Rechitsky, Oleg Verlinsky, et al.. (1999). Prepregnancy Testing for Single-Gene Disorders by Polar Body Analysis. Genetic Testing. 3(2). 185–190. 30 indexed citations

Levine, Elliot M., Vivek Ghai, John Barton, & C. Ström. (1999). Intrapartum antibiotic prophylaxis increases the incidence of gram-negative neonatal sepsis. Infectious Diseases in Obstetrics and Gynecology. 7(4). 210–213. 68 indexed citations

Verlinsky, Yury, J. Cieslak, V. Ivakhnenko, et al.. (1999). Prevention of Age-Related Aneuploidies by Polar Body Testing of Oocytes. Journal of Assisted Reproduction and Genetics. 16(4). 165–169. 80 indexed citations

Kuliev, Anver, Svetlana Rechitsky, Oleg Verlinsky, et al.. (1999). Birth of Healthy Children After Preimplantation Diagnosis of Thalassemias. Journal of Assisted Reproduction and Genetics. 16(4). 207–211. 46 indexed citations

10.

Verlinsky, Yury, J. Cieslak, V. Ivakhnenko, et al.. (1998). Preimplantation Diagnosis of Common Aneuploidies by the First- and Second-Polar Body FISH Analysis. Journal of Assisted Reproduction and Genetics. 15(5). 285–289. 88 indexed citations

11.

Verlinsky, Oleg, Svetlana Rechitsky, V. I. Kukharenko, et al.. (1998). Sequence Analysis of Libraries from Individual Human Blastocysts. Journal of Assisted Reproduction and Genetics. 15(5). 338–343. 7 indexed citations

12.

Rechitsky, Svetlana, C. Ström, Oleg Verlinsky, et al.. (1998). Allele Dropout in Polar Bodies and Blastomeres. Journal of Assisted Reproduction and Genetics. 15(5). 253–257. 104 indexed citations

13.

Ström, C., Svetlana Rechitsky, George Wolf, et al.. (1998). Preimplantation diagnosis of autosomal dominant retinitis pigmentosum using two simultaneous single cell assays for a point mutation in the rhodopsin gene. Molecular Human Reproduction. 4(4). 351–355. 12 indexed citations

14.

Verlinsky, Yury, Oleg Verlinsky, Svetlana Rechitsky, et al.. (1998). Isolation of cDNA libraries from individual human preimplantation embryos. Molecular Human Reproduction. 4(6). 571–575. 14 indexed citations

15.

Verlinsky, Yury, J. Cieslak, V. Ivakhnenko, et al.. (1997). Prepregnancy Genetic Testing for Age-Related Aneuploidies by Polar Body Analysis. Genetic Testing. 1(4). 231–235. 27 indexed citations

16.

Verlinsky, Yury, S. Munné, Joe Leigh Simpson, et al.. (1997). Current status of preimplantation diagnosis. Journal of Assisted Reproduction and Genetics. 14(2). 72–75. 17 indexed citations

17.

Cadkin, A V, et al.. (1997). Prenatal diagnosis of body stalk anomaly in the first trimester of pregnancy. Ultrasound in Obstetrics and Gynecology. 10(6). 419–421. 25 indexed citations

18.

Verlinsky, Yury, Norman Ginsberg, Michael Freidine, et al.. (1995). Cross‐hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common chromosomal aneuploidies by fish. Prenatal Diagnosis. 15(9). 831–834. 22 indexed citations

19.

Verlinsky, Yury, J. Cieslak, Michael Freidine, et al.. (1995). Diagnosing and preventing inherited disease: Pregnancies following pre-conception diagnosis of common aneuploidies by fluorescent in-situ hybridization. Human Reproduction. 10(7). 1923–1927. 123 indexed citations

20.

Ström, C.. (1988). A three allele restriction fragment length polymorphism within the human Col2A1 gene. Nucleic Acids Research. 16(18). 9077–9077. 9 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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