R Leśniewicz

643 total citations
20 papers, 347 citations indexed

About

R Leśniewicz is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, R Leśniewicz has authored 20 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 5 papers in Pediatrics, Perinatology and Child Health and 3 papers in Molecular Biology. Recurrent topics in R Leśniewicz's work include Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Connective tissue disorders research (3 papers). R Leśniewicz is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Prenatal Screening and Diagnostics (5 papers) and Connective tissue disorders research (3 papers). R Leśniewicz collaborates with scholars based in Poland, Germany and Austria. R Leśniewicz's co-authors include W. Paul Dmowski, Alina T. Midro, Sławomir Wołczyński, Barbara Panasiuk, Dieter Meschede, Martin Erdel, J. Horst, Gerd Scherer, Ewa Wiland and Maciej Kurpisz and has published in prestigious journals such as European Journal of Biochemistry, Fertility and Sterility and Cytogenetic and Genome Research.

In The Last Decade

R Leśniewicz

20 papers receiving 303 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R Leśniewicz Poland 9 154 154 101 98 47 20 347
Jae-Wook Jeong United States 9 149 1.0× 198 1.3× 118 1.2× 176 1.8× 13 0.3× 11 458
Shu‐Chin Chien Taiwan 10 73 0.5× 50 0.3× 42 0.4× 84 0.9× 67 1.4× 32 309
Elizabeth R Perdeaux United Kingdom 4 116 0.8× 93 0.6× 46 0.5× 283 2.9× 46 1.0× 4 403
Zhaowei Tu China 10 40 0.3× 105 0.7× 108 1.1× 194 2.0× 41 0.9× 11 369
Dong-Kee Lee United States 8 153 1.0× 223 1.4× 106 1.0× 217 2.2× 10 0.2× 8 540
Tong-Song Wang China 10 49 0.3× 208 1.4× 148 1.5× 81 0.8× 34 0.7× 17 426
RobertS. Sparkes United States 6 114 0.7× 114 0.7× 140 1.4× 94 1.0× 21 0.4× 8 384
Beike Leegte Netherlands 11 428 2.8× 103 0.7× 20 0.2× 189 1.9× 118 2.5× 15 531
Benoît Souquet France 8 100 0.6× 63 0.4× 23 0.2× 228 2.3× 25 0.5× 9 325
V. Sele Denmark 13 212 1.4× 176 1.1× 29 0.3× 136 1.4× 60 1.3× 26 477

Countries citing papers authored by R Leśniewicz

Since Specialization
Citations

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

Fields of papers citing papers by R Leśniewicz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R Leśniewicz

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

All Works

20 of 20 papers shown
1.
Posmyk, Renata, R Leśniewicz, Monika Chorąży, et al.. (2014). The smallest de novo deletion of 20q11.21–q11.23 in a girl with feeding problems, retinal dysplasia, and skeletal abnormalities. American Journal of Medical Genetics Part A. 164(4). 1056–1061. 19 indexed citations
2.
Jarząbek, Katarzyna, et al.. (2012). Evidence that FGFR1 loss-of-function mutations may cause variable skeletal malformations in patients with Kallmann syndrome. Advances in Medical Sciences. 57(2). 314–321. 29 indexed citations
3.
Chorąży, Monika, et al.. (2011). The natural history of Möbius syndrome in a 32-year-old man. Neurologia i Neurochirurgia Polska. 45(1). 74–79. 1 indexed citations
4.
Koda, Mariusz, Z Piotrowski, S Sułkowski, et al.. (2011). IGF-IR in patients with advanced colorectal cancer in correlation with certain clinico-morphological factors: Initial report. Oncology Letters. 2(6). 1155–1159. 12 indexed citations
5.
Posmyk, Renata, R Leśniewicz, Monika Chorąży, & Sławomir Wołczyński. (2011). New case of Primrose syndrome with mild intellectual disability. American Journal of Medical Genetics Part A. 155(11). 2838–2840. 9 indexed citations
6.
Baltaziak, M, et al.. (2011). [Gap junction intercellular communication in carcinogenesis of endometrial cancer].. PubMed. 82(7). 520–4. 1 indexed citations
7.
Leśniewicz, R, et al.. (2010). Prenatal evaluation of a fetus with trisomy 18 and additional balanced de novo Rob(13;14).. Folia Histochemica et Cytobiologica. 47(5). S137–40. 5 indexed citations
8.
Panasiuk, Barbara, Jacqueline Suk Danik, Beata Stasiewicz‐Jarocka, et al.. (2009). Reciprocal chromosome translocations involving short arm of chromosome 9 as a risk factor of unfavorable pregnancy outcomes after meiotic malsegregation 2:2. Advances in Medical Sciences. 54(2). 203–10. 19 indexed citations
9.
Panasiuk, Barbara, et al.. (2007). Translocation form of Wolf-Hirschhorn syndrome --assessment of recurrence rate probability.. PubMed. 52 Suppl 1. 166–70. 6 indexed citations
10.
Midro, Alina T., Ewa Wiland, Barbara Panasiuk, R Leśniewicz, & Maciej Kurpisz. (2006). Risk evaluation of carriers with chromosome reciprocal translocation t(7;13)(q34;q13) and concomitant meiotic segregation analyzed by FISH on ejaculated spermatozoa. American Journal of Medical Genetics Part A. 140A(3). 245–256. 33 indexed citations
11.
Galicka, Anna, Sławomir Wołczyński, R Leśniewicz, L Chyczewski, & A Gindzieński. (2002). A novel Gly to Arg substitution at position 388 of the alpha1 chain of type I collagen in lethal form of osteogenesis imperfecta.. Acta Biochimica Polonica. 49(2). 443–450. 3 indexed citations
12.
Galicka, Anna, et al.. (2001). Defects of type I procollagen metabolism correlated with decrease of prolidase activity in a case of lethal osteogenesis imperfecta. European Journal of Biochemistry. 268(7). 2172–2178. 27 indexed citations
13.
Scherer, Gerd, Martin Erdel, Dieter Meschede, et al.. (1998). Three novel SRY mutations in XY gonadal dysgenesis and the enigma of XY gonadal dysgenesis cases without SRY mutations. Cytogenetic and Genome Research. 80(1-4). 188–192. 55 indexed citations
14.
Leśniewicz, R, et al.. (1998). [The case of intrauterine pregnancy coexisting with extrauterine pregnancy which was surgically removed].. PubMed. 69(4). 210–2. 1 indexed citations
15.
Sawicka, Anna, R Leśniewicz, M Zawada, Beata Stasiewicz‐Jarocka, & Alina T. Midro. (1998). [Familial complex chromosome translocation of t(1;4;10)(q21.3;q27;q26.1) verified by FISH].. PubMed. 69(4). 200–6. 3 indexed citations
16.
Leśniewicz, R & Alina T. Midro. (1998). [Ultrasound diagnosis of four fetuses with Fraser syndrome during pregnancy].. PubMed. 69(3). 152–7. 1 indexed citations
17.
Leśniewicz, R, Barbara Panasiuk, & Alina T. Midro. (1998). [Spontaneous menstruation in patients with Turner syndrome in our observations].. PubMed. 69(12). 1245–52. 1 indexed citations
18.
19.
Midro, Alina T., et al.. (1993). [Clinical examinations, chromosomal and molecular DNA in patients with Swyer syndrome].. PubMed. 64(5). 257–62. 2 indexed citations
20.
Midro, Alina T., et al.. (1992). Different risks in two familial translocations t(9;12) with similar breakpoints.. PubMed. 35(1). 33–40. 1 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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