L. Wiśniewski

471 total citations
28 papers, 390 citations indexed

About

L. Wiśniewski is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, L. Wiśniewski has authored 28 papers receiving a total of 390 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in L. Wiśniewski's work include Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (8 papers) and Chromosomal and Genetic Variations (8 papers). L. Wiśniewski is often cited by papers focused on Genomic variations and chromosomal abnormalities (16 papers), Prenatal Screening and Diagnostics (8 papers) and Chromosomal and Genetic Variations (8 papers). L. Wiśniewski collaborates with scholars based in Poland, United States and Belgium. L. Wiśniewski's co-authors include Jerry Higgins, Kurt Hirschhorn, James R. Heffelfinger, Terry Hassold, Richard A. Doherty, Fredda Ginsberg‐Fellner, Robert J. Desnick, Mary E. Witt, Małgorzata Krajewska‐Walasek and J. P. Fryns and has published in prestigious journals such as Journal of Medical Genetics, Human Genetics and American Journal of Hematology.

In The Last Decade

L. Wiśniewski

28 papers receiving 375 citations

Peers

L. Wiśniewski

GENET

PPCH

GENET

Petrea Jacobsen Denmark

Rethoré Mo France

F. Prieto Spain

Franca Bernardi Italy

F. R. Sergovich Canada

D R Romain New Zealand

G. R. Stalder Switzerland

Catherine Metaxotou Greece

Judith Dagan Israel

Michael J. Macera United States

Petrea Jacobsen Denmark

L. Wiśniewski

347 ×1.1

GENET

195 ×1.5

97 ×0.8

90 ×0.8

PPCH

35 ×0.8

GENET

Citations per year, relative to L. Wiśniewski L. Wiśniewski (= 1×) peers Petrea Jacobsen

Countries citing papers authored by L. Wiśniewski

Since Specialization

Citations

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

Fields of papers citing papers by L. Wiśniewski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of L. Wiśniewski

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

Chrzańowska, Krystyńa, J P Fryns, Małgorzata Krajewska‐Walasek, Herman Van den Berghe, & L. Wiśniewski. (1991). Nager type of Acrofacial dysostosis: an example of autosomal dominant transmission with variable expression. Genetica Polonica. 32. 2 indexed citations

Chrzańowska, Krystyńa, J. P. Fryns, Małgorzata Krajewska‐Walasek, L. Wiśniewski, & Herman Van den Berghe. (1989). Phenotype variability in the Miller acrofacial dysostosis syndrome. Report of two further patients. Clinical Genetics. 35(2). 157–160. 13 indexed citations

Chrzańowska, Krystyńa, J. P. Fryns, Małgorzata Krajewska‐Walasek, Herman Van den Berghe, & L. Wiśniewski. (1989). Skeletal dysplasia syndrome with progeroid appearance, characteristic facial and limb anomalies, multiple synostoses, and distinct skeletal changes: A variant example of the Lenz–Majewski syndrome. American Journal of Medical Genetics. 32(4). 470–474. 10 indexed citations

Wiśniewski, L., et al.. (1987). Clinical Features and Computer-Aided Analysis of Chromosome Aberration in a Case with Incontinentia Pigmenti. Klinische Pädiatrie. 199(1). 32–36. 2 indexed citations

Wiśniewski, L., et al.. (1985). A new case of partial trisomy of 17 long arm. Densitometric analysis of aberrations. European Journal of Pediatrics. 143(4). 314–316. 6 indexed citations

Wiśniewski, L., et al.. (1985). Clinical features in a case with ring chromosome 13. European Journal of Pediatrics. 144(4). 409–412. 4 indexed citations

Wiśniewski, L. & Richard A. Doherty. (1985). Supernumerary microchromosomes identified as inverted duplications of chromosome 15: A report of three cases. Human Genetics. 69(2). 161–163. 24 indexed citations

Krajewska‐Walasek, Małgorzata, et al.. (1985). Ring chromosome 4 : 46, XY, r (4) (p16q35) in a boy. Klinische Pädiatrie. 197(4). 294–296. 7 indexed citations

Wiśniewski, L., et al.. (1982). [DNA content and the size of Y chromosome in a patient with mixed gonadal dysgenesis and 45,X/46,Xt(Y:Y) (pter leads to q12::q12 leads to q11) karyotype].. PubMed. 53(12). 889–95. 1 indexed citations

10.

Wiśniewski, L. & Kurt Hirschhorn. (1982). Distamycin A-DAPI banding of nonfluorescent Y (Ynf) chromosomes in 45,X/46,XYnf mosaicism. Human Genetics. 60(2). 130–132. 11 indexed citations

11.

Wiśniewski, L., et al.. (1982). Prader-Willi Syndrome in a Girl with 47,XX, + mar Karyotype. Klinische Pädiatrie. 194(5). 328–331. 1 indexed citations

12.

Wiśniewski, L., et al.. (1980). Prader‐Willi syndrome and a bisatellited derivative of chromosome 15. Clinical Genetics. 18(1). 42–47. 58 indexed citations

13.

Wiśniewski, L., et al.. (1980). Two new cases of 9p- syndrome. Klinische Pädiatrie. 192(3). 270–274. 3 indexed citations

14.

Wiśniewski, L., et al.. (1979). Contraction of C-bands of human chromosomes No. 1 and No. 9. Genetica Polonica. 20(2). 1 indexed citations

15.

Wiśniewski, L., et al.. (1979). The child with chromosome ring 15.. PubMed. 191(4). 429–32. 6 indexed citations

16.

Wiśniewski, L., et al.. (1978). Partial trisomy 2q and familial translocation t(2;18)(q31;p11). Human Genetics. 45(2). 225–228. 8 indexed citations

17.

Wiśniewski, L. & Jerry Higgins. (1977). Mosaicism presumably related to a Y/6 translocation in a boy with multiple congenital abnormalities.. Journal of Medical Genetics. 14(5). 378–381. 6 indexed citations

18.

Wiśniewski, L., et al.. (1976). Cytogenetic studies in lymphoproliferative disorders. 17(3). 2 indexed citations

19.

Higgins, Jerry, et al.. (1976). Two informative translocations involving chromosome 2. Cytogenetic and Genome Research. 16(1-5). 314–316. 3 indexed citations

20.

Wiśniewski, L., et al.. (1967). Cytologic evaluation of fetal death and an attempt to determine the time of its occurrence.. PubMed. 11(5). 403–9. 2 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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