Barbara Pawlik

717 total citations
8 papers, 252 citations indexed

About

Barbara Pawlik is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Barbara Pawlik has authored 8 papers receiving a total of 252 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Barbara Pawlik's work include Hedgehog Signaling Pathway Studies (3 papers), Congenital limb and hand anomalies (2 papers) and Genetic Syndromes and Imprinting (1 paper). Barbara Pawlik is often cited by papers focused on Hedgehog Signaling Pathway Studies (3 papers), Congenital limb and hand anomalies (2 papers) and Genetic Syndromes and Imprinting (1 paper). Barbara Pawlik collaborates with scholars based in Germany, Türkiye and France. Barbara Pawlik's co-authors include Bernd Wollnik, Yun Li, Sevim Balcı, Dagmar Wieczorek, Nurten Akarsu, Almuth Caliebe, Bernd Schweiger, Fernando Regla Vargas, Gabriele Gillessen‐Kaesbach and Fritz Hans Schweingruber and has published in prestigious journals such as FEBS Journal, Human Mutation and European Journal of Human Genetics.

In The Last Decade

Barbara Pawlik

8 papers receiving 246 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Barbara Pawlik Germany 6 142 95 70 49 28 8 252
Timothy Hutchin United States 7 279 2.0× 10 0.1× 26 0.4× 71 1.4× 44 1.6× 7 424
Lynn Mar Canada 9 199 1.4× 102 1.1× 3 0.0× 8 0.2× 6 0.2× 10 245
Sawitree Rattanasopha Thailand 4 227 1.6× 112 1.2× 7 0.1× 4 0.1× 3 0.1× 5 297
Madoka Kumai Japan 6 279 2.0× 29 0.3× 3 0.0× 10 0.2× 7 0.3× 7 337
B. B. Roa United States 9 219 1.5× 112 1.2× 3 0.0× 3 0.1× 36 1.3× 13 357
Annie Dumouchel Canada 6 248 1.7× 69 0.7× 18 0.3× 2 0.0× 5 0.2× 7 311
Jiale Xiang China 9 172 1.2× 88 0.9× 85 1.7× 23 0.8× 24 345
Leanne Moynihan United Kingdom 7 111 0.8× 71 0.7× 1 0.0× 34 0.7× 30 1.1× 7 226
Jennifer Lin‐Jones United States 9 198 1.4× 23 0.2× 7 0.1× 36 0.7× 13 0.5× 11 264
Adam Diehl United States 7 330 2.3× 138 1.5× 4 0.1× 3 0.1× 8 0.3× 10 458

Countries citing papers authored by Barbara Pawlik

Since Specialization
Citations

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

Fields of papers citing papers by Barbara Pawlik

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Barbara Pawlik

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

All Works

8 of 8 papers shown
1.
Yüksel‐Apak, Memnune, Nina Bögershausen, Barbara Pawlik, et al.. (2012). A large duplication involving the IHH locus mimics acrocallosal syndrome. European Journal of Human Genetics. 20(6). 639–644. 11 indexed citations
2.
Pawlik, Barbara, Asif Mir, Hina Iqbal, et al.. (2010). A Novel Familial <i>BBS12</i> Mutation Associated with a Mild Phenotype: Implications for Clinical and Molecular Diagnostic Strategies. Molecular Syndromology. 1(1). 27–34. 30 indexed citations
4.
Pawlik, Barbara, et al.. (2009). A novel loss-of-function mutation in the GNS gene causes Sanfilippo syndrome type D.. PubMed. 20(2). 133–9. 4 indexed citations
5.
Hilgert, Nele, Fatemeh Alasti, Nele Dieltjens, et al.. (2008). Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11. Clinical Genetics. 74(3). 223–232. 55 indexed citations
6.
7.
Paradowski, Bogusław & Barbara Pawlik. (2005). [Diaschisis phenomenon in different neurological diseases].. PubMed. 58(11-12). 675–7. 1 indexed citations
8.
Schoch, Werner H., Barbara Pawlik, & Fritz Hans Schweingruber. (1988). Botanische Makroreste : ein Atlas zur Bestimmung häufig gefundender und ökologisch wichtiger Pflanzensamen = Botanical macro-remains : an atlas for the determination of frequently encountered and ecologically important plant seeds = Macrorestes botaniques : atlas pour la détermination des graines fréquemment trouvées et écologiquement importantes. 16 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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