Carola Lauster

1.6k total citations
10 papers, 155 citations indexed

About

Carola Lauster is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Carola Lauster has authored 10 papers receiving a total of 155 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in Carola Lauster's work include Cleft Lip and Palate Research (9 papers), Craniofacial Disorders and Treatments (6 papers) and dental development and anomalies (5 papers). Carola Lauster is often cited by papers focused on Cleft Lip and Palate Research (9 papers), Craniofacial Disorders and Treatments (6 papers) and dental development and anomalies (5 papers). Carola Lauster collaborates with scholars based in Germany, Netherlands and United States. Carola Lauster's co-authors include Gül Schmidt, Roland Lauster, Franz‐Josef Kramer, Elisabeth Mangold, Heiko Reutter, Martin Scheer, Stefanie Birnbaum, Markus Martini, Michael Knapp and Bert Braumann and has published in prestigious journals such as Differentiation, European Journal Of Oral Sciences and The Cleft Palate-Craniofacial Journal.

In The Last Decade

Carola Lauster

10 papers receiving 148 citations

Peers

Carola Lauster
Toby Goldstein United States
Sixto García‐Miñaúr Spain
Satoshi Suzuki Japan
Yukiho Kobayashi Japan
Anne Dieux France
Fabrizia Franchi Italy
Philip K. Chen Taiwan
Jennifer M. Feenstra United States
Ornella Rodeschini Italy
Ann‐Leslie Zaslav United States
Toby Goldstein United States
Carola Lauster
Citations per year, relative to Carola Lauster Carola Lauster (= 1×) peers Toby Goldstein

Countries citing papers authored by Carola Lauster

Since Specialization
Citations

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

Fields of papers citing papers by Carola Lauster

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carola Lauster

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

All Works

10 of 10 papers shown
1.
2.
Assis, Nilma Almeida de, Stefanie Nowak, Kerstin U. Ludwig, et al.. (2010). SUMO1 as a candidate gene for non-syndromic cleft lip with or without cleft palate: No evidence for the involvement of common or rare variants in Central European patients. International Journal of Pediatric Otorhinolaryngology. 75(1). 49–52. 9 indexed citations
3.
Birnbaum, Stefanie, Heiko Reutter, Meinhard Mende, et al.. (2009). Further evidence for the involvement ofMYH9in the etiology of non‐syndromic cleft lip with or without cleft palate. European Journal Of Oral Sciences. 117(2). 200–203. 19 indexed citations
4.
Reutter, Heiko, Stefanie Birnbaum, Meinhard Mende, et al.. (2009). Transforming growth factor-beta receptor type 1 (TGFBR1) is not associated with non-syndromic cleft lip with or without cleft palate in patients of Central European descent. International Journal of Pediatric Otorhinolaryngology. 73(10). 1334–1338. 3 indexed citations
5.
Reutter, Heiko, Stefanie Birnbaum, Meinhard Mende, et al.. (2008). TGFB3 displays parent-of-origin effects among central Europeans with nonsyndromic cleft lip and palate. Journal of Human Genetics. 53(7). 656–661. 28 indexed citations
6.
Reutter, Heiko, Stefanie Birnbaum, Meinhard Mende, et al.. (2008). Family-Based Association Study of the MTHFR Polymorphism C677T in Patients with Nonsyndromic Cleft Lip and Palate from Central Europe. The Cleft Palate-Craniofacial Journal. 45(3). 267–271. 17 indexed citations
7.
Thiele, Hölger, et al.. (2008). Cleft Lip and/or Palate with Monogenic Autosomal Recessive Transmission in Pyrenees Shepherd Dogs. The Cleft Palate-Craniofacial Journal. 46(1). 81–88. 21 indexed citations
8.
Birnbaum, Stefanie, Heiko Reutter, Carola Lauster, et al.. (2008). Mutation screening in theIRF6‐gene in patients with apparently nonsyndromic orofacial clefts and a positive family history suggestive of autosomal‐dominant inheritance. American Journal of Medical Genetics Part A. 146A(6). 787–790. 18 indexed citations
9.
10.
Birnbaum, Stefanie, Heiko Reutter, Meinhard Mende, et al.. (2006). A family‐based association study in Central Europeans: No evidence for the cystathionine beta‐synthase c.844ins68 gene variant as a risk factor for non‐syndromic cleft lip and palate. American Journal of Medical Genetics Part A. 143A(2). 205–207. 6 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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