Frank Majewski

2.3k total citations
26 papers, 1.3k citations indexed

About

Frank Majewski is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Frank Majewski has authored 26 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 12 papers in Molecular Biology and 6 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Frank Majewski's work include Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and Craniofacial Disorders and Treatments (5 papers). Frank Majewski is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Prenatal Screening and Diagnostics (5 papers) and Craniofacial Disorders and Treatments (5 papers). Frank Majewski collaborates with scholars based in Germany, United States and Poland. Frank Majewski's co-authors include Gabriele Gillessen‐Kaesbach, James F. Reynolds, Dagmar Wieczorek, Wolfgang Küster, Beate Albrecht, Denise Horn, Peter Meinecke, Frances R. Goodman, Amanda Collins and Peter Scambler and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics and Journal of the American Academy of Dermatology.

In The Last Decade

Frank Majewski

26 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Frank Majewski Germany 16 755 579 271 200 157 26 1.3k
Sevim Balcı Türkiye 17 463 0.6× 552 1.0× 181 0.7× 200 1.0× 92 0.6× 70 1.2k
Louise Brueton United Kingdom 24 604 0.8× 908 1.6× 205 0.8× 154 0.8× 198 1.3× 34 1.5k
Carol L. Clericuzio United States 29 872 1.2× 834 1.4× 377 1.4× 393 2.0× 112 0.7× 58 1.9k
Beate Albrecht Germany 23 1.0k 1.4× 862 1.5× 264 1.0× 214 1.1× 126 0.8× 45 1.7k
Mark Lubinsky United States 25 577 0.8× 734 1.3× 401 1.5× 399 2.0× 94 0.6× 73 1.6k
Ursula G. Froster Germany 23 886 1.2× 900 1.6× 371 1.4× 334 1.7× 139 0.9× 79 2.0k
Ikuko Teshima Canada 23 797 1.1× 731 1.3× 292 1.1× 139 0.7× 112 0.7× 61 1.5k
Mahin Golabi United States 26 1.2k 1.5× 1.3k 2.2× 386 1.4× 470 2.4× 107 0.7× 59 2.4k
J P Fryns Belgium 25 1.2k 1.6× 1.1k 1.9× 430 1.6× 304 1.5× 130 0.8× 90 2.2k
Boris G. Kousseff United States 25 785 1.0× 603 1.0× 276 1.0× 307 1.5× 88 0.6× 83 1.6k

Countries citing papers authored by Frank Majewski

Since Specialization
Citations

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

Fields of papers citing papers by Frank Majewski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frank Majewski

This figure shows the co-authorship network connecting the top 25 collaborators of Frank Majewski. A scholar is included among the top collaborators of Frank Majewski 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 Frank Majewski. Frank Majewski 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.
Majewski, Frank, Stefan Böhringer, Sven Fischer, et al.. (2006). A family with autosomal dominant oculo-auriculo-vertebral spectrum. Clinical Dysmorphology. 16(1). 1–7. 59 indexed citations
2.
Böhringer, Stefan, Sven Fischer, Hermann‐Josef Lüdecke, et al.. (2005). Oculo-auriculo-vertebral spectrum (OAVS): clinical evaluation and severity scoring of 53 patients and proposal for a new classification. European Journal of Medical Genetics. 48(4). 397–411. 157 indexed citations
3.
Leube, Barbara, Frank Majewski, Matthias Drechsler, & Brigitte Royer‐Pokora. (2003). Unbalanced cryptic translocation der(14)t(9;14)(q34.3;q32.33) identified by subtelomeric FISH. Clinical Dysmorphology. 12(4). 261–265. 5 indexed citations
4.
Musante, Luciana, Hans-Gerd Kehl, Frank Majewski, et al.. (2003). Spectrum of mutations in PTPN11 and genotype–phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome. European Journal of Human Genetics. 11(2). 201–206. 111 indexed citations
5.
Türkmen, Seval, Gabriele Gillessen‐Kaesbach, Peter Meinecke, et al.. (2003). Mutations in NSD1 are responsible for Sotos syndrome, but are not a frequent finding in other overgrowth phenotypes. European Journal of Human Genetics. 11(11). 858–865. 97 indexed citations
6.
Leube, Barbara, et al.. (2003). Clinical, cytogenetic, and molecular observations in a patient with Pallister‐Killian‐syndrome with an unusual karyotype. American Journal of Medical Genetics Part A. 123A(3). 296–300. 19 indexed citations
7.
Goodman, Frances R., Frank Majewski, Amanda Collins, & Peter Scambler. (2002). A 117-kb Microdeletion Removing HOXD9–HOXD13 and EVX2 Causes Synpolydactyly. The American Journal of Human Genetics. 70(2). 547–555. 77 indexed citations
8.
Majewski, Frank. (2000). Lenz-Majewski hyperostotic dwarfism: Reexamination of the original patient. American Journal of Medical Genetics. 93(4). 335–338. 12 indexed citations
9.
Bartsch, Oliver, et al.. (1999). FISH studies in 45 patients with Rubinstein-Taybi syndrome: deletions associated with polysplenia, hypoplastic left heart and death in infancy. European Journal of Human Genetics. 7(7). 748–756. 65 indexed citations
10.
Majewski, Frank & Timm O. Goecke. (1998). Microcephalic osteodysplastic primordial dwarfism type ii: Report of three cases and review. American Journal of Medical Genetics. 80(1). 25–31. 29 indexed citations
11.
12.
Schubert, Regine, et al.. (1997). Partial trisomy 6p from a de novo translocation (6; 18) with variable mosaicism in different tissues. Clinical Genetics. 52(2). 126–129. 11 indexed citations
13.
Thiele, Hannelore, et al.. (1996). Familial arhinia, choanal atresia, and microphthalmia. American Journal of Medical Genetics. 63(1). 310–313. 32 indexed citations
14.
Megahed, Mosaad, et al.. (1995). Ichthyotic and psoriasiform skin lesions along Blaschko's lines in a woman with X-linked dominant chondrodysplasia punctata. Journal of the American Academy of Dermatology. 33(2). 356–360. 10 indexed citations
15.
Preis, S., et al.. (1995). Acrofacial dysostosis of unknown type: Nosology of the acrofacial dysostoses. American Journal of Medical Genetics. 56(2). 155–160. 11 indexed citations
16.
Horneff, Gerd, et al.. (1993). Pallister-Killian syndrome in older children and adolescents. Pediatric Neurology. 9(4). 312–315. 26 indexed citations
17.
Buntinx, Inge & Frank Majewski. (1990). Blepharophimosis, iris coloboma, microgenia, hearing loss, postaxial polydactyly, aplasia of corpus callosum, hydroureter, and developmental delay. American Journal of Medical Genetics. 36(3). 273–274. 13 indexed citations
18.
Küster, Wolfgang, Leigh Pascoe, J Purrmann, et al.. (1989). The genetics of Crohn disease: Complex segregation analysis of a family study with 265 patients with Crohn disease and 5,387 relatives. American Journal of Medical Genetics. 32(1). 105–108. 84 indexed citations
19.
Ardinger, Holly H, Joan Atkin, R. Dwain Blackston, et al.. (1988). Verification of the fetal valproate syndrome phenotype. American Journal of Medical Genetics. 29(1). 171–185. 217 indexed citations
20.
Küster, Wolfgang, W. Lenz, Helena Kääriäinen, et al.. (1988). Congenital scalp defects with distal limb anomalies (Adams‐Oliver syndrome): Report of ten cases and review of the literature. American Journal of Medical Genetics. 31(1). 99–115. 68 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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