Beate Mitulla
Impact in
- Genetics top 10%
- Craniofacial Disorders and Treatments
- Cleft Lip and Palate Research
- Genomic variations and chromosomal abnormalities
- Neurogenetic and Muscular Disorders Research
- Connective tissue disorders research
- Ocular Disorders and Treatments
- Clinical Biochemistry top 10%
Papers in
-
- Hedgehog Signaling Pathway Studies 2
- Genetics 6
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
- Neurogenetic and Muscular Disorders Research 2
- Cleft Lip and Palate Research 2
- Genomic variations and chromosomal abnormalities 2
- Co-authors
- Beate Albrecht (3 shared papers)Christiane Zweier (3 shared papers)Andrea Thieme (2 shared papers)Rainer König (2 shared papers)R. Behrens (2 shared papers)Hans‐Dieter Rott (2 shared papers)Anita Rauch (2 shared papers)Gabriele Gillessen‐Kaesbach (3 shared papers)
In The Last Decade
Beate Mitulla
13 papers receiving 494 citations
Peers
Comparison fields: 5 of 48
- Genetics 263
- Genetics 93
- Clinical Biochemistry 35
- Surgery 161
- Molecular Biology 185
Countries citing papers authored by Beate Mitulla
This map shows the geographic impact of Beate Mitulla'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 Beate Mitulla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Beate Mitulla more than expected).
Fields of papers citing papers by Beate Mitulla
This network shows the impact of papers produced by Beate Mitulla. 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 Beate Mitulla. The network helps show where Beate Mitulla may publish in the future.
Co-authors
The 25 scholars most cited alongside Beate Mitulla, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2005 | 163 | |
| 2 | 2002 | 91 | |
| 3 | 2005 | 63 | |
| 4 | 1993 | 37 | |
| 5 | 1990 | 33 | |
| 6 | 1996 | 30 | |
| 7 | 2004 | 29 | |
| 8 | 2009 | 27 | |
| 9 | 1994 | 18 | |
| 10 | 2002 | 12 | |
| 11 | 2007 | 6 | |
| 12 | 2002 | 6 | |
| 13 | 2000 | 1 |
About Beate Mitulla
Beate Mitulla is a scholar working on Molecular Biology, Genetics, Surgery, Genetics and Pediatrics, Perinatology and Child Health, having authored 13 papers that have together received 516 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Child Nutrition and Feeding Issues (2 papers), Cleft Lip and Palate Research (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Congenital gastrointestinal and neural anomalies (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Genetics (263 citations), Genetics (93 citations), Clinical Biochemistry (35 citations), Surgery (161 citations) and Molecular Biology (185 citations). Beate Mitulla has collaborated with scholars based in Germany, Austria and Estonia. Frequent co-authors include Beate Albrecht, Christiane Zweier, Andrea Thieme, Rainer König, R. Behrens, Hans‐Dieter Rott, Anita Rauch, Gabriele Gillessen‐Kaesbach, Christopher Mohr and Frank Majewski. Their work appears in journals such as Human Genetics, Annals of Human Genetics, Journal of Inherited Metabolic Disease, European Journal of Medical Genetics and Prenatal Diagnosis.
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.