Beate Mitulla

1.0k citations
13 papers · 477 · h-index 10

Impact in

  • Genetics top 10%
    • Craniofacial Disorders and Treatments
    • Cleft Lip and Palate Research
    • Genomic variations and chromosomal abnormalities
    • Ocular Disorders and Treatments
    • Neurogenetic and Muscular Disorders Research
    • Congenital Ear and Nasal Anomalies

Papers in

    • Hedgehog Signaling Pathway Studies 2
    • Genomic variations and chromosomal abnormalities 2
    • Cleft Lip and Palate Research 2
    • Craniofacial Disorders and Treatments 2
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2

Beate Mitulla

13 papers receiving 463 citations

Peers

Beate Mitulla
Comparison fields: 5 of 50
  • Genetics 102
  • Genetics 262
  • Clinical Biochemistry 31
  • Surgery 160
  • Developmental Biology 6
Replace Christine A. Oley with:
Christine A. Oley Australia
Baiba Lāce Latvia
B. G. A. ter Haar Netherlands
Marjan M. Nezarati Canada
R M Winter United Kingdom
Magdalena Badura‐Stronka Poland
Esther Geán Spain
Carole Brewer United Kingdom
Vanesa López‐González Spain
Hermine E. Veenstra‐Knol Netherlands
Beate Mitulla relative to Christine A. Oley Australia Christine A. Oley's profile →
Citations per field
00.5×4.4×
Christine A. Oley · 1×
Citations per year

Countries citing papers authored by Beate Mitulla

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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.

Border = papers with Beate Mitulla Line = papers co-authored together Beate Mitulla links everyone, so they are left out of the graph.

All Works

13 of 13 papers shown
#Work
1 2005157
2 200289
3 200554
4 199329
5 199029
6 199627
7 200426
8 200924
9 199417
10 200212
11 20076
12 20026
13 20001

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 477 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (2 papers), Child Nutrition and Feeding Issues (2 papers), Cleft Lip and Palate Research (2 papers), Hedgehog Signaling Pathway Studies (2 papers), Craniofacial Disorders and Treatments (2 papers), Congenital gastrointestinal and neural anomalies (2 papers), Prenatal Screening and Diagnostics (2 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Genetics (102 citations), Genetics (262 citations), Clinical Biochemistry (31 citations), Surgery (160 citations) and Developmental Biology (6 citations). Beate Mitulla has collaborated with scholars based in Germany, Finland and Estonia. Frequent co-authors include Beate Albrecht, Christiane Zweier, Andrea Thieme, Anita Rauch, Hans‐Dieter Rott, Rainer König, R. Behrens, Gabriele Gillessen‐Kaesbach, Sven Fischer and Christopher Mohr. Their work appears in journals such as Human Genetics, Annals of Human Genetics, Journal of Inherited Metabolic Disease, European Journal of Medical Genetics and Journal of Neurology.

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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