Sara Halbach

859 citations
6 papers · 102 · h-index 5

Impact in

    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders
    • Vascular Anomalies and Treatments

Papers in

    • Genomic variations and chromosomal abnormalities 3
    • Congenital Ear and Nasal Anomalies 3
    • Genetics and Neurodevelopmental Disorders 2
    • Genomics and Rare Diseases 1
    • Cleft Lip and Palate Research 1
    • Cancer-related gene regulation 1

Sara Halbach

6 papers receiving 98 citations

Peers

Sara Halbach
Comparison fields: 5 of 33
  • Genetics 44
  • Genetics 14
  • Clinical Biochemistry 6
  • Neurology 12
  • Surgery 28
Replace François Lecoquierre with:
François Lecoquierre France
Gaku Minase Japan
Theresa Brunet Germany
Aurelio Hernández‐Laín Spain
Kelly Radtke United States
Akshata Sonni United States
Abdulaziz Alsaman Saudi Arabia
Mehmed M. Atik United States
Birgitta Bernhard United Kingdom
Anne‐Karin Kahlert Germany
Sara Halbach relative to François Lecoquierre France François Lecoquierre's profile →
Citations per field
00.5×2×4×6.3×
François Lecoquierre · 1×
Citations per year

Countries citing papers authored by Sara Halbach

Since Specialization
Citations

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

Fields of papers citing papers by Sara Halbach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Sara Halbach, 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 Sara Halbach Line = papers co-authored together Sara Halbach links everyone, so they are left out of the graph.

All Works

6 of 6 papers shown
#Work
1 201332
2 201626
3 201319
4 200815
5 20158
6 20152

About Sara Halbach

Sara Halbach is a scholar working on Genetics, Genetics, Molecular Biology, Surgery and Dermatology, having authored 6 papers that have together received 102 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (3 papers), Congenital Ear and Nasal Anomalies (3 papers), Genetics and Neurodevelopmental Disorders (2 papers), Vascular Tumors and Angiosarcomas (1 paper), Genomics and Rare Diseases (1 paper), Cleft Lip and Palate Research (1 paper), Cancer-related gene regulation (1 paper) and Dermatologic Treatments and Research (1 paper). The work is most often cited by research in Genetics (44 citations), Genetics (14 citations), Clinical Biochemistry (6 citations), Neurology (12 citations) and Surgery (28 citations). Sara Halbach has collaborated with scholars based in United States, Belgium and India. Frequent co-authors include Darrel Waggoner, Donna M. McDonald‐McGinn, Elaine H. Zackai, Christopher Tan, Elizabeth Bhoj, Bridget O’Connor, Anne M. Connolly, Yufeng Shen, Marwan Shinawi and Francesca Forzano. Their work appears in journals such as European Journal of Medical Genetics, Genes & Diseases, Neurogenetics, American Journal of Medical Genetics Part A and Molecular Syndromology.

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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