Milly Andrle

416 citations
11 papers · 346 · h-index 6

Impact in

  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Animal Genetics and Reproduction
    • Chromosomal and Genetic Variations

Papers in

    • Genomic variations and chromosomal abnormalities 4
    • Genetics and Neurodevelopmental Disorders 1
    • DNA and Nucleic Acid Chemistry 3
    • DNA Repair Mechanisms 2
    • Genomics and Chromatin Dynamics 2

Milly Andrle

9 papers receiving 320 citations

Peers

Milly Andrle
Comparison fields: 5 of 45
  • Genetics 233
  • Plant Science 177
  • Developmental Biology 10
  • Pediatrics, Perinatology and Child Health 74
  • Molecular Biology 185
Replace M Ferguson-Smith with:
M Ferguson-Smith United Kingdom
H.E. Wyandt United States
P Balícek Czechia
Paula R. Martens United States
John Chamberlin United States
Frank S. Grass United States
Laurie A. Christ United States
Ahmed B. Hamid Germany
M. Crocker United Kingdom
M.R. Verschraegen-Spae Belgium
Milly Andrle relative to M Ferguson-Smith United Kingdom M Ferguson-Smith's profile →
Citations per field
00.5×1.7×
M Ferguson-Smith · 1×
Citations per year

Countries citing papers authored by Milly Andrle

Since Specialization
Citations

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

Fields of papers citing papers by Milly Andrle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 7 scholars most cited alongside Milly Andrle, 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 Milly Andrle Line = papers co-authored together Milly Andrle links everyone, so they are left out of the graph.

All Works

11 of 11 papers shown
#Work
1 1978257
2 197524
3 197917
4 197814
5 197613
6 200811
7
HLA and trisomy 21.
19855
8
[Inversion 8 and consecutive trisomy of region 8q22----qter].
19874
9
[Partial monosomy and trisomy 5 p due to balanced translocation t (3,5) in the father (author's transl)].
19811
10 20080
11
[Satellite associations in trisomy 21 (author's transl)].
19810

About Milly Andrle

Milly Andrle is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Immunology and Pathology and Forensic Medicine, having authored 11 papers that have together received 346 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (4 papers), DNA and Nucleic Acid Chemistry (3 papers), Prenatal Screening and Diagnostics (3 papers), DNA Repair Mechanisms (2 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Genomics and Chromatin Dynamics (2 papers), Cancer Mechanisms and Therapy (1 paper) and Genetics and Neurodevelopmental Disorders (1 paper). The work is most often cited by research in Genetics (233 citations), Plant Science (177 citations), Developmental Biology (10 citations), Pediatrics, Perinatology and Child Health (74 citations) and Molecular Biology (185 citations). Milly Andrle has collaborated with scholars based in Austria, Czechia and Switzerland. Frequent co-authors include Peter F. Ambros, Dieter Schweizer, A Rett, Wolfgang R. Mayr, E. Bühler, T. Tsuchimoto and Wolfgang Fiedler. Their work appears in journals such as Human Genetics, Experimental Cell Research, PubMed and Cytogenetics and Cell Genetics.

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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