Elke Back

1.1k citations
36 papers · 829 indexed · h-index 15

Impact in

  • Genetics top 5%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders

Papers in

    • Genomic variations and chromosomal abnormalities 24
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 5
    • Genetics and Neurodevelopmental Disorders 4
    • Animal Genetics and Reproduction 3
    • Prenatal Screening and Diagnostics 6

Elke Back

35 papers receiving 783 citations

Peers

Elke Back
Comparison fields: 5 of 61
  • Genetics 576
  • Developmental Biology 25
  • Pediatrics, Perinatology and Child Health 138
  • Reproductive Medicine 58
  • Plant Science 247
Replace de Grouchy J with:
de Grouchy J France
Claude‐Lise Richer Canada
Maxine J. Sutcliffe United States
Annelyse Mertz Germany
E. Boyd United Kingdom
Ernest Lieber United States
Herman E. Wyandt United States
Alina T. Midro Poland
Ercole Rao Germany
M. Winkelmann Germany
Elke Back relative to de Grouchy J France de Grouchy J's profile →
Citations per field
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de Grouchy J · 1×
Citations per year

Countries citing papers authored by Elke Back

Since Specialization
Citations

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

Fields of papers citing papers by Elke Back

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 201529
2 20080
3 1999153
4 199864
5 19978
6 19974
7 19975
8 199618
9 199512
10 199412
11 199211
12 19916
13 198933
14 198917
15 198626
16
Two cases of partial trisomy 10q in the same family caused by parental direct insertion [ins. (15;10) (q15;q24q26)].
197910
17 197823
18
Deletion of the long arm of chromosome 4 [46,XX,del(4)(q31)] in a patient with congenital anomalies.
19779
19 19695
20 196714

About Elke Back

Elke Back is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Plant Science, Molecular Biology and Cancer Research, having authored 36 papers that have together received 829 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (24 papers), Chromosomal and Genetic Variations (11 papers), Prenatal Screening and Diagnostics (6 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Genomics and Chromatin Dynamics (4 papers), Genetics and Neurodevelopmental Disorders (4 papers), Animal Genetics and Reproduction (3 papers) and Sexual Differentiation and Disorders (2 papers). The work is most often cited by research in Genetics (576 citations), Developmental Biology (25 citations), Pediatrics, Perinatology and Child Health (138 citations), Reproductive Medicine (58 citations) and Plant Science (247 citations). Elke Back has collaborated with scholars based in Germany, Austria and Denmark. Frequent co-authors include K. D. Zang, G. Wolff, I. Voiculescu, Ralf Kist, Ken Dewar, Dietmar Pfeifer, Bruce W. Birren, Eric S. Lander, L Korniszewski and W. Schempp. Their work appears in journals such as Clinical Genetics, Human Genetics, Cytogenetic and Genome Research, The American Journal of Human Genetics and European Journal of Human 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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