Iben Bache

1.8k citations
29 papers · 731 · h-index 15

Impact in

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

Papers in

    • Genomic variations and chromosomal abnormalities 12
    • Genetics and Neurodevelopmental Disorders 8
    • Genomics and Rare Diseases 4
    • Diabetes and associated disorders 3
    • Congenital heart defects research 5

Iben Bache

27 papers receiving 702 citations

Peers

Iben Bache
Comparison fields: 5 of 96
  • Genetics 341
  • Human-Computer Interaction 32
  • General Dentistry 8
  • Endocrinology, Diabetes and Metabolism 72
  • Developmental and Educational Psychology 47
Replace Jill Smith with:
Jill Smith Australia
James M. Farnham United States
Gabriel Levi United States
Noriko Miyake Japan
Robert Johnson Australia
Roberta La Piana Canada
David A. Muzykewicz United States
Cecilia Chang United States
Patrick Callier France
Kristina Allen‐Brady United States
Iben Bache relative to Jill Smith Australia Jill Smith's profile →
Citations per field
00.5×4.2×
Jill Smith · 1×
Citations per year

Countries citing papers authored by Iben Bache

Since Specialization
Citations

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

Fields of papers citing papers by Iben Bache

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 29 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2010122
2 2016117
3 201072
4 200763
5 201650
6 199933
7 201031
8 201725
9 201225
10 200722
11 200022
12 200619
13 201419
14 201616
15 201014
16 200814
17 201912
18 200511
19 20069
20 20078

About Iben Bache

Iben Bache is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Surgery and Pathology and Forensic Medicine, having authored 29 papers that have together received 731 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Genetics and Neurodevelopmental Disorders (8 papers), Prenatal Screening and Diagnostics (5 papers), Congenital heart defects research (5 papers), Genomics and Rare Diseases (4 papers), Diabetes and associated disorders (3 papers), Assisted Reproductive Technology and Twin Pregnancy (3 papers) and Diabetes Management and Research (2 papers). The work is most often cited by research in Genetics (341 citations), Human-Computer Interaction (32 citations), General Dentistry (8 citations), Endocrinology, Diabetes and Metabolism (72 citations) and Developmental and Educational Psychology (47 citations). Iben Bache has collaborated with scholars based in Denmark, Germany and Netherlands. Frequent co-authors include Niels Tommerup, Zeynep Tümer, Klaus Rostgaard, Nete Munk Nielsen, Morten Frisch, Robert J. Biggar, Kristian Tore Jørgensen, Asli Silahtaroglu, Anne Nørremølle and Karsten Buschard. Their work appears in journals such as European Journal of Human Genetics, Behavior Genetics, Obstetrical & Gynecological Survey, Orphanet Journal of Rare Diseases and Diabetic Medicine.

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.

Explore authors with similar magnitude of impact