Malte Spielmann

15.7k citations
90 papers · 5.7k indexed · 4 hit papers · h-index 27
    • Genomics and Chromatin Dynamics 12
    • Single-cell and spatial transcriptomics 10
    • Congenital heart defects research 8
    • RNA Research and Splicing 7
  • Biophysics top 1%
  • Neurology top 2%
  • Genetics top 1%
    • Genomic variations and chromosomal abnormalities 21
    • Genomics and Rare Diseases 15
    • Connective tissue disorders research 7
    • Congenital limb and hand anomalies 8

Malte Spielmann

83 papers receiving 5.7k citations

Hit Papers

Single-cell sequencing of human midbrain reveals glial...306201820262020202350010001.5k2.0k

Peers

Malte Spielmann
Comparison fields: 5 of 149
  • Molecular Biology 3.9k
  • Biophysics 277
  • Cancer Research 678
  • Neurology 361
  • Genetics 1.2k
Replace Alistair R. R. Forrest with:
Alistair R. R. Forrest Australia
Simone Picelli Sweden
Susana M. Chuva de Sousa Lopes Netherlands
Arthur S. Alberts United States
Tim Stuart United States
Maria Kasper Sweden
Jeanne F. Loring United States
Omid R. Faridani Sweden
H. Amalia Pasolli United States
Malte Spielmann relative to Alistair R. R. Forrest Australia Alistair R. R. Forrest's profile →
Citations per field
00.5×7.7×
Alistair R. R. Forrest · 1×
Citations per year

Countries citing papers authored by Malte Spielmann

Since Specialization
Citations

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

Fields of papers citing papers by Malte Spielmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

20 of 20 papers shown
#Work
1 20250
2 20241
3 20240
4 20237
5 20231
6 202328
7 20231
8 20231
9 20230
10 20236
11 202285
12
Single-cell sequencing of human midbrain reveals glial activation and a Parkinson-specific neuronal statebreakdown →
2021306
13 20215
14 2021170
15 20216
16
A human cell atlas of fetal gene expressionbreakdown →
2020383
17 20192
18 201515
19 200912
20
[Factors of severity in placental choriocarcinoma].
19822

About Malte Spielmann

Malte Spielmann is a scholar working on Developmental Biology, Genetics and Molecular Biology, having authored 90 papers that have together received 5.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (21 papers), Genomics and Rare Diseases (15 papers), Genomics and Chromatin Dynamics (12 papers), Single-cell and spatial transcriptomics (10 papers), Congenital heart defects research (8 papers), Congenital limb and hand anomalies (8 papers), Connective tissue disorders research (7 papers) and RNA Research and Splicing (7 papers). The work is most often cited by research in Molecular Biology (3.9k citations), Biophysics (277 citations) and Cancer Research (678 citations). Malte Spielmann has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Stefan Mundlos, Darío G. Lupiáñez, Jay Shendure, Cole Trapnell, Junyue Cao, Fan Zhang, Frank J. Steemers, Daniel M. Ibrahim, Xingfan Huang and Xiaojie Qiu. Their work appears in journals such as Journal of Medical Genetics, European Journal of Human Genetics, The American Journal of Human Genetics, European Journal of Medical Genetics and Clinical 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026