André Heimbach

2.9k citations
14 papers · 1.2k · 1 hit paper · h-index 7

Impact in

Papers in

André Heimbach

12 papers receiving 1.2k citations

André Heimbach's Hit Papers

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase 2006 · 962 citations
9620+6+13Years since publication250500750

Peers

André Heimbach
Comparison fields: 5 of 73
  • Neurology 692
  • Neurology 272
  • Cellular and Molecular Neuroscience 307
  • Physiology 321
  • Physiology 49
Replace Janos Groh with:
Janos Groh Germany
Ammar F. Mubaidin Jordan
Faisal Fecto United States
Insup Choi United States
Luis Bonet‐Ponce United States
Konstantin Senkevich Russia
Aleksandar Raković Germany
Hiroyuki Morino Japan
James Velier United States
Julia S. Schlehe United States
André Heimbach relative to Janos Groh Germany Janos Groh's profile →
Citations per field
00.5×1.5×2.3×
Janos Groh · 1×
Citations per year

Countries citing papers authored by André Heimbach

Since Specialization
Citations

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

Fields of papers citing papers by André Heimbach

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

14 of 14 papers shown
#Work
1
Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase
Hit paper breakdown →
2006962
2 2011101
3 201870
4 201132
5 202216
6 201811
7 201911
8 20225
9 20165
10 20165
11 20172
12 20162
13 20161
14 20220

About André Heimbach

André Heimbach is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Neurology and Neurology, having authored 14 papers that have together received 1.2k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Cancer Genomics and Diagnostics (2 papers), Lysosomal Storage Disorders Research (2 papers), Cellular transport and secretion (2 papers), Ovarian cancer diagnosis and treatment (2 papers), Neuroinflammation and Neurodegeneration Mechanisms (2 papers), Peroxisome Proliferator-Activated Receptors (1 paper) and Traumatic Brain Injury and Neurovascular Disturbances (1 paper). The work is most often cited by research in Neurology (692 citations), Neurology (272 citations), Cellular and Molecular Neuroscience (307 citations), Physiology (321 citations) and Physiology (49 citations). André Heimbach has collaborated with scholars based in Germany, Switzerland and United Kingdom. Frequent co-authors include Barbara Stiller, Christian Kubisch, Birgit Liss, A. S. Najim Al-Din, C. Geoffrey Woods, Alfredo Ramı́rez, Meliha Karsak, Jan Gründemann, Ingrid Goebel and María Isabel Behrens. Their work appears in journals such as Journal of Clinical Oncology, Frontiers in Genetics, Seizure, Translational Psychiatry and Journal Of Clinical Periodontology.

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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