André Heimbach

2.8k total citations · 1 hit paper
14 papers, 1.1k citations indexed

About

André Heimbach is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, André Heimbach has authored 14 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Pathology and Forensic Medicine. Recurrent topics in André Heimbach's work include BRCA gene mutations in cancer (5 papers), Cellular transport and secretion (2 papers) and Ovarian cancer diagnosis and treatment (2 papers). André Heimbach is often cited by papers focused on BRCA gene mutations in cancer (5 papers), Cellular transport and secretion (2 papers) and Ovarian cancer diagnosis and treatment (2 papers). André Heimbach collaborates with scholars based in Germany, Switzerland and United Kingdom. André Heimbach's co-authors include Christian Kubisch, Barbara Stiller, Birgit Liss, Axel M. Hillmer, María Isabel Behrens, Ingrid Goebel, C. Geoffrey Woods, Jan Gründemann, Alfredo Ramı́rez and L. Pablo Cid and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Applied and Environmental Microbiology.

In The Last Decade

André Heimbach

12 papers receiving 1.1k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase

2006 881 citations Alfredo Ramı́rez, André Heimbach et al. Nature Genetics profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
André Heimbach Germany	7	667	380	320	292	276	14	1.1k
Janos Groh Germany	22	327 0.5×	311 0.8×	235 0.7×	476 1.6×	356 1.3×	38	1.1k
Konstantin Senkevich Russia	13	484 0.7×	198 0.5×	345 1.1×	146 0.5×	131 0.5×	51	761
Hiroyuki Morino Japan	20	494 0.7×	685 1.8×	163 0.5×	564 1.9×	216 0.8×	78	1.2k
Ammar F. Mubaidin Jordan	4	605 0.9×	395 1.0×	275 0.9×	293 1.0×	246 0.9×	7	1.1k
Gerald Goodall United Kingdom	15	801 1.2×	457 1.2×	317 1.0×	108 0.4×	321 1.2×	19	1.3k
Aline Perrin France	5	518 0.8×	268 0.7×	204 0.6×	341 1.2×	606 2.2×	5	1.0k
Faisal Fecto United States	13	984 1.5×	669 1.8×	238 0.7×	287 1.0×	314 1.1×	19	1.6k
Michael Klinkenberg Germany	17	634 1.0×	737 1.9×	313 1.0×	333 1.1×	134 0.5×	19	1.4k
Norman Kock Germany	18	785 1.2×	492 1.3×	118 0.4×	484 1.7×	98 0.4×	26	1.3k

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-authorship network of co-authors of André Heimbach

This figure shows the co-authorship network connecting the top 25 collaborators of André Heimbach. A scholar is included among the top collaborators of André Heimbach based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with André Heimbach. André Heimbach is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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14 of 14 papers shown

Heimbach, André, et al.. (2025). The role of Pantoea stewartii subsp. stewartii leucine-responsive regulatory protein (Lrp) during maize xylem growth. Applied and Environmental Microbiology. 91(7). e0085325–e0085325.

Zillich, Lea, Josef Frank, Jerome C. Foo, et al.. (2022). Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum. Translational Psychiatry. 12(1). 190–190. 16 indexed citations

Vennin, Constance, Charlotte Hewel, Hristo Todorov, et al.. (2022). A Resilience Related Glial-Neurovascular Network Is Transcriptionally Activated after Chronic Social Defeat in Male Mice. Cells. 11(21). 3405–3405. 5 indexed citations

Sharma, Amit, et al.. (2019). F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis. Frontiers in Genetics. 10. 508–508. 11 indexed citations

Fickl, Stefan, Fabian Hüttig, André Heimbach, et al.. (2018). The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis. Journal Of Clinical Periodontology. 45(12). 1498–1509. 69 indexed citations

Domingues, Francisco S., Christine Schwienbacher, Cláudia B. Volpato, et al.. (2018). Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly. Seizure. 66. 81–85. 11 indexed citations

Richters, Lisa, Philip C. Schouten, Stefan Kommoss, et al.. (2017). BRCA-like classification in ovarian cancer: Results from the AGO-TR1-trial.. Journal of Clinical Oncology. 35(15_suppl). 5546–5546. 2 indexed citations

Hauke, Jan, André Heimbach, Lisa Richters, et al.. (2016). Next-generation sequencing in BRCA1/2-negative breast and ovarian cancer families.. Journal of Clinical Oncology. 34(15_suppl). 1533–1533. 1 indexed citations

Hahnen, Eric, Klaus Baumann, André Heimbach, et al.. (2016). Prevalence of somatic mutations in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1 study).. Journal of Clinical Oncology. 34(15_suppl). 5544–5544. 5 indexed citations

10.

Kommoss, Stefan, Jan Hauke, Florian Heitz, et al.. (2016). Incidence of germline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1). Geburtshilfe und Frauenheilkunde. 76(10). 5 indexed citations

11.

Harter, Philipp, Jan Hauke, Florian Heitz, et al.. (2016). Incidence of germline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1).. Journal of Clinical Oncology. 34(15_suppl). 5538–5538. 2 indexed citations

12.

Brockschmidt, Antje, Byung Ha Chung, Stefanie Weber, et al.. (2011). CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT). Nephrology Dialysis Transplantation. 27(6). 2355–2364. 28 indexed citations

13.

Park, Jin‐Sung, Prachi Mehta, Antony A. Cooper, et al.. (2011). Pathogenic effects of novel mutations in the P‐type ATPase ATP13A2 ( PARK9 ) causing Kufor‐Rakeb syndrome, a form of early‐onset parkinsonism. Human Mutation. 32(8). 956–964. 97 indexed citations

14.

Ramı́rez, Alfredo, André Heimbach, Jan Gründemann, et al.. (2006). Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase. Nature Genetics. 38(10). 1184–1191. 881 indexed citations breakdown →

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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