André Heimbach

2.8k citations

14 papers · 1.1k indexed · 1 hit paper · h-index 7

Impact in

Neurology top 2%
- Parkinson's Disease Mechanisms and Treatments
- Neurological diseases and metabolism
- Neurological disorders and treatments
Cellular and Molecular Neuroscience top 5%
- Nuclear Receptors and Signaling

Papers in ⓘ

Co-authors: Barbara Stiller (2 shared papers)Christian Kubisch (2 shared papers)Jan Gründemann (1 shared paper)Ingrid Goebel (1 shared paper)Meliha Karsak (1 shared paper)María Isabel Behrens (1 shared paper)Alfredo Ramı́rez (1 shared paper)Jochen Roeper (1 shared paper)
Journals: Journal of Clinical Oncology (4 papers)Human Mutation (1 paper)Nature Genetics (1 paper)Cells (1 paper)Frontiers in Genetics (1 paper)
Partner nations: Germany Switzerland United Kingdom

In The Last Decade

André Heimbach

12 papers receiving 1.1k citations

Hit Papers

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Hereditary parkinsonism with dementia is caused by mutations in ATP13A2, encoding a lysosomal type 5 P-type ATPase 2006 · 881 citations

Peers

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

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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 Nature Genetics ·Alfredo Ramı́rez, André Heimbach, Jan Gründemann, Barbara Stiller, D. J Hampshire, L. Pablo Cid, Ingrid Goebel, Ammar F. Mubaidin, Abdul-Latif Wriekat, Jochen Roeper, A. S. Najim Al-Din, Axel M. Hillmer, Meliha Karsak, Birgit Liss, C. Geoffrey Woods, María Isabel Behrens, Christian Kubisch Hit paper breakdown →	2006	881
2	Pathogenic effects of novel mutations in the P‐type ATPase ATP13A2 ( PARK9 ) causing Kufor‐Rakeb syndrome, a form of early‐onset parkinsonism Human Mutation ·Jin‐Sung Park, Prachi Mehta, Antony A. Cooper, David Veivers, André Heimbach, Barbara Stiller, Christian Kubisch, Victor S.C. Fung, Dimitri Krainc, Alan Mackay‐Sim, Carolyn M. Sue	2011	97
3	The severity of human peri‐implantitis lesions correlates with the level of submucosal microbial dysbiosis Journal Of Clinical Periodontology ·Annika Kröger, Claudia Hülsmann, Stefan Fickl, Thomas Spinell, Fabian Hüttig, Frederic Kaufmann, André Heimbach, Per Hoffmann, Norbert Enkling, Stefan Renvert, Frank Schwarz, Ryan T. Demmer, Panos N. Papapanou, Søren Jepsen, Moritz Kebschull	2018	69
4	CHD1L: a new candidate gene for congenital anomalies of the kidneys and urinary tract (CAKUT) Nephrology Dialysis Transplantation ·Antje Brockschmidt, Byung Ha Chung, Stefanie Weber, Dagmar‐Christiane Fischer, Maria Kolatsi‐Joannou, Lori Christ, André Heimbach, Diamant Shtiza, G. G. B. Klaus, G Simonetti, Moira Konrad, Paul J.D. Winyard, Dieter Haffner, Franz Schaefer, Ruthild G. Weber	2011	28
5	Multi-omics signatures of alcohol use disorder in the dorsal and ventral striatum Translational Psychiatry ·Lea Zillich, Eric Poisel, Josef Frank, Jerome C. Foo, Marion M. Friske, Fabian Streit, Lea Sirignano, Stefanie Heilmann‐Heimbach, André Heimbach, Per Hoffmann, Franziska Degenhardt, Anita C. Hansson, Georgy Bakalkin, Markus M. Nöthen, Marcella Rietschel, Rainer Spanagel, Stephanie H. Witt	2022	16
6	Compound heterozygous SZT2 mutations in two siblings with early-onset epilepsy, intellectual disability and macrocephaly Seizure ·Francisco S. Domingues, Eva König, Christine Schwienbacher, Cláudia B. Volpato, Anne Picard, Chiara Cantaloni, Deborah Mascalzoni, Peter Lackner, André Heimbach, Per Hoffmann, Franco Stanzial, Andrew A. Hicks, Lucio Parmeggiani, Francesco Benedicenti, Serena De Pellegrin, Gianluca Casara, Peter P. Pramstaller	2018	11
7	F8 Inversions at Xq28 Causing Hemophilia A Are Associated With Specific Methylation Changes: Implication for Molecular Epigenetic Diagnosis Frontiers in Genetics ·Muhammad Ahmer Jamil, Amit Sharma, Nicole Nuesgen, Behnaz Pezeshkpoor, André Heimbach, A. I. Pavlova, Johannes Oldenburg, Osman El‐Maarri	2019	11
8	A Resilience Related Glial-Neurovascular Network Is Transcriptionally Activated after Chronic Social Defeat in Male Mice Cells ·Constance Vennin, Charlotte Hewel, Hristo Todorov, Marlon Wendelmuth, Konstantin Radyushkin, André Heimbach, Illia Horenko, Sarah Ayash, Marianne B. Müller, Susann Schweiger, Susanne Gerber, Beat Lutz	2022	5
9	Prevalence of somatic mutations in risk genes including BRCA1/2 in consecutive ovarian cancer patients (AGO-TR-1 study). Journal of Clinical Oncology ·Eric Hahnen, Klaus Baumann, André Heimbach, Alexander Reuß, Christian Jackisch, Jan Hauke, Tjoung‐Won Park‐Simon, Lisa Richters, Lars Hanker, Sandra Kroeber, Jacobus Pfisterer, Heidrun Gevensleben, Andreas Schnelzer, Dimo Dietrich, Stephanie E. Schneider, Stefan Kommoss, Frederic Marmé, Katharina Prieske, Rita K. Schmutzler, Philipp Harter	2016	5
10	Incidence of germline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1) Geburtshilfe und Frauenheilkunde ·Stefan Kommoss, P. Harter, Jan Hauke, Florian Heitz, (unknown), F Marmé, André Heimbach, Katharina Prieske, Lisa Richters, Alexander Burges, Guido Neidhardt, N de Gregorio, Ahmed El‐Balat, Felix Hilpert, Werner Meier, Martin Heubner, Karin Kast, Elena Ioana Braicu, Eric Hahnen, Rita K. Schmutzler	2016	5
11	BRCA-like classification in ovarian cancer: Results from the AGO-TR1-trial. Journal of Clinical Oncology ·Lisa Richters, Philip C. Schouten, Stefan Kommoss, Jan Hauke, Alexander Burges, Dimo Dietrich, Ahmed El‐Balat, Felix Hilpert, Roel Kluin, Martin Heubner, Karin Kast, André Heimbach, Elena Ioana Braicu, Sandra Schmidt, Klaus Baumann, Christian Jackisch, Sabine C. Linn, Rita K. Schmutzler, Philipp Harter, Eric Hahnen	2017	2
12	Incidence of germline mutations in risk genes including BRCA1/2 in consecutive ovarian cancer (OC) patients (AGO TR-1). Journal of Clinical Oncology ·Philipp Harter, Jan Hauke, Florian Heitz, Alexander Reuß, Stefan Kommoss, Frederik Marmé, André Heimbach, Katharina Prieske, Lisa Richters, Alexander Burges, Guido Neidhardt, Nikolaus de Gregorio, Ahmed El‐Balat, Felix Hilpert, Werner Meier, Martin Heubner, Karin Kast, Elena Ioana Braicu, Eric Hahnen, Rita K. Schmutzler	2016	2
13	Next-generation sequencing in BRCA1/2-negative breast and ovarian cancer families. Journal of Clinical Oncology ·Jan Hauke, André Heimbach, Lisa Richters, Sandra Kroeber, Janine Altmüller, Hölger Thiele, Peter Nüernberg, Barbara Wappenschmidt, Guido Neidhardt, Kerstin Rhiem, Rita K. Schmutzler, Eric Hahnen	2016	1
14	The role of Pantoea stewartii subsp. stewartii leucine-responsive regulatory protein (Lrp) during maize xylem growth Applied and Environmental Microbiology ·Wilson M. Farthing, André Heimbach, Ann M. Stevens	2025	0

About André Heimbach

André Heimbach is a scholar working on Biological Psychiatry, Behavioral Neuroscience, Neurology, Reproductive Medicine and Genetics, having authored 14 papers that have together received 1.1k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (5 papers), Ovarian cancer diagnosis and treatment (2 papers), Cancer Genomics and Diagnostics (2 papers), Neuroinflammation and Neurodegeneration Mechanisms (2 papers), Lysosomal Storage Disorders Research (2 papers), Cellular transport and secretion (2 papers), Hemophilia Treatment and Research (1 paper) and Plant-Microbe Interactions and Immunity (1 paper). The work is most often cited by research in Neurology (667 citations), Neurology (276 citations), Cellular and Molecular Neuroscience (292 citations), Physiology (320 citations) and Periodontics (56 citations). André Heimbach has collaborated with scholars based in Germany, Switzerland and United Kingdom. Frequent co-authors include Barbara Stiller, Christian Kubisch, Jan Gründemann, Ingrid Goebel, Meliha Karsak, María Isabel Behrens, Alfredo Ramı́rez, Jochen Roeper, C. Geoffrey Woods and Ammar F. Mubaidin. Their work appears in journals such as Journal of Clinical Oncology, Human Mutation, Nature Genetics, Cells and Frontiers in Genetics.

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