Christiane Kehrer

1.2k total citations
21 papers, 594 citations indexed

About

Christiane Kehrer is a scholar working on Physiology, Psychiatry and Mental health and Molecular Biology. According to data from OpenAlex, Christiane Kehrer has authored 21 papers receiving a total of 594 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Physiology, 8 papers in Psychiatry and Mental health and 6 papers in Molecular Biology. Recurrent topics in Christiane Kehrer's work include Lysosomal Storage Disorders Research (19 papers), Cerebral Palsy and Movement Disorders (6 papers) and Neuroinflammation and Neurodegeneration Mechanisms (6 papers). Christiane Kehrer is often cited by papers focused on Lysosomal Storage Disorders Research (19 papers), Cerebral Palsy and Movement Disorders (6 papers) and Neuroinflammation and Neurodegeneration Mechanisms (6 papers). Christiane Kehrer collaborates with scholars based in Germany, United States and Netherlands. Christiane Kehrer's co-authors include Ingeborg Krägeloh‐Mann, Samuel Groeschel, Gunnar Blumenstock, Judith Böhringer, Annette Bley, Volkmar Gieselmann, Ingo Müller, Alfried Kohlschütter, Christine í Dali and Robert Steinfeld and has published in prestigious journals such as Blood, Neurology and Developmental Medicine & Child Neurology.

In The Last Decade

Christiane Kehrer

20 papers receiving 581 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Christiane Kehrer Germany 15 436 239 208 85 70 21 594
Christine í Dali Denmark 14 323 0.7× 199 0.8× 115 0.6× 43 0.5× 73 1.0× 28 532
Vĕra Malinová Czechia 15 400 0.9× 126 0.5× 135 0.6× 28 0.3× 37 0.5× 24 573
Céline Cluzeau United States 12 250 0.6× 274 1.1× 57 0.3× 41 0.5× 33 0.5× 15 529
Maria Prociuk United States 8 286 0.7× 112 0.5× 79 0.4× 26 0.3× 36 0.5× 10 396
Hernán Amartino Argentina 15 400 0.9× 102 0.4× 139 0.7× 20 0.2× 82 1.2× 47 596
Mahesh Kamate India 11 149 0.3× 142 0.6× 67 0.3× 33 0.4× 55 0.8× 59 426
Therese Ruane United States 7 294 0.7× 176 0.7× 96 0.5× 13 0.2× 23 0.3× 11 510
Yasmina Amraoui Germany 10 297 0.7× 109 0.5× 79 0.4× 22 0.3× 51 0.7× 15 382
Heather Cahan United States 7 265 0.6× 119 0.5× 64 0.3× 19 0.2× 44 0.6× 16 418
Rosario Domingo‐Jiménez Spain 14 179 0.4× 224 0.9× 50 0.2× 9 0.1× 64 0.9× 48 648

Countries citing papers authored by Christiane Kehrer

Since Specialization
Citations

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

Fields of papers citing papers by Christiane Kehrer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Christiane Kehrer

This figure shows the co-authorship network connecting the top 25 collaborators of Christiane Kehrer. A scholar is included among the top collaborators of Christiane Kehrer 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 Christiane Kehrer. Christiane Kehrer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Böhringer, Judith, Samuel Groeschel, Christiane Kehrer, et al.. (2022). Hematopoietic Stem Cell Transplantation with Mesenchymal Stromal Cells in Children with Metachromatic Leukodystrophy. Stem Cells and Development. 31(7-8). 163–175. 8 indexed citations
2.
Groeschel, Samuel, K. Harzer, Christiane Kehrer, et al.. (2022). Predicting clinical phenotypes of metachromatic leukodystrophy based on the arylsulfatase A activity and the ARSA genotype? – Chances and challenges. Molecular Genetics and Metabolism. 137(3). 273–282. 15 indexed citations
3.
Groeschel, Samuel, et al.. (2021). The impact of severe rare chronic neurological disease in childhood on the quality of life of families—a study on MLD and PCH2. Orphanet Journal of Rare Diseases. 16(1). 211–211. 30 indexed citations
4.
Krägeloh‐Mann, Ingeborg, Samuel Groeschel, Stefanie Beck‐Wödl, et al.. (2020). Natural history of Krabbe disease – a nationwide study in Germany using clinical and MRI data. Orphanet Journal of Rare Diseases. 15(1). 243–243. 19 indexed citations
5.
Beck‐Wödl, Stefanie, Christiane Kehrer, K. Harzer, et al.. (2020). Long‐term disease course of two patients with multiple sulfatase deficiency differs from metachromatic leukodystrophy in a broad cohort. JIMD Reports. 58(1). 80–88. 5 indexed citations
6.
Döring, Michaela, Christiane Kehrer, Judith Böhringer, et al.. (2020). Early clinical course after hematopoietic stem cell transplantation in children with juvenile metachromatic leukodystrophy. PubMed. 7(1). 12–12. 20 indexed citations
7.
Kehrer, Christiane, Judith Böhringer, Stefanie Beck‐Wödl, et al.. (2020). Association of Age at Onset and First Symptoms With Disease Progression in Patients With Metachromatic Leukodystrophy. Neurology. 96(2). e255–e266. 42 indexed citations
8.
Adang, Laura, Lars Schlotawa, Samuel Groeschel, et al.. (2020). Natural history of multiple sulfatase deficiency: Retrospective phenotyping and functional variant analysis to characterize an ultra‐rare disease. Journal of Inherited Metabolic Disease. 43(6). 1298–1309. 18 indexed citations
9.
Kehrer, Christiane, Judith Böhringer, Stefanie Beck‐Wödl, et al.. (2019). Phenotypic variation between siblings with Metachromatic Leukodystrophy. Orphanet Journal of Rare Diseases. 14(1). 136–136. 25 indexed citations
10.
11.
Krägeloh‐Mann, Ingeborg, et al.. (2017). Demyelination load as predictor for disease progression in juvenile metachromatic leukodystrophy. Annals of Clinical and Translational Neurology. 4(6). 403–410. 17 indexed citations
12.
Kehrer, Christiane, et al.. (2017). Rare Variant of GM2 Gangliosidosis through Activator-Protein Deficiency. Neuropediatrics. 48(2). 127–130. 5 indexed citations
13.
Groeschel, Samuel, Jörn‐Sven Kühl, Annette Bley, et al.. (2016). Long-term Outcome of Allogeneic Hematopoietic Stem Cell Transplantation in Patients With Juvenile Metachromatic Leukodystrophy Compared With Nontransplanted Control Patients. JAMA Neurology. 73(9). 1133–1133. 90 indexed citations
14.
Kehrer, Christiane, Samuel Groeschel, B. Kustermann‐Kuhn, et al.. (2014). Language and cognition in children with metachromatic leukodystrophy: onset and natural course in a nationwide cohort. Orphanet Journal of Rare Diseases. 9(1). 18–18. 48 indexed citations
15.
Krägeloh‐Mann, Ingeborg, Samuel Groeschel, Christiane Kehrer, et al.. (2012). Juvenile metachromatic leukodystrophy 10 years post transplant compared with a non-transplanted cohort. Bone Marrow Transplantation. 48(3). 369–375. 39 indexed citations
16.
Groeschel, Samuel, Christine í Dali, Judith Böhringer, et al.. (2012). Cerebral gray and white matter changes and clinical course in metachromatic leukodystrophy. Neurology. 79(16). 1662–1670. 33 indexed citations
17.
Kehrer, Christiane, et al.. (2011). The natural course of gross motor deterioration in metachromatic leukodystrophy. Developmental Medicine & Child Neurology. 53(9). 850–855. 62 indexed citations
18.
Groeschel, Samuel, Christiane Kehrer, Corinna Engel, et al.. (2011). Metachromatic leukodystrophy: natural course of cerebral MRI changes in relation to clinical course. Journal of Inherited Metabolic Disease. 34(5). 1095–1102. 57 indexed citations
19.
Kehrer, Christiane, et al.. (2010). Development and reliability of a classification system for gross motor function in children with metachromatic leucodystrophy. Developmental Medicine & Child Neurology. 53(2). 156–160. 58 indexed citations
20.
Böhringer, Judith, B. Kustermann‐Kuhn, Friederike Gieseke, et al.. (2010). Hematopoietic Stem Cell Therapy In Eight Patients with Metachromatic Leukodystrophy – Relevance of Post-Transplant Medication.. Blood. 116(21). 3727–3727. 1 indexed citations

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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