Ingeborg Krägeloh‐Mann

11.8k total citations · 1 hit paper
178 papers, 6.1k citations indexed

About

Ingeborg Krägeloh‐Mann is a scholar working on Pediatrics, Perinatology and Child Health, Physiology and Psychiatry and Mental health. According to data from OpenAlex, Ingeborg Krägeloh‐Mann has authored 178 papers receiving a total of 6.1k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Pediatrics, Perinatology and Child Health, 39 papers in Physiology and 37 papers in Psychiatry and Mental health. Recurrent topics in Ingeborg Krägeloh‐Mann's work include Neonatal and fetal brain pathology (45 papers), Lysosomal Storage Disorders Research (38 papers) and Cerebral Palsy and Movement Disorders (31 papers). Ingeborg Krägeloh‐Mann is often cited by papers focused on Neonatal and fetal brain pathology (45 papers), Lysosomal Storage Disorders Research (38 papers) and Cerebral Palsy and Movement Disorders (31 papers). Ingeborg Krägeloh‐Mann collaborates with scholars based in Germany, United States and Netherlands. Ingeborg Krägeloh‐Mann's co-authors include Christine Cans, Martin Staudt, Wolfgang Grodd, Marina A. Pavlova, Marko Wilke, Alexander N. Sokolov, Niels Birbaumer, Javier de la Cruz, Christiane Kehrer and Volkmar Gieselmann and has published in prestigious journals such as The Lancet, Nature Genetics and Blood.

In The Last Decade

Ingeborg Krägeloh‐Mann

167 papers receiving 6.0k 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.

Decreasing prevalence in cerebral palsy: a multi‐site European population‐based study, 1980 to 2003

2015 330 citations Ingeborg Krägeloh‐Mann et al. Developmental Medicine & Child Neurology profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ingeborg Krägeloh‐Mann Germany	42	2.2k	2.0k	1.3k	1.1k	831	178	6.1k
Diane C. Chugani United States	56	1.7k 0.8×	2.8k 1.4×	1.4k 1.1×	3.1k 2.9×	830 1.0×	157	9.0k
Johan S.H. Vles Netherlands	41	1.4k 0.6×	1.9k 1.0×	878 0.7×	1.2k 1.1×	433 0.5×	192	5.4k
Csaba Juhász United States	49	1.4k 0.6×	2.6k 1.3×	572 0.4×	2.4k 2.2×	677 0.8×	221	7.7k
Nathalie Boddaert France	60	1.7k 0.8×	1.2k 0.6×	4.4k 3.5×	2.2k 2.0×	539 0.6×	389	12.7k
Peter R. Huttenlocher United States	43	1.9k 0.9×	1.3k 0.6×	1.8k 1.4×	3.4k 3.2×	1.2k 1.5×	94	9.6k
Coriene E. Catsman‐Berrevoets Netherlands	41	1.0k 0.5×	469 0.2×	857 0.7×	862 0.8×	564 0.7×	142	5.6k
Pamela J. Thompson United Kingdom	53	2.1k 0.9×	4.8k 2.4×	584 0.5×	2.8k 2.6×	413 0.5×	159	7.4k
Onno van Nieuwenhuizen Netherlands	33	1.2k 0.6×	1.5k 0.8×	687 0.5×	328 0.3×	707 0.9×	117	3.5k
Nicholas M. Barbaro United States	62	1.7k 0.8×	2.8k 1.4×	1.5k 1.2×	2.3k 2.1×	1.4k 1.7×	161	11.9k
Elisa Fazzi Italy	36	1.3k 0.6×	859 0.4×	1.2k 0.9×	463 0.4×	143 0.2×	159	4.2k

Countries citing papers authored by Ingeborg Krägeloh‐Mann

Since Specialization

Citations

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

Fields of papers citing papers by Ingeborg Krägeloh‐Mann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ingeborg Krägeloh‐Mann. 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 Ingeborg Krägeloh‐Mann. The network helps show where Ingeborg Krägeloh‐Mann may publish in the future.

Co-authorship network of co-authors of Ingeborg Krägeloh‐Mann

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

All Works

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20 of 20 papers shown

Gavazzi, Francesco, Sarah Woidill, Samuel Groeschel, et al.. (2025). Exploration Into Lived Experiences of Multiple Sulfatase Deficiency–Affected Individuals and Their Families. Journal of Child Neurology. 40(10). 852–861.

Al‐Fatly, Bassam, et al.. (2025). Lesion distribution and network mapping in dyskinetic cerebral palsy. Brain Communications. 7(3). fcaf228–fcaf228. 1 indexed citations

Mayer, Simone, et al.. (2025). Constructed growth charts and nutrition for pontocerebellar hypoplasia type 2A. Developmental Medicine & Child Neurology. 68(1). 82–90.

Franz, Axel R., Corinna Engel, Dirk Bassler, et al.. (2025). Effects of liberal versus restrictive transfusion strategies on intermittent hypoxaemia in extremely low birthweight infants: secondary analyses of the ETTNO randomised controlled trial. Archives of Disease in Childhood Fetal & Neonatal. 110(6). 564–570.

Gburek‐Augustat, Janina, Ina Sorge, Jan Marco Kern, et al.. (2023). Acute and Chronic Kernicterus: MR Imaging Evolution of Globus Pallidus Signal Change during Childhood. American Journal of Neuroradiology. 44(9). 1090–1095. 3 indexed citations

Kern, Jan Marco, Judith Böhringer, Dagmar Timmann, et al.. (2023). Clinical, Imaging, Genetic, and Disease Course Characteristics in Patients With GM2 Gangliosidosis. Neurology. 102(1). e207898–e207898. 2 indexed citations

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

Knaap, Marjo S. van der, Joshua L. Bonkowsky, Adeline Vanderver, et al.. (2022). Therapy Trial Design in Vanishing White Matter. Neurology Genetics. 8(2). e657–e657. 11 indexed citations

Antony, Justin S., Jun-Hoe Lee, Lukas Heumos, et al.. (2021). A Mutation-Agnostic Hematopoietic Stem Cell Gene Therapy for Metachromatic Leukodystrophy. The CRISPR Journal. 5(1). 66–79. 11 indexed citations

10.

Harting, Inga, Ingeborg Krägeloh‐Mann, Annette Bley, et al.. (2020). POLR3A variants with striatal involvement and extrapyramidal movement disorder. Neurogenetics. 21(2). 121–133. 26 indexed citations

11.

Wilke, Marko, Samuel Groeschel, Sabine Rona, et al.. (2018). Clinical application of advanced MR methods in children: points to consider. Annals of Clinical and Translational Neurology. 5(11). 1434–1455. 9 indexed citations

12.

Kehrer, Christiane, et al.. (2018). FV 300. Living with Severe Rare Chronic Neurological Disease in Childhood: Family Burden and Quality of Life in Families with MLD and PCH2. Neuropediatrics. 49.

13.

Lidzba, Karen, Bianca de Haan, Marko Wilke, Ingeborg Krägeloh‐Mann, & Martin Staudt. (2017). Lesion characteristics driving right-hemispheric language reorganization in congenital left-hemispheric brain damage. Brain and Language. 173. 1–9. 27 indexed citations

14.

Schicks, Julia, Jennifer Müller vom Hagen, Peter Bauer, et al.. (2013). Niemann-Pick type C is frequent in adult ataxia with cognitive decline and vertical gaze palsy. Neurology. 80(12). 1169–1170. 24 indexed citations

15.

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

16.

Pavlova, Marina A., et al.. (2010). Social Interaction Revealed by Motion: Dynamics of Neuromagnetic Gamma Activity. Cerebral Cortex. 20(10). 2361–2367. 27 indexed citations

17.

Kuchař, Ladislav, J. Ledvinová, Martin Hřebı́ček, et al.. (2009). Prosaposin deficiency and saposin B deficiency (activator‐deficient metachromatic leukodystrophy): Report on two patients detected by analysis of urinary sphingolipids and carrying novel PSAP gene mutations. American Journal of Medical Genetics Part A. 149A(4). 613–621. 60 indexed citations

18.

Pohlmann‐Eden, Bernd, Ulrich Stephani, Ingeborg Krägeloh‐Mann, et al.. (2007). Management des refraktären Status epilepticus. Der Nervenarzt. 78(8). 871–882. 1 indexed citations

19.

Mader, Irina, et al.. (2001). Congenital disorder of glycosylation type Ia: benign clinical course in a new genetic variant. Child s Nervous System. 18(1-2). 77–80. 17 indexed citations

20.

Grodd, Wolfgang, Ingeborg Krägeloh‐Mann, Uwe Klose, & R. Sauter. (1991). Metabolic and destructive brain disorders in children: findings with localized proton MR spectroscopy.. Radiology. 181(1). 173–181. 132 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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