Sandra Pohl

1.7k citations

42 papers · 1.1k indexed · h-index 19

Impact in

Physiology top 1%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
Cell Biology top 5%
- Cellular transport and secretion

Papers in ⓘ

Physiology 16
- Lysosomal Storage Disorders Research 30
- Calcium signaling and nucleotide metabolism 16
Cell Biology 20
- Cellular transport and secretion 20

Co-authors: Thomas Braulke (23 shared papers)Jürgen Bereiter‐Hahn (3 shared papers)Marina Jendrach (3 shared papers)Monika Vöth (2 shared papers)Stephan Storch (8 shared papers)Katrin Marschner (5 shared papers)Katrin Kollmann (6 shared papers)Sören Mai (1 shared paper)
Journals: Human Molecular Genetics (3 papers)Journal of Biological Chemistry (3 papers)Journal of Clinical Medicine (3 papers)Human Mutation (3 papers)Biochimica et Biophysica Acta (BBA) - Molecular Cell Research (2 papers)
Partner nations: Germany United Kingdom United States

In The Last Decade

Sandra Pohl

41 papers receiving 1.1k citations

Peers

Countries citing papers authored by Sandra Pohl

Since Specialization

Citations

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

Fields of papers citing papers by Sandra Pohl

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Short- and long-term alterations of mitochondrial morphology, dynamics and mtDNA after transient oxidative stress Mitochondrion ·Marina Jendrach, Sören Mai, Sandra Pohl, Monika Vöth, Jürgen Bereiter‐Hahn	2008	197
2	Morpho-dynamic changes of mitochondria during ageing of human endothelial cells Mechanisms of Ageing and Development ·Marina Jendrach, Sandra Pohl, Monika Vöth, Axel Kowald, Peter Hammerstein, Jürgen Bereiter‐Hahn	2005	127
3	A Key Enzyme in the Biogenesis of Lysosomes Is a Protease That Regulates Cholesterol Metabolism Science ·Katrin Marschner, Katrin Kollmann, Michaela Schweizer, Thomas Braulke, Sandra Pohl	2011	123
4	Mannose phosphorylation in health and disease European Journal of Cell Biology ·Katrin Kollmann, Sandra Pohl, Katrin Marschner, Marisa Encarnação, Imme Sakwa, Stephan Tiede, Ben J. Poorthuis, Torben Lübke, Sven Müller‐Loennies, Stephan Storch, Thomas Braulke	2009	88
5	Lysosomal dysfunction causes neurodegeneration in mucolipidosis II ‘knock-in’ mice Brain ·Katrin Kollmann, (unknown), Sandra Markmann, Willy Morelle, Michaela Schweizer, Irm Hermans‐Borgmeyer, A. K. Röchert, Sandra Pohl, Torben Lübke, J.-C. Michalski, Reijo Käkelä, Steven U. Walkley, Thomas Braulke	2012	67
6	A Dileucine Motif and a Cluster of Acidic Amino Acids in the Second Cytoplasmic Domain of the Batten Disease-related CLN3 Protein Are Required for Efficient Lysosomal Targeting Journal of Biological Chemistry ·Stephan Storch, Sandra Pohl, Thomas Braulke	2004	50
7	Analysis of Potential Biomarkers and Modifier Genes Affecting the Clinical Course of CLN3 Disease Molecular Medicine ·Anne-Hélène Lebrun, Parisa Moll-Khosrawi, Sandra Pohl, G. Makrypidi, Stephan Storch, Dirk Kilian, Thomas Streichert, Benjamin Otto, Sara Mole, Kurt Ullrich, Susan L. Cotman, Alfried Kohlschütter, Thomas Braulke, Angela Schulz	2011	47
8	On the relevance of mitochondrial fusions for the accumulation of mitochondrial deletion mutants: A modelling study Aging Cell ·Axel Kowald, Marina Jendrach, Sandra Pohl, Jürgen Bereiter‐Hahn, Peter Hammerstein	2005	35
9	C‐Terminal Prenylation of the CLN3 Membrane Glycoprotein Is Required for Efficient Endosomal Sorting to Lysosomes Traffic ·Stephan Storch, Sandra Pohl, Arne Quitsch, Katrin Falley, Thomas Braulke	2007	35
10	Glycosylation- and phosphorylation-dependent intracellular transport of lysosomal hydrolases Biological Chemistry ·Sandra Pohl, Katrin Marschner, Stephan Storch, Thomas Braulke	2009	30
11	Increased expression of lysosomal acid phosphatase in CLN3‐defective cells and mouse brain tissue Journal of Neurochemistry ·Sandra Pohl, Hannah M. Mitchison, Alfried Kohlschütter, Otto van Diggelen, Thomas Braulke, Stephan Storch	2007	28
12	Molecular analysis of the GlcNac‐1‐phosphotransferase Journal of Inherited Metabolic Disease ·Thomas Braulke, Sandra Pohl, Stephan Storch	2008	25
13	Site-1 and site-2 proteases: A team of two in regulated proteolysis Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Tatyana Danyukova, Kenneth Schöneck, Sandra Pohl	2021	21
14	Compensatory expression of human N-Acetylglucosaminyl-1-phosphotransferase subunits in mucolipidosis type III gamma Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Sandra Pohl, Stephan Tiede, Monica Castrichini, Michael Cantz, Volkmar Gieselmann, Thomas Braulke	2009	20
15	Site-1 protease and lysosomal homeostasis Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Renata Voltolini Velho, Raffaella De Pace, Sarah Klünder, Giorgia Di Lorenzo, Michaela Schweizer, Thomas Braulke, Sandra Pohl	2017	19
16	Loss of N‐acetylglucosamine‐1‐phosphotransferase gamma subunit due to intronic mutation in GNPTG causes mucolipidosis type III gamma: Implications for molecular and cellular diagnostics American Journal of Medical Genetics Part A ·Sandra Pohl, Marisa Encarnação, Monica Castrichini, Sven Müller‐Loennies, Nicole Muschol, Thomas Braulke	2009	19
17	Mucolipidosis II-Related Mutations Inhibit the Exit from the Endoplasmic Reticulum and Proteolytic Cleavage of GlcNAc-1-Phosphotransferase Precursor Protein (GNPTAB) Human Mutation ·Raffaella De Pace, Maria Francisca Coutinho, Friedrich Koch‐Nolte, Friedrich Haag, Maria João Prata, Sandra Alves, Thomas Braulke, Sandra Pohl	2013	19
18	Lysosomal Proteome and Secretome Analysis Identifies Missorted Enzymes and Their Nondegraded Substrates in Mucolipidosis III Mouse Cells Molecular & Cellular Proteomics ·Giorgia Di Lorenzo, Renata Voltolini Velho, Dominic Winter, Melanie Thelen, Shiva Ahmadi, Michaela Schweizer, Raffaella De Pace, Kerstin Cornils, Timur Yorgan, Saskia Grüb, Irm Hermans‐Borgmeyer, Thorsten Schinke, Sven Müller‐Loennies, Thomas Braulke, Sandra Pohl	2018	18
19	Analyses of disease-related GNPTAB mutations define a novel GlcNAc-1-phosphotransferase interaction domain and an alternative site-1 protease cleavage site Human Molecular Genetics ·Renata Voltolini Velho, Raffaella De Pace, Sarah Klünder, Fernanda Sperb‐Ludwig, Charles Marques Lourenço, Ida Vanessa Döederlein Schwartz, Thomas Braulke, Sandra Pohl	2015	18
20	Mucolipidosis type II and type III: a systematic review of 843 published cases Genetics in Medicine ·Emma J. Dogterom, Margreet A.E.M. Wagenmakers, Martina Wilke, Serwet Demirdas, Nicole Muschol, Sandra Pohl, Jan C. van der Meijden, Dimitris Rizopoulos, Ans T. van der Ploeg, Esmée Oussoren	2021	15

About Sandra Pohl

Sandra Pohl is a scholar working on Physiology, Cell Biology, Physiology, Aging and Genetics, having authored 42 papers that have together received 1.1k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (30 papers), Cellular transport and secretion (20 papers), Calcium signaling and nucleotide metabolism (16 papers), Glycosylation and Glycoproteins Research (5 papers), Carbohydrate Chemistry and Synthesis (4 papers), ATP Synthase and ATPases Research (3 papers), Mitochondrial Function and Pathology (3 papers) and Trypanosoma species research and implications (3 papers). The work is most often cited by research in Physiology (277 citations), Cell Biology (407 citations), Physiology (584 citations), Aging (32 citations) and Clinical Biochemistry (62 citations). Sandra Pohl has collaborated with scholars based in Germany, United Kingdom and United States. Frequent co-authors include Thomas Braulke, Jürgen Bereiter‐Hahn, Marina Jendrach, Monika Vöth, Stephan Storch, Katrin Marschner, Katrin Kollmann, Sören Mai, Michaela Schweizer and Peter Hammerstein. Their work appears in journals such as Human Molecular Genetics, Journal of Biological Chemistry, Journal of Clinical Medicine, Human Mutation and Biochimica et Biophysica Acta (BBA) - Molecular Cell Research.

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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