Angela Schulz

3.1k citations

93 papers · 1.9k · h-index 22

Impact in

Physiology top 1%
- Lysosomal Storage Disorders Research
- Calcium signaling and nucleotide metabolism
Cell Biology top 2%
- Cellular transport and secretion

Papers in

Physiology 78
- Lysosomal Storage Disorders Research 78
- Calcium signaling and nucleotide metabolism 10
Rheumatology 23
- Glycogen Storage Diseases and Myoclonus 23

Co-authors: Alfried Kohlschütter (29 shared papers)Alessandro Simonati (6 shared papers)Peter Slasor (16 shared papers)Miriam Nickel (35 shared papers)David Jacoby (11 shared papers)Temitayo Ajayi (10 shared papers)Nicola Specchio (20 shared papers)Ruth Williams (3 shared papers)
Journals: Molecular Genetics and Metabolism (15 papers)Neuropediatrics (12 papers)European Journal of Paediatric Neurology (5 papers)Orphanet Journal of Rare Diseases (4 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (4 papers)
Partner nations: Germany United States United Kingdom

In The Last Decade

Angela Schulz

83 papers receiving 1.8k citations

Peers

Countries citing papers authored by Angela Schulz

Since Specialization

Citations

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

Fields of papers citing papers by Angela Schulz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Angela Schulz, 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 Angela Schulz Line = papers co-authored together Angela Schulz 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 93 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Study of Intraventricular Cerliponase Alfa for CLN2 Disease New England Journal of Medicine ·Angela Schulz, Temitayo Ajayi, Nicola Specchio, Emily de los Reyes, Paul Gissen, Douglas Ballon, Jonathan P. Dyke, Heather Cahan, Peter Slasor, David Jacoby, Alfried Kohlschütter	2018	318
2	NCL diseases — clinical perspectives Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Angela Schulz, Alfried Kohlschütter, Jonathan W. Mink, Alessandro Simonati, Ruth Williams	2013	180
3	Clinical challenges and future therapeutic approaches for neuronal ceroid lipofuscinosis The Lancet Neurology ·Sara Mole, Glenn Anderson, Heather Band, Samuel F. Berkovic, Jonathan D. Cooper, Sophia-Martha kleine Holthaus, Tristan R. McKay, Diego L. Medina, (unknown), Angela Schulz, Alexander J. Smith	2018	118
4	Disease characteristics and progression in patients with late-infantile neuronal ceroid lipofuscinosis type 2 (CLN2) disease: an observational cohort study The Lancet Child & Adolescent Health ·Miriam Nickel, Alessandro Simonati, David Jacoby, Susanne Lezius, Dirk Kilian, Benjamin Van de Graaf, Odelya E. Pagovich, Barry E. Kosofsky, Kaleb Yohay, Matthew Downs, Peter Slasor, Temitayo Ajayi, Ronald G. Crystal, Alfried Kohlschütter, Dolan Sondhi, Angela Schulz	2018	93
5	Current and Emerging Treatment Strategies for Neuronal Ceroid Lipofuscinoses CNS Drugs ·Alfried Kohlschütter, Angela Schulz, Udo Bartsch, Stephan Storch	2019	78
6	Diagnosis of neuronal ceroid lipofuscinosis type 2 (CLN2 disease): Expert recommendations for early detection and laboratory diagnosis Molecular Genetics and Metabolism ·Michael Fietz, Moeenaldeen AlSayed, Derek Burke, Jessica Cohen‐Pfeffer, Jonathan D. Cooper, Lenka Dvořáková, Roberto Giugliani, Emanuela Izzo, Helena Jahnová, Zoltán Lukács, Sara Mole, Inés Noher de Halac, David A. Pearce, Helena Poupětová, Angela Schulz, Nicola Specchio, Winnie Xin, Nicole L. Miller	2016	67
7	The CLN9 Protein, a Regulator of Dihydroceramide Synthase Journal of Biological Chemistry ·Angela Schulz, Talal Mousallem, Maya Venkataramani, Dixie‐Ann Persaud‐Sawin, Adam Zucker, Chiara Luberto, Alicja Bielawska, Jacek Bielawski, Joost C. M. Holthuis, S. Michal Jazwinski, Lina Kozhaya, Ghassan Dbaibo, Rose‐Mary Boustany	2005	63
8	Towards understanding the neuronal ceroid lipofuscinoses Brain and Development ·Alfried Kohlschütter, Angela Schulz	2009	61
9	Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene Journal of Medical Genetics ·Maria Kousi, Verneri Anttila, Angela Schulz, Stella Calafato, Eveliina Jakkula, Erik Riesch, Liisa Myllykangas, Hannu Kalimo, Meral Topçu, Sarenur Gökben, Füsun Alehan, Johannes R. Lemke, Michael Alber, Aarno Palotie, Outi Kopra, Anna‐Elina Lehesjoki	2012	56
10	Treatment of brain disease in the mucopolysaccharidoses Molecular Genetics and Metabolism ·Maurizio Scarpa, Paul J. Orchard, Angela Schulz, Patricia Dickson, Mark E. Haskins, Maria L. Escolar, Roberto Giugliani	2017	53
11	Impaired cell adhesion and apoptosis in a novel CLN9 Batten disease variant Annals of Neurology ·Angela Schulz, Sumeer Dhar, Svetlana N. Rylova, Ghassan Dbaibo, Joseph Alroy, Christian Hagel, Isabelo Artacho, Alfried Kohlschütter, Simon Lin, Rose‐Mary Boustany	2004	50
12	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	48
13	Lysoplex: An efficient toolkit to detect DNA sequence variations in the autophagy-lysosomal pathway Autophagy ·Giuseppina Di Fruscio, Angela Schulz, Rossella De Cegli, Marco Savarese, Margherita Mutarelli, Giancarlo Parenti, Sandro Banfi, Thomas Braulke, Vincenzo Nigro, Andrea Ballabio	2015	46
14	Lysosomal proteome analysis reveals that CLN3-defective cells have multiple enzyme deficiencies associated with changes in intracellular trafficking Journal of Biological Chemistry ·Carolin Schmidtke, Stephan Tiede, Melanie Thelen, Reijo Käkelä, Sabrina Jabs, G. Makrypidi, Marc Sylvester, Michaela Schweizer, Ingke Braren, Nahal Brocke‐Ahmadinejad, Susan L. Cotman, Angela Schulz, Volkmar Gieselmann, Thomas Braulke	2019	43
15	Retention of lysosomal protein CLN5 in the endoplasmic reticulum causes neuronal ceroid lipofuscinosis in Asian Sibship Human Mutation ·Anne-Hélène Lebrun, Stephan Storch, Franz Rüschendorf, Mia-Lisa Schmiedt, Aija Kyttälä, Sara Mole, Claudia Kitzmüller, Kathrin Saar, Leena Mewasingh, Volker Boda, Alfried Kohlschütter, Kurt Ullrich, Thomas Braulke, Angela Schulz	2009	43
16	Mutation update: Review of TPP1 gene variants associated with neuronal ceroid lipofuscinosis CLN2 disease Human Mutation ·Emily Gardner, Mitch Bailey, Angela Schulz, Mikel Aristorena, Nicole L. Miller, Sara Mole	2019	40
17	CLN2 Disease (Classic Late Infantile Neuronal Ceroid Lipofuscinosis). PubMed ·Alfried Kohlschütter, Angela Schulz	2016	33
18	An Adapted Clinical Measurement Tool for the Key Symptoms of CLN2 Disease LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) ·Kathleen W. Wyrwich, Angela Schulz, Miriam Nickel, Peter Slasor, Temitayo Ajayi, David Jacoby, Alfried Kohlschütter	2018	29
19	Phenotype and natural history of variant late infantile ceroid‐lipofuscinosis 5 Developmental Medicine & Child Neurology ·Alessandro Simonati, Ruth Williams, Nardo Nardocci, Minna Laine, Roberta Battini, Angela Schulz, Barbara Garavaglia, Francesca Moro, Francesco Pezzini, Filippo M. Santorelli	2017	27
20	Brain iron quantification by MRI in mitochondrial membrane protein‐associated neurodegeneration under iron‐chelating therapy Annals of Clinical and Translational Neurology ·Ulrike Löbel, Ferdinand Schweser, Miriam Nickel, Andreas Deistung, Regine Grosse, Christian Hagel, Jens Fiehler, Angela Schulz, Monika Hartig, Jürgen R. Reichenbach, Alfried Kohlschütter, Jan Sedlacik	2014	23

About Angela Schulz

Angela Schulz is a scholar working on Physiology, Rheumatology, Molecular Biology, Cell Biology and Physiology, having authored 93 papers that have together received 1.9k indexed citations. Recurring topics across this work include Lysosomal Storage Disorders Research (78 papers), Glycogen Storage Diseases and Myoclonus (23 papers), Cellular transport and secretion (17 papers), Calcium signaling and nucleotide metabolism (10 papers), Glycosylation and Glycoproteins Research (7 papers), Biochemical and Molecular Research (7 papers), Galectins and Cancer Biology (4 papers) and Carbohydrate Chemistry and Synthesis (4 papers). The work is most often cited by research in Physiology (1.3k citations), Physiology (182 citations), Cell Biology (556 citations), Rheumatology (258 citations) and Clinical Biochemistry (73 citations). Angela Schulz has collaborated with scholars based in Germany, United States and United Kingdom. Frequent co-authors include Alfried Kohlschütter, Alessandro Simonati, Peter Slasor, Miriam Nickel, David Jacoby, Temitayo Ajayi, Nicola Specchio, Ruth Williams, Jonathan W. Mink and Paul Gissen. Their work appears in journals such as Molecular Genetics and Metabolism, Neuropediatrics, European Journal of Paediatric Neurology, Orphanet Journal of Rare Diseases and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

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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