H. Moser

2.6k total citations
27 papers, 1.7k citations indexed

About

H. Moser is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, H. Moser has authored 27 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 7 papers in Physiology. Recurrent topics in H. Moser's work include Peroxisome Proliferator-Activated Receptors (11 papers), Metabolism and Genetic Disorders (7 papers) and Adipose Tissue and Metabolism (5 papers). H. Moser is often cited by papers focused on Peroxisome Proliferator-Activated Receptors (11 papers), Metabolism and Genetic Disorders (7 papers) and Adipose Tissue and Metabolism (5 papers). H. Moser collaborates with scholars based in United States, Switzerland and France. H. Moser's co-authors include William Krivit, Daniel J. Loes, Elsa Shapiro, Lawrence A. Lockman, Yuka Kishimoto, James A. Hamilton, Arthur E. Stillman, Stephen H. Hite, Richard E. Latchaw and Angus Clarke and has published in prestigious journals such as The Lancet, Journal of Clinical Investigation and Brain.

In The Last Decade

H. Moser

27 papers receiving 1.7k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
H. Moser United States 17 1.4k 422 403 196 190 27 1.7k
Denise Cassandrini Italy 23 735 0.5× 228 0.5× 252 0.6× 176 0.9× 132 0.7× 62 1.3k
Alessandro Malandrini Italy 26 973 0.7× 242 0.6× 287 0.7× 217 1.1× 184 1.0× 95 2.2k
Andreina Bordoni Italy 29 2.0k 1.4× 943 2.2× 201 0.5× 216 1.1× 406 2.1× 73 2.6k
Norma B. Romero France 22 1.2k 0.8× 151 0.4× 174 0.4× 168 0.9× 324 1.7× 44 1.7k
Ikuya Nonaka Japan 17 977 0.7× 131 0.3× 195 0.5× 116 0.6× 124 0.7× 31 1.2k
Chiara Fiorillo Italy 22 836 0.6× 113 0.3× 180 0.4× 134 0.7× 184 1.0× 93 1.4k
A E Harding United Kingdom 31 1.7k 1.2× 666 1.6× 150 0.4× 141 0.7× 234 1.2× 61 3.1k
Konrad Oexle Germany 20 609 0.4× 115 0.3× 175 0.4× 312 1.6× 114 0.6× 63 1.3k
Simon Hammans United Kingdom 25 1.4k 1.0× 825 2.0× 96 0.2× 142 0.7× 103 0.5× 45 1.7k
Nobuyoshi Fukuhara Japan 17 693 0.5× 261 0.6× 120 0.3× 63 0.3× 48 0.3× 35 1.1k

Countries citing papers authored by H. Moser

Since Specialization
Citations

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

Fields of papers citing papers by H. Moser

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of H. Moser

This figure shows the co-authorship network connecting the top 25 collaborators of H. Moser. A scholar is included among the top collaborators of H. Moser 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 H. Moser. H. Moser 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.
Pillion, Joseph P., et al.. (2006). Auditory brainstem response findings and peripheral auditory sensitivity in adrenoleukodystrophy. Journal of the Neurological Sciences. 247(2). 130–137. 2 indexed citations
2.
Shapiro, Elsa, William Krivit, Lawrence A. Lockman, et al.. (2000). Long-term effect of bone-marrow transplantation for childhood-onset cerebral X-linked adrenoleukodystrophy. The Lancet. 356(9231). 713–718. 206 indexed citations
3.
Green, A., et al.. (2000). Proceedings of the 4th International Workshop of the Adrenoleukodystrophy International Research Group (ALD‐IRG), University of York, 3 September 1998. Journal of Inherited Metabolic Disease. 23(5). 449–452. 1 indexed citations
4.
Moser, H.. (1997). Adrenoleukodystrophy: phenotype, genetics, pathogenesis and therapy. Brain. 120(8). 1485–1508. 327 indexed citations
5.
Moser, H., et al.. (1995). Interactions of a very long chain fatty acid with model membranes and serum albumin. Implications for the pathogenesis of adrenoleukodystrophy.. Journal of Clinical Investigation. 96(3). 1455–1463. 158 indexed citations
6.
Maris, Thomas G., et al.. (1995). X‐linked adrenoleukodystrophy presenting as neurologically pure familial spastic paraparesis. Neurology. 45(6). 1101–1104. 18 indexed citations
7.
Wallgren‐Pettersson, Carina, Angus Clarke, Françoise Samson, et al.. (1995). The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies.. Journal of Medical Genetics. 32(9). 673–679. 97 indexed citations
8.
Loes, Daniel J., Arthur E. Stillman, Stephen H. Hite, et al.. (1994). Childhood cerebral form of adrenoleukodystrophy: short-term effect of bone marrow transplantation on brain MR observations.. American Journal of Neuroradiology. 15(9). 1767–71. 48 indexed citations
9.
Gärtner, Jutta, Cassandra Obie, H. Moser, & David Valle. (1992). A polymorphic synonymous mutation (K54K) in the human 70 kD peroxisomal membrane protein gene (PMP1). Human Molecular Genetics. 1(8). 654–654. 1 indexed citations
10.
Liechti‐Gallati, Sabina, Bernhard Müller, T. Grimm, et al.. (1991). X-linked centronuclear myopathy: Mapping the gene to Xq28. Neuromuscular Disorders. 1(4). 239–245. 27 indexed citations
11.
Wenk, Gary L., Sakkubai Naidu, Manuel F. Casanova, C. A. Kitt, & H. Moser. (1991). Altered neurochemical markers in Rett's syndrome. Neurology. 41(11). 1753–1753. 57 indexed citations
12.
Braga, Suzanne, et al.. (1990). Severe neonatal asphyxia due to X-linked centronuclear myopathy. European Journal of Pediatrics. 150(2). 132–135. 14 indexed citations
13.
Aubourg, Patrick, et al.. (1990). The red-green visual pigment gene region in adrenoleukodystrophy.. PubMed. 46(3). 459–69. 19 indexed citations
14.
Wısnıewskı, Thomas, et al.. (1989). ULTRASTRUCTURAL EVIDENCE FOR A GLIOPATHY IN CEREBRO-HEPATO-RENAL (ZELLWEGER) SYNDROME. Journal of Neuropathology & Experimental Neurology. 48(3). 366–366. 1 indexed citations
15.
Naidu, S., et al.. (1988). Galactosylceramide-β-Galactosidase Deficiency in Association with Cherry Red Spot. Neuropediatrics. 19(1). 46–48. 5 indexed citations
16.
Schneller, M., et al.. (1983). Congenital nephrotic syndrome: clinico-pathological heterogeneity and prenatal diagnosis.. PubMed. 19(5). 243–9. 18 indexed citations
17.
Moser, H., et al.. (1981). [Twin pregnancy with operative removaL of one fetus with chromosomal mosaicism 46,XX/45,XO and term delivery of a healthy baby].. PubMed. 185(6). 365–6. 4 indexed citations
18.
Iwamori, Masao, et al.. (1976). HUMAN DIABETIC NEUROPATHY. Journal of Neuropathology & Experimental Neurology. 35(3). 336–336. 5 indexed citations
19.
Vassella, F, Marco Mumenthaler, E. Rossi, H. Moser, & Ulrich Wiesmann. (1967). Die kongenitale muskeldystrophie. Journal of Neurology. 190(4). 349–374. 26 indexed citations
20.
Moser, H. & P Wurnig. (1954). [Results of experimental studies and clinical observations in fat embolism; pathophysiological and therapeutic contribution].. PubMed. 278(1). 72–86. 5 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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