Hans Moser

4.4k citations

86 papers · 2.6k indexed · 1 hit paper · h-index 21

Impact in

Agronomy and Crop Science top 2%
- Animal Disease Management and Epidemiology
Genetics top 5%
- Neurogenetic and Muscular Disorders Research
- Virus-based gene therapy research

Papers in

Genetics 8
- Neurogenetic and Muscular Disorders Research 7
- Genomic variations and chromosomal abnormalities 4
Anatomy 1

Co-authors: Sabina Liechti‐Gallati Louis M. Kunkel Corlee J. Bertelson Anthony P. Monaco Alan E H Emery Frits Pluimers J Smak A.R.W. Elbers
Journals: Human Genetics (6 papers)Physical review. B, Condensed matter (4 papers)Langenbeck s Archives of Surgery (4 papers)Journal of Molecular Medicine (3 papers)Preventive Veterinary Medicine (2 papers)
Partner nations: Switzerland Germany United States

In The Last Decade

Hans Moser

79 papers receiving 2.4k citations

Hit Papers

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An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus 1988 · 934 citations

Peers

Countries citing papers authored by Hans Moser

Since Specialization

Citations

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

Fields of papers citing papers by Hans Moser

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

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

All Works

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20 of 20 papers shown

#	Work
1	Private Krankenversicherung : Kommentar zu den 192-208,213 VVG, zu den MB/KK und MB/KT sowie zu weiteren Gesetzes- und Regelwerken in der privaten Krankenversicherung C.H.Beck eBooks ·Peter B. Bach, Hans Moser, Paredes Valencia, Karin Zamora Preuthun	2015	1
2	Private Krankenversicherung : MB/KK- und MB/KT-Kommentar : Kommentar zu den §§ 192 ff., 213 VVG, zu den MB/KK und MB/KT und zu weiteren Gesetzes- und Regelwerken der Rechtspraxis in der Privaten Krankenversicherung C.H.Beck eBooks ·Peter B. Bach, Hans Moser, VJ James, Karin Zamora Preuthun	2002	0
3	Tracing systems used during the epidemic of classical swine fever in the Netherlands, 1997-1998 Revue Scientifique et Technique de l OIE ·A.R.W. Elbers, Hans Moser, Niken Murti, Q Qomariah, Arjan Stegeman, J Smak, Frits Pluimers	2001	41
4	Abnormal myelination in a patient with deletion 14q11.2q13.1 Pediatric Neurology ·Gian Paolo Ramelli, Luca Remonda, Karl‐Olof Lövblad, Paredes Tello, Hans Moser	2000	12
5	The 1997–1998 epidemic of classical swine fever in the Netherlands Veterinary Microbiology ·Arjan Stegeman, A.R.W. Elbers, S. Gomatti, Hans Moser, J Smak, Frits Pluimers	2000	83
6	The classical swine fever epidemic 1997–1998 in the Netherlands: descriptive epidemiology Preventive Veterinary Medicine ·A.R.W. Elbers, Arjan Stegeman, Hans Moser, Niken Murti, J Smak, Frits Pluimers	1999	196
7	The 1997–1998 classical swine fever epidemic in The Netherlands — a survival analysis Preventive Veterinary Medicine ·Rod Meade, Katharina D.C. Stärk, ROGER S. MORRIS, Dirk U. Pfeiffer, Hans Moser	1999	19
8	A new mutation, 3905insT, accounts for 4.8% of 1173 CF chromosomes in Switzerland and causes a severe phenotype Human Genetics ·Martin Hergersberg, P.C. Ferreira da Silva, Thomas Bettecken, Yu Huan Zhang, S.W. Kim, ArifinSRM, Inge Einschenk, Sabina Liechti‐Gallati, Michael A. Morris, Daniel F. Schorderet, ABDULLAH AL-ABDULLAH, Hans Moser, Naseem Malik	1997	11
9	Uniparental Origin of Sex Chromosome Polysomies Human Heredity ·Isabel Lorda‐Sánchez, Franz Binkert, Kaye L. Bennett, Hans Moser, W Rosenkranz, Fina Alfiana Damayanti, Albert Schinzel	1992	19
10	An EcoRI polymorphism for the glutaminyl-tRNA synthetase (QARS) gene on chromosome 1q Human Molecular Genetics ·Achim Sander, Sabina Liechti‐Gallati, M. C. V. R. De Oliveira, Hans Moser, Markus Zingg, Joram Raveh	1992	1
11	RFLPs for Duchenne muscular dystrophy cDNA clones 9 and 10. Europe PMC (PubMed Central) ·Sabina Liechti‐Gallati, Volker Schneider, P E Mullis, Hans Moser	1990	2
12	Haplotype analysis for CF‐linked DNA polymorphisms in Switzerland Clinical Genetics ·Sabina Liechti‐Gallati, de Nooy-van Heel A, Volker Schneider, Marco Mächler, M. Alkan, Naseem Malik, Suzanne Braga, Hans Moser	1990	3
13	Ausländische Direktinvestitionen in Österreich : Auswirkungen auf Beschäftigung, Wachstum und Wettbewerbsfähigkeit der Industrie Campus eBooks ·Mohammed Mohammed Khaled Hussein Mohammedin, Hans Moser	1989	2
14	Molecular deletion patterns in Duchenne and Becker type muscular dystrophy Human Genetics ·Sabina Liechti‐Gallati, M. Kœnig, Louis M. Kunkel, Daniel Frey, Eugen Boltshauser, Volker Schneider, Suzanne Braga, Hans Moser	1989	67
15	Intracellular calcium changes in Balanus photoreceptor. A study with calcium ion-selective electrodes and Arsenazo III Cell Calcium ·Hugh M. Brown, B. Rydqvist, Hans Moser	1988	18
16	An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus Genomics ·Anthony P. Monaco, Corlee J. Bertelson, Sabina Liechti‐Gallati, Hans Moser, Louis M. Kunkel Hit paper breakdown →	1988	934
17	Familial deletion in Becker type muscular dystrophy within the pXJ region Human Genetics ·Sabina Liechti‐Gallati, Suzanne Braga, Paredes Tello, Hans Moser	1987	7
18	Private Krankenversicherung : MB/KK- und MB/KT-Kommentar Beck eBooks ·Peter B. Bach, Hans Moser, Paredes Valencia	1984	1
19	[Carrier detection and genetic counselling in duchenne muscular dystrophy (author's transl)]. PubMed ·Hans Moser	1977	6
20	[PROGRESSIVE MUSCULAR DYSTROPHY. VI. INCIDENCE, CLINICAL ASPECTS AND GENETICS OF THE DUCHENNE TYPE]. PubMed ·Hans Moser, Ulrich Wiesmann, R. Richterich, Eleonora Rossi	1964	31

About Hans Moser

Hans Moser is a scholar working on Genetics, Anatomy, Genetics, Molecular Biology and Surfaces, Coatings and Films, having authored 86 papers that have together received 2.6k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (10 papers), Neurogenetic and Muscular Disorders Research (7 papers), Advanced Chemical Physics Studies (7 papers), Herpesvirus Infections and Treatments (6 papers), Nonlinear Dynamics and Pattern Formation (4 papers), Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Cytomegalovirus and herpesvirus research (4 papers). The work is most often cited by research in Agronomy and Crop Science (309 citations), Genetics (300 citations), Cardiology and Cardiovascular Medicine (505 citations), Molecular Biology (1.4k citations) and Genetics (466 citations). Hans Moser has collaborated with scholars based in Switzerland, Germany and United States. Frequent co-authors include Sabina Liechti‐Gallati, Louis M. Kunkel, Corlee J. Bertelson, Anthony P. Monaco, Alan E H Emery, Frits Pluimers, J Smak, A.R.W. Elbers, Arjan Stegeman and Wolf‐Dieter Schneider. Their work appears in journals such as Human Genetics, Physical review. B, Condensed matter, Langenbeck s Archives of Surgery, Journal of Molecular Medicine and Preventive Veterinary Medicine.

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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